Hybrid III 10-Year-Old Child Test Dummy, 11651-11676 [2012-4129]
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Federal Register / Vol. 77, No. 38 / Monday, February 27, 2012 / Rules and Regulations
[FR Doc. 2012–4134 Filed 2–21–12; 11:15 am]
BILLING CODE 4910–59–C
DEPARTMENT OF TRANSPORTATION
National Highway Traffic Safety
Administration
49 CFR Part 572
[Docket No. NHTSA–2011–0175]
RIN 2127–AJ49
Hybrid III 10-Year-Old Child Test
Dummy
National Highway Traffic
Safety Administration (NHTSA),
Department of Transportation (DOT).
ACTION: Final rule.
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AGENCY:
This final rule establishes
regulations setting forth specifications
and qualification requirements for a
Hybrid III 10-year-old size child test
SUMMARY:
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dummy (HIII–10C). In a companion
document published elsewhere in this
issue of the Federal Register, NHTSA is
adopting use of the dummy to test child
restraints recommended for children
weighing more than 65 pounds (lb) for
compliance with the Federal motor
vehicle safety standard for child
restraint systems. The HIII–10C dummy
enables NHTSA to assess the
performance of child restraint systems
in restraining children in the 8- to 12year-old age range.
DATES: Effective date: April 27, 2012.
The incorporation by reference of the
publications listed in the rule has been
approved by the Director of the Federal
Register as of April 27, 2012.
If you wish to petition for
reconsideration of this rule, your
petition must be received by April 12,
2012.
ADDRESSES: If you wish to petition for
reconsideration of this rule, you should
refer in your petition to the docket
number of this document and submit
your petition to: Administrator,
National Highway Traffic Safety
PO 00000
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Administration, 1200 New Jersey
Avenue SE., West Building,
Washington, DC 20590. For more
information, see Section V, Rulemaking
Analyses and Notices.
For
non-legal issues, you may call Peter
Martin, NHTSA Office of
Crashworthiness Standards (telephone
202–366–5668) (fax 202–493–2990). For
legal issues, you may call Deirdre Fujita,
NHTSA Office of Chief Counsel
(telephone 202–366–2992) (fax 202–
366–3820). The mailing address for
these officials is the National Highway
Traffic Safety Administration, 1200 New
Jersey Avenue SE., Washington, DC
20590.
FOR FURTHER INFORMATION CONTACT:
Petitions
for reconsideration of this rule: The
petition will be placed in the docket.
Anyone is able to search the electronic
form of all documents received into any
of our dockets by the name of the
individual submitting the comment (or
signing the comment, if submitted on
behalf of an association, business, labor
SUPPLEMENTARY INFORMATION:
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ER27FE12.002
Issued on: February 16, 2012.
David L. Strickland,
Administrator.
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union, etc.). You may review DOT’s
complete Privacy Act Statement in the
Federal Register published on April 11,
2000 (Volume 65, Number 70; Pages
19477–78).
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Table of Contents
I. Executive Summary
II. Background
a. 2005 NPRM
b. Developments Since 2005
c. Summary of Decision
III. Summary of Comments
IV. Response to Comments
a. Functionality of the HIII–10C as a Part
572 ATD
1. Chin-to-Chest Contact
2. Shock Emanating From Shoulder and
Neck
i. Shoulder Revision
ii. Lower Neck Revision
3. Stiffness of Vinyl Insert
4. Dummy Availability
b. Durability of the HIII–10C
1. Proximal Femur
2. Bib Assembly
3. Shoulder Rotation Stop Screws
4. Agency Part Replacement Records
i. Pelvis Helicoil Insert
ii. Neck and Ribcage Replacement
iii. Other Replacements
5. Durability Summary
c. Qualification Procedures and
Requirements
1. Response Corridors
i. Head
ii. Neck
iii. Thorax
iv. Torso Flexion
v. Knee Impact
2. Summary of Qualification Requirements
3. Impact Probes
4. Instrumentation
i. Rotary Potentiometers
ii. Sternum Displacement
d. Technical Data Package
1. Changes to the Engineering Drawings
and PADI
2. Organization of Materials
i. Searchable Text
ii. Order of Engineering Drawings
iii. Part Quantity Specification
iv. Part Numbering Scheme
3. Specifications for Soft Parts
4. Use of 3D Computer Renderings
e. Other
1. Labeling the Dummy as a ‘‘Ten Year
Old’’
2. Best Practices for Belt Routing
3. Abdominal Injury Correlates
4. Repeatability in Systems Testing
f. Dummy Development Efforts
1. Hybrid III Child Dummy Revisions—
Abdomen and Pelvis
2. Pediatric Research
3. Status of HIC
V. Rulemaking Analyses and Notices
I. Executive Summary
The agency has determined that the
HIII–10C dummy, configured as
described in this document, is a suitable
and useful test device for quantitative
assessment of child restraint systems
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(CRSs) and other safety devices for older
children. The dummy, with a weight of
35.2 kilograms (kg) (77.6 pounds (lb))
and sitting height of 71 centimeters (28
inches), is ideally suited to test the
upper load and height limits of safety
restraints for children.
The dummy is specified by this rule
by a technical data package (TDP)
consisting of a set of engineering
drawings, a parts list, and a set of
procedures for assembly, disassembly,
and inspection (PADI) of the dummy.
Additionally, this rule amends 49 CFR
part 572 to specify qualification
requirements for the dummy, to assure
that the HIII–10C responses are within
established performance corridors, and
further ensure the uniformity of dummy
assembly, structural integrity,
consistency of response and adequacy of
instrumentation. The TDP and
qualification requirements assure that
HIII–10C dummies are uniform in their
design, construction and kinematics.
The drawings and the PADI for the
HIII–10C are available for examination
in the docket for this final rule.
Technical reports and other materials
pertaining to this final rule have also
been placed in the docket for this final
rule.
The notice of proposed rulemaking
(NPRM) on which this final rule is
based was published July 13, 2005 (70
FR 40281).
The agency is concurrently publishing
in this issue of the Federal Register a
final rule to amend Federal Motor
Vehicle Safety Standard (FMVSS) No.
213, ‘‘Child restraint systems’’ (49 CFR
571.213), to adopt use of the HIII–10C
dummy in agency compliance tests of
CRSs. (RIN 2127–AL10, formerly RIN
2127–AJ44.)
The final rules bring to a close
NHTSA’s work on Public Law 107–318,
116 Stat. 2772 (‘‘Anton’s Law’’), which
contained provisions for NHTSA to
develop and evaluate a test dummy that
represents a 10-year-old child for use in
testing CRSs. Public Law 107–318
required us to initiate rulemaking on the
Anthropomorphic Test Device (ATD), a
mandate we satisfied in 2005 when we
published an NPRM to adopt the HIII–
10C into FMVSS No. 213.1
When we published the 2005
proposal to include the dummy in
FMVSS No. 213, we proposed that
1 70 FR 51720 (August 31, 2005). Among other
matters, Public Law 107–318 directed NHTSA to
evaluate an anthropomorphic test device (ATD) that
simulates a 10-year-old child for use in testing CRSs
and to initiate a rulemaking proceeding for the
adoption of the ATD. NHTSA addressed other
provisions of Public Law 107–318 in earlier agency
actions. These actions are discussed in the
preamble of the August 31, 2005 NPRM.
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booster seats must conform to several
new requirements based on HIII–10C
measurements, including a head injury
criterion (HIC). As part of our
assessment, we demonstrated in our
pre-proposal testing that, while most
CRSs conformed to the new
requirements, there were some failures,
including those where HIC was
exceeded. However, during extensive
post-NPRM booster seat testing,
inconsistencies in the test protocol
revealed variability in the kinematics
and measurements of the HIII–10C. In
particular, the agency discovered that a
slight perturbation in the test protocol
could create a large change in HIC. The
variability in HIC measurements is
attributable to a design feature unique to
the HIII–10C in which chin-to-chest
contact during the impact event can be
excessively hard, but not easily
controlled through CRS design.
Subsequently, the agency devoted
substantial rulemaking and research
efforts to try to address test variability.
The August 31, 2005 (FMVSS No. 213)
NPRM was followed by a supplemental
NPRM (SNPRM) published in 2008 2
and an SNPRM published in 2010.3
Throughout the rulemaking proceeding,
NHTSA informed the public of its
research findings, concerns and ideas
about using the HIII–10C in FMVSS No.
213, and in turn learned from comments
from research organizations, consumer
groups, CRS, vehicle, and ATD
manufacturers, and others. Considerable
effort was devoted to revising the test
protocol to eliminate variability in HIC.
The endeavor has led to a new
dummy positioning procedure that
improves test repeatability with no
substantial change to the HIII–10C. The
agency has determined that the HIII–
10C is an important ATD that will
enhance our ability to assess the
performance of CRSs and other
occupant protection systems in
protecting children.4 In the
accompanying FMVSS No. 213 final
rule published today, we adopt the HIII–
10C into FMVSS No. 213, but due to the
recurrence of hard chin-to-chest
2 73 FR 3901 (January 23, 2008). This SNPRM
proposed a seating procedure for the HIII–10C to
minimize the chin-to-chest impacts. Commenters
were generally unsupportive of the procedure.
3 75 FR 71648 (November 24, 2010). This second
SNPRM proposed an alternative seating procedure
for the ATD.
4 The HIII–10C represents children of a size
heretofore not represented by the ATDs used in
NHTSA regulations. The child ATDs in 49 CFR part
572 that NHTSA uses for testing CRSs are ATDs
representing a newborn infant, a 12-month-old, a
3-year-old, a 6-year-old, and a weighted 6-year-old.
In 49 CFR part 572, there is also specified a 5th
percentile adult female ATD, which is
approximately the size of a 12-year-old.
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contacts, we will not adopt HIC as an
FMVSS No. 213 injury criterion.
The agency has thus decided that the
HIII–10C is a suitable device for use in
FMVSS No. 213. The HIII–10C test
dummy will provide an enhanced
assessment of child restraint
performance, and is worthy of adoption
into 49 CFR part 572 as implemented by
this final rule.
II. Background
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a. 2005 NPRM
In July 2005, NHTSA issued an NPRM
proposing specifications and
certification requirements for a new test
dummy representative of a 10-year-old
child (70 FR 40281, July 13, 2005). The
dummy was proposed to be included
among the descriptions of
anthropomorphic test devices in 49 CFR
part 572, so that it could be called out
for use in FMVSS test procedures and
other regulations. Concurrently, NHTSA
proposed to use the new dummy to
assess CRSs recommended for older
children under FMVSS No. 213 (70 FR
51720, August 31, 2005). These two
NPRMs are referred to herein as the Part
572 NPRM and the FMVSS No. 213
NPRM, respectively.
b. Developments Since 2005
Additional rulemaking notices. Since
the two NPRMs were published in 2005,
the agency issued two supplemental
NPRMs that dealt with the unrealistic
‘‘chin-to-chest’’ condition that occurred
when the HIII–10C was used in the
FMVSS No. 213 sled test environment.
This condition was first observed in
agency tests that led up to the 2005
NPRMs. In several of the tests, as the
HIII–10C’s head flung forward, the neck
flexed to the point where the dummy’s
chin came into hard contact with its
upper thorax. This chin-to-chest contact
at times produced elevated head
accelerations. However, in the testing
that led up to the 2005 NPRMs, we did
not foresee a problem with the chin-tochest contact because the majority of
booster seats tested met the FMVSS No.
213 head injury criterion (HIC) limit of
1000.5
Commenters to both NPRMs of 2005
also observed hard chin-to-chest contact
in their own tests. Some commenters
(Dorel Juvenile Group (Dorel), Graco
Children’s Products (Graco)) expressed
concerns the chin-to-chest contact was
an indication of poor spine biofidelity
and urged NHTSA to undertake
additional testing of the HIII–10C to
ensure that the test dummy is
appropriate for use in FMVSS No. 213
testing.
5 70
FR at 51724.
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Following these comments, NHTSA
conducted further testing of the HIII–
10C to investigate the chin-to-chest
contact. We concurred with the
commenters that the hard chin-to-chest
contact exhibited by the HIII–10C in
sled tests was an undesirable
occurrence. The hard contact was
unrealistic, as real-world accident data
indicated that children do not sustain
head injuries in that manner. The chinto-chest contact is much less prevalent
in the kinematics of actual children
because the child’s spine is more
flexible than that of the ATD. The added
flexibility of a child’s spine allows
greater forward translation and rotation
of the head. When chin-to-chest contact
occurs in children, it does not produce
as hard of a contact as the dummy and
does not result in severe injuries.
Moreover, we found that HIC values
produced by the HIII–10C were highly
variable when chin-to-chest contact
occurs, as the dummy was not designed
to achieve repeatable or reproducible
responses under this condition.
In consideration of the likelihood of
unreasonably high HIC values, the
agency issued the 2008 SNPRM that
mitigated chin-to-chest contact by
specifying a posture that was about 10
degrees more upright than the HIII–10C
positioned in a CRS under the original
NPRM (73 FR 3901). However, this
proposal was widely criticized in
comments to the SNPRM. Some
commenters believed that the upright
positioning procedure was unrealistic
because it did not reflect the way
children actually sit in booster seats.
Some also indicated that a belt routing
system or harness designed for an
upright ATD may introduce unwanted
belt slack when applied to a fully
reclined child. They believed this could
add to head excursion and preclude a
CRS from performing its primary
function of properly positioning a
vehicle’s seat belt to a child occupant.
Additionally, some commenters found
the procedure to be cumbersome and
difficult to follow.
Following a test program conducted
in response to these comments, on
November 24, 2010 the agency issued a
second SNPRM for positioning the HIII–
10C (75 FR 71648). The 2010 SNPRM
replaced the proposal for the upright
positioning procedure with a procedure
developed by the University of
Michigan Transportation Research
Institute (UMTRI). The UMTRI
procedure emphasizes fitting the
dummy to the CRS rather than
achieving a specific dummy posture. In
trial tests run by the agency using the
UMTRI procedure, we found the
repeatability of all test measurements to
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be greatly improved relative to those
observed under the seating procedures
we had proposed previously. Because
the UMTRI procedure typically results
in an ATD posture similar to that
associated with the seating procedure
used in the original NPRM of 2005,
chin-to-chest contact continued to
occur. Thus, we proposed using the
UMTRI procedure when positioning the
HIII–10C in FMVSS No. 213 tests, but
proposed that HIC would not be used as
a performance criterion in FMVSS No.
213 when using the HIII–10C.
Supplemental testing. Since the
NPRMs of 2005, the agency has used the
HIII–10C in about two hundred sled
tests to support the FMVSS No. 213
SNPRMs, to address the comments to
the Part 572 NPRM, and to arrive at the
final configuration of the dummy. We
have acquired four additional HIII–10C
units to add to our repeatability and
reproducibility assessment. In this
period since 2005, we have made a
comprehensive assessment of the ATD
to examine the many issues brought up
in comments received on the four
rulemaking proposals.
The test results permitted us to
examine and evaluate the consistency of
the data and adequacy of the dummy in
a broad range of CRSs available in the
market. Of the approximately 80 models
of booster seats manufactured since
2006,6 twenty seats from eight different
manufacturers have been tested with the
HIII–10C since the Part 572 NPRM.
Another fourteen seat models
manufactured prior to 2006 have also
been tested. This spectrum represents a
good cross-section of the booster seat
market and demonstrates well the utility
of the HIII–10C under all installations.
Utility of the HIII–10C. Our
supplementary testing has reaffirmed
that the HIII–10C is a meaningful ATD
for use in FMVSS No. 213 and merits
incorporation into 49 CFR part 572 even
without NHTSA’s use of HIC as an
FMVSS No. 213 pass/fail criterion.
Additional qualification data obtained
since 2005 has confirmed the high level
of repeatability and reproducibility that
was demonstrated in the NPRM on a
limited data set.7 As reported in this
6 To assist consumers in deciding which CRS to
purchase, NHTSA provides ease of use ratings for
child seats. We attempt to select and rate all seats
on the market. Currently, we provide about 80
ratings of seats designed for children weighing 36.3
kg (80 lb) or more and manufactured since 2006.
There are 23 different manufacturers represented in
our selection of seats.
7 Except to the extent discussed in this document
regarding chin-to-chest contact, NHTSA confirms
the NPRM’s discussion of the findings that the HIII–
10C is a biofidelic ATD that produces repeatable
and reproducible results. A detailed discussion of
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preamble, the qualification corridors
indicate outstanding dummy
repeatability and reproducibility.
Throughout the entire test experience,
the HIII–10C has proven to be a durable
test instrument.
The additional data also confirms the
qualification of HIII–10C-based injury
metrics. Other than HIC, all other
dummy-based measurements used in
FMVSS No. 213—head excursion, knee
excursion, and chest acceleration—have
proven to be sound metrics appropriate
for CRS testing. A NHTSA-sponsored
study published in 2008 found the head
excursion of the HIII–10C to be very
similar to a human subject in matched
pair tests.8 Also, the agency has
observed a strong correlation between
knee excursion and submarining in
child dummies. As such, knee excursion
correlates indirectly with abdominal
injuries. The limit on knee excursion
prevents CRS manufacturers from
controlling head excursion by designing
their restraints so that children
submarine in a crash.
The limit on chest acceleration
ensures that a CRS provides a child with
sufficient ‘‘ride down’’ or absorption of
crash forces over a period of time in a
manner that avoids injury. The revisions
to the HIII–10C described in this
preamble assure that the chest
acceleration measurements are devoid
of any signal irregularities. The HIII–
10C will also be used in FMVSS No. 213
to assess the structural integrity of CRSs
for older children.
Recent agency studies have also
demonstrated that the HIII–10C has
sufficient biofidelity to be used in
possible belt fit programs. Our research
has found lap and shoulder belts to fit
the HIII–10C much like they do a
human.9 The dummy was found to sit
in a seat like a human child and don the
belt like a human child.
The agency has also recently
completed studies on the HIII–10C’s
utility and biofidelity in assessing
the HIII–10C’s biofidelity can be found in the
NPRM, see 70 FR at 40284. The repeatability and
reproducibility of the HII–10C is discussed in the
NPRM at 70 FR at 40285. Commenters did not
disagree with these aspects of the dummy, except
as discussed in this document regarding the chinto-chest contact.
8 Ash, JH, Sherwood, CP, Abdelilah, Y, Crandall,
JR, Parent, DP, Kallieris, D., ‘‘Comparison of
Anthropomorphic Test Dummies with a Pediatric
Cadaver Restrained by a Three-point Belt in Frontal
Sled Tests,’’ Proceedings of the 21st International
Technical Conference on the Enhanced Safety of
Vehicles, June 2009.
9 Reed, M., Ebert-Hamilton, S., Klinich, K.,
Manary, M., Rupp, J., ‘‘Assessing Child Belt Fit,
Volume I: Effects of Vehicle Seat and Belt Geometry
on Belt Fit,’’ UMTRI Report No. UMTRI–2008–49–
1, University of Michigan, Ann Arbor, MI,
September 2008.
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submarining and abdominal injury.10 In
summary, we have found the HIII–10C
to be sufficiently biofidelic to mimic the
kinematics of a belted human child. The
dummy was found to be sensitive to a
range of lap belt and torso belt
anchorage configurations and its
propensity to submarine was consistent
with that of a belted child. Given these
positive results, the agency is pursuing
the development of an HIII–10C
modification consisting of an abdominal
insert that measures abdominal
deformation, thus providing a direct
assessment of injury risk.
c. Summary of Decision
The data available since 2005 support
a decision that the HIII–10C is a suitable
device for use in FMVSS No. 213.
Adopting the HIII–10C in 49 CFR part
572 enables NHTSA to expand the
applicability of FMVSS No. 213 to CRSs
that are recommended for children over
the current 35.2 kg (65 lb) weight limit
in a meaningful way. There has been
considerable interest over the years in
expanding the applicability of FMVSS
No. 213 to increase the likelihood that
child restraints for older children (e.g.,
booster seats) will perform adequately
in a crash. This interest goes hand-inhand with efforts to prolong CRS use
among children who have outgrown
their child safety seat, but who cannot
adequately fit a vehicle’s lap and
shoulder belt system. Adopting the
HIII–10C into 49 CFR part 572 enhances
NHTSA’s ability to reduce unreasonable
risks of traffic crashes to older children.
which we discuss in this document as
appropriate. Additional organizations
commenting on the FMVSS No. 213
rulemaking include Graco, the Juvenile
Product Manufacturers Association
(JPMA), and Consumers Union.
Commenters were very supportive of
the idea of incorporating an ATD
representing children in the 8- to 12year-old age range. There was general
support for the HIII–10C’s incorporation
into Part 572, but as indicated above,
concerns were raised about the chin-tochest contact. Dorel expressed
opposition to the adoption of the HIII–
10C, citing concerns about the ATD’s
biofidelity, durability, and compatibility
with the FMVSS No. 213 test
environment. Some comments
suggested adjustments and clarifications
to the Part 572 proposed regulatory text,
to improve the procedures for qualifying
an ATD and the performance
assessments.
The following major categories of
issues were raised: (a) Functionality of
the HIII–10C as a Part 572 ATD; (b)
durability of the ATD; (c) qualification
procedures and requirements; (d) the
TDP (the engineering drawings and
PADI); (e) other issues (clarifying agency
statements in the preamble); and (f)
dummy development efforts. Each of
these areas is discussed below.
IV. Response to Comments
a. Functionality of the HIII–10C as a
Part 572 ATD
1. Chin-to-Chest Contact
As described earlier in this preamble,
III. Summary of Comments
the agency received many comments
We received comments on the Part
regarding the undesirable chin-to-chest
572 NPRM from: The American
contact exhibited by the HIII–10C,
Academy of Pediatrics (AAP),
which is related to the biofidelity of the
Children’s Hospital of Philadelphia
HIII–10C’s spine. Dorel, the Alliance
(CHOP), Advocates for Highway and
and others reported chin-to-chest
Auto Safety (Advocates), Dorel,
contact during normal use of the
Chrysler, the Alliance of Automobile
dummy, which was believed to be
Manufacturers 11 (Alliance), and a joint
brought on by an overly stiff thoracic
submission from ATD manufacturers
spine relative to human children.
First Technology Safety Systems (FTSS)
We agree that the hard chin-to-chest
and Denton ATD (Denton) (FTSS/
contact in FMVSS No. 213 sled tests is
Denton).12 Some of the comments on the an undesirable characteristic of the
FMVSS No. 213 SNPRMs raised issues
HIII–10C. Chin-to-chest contact has also
pertaining to the Part 572 rulemaking,
been observed in tests run by the
agency. In most cases, the time interval
10 Reed, M., Ebert-Hamilton, S., Klinich, K.,
producing the highest calculation of HIC
Manary, M., Rupp, J., ‘‘Assessing Child Belt Fit,
Volume II: Effect of Restraint Configuration, Booster enveloped the instant when chin-tochest contact occurred, including cases
Seat Designs, Seating Procedure, and Belt Fit on the
Dynamic Response of the Hybrid III 10-year-old
where head acceleration was very high.
ATD in Sled Tests,’’ UMTRI Report No. UMTRI–
In other words, chin-to-chest contact
2008–49–2, University of Michigan, Ann Arbor, MI,
often caused HIC to exceed the injury
September 2008.
11 At the date of the October 3, 2005 comment,
assessment reference value (HIC36 =
the Alliance consisted of: BMW Group,
1000).
DaimlerChrysler; Ford Motor Company; General
The design of the neck-to-thorax joint
Motors; Mazda; Mitsubishi Motors; Porsche; Toyota;
in the HIII–10C differs from other
and Volkswagen.
dummies in the Hybrid III family. In the
12 In 2010, FTSS and Denton announced that they
have merged into one company, Humanetics, Inc.
other dummies, the neck is off-set or
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cantilevered anterior to the thorax,
which is not optimal
anthropometrically. In the HIII–10C, the
upper part of the thorax spine structure
has been designed such that the neckto-thorax joint is an in-line connection
following more closely the
anthropometry of a human. The lower
neck bracket described earlier serves at
the neck-to-thorax joint.
The downside to the improved
anthropometry is that it creates a ‘‘hard
spot’’ during chin-to-chest contact. The
stiff lower neck bracket is where the
chin comes into contact with the chest
and where only a thin layer of soft flesh
material offers any buffer. Beyond a few
millimeters of flesh material
compression, chin-to-chest contact
forces—and head accelerations—
increase exponentially. As a result, a
small deviation in head motion causes
a very large change in head acceleration
and HIC. The change is difficult to
control and may be in conflict with
good CRS design. In some cases, HIC
scores have been shown to improve
when the torso belt fit is degraded.13
Since chin contact to the thorax is not
a natural brain injury path in actual
children, any such attempt to lessen HIC
through booster seat design may
compromise the overall safety
performance of the seat.
Due to the non-biofidelic chin-tochest contact, we have decided not to
require CRSs to meet the HIC criterion
when tested with the HIII–10C in the
compliance of FMVSS No. 213, as
announced in the FMVSS No. 213 final
rule published today. When we
followed the UMTRI seating procedure
adopted in the final rule for FMVSS No.
213, we found that the seating
procedure reduces HIC variability in
repeat tests of the same booster seat,
including those in which hard chin-tochest contact occurs. However, hard
chin-to-chest contact was still observed
in many agency tests. Mitigating this
effect altogether, as recommended in
comments by Dorel, would require a
major redesign of the entire thorax and
spine, which is not feasible. Instead, the
agency is concentrating efforts on
developing an entirely new pediatric
dummy for future use, as discussed later
in this preamble.
Nonetheless, we did make minor
changes to the HIII–10C to mitigate
some of the effects of the chin-to-chest
contact in accordance with a recent
agency study.14 This Part 572 final rule
13 2008
UMTRI Vol. 2 Report
14 Stammen, J., Bolte, J., Shaw, J., ‘‘Biomechanical
Impact Response of the Human Chin and
Manubrium,’’ Annals of Biomedical Engineering
(2011, in press).
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specifies the thickness of the HIII–10C’s
chin flesh in the inferior-superior
direction. The new specification is
aimed at lessening the variability of
head accelerations among different
dummies when chin-to-chest contact
does occur.
The chin flesh specification improves
the functionality of the HIII–10C as an
ATD, even though we have decided not
to use HIC as an FMVSS No. 213 pass/
fail criterion when using the dummy.
HIC may continue to be measured in
FMVSS No. 213 tests with the HIII–10C
for research purposes, and could be
used as a performance metric in other
NHTSA programs (e.g., out-of-position
(OOP) air bag tests, New Car Assessment
Programs). Standardizing the thickness
of the chin will improve the
repeatability of the HIC measurements
from different dummies when chin-tochest contact occurs. Hard chin-to-chest
contact may be a concern to researchers
investigating the whipping actions of
the head. The chin specification will
better enable them to compare HIC
measurements in tests with different
dummies.15
2. Shock Emanating From Shoulder and
Neck
Chrysler16 and Graco were concerned
that spikes or ‘‘noise’’ is present in the
signal traces of accelerometers and load
cells in the head and upper torso of the
HIII–10C. In evaluating these comments,
we determined that the presence of
these spikes has no consequence on the
use of the HIII–10C as a regulatory tool
as specified in the final rule for FMVSS
No. 213. The only instruments within
the HIII–10C that will be used in
FMVSS No. 213 are accelerometers
arranged triaxially at the center of
gravity (CG) of the chest. In all agency
tests in which these spikes appeared in
the accelerometer signals, they were
removed by the signal processing
algorithms used to compute the chest
acceleration criterion.17
The routines used to compute chest
G’s include a standard SAE
International (SAE) Channel Frequency
Class (CFC) 180 filter and a 3
millisecond (ms) clip.18 The 3 ms clip
originated in 1970 for use in FMVSS No.
208, ‘‘Occupant crash protection,’’ in
recognition that such spikes are
15 Because we are measuring HIC for research
purposes, this final rule adopts the proposed
qualification test for the HIII–10C head
measurements.
16 Docket No. NHTSA–2005–21247–0016.
17 The chest acceleration criterion specified in
FMVSS No. 213 is 60 G’s.
18 The 3 ms clip truncates the peak acceleration
portion of a continuous signal having a duration
less than 3 milliseconds.
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insignificant as injury contributors (35
FR 14941). The spikes in the data of the
HIII–10C were caused by two sources
other than by chin-to-chest contact:
part-to-part contact between
components of the shoulder assembly,
and a loose fitting neck cable that
interfered with the lower neck load cell.
Spikes emanating from the shoulder and
neck of the HIII–10C were not always
completely removed by CFC180 filtering
of the chest acceleration signals, but
once they were ‘‘clipped’’ by the 3 ms
algorithm, they had no measureable
effect on the computation of chest G’s.
Moreover, in most cases the time
interval containing the peak
acceleration identified by the algorithm
did not contain the spike, which usually
occurred later in the event. Thus, the
injury reference measures for the HIII–
10C’s immediate use in FMVSS No. 213
(chest acceleration, head and knee
excursion) are not affected by this
condition.
The shock emanating from the
shoulder and neck is benign in terms of
its effect on the dummy itself (the
acceleration spikes are no greater than
150 G’s). It does not affect the
kinematics of the dummy in any way
(i.e., the head trajectory and knee
excursion are unaffected). The
magnitude of the spikes is well within
the typical operating range of +/¥ 2000
G’s for the specified accelerometers, so
shock damage to the instruments is
unlikely.
Nonetheless, although the shocks do
not influence the outcomes of FMVSS
No. 213 tests, we made the following
simple modifications to the HIII–10C’s
shoulder and neck to lessen the shock
effect. Improving the ATD in this
manner assures that the dummy is better
suited for possible future uses in tests
where computations for head injury
assessments based on head
accelerometer signals are more sensitive
to the condition (e.g., OOP air bag
tests).19
i. Shoulder Revision
The TDP of this final rule modifies
the shoulder design of the HIII–10C.
Similar to a human, the shoulder of
the HIII–10C provides the load bearing
surface for the shoulder belt. On the
dummy, the part that provides this
surface is a one-piece aluminum casting
that is connected to the spine via a yoke
that extends laterally from the spine.
The yoke-to-shoulder connection is a
19 The computation of HIC applies a higher signal
filter class (CFC 1000 vs. CFC 180) and does not
impose a 3 ms clip. The revisions do not affect the
assessment of CRSs with regard to FMVSS No. 213,
so this change will not delay the incorporation of
the HIII–10C into Part 572.
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pivot which provides medial-lateral
movement (i.e., pivoting about the zaxis) in a direction that is dependent
upon the position of the shoulder belt.
If the belt lies close to the neck, the
shoulder will pivot inward; if it is on
the edge of the shoulder it will pivot
outward. The piece of the shoulder
casting that contains the pivot hole has
a finger-like protrusion. As the shoulder
pivots, the finger acts as a cam by
compressing a rubber pad that is glued
within the yoke. This provides
resistance to the z-axis pivoting.
Compared to Hybrid III adult
dummies, the shoulder design of the
HIII–10C is anthropometrically
improved. For the adult dummies, the
shoulder is an assembly of two halves
that are joined medially-laterally. The
mid-joint provides the z-axis pivoting
for each half. By eliminating the midjoint, the HIII–10C is able to provide a
more biofidelic interaction with the
shoulder belt during a dynamic event.
Because it is made from one part instead
of two, the HIII–10C shoulder was able
to be designed with a sloped, uniform
shoulder belt bearing surface.
The improved design of the HIII–10C
is made possible by the new
configuration of the upper thorax in
which the offset of the neck has been
eliminated. The HIII–10C shoulder
design allows more realistic movement
of the belt along the shoulder during a
dynamic event. Furthermore, since the
surface that bears the load of the
shoulder belt is a one-piece casting, the
designers of the dummy were able to
build in a shoulder load cell. Although
it is not currently used for regulatory
purposes, the load cell is very useful in
research and development activities to
study belt load distributions across the
torso.
Notwithstanding its simpler design,
the new shoulder has had problems over
the years. In early versions of the design
(pre-NPRM), the shoulder had a
tendency to over-pivot to the point
where the finger protrusion was
bottoming out the rubber pad. In the
2001–2002 timeframe, the shoulder
went through two design revisions in an
attempt to rectify the situation by
relocating the shoulder pivot hole and
trimming the yoke.
As indicated by the Graco and
Chrysler comments, the Part 572 NPRM
version of the shoulder could still be
improved. Before the finger bottoms out
the pad, metal-to-metal contact occurs
between the yoke and the shoulder in
one or more places. Shock from this
contact appears as short-duration spikes
of up to 150 G’s in the signals of
accelerometers closest to the shoulder.
Spikes of a lesser extent also appear in
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neck load cell signals. Chrysler ran sled
tests to identify the shoulder-yoke
contact points by means of transfer
paint, and reported these results to the
agency.20
To address the spikes, as reflected in
the TDP for this final rule, we have
revised the shoulder and yoke assembly
to lessen the effect of the two parts
bottoming out against each other. More
clearance has been created for the
shoulder to move by reconfiguring the
shoulder casting and the yoke assembly
by making them both narrower. This
modification does not affect the
biofidelity of the ATD or the
reproducibility or repeatability of the
responses because the neck response
and sled kinematics were not affected
by the shoulder revisions.
Complete details of the modifications
are described in an agency technical
report that may be found in the docket
for this final rule.21
ii. Lower Neck Revision
This final rule makes simple
modifications to the HIII–10C’s lower
neck load cell and fasteners associated
with the neck safety cable to lessen the
shock effect.
The safety cable of the HIII–10C neck
is common to all ATDs in Part 572. It
is a steel wire rope that runs through the
center of the molded neck to prevent
total separation of the head from the
torso under an extreme test condition.
The rope is fitted with swages at both
ends: a ball-end at the superior end and
a threaded stud-end at the inferior end.
The ball-end is larger than the diameter
of the neck’s through-hole to prevent it
from passing through the neck. On the
inferior end, a nut is used to tighten the
threaded swage, which places the cable
under tension and the molded neck
under compression. A secondary jam
nut serves as a lock. According to the
NPRM and final rule specifications, the
nut should be tightening to a torque
setting of 8 +/¥ 2 inch-pounds (in-lbs)
before each test.
The entire neck assembly is joined to
the spine by means of a specialized
bracket that allows the neck to be set at
different forward tilt angles. A throughhole runs through the center of this
bracket allowing access to the end
fitting of the wire rope so that it may be
tightened without removing the bracket
from the neck. In lieu of the bracket, an
optional part is available for the HIII–
10C containing a lower neck load cell.
It has the same general configuration as
20 Id.
21 ‘‘Revisions to the HIII–10C Technical Data
Package,’’ NHTSA, August 2011.
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the un-instrumented bracket, except the
through hole has a smaller bore.
Shock emanating from the neck has
been observed when either the bracket
or an optional part containing a lower
neck load cell is used. (The load cell is
not needed in tests carried out under
FMVSS No. 213.) When the neck goes
into extreme flexion (a 90 degree bend
is specified in the qualification test), the
center cable is not sufficiently taut to
prevent its movement within the center
channel of the neck. As a result, the
steel washer and nuts on the threaded
swage move within the free space
provided by the center hole and can
come into contact with the inner walls
of the through-hole. To mitigate this
condition, the washer has been changed
from steel to nylon. Also, the lower neck
load cell and its structural replacement
have been revised since the Part 572
NPRM. For each of these two parts, a
sleeve made of soft, dampening material
is now used to line the through-hole and
prevent rattling of the nuts. The load
cell revision also carries over the
capacities specified in the NPRM which
were increased for some channels where
data was truncated in pre-NPRM agency
tests using a previous load cell.22
In a related problem, a premature
wear problem has been observed in the
agency’s HIII–10C units and reported in
comments provided by Dorel. The
molded neck itself has two polymeric
bushings, one at each end of the neck,
through which the cable passes. The
bushings prevent the steel rope from
abrading the internal through-hole of
the neck. However, the aforementioned
cable movement tends to abrade the
neck channel and chafe the lower
polymeric cable bushing.
To avoid problems such as those
noted by Dorel, the polymeric bushing
should be inspected on a periodic basis.
The bushing is an inexpensive part that
may be readily inspected and replaced
during the course of running the neck
qualification tests. We note that setting
the neck cable to the proper torque is
key to the longevity of the bushing. The
torque setting is also critical to passing
the qualification requirement for the
neck. In addition, we also found that the
torque setting of the neck cable nut
significantly affects the head excursion
and the upper neck moment within the
sagittal plane (about the y-axis).
We also found that, when left
unchecked, the threaded stud-end could
wear through the plastic collar and
chafe the outer aluminum disc of the
22 The revised load cell is a six-axis load cell.
Maximum load capacities and several other load
cell specifications are given on Drawing SA572–40
in the TDP.
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molded neck after extended use. When
the neck goes into extreme flexion, a
chafed bushing can partially work its
way out of the center through hole of
the molded neck. This allows the wire
rope to rub directly against the
aluminum end plate of the neck,
sending shock through the entire spine,
which appears as noise in the signals of
nearby sensors.
As described earlier, the signal noise
emanating from the neck has no
consequence on the use of the HIII–10C
in FMVSS No. 213 because the noise is
removed by signal processing
algorithms. Nonetheless, the agency has
implemented simple revisions to
mitigate any shock emanating from the
shoulder and lower neck. In addition to
revising the lower neck load cell to
preclude rattling, we have taken steps to
lessen the effects of the chafing. A new
bushing has been specified in the TDP
with an increase to the flange thickness
and with a smaller inner diameter,
which reduces the clearance of the wire
rope. The inner diameter of the cable
washer has also been decreased to
prevent it from sliding. Details of the
new load cell, bushing, and washer,
along with their effects, are reported in
NHTSA’s technical report, ‘‘Revisions to
the HIII–10C Technical Data Package,’’
August 2011.
3. Stiffness of Vinyl Insert
Dorel indicated in its comments that
it was having difficulty meeting the
torso flexion test because the vinyl
abdominal inserts it used were too stiff
or too soft. Dorel had to mix and match
inserts and lumbar flex joints in an
attempt to pass the test. The commenter
was concerned that the manufacturing
variability for the inserts is too wide.
The agency has revised the
specification of the abdominal insert by
adding new dimensional requirements
that improve manufacturing consistency
and fit. The agency has also revised the
PADI to include a section on how to
position the abdominal insert within the
pelvis cavity when running the torso
flexion test. The specified setting of the
insert governs its interaction with the
chest jacket, lumbar spine, and ribcage,
all of which influences the outcome of
the torso flexion test. In agency tests, the
new insert setting provided sufficient
instruction to successfully carry out the
torso flexion tests without having to mix
or match inserts.
4. Dummy Availability
In its 2005 comments, Dorel claimed
that no dummies were available on the
market prior to the NPRMs of 2005 that
satisfied the proposed Part 572
specifications. It listed nine changes to
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its version of the dummy relative to the
version specified by the Part 572 NPRM
of 2005. Thus, Dorel claimed that it was
not given adequate opportunity to
evaluate the proposed dummy.
We see no merit to delaying the final
rule to either FMVSS No. 213 or Part
572 on the basis of HIII–10C availability.
Several years have passed since the
NPRMs were published in 2005, during
which two additional NPRMs have been
published on the use of the HIII–10C in
FMVSS No. 213. This has provided
commenters with ample time and
opportunity to acquire, test, and submit
comments to the docket about the HIII–
10C. We note that in Dorel’s comments
to the SNPRM of 2008, it did not discuss
any specifics on the HIII–10C other than
those already provided in 2005 and
addressed herein.
b. Durability of the HIII–10C
In its comments, Dorel reported on
observed durability problems and
breakage of the HIII–10C in its sled tests.
No other commenters noted any
problems related to these observations
or any other damage.
As described earlier in this preamble,
the agency has expanded our dataset of
HIII–10C sled tests by about 200 tests
and many more qualification tests since
the NPRMs were published in 2005. In
the whole of this extensive test regimen,
the agency has studied many aspects of
the dummy’s performance including its
functionality and durability. We have
not observed any significant
functionality or durability problems that
would preclude the use of the HIII–10C
use in FMVSS No. 213 or any other
standardized test.
Each problem raised by Dorel is
discussed below. Also included is a
discussion of our own part replacement
records assembled during the course of
our post-NPRM evaluation of the
dummy. No further changes to the
dummy have been implemented as a
result of these observations.
1. Proximal Femur
Dorel reported a broken casting in one
of its HIII–10C units representing the
proximal femur. Although Dorel did not
describe how the failure occurred, we
assume it was brought on by the
‘‘flailing legs’’ seen in FMVSS No. 213
tests. During the impact event, the lap
belt retains the pelvis, while the legs
spring forward placing a tensile load on
the joint connecting the legs to the
pelvis.
We had observed this type of failure
in testing of an earlier, pre-NPRM
version of the dummy. Since then, the
dummy part representing the proximal
femur was redesigned to eliminate the
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11657
fracture problem. The part is now made
of 4140 steel rather than C954
aluminum bronze, and a sharp corner
stress riser has been rounded. In the
photographs provided by Dorel, it
appears that its failed unit had the older
aluminum bronze casting. The new
design was incorporated into the Part
572 NPRM version of the dummy and is
specified in the version described in
this final rule.
The femur has held up in all agency
tests since the change was implemented
to the pre-NPRM version. No further
change to the dummy is necessary.
2. Bib Assembly
Dorel provided a picture of a torn bib
assembly, without further discussion, in
its response to the Part 572 NPRM. The
extent of the testing to produce this
damage was not described.
The agency has not encountered any
instances of torn bib assemblies in our
extensive testing experience with the
HIII–10C, but we have seen occasional
abrasions on some bib assemblies of
other Part 572 dummies. They were
caused by the shoulder belt pressing
against and eventually rubbing through
the chest jacket during multiple severe
test exposures. This may have been the
case for Dorel, based on its general
comment that it had performed ‘‘65
dynamic sled tests run at DJG [Dorel
Juvenile Group] to the new [FMVSS
No.] 213 standard bench and pulse
using the HIII–10C dummy,’’ in addition
to other dynamic sled tests conducted at
a contract laboratory. Given that the tear
is likely caused by excessive wear-andtear, the agency has not revised the bib
assembly.
3. Shoulder Rotation Stop Screws
The arm of the HIII–10C is connected
to the shoulder through a yoke that acts
as a two degree of freedom joint which
allows the arm to flex, extend, and
rotate axially. Affixed to the yoke is a
protrusion, or ‘‘shoulder rotation stop,’’
that limits the range of motion of the
shoulder in axial rotation (i.e., it cannot
complete a 360 degree circuit). So, when
the arms of the HIII–10C flail forward
and extend during a dynamic test, the
stops prevent the arms from rotating all
the way up and around behind the
body.
Dorel provided photos showing that
the screws holding the rotation stop in
place in its HIII–10C unit had sheared
off. Dorel stated that it repaired the part
by welding the stop into place, but the
commenter provided no further
discussion.
The agency has not experienced this
type of failure in any of our tests of the
HIII–10C, and we do not know the
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circumstances that led to the failure in
the Dorel unit. In the absence of
information that a problem exists or that
it is recurring, we find no need to
change the HIII–10C with regard to the
shoulder stop.
4. Agency Part Replacement Records
Since the NPRMs of 2005, NHTSA has
continued to monitor the durability of
the HIII–10C, as we do routinely with
all of our ATDs. A summary of our
records is provided below. In general, a
part within a dummy is replaced for one
of two reasons: Because it was damaged
during a test or because it has become
worn and unserviceable after extensive
use. As described below, our experience
indicates that all part replacements were
made under the latter circumstance. The
records thus show good durability of the
HIII–10C.
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i. Pelvis Helicoil Insert
Throughout our post-NPRM testing
experience of about 200 sled tests, the
agency observed only one instance of a
part failure that appeared to have
affected the outcome of the test. This
failure was brought on by flailing legs,
which caused the femur to separate
from the pelvis due to the failure of a
helicoil.23 ‘‘Helicoil’’ is the product
name of a steel fastener that provides
positive thread locking into soft metals
like aluminum or bronze.
Three helicoils are inserted into the
HIII–10C’s aluminum pelvis casting so
that the flange that retains the proximal
head of the femur may be bolted directly
to the casting. After one of our tests, we
noticed that the flange had separated
from the pelvis. Upon closer inspection,
we found that a helicoil had disengaged
from the pelvis. This failure has not
recurred. Moreover, a helicoil failure is
typically gradual as its threads loosen
from the base material over time. A
thorough pre-test inspection can usually
spot helicoil looseness so that repairs
may be made, thus mitigating the
likelihood of a test failure. Therefore, a
revision to the flange fastening system is
unnecessary.
ii. Neck and Ribcage Replacement
Like all ATDs in the Hybrid III family
of dummies, the deformable parts of the
HIII–10C have the shortest service lives.
The two most often replaced parts on
the HIII–10C are the ribcage and the
molded neck. Worn ribs are usually
detectable by examining them for overly
gouged or delaminated damping
material. Unserviceable molded neck
assemblies are not noticeable by visual
23 This was not the proximal femur casting part
reported by Dorel.
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inspection, with the exception of chafed
cable bushings as described earlier.
The conditions of the ribs and neck
are monitored directly through the Part
572 qualification procedures. In our
experiences with the HIII–10C, the
decision to remove a rib set or neck
from service has always been made
during pre-test qualification procedures
when the thorax impact or the neck
flexion/extension test qualifications
cannot be met after a few trials. The
typical service life for HIII–10C rib sets
and neck assemblies alike are about
thirty sled tests. We have not had a
situation where failure occurred during
a sled test of any kind.
iii. Other Replacements
According to our records, flesh
materials—particularly the chest flesh—
are the only other parts that have been
replaced on a recurring basis. As with
flesh materials of all ATDs, those of the
HIII–10C are replaced periodically as
they become aged, abraded, or torn.
Deterioration of these parts is easy to
identify so that they may be repaired or
replaced well before they deteriorate to
the point where their condition may
affect test results. They are also
relatively inexpensive (chest flesh is the
highest priced flesh material item: $650)
and easy to service.
5. Durability Summary
Given the record of low maintenance
to our own HIII–10C units and the
relatively few complaints noted by
commenters, we consider the dummy to
be highly suitable for use in FMVSS No.
213 in terms of its durability. Our
records indicate that there have been
relatively few instances of HIII–10C part
replacements of any sort. When we have
replaced parts, it has always been due
to extensive service, not a sudden
failure. Replacement of worn parts
constitutes preventative maintenance
that, when scheduled at regular
intervals, will help to ensure valid test
results.
c. Qualification Procedures and
Requirements
Qualification procedures for the HIII–
10C are basically the same as those
proposed in the Part 572 NPRM, though
some of the response corridors have
been modified in consideration of
additional qualification test data
accumulated by the agency during our
post-NPRM test experience. We also
considered in our analysis a large
qualification test dataset provided by
the Alliance, amassed by members of
the SAE International (SAE) Dummy
Testing Equipment Subcommittee
(DTESC). The much larger data set now
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allows us to base the setting of the
corridors on an enhanced statistical
analysis, providing even better
assurance that the mean and the
dispersion of the responses are
representative of the dummies that the
users will have to work with in the
field.
Comments provided by the Alliance
and echoed by FTSS/Denton
recommended several changes to the
performance corridors for the HIII–10C.
In most instances, the commenters
recommended changes that were
specified by the DTESC based on a large
dataset of qualification test results
provided by participating organizations,
including Chrysler, Ford, and General
Motors, FTSS/Denton, Delphi, MGA,
and TRW. The Alliance also
recommended changes to the
specification for impact probes and
dummy instrumentation. The comments
and our response thereto are discussed
below.
1. Response Corridors
The corridors suggested by the
Alliance are based on a range of 98 to
275 qualification tests per body segment
from about 25 dummies. The Part 572
NPRM corridors were based on a range
of 6 to 28 qualification tests per
component performed on 2 dummies.
Post-NPRM data accumulated by the
agency contained qualification results
from an additional 4 HIII–10C units.
The agency analyzed the data
submitted by the Alliance and found
that the suggested corridors and the
coefficients of variation (CVs) were
generally in good agreement with
agency data. This good correspondence
lent confidence that the data were of
sufficient quality to be considered with
agency data towards the establishment
of performance corridors. The advantage
of a larger sample size is that it allows
for consideration of such factors as labto-lab, operator-to-operator, and
dummy-to-dummy variability.
Upon consideration of the larger
dataset, we found that our original
corridors proposed in the Part 572
NPRM needed only fine-tuning.
Summaries of the changes to each body
region are given below. Full details of
our analyses are contained in the
technical report, ‘‘Development of
Qualification Performance
Specifications for the HIII–10C Crash
Test Dummy,’’ December 2011, which
has been placed in the docket for this
final rule.
i. Head
The head qualification test consists of
dropping the head onto a rigid surface
from a height of 376 millimeters (mm)
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(14.8 inch (in.)). Since the HIII–10C
head is a Hybrid III 5th percentile adult
female (HIII–5F) head, the same test
procedure is specified as in 49 CFR part
572, Subpart O, which contains the
specification for the HIII–5F ATD. The
head drop is designed for the forehead
to impact a flat, rigid surface at the
midsagittal plane. The head response
limit in these impacts is specified
between 250 and 300 G’s as proposed in
the NPRM. No change was necessary to
these limits, as the majority of data fit
well and is well centered within the
corridors.
ii. Neck
The head and neck assembly and the
test procedures are the same as
proposed in the Part 572 NPRM. The
neck is evaluated for flexion and
extension kinematics similar to that
defined in 49 CFR part 572, Figure 15
and Figure 21. The head-neck assembly
is mounted to the bottom of a pendulum
that is being decelerated from a speed of
11659
6.1 meter/sec (m/s) (20 feet/sec (ft/s)) for
flexion and 5.03 m/s (16.5 ft/s) for
extension at velocity reduction rates
indicated in Table 1. The only
difference between the final rule and the
Part 572 NPRM is a corrected reduction
in velocity specification at 10 ms for
neck extension, changing from 1.59–
1.89 ft/s to 1.49–1.89 ft/s. (The metric
specification was correct.) The 1.59 ft/
s specification reflected a typographical
error.
TABLE 1—NECK REDUCTION IN IMPACT VELOCITY FROM INITIAL IMPACT IN FLEXION AND EXTENSION
Body region
Reduction in impact velocity from initial impact
Final rule
NPRM
Neck (flexion)
ft/s
at 10ms ............................................................................................
at 20ms ............................................................................................
at 30ms ............................................................................................
Neck (Extension)
srobinson on DSK4SPTVN1PROD with RULES2
Neck flexion. The final rule
performance corridors for maximum Dplane rotation of the head and moment
decay time were revised from those
proposed in the Part 572 NPRM. Even
though the width of the D-plane rotation
corridor remained unchanged,
additional agency data and comments
by the Alliance supported a statistically
justifiable shift of the range upward
from 74–88 degrees to 76–90 degrees
(the Alliance recommended a 76.5–88.5
degree range). The corridor for moment
decay time was adjusted to a slightly
narrower range from 85–105 ms to 86–
105 ms in the final rule. The combined
NHTSA–Alliance data did not justify
the selection of a narrower corridor
suggested by the Alliance at 91–101 ms.
In light of the good fit of the new
qualification data within the previously
established limits, the peak moment
range within the rotation corridor
remains unchanged from that proposed
in the NPRM at 50–62 ms. The Alliance
did not comment on this item.
Neck extension. All three neck
extension performance corridors in this
qualification test were adjusted slightly
from those proposed in the Part 572
NPRM. The adjustments were needed to
account for data received from the
Alliance and the additional data
generated in agency tests. The
maximum D-plane rotation corridor was
widened and shifted downward from
99–114 degrees proposed in the NPRM
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1.64–2.04
3.04–4.04
4.45–5.65
1.49–1.89
2.88–3.68
4.20–5.20
The thorax qualification procedure is
the same as that proposed in the Part
572 NPRM. It specifies a 6.0 m/s (19.7
ft/s) frontal impact within the
midsagittal plane by a 6.89 kg (15.2 lb)
round faced 121 millimeter (mm) (4.76
in) diameter probe into the mid-sternum
of a seated dummy. Thorax impact
responses are specified as the maximum
sternum displacement, the maximum
probe force at the time of maximum
sternum displacement, the maximum
probe force when the sternum
displacement is between 20 mm and the
lower bound of maximum displacement,
and the internal hysteresis percentage
between loading and unloading curves.
The NPRM proposed chest deflection
limits of 40.5–48.5 mm, while the
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ft/s
4.89–6.20
9.45–12.07
13.78–17.06
iii. Thorax
Frm 00035
1.64–2.04
3.04–4.04
4.45–5.65
m/s
to 96–115 degrees for the final rule. The
limits suggested by the Alliance were
also 96–115 degrees.
Also, based on the additional data, in
the final rule the corridor for peak
occipital-condyle moment during the
maximum rotation interval is revised to
(¥46)–(¥37) Newton-meters (N-m), as
compared to (¥47)–(¥35) N-m
proposed in the NPRM, and (¥47)–
(¥36) N-m recommended by the
Alliance. The final rule specifies a
moment decay time of 100–116 ms, as
compared to 100–120 ms proposed in
the NPRM, and 100–114 ms
recommended by the Alliance.
PO 00000
ft/s
5.38–6.69
9.97–13.25
14.60–18.53
ft/s
at 10ms ............................................................................................
at 20ms ............................................................................................
at 30ms ............................................................................................
VerDate Mar<15>2010
m/s
1.59–1.89
2.88–3.68
4.20–5.20
m/s
5.38–6.69
9.97–13.25
14.60–18.53
m/s
4.89–6.20
9.45–12.07
13.78–17.06
Alliance recommended 38.5–48.5 mm.
Upon consideration of the full dataset,
our analysis has led us to set the limits
at 37–46 mm for the final rule. This
downward shift was necessitated by a
stiffer response seen in the most recent
data in both NHTSA testing and in
results submitted by the Alliance.
In light of the modified maximum
chest deflection corridor, the limits of
the peak probe force at maximum
deflection and the peak probe force in
the deflection transition zone (prior to
the rib deflection reaching the lower
corridor limit) were raised
correspondingly. The former was
changed from 1.83–2.33 kN in the
NPRM to 2.0–2.45 kN in the final rule,
while the latter was changed from
<2.33kN in the NPRM to <2.52 kN in the
final rule. Comparable Alliance
recommendations were 1.95–2.45 kN for
peak force at maximum deflection and
<2.45 kN in the transition zone. Limits
for hysteresis proposed in the NPRM
were well-supported by the data and
remained unchanged at 69–85 percent.
iv. Torso Flexion
The torso flexion test involves the
determination of bending resistance of
the upright seated dummy’s lumbar
spine/mid-torso area when the upper
torso is quasi-statically flexed from its
upright seated posture by 35 degrees
relative to a lower torso. The resistance
to bending is defined as the highest load
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encountered during the bending
process.
The final rule specifies a resistance of
180 to 250 N compared to that in the
NPRM of 190–240 N. The adjustment
was made in response to Alliance
comments recommending a range of
178–249 N. The final rule limits are in
near agreement with the Alliance
recommendation, and are well
supported by the combined AllianceNHTSA data set. The final rule also
specifies that upon removal of the
flexion force the torso, the torso is
required to return to within 8 degrees of
its initial position. This is the same
requirement that was proposed in the
NPRM. Commenters did not recommend
a revision to this requirement.
v. Knee Impact
The knee impact test is the same as
that proposed in the Part 572 NPRM,
consisting of a 2.1 m/s (6.9 ft/s) impact
by a 1.91 kg (4.21 lb) flat-faced 76.2 mm
(3.0 in.) diameter rigid probe into the
knee of a HIII–10C leg assembly
(including the tibia and foot), where the
distal end of the femur is mounted
rigidly to a reaction mass. For the final
rule, the corridor for the force applied
to the knee by the impactor is specified
to be between 2.6 and 3.2 kN, as
compared to 2.56 to 3.14 kN in the
NPRM. The final rule specification is in
agreement with recommendations made
by the Alliance.
2. Summary of Qualification
Requirements
A summary of performance
specifications for the entire dummy,
including those proposed in the Part
572 NPRM and those advocated by the
Alliance, is provided in Table 2. Based
on our analysis, the agency data were
found in most instances to be in
reasonably good agreement with the
corridors suggested by the Alliance
corridors. For measurements where our
analysis of the data did not justify
setting the corridors at Alliance
recommendations, we searched for the
best justifiable accommodation of both
datasets within the limits of the
biofidelity data.
As a general rule, performance
corridors were set around ± 3 standard
deviations from the mean for
measurements with a CV<3 percent, at
± 2 standard deviations from the mean
for measurements with a CV from 3 to
5 percent, and at ± 10 percent from the
mean for measurements with a CV from
5 to 10 percent.
Table 2 indicates that all of the data
leading to CVs for the final rule are
within the 10 percent limit.
Accordingly, all of the dummy based
measurements related to their projected
use as Injury Assessment Reference
Values (IARVs) meet the requirements
for inclusion into Part 572.
TABLE 2—FINAL RULE QUALIFICATION CORRIDORS AND COMPARISON WITH NPRM AND ALLIANCE RECOMMENDATIONS
Response measurement or test parameter
Test
Head drop ...............
Neck pendulum,
flexion.
Neck pendulum, extension.
Thorax pendulum
impact.
Torso flexion ...........
Knee impact ...........
Final rule
corridor
NPRM corridor
Alliance suggested corridor
Full alliance/NHTSA dataset
Mean
S.D.
%CV
Acceleration (g) .......................................
Max D-plane rotation (deg) .....................
250–300
76–90
250–300
74–88
250–300
76.5–88.5
271
83.05
11.6
3.28
4.29
3.95
Peak O–C moment (N-m) .......................
Moment decay time to 10 N-m (ms) .......
Max D-Plane rotation (deg) ....................
50–62
86–105
96–115
50–62
85–105
99–114
n/a
91–101
96–115
55.38
96.63
105.4
3.30
3.88
4.35
5.96
4.01
4.12
Peak O–C moment (N-m) .......................
Moment decay to –10 N-m (ms) .............
Sternum displacement (mm) ...................
(¥46)–(¥37)
100–116
37–46
(¥47)–(¥35)
100–120
40.5–48.5
(¥47)–(¥36)
100–114
38.5–48.5
¥41.8
107.2
41.3
2.37
3.17
2.1
5.67
2.95
5.04
Peak probe force defining the displacement corridor (kN).
Peak probe force during the time when
sternum displ. is 20 to 40.5 mm (kN).
Thorax hysteresis ....................................
Peak force at 35 deg from vertical (N) ...
Return angle (degrees) ...........................
Peak force (kN) .......................................
2.0–2.45
1.83–2.33
1.95–2.45
2.227
0.113
5.06
<2.52
<2.33
<2.45
2.287
0.154
6.74
69–85%
180–250
< 8, >¥8
2.6–3.2
69–85%
190–240
< 8, >¥8
2.56–3.14
69–85%
178–249
......................
2.60–3.20
80.3
213.3
5.2
2.92
2.3
18.7
1.7
0.157
2.91
8.8
note 1
5.37
(1) The %CV does not apply to this measurement since the nominal requirement of zero degrees renders a %CV of infinite magnitude.
srobinson on DSK4SPTVN1PROD with RULES2
3. Impact Probes
For the dummies specified in Part 572
before 2000, impact probes used in
qualification testing were assumed to
take the form of a nearly perfect
cylinder that could be specified by a
material, weight, and diameter. In
practice, a perfectly cylindrical probe is
rare. Also, the addition of several new
child dummies to 49 CFR part 572
called for a new assortment of lighter
probes that were even more difficult to
design in a pure cylindrical form due to
their low weight. This created a
situation where testing laboratories
maintained a limited assortment of
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probe bodies, and then attained the
proper probe characteristics by
interchanging probe faces.
Beginning with our final rule for the
Hybrid III 6-year-old child dummy
(HIII–6C) in January 2000, the agency
began to specify the minimum mass
moment of inertia (MOI) and free air
resonance for the various probes used in
Part 572 qualification testing. This
assured that vibratory effects were not
present and that various probe
configurations did not introduce
differences in dummy response due to
probe shape variations. At the same
time, laboratories retained ample
latitude to design impact probes. For the
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HIII–10C, the Part 572 NPRM specified
a minimum mass moment of inertia as
well.
In its comment, the Alliance took
issue with our proposed specifications.
It pointed out that the minimum thorax
and knee pendulum mass moments of
inertia as proposed in the NPRM at
2,040 kg-cm2 and 140 kg-cm2,
respectively, were higher than those
recommended by the SAE Hybrid III
Dummy Family Task Group. In its
comments, the Alliance included thorax
and knee qualification data collected
from multiple test facilities indicating
minimal performance differences in
qualification tests despite a variety of
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test probes with different MOIs. It
recommended that we revise our
minimum specification to 1,463 kg-cm2
for the thorax probe and 117 kg-cm2 for
the knee probe, as was called out in the
original SAE specification of the
dummy.
In our analysis of Alliance data, we
examined round-robin tests performed
on the same knee (or thorax) to isolate
the effect of the different probe MOI on
the response of that part. By only
considering these tests, we eliminated
the possibility that dummy
reproducibility would confound the
response data. Also, we only considered
data from the sources where MOIs were
known. Though it submitted test data
from several laboratories, the Alliance
provided probe MOIs from just three
sources.
In comparing qualification test data
using the Alliance probes with the
lowest MOIs against data using our own
probes, we found peak force
measurements to be consistently lower
with the Alliance probes. We note that
the Alliance knee probe with the lowest
MOI was still above our lower limit (152
kg-cm2 vs. 140 kg-cm2), and the Alliance
thorax probe with the lowest MOI was
only narrowly under our limit (1,960 kgcm2 vs. 2,040 kg-cm2). Given the trend
towards lower force response with
lower MOIs and that the majority of
Alliance probes are already within our
MOI specification, the agency will not
revise the probe specifications.
4. Instrumentation
i. Rotary Potentiometers
The Alliance pointed out an omission
to the filter specification for rotary
potentiometers that are typically used in
the neck flexion and extension
qualification tests. The potentiometers
are used to measure the rotation of the
head relative to the pendulum. The
agency inadvertently overlooked the
filter call-out in the Part 572 NPRM. We
have revised the specification to include
a 60 CFC call-out as was recommended
by the Alliance. This call-out is
consistent with SAE J211 and that of
other Part 572 ATD specifications.
srobinson on DSK4SPTVN1PROD with RULES2
ii. Sternum Displacement
The Alliance pointed out that the CFC
180 filter specification for sternum
displacement was not consistent with
the SAE Recommended Practice J211,
Rev. Mar 95, ‘‘Instrumentation for
Impact Tests—Part 1—Electronic
Instrumentation,’’ (SAE J211). It noted
that Hybrid III dummies specified in 49
CFR part 572 subparts N (HIII–6C) and
O (HIII–5F) call for the use of a CFC 600
filter for sternum displacement. This
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was a mistake in the Part 572 NPRM.
We have revised the final rule to specify
a CFC 600 filter for sternum
displacement potentiometer signals.
d. Technical Data Package
The HIII–10C as specified herein is
essentially the same as that defined in
the Part 572 NPRM. A few minor
revisions to the TDP have come about as
a result of our experiences during
extensive use of multiple HIII–10C
dummies in the post-NPRM tests of
booster seats. The revisions were
corrective in nature; they do not affect
the response of the dummy other than
to remove unwanted artifacts. These
include changes associated with
improved functionality to the shoulder,
neck cable bushing, and chin as
described earlier. In addition, several
typographical errors and other mistakes
in print were uncovered. Comments
associated with the TDP are discussed
below.
1. Changes to the Engineering Drawings
and PADI
FTSS/Denton requested a number of
changes to the engineering drawings
and PADI. These requests were echoed
by the Alliance. For the most part, we
agree with FTSS/Denton’s requests and
we have revised the TDP accordingly.
The revisions are all aimed at
manufacturing, machining, assembly,
and inspection of dummy parts. They
fell into four categories: errors,
dimensioning changes, clarifications
expressed in notes, and changes
associated with the introduction of new
part numbers.
Errors consisted of misnumberings,
typographical errors, and other mistakes
in print.
An example of a dimension change
can be seen on the Shoulder Yoke
Assembly, drawing 420–3430. For this
part, the yoke was widened by 0.003
inches. This minor change provides the
proper clearance needed to account for
tolerance stack up so that the arm may
always be attached to the shoulder
without force-fitting.
An example of a clarifying revision is
the added set of dimensions placed on
sheet 3 of drawing 420–0000, Complete
Assembly, HIII–10C. These reference
dimensions indicate the location of
safety belt plateaus on the dummy’s
shoulder and pelvis. They are useful
when inspecting the dummy in
accordance with the instructions
provided in the PADI and when
conducting the torso flexion
qualification test. This additional
information does not alter the dummy’s
design or its construction.
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11661
In the TDP proposed in the Part 572
NPRM, many parts were identified with
part numbers associated with other
ATDs. In the final drawing package we
assigned new part numbers to these
parts, using the HIII–10C’s ‘‘420’’ prefix,
to identify these as HIII–10C parts. This
was strictly a documentation change to
better identify HIII–10C parts and did
not affect the construction of the
dummy in any way. However, it did
generate many drawing revisions since
many of the newly assigned part
numbers are referenced on many HIII–
10C drawings.
None of the revisions affect the
performance of the HIII–10C in
qualification testing or in FMVSS No.
213. Therefore, they are not discussed
exhaustively in this document. A full
accounting of the revisions can be found
in the supplementary technical report
cited earlier, ‘‘Revisions to the HIII–10C
Technical Data Package,’’ NHTSA,
August 2011.
2. Organization of Materials
i. Searchable Text
FTSS/Denton and the Alliance
recommended that the part numbers be
searchable in electronic PDF drawing
files. The agency concurs that it would
be an improvement for text to be
searchable in the electronic PDF
drawing files to facilitate use.
Accordingly, the agency has converted
the drawing files to an electronic format
with searchable text capability. A
searchable text is now available in the
electronic drawing files.
ii. Order of Engineering Drawings
FTSS/Denton and the Alliance
recommended that the drawing package
be arranged into ascending order by part
number. We disagree. We believe that
the drawing package should be left in
segment order to be able to quickly
identify parts belonging to a particular
segment cluster. Moreover, the
numbering system should be consistent
with the PADI to facilitate inspection
and service of the dummy. Given that
the drawing package is electronically
searchable, it will be an easy matter for
users to search for drawings and order
them in the manner they prefer.
Accordingly, the HIII–10C drawing
package remains ordered by body
segment (as proposed in the Part 572
NPRM).
iii. Part Quantity Specification
The HIII–10C parts list is arranged
such that each assembly is listed
together with its associated parts. In
many instances the same part (such as
a fastener) is used on multiple
assemblies and is thus listed more than
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once on the parts list. The parts list
proposed in the Part 572 NPRM only
identifies how many times a part is used
on the assembly immediately preceding
it on the list, not the entire dummy.
FTSS/Denton and the Alliance
recommend that the parts list should
include a column giving the total
quantity of that part in the dummy the
first time it appears on the list. The
agency agrees that such information
would be useful for procurement of
parts and servicing of the dummy.
Accordingly, a column has been added
in the parts list showing the total
number of times a part appears in the
dummy.
srobinson on DSK4SPTVN1PROD with RULES2
iv. Part Numbering Scheme
A number of HIII–10C dummy parts
are common with parts of other
dummies. For example, the HIII–10C
has the same head as the HIII 5th
female, but the TDP’s for each dummy
have their own numbering scheme with
different part numbers for the head.
FTSS/Denton commented that it
believes the same part numbers should
be used for identical parts. This
comment was echoed by the Alliance.
The agency has not revised our part
numbering scheme as recommended by
FTSS/Denton. If the same part numbers
were used, substantial documentation
problems could be encountered. A
revision to the design of a shared part
may be needed for one dummy, but
detrimental to the function of another
dummy. A distinct numbering system,
by cross-referencing the shared part
numbers, poses no such problems.
The main benefits of using identical
part numbers are related to part
inventory control and sequencing of
production processes. For dummy
manufacturers like FTSS/Denton, the
economics of production may be aided
by a numbering scheme that identifies
common parts so that batch processing
of identical parts could be scheduled
readily. However, we believe that
interested parties can realize these
advantages easily enough by developing
their own internal part numbering
scheme as they see fit. This may be
cross-referenced against the HIII–10C
TDP without resorting to a common part
numbering scheme for Part 572.
3. Specifications for Soft Parts
The Alliance and FTSS/Denton
recommended that the agency and
industry work together to define
dimensions that are critical to
controlling performance of the vinyl,
rubber, and other deformable parts and
to identify suitable measurement jigs
and part tolerances. The Alliance cited
the jacket of the 49 CFR part 572 subpart
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O Hybrid III 5th percentile adult female
dummy as an example of unwanted
reproducibility variations among
dummy manufacturers. FTSS/Denton
requested further that the agency work
directly with them to set longevity
specifications for the useful life of
deformable parts. Citing customer
dissatisfaction, FTSS/Denton was
concerned that vinyl and rubber ATD
components typically shrink or change
shape over time.
We do not believe it is feasible or
practical for NHTSA to undertake the
work suggested by the commenters at
this time, nor is it necessary for the
HIII–10C. The HIII–10C was developed
cooperatively under the direction of the
SAE Hybrid III Dummy Family Task
Force to limit the variability of parts. At
the time, FTSS and Denton collaborated
jointly on the design. SAE provided the
general specifications, and the two
manufacturers shared the responsibility
of designing the hardware and
producing the prototypes. The
cooperation assured that variations in
reproducibility were avoided.
Even before the companies merged,
HIII–10C parts built by FTSS and
Denton had a good record of
reproducibility and interchangeability,
as highlighted in the Part 572 NPRM.
Now that the two companies have
merged, HIII–10C vinyl and rubber parts
can be created from a common set of
molds, thus precluding any variability
in the form and fit of soft parts. As for
longevity, the decision on when to
replace worn HIII–10C parts should be
based on conformity to part
specifications and qualification testing.
4. Use of 3D Computer Renderings
The Part 572 NPRM mentioned that
‘‘three-dimensional engineering aids are
available from the NHTSA Web site for
complex dummy part dimensions.
While these aids are not part of this
specification, they can be used by the
public for reference purposes.’’ These
aids take the form of computer-aided
design (CAD) files that appear as threedimensional (3D) renderings of various
parts. They were received by NHTSA
from the SAE Hybrid III Dummy Family
Task Group in 2004 at the time we
received the two-dimensional (2D)
engineering drawings.24 The Alliance
commented that it believes that the 3D
renderings should be formally entered
into Part 572 to specify the HIII–10C.
Although we see much merit to 3D
renderings, we will not implement the
24 Two sets of 3D renderings were received: one
originating from FTSS and the other from Denton
before the merger of the two companies into
Humanetics.
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suggestion to enter them into Part 572.
We understand that all contemporary
ATD designs originate using CAD tools
which are valuable assets to designers
and researchers. Within NHTSA, CAD
files of ATDs have been used in our
research activities to construct finite
element models to simulate dummies in
dynamic events. We have also used
them to investigate possible ATD design
modifications and to study static
interactions with seat belts and vehicle
interiors.
However, 3D CAD renderings are not
currently used for regulatory purposes
in Part 572. As applied within our
research activities, a 3D computer
rendering is akin to an actual part. But
the part alone—without dimensions or
any other information—cannot be used
to specify itself. Part specifications
communicate information on how to
fabricate and verify the part. This is
done by applying dimensions and
tolerances to parts, along with
information on material, surface finish,
and other features required by the
specification-holder. The most objective
way to convey this information is to
render the part on a standard 2D
engineering drawing, showing multiple
views of the part when necessary.
Drawing standards have long been
developed to systematically and
unambiguously convey this information,
as reflected in Part 572 engineering
drawings of ATDs. Thus, the 2D
drawings ultimately serve to specify
ATD parts.
Neither the Alliance nor FTSS/Denton
(the originator of the 3D renderings) has
proposed a systematic and unambiguous
means by which the 3D renderings may
be used to specify ATDs. Until such a
means is devised, we will not include
them in 49 CFR part 572 to specify the
HIII–10C. Our basis for acceptance of
the dummy will continue to be
conformance to 2D drawings, together
with the qualification test requirements
in Part 572.
We continue to believe that 3D
renderings serve as very helpful
engineering aids as described in the
NPRM and hold promise in specifying
ATD parts. However, in the case of the
3D renderings of the HIII–10C received
from the SAE Hybrid III Dummy Family
Task Group, the agency will not post the
CAD files on our Web site. Upon further
review of these renderings, we have
found many instances where they do
not conform to the 2D specifications
shown on drawings. Since we cannot
vouch for their accuracy, we decline to
post them.
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e. Other
In response to some of the comments,
this section clarifies or explains some of
the statements in the preamble of the
Part 572 NPRM. These clarifications do
not affect the regulatory text or TDP
specifying the HIII–10C for
incorporation into Part 572.
srobinson on DSK4SPTVN1PROD with RULES2
1. Labeling the Dummy as a ‘‘Ten Year
Old’’
As noted earlier in this preamble,
among the ATDs described in 49 CFR
part 572, the HIII–10C successfully fills
the size gap between the existing HIII–
6C and the Hybrid III 5th percentile
adult female dummy. The majority of
the commenters were supportive of the
use of the HIII–10C. However, AAP
noted that the height and weight of the
HIII–10C do not correspond to an
average 10-year-old child as indicated
by growth charts published by the
Center for Disease Control (CDC). AAP
stated that, according to growth charts
from 2000, the HIII–10C falls into the
50th–75th percentile in weight, but at
130 centimeters (cm) tall, it is only in
the 5th–10th percentile in standing
height. AAP believed that these
proportions do not represent any
average human child and may better
represent a nine-year-old child than a
ten-year-old. This comment was echoed
by Advocates. Although neither
organization objected to the use of the
dummy in the FMVSS, both apparently
believe that the discrepancy in the
proportions of the HIII–10C may
confuse or mislead the general public on
the applicability of booster seats. Thus,
both organizations believe the agency
should explain how we defined ‘‘tenyear-old’’ as it relates to human children
and the description of the HIII–10C.
Agency response. The target design
for the HIII–10C dummy was an ATD
that was suitable for assessing CRSs
rated for children weighing about 36.3
kg (80 lb). At 35.4 kg (78 lb), the HIII–
10C fulfills this objective. As such, the
design intent of the dummy was not to
conform rigorously to the
anthropometry of a child of a particular
age, weight, or height percentile.
Furthermore, the sitting height—not the
standing height—is of primary
importance when evaluating booster
seats because the overlay of the seat belt
system onto the dummy is depended on
its seated posture. As pointed out by
AAP, the sitting height of the HIII–10C
falls into the same growth chart range
for sitting height as it does for weight.
Nevertheless, the agency believes that
the proportions of the HIII–10C are more
consistent with an average 10-year-old
than indicated by AAP’s comments.
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Characteristic dimensions and segment
weights of the HIII–10C are based on the
anthropometry of the average 10-yearold as identified by Mertz et al.,25 to
which the dummy is shown to match
closely.
Moreover, we note that our declared
standing height of 130 cm is only an
approximation, not a direct
measurement. The HIII–10C has no oneto-one correspondence with the heights
shown on CDC growth charts. The CDC
reference for standing height is one that
is taken when subjects are maximally
erect. Like all full ATDs in Part 572, the
HIII–10C is a sitting dummy. Since it
cannot be placed in a standing position,
its ‘‘standing height’’ cannot be
measured directly. Instead, it is
approximated by summing the lengths
of its body segments. However, since the
dummy is constructed to represent a
reclined and supported seated posture,
not an erect posture, the summed
lengths underestimate the CDC standing
height. This means that if an actual
child with sitting dimensions equal to
those of the HIII–10C stood in a
maximally erect posture, his/her height
would probably be greater than 130 cm.
2. Best Practices for Belt Routing
In citing a 2005 paper by Tylko and
Dalmotas,26 the Alliance observed that
the chest deflection of the HIII–10C in
the booster seat was higher than it was
when it was used without the booster
seat. In the non-booster test, the belt was
routed close to the neck where that the
dummy’s central sternal potentiometer
was not sensitive to high belt loading.
(This insensitivity is common to all
ATDs in the Hybrid III family of
dummies.) The Alliance has asked the
agency to raise awareness of this issue
so that the positive effects of booster
seats are not mistakenly maligned.
Agency response. As a point of
clarification, we note that an injury
criterion based on chest deflection is not
included in FMVSS No. 213. Further,
we also note that the authors of the
study make the point that limiting the
analysis to chest responses could lead to
false conclusions, and that multiple
injury metrics should be used, not just
chest deflection.
The agency agrees that low chest
deflections alone are not always a good
indicator of a safe condition. Low
deflections often accompany cases of
25 Mertz HJ, Jarrett K, Moss S, Salloum M, ZhaoY,
The Hybrid III 10-Year-Old Dummy, Stapp Car
Crash Journal, Vol. 45, November 2001.
26 Tylko S, Dalmotas D (2005), ‘‘Protection of Rear
Seat Occupants in Frontal Crashes,’’ Proceedings of
the 19th International Technical Conference on the
Enhanced Safety of Vehicles Conference, Paper No.
05–258.
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submarining and high knee excursion.
Low chest deflections can also occur
when the belt migrates laterally off the
shoulder so that the thorax is not held
back and head excursion is exceedingly
high. This exemplifies why multiple
injury metrics are usually needed to
evaluate a safety system. For FMVSS
No. 213, we assess booster seats by
evaluating the HIII–10C’s chest
acceleration, head excursion, and knee
excursion concurrently. The agency
does not believe that either FMVSS No.
213 or the HIII–10C promotes a poor
booster seat design in which the
shoulder belt is routed close to the neck.
As discussed in this rulemaking, we
have found that the HIII–10C dummy
adequately distinguishes good vs. bad
belt routing in the CRS test
environment.
3. Abdominal Injury Correlates
The August 31, 2005 NPRM on
FMVSS No. 213 discussed NHTSA’s
work developing abdominal injury
criteria for the HIII–10C, including our
work on the ‘‘abdominal injury ratio’’
(AIR), which uses impulse calculations
from the iliac compressive and lumbar
shear forces to identify dummy
kinematics associated with
submarining. A high AIR value occurs
with diminished iliac loads in the
presence of high lumbar shear loads.
This indicates that the belt may have
slipped off the iliac and the dummy
may have submarined. Thus, greater
AIR values correlate indirectly to
abdominal injuries.
In comments to the Part 572 NPRM,
Advocates requested that the agency
implement AIR until such time as an
alternative abdominal injury measure
has been established.
Agency response. AIR was not
proposed in the FMVSS No. 213 NPRM
or SNPRMs due to limited data and is
not included in the final rule. We note
that AIR is empirical; it is not founded
upon the biomechanics of injury. (I.e.,
reduced iliac loads do not cause
abdominal injuries. They only identify
instances where a belt may have slipped
into the abdomen of the dummy, which
may or may not lead to injury.) If the
AIR criterion were to be imposed, CRS
manufacturers could maximize iliac
loads to achieve a good AIR score. We
have concerns about criteria that
encourage high loads of any sort, as this
could potentially increase injury risk in
another body region or produce some
other unexpected consequence.
For immediate use now, the agency
has adopted the use of a correlate to
abdominal injuries, i.e., knee excursion.
The final rule for FMVSS No. 213
imposes limits on knee excursion and
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head excursion for the HIII–10C. The
limit on knee excursion prevents
restraint manufacturers from controlling
head excursion by designing their
restraints so that children submarine
excessively during a crash. The agency
has observed a strong correlation
between knee excursion and
submarining in the child dummies.27
Ultimately, a direct biomechanicallybased measure of abdominal
deformation provides the best means to
assess abdominal injuries. Our research
plan for the HIII–10C includes
developing a pelvis and abdominal
modification that will provide such a
measurement.
4. Repeatability in Systems Testing
In the Part 572 NPRM, the agency
reported on a series of repeatability tests
using a dynamic sled. The tests were
carried out using a specialized booster
seat designed for repeated use. Dorel
commented that they cannot follow this
protocol when certifying its own seats.
Dorel also commented that our
repeatability tests seemed to assure a
best-case outcome in terms of dummy
injury metrics.
Agency response. Dorel may have
misconstrued our reporting of these
tests as a mandate for additional
procedures necessary to qualify the
HIII–10C and certify booster seats. This
was not our intent. The series of tests
were not directly applicable to
compliance testing of booster seats. The
purpose of the sled tests was to evaluate
the repeatability and durability of the
HIII–10C dummy kinematics in a pulse
approaching FMVSS No. 213 severity.
The tests were not to create a best-case
scenario for injury reference values. We
chose to use a rigid bench seat in
conjunction with a limited number of
CRS models to minimize the effects of
set-up related variables which otherwise
could interfere with the assessment of
the dummy’s own true consistency.
f. Dummy Development Efforts
srobinson on DSK4SPTVN1PROD with RULES2
1. Hybrid III Child Dummy Revisions—
Abdomen and Pelvis
Citing the significance of abdominal
injuries in children and the lack of
instrumentation in the HIII–10C, both
CHOP and Advocates urged the agency
to redouble our efforts to come up with
an appropriate means to assess
abdominal injuries with the dummy.
Dorel, AAP, and UMTRI also
27 Klinich, K., Reed, M., Orton, N., Manary, M.,
Rupp, J., ‘‘Optimizing Protection for Rear Seat
Occupants: Assessing Booster Performance with
Realistic Belt Geometry Using the Hybrid III 6YO
ATD,’’ UMTRI Report, University of Michigan, Ann
Arbor, MI, March 2011.
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commented on importance of assessing
abdominal injuries.
Since the NPRMs of 2005, NHTSA has
been actively involved in two principal
research efforts aimed at improving
abdominal injury assessment in Hybrid
III child ATDs. The two efforts focus on
the development of a biofidelic,
instrumented abdomen along with an
appropriately proportioned pelvis.
One effort involves a concept for a
fluid-filled abdomen that was reported
in 2001.28 Since then, it has been
developed into a silicone shell filled
with silicone gel with instrumentation
to measure deformation. The shell takes
the form of an insert that fills the
abdominal cavity of the HIII–6C. The
abdominal insert has proven to be
reasonably biofidelic when compared
with the response of an age-matched
animal surrogate.29 The other effort
involves the modification of a standard
HIII–6C pelvis to more closely reflect
child anthropometry based on data
collected by UMTRI on child
participants.30
NHTSA has also begun work with an
SAE working group devoted to
integrating abdomen and pelvis
technology into the HIII–6C (the SAE
dummy abdomen pelvis round robin
(DAPRR) working group (August 2008)).
In DAPRR, NHTSA is facilitating the
development of prototype pelves using
UMTRI design criteria 31 to develop a
biofidelic retrofit package suitable for
assessing pediatric abdominal injuries.
Round-robin testing of the prototypes is
planned for 2012. The HIII–6C is the
primary target of the developing
modifications given the greater use rates
of six-year-olds vs. ten-year-olds in
child restraint systems regulated by
FMVSS No. 213. The new pelvis and
abdomen designs could possibly be
transitioned to the ten-year-old size
through dimensional scaling and
considerations for biomechanical
response differences.
28 Rouhana et al. (2001), ‘‘Development of a
Reusable, Rate-sensitive Abdomen for the Hybrid III
Family of Dummies,’’ Stapp Car Crash Journal, V45.
29 Kent R, Stacey S, Kindig M, Forman J, Woods
W (2006), ‘‘Biomechanical Response of the Pediatric
Abdomen, Part 1: Development of an Experimental
Model and Quantification of Structural Response to
Dynamic Belt Loading,’’ Stapp Car Crash Journal,
V50, 2006–22–0001.
30 Klinich, K et al. (2010), ‘‘Development and
Testing of a More Realistic Pelvis for the Hybrid III
6-Year-Old ATD,’’ Traffic Injury Prevention,
11:606–612.
31 Reed MP, Sochor MM, Rupp JD, Klinich KD,
Manary MA (2009), ‘‘Anthropometric Specification
of Child Crash Dummy Pelves through Statistical
Analysis of Skeletal Geometry,’’ Journal of
Biomechanics, V42: 1143–1145.
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2. Pediatric Research
CHOP, AAP, and Advocates have
asked the agency to intensify our
research efforts in child biomechanics
in general. Many noted that current
pediatric crash test dummies have been
developed based on biofidelity
requirements that were scaled from
adult response data.
Since the NPRMs of 2005, the agency
has been engaged in several activities
aimed at new child specific biofidelity
requirements for use in the development
of new frontal impact child dummies.
These are summarized below and
discussed more fully in NHTSA’s
Biomechanics Research Plan, 2011–
2015.32
Child anthropometry. In order to
properly assess a child’s interaction
with a booster seat and belt system, we
are building a child anthropometry
database by collecting whole-body laser
scans of 3-, 6- and 10-year-old age
ranges in automotive seating positions.
Biomechanical response. We have
several projects focused on getting
response data that is unique to the
pediatric human and not scaled from
adult data. For example, to better
understand the deformation
characteristics of a pediatric thorax, we
are collecting force versus deflection
data during cardiopulmonary
resuscitation of pediatric hospital
patients. Additionally, we are collecting
data from sled tests of pediatric agematched surrogates that are being used
to quantify thoracic response and spinal
kinematics.
Biomechanics of injury. We are
studying the relationship between local
brain tissue strain and axonal injury in
a prepubescent human. This has
potential to be used for the basis of new
brain injury criteria for children.
Child dummy development. The
agency has begun assessing current
child ATDs (including those in the
Hybrid III family as well as the Q-series)
against new pediatric response data.
Our first consideration is the need for
developing an all-new 6-year-old ATD
versus enhancement of the existing
HIII–6C. Thereafter, we will consider
the need for an advanced 10-year-old
ATD.
3. Status of HIC
Advocates have asked the agency to
work expeditiously to reinstate a head
injury criterion for the HIII–10C.
The agency is committed to resolving
the problem that led to our decision to
omit HIC as a criterion in FMVSS No.
32 NHTSA’s Biomechanics Research Plan, 2011–
2015, Report No. DOT HS 811 474, U.S. Department
of Transportation, Washington DC, June 2011.
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213 when testing with the HIII–10C. The
problem, explained earlier, stems from
ATD whole-body motions that induce a
hard chin-to-chest contact, not HIC
itself. We are working to improve the
ATD’s chin and sternum designs to
mitigate this effect. As described under
the heading of child biomechanics
within the NHTSA Biomechanics
Research Plan,33 we are also working to
attain a better understanding of
pediatric body motions in order to
engineer a biofidelic head response into
an ATD. This includes efforts to
characterize the flexibility of an
adolescent thoracic spine and its effect
on head excursion and upper neck
loads. Furthermore, research is
underway to better understand the
interaction between the shoulder belt
and clavicle and its effect on head
motion. We are also examining the
extent to which chin-to-chest contacts
actually occur to children in booster
seats in order to model the interaction
correctly with a child ATD.
srobinson on DSK4SPTVN1PROD with RULES2
V. Rulemaking Analyses and Notices
Executive Order (E.O.) 12866, E.O.
13563 and DOT Regulatory Policies and
Procedures
This rulemaking action has
considered the impact of this regulatory
action under E.O. 12866 and E.O.13563
and the Department of Transportation’s
(DOT) regulatory policies and
procedures. This rulemaking action was
not reviewed by the Office of
Management and Budget under E.O.
12866. The rulemaking has also been
determined not to be significant under
DOT’s regulatory policies and
procedures (44 FR 11034, February 26,
1979).
There are benefits associated with this
rulemaking but they cannot be
quantified. The incorporation of the test
dummy into 49 CFR part 572 will
permit NHTSA to use the ATD in
FMVSS No. 213 compliance testing of
CRSs for children weighing over 65 lb.
In addition, the availability of this
dummy in a regulated format will
benefit safety by providing a more
suitable, stabilized, and objective test
tool to the safety community for use in
research and development of child
passenger safety products.
Based on our dummy purchase
contract with FTSS/Denton, the
estimated cost of an uninstrumented
HIII–10C dummy is approximately
$35,000. Instruments necessary to
qualify the dummy in accordance with
33 NHTSA’s Biomechanics Research Plan, 2011–
2015, Report No. DOT HS 811 474, U.S. Department
of Transportation, Washington DC, June 2011,
pp. 6–10.
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Part 572 include 3 accelerometers for
the head (about $500 apiece) and an
upper neck load cell (about $10,000).
The central sternal potentiometer,
needed for the thorax qualification
procedure, is included in the base cost
of the dummy. For compliance testing,
only three accelerometers are needed;
they are located at the CG of the thorax
rather than the head. All sensors
required in compliance and certification
procedures are common with other 49
CFR part 572 dummies, so the cost of
those instruments may be defrayed to
some extent for those who already own
them. If the dummy is outfitted with all
instrumentation up to its full capability,
the total instrumentation cost is about
$65,000 in addition to the cost of the
dummy.
This document amends 49 CFR part
572 by adding design and performance
specifications for a test dummy
representative of a ten-year-old child
that the agency will use in compliance
tests of the Federal child restraint
system safety standard, and may use for
research purposes. This Part 572 rule
does not impose any requirements on
anyone. Businesses are affected only if
they choose to manufacture or test with
the dummy. Because the economic
impacts of this final rule are minimal,
no further regulatory evaluation is
necessary.
Regulatory Flexibility Act
Pursuant to the Regulatory Flexibility
Act (5 U.S.C. 601 et seq., as amended by
the Small Business Regulatory
Enforcement Fairness Act (SBREFA) of
1996), whenever an agency is required
to publish a proposed or final rule, it
must prepare and make available for
public comment a regulatory flexibility
analysis that describes the effect of the
rule on small entities (i.e., small
businesses, small organizations, and
small governmental jurisdictions),
unless the head of the agency certifies
the rule will not have a significant
economic impact on a substantial
number of small entities. The Small
Business Administration’s regulations at
13 CFR part 121 define a small business,
in part, as a business entity ‘‘which
operates primarily within the United
States.’’ (13 CFR 121.105(a)).
We have considered the effects of this
rulemaking under the Regulatory
Flexibility Act. I hereby certify that this
rulemaking action will not have a
significant economic impact on a
substantial number of small entities.
This action will not have a significant
economic impact on a substantial
number of small entities because the
addition of the test dummy to Part 572
does not impose any requirements on
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anyone. NHTSA will not require anyone
to manufacture the dummy or to test
motor vehicles or motor vehicle
equipment with it.
National Environmental Policy Act
NHTSA has analyzed this final rule
for the purposes of the National
Environmental Policy Act and
determined that it will not have any
significant impact on the quality of the
human environment.
Executive Order 13045 and 12132
(Federalism)
Executive Order 13045 (62 FR 19885,
April 23, 1997) applies to any rule that:
(1) is determined to be ‘‘economically
significant’’ as defined under E.O.
12866, and (2) concerns an
environmental, health, or safety risk that
NHTSA has reason to believe may have
a disproportionate effect on children. If
the regulatory action meets both criteria,
we must evaluate the environmental
health or safety effects of the planned
rule on children, and explain why the
planned regulation is preferable to other
potentially effective and reasonably
feasible alternatives considered by us.
This final rule is not subject to the
Executive Order because it is not
economically significant as defined in
E.O. 12866.
NHTSA has examined this final rule
pursuant to Executive Order 13132 (64
FR 43255, August 10, 1999) and
concluded that no additional
consultation with States, local
governments or their representatives is
mandated beyond the rulemaking
process. The agency has concluded that
the final rule does not have federalism
implications because the rule does not
have ‘‘substantial direct effects on the
States, on the relationship between the
national government and the States, or
on the distribution of power and
responsibilities among the various
levels of government.’’ This rule will
not impose any requirements on
anyone. Businesses will be affected only
if they choose to manufacture or test
with the dummy.
Further, no consultation is needed to
discuss the preemptive effect of this
final rule. NHTSA’s safety standards can
have preemptive effect in two ways.
This final rule amends 49 CFR part 572
and is not a safety standard.34 This Part
34 With respect to the safety standards, the
National Traffic and Motor Vehicle Safety Act
contains an express preemptive provision: ‘‘When
a motor vehicle safety standard is in effect under
this chapter, a State or a political subdivision of a
State may prescribe or continue in effect a standard
applicable to the same aspect of performance of a
motor vehicle or motor vehicle equipment only if
the standard is identical to the standard prescribed
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572 final rule does not impose any
requirements on anyone.
Civil Justice Reform
With respect to the review of the
promulgation of a new regulation,
section 3(b) of Executive Order 12988,
‘‘Civil Justice Reform’’ (61 FR 4729,
February 7, 1996) requires that
Executive agencies make every
reasonable effort to ensure that the
regulation: (1) Clearly specifies the
preemptive effect; (2) clearly specifies
the effect on existing Federal law or
regulation; (3) provides a clear legal
standard for affected conduct, while
promoting simplification and burden
reduction; (4) clearly specifies the
retroactive effect, if any; (5) adequately
defines key terms; and (6) addresses
other important issues affecting clarity
and general draftsmanship under any
guidelines issued by the Attorney
General. This document is consistent
with that requirement.
Pursuant to this Order, NHTSA notes
as follows.
The issue of preemption is discussed
above in connection with E.O. 13132.
NHTSA notes further that there is no
requirement that individuals submit a
petition for reconsideration or pursue
other administrative proceeding before
they may file suit in court.
Paperwork Reduction Act
Under the Paperwork Reduction Act
of 1995, a person is not required to
respond to a collection of information
by a Federal agency unless the
collection displays a valid control
number from the Office of Management
and Budget (OMB). This rule will not
have any requirements that are
considered to be information collection
requirements as defined by the OMB in
5 CFR part 1320.
srobinson on DSK4SPTVN1PROD with RULES2
National Technology Transfer and
Advancement Act
Section 12(d) of the National
Technology Transfer and Advancement
Act of 1995 (NTTAA), Public Law 104–
113, section 12(d) (15 U.S.C. 272)
directs NHTSA to use voluntary
consensus standards in its regulatory
activities unless doing so would be
inconsistent with applicable law or
otherwise impractical. Voluntary
under this chapter.’’ 49 U.S.C. 30103(b)(1). Second,
the Supreme Court has recognized the possibility of
implied preemption: State requirements imposed
on motor vehicle manufacturers, including
sanctions imposed by State tort law, can stand as
an obstacle to the accomplishment and execution of
a NHTSA safety standard. When such a conflict
exists, the Supremacy Clause of the Constitution
makes the State requirements unenforceable. See
Geier v. American Honda Motor Co., 529 U.S. 861
(2000).
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consensus standards are technical
standards (e.g., materials specifications,
test methods, sampling procedures, and
business practices) that are developed or
adopted by voluntary consensus
standards bodies. The NTTAA directs
NHTSA to provide Congress, through
OMB, explanations when the agency
decides not to use available and
applicable voluntary consensus
standards.
The test dummy and qualification
requirements are based on the work of
the SAE Hybrid III Dummy Family Task
Group (DFTG). Differences between the
DFTG recommendations and this final
rule are minor and are based on
additional research performed by the
agency and on comments to the NPRM.
The following voluntary consensus
standards have been used in developing
the HIII–10C dummy:
• SAE Recommended Practice J211,
Rev. Mar 95, ‘‘Instrumentation for
Impact Tests—Part 1—Electronic
Instrumentation’’; and,
• SAE J1733 of 1994–12 ‘‘Sign
Convention for Vehicle Crash Testing.’’
Unfunded Mandates Reform Act
Section 202 of the Unfunded
Mandates Reform Act of 1995 (UMRA),
Public Law 104–4, requires Federal
agencies to prepare a written assessment
of the costs, benefits, and other effects
of proposed or final rules that include
a Federal mandate likely to result in the
expenditure by State, local, or tribal
governments, in the aggregate, or by the
private sector, of more than $100
million annually (adjusted for inflation
with base year of 1995). Before
promulgating a NHTSA rule for which
a written statement is needed, section
205 of the UMRA generally requires the
agency to identify and consider a
reasonable number of regulatory
alternatives and adopt the least costly,
most cost-effective, or least burdensome
alternative that achieves the objectives
of the rule.
This final rule does not impose any
unfunded mandates under the UMRA.
This rule does not meet the definition
of a Federal mandate because it does not
impose requirements on anyone. It
amends 49 CFR part 572 by adding
design and performance specifications
for a 10-year-old test dummy that the
agency will use in FMVSS No. 213 and
for research purposes. This final rule
affects only those businesses that choose
to manufacture or test with the dummy.
It would not result in costs of $100
million or more to either State, local, or
tribal governments, in the aggregate, or
to the private sector.
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Plain Language
Executive Order 12866 requires each
agency to write all rules in plain
language. Application of the principles
of plain language includes consideration
of the following questions:
—Has the agency organized the material
to suit the public’s needs?
—Are the requirements in the rule
clearly stated?
—Does the rule contain technical
language or jargon that is not clear?
—Would a different format (grouping
and order of sections, use of headings,
paragraphing) make the rule easier to
understand?
—Would more (but shorter) sections be
better?
—Could the agency improve clarity by
adding tables, lists, or diagrams?
—What else could the agency do to
make this rulemaking easier to
understand?
If you have any responses to these
questions, please send them to NHTSA.
Regulation Identifier Number
The Department of Transportation
assigns a regulation identifier number
(RIN) to each regulatory action listed in
the Unified Agenda of Federal
Regulations. The Regulatory Information
Service Center publishes the Unified
Agenda in April and October of each
year. You may use the RIN contained in
the heading at the beginning of this
document to find this action in the
Unified Agenda.
Petitions for Reconsideration of This
Rule
The petition will be placed in the
docket. Anyone is able to search the
electronic form of all documents
received into any of our dockets by the
name of the individual submitting the
comment (or signing the comment, if
submitted on behalf of an association,
business, labor union, etc.). You may
review DOT’s complete Privacy Act
Statement in the Federal Register
published on April 11, 2000 (Volume
65, Number 70; Pages 19477–78).
List of Subjects in 49 CFR Part 572
Motor vehicle safety, Incorporation by
reference.
In consideration of the foregoing,
NHTSA amends 49 CFR Part 572 as
follows:
PART 572—ANTHROPOMORPHIC
TEST DUMMIES
1. The authority citation for Part 572
continues to read as follows:
■
Authority: 49 U.S.C. 322, 30111, 30115,
30117 and 30166; delegation of authority at
49 CFR 1.50.
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2. 49 CFR Part 572 is amended by
adding a new Subpart T consisting of
572.170—572.177 to read as follows:
■
Subpart T—Hybrid III 10-Year-Old Child
Test Dummy (HIII–10C)
Sec.
572.170 Incorporation by reference.
572.171 General description.
572.172 Head assembly and test procedure.
572.173 Neck assembly and test procedure.
572.174 Thorax assembly and test
procedure.
572.175 Upper and lower torso assemblies
and torso flexion test procedure.
572.176 Knees and knee impact test
procedure.
572.177 Test conditions and
instrumentation.
Appendix—Figures to Subpart T of Part 572
§ 572.170
Incorporation by reference.
(a) Certain material is incorporated by
reference (IBR) into this part with the
approval of the Director of the Federal
Register under 5 U.S.C. 552(a) and 1
CFR part 51. To enforce any edition
other than that specified in this section,
NHTSA must publish notice of change
in the Federal Register and the material
must be available to the public. All
approved material is available for
inspection at the Department of
Transportation, Docket Operations,
Room W12–140, telephone 202–366–
9826, and is available from the sources
listed below. The material is available in
electronic format through
Regulations.gov, call 1–877–378–5457
or go to www.regulations.gov. It is also
available for inspection at the National
Archives and Records Administration
(NARA). For information on the
availability of this material at NARA,
call 202–741–6030 or go to https://
www.archives.gov/federal-register/cfr/
ibr-locations.html.
(b) NHTSA Technical Information
Services, 1200 New Jersey Ave., SE.,
Washington, DC 20590, telephone 202–
366–5965.
(1) A parts/drawing list entitled,
‘‘Parts/Drawing List, Part 572 Subpart T,
Hybrid III 10-Year-Old Child Test
Dummy (HIII–10C), August 2011,’’ IBR
approved for § 572.171.
(2) A drawings and inspection
package entitled, ‘‘Parts List and
Drawings, Part 572 Subpart T, Hybrid III
10-Year-Old Child Test Dummy (HIII–
10C), August 2011,’’ IBR approved for
§ 572.171, including:
(i) Drawing No. 420–0000, Complete
Assembly HIII 10-year-old, IBR
approved for §§ 572.171, 572.172,
572.173, 572.174, 572.176, and 572.177.
(ii) Drawing No. 420–1000, Head
Assembly, IBR approved for § 572.171,
§ 572.172, § 572.173, and § 572.177.
(iii) Drawing No. 420–2000, Neck
Assembly, IBR approved for §§ 572.171,
572.173, and 572.177.
(iv) Drawing No. 420–3000, Upper
Torso Assembly, IBR approved for
§§ 572.171, 572.174, 572.175, and
572.177.
(v) Drawing No. 420–4000, Lower
Torso Assembly, IBR approved for
§§ 572.171, 572.174, 572.175, and
572.177.
(vi) Drawing No. 420–5000–1,
Complete Leg Assembly—left, IBR
approved for §§ 572.171, 572.176, and
572.177.
(vii) Drawing No. 420–5000–2,
Complete Leg Assembly—right, IBR
approved for §§ 572.171, 572.176, and
572.177.
(viii) Drawing No. 420–7000–1,
Complete Arm Assembly—left, IBR
approved for § 572.171, and,
(ix) Drawing No. 420–7000–2,
Complete Arm Assembly—right, IBR
approved for § 572.171.
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(3) A procedures manual entitled
‘‘Procedures for Assembly, Disassembly
and Inspection (PADI) of the Hybrid III
10-Year-Old Child Test Dummy (HIII–
10C), August 2011’’; IBR approved for
§§ 572.171 and 572.177.
(c) SAE International, 400
Commonwealth Drive, Warrendale, PA
15096, call 1–877–606–7323.
(1) SAE Recommended Practice J211/
1, Rev. Mar 95, ‘‘Instrumentation for
Impact Tests—Part 1—Electronic
Instrumentation,’’ IBR approved for
§ 572.177.
(2) SAE Information Report J1733 of
1994–12, ‘‘Sign Convention for Vehicle
Crash Testing,’’ December 1994, IBR
approved for § 572.177.
§ 572.171
General description.
(a) The Hybrid III 10-year-old Child
Test Dummy (HIII–10C) is defined by
drawings and specifications containing
the following materials:
(1) The parts enlisted in ‘‘Parts/
Drawing List, Part 572 Subpart T,
Hybrid III 10-Year-Old Child Test
Dummy (HIII–10C), August 2011’’
(incorporated by reference, see
§ 572.170),
(2) The engineering drawings and
specifications contained in ‘‘Parts List
and Drawings, Part 572 Subpart T,
Hybrid III 10-Year-Old Child Test
Dummy (HIII–10C), August 2011,’’
which includes the engineering
drawings and specifications described
in Drawing 420–0000, the titles of the
assemblies of which are listed in Table
A, and,
(3) A manual entitled ‘‘Procedures for
Assembly, Disassembly and Inspection
(PADI) of the Hybrid III 10-Year-Old
Child Test Dummy (HIII–10C), August
2011.’’
TABLE A
Component assembly
Drawing No.
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(i) Head Assembly .......................................................................................................................................................................
(ii) Neck Assembly .......................................................................................................................................................................
(iii) Upper Torso Assembly ..........................................................................................................................................................
(iv) Lower Torso Assembly ..........................................................................................................................................................
(v) Complete Leg Assembly—left ................................................................................................................................................
(vi) Complete Leg Assembly—right .............................................................................................................................................
(vii) Complete Arm Assembly—left ..............................................................................................................................................
(viii) Complete Arm Assembly—right ...........................................................................................................................................
(b) The structural properties of the
dummy are such that the dummy
conforms to this Subpart in every
respect before use in any test.
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§ 572.172 Head assembly and test
procedure.
(a) The head assembly for this test
consists of the complete head (drawing
420–1000), a six-axis neck transducer
(drawing SA572–S11, included in
drawing 420–0000), or its structural
replacement (drawing 420–383X), and 3
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420–1000
420–2000
420–3000
420–4000
420–5000–1
420–5000–2
420–7000–1
420–7000–2
accelerometers (drawing SA572–S4,
included in drawing 420–0000) (all
incorporated by reference, see
§ 572.170).
(b) When the head assembly is
dropped from a height of 376.0 ± 1.0
mm (14.8 ± 0.04 in) in accordance with
paragraph (c) of this section, the peak
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resultant acceleration at the location of
the accelerometers at the head CG may
not be less than 250 G or more than 300
G. The resultant acceleration vs. time
history curve shall be unimodal;
oscillations occurring after the main
pulse must be less than 10 percent of
the peak resultant acceleration. The
lateral acceleration shall not exceed 15
G (zero to peak).
(c) Head test procedure. The test
procedure for the head is as follows:
(1) Soak the head assembly in a
controlled environment at any
temperature between 18.9 and 25.6 °C
(66 and 78 °F) and a relative humidity
from 10 to 70 percent for at least four
hours prior to a test.
(2) Prior to the test, clean the impact
surface of the skin and the impact plate
surface with isopropyl alcohol,
trichloroethane, or an equivalent. The
skin of the head must be clean and dry
for testing.
(3) Suspend and orient the head
assembly as shown in Figure T1. The
lowest point on the forehead must be
376.0 ± 1.0 mm (14.8 ± 0.04 in) from the
impact surface. The 1.57 mm (0.062 in)
diameter holes located on either side of
the dummy’s head shall be used to
ensure that the head is level with
respect to the impact surface.
(4) Drop the head assembly from the
specified height by means that ensure a
smooth, instant release onto a rigidly
supported flat horizontal steel plate
which is 50.8 mm (2 in) thick and 610
mm (24 in) square. The impact surface
shall be clean, dry and have a micro
finish of not less than 203.2 × 10¥6 mm
(8 micro inches) (RMS) and not more
than 2032.0 × 10¥6 mm (80 micro
inches) (RMS).
(5) Allow at least 2 hours between
successive tests on the same head.
§ 572.173 Neck assembly and test
procedure.
(a) The neck assembly for the
purposes of this test consists of the
assembly of components shown in
drawing 420–2000 (incorporated by
reference, see § 572.170).
(b) When the head-neck assembly
consisting of the head (drawing 420–
1000), neck (drawing 420–2000), six-
channel neck transducer (SA572–S11,
included in drawing 420–0000), lower
neck bracket assembly (drawing 420–
2070), and either three uniaxial
accelerometers (drawing SA572–S4,
included in drawing 420–0000) or their
mass equivalent installed in the head
assembly as specified in drawing 420–
1000 (all incorporated by reference, see
§ 572.170), is tested according to the test
procedure in paragraph (c) of this
section, it shall have the following
characteristics:
(1) Flexion. (i) Plane D, referenced in
Figure T2, shall rotate in the direction
of preimpact flight with respect to the
pendulum’s longitudinal centerline
between 76 degrees and 90 degrees.
During the time interval while the
rotation is within the specified corridor,
the peak moment, measured by the neck
transducer (drawing SA572–S11,
included in drawing 420–0000)
(incorporated by reference, see
§ 572.170), about the occipital condyles
may not be less than 50 N-m (36.9 ft-lbf)
and not more than 62 N-m (45.7 ft-lbf).
The positive moment shall decay for the
first time to 10 N-m (7.4 ft-lbf) between
86 ms and 105 ms after time zero.
(ii) The moment shall be calculated by
the following formula: Moment (N-m) =
My ¥ (0.01778) × (Fx).
(iii) My is the moment about the y-axis
in Newton-meters, Fx is the shear force
measured by the neck transducer
(drawing SA572–S11) in Newtons, and
0.01778 is the distance in meters from
the load center of the neck transducer to
the occipital condyle.
(2) Extension. (i) Plane D, referenced
in Figure T3, shall rotate in the
direction of preimpact flight with
respect to the pendulum’s longitudinal
centerline between 96 degrees and 115
degrees. During the time interval while
the rotation is within the specified
corridor, the peak moment, measured by
the neck transducer (drawing SA572–
S11, included in drawing 420–0000)
(incorporated by reference, see
§ 572.170), about the occipital condyles
may not be more than ¥37 N-m (¥27.3
ft-lbf) and not less than ¥46 N-m
(¥33.9 ft-lbf). The positive moment
shall decay for the first time to ¥10 N-
m (¥7.4 ft-lbf) between 100 ms and 116
ms after time zero.
(ii) The moment shall be calculated by
the following formula: Moment (N-m) =
My ¥ (0.01778) × (Fx).
(iii) My is the moment about the y-axis
in Newton-meters, Fx is the shear force
measured by the neck transducer
(drawing SA572–S11, included in
drawing 420–0000) (incorporated by
reference, see § 572.170) in Newtons,
and 0.01778 is the distance in meters
from the load center of the neck
transducer to the occipital condyle.
(3) Time zero is defined as the time
of initial contact between the pendulum
striker plate and the honeycomb
material. All data channels shall be at
the zero level at this time.
(c) Test procedure. The test procedure
for the neck assembly is as follows:
(1) Soak the neck assembly in a
controlled environment at any
temperature between 20.6 and 22.2 °C
(69 and 72 °F) and a relative humidity
between 10 and 70 percent for at least
four hours prior to a test.
(2) Torque the hex nut (drawing 420–
2000, part 9000130) on the neck cable
(drawing 420–2060) (both incorporated
by reference, see § 572.170) to 0.9 ± 0.2
N-m (8 ± 2 in-lbf) before each test on the
same neck.
(3) Mount the head-neck assembly,
defined in paragraph (b) of this section,
on the pendulum described in Figure 22
of 49 CFR part 572 so that the leading
edge of the lower neck bracket coincides
with the leading edge of the pendulum
as shown in Figure T2 for flexion tests
and Figure T3 for extension tests.
(4)(i) Release the pendulum and allow
it to fall freely from a height to achieve
an impact velocity of 6.1 ± 0.12 m/s
(20.0 ± 0.4 ft/s) for flexion tests and 5.03
± 0.12 m/s (16.50 ± 0.40 ft/s) for
extension tests, measured by an
accelerometer mounted on the
pendulum as shown in Figure T2 at the
instant of contact with the honeycomb.
(ii) Stop the pendulum from the
initial velocity with an acceleration vs.
time pulse that meets the velocity
change as specified below. Integrate the
pendulum acceleration data channel to
obtain the velocity vs. time curve:
srobinson on DSK4SPTVN1PROD with RULES2
TABLE B—PENDULUM PULSE
Flexion
Time
(ms)
M/s
10 .....................................................................................................................
20 .....................................................................................................................
30 .....................................................................................................................
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1.64–2.04
3.04–4.04
4.45–5.65
Extension
ft/s
m/s
5.38–6.69
9.97–13.25
14.60–18.53
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1.49–1.89
2.88–3.68
4.20–5.20
ft/s
4.89–6.20
9.45–12.07
13.78–17.06
Federal Register / Vol. 77, No. 38 / Monday, February 27, 2012 / Rules and Regulations
srobinson on DSK4SPTVN1PROD with RULES2
§ 572.174 Thorax assembly and test
procedure.
(a) The thorax consists of the part of
the torso assembly designated as the
upper torso (drawing 420–3000)
(incorporated by reference, see
§ 572.170).
(b) When the anterior surface of the
thorax of a completely assembled
dummy (drawing 420–0000)
(incorporated by reference, see
§ 572.170) is impacted by a test probe
conforming to section 572.177 at 6.00 ±
0.12 m/s (22.0 ± 0.4 ft/s) according to
the test procedure in paragraph (c) of
this section:
(1) Maximum sternum displacement
(compression) relative to the spine,
measured with chest deflection
transducer (drawing SA572–T4,
included in drawing 420–0000)
(incorporated by reference, see
§ 572.170), must be not less than 37 mm
(1.46 in) and not more than 46 mm (1.81
in). Within this specified compression
corridor, the peak force, measured by
the impact probe as defined in section
572.177 and calculated in accordance
with paragraph (b)(3) of this section,
shall not be less than 2.0 kN (450 lbf)
and not more than 2.45 kN (551 lbf).
The peak force after 20 mm (0.79 in.) of
sternum displacement but before
reaching the minimum required 37 mm
(1.46 in.) sternum displacement limit
shall not exceed 2.52 kN (567 lbf).
(2) The internal hysteresis of the
ribcage in each impact as determined by
the plot of force vs. deflection in
paragraph (a)(1) of this section shall be
not less than 69 percent but not more
than 85 percent. The hysteresis shall be
calculated by determining the ratio of
the area between the loading (from time
zero to maximum deflection) and
unloading portions (from maximum
deflection to zero force) of the force
deflection curve to the area under the
loading portion of the curve.
(3) The force shall be calculated by
the product of the impactor mass and its
measured deceleration.
(c) Test Procedure. The test procedure
for the thorax assembly is as follows:
(1) The dummy is clothed in a form
fitting cotton stretch above-the-elbow
sleeved shirt and above-the-knees pants.
The weight of the shirt and pants shall
not exceed 0.14 kg (0.30 lb) each.
(2) Torque the lumbar cable (drawing
420–4130) (incorporated by reference,
see § 572.170) to 0.9 ± 0.2 N-m (8 ± 2
in-lbf) and set the lumbar adjustment
angle to 12 degrees. Set the neck angle
to 16 degrees.
(3) Soak the dummy in a controlled
environment at any temperature
between 20.6 and 22.2 °C (69 and 72 °F)
and a relative humidity between 10 and
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70 percent for at least four hours prior
to a test.
(4) Seat and orient the dummy on a
seating surface without back support as
shown in Figure T4, with the limbs
extended horizontally and forward,
parallel to the midsagittal plane, the
midsagittal plane vertical within ± 1
degree and the ribs level in the anteriorposterior and lateral directions within ±
0.5 degrees.
(5) Establish the impact point at the
chest midsagittal plane so that the
impact point of the longitudinal
centerline of the probe coincides with
the midsagittal plane of the dummy
within ± 2.5 mm (0.1 in) and is 12.7 ±
1.1 mm (0.5 ± 0.04 in) below the
horizontal-peripheral centerline of the
No. 3 rib and is within 0.5 degrees of a
horizontal line in the dummy’s
midsagittal plane.
(6) Impact the thorax with the test
probe so that at the moment of contact
the probe’s longitudinal centerline falls
within 2 degrees of a horizontal line in
the dummy’s midsagittal plane.
(7) Guide the test probe during impact
so that there is no significant lateral,
vertical, or rotational movement.
(8) No suspension hardware,
suspension cables, or any other
attachments to the probe, including the
velocity vane, shall make contact with
the dummy during the test.
§ 572.175 Upper and lower torso
assemblies and torso flexion test
procedure.
(a) The test objective is to determine
the stiffness of the molded lumbar
assembly (drawing 420–4100),
abdominal insert (drawing 420–4300),
and chest flesh assembly (drawing 420–
3560) on resistance to articulation
between the upper torso assembly
(drawing 420–3000) and lower torso
assembly (drawing 420–4000) (all
incorporated by reference, see
§ 572.170).
(b) When the upper torso assembly of
a seated dummy is subjected to a force
continuously applied at the head to
neck pivot pin level through a rigidly
attached adaptor bracket as shown in
Figure T5 according to the test
procedure set out in paragraph (c) of
this section:
(1) The lumbar spine-abdomen-chest
flesh assembly shall flex by an amount
that permits the upper torso assembly to
translate in angular motion relative to
the vertical transverse plane 35 ± 0.5
degrees at which time the force applied
must be not less than 180 N (40.5 lbf)
and not more than 250 N (56.2 lbf).
(2) Upon removal of the force, the
torso assembly must return to within 8
degrees of its initial position.
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(c) Test Procedure. The test procedure
for the upper/lower torso assembly is as
follows:
(1) Torque the lumbar cable (drawing
420–4130) (incorporated by reference,
see § 572.170) to 0.9 ± 0.2 N-m (8 ± 2
in-lbf) and set the lumbar adjustment
angle to 12 degrees. Set the neck angle
to 16 degrees.
(2) Soak the dummy in a controlled
environment at any temperature
between 20.6 and 22.2 °C (69 and 72 °F)
and a relative humidity between 10 and
70 percent for at least four hours prior
to a test.
(3) Assemble the complete dummy
(with or without the legs below the
femurs) and attach to the fixture in a
seated posture as shown in Figure T5.
(4) Secure the pelvis to the fixture at
the pelvis instrument cavity rear face by
threading four 1⁄4-inch cap screws into
the available threaded attachment holes.
Tighten the mountings so that the test
material is rigidly affixed to the test
fixture and the pelvic-lumbar joining
surface is 18 degrees from horizontal
and the legs are parallel with the test
fixture.
(5) Attach the loading adaptor bracket
to the spine of the dummy as shown in
Figure T5.
(6) Inspect and adjust, if necessary,
the seating of the abdominal insert
within the pelvis cavity and with
respect to the chest flesh, assuring that
the chest flesh provides uniform fit and
overlap with respect to the outside
surface of the pelvis flesh.
(7) Flex the dummy’s upper torso
three times between the vertical and
until the torso reference frame, as
shown in Figure T5, reaches 30 degrees
from the vertical transverse plane. Bring
the torso to vertical orientation and wait
for 30 minutes before conducting the
test. During the 30-minute waiting
period, the dummy’s upper torso shall
be externally supported at or near its
vertical orientation to prevent it from
drooping.
(8) Remove all external support and
wait two minutes. Measure the initial
orientation angle of the torso reference
plane of the seated, unsupported
dummy as shown in Figure T5. The
initial orientation angle may not exceed
20 degrees.
(9) Attach the pull cable and the load
cell as shown in Figure T5.
(10) Apply a tension force in the
midsagittal plane to the pull cable as
shown in Figure T5 at any upper torso
deflection rate between 0.5 and 1.5
degrees per second, until the angle
reference plane is at 35 ± 0.5 degrees of
flexion relative to the vertical transverse
plane.
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(11) Continue to apply a force
sufficient to maintain 35 ± 0.5 degrees
of flexion for
10 seconds, and record the highest
applied force during the 10-second
period.
(12) Release all force at the
attachment bracket as rapidly as
possible, and measure the return angle
with respect to the initial angle
reference plane as defined in paragraph
(c)(7) of this section three minutes after
the release.
srobinson on DSK4SPTVN1PROD with RULES2
§ 572.176 Knees and knee impact test
procedure.
(a) The knee assembly for the purpose
of this test is the part of the leg assembly
shown in drawing 420–5000
(incorporated by reference, see
§ 572.170).
(b) When the knee assembly,
consisting of lower upper leg assembly
(420–5200), femur load transducer
(SA572–S10, included in drawing 420–
0000) or its structural replacement (420–
5121), lower leg assembly (420–5300),
ankle assembly (420–5400), and foot
molded assembly (420–5500) (all
incorporated by reference, see
§ 572.170) is tested according to the test
procedure in subsection (c) of this
section:
(1) The peak resistance force as
measured with the test probe-mounted
accelerometer must not be less than 2.6
kN (585 lbf) and not more than 3.2 kN
(719 lbf).
(2) The force shall be calculated by
the product of the impactor mass and its
deceleration.
(c) Test Procedure. The test procedure
for the knee assembly is as follows:
(1) Soak the knee assembly in a
controlled environment at any
temperature between 20.6 and 22.2 °C
(69 and 72 °F) and a relative humidity
between 10 and 70 percent for at least
four hours prior to a test.
(2) Mount the test material and secure
it to a rigid test fixture as shown in
Figure T6. No part of the foot or tibia
may contact any exterior surface.
(3) Align the test probe so that
throughout its stroke and at contact with
the knee it is within 2 degrees of
horizontal and collinear with the
longitudinal centerline of the femur.
(4) Guide the pendulum so that there
is no significant lateral, vertical, or
rotational movement at the time of
initial contact between the impactor and
the knee.
(5) The test probe velocity at the time
of contact shall be 2.1 ± 0.03 m/s (6.9
± 0.1 ft/s).
(6) No suspension hardware,
suspension cables, or any other
attachments to the probe, including the
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velocity vane, shall make contact with
the dummy during the test.
§ 572.177 Test conditions and
instrumentation.
(a) The following test equipment and
instrumentation is needed for
qualification as set forth in this subpart:
(1) The test probe for thoracic impacts
is of rigid metallic construction,
concentric in shape, and symmetric
about its longitudinal axis. It has a mass
of 6.89 ± 0.012 kg (15.2 ± 0.05 lb) and
a minimum mass moment of inertia of
2040 kg-cm2 (1.81 lbf-in-sec2) in yaw
and pitch about the CG. One-third (1⁄3)
of the weight of the suspension cables
and their attachments to the impact
probe is included in the calculation of
mass, and such components may not
exceed five percent of the total weight
of the test probe. The impacting end of
the probe, perpendicular to and
concentric with the longitudinal axis, is
at least 25.4 mm (1.0 in) long, and has
a flat, continuous, and non-deformable
121 ± 0.25 mm (4.76 ± 0.01 in) diameter
face with a maximum edge radius of
12.7 mm (0.5 in). The probe’s end
opposite to the impact face has
provisions for mounting of an
accelerometer with its sensitive axis
collinear with the longitudinal axis of
the probe. No concentric portions of the
impact probe may exceed the diameter
of the impact face. The impact probe has
a free air resonant frequency of not less
than 1000 Hz, which may be determined
using the procedure listed in the PADI
(incorporated by reference, see
§ 572.170).
(2) The test probe for knee impacts is
of rigid metallic construction,
concentric in shape, and symmetric
about its longitudinal axis. It has a mass
of 1.91 ± 0.01 kg (4.21 ± 0.02 lb) and a
minimum mass moment of inertia of
140 kg-cm2 (0.124 lbf-in-sec2) in yaw
and pitch about the CG. One third (1⁄3)
of the weight of the suspension cables
and their attachments to the impact
probe may be included in the
calculation of mass, and such
components may not exceed five
percent of the total weight of the test
probe. The impacting end of the probe,
perpendicular to and concentric with
the longitudinal axis, is at least 12.5 mm
(0.5 in) long, and has a flat, continuous,
and non-deformable 76.2 ± 0.2 mm (3.00
± 0.01 in) diameter face with a
maximum edge radius of 12.7 mm (0.5
in). The probe’s end opposite to the
impact face has provisions for mounting
an accelerometer with its sensitive axis
collinear with the longitudinal axis of
the probe. No concentric portions of the
impact probe may exceed the diameter
of the impact face. The impact probe has
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a free air resonant frequency of not less
than 1000 Hz, which may be determined
using the procedure listed in the PADI
(incorporated by reference, see
§ 572.170).
(3) Head accelerometers have
dimensions, response characteristics,
and sensitive mass locations specified
in drawing SA572–S4 (included in
drawing 420–0000) and are mounted in
the head as shown in drawing 420–0000
(both incorporated by reference, see
§ 572.170), sheet 2 of 6.
(4) The upper neck force and moment
transducer has the dimensions, response
characteristics, and sensitive axis
locations specified in drawing SA572–
S11 (included in drawing 420–0000)
and is mounted in the head-neck
assembly as shown in drawing 420–
0000 (both incorporated by reference,
see § 572.170), sheet 2 of 6.
(5) The chest deflection transducer
has the dimensions and response
characteristics specified in drawing
SA572–S50 (included in drawing 420–
0000) and is mounted to the upper torso
assembly as shown in drawing 420–
0000 (both incorporated by reference,
see § 572.170), sheet 2 of 6.
(b) The following instrumentation
may be required for installation in the
dummy for compliance testing. If so, it
is installed during qualification
procedures as described in this subpart:
(1) The thorax CG accelerometers
have the dimensions, response
characteristics, and sensitive mass
locations specified in drawing SA572–
S4 (included in drawing 420–0000)
(incorporated by reference, see
§ 572.170) and are mounted in the torso
assembly in a triaxial configuration
within the spine box instrumentation
cavity.
(2) The lower neck force and moment
transducer has the dimensions, response
characteristics, and sensitive axis
locations specified in drawing SA572–
S40 (included in drawing 420–0000)
and is mounted to the neck assembly by
replacing the lower neck mounting
bracket 420–2070 as shown in drawing
420–2000 (all incorporated by reference,
see § 572.170).
(3) The clavicle force transducers
have the dimensions, response
characteristics, and sensitive axis
locations specified in drawing SA572–
S41 (included in drawing 420–0000)
and are mounted in the shoulder
assembly as shown in drawing 420–
3800 (both incorporated by reference,
see § 572.170).
(4) The IR–Tracc chest deflection
transducers have the dimensions and
response characteristics specified in
drawing SA572–S43 (included in
drawing 420–0000) and are mounted to
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the spine box assembly as shown in
drawing 420–8000 (both incorporated
by reference, see § 572.170).
(5) The spine and sternum
accelerometers have the dimensions,
response characteristics, and sensitive
mass locations specified in drawing
SA572–S4 (included in drawing 420–
0000) and are mounted in the torso
assembly in uniaxial fore-and-aft
oriented configuration arranged as
corresponding pairs in two locations
each on the sternum and at the spine
box of the upper torso assembly as
shown in drawing 420–0000 (both
incorporated by reference, see
§ 572.170), sheet 2 of 6.
(6) The lumbar spine force-moment
transducer has the dimensions, response
characteristics, and sensitive axis
locations specified in drawing SA572–
S12 (included in drawing 420–0000)
and is mounted in the lower torso
assembly as shown in drawing 420–
4000 (both incorporated by reference,
see § 572.170).
(7) The iliac force transducers have
the dimensions and response
characteristics specified in drawing
SA572–S13 L and R (included in
drawing 420–0000) and are mounted in
the lower torso assembly as shown in
drawing 420–4000 (both incorporated
by reference, see § 572.170).
(8) The pelvis accelerometers have the
dimensions, response characteristics,
and sensitive mass locations specified
in drawing SA572–S4 (included in
drawing 420–0000) and are mounted in
the torso assembly in triaxial
configuration in the pelvis bone as
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shown in drawing 420–0000 (both
incorporated by reference, see
§ 572.170), sheet 2 of 6.
(9) The femur force and moment
transducers (SA572–S10, included in
drawing 420–0000) have the
dimensions, response characteristics,
and sensitive axis locations specified in
the appropriate drawing and are
mounted in the upper leg assembly,
replacing the femur load cell simulator
(drawing 420–5121) as shown in
drawing 420–5100 (all incorporated by
reference, see § 572.170).
(10) The tilt sensors have the
dimensions and response characteristics
specified in drawing SA572–S42
(included in drawing 420–0000) and are
mounted to the head, thorax, and pelvis
assemblies as shown in drawing 420–
0000 (both incorporated by reference,
see § 572.170), sheet 2 of 6.
(c) The outputs of transducers
installed in the dummy and in the test
equipment specified by this part are to
be recorded in individual data channels
that conform to SAE Recommended
Practice J211 (incorporated by reference,
see § 572.170) except as noted, with
channel frequency classes as follows:
(1) Pendulum acceleration, CFC 180,
(2) Pendulum D-plane rotation (if
transducer is used), CFC 60,
(3) Torso flexion pulling force (if
transducer is used), CFC 60,
(4) Head acceleration, CFC 1000,
(5) Neck forces, upper and lower, CFC
1000,
(6) Neck moments, upper and lower,
CFC 600,
(7) Thorax CG acceleration, CFC 180,
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11671
(8) Sternum deflection, Class 600,
(9) Sternum and rib accelerations,
Class 1000,
(10) Spine accelerations, CFC 180,
(11) Lumbar forces, CFC 1000,
(12) Lumbar moments, CFC 600,
(13) Shoulder forces, CFC 180,
(14) Pelvis accelerations, CFC 1000,
(15) Iliac forces, CFC 180,
(16) Femur and tibia forces, CFC 600,
(17) Femur and tibia moments, CFC
600.
(d) Coordinate signs for
instrumentation polarity are to conform
to SAE Information Report J1733
(incorporated by reference, see
§ 572.170).
(e) The mountings for sensing devices
have no resonant frequency less than 3
times the frequency range of the
applicable channel class.
(f) Limb joints are set at one G, barely
restraining the weight of the limb when
it is extended horizontally. The force
needed to move a limb segment is not
to exceed 2G throughout the range of
limb motion.
(g) Performance tests of the same
component, segment, assembly, or fully
assembled dummy are separated in time
by not less than 30 minutes unless
otherwise noted.
(h) Surfaces of dummy components
may not be painted except as specified
in this subpart or in drawings subtended
by this subpart.
Appendix—Figures to Subpart T of Part
572
BILLING CODE 4910–59–P
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11676
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Issued on: February 16, 2012.
David L. Strickland,
Administrator.
[FR Doc. 2012–4129 Filed 2–21–12; 11:15 am]
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BILLING CODE 4910–59–C
Agencies
[Federal Register Volume 77, Number 38 (Monday, February 27, 2012)]
[Rules and Regulations]
[Pages 11651-11676]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-4129]
-----------------------------------------------------------------------
DEPARTMENT OF TRANSPORTATION
National Highway Traffic Safety Administration
49 CFR Part 572
[Docket No. NHTSA-2011-0175]
RIN 2127-AJ49
Hybrid III 10-Year-Old Child Test Dummy
AGENCY: National Highway Traffic Safety Administration (NHTSA),
Department of Transportation (DOT).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This final rule establishes regulations setting forth
specifications and qualification requirements for a Hybrid III 10-year-
old size child test dummy (HIII-10C). In a companion document published
elsewhere in this issue of the Federal Register, NHTSA is adopting use
of the dummy to test child restraints recommended for children weighing
more than 65 pounds (lb) for compliance with the Federal motor vehicle
safety standard for child restraint systems. The HIII-10C dummy enables
NHTSA to assess the performance of child restraint systems in
restraining children in the 8- to 12-year-old age range.
DATES: Effective date: April 27, 2012. The incorporation by reference
of the publications listed in the rule has been approved by the
Director of the Federal Register as of April 27, 2012.
If you wish to petition for reconsideration of this rule, your
petition must be received by April 12, 2012.
ADDRESSES: If you wish to petition for reconsideration of this rule,
you should refer in your petition to the docket number of this document
and submit your petition to: Administrator, National Highway Traffic
Safety Administration, 1200 New Jersey Avenue SE., West Building,
Washington, DC 20590. For more information, see Section V, Rulemaking
Analyses and Notices.
FOR FURTHER INFORMATION CONTACT: For non-legal issues, you may call
Peter Martin, NHTSA Office of Crashworthiness Standards (telephone 202-
366-5668) (fax 202-493-2990). For legal issues, you may call Deirdre
Fujita, NHTSA Office of Chief Counsel (telephone 202-366-2992) (fax
202-366-3820). The mailing address for these officials is the National
Highway Traffic Safety Administration, 1200 New Jersey Avenue SE.,
Washington, DC 20590.
SUPPLEMENTARY INFORMATION: Petitions for reconsideration of this rule:
The petition will be placed in the docket. Anyone is able to search the
electronic form of all documents received into any of our dockets by
the name of the individual submitting the comment (or signing the
comment, if submitted on behalf of an association, business, labor
[[Page 11652]]
union, etc.). You may review DOT's complete Privacy Act Statement in
the Federal Register published on April 11, 2000 (Volume 65, Number 70;
Pages 19477-78).
Table of Contents
I. Executive Summary
II. Background
a. 2005 NPRM
b. Developments Since 2005
c. Summary of Decision
III. Summary of Comments
IV. Response to Comments
a. Functionality of the HIII-10C as a Part 572 ATD
1. Chin-to-Chest Contact
2. Shock Emanating From Shoulder and Neck
i. Shoulder Revision
ii. Lower Neck Revision
3. Stiffness of Vinyl Insert
4. Dummy Availability
b. Durability of the HIII-10C
1. Proximal Femur
2. Bib Assembly
3. Shoulder Rotation Stop Screws
4. Agency Part Replacement Records
i. Pelvis Helicoil Insert
ii. Neck and Ribcage Replacement
iii. Other Replacements
5. Durability Summary
c. Qualification Procedures and Requirements
1. Response Corridors
i. Head
ii. Neck
iii. Thorax
iv. Torso Flexion
v. Knee Impact
2. Summary of Qualification Requirements
3. Impact Probes
4. Instrumentation
i. Rotary Potentiometers
ii. Sternum Displacement
d. Technical Data Package
1. Changes to the Engineering Drawings and PADI
2. Organization of Materials
i. Searchable Text
ii. Order of Engineering Drawings
iii. Part Quantity Specification
iv. Part Numbering Scheme
3. Specifications for Soft Parts
4. Use of 3D Computer Renderings
e. Other
1. Labeling the Dummy as a ``Ten Year Old''
2. Best Practices for Belt Routing
3. Abdominal Injury Correlates
4. Repeatability in Systems Testing
f. Dummy Development Efforts
1. Hybrid III Child Dummy Revisions--Abdomen and Pelvis
2. Pediatric Research
3. Status of HIC
V. Rulemaking Analyses and Notices
I. Executive Summary
The agency has determined that the HIII-10C dummy, configured as
described in this document, is a suitable and useful test device for
quantitative assessment of child restraint systems (CRSs) and other
safety devices for older children. The dummy, with a weight of 35.2
kilograms (kg) (77.6 pounds (lb)) and sitting height of 71 centimeters
(28 inches), is ideally suited to test the upper load and height limits
of safety restraints for children.
The dummy is specified by this rule by a technical data package
(TDP) consisting of a set of engineering drawings, a parts list, and a
set of procedures for assembly, disassembly, and inspection (PADI) of
the dummy. Additionally, this rule amends 49 CFR part 572 to specify
qualification requirements for the dummy, to assure that the HIII-10C
responses are within established performance corridors, and further
ensure the uniformity of dummy assembly, structural integrity,
consistency of response and adequacy of instrumentation. The TDP and
qualification requirements assure that HIII-10C dummies are uniform in
their design, construction and kinematics.
The drawings and the PADI for the HIII-10C are available for
examination in the docket for this final rule. Technical reports and
other materials pertaining to this final rule have also been placed in
the docket for this final rule.
The notice of proposed rulemaking (NPRM) on which this final rule
is based was published July 13, 2005 (70 FR 40281).
The agency is concurrently publishing in this issue of the Federal
Register a final rule to amend Federal Motor Vehicle Safety Standard
(FMVSS) No. 213, ``Child restraint systems'' (49 CFR 571.213), to adopt
use of the HIII-10C dummy in agency compliance tests of CRSs. (RIN
2127-AL10, formerly RIN 2127-AJ44.)
The final rules bring to a close NHTSA's work on Public Law 107-
318, 116 Stat. 2772 (``Anton's Law''), which contained provisions for
NHTSA to develop and evaluate a test dummy that represents a 10-year-
old child for use in testing CRSs. Public Law 107-318 required us to
initiate rulemaking on the Anthropomorphic Test Device (ATD), a mandate
we satisfied in 2005 when we published an NPRM to adopt the HIII-10C
into FMVSS No. 213.\1\
---------------------------------------------------------------------------
\1\ 70 FR 51720 (August 31, 2005). Among other matters, Public
Law 107-318 directed NHTSA to evaluate an anthropomorphic test
device (ATD) that simulates a 10-year-old child for use in testing
CRSs and to initiate a rulemaking proceeding for the adoption of the
ATD. NHTSA addressed other provisions of Public Law 107-318 in
earlier agency actions. These actions are discussed in the preamble
of the August 31, 2005 NPRM.
---------------------------------------------------------------------------
When we published the 2005 proposal to include the dummy in FMVSS
No. 213, we proposed that booster seats must conform to several new
requirements based on HIII-10C measurements, including a head injury
criterion (HIC). As part of our assessment, we demonstrated in our pre-
proposal testing that, while most CRSs conformed to the new
requirements, there were some failures, including those where HIC was
exceeded. However, during extensive post-NPRM booster seat testing,
inconsistencies in the test protocol revealed variability in the
kinematics and measurements of the HIII-10C. In particular, the agency
discovered that a slight perturbation in the test protocol could create
a large change in HIC. The variability in HIC measurements is
attributable to a design feature unique to the HIII-10C in which chin-
to-chest contact during the impact event can be excessively hard, but
not easily controlled through CRS design.
Subsequently, the agency devoted substantial rulemaking and
research efforts to try to address test variability. The August 31,
2005 (FMVSS No. 213) NPRM was followed by a supplemental NPRM (SNPRM)
published in 2008 \2\ and an SNPRM published in 2010.\3\ Throughout the
rulemaking proceeding, NHTSA informed the public of its research
findings, concerns and ideas about using the HIII-10C in FMVSS No. 213,
and in turn learned from comments from research organizations, consumer
groups, CRS, vehicle, and ATD manufacturers, and others. Considerable
effort was devoted to revising the test protocol to eliminate
variability in HIC.
---------------------------------------------------------------------------
\2\ 73 FR 3901 (January 23, 2008). This SNPRM proposed a seating
procedure for the HIII-10C to minimize the chin-to-chest impacts.
Commenters were generally unsupportive of the procedure.
\3\ 75 FR 71648 (November 24, 2010). This second SNPRM proposed
an alternative seating procedure for the ATD.
---------------------------------------------------------------------------
The endeavor has led to a new dummy positioning procedure that
improves test repeatability with no substantial change to the HIII-10C.
The agency has determined that the HIII-10C is an important ATD that
will enhance our ability to assess the performance of CRSs and other
occupant protection systems in protecting children.\4\ In the
accompanying FMVSS No. 213 final rule published today, we adopt the
HIII-10C into FMVSS No. 213, but due to the recurrence of hard chin-to-
chest
[[Page 11653]]
contacts, we will not adopt HIC as an FMVSS No. 213 injury criterion.
---------------------------------------------------------------------------
\4\ The HIII-10C represents children of a size heretofore not
represented by the ATDs used in NHTSA regulations. The child ATDs in
49 CFR part 572 that NHTSA uses for testing CRSs are ATDs
representing a newborn infant, a 12-month-old, a 3-year-old, a 6-
year-old, and a weighted 6-year-old. In 49 CFR part 572, there is
also specified a 5th percentile adult female ATD, which is
approximately the size of a 12-year-old.
---------------------------------------------------------------------------
The agency has thus decided that the HIII-10C is a suitable device
for use in FMVSS No. 213. The HIII-10C test dummy will provide an
enhanced assessment of child restraint performance, and is worthy of
adoption into 49 CFR part 572 as implemented by this final rule.
II. Background
a. 2005 NPRM
In July 2005, NHTSA issued an NPRM proposing specifications and
certification requirements for a new test dummy representative of a 10-
year-old child (70 FR 40281, July 13, 2005). The dummy was proposed to
be included among the descriptions of anthropomorphic test devices in
49 CFR part 572, so that it could be called out for use in FMVSS test
procedures and other regulations. Concurrently, NHTSA proposed to use
the new dummy to assess CRSs recommended for older children under FMVSS
No. 213 (70 FR 51720, August 31, 2005). These two NPRMs are referred to
herein as the Part 572 NPRM and the FMVSS No. 213 NPRM, respectively.
b. Developments Since 2005
Additional rulemaking notices. Since the two NPRMs were published
in 2005, the agency issued two supplemental NPRMs that dealt with the
unrealistic ``chin-to-chest'' condition that occurred when the HIII-10C
was used in the FMVSS No. 213 sled test environment. This condition was
first observed in agency tests that led up to the 2005 NPRMs. In
several of the tests, as the HIII-10C's head flung forward, the neck
flexed to the point where the dummy's chin came into hard contact with
its upper thorax. This chin-to-chest contact at times produced elevated
head accelerations. However, in the testing that led up to the 2005
NPRMs, we did not foresee a problem with the chin-to-chest contact
because the majority of booster seats tested met the FMVSS No. 213 head
injury criterion (HIC) limit of 1000.\5\
---------------------------------------------------------------------------
\5\ 70 FR at 51724.
---------------------------------------------------------------------------
Commenters to both NPRMs of 2005 also observed hard chin-to-chest
contact in their own tests. Some commenters (Dorel Juvenile Group
(Dorel), Graco Children's Products (Graco)) expressed concerns the
chin-to-chest contact was an indication of poor spine biofidelity and
urged NHTSA to undertake additional testing of the HIII-10C to ensure
that the test dummy is appropriate for use in FMVSS No. 213 testing.
Following these comments, NHTSA conducted further testing of the
HIII-10C to investigate the chin-to-chest contact. We concurred with
the commenters that the hard chin-to-chest contact exhibited by the
HIII-10C in sled tests was an undesirable occurrence. The hard contact
was unrealistic, as real-world accident data indicated that children do
not sustain head injuries in that manner. The chin-to-chest contact is
much less prevalent in the kinematics of actual children because the
child's spine is more flexible than that of the ATD. The added
flexibility of a child's spine allows greater forward translation and
rotation of the head. When chin-to-chest contact occurs in children, it
does not produce as hard of a contact as the dummy and does not result
in severe injuries. Moreover, we found that HIC values produced by the
HIII-10C were highly variable when chin-to-chest contact occurs, as the
dummy was not designed to achieve repeatable or reproducible responses
under this condition.
In consideration of the likelihood of unreasonably high HIC values,
the agency issued the 2008 SNPRM that mitigated chin-to-chest contact
by specifying a posture that was about 10 degrees more upright than the
HIII-10C positioned in a CRS under the original NPRM (73 FR 3901).
However, this proposal was widely criticized in comments to the SNPRM.
Some commenters believed that the upright positioning procedure was
unrealistic because it did not reflect the way children actually sit in
booster seats. Some also indicated that a belt routing system or
harness designed for an upright ATD may introduce unwanted belt slack
when applied to a fully reclined child. They believed this could add to
head excursion and preclude a CRS from performing its primary function
of properly positioning a vehicle's seat belt to a child occupant.
Additionally, some commenters found the procedure to be cumbersome and
difficult to follow.
Following a test program conducted in response to these comments,
on November 24, 2010 the agency issued a second SNPRM for positioning
the HIII-10C (75 FR 71648). The 2010 SNPRM replaced the proposal for
the upright positioning procedure with a procedure developed by the
University of Michigan Transportation Research Institute (UMTRI). The
UMTRI procedure emphasizes fitting the dummy to the CRS rather than
achieving a specific dummy posture. In trial tests run by the agency
using the UMTRI procedure, we found the repeatability of all test
measurements to be greatly improved relative to those observed under
the seating procedures we had proposed previously. Because the UMTRI
procedure typically results in an ATD posture similar to that
associated with the seating procedure used in the original NPRM of
2005, chin-to-chest contact continued to occur. Thus, we proposed using
the UMTRI procedure when positioning the HIII-10C in FMVSS No. 213
tests, but proposed that HIC would not be used as a performance
criterion in FMVSS No. 213 when using the HIII-10C.
Supplemental testing. Since the NPRMs of 2005, the agency has used
the HIII-10C in about two hundred sled tests to support the FMVSS No.
213 SNPRMs, to address the comments to the Part 572 NPRM, and to arrive
at the final configuration of the dummy. We have acquired four
additional HIII-10C units to add to our repeatability and
reproducibility assessment. In this period since 2005, we have made a
comprehensive assessment of the ATD to examine the many issues brought
up in comments received on the four rulemaking proposals.
The test results permitted us to examine and evaluate the
consistency of the data and adequacy of the dummy in a broad range of
CRSs available in the market. Of the approximately 80 models of booster
seats manufactured since 2006,\6\ twenty seats from eight different
manufacturers have been tested with the HIII-10C since the Part 572
NPRM. Another fourteen seat models manufactured prior to 2006 have also
been tested. This spectrum represents a good cross-section of the
booster seat market and demonstrates well the utility of the HIII-10C
under all installations.
---------------------------------------------------------------------------
\6\ To assist consumers in deciding which CRS to purchase, NHTSA
provides ease of use ratings for child seats. We attempt to select
and rate all seats on the market. Currently, we provide about 80
ratings of seats designed for children weighing 36.3 kg (80 lb) or
more and manufactured since 2006. There are 23 different
manufacturers represented in our selection of seats.
---------------------------------------------------------------------------
Utility of the HIII-10C. Our supplementary testing has reaffirmed
that the HIII-10C is a meaningful ATD for use in FMVSS No. 213 and
merits incorporation into 49 CFR part 572 even without NHTSA's use of
HIC as an FMVSS No. 213 pass/fail criterion. Additional qualification
data obtained since 2005 has confirmed the high level of repeatability
and reproducibility that was demonstrated in the NPRM on a limited data
set.\7\ As reported in this
[[Page 11654]]
preamble, the qualification corridors indicate outstanding dummy
repeatability and reproducibility. Throughout the entire test
experience, the HIII-10C has proven to be a durable test instrument.
---------------------------------------------------------------------------
\7\ Except to the extent discussed in this document regarding
chin-to-chest contact, NHTSA confirms the NPRM's discussion of the
findings that the HIII-10C is a biofidelic ATD that produces
repeatable and reproducible results. A detailed discussion of the
HIII-10C's biofidelity can be found in the NPRM, see 70 FR at 40284.
The repeatability and reproducibility of the HII-10C is discussed in
the NPRM at 70 FR at 40285. Commenters did not disagree with these
aspects of the dummy, except as discussed in this document regarding
the chin-to-chest contact.
---------------------------------------------------------------------------
The additional data also confirms the qualification of HIII-10C-
based injury metrics. Other than HIC, all other dummy-based
measurements used in FMVSS No. 213--head excursion, knee excursion, and
chest acceleration--have proven to be sound metrics appropriate for CRS
testing. A NHTSA-sponsored study published in 2008 found the head
excursion of the HIII-10C to be very similar to a human subject in
matched pair tests.\8\ Also, the agency has observed a strong
correlation between knee excursion and submarining in child dummies. As
such, knee excursion correlates indirectly with abdominal injuries. The
limit on knee excursion prevents CRS manufacturers from controlling
head excursion by designing their restraints so that children submarine
in a crash.
---------------------------------------------------------------------------
\8\ Ash, JH, Sherwood, CP, Abdelilah, Y, Crandall, JR, Parent,
DP, Kallieris, D., ``Comparison of Anthropomorphic Test Dummies with
a Pediatric Cadaver Restrained by a Three-point Belt in Frontal Sled
Tests,'' Proceedings of the 21st International Technical Conference
on the Enhanced Safety of Vehicles, June 2009.
---------------------------------------------------------------------------
The limit on chest acceleration ensures that a CRS provides a child
with sufficient ``ride down'' or absorption of crash forces over a
period of time in a manner that avoids injury. The revisions to the
HIII-10C described in this preamble assure that the chest acceleration
measurements are devoid of any signal irregularities. The HIII-10C will
also be used in FMVSS No. 213 to assess the structural integrity of
CRSs for older children.
Recent agency studies have also demonstrated that the HIII-10C has
sufficient biofidelity to be used in possible belt fit programs. Our
research has found lap and shoulder belts to fit the HIII-10C much like
they do a human.\9\ The dummy was found to sit in a seat like a human
child and don the belt like a human child.
---------------------------------------------------------------------------
\9\ Reed, M., Ebert-Hamilton, S., Klinich, K., Manary, M., Rupp,
J., ``Assessing Child Belt Fit, Volume I: Effects of Vehicle Seat
and Belt Geometry on Belt Fit,'' UMTRI Report No. UMTRI-2008-49-1,
University of Michigan, Ann Arbor, MI, September 2008.
---------------------------------------------------------------------------
The agency has also recently completed studies on the HIII-10C's
utility and biofidelity in assessing submarining and abdominal
injury.\10\ In summary, we have found the HIII-10C to be sufficiently
biofidelic to mimic the kinematics of a belted human child. The dummy
was found to be sensitive to a range of lap belt and torso belt
anchorage configurations and its propensity to submarine was consistent
with that of a belted child. Given these positive results, the agency
is pursuing the development of an HIII-10C modification consisting of
an abdominal insert that measures abdominal deformation, thus providing
a direct assessment of injury risk.
---------------------------------------------------------------------------
\10\ Reed, M., Ebert-Hamilton, S., Klinich, K., Manary, M.,
Rupp, J., ``Assessing Child Belt Fit, Volume II: Effect of Restraint
Configuration, Booster Seat Designs, Seating Procedure, and Belt Fit
on the Dynamic Response of the Hybrid III 10-year-old ATD in Sled
Tests,'' UMTRI Report No. UMTRI-2008-49-2, University of Michigan,
Ann Arbor, MI, September 2008.
---------------------------------------------------------------------------
c. Summary of Decision
The data available since 2005 support a decision that the HIII-10C
is a suitable device for use in FMVSS No. 213. Adopting the HIII-10C in
49 CFR part 572 enables NHTSA to expand the applicability of FMVSS No.
213 to CRSs that are recommended for children over the current 35.2 kg
(65 lb) weight limit in a meaningful way. There has been considerable
interest over the years in expanding the applicability of FMVSS No. 213
to increase the likelihood that child restraints for older children
(e.g., booster seats) will perform adequately in a crash. This interest
goes hand-in-hand with efforts to prolong CRS use among children who
have outgrown their child safety seat, but who cannot adequately fit a
vehicle's lap and shoulder belt system. Adopting the HIII-10C into 49
CFR part 572 enhances NHTSA's ability to reduce unreasonable risks of
traffic crashes to older children.
III. Summary of Comments
We received comments on the Part 572 NPRM from: The American
Academy of Pediatrics (AAP), Children's Hospital of Philadelphia
(CHOP), Advocates for Highway and Auto Safety (Advocates), Dorel,
Chrysler, the Alliance of Automobile Manufacturers \11\ (Alliance), and
a joint submission from ATD manufacturers First Technology Safety
Systems (FTSS) and Denton ATD (Denton) (FTSS/Denton).\12\ Some of the
comments on the FMVSS No. 213 SNPRMs raised issues pertaining to the
Part 572 rulemaking, which we discuss in this document as appropriate.
Additional organizations commenting on the FMVSS No. 213 rulemaking
include Graco, the Juvenile Product Manufacturers Association (JPMA),
and Consumers Union.
---------------------------------------------------------------------------
\11\ At the date of the October 3, 2005 comment, the Alliance
consisted of: BMW Group, DaimlerChrysler; Ford Motor Company;
General Motors; Mazda; Mitsubishi Motors; Porsche; Toyota; and
Volkswagen.
\12\ In 2010, FTSS and Denton announced that they have merged
into one company, Humanetics, Inc.
---------------------------------------------------------------------------
Commenters were very supportive of the idea of incorporating an ATD
representing children in the 8- to 12-year-old age range. There was
general support for the HIII-10C's incorporation into Part 572, but as
indicated above, concerns were raised about the chin-to-chest contact.
Dorel expressed opposition to the adoption of the HIII-10C, citing
concerns about the ATD's biofidelity, durability, and compatibility
with the FMVSS No. 213 test environment. Some comments suggested
adjustments and clarifications to the Part 572 proposed regulatory
text, to improve the procedures for qualifying an ATD and the
performance assessments.
The following major categories of issues were raised: (a)
Functionality of the HIII-10C as a Part 572 ATD; (b) durability of the
ATD; (c) qualification procedures and requirements; (d) the TDP (the
engineering drawings and PADI); (e) other issues (clarifying agency
statements in the preamble); and (f) dummy development efforts. Each of
these areas is discussed below.
IV. Response to Comments
a. Functionality of the HIII-10C as a Part 572 ATD
1. Chin-to-Chest Contact
As described earlier in this preamble, the agency received many
comments regarding the undesirable chin-to-chest contact exhibited by
the HIII-10C, which is related to the biofidelity of the HIII-10C's
spine. Dorel, the Alliance and others reported chin-to-chest contact
during normal use of the dummy, which was believed to be brought on by
an overly stiff thoracic spine relative to human children.
We agree that the hard chin-to-chest contact in FMVSS No. 213 sled
tests is an undesirable characteristic of the HIII-10C. Chin-to-chest
contact has also been observed in tests run by the agency. In most
cases, the time interval producing the highest calculation of HIC
enveloped the instant when chin-to-chest contact occurred, including
cases where head acceleration was very high. In other words, chin-to-
chest contact often caused HIC to exceed the injury assessment
reference value (HIC36 = 1000).
The design of the neck-to-thorax joint in the HIII-10C differs from
other dummies in the Hybrid III family. In the other dummies, the neck
is off-set or
[[Page 11655]]
cantilevered anterior to the thorax, which is not optimal
anthropometrically. In the HIII-10C, the upper part of the thorax spine
structure has been designed such that the neck-to-thorax joint is an
in-line connection following more closely the anthropometry of a human.
The lower neck bracket described earlier serves at the neck-to-thorax
joint.
The downside to the improved anthropometry is that it creates a
``hard spot'' during chin-to-chest contact. The stiff lower neck
bracket is where the chin comes into contact with the chest and where
only a thin layer of soft flesh material offers any buffer. Beyond a
few millimeters of flesh material compression, chin-to-chest contact
forces--and head accelerations--increase exponentially. As a result, a
small deviation in head motion causes a very large change in head
acceleration and HIC. The change is difficult to control and may be in
conflict with good CRS design. In some cases, HIC scores have been
shown to improve when the torso belt fit is degraded.\13\ Since chin
contact to the thorax is not a natural brain injury path in actual
children, any such attempt to lessen HIC through booster seat design
may compromise the overall safety performance of the seat.
---------------------------------------------------------------------------
\13\ 2008 UMTRI Vol. 2 Report
---------------------------------------------------------------------------
Due to the non-biofidelic chin-to-chest contact, we have decided
not to require CRSs to meet the HIC criterion when tested with the
HIII-10C in the compliance of FMVSS No. 213, as announced in the FMVSS
No. 213 final rule published today. When we followed the UMTRI seating
procedure adopted in the final rule for FMVSS No. 213, we found that
the seating procedure reduces HIC variability in repeat tests of the
same booster seat, including those in which hard chin-to-chest contact
occurs. However, hard chin-to-chest contact was still observed in many
agency tests. Mitigating this effect altogether, as recommended in
comments by Dorel, would require a major redesign of the entire thorax
and spine, which is not feasible. Instead, the agency is concentrating
efforts on developing an entirely new pediatric dummy for future use,
as discussed later in this preamble.
Nonetheless, we did make minor changes to the HIII-10C to mitigate
some of the effects of the chin-to-chest contact in accordance with a
recent agency study.\14\ This Part 572 final rule specifies the
thickness of the HIII-10C's chin flesh in the inferior-superior
direction. The new specification is aimed at lessening the variability
of head accelerations among different dummies when chin-to-chest
contact does occur.
---------------------------------------------------------------------------
\14\ Stammen, J., Bolte, J., Shaw, J., ``Biomechanical Impact
Response of the Human Chin and Manubrium,'' Annals of Biomedical
Engineering (2011, in press).
---------------------------------------------------------------------------
The chin flesh specification improves the functionality of the
HIII-10C as an ATD, even though we have decided not to use HIC as an
FMVSS No. 213 pass/fail criterion when using the dummy. HIC may
continue to be measured in FMVSS No. 213 tests with the HIII-10C for
research purposes, and could be used as a performance metric in other
NHTSA programs (e.g., out-of-position (OOP) air bag tests, New Car
Assessment Programs). Standardizing the thickness of the chin will
improve the repeatability of the HIC measurements from different
dummies when chin-to-chest contact occurs. Hard chin-to-chest contact
may be a concern to researchers investigating the whipping actions of
the head. The chin specification will better enable them to compare HIC
measurements in tests with different dummies.\15\
---------------------------------------------------------------------------
\15\ Because we are measuring HIC for research purposes, this
final rule adopts the proposed qualification test for the HIII-10C
head measurements.
---------------------------------------------------------------------------
2. Shock Emanating From Shoulder and Neck
Chrysler\16\ and Graco were concerned that spikes or ``noise'' is
present in the signal traces of accelerometers and load cells in the
head and upper torso of the HIII-10C. In evaluating these comments, we
determined that the presence of these spikes has no consequence on the
use of the HIII-10C as a regulatory tool as specified in the final rule
for FMVSS No. 213. The only instruments within the HIII-10C that will
be used in FMVSS No. 213 are accelerometers arranged triaxially at the
center of gravity (CG) of the chest. In all agency tests in which these
spikes appeared in the accelerometer signals, they were removed by the
signal processing algorithms used to compute the chest acceleration
criterion.\17\
---------------------------------------------------------------------------
\16\ Docket No. NHTSA-2005-21247-0016.
\17\ The chest acceleration criterion specified in FMVSS No. 213
is 60 G's.
---------------------------------------------------------------------------
The routines used to compute chest G's include a standard SAE
International (SAE) Channel Frequency Class (CFC) 180 filter and a 3
millisecond (ms) clip.\18\ The 3 ms clip originated in 1970 for use in
FMVSS No. 208, ``Occupant crash protection,'' in recognition that such
spikes are insignificant as injury contributors (35 FR 14941). The
spikes in the data of the HIII-10C were caused by two sources other
than by chin-to-chest contact: part-to-part contact between components
of the shoulder assembly, and a loose fitting neck cable that
interfered with the lower neck load cell. Spikes emanating from the
shoulder and neck of the HIII-10C were not always completely removed by
CFC180 filtering of the chest acceleration signals, but once they were
``clipped'' by the 3 ms algorithm, they had no measureable effect on
the computation of chest G's. Moreover, in most cases the time interval
containing the peak acceleration identified by the algorithm did not
contain the spike, which usually occurred later in the event. Thus, the
injury reference measures for the HIII-10C's immediate use in FMVSS No.
213 (chest acceleration, head and knee excursion) are not affected by
this condition.
---------------------------------------------------------------------------
\18\ The 3 ms clip truncates the peak acceleration portion of a
continuous signal having a duration less than 3 milliseconds.
---------------------------------------------------------------------------
The shock emanating from the shoulder and neck is benign in terms
of its effect on the dummy itself (the acceleration spikes are no
greater than 150 G's). It does not affect the kinematics of the dummy
in any way (i.e., the head trajectory and knee excursion are
unaffected). The magnitude of the spikes is well within the typical
operating range of +/- 2000 G's for the specified accelerometers, so
shock damage to the instruments is unlikely.
Nonetheless, although the shocks do not influence the outcomes of
FMVSS No. 213 tests, we made the following simple modifications to the
HIII-10C's shoulder and neck to lessen the shock effect. Improving the
ATD in this manner assures that the dummy is better suited for possible
future uses in tests where computations for head injury assessments
based on head accelerometer signals are more sensitive to the condition
(e.g., OOP air bag tests).\19\
---------------------------------------------------------------------------
\19\ The computation of HIC applies a higher signal filter class
(CFC 1000 vs. CFC 180) and does not impose a 3 ms clip. The
revisions do not affect the assessment of CRSs with regard to FMVSS
No. 213, so this change will not delay the incorporation of the
HIII-10C into Part 572.
---------------------------------------------------------------------------
i. Shoulder Revision
The TDP of this final rule modifies the shoulder design of the
HIII-10C.
Similar to a human, the shoulder of the HIII-10C provides the load
bearing surface for the shoulder belt. On the dummy, the part that
provides this surface is a one-piece aluminum casting that is connected
to the spine via a yoke that extends laterally from the spine. The
yoke-to-shoulder connection is a
[[Page 11656]]
pivot which provides medial-lateral movement (i.e., pivoting about the
z-axis) in a direction that is dependent upon the position of the
shoulder belt. If the belt lies close to the neck, the shoulder will
pivot inward; if it is on the edge of the shoulder it will pivot
outward. The piece of the shoulder casting that contains the pivot hole
has a finger-like protrusion. As the shoulder pivots, the finger acts
as a cam by compressing a rubber pad that is glued within the yoke.
This provides resistance to the z-axis pivoting.
Compared to Hybrid III adult dummies, the shoulder design of the
HIII-10C is anthropometrically improved. For the adult dummies, the
shoulder is an assembly of two halves that are joined medially-
laterally. The mid-joint provides the z-axis pivoting for each half. By
eliminating the mid-joint, the HIII-10C is able to provide a more
biofidelic interaction with the shoulder belt during a dynamic event.
Because it is made from one part instead of two, the HIII-10C shoulder
was able to be designed with a sloped, uniform shoulder belt bearing
surface.
The improved design of the HIII-10C is made possible by the new
configuration of the upper thorax in which the offset of the neck has
been eliminated. The HIII-10C shoulder design allows more realistic
movement of the belt along the shoulder during a dynamic event.
Furthermore, since the surface that bears the load of the shoulder belt
is a one-piece casting, the designers of the dummy were able to build
in a shoulder load cell. Although it is not currently used for
regulatory purposes, the load cell is very useful in research and
development activities to study belt load distributions across the
torso.
Notwithstanding its simpler design, the new shoulder has had
problems over the years. In early versions of the design (pre-NPRM),
the shoulder had a tendency to over-pivot to the point where the finger
protrusion was bottoming out the rubber pad. In the 2001-2002
timeframe, the shoulder went through two design revisions in an attempt
to rectify the situation by relocating the shoulder pivot hole and
trimming the yoke.
As indicated by the Graco and Chrysler comments, the Part 572 NPRM
version of the shoulder could still be improved. Before the finger
bottoms out the pad, metal-to-metal contact occurs between the yoke and
the shoulder in one or more places. Shock from this contact appears as
short-duration spikes of up to 150 G's in the signals of accelerometers
closest to the shoulder. Spikes of a lesser extent also appear in neck
load cell signals. Chrysler ran sled tests to identify the shoulder-
yoke contact points by means of transfer paint, and reported these
results to the agency.\20\
---------------------------------------------------------------------------
\20\ Id.
---------------------------------------------------------------------------
To address the spikes, as reflected in the TDP for this final rule,
we have revised the shoulder and yoke assembly to lessen the effect of
the two parts bottoming out against each other. More clearance has been
created for the shoulder to move by reconfiguring the shoulder casting
and the yoke assembly by making them both narrower. This modification
does not affect the biofidelity of the ATD or the reproducibility or
repeatability of the responses because the neck response and sled
kinematics were not affected by the shoulder revisions.
Complete details of the modifications are described in an agency
technical report that may be found in the docket for this final
rule.\21\
---------------------------------------------------------------------------
\21\ ``Revisions to the HIII-10C Technical Data Package,''
NHTSA, August 2011.
---------------------------------------------------------------------------
ii. Lower Neck Revision
This final rule makes simple modifications to the HIII-10C's lower
neck load cell and fasteners associated with the neck safety cable to
lessen the shock effect.
The safety cable of the HIII-10C neck is common to all ATDs in Part
572. It is a steel wire rope that runs through the center of the molded
neck to prevent total separation of the head from the torso under an
extreme test condition. The rope is fitted with swages at both ends: a
ball-end at the superior end and a threaded stud-end at the inferior
end. The ball-end is larger than the diameter of the neck's through-
hole to prevent it from passing through the neck. On the inferior end,
a nut is used to tighten the threaded swage, which places the cable
under tension and the molded neck under compression. A secondary jam
nut serves as a lock. According to the NPRM and final rule
specifications, the nut should be tightening to a torque setting of 8
+/- 2 inch-pounds (in-lbs) before each test.
The entire neck assembly is joined to the spine by means of a
specialized bracket that allows the neck to be set at different forward
tilt angles. A through-hole runs through the center of this bracket
allowing access to the end fitting of the wire rope so that it may be
tightened without removing the bracket from the neck. In lieu of the
bracket, an optional part is available for the HIII-10C containing a
lower neck load cell. It has the same general configuration as the un-
instrumented bracket, except the through hole has a smaller bore.
Shock emanating from the neck has been observed when either the
bracket or an optional part containing a lower neck load cell is used.
(The load cell is not needed in tests carried out under FMVSS No. 213.)
When the neck goes into extreme flexion (a 90 degree bend is specified
in the qualification test), the center cable is not sufficiently taut
to prevent its movement within the center channel of the neck. As a
result, the steel washer and nuts on the threaded swage move within the
free space provided by the center hole and can come into contact with
the inner walls of the through-hole. To mitigate this condition, the
washer has been changed from steel to nylon. Also, the lower neck load
cell and its structural replacement have been revised since the Part
572 NPRM. For each of these two parts, a sleeve made of soft, dampening
material is now used to line the through-hole and prevent rattling of
the nuts. The load cell revision also carries over the capacities
specified in the NPRM which were increased for some channels where data
was truncated in pre-NPRM agency tests using a previous load cell.\22\
---------------------------------------------------------------------------
\22\ The revised load cell is a six-axis load cell. Maximum load
capacities and several other load cell specifications are given on
Drawing SA572-40 in the TDP.
---------------------------------------------------------------------------
In a related problem, a premature wear problem has been observed in
the agency's HIII-10C units and reported in comments provided by Dorel.
The molded neck itself has two polymeric bushings, one at each end of
the neck, through which the cable passes. The bushings prevent the
steel rope from abrading the internal through-hole of the neck.
However, the aforementioned cable movement tends to abrade the neck
channel and chafe the lower polymeric cable bushing.
To avoid problems such as those noted by Dorel, the polymeric
bushing should be inspected on a periodic basis. The bushing is an
inexpensive part that may be readily inspected and replaced during the
course of running the neck qualification tests. We note that setting
the neck cable to the proper torque is key to the longevity of the
bushing. The torque setting is also critical to passing the
qualification requirement for the neck. In addition, we also found that
the torque setting of the neck cable nut significantly affects the head
excursion and the upper neck moment within the sagittal plane (about
the y-axis).
We also found that, when left unchecked, the threaded stud-end
could wear through the plastic collar and chafe the outer aluminum disc
of the
[[Page 11657]]
molded neck after extended use. When the neck goes into extreme
flexion, a chafed bushing can partially work its way out of the center
through hole of the molded neck. This allows the wire rope to rub
directly against the aluminum end plate of the neck, sending shock
through the entire spine, which appears as noise in the signals of
nearby sensors.
As described earlier, the signal noise emanating from the neck has
no consequence on the use of the HIII-10C in FMVSS No. 213 because the
noise is removed by signal processing algorithms. Nonetheless, the
agency has implemented simple revisions to mitigate any shock emanating
from the shoulder and lower neck. In addition to revising the lower
neck load cell to preclude rattling, we have taken steps to lessen the
effects of the chafing. A new bushing has been specified in the TDP
with an increase to the flange thickness and with a smaller inner
diameter, which reduces the clearance of the wire rope. The inner
diameter of the cable washer has also been decreased to prevent it from
sliding. Details of the new load cell, bushing, and washer, along with
their effects, are reported in NHTSA's technical report, ``Revisions to
the HIII-10C Technical Data Package,'' August 2011.
3. Stiffness of Vinyl Insert
Dorel indicated in its comments that it was having difficulty
meeting the torso flexion test because the vinyl abdominal inserts it
used were too stiff or too soft. Dorel had to mix and match inserts and
lumbar flex joints in an attempt to pass the test. The commenter was
concerned that the manufacturing variability for the inserts is too
wide.
The agency has revised the specification of the abdominal insert by
adding new dimensional requirements that improve manufacturing
consistency and fit. The agency has also revised the PADI to include a
section on how to position the abdominal insert within the pelvis
cavity when running the torso flexion test. The specified setting of
the insert governs its interaction with the chest jacket, lumbar spine,
and ribcage, all of which influences the outcome of the torso flexion
test. In agency tests, the new insert setting provided sufficient
instruction to successfully carry out the torso flexion tests without
having to mix or match inserts.
4. Dummy Availability
In its 2005 comments, Dorel claimed that no dummies were available
on the market prior to the NPRMs of 2005 that satisfied the proposed
Part 572 specifications. It listed nine changes to its version of the
dummy relative to the version specified by the Part 572 NPRM of 2005.
Thus, Dorel claimed that it was not given adequate opportunity to
evaluate the proposed dummy.
We see no merit to delaying the final rule to either FMVSS No. 213
or Part 572 on the basis of HIII-10C availability. Several years have
passed since the NPRMs were published in 2005, during which two
additional NPRMs have been published on the use of the HIII-10C in
FMVSS No. 213. This has provided commenters with ample time and
opportunity to acquire, test, and submit comments to the docket about
the HIII-10C. We note that in Dorel's comments to the SNPRM of 2008, it
did not discuss any specifics on the HIII-10C other than those already
provided in 2005 and addressed herein.
b. Durability of the HIII-10C
In its comments, Dorel reported on observed durability problems and
breakage of the HIII-10C in its sled tests. No other commenters noted
any problems related to these observations or any other damage.
As described earlier in this preamble, the agency has expanded our
dataset of HIII-10C sled tests by about 200 tests and many more
qualification tests since the NPRMs were published in 2005. In the
whole of this extensive test regimen, the agency has studied many
aspects of the dummy's performance including its functionality and
durability. We have not observed any significant functionality or
durability problems that would preclude the use of the HIII-10C use in
FMVSS No. 213 or any other standardized test.
Each problem raised by Dorel is discussed below. Also included is a
discussion of our own part replacement records assembled during the
course of our post-NPRM evaluation of the dummy. No further changes to
the dummy have been implemented as a result of these observations.
1. Proximal Femur
Dorel reported a broken casting in one of its HIII-10C units
representing the proximal femur. Although Dorel did not describe how
the failure occurred, we assume it was brought on by the ``flailing
legs'' seen in FMVSS No. 213 tests. During the impact event, the lap
belt retains the pelvis, while the legs spring forward placing a
tensile load on the joint connecting the legs to the pelvis.
We had observed this type of failure in testing of an earlier, pre-
NPRM version of the dummy. Since then, the dummy part representing the
proximal femur was redesigned to eliminate the fracture problem. The
part is now made of 4140 steel rather than C954 aluminum bronze, and a
sharp corner stress riser has been rounded. In the photographs provided
by Dorel, it appears that its failed unit had the older aluminum bronze
casting. The new design was incorporated into the Part 572 NPRM version
of the dummy and is specified in the version described in this final
rule.
The femur has held up in all agency tests since the change was
implemented to the pre-NPRM version. No further change to the dummy is
necessary.
2. Bib Assembly
Dorel provided a picture of a torn bib assembly, without further
discussion, in its response to the Part 572 NPRM. The extent of the
testing to produce this damage was not described.
The agency has not encountered any instances of torn bib assemblies
in our extensive testing experience with the HIII-10C, but we have seen
occasional abrasions on some bib assemblies of other Part 572 dummies.
They were caused by the shoulder belt pressing against and eventually
rubbing through the chest jacket during multiple severe test exposures.
This may have been the case for Dorel, based on its general comment
that it had performed ``65 dynamic sled tests run at DJG [Dorel
Juvenile Group] to the new [FMVSS No.] 213 standard bench and pulse
using the HIII-10C dummy,'' in addition to other dynamic sled tests
conducted at a contract laboratory. Given that the tear is likely
caused by excessive wear-and-tear, the agency has not revised the bib
assembly.
3. Shoulder Rotation Stop Screws
The arm of the HIII-10C is connected to the shoulder through a yoke
that acts as a two degree of freedom joint which allows the arm to
flex, extend, and rotate axially. Affixed to the yoke is a protrusion,
or ``shoulder rotation stop,'' that limits the range of motion of the
shoulder in axial rotation (i.e., it cannot complete a 360 degree
circuit). So, when the arms of the HIII-10C flail forward and extend
during a dynamic test, the stops prevent the arms from rotating all the
way up and around behind the body.
Dorel provided photos showing that the screws holding the rotation
stop in place in its HIII-10C unit had sheared off. Dorel stated that
it repaired the part by welding the stop into place, but the commenter
provided no further discussion.
The agency has not experienced this type of failure in any of our
tests of the HIII-10C, and we do not know the
[[Page 11658]]
circumstances that led to the failure in the Dorel unit. In the absence
of information that a problem exists or that it is recurring, we find
no need to change the HIII-10C with regard to the shoulder stop.
4. Agency Part Replacement Records
Since the NPRMs of 2005, NHTSA has continued to monitor the
durability of the HIII-10C, as we do routinely with all of our ATDs. A
summary of our records is provided below. In general, a part within a
dummy is replaced for one of two reasons: Because it was damaged during
a test or because it has become worn and unserviceable after extensive
use. As described below, our experience indicates that all part
replacements were made under the latter circumstance. The records thus
show good durability of the HIII-10C.
i. Pelvis Helicoil Insert
Throughout our post-NPRM testing experience of about 200 sled
tests, the agency observed only one instance of a part failure that
appeared to have affected the outcome of the test. This failure was
brought on by flailing legs, which caused the femur to separate from
the pelvis due to the failure of a helicoil.\23\ ``Helicoil'' is the
product name of a steel fastener that provides positive thread locking
into soft metals like aluminum or bronze.
---------------------------------------------------------------------------
\23\ This was not the proximal femur casting part reported by
Dorel.
---------------------------------------------------------------------------
Three helicoils are inserted into the HIII-10C's aluminum pelvis
casting so that the flange that retains the proximal head of the femur
may be bolted directly to the casting. After one of our tests, we
noticed that the flange had separated from the pelvis. Upon closer
inspection, we found that a helicoil had disengaged from the pelvis.
This failure has not recurred. Moreover, a helicoil failure is
typically gradual as its threads loosen from the base material over
time. A thorough pre-test inspection can usually spot helicoil
looseness so that repairs may be made, thus mitigating the likelihood
of a test failure. Therefore, a revision to the flange fastening system
is unnecessary.
ii. Neck and Ribcage Replacement
Like all ATDs in the Hybrid III family of dummies, the deformable
parts of the HIII-10C have the shortest service lives. The two most
often replaced parts on the HIII-10C are the ribcage and the molded
neck. Worn ribs are usually detectable by examining them for overly
gouged or delaminated damping material. Unserviceable molded neck
assemblies are not noticeable by visual inspection, with the exception
of chafed cable bushings as described earlier.
The conditions of the ribs and neck are monitored directly through
the Part 572 qualification procedures. In our experiences with the
HIII-10C, the decision to remove a rib set or neck from service has
always been made during pre-test qualification procedures when the
thorax impact or the neck flexion/extension test qualifications cannot
be met after a few trials. The typical service life for HIII-10C rib
sets and neck assemblies alike are about thirty sled tests. We have not
had a situation where failure occurred during a sled test of any kind.
iii. Other Replacements
According to our records, flesh materials--particularly the chest
flesh--are the only other parts that have been replaced on a recurring
basis. As with flesh materials of all ATDs, those of the HIII-10C are
replaced periodically as they become aged, abraded, or torn.
Deterioration of these parts is easy to identify so that they may be
repaired or replaced well before they deteriorate to the point where
their condition may affect test results. They are also relatively
inexpensive (chest flesh is the highest priced flesh material item:
$650) and easy to service.
5. Durability Summary
Given the record of low maintenance to our own HIII-10C units and
the relatively few complaints noted by commenters, we consider the
dummy to be highly suitable for use in FMVSS No. 213 in terms of its
durability. Our records indicate that there have been relatively few
instances of HIII-10C part replacements of any sort. When we have
replaced parts, it has always been due to extensive service, not a
sudden failure. Replacement of worn parts constitutes preventative
maintenance that, when scheduled at regular intervals, will help to
ensure valid test results.
c. Qualification Procedures and Requirements
Qualification procedures for the HIII-10C are basically the same as
those proposed in the Part 572 NPRM, though some of the response
corridors have been modified in consideration of additional
qualification test data accumulated by the agency during our post-NPRM
test experience. We also considered in our analysis a large
qualification test dataset provided by the Alliance, amassed by members
of the SAE International (SAE) Dummy Testing Equipment Subcommittee
(DTESC). The much larger data set now allows us to base the setting of
the corridors on an enhanced statistical analysis, providing even
better assurance that the mean and the dispersion of the responses are
representative of the dummies that the users will have to work with in
the field.
Comments provided by the Alliance and echoed by FTSS/Denton
recommended several changes to the performance corridors for the HIII-
10C. In most instances, the commenters recommended changes that were
specified by the DTESC based on a large dataset of qualification test
results provided by participating organizations, including Chrysler,
Ford, and General Motors, FTSS/Denton, Delphi, MGA, and TRW. The
Alliance also recommended changes to the specification for impact
probes and dummy instrumentation. The comments and our response thereto
are discussed below.
1. Response Corridors
The corridors suggested by the Alliance are based on a range of 98
to 275 qualification tests per body segment from about 25 dummies. The
Part 572 NPRM corridors were based on a range of 6 to 28 qualification
tests per component performed on 2 dummies. Post-NPRM data accumulated
by the agency contained qualification results from an additional 4
HIII-10C units.
The agency analyzed the data submitted by the Alliance and found
that the suggested corridors and the coefficients of variation (CVs)
were generally in good agreement with agency data. This good
correspondence lent confidence that the data were of sufficient quality
to be considered with agency data towards the establishment of
performance corridors. The advantage of a larger sample size is that it
allows for consideration of such factors as lab-to-lab, operator-to-
operator, and dummy-to-dummy variability.
Upon consideration of the larger dataset, we found that our
original corridors proposed in the Part 572 NPRM needed only fine-
tuning. Summaries of the changes to each body region are given below.
Full details of our analyses are contained in the technical report,
``Development of Qualification Performance Specifications for the HIII-
10C Crash Test Dummy,'' December 2011, which has been placed in the
docket for this final rule.
i. Head
The head qualification test consists of dropping the head onto a
rigid surface from a height of 376 millimeters (mm)
[[Page 11659]]
(14.8 inch (in.)). Since the HIII-10C head is a Hybrid III 5th
percentile adult female (HIII-5F) head, the same test procedure is
specified as in 49 CFR part 572, Subpart O, which contains the
specification for the HIII-5F ATD. The head drop is designed for the
forehead to impact a flat, rigid surface at the midsagittal plane. The
head response limit in these impacts is specified between 250 and 300
G's as proposed in the NPRM. No change was necessary to these limits,
as the majority of data fit well and is well centered within the
corridors.
ii. Neck
The head and neck assembly and the test procedures are the same as
proposed in the Part 572 NPRM. The neck is evaluated for flexion and
extension kinematics similar to that defined in 49 CFR part 572, Figure
15 and Figure 21. The head-neck assembly is mounted to the bottom of a
pendulum that is being decelerated from a speed of 6.1 meter/sec (m/s)
(20 feet/sec (ft/s)) for flexion and 5.03 m/s (16.5 ft/s) for extension
at velocity reduction rates indicated in Table 1. The only difference
between the final rule and the Part 572 NPRM is a corrected reduction
in velocity specification at 10 ms for neck extension, changing from
1.59-1.89 ft/s to 1.49-1.89 ft/s. (The metric specification was
correct.) The 1.59 ft/s specification reflected a typographical error.
Table 1--Neck Reduction in Impact Velocity From Initial Impact in Flexion and Extension
----------------------------------------------------------------------------------------------------------------
Body region Reduction in impact velocity from initial impact
----------------------------------------------------------------------------------------------------------------
Final rule NPRM
Neck (flexion) -----------------------------------------------------------------------
ft/s m/s ft/s m/s
----------------------------------------------------------------------------------------------------------------
at 10ms................................. 1.64-2.04 5.38-6.69 1.64-2.04 5.38-6.69
at 20ms................................. 3.04-4.04 9.97-13.25 3.04-4.04 9.97-13.25
at 30ms................................. 4.45-5.65 14.60-18.53 4.45-5.65 14.60-18.53
----------------------------------------------------------------------------------------------------------------
Neck (Extension) ft/s m/s ft/s m/s
----------------------------------------------------------------------------------------------------------------
at 10ms................................. 1.49-1.89 4.89-6.20 1.59-1.89 4.89-6.20
at 20ms................................. 2.88-3.68 9.45-12.07 2.88-3.68 9.45-12.07
at 30ms................................. 4.20-5.20 13.78-17.06 4.20-5.20 13.78-17.06
----------------------------------------------------------------------------------------------------------------
Neck flexion. The final rule performance corridors for maximum D-
plane rotation of the head and moment decay time were revised from
those proposed in the Part 572 NPRM. Even though the width of the D-
plane rotation corridor remained unchanged, additional agency data and
comments by the Alliance supported a statistically justifiable shift of
the range upward from 74-88 degrees to 76-90 degrees (the Alliance
recommended a 76.5-88.5 degree range). The corridor for moment decay
time was adjusted to a slightly narrower range from 85-105 ms to 86-105
ms in the final rule. The combined NHTSA-Alliance data did not justify
the selection of a narrower corridor suggested by the Alliance at 91-
101 ms. In light of the good fit of the new qualification data within
the previously established limits, the peak moment range within the
rotation corridor remains unchanged from that proposed in the NPRM at
50-62 ms. The Alliance did not comment on this item.
Neck extension. All three neck extension performance corridors in
this qualification test were adjusted slightly from those proposed in
the Part 572 NPRM. The adjustments were needed to account for data
received from the Alliance and the additional data generated in agency
tests. The maximum D-plane rotation corridor was widened and shifted
downward from 99-114 degrees proposed in the NPRM to 96-115 degrees for
the final rule. The limits suggested by the Alliance were also 96-115
degrees.
Also, based on the additional data, in the final rule the corridor
for peak occipital-condyle moment during the maximum rotation interval
is revised to (-46)-(-37) Newton-meters (N-m), as compared to (-47)-(-
35) N-m proposed in the NPRM, and (-47)-(-36) N-m recommended by the
Alliance. The final rule specifies a moment decay time of 100-116 ms,
as compared to 100-120 ms proposed in the NPRM, and 100-114 ms
recommended by the Alliance.
iii. Thorax
The thorax qualification procedure is the same as that proposed in
the Part 572 NPRM. It specifies a 6.0 m/s (19.7 ft/s) frontal impact
within the midsagittal plane by a 6.89 kg (15.2 lb) round faced 121
millimeter (mm) (4.76 in) diameter probe into the mid-sternum of a
seated dummy. Thorax impact responses are specified as the maximum
sternum displacement, the maximum probe force at the time of maximum
sternum displacement, the maximum probe force when the sternum
displacement is between 20 mm and the lower bound of maximum
displacement, and the internal hysteresis percentage between loading
and unloading curves.
The NPRM proposed chest deflection limits of 40.5-48.5 mm, while
the Alliance recommended 38.5-48.5 mm. Upon consideration of the full
dataset, our analysis has led us to set the limits at 37-46 mm for the
final rule. This downward shift was necessitated by a stiffer response
seen in the most recent data in both NHTSA testing and in results
submitted by the Alliance.
In light of the modified maximum chest deflection corridor, the
limits of the peak probe force at maximum deflection and the peak probe
force in the deflection transition zone (prior to the rib deflection
reaching the lower corridor limit) were raised correspondingly. The
former was changed from 1.83-2.33 kN in the NPRM to 2.0-2.45 kN in the
final rule, while the latter was changed from <2.33kN in the NPRM to
<2.52 kN in the final rule. Comparable Alliance recommendations were
1.95-2.45 kN for peak force at maximum deflection and <2.45 kN in the
transition zone. Limits for hysteresis proposed in the NPRM were well-
supported by the data and remained unchanged at 69-85 percent.
iv. Torso Flexion
The torso flexion test involves the determination of bending
resistance of the upright seated dummy's lumbar spine/mid-torso area
when the upper torso is quasi-statically flexed from its upright seated
posture by 35 degrees relative to a lower torso. The resistance to
bending is defined as the highest load
[[Page 11660]]
encountered during the bending process.
The final rule specifies a resistance of 180 to 250 N compared to
that in the NPRM of 190-240 N. The adjustment was made in response to
Alliance comments recommending a range of 178-249 N. The final rule
limits are in near agreement with the Alliance recommendation, and are
well supported by the combined Alliance-NHTSA data set. The final rule
also specifies that upon removal of the flexion force the torso, the
torso is required to return to within 8 degrees of its initial
position. This is the same requirement that was proposed in the NPRM.
Commenters did not recommend a revision to this requirement.
v. Knee Impact
The knee impact test is the same as that proposed in the Part 572
NPRM, consisting of a 2.1 m/s (6.9 ft/s) impact by a 1.91 kg (4.21 lb)
flat-faced 76.2 mm (3.0 in.) diameter rigid probe into the knee of a
HIII-10C leg assembly (including the tibia and foot), where the distal
end of the femur is mounted rigidly to a reaction mass. For the final
rule, the corridor for the force applied to the knee by the impactor is
specified to be between 2.6 and 3.2 kN, as compared to 2.56 to 3.14 kN
in the NPRM. The final rule specification is in agreement with
recommendations made by the Alliance.
2. Summary of Qualification Requirements
A summary of performance specifications for the entire dummy,
including those proposed in the Part 572 NPRM and those advocated by
the Alliance, is provided in Table 2. Based on our analysis, the agency
data were found in most instances to be in reasonably good agreement
with the corridors suggested by the Alliance corridors. For
measurements where our analysis of the data did not justify setting the
corridors at Alliance recommendations, we searched for the best
justifiable accommodation of both datasets within the limits of the
biofidelity data.
As a general rule, performance corridors were set around 3 standard deviations from the mean for measurements with a CV<3
percent, at 2 standard deviations from the mean for
measurements with a CV from 3 to 5 percent, and at 10
percent from the mean for measurements with a CV from 5 to 10 percent.
Table 2 indicates that all of the data leading to CVs for the final
rule are within the 10 percent limit. Accordingly, all of the dummy
based measurements related to their projected use as Injury Assessment
Reference Values (IARVs) meet the requirements for inclusion into Part
572.
Table 2--Final Rule Qualification Corridors and Comparison With NPRM and Alliance Recommendations
--------------------------------------------------------------------------------------------------------------------------------------------------------
Alliance Full alliance/NHTSA dataset
Test Response measurement or test Final rule NPRM suggested -----------------------------
parameter corridor corridor corridor Mean S.D. %CV
--------------------------------------------------------------------------------------------------------------------------------------------------------
Head drop..................................... Acceleration (g)................ 250-300 250-300 250-300 271 11.6 4.29
Neck pendulum, flexion........................ Max D-plane rotation (deg)...... 76-90 74-88 76.5-88.5 83.05 3.28 3.95
Peak O-C moment (N-m)........... 50-62 50-62 n/a 55.38 3.30 5.96
Moment decay time to 10 N-m (ms) 86-105 85-105 91-101 96.63 3.88 4.01
Neck pendulum, extension...................... Max D-Plane rotation (deg)...... 96-115 99-114 96-115 105.4 4.35 4.12
Peak O-C moment (N-m)........... (-46)-(-37) (-47)-(-35) (-47)-(-36) -41.8 2.37 5.67
Moment decay to -10 N-m (ms).... 100-116 100-120 100-114 107.2 3.17 2.95
Thorax pendulum impact........................ Sternum displacement (mm)....... 37-46 40.5-48.5 38.5-48.5 41.3 2.1 5.04
Peak probe force defining the 2.0-2.45 1.83-2.33 1.95-2.45 2.227 0.113 5.06
displacement corridor (kN).
Peak probe force during the time <2.52 <2.33 <2.45 2.287 0.154 6.74
when sternum displ. is 20 to
40.5 mm (kN).
Thorax hysteresis............... 69-85% 69-85% 69-85% 80.3 2.3 2.91
Torso flexion................................. Peak force at 35 deg from 180-250 190-240 178-249 213.3 18.7 8.8
vertical (N).
Return angle (degrees).......... < 8, >-8 < 8, >-8 ............ 5.2 1.7 note 1
Knee impact................................... Peak force (kN)................. 2.6-3.2 2.56-3.14 2.60-3.20 2.92 0.157 5.37
--------------------------------------------------------------------------------------------------------------------------------------------------------
(1) The %CV does not apply to this measurement since the nominal requirement of zero degrees renders a %CV of infinite magnitude.
3. Impact Probes
For the dummies specified in Part 572 before 2000, impact probes
used in qualification testing were assumed to take the form of a nearly
perfect cylinder that could be specified by a material, weight, and
diameter. In practice, a perfectly cylindrical probe is rare. Also, the
addition of several new child dummies to 49 CFR part 572 called for a
new assortment of lighter probes that were even more difficult to
design in a pure cylindrical form due to their low weight. This created
a situation where testing laboratories maintained a limited assortment
of probe bodies, and then attained the proper probe characteristics by
interchanging probe faces.
Beginning with our final rule for the Hybrid III 6-year-old child
dummy (HIII-6C) in January 2000, the agency began to specify the
minimum mass moment of inertia (MOI) and free air resonance for the
various probes used in Part 572 qualification testing. This assured
that vibratory effects were not present and that various probe
configurations did not introduce differences in dummy response due to
probe shape variations. At the same time, laboratories retained ample
latitude to design impact probes. For the HIII-10C, the Part 572 NPRM
specified a minimum mass moment of inertia as well.
In its comment, the Alliance took issue with our proposed
specifications. It pointed out that the minimum thorax and knee
pendulum mass moments of inertia as proposed in the NPRM at 2,040 kg-
cm\2\ and 140 kg-cm\2\, respectively, were higher than those
recommended by the SAE Hybrid III Dummy Family Task Group. In its
comments, the Alliance included thorax and knee qualification data
collected from multiple test facilities indicating minimal performance
differences in qualification tests despite a variety of
[[Page 11661]]
test probes with different MOIs. It recommended that we revise our
minimum specification to 1,463 kg-cm\2\ for the thorax probe and 117
kg-cm\2\ for the knee probe, as was called out in the original SAE
specification of the dummy.
In our analysis of Alliance data, we examined round-robin tests
performed on the same knee (or thorax) to isolate the effect of the
different probe MOI on the response of that part. By only considering
these tests, we eliminated the possibility that dummy reproducibility
would confound the response data. Also, we only considered data from
the sources where MOIs were known. Though it submitted test data from
several laboratories, the Alliance provided probe MOIs from just three
sources.
In comparing qualification test data using the Alliance probes with
the lowest MOIs against data using our own probes, we found peak force
measurements to be consistently lower with the Alliance probes. We note
that the Alliance knee probe with the lowest MOI was still above our
lower limit (152 kg-cm\2\ vs. 140 kg-cm\2\), and the Alliance thorax
probe with the lowest MOI was only narrowly under our limit (1,960 kg-
cm\2\ vs. 2,040 kg-cm\2\). Given the trend towards lower force response
with lower MOIs and that the majority of Alliance probes are already
within our MOI specification, the agency will not revise the probe
specifications.
4. Instrumentation
i. Rotary Potentiometers
The Alliance pointed out an omission to the filter specification
for rotary potentiometers that are typically used in the neck flexion
and extension qualification tests. The potentiometers are used to
measure the rotation of the head relative to the pendulum. The agency
inadvertently overlooked the filter call-out in the Part 572 NPRM. We
have revised the specification to include a 60 CFC call-out as was
recommended by the Alliance. This call-out is consistent with SAE J211
and that of other Part 572 ATD specifications.
ii. Sternum Displacement
The Alliance pointed out that the CFC 180 filter specification for
sternum displacement was not consistent with the SAE Recommended
Practice J211, Rev. Mar 95, ``Instrumentation for Impact Tests--Part
1--Electronic Instrumentation,'' (SAE J211). It noted that Hybrid III
dummies specified in 49 CFR part 572 subparts N (HIII-6C) and O (HIII-
5F) call for the use of a CFC 600 filter for sternum displacement. This
was a mistake in the Part 572 NPRM. We have revised the final rule to
specify a CFC 600 filter for sternum displacement potentiometer
signals.
d. Technical Data Package
The HIII-10C as specified herein is essentially the same as that
defined in the Part 572 NPRM. A few minor revisions to the TDP have
come about as a result of our experiences during extensive use of
multiple HIII-10C dummies in the post-NPRM tests of booster seats. The
revisions were corrective in nature; they do not affect the response of
the dummy other than to remove unwanted artifacts. These include
changes associated with improved functionality to the shoulder, neck
cable bushing, and chin as described earlier. In addition, several
typographical errors and other mistakes in print were uncovered.
Comments associated with the TDP are discussed below.
1. Changes to the Engineering Drawings and PADI
FTSS/Denton requested a number of changes to the engineering
drawings and PADI. These requests were echoed by the Alliance. For the
most part, we agree with FTSS/Denton's requests and we have revised the
TDP accordingly. The revisions are all aimed at manufacturing,
machining, assembly, and inspection of dummy parts. They fell into four
categories: errors, dimensioning changes, clarifications expressed in
notes, and changes associated with the introduction of new part
numbers.
Errors consisted of misnumberings, typographical errors, and other
mistakes in print.
An example of a dimension change can be seen on the Shoulder Yoke
Assembly, drawing 420-3430. For this part, the yoke was widened by
0.003 inches. This minor change provides the proper clearance needed to
account for tolerance stack up so that the arm may always be attached
to the shoulder without force-fitting.
An example of a clarifying revision is the added set of dimensions
placed on sheet 3 of drawing 420-0000, Complete Assembly, HIII-10C.
These reference dimensions indicate the location of safety belt
plateaus on the dummy's shoulder and pelvis. They are useful when
inspecting the dummy in accordance with the instructions provided in
the PADI and when conducting the torso flexion qualification test. This
additional information does not alter the dummy's design or its
construction.
In the TDP proposed in the Part 572 NPRM, many parts were
identified with part numbers associated with other ATDs. In the final
drawing package we assigned new part numbers to these parts, using the
HIII-10C's ``420'' prefix, to identify these as HIII-10C parts. This
was strictly a documentation change to better identify HIII-10C parts
and did not affect the construction of the dummy in any way. However,
it did generate many drawing revisions since many of the newly assigned
part numbers are referenced on many HIII-10C drawings.
None of the revisions affect the performance of the HIII-10C in
qualification testing or in FMVSS No. 213. Therefore, they are not
discussed exhaustively in this document. A full accounting of the
revisions can be found in the supplementary technical report cited
earlier, ``Revisions to the HIII-10C Technical Data Package,'' NHTSA,
August 2011.
2. Organization of Materials
i. Searchable Text
FTSS/Denton and the Alliance recommended that the part numbers be
searchable in electronic PDF drawing files. The agency concurs that it
would be an improvement for text to be searchable in the electronic PDF
drawing files to facilitate use. Accordingly, the agency has converted
the drawing files to an electronic format with searchable text
capability. A searchable text is now available in the electronic
drawing files.
ii. Order of Engineering Drawings
FTSS/Denton and the Alliance recommended that the drawing package
be arranged into ascending order by part number. We disagree. We
believe that the drawing package should be left in segment order to be
able to quickly identify parts belonging to a particular segment
cluster. Moreover, the numbering system should be consistent with the
PADI to facilitate inspection and service of the dummy. Given that the
drawing package is electronically searchable, it will be an easy matter
for users to search for drawings and order them in the manner they
prefer. Accordingly, the HIII-10C drawing package remains ordered by
body segment (as proposed in the Part 572 NPRM).
iii. Part Quantity Specification
The HIII-10C parts list is arranged such that each assembly is
listed together with its associated parts. In many instances the same
part (such as a fastener) is used on multiple assemblies and is thus
listed more than
[[Page 11662]]
once on the parts list. The parts list proposed in the Part 572 NPRM
only identifies how many times a part is used on the assembly
immediately preceding it on the list, not the entire dummy. FTSS/Denton
and the Alliance recommend that the parts list should include a column
giving the total quantity of that part in the dummy the first time it
appears on the list. The agency agrees that such information would be
useful for procurement of parts and servicing of the dummy.
Accordingly, a column has been added in the parts list showing the
total number of times a part appears in the dummy.
iv. Part Numbering Scheme
A number of HIII-10C dummy parts are common with parts of other
dummies. For example, the HIII-10C has the same head as the HIII 5th
female, but the TDP's for each dummy have their own numbering scheme
with different part numbers for the head. FTSS/Denton commented that it
believes the same part numbers should be used for identical parts. This
comment was echoed by the Alliance.
The agency has not revised our part numbering scheme as recommended
by FTSS/Denton. If the same part numbers were used, substantial
documentation problems could be encountered. A revision to the design
of a shared part may be needed for one dummy, but detrimental to the
function of another dummy. A distinct numbering system, by cross-
referencing the shared part numbers, poses no such problems.
The main benefits of using identical part numbers are related to
part inventory control and sequencing of production processes. For
dummy manufacturers like FTSS/Denton, the economics of production may
be aided by a numbering scheme that identifies common parts so that
batch processing of identical parts could be scheduled readily.
However, we believe that interested parties can realize these
advantages easily enough by developing their own internal part
numbering scheme as they see fit. This may be cross-referenced against
the HIII-10C TDP without resorting to a common part numbering scheme
for Part 572.
3. Specifications for Soft Parts
The Alliance and FTSS/Denton recommended that the agency and
industry work together to define dimensions that are critical to
controlling performance of the vinyl, rubber, and other deformable
parts and to identify suitable measurement jigs and part tolerances.
The Alliance cited the jacket of the 49 CFR part 572 subpart O Hybrid
III 5th percentile adult female dummy as an example of unwanted
reproducibility variations among dummy manufacturers. FTSS/Denton
requested further that the agency work directly with them to set
longevity specifications for the useful life of deformable parts.
Citing customer dissatisfaction, FTSS/Denton was concerned that vinyl
and rubber ATD components typically shrink or change shape over time.
We do not believe it is feasible or practical for NHTSA to
undertake the work suggested by the commenters at this time, nor is it
necessary for the HIII-10C. The HIII-10C was developed cooperatively
under the direction of the SAE Hybrid III Dummy Family Task Force to
limit the variability of parts. At the time, FTSS and Denton
collaborated jointly on the design. SAE provided the general
specifications, and the two manufacturers shared the responsibility of
designing the hardware and producing the prototypes. The cooperation
assured that variations in reproducibility were avoided.
Even before the companies merged, HIII-10C parts built by FTSS and
Denton had a good record of reproducibility and interchangeability, as
highlighted in the Part 572 NPRM. Now that the two companies have
merged, HIII-10C vinyl and rubber parts can be created from a common
set of molds, thus precluding any variability in the form and fit of
soft parts. As for longevity, the decision on when to replace worn
HIII-10C parts should be based on conformity to part specifications and
qualification testing.
4. Use of 3D Computer Renderings
The Part 572 NPRM mentioned that ``three-dimensional engineering
aids are available from the NHTSA Web site for complex dummy part
dimensions. While these aids are not part of this specification, they
can be used by the public for reference purposes.'' These aids take the
form of computer-aided design (CAD) files that appear as three-
dimensional (3D) renderings of various parts. They were received by
NHTSA from the SAE Hybrid III Dummy Family Task Group in 2004 at the
time we received the two-dimensional (2D) engineering drawings.\24\ The
Alliance commented that it believes that the 3D renderings should be
formally entered into Part 572 to specify the HIII-10C.
---------------------------------------------------------------------------
\24\ Two sets of 3D renderings were received: one originating
from FTSS and the other from Denton before the merger of the two
companies into Humanetics.
---------------------------------------------------------------------------
Although we see much merit to 3D renderings, we will not implement
the suggestion to enter them into Part 572. We understand that all
contemporary ATD designs originate using CAD tools which are valuable
assets to designers and researchers. Within NHTSA, CAD files of ATDs
have been used in our research activities to construct finite element
models to simulate dummies in dynamic events. We have also used them to
investigate possible ATD design modifications and to study static
interactions with seat belts and vehicle interiors.
However, 3D CAD renderings are not currently used for regulatory
purposes in Part 572. As applied within our research activities, a 3D
computer rendering is akin to an actual part. But the part alone--
without dimensions or any other information--cannot be used to specify
itself. Part specifications communicate information on how to fabricate
and verify the part. This is done by applying dimensions and tolerances
to parts, along with information on material, surface finish, and other
features required by the specification-holder. The most objective way
to convey this information is to render the part on a standard 2D
engineering drawing, showing multiple views of the part when necessary.
Drawing standards have long been developed to systematically and
unambiguously convey this information, as reflected in Part 572
engineering drawings of ATDs. Thus, the 2D drawings ultimately serve to
specify ATD parts.
Neither the Alliance nor FTSS/Denton (the originator of the 3D
renderings) has proposed a systematic and unambiguous means by which
the 3D renderings may be used to specify ATDs. Until such a means is
devised, we will not include them in 49 CFR part 572 to specify the
HIII-10C. Our basis for acceptance of the dummy will continue to be
conformance to 2D drawings, together with the qualification test
requirements in Part 572.
We continue to believe that 3D renderings serve as very helpful
engineering aids as described in the NPRM and hold promise in
specifying ATD parts. However, in the case of the 3D renderings of the
HIII-10C received from the SAE Hybrid III Dummy Family Task Group, the
agency will not post the CAD files on our Web site. Upon further review
of these renderings, we have found many instances where they do not
conform to the 2D specifications shown on drawings. Since we cannot
vouch for their accuracy, we decline to post them.
[[Page 11663]]
e. Other
In response to some of the comments, this section clarifies or
explains some of the statements in the preamble of the Part 572 NPRM.
These clarifications do not affect the regulatory text or TDP
specifying the HIII-10C for incorporation into Part 572.
1. Labeling the Dummy as a ``Ten Year Old''
As noted earlier in this preamble, among the ATDs described in 49
CFR part 572, the HIII-10C successfully fills the size gap between the
existing HIII-6C and the Hybrid III 5th percentile adult female dummy.
The majority of the commenters were supportive of the use of the HIII-
10C. However, AAP noted that the height and weight of the HIII-10C do
not correspond to an average 10-year-old child as indicated by growth
charts published by the Center for Disease Control (CDC). AAP stated
that, according to growth charts from 2000, the HIII-10C falls into the
50th-75th percentile in weight, but at 130 centimeters (cm) tall, it is
only in the 5th-10th percentile in standing height. AAP believed that
these proportions do not represent any average human child and may
better represent a nine-year-old child than a ten-year-old. This
comment was echoed by Advocates. Although neither organization objected
to the use of the dummy in the FMVSS, both apparently believe that the
discrepancy in the proportions of the HIII-10C may confuse or mislead
the general public on the applicability of booster seats. Thus, both
organizations believe the agency should explain how we defined ``ten-
year-old'' as it relates to human children and the description of the
HIII-10C.
Agency response. The target design for the HIII-10C dummy was an
ATD that was suitable for assessing CRSs rated for children weighing
about 36.3 kg (80 lb). At 35.4 kg (78 lb), the HIII-10C fulfills this
objective. As such, the design intent of the dummy was not to conform
rigorously to the anthropometry of a child of a particular age, weight,
or height percentile. Furthermore, the sitting height--not the standing
height--is of primary importance when evaluating booster seats because
the overlay of the seat belt system onto the dummy is depended on its
seated posture. As pointed out by AAP, the sitting height of the HIII-
10C falls into the same growth chart range for sitting height as it
does for weight.
Nevertheless, the agency believes that the proportions of the HIII-
10C are more consistent with an average 10-year-old than indicated by
AAP's comments. Characteristic dimensions and segment weights of the
HIII-10C are based on the anthropometry of the average 10-year-old as
identified by Mertz et al.,\25\ to which the dummy is shown to match
closely.
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\25\ Mertz HJ, Jarrett K, Moss S, Salloum M, ZhaoY, The Hybrid
III 10-Year-Old Dummy, Stapp Car Crash Journal, Vol. 45, November
2001.
---------------------------------------------------------------------------
Moreover, we note that our declared standing height of 130 cm is
only an approximation, not a direct measurement. The HIII-10C has no
one-to-one correspondence with the heights shown on CDC growth charts.
The CDC reference for standing height is one that is taken when
subjects are maximally erect. Like all full ATDs in Part 572, the HIII-
10C is a sitting dummy. Since it cannot be placed in a standing
position, its ``standing height'' cannot be measured directly. Instead,
it is approximated by summing the lengths of its body segments.
However, since the dummy is constructed to represent a reclined and
supported seated posture, not an erect posture, the summed lengths
underestimate the CDC standing height. This means that if an actual
child with sitting dimensions equal to those of the HIII-10C stood in a
maximally erect posture, his/her height would probably be greater than
130 cm.
2. Best Practices for Belt Routing
In citing a 2005 paper by Tylko and Dalmotas,\26\ the Alliance
observed that the chest deflection of the HIII-10C in the booster seat
was higher than it was when it was used without the booster seat. In
the non-booster test, the belt was routed close to the neck where that
the dummy's central sternal potentiometer was not sensitive to high
belt loading. (This insensitivity is common to all ATDs in the Hybrid
III family of dummies.) The Alliance has asked the agency to raise
awareness of this issue so that the positive effects of booster seats
are not mistakenly maligned.
---------------------------------------------------------------------------
\26\ Tylko S, Dalmotas D (2005), ``Protection of Rear Seat
Occupants in Frontal Crashes,'' Proceedings of the 19th
International Technical Conference on the Enhanced Safety of
Vehicles Conference, Paper No. 05-258.
---------------------------------------------------------------------------
Agency response. As a point of clarification, we note that an
injury criterion based on chest deflection is not included in FMVSS No.
213. Further, we also note that the authors of the study make the point
that limiting the analysis to chest responses could lead to false
conclusions, and that multiple injury metrics should be used, not just
chest deflection.
The agency agrees that low chest deflections alone are not always a
good indicator of a safe condition. Low deflections often accompany
cases of submarining and high knee excursion. Low chest deflections can
also occur when the belt migrates laterally off the shoulder so that
the thorax is not held back and head excursion is exceedingly high.
This exemplifies why multiple injury metrics are usually needed to
evaluate a safety system. For FMVSS No. 213, we assess booster seats by
evaluating the HIII-10C's chest acceleration, head excursion, and knee
excursion concurrently. The agency does not believe that either FMVSS
No. 213 or the HIII-10C promotes a poor booster seat design in which
the shoulder belt is routed close to the neck. As discussed in this
rulemaking, we have found that the HIII-10C dummy adequately
distinguishes good vs. bad belt routing in the CRS test environment.
3. Abdominal Injury Correlates
The August 31, 2005 NPRM on FMVSS No. 213 discussed NHTSA's work
developing abdominal injury criteria for the HIII-10C, including our
work on the ``abdominal injury ratio'' (AIR), which uses impulse
calculations from the iliac compressive and lumbar shear forces to
identify dummy kinematics associated with submarining. A high AIR value
occurs with diminished iliac loads in the presence of high lumbar shear
loads. This indicates that the belt may have slipped off the iliac and
the dummy may have submarined. Thus, greater AIR values correlate
indirectly to abdominal injuries.
In comments to the Part 572 NPRM, Advocates requested that the
agency implement AIR until such time as an alternative abdominal injury
measure has been established.
Agency response. AIR was not proposed in the FMVSS No. 213 NPRM or
SNPRMs due to limited data and is not included in the final rule. We
note that AIR is empirical; it is not founded upon the biomechanics of
injury. (I.e., reduced iliac loads do not cause abdominal injuries.
They only identify instances where a belt may have slipped into the
abdomen of the dummy, which may or may not lead to injury.) If the AIR
criterion were to be imposed, CRS manufacturers could maximize iliac
loads to achieve a good AIR score. We have concerns about criteria that
encourage high loads of any sort, as this could potentially increase
injury risk in another body region or produce some other unexpected
consequence.
For immediate use now, the agency has adopted the use of a
correlate to abdominal injuries, i.e., knee excursion. The final rule
for FMVSS No. 213 imposes limits on knee excursion and
[[Page 11664]]
head excursion for the HIII-10C. The limit on knee excursion prevents
restraint manufacturers from controlling head excursion by designing
their restraints so that children submarine excessively during a crash.
The agency has observed a strong correlation between knee excursion and
submarining in the child dummies.\27\ Ultimately, a direct
biomechanically-based measure of abdominal deformation provides the
best means to assess abdominal injuries. Our research plan for the
HIII-10C includes developing a pelvis and abdominal modification that
will provide such a measurement.
---------------------------------------------------------------------------
\27\ Klinich, K., Reed, M., Orton, N., Manary, M., Rupp, J.,
``Optimizing Protection for Rear Seat Occupants: Assessing Booster
Performance with Realistic Belt Geometry Using the Hybrid III 6YO
ATD,'' UMTRI Report, University of Michigan, Ann Arbor, MI, March
2011.
---------------------------------------------------------------------------
4. Repeatability in Systems Testing
In the Part 572 NPRM, the agency reported on a series of
repeatability tests using a dynamic sled. The tests were carried out
using a specialized booster seat designed for repeated use. Dorel
commented that they cannot follow this protocol when certifying its own
seats. Dorel also commented that our repeatability tests seemed to
assure a best-case outcome in terms of dummy injury metrics.
Agency response. Dorel may have misconstrued our reporting of these
tests as a mandate for additional procedures necessary to qualify the
HIII-10C and certify booster seats. This was not our intent. The series
of tests were not directly applicable to compliance testing of booster
seats. The purpose of the sled tests was to evaluate the repeatability
and durability of the HIII-10C dummy kinematics in a pulse approaching
FMVSS No. 213 severity. The tests were not to create a best-case
scenario for injury reference values. We chose to use a rigid bench
seat in conjunction with a limited number of CRS models to minimize the
effects of set-up related variables which otherwise could interfere
with the assessment of the dummy's own true consistency.
f. Dummy Development Efforts
1. Hybrid III Child Dummy Revisions--Abdomen and Pelvis
Citing the significance of abdominal injuries in children and the
lack of instrumentation in the HIII-10C, both CHOP and Advocates urged
the agency to redouble our efforts to come up with an appropriate means
to assess abdominal injuries with the dummy. Dorel, AAP, and UMTRI also
commented on importance of assessing abdominal injuries.
Since the NPRMs of 2005, NHTSA has been actively involved in two
principal research efforts aimed at improving abdominal injury
assessment in Hybrid III child ATDs. The two efforts focus on the
development of a biofidelic, instrumented abdomen along with an
appropriately proportioned pelvis.
One effort involves a concept for a fluid-filled abdomen that was
reported in 2001.\28\ Since then, it has been developed into a silicone
shell filled with silicone gel with instrumentation to measure
deformation. The shell takes the form of an insert that fills the
abdominal cavity of the HIII-6C. The abdominal insert has proven to be
reasonably biofidelic when compared with the response of an age-matched
animal surrogate.\29\ The other effort involves the modification of a
standard HIII-6C pelvis to more closely reflect child anthropometry
based on data collected by UMTRI on child participants.\30\
---------------------------------------------------------------------------
\28\ Rouhana et al. (2001), ``Development of a Reusable, Rate-
sensitive Abdomen for the Hybrid III Family of Dummies,'' Stapp Car
Crash Journal, V45.
\29\ Kent R, Stacey S, Kindig M, Forman J, Woods W (2006),
``Biomechanical Response of the Pediatric Abdomen, Part 1:
Development of an Experimental Model and Quantification of
Structural Response to Dynamic Belt Loading,'' Stapp Car Crash
Journal, V50, 2006-22-0001.
\30\ Klinich, K et al. (2010), ``Development and Testing of a
More Realistic Pelvis for the Hybrid III 6-Year-Old ATD,'' Traffic
Injury Prevention, 11:606-612.
---------------------------------------------------------------------------
NHTSA has also begun work with an SAE working group devoted to
integrating abdomen and pelvis technology into the HIII-6C (the SAE
dummy abdomen pelvis round robin (DAPRR) working group (August 2008)).
In DAPRR, NHTSA is facilitating the development of prototype pelves
using UMTRI design criteria \31\ to develop a biofidelic retrofit
package suitable for assessing pediatric abdominal injuries. Round-
robin testing of the prototypes is planned for 2012. The HIII-6C is the
primary target of the developing modifications given the greater use
rates of six-year-olds vs. ten-year-olds in child restraint systems
regulated by FMVSS No. 213. The new pelvis and abdomen designs could
possibly be transitioned to the ten-year-old size through dimensional
scaling and considerations for biomechanical response differences.
---------------------------------------------------------------------------
\31\ Reed MP, Sochor MM, Rupp JD, Klinich KD, Manary MA (2009),
``Anthropometric Specification of Child Crash Dummy Pelves through
Statistical Analysis of Skeletal Geometry,'' Journal of
Biomechanics, V42: 1143-1145.
---------------------------------------------------------------------------
2. Pediatric Research
CHOP, AAP, and Advocates have asked the agency to intensify our
research efforts in child biomechanics in general. Many noted that
current pediatric crash test dummies have been developed based on
biofidelity requirements that were scaled from adult response data.
Since the NPRMs of 2005, the agency has been engaged in several
activities aimed at new child specific biofidelity requirements for use
in the development of new frontal impact child dummies. These are
summarized below and discussed more fully in NHTSA's Biomechanics
Research Plan, 2011-2015.\32\
---------------------------------------------------------------------------
\32\ NHTSA's Biomechanics Research Plan, 2011-2015, Report No.
DOT HS 811 474, U.S. Department of Transportation, Washington DC,
June 2011.
---------------------------------------------------------------------------
Child anthropometry. In order to properly assess a child's
interaction with a booster seat and belt system, we are building a
child anthropometry database by collecting whole-body laser scans of 3-
, 6- and 10-year-old age ranges in automotive seating positions.
Biomechanical response. We have several projects focused on getting
response data that is unique to the pediatric human and not scaled from
adult data. For example, to better understand the deformation
characteristics of a pediatric thorax, we are collecting force versus
deflection data during cardiopulmonary resuscitation of pediatric
hospital patients. Additionally, we are collecting data from sled tests
of pediatric age-matched surrogates that are being used to quantify
thoracic response and spinal kinematics.
Biomechanics of injury. We are studying the relationship between
local brain tissue strain and axonal injury in a prepubescent human.
This has potential to be used for the basis of new brain injury
criteria for children.
Child dummy development. The agency has begun assessing current
child ATDs (including those in the Hybrid III family as well as the Q-
series) against new pediatric response data. Our first consideration is
the need for developing an all-new 6-year-old ATD versus enhancement of
the existing HIII-6C. Thereafter, we will consider the need for an
advanced 10-year-old ATD.
3. Status of HIC
Advocates have asked the agency to work expeditiously to reinstate
a head injury criterion for the HIII-10C.
The agency is committed to resolving the problem that led to our
decision to omit HIC as a criterion in FMVSS No.
[[Page 11665]]
213 when testing with the HIII-10C. The problem, explained earlier,
stems from ATD whole-body motions that induce a hard chin-to-chest
contact, not HIC itself. We are working to improve the ATD's chin and
sternum designs to mitigate this effect. As described under the heading
of child biomechanics within the NHTSA Biomechanics Research Plan,\33\
we are also working to attain a better understanding of pediatric body
motions in order to engineer a biofidelic head response into an ATD.
This includes efforts to characterize the flexibility of an adolescent
thoracic spine and its effect on head excursion and upper neck loads.
Furthermore, research is underway to better understand the interaction
between the shoulder belt and clavicle and its effect on head motion.
We are also examining the extent to which chin-to-chest contacts
actually occur to children in booster seats in order to model the
interaction correctly with a child ATD.
---------------------------------------------------------------------------
\33\ NHTSA's Biomechanics Research Plan, 2011-2015, Report No.
DOT HS 811 474, U.S. Department of Transportation, Washington DC,
June 2011, pp. 6-10.
---------------------------------------------------------------------------
V. Rulemaking Analyses and Notices
Executive Order (E.O.) 12866, E.O. 13563 and DOT Regulatory Policies
and Procedures
This rulemaking action has considered the impact of this regulatory
action under E.O. 12866 and E.O.13563 and the Department of
Transportation's (DOT) regulatory policies and procedures. This
rulemaking action was not reviewed by the Office of Management and
Budget under E.O. 12866. The rulemaking has also been determined not to
be significant under DOT's regulatory policies and procedures (44 FR
11034, February 26, 1979).
There are benefits associated with this rulemaking but they cannot
be quantified. The incorporation of the test dummy into 49 CFR part 572
will permit NHTSA to use the ATD in FMVSS No. 213 compliance testing of
CRSs for children weighing over 65 lb. In addition, the availability of
this dummy in a regulated format will benefit safety by providing a
more suitable, stabilized, and objective test tool to the safety
community for use in research and development of child passenger safety
products.
Based on our dummy purchase contract with FTSS/Denton, the
estimated cost of an uninstrumented HIII-10C dummy is approximately
$35,000. Instruments necessary to qualify the dummy in accordance with
Part 572 include 3 accelerometers for the head (about $500 apiece) and
an upper neck load cell (about $10,000). The central sternal
potentiometer, needed for the thorax qualification procedure, is
included in the base cost of the dummy. For compliance testing, only
three accelerometers are needed; they are located at the CG of the
thorax rather than the head. All sensors required in compliance and
certification procedures are common with other 49 CFR part 572 dummies,
so the cost of those instruments may be defrayed to some extent for
those who already own them. If the dummy is outfitted with all
instrumentation up to its full capability, the total instrumentation
cost is about $65,000 in addition to the cost of the dummy.
This document amends 49 CFR part 572 by adding design and
performance specifications for a test dummy representative of a ten-
year-old child that the agency will use in compliance tests of the
Federal child restraint system safety standard, and may use for
research purposes. This Part 572 rule does not impose any requirements
on anyone. Businesses are affected only if they choose to manufacture
or test with the dummy. Because the economic impacts of this final rule
are minimal, no further regulatory evaluation is necessary.
Regulatory Flexibility Act
Pursuant to the Regulatory Flexibility Act (5 U.S.C. 601 et seq.,
as amended by the Small Business Regulatory Enforcement Fairness Act
(SBREFA) of 1996), whenever an agency is required to publish a proposed
or final rule, it must prepare and make available for public comment a
regulatory flexibility analysis that describes the effect of the rule
on small entities (i.e., small businesses, small organizations, and
small governmental jurisdictions), unless the head of the agency
certifies the rule will not have a significant economic impact on a
substantial number of small entities. The Small Business
Administration's regulations at 13 CFR part 121 define a small
business, in part, as a business entity ``which operates primarily
within the United States.'' (13 CFR 121.105(a)).
We have considered the effects of this rulemaking under the
Regulatory Flexibility Act. I hereby certify that this rulemaking
action will not have a significant economic impact on a substantial
number of small entities. This action will not have a significant
economic impact on a substantial number of small entities because the
addition of the test dummy to Part 572 does not impose any requirements
on anyone. NHTSA will not require anyone to manufacture the dummy or to
test motor vehicles or motor vehicle equipment with it.
National Environmental Policy Act
NHTSA has analyzed this final rule for the purposes of the National
Environmental Policy Act and determined that it will not have any
significant impact on the quality of the human environment.
Executive Order 13045 and 12132 (Federalism)
Executive Order 13045 (62 FR 19885, April 23, 1997) applies to any
rule that: (1) is determined to be ``economically significant'' as
defined under E.O. 12866, and (2) concerns an environmental, health, or
safety risk that NHTSA has reason to believe may have a
disproportionate effect on children. If the regulatory action meets
both criteria, we must evaluate the environmental health or safety
effects of the planned rule on children, and explain why the planned
regulation is preferable to other potentially effective and reasonably
feasible alternatives considered by us.
This final rule is not subject to the Executive Order because it is
not economically significant as defined in E.O. 12866.
NHTSA has examined this final rule pursuant to Executive Order
13132 (64 FR 43255, August 10, 1999) and concluded that no additional
consultation with States, local governments or their representatives is
mandated beyond the rulemaking process. The agency has concluded that
the final rule does not have federalism implications because the rule
does not have ``substantial direct effects on the States, on the
relationship between the national government and the States, or on the
distribution of power and responsibilities among the various levels of
government.'' This rule will not impose any requirements on anyone.
Businesses will be affected only if they choose to manufacture or test
with the dummy.
Further, no consultation is needed to discuss the preemptive effect
of this final rule. NHTSA's safety standards can have preemptive effect
in two ways. This final rule amends 49 CFR part 572 and is not a safety
standard.\34\ This Part
[[Page 11666]]
572 final rule does not impose any requirements on anyone.
---------------------------------------------------------------------------
\34\ With respect to the safety standards, the National Traffic
and Motor Vehicle Safety Act contains an express preemptive
provision: ``When a motor vehicle safety standard is in effect under
this chapter, a State or a political subdivision of a State may
prescribe or continue in effect a standard applicable to the same
aspect of performance of a motor vehicle or motor vehicle equipment
only if the standard is identical to the standard prescribed under
this chapter.'' 49 U.S.C. 30103(b)(1). Second, the Supreme Court has
recognized the possibility of implied preemption: State requirements
imposed on motor vehicle manufacturers, including sanctions imposed
by State tort law, can stand as an obstacle to the accomplishment
and execution of a NHTSA safety standard. When such a conflict
exists, the Supremacy Clause of the Constitution makes the State
requirements unenforceable. See Geier v. American Honda Motor Co.,
529 U.S. 861 (2000).
---------------------------------------------------------------------------
Civil Justice Reform
With respect to the review of the promulgation of a new regulation,
section 3(b) of Executive Order 12988, ``Civil Justice Reform'' (61 FR
4729, February 7, 1996) requires that Executive agencies make every
reasonable effort to ensure that the regulation: (1) Clearly specifies
the preemptive effect; (2) clearly specifies the effect on existing
Federal law or regulation; (3) provides a clear legal standard for
affected conduct, while promoting simplification and burden reduction;
(4) clearly specifies the retroactive effect, if any; (5) adequately
defines key terms; and (6) addresses other important issues affecting
clarity and general draftsmanship under any guidelines issued by the
Attorney General. This document is consistent with that requirement.
Pursuant to this Order, NHTSA notes as follows.
The issue of preemption is discussed above in connection with E.O.
13132. NHTSA notes further that there is no requirement that
individuals submit a petition for reconsideration or pursue other
administrative proceeding before they may file suit in court.
Paperwork Reduction Act
Under the Paperwork Reduction Act of 1995, a person is not required
to respond to a collection of information by a Federal agency unless
the collection displays a valid control number from the Office of
Management and Budget (OMB). This rule will not have any requirements
that are considered to be information collection requirements as
defined by the OMB in 5 CFR part 1320.
National Technology Transfer and Advancement Act
Section 12(d) of the National Technology Transfer and Advancement
Act of 1995 (NTTAA), Public Law 104-113, section 12(d) (15 U.S.C. 272)
directs NHTSA to use voluntary consensus standards in its regulatory
activities unless doing so would be inconsistent with applicable law or
otherwise impractical. Voluntary consensus standards are technical
standards (e.g., materials specifications, test methods, sampling
procedures, and business practices) that are developed or adopted by
voluntary consensus standards bodies. The NTTAA directs NHTSA to
provide Congress, through OMB, explanations when the agency decides not
to use available and applicable voluntary consensus standards.
The test dummy and qualification requirements are based on the work
of the SAE Hybrid III Dummy Family Task Group (DFTG). Differences
between the DFTG recommendations and this final rule are minor and are
based on additional research performed by the agency and on comments to
the NPRM.
The following voluntary consensus standards have been used in
developing the HIII-10C dummy:
SAE Recommended Practice J211, Rev. Mar 95,
``Instrumentation for Impact Tests--Part 1--Electronic
Instrumentation''; and,
SAE J1733 of 1994-12 ``Sign Convention for Vehicle Crash
Testing.''
Unfunded Mandates Reform Act
Section 202 of the Unfunded Mandates Reform Act of 1995 (UMRA),
Public Law 104-4, requires Federal agencies to prepare a written
assessment of the costs, benefits, and other effects of proposed or
final rules that include a Federal mandate likely to result in the
expenditure by State, local, or tribal governments, in the aggregate,
or by the private sector, of more than $100 million annually (adjusted
for inflation with base year of 1995). Before promulgating a NHTSA rule
for which a written statement is needed, section 205 of the UMRA
generally requires the agency to identify and consider a reasonable
number of regulatory alternatives and adopt the least costly, most
cost-effective, or least burdensome alternative that achieves the
objectives of the rule.
This final rule does not impose any unfunded mandates under the
UMRA. This rule does not meet the definition of a Federal mandate
because it does not impose requirements on anyone. It amends 49 CFR
part 572 by adding design and performance specifications for a 10-year-
old test dummy that the agency will use in FMVSS No. 213 and for
research purposes. This final rule affects only those businesses that
choose to manufacture or test with the dummy. It would not result in
costs of $100 million or more to either State, local, or tribal
governments, in the aggregate, or to the private sector.
Plain Language
Executive Order 12866 requires each agency to write all rules in
plain language. Application of the principles of plain language
includes consideration of the following questions:
--Has the agency organized the material to suit the public's needs?
--Are the requirements in the rule clearly stated?
--Does the rule contain technical language or jargon that is not clear?
--Would a different format (grouping and order of sections, use of
headings, paragraphing) make the rule easier to understand?
--Would more (but shorter) sections be better?
--Could the agency improve clarity by adding tables, lists, or
diagrams?
--What else could the agency do to make this rulemaking easier to
understand?
If you have any responses to these questions, please send them to
NHTSA.
Regulation Identifier Number
The Department of Transportation assigns a regulation identifier
number (RIN) to each regulatory action listed in the Unified Agenda of
Federal Regulations. The Regulatory Information Service Center
publishes the Unified Agenda in April and October of each year. You may
use the RIN contained in the heading at the beginning of this document
to find this action in the Unified Agenda.
Petitions for Reconsideration of This Rule
The petition will be placed in the docket. Anyone is able to search
the electronic form of all documents received into any of our dockets
by the name of the individual submitting the comment (or signing the
comment, if submitted on behalf of an association, business, labor
union, etc.). You may review DOT's complete Privacy Act Statement in
the Federal Register published on April 11, 2000 (Volume 65, Number 70;
Pages 19477-78).
List of Subjects in 49 CFR Part 572
Motor vehicle safety, Incorporation by reference.
In consideration of the foregoing, NHTSA amends 49 CFR Part 572 as
follows:
PART 572--ANTHROPOMORPHIC TEST DUMMIES
0
1. The authority citation for Part 572 continues to read as follows:
Authority: 49 U.S.C. 322, 30111, 30115, 30117 and 30166;
delegation of authority at 49 CFR 1.50.
[[Page 11667]]
0
2. 49 CFR Part 572 is amended by adding a new Subpart T consisting of
572.170--572.177 to read as follows:
Subpart T--Hybrid III 10-Year-Old Child Test Dummy (HIII-10C)
Sec.
572.170 Incorporation by reference.
572.171 General description.
572.172 Head assembly and test procedure.
572.173 Neck assembly and test procedure.
572.174 Thorax assembly and test procedure.
572.175 Upper and lower torso assemblies and torso flexion test
procedure.
572.176 Knees and knee impact test procedure.
572.177 Test conditions and instrumentation.
Appendix--Figures to Subpart T of Part 572
Sec. 572.170 Incorporation by reference.
(a) Certain material is incorporated by reference (IBR) into this
part with the approval of the Director of the Federal Register under 5
U.S.C. 552(a) and 1 CFR part 51. To enforce any edition other than that
specified in this section, NHTSA must publish notice of change in the
Federal Register and the material must be available to the public. All
approved material is available for inspection at the Department of
Transportation, Docket Operations, Room W12-140, telephone 202-366-
9826, and is available from the sources listed below. The material is
available in electronic format through Regulations.gov, call 1-877-378-
5457 or go to www.regulations.gov. It is also available for inspection
at the National Archives and Records Administration (NARA). For
information on the availability of this material at NARA, call 202-741-
6030 or go to https://www.archives.gov/federal-register/cfr/ibr-locations.html.
(b) NHTSA Technical Information Services, 1200 New Jersey Ave.,
SE., Washington, DC 20590, telephone 202-366-5965.
(1) A parts/drawing list entitled, ``Parts/Drawing List, Part 572
Subpart T, Hybrid III 10-Year-Old Child Test Dummy (HIII-10C), August
2011,'' IBR approved for Sec. 572.171.
(2) A drawings and inspection package entitled, ``Parts List and
Drawings, Part 572 Subpart T, Hybrid III 10-Year-Old Child Test Dummy
(HIII-10C), August 2011,'' IBR approved for Sec. 572.171, including:
(i) Drawing No. 420-0000, Complete Assembly HIII 10-year-old, IBR
approved for Sec. Sec. 572.171, 572.172, 572.173, 572.174, 572.176,
and 572.177.
(ii) Drawing No. 420-1000, Head Assembly, IBR approved for Sec.
572.171, Sec. 572.172, Sec. 572.173, and Sec. 572.177.
(iii) Drawing No. 420-2000, Neck Assembly, IBR approved for
Sec. Sec. 572.171, 572.173, and 572.177.
(iv) Drawing No. 420-3000, Upper Torso Assembly, IBR approved for
Sec. Sec. 572.171, 572.174, 572.175, and 572.177.
(v) Drawing No. 420-4000, Lower Torso Assembly, IBR approved for
Sec. Sec. 572.171, 572.174, 572.175, and 572.177.
(vi) Drawing No. 420-5000-1, Complete Leg Assembly--left, IBR
approved for Sec. Sec. 572.171, 572.176, and 572.177.
(vii) Drawing No. 420-5000-2, Complete Leg Assembly--right, IBR
approved for Sec. Sec. 572.171, 572.176, and 572.177.
(viii) Drawing No. 420-7000-1, Complete Arm Assembly--left, IBR
approved for Sec. 572.171, and,
(ix) Drawing No. 420-7000-2, Complete Arm Assembly--right, IBR
approved for Sec. 572.171.
(3) A procedures manual entitled ``Procedures for Assembly,
Disassembly and Inspection (PADI) of the Hybrid III 10-Year-Old Child
Test Dummy (HIII-10C), August 2011''; IBR approved for Sec. Sec.
572.171 and 572.177.
(c) SAE International, 400 Commonwealth Drive, Warrendale, PA
15096, call 1-877-606-7323.
(1) SAE Recommended Practice J211/1, Rev. Mar 95, ``Instrumentation
for Impact Tests--Part 1--Electronic Instrumentation,'' IBR approved
for Sec. 572.177.
(2) SAE Information Report J1733 of 1994-12, ``Sign Convention for
Vehicle Crash Testing,'' December 1994, IBR approved for Sec. 572.177.
Sec. 572.171 General description.
(a) The Hybrid III 10-year-old Child Test Dummy (HIII-10C) is
defined by drawings and specifications containing the following
materials:
(1) The parts enlisted in ``Parts/Drawing List, Part 572 Subpart T,
Hybrid III 10-Year-Old Child Test Dummy (HIII-10C), August 2011''
(incorporated by reference, see Sec. 572.170),
(2) The engineering drawings and specifications contained in
``Parts List and Drawings, Part 572 Subpart T, Hybrid III 10-Year-Old
Child Test Dummy (HIII-10C), August 2011,'' which includes the
engineering drawings and specifications described in Drawing 420-0000,
the titles of the assemblies of which are listed in Table A, and,
(3) A manual entitled ``Procedures for Assembly, Disassembly and
Inspection (PADI) of the Hybrid III 10-Year-Old Child Test Dummy (HIII-
10C), August 2011.''
Table A
------------------------------------------------------------------------
Component assembly Drawing No.
------------------------------------------------------------------------
(i) Head Assembly.................................. 420-1000
(ii) Neck Assembly................................. 420-2000
(iii) Upper Torso Assembly......................... 420-3000
(iv) Lower Torso Assembly.......................... 420-4000
(v) Complete Leg Assembly--left.................... 420-5000-1
(vi) Complete Leg Assembly--right.................. 420-5000-2
(vii) Complete Arm Assembly--left.................. 420-7000-1
(viii) Complete Arm Assembly--right................ 420-7000-2
------------------------------------------------------------------------
(b) The structural properties of the dummy are such that the dummy
conforms to this Subpart in every respect before use in any test.
Sec. 572.172 Head assembly and test procedure.
(a) The head assembly for this test consists of the complete head
(drawing 420-1000), a six-axis neck transducer (drawing SA572-S11,
included in drawing 420-0000), or its structural replacement (drawing
420-383X), and 3 accelerometers (drawing SA572-S4, included in drawing
420-0000) (all incorporated by reference, see Sec. 572.170).
(b) When the head assembly is dropped from a height of 376.0 1.0 mm (14.8 0.04 in) in accordance with paragraph
(c) of this section, the peak
[[Page 11668]]
resultant acceleration at the location of the accelerometers at the
head CG may not be less than 250 G or more than 300 G. The resultant
acceleration vs. time history curve shall be unimodal; oscillations
occurring after the main pulse must be less than 10 percent of the peak
resultant acceleration. The lateral acceleration shall not exceed 15 G
(zero to peak).
(c) Head test procedure. The test procedure for the head is as
follows:
(1) Soak the head assembly in a controlled environment at any
temperature between 18.9 and 25.6 [deg]C (66 and 78 [deg]F) and a
relative humidity from 10 to 70 percent for at least four hours prior
to a test.
(2) Prior to the test, clean the impact surface of the skin and the
impact plate surface with isopropyl alcohol, trichloroethane, or an
equivalent. The skin of the head must be clean and dry for testing.
(3) Suspend and orient the head assembly as shown in Figure T1. The
lowest point on the forehead must be 376.0 1.0 mm (14.8
0.04 in) from the impact surface. The 1.57 mm (0.062 in)
diameter holes located on either side of the dummy's head shall be used
to ensure that the head is level with respect to the impact surface.
(4) Drop the head assembly from the specified height by means that
ensure a smooth, instant release onto a rigidly supported flat
horizontal steel plate which is 50.8 mm (2 in) thick and 610 mm (24 in)
square. The impact surface shall be clean, dry and have a micro finish
of not less than 203.2 x 10-\6\ mm (8 micro inches) (RMS)
and not more than 2032.0 x 10-\6\ mm (80 micro inches)
(RMS).
(5) Allow at least 2 hours between successive tests on the same
head.
Sec. 572.173 Neck assembly and test procedure.
(a) The neck assembly for the purposes of this test consists of the
assembly of components shown in drawing 420-2000 (incorporated by
reference, see Sec. 572.170).
(b) When the head-neck assembly consisting of the head (drawing
420-1000), neck (drawing 420-2000), six-channel neck transducer (SA572-
S11, included in drawing 420-0000), lower neck bracket assembly
(drawing 420-2070), and either three uniaxial accelerometers (drawing
SA572-S4, included in drawing 420-0000) or their mass equivalent
installed in the head assembly as specified in drawing 420-1000 (all
incorporated by reference, see Sec. 572.170), is tested according to
the test procedure in paragraph (c) of this section, it shall have the
following characteristics:
(1) Flexion. (i) Plane D, referenced in Figure T2, shall rotate in
the direction of preimpact flight with respect to the pendulum's
longitudinal centerline between 76 degrees and 90 degrees. During the
time interval while the rotation is within the specified corridor, the
peak moment, measured by the neck transducer (drawing SA572-S11,
included in drawing 420-0000) (incorporated by reference, see Sec.
572.170), about the occipital condyles may not be less than 50 N-m
(36.9 ft-lbf) and not more than 62 N-m (45.7 ft-lbf). The positive
moment shall decay for the first time to 10 N-m (7.4 ft-lbf) between 86
ms and 105 ms after time zero.
(ii) The moment shall be calculated by the following formula:
Moment (N-m) = My - (0.01778) x (Fx).
(iii) My is the moment about the y-axis in Newton-
meters, Fx is the shear force measured by the neck
transducer (drawing SA572-S11) in Newtons, and 0.01778 is the distance
in meters from the load center of the neck transducer to the occipital
condyle.
(2) Extension. (i) Plane D, referenced in Figure T3, shall rotate
in the direction of preimpact flight with respect to the pendulum's
longitudinal centerline between 96 degrees and 115 degrees. During the
time interval while the rotation is within the specified corridor, the
peak moment, measured by the neck transducer (drawing SA572-S11,
included in drawing 420-0000) (incorporated by reference, see Sec.
572.170), about the occipital condyles may not be more than -37 N-m (-
27.3 ft-lbf) and not less than -46 N-m (-33.9 ft-lbf). The positive
moment shall decay for the first time to -10 N-m (-7.4 ft-lbf) between
100 ms and 116 ms after time zero.
(ii) The moment shall be calculated by the following formula:
Moment (N-m) = My - (0.01778) x (Fx).
(iii) My is the moment about the y-axis in Newton-
meters, Fx is the shear force measured by the neck
transducer (drawing SA572-S11, included in drawing 420-0000)
(incorporated by reference, see Sec. 572.170) in Newtons, and 0.01778
is the distance in meters from the load center of the neck transducer
to the occipital condyle.
(3) Time zero is defined as the time of initial contact between the
pendulum striker plate and the honeycomb material. All data channels
shall be at the zero level at this time.
(c) Test procedure. The test procedure for the neck assembly is as
follows:
(1) Soak the neck assembly in a controlled environment at any
temperature between 20.6 and 22.2 [deg]C (69 and 72 [deg]F) and a
relative humidity between 10 and 70 percent for at least four hours
prior to a test.
(2) Torque the hex nut (drawing 420-2000, part 9000130) on the neck
cable (drawing 420-2060) (both incorporated by reference, see Sec.
572.170) to 0.9 0.2 N-m (8 2 in-lbf) before
each test on the same neck.
(3) Mount the head-neck assembly, defined in paragraph (b) of this
section, on the pendulum described in Figure 22 of 49 CFR part 572 so
that the leading edge of the lower neck bracket coincides with the
leading edge of the pendulum as shown in Figure T2 for flexion tests
and Figure T3 for extension tests.
(4)(i) Release the pendulum and allow it to fall freely from a
height to achieve an impact velocity of 6.1 0.12 m/s (20.0
0.4 ft/s) for flexion tests and 5.03 0.12 m/s
(16.50 0.40 ft/s) for extension tests, measured by an
accelerometer mounted on the pendulum as shown in Figure T2 at the
instant of contact with the honeycomb.
(ii) Stop the pendulum from the initial velocity with an
acceleration vs. time pulse that meets the velocity change as specified
below. Integrate the pendulum acceleration data channel to obtain the
velocity vs. time curve:
Table B--Pendulum Pulse
----------------------------------------------------------------------------------------------------------------
Flexion Extension
Time (ms) ---------------------------------------------------------------
M/s ft/s m/s ft/s
----------------------------------------------------------------------------------------------------------------
10.............................................. 1.64-2.04 5.38-6.69 1.49-1.89 4.89-6.20
20.............................................. 3.04-4.04 9.97-13.25 2.88-3.68 9.45-12.07
30.............................................. 4.45-5.65 14.60-18.53 4.20-5.20 13.78-17.06
----------------------------------------------------------------------------------------------------------------
[[Page 11669]]
Sec. 572.174 Thorax assembly and test procedure.
(a) The thorax consists of the part of the torso assembly
designated as the upper torso (drawing 420-3000) (incorporated by
reference, see Sec. 572.170).
(b) When the anterior surface of the thorax of a completely
assembled dummy (drawing 420-0000) (incorporated by reference, see
Sec. 572.170) is impacted by a test probe conforming to section
572.177 at 6.00 0.12 m/s (22.0 0.4 ft/s)
according to the test procedure in paragraph (c) of this section:
(1) Maximum sternum displacement (compression) relative to the
spine, measured with chest deflection transducer (drawing SA572-T4,
included in drawing 420-0000) (incorporated by reference, see Sec.
572.170), must be not less than 37 mm (1.46 in) and not more than 46 mm
(1.81 in). Within this specified compression corridor, the peak force,
measured by the impact probe as defined in section 572.177 and
calculated in accordance with paragraph (b)(3) of this section, shall
not be less than 2.0 kN (450 lbf) and not more than 2.45 kN (551 lbf).
The peak force after 20 mm (0.79 in.) of sternum displacement but
before reaching the minimum required 37 mm (1.46 in.) sternum
displacement limit shall not exceed 2.52 kN (567 lbf).
(2) The internal hysteresis of the ribcage in each impact as
determined by the plot of force vs. deflection in paragraph (a)(1) of
this section shall be not less than 69 percent but not more than 85
percent. The hysteresis shall be calculated by determining the ratio of
the area between the loading (from time zero to maximum deflection) and
unloading portions (from maximum deflection to zero force) of the force
deflection curve to the area under the loading portion of the curve.
(3) The force shall be calculated by the product of the impactor
mass and its measured deceleration.
(c) Test Procedure. The test procedure for the thorax assembly is
as follows:
(1) The dummy is clothed in a form fitting cotton stretch above-
the-elbow sleeved shirt and above-the-knees pants. The weight of the
shirt and pants shall not exceed 0.14 kg (0.30 lb) each.
(2) Torque the lumbar cable (drawing 420-4130) (incorporated by
reference, see Sec. 572.170) to 0.9 0.2 N-m (8 2 in-lbf) and set the lumbar adjustment angle to 12 degrees. Set
the neck angle to 16 degrees.
(3) Soak the dummy in a controlled environment at any temperature
between 20.6 and 22.2 [deg]C (69 and 72 [deg]F) and a relative humidity
between 10 and 70 percent for at least four hours prior to a test.
(4) Seat and orient the dummy on a seating surface without back
support as shown in Figure T4, with the limbs extended horizontally and
forward, parallel to the midsagittal plane, the midsagittal plane
vertical within 1 degree and the ribs level in the
anterior-posterior and lateral directions within 0.5
degrees.
(5) Establish the impact point at the chest midsagittal plane so
that the impact point of the longitudinal centerline of the probe
coincides with the midsagittal plane of the dummy within
2.5 mm (0.1 in) and is 12.7 1.1 mm (0.5 0.04
in) below the horizontal-peripheral centerline of the No. 3 rib and is
within 0.5 degrees of a horizontal line in the dummy's midsagittal
plane.
(6) Impact the thorax with the test probe so that at the moment of
contact the probe's longitudinal centerline falls within 2 degrees of a
horizontal line in the dummy's midsagittal plane.
(7) Guide the test probe during impact so that there is no
significant lateral, vertical, or rotational movement.
(8) No suspension hardware, suspension cables, or any other
attachments to the probe, including the velocity vane, shall make
contact with the dummy during the test.
Sec. 572.175 Upper and lower torso assemblies and torso flexion test
procedure.
(a) The test objective is to determine the stiffness of the molded
lumbar assembly (drawing 420-4100), abdominal insert (drawing 420-
4300), and chest flesh assembly (drawing 420-3560) on resistance to
articulation between the upper torso assembly (drawing 420-3000) and
lower torso assembly (drawing 420-4000) (all incorporated by reference,
see Sec. 572.170).
(b) When the upper torso assembly of a seated dummy is subjected to
a force continuously applied at the head to neck pivot pin level
through a rigidly attached adaptor bracket as shown in Figure T5
according to the test procedure set out in paragraph (c) of this
section:
(1) The lumbar spine-abdomen-chest flesh assembly shall flex by an
amount that permits the upper torso assembly to translate in angular
motion relative to the vertical transverse plane 35 0.5
degrees at which time the force applied must be not less than 180 N
(40.5 lbf) and not more than 250 N (56.2 lbf).
(2) Upon removal of the force, the torso assembly must return to
within 8 degrees of its initial position.
(c) Test Procedure. The test procedure for the upper/lower torso
assembly is as follows:
(1) Torque the lumbar cable (drawing 420-4130) (incorporated by
reference, see Sec. 572.170) to 0.9 0.2 N-m (8 2 in-lbf) and set the lumbar adjustment angle to 12 degrees. Set
the neck angle to 16 degrees.
(2) Soak the dummy in a controlled environment at any temperature
between 20.6 and 22.2 [deg]C (69 and 72 [deg]F) and a relative humidity
between 10 and 70 percent for at least four hours prior to a test.
(3) Assemble the complete dummy (with or without the legs below the
femurs) and attach to the fixture in a seated posture as shown in
Figure T5.
(4) Secure the pelvis to the fixture at the pelvis instrument
cavity rear face by threading four \1/4\-inch cap screws into the
available threaded attachment holes. Tighten the mountings so that the
test material is rigidly affixed to the test fixture and the pelvic-
lumbar joining surface is 18 degrees from horizontal and the legs are
parallel with the test fixture.
(5) Attach the loading adaptor bracket to the spine of the dummy as
shown in Figure T5.
(6) Inspect and adjust, if necessary, the seating of the abdominal
insert within the pelvis cavity and with respect to the chest flesh,
assuring that the chest flesh provides uniform fit and overlap with
respect to the outside surface of the pelvis flesh.
(7) Flex the dummy's upper torso three times between the vertical
and until the torso reference frame, as shown in Figure T5, reaches 30
degrees from the vertical transverse plane. Bring the torso to vertical
orientation and wait for 30 minutes before conducting the test. During
the 30-minute waiting period, the dummy's upper torso shall be
externally supported at or near its vertical orientation to prevent it
from drooping.
(8) Remove all external support and wait two minutes. Measure the
initial orientation angle of the torso reference plane of the seated,
unsupported dummy as shown in Figure T5. The initial orientation angle
may not exceed 20 degrees.
(9) Attach the pull cable and the load cell as shown in Figure T5.
(10) Apply a tension force in the midsagittal plane to the pull
cable as shown in Figure T5 at any upper torso deflection rate between
0.5 and 1.5 degrees per second, until the angle reference plane is at
35 0.5 degrees of flexion relative to the vertical
transverse plane.
[[Page 11670]]
(11) Continue to apply a force sufficient to maintain 35 0.5 degrees of flexion for 10 seconds, and record the highest
applied force during the 10-second period.
(12) Release all force at the attachment bracket as rapidly as
possible, and measure the return angle with respect to the initial
angle reference plane as defined in paragraph (c)(7) of this section
three minutes after the release.
Sec. 572.176 Knees and knee impact test procedure.
(a) The knee assembly for the purpose of this test is the part of
the leg assembly shown in drawing 420-5000 (incorporated by reference,
see Sec. 572.170).
(b) When the knee assembly, consisting of lower upper leg assembly
(420-5200), femur load transducer (SA572-S10, included in drawing 420-
0000) or its structural replacement (420-5121), lower leg assembly
(420-5300), ankle assembly (420-5400), and foot molded assembly (420-
5500) (all incorporated by reference, see Sec. 572.170) is tested
according to the test procedure in subsection (c) of this section:
(1) The peak resistance force as measured with the test probe-
mounted accelerometer must not be less than 2.6 kN (585 lbf) and not
more than 3.2 kN (719 lbf).
(2) The force shall be calculated by the product of the impactor
mass and its deceleration.
(c) Test Procedure. The test procedure for the knee assembly is as
follows:
(1) Soak the knee assembly in a controlled environment at any
temperature between 20.6 and 22.2 [deg]C (69 and 72 [deg]F) and a
relative humidity between 10 and 70 percent for at least four hours
prior to a test.
(2) Mount the test material and secure it to a rigid test fixture
as shown in Figure T6. No part of the foot or tibia may contact any
exterior surface.
(3) Align the test probe so that throughout its stroke and at
contact with the knee it is within 2 degrees of horizontal and
collinear with the longitudinal centerline of the femur.
(4) Guide the pendulum so that there is no significant lateral,
vertical, or rotational movement at the time of initial contact between
the impactor and the knee.
(5) The test probe velocity at the time of contact shall be 2.1
0.03 m/s (6.9 0.1 ft/s).
(6) No suspension hardware, suspension cables, or any other
attachments to the probe, including the velocity vane, shall make
contact with the dummy during the test.
Sec. 572.177 Test conditions and instrumentation.
(a) The following test equipment and instrumentation is needed for
qualification as set forth in this subpart:
(1) The test probe for thoracic impacts is of rigid metallic
construction, concentric in shape, and symmetric about its longitudinal
axis. It has a mass of 6.89 0.012 kg (15.2
0.05 lb) and a minimum mass moment of inertia of 2040 kg-cm\2\ (1.81
lbf-in-sec\2\) in yaw and pitch about the CG. One-third (\1/3\) of the
weight of the suspension cables and their attachments to the impact
probe is included in the calculation of mass, and such components may
not exceed five percent of the total weight of the test probe. The
impacting end of the probe, perpendicular to and concentric with the
longitudinal axis, is at least 25.4 mm (1.0 in) long, and has a flat,
continuous, and non-deformable 121 0.25 mm (4.76 0.01 in) diameter face with a maximum edge radius of 12.7 mm
(0.5 in). The probe's end opposite to the impact face has provisions
for mounting of an accelerometer with its sensitive axis collinear with
the longitudinal axis of the probe. No concentric portions of the
impact probe may exceed the diameter of the impact face. The impact
probe has a free air resonant frequency of not less than 1000 Hz, which
may be determined using the procedure listed in the PADI (incorporated
by reference, see Sec. 572.170).
(2) The test probe for knee impacts is of rigid metallic
construction, concentric in shape, and symmetric about its longitudinal
axis. It has a mass of 1.91 0.01 kg (4.21
0.02 lb) and a minimum mass moment of inertia of 140 kg-cm\2\ (0.124
lbf-in-sec\2\) in yaw and pitch about the CG. One third (\1/3\) of the
weight of the suspension cables and their attachments to the impact
probe may be included in the calculation of mass, and such components
may not exceed five percent of the total weight of the test probe. The
impacting end of the probe, perpendicular to and concentric with the
longitudinal axis, is at least 12.5 mm (0.5 in) long, and has a flat,
continuous, and non-deformable 76.2 0.2 mm (3.00 0.01 in) diameter face with a maximum edge radius of 12.7 mm
(0.5 in). The probe's end opposite to the impact face has provisions
for mounting an accelerometer with its sensitive axis collinear with
the longitudinal axis of the probe. No concentric portions of the
impact probe may exceed the diameter of the impact face. The impact
probe has a free air resonant frequency of not less than 1000 Hz, which
may be determined using the procedure listed in the PADI (incorporated
by reference, see Sec. 572.170).
(3) Head accelerometers have dimensions, response characteristics,
and sensitive mass locations specified in drawing SA572-S4 (included in
drawing 420-0000) and are mounted in the head as shown in drawing 420-
0000 (both incorporated by reference, see Sec. 572.170), sheet 2 of 6.
(4) The upper neck force and moment transducer has the dimensions,
response characteristics, and sensitive axis locations specified in
drawing SA572-S11 (included in drawing 420-0000) and is mounted in the
head-neck assembly as shown in drawing 420-0000 (both incorporated by
reference, see Sec. 572.170), sheet 2 of 6.
(5) The chest deflection transducer has the dimensions and response
characteristics specified in drawing SA572-S50 (included in drawing
420-0000) and is mounted to the upper torso assembly as shown in
drawing 420-0000 (both incorporated by reference, see Sec. 572.170),
sheet 2 of 6.
(b) The following instrumentation may be required for installation
in the dummy for compliance testing. If so, it is installed during
qualification procedures as described in this subpart:
(1) The thorax CG accelerometers have the dimensions, response
characteristics, and sensitive mass locations specified in drawing
SA572-S4 (included in drawing 420-0000) (incorporated by reference, see
Sec. 572.170) and are mounted in the torso assembly in a triaxial
configuration within the spine box instrumentation cavity.
(2) The lower neck force and moment transducer has the dimensions,
response characteristics, and sensitive axis locations specified in
drawing SA572-S40 (included in drawing 420-0000) and is mounted to the
neck assembly by replacing the lower neck mounting bracket 420-2070 as
shown in drawing 420-2000 (all incorporated by reference, see Sec.
572.170).
(3) The clavicle force transducers have the dimensions, response
characteristics, and sensitive axis locations specified in drawing
SA572-S41 (included in drawing 420-0000) and are mounted in the
shoulder assembly as shown in drawing 420-3800 (both incorporated by
reference, see Sec. 572.170).
(4) The IR-Tracc chest deflection transducers have the dimensions
and response characteristics specified in drawing SA572-S43 (included
in drawing 420-0000) and are mounted to
[[Page 11671]]
the spine box assembly as shown in drawing 420-8000 (both incorporated
by reference, see Sec. 572.170).
(5) The spine and sternum accelerometers have the dimensions,
response characteristics, and sensitive mass locations specified in
drawing SA572-S4 (included in drawing 420-0000) and are mounted in the
torso assembly in uniaxial fore-and-aft oriented configuration arranged
as corresponding pairs in two locations each on the sternum and at the
spine box of the upper torso assembly as shown in drawing 420-0000
(both incorporated by reference, see Sec. 572.170), sheet 2 of 6.
(6) The lumbar spine force-moment transducer has the dimensions,
response characteristics, and sensitive axis locations specified in
drawing SA572-S12 (included in drawing 420-0000) and is mounted in the
lower torso assembly as shown in drawing 420-4000 (both incorporated by
reference, see Sec. 572.170).
(7) The iliac force transducers have the dimensions and response
characteristics specified in drawing SA572-S13 L and R (included in
drawing 420-0000) and are mounted in the lower torso assembly as shown
in drawing 420-4000 (both incorporated by reference, see Sec.
572.170).
(8) The pelvis accelerometers have the dimensions, response
characteristics, and sensitive mass locations specified in drawing
SA572-S4 (included in drawing 420-0000) and are mounted in the torso
assembly in triaxial configuration in the pelvis bone as shown in
drawing 420-0000 (both incorporated by reference, see Sec. 572.170),
sheet 2 of 6.
(9) The femur force and moment transducers (SA572-S10, included in
drawing 420-0000) have the dimensions, response characteristics, and
sensitive axis locations specified in the appropriate drawing and are
mounted in the upper leg assembly, replacing the femur load cell
simulator (drawing 420-5121) as shown in drawing 420-5100 (all
incorporated by reference, see Sec. 572.170).
(10) The tilt sensors have the dimensions and response
characteristics specified in drawing SA572-S42 (included in drawing
420-0000) and are mounted to the head, thorax, and pelvis assemblies as
shown in drawing 420-0000 (both incorporated by reference, see Sec.
572.170), sheet 2 of 6.
(c) The outputs of transducers installed in the dummy and in the
test equipment specified by this part are to be recorded in individual
data channels that conform to SAE Recommended Practice J211
(incorporated by reference, see Sec. 572.170) except as noted, with
channel frequency classes as follows:
(1) Pendulum acceleration, CFC 180,
(2) Pendulum D-plane rotation (if transducer is used), CFC 60,
(3) Torso flexion pulling force (if transducer is used), CFC 60,
(4) Head acceleration, CFC 1000,
(5) Neck forces, upper and lower, CFC 1000,
(6) Neck moments, upper and lower, CFC 600,
(7) Thorax CG acceleration, CFC 180,
(8) Sternum deflection, Class 600,
(9) Sternum and rib accelerations, Class 1000,
(10) Spine accelerations, CFC 180,
(11) Lumbar forces, CFC 1000,
(12) Lumbar moments, CFC 600,
(13) Shoulder forces, CFC 180,
(14) Pelvis accelerations, CFC 1000,
(15) Iliac forces, CFC 180,
(16) Femur and tibia forces, CFC 600,
(17) Femur and tibia moments, CFC 600.
(d) Coordinate signs for instrumentation polarity are to conform to
SAE Information Report J1733 (incorporated by reference, see Sec.
572.170).
(e) The mountings for sensing devices have no resonant frequency
less than 3 times the frequency range of the applicable channel class.
(f) Limb joints are set at one G, barely restraining the weight of
the limb when it is extended horizontally. The force needed to move a
limb segment is not to exceed 2G throughout the range of limb motion.
(g) Performance tests of the same component, segment, assembly, or
fully assembled dummy are separated in time by not less than 30 minutes
unless otherwise noted.
(h) Surfaces of dummy components may not be painted except as
specified in this subpart or in drawings subtended by this subpart.
Appendix--Figures to Subpart T of Part 572
BILLING CODE 4910-59-P
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Issued on: February 16, 2012.
David L. Strickland,
Administrator.
[FR Doc. 2012-4129 Filed 2-21-12; 11:15 am]
BILLING CODE 4910-59-C