I. Criteria for cathodic protection.
A. Steel, cast iron, and ductile iron
structures.
(1) A negative (cathodic) voltage
of at least 0.85 volt, with reference to a saturated copper-copper sulfate half
cell. Determination of this voltage must be made with the protective current
applied, and in accordance with sections II and IV.
(2) A negative (cathodic) voltage shift of at
least 300 millivolts. Determination of this voltage shift must be made with the
protective current applied, and in accordance with sections II and IV. This
criterion of voltage shift applies to structures not in contact with metals of
different anodic potentials.
(3) A
minimum negative (cathodic) polarization voltage shift of 100 millivolts. This
polarization voltage shift must be determined in accordance with sections III
and IV.
(4) A voltage at least as
negative (cathodic) as that originally established at the beginning of the
Tafel segment of the E-log-l curve. This voltage must be measured in accordance
with section IV.
(5) A net
protective current from the electrolyte into the structure surface as measured
by an earth current technique applied at predetermined current discharge
(anodic) points of the structure.
B. Aluminum structures.
(1) Except as provided in paragraphs (3) and
(4), a minimum negative (cathodic) voltage shift of 150 millivolts, produced by
the application of protective current. The voltage shift must be determined in
accordance with sections II and IV.
(2) Except as provided in paragraphs (3) and
(4), a minimum negative (cathodic) polarization voltage shift of 100
millivolts. This polarization voltage shift must be determined in accordance
with sections III and IV.
(3)
Notwithstanding the alterative minimum criteria in paragraphs (1) and (2),
aluminum, if cathodically protected at voltages in excess of 1.20 volts as
measured with reference to a copper-copper sulfate half cell, in accordance
with section IV, and compensated for the voltage (IR) drops other than those
across the structure-electrolyte boundary may suffer corrosion resulting from
the build up of alkali on the metal surface. A voltage in excess of 1.20 volts
may not be used unless previous test results indicate no appreciable corrosion
will occur in the particular environment.
(4) Since aluminum may suffer from corrosion
under high pH conditions, and since application of cathodic protection tends to
increase the pH at the metal surface, careful investigation or testing must be
made before applying cathodic protection to stop pitting attack on aluminum
structures in environments with a natural pH in excess of 8.
C. Copper structures. A minimum
negative (cathodic) polarization voltage shift of 100 millivolts. This
polarization voltage shift must be determined in accordance with sections III
and IV.
D. Metals of different
anodic potentials. A negative (cathodic) voltage, measured in accordance with
section IV, equal to that required for the most anodic metal in the system must
be maintained. If amphoteric structures are involved that could be damaged by
high alkalinity covered by paragraphs B(3) and B(4), they must be electrically
isolated with insulating flanges, or the equivalent.
II. Interpretation of voltage measurement.
Voltage (IR) drops other than those across the structure electrolyte boundary
must be considered for valid interpretation of the voltage measurement in
paragraphs A(1) and A(2) and paragraph B(1) of section I.
III. Determination of polarization voltage
shift. The polarization voltage shift must be determined by interrupting the
protective current and measuring the polarization decay. When the current is
initially interrupted, an immediate voltage shift occurs. The voltage reading
after the immediate shift must be used as the base reading from which to
measure polarization decay in paragraphs A(3), B(2), and C of section
I.
IV. Reference half cells.
A. Except as provided in paragraphs B and C,
negative (cathodic) voltage must be measured between the structure surface and
saturated copper-copper sulfate half cell contacting the electrolyte.
B. Other standard reference half cells may be
substituted for the saturated copper-copper sulfate half cell. Two commonly
used reference half cells are listed below along with their voltage equivalent
to 0.85 volt as referred to a saturated copper-copper sulfate half cell:
(1) Saturated KCI calomel half cell: 0.78
volt.
(2) Silver-silver chloride
half cell used in sea water: -0.80 volt.
C. "In addition to the standard reference
half cells, an alternate metallic material or structure may be used in place of
the saturated copper-copper sulfate half cell if its potential stability is
assured and if its voltage equivalent referred to a saturated copper copper
sulfate half cell is established."