STD-INSP-0123 IGC Practice - A - (ASTM G28)
STD-INSP-0123 IGC Practice - A - (ASTM G28)
STD-INSP-0123 IGC Practice - A - (ASTM G28)
Issue 02
Issue Date
TEST METHOD
Revision 00
Revision Date -
IGC Practice ‘A’ (ASTM G28)
Page 1 of 7
1.0 Purpose:
To establish and maintain the documented Procedure to ensure that the testing is carried out as per the
applicable specifications / standards.
2.0 Scope:
This test method describes the procedure for conducting the boiling ferric sulfate—50 %
sulfuric acid test which measures the susceptibility of certain nickel-rich, chromium-
bearing alloys to intergranular corrosion.
The uniform corrosion rate obtained by this test method, which is a function of minor
variations in alloy composition, may easily mask the intergranular corrosion components of
the overall corrosion rate on alloys N10276, N06022, N06059, and N06455.
The presence of intergranular corrosion is usually determined by comparing the calculated corrosion
rate to that for properly annealed material.
6.0 Instrument :
A1-L glass Erlenmeyer flask with a ground 45/50 glass joint and four-bulb (minimum)
Allihn condenser with 45/50 ground glass joint are required and Hot Plate.
Specimen Supports—an open glass cradle capable of supporting the specimens with three –
four holes to increase circulation of the test solution around the specimen.
The intent is to test a specimen representing as nearly as possible the material as used in service.
Sample with inclusion, porosity and slag is not allowed. Sample should be smooth machined,
cleaned and polished by 80, 120, 180 grit paper.
The size of the sample submitted for test and the area from which it is to be taken (end or middle of
coil, midway surface and center, and so forth) shall be specified by the customer. The testing
apparatus dictates the final size of the specimen. The size should be such that it should provide easy
entrance and removal from the neck of the container.
Specimens obtained by shearing should have the sheared edges machined or ground off prior to the
testing. Care should be taken while grinding to avoid overheating or burning.
Any scale on the surface should be removed mechanically unless specific surface finish is to be
evaluated. Chemical removal is allowed in this case. Mechanical removal should be done by 120
grit iron free aluminum oxide abrasive.
Each specimen sample should be de-greased using a cleansing solvent like acetone, ether prior to
testing.
First, measure 400ml. of Type IV reagent water in a 500ml. graduate and pour into the flask.
Then measure 236 ml. of reagent-grade sulfuric acid (H2SO4) of a concentration which must be in
the range from 95.0 to 98.0 weight percent in a 250ml. graduate. Add the acid slowly to the water in
the flask to avoid boiling by the heat evolved. Externally cooling the flask with water during the
mixing will also reduce overheating.
Add boiling chips & Lubricate the ground glass of the condenser joint with silicone grease.
Cover the flask with the condenser and circulate cooling water & Boil the solution until all ferric
sulfate is dissolved.
Mark the liquid level on the flask with wax crayon to provide a check on vapor loss which would
result in concentration of the acid. If there is an appreciable change in the level (a 0.5-cm or more
drop), repeat the test with fresh solution and with a fresh specimen or a reground specimen.
Weigh the specimen and subtract this mass from the original mass.
If the corrosion rate is extraordinarily high in Method A, as evidenced by a change in color (green)
of the solution, additional ferric sulfate must be added during the test. The amount of ferric sulfate
that must be added, if the total mass loss of all specimens exceeds 2 g as indicated by an
intermediate weight, is 10 g for each 1 g of dissolved alloy. This does not apply to Method B.
In this method, several specimens of the same alloy may be tested simultaneously. The number (3 or
4) is limited only by the number of glass cradles that can be fitted into the flask and the
consumption of ferric sulfate. Only one sample should be tested in a flask for Method B.
9.1 Calculation:
Measure the effect of the acid solution on the material.
Corrosion rate = (K x W) / (A x T x D)
Where:
K = a constant (see below table),
T = time of exposure, h, to the nearest 0.01 h,
A = area, cm2, to the nearest 0.01 cm2,
W = mass loss, g, to the nearest 0.001 g, and
D = density, g/cm3 (see below table).
The presence of intergranular corrosion is usually determined by comparing the calculated corrosion
rate to that for properly annealed material.
As an alternative or in addition to calculating a corrosion rate from mass loss data, metallographic
examination may be used to evaluate the degree of intergranular corrosion. The depth of attack
considered acceptable shall be determined between buyer and seller.