Standard Practice for Determining the Susceptibility of Stainless Steels and Related Nickel-Chromium-Iron Alloys to Stress-Corrosion Cracking in Polythionic Acids

SIGNIFICANCE AND USE
This environment provides a way of evaluating the resistance of stainless steels and related alloys to intergranular stress corrosion cracking. Failure is accelerated by the presence of increasing amounts of intergranular precipitate. Results for the polythionic acid test have not been correlated exactly with those of intergranular corrosion tests. Also, this test may not be relevant to stress corrosion cracking in chlorides or caustic environments.
The polythionic acid environment may produce areas of shallow intergranular attack in addition to the more localized and deeper cracking mode of attack. Examination of failed specimens is necessary to confirm that failure occurred by cracking rather than mechanical failure of reduced sections.
SCOPE
1.1 This practice describes procedures for preparing and conducting the polythionic acid test at room temperature, 22 to 25°C (72 to 77°F), to determine the relative susceptibility of stainless steels or other related materials (nickel-chromium-iron alloys) to intergranular stress corrosion cracking.  
1.2 This practice can be used to evaluate stainless steels or other materials in the "as received" condition or after being subjected to high-temperature service, 482 to 815°C (900 to 1500°F), for prolonged periods of time.  
1.3 This practice can be applied to wrought products, castings, and weld metal of stainless steels or other related materials to be used in environments containing sulfur or sulfides. Other materials capable of being sensitized can also be tested in accordance with this test.  
1.4 This practice may be used with a variety of stress corrosion test specimens, surface finishes, and methods of applying stress.  
1.5 This standard may involve hazardous materials, operations, and equipment. This standard does not purport to address all of the safety problems associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. For more specific precautionary statements, see Section 7.

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30-Apr-2004
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ASTM G35-98(2004) - Standard Practice for Determining the Susceptibility of Stainless Steels and Related Nickel-Chromium-Iron Alloys to Stress-Corrosion Cracking in Polythionic Acids
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NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
Contact ASTM International (www.astm.org) for the latest information
Designation:G35–98(Reapproved 2004)
Standard Practice for
Determining the Susceptibility of Stainless Steels and
Related Nickel-Chromium-Iron Alloys to Stress-Corrosion
Cracking in Polythionic Acids
ThisstandardisissuedunderthefixeddesignationG35;thenumberimmediatelyfollowingthedesignationindicatestheyearoforiginal
adoption or, in the case of revision, the year of last revision.Anumber in parentheses indicates the year of last reapproval.Asuperscript
epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope G30 Practice for Making and Using U-Bend Stress-
Corrosion Test Specimens
1.1 This practice describes procedures for preparing and
conducting the polythionic acid test at room temperature, 22 to
3. Summary of Practice
25°C (72 to 77°F), to determine the relative susceptibility of
3.1 Thestressedspecimensareplacedinthecontaineralong
stainless steels or other related materials (nickel-chromiumiron
with a sensitized and stressedAISIType 302 (UNS S30200) or
alloys) to intergranular stress corrosion cracking.
Type 304 (UNS S30400) stainless steel control specimen. A
1.2 This practice can be used to evaluate stainless steels or
sufficient amount of the previously prepared polythionic acid
other materials in the “as received” condition or after being
solution is added to the container to immerse the test speci-
subjected to high-temperature service, 482 to 815°C (900 to
mens.Acover is placed on the container and the test is carried
1500°F), for prolonged periods of time.
out at room temperature.
1.3 This practice can be applied to wrought products,
castings, and weld metal of stainless steels or other related
4. Significance and Use
materials to be used in environments containing sulfur or
4.1 This environment provides a way of evaluating the
sulfides. Other materials capable of being sensitized can also
resistance of stainless steels and related alloys to intergranular
be tested in accordance with this test.
stresscorrosioncracking.Failureisacceleratedbythepresence
1.4 This practice may be used with a variety of stress
of increasing amounts of intergranular precipitate. Results for
corrosion test specimens, surface finishes, and methods of
the polythionic acid test have not been correlated exactly with
applying stress.
those of intergranular corrosion tests.Also, this test may not be
1.5 This standard does not purport to address all of the
relevant to stress corrosion cracking in chlorides or caustic
safety concerns, if any, associated with its use. It is the
environments.
responsibility of the user of this standard to establish appro-
4.2 The polythionic acid environment may produce areas of
priate safety and health practices and determine the applica-
shallow intergranular attack in addition to the more localized
bility of regulatory limitations prior to use. For more specific
and deeper cracking mode of attack. Examination of failed
precautionary statements, see Section 7.
specimens is necessary to confirm that failure occurred by
2. Referenced Documents cracking rather than mechanical failure of reduced sections.
2.1 ASTM Standards:
5. Apparatus
D1193 Specification for Reagent Water
5.1 Any suitable glass or other transparent, inert container
G1 Practice for Preparing, Cleaning, and Evaluating Corro-
can be used to contain the acid solution and stressed specimens
sion Test Specimens
during the period of test at room temperature, 22 to 25°C (72
G15 Terminology Relating to Corrosion and Corrosion
to 77°F). The container should be fitted with a removable top
Testing
to reduce evaporation and to allow access to the stressed
specimen (or specimens) for the periodic inspection.
This practice is under the jurisdiction of ASTM Committee G01 on Corrosion
of Metals, and is the direct responsibility of Subcommittee G01.06 on Environmen-
6. Reagents
tally Assisted Cracking.
6.1 Purity of Reagents—The polythionic acid solution shall
Current edition approved May 1, 2004. Published May 2004. Originally
approved in 1988. Last previous edition approved in 1998 as G35 – 98. DOI: be prepared using reagent grade sulfurous acid and technical
10.1520/G0035-98R04.
grade hydrogen sulfide; or, distilled water, commercial grade
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
sulfur dioxide, and technical grade hydrogen sulfide.
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
Standards volume information, refer to the standard’s Document Summary page on
the ASTM website.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.
G35–98 (2004)
6.2 Purity of Water—Reagent water Type IV (Specification various types of test specimens available, see Ref (7), as well
D1193) shall be used to prepare the test solutions. as Practices G1 and G30, and Terminology G15.
6.3 Wackenroder’s or Polythionic Acid Solution (1) —A
8.2 The AISI Type 302 control specimens should be sensi-
slow current of hydrogen sulfide is passed for an hour through
tized by heating in a furnace for 4 h at 650°C (1200°F) and
a fritted glass tube into a flask containing chilled (0°C, 32°F)
thenallowingtoaircool.TheAISIType304controlspecimens
6 % sulfurous acid, after which the liquid is kept in the
should be sensitized by heating in a furnace for2hat 677°C
stoppered flask for 48 h at room temperature. This operation is
(1250°F) and then allowing to air cool.
repeated until the liquid no longer gives off the odor of sulfur
dioxide after standing at room temperature for a few hours.
9. Procedure
Note safety precautions in Section 7.
9.1 Prepare the polythionic acid test solution as described in
6.3.1 In an alternative method (2), the polythionic acid
6.3 and 6.3.1.
solution is prepared by passing a slow current of sulfur dioxide
9.2 Prior to usage, filter the acid solution to remove the
gas through a fritted glass bubbler submerged in a container of
excesssulfurandtestforthepresenceofpolythionicacids.The
distilled water. This is continued until the solution becomes
simplest method of testing
...

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