ASTM A967-05
美标标准
评定在沸腾的氯化镁溶液中金属及其合金的抗应力腐蚀断裂的一般方法
39
ASTM G41-90(94)
测定金属在热盐环境下应力断裂敏感性的一般方法
40
ASTM G44-99
在3.5%氯化钠溶液中交替浸渍法评定金属及合金的抗应力腐蚀破裂的一般方法
41
ASTM G46-94
局部腐蚀的检测和评定
腐蚀场所或高温下使用的焊接大口径奥氏体钢管
10
ASTM A480/A480M-03
平轧不锈和抗热钢板材﹑薄板材和带材通用要求技术规范
11
ASTM A484/A484M-03
不锈和抗热钢棒﹑钢坯和锻件
12
ASTM A450/A450M-04
碳素铁素体和奥氏体合金钢管
13
ASTM A511-04
无缝不锈钢机械管件的技术规范
42
ASTM G48-03
用氯化铁溶液测定不锈钢及有关合金耐斑点腐蚀及裂隙腐蚀的试验方法
43
ASTM G78-95
海水及其它含氯化物的水文环境中铁基和镍基不锈合金的裂隙腐蚀试验
44
ASTM G85-02
改进的盐喷雾(物化)试验
纵向焊接管的超声检测
24
ASTM E309-95
用磁刨和法做管状钢产品的涡流检验
25
ASTM E340-00
金属和合金宏观腐蚀的测试方法
26
ASTM E381-98
钢制品(包括棒﹑方钢坯﹑大方坯和锻件)的宏观腐蚀测试检查和评定
27
ASTM E384-99
材料显微硬度的试验方法
28
ASTM E407-99
7
ASTM A967-01
ASTM材料查询索引
容压零件用奥氏体及奥氏体铁素体铸铁的技术规范
ASTM A352/A352M-03 ASTM A353/A353M-93(1999)
ASTM A354-04 ASTM A355-89(2000) ASTM A356/A356M-98(2003)
无缝和焊接奥氏体不锈钢管 不锈钢弹簧丝技术规范
锻造用不锈及耐热钢坯及钢棒规格 高温无压部件用灰铁铸件 低温用合金钢螺栓材料规格 经淬火和回火的碳素钢棒 合金钢棒材.级别 硼铁规格
ASTM A324-73(2000) ASTM A325-04a ASTM A325M-04a
ASTM A327-91(1997) ASTM A327M-91(1997) ASTM A328/A328M-03 ASTM A333/A333M-04a ASTM A334/A334M-04a ASTM A335/A335M-03 ASTM A336/A336M-03a
有关磁性试验用符号和定义的术语
用直流磁导计和冲击试验法测定材料的直流磁性能的试验方法
磁铁材料导磁率的试验方法 在电力频率下用瓦特计-安培计-伏特计法(100-1000赫兹)和25 厘米艾普斯亭(EPSTEIN) 机架测定材料的交流电磁性能的试验
方法
磁设备用平轧电炉钢
用瓦特计--安培计--伏特计法(100-10000赫兹)和25厘米艾普斯 亭框测定材料的交流磁性能的试验方法
标准号
ASTM A1-00
ASTM A2-02
ASTM A3-01
ASTM A6/A6M-04a
ASTM A20/A20M-04a
ASTM A27/A27M-03
ASTM A29/A29M-04
ASTM A967-2001 不锈钢零件化学钝化处理的标准规范
Designation:A967–01e1Standard Specification forChemical Passivation Treatments for Stainless Steel Parts1 This standard is issued under thefixed designation A967;the number immediately following the designation indicates the year of original adoption or,in the case of revision,the year of last revision.A number in parentheses indicates the year of last reapproval.A superscript epsilon(e)indicates an editorial change since the last revision or reapproval.e1N OTE—Paragraph3.1.1.5was deleted editorially in April2002.Paragraph10.2was corrected editorially in April2002.1.Scope1.1This specification covers several different types of chemical passivation treatments for stainless steel parts.It includes recommendations and precautions for descaling, cleaning,and passivation of stainless steel parts.It includes several alternative tests,with acceptance criteria,for confirma-tion of effectiveness of such treatments for stainless steel parts.1.2Practices for the mechanical and chemical treatments of stainless steel surfaces are discussed more thoroughly in Practice A380.1.3Several alternative chemical treatments are defined for passivation of stainless steel parts.Appendix X1gives some nonmandatory information and provides some general guide-lines regarding the selection of passivation treatment appropri-ate to particular grades of stainless steel but makes no recommendations regarding the suitability of any grade,treat-ment,and acceptance criteria for any particular application or class of applications.1.4The tests in this specification are intended to confirm the effectiveness of passivation,particularly with regard to the removal of free iron and other exogenous matter.These tests include the following practices:1.4.1Practice A—Water Immersion Test,1.4.2Practice B—High Humidity Test,1.4.3Practice C—Salt Spray Test,1.4.4Practice D—Copper Sulfate Test,1.4.5Practice E—Potassium Ferricyanide–Nitric Acid Test, and1.4.6Practice F—Free Iron Test.1.5The values stated in inch-pound units are to be regarded as the standard.The SI units given in parentheses are for information only.1.6The following precautionary caveat pertains only to the test method portions,Sections14through18of this specifica-tion:This standard does not purport to address all of the safety concerns,if any,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.2.Referenced Documents2.1ASTM Standards:A380Practice for Cleaning,Descaling,and Depassivation of Stainless Steel Parts,Equipment,and Systems2B117Practice for Operating Salt Spray(Fog)Apparatus3 B254Practice for Preparation of and Electroplating on Stainless Steel42.2Federal Specification:QQ-P-35C Passivation Treatments for Corrosion-Resistant Steels53.Terminology3.1Definition of Term Specific to This Standard—It is necessary to define which of the several commonly used definitions of the term passivation will be used in this specification.(See Discussion.)3.1.1Discussion—Stainless steels are autopassivating in the sense that the protective passivefilm is formed spontaneously on exposure to air or moisture.The presence of exogenous surface contamination,including dirt,grease,free iron from contact with steel tooling,and so forth,may interfere with the formation of the passivefilm.The cleaning of these contami-nants from the stainless steel surface will facilitate the spon-taneous passivation by allowing the oxygen uniform access to the surface.The passivefilm may be augmented by chemical treatments that provide an oxidizing environment for the stainless steel surface.3.1.1.1In this specification,passivation,unless otherwise specified,is defined as the chemical treatment of a stainless steel with a mild oxidant,such as a nitric acid solution,for the purpose of the removal of free iron or other foreign matter,but which is generally not effective in removal of heat tint or oxide scale on stainless steel.In the case of stainless steels with additions of sulfur for the purpose of improved machinability,1This specification is under the jurisdiction of ASTM Committee A01on Steel, Stainless Steel,and Related Alloys and is the direct responsibility of Subcommittee A01.14on Methods of Corrosion Testing.Current edition approved Oct.10,2001.Published December2001.Originally published as A967–st previoius edition A967–99.2Annual Book of ASTM Standards,V ol01.03.3Annual Book of ASTM Standards,V ol03.02.4Annual Book of ASTM Standards,V ol02.05.5Available from Superintendent of Documents,ernment Printing Office,Washington,DC20402.1Copyright©ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959,United States.passivation may also include the removal of sulfides from the surface of the metal for the purpose of maximizing corrosion resistance.3.1.1.2The formation of the protective passivefilm on a stainless steel,also called passivation in a more general context,will occur spontaneously in air or other oxygen-containing environment when the stainless steel surface is free of oxide scale and exogenous matter.3.1.1.3Chemical treatments,such as sodium dichromate solutions,may facilitate the more rapid formation of the passivefilm on a stainless steel surface already free of scale or foreign matter.Such treatments,also sometimes called passi-vation in common usage,are designated as post-cleaning treatments in this specification in order to distinguish them from chemical treatments capable of removing free iron from stainless steels.3.1.1.4The chemical treatments capable of removing heat tint or oxide scale from stainless steel and capable of dissolving the stainless steel itself,typically called pickling,are substan-tially more aggressive than treatments used for passivation,as defined in3.1.1.1.The surface of stainless steel that has been pickled is free of scale,free iron,and exogenous foreign matter,and does not require a separate treatment for passiva-tion as defined in3.1.1.1.The passivation process defined in 3.1.1.2will occur without further chemical treatment but may be augmented and improved by the post-cleaning treatments defined in3.1.1.3.3.1.1.5Electrochemical treatments,including electropick-ling and electropolishing capable of removing heat tint or oxide scale from stainless steel and capable of dissolving the stainless steel itself,are substantially more aggressive than treatments used for passivation,as defined in3.1.1.1.The surface of stainless steel resulting from these treatments is free of scale, free iron,and exogenous foreign matter,and does not require a separate treatment for passivation as defined in3.1.1.1.The passivation process defined in 3.1.1.2will occur without further chemical treatment,but may be augmented and im-proved by the post-cleaning treatments defined in 3.1.1.3. Statements regarding chemical treatments,unless otherwise specified,are taken to include electrochemical treatments.4.Ordering Information4.1It is the responsibility of the purchaser to specify a test practice appropriate to any particular material and application. This specification was written for the purpose of providing an alternative to United States Federal Specification QQ-P-35C. Determination of the suitability of this specification for that purpose is the responsibility of the purchaser.4.2Unless specified by the purchaser,the chemical treat-ment applied to the stainless steel parts shall be selected by the seller from among the listed passivation treatments.5.Materials and Preparation for Passivation Treatments 5.1The passivation treatments shall be of one or more of the following types.The effectiveness of a particular treatment for a particular grade of stainless steel in a particular application is demonstrated by meeting the specified testing requirements: 5.1.1Treatments in nitric acid,5.1.2Treatments in citric acid,5.1.3Other chemical treatments,including electrochemical treatments,5.1.4Neutralization,and5.1.5Post-cleaning treatments.5.2Materials:5.2.1The chemicals used for passivation treatments shall produce passivated surfaces that meet the requirements of one or more of the tests of this specification.Attention shall be given to maintaining adequate volume,concentration,purity, and temperature control appropriate to the size and amount of stainless steel to be treated.5.2.2The processor shall maintain a record with regard to concentration and temperature of the passivation solution sufficient to demonstrate that the specified passivation condi-tions were maintained for each lot of stainless steel parts processed.Such records shall be available for inspection when specified in the purchase order.The processor is not required to reveal the precise composition of proprietary chemical mix-tures but shall maintain a unique identification of the mixture that will ensure its accurate representation for subsequent use.5.2.3The processor shall be responsible for the safe dis-posal of all material generated by this process.5.3Preparation for Passivation Treatments:5.3.1The pretreatment methods and procedures used prior to the passivation treatment,including mechanical and chemi-cal methods,singly or in combination,for descaling and pickling,shall be in accordance with Practice A380.When electrochemical cleaning is required,it shall be performed in accordance with Practice B254.5.3.2The resulting pretreated surface shall be substantially free of oil,grease,rust,scale,and other foreign matter.5.3.3When thefinal pretreatment of a part includes pickling of the entire surface of the part,no further passivation treatment is required prior to testing of the surface unless specified by the purchaser.6.Treatments in Nitric Acid Solutions6.1Passivation Treatment:6.1.1Stainless steel parts shall be treated in one of the following aqueous solutions and maintained within the speci-fied temperature range for the specified time.6.1.1.1Nitric1—The solution shall contain20to25volume percent of nitric acid and2.5+0.5weight percent of sodium dichromate.The parts shall be immersed for a minimum of20 min at a temperature in the range from120to130°F(49to 54°C).6.1.1.2Nitric2—The solution shall contain20to45volume percent of nitric acid.The parts shall be immersed for a minimum of30min at a temperature in the range from70to 90°F(21to32°C).6.1.1.3Nitric3—The solution shall contain20to25volume percent nitric acid.The parts shall be immersed for a minimum of20min at a temperature in the range from120to140°F(49 to60°C).6.1.1.4Nitric4—The solution shall contain45to55volume percent of nitric acid.The parts shall be immersed for a minimum of30min at a temperature in the range from120to 130°F(49to54°C).6.1.1.5Nitric5—Other combinations of temperature,time, and concentration of nitric acid,with or without other chemi-cals,including accelerants,inhibitors,or proprietary solutions, capable of producing parts that pass the specified test require-ments.6.2Water Rinse—Immediately after removal from the pas-sivating solution the parts shall be thoroughly rinsed,using stagnant,countercurrent,or spray washes singly or in combi-nation,with or without a separate chemical treatment for neutralization(see9.1)of the passivation media,with afinal rinse being carried out using water with a maximum total solids content of200ppm.7.Treatments in Citric Acid7.1Passivation Treatment:7.1.1Stainless steel parts shall be treated in one of the following aqueous solutions and maintained within the speci-fied temperature range for the specified time.7.1.1.1Citric1—The solution shall contain4to10weight percent of citric acid.The parts shall be immersed for a minimum of4min at a temperature in the range from140to 160°F(60to71°C).7.1.1.2Citric2—The solution shall contain4to10weight percent of citric acid.The parts shall be immersed for a minimum of10min at a temperature in the range from120to 140°F(49to60°C).7.1.1.3Citric3—The solution shall contain4to10weight percent of citric acid.The parts shall be immersed for a minimum of20min at a temperature in the range from70to 120°F(21to49°C).7.1.1.4Citric4—Other combinations of temperature,time, and concentration of citric acid,with or without other chemi-cals to enhance cleaning,including accelerants,inhibitors,or proprietary solutions capable of producing parts that pass the specified test requirements.7.1.1.5Citric5—Other combinations of temperature,time, and concentrations of citric acid,with or without other chemi-cals to enhance cleaning,including accelerants,inhibitors,or proprietary solutions capable of producing parts that pass the specified test requirements.Immersion bath to be controlled ata pH of1.8–2.2.7.2Water Rinse—Immediately after removal from the pas-sivating solution,the parts shall be thoroughly rinsed,using stagnant,countercurrent,or spray washes,singly or in combi-nation,with or without a separate chemical treatment for neutralization of the passivation media(see9.2),with afinal rinse being carried out using water with a maximum total solids content of200ppm.8.Treatments in Other Chemical Solutions,IncludingElectrochemical Treatments8.1It is recognized that the purpose of removal of all exogenous matter from a stainless steel surface,including the removal of free iron,can be accomplished by different media, with potential for benefits to be gained from use of proprietary skills and art,including proprietary passivation media.Such treatments may include externally applying an electrical po-tential on the stainless steel parts,as in the case of electropol-ishing.The suitability of such passivation treatments for use in meeting the requirements of this specification shall be deter-mined by the capability of the processed parts meeting the specified test requirements.8.2Stainless steel parts shall be treated in a specified aqueous solution,with or without externally applied electrical potential,and maintained within a specified temperature range for a time sufficient for the processed parts to meet the specified test requirement.8.3Water Rinse—Immediately after removal from the pas-sivating solution,the parts shall be thoroughly rinsed,using stagnant,countercurrent,or spray washes,singly or in combi-nation,with or without a separate chemical treatment for neutralization of the passivation media(see9.2),with afinal rinse being carried out using water with a maximum total solids content of200ppm.9.Neutralization9.1The chemical reactions of the passivating media on the surface of the stainless steel shall be stopped by rinsing of the stainless steel part,with or without a separate neutralization treatment.9.2The suitability of a neutralization procedure is deter-mined by the capability of the processed parts meeting the specified test requirements.(See Note1.)N OTE1—The selection of medium and procedures for a neutralization depends of the chemistry of the passivation and on economic consider-ations.An example of a neutralizing treatment would be immersion of the part for a minimum of30min in a solution of5%NaOH at160to180°F (71to82°C),followed by a water rinse.10.Post-Cleaning Treatments10.1Although the passivefilm characteristic of stainless steel will form spontaneously in air or any other oxygen-containing environment,the processor shall,when specified, apply a chemical treatment that will accelerate the formation of the passivefilm on a chemically clean stainless steel surface. An example of a medium that serves to accelerate the forma-tion of the passivefilm but does not contribute to the removal of free iron from the stainless steel surface would be an aqueous solution of sodium dichromate.10.2When specified,within one hour after thefinal water rinse as required in6.2,7.2,or8.3,all ferritic and martensitic steel parts shall be immersed in an aqueous solution containing 4to6weight percent of sodium dichromate at a temperature in the range from140to160°F(60to71°C)for a minimum of30 min,followed by a rinse in accordance with6.2,7.2,or8.3. The parts shall then be thoroughly dried.10.3The purchaser may specify other post-cleaning treat-ments.11.Finish11.1The passivated parts shall exhibit a chemically clean surface and shall,on visual inspection,show no etching, pitting,or frosting resulting from the passivation procedures.12.Testing Agency12.1When required,the purchaser shall be permitted to perform such inspections as necessary to determine that the testing agency is capable of performing the specifiedtest.13.Lot,Frequency of Testing,and Selection of Test13.1Definition of Lot—A lot shall consist of one of the following,at the option of the processor:13.1.1The passivated parts of similar alloy and manufac-turing methods that are pretreated and passivated in a single day or within a time frame that will ensure consistent passiva-tion results;13.1.2The passivated parts of the same product of one size from one heat in one shipment;or13.1.3When few parts are involved,the passivated parts from an entire production run.13.2Unless a greater frequency of testing is specified on the purchase order,one test per lot shall be sufficient.13.3One or more of the following tests,when specified on the purchase order,shall be performed on each lot of stainless steel parts.Not all of the following tests are suitable for all grades of stainless steel.(See Note2.)13.3.1Practice A—Water Immersion Test,13.3.2Practice B—High Humidity Test,13.3.3Practice C—Salt Spray Test,13.3.4Practice D—Copper Sulfate Test,and13.3.5Practice E—Potassium Ferricyanide–Nitric Acid Test.N OTE2—Some of the tests may produce positive indications not associated with the presence of free iron on the stainless steel surface.An example would be application of Practice C on some lesser-alloyed martensitic or ferritic stainless steels.14.Practice A—Water Immersion Test14.1This test is used for the detection of free iron or any other anodic surface contaminants on stainless steel.14.2The sample representing the lot of passivated parts shall be alternately immersed in a non-rusting tank of distilled water for1h and allowed to dry in air for1h.This cycle shall be repeated a minimum of twelve times.14.3The tested sample shall not exhibit rust or staining attributable to the presence of free iron particles embedded in the surface.15.Practice B—High Humidity Test15.1This test is used for the detection of free iron or any other anodic surface contaminants on stainless steel.15.2The test shall be performed using a humidity cabinet capable of maintaining the specified test conditions.15.3The sample representing the lot of passivated parts shall be cleaned by immersion in acetone or methyl alcohol or by swabbing with a clean gauze saturated with acetone or methyl alcohol,and dried in an inert atmosphere or desiccated container.The cleaned and dried part shall be subjected to97 63%humidity at10065°F(3863°C)for a minimum of 24h.15.4The tested sample shall not exhibit rust or staining attributable to the presence of free iron particles imbedded in the surface.16.Practice C—Salt Spray Test16.1This test is used for the detection of free iron or any other anodic surface contaminants on stainless steel.16.2The sample representing the lot of passivated parts shall be tested by the salt spray test conducted in accordance with Practice B117for a minimum of2h using a5%salt solution.16.3The tested sample shall not exhibit rust or staining attributable to the presence of free iron particles imbedded in the surface.17.Practice D—Copper Sulfate Test17.1This test is recommended for the detection of free iron on the surface of austenitic stainless steels in the200and300 series,precipitation hardened stainless steels,and ferritic400 series stainless steels having a minimum of16%chromium. This test is not recommended for martensitic400series stainless steels or for ferritic400series stainless steels with less than16%chromium because these steels will give a positive indication irrespective of the presence or absence of anodic surface contaminants.This test shall not be applied to parts to be used in food processing.17.2The test solution is prepared by dissolving4g of copper sulfate pentahydrate(CuSO4·5H2O)in250mL of distilled water to which1mL of sulfuric acid(H2SO4,sp gr 1.84)has been added.Aqueous copper sulfate solutions more than two weeks old shall not be used for this test.17.3The test solution is swabbed on the surface of the sample representing the lot of passivated parts,applying additional solution as needed to keep the surface wet for a period of at least6min.At the end of this period,the surface shall be carefully rinsed and dried with care taken not to disturb copper deposits if present.17.4The tested sample shall not exhibit copper deposits.18.Practice E—Potassium Ferricyanide–Nitric Acid Test 18.1This test is recommended when detection of very small amounts of free iron is required.It is recommended for detection of free iron on austenitic200and300series stainless steels.This test is not recommended for detection of free iron on ferritic or martensitic400series stainless steels,because these steels will give a positive indication irrespective of the presence or absence of anodic surface contaminants.This test shall not be applied to parts to be used in food processing. 18.2The test solution is prepared by adding10g of chemically pure potassium ferricyanide to500mL of distilled water,adding30mL of70%nitric acid,agitating until all of the ferricyanide is dissolved,and diluting to1000mL with distilled water.The test solution shall be mixed fresh on the day of the test.18.3The test solution is swabbed on the surface of the sample representing the lot of passivated parts.The formation of a dark blue color within30s denotes the presence of metallic iron.18.4The tested sample shall not exhibit the dark blue color indicative of free iron on the surface.18.5When the test is negative,the surface shall be thor-oughly washed with warm water to removal all traces of the test solution.When the test is positive,the dark blue stain shall be removed with a solution of10%acetic acid and8%oxalic acid,followed by a thorough hot waterrinse.19.Practice F—Free Iron Test19.1This test is used for the detection of free iron on the surface of stainless steel.It is especially useful for large parts that have been uniformly cleaned but that are inconvenient for reasons of size of equipment or ease of handling of the part to place in the environments defined in Practice A(Section14)or Practice B(Section15).Unless otherwise specified by the purchaser,the number of tests and the locations of the tests shall be at the option of the processor to assure a representative testing of the part.19.2The test is performed by placing a clean cloth pad that has been thoroughly soaked with distilled or deminaralized water on the surface of the part at a part temperature of50°F (10°C)or greater for a period of not less than60minutes.The cloth shall be in contact with the steel for an area of at least20 square inches(130cm2).The pad shall be maintained wet through the test period,either by a method of retarding external evaporation,by the further addition of potable water,or by backing the pad with a sponge or similar water source.The cloth pad used shall be used for only one such test,being changed for each test so as to avoid risk of contamination. After removal of the cloth pad,the surface of the part shall be allowed to dry in air before inspection.19.3The tested part shall not exhibit rust or staining attributable to the presence of free iron particles embedded in the surface.20.Rejection and Retest20.1Any lot failing to meet the specified test requirements of the purchase order shall be rejected.A rejected lot may,at the option of the processor,be re-passivated,with or without re-pretreatment,and then be retested.The number of samples tested from a lot subject to retest shall be twice the original specified test frequency,to the limit of the number of pieces in the lot.All samples must pass the specified acceptance criterion for the specified test for the retested lot to be accepted. 21.Precision and Bias21.1No statement is made concerning either the precision or bias of Practices A,B,C,D,and E because the results state merely whether there is conformance to the criteria for success specified in the procedure.22.Certification22.1When specified in the purchase order,a report of the practice and tests used,including the record of process condi-tions when specified in accordance with 3.1.1.2,shall be supplied to the purchaser.APPENDIX(Nonmandatory Information)RMATION REGARDING PASSIV ATION TREATMENTSN OTE X1.1—The following information is based on a section of Federal Specification QQ-P-35C(Oct.28,1988)identified as information of a general or explanatory nature that may be helpful,but is not mandatory. Minor changes have been made in the text to facilitate references to the main document and to correct technical inaccuracies.X1.1Intended Use—The passivation treatments provided by this specification are intended to improve the corrosion resistance of parts made from stainless steels of all types.X1.1.1During processing operations such as forming,ma-chining,tumbling,and lapping,iron particles or other foreign particles may become smeared over or imbedded into the surface of stainless steel parts.These particles must be re-moved or they will appear as rust or stain spots.This condition may be prevented by chemically treating the parts to remove the iron particles or other foreign particles,and then allowing the passivefilm to form on the cleaned surface,with or without chemical enhancement of the formation of this oxidefilm.X1.1.2This specification is not intended for the black oxide coating of parts typically used for photographic or optical instruments.X1.2Ordering Data—Purchasers should select the pre-ferred options permitted by this specification and include the following information in the purchase order:X1.2.1Title,number,and date of this specification;X1.2.2Identification of material by type and applicable product specification;X1.2.3Test practices to be imposed(see1.4);X1.2.4Definition of lot size,if other than described in this specification;andX1.2.5Required documentation,if other than the minimum required by this specification.X1.3Grades of Stainless Steel—Different types of stainless steel are selected on a basis of properties required,for example, corrosion resistance and design criteria,and fabrication re-quirements.Table X1.1is a compilation that serves as a guide for the selection of passivation treatment for different grades, but is far from complete either in grades or in passivation treatments.X1.4Clean Water—Clean water is defined as water con-taining a maximum total solid content of200ppm.Rinsing can be accomplished by a combination of stagnant,countercurrent or spray rinses,or both,prior tofinal rinse.X1.5Chemically Clean Surface—A chemically clean sur-face is defined as a surface upon which water,when applied momentarily to the surface,will remain on that surface in an even,continuousfilm,and in addition is free of any foreign material or residualfilm deposit which would be detrimental to the quality of thepart.X1.6Test Specimens —When using test specimens instead of parts,the specimens can effectively represent the parts only if they have been exposed to the same processing steps,such as machining,grinding,heat treating,welding,and so forth,as the parts they are to represent.X1.7Carburized Surfaces —Stainless steel parts with car-burized surfaces cannot be passivated because the carbon combines with the chromium forming chromium carbides on the surface.X1.8Nitrided Surfaces —Stainless steel parts with nitrided surfaces should not be passivated because the treatment will severely corrode the nitrided case.X1.9This specification provides for the same passivation treatments as Fed.Spec.QQ-P-35C,but also includes a number of alternative passivation treatments.The effectiveness of any passivation treatment is demonstrated by the parts meeting the specified testing requirements after treatment.X1.10Martensitic Grade 440C —High-strength grades such as 440C are subject to hydrogen embrittlement or intergranular attack when exposed to acids.Cleaning by mechanical methods or other chemical methods is recom-mended.X1.11The salt spray test is typically used to evaluate austenitic stainless steels and may not be applicable to all martensitic or ferritic stainless steels.ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentioned in this ers of this standard are expressly advised that determination of the validity of any such patent rights,and the risk of infringement of such rights,are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years and if not revised,either reapproved or withdrawn.Your comments are invited either for revision of this standard or for additional standards and should be addressed to ASTM International Headquarters.Your comments will receive careful consideration at a meeting of the responsible technical committee,which you may attend.If you feel that your comments have not received a fair hearing you should make your views known to the ASTM Committee on Standards,at the address shownbelow.FIG.X1.1Recommended Nitric Acid Passivation Treatments for Different Grades of StainlessSteel。
ASTM A967
ASTM A967-01E1Standard Specification for Chemical Passivation Treatments for Stainless Steel PartsASTM International / 10-Oct-2001 / 6 pagesREPLACED by ASTM A967-051.1 This specification covers several different types of chemical passivation treatments for stainless steel parts. It includes recommendations and precautions for descaling, cleaning, and passivation of stainless steel parts. It includes several alternative tests, with acceptance criteria, for confirmation of effectiveness of such treatments for stainless steel parts.1.2 Practices for the mechanical and chemical treatments of stainless steel surfaces are discussed more thoroughly in Practice A 380.1.3 Several alternative chemical treatments are defined for passivation of stainless steel parts. gives some nonmandatory information and provides some general guidelines regarding the selection of passivation treatment appropriate to particular grades of stainless steel but makes no recommendations regarding the suitability of any grade, treatment, and acceptance criteria for any particular application or class of applications.1.4 The tests in this specification are intended to confirm the effectiveness of passivation, particularly with regard to the removal of free iron and other exogenous matter. These tests include the following practices:1.4.1 Practice A - Water Immersion Test,1.4.2 Practice B - High Humidity Test,1.4.3 Practice C - Salt Spray Test,1.4.4 Practice D - Copper Sulfate Test,1.4.5 Practice E - Potassium Ferricyanide-Nitric Acid Test, and1.4.6 Practice F - Free Iron Test.1.5 The values stated in inch-pound units are to be regarded as the standard. The SI units given in parentheses are for information only.1.6 The following precautionary caveat pertains only to the test method portions, Sections 14 through 18 of this specification: This standard does not purport to address all of the safety concerns, if any, 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.Keywords: chemical passivation; stainless steel; passivation treatments; water immersion, steel; high humidity, steel; 77.140.20This product replaced by:ASTM A967-05 - Standard Specification for Chemical Passivation Treatments for Stainless Steel Parts This product replaces:∙ASTM A967-99 - Standard Specification for Chemical Passivation Treatments for Stainless Steel Parts∙ASTM A967-01 - Standard Specification for Chemical Passivation Treatments for Stainless Steel Parts。
不锈钢钝化
不锈钢钝化什么是钝化?钝化过程是什么样的?怎么样钝化?工作原理是什么?不锈钢部件加工后怎么钝化?什么是钝化?回答这个问题前我们得先知道什么是不锈钢?不锈钢具有天然的耐腐蚀性能,这可能意味着它们的钝化是不必要的,但不锈钢并非完全不受腐蚀。
不锈钢的抗腐蚀性能主要来源于铬的组成成分。
. 铬接触空气(氧),在不锈钢表面形成一层很薄的氧化铬薄膜。
材料中的铬使不锈钢具有耐腐蚀性能是因为氧化铬(是不锈钢中的铬可以被空气钝化形成的)。
在理想的条件下,纯净的,清洁的不锈钢暴露在大气中与氧气接触,形成一个氧化铬薄层,这个薄层可以保护不锈钢不被腐蚀。
在现实普通情况下,制造环境中的杂质,不锈钢中加入硫化物等来提高机械加工性能,或则加工过程产生的铁颗粒可能粘附在不锈钢部件的表面,这些都可能破坏不锈钢表面氧化铬薄层的形成,因此,不锈钢表面的这些污染物需要移除。
这些去除污染物和形成氧化层的过程叫做钝化。
钝化是一种非电解过程,通常使用硝酸或柠檬酸,从表面除去游离铁,形成惰性、保护性的氧化层,进而使不锈钢因缺乏铁与大气反应而变得更耐锈。
不锈钢钝化工艺从化学上去除了这些游离铁,形成了被动氧化物“膜”层,进一步提高了耐蚀性。
当接触空气(氧气)时,处于钝化状态的不锈钢会形成化学上不活泼或惰性的氧化铬表面。
根据ASTM A380&A967的钝化描述,钝化是通过化学溶解从不锈钢表面去除外源铁或铁化合物,最典型的方法是用酸性溶液去除表面污染,但不会对不锈钢本身产生重大影响ASTM A380 关于钝化的更多描述“”用温和氧化剂如硝酸溶液对不锈钢进行化学处理,目的是加强保护被动薄膜的自发形成。
因此,一种“温和氧化剂”,如硝酸或柠檬酸(矿物或有机酸溶液),可以从不锈钢表面去除多余的铁和相关污染物,并可以在暴露空气中时形成铬氧化层,从而使不锈钢具有抗腐蚀性能。
钝化过程是怎么样的?.有许多钝化规范(ASTM A967,AMS2700,ASTM A 380)用于指导如何对不锈钢,钛和其他材料进行钝化,其中一些如下:通常所有规范都是:清洗表面免受上面列出的任何污染物的污染,通过浸泡在酸浴中进行化学处理(通常为硝酸或柠檬酸),并测试新钝化的不锈钢表面,以确保工艺步骤。
不锈钢表面处理
6
1.5.6表面处理标准—不锈钢钝化
Chemical Passivation Treatments(ASTM-A-967)
类别 class 描述 DESCRIPTION
Citric 1 Citric 2
Citric 3 Citric 4 Citric 5
电解抛光(Electropolishing)
原理
- 以工件为阳极,不溶性金属为阴极,在特定的电解液中,在通电的条 件下发生选择性溶解,从而达到微观整平,增大光亮度的效果
应用范围
- 生化,医药领域,食品,化妆,半导体,印刷,过滤,化工领 域
特性
- 1.色泽一致,清洁光亮,2.可以去除零件表面的毛刺3.提高零件 表面的耐蚀性,6.生产效率高,成本较低
60℃-71℃,20min 49℃-60℃,30min
21℃-49℃,20min / /
7
8
工件表面要保持平滑,不要有明显的凹痕.
热处理后的氧化皮要清除干净.表面渗碳,渗氮的零件不能进行钝化处理.
不要用铁及其氧化物做成的工具清理零件表面.
440C和S136材料,必须经过热处理,方可进行钝化
3
1.2.3不锈钢钝化—测试要求
沸水测试
硝酸 铁氰化钾测试
湿度测试
硫酸铜测试
盐雾测试
4
1.2.4不锈钢表面处理——电解抛光
深圳泰瑞电镀厂培训教材 ——不锈钢表面处理
Logo
1
1.2.1不锈钢钝化—原理
原理
不锈钢表面的金属成分与氧化性溶液发生反应,生成一层薄 的保护膜的过程。
●特点与用途
1.尺寸无变化
astm-a967-01e1 不锈钢部件化学钝化处理的标准规范
洗,可在流动的水中清洗,也可进行喷洗,或者几种方法结合起来清洗。清洗时也可使用单 独的化学方法来中和(详见9.2)钝化媒介。最后的漂洗液固体含量最多为200%。
8. 包括电化学处理方法在内的其他化学溶液处理方法
8.1 众所周知去除不锈钢表面的外源物质,包括去除游离铁,可通过不同的媒介来实现,利 用合适的技艺和方法、适合的钝化媒介还可得到益处。电解时,该处理方法从外部对不锈钢 部件供电。符合该标准的此类钝化处理方法是否适用取决于反应后的部件是否符合测试的要 求。 8.2 不锈钢部件要求在水溶液中进行处理,不管是否从外部供电,也必须在规定的温度范围 内进行处理以此保证处理过的不锈钢部件符合测试的要求。 8.3 清水漂洗 - 从钝化溶液中去除不锈钢部件后立即进行全面的清洗。可在静止的水中清 洗,可在流动的水中清洗,也可进行喷洗,或者几种方法结合起来清洗。清洗时也可使用单 独的化学方法来中和(详见9.2)钝化媒介。最后的漂洗液固体含量最多为200%。
10. 后清洗处理方法
10.1 尽管不锈钢在空气或其他氧化环境下会自行形成钝化层,有具体要求时,操作者应该 采用能加快化学清洗处理过的不锈钢表面形成钝化层的化学处理方法。例如能加快钝化层的 形成但是不能去除不锈钢表面游离铁的媒介的溶液应该是重铬酸钠溶液。 10.2 如果用户要求,按照6.2,7.2,或8.3要求的方法进行最后漂洗后的一小时以内,所有铁 素体和马氏体钢部件必须浸泡在含有4-6%(重量百分比)重铬酸钠溶液的水溶液中,温度 控制在140-160华氏度(60-71摄氏度),至少浸泡30分钟。然后根据6.2,7.2或8.3条的要求 进行漂洗。最后使不锈钢部件充分干燥。 10.3 购买者会具体要求其他的后清洗处理方法。
3. 术语
3.1 该标准特定的术语定义 - 在该标准规范中定义常用的术语 passivation 是必要的(详见 讨论)。 3.1.1 讨论 - 如果不锈钢暴露在空气或潮湿的环境下产生了防钝化膜,它会自动钝化。外界 表面污染物的存在,包括灰尘,油脂,游离铁等等物质可能会干涉钝化层的形成。清洗这些 污染物会同时使不锈钢钝化,因为有氧化物质接触不锈钢的表面。可形成氧化生锈环境的化 学处理方法也会使不锈钢表面的钝化层扩大。 3.1.1.1 在该规范中,除非有特殊的定义,否则钝化即定义为使用温和氧化物的化学方法处 理不锈钢的过程,例如硝酸盐溶液。该处理方法目的在于去除游离铁及其他异物,但不会去 除不锈钢上的热色调和氧化铁皮。假如为了提高不锈钢的切削加工性而多加了硫元素,钝化
ASTM美国材料实验协会AB类标准大全
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ASTM B131-07铜合金子弹壳帽规格
ASTM B134/B134M-05黄铜丝规格
ASTM B135-02标准无缝铜管
ASTM B135M-00(2006)无缝黄铜管规格(米制)
ASTM A929/A929M-01(被ASTM A929/A929M-01(2007)代替)??波纹钢管用热浸金属镀层薄钢板规格
ASTM A930-03??涵管、雨水管和其它地下排水管用波纹金属管的寿命周期成本分析规程
ASTM A931-96(2002)钢丝绳和绞线拉伸试验的试验方法
ASTM A932/A932M-01(2006)??用瓦特计-安培计-伏特计和薄钢板样品测试在电源频率下非晶体材料交流磁性能的标准试验方法
ASTM B154-05铜和铜合金硝酸亚汞试验的试验方法
ASTM B159/B159M-05磷青铜丝技术规范
ASTM B16/B16M-05制螺钉机用易切削黄铜条材、棒材和型材
ASTM B160-05??镍线材和棒材规格
ASTM B161-05镍无缝管规格
ASTM B162-99(2005)??镍中厚板、薄板和带材规格
ASTM A950/A950M-99(2007)??熔接环氧树脂涂层结构钢工字桩和打板桩规格
ASTM A951/A951M-06砌筑嵌缝配筋用钢丝规格
ASTM A952/A952M-02??锻造等级80和等级100的钢提升组件及焊接连接杆规格
ASTM A955/A955M-07(被ASTM A955/A955M-07a代替)??混凝土加固用异形不锈钢钢筋及普通不锈钢钢筋规格
ASTM
2006/6/1
Reagents
Standard Test Method for Tensile Properties of Plastics
2003/12/1
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ASTM D 3578
2001/11/10
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Standard Specification for Rubber Examination Gloves
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Standard Specification for Rubber Examination Gloves
2005/5/1
ASTM D 4003
Standard Test Methods for Programmable Horizontal Impact Test for
04/10/1998
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Shipping Containers and Systems R(2003)
ASTM D 4169
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14 ASTMD 737- 04
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ASTM美国材料实验协会AB类标准大全
A S T M美国材料实验协会A B类标准大全TTA standardization office【TTA 5AB- TTAK 08- TTA 2C】A S T M美国材料实验协会A类标准大全?ASTM是美国材料实验协会(American Society of Testing Materials )所制定的相关标准。
其中A类标准有:ASTM A918-06 要求标出每个表面镀层质量的用途用电解镀锌-镍合金钢板规格ASTM A920/A920M-02A 具有机械特性的微合金热锻特种钢棒规格ASTM A921/A921M-93(2005) 后热锻用微合金特种热锻钢棒规格ASTM A922-05?硅金属规格ASTM A923-06 测定锻造双联奥氏体/铁素体不锈钢不稳定金属间相的试验方法ASTM A924/A924M-07 热浸法镀金属镀层薄钢板通用要求规格ASTM A925-03?锌-5%铝-铈合金涂覆钢架空金属绞线规格ASTM A926-03 波纹金属管用涂覆材料抗磨性比较的试验方法ASTM A927/A927M-04?使用伏特计-电流计-瓦特计方法的环形铁芯交流磁性能的标准试验方法ASTM A928/A928M-05 用添加填料金属电熔焊接的铁素体/奥氏体(双联)不锈钢管电熔焊接规格ASTM A929/A929M-01(2007)波纹钢管用热浸金属镀层薄钢板规格ASTM A929/A929M-01(被ASTM A929/A929M-01(2007)代替)波纹钢管用热浸金属镀层薄钢板规格ASTM A930-03?涵管、雨水管和其它地下排水管用波纹金属管的寿命周期成本分析规程ASTM A931-96(2002) 钢丝绳和绞线拉伸试验的试验方法ASTM A932/A932M-01(2006)用瓦特计-安培计-伏特计和薄钢板样品测试在电源频率下非晶体材料交流磁性能的标准试验方法ASTM A933/A933M-07?加固用聚氯乙烯涂层钢丝和焊接钢丝网规格ASTM A934/A934M-04 环氧基树脂涂覆的预制钢筋规格ASTM A937/A937M-06?使用临界试验面测定绝缘涂层层间阻力的标准测试方法ASTM A938-04(被ASTM A938-04代替) 钢丝扭转试验的试验方法ASTM A939-07?圆柱形锻件镗孔表面超声波检验规程ASTM A939-96(2006)(被ASTM A939-07代替)圆柱形锻件镗孔表面超声波检验规程ASTM A940/A940M-06 涡轮机转轮用经局部热处理的真空处理合金钢锻件规格ASTM A941-06A 有关钢、不锈钢、相关合金和铁基合金的术语ASTM A942-95(2007)离心铸造白口铁/灰口铁双金属耐磨滚轮外壳标准规范ASTM A943/A943M-01(2005) 喷涂成形无缝奥氏体不锈钢管规格ASTM A944-05 用梁端试样比较钢筋与混凝土粘结强度的试验方法ASTM A945/A945M-06e1?带经改进可焊接性、可成形性及韧性的低碳限硫的高强度低合金结构钢薄板规格ASTM A946-95(2004) 耐腐蚀和耐热用铬、铬-镍及硅合金钢板规格ASTM A947M-95(2004) 有纹理不锈钢薄钢板(米制)规格ASTM A949/A949M-01(2005) 喷涂成形无缝铁素体/奥氏体不锈钢管规格ASTM A950/A950M-99(2003)(被ASTM A950/A950M-99(2007)代替)熔接环氧树脂涂层结构钢工字桩和打板桩规格ASTM A950/A950M-99(2007)熔接环氧树脂涂层结构钢工字桩和打板桩规格ASTM A951/A951M-06 砌筑嵌缝配筋用钢丝规格ASTM A952/A952M-02?锻造等级 80 和等级100 的钢提升组件及焊接连接杆规格ASTM A955/A955M-07(被ASTM A955/A955M-07a代替)混凝土加固用异形不锈钢钢筋及普通不锈钢钢筋规格ASTM A955/A955M-07a?混凝土加固用异形不锈钢钢筋及普通不锈钢钢筋规格ASTM A956-06 测试钢产品里氏硬度的试验方法ASTM A957/A957M-06 一般工业用钢和合金熔模铸件通用要求规格ASTM A958-00(2006)类似于锻造等级的碳素钢和合金钢铸件拉伸要求及化学要求的规格ASTM A959-04?规定锻造不锈钢统一标准等级成份的指南ASTM A960/A960M-07 锻制钢管管件通用要求规格ASTM A961/A961M-07 管道设备用钢法兰、锻制配件、阀门和部件的普通要求ASTM A962/A962M-07(被ASTM A962/A962M-07a代替)低温至蠕变任何温度范围下用钢紧固件或紧固件材料或两者的通用要求规格ASTM A962/A962M-07a?低温至蠕变任何温度范围下用钢紧固件或紧固件材料或两者的通用要求规格ASTM A964/A964M-03?波纹钢箱形涵洞规格ASTM A965/A965M-06A 压力和高温部件用奥氏体钢锻件规格ASTM A966/A966M-07?使用交流电的钢锻件磁粉探伤试验方法ASTM A966/A966M-96(2006)(被ASTM A966/A966M-07代替)使用交流电的钢锻件磁粉探伤试验方法ASTM A967-05(被ASTM A967-05e1代替) 不锈钢部件化学钝化处理规格ASTM A967-05e1?不锈钢部件化学钝化处理规格ASTM A968/A968M-96(2001) 腐蚀和耐热用铬、铬-镍和硅合金钢棒及形状的规格ASTM A970/A970M-06 混凝土加固用撑帽式钢筋规格ASTM A971/A971M-05?测量平轧电工用钢卷材边缘锥度和凸顶的试验方法ASTM A972/A972M-00(2004)熔合的环氧涂层钢管桩规格ASTM A973/A973M-01 等级100的合金钢链规格ASTM A974-97(2003)焊接钢丝围栅石笼和石笼钢筋网(金属镀层或聚氯乙烯涂敷)规格ASTM A975-97(2003) 双层扭曲六边形网眼筐和护坡钢筋网(金属镀层钢丝或带聚氯乙烯(PVC)敷层的金属镀层钢丝)规格ASTM A976-03?按照成份、相对绝缘能力及用途对绝缘涂层进行分类方法ASTM A977/A977M-02?用磁滞曲线图测定高矫顽力永久磁性材料磁性的标准试验方法ASTM A978/A978M-97(2002)e1?自流式生活污水管、雨水管和其他专用设施用预涂层及聚乙烯衬里复合肋式钢管规格ASTM A979/A979M-03 安装在野外波纹钢结构内的混凝土路面和衬层规格ASTM A980-97(2003) 超高强度冷轧碳素钢薄板ASTM A981-97(2002)(被ASTM A981-97(2007)代替) 评定预应力地锚中用等级270未镀敷的 mm in.)直径钢绞线结合强度的试验方法ASTM A981-97(2007) 评定加预应力地锚使用的270号、直径为毫米英寸)加预应力连铸钢坯结合强度的标准试验方法ASTM A982/A982M-05?压缩机与轮机翼用不锈钢锻件规格ASTM A983/A983M-06 中速柴油机连续晶粒流动锻造碳素及合金钢曲轴规格ASTM A984/A984M-03 电阻焊接干线用平端黑钢管规格ASTM A985/A985M-04A 承压部件用钢围模料铸件通用要求规格ASTM A986/A986M-01(2006)连续晶粒流动曲轴锻件磁粉探伤规格ASTM A987-05?测量锡轧制成品形状性能的试验方法ASTM A988/A988M-05 高温设备用热等静压不锈钢法兰、配件、阀门和部件规格ASTM A989/A989M-05?高温设备用热等静压合金钢法兰、配件、阀门和部件规格ASTM A990-06?腐蚀环境下保压部件控制用铁-镍-铬及镍合金铸件规格ASTM A99-03?锰铁规格ASTM A991/A991M-98(2004) 测量热处理钢产品用炉温度均匀性的试验方法ASTM A992/A992M-06A 结构钢形状规格ASTM A994-05?钢、不锈钢和相关合金产品规格的编写程序及格式的指南ASTM A995/A995M-98(2003) 承压部件用奥氏体-铁素体(双联)不锈钢铸件规格ASTM A996/A996M-06A 混凝土加固用轨道钢和轮轴钢异形棒材规格ASTM A997-07?熔模铸件表面目测验收标准规程ASTM A998/A998M-98(2003) 下水道和其他设施用工厂制波纹钢管管件钢筋的结构设计规程ASTM A999/A999M-04A 合金和不锈钢管通用要求规格ASTM A1007-07 钢丝绳用碳素钢丝规格ASTM A325-07 经热处理最小抗拉强度为830Mpa的热处理钢结构螺栓ASTM A938-07 钢丝扭转试验的试验方法ASTM美国材料实验协会B类标准大全?ASTM是美国材料实验协会(American Society of Testing Materials )所制定的相关标准。
不锈钢硝酸与柠檬酸钝化的工艺
不锈钢硝酸与柠檬酸钝化的工艺不锈钢是一种固有的抗腐蚀材料,但是当对不锈钢进行机械加工,成型或加工时,可以将游离铁引入到基材表面上。
用诸如硝酸或柠檬酸之类的氧化性酸对不锈钢进行适当的钝化处理会除去这种游离铁,并促进薄而致密的保护性氧化层的生长,从而使不锈钢的耐腐蚀性最大化。
对于不锈钢的类型和最终应用,某些钝化工艺可能会比其他钝化工艺表现更好。
就让我们杰昌电镀来说说吧,我们将比较硝酸和柠檬酸的钝化作用,这是ASTM A967和AMS 2700中指定的两种主要化学方法。
硝酸钝化硝酸钝化在比较硝酸钝化与柠檬酸钝化时,整个行业中最常用的方法是硝酸钝化。
硝酸钝化工艺是QQ-P-35中规定的原始钝化工艺,这是第一个涉及钝化的军事规范。
硝酸钝化提供了多种选项,可自定义酸的氧化电位,以适合特定等级的不锈钢。
硝酸钝化的各种方法和类型包括几种加热选项以及包括重铬酸钠的选项。
硝酸浓度越高,硝酸温度越高,钝化化学物质的氧化电位越高。
也可以将重铬酸钠添加到硝酸中,以提高镀液的氧化能力,使其更适合用于耐蚀性较低的不锈钢,例如沉淀硬化,马氏体和铁素体等级的不锈钢。
这些等级的不锈钢中的镍和铬含量较低,这使其更易于被腐蚀。
化学物质的氧化电位越高,在表面上形成钝化氧化物阻挡层的速度越快,效果越好,从而降低了腐蚀电位。
以下是根据ASTM A967进行的各种硝酸钝化方法的浓度和时间:钝化化学物的污染会导致表面的点蚀,从而产生严重腐蚀或变暗的表面。
导致点蚀的常见物质是氯化物,其来源多种多样,包括拖入酸中或在水中使用氯化物。
此外,钝化槽中的有机物堆积,例如未正确清洁的零件所产生的机加工油的引入,都可能导致不锈钢腐蚀。
因此,需要定期进行分析并维护钝化化学物质。
某些钝化方法也比其他方法更能抵抗点蚀。
用于硝酸钝化氧化电位增加的镀液也更能抵抗点蚀。
与柠檬酸相比,硝酸还具有更强的抗点腐蚀性。
柠檬酸钝化柠檬酸钝化是由Adolf Coors酿酒公司开发的,用于啤酒桶内部的钝化。
astm热处理标准
astm热处理标准
ASTM(美国材料与试验协会)制定了许多与热处理相关的标准。
以下是一些常见的ASTM热处理标准的介绍:
1. ASTM A255,该标准规定了金属材料的宏观脆性测定方法,
可以用于评估热处理过程中的脆性。
2. ASTM A304,该标准涵盖了碳钢和合金钢的热处理要求,包
括退火、正火、淬火和回火等。
3. ASTM A519,该标准适用于无缝碳钢和合金钢机械管的热处
理要求。
4. ASTM A615,该标准规定了混凝土用热轧钢筋的热处理要求,包括冷弯和热弯试验。
5. ASTM A681,该标准适用于刀具钢、模具钢和合金钢的热处
理要求,包括淬火、回火和表面硬化等。
6. ASTM A967,该标准规定了不锈钢表面处理的热处理要求,
包括酸洗、电解抛光和钝化等。
7. ASTM E112,该标准涵盖了金属材料的晶粒度测定方法,可以用于评估热处理对材料微观结构的影响。
8. ASTM E562,该标准规定了金属材料的宏观残余应力测定方法,可以用于评估热处理对材料应力状态的影响。
需要注意的是,上述只是一小部分与热处理相关的ASTM标准,ASTM还有许多其他与材料测试和性能评估相关的标准。
具体的热处理标准选择应根据具体材料和应用要求进行确定。
ASTM_A967-05 钝化验证方法A~E译文
A 水浸测试:这个测试在不锈钢中用于检测游离铁或任何其他阳极表面污染物。
同一钝化批次的样本应轮流浸在不锈槽的蒸馏水中1 h和在空气中干燥1 h。
这个周期应被重复至少12次。
被测样品不能因为游离铁的存在而生锈或着色。
B 高湿度测试:这个测试在不锈钢中用于检测游离铁或任何其他阳极表面污染物。
试验应用一个湿度箱能够维护指定的测试条件。
被测钝化样品应浸在丙酮或甲醇中清洁或用带有丙酮或甲醇的渗透纱布擦拭,在惰性气体或干燥容器中干燥。
清洁干燥的部分应在温度38±3°C 湿度97±3 %环境中24H。
被测样品不能因为游离铁的存在而生锈或着色。
C 喷盐测试:这个测试在不锈钢中用于检测游离铁或任何其他阳极表面污染物。
被测钝化样品的喷盐测试按Practice B117 用5 %盐液浸泡至少2H。
被测样品不能因为游离铁的存在而生锈或着色。
D 硫酸铜测试:本测试建议用于200和300系列奥氏体钢等铬含量大于16%的表面游离铁测试。
本测试不能用于用在食品程序的样品。
试验方案用到4克CuSO4·5H2O在250毫升蒸馏水加1毫升硫酸(比重1.84)(注:先加水,后加酸!),擦拭在样品表面,至少保持样品潮湿6分钟,试样应以不去除任何沉积铜的方式冲洗和干燥。
铜的沉积指示游离铁的存在。
E 铁氰化钾硝酸盐测试:(国内俗称:蓝点测试)本测试建议用于200和300奥氏体钢需要检测极少量游离铁。
不能用于用在食品程序的样品。
需要准备加10克化学纯铁氰化钾于500毫升蒸馏水中,加30毫升70%硝酸溶液,搅拌至溶解并用蒸馏水稀释到1000毫升。
本试剂应在试验当天勾兑。
试剂在样品上擦拭,30秒内形成深蓝色表明游离铁的存在。
测试后样品表面不能有象征游离铁的深蓝色存在。
若测试没有变色,应彻底用温水冲洗去除所有溶剂痕迹;若测试变色,深蓝色的污垢应用10%的醋酸和8%的草酸,然后用开水彻底清洗F 游离铁测试:本测试对大部分均匀清洗样品有效但不便用于测试A和B的环境。
OPENCIRCUITPOTENTIALTECHNOLOGY:开路电位技术
CWA Conference 2012Quebec City, QCSeptember 10-11, 2012MONITORING PASSIVATION ON STAINLESS STEEL WITHOPEN CIRCUIT POTENTIAL TECHNOLOGYNathalie VézinaProduct Manager, Research & DevelopmentSURFOX systemsWalter Surface TechnologiesABSTRACTPassivation of stainless steel parts is of crucial importance in order to maintain its corrosion protection properties. Mostspecifically, heat affected zones on welded stainless steel are vulnerable areas that require specific care and should be thoroughly tested for passivation in order to avoid corrosion issues. The optimization of the passivation on stainless steelparts depends largely on our knowledge of the passivation process itself and the methods used to test the manufactured parts.A suitable test method is instrumental in validating proper passivation of parts for various industries such as food & bever-age, pharmaceutical and other industries using stainless steel components for their specific needs. Several existing methodsare currently available and are well known to most manufacturers, but do they really meet their specific needs?Over time, other methods have been developed to meet the growing needs of manufacturers. Particular attention will begiven in this document to the Open Circuit Potential technology and the added value of this new test method that offersflexibility, a clear economic advantage and accuracy that was previously unattainable.PROBLEM STATEMENTOften microscopic cells are present on the surface of the delivered work piece, but cannot be located and detected visuallyprior to shipment. These later spread and become visible, creating a phenomenon known as pitting and corrosion. That iswhy it is important for a manufacturer to ensure that the work piece is properly passivated before it is put in service. On siterepair and refurbishment is costly for the manufacturer and the need exists for a clear diagnostic tool capable of monitoringthe state of the passivation before it leaves the shop.PASSIVATIONStainless steel is an alloy that contains iron and at least 10.5% chromium. Other elements such as nickel, molybdenum, and many more may also be present depending on the grade of stainless steel. Stainless steel gets its amazing corrosion protection proper-ties from the presence of chromium in the alloy. The chromium present reacts with oxygen to form a thin chromium oxide layer on the surface of the workpiece, thus preventing the reaction of iron with oxygen which forms iron oxide: rust. The thin chromium oxide layer acts as a barrier between the iron rich bulk alloy and the oxygen rich ambient air.To passivate, the surface of stainless steel must be completely free of contaminants. Heat tint from welding as an example is a major contaminant that must be removed from the surface, not only for aesthetic reasons, but specifically to allow the stainless steel to passivate itself.The passivation process begins immediately after the contaminants are completely removed from the surface of the material. The chromium content in stainless steel at the surface of the material then reacts with oxygen in ambient air to form a passive layer of chromium oxide on the surface of stainless steel. It takes between 24 to 48 hours to achieve a uniform and stable passive layer.The chromium oxide layer can be damaged by:• Thermal treatments such as welding• Mechanicalabrasion• Galvaniccorrosion• Strongacids PASSIVATION PROCESSFe + C + Cr (min. 10.5%)Stainless steel part free of contaminant.ChromiumOxygenThe chromium content in the stainless steelreacts with oxygen in ambient air.The chromium oxide layer is reformedand protects against corrosion.2 3Several methods are available for restoring thermally damaged (from welding) stainless steel:Grinding and polishingGrinding the welds off completely removes the heat tint. However, there might be traces of free iron left behind which can cause pitting and corrosion. To ensure that this free iron is removed, a post chemical treatment with an acidic product is required. The situation is different for mirror finishes where the corrosion resistance of the stainless steel parts are greatly enhanced due to the uniformity of the material itself after the polishing process. The drawback of this method is that it is labour intensive and will alter the surface fininsh.Sand blastingSand blasting will remove the heat tint, but will embed a plethora of other contaminants into the stainless steel, which could hinder and limit the self passivation of material. This method is not considered ideal for repairing damaged stainless steel.Pickling pastes and gelsPickling pastes and gels will remove the heat tint and every other inorganic contaminant from stainless steel parts. However, these pastes and gels usually contain mixtures of nitric and hydrofluoric acids. Nitric acid vapours are very harmful to the human respiratory system and hydrofluoric acid will cause severe damage to the skin. Not only are the pickling pastes and gels very toxic to human beings, but they also alter the surface of stainless steel.Electrochemical cleaning and polishingElectrochemical cleaning and polishing is by far the safest and most efficient method of removing heat tint and other contami-nants from stainless steel surfaces. Electrochemical polishing removes more iron and nickel, leaving the surface rich in chrome. Walter offers a weld cleaning and polishing system known as SURFOX which will remove heat tint from surfaces at a speed of 3 to 5 feet per minute. This system uses food grade acids and electricity to remove the heat tint. SURFOX is certified ASTM A967-05/A380* for passivation.* ASTM A380 Standard provides definitions and describes best practices for cleaning, descaling and passivation of Stainless Steel Parts, Equipment and Systems. ASTM A967 Standard provides tests with acceptance criteria to demonstrate that the passivation procedures have been successful.As per ASTM International Standards; “passivation testing is the process by which stainless steel will spontaneously form a chemically inactive surface when exposed to air or other oxygen containing environments. Passivation testing involves the removal of exogenous iron or iron compounds from the surface of the stainless steel, by means of a chemical dissolution, most typically with an acid solution that will remove the surface contamination but will not significantly affect the stainless steel itself.”EXISTING PASSIVATION TEST METHODSAny steel or iron that comes in contact with stainless steel is a potential source of contamination. Tools such as grinding wheels and wire brushes previously used on steel or iron parts are susceptible to transfer iron to stainless steel surfaces. One of the most difficult sources of iron to avoid is the atmosphere itself. Industrial areas have a surprising amount of iron in the air. This iron falls onto exposed items, including previously cleaned stainless steel parts. To ensure proper passivation of stainless steel compo-nents, the surface must be free of contaminants such as free iron. Test methods exist to determine the presence of free iron on stainless steel surfaces.Stainless steel manufacturers need to select a test method which fulfills all of their needs. One important selection criteria is how quickly the test can generate results; quicker is normally better. The accessibility and the ability to perform the test on site are also important considerations. The fact that most of the known tests will damage and stain the stainless steel parts also reduces the range of solutions offered to manufacturers.The following tests will detect free-iron on parts and will provide pass or fail results:Water immersion testThis test may seem attractive at first sight since water is often easily accessible. However, it may take several hours before being able to see any results. Not to mention that if the part is improperly passivated, it will have a tendency to rust and will probably need to be reworked before being tested again.It is also important to ensure that the water is clean. The water used for the test should not contain iron (from plumbing for instance) or chemicals, otherwise the test result may falsely indicate that iron is present on the surface the part.Humidity testThe humidity chamber test requires specific equipment and a capital investment. Unless the manufacturer is properly equipped, stainless steel parts will be sent to an external laboratory. It may be easy to outsource humidity testing for small stainless steel parts, but larger parts may be problematic. Obtaining the results will also take time and failed parts will require a rework.Salt spray testThe inconveniences of the salt spray test are similar to the humidity chamber test.Copper Sulfate testThis test is rarely accepted in the food industry because of its toxic nature. Moreover, this test will leave undesirable marks on the stainless steel parts.Potassiunm ferricyanide – nitric acid testThis last test is very sensitive. The potassium ferricyanide solution must be made fresh every day. The reaction is highly visible as it turns blue in presence of free iron, but will often give false positives.ALTERNATE METHODOpen Circuit Potential TestersWalter Surface Technologies has recently launched a compact and portable testing device which is capable of qualifying the stability and thickness of the passive chromium oxide layer of stainless steel. This device works on the principle of Open Circuit Potential. Open Circuit Potential is the difference of electrical potential between two terminals. The tester measures the interface potential of the chromium oxide layer versus the underlying steel. A numeric value of the quality of the passive layer will then be read in about 20 seconds. This tester can also be used to monitor the evolution in time of the passive layer. The passivation tester will indicate a positive reading within a couple of hours of properly cleaning and decontaminating the stainless steel surface.The thin profile of the test probe allows for the collection of readings in small and very specific areas. Multiple readings can be taken in order to maximize reliability and reproducibility. A negative value will indicate that the part being tested is not passivated.A positive value will indicate that the part is passivated. The higher the value, the thicker and more resistant the passive layer.Walter’s new generation of passivation testers are also supplied with a software and USB cable in order to record data from the tester and upload data to a computer. This feature can be used to implement quality control procedures at the manufacturing location.To summarize, the Open Circuit Potential method offers the following advantages:* Qualifies the quality and thickness of the protective chromium oxide layer* Provides a numeric value instead of a pass and fail result only* Provides fast and accurate readings (about 20 secs.)* Will not damage the surface being tested* Allows for onsite measurements* Allows recording and uploading of measured dataCONCLUSIONPassivation of stainless steel parts and structures are unquestionably a concern for welders and manufacturers in many indus-tries. For economic reasons, manufacturers want to minimize rework costs of rusted parts and structures in the field. Fortunately, new techniques are being developed to help manufacturers ensure the quality of their parts. The Open Circuit Potential method is a reliable, effective and accurate method to measure passivation and minimize rework costs.About Walter Surface TechnologiesWalter Surface Technologies has been a leader in the surface treatment technologies for 60 years, and has been providing high productivity abrasives, power tools, tooling, chemical tools and environmental solutions for the metal working industry. Founded in Montreal in 1952, Walter Surface Technologies is now established in multiple countries in North America, South America and Europe. For additional informa-tion, visit us at . Visit for more information pertaining to the Surfox line of products.。
astm967标准内容
astm967标准内容
ASTM 967标准内容是涂层在金属和非金属基材上使用的清洗方法的指南。
该
标准的目的是确保涂层能够附着牢固且持久,并且能够提供所需的保护性能。
ASTM 967标准详细描述了几种不同的清洗方法,包括机械清洗、溶剂清洗和
表面活性剂清洗。
机械清洗方法使用机器或设备对基材表面进行清洗,以去除表面的污垢和杂质。
溶剂清洗方法则使用溶剂来溶解和清除表面的油脂、沉积物和其他污垢。
表面活性剂清洗方法通过使用表面活性剂来降低液体的表面张力,以便更好地清洗表面。
ASTM 967标准还规定了清洗剂的使用和评估,包括对清洗剂的配方、浓度、
温度和清洗时间的要求。
此外,该标准还提供了评估清洗效果的方法,包括对清洗后表面的外观、油迹和残留物的检查。
符合ASTM 967标准的清洗方法可以确保涂层在应用过程中的可靠性和耐久性。
通过正确清洗基材表面,涂层能够更好地附着,并能够提供所需的保护性能,如耐腐蚀性、耐磨性和耐候性。
总之,ASTM 967标准对于涂层应用中的清洗过程具有重要的指导作用。
遵循
该标准的要求,可以确保清洁的基材表面,从而提供高质量的涂层。
304不锈钢材质药水检测标准
304不锈钢是一种常见的不锈钢材料,常用于制造医疗设备、制药设备和食品加工设备等领域。
药水检测标准通常用于评估不锈钢材料在与药水接触时的耐腐蚀性和化学稳定性。
以下是一些可能适用于304不锈钢材质药水检测的标准和测试方法的一般指导:ASTM A380 - "Standard Practice for Cleaning, Descaling, and Passivation of Stainless Steel Parts,Equipment, and Systems":这一标准涵盖了不锈钢材料的清洁、除垢和钝化处理。
钝化是一种通过化学方法来增强不锈钢材料对腐蚀的抵抗力的过程。
该标准可以用于确保不锈钢在与药水接触时不会受到腐蚀的影响。
ASTM A967 - "Standard Specification for Chemical Passivation Treatments for Stainless Steel Parts":这个标准详细描述了化学钝化不锈钢材料的要求和测试方法。
它确保了钝化过程的质量,从而提高了不锈钢的耐腐蚀性。
ASTM A262 - "Standard Practices for Detecting Susceptibility to Intergranular Attack in AusteniticStainless Steels":这个标准用于检测奥氏体不锈钢(包括304不锈钢)的晶间腐蚀敏感性。
如果不锈钢材料在与药水接触时有晶间腐蚀的风险,可以使用这个标准来评估其耐腐蚀性。
使用pH值和化学成分监测:根据药水的特性,可以使用pH值计或化学成分分析来监测不锈钢材料与药水之间的相互作用。
这可以帮助确定是否需要额外的保护措施或测试。
请注意,具体的检测标准和测试方法可能会根据不同的应用、药水的成分以及设备的设计和使用条件而有所不同。
酸洗钝化在制药行业中的应用
酸洗钝化在制药行业中的应用摘要:随着国家对医药事业越来越重视,相关法律法规不断出台,我国的制药行业也在不断的发展。
制药行业尤其是无菌和生物制药生产企业会用到大量的不锈钢材质设备,都与药品直接接触。
这些不锈钢设备都需要进行防腐蚀处理,保证药品生产质量,所以要充分研究酸洗钝化技术的开发和应用,从而更好的在制药行业中进行应用。
关键词:医药事业;制药行业;酸洗钝化;红锈;生物膜现如今制药行业尤其是无菌和生物制药生产企业会用到大量的不锈钢材质设备,都与药品直接接触,包括传统的纯化水系统、注射用水系统、CIP系统、配料系统、制剂的溶液分装等等。
如此大量的不锈钢系统在日常的使用以及定期的维保方面,酸洗钝化【1】是非常重要的,如果说不锈钢表面缺失了钝化的效果和钝化膜,那么它就起不到GMP所要求的抗腐蚀性。
所有的管道、储罐、阀门、喷淋球等等基础的原材料在供应商的工厂已经做过酸洗钝化,但为什么不锈钢系统在现场安装施工完成后还需要进行额外的酸洗钝化?主要是因为在现场的机加工后破坏了原有的不锈钢钝化膜,比如现场的一些切割、焊接加工处理,不管是手工焊还是自动焊都会破坏原有的钝化效果。
由于此原因,只要是对于管道、阀门等现场进行切割、焊接加工处理的都需要进行酸洗钝化。
1.基本概念钝化是指使金属表面转化为难氧化的状态而延缓金属腐蚀速度的方法。
钝化深度和表面金属元素的优化分布(如铬铁比)将决定金属钝化后的抗腐蚀性和腐蚀速率。
就提高标准等级不锈钢的抗腐蚀性而言,钝化处理是最佳选择,也是必要程序。
钝化是洁净表面有氧气存在时的自发现象,可在不锈钢表面生成致密的钝化膜。
通过化学处理,不锈钢表面的钝化膜可实现一定程度增强。
钝化的一个先决条件是对表面的清洗程序,不锈钢表面的清洗程序应包含所有必要的表面污物的清除(油脂、颗粒等)以保证合金表面最佳的抗腐蚀性能、保护产品不被污染的性能和合金表面外观的达标【2】。
最终化学钝化处理的目的是确保合金表面无铁元素及其他污物存在以实现最佳抗腐蚀状态。
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Designation:A967–05Standard Specification forChemical Passivation Treatments for Stainless Steel Parts1 This standard is issued under thefixed designation A967;the number immediately following the designation indicates the year of original adoption or,in the case of revision,the year of last revision.A number in parentheses indicates the year of last reapproval.A superscript epsilon(e)indicates an editorial change since the last revision or reapproval.1.Scope*1.1This specification covers several different types of chemical passivation treatments for stainless steel parts.It includes recommendations and precautions for descaling, cleaning,and passivation of stainless steel parts.It includes several alternative tests,with acceptance criteria,for confirma-tion of effectiveness of such treatments for stainless steel parts.1.2Practices for the mechanical and chemical treatments of stainless steel surfaces are discussed more thoroughly in Practice A380.1.3Several alternative chemical treatments are defined for passivation of stainless steel parts.Appendix X1gives some nonmandatory information and provides some general guide-lines regarding the selection of passivation treatment appropri-ate to particular grades of stainless steel.It makes no recom-mendations regarding the suitability of any grade,treatment,or acceptance criteria for any particular application or class of applications.1.4The tests in this specification are intended to confirm the effectiveness of passivation,particularly with regard to the removal of free iron and other exogenous matter.These tests include the following practices:1.4.1Practice A—Water Immersion Test,1.4.2Practice B—High Humidity Test,1.4.3Practice C—Salt Spray Test,1.4.4Practice D—Copper Sulfate Test,1.4.5Practice E—Potassium Ferricyanide–Nitric Acid Test, and1.4.6Practice F—Free Iron Test.1.5The values stated in inch-pound units are to be regarded as the standard.The SI units given in parentheses are for information only.1.6The following precautionary caveat pertains only to the test method portions,Sections14through18of this specifica-tion:This standard does not purport to address all of the safety concerns,if any,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.2.Referenced Documents2.1ASTM Standards:2A380Practice for Cleaning,Descaling,and Depassivation of Stainless Steel Parts,Equipment,and SystemsB117Practice for Operating Salt Spray(Fog)Apparatus B254Practice for Preparation of and Electroplating on Stainless Steel2.2Federal Specification:3QQ-P-35C Passivation Treatments for Corrosion-Resistant Steels3.Terminology3.1Definition of Term Specific to This Standard—It is necessary to define which of the several commonly used definitions of the term passivation will be used in this specification.(See Discussion.)3.1.1Discussion—Stainless steels are autopassivating in the sense that the protective passivefilm is formed spontaneously on exposure to air or moisture.The presence of exogenous surface contamination,including dirt,grease,free iron from contact with steel tooling,and so forth,may interfere with the formation of the passivefilm.The cleaning of these contami-nants from the stainless steel surface will facilitate the spon-taneous passivation by allowing the oxygen uniform access to the surface.The passivefilm may be augmented by chemical treatments that provide an oxidizing environment for the stainless steel surface.3.1.1.1In this specification,passivation,unless otherwise specified,is defined as the chemical treatment of a stainless steel with a mild oxidant,such as a nitric acid solution,for the purpose of the removal of free iron or other foreign matter,but which is generally not effective in removal of heat tint or oxide scale on stainless steel.In the case of stainless steels with additions of sulfur for the purpose of improved machinability,1This specification is under the jurisdiction of ASTM Committee A01on Steel, Stainless Steel and Related Alloys and is the direct responsibility of Subcommittee A01.14on Methods of Corrosion Testing.Current edition approved Sept.1,2005.Published September2005.Originally approved st previous edition approved in2001as A967–01e1.2For referenced ASTM standards,visit the ASTM website,,or contact ASTM Customer Service at service@.For Annual Book of ASTM Standards volume information,refer to the standard’s Document Summary page on the ASTM website.3Available from Superintendent of Documents,ernment Printing Office,Washington,DC20402.*A Summary of Changes section appears at the end of this standard. Copyright©ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959,United States.passivation may also include the removal of sulfides from the surface of the metal for the purpose of maximizing corrosion resistance.3.1.1.2The formation of the protective passivefilm on a stainless steel,also called passivation in a more general context,will occur spontaneously in air or other oxygen-containing environment when the stainless steel surface is free of oxide scale and exogenous matter.3.1.1.3Chemical treatments,such as sodium dichromate solutions,may facilitate the more rapid formation of the passivefilm on a stainless steel surface already free of scale or foreign matter.Such treatments,also sometimes called passi-vation in common usage,are designated as post-cleaning treatments in this specification in order to distinguish them from chemical treatments capable of removing free iron from stainless steels.3.1.1.4The chemical treatments capable of removing heat tint or oxide scale from stainless steel and capable of dissolving the stainless steel itself,typically called pickling,are substan-tially more aggressive than treatments used for passivation,as defined in3.1.1.1.The surface of stainless steel that has been pickled is free of scale,free iron,and exogenous foreign matter,and does not require a separate treatment for passiva-tion as defined in3.1.1.1.The passivation process defined in 3.1.1.2will occur without further chemical treatment but may be augmented and improved by the post-cleaning treatments defined in3.1.1.3.3.1.1.5Electrochemical treatments,including electropick-ling and electropolishing capable of removing heat tint or oxide scale from stainless steel and capable of dissolving the stainless steel itself,are substantially more aggressive than treatments used for passivation,as defined in3.1.1.1.The surface of stainless steel resulting from these treatments is free of scale, free iron,and exogenous foreign matter,and does not require a separate treatment for passivation as defined in3.1.1.1.The passivation process defined in 3.1.1.2will occur without further chemical treatment,but may be augmented and im-proved by the post-cleaning treatments defined in 3.1.1.3. Statements regarding chemical treatments,unless otherwise specified,are taken to include electrochemical treatments.4.Ordering Information4.1It is the responsibility of the purchaser to specify a test practice appropriate to any particular material and application. This specification was written for the purpose of providing an alternative to United States Federal Specification QQ-P-35C. Determination of the suitability of this specification for that purpose is the responsibility of the purchaser.4.2Unless specified by the purchaser,the chemical treat-ment applied to the stainless steel parts shall be selected by the seller from among the listed passivation treatments.5.Materials and Preparation for Passivation Treatments 5.1The passivation treatments shall be of one or more of the following types.The effectiveness of a particular treatment for a particular grade of stainless steel in a particular application is demonstrated by meeting the specified testing requirements: 5.1.1Treatments in nitric acid,5.1.2Treatments in citric acid,5.1.3Other chemical treatments,including electrochemical treatments,5.1.4Neutralization,and5.1.5Post-cleaning treatments.5.2Materials:5.2.1The chemicals used for passivation treatments shall produce passivated surfaces that meet the requirements of one or more of the tests of this specification.Attention shall be given to maintaining adequate volume,concentration,purity, and temperature control appropriate to the size and amount of stainless steel to be treated.5.2.2The processor shall maintain a record with regard to concentration and temperature of the passivation solution sufficient to demonstrate that the specified passivation condi-tions were maintained for each lot of stainless steel parts processed.Such records shall be available for inspection when specified in the purchase order.The processor is not required to reveal the precise composition of proprietary chemical mix-tures but shall maintain a unique identification of the mixture that will ensure its accurate representation for subsequent use.5.2.3The processor shall be responsible for the safe dis-posal of all material generated by this process.5.3Preparation for Passivation Treatments:5.3.1The pretreatment methods and procedures used prior to the passivation treatment,including mechanical and chemi-cal methods,singly or in combination,for descaling and pickling,shall be in accordance with Practice A380.When electrochemical cleaning is required,it shall be performed in accordance with Practice B254.5.3.2The resulting pretreated surface shall be substantially free of oil,grease,rust,scale,and other foreign matter.5.3.3When thefinal pretreatment of a part includes pickling of the entire surface of the part,no further passivation treatment is required prior to testing of the surface unless specified by the purchaser.6.Treatments in Nitric Acid Solutions6.1Passivation Treatment:6.1.1Stainless steel parts shall be treated in one of the following aqueous solutions and maintained within the speci-fied temperature range for the specified time.6.1.1.1Nitric1—The solution shall contain20to25volume percent of nitric acid and2.5+0.5weight percent of sodium dichromate.The parts shall be immersed for a minimum of20 min at a temperature in the range from120to130°F(49to 54°C).6.1.1.2Nitric2—The solution shall contain20to45volume percent of nitric acid.The parts shall be immersed for a minimum of30min at a temperature in the range from70to 90°F(21to32°C).6.1.1.3Nitric3—The solution shall contain20to25volume percent nitric acid.The parts shall be immersed for a minimum of20min at a temperature in the range from120to140°F(49 to60°C).6.1.1.4Nitric4—The solution shall contain45to55volume percent of nitric acid.The parts shall be immersed for a minimum of30min at a temperature in the range from120to 130°F(49to54°C).6.1.1.5Nitric5—Other combinations of temperature,time, and concentration of nitric acid,with or without other chemi-cals,including accelerants,inhibitors,or proprietary solutions, capable of producing parts that pass the specified test require-ments.6.2Water Rinse—Immediately after removal from the pas-sivating solution the parts shall be thoroughly rinsed,using stagnant,countercurrent,or spray washes singly or in combi-nation,with or without a separate chemical treatment for neutralization(see9.1)of the passivation media,with afinal rinse being carried out using water with a maximum total solids content of200ppm.7.Treatments in Citric Acid7.1Passivation Treatment:7.1.1Stainless steel parts shall be treated in one of the following aqueous solutions and maintained within the speci-fied temperature range for the specified time.7.1.1.1Citric1—The solution shall contain4to10weight percent of citric acid.The parts shall be immersed for a minimum of4min at a temperature in the range from140to 160°F(60to71°C).7.1.1.2Citric2—The solution shall contain4to10weight percent of citric acid.The parts shall be immersed for a minimum of10min at a temperature in the range from120to 140°F(49to60°C).7.1.1.3Citric3—The solution shall contain4to10weight percent of citric acid.The parts shall be immersed for a minimum of20min at a temperature in the range from70to 120°F(21to49°C).7.1.1.4Citric4—Other combinations of temperature,time, and concentration of citric acid,with or without other chemi-cals to enhance cleaning,including accelerants,inhibitors,or proprietary solutions capable of producing parts that pass the specified test requirements.7.1.1.5Citric5—Other combinations of temperature,time, and concentrations of citric acid,with or without other chemi-cals to enhance cleaning,including accelerants,inhibitors,or proprietary solutions capable of producing parts that pass the specified test requirements.Immersion bath to be controlled ata pH of1.8–2.2.7.2Water Rinse—Immediately after removal from the pas-sivating solution,the parts shall be thoroughly rinsed,using stagnant,countercurrent,or spray washes,singly or in combi-nation,with or without a separate chemical treatment for neutralization of the passivation media(see9.2),with afinal rinse being carried out using water with a maximum total solids content of200ppm.8.Treatments in Other Chemical Solutions,IncludingElectrochemical Treatments8.1It is recognized that the purpose of removal of all exogenous matter from a stainless steel surface,including the removal of free iron,can be accomplished by different media, with potential for benefits to be gained from use of proprietary skills and art,including proprietary passivation media.Such treatments may include externally applying an electrical po-tential on the stainless steel parts,as in the case of electropol-ishing.The suitability of such passivation treatments for use in meeting the requirements of this specification shall be deter-mined by the capability of the processed parts meeting the specified test requirements.8.2Stainless steel parts shall be treated in a specified aqueous solution,with or without externally applied electrical potential,and maintained within a specified temperature range for a time sufficient for the processed parts to meet the specified test requirement.8.3Water Rinse—Immediately after removal from the pas-sivating solution,the parts shall be thoroughly rinsed,using stagnant,countercurrent,or spray washes,singly or in combi-nation,with or without a separate chemical treatment for neutralization of the passivation media(see9.2),with afinal rinse being carried out using water with a maximum total solids content of200ppm.9.Neutralization9.1The chemical reactions of the passivating media on the surface of the stainless steel shall be stopped by rinsing of the stainless steel part,with or without a separate neutralization treatment.9.2The suitability of a neutralization procedure is deter-mined by the capability of the processed parts meeting the specified test requirements(see Note1).N OTE1—The selection of medium and procedures for a neutralization depends of the chemistry of the passivation and on economic consider-ations.An example of a neutralizing treatment would be immersion of the part for a minimum of30min in a solution of5%NaOH at160to180°F (71to82°C),followed by a water rinse.10.Post-Cleaning Treatments10.1Although the passivefilm characteristic of stainless steel will form spontaneously in air or any other oxygen-containing environment,the processor shall,when specified, apply a chemical treatment that will accelerate the formation of the passivefilm on a chemically clean stainless steel surface. An example of a medium that serves to accelerate the forma-tion of the passivefilm but does not contribute to the removal of free iron from the stainless steel surface would be an aqueous solution of sodium dichromate.10.2When specified,within one hour after thefinal water rinse as required in6.2,7.2,or8.3,all ferritic and martensitic steel parts shall be immersed in an aqueous solution containing 4to6weight percent of sodium dichromate at a temperature in the range from140to160°F(60to71°C)for a minimum of30 min,followed by a rinse in accordance with6.2,7.2,or8.3. The parts shall then be thoroughly dried.10.3The purchaser may specify other post-cleaning treat-ments.11.Finish11.1The passivated parts shall exhibit a chemically clean surface and shall,on visual inspection,show no etching, pitting,or frosting resulting from the passivation procedures.12.Testing Agency12.1When required,the purchaser shall be permitted to perform such inspections as necessary to determine that the testing agency is capable of performing the specifiedtest.13.Lot,Frequency of Testing,and Selection of Test13.1Definition of Lot—A lot shall consist of one of the following,at the option of the processor:13.1.1The passivated parts of similar alloy and manufac-turing methods that are pretreated and passivated in a single day or within a time frame that will ensure consistent passiva-tion results;13.1.2The passivated parts of the same product of one size from one heat in one shipment;or13.1.3When few parts are involved,the passivated parts from an entire production run.13.2Unless a greater frequency of testing is specified on the purchase order,one test per lot shall be sufficient.13.3One or more of the following tests,when specified on the purchase order,shall be performed on each lot of stainless steel parts.Not all of the following tests are suitable for all grades of stainless steel.(See Note2.)13.3.1Practice A—Water Immersion Test,13.3.2Practice B—High Humidity Test,13.3.3Practice C—Salt Spray Test,13.3.4Practice D—Copper Sulfate Test,and13.3.5Practice E—Potassium Ferricyanide–Nitric Acid Test.N OTE2—Some of the tests may produce positive indications not associated with the presence of free iron on the stainless steel surface.An example would be application of Practice C on some lesser-alloyed martensitic or ferritic stainless steels.14.Practice A—Water Immersion Test14.1This test is used for the detection of free iron or any other anodic surface contaminants on stainless steel.14.2The sample representing the lot of passivated parts shall be alternately immersed in a non-rusting tank of distilled water for1h and allowed to dry in air for1h.This cycle shall be repeated a minimum of twelve times.14.3The tested sample shall not exhibit rust or staining attributable to the presence of free iron particles embedded in the surface.15.Practice B—High Humidity Test15.1This test is used for the detection of free iron or any other anodic surface contaminants on stainless steel.15.2The test shall be performed using a humidity cabinet capable of maintaining the specified test conditions.15.3The sample representing the lot of passivated parts shall be cleaned by immersion in acetone or methyl alcohol or by swabbing with a clean gauze saturated with acetone or methyl alcohol,and dried in an inert atmosphere or desiccated container.The cleaned and dried part shall be subjected to97 63%humidity at10065°F(3863°C)for a minimum of 24h.15.4The tested sample shall not exhibit rust or staining attributable to the presence of free iron particles imbedded in the surface.16.Practice C—Salt Spray Test16.1This test is used for the detection of free iron or any other anodic surface contaminants on stainless steel.16.2The sample representing the lot of passivated parts shall be tested by the salt spray test conducted in accordance with Practice B117for a minimum of2h using a5%salt solution.16.3The tested sample shall not exhibit rust or staining attributable to the presence of free iron particles imbedded in the surface.17.Practice D—Copper Sulfate Test17.1This test is recommended for the detection of free iron on the surface of austenitic stainless steels in the200and300 series,precipitation hardened stainless steels,and ferritic400 series stainless steels having a minimum of16%chromium. This test is not recommended for martensitic400series stainless steels or for ferritic400series stainless steels with less than16%chromium because these steels will give a positive indication irrespective of the presence or absence of anodic surface contaminants.This test shall not be applied to parts to be used in food processing.17.2The test solution is prepared by dissolving4g of copper sulfate pentahydrate(CuSO4·5H2O)in250mL of distilled water to which1mL of sulfuric acid(H2SO4,sp gr 1.84)has been added.17.3The test solution is swabbed on the surface of the sample representing the lot of passivated parts,applying additional solution as needed to keep the surface wet for a period of at least6min.At the end of this period,the surface shall be carefully rinsed and dried with care taken not to disturb copper deposits if present.17.4The tested sample shall not exhibit copper deposits.18.Practice E—Potassium Ferricyanide–Nitric Acid Test 18.1This test is recommended when detection of very small amounts of free iron is required.It is recommended for detection of free iron on austenitic200and300series stainless steels.This test is not recommended for detection of free iron on ferritic or martensitic400series stainless steels,because these steels will give a positive indication irrespective of the presence or absence of anodic surface contaminants.This test shall not be applied to parts to be used in food processing.18.2The test solution is prepared by adding10g of chemically pure potassium ferricyanide to500mL of distilled water,adding30mL of70%nitric acid,agitating until all of the ferricyanide is dissolved,and diluting to1000mL with distilled water.The test solution shall be mixed fresh on the day of the test.18.3The test solution is swabbed on the surface of the sample representing the lot of passivated parts.The formation of a dark blue color within30s denotes the presence of metallic iron.18.4The tested sample shall not exhibit the dark blue color indicative of free iron on the surface.18.5When the test is negative,the surface shall be thor-oughly washed with warm water to removal all traces of the test solution.When the test is positive,the dark blue stain shall be removed with a solution of10%acetic acid and8%oxalic acid,followed by a thorough hot waterrinse.19.Practice F—Free Iron Test19.1This test is used for the detection of free iron on the surface of stainless steel.It is especially useful for large parts that have been uniformly cleaned but that are inconvenient for reasons of size of equipment or ease of handling of the part to place in the environments defined in Practice A(Section14)or Practice B(Section15).Unless otherwise specified by the purchaser,the number of tests and the locations of the tests shall be at the option of the processor to assure a representative testing of the part.19.2The test is performed by placing a clean cloth pad that has been thoroughly soaked with distilled or deminaralized water on the surface of the part at a part temperature of50°F (10°C)or greater for a period of not less than60minutes.The cloth shall be in contact with the steel for an area of at least20 square inches(130cm2).The pad shall be maintained wet through the test period,either by a method of retarding external evaporation,by the further addition of potable water,or by backing the pad with a sponge or similar water source.The cloth pad used shall be used for only one such test,being changed for each test so as to avoid risk of contamination. After removal of the cloth pad,the surface of the part shall be allowed to dry in air before inspection.19.3The tested part shall not exhibit rust or staining attributable to the presence of free iron particles embedded in the surface.20.Rejection and Retest20.1Any lot failing to meet the specified test requirements of the purchase order shall be rejected.A rejected lot may,at the option of the processor,be re-passivated,with or without re-pretreatment,and then be retested.The number of samples tested from a lot subject to retest shall be twice the original specified test frequency,to the limit of the number of pieces in the lot.All samples must pass the specified acceptance criterion for the specified test for the retested lot to be accepted.21.Precision and Bias21.1No statement is made concerning either the precision or bias of Practices A,B,C,D,and E because the results state merely whether there is conformance to the criteria for success specified in the procedure.22.Certification22.1When specified in the purchase order,a report of the practice and tests used,including the record of process condi-tions when specified in accordance with 3.1.1.2,shall be supplied to the purchaser.23.Keywords23.1cleaning of stainless steel;descaling;passivation;tests for cleanliness of stainless steels;APPENDIX(Nonmandatory Information)RMATION REGARDING PASSIV ATION TREATMENTSN OTE X1.1—The following information is based on a section of Federal Specification QQ-P-35C(Oct.28,1988)identified as information of a general or explanatory nature that may be helpful,but is not mandatory. Minor changes have been made in the text to facilitate references to the main document and to correct technical inaccuracies.X1.1Intended Use—The passivation treatments provided by this specification are intended to improve the corrosion resistance of parts made from stainless steels of all types.X1.1.1During processing operations such as forming,ma-chining,tumbling,and lapping,iron particles or other foreign particles may become smeared over or imbedded into the surface of stainless steel parts.These particles must be re-moved or they will appear as rust or stain spots.This condition may be prevented by chemically treating the parts to remove the iron particles or other foreign particles,and then allowing the passivefilm to form on the cleaned surface,with or without chemical enhancement of the formation of this oxidefilm.X1.1.2This specification is not intended for the black oxide coating of parts typically used for photographic or optical instruments.X1.2Ordering Data—Purchasers should select the pre-ferred options permitted by this specification and include the following information in the purchase order:X1.2.1Title,number,and date of this specification;X1.2.2Identification of material by type and applicable product specification;X1.2.3Test practices to be imposed(see1.4);X1.2.4Definition of lot size,if other than described in this specification;andX1.2.5Required documentation,if other than the minimum required by this specification.X1.3Grades of Stainless Steel—Different types of stainless steel are selected on a basis of properties required,for example, corrosion resistance and design criteria,and fabrication re-quirements.Table X1.1is a compilation that serves as a guide for the selection of passivation treatment for different grades, but is far from complete either in grades or in passivation treatments.X1.4Clean Water—Clean water is defined as water con-taining a maximum total solid content of200ppm.Rinsing can be accomplished by a combination of stagnant,countercurrent or spray rinses,or both,prior tofinal rinse.X1.5Chemically Clean Surface—A chemically clean sur-face is defined as a surface upon which water,when applied momentarily to the surface,will remain on that surface inaneven,continuous film,and in addition is free of any foreign material or residual film deposit which would be detrimental to the quality of the part.X1.6Test Specimens —When using test specimens instead of parts,the specimens can effectively represent the parts only if they have been exposed to the same processing steps,such as machining,grinding,heat treating,welding,and so forth,as the parts they are to represent.X1.7Carburized Surfaces —Stainless steel parts with car-burized surfaces cannot be passivated because the carbon combines with the chromium forming chromium carbides on the surface.X1.8Nitrided Surfaces —Stainless steel parts with nitrided surfaces should not be passivated because the treatment willseverely corrode the nitrided case.X1.9This specification provides for the same passivation treatments as Fed.Spec.QQ-P-35C ,but also includes a number of alternative passivation treatments.The effectiveness of any passivation treatment is demonstrated by the parts meeting the specified testing requirements after treatment.X1.10Martensitic Grade 440C —High-strength grades such as 440C are subject to hydrogen embrittlement or intergranular attack when exposed to acids.Cleaning by mechanical methods or other chemical methods is recom-mended.X1.11The salt spray test is typically used to evaluate austenitic stainless steels and may not be applicable to all martensitic or ferritic stainlesssteels.FIG.X1.1Recommended Nitric Acid Passivation Treatments for Different Grades of StainlessSteel。