化学镀镍相关标准与规范
- 格式:docx
- 大小:21.82 KB
- 文档页数:4
化学镀镍的质量检测与相关标准一、化学镀镍的质量检测:※外观按主要表面的外观可为光亮、半光亮或无光泽。
除另有规定,当用目视检查,表面应均匀,不应有麻点、裂纹、起泡、分层或结瘤等缺陷。
※表面粗糙度如果需方规定了粗糙度,应按GB 3505的规定进行测定。
镀层的表面粗糙度一般不会优于镀前基体的表面粗糙度。
※厚度主要表面镀覆的自催化镍-磷合金和底层的最小厚度及测量方法应由需方规定。
※弯曲试验将试样沿直径最小为12mm的或试样厚度4倍的心轴绕180°用4倍的放大镜检查,有无脱皮,起泡。
※硬度如果需方要求硬度值,应按GB 9790规定的方法,在热处理后测量,其结果应在需方规定的硬度值的±10%以内。
※镀层的耐蚀性参照ASTM-B-117进行, 如果需要,需方应规定镀层的耐蚀性及其试验和评价方法。
二. 化学镀镍的相关标准: 序号 标准号 标准名1 GB/T13913—92 自催化镍-磷镀层技术要求和试验方法2 ISO 4527—1987 自催化镍磷镀层——规范和试验方法3 ASTM B656—79 金属上工程用自催化镀镍标准实施方法4 MIL-C -26074—B 美国 军用规范 化学镀镍层技术要求5 AMS- 2404—A航空材料规范 化学镀镍7 NACE T—6A—54美国 腐蚀工程师学会文件 化学镀镍层8 DEF STD 03-5/1 英国 材料的化学镀镍9 NFA-91—105 法国 化学镀镍层特性和测试方法10 DIN50966—1987 德国 功能用化学镀镍11 RAL-RG660 德国 硬铬和化学镀镍层的质量保证12 ONORMC2550—1987 化学镀镍磷镀层—技术要求杰昌金属表面处理技术有限公司提供。
化学镀镍1.什么是化学镀镍化学镀镍,⼜称为⽆电解镀镍或⾃催化镀镍,是通过溶液中适当的还原剂使⾦属离⼦在⾦属表⾯靠⾃催化的还原作⽤⽽进⾏的⾦属沉积过程。
化学镀溶液的分类⽅法很多,根据不同的原则有不同的分类法。
按PH值分为酸性镀液和碱性镀液,酸性镀液PH值⼀般在4~6,碱性镀液PH值⼀般⼤于8,碱性镀液因其操作温度较低,主要⽤于⾮⾦属材料的⾦属化(如塑料,陶瓷等);按还原剂类型不同有次亚磷酸盐、胺基硼烷、硼氢化物以及肼做还原剂的化学镀镍溶液;按温度分类则有⾼温镀液(80~95℃)、低温镀液(60~70℃)以及室温镀液;按镀层磷含量可分为⾼磷镀液、中磷镀液和低磷镀液,⾼磷镀液含磷量9%~12%(质量),镀层呈⾮磁性、⾮晶态,在酸性介质中有很⾼的耐腐蚀性。
利⽤镀层⾮磁性,主要⽤于计算机硬盘的底镀层、电⼦仪器防电磁波⼲扰的屏蔽等以及⼯件的防腐镀层;中磷镀液获得的镀层含磷量为6%~9%(质量),此类镀液沉积速率快、稳定性好、寿命长,镀层既耐腐蚀⼜耐磨,在⼯业中应⽤最为⼴泛,如汽车、电⼦、纺织机械、⽯油化⼯机械、⾷品⼯业、办公设备、精密机械⼯业等;低磷镀液含磷量0.5%~5%(质量),此类溶液所得到的镀层硬度⾼、耐磨,特别是在碱性介质中的耐腐蚀性能明显优于中磷和⾼磷镀层。
近年来还开发了三元镍-磷合⾦镀液,有镍铬磷、镍铜磷、镍钴磷等多种镀液。
2.检测标准GB/T13913—92⾃催化镍-磷镀层技术要求和试验⽅法ISO4527(1987),ISO/TC107⾃催化镍磷镀层——规范和试验⽅法ASTM B656——79美国⾦属上⼯程⽤⾃催化镀镍标准实施⽅法 MILC 26074B美国军⽤规范化学镀镍层技术要求AMS 2404A——航空材料规范化学镀镍AMS 2404——航空材料规范化学镀镍,低磷NACE T—6A—54美国腐蚀⼯程师学会⽂件化学镀镍层DEF STD 03-5/1英国材料的化学镀镍NFA-91-105 法国化学镀镍层特性和测试⽅法DIN 50966(1987)德国功能⽤化学镀镍RAL-RG660第⼆部分(1984)德国硬铬和化学镀镍层的质量保证ONORM C2550(1987)奥地利化学镀镍磷镀层—技术要求和测试3.化学镀镍溶液成分分析为了保证化学镀镍的质量,必须始终保持镀浴的化学成分、⼯艺技术参数在最佳范围(状态),这就要求操作者经常进⾏镀液化学成分的分析与调整。
化学镀镍的一般操作规范简介成形的化学镀镍工艺是在1946年被发现及发展的,1955年美国通用运输公司(GA TC)建成了第一条化学镀镍生产线和第一个商品化学镀镍溶液。
20世纪80年代,化学镀镍工艺有了巨大的发展,研究和应用达到一个新的水平。
按照合金成分分类,化学镀镍可以分为镍-磷合金和镍-硼合金两大类。
从应用领域来讲,镍-磷合金使用更为普遍。
化学镀镍-磷合金按照溶液的pH可以分为碱性和酸性化学镀镍,碱性化学镀镍主要用于预镀的打底层,以提高电镀层与基体的结合力,在铝轮毂的电镀中有较成功的应用。
酸性化学镀镍工艺是目前化学镀镍中应用最为广泛的工艺,按镀层中的磷含量又可分为低磷(2%~5%)、中磷(6%~9%)和高磷(10%以上)。
化学镀镍工艺因为镀层均匀,亮度好,耐蚀性及耐磨性优良而被广泛应用于多个领域。
1. 化学镀镍的周期定义化学镀镍溶液在使用中的管理与维护非常重要,它与电镀液的管理与维护不同,化学镀镍液中的镍离子等多种成分时刻在不断变化,均需要外加补充,否则溶液不能正常进行。
化学镀镍溶液的好坏一般通过能够获得质量稳定镀层的周期(循环系数MTO)来评判。
目前市场销售的化学镀镍溶液多数分为A、B、C三种组份,周期数可以做到6~8,对镀层质量要求不严格的可以做到12个周期甚至以上。
1个周期的定义是,当溶液中主盐的添加量达到了开缸剂量时为一个周期,以1L溶液为例,开缸量一般为60毫升/升,在使用过程中,当A剂的补充量达到了60毫升时,该化学镀镍溶液就已使用一个周期。
2. 化学镀镍溶液的过程控制2.1应准确计算槽体容积和零件的表面积看似再简单不过的问题,但很多时候都难以做到。
化学镀镍溶液的消耗及补充与装载量有直接的关系,因此,溶液的装载量应得到重视。
装载量就是所要施镀零件的表面积与溶液体积之比值。
一般控制在1~1.5 dm2/L为最佳,过大(>2.5 dm2/L)或过小(<0.5 dm2/L)对溶液的稳定性都不好。
Designation:B733–97Standard Specification forAutocatalytic(Electroless)Nickel-Phosphorus Coatings on Metal1This standard is issued under thefixed designation B733;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.This standard has been approved for use by agencies of the Department of Defense.1.Scope1.1This specification covers requirements for autocatalytic (electroless)nickel-phosphorus coatings applied from aqueous solutions to metallic products for engineering(functional)uses.1.2The coatings are alloys of nickel and phosphorus pro-duced by autocatalytic chemical reduction with hypophosphite. Because the deposited nickel alloy is a catalyst for the reaction, the process is self-sustaining.The chemical and physical properties of the deposit vary primarily with its phosphorus content and subsequent heat treatment.The chemical makeup of the plating solution and the use of the solution can affect the porosity and corrosion resistance of the deposit.For more details,see ASTM STP265(1)2and Refs(2)(3)(4)and(5) also refer to Figs.X1.1,Figs.X1.2,and Figs.X1.3in the Appendix of Guide B656.1.3The coatings are generally deposited from acidic solu-tions operating at elevated temperatures.1.4The process produces coatings of uniform thickness on irregularly shaped parts,provided the plating solution circu-lates freely over their surfaces.1.5The coatings have multifunctional properties,such as hardness,heat hardenability,abrasion,wear and corrosion resistance,magnetics,electrical conductivity provide diffusion barrier,and solderability.They are also used for the salvage of worn or mismachined parts.1.6The low phosphorus(2to4%P)coatings are microc-rystalline and possess high as-plated hardness(620to750HK 100).These coatings are used in applications requiring abra-sion and wear resistance.1.7Lower phosphorus deposits in the range between1and 3%phosphorus are also microcrystalline.These coatings are used in electronic applications providing solderability,bond-ability,increased electrical conductivity,and resistance to strong alkali solutions.1.8The medium phosphorous coatings(5to9%P)are most widely used to meet the general purpose requirements of wear and corrosion resistance.1.9The high phosphorous(more than10%P)coatings have superior salt-spray and acid resistance in a wide range of applications.They are used on beryllium and titanium parts for low stress properties.Coatings with phosphorus contents greater than11.2%P are not considered to be ferromagnetic.1.10The values stated in SI units are to be regarded as standard.1.11The following precautionary statement pertains only to the test method portion,Section9,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 limita-tions prior to use.2.Referenced Documents2.1ASTM Standards:B368Test Method for Copper-Accelerated Acetic Acid-Salt Spray(Fog)Testing(CASS Testing)3B374Terminology Relating to Electroplating3B380Test Method of Corrosion by the Corrodkote Proce-dure3B487Test Method for Measurement of Metal and Oxide Coating Thicknesses by Microscopical Examination of a Cross Section3B499Test Method for Measurement of Coating Thick-nesses by the Magnetic Method:Nonmagnetic Coatings on Magnetic Basis Metals3B504Test Method for Measurement of Thickness of Me-tallic Coatings by the Coulometric Method3B537Practice for Rating of Electroplated Panels Subjected to Atmospheric Exposure3B567Method for Measurement of Coating Thickness by the Beta Backscatter Method3B568Method for Measurement of Coating Thickness by X-Ray Spectrometry31This specification is under the jurisdiction of ASTM Committee B-08on MetalPowders and Metal Powder Products and is the direct responsibility of Subcom-mittee B08.08.01on Engineering Coatings.Current edition approved July10,1997.Published October1997.Originallypublished as B733–st previous edition B733–90(1994).2The boldface numbers given in parentheses refer to a list of references at theend of the text.3Annual Book of ASTM Standards,V ol02.05.1Copyright©ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959,United States.B571Test Methods for Adhesion of Metallic Coatings3B578Test Method for Microhardness of Electroplated Coatings3B602Test Method for Attribute Sampling of Metallic and Inorganic Coating3B656Guide for Autocatalytic Nickel-Phosphorus Deposi-tion on Metals for Engineering Use3B667Practice for Construction and Use of a Probe for Measuring Electrical Contact Resistance4B678Test Method for Solderability of Metallic-Coated Products3B697Guide for Selection of Sampling Plans for Inspection of Electrodeposited Metallic and Inorganic Coatings3B762Method for Variable Sampling of Metallic and Inor-ganic Coatings3B849Specification for Pre-Treatment of Iron or Steel for Reducing the Risk of Hydrogen Embrittlement3B850Specification for Post-Coating Treatments of Iron orSteel for Reducing the Risk of Hydrogen Embrittlement3 B851Specification for Automated Controlled Shot Peening of Metallic Articles Prior to Nickel,Autocatalytic Nickel, Chromium,or As A Final Finish3D1193Specification for Reagent Water5D2670Method for Measuring Wear Properties of Fluid Lubricants(Falex Method)6D2714Method for Calibration and Operation of an Alpha LFW-1Friction and Wear Testing Machine6D3951Practice for Commercial Packaging7D4060Test Method for Abrasion Resistance of Organic Coatings by the Taber Abraser8E60Practice for Photometric Methods for Chemical Analy-sis of Metals9E156Test Method for Determination of Phosphorus in High-Phosphorus Brazing Alloys(Photometric Method)10 E352Test Methods for Chemical Analysis of Tool Steels and Other Similar Medium-and High-Alloy Steel9F519Test Method for Mechanical Hydrogen Embrittle-ment11G5Practice for Standard Reference Method for Making Potentiostatic and Potentiodynamic Anodic Polarization Measurements12G31Practice for Laboratory Immersion Corrosion Testing of Metals12G59Practice for Conducting Potentiodynamic Polarization Resistance Measurements12G85Practice for Modified Salt Spray(Fog)Testing122.2Military Standards:MIL-R-81841Rotary Flap Peening of Metal Parts13MIL-S-13165Shot Peening of Metal Parts13MIL-STD-105Sampling Procedures and Tables for Inspec-tion by Attribute132.3ISO Standards:ISO4527Autocatalytic Nickel-Phosphorus Coatings—Specification and Test Methods143.Terminology3.1Definition:3.1.1significant surfaces—those substrate surfaces which the coating must protect from corrosion or wear,or both,and that are essential to the performance.3.2Other Definitions—Terminology B374defines most of the technical terms used in this specification.4.Coating Classification4.1The coating classification system provides for a scheme to select an electroless nickel coating to meet specific perfor-mance requirements based on alloy composition,thickness and hardness.4.1.1TYPE describes the general composition of the de-posit with respect to the phosphorus content and is divided into five categories which establish deposit properties(see Table1). N OTE1—Due to the precision of some phosphorus analysis methods a deviation of0.5%has been designed into this classification scheme. Rounding of the test results due to the precision of the limits provides for an effective limit of4.5and9.5%respectively.For example,coating with a test result for phosphorus of9.7%would have a classification of TYPE V,see Appendix X4,Alloy TYPEs.4.2Service Condition Based on Thickness:4.2.1Service condition numbers are based on the severity of the exposure in which the coating is intended to perform and minimum coating thickness to provide satisfactory perfor-mance(see Table2).4.2.2SC0Minimum Service,0.1µm—This is defined by a minimum coating thickness to provide specific material prop-erties and extend the life of a part or its function.Applications4Annual Book of ASTM Standards,V ol03.04.5Annual Book of ASTM Standards,V ol11.01.6Annual Book of ASTM Standards,V ol05.02.7Annual Book of ASTM Standards,V ol09.02.8Annual Book of ASTM Standards,V ol06.01.9Annual Book of ASTM Standards,V ol03.05.10Discontinued;see1992Annual Book of ASTM Standards,V ol03.05. 11Annual Book of ASTM Standards,V ol15.03.12Annual Book of ASTM Standards,V ol03.02.13Available from Standardization Documents Order Desk,Bldg.4Section D, 700Robbins Ave.,Philadelphia,PA19111-5094,Attn:NPODS.14Available from American National Standards Institute,11W.42nd St.,13th Floor,New York,NY10036.TABLE1Deposit Alloy TypesType Phosphorus%wtI No Requirement for PhosphorusII1to3III2to4IV5to9V10and aboveTABLE2Service ConditionsCoating Thickness RequirementsService ConditionMinimum CoatingThicknessSpecificationµm in.(mm)SC0Minimun Thickness0.10.000004()SC1Light Service50.0002()SC2Mild Service130.0005()SC3Moderate Service250.001()SC4Severe Service750.003()include requirements for diffusion barrier,undercoat,electrical conductivity and wear and corrosion protection in specialized environments.4.2.3SC1Light Service ,5µm—This is defined by a minimum coating thickness of 5µm for extending the life of the part.Typical environments include light-load lubricated wear,indoor corrosion protection to prevent rusting,and for soldering and mild abrasive wear.4.2.4SC2Mild Service ,13µm—This is defined by mild corrosion and wear environments.It is characterized by indus-trial atmosphere exposure on steel substrates in dry or oiled environments.4.2.5SC3Moderate Service ,25µm—This is defined by moderate environments such as non marine outdoor exposure,alkali salts at elevated temperature,and moderate wear.4.2.6SC4Severe Service ,75µm—This is defined by a very aggressive environment.Typical environments would include acid solutions,elevated temperature and pressure,hydrogen sulfide and carbon dioxide oil service,high-temperature chlo-ride systems,very severe wear,and marine immersion.N OTE 2—The performance of the autocatalytic nickel coating depends to a large extent on the surface finish of the article to be plated and how it was pretreated.Rough,non uniform surfaces require thicker coatings than smooth surfaces to achieve maximum corrosion resistance and minimum porosity.4.3Post Heat Treatment Class —The nickel-phosphorus coatings shall be classified by heat treatment after plating to increase coating adhesion and or hardness (see Table 3).4.3.1Class 1—As-deposited,no heat treatment.4.3.2Class 2—Heat treatment at 260to 400°C to produce a minimum hardness of 850HK100.4.3.3Class 3—Heat treatment at 180to 200°C for 2to 4h to improve coating adhesion on steel and to provide for hydrogen embrittlement relief (see section 6.6).4.3.4Class 4—Heat treatment at 120to 130°C for at least 1h to increase adhesion of heat-treatable (age-hardened)alumi-num alloys and carburized steel (see Note 3).4.3.5Class 5—Heat treatment at 140to 150°C for at least 1h to improve coating adhesion for aluminum,non age-hardened aluminum alloys,copper,copper alloys and beryl-lium.4.3.6Class 6—Heat treatment at 300to 320°C for at least 1h to improve coating adhesion for titanium alloys.N OTE 3—Heat-treatable aluminum alloys such as Type 7075can undergo microstructural changes and lose strength when heated to over 130°C.5.Ordering Information5.1The following information shall be supplied by the purchaser in either the purchase order or on the engineering drawing of the part to be plated:5.1.1Title,ASTM designation number,and year of issue of this specification.5.1.2Classification of the deposit by type,service condi-tion,class,(see 4.1,4.2and 4.3).5.1.3Specify maximum dimension and tolerance require-ments,if any.5.1.4Peening,if required (see6.5).5.1.5Stress relief heat treatment before plating,(see6.3).5.1.6Hydrogen Embrittlement Relief after plating,(see 6.6).5.1.7Significant surfaces and surfaces not to be plated must be indicated on drawings or sample.5.1.8Supplemental or Special Government Requirements such as,specific phosphorus content,abrasion wear or corro-sion resistance of the coating,solderability,contact resistance and packaging selected from Supplemental Requirements.5.1.9Requirement for a vacuum,inert or reducing atmo-sphere for heat treatment above 260°C to prevent surface oxidation of the coating (see S3).5.1.10Test methods for coating adhesion,composition,thickness,porosity,wear and corrosion resistance,if required,selected from those found in Section 9and Supplemental Requirements.5.1.11Requirements for sampling (see Section 8).N OTE 4—The purchaser should furnish separate test specimens or coupons of the basis metal for test purposes to be plated concurrently with the articles to be plated (see 8.4).6.Materials and Manufacture6.1Substrate —Defects in the surface of the basis metal such as scratches,porosity,pits,inclusions,roll and die marks,laps,cracks,burrs,cold shuts,and roughness may adversely affect the appearance and performance of the deposit,despite the observance of the best plating practice.Any such defects on significant surfaces shall be brought to the attention of the purchaser before plating.The producer shall not be responsible for coatings defects resulting from surface conditions of the metal,if these conditions have been brought to the attention of the purchaser.6.2Pretreatment —Parts to be autocatalytic nickel plated may be pretreated in accordance with Guide B 656.A suitable method shall activate the surface and remove oxide and foreign materials,which may cause poor adhesion and coating poros-ity.N OTE 5—Heat treatment of the base material may effect its metallur-gical properties.An example is leaded steel which may exhibit liquid or solid embrittlement after heat treatment.Careful selection of the pre and post heat treatments are recommended.TABLE 3Classification of Post Heat TreatmentCLASS DescriptionTemperature(°C)Time (h)1No Heat Treatment,As Plated2Heat Treatment for Maximum Hardness TYPE I260202851632084001TYPE II 350to 3801TYPE III 360to 3901TYPE IV 365to 4001TYPE V375to 40013Hydrogen Embrittlement and Adhesion on Steel180to 2002to 44Adhesion,Carburized Steel and Age Hardened Aluminum 120to 1301to 65Adhesion on Beryllium and Aluminum140to 1501to 26Adhesion on Titanium300–3201–46.3Stress Relief:6.3.1Pretreatment of Iron and Steel for Reducing the Risk of Hydrogen Embrittlement—Parts that are made of steel with ultimate tensile strength of greater than1000Mpa(hardness of 31HRC or greater),that have been machined,ground,cold formed,or cold straightened subsequent to heat treatment,shall require stress relief heat treatment when specified by the purchaser,the tensile strength to be supplied by the purchaser, Specification B849may be consulted for a list of pre-treatments that are widely used.6.3.2Peening—Peening prior to plating may be required on high-strength steel parts to induce residual compressive stresses in the surface,which can reduce loss of fatigue strength and improve stress corrosion resistance after plating. (See Supplementary Requirements).6.3.3Steel parts which are designed for unlimited life under dynamic loads shall be shot peened or rotaryflap peened.N OTE6—Controlled shot peening is the preferred method because there are geometry’s where rotaryflap peening is not effective.See S11.2. 6.3.3.1Unless otherwise specified,the shot peening shall be accomplished on all surfaces for which the coating is required and all immediate adjacent surfaces when they contain notches,fillets,or other abrupt changes of section size where stresses will be concentrated.6.4Racking—Parts should be positioned so as to minimize trapping of hydrogen gas in cavities and holes,allowing free circulation of solution over all surfaces to obtain uniform coating thickness.The location of rack or wire marks in the coating shall be agreed upon between the producer and purchaser.6.5Plating Process:6.5.1To obtain consistent coating properties,the bath must be monitored periodically for pH,temperature,nickel and hypophosphite.Replenishments to the plating solution should be as frequent as required to maintain the concentration of the nickel and hypophosphite between90and100%of set point. The use of a statistical regimen to establish the control limits and frequency of analysis may be employed to ensure quality deposits are produced.6.5.2Mechanical movement of parts and agitation of the bath is recommended to increase coating smoothness and uniformity and prevent pitting or streaking due to hydrogen bubbles.6.6Post Coating Treatment for Iron and Steel for Reducing the Risk of Hydrogen Embrittlement—Parts that are made of steel with ultimate tensile strengths of1000Mpa(hardness of 31HRC or greater),as well as surface hardened parts,shall require post coating hydrogen embrittlement relief baking when specified by the purchaser,the tensile strength to be supplied by the purchaser.Specification B850may be con-sulted for a list of post treatments that are widely used.6.6.1Heat treatment shall be performed preferably within1h but not more than3h of plating on plated after plating of steel parts to reduce the risk of hydrogen embrittlement.In all cases,the duration of the heat treatment shall commence from the time at which the whole of each part attains the specified temperature.6.6.2High-strength steel parts with actual tensile strengths greater than1000MPa(corresponding hardness values300 HV10,303HB or31HRC)and surface hardened parts shall be processed after coating in accordance with Specification B850.6.7Heat Treatment After Plating to Improve Adhesion—To improve the adhesion of the coating to various substrates,the heat treatments in Table3should be performed as soon as practical after plating(see4.3).6.8Heat Treatment After Plating to Increase Hardness: 6.8.1To increase the hardness of the coating a heat treat-ment of over260°C is required.Table3describes the heat treatment for maximum hardness.6.8.2See Appendixes3and4and Guide B656;Figs.X1.2 and Figs.X1.3.6.8.3A heat treatment at260°C for greater than20h should be used to reduce the loss of surface hardness and strength of some ferrous basis metals.Avoid rapid heating and cooling of plated parts.Sufficient time must be allowed for large parts to reach oven temperature.N OTE7—The length of time to reach maximum hardness varies with the phosphorus content of the deposit.High phosphorus deposits may require longer time or a higher temperature,or both.Individual alloys should be tested for maximum hardness attainable,especially for condi-tions of lower temperatures and longer times.N OTE8—Inert or reducing atmosphere or vacuum sufficient to prevent oxidation is recommended for heat treatment above260°C.Do not use gas containing hydrogen with high-strength steel parts.7.Requirements7.1Process—The coating shall be produced from an aque-ous solution through chemical reduction reaction.7.2Acceptance Requirements—These requirements are placed on each lot or batch and can be evaluated by testing the plated part.7.2.1Appearance:7.2.1.1The coating surface shall have a uniform,metallic appearance without visible defects such as blisters,pits, pimples,and cracks(see9.2).7.2.1.2Imperfections that arise from surface conditions of the substrate which the producer is unable to remove using conventional pretreatment techniques and that persist in the coating shall not be cause for rejection(see 6.1).Also, discoloration due to heat treatment shall not be cause for rejection unless special heat treatment atmosphere is specified (see section5.1.9).7.2.2Thickness—The thickness of the coating shall exceed the minimum requirements in Table2as specified by the service condition agreed to prior to plating(see9.3).After coating and if specified,the part shall not exceed maximum dimension on significant surface(see section5.1.3).N OTE9—The thickness of the coating cannot be controlled in blind or small diameter deep holes or where solution circulation is restricted. 7.2.3Adhesion—The coating shall have sufficient adhesion to the basis metal to pass the specified adhesion test(see9.4 and Test Methods B571).7.2.4Porosity—The coatings shall be essentially pore free when tested according to one of the methods of9.6.The test method,the duration of the test,and number of allowable spots per unit area shall be specified(see section5.1.10and9.6).7.3Qualification Requirements—These requirements are placed on the deposit and process and are performed on specimens to qualify the deposit and plating process.The tests for these qualification requirements shall be performed monthly or more frequently.7.3.1Composition—Type II,III,IV,V deposits shall be analyzed for alloy composition by testing for phosphorus(see 9.1).The weight percent of phosphorus shall be in the range designated by type classification(see4.1).7.3.2Microhardness—The microhardness of Class2depos-its shall be determined by Test Method B578(Knoop).For Class2coatings,the microhardness shall equal or exceed a minimum of850(HK100(or equivalent Vickers)(see4.3and 9.5).The conversion of Vickers to Knoop using Tables E140 is not recommended.7.3.3Hydrogen Embrittlement—The process used to de-posit a coating onto high strength steels shall be evaluated for hydrogen embrittlement by Test Method F519.8.Sampling8.1The purchaser and producer are urged to employ statis-tical process control in the coating process.Properly performed this will ensure coated products of satisfactory quality and will reduce the amount of acceptance inspection.8.1.1Sampling plans can only screen out unsatisfactory products without assurance that none of them will be accepted.(7)8.2The sampling plan used for the inspection of a quantity of coated parts(lot)shall be Test Method B602unless otherwise specified by purchaser in the purchase order or contract(see section5.1.11and S.11.1).N OTE10—Usually,when a collection of coated parts(the inspection lot8.2)is examined for compliance with the requirements placed on the partsa relatively small number of parts,the sample,is selected at random and inspected.The inspection lot is then classified as complying or not complying with the requirements based on the results of the inspection sample.The size of the sample and the criteria of compliance are determined by the application of statistics.The procedure is known as sampling inspection.Three standards Test Method B602,Guide B697, and Test Method B762contain sampling plans that are designed for the sampling inspection of coatings.Test Method B602contains four sampling plans,three for use with tests that are nondestructive and one for use with tests that are destructive.The purchaser and producer may agree on the plan(s)to be used.If they do not, Test Method B602identifies the plan to be used.Guide B697provides a large number of plans and also gives guidance on the selection of a plan.When Guide B697is specified,the purchaser and producer need to agree on the plan to be used.Test Method B762can be used only for coating requirements that have a numerical limit,such as coating thickness.The last must yield a numerical value and certain statistical requirements must be met.Test Method B762contains several plans and also gives instructions for calculating plans to meet special needs.The purchaser and producer may agree on the plan(s)to be used.If they do not,Test Method B762 identifies the plan to be used.An inspection lot shall be defined as a collection of coated parts which are of the same kind,that have been produced to the same specification, that have been coated by a single producer at one time or approximately the same time under essentially identical conditions,and that are submit-ted for acceptance or rejection as a group.8.3All specimens used in the sampling plan for acceptance tests shall be made of the same basis material and in the same metallurgical condition as articles being plated to this specifi-cation.8.4All specimens shall be provided by the purchaser unless otherwise agreed to by the producer.N OTE11—The autocatalytic nickel process is dynamic and a daily sampling is recommended.For Coatings requiring alloy analysis and corrosion testing weekly sampling should be considered as an option. 9.Test Methods9.1Deposit Analysis for Phosphorus:9.1.1Phosphorus Determination—Determine mass% phosphorus content according to Practice E60,Test Methods E352,or Test Method E156on known weight of deposit dissolved in warm concentrated nitric acid.9.1.2Composition can be determined by atomic absorption, emission or X-rayfluorescence spectrometry.N OTE12—Inductively coupled plasma techniques can determine the alloy to within0.5%.The following analysis wavelength lines have been used with minimum interference to determine the alloy.Ni216.10nm Cd214.44nm Fe238.20nmP215.40nm Co238.34nm Pb283.30nmP213.62nm Cr284.32nm Sn198.94nmAl202.55nm Cu324.75nm Zn206.20nm9.2Appearance—Examine the coating visually for compli-ance with the requirements of7.2.1.9.3Thickness:N OTE13—Eddy-current type instruments give erratic measurements due to variations in conductivity of the coatings with changes in phosphorus content.9.3.1Microscopical Method—Measure the coating thick-ness of a cross section according to Test Method B487.N OTE14—To protect the edges,electroplate the specimens with a minimum of5µm of nickel or copper prior to cross sectioning.9.3.2Magnetic Induction Instrument Method—Test Method B499is applicable to magnetic substrates plated with auto-catalytic nickel deposits,that contain more than11mass% phosphorus(not ferromagnetic)and that have not been heat-treated.The instrument shall be calibrated with deposits plated in the same solution under the same conditions on magnetic steel.9.3.3Beta Backscatter Method—Test Method B567is only applicable to coatings on aluminum,beryllium,magnesium, and titanium.The instrument must be calibrated with standards having the same composition as the coating.N OTE15—The density of the coating varies with its mass%phospho-rus content(See Appendix X2).9.3.4Micrometer Method—Measure the part,test coupon, or pin in a specific spot before and after plating using a suitable micrometer.Make sure that the surfaces measured are smooth, clean,and dry.9.3.5Weigh,Plate,Weigh Method—Using a similar sub-strate material of known surface area,weigh to the nearest milligram before and after plating making sure that the part or coupon is dry and at room temperature for eachmeasurement.Calculate the thickness from the increase in weight,specific gravity,and area as follows:coating thickness,µm510W/~A3D!(1) where:W=weight gain in milligrams,A=total surface area in square centimetres,andD=grams per cubic centimetres(see Appendix X2).9.3.6Coulometric Method—Measure the coating thickness in accordance with Test Method B504.The solution to be used shall be in accordance with manufacturer’s recommendations. The surface of the coating shall be cleaned prior to testing(see Note14).9.3.6.1Calibrate standard thickness specimens with depos-its plated in the same solution under the same conditions. 9.3.7X-Ray Spectrometry—Measure the coating thickness in accordance with Test Method B568.The instrument must be calibrated with standards having the same composition as the coating.N OTE16—This method is only recommended for deposits in the as-plated condition.The phosphorus content of the coating must be known to calculate the thickness of the deposit.Matrix effect due to the distribution of phosphorus in layers of the coating also effect the measurement accuracy and require that calibration standards be made under the same conditions as the production process.9.4Adhesion:9.4.1Bend Test(Test Methods B571)—A sample specimen is bent180°over a mandrel diameter43the thickness(10mm minimum)of the specimen and examined at43power magnification forflaking or separation at the interface.Fine cracks in the coating on the tension side of the bend are not an indication of poor adhesion.Insertion of a sharp probe at the interface of the coating and basis metal to determine the adhesion is suggested.N OTE17—Appropriate test specimens are strips approximately25to50 mm wide,200to300mm long and3to6mm thick.9.4.2Impact Test—A spring-loaded center punch with a point having2to3mm radius is used to test adhesion of the coating on nonsignificant surfaces of the plated part.Make three closely spaced indentations and examine under103 magnification forflaking or blistering of the coating,which is cause for rejection.9.4.3Thermal Shock—The coated part is heated to200°C in an oven and then quenched in room temperature water.The coating is examined for blistering or other evidence of poor adhesion at43magnification.9.5Microhardness—The microhardness of the coating can be measured by Test Method B578using Knoop indenter and is reported in Knoop Hardness Number(HK).It will vary depending on loads,type of indenter,and operator.A100g load is recommended.The rhombic Knoop indenter gives higher hardness readings than the square-base pyramidal Vickers diamond indenter for100to300g loads,see Ref(6).For maximum accuracy,a minimum coating thickness of75µm is recommended.Conversions of Vickers or Knoop hardness number to Rockwell C is not recommended.N OTE18—On thick(75µm+)coatings on steel a surface microhardness determination is permissible.9.6Porosity—There is no universally accepted test for porosity.When required,one of the following tests can be used on the plated part or specimen.9.6.1Ferroxyl Test for Iron Base Substrates—Prepare the test solution by dissolving25g of potassium ferricyanide and 15g of sodium chloride in1L of distilled water.After cleaning,immerse the part for30s in the test solution at25°C. After rinsing and air drying,examine the part for blue spots, which form at pore sites.9.6.2Boiling Water Test for Iron-Base Substrates—Completely immerse the part to be treated in a vesselfilled with aerated water at room temperature.Apply heat to the beaker at such a rate that the water begins to boil in not less than15min,nor more than20min after the initial application of heat.Continue to boil the water for30min.Then remove the part,air dry,and examine for rust spots,which indicate pores. N OTE19—Aerated water is prepared by bubbling clean compressed air through distilled water by means of a glass diffusion disk at room temperature for12h.The pH of the aerated water should be6.7+0.5.9.6.3Aerated Water Test for Iron-Base Substrates—Immerse the part for4h in vigorously aerated Type IV or better water(see Specification D1193)at2562°C temperature and then examine the part for rust spots.9.6.4Alizarin Test for Aluminum Alloys—Wipe the plated part or specimen with10mass%sodium hydroxide solution. After3min contact,rinse,and apply a solution of alizarin sulfonate prepared by dissolving1.5g of methyl cellulose in90 mL of boiling water to which,after cooling,0.1g sodium alizarin sulfonate,dissolved in5mL of ethanol is added.After 4min contact,apply glacial acetic acid until the violet color disappears.Any red spots remaining indicate pores.9.6.5Porosity Test for Copper Substrates—Wipe the plated part or specimen with glacial acetic acid.After3min,apply a solution of potassium ferrocyanide prepared by dissolving1g of potassium ferrocyanide and1.5g methyl cellulose in90mL of boiling distilled water.The appearance of brown spots after 2min indicate pores.9.7Other Test Methods—Test methods which have been developed that are equal to or better than these may be substituted.The precision and bias requirements will vary for each type of test.If an alternate test is specified it shall be agreed upon between the producer and the purchaser.10.Rejection and Rehearing10.1Part(s)that fail to conform to the requirements of this standard may be rejected.Rejection shall be reported to the producer promptly in writing.In the case of dissatisfaction occurs with the results of a test,the producer may make a claim for a hearing.Coatings that show imperfections may be rejected.11.Certification11.1When specified in the purchase order or contract,the purchaser shall be furnished certification that the samples representing each lot have been processed,tested and inspected as directed in this specification and the requirements havebeen。
、化学镀镍溶液的成分分析为了保证化学镀镍的质量,必须始终保持镀浴的化学成分、工艺技术参数在最佳范围(状态),这就要求操作者经常进行镀液化学成分的分析与调整。
l.Ni2+浓度镀液中镍离子浓度常规测定方法是用EDTA络合滴定,紫脲酸胺为指示剂。
试剂(1)浓氨水(密度:0.91g/ml)。
(2)紫脲酸胺指示剂(紫脲酸胺:氯化钠=1:100)。
(3)EDTA容液0.05mol,按常规标定。
分析方法:用移液管取出10ml冷却后的化学镀镍液于250ml的锥形瓶中,并加入100ml蒸馏水、15ml浓氨水、约0.2g指示剂,用标定后的EDTA溶液滴定,当溶液颜色由浅棕色变至紫色即为终点。
镍含量的计算:CNi2+=5.87M・V(g/L)式中M——标准EDTA溶液的摩尔浓度;V——耗用标准EDTA溶液的毫升数。
2.还原剂浓度次亚磷酸钠NaH2PO2・H2O浓度的测定其原理是在酸性条件下,用过量的碘氧化次磷酸钠,然后用硫代硫酸钠溶液反滴定自剩余的碘,淀粉为指示剂。
试剂(1)盐酸1:1。
(2)碘标准溶液0.1mol按常规标定。
(3)淀粉指示剂1%。
(4)硫代硫酸钠0.1mol按常规标定。
分析方法:用移液管量取冷却后的镀液5ml于带盖的250mL锥形瓶中;加入盐酸25mL碘标准溶液于此锥形瓶中,加盖,置于暗处0.5h(温度不得低于25°C);打开瓶盖,加入1mL淀粉指示剂,并用硫代硫酸钠标准溶液滴定至蓝色消失为终点。
计算:CNaH2PO2・H2O=10.6(2M1V1-M2V2)(g/L)式中M1——标准碘溶液的摩尔浓度;VI——标准碘溶液毫升数;M2——标准硫代硫酸钠溶液的摩尔浓度;V2——耗用标准硫代硫酸钠溶液毫升数。
3.NaHPO3・5H2O的浓度化学镀镍浴还原剂反应产物中影响最大的是次磷酸钠的反应产物亚磷酸钠。
其他种类的还原剂的反应产物的影响较小甚至几乎无影响,如DMAB。
其测定原理是在碱性条件下,用过量的碘氧化亚磷酸,但次磷酸不参加反应;然而,用硫代硫酸钠反滴定剩余的碘;淀粉为指示剂。
化学镀镍综述化学镀镍,又称为无电解镀镍,是在金属盐和还原剂共同存在的溶液中靠自催化的化学反应而在金属表面沉积了金属镀层的新的成膜技术。
电镀是利用外电流将电镀液中的金属离子在阴极上还原成金属的过程。
而化学镀是不外加电流,在金属表面的催化作用下经控制化学还原法进行的金属沉积过程。
因不用外电源直译为无电镀或不通电镀。
由于反应必须在具有自催化性的材料表面进行,美国材料试验协会(ASTMB-347)推荐用自催化镀一词(Autocatalytic plating)。
对化学镀镍而言,我国1992年颁布的国家标准(GB/T13913-92)则称为自催化镍-磷镀层(Autocatalytic Nickel Phosphorus Coating),其意义与美国材料试验协会的名称相同。
由于金属的沉积过程是纯化学反应(催化作用当然是重要的),所以将这种金属沉积工艺称为“化学镀”最为恰当,这样它才能充分反映该工艺过程的本质。
从语言学角度看Chemical,Non electrolytic,Electroless三个词主是一个意义了,直译为无电镀一词是不确切的。
“化学镀”这个术语目前在国内外已被大家认同和采用。
化学镀镍所镀出的镀层为镍磷合金,按其磷含量的不同可分为低磷、中磷、高磷三大类:·磷含量低于3%的称为低磷;·磷含量在3-10%的为中磷;·磷含量高于10%的为高磷;其中中磷的跨度比较大,一般我们常见的中磷镀层为6-9%的磷含量。
当然,本站主要介绍的是化学镀镍磷合金,有时为了方便我们简称化学镀了,而且EN也是化学镀镍简称。
但化学镀不仅此一种镀种,比较成熟的还有化学镀铜,化学镀金,化学镀锡,还有一种复合镀层。
其它镀种的市场占有量不足总量的1%,本站不做重点介绍。
化学镀层的物理性质与化学性质密度:镍的密度在20℃时为8.91。
含磷量1%-4%时为8.5;含磷量7%-9%时为8.1;含磷量10%-12%时为7.9。
AMS2404D化学镀镍(中文)化学镀镍1. 范围 1.1. 目的这个规格说明涵盖在不同材料上度化学镍的工艺要求。
1.2.应用这种材料过去常被用作提供统一的构造形状,去提高抵抗防腐蚀性,或改善它的可焊性,但它的作用不仅仅局限在这些应用上,这种材料已被用做服务于 1000°F(540℃)尽管它的抗腐蚀作用会随着服务的温度增加而消弱。
1.3.分类这种规格的电镀分类如下:等级一. 除了氢脆化的减除,不进行电镀加热处理。
等级二. 加热处理在 450°F(232℃)或者以上,使材料变坚硬。
等级三. 加热处理在 375°F(191℃)去核实非热处理合金的粘附性。
等级四. 加热处理在 250°F(121℃)去核实热处理合金的粘附性。
1.3.1 除非有细节的规定,一般采用等级一。
1.4.安全或危险材料:当描述和被引用的材料,方法,应用和步骤在这个规格中也许会涉及使用危险材料。
这个规格没有指明在这种使用中会涉及到危险。
这是使用者的责任去确保和熟悉危险材料的安全和正当使用,以及采取必要预防措施确保参与人员的健康和安全。
2.应用文件:下面出版的版本是这个指定范围类规格下的一部分,引用的最新版本在购买订单之日起生效。
2.1.ASTM 出版: ASTM B 117:盐沫测试装置。
ASTM B 487:在横截面下用显微镜测量金属和氧化层厚度。
ASTM B 499:通过磁性法测量膜厚度,无磁性膜在磁性金属上。
ASTM B 568:通过 X 射线的光谱学去测量膜的厚度。
ASTM B 571:金属膜的粘附性。
ASTM B636:螺旋状镀金属膜的内部压力测试。
ASTM748:通过显微镜扫描横截面测量金属膜的厚度。
ASTM764:对不同镍材料进行逐个表层的厚度测试(STEP 测试)。
ASTM384: 材料显微硬度测试。
ASTM519:电镀过程和飞机维修化学中,机械氢脆化测试。
化学镀镍相关标准与规范化学镀镍过程的标准和规范有许多,几乎各国都有自己的标准,这些标准和规范是由许多学科的专业人员共同制定的,为了方便我国技术人员参考,现将其中比较重要的一些标准名称列出:国际标准:ISO 4527(1987),ISO/TC107 自催化镍磷镀层-规范和试验方法(Autocatalyticnickel-phosphoruscoatings-specification and test methods)中国:自催化镍-磷镀层技术要求和试验方法 GB/T 13913-92美国:ASTM B733-97 金属上自催化镍磷镀层标准规范(Standard Specification for Autocatalytic(Electroless) Nickel-Phosphorous Coatings on Metal)ASTMB656-91 工程用金属自催化镍磷沉积标准(Standard Guide for Autocatalytic (Electroless)Nickel-Phosphorus on Metals for Engineering Use)ASTM B656-79 金属上工程用自催化镀镍标准实施办法(该标准于2000年废止)MILC 26074B-军用规范,化学镀镍层的技术要求(Coatings,Electroless Nickel Requirements for Military)AMS 2404A-航空材料规范化学镀镍(Electroless Nickel Plating)AMS 2405-航空材料规范化学镀镍,低磷(Electroless Nickel Plating,Low Phosphrous) NACE T-6A-54 美国腐蚀工程师学会文件化学镀镍层英国:DEE STD 03-5/1 材料的化学镀镍层(Electroless Nickel Coatings of Material)法国:NFA 91-105 化学镀镍层特性和测试方法(Dépôt Chimique s de Nickel-Propciétés Caractéristiques atMéthodes Déssais德国:DIN 50966(1987) 功能化学镀镍层RAL-RG 660(第二部分)(1984)硬铬和化学镀镍层的质量保证苏联标准:ΓOCT 9.305-84奥地利:ÖNOrm c2550(1987) 化学镀镍磷镀层-技术要求和测试日本标准:JISH 8654-89 金属上自催化镍磷镀层H8645-99 ??解ンツケル?りんめフき11.1 国际标准ISO4527该国际标准于1987年发布,论述了含磷2~15wt%的化学镀镍,并阐述了实际的沉积和预处理步骤。
化学镀镍盐雾试验标准《化学镀镍盐雾试验标准》嘿,同学们!今天咱们来聊聊化学镀镍盐雾试验标准相关的化学知识。
不过在这之前,咱们得先把一些化学概念搞清楚,这样才能更好地理解这个标准哦。
咱们先说说化学键。
化学键就像是原子之间的小钩子,把原子们连接在一起。
这里面有离子键和共价键两种主要的“小钩子”。
离子键呢,就好比是带正电和带负电的原子像超强磁铁一样吸在一起。
比如说氯化钠,钠原子带正电,氯原子带负电,它们之间就有很强的吸引力,就像磁铁的两极一样,紧紧地吸住,这就是离子键。
而共价键呢,是原子们共用“小钩子”连接起来的。
就像两个小伙伴,他们共享一些东西,把彼此连接在一起。
再说说化学平衡,这个就像拔河比赛。
反应物和生成物就像是两队人在拔河。
刚开始的时候,可能一方比较强,但是随着比赛进行,最后会达到一个状态,就是两队人拉扯的力量一样大了,这时候正反应和逆反应的速率相等了,就像两边拉扯的速度一样。
而且这时候两边的人数(浓度)也不再变化了,这就是化学平衡状态。
分子的极性也很有趣。
咱们可以把分子想象成小磁针。
像水这种极性分子,氧一端就像磁针的南极,带负电,氢一端就像北极,带正电。
而二氧化碳就不一样了,它是直线对称的,就像一个两边完全一样的东西,所以它是非极性分子,就没有像小磁针那样的正负电两端。
配位化合物呢,就像是一场聚会。
中心离子就是聚会的主角,而配体就是那些提供孤对电子共享的小伙伴。
它们聚在一起,就形成了配位化合物。
还有氧化还原反应中的电子转移,这个就像做交易。
比如说锌和硫酸铜反应,锌原子就像一个慷慨的商人,把自己的电子给了铜离子,就像把自己的货物给了别人。
结果锌自己变成了离子,而铜离子得到电子就变成了原子,这就是电子的转移。
化学反应速率的影响因素也很好理解。
温度就像是天气。
天气热的时候,就像高温的时候,原子们就像人一样更有活力,动得更快,反应也就更快了。
浓度就像是跑道上的人多少。
如果跑道上的人(反应物分子)很多,那相互碰撞反应的机会就大,反应就快;如果人少,反应就慢。
化学镀镍的一般操作规范简介成形的化学镀镍工艺是在1946年被发现及发展的,1955年美国通用运输公司(GA TC)建成了第一条化学镀镍生产线和第一个商品化学镀镍溶液。
20世纪80年代,化学镀镍工艺有了巨大的发展,研究和应用达到一个新的水平。
按照合金成分分类,化学镀镍可以分为镍-磷合金和镍-硼合金两大类。
从应用领域来讲,镍-磷合金使用更为普遍。
化学镀镍-磷合金按照溶液的pH可以分为碱性和酸性化学镀镍,碱性化学镀镍主要用于预镀的打底层,以提高电镀层与基体的结合力,在铝轮毂的电镀中有较成功的应用。
酸性化学镀镍工艺是目前化学镀镍中应用最为广泛的工艺,按镀层中的磷含量又可分为低磷(2%~5%)、中磷(6%~9%)和高磷(10%以上)。
化学镀镍工艺因为镀层均匀,亮度好,耐蚀性及耐磨性优良而被广泛应用于多个领域。
1. 化学镀镍的周期定义化学镀镍溶液在使用中的管理与维护非常重要,它与电镀液的管理与维护不同,化学镀镍液中的镍离子等多种成分时刻在不断变化,均需要外加补充,否则溶液不能正常进行。
化学镀镍溶液的好坏一般通过能够获得质量稳定镀层的周期(循环系数MTO)来评判。
目前市场销售的化学镀镍溶液多数分为A、B、C三种组份,周期数可以做到6~8,对镀层质量要求不严格的可以做到12个周期甚至以上。
1个周期的定义是,当溶液中主盐的添加量达到了开缸剂量时为一个周期,以1L溶液为例,开缸量一般为60毫升/升,在使用过程中,当A剂的补充量达到了60毫升时,该化学镀镍溶液就已使用一个周期。
2. 化学镀镍溶液的过程控制2.1应准确计算槽体容积和零件的表面积看似再简单不过的问题,但很多时候都难以做到。
化学镀镍溶液的消耗及补充与装载量有直接的关系,因此,溶液的装载量应得到重视。
装载量就是所要施镀零件的表面积与溶液体积之比值。
一般控制在1~1.5 dm2/L为最佳,过大(>2.5 dm2/L)或过小(<0.5 dm2/L)对溶液的稳定性都不好。
化学镀镍知识概述一、化学镀镍溶液的组成与镀液成分设计常识优异的镀液配方对于产生最优质的化学镀镍层是必不可少的。
化学镀镍溶液应包括:镍盐、还原剂、络合剂、缓冲剂、促进剂、稳定剂、光亮剂、润湿剂等。
主盐化学镀镍溶液中的主盐就是镍盐,如硫酸镍、氯化镍、醋酸镍等,由它们提供化学镀反应过程中所需要的镍离子。
早期曾用过氯化镍做主盐,但由于氯离子的存在不仅会降低镀层的耐蚀性,还产生拉应力,所以目前已很少有人使用。
同硫酸镍相比用醋酸镍做主盐对镀层性能是有益的。
但因其价格昂贵而无人使用。
其实最理想的镍离子来源应该是次磷酸镍,使用它不至于在镀浴中积存大量的硫酸根,也不至于在使用中随着补加次磷酸钠而带入大量钠离子,同样因其价格因素而不能被工业化应用。
目前应用最多的就是硫酸镍,由于制造工艺稍有不同而有两种结晶水的硫酸镍。
因为硫酸镍是主盐,用量大,在镀中还要进行不断的补加,所含杂质元素会在镀液的积累,造成镀液镀速下降、寿命缩短,还会影响到镀层性能,尤其是耐蚀性。
所以在采购硫酸镍时应该力求供货方提供可靠的成分化验单,做到每个批量的质量稳定,尤其要注意对镀液有害的杂质尤其是重金属元素的控制。
还原剂用得最多的还原剂是次磷酸钠,原因在于它的价格低、镀液容易控制,而且合金镀层性能良好。
次磷酸钠在水中易于溶解,水溶液的pH值为6。
是白磷溶于NaOH中,加热而得到的产物。
目前国内的次磷酸钠制造水平很高,除了国内需求外还大量出口。
络合剂化学镀镍溶液中除了主盐与还原剂以外,最重要的组成部分就是络合剂。
镀液性能的差异、寿命长短主要取决于络合剂的选用及其搭配关系。
络合剂的第一个作用就是防止镀液析出沉淀,增加镀液稳定性并延长使用寿命。
如果镀液中没有络合剂存在,由于镍的氢氧化物溶解度较小,在酸性镀液中便可析出浅绿色絮状含水氢氧化镍沉淀。
硫酸镍溶于水后形成六水合镍离子,它有水解倾向,水解后呈酸性,这时即析出了氢氧化物沉淀。
如果六水合镍离子中有部分络合剂存在则可以明显提高其抗水解能力,甚至有可能在碱性环境中以镍离子形式存在。
化学镀镍(EPN)工艺技术ENP俗称化学镀镍或自催化镀镍或镍磷镀及无电镀镍,是一种用化学的方法,在金属表面沉积出十分均匀、光亮、坚硬的镍磷(硼)合金镀层的表面处理工艺技术。
它具有高均匀性、高结合强度、高耐磨性、高耐腐蚀及绿色环保等品质特征。
化学镀镍(ENP)工艺技术ENP(Electroless Nickel plating)工艺是一种用非电镀(化学)的方法,在零部件表面沉镀出十分均匀、光亮、坚硬的镍磷硼合金镀层的先进表面处理工艺。
它兼有高匀性、高结合强度、高耐磨性、高耐腐蚀性和无漏镀缺陷及仿真性极好六大优点,其综合性能优于电镀铬。
在很多环境介质中甚至比不锈钢更耐腐蚀,用来代替不锈钢可以降低工件成本。
在工艺方面,化学镀镍是靠化学方法形成镀层,不受零件形状和尺寸的限制,任何复杂形状的零件各部位镀层厚度均匀一致,施镀过程中厚度精度为±2μm,能够满足各种复杂精密部件的尺寸要求,而且镍合金镀层质密光滑,镀后无需任何加工,还可以反复修镀。
该技术是目前发达国家重点推广的表面处理新技术。
一、ENP的基本原理ENP的基本原理是以次亚磷酸盐为还原剂,将镍盐还原成镍,同时使金属层中含有一定的磷,沉淀的镍膜具有催化性,可使反应继续进行下去。
关于ENP的具体反应机理,目前尚无统一认识,现为大多数人所接受的原子氢态理论是:1、镀液在加热时,通过次亚磷酸根在水溶液中脱氢,而形成亚磷酸根,同时放出生态原子氢,即:H2PO2-+H2O→H2PO32-+H++2[H]2、初生态的原子氢吸附催化金属表面而使之活化,使镀液中的镍离子还原,在催化金属表面上沉积金属镍:Ni2++2[H]→Nio+2H+3、随着次亚磷酸根的分解,还原成磷:H2PO2-+[H]→H2O+OH-+Po镍原子和磷原子共同沉积而形成Ni-P合金,因此,ENP的基本原理也就是通过镀液中离子还原,同时伴随着次亚磷酸盐的分解而产生磷原子进入镀层,形成过饱和的Ni-P固溶体。
化学镀镍相关标准与规范化学镀镍过程的标准和规范有许多,几乎各国都有自己的标准,这些标准和规范是由许多学科的专业人员共同制定的,为了方便我国技术人员参考,现将其中比较重要的一些标准名称列出:国际标准:ISO 4527(1987),ISO/TC107 自催化镍磷镀层-规范和试验方法(Autocatalyticnickel-phosphoruscoatings-specification and test methods)中国:自催化镍-磷镀层技术要求和试验方法 GB/T 13913-92美国:ASTM B733-97 金属上自催化镍磷镀层标准规范(Standard Specification for Autocatalytic(Electroless) Nickel-Phosphorous Coatings on Metal)ASTMB656-91 工程用金属自催化镍磷沉积标准(Standard Guide for Autocatalytic (Electroless)Nickel-Phosphorus on Metals for Engineering Use)ASTM B656-79 金属上工程用自催化镀镍标准实施办法(该标准于2000年废止)MILC 26074B-军用规范,化学镀镍层的技术要求(Coatings,Electroless Nickel Requirements for Military)AMS 2404A-航空材料规范化学镀镍(Electroless Nickel Plating)AMS 2405-航空材料规范化学镀镍,低磷(Electroless Nickel Plating,Low Phosphrous) NACE T-6A-54 美国腐蚀工程师学会文件化学镀镍层英国:DEE STD 03-5/1 材料的化学镀镍层(Electroless Nickel Coatings of Material)法国:NFA 91-105 化学镀镍层特性和测试方法(Dépôt Chimique s de Nickel-Propciétés Caractéristiques atMéthodes Déssais德国:DIN 50966(1987) 功能化学镀镍层RAL-RG 660(第二部分)(1984)硬铬和化学镀镍层的质量保证苏联标准:ΓOCT 9.305-84奥地利:ÖNOrm c2550(1987) 化学镀镍磷镀层-技术要求和测试日本标准:JISH 8654-89 金属上自催化镍磷镀层H8645-99 ??解ンツケル?りんめフき11.1 国际标准ISO4527该国际标准于1987年发布,论述了含磷2~15wt%的化学镀镍,并阐述了实际的沉积和预处理步骤。
化学镀镍流程化学镀镍是一种常见的表面处理工艺,通过在金属表面沉积一层镍来提高其耐腐蚀性、耐磨性和美观度。
下面将介绍化学镀镍的流程及相关注意事项。
首先,准备工作。
在进行化学镀镍之前,需要对待镀件进行表面处理,包括去油、酸洗、水洗等工序,确保表面干净,无杂质。
同时,准备镀液和镀液搅拌设备,确保镀液的配制和搅拌均匀。
其次,浸泡清洗。
将经过表面处理的待镀件浸入预处理槽中,进行清洗。
清洗的目的是去除表面残留的杂质和氧化物,确保镀层的附着力和光洁度。
然后,进行化学镀镍。
将清洗后的待镀件浸入镀液中,通电进行镀镍。
镀液中的主要成分包括镍盐、氨水、硼砂等,通过控制电流密度和镀液温度来控制镀层的厚度和均匀度。
接着,水洗。
在镀镍结束后,将镀件取出,进行水洗。
水洗的目的是去除镀液残留在表面的化学物质,防止对镀层质量的影响。
最后,烘干和包装。
将水洗后的镀件进行烘干,确保表面无水痕。
然后进行包装,以防止镀层在运输和储存过程中受到损坏。
在进行化学镀镍的过程中,需要注意以下几点:1. 控制镀液的配制和搅拌,保持镀液的均匀性和稳定性,以确保镀层的质量。
2. 控制镀液的温度和PH值,这对镀层的光洁度和均匀度有重要影响。
3. 控制电流密度和镀液的流速,以确保镀层的厚度和均匀度。
4. 定期对镀液进行分析和调整,确保镀液的成分和性能符合要求。
5. 在操作过程中,要严格遵守安全操作规程,避免镀液的溅洒和工作场所的污染。
综上所述,化学镀镍是一项重要的表面处理工艺,通过严格控制每个环节,可以获得高质量的镀层,提高金属制品的使用性能和外观质量。
希望以上内容对您有所帮助,谢谢阅读!。
化学镀镍相关标准与规范
化学镀镍过程的标准和规范有许多,几乎各国都有自己的标准,这些标准和规范是由许多学科的专业人员共同制定的,为了方便我国技术人员参考,现将其中比较重要的一些标准名称列出:
国际标准:
ISO 4527(1987),ISO/TC107 自催化镍磷镀层-规范和试验方法(Autocatalytic
nickel-phosphorus
coatings-specification and test methods)
中国:
自催化镍-磷镀层技术要求和试验方法 GB/T 13913-92
美国:
ASTM B733-97 金属上自催化镍磷镀层标准规范(Standard Specification for Autocatalytic
(Electroless) Nickel-Phosphorous Coatings on Metal)
ASTMB656-91 工程用金属自催化镍磷沉积标准(Standard Guide for Autocatalytic (Electroless)
Nickel-Phosphorus on Metals for Engineering Use)
ASTM B656-79 金属上工程用自催化镀镍标准实施办法(该标准于2000年废止)
MILC 26074B-军用规范,化学镀镍层的技术要求(Coatings,Electroless Nickel Requirements for Military)
AMS 2404A-航空材料规范化学镀镍(Electroless Nickel Plating)
AMS 2405-航空材料规范化学镀镍,低磷(Electroless Nickel Plating,Low Phosphrous) NACE T-6A-54 美国腐蚀工程师学会文件化学镀镍层
英国:
DEE STD 03-5/1 材料的化学镀镍层(Electroless Nickel Coatings of Material)
法国:
NFA 91-105 化学镀镍层特性和测试方法(Dépôt Chimique s de Nickel-Propciétés Caractéristiques at
Méthodes Déssais
德国:
DIN 50966(1987) 功能化学镀镍层
RAL-RG 660(第二部分)(1984)硬铬和化学镀镍层的质量保证
苏联标准:
ΓOCT 9.305-84
奥地利:
ÖNOrm c2550(1987) 化学镀镍磷镀层-技术要求和测试
日本标准:
JISH 8654-89 金属上自催化镍磷镀层
H8645-99 ??解ンツケル?りんめフき
11.1 国际标准ISO4527
该国际标准于1987年发布,论述了含磷2~15wt%的化学镀镍,并阐述了实际的沉积和预处理步骤。
为了消除钢中的内应力,推荐了热处理的范围,同时也论及了喷砂和喷丸处理。