ASTM B629-1977(2013) Standard Practice for Preparation of Molybdenum and Molybdenum Alloys for Electroplating《电镀用钼和钼合金的制备的标准实施规程》.pdf

《ASTM B629-1977(2013) Standard Practice for Preparation of Molybdenum and Molybdenum Alloys for Electroplating《电镀用钼和钼合金的制备的标准实施规程》.pdf》由会员分享，可在线阅读，更多相关《ASTM B629-1977(2013) Standard Practice for Preparation of Molybdenum and Molybdenum Alloys for Electroplating《电镀用钼和钼合金的制备的标准实施规程》.pdf（2页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: B629 77 (Reapproved 2013)Standard Practice forPreparation of Molybdenum and Molybdenum Alloys forElectroplating1This standard is issued under the fixed designation B629; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision,

2、the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This practice covers a procedure for preparing molyb-denum and its alloys for electroplating. The procedur

3、e utilizestechniques, equipment, and chemicals that are common toelectroplating. Specialized procedures such as hydrogen heattreatment and fused salt pickling are not included. These andother procedures can be found in the references listed at the endof this practice.1.2 This standard does not purpo

4、rt to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Significance and Use2.1 Molybdenum is used i

5、n engineering applications wherestrength and rigidity of component parts are needed, especiallyat high temperatures. Its good strength at high temperatures,low vapor pressure, and good impact and creep resistancemake it attractive for load-bearing items such as turbine blades,mechanical seals, rocke

6、t motor parts, heating elements, andelectronic devices. Molybdenum, however, is easily oxidized,and the oxides are not protective. The volatility of the oxidesabove 800C can lead, in the case of unprotected parts, tocatastrophic oxidation and to losses in dimensions. Electro-plated coatings are appl

7、ied to molybdenum to preventoxidation, to prevent seizing and galling, and to assist joiningby soldering, brazing, and diffusion bonding.3. Procedure3.1 Precleaning:3.1.1 The principles of electroplating on molybdenum aresimilar to those of other metals. The surfaces must be free ofdirt, grease, and

8、 other foreign matter. Solvent, emulsion, andsoak cleaners are suitable for precleaning to remove grosssurface contaminants. If a molybdenum specimen is subjectedto severe forming operations and retains a carbonaceoussurface layer, descale the part by immersion in a 110 g/Lsolution of sodium hydroxi

9、de at or near boiling, or bymechanical finishing. Glass bead blasting can be used toremove uneven coatings of scale without disturbing the finishof the metal.3.1.2 Cathodic alkaline cleaning is preferred for the finalprecleaning so as to avoid anodic oxidation. Proprietaryformulations used for catho

10、dic alkaline cleaning of othermetals are suitable. Cathodic treatment at about 6 V for 30 to60 s is usually adequate, using a cleaner concentration of 60 to75g/L and a solution temperature of 60 to 75C.3.2 RinseHere, and throughout the procedure, the waterrinses should be warm (approximately 50C).3.

11、3 ElectropolishingEither of the following electropol-ishes may be used. The choice of electropolish and timedepends on the amount of material that can be removed and thedegree of surface improvement desired. The cathodes may belead or carbon. The sulfuric acid bath produces a blue film thatis partly

12、 removed in the rinse and completely removed in thealkaline dip.3.3.1 Sulfuric Acid:H2SO4(sp gr 1.83) 80 mass % (755 mL of acid/L)Temperature 20 to 30CCurrent density 1100 to 2200 A/m2anodicTime 30 s3.3.2 Sulfuric - Phosphoric Acid:H2SO4(sp gr 1.83) 50 % vol (500 mL/L)H3PO4(85 %) 50 % vol (500 mL/L)

13、Temperature 50 to 55CCurrent density 2500 A/m2anodicTime 180 s3.4 Rinse.3.5 Alkaline DipBriefly immerse the specimen in a 45-g/Lsolution of sodium hydroxide at room temperature.3.6 Rinse.3.7 Acid DipBriefly immerse the specimen in a 10-mass % solution of sulfuric acid (58 mL of 1.83 sp gr acid/L)at

14、room temperature.3.8 Rinse.1This practice is under the jurisdiction of ASTM Committee B08 on Metallicand Inorganic Coatingsand is the direct responsibility of Subcommittee B08.02 onPre Treatment.Current edition approved Dec. 1, 2013. Published December 2013. Originallyapproved in 1977. Last previous

15、 edition approved in 2008 as B629 77 (2008).DOI: 10.1520/B0629-77R13.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States13.9 Chromium StrikingElectroplate the specimen in aconventional chromium electroplating solution for 1 to 5 min at150

16、0 to 2500 A/m2at a temperature of 50C minimum. Insome cases, it may be necessary to first make the part anodic inthe chromium solution for 1 min at 2200A/m2in order to attaingood adhesion.3.10 Rinse.3.11 Nickel StrikingElectroplate the specimen in the fol-lowing solution at 800 A/m2for 120 s.NiCl26H

17、2O 240 g/LHCl (sp gr 1.18) 10 vol % (100 mL/L)Temperature 20 to 30CAnode nickel or carbon3.12 Rinse.3.13 Electroplate the specimen with the desired metal.REFERENCES(1) Beach, J. G., et al. U. S. Patent 2,928,169 (March 15, 1960).(2) Brenner, A., Plating, Vol 43, 1956, p. 1143.(3) Domnikov, L., Metal

18、 Finishing, Vol 61, April 1963, p. 64.(4) Finne, R. M., and Bracht, W. R., Journal of Electrochemical Society,Vol 113, 1966, p. 551.(5) Freeman, R. R., and Briggs, J. Z., “Electroplating on MolybdenumMetal,” Climax Molybdenum Co., Ann Arbor, MI, September 1958.(6) Korbelak, A., Plating, Vol 40, 1953

19、, p. 1126, U. S. Patent 2,697,316.(7) Safranek, W. H., and Schaer, G. R., Proceedings, American Electro-platers Society, Vol 43, 1956, p. 105.(8) Schaer, G. R., U. S. Patent 2,859,158 (November 4, 1958).(9) Schaer, G. R., et al, U. S. Patent 2,886,499 (May 12, 1959).(10) Seegmiller, et al, Proceedin

20、gs, American Electroplaters Society, Vol49, 1962, p. 67.(11) Valler, L. E., et al. USAED Report No. BMI 813, (April 1, 1953 )(Obtainable from National Technical Information Service,Springfield, VA).ASTM International takes no position respecting the validity of any patent rights asserted in connecti

21、on with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the responsible

22、 technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive careful consi

23、deration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International, 100 Ba

24、rr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).B629 77 (2013)2