ASTM A239-1995(2004) Standard Practice for Locating the Thinnest Spot in a Zinc (Galvanized) Coating on Iron or Steel Articles《用普力斯试验法(硫酸铜浸蚀)确定铁或钢制品上镀锌层最薄点的标准测试方法》.pdf

《ASTM A239-1995(2004) Standard Practice for Locating the Thinnest Spot in a Zinc (Galvanized) Coating on Iron or Steel Articles《用普力斯试验法(硫酸铜浸蚀)确定铁或钢制品上镀锌层最薄点的标准测试方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM A239-1995(2004) Standard Practice for Locating the Thinnest Spot in a Zinc (Galvanized) Coating on Iron or Steel Articles《用普力斯试验法(硫酸铜浸蚀)确定铁或钢制品上镀锌层最薄点的标准测试方法》.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: A 239 95 (Reapproved 2004)Standard Practice forLocating the Thinnest Spot in a Zinc (Galvanized) Coatingon Iron or Steel Articles1, 2This standard is issued under the fixed designation A 239; the number immediately following the designation indicates the year oforiginal adoption or, in

2、the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript 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. Scope1.1 Th

3、is practice covers the procedure for locating, by theuse of a solution of copper sulfate, the thinnest spot in a zinccoating (hot dipped, electroplated, or sprayed) on iron or steelarticles that are coated after the shape is produced by casting,drawing, pressing, or other forming methods. Examples a

4、re:electrical metallic tubing and rigid conduit pipe, castings andforgings, and structural steel; on special hardware, such aspoleline, builders, and farm implement hardware; bolts, nuts,screws, and other miscellaneous general hardware.1.2 The use of this practice with zinc coating depositedthrough

5、different processes (such as hot dipped, electroplated,or sprayed) requires caution in interpretation since the endpoint may vary considerably between different zinc-coatingsystems.1.3 Excluded from this practice is sheet steel from hot-dipor electrocoating lines as the sheet products are normallysu

6、bject to additional forming after the coating process. Alsoexcluded from this practice are all zinc-coated wire and wireproducts either continuously or batch coated before or afterforming. WarningPast research (dating from around 1963)has indicated that this practice can be influenced by operatortec

7、hnique. Variations can be due to the difference in handpressure used to wipe the sample or the inability of the operatorto recognize the end point.1.4 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this sta

8、ndard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Significance and Use2.1 This practice is designed to locate the thinnest portionsof the zinc coating on newly coated items (see Appendix X1).Variations in coating th

9、ickness can be due to the process bywhich the zinc is applied (hot dipped, electroplated, or sprayed)or by the geometry of the part that is coated. During hot-dipgalvanizing, the coating thickness is affected by the drainagepattern of the molten zinc, while during zinc spraying (metal-lizing), coati

10、ng thickness can be dependent on the operatorsmanipulation of the spray nozzle. The geometry of the part canalso influence coating thickness especially during hot-dipgalvanizing, where peaks and valleys on the part can causemolten zinc to build up or thin out. This practice is designed toidentify th

11、ose areas of the part where the coating is thin.3. Copper Sulfate Solution3.1 The copper sulfate solution shall be made by dissolvingapproximately 36 parts by weight of commercial cupric sulfatecrystals (CuSO45H2O) in 100 parts by weight of distilledwater (see 3.1.1). Heat may be used to complete th

12、e solution ofcupric sulfate crystals. If heated, the solution shall be allowedto cool. The solution shall then be agitated with an excess ofpowdered cupric hydroxide (Cu(OH)2), about 0.13 oz/gal 1.0g/L of solution. The presence of an excess of cupric hydroxidewill be shown by the sediment of this re

13、agent at the bottom ofthe vessel. The neutralized solution shall be allowed to standfor 24 h and then filtered or decanted.3.1.1 Cupric oxide (CuO), 0.11 oz/gal 0.8 g/L may besubstituted for cupric hydroxide, provided the solution isallowed to stand not less than 48 h after this addition beforedecan

14、ting or filtering.3.2 The solution shall have a specific gravity of 1.186 at18C 65F. To adjust a solution of improper specific gravity,add distilled water when the specific gravity is high, and add a1This practice is under the jurisdiction of ASTM Committee A05 on Metallic-Coated Iron and Steel Prod

15、ucts and is the direct responsibility of SubcommitteeA05.07 on Methods of Testing.Current edition approved May 1, 2004. Published June 2004. Originallyapproved in 1940. Last previous edition approved in 1999 as A 239 - 95 (1999).2This practice is used to locate the thinnest spot only, and is not int

16、ended as atest for coating weight. This practice is to be used only within the limits of Section1, Scope.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.copper sulfate solution of a higher specific gravity when thesolution is low in

17、specific gravity.4. Specimen Rinse Water4.1 Ordinary, clean tap water may be used for rinsingspecimens. If no running tap water is available, the rinse watershall be changed after each dip. The temperature of the rinsewater shall be from 15 to 21C 60 to 70F.5. Quantity of Copper Sulfate Solution5.1

18、Hardware and Similar Articles For evaluating hard-ware and similar articles, the quantity of copper sulfatesolution required for each evaluation will depend on thesuperficial area of the specimen being evaluated and the weightof coating. The quantity should not be less than 1.2 qt/oz/ft240.5 mL/g/m2

19、 of zinc coating on the specimen (Note 1) andshall be sufficient to cover the specimen so that the top surfaceof the solution is at least12 in. 12.7 mm above the top of thesection of the specimen under evaluation. The solution shall bediscarded after completion of the evaluation, and fresh solutions

20、hall be used for any additional evaluations.NOTE 1The theoretical minimum amount of copper sulfate solutionrequired to dissolve zinc is 0.4 qt/oz 13.5 mL/g. The quantity specifiedin 5.1 is three times this minimum to ensure adequate rate of solution.6. Preparation of Specimens6.1 The specimens selec

21、ted for evaluation shall be free ofabrasion or cuts in the zinc coating, except those which mayoccur during manufacture of the specimen. Where the area ofuncoated surface to be immersed is more than 10 % of the totalimmersed surface area, precautions, such as plugs for tubularmaterial, or lacquer, p

22、araffin, or other suitable coatings for theuncoated surfaces must be taken so as not to deplete thestrength of copper sulfate solution.6.2 Clean the specimens with a suitable volatile organicsolvent and finally, thoroughly wash with clean water and wipedry with a clean cotton cloth. Unless otherwise

23、 specified,remove lacquer or varnish coatings with a suitable clean,volatile organic solvent such as acetone, which will not attackthe zinc coating or leave a greasy or waxy deposit. Thoroughlyrinse the specimens in clean water and wipe dry with a cleancotton cloth. Bring the specimens to a temperat

24、ure between 15and 21C 60 and 70F prior to the beginning of theimmersion series.6.3 Abnormal cases may arise when, by reason of unusualsurface conditions, the copper sulfate solution will not actnormally on the zinc coating. For example, the solution mayhave no apparent attack on all or part of the s

25、urface, or falsedeposits of copper may appear on the zinc coating. If there isany question of abnormality of performance of specimens,discard the specimens and select new ones. Clean the newspecimens in alcohol, rinse, and wipe dry. Then immerse for 3min in a solution consisting of 1 part by volume

26、of ammoniumhydroxide (sp gr 0.90) and 9 parts of water. The specimens maybe scrubbed with a cotton cloth during this immersion. Aftercleaning, wash the specimens and wipe dry, then subject themto the procedure described in Section 7.7. Procedure7.1 Immerse the specimens in the copper sulfate solutio

27、n,which shall be maintained at a temperature of 16 to 20C 61to 68F. Allow the specimens to remain in a fixed position inthe solution for exactly 1 min. Do not agitate the solutionduring the immersion period, nor allow the specimens to toucheach other or the sides of the container. After each 1-minim

28、mersion, wash the specimens immediately in the rinse water,and use a fiber bristle brush to remove any copper deposit thatmay have formed on the zinc coating. Before returning thespecimens to the copper sulfate solution, drain thoroughly ofexcess rinse water and wipe dry with a clean cloth.7.2 Conti

29、nue successive immersions of 1 min each, washingand wiping the specimens after each immersion until the endpoint has been reached (see Appendix X2).NOTE 2Zinc coatings on threads are usually difficult to test. It hasbeen found advantageous to saw female-threaded parts longitudinally,exposing the thr

30、eads to full view and facilitating cleaning to removesponge copper after each immersion in the copper sulfate solution.Brushing should be parallel to the threads.8. End Point8.1 The end point shall be recognized by the appearance ofbright, adherent copper deposits. However, if such a depositfails to

31、 form after the complete disappearance of the zinccoating, the immersion succeeding the disappearance of thezinc shall be recognized as representing the end point.8.2 Confirm adherence of the bright copper deposit by apeeling test. If it is possible to remove the copper with an inkeraser or to peel

32、the copper with the edge of a blunt tool suchas the back of a knife blade, and zinc appears underneath thecopper, such an appearance of deposited copper shall not beconstrued as an end point.8.3 A fine line appearance of copper on the top of screwthreads or on sharp edges of articles, or within 1 in

33、. 25 mmof a cut portion of a specimen, shall not be judged as an endpoint. Likewise, the indication of bright adherent deposits ofcopper at or adjacent to any cut or abrasion present on theoriginal specimen shall not be considered an end point.9. Supplementary Tests9.1 If at any time during the imme

34、rsion procedure there isany doubt as to the presence of exposed base metal, asdetermined by visual inspection, there are several supplemen-tary tests described in Section 10, one or more of which may beused depending on the type of coating being evaluated.10. Supplementary Test for All Types of Zinc

35、 Coatings10.1 Microscopical TestSection the specimen through thecopper deposit, mount, and polish it for metallographic analy-sis. Etch the polished surface using an etching solutioncomposed of 20 g of chromic acid, 1.5 g of sodium sulfate, and100 mL of distilled water (Palmerton reagent). After etc

36、hing,wash the specimen with alcohol. Examine the etched specimenunder a microscope, using a magnification of 100 diameters orgreater if necessary.A 239 95 (2004)210.2 Qualitative Test for Zinc3Apply a drop (or severaldrops) of diluted hydrochloric acid to the area in question(depending on its size).

37、 The presence of zinc is indicated byimmediate vigorous effervescence (evolution of hydrogen). Ifno appreciable zinc is present, the effervescence will be mild.By carefully removing the acid, a confirming test for zinc maybe made as follows: neutralize the acid with ammoniumhydroxide, acidify with a

38、cetic acid, and pass hydrogen sulfideinto the solution; a white precipitate (zinc sulfide, ZnS)confirms the presence of zinc.11. Keywords11.1 bolts; electroplated; hardware; hot dipped; nuts;screws; thinnest spot; zinc coating thicknessAPPENDIXES(Nonmandatory Information)X1. APPLICATION OF THIS PRAC

39、TICE TO WEATHERED GALVANIZED WAREX1.1 This practice is not applicable to aged or weatheredmaterial because of the corrosion film present on the zinccoating. If it is desired to use this practice on such material, thecorrosion film should be removed before conducting thisprocedure by immersing the sp

40、ecimens for 3 min in anammonium hydroxide solution (1 part by volume of ammo-nium hydroxide (sp gr 0.90) to 9 parts by volume of distilledwater) then rinsing the specimens in clean water and wipingthem dry.X2. STANDARD FOR COMPARISONX2.1 If it is desired to show the character of the brightmetallic c

41、opper deposit on an exposed iron or steel surface, areference standard for comparison may be prepared as follows:Partially submerge a zinc-coated specimen in strong hydro-chloric acid until violent action ceases. Immediately removethe specimen, wash, and wipe it dry. The specimen with an areaof bare

42、 surface thus exposed, including a portion with zinccoating intact, is then dipped for a few seconds in the coppersulfate solution at a temperature of 16 to 20C 61 to 68F,removed, washed, and wiped dry. This copper-coated referencestandard should be prepared at the time this practice is beingconduct

43、ed.X3. ACTION OF COPPER SULFATE SOLUTION ON ZINC COATINGSX3.1 The fact that this practice cannot be used for deter-mining the weight of zinc coating is due to the wide variationin the rate of solubility of the various types of coating resultingfrom differences in the composition and structure of the

44、coatings. For instance, electroplated and sprayed-zinc coatingsconsist essentially of pure zinc; the outer part of hot-dippedcoatings consists of nearly pure zinc; whereas, the portion nextto the steel base is composed of zinc-iron alloys; in the case ofhot-dipped coatings heated after galvanizing,

45、the coating con-sists almost entirely of zinc-iron alloys.X3.2 In view of these differences in the makeup of the zinccoatings applied by the different processes, it has been foundby Groesbeck and Walkup4in tests on a limited number ofsamples that electroplated and flame-sprayed coatings, byreason of

46、 their high pure-zinc content, dissolve rather rapidlyin the copper sulfate solution; that the conventional hot-dipcoatings dissolve only about two thirds as fast as the pure zinccoatings; and that the hot-dip coatings heated after galvanizingdissolve only about half as fast as the pure zinc coating

47、s.3Only an outline of the test is given. The details of the test may be found intechnical literature.4For further information on this test method, reference may be made to thefollowing papers:Walkup, H. H., and Groesbeck, E. C., “Some Factors Affecting the Preece Testfor Zinc Coatings,” Proceedings,

48、 ASTM, Vol 32, Part II, 1932, p. 453.Groesbeck, E. C., and Walkup, H. H., “Preece Test (Copper Sulphate Dip) forZinc Coatings,” National Institute of Standards and Technology Journal ofResearch, Vol 12, No. 6, June 1934, p. 785 (Research Paper RP688).A 239 95 (2004)3ASTM International takes no posit

49、ion respecting the validity of any patent rights asserted in connection 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 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 a