ASTM D1845-1986(2003) Standard Test Methods for Chemical Analysis of Strontium Chromate Pigment《铬酸锶颜料的化学分析测试方法》.pdf

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1、Designation: D 1845 86 (Reapproved 2003)Standard Test Methods forChemical Analysis of Strontium Chromate Pigment1This standard is issued under the fixed designation D 1845; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year o

2、f 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 These test methods cover the chemi

3、cal analysis ofstrontium chromate pigment.1.2 The analytical procedures appear in the following order:SectionsStrontium by the Strontium Sulfate Method 7to10Chromium by the Thiosulfate Method 11to14Chloride Content 15Sulfate Content 16Moisture and Other Volatile Matter 17Coarse Particles 18Mass Colo

4、r and Tinting Strength 191.3 This values stated in SI units are to be considered thestandard. The values given in parentheses are for informationonly.1.4 This standard does not purport to address the safetyconcerns associated with its use. It is the responsibility of theuser of this standard to esta

5、blish appropriate safety and healthpractices and determine the applicability of regulatory limita-tions prior to use.2. Referenced Documents2.1 ASTM Standards:2D 185 Test Methods for Coarse Particles in PigmentsD 280 Test Methods for Hygroscopic Moisture (and OtherMatter Volatile Under the Test Cond

6、itions) in PigmentsD 387 Test Method for Color and Strength of ChromaticPigments with a Mechanical MullerD 444 Test Methods for Chemical Analysis of Zinc YellowPigment (Zinc Chromate Yellow)D 1193 Specification for Reagent Water3. Significance and Use3.1 These test methods may be used to confirm the

7、 statedstrontium oxide and chromium oxide content of strontiumchromate.4. Apparatus4.1 Gooch crucible.4.2 Electric Furnace, capable of 800C.5. Purity of Reagents5.1 Reagent grade chemicals shall be used in all tests.Unless otherwise indicated, it is intended that all reagents shallconform to the spe

8、cifications of the Committee on AnalyticalReagents of the American Chemical Society, where suchspecifications are available.3Other grades may be used, pro-vided it is first ascertained that the reagent is of sufficientlyhigh purity to permit its use, without lessening the accuracy ofthe determinatio

9、n.5.2 Unless otherwise indicated, references to water shall beunderstood to mean Type II of Specification D 1193.6. Preparation of Sample6.1 Mix the sample thoroughly. Take a sufficient quantityfor chemical analysis and pass it through a No. 325 (4-m)sieve.STRONTIUM BY THE STRONTIUM SULFATEMETHOD7.

10、Reagents7.1 Acetic Acid (glacial).7.2 Ammonium Hydroxide (1+3)Mix 1 volume of con-centrated ammonium hydroxide (NH4OH, sp gr 0.90) with 3volumes of water.1 These test methods are under the jurisdiction of ASTM CommitteePaint and Related Coatings, Materials, and Applications and are the directrespons

11、ibility of Subcommittee D01.31 on Pigment Specifications.Current edition approved Dec. 1, 2003. Published December 2003. Originallyapproved in 1961. Last previous edition approved in 1986 as D 1845 86 (1999).2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Custome

12、r Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents notlis

13、ted by the American Chemical Society, see Analar Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, Wes

14、t Conshohocken, PA 19428-2959, United States.7.3 Ethyl Alcohol, conforming to Formula No. 2B or No. 30of the U.S. Bureau of Alcohol, Tobacco, and Firearms.7.4 Hydrochloric Acid (1+1)Mix equal volumes of con-centrated hydrochloric acid (HCl, sp gr 1.19) and water.7.5 Sulfuric Acid (1+19)Mix 1 volume

15、of concentratedsulfuric acid (H2SO4, sp gr 1.84) with 19 volumes of water.8. Procedure8.1 Weigh to 0.1 mg about 0.5 g of the sample into a400-mL beaker. Add 40 mL of HCl (1+1) and heat the solutionto dissolve the pigment. Add 40 mL of ethyl alcohol until thechromium is reduced, as this is indicated

16、by a dark colorationof the solution. Add to the solution 100 mL of water andsufficient NH4OH (1+3) to form a slight persistent precipitate.8.2 Add HCl dropwise until the precipitate just redissolves(Note 1). Heat the solution to just under boiling and add 20 mLof H2SO4(1+19). Add 100 mL of ethyl alc

17、ohol and allow theprecipitate to settle for several hours or overnight.NOTE 1For a cleaner precipitate, add HCl until a pH of 2.0 is reached,instead of adding HCl dropwise until the precipitate is just dissolved. Thenadd 25 mL of acetic acid to minimize the tendency of the sulfate to forma complex w

18、ith trivalent chromium. Finally, heat the solution, and addH2SO4(1 + 19).8.3 Filter the precipitate through a Gooch crucible that hasbeen previously dried to constant weight. Wash the precipitateseveral times with a solution of equal volumes of ethyl alcohol,water, and H2SO4(1+19). Dry the crucible

19、in an oven and thenignite for12 h at 800C or until constant weight is attained(weight loss less than 0.1 mg). Cool and weigh the crucible.9. Calculation9.1 Calculate the percent of strontium oxide (SrO) asfollows:SrO, % 5 P 3 0.56416!/S 3 100where:P = SrSO4precipitate, g, andS = pigment specimen, g.

20、0.56416 5molecular weight of SrOmolecular weight of SrSO45103.63163.7010. Precision10.1 Within LaboratoryThe usual difference between du-plicate runs performed by the same analyst is approximately0.2 % of the SrO content of the pigment tested.10.2 Between LaboratoriesThe average difference be-tween

21、two determinations performed by different analysts indifferent laboratories is approximately 0.5 % of the SrOcontent of the pigment tested.CHROMIUM BY THE THIOSULFATE METHOD11. Reagents11.1 Hydrochloric Acid (1+5)Mix 1 volume of concen-trated hydrochloric acid (HCl, sp gr 1.19) with 5 volumes ofwate

22、r.11.2 Potassium Iodide Solution (150 g per L)Dissolve150 g of potassium iodide (KI) in water and dilute to 1 L.11.3 Sodium Thiosulfate Standard Solution (0.1 N)Dissolve 24.8 g of reagent grade Na2S2O35H2O in recentlyboiled water and dilute to 1 L with additional recently boiledwater. To standardize

23、, pipet 25 mL of the standard potassiumdichromate solution (exactly 0.1000 N) into a 250-mL Erlen-meyer flask. Add 100 mL of water, 15 mL of potassium iodidesolution, and 15 mL of concentrated hydrochloric acid (sp gr1.19). Titrate the liberated iodine with sodium thiosulfatesolution until the reddi

24、sh-brown color becomes quite faint.Add5 mL of starch solution and continue the titration dropwiseuntil the blue color changes to a pale green. Calculate thenormality of the sodium thiosulfate solution as follows:N 52.5000Mwhere:N = normality, andM = sodium thiosulfate solution, g.11.4 Starch Indicat

25、or SolutionMake a homogenous pasteof 10 g of soluble starch in cold water. Add to this 1 L ofboiling water, stir rapidly, and cool. Salicylic acid (1.25 g/L)may be added to preserve the indicator. If long storage isrequired, the solution should be kept in a refrigerator at 4 to10C (40 to 50F). Prepa

26、re fresh indicator when the end pointof the titration from blue to colorless or blue to light green failsto be sharp.12. Procedure12.1 Weigh accurately approximately 0.2 g of the sampleinto a 250-mL iodine flask. Add 50 mL of water and 50 mL ofHCl (1 + 5); swirl the flask to complete solution.Add 20

27、 mL ofKI solution and allow the solution to stand for several minutes.12.2 Titrate the liberated iodine with 0.1 N Na2S2O3solu-tion until the reddish brown iodine color becomes faint. Add 1mL of starch solution and continue the titration cautiously tothe end point which is easily discernible when th

28、e colorchanges from blue to a light green with no blue tinge.13. Calculation13.1 Calculate the percent of chromium as chromic oxide(CrO3) as follows:CrO3,%5 VN 3 0.03334!/S 3 100where:V =Na2S2O3solution required for titration of specimen,mL,N = normality of the Na2S2O3solution, andS = sample used, g

29、.14. Precision and Bias14.1 Within LaboratoriesThe usual difference betweenduplicate runs performed by the same analyst is approximately0.3 % of the CrO3content of the pigment tested.14.2 Between LaboratoriesThe average difference be-tween two determinations performed by different analysts indiffere

30、nt laboratories is approximately 0.5 % of the CrO3content of the pigment tested.D 1845 86 (2003)20.0334 5molecular weight CrO21000 3 3 volume!599.991000 3 35 milliequivalent weightCHLORIDE CONTENT15. Procedure15.1 Determine the chloride content in accordance with TestMethods D 444.SULFATE CONTENT16.

31、 Procedure16.1 Determine the sulfate content in accordance with theTest Methods D 444.MOISTURE AND OTHER VOLATILE MATTER17. Procedure17.1 Determine moisture and other volatile matter in accor-dance with Method A of Test Methods D 280.COARSE PARTICLES18. Procedure18.1 Determine the percentage of coar

32、se particles in thepigment as received in accordance with Test Methods D 185.MASS COLOR AND TINTING STRENGTH19. Procedure19.1 Determine mass color and tinting strength in accor-dance with Test Method D 387.20. Keywords20.1 chromium; strontium chromate pigment; thiosulfatemethodASTM International tak

33、es no position 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 re

34、sponsibility.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 additional standardsand should be addres

35、sed to ASTM International Headquarters. Your comments will receive careful consideration 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 th

36、e address shown below.This standard is copyrighted by ASTM International, 100 Barr 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).D 1845 86 (2003)3