ASTM D715-1986(2014) Standard Test Methods for Analysis of Barium Sulfate Pigment《分析硫酸钡颜料的标准试验方法》.pdf

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1、Designation: D715 86 (Reapproved 2014)Standard Test Methods forAnalysis of Barium Sulfate Pigment1This standard is issued under the fixed designation D715; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision.

2、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 These test methods cover the analysis of barium sulfatepigment.1.2 The values stated in SI units are to be regarded as thestandard. T

3、he values given in parentheses are for informationonly.1.3 This standard does not purport to address the safetyconcerns associated with its use. It is the responsibility of theuser of this standard to establish appropriate safety and healthpractices and determine the applicability of regulatory limi

4、ta-tions prior to use.2. Referenced Documents2.1 ASTM Standards:2D185 Test Methods for Coarse Particles in PigmentsD280 Test Methods for Hygroscopic Moisture (and OtherMatter Volatile Under the Test Conditions) in PigmentsD1193 Specification for Reagent WaterD1208 Test Methods for Common Properties

5、of CertainPigmentsE832 Specification for Laboratory Filter Papers3. Significance and Use3.1 These test methods are used to determine the purity ofbarium sulfate and to determine the concentration of knownimpurities. This information is useful to producers and users asan aid in the manufacture of coa

6、tings.4. Purity of Reagents4.1 Reagent grade chemicals shall be used in all tests.Unless otherwise indicated, it is intended that all reagents shallconform to the specifications of the Committee on AnalyticalReagents of the American Chemical Society, where suchspecifications are available.3Other gra

7、des 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 determination.4.2 Unless otherwise indicated, references to water shall beunderstood to mean reagent water conforming to Type II ofSpecification D1

8、193.BARIUM SULFATE5. Reagents5.1 Ammonium Hydroxide (sp gr 0.90)Concentrated am-monium hydroxide (NH4OH).5.2 Ammonium Sulfate (NH4)2SO4).5.3 Hydrochloric Acid (sp gr 1.19)Concentrated hydro-chloric acid (HCl).5.4 Hydrochloric Acid (1+1)Mix equal volumes of con-centrated HCl (sp gr 1.19) and water.5.

9、5 Methyl Red Indicator SolutionDissolve 0.2 g ofmethyl red in 100 mL of methanol, ethanol, or isopropanol.5.6 Sodium Carbonate Solution (30 g/L)Dissolve 30 g ofNa2CO3in water and dilute to 1 L.6. Procedure6.1 Weigh to 0.1 mg approximately 0.5 g of the sample intoa platinum crucible, add3gofNa2CO3, m

10、ix thoroughly, andfuse until the melt is clear. Allow the melt to cool and thenleach in a platinum dish with hot water until it is entirelydisintegrated. Filter on a close-texture paper and wash thor-oughly with hot Na2CO3solution (30 g/L).6.2 Transfer the filter paper containing the insoluble carbo

11、n-ates to a 250-mL beaker and acidify with concentrated HCl (spgr 1.19). Wash the fusion crucible with HCl (sp gr 1.19) so thatno barium is lost. Boil the solution, filter into a 600-mL beaker,and wash well with water. Add methyl red indicator solution,1These test methods are under the jurisdiction

12、of ASTM Committee D01 onPaint and Related Coatings, Materials, and Applications and are the directresponsibility of Committee D01.31 on Pigment Specifications.Current edition approved Dec. 1, 2014. Published December 2014. Originallyapproved in 1943. Last previous edition approved in 2008 as D715 86

13、 (2008).DOI: 10.1520/D0715-86R14.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Reagent Chemicals, American

14、 Chemical Society Specifications, AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents notlisted by the American Chemical Society, see Analar Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.

15、S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States1and add NH4OH (sp gr 0.90) until the solution is slightlyalkaline. Add 6 mL of HCl (1+1), and dilute to 300 mL.6.3 Heat the solutio

16、n to boiling, and add5gof(NH4)2SO4dissolved in 40 mL of water. If low-grade material is beinganalyzed, the (NH4)2SO4solution should be added drop bydrop from a buret to minimize inclusion. If the barytes is arather pure product (95 to 99 % BaSO4), this is not necessary,since the only nonvolatile con

17、stituents of the solution will bebarium salts. Allow the precipitate of BaSO4to digest for 4 hor overnight, and filter through a close-texture paper. Wash theprecipitate with as little cold water as possible (consistent withthe purity of the precipitate), ignite in an oxidizing atmosphere,and weigh

18、as BaSO4.7. Calculation7.1 Calculate the percent of BaSO4as follows:BaSO4,%5P/S1!3100 (1)where:P = BaSO4,g,andS1= sample used, g.FERRIC OXIDE8. Apparatus8.1 Colorimetric ApparatusNessler type or other similar100-mL colorimetric tubes.9. Reagents9.1 Ammonium Thiocyanate Solution (76.1 g/L)Dissolve76

19、g of ammonium thiocyanate (NH4CNS) in water and diluteto1L.9.2 Iron, Standard Solution (100 mL = 0.00002 g Fe)Dilute and divide a ferric solution of known iron content so asto obtain 0.4 mg of iron. Dilute the solution to 2 L with watercontaining 200 mL of iron-free H2SO4.9.3 Potassium Permanganate

20、Solution (0.1 g/L)Dissolve0.1 g of potassium permanganate (KMnO4) in water and diluteto1L.9.4 Standard Color SolutionMix thoroughly 10 parts byvolume of NH4CNS and 90 parts by volume of standard ironsolution (100 mL = 0.02 mg Fe). One hundred millilitres of thesolution will thus contain 0.000018 mg

21、of Fe.9.5 Sulfuric Acid (sp gr 1.84)Concentrated sulfuric acid(H2SO4).9.6 Sulfuric Acid (1+1)Carefully mix 1 volume of con-centrated H2SO4(sp gr 1.84) with 1 volume of water.10. Procedure10.1 Dissolve the soluble portion of a 1-g specimen inH2SO4(1+1), filter, and wash, keeping the volume of thesolu

22、tion under 100 mL. Oxidize any iron present in the filtrateby adding potassium permanganate (KMnO4) until a faint pinkcolor is obtained. Dilute the solution to 100 mL and pour intoa buret graduated in 0.1-mL divisions.10.2 Pour 100 mL of the standard color solution into a100-mL colorimetric tube. In

23、to a second colorimetric tube pour10 mL of concentrated H2SO4(sp gr 1.84) and 10 mL ofNH4CNS, dilute to 60 or 70 mL and then add the test solutionfrom the buret until the depth of color thus produced ondilution to 100 mLexactly matches that of the standard. Recordthe number of millilitres required.1

24、1. Calculation11.1 Calculate the percent of Fe2O3as follows:Fe2O3,%5 I 31.4298!/S2# 3100 (2)where:I = iron in standard, g,1.4298 =Fe2O3Fe25159.694111.694, andS2= sample used, g.HYDROGEN ION CONCENTRATION12. Procedure12.1 Determine the pH in accordance with Test MethodsD1208.MATTER SOLUBLE IN WATER13

25、. Procedure13.1 Determine the amount of water soluble material pres-ent in accordance with Test Methods D1208.MOISTURE AND OTHER VOLATILE MATTER14. Procedure14.1 Determine the moisture and other volatile matter inaccordance with Test Methods D280.COARSE PARTICLES(Total Residue Retained on No. 325 (4

26、5-m)Sieve)15. Procedure15.1 Determine the coarse particles in accordance with TestMethods D185.FREE SILICA16. Reagent16.1 Heavy Liquid (sp gr 2.9)Dissolve 4 parts by weightof potassium iodide (KI) in 6 parts of warm water, and add,while stirring constantly, 5 parts of mercuric iodide (HgI2).Evaporat

27、e over a hot plate or gas flame, protected by screencloth, until a light crystalline scum forms. Cool, and filterthrough heavy paper. The solution will be a clear, deep, ambercolor of about 3.2 specific gravity. All filter washings showinga yellow color should be saved and evaporated. Determine the3

28、.2 specific gravity accurately by means of a specific gravitybottle, and correct the solution to a specific gravity of 2.9 atroom temperature by adding water. Prepare approximately 200mL of the solution.17. Procedure17.1 Carefully weigh 10 g of the finely ground dry bariumsulfate pigment and transfe

29、r to a carefully dried 125-mL clearD715 86 (2014)2glass separatory funnel of the long narrow type. Add 100 mLof the heavy liquid (sp gr 2.9), stopper, and shake well toliberate any air bubbles that might adhere to the particles, andalso to break up all agglomerates. Set the separatory funnelaside an

30、d allow to stand in a perpendicular position for 2 h, orfor a sufficient time for the particles to rise or sink.17.2 Draw off the heavy particles through the stopcock intoa beaker along with 75 mL of the liquid. Add 50 mL of freshheavy liquid (sp gr 2.9) to the float particles and liquidremaining in

31、 the separatory funnel and repeat the procedure asdescribed in 17.1.17.3 Draw off the heavy particles along with 75 mL of theliquid and add to those drawn off in accordance with 17.1,leaving the float particles in the funnel. Wash the particlesremaining in the funnel with fresh heavy liquid (sp gr 2

32、.9),filter through a No. 2/0 paper (see Specification E832), andwash free of solution with warm water.17.4 Transfer the filter paper and silica to an ignition cup,dry, and ignite carefully in an electric furnace or over a flameto keep mechanical loss at a minimum. Weigh the floatedmaterial, and tran

33、sfer to a tared platinum dish or crucible. Add20 mL of hydrofluoric acid (HF) and 3 drops of H2SO4(1+1),evaporate to dryness, and ignite carefully to expel all fumes.Cool and weigh. The loss in weight represents the free silica inthe floated material.18. Calculation18.1 Calculate the percent of free

34、 SiO2as follows:Free SiO2,%5 A/S3! 3100 (3)where:A = SiO2,g,andS3= sample used, g.19. Precision and Bias19.1 The precision and bias of these test methods has notbeen determined.20. Keywords20.1 analysis of pigment; barium sulfate; barium sulfatecontent; barium sulfate pigment; ferric oxide in barium

35、 sulfate;free silica in barium sulfateASTM International takes 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 r

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38、e your views known to the ASTM Committee on Standards, at the 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 b

39、y 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 Copyright Clearance Center, 222Rosewood Drive, Danvers, MA 01923, Tel: (978) 646-2600; http:/ 86 (2014)3