ASTM D3989-2001(2012) Standard Test Method for Total Rare Earth Metals in Paint Driers by EDTA Method《用EDTA法对涂料催干剂中稀土金属总量测定的标准试验方法》.pdf

《ASTM D3989-2001(2012) Standard Test Method for Total Rare Earth Metals in Paint Driers by EDTA Method《用EDTA法对涂料催干剂中稀土金属总量测定的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D3989-2001(2012) Standard Test Method for Total Rare Earth Metals in Paint Driers by EDTA Method《用EDTA法对涂料催干剂中稀土金属总量测定的标准试验方法》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D3989 01 (Reapproved 2012)Standard Test Method forTotal Rare Earth Metals in Paint Driers by EDTA Method1This standard is issued under the fixed designation D3989; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the ye

2、ar 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 test method covers the titrimetric determination ofrare earth metals in liquid rare earth metal driers and

3、utilizesthe disodium salt of ethylenediaminetetraacetic acid dihydrate(EDTA).1.2 This test method is limited to the determination of therare earth metal content of a liquid rare earth metal drier thatdoes not contain other drier elements. The method is notapplicable to drier blends.1.3 This test met

4、hod has been tested in concentrations of6 % cerium and 6 % rare earth metals, but there is no reason tobelieve that it is not suitable for higher or lower drier metalconcentrations provided specimen size is adjusted accordingly.1.4 The values stated in SI units are to be regarded as thestandard. The

5、 values given in parentheses are for informationonly.1.5 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 standard to establish appro-priate safety and health practices and determine the applica-bility o

6、f regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D600 Specification for Liquid Paint DriersD1193 Specification for Reagent WaterE180 Practice for Determining the Precision of ASTMMethods for Analysis and Testing of Industrial and Spe-cialty Chemicals (Withdrawn 2009)3

7、E300 Practice for Sampling Industrial Chemicals3. Summary of Test Method3.1 A diluted solution of the drier is complexed with anexcess of EDTA, the pH adjusted to 5.0, and then titrated withzinc chloride solution to a xylenol orange end point.4. Significance and Use4.1 This test method may be used t

8、o confirm the statedcontent of a pure, liquid rare earth metal drier manufactured foruse in the coatings industry.5. Interferences5.1 Calcium does not interfere at low pH.5.2 All other cations that can be titrated with EDTAin acidicmedia will interfere and must not be present in the drier.6. Reagent

9、s6.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical Society,where such specifications are available.4Other grades ma

10、y beused, provided it is first ascertained that the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of the determination.6.2 Purity of WaterUnless otherwise indicated, referenceto water shall be understood to mean reagent water conformingto Type II of Specificat

11、ion D1193.6.3 Ammonium ChlorideAmmonium Hydroxide BufferSolutionAdd 350 mL of concentrated ammonium hydroxide(NH4OH) to 54 g of ammonium chloride (NH4Cl), and diluteto 1 L with water.6.4 Ammonium Hydroxide (NH4OH), (1+1).6.5 Ascorbic Acid.6.6 Eriochrome Black T IndicatorMix and grind thor-oughly in

12、a mortar a mixture of 0.2 g of Eriochrome Black T1This test method is under the jurisdiction of ASTM Committee D01 on Paintand Related Coatings, Materials, andApplications and is the direct responsibility ofSubcommittee D01.21 on Chemical Analysis of Paints and Paint Materials.Current edition approv

13、ed June 1, 2012. Published July 2012. Originally approvedin 1981. Last previous edition approved in 2006 as D3989 01 (2006). DOI:10.1520/D3989-01R12.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStanda

14、rds volume information, refer to the standards Document Summary page onthe ASTM website.3The last approved version of this historical standard is referenced onwww.astm.org.4Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For suggestions on the t

15、esting 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.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.Copyright ASTM International, 100 Barr Harbor

16、 Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States1and 100 g of sodium chloride. Store the mixture in a tightlystoppered bottle where it is stable indefinitely.6.7 EDTA, Standard Solution (0.01 M)Weigh about 3.73 gof disodium salt of ethylenediaminetetraacetic acid dihydrateto the

17、nearest 0.01 g, dissolve in water, and dilute to approxi-mately 1 L in a glass-stoppered bottle.6.8 Hydrochloric Acid (HCL), (1+1).6.9 Isopropyl Alcohol (99.5 %).6.10 Sodium Acetate-Acetic Acid Buffer SolutionDissolve82 g of sodium acetate in water and dilute to 1 L.Adjust pH to5.0 with glacial acet

18、ic acid using a pH meter.6.11 Xylenol Orange IndicatorDissolve 0.2 g in 100 mLof water. Prepare fresh daily as required.6.12 Zinc Chloride Solution, Standard (0.01 M)Weighabout 0.65 g of zinc ribbon (Note 1) to the nearest 5 mg on aglazed paper. Transfer to a 1-Lvolumetric flask and add 25 mLof dilu

19、te hydrochloric acid (1 + 3). Warm if necessary on asteam bath to dissolve the material completely. Cool, dilute tothe mark with water, and mix thoroughly.NOTE 1Store the zinc ribbon in a tight container to prevent the surfaceof the zinc from oxidizing.7. Sampling7.1 Take a small sample of liquid dr

20、ier from bulk using theprocedure in Practice E300 appropriate for the size of thecontainer, Section 19 for tanks and tank cars or Section 23 fordrums and cans.NOTE 2Liquid driers are normally homogeneous so that only simplephysical tests, such as specific gravity or solids content, on top and bottom

21、samples from tanks are required to confirm that separation has notoccurred. Agitate the drums in accordance with the section on ThiefSampling of Practice E300.7.2 Examine the sample of drier for sediment or suspendedmatter which if present is evidence of noncompliance with thesection on Chemical and

22、 Physical Requirements of Specifica-tion D600.7.3 If the sample is homogeneous keep it in a stopperedvessel to prevent solvent evaporation prior to analysis.8. Standardization8.1 Zinc Chloride Solution, Standard (0.01 M)Calculatethe molarity, M1, of the zinc chloride (ZnCl2) solution asfollows:M15 S

23、1/65.37 (1)where:M1= molarity of ZnCl2solution,S1= grams of zinc used, and65.37 = grams of zinc per litre to producea1Msolution.8.2 EDTA Solution, Standard (0.01 M)Transfer 40.00 mLof this solution from a buret into a 250-mL assay beaker orwide-mouth flask. Add 50 mL of isopropyl alcohol, 10 mL ofam

24、monium chloride-ammonium hydroxide buffer solution, andabout 0.2 g of Eriochrome Black T indicator mixture (Note 3).Mix thoroughly by swirling. Titrate with the standard ZnCl2solution to the first permanent appearance of a red color.NOTE 3If the end point is overstepped, add 1.0 mL of the EDTAsoluti

25、on to the mixture and titrate again with standard ZnCl2solution. Usetotal volume of each solution for the calculation.8.2.1 Calculate the molarity, M2, of the EDTA solution asfollows:M25 V1M1/V2(2)where:V1= volume of ZnCl2solution, mL,M1= molarity of ZnCl2solution,V2= volume of EDTA solution, mL, an

26、dM2= molarity of EDTA solution.9. Procedure9.1 Check the clarity of the drier. If not clear, centrifuge aportion of the sample until it is clear, keeping the centrifugetube stoppered to prevent solvent evaporation.9.2 Place a few grams of the drier in a 50-mL Erlenmeyerflask fitted with a cork, thro

27、ugh which passes a dropping tubeand a rubber bulb (or medicine dropper) and obtain the totalweight. Into a 400-mL beaker weigh by difference to thenearest 0.5 mg the following specimen sizes: (a) 0.5 to 0.7 gfor 6 % rare earth metals or cerium, (b) 0.25 to 0.35 g for 12 %rare earth metals, and (c) p

28、roportionate amounts for more orless rare earth metals or cerium.9.3 Add about 5 mL of isopropyl alcohol and 2 mL of diluteHCl. Warm on a hot plate until the specimen dissolves.9.4 While still warm, add 0.4 to 0.5 g of ascorbic acid toreduce Ce (IV) and warm until any yellow color disappears.Add 70

29、mL of isopropyl alcohol and 40.0 mL of EDTAsolution.9.5 Place on the magnetic stirrer and add a stirring bar andthe electrodes from the pH meter. Adjust the pH to approxi-mately 4.0 with 1 + 1 NH4OH, add 25 mL of sodium acetatebuffer, and adjust pH to 5.0 with 1 + 1 NH4OH or 1 + 1 HCl.9.6 Add approx

30、imately 1 mLof xylenol orange solution andtitrate with standardized zinc chloride solution from a yellow toorange end point.NOTE 4Use a good titration light to assist in detecting the end point.10. Calculation10.1 Calculate the percent total rare earth metals, T, presentas follows:T 5 V3M22 V4M1!14.

31、0/S2(3)where:V3= volume of EDTA solution, mL,M2= molarity of EDTA solution,V4= volume of ZnCl2solution, mL,M1= molarity of ZnCl2solution,14.0 = millimolar weight of rare earth metals 100, andD3989 01 (2012)2S2= grams of specimen used.11. Precision and Bias511.1 PrecisionThe precision estimates are b

32、ased on aninterlaboratory study in which one operator in five differentlaboratories analyzed in duplicate on two different dayssamples of 6 % rare earth metal drier and 6 % cerium drier.Thedriers were commercially supplied. The results were analyzedstatistically in accordance with Practice E180 and

33、the within-laboratory coefficient of variation was found to be 0.4 %relative at 10 df and the between-laboratory coefficient ofvariation was 1.6 % relative at 8 df. Based on these coeffi-cients, the following criteria should be used for judging theacceptability of results at the 95 % confidence leve

34、l:11.1.1 RepeatabilityTwo results, each the mean of dupli-cate determinations, obtained by the same operator on differentdays should be considered suspect if they differ by more than1.25 % relative.11.1.2 ReproducibilityTwo results, each the mean of du-plicate determinations, obtained by operators i

35、n different labo-ratories should be considered suspect if they differ by morethan 5.3 % relative.11.2 BiasBias cannot be determined because there are noaccepted standards for rare earth metals in paint driers.12. Keywords12.1 analysis rare earth drier; EDTA; paint driersASTM International takes no p

36、osition 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 responsib

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38、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 the addre

39、ss 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), 6

40、10-832-9555 (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/).5Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Research Report RR:D01-1030.D3989 01 (2012)3