1、Designation: D 3988 05Standard Test Method forVanadium in Paint Driers by EDTA Method1This standard is issued under the fixed designation D 3988; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number i
2、n parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers the titrimetric determination ofvanadium in liquid vanadium driers and utilizes the disodiumsalt of ethylenediaminetet
3、raacetic acid dihydrate (EDTA).1.2 This test method is limited to the determination of thevanadium content of a liquid vanadium drier that does notcontain other drier elements. This test method is not applicableto drier blends.1.3 All cations that can be titrated with EDTA in alkalinemedia interfere
4、 and must not be present in the sample.1.4 This test method has been tested for concentrations of 3and 4 % vanadium, but there is no reason to believe that it isnot suitable for higher or lower vanadium concentrationsprovided specimen size is adjusted proportionately.1.5 The values stated in SI unit
5、s are to be regarded as thestandard. The values given in parentheses are for informationonly.1.6 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 prac
6、tices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D 600 Specification for Liquid Paint DriersD 1193 Specification for Reagent WaterE 180 Practice for Determining the Precision of ASTMMethods for Analysis and Testing of Industrial
7、 ChemicalsE 300 Practice for Sampling Industrial Chemicals3. Summary of Test Method3.1 The amount of vanadium drier used in oxidizing-typecoatings significantly affects their drying properties. The vana-dium drier is acidified and heated to make the vanadiumavailable for chelation with EDTA. It is t
8、hen chelated, the pHadjusted, and the excess titrated with zinc chloride solution,using Eriochrome Black T as the indicator.4. Significance and Use4.1 This test method may be used to confirm the statedcontent of a pure liquid vanadium drier manufactured for useby the coatings industry.5. Apparatus5.
9、1 Centrifuge, capable of developing 1000 to 2000 g.6. Reagents6.1 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 Soc
10、iety,where such specifications are available.3Other grades may 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 unders
11、tood to mean reagent water conformingto Type II of Specification D 1193.6.3 Ammonium Hydroxide (sp gr 0.90)Concentrated am-monium hydroxide (NH4OH).6.4 Ascorbic Acid.6.5 Buffer SolutionAdd 350 mL of concentrated NH4OHto 54 g of ammonium chloride and dilute to 1 L with water.6.6 Eriochrome Black T In
12、dicatorMix and grind thor-oughly in a mortar a mixture of 0.2 g of Eriochrome Black Tand 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 3.73g of EDTA to the nearest 0.01 g, dissolve in water, an
13、d diluteto approximately 1 L in a glass-stoppered bottle.6.8 Hydrochloric Acid (sp gr 1.19)Concentrated hydro-chloric acid (HCl).1This test method is under the jurisdiction of ASTM Committee D01 on Paintand Related Coatings, Materials, and Applications and is the direct responsibility ofSubcommittee
14、 D01.21 on Chemical Analysis of Paints and Paint Materials.Current edition approved Jan. 1, 2005. Published February 2005. Originallyapproved in 1981. Last previous edition approved in 1999 as D 3988 85 (1999).2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Custo
15、mer 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 notl
16、isted 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, W
17、est Conshohocken, PA 19428-2959, United States.6.9 Isopropyl Alcohol, 99.5 %.6.10 Zinc Chloride, Standard Solution (ZnCl2) (0.01 M)Weigh about 0.65 g of zinc (Note 1) to 5 mg. Transfer to a 1-Lvolumetric flask, and add 25 mL of dilute hydrochloric acid(1 + 3). Warm if necessary on a steam bath to di
18、ssolve thematerial completely. Cool, dilute to the mark with water andmix thoroughly.NOTE 1Store the zinc ribbon in a tightly closed container to preventthe surface of the zinc from oxidizing.7. Sampling7.1 Take a small sample of liquid drier from bulk using theprocedure in Practice E 300 appropriat
19、e for the size of thecontainer: section on Bottle Sampling for tanks and tank cars,or section on Tube Sampling for drums and cans.NOTE 2Liquid driers are normally homogeneous so that only simplephysical tests, such as specific gravity or solids content, on top and bottomsamples from tanks, are requi
20、red to confirm that separation has notoccurred. Agitate the drums in accordance with the section on TubeSampling of Practice E 300.7.2 Examine the sample of drier for sediment or suspendedmatter which, if present, is evidence of noncompliance withSpecification D 600.7.3 If the sample is homogeneous
21、keep it in a stopperedvessel to prevent solvent evaporation prior to analysis.8. Standardization8.1 Zinc Chloride, Standard Solution (0.01 M)Calculatethe molarity, M1as follows:M15 S1/65.37 (1)where:S1= zinc used, g, and65.37 = zinc to producea1Msolution, g/L.8.2 EDTA, Standard Solution (0.01 M)Tran
22、sfer 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 ofbuffer solution, and about 0.2 g of indicator mixture. Mixthoroughly by swirling. Titrate with the standard ZnCl2solu-tion to the first permanent appearance of a red colo
23、r.NOTE 3If the end point is overstepped, add 1.0 mL of the EDTAsolution to the mixture and titrate again with standard ZnCl2solution. Usetotal volume of each solution for the calculation.8.2.1 Calculate the molarity of the EDTA solution, M2,asfollows:M25 V1M1/V2(2)where:V1= volume of ZnCl2solution,
24、mL,M1= molarity of ZnCl2solution, andV2= volume of EDTA solution, mL.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 Er
25、lenmeyerflask fitted with a cork through which passes a dropping tubeand rubber bulb (or eye dropper) and obtain the total weight.Weigh by difference to 0.5 mg two or three 0.18 to 0.22-gspecimens into 250-mL wide-mouth flasks.NOTE 4This is the correct specimen weight range for a vanadiumdrier conta
26、ining 3 to 6 % of vanadium (16 to 24 mL of standard 0.01 MZnCl2solution is required for the titration).9.3 Add to each flask, 15 mL of isopropyl alcohol and 1.0mL of concentrated HCl. Boil the solutions (use a steam bathif possible, and boiling aids) gently for 5 min, then cool for 5to 10 min in a c
27、old water bath (Note 5). Add 35 mL more ofisopropyl alcohol to each flask.NOTE 5Boiling with HCl converts, bi-, tri-, and tetravalent vanadiumto the relativity stable vanadyl ion, VO+. The latter chelates with EDTAina1to1molar ratio as do other metallic ions.9.4 From a buret, measure 40.0 mL of EDTA
28、 solution intoeach flask. Add 0.1 g of ascorbic acid (solution should be blue)and swirl to dissolve (Note 6). Add 15 to 20 mL of buffersolution and about 0.3 g of indicator mixture (Note 7). Mixthoroughly by swirling.NOTE 6Ascorbic acid, a reducing agent, is added to reduce anymetavanadate ion, VO3+
29、, to vanadyl ion, VO+.NOTE 7The amounts of ascorbic acid and indicator mixture are notcritical. With a little experience, these may be added from the tip of aspatula.9.5 Titrate with standard ZnCl2solution to the first perma-nent tinge of red (see Note 8 and Note 9). Maintain vigorousswirling during
30、 the titration to ensure thorough mixing of thetwo phases that may appear.NOTE 8The color change at the end point is from blue to blue with ared tinge. Adding more ZnCl2solution gives a violet color.NOTE 9Use a good titration light to assist in detecting the end point.10. Calculation10.1 Calculate t
31、he percent of the vanadium present, A,asfollows:A 5V3M22 V4M1! 5.10S2(3)where:V3= volume of EDTA solution, mL,M2= molarity of EDTA solution,V4= volume of ZnCl2solution, mL,M1= molarity of ZnCl2solution,5.10 = millimolar weight of vanadium 3 100, andS2= specimen used, g.11. Precision411.1 The precisi
32、on estimates are based on an interlaboratorystudy in which one operator in five different laboratoriesanalyzed in duplicate on two different days two samples ofvanadium drier containing 3 and 4 % vanadium. The vanadiumdrier was commercially supplied. The results were analyzedstatistically in accorda
33、nce with Practice E 180 and the within-laboratory standard deviation was found to be 0.025 % vana-dium at 9 df and the between-laboratory standard deviation4Supporting data are available from ASTM International Headquarters. RequestRR: D01-1029.D39880520.07 % vanadium at 7 df. Based on these standar
34、d deviations,the following criteria should be used for judging the accept-ability of results at the 95 % confidence level: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 th
35、an0.08 % absolute at concentrations of 3 to 4 % vanadium.11.1.2 ReproducibilityTwo results, each the mean of du-plicate determinations, obtained by operators in different labo-ratories should be considered suspect if they differ by morethan 0.22 % absolute at concentrations of 3 to 4 % vanadium.12.
36、Bias12.1 Bias cannot be determined for this method becausethere are no accepted standards for vanadium in paint driers.13. Keywords13.1 EDTA-analysis; liquid drier; paint driers; vanadiumdrierASTM International takes no position respecting the validity of any patent rights asserted in connection wit
37、h 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 techn
38、ical 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 considerati
39、on 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 Barr Har
40、bor 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).D3988053
