ASTM D2086-2008 Standard Test Method for Acidity in Vinyl Acetate and Acetaldehyde《乙酸基乙烯脂和乙醛的酸度标准试验方法》.pdf

1、Designation: D 2086 08Standard Test Method forAcidity in Vinyl Acetate and Acetaldehyde1This standard is issued under the fixed designation D 2086; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number

2、 in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope*1.1 This test method covers the determination of totalacidity as acetic acid in refined vinyl acetate and acetaldehyde.1.2 The values stated in

3、SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.3 For purposes of determining conformance of an ob-served value or a calculated value using this test method torelevant specifications, test result(s) shall be rounded off “tothe nearest unit” in the

4、 last right-hand digit used in expressingthe specification limit, in accordance with the rounding-offmethod of Practice E29.1.4 For hazard information and guidance, see the suppliersMaterial Safety Data Sheet.1.5 This standard does not purport to address all of thesafety concerns, if any, associated

5、 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 of regulatory limitations prior to use. For specific hazardstatements, see Section 8.2. Referenced Documents2.1 ASTM Standards:2D 1193 Specificat

6、ion for Reagent WaterE29 Practice for Using Significant Digits in Test Data toDetermine Conformance with SpecificationsE 200 Practice for Preparation, Standardization, and Stor-age of Standard and Reagent Solutions for ChemicalAnalysis3. Summary of Test Method3.1 The specimen is mixed with either an

7、 equal volume ofchilled water or an equal volume of ethyl alcohol and titratedat reduced temperature with aqueous sodium hydroxide solu-tion to a phenolphthalein end point.4. Significance and Use4.1 This test method provides a measurement of total acidityin vinyl acetate and acetaldehyde. The result

8、s of these mea-surements can be used for specification acceptance.5. Interferences5.1 Any material or contaminant that will react with NaOHunder the test conditions will affect the results.5.2 Vinyl acetate will decompose on storage, typically byway of hydrolysis, to form acetic acid.5.3 Acetaldehyd

9、e will react with oxygen, either dissolved orin a storage container, to form acetic acid.5.4 Various acids or other acidic materials may be present.Common practice, including the method used here, calculatesthese as acetic acid. The actual weight percent of acidicmaterials may be different.6. Appara

10、tus6.1 Buret, 10-mL, graduated in 0.05-mL subdivisions.6.2 Erlenmeyer Flask, 250-mL capacity.6.3 Graduated Cylinder, 50 or 100-mL capacity.6.4 Cold Bath, maintained at 0C or below.7. Reagents7.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is in

11、tended thatall reagents shall conform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical Society,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 wi

12、thout lessening theaccuracy of the determination.7.2 Purity of WaterUnless otherwise indicated, referencesto water shall be understood to mean reagent water as definedby Type IV or higher purity of Specification D 1193.7.3 Ethyl Alcohol (Ethanol), 95 volume %, minimum.NOTE 1Denatured ethyl alcohol c

13、onforming to Formula No. 3Aof the1This test method is under the jurisdiction of ASTM Committee D01 on Paintand Related Coatings, Materials, and Applications and is the direct responsibility ofSubcommittee D01.35 on Solvents, Plasticizers, and Chemical Intermediates.Current edition approved Nov. 1, 2

14、008. Published November 2008. Originallyapproved in 1962. Last previous edition approved in 2003 as D 2086 03.2For 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 st

15、andards Document Summary page onthe ASTM website.3Reagent Chemicals, American 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., Pool

16、e, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.1*A Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, U

17、nited States.U.S. Bureau of Alcohol, Tobacco and Firearms is suitable for use as asolvent.7.4 Phenolphthalein Indicator Solution (10 g/L)Dissolve1 g of phenolphthalein in 100 mL of methanol, ethanol, orisopropanol.7.5 Sodium Hydroxide, Standard Solution (0.05 N)Prepare and standardize a 0.05 N sodiu

18、m hydroxide (NaOH)solution (Note 2) in accordance with the Sodium HydroxideSolution sections of Practice E 200.NOTE 2Alternatively, potassium hydroxide (KOH) solution may beused.7.6 Bromothymol Blue Indicator (10g/L)Dissolve1gofbromothymol blue in 100 mL of methanol, ethanol, or isopro-panol.7.7 Sod

19、ium Hydroxide, Standard Solution (0.02 N)Prepare and standardize a 0.02 N sodium hydroxide (NaOH)solution (Note 3) in accordance with the Sodium HydroxideSolution sections of Practice E 200.NOTE 3Alternatively, potassium hydroxide (KOH) solution may beused. If the titration solution becomes cloudy d

20、ue to water saturationduring titrations, 0.02 N alcoholic KOH may be used as the titrant.8. Hazards8.1 Vinyl acetate and acetaldehyde are flammable andhazardous as their vapors form explosive mixtures with air.8.2 Acetaldehyde boils at 21C; therefore, store in pressurecontainers or refrigerate if ke

21、pt in glass containers. Wear safetygoggles or a full face shield when handling acetaldehyde.9. Procedure for Vinyl Acetate (Warningsee Section 8)9.1 If a solvent is to be utilized, add 50 mL of ethanol oranhydrous methanol. Alternatively, the vinyl acetate may betitrated neat.9.2 If a solvent is uti

22、lized, add 0.5 mL bromothymol blueindicator to the solvent and titrate with 0.02 N NaOH solutionto the first blue color.9.3 Add 50 mL of the specimen from a graduated cylinderand cool the solution to approximately 0C in a cold bath(alternatively, chill in refrigerator for 15 min. If a solvent is not

23、used and the indicator was not added in 9.2, add 0.5 mL ofbromothymol blue indicator. The solution may be purged toremove any absorbed carbon dioxide.9.4 Titrate with the 0.02 N NaOH solution to the blue color.10. Procedure for Acetaldehyde (Warningsee Section 8)10.1 Measure into a 250-mL Erlenmeyer

24、 flask 50 mL ofwater and add sufficient crushed ice (prepared from reagentwater) so that some ice will remain at the end of thedetermination.NOTE 4Titration at low temperature avoids interference and is re-quired because of the low boiling point of acetaldehyde.10.2 Add 0.5 mL of phenolphthalein ind

25、icator solution andtitrate with 0.05 N NaOH solution to the first perceptible pinkcolor.10.3 By means of a graduated cylinder add 50 mL of theacetaldehyde specimen that previously has been chilled to 0 to5C.10.4 Titrate immediately with the 0.05 N NaOH solution tothe same first perceptible pink colo

26、r originally obtained in 10.2.11. Calculation11.1 Calculate the acidity A of the specimen as follows:11.1.1 Acidity as weight % acetic acid:A 5 VN 3 0.060 3 100!/50 D 5 VN 3 0.12!/D (1)or11.1.2 Acidity as milligrams KOH per gram of specimen:5 VN 3 0.056 3 1000!/50 D 5 VN 3 1.12!/D (2)where:V = volum

27、e of NaOH solution required for titration ofthe specimen, mL,N = normality of the NaOH solution,D = density of specimen in g/mL,0.060 = milliequivalent weight of acetic acid, and0.056 = milliequivalent weight of KOH.12. Report12.1 Report the following information:12.1.1 The percent of acetic acid to

28、 the nearest 0.0001 %.12.1.2 Vinyl AcetateAcceptable duplicate determinationsfor averaging have not yet been determined.12.1.3 AcetaldehydeDuplicate determinations that agreewithin 0.010 %, absolute, are acceptable for averaging (95 %confidence level).13. Precision and Bias13.1 The following criteri

29、a should be used for determiningthe acceptability of results at the 95 % confidence level.13.2 Vinyl Acetate:13.2.1 RepeatabilityThe repeatability of this test methodhas not yet been determined.13.2.2 ReproducibilityThe standard deviation of results(each the average of duplicates), obtained by analy

30、sts indifferent laboratories, has been estimated at 0.0002 wt. %absolute with 3 df. The 95 % limit for differences between twosuch averages is estimated at 0.0006 wt. %.NOTE 5The statistical data was determined with only two laboratoryparticipants and will be utilized only until a complete round rob

31、in studycan be completed.13.3 Acetaldehyde:13.3.1 RepeatabilityTwo results, each the mean of dupli-cate determinations, obtained by the same analyst should beconsidered suspect if they differ by more than 0.014 %absolute.13.3.2 ReproducibilityTwo results, each the mean of du-plicate determinations,

32、obtained by analysts in different labo-ratories should be considered suspect if they differ by morethan 0.035 %, absolute.NOTE 6The above precision estimates are based on an interlaboratorystudy on samples of acetaldehyde containing 0.034 and 0.146 % aceticacid. Each sample was analyzed in duplicate

33、 by two analysts in each offive different laboratories on two different days.13.4 BiasBias has not been determined for this testmethod because an appropriate standard is not available (seeSection 5).D208608214. Keywords14.1 acetaldehyde; acidity; vinyl acetateSUMMARY OF CHANGESCommittee D01.35 has i

34、dentified the location of selected changes to this standard since the last issue(D 2086 - 03) that may impact the use of this standard. (Approved November 1, 2008.)(1) Revised 7.2.ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item m

35、entionedin 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 committ

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37、ing 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 Harbor Drive, P

38、O 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).D2086083