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本文(ASTM D3443-2000(2010)e1 Standard Test Method for Chloride in Trichlorotrifluoroethane《三氯三氟乙烷中氯化物含量的标准试验方法》.pdf)为本站会员(deputyduring120)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM D3443-2000(2010)e1 Standard Test Method for Chloride in Trichlorotrifluoroethane《三氯三氟乙烷中氯化物含量的标准试验方法》.pdf

1、Designation: D3443 00 (Reapproved 2010)1Standard Test Method forChloride in Trichlorotrifluoroethane1This standard is issued under the fixed designation D3443; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revisi

2、on. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the Department of Defense.1NOTEAdded research report information to Section 8 editoria

3、lly in September 2010.1. Scope1.1 This test method covers the determination of chloride intrichlorotrifluoroethane and other halocarbons that are liquid atroom temperature.1.2 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.3

4、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 of regulatory limitations prior to use.2. Summary of Test

5、Method2.1 This test method is based on the determination ofionizable chloride by titration with mercuric acetate solutionusing s-diphenylcarbazone as the indicator.3. Significance and Use3.1 This test method determines ionizable chloride that canbe aqueously extracted from trichlorotrifluoroethane.3

6、.2 This test method can be used to establish production andpurchasing specifications.4. Apparatus4.1 Separatory Funnels, two 250-mL, with polytetra-fluoroethylene stopcocks.4.2 Erlenmeyer Flask, 125-mL.5. Reagents5.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwi

7、se 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.2Other grades may beused, provided it is first ascertained that the reagent is ofsufficiently high purit

8、y to permit its use without lessening theaccuracy of the determination.5.2 Purity of WaterUnless otherwise indicated, referencesto water shall be understood to mean halide-free distilled water.5.3 s-Diphenylcarbazone SolutionDissolve 0.5 g ofs-diphenylcarbazone, in 100 mL of methanol.5.4 Silver Nitr

9、ate SolutionDissolve 8.5 g of silver nitrate(AgNO3) in 500 mL of water.5.5 Standard Mercuric Acetate SolutionDilute 40 mL ofstock mercuric acetate solution, reagent 2, to 1000 mL andadjust the pH to 1.6 with nitric acid. Standardize as follows:5.5.1 Pipet 10.00 mL of standard sodium chloride solutio

10、ninto a 250-mL Erlenmeyer flask. Add 20 mL of chloride-freewater and 5 drops of s-diphenylcarbazone solution. Titrate withstandard mercuric acetate solution to the faint purple end point.Then:mL NaCl 3 1.000mL mercuric acetate5 F 5 g Cl/mL (1)whereF = factor for the mercuric acetate solution (see 7.

11、1).5.6 Standard Sodium Chloride SolutionDissolve 0.0660 gof sodium chloride in water and dilute to 1000 mL. Pipet 25mL of this solution into a 1000-mL volumetric flask, dilute tovolume, and mix. One millilitre of this solution contains 1.00g of chloride ion.1This test method is under the jurisdictio

12、n of ASTM Committee D26 onHalogenated Organic Solvents and Fire Extinguishing Agents and is the directresponsibility of Subcommittee D26.04 on Test Methods.Current edition approved June 1, 2010. Published July 2010. Originally approvedin 1975. Last previous edition approved in 2005 as D3443 00(2005)

13、. DOI:10.1520/D3443-00R10E01.2Reagent 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., Poole, Dorset, U.K., an

14、d the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.5.7 Stock Mercuric Acetate SolutionDissolve 1.6 g ofmercuric acetate in

15、500 mLof water containing 3.5 mLof nitricacid. Dilute to 1000 mL and mix.6. Procedure6.1 Wash all glassware with chloride-free water until 10 mLof the washings show no trace of turbidity when 1 mL of silvernitrate solution is added.6.2 Transfer 100 mL of the sample into a 250-mL separatoryfunnel, ad

16、d 25 mL of chloride-free water to the sample andshake for 1 min. Transfer the sample to a second 250-mLseparatory funnel and drain the water into a 125-mL Erlenm-eyer flask. Repeat the extraction once with another 25 mL ofwater. Combine the water extracts in the Erlenmeyer flask.6.3 Warm the water e

17、xtract to 60C to drive off anyremaining sample. Cool to room temperature.6.4 Add 5 drops of s-diphenylcarbazone solution and titratewith standard mercuric acetate solution to the pale purple endpoint.7. Calculation7.1 Calculate parts per million chloride as follows:Chloride, ppm 5 A 3 F!/S 3 G! (2)w

18、here:A = millilitres of mercuric acetate solution required for thetitration,F = factor for the solution (see 5.5.1),S = millilitres of sample, andG = specific gravity of the sample.8. Precision and Bias38.1 Repeatability (Single Analyst): The standard deviationof results (each the average of triplic

19、ates obtained by the sameanalyst on two different days) has been estimated to be 0.005wt. ppm at four degrees of freedom. Two such values should beconsidered suspect (95 % confidence level) if they differ bymore than 0.02 wt. ppm.8.2 Reproducibility (Multilaboratory): The standard devia-tion of resu

20、lts (each the average of triplicates in four differentlaboratories) has been estimated to be 0.06 wt. ppm at threedegrees of freedom. Two such values should be consideredsuspect (95 % confidence level) if they differ by more than 0.3wt. ppm.9. Keywords9.1 CFC-113; chloride; trichlorotrifluoroethaneA

21、STM 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 riskof infringement of such rights, are

22、entirely their own responsibility.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 standard

23、sand should be addressed 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 Committe

24、e 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 by contacting ASTM at the aboveaddress o

25、r 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 ASTM website (www.astm.org/COPYRIGHT/).3Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting RR:D26-1000 and RR:D26-1010.D3443 00 (2010)12

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