ASTM D2106-2007(2012) Standard Test Methods for Determination of Amine Acid Acceptance (Alkalinity) of Halogenated Organic Solvents《测定卤代有机溶剂的氨基酸接受性(碱度)的标准试验方法》.pdf

《ASTM D2106-2007(2012) Standard Test Methods for Determination of Amine Acid Acceptance (Alkalinity) of Halogenated Organic Solvents《测定卤代有机溶剂的氨基酸接受性(碱度)的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D2106-2007(2012) Standard Test Methods for Determination of Amine Acid Acceptance (Alkalinity) of Halogenated Organic Solvents《测定卤代有机溶剂的氨基酸接受性(碱度)的标准试验方法》.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D2106 07 (Reapproved 2012)Standard Test Methods forDetermination of Amine Acid Acceptance (Alkalinity) ofHalogenated Organic Solvents1This standard is issued under the fixed designation D2106; the number immediately following the designation indicates the year oforiginal adoption or, in

2、 the case of revision, the year 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.This standard has been approved for use by agencies of the Department of Defense.1. Scope1.1 Th

3、ese test methods, where applicable, cover the deter-mination of the acid acceptance of halogenated organic sol-vents due to the presence therein of an organic amine titratableby standard acid. These test methods are suitable for samples of0.001 to 0.02 weight percent (10 200 ppm) alkalinity asNaOH.

4、Two test methods are covered as follows:1.1.1 Test Method A pH Method, and1.1.2 Test Method B Indicator Method.1.1.3 Test Method CGC Method.1.2 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 t

5、o establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D6806 Practice for Analysis of Halogenated Organic Sol-vents and Their Admixtures by Gas ChromatographyE70 Test Method for pH of Aqu

6、eous Solutions With theGlass ElectrodeE200 Practice for Preparation, Standardization, and Storageof Standard and Reagent Solutions for Chemical Analysis3. Terminology3.1 Definitions:3.1.1 amine acid acceptancethe degree to which an or-ganic amine present in the halogenated organic solvent iscapable

7、of absorbing or neutralizing acid generated by thesolvent or introduced into it from an external source.4. Significance and Use4.1 This test method is useful for the determination of theamount of acid acceptance contributed by amines or bases ascompared to other acid-accepting compounds.5. Purity of

8、 Reagents5.1 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 grades may be used, p

9、ro-vided it is first ascertained that the reagent is of sufficientlyhigh purity to permit its use without lessening the accuracy ofthe determination.5.2 Purity of Water Unless otherwise indicated, referencesto water shall be understood to mean distilled water or water ofequal purity. Additional requ

10、irements are specified in 8.1 and12.1.TEST METHOD ApH METHOD6. Summary of Test Method6.1 The amine acid acceptance of the halogenated organicsolvent is determined, after extraction into a volume of waterpreadjusted to a pH of 3.9, by titrating with standard acid to apH of 3.9. The extraction is perf

11、ormed either by stirring theimmiscible liquids mechanically or by shaking the immisciblelayers of liquids manually.7. Apparatus7.1 pH Meter, equipped with a pH indicating electrode andpH reference electrode or combination electrode.7.2 Stirrer, electric stirring bar, air-driven or magnetic.1These te

12、st methods are under the jurisdiction of ASTM Committee D26 onHalogenated Organic Solvents and Fire Extinguishing Agents and are the directresponsibility of Subcommittee D26.04 on Test Methods.Current edition approved Sept. 1, 2012. Published November 2012. Originallyapproved in 1962. Last previous

13、edition approved in 2007 as D2106 07. DOI:10.1520/D2106-07R12.2For 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

14、.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., Poole, Dorset, U.K., and the United States Pharmaco

15、peiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States18. Reagents8.1 WaterAdjust the pH of 1 L (or any convenientquantity) of water to 3.9. Boil 1 L of dis

16、tilled water for 5 minin a borosilicate glass or stainless steel container, then coverand cool to room temperature. Titrate a 50-mL aliquot to a pHof 3.8 to 4.0 with 0.01 N hydrochloric acid (HCl) (or 0.01 NNaOH if the pH is below 3.8). From this titer, calculate thevolume of 0.01 N HCl (or NaOH) re

17、quired to adjust the pH ofthe remaining 950 mL of boiled distilled water to a pH of 3.8to 4.0. The calculation is as follows:950503titer (1)Add the calculated amount of 0.01 N HCl (or NaOH)together with the titrated 50 mL aliquot of water to the 950 mLstock and mix thoroughly. Determine the pH of a

18、secondaliquot. If further adjustment is necessary to obtain a pH of 3.8to 4.0, repeat the preceding procedure.8.2 Hydrochloric Acid, Standard (0.01 N)Dilute 1.8 mLof concentrated hydrochloric acid (HCl, sp gr 1.19) to 1 L withwater and standardize in accordance with Practice E200,Sections 20 through

19、 23. Certified reagent of 0.01 N HCl may bepurchased from supply houses.8.3 pH 4.0 Buffer Solution, available from most supplyhouses.8.4 pH 7.0 Buffer Solution, available from most supplyhouses.NOTE 1Hydrochloric acid of about 0.01 to about 0.02 N can be used.It can be difficult to see the end point

20、 when using hydrochloric acid muchbelow about 0.01 N and concentrations much above 0.02 N increase thelikelihood of over-titrating the end point when titrating samples of lowalkalinity. For alkalinity below about 0.00075 % (75 ppm), 0.01 N HCl isappropriate. For alkalinity above about 75 ppm, 0.02 N

21、 HCl is appropriate.9. Procedure9.1 Calibrate the pH meter in accordance with Test MethodE70.9.1.1 Prepare a blank using 100 mL of water previouslyadjusted to pH 3.9, and subject it to the same type and degreeof agitation as the test samples. Titrate the blank to pH 3.9 andrecord the volume of titra

22、nt as B.9.2 Using Mechanical AgitationTransfer 50 mL of thehalogenated organic solvent to a 150-mL beaker and add 50mL of water previously adjusted to a pH of 3.9. Insert a stirrer,and stir as vigorously as possible for 10 s. Stop the stirrer andlift it out of the beaker. Allow the liquids to separa

23、te. Insert thepH meter electrodes into the separated aqueous upper layer,avoiding contact of the electrodes with the solvent layer, andtitrate the water layer with 0.01 N HCl to a pH of 3.9. When theend point has been reached, remove the electrodes and reinsertthe stirrer. Stir vigorously for 10 s a

24、gain. Remove the stirrer,insert the electrodes, and again titrate to a pH of 3.9. Repeat thesteps until additional stirring does not result in a change of pH(Note 2). Record the final titration and calculate the amine acidacceptance. When a magnetic stirring bar is used, it is notnecessary to remove

25、 it between agitation periods.NOTE 2If the readings of the pH meter are erratic because theelectrodes have been wet with halogenated solvent, it may be treated byrinsing the electrode with acetone or alcohol, followed by thoroughrinsing with water and soaking in water for a short time.9.3 Using Hand

26、 AgitationIf no stirrer is available, theextraction and titration may be carried out as follows: Transfer50 mL of the halogenated organic solvent to a 250-mLglass-stoppered Erlenmeyer flask, add 50 mL of water pread-justed to a pH of 3.9, and stopper the flask. Shake vigorouslyfor 5 s. Pour the cont

27、ents into a 150-mL beaker and allow theimmiscible liquids to separate into layers. Insert the pH meterelectrodes and titrate the water layer with 0.01 N HCl to a pHof 3.9. When the end point has been reached, remove theelectrodes, return the liquids to the flask, and extract again for5 s. Repeat the

28、 titration. Repeat the extraction and titration untilno change in pH results from additional shaking (Note 2).Record the final titration and calculate the amine acid accep-tance.10. Calculation10.1 Calculate the Amine Acid Acceptance (alkalinity) asNaOH, in weight percent as follows:Amine Acid Accep

29、tance alkalinity!, as NaOH, Weight Percent5 (2)$V 2 B/2! 3 NX0.040#/W% 3100or as parts per million as follows:Amine Acid Acceptance alkalinity!, as NaOH, ppm5 (3)$V 2 B/2! 3 NX0.040#/W% 31000000where:V = millilitres HCl required for titration of the sample, mL,N = normality of the HCl,B = millilitre

30、s HCl required for titration of the blank, mL,andW = weight sample used (or volume in millilitres times itsspecific gravity), g.11. Precision and Bias11.1 The precision limits of this test have been determinedas 0.0005 % (equivalent NaOH, weight percent).TEST METHOD BINDICATOR METHOD12. Summary of T

31、est Method12.1 The amine acid acceptance of the halogenated organicsolvent is determined, after extraction into a volume of waterpreadjusted to the bromphenol blue end point yellow, bytitrating with standard acid to the bromphenol blue end point,blue to yellow.13. Reagents13.1 WaterAdd bromphenol bl

32、ue indicator solution (1drop for each 10 mL of water) to 1 L (or any convenientvolume) of water and adjust to the bromphenol blue colorchange end point.13.2 Bromphenol Blue Indicator Solution (10 g/L)Dissolve1gofbromphenol blue in 100 mL of water.13.3 Hydrochloric Acid, Standard (0.01 N)See 8.2.D210

33、6 07 (2012)214. Procedure14.1 Prepare a blank using 100 mL of water previouslyadjusted to the color change point of the indicator being used,and subject it to the same type and degree of agitation as thetest samples. Titrate the blank to the color change point of theindicator and record the volume o

34、f titrant as B.14.2 Transfer 50 mL of the halogenated organic solvent to aclean 250-mL glass-stoppered Erlenmeyer flask, and add 50mL of water adjusted to the bromphenol blue end point (Note3). Stopper the flask and shake for 10 s. Allow the immiscibleliquids to separate, and titrate the aqueous upp

35、er layer with0.01 N HCl to the bromphenol blue end point. Stopper theflask, and again shake for 5 s. If the end point has changed,titrate to the bromphenol blue end point again. Repeat until nochange in indicator results when additional shaking is done.Record the titration and calculate the amine ac

36、id acceptance.NOTE 3Methyl orange indicator solution, modified methyl orangeindicator solution, or bromothymol blue indicator solution may besubstituted for bromphenol blue indicator solution where an operator hasdifficulty observing certain color changes.14.3 Mechanical agitation may be used as des

37、cribed in 9.2.15. Calculation15.1 See Section 10.16. Precision and Bias416.1 Precision determinations were performed at concentra-tions of 0.0009, 0.0018, and 0.0194 weight percent as NaOH.16.2 The standard deviation of results (each the average of5 replicates) obtained by different analysts on diff

38、erent dayswithin the same laboratory has been estimated to be 0.0002weight percent absolute at 12 degrees of freedom. The 95 %limit for the difference between two such averages is 0.0005weight percent absolute.16.3 The standard deviation of results (each the average of5 replicates) obtained by analy

39、sts in different laboratories hasbeen estimated to be 0.0003 weight percent absolute at 4degrees of freedom. The 95 % limit for the difference betweentwo such averages has been estimated to be 0.0008 weightpercent absolute.16.4 The bias of this test method was not determined.TEST METHOD CGAS CHROMAT

40、OGRAPHYMETHOD17. Procedure17.1 Determine the weight ppm or weight percent of theamine or amines present using gas chromatography with a gaschromatographic method that is in compliance with PracticeD6806.17.2 It will be necessary to calibrate the gas chromatographwith a known standard of the amine or

41、 amines present. Theknown standard should be of approximately the same concen-tration as the amine to be measured.17.3 If the amine is unknown it can be identified by GCmass spectroscopy.17.4 Calculate the Amine Acid Acceptance (alkalinity) bythe following formula:Amine Acid Acceptance alkalinity!,

42、as NaOH5 (4)40 3ppmMWor40 3wt %MWwhere:40 = the molecular weight of NaOH,ppm = ppm of the amine as determined in 17.1,wt % = weight percent of the amine as determined in 17.1,andMW = the molecular weight of the amine.17.5 If more than one amine is present the amine acidacceptance (alkalinity) will b

43、e the sum of the acid acceptance(alkalinity) of the individual amines.18. Precision and Bias518.1 Precision and bias data was obtained with two differentamines, n-methyl morpholine at about 20 ppm as NaOH inperchloroethylene, and diisopropyl amine, at about 3 ppm intrichloroethylene.18.2 There was n

44、o statistically significant difference be-tween alkalinity as determined between Methods B (titrationwith indicator) and Method C (determination of amine by GC).No bias is present.18.3 The reproducibility of the method was found to aver-age 2.1 % Relative Standard Deviation at 3 and 20 ppm.18.4 Repe

45、atability was calculated at 6.39 % RDS, that istwo determinations should differ less than 6.39 % RSD (1.3ppm at 20 ppm alkalinity).19. Keywords19.1 acid acceptance; alkalinity; amine acid acceptance;halogenated organic solvents4A Research Report is available from ASTM International Headquarters.Requ

46、est RR:D26-1012.5A Research Report is available from ASTM International Headquarters.Request RR:D26-1019.D2106 07 (2012)3ASTM 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 expres

47、sly 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 committee and must be reviewed every five years andif not revised,

48、 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 consideration at a meeting of theresponsible technical committee, which you may at

49、tend. 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, 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). Permission rig