ASTM D5070-1990(2014) Standard Test Method for Synthetic Quaternary Ammonium Salts in Fabric Softeners by Potentiometric Titrations《采用电位滴定法的织物软化剂中合成季胺盐的标准试验方法》.pdf

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ASTM D5070-1990(2014) Standard Test Method for Synthetic Quaternary Ammonium Salts in Fabric Softeners by Potentiometric Titrations《采用电位滴定法的织物软化剂中合成季胺盐的标准试验方法》.pdf_第1页
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ASTM D5070-1990(2014) Standard Test Method for Synthetic Quaternary Ammonium Salts in Fabric Softeners by Potentiometric Titrations《采用电位滴定法的织物软化剂中合成季胺盐的标准试验方法》.pdf_第3页
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1、Designation: D5070 90 (Reapproved 2014)Standard Test Method forSynthetic Quaternary Ammonium Salts in Fabric Softenersby Potentiometric Titrations1This standard is issued under the fixed designation D5070; 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.1. Scope1.1 This test method describes a potentiometric titrationprocedure for the determinatio

3、n of quaternary ammonium saltsin fabric softeners. This test method is intended for the analysisof known quaternary ammonium salts such as the dialkyldimethyl quaternary ammonium compound type and the di-amidoamine based quaternary ammonium compound type.1.2 The quaternary ammonium salts conform to

4、the struc-tures shown in Fig. 1 and Fig. 2.1.3 The analytical procedure appears in the following order:SectionApparatus 5Reagents 6Preparation of standard reagents 7Standardization of hyamine solution 9Safety precautions 8Procedure for determination of dialkyl dimethyl quaternaries 10Procedure for d

5、etermination of diamidoamine based quaternaries 111.4 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.5 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibil

6、ity 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. See 6.4, 6.6, 6.7and Section 8 for specific warning statements.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Reagent Wa

7、terD3049 Test Method for Synthetic Anionic Ingredient byCationic Titration3. Summary of Test Method3.1 Quaternary ammonium compounds present in fabricsofteners, as the active materials, are titrated potentiometricallyin an aqueous medium with a standard solution of sodiumlauryl sulfate using a nitra

8、te ion-selective electrode. In thispotentiometric titration, the reaction involves the formation ofa complex between the quaternary ammonium compound andthe anionic surfactant which then precipitates.At the end point,the nitrate ion electrode appears to respond to an excess oftitrant with a potentia

9、l change large enough to give a welldefined inflection in the titration curve. Alternatively thequaternary ammonium compound can be first complexed withan excess of standard sodium lauryl sulfate; the excess sodiumlauryl sulfate is titrated potentiometrically with standardHyamine 1622.34. Significan

10、ce and Use4.1 This test method is used to determine the quaternaryammonium salts commonly found in fabric softeners. Quater-nary ammonium compounds being the active ingredients infabric softeners requires accurate determination to assess thecost and performance of such compounds.5. Apparatus5.1 Auto

11、titration Systemburet with 10 or 20 mLcapacity;4magnetic stirrer;5evaluating ruler.65.2 Electrodes(1) nitrate specific ion electrode;7(2) sur-factant electrode;8(3) Ag/AgCl reference electrode.91This test method is under the jurisdiction of ASTM Committee D12 on Soapsand Other Detergents and is the

12、direct responsibility of Subcommittee D12.12 onAnalysis and Specifications of Soaps, Synthetics, Detergents and their Components.Current edition approved Jan. 1, 2014. Published February 2014. Originallyapproved in 1990. Last previous edition approved in 2005 as D5070-90(2005). DOI:10.1520/D5070-90R

13、14.2For 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.3The sole source of supply of Hyamine 1622 known to the co

14、mmittee at thistime is Gallard Schlesinger Manufacturing Corp., 584 Mineola Ave., Carle Place,NY 11514. If you are aware of alternative suppliers, please provide this informationto ASTM Headquarters. Your comments will receive careful consideration at ameeting of the responsible technical committee,

15、 which you may attend.4Metrohm-Brinkman E-536, or equivalent, has been found satisfactory. Avail-able from Brinkman Instruments Inc., Cantiague Rd., Westbury, NY 11590.5Potentiograph/E-535 and Dosimat/E-459, or equivalent, have been foundsatisfactory. Available from Brinkman Instruments Inc., Cantia

16、gue Rd., Westbury,NY 11590.6Evaluating Ruler EA-893, or equivalent, has been found satisfactory. Availablefrom Brinkman Instruments Inc., Cantiague Rd., Westbury, NY 11590.7Orion Model 93.07, or equivalent, has been found satisfactory. Available fromOrion Research Inc., 529 Main St., Boston, MA 0212

17、9.8Orion Model 93.42, or equivalent, has been found satisfactory. Available fromOrion Research Inc., 529 Main St., Boston, MA 02129.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States15.3 Adaptors(1) coaxial adaptor, required for indicato

18、relectrode,10(2) banana plug adaptor, required for referenceelectrode.NOTE 1To ensure electrical continuity (after assembly) shake downelectrode in the manner of a clinical thermometer. Also, the conditioningof the electrode is essential for obtaining a good break in the titrationcurve. Conditioning

19、 new electrodes in 0.01 M KNO3, aqueous solution for60 min (or more) prior to use is recommended.NOTE 2Other electrodes (for example, a calomel electrode) aresuitable as the reference electrode provided they give a stable referencepotential during the titration. Reference electrodes having a ceramic

20、 or anasbestos junction tend to clog with use. Therefore, a ground-glass sleeveelectrode (such as the Metrohm EA 440 or equivalent)11is suggested.6. Reagents6.1 Hyamine 1622,3diisobutylphenoxyethoxyethyl dimethylbenzyl ammonium chloride monohydrate.6.2 Sodium Lauryl Sulfate,12primary standard (Note

21、3).NOTE 3Sodium lauryl sulfate must be analyzed for purity accordingto the Reagent section of Test Method D3049, before its use as a primarystandard.6.3 Water, type III reagent water conforming to Specifica-tion D1193.6.4 Isopropanol, reagent grade. (WarningHighly flam-mable.)6.5 Sodium Borate Decah

22、ydrate(Na2B4O710H2O), re-agent grade.6.6 Boric Acid (H3BO3), reagent grade. (WarningCausesirritation.)6.7 Sulfuric Acid (H2SO4), reagent grade. (WarningCauses severe burns on contact with skin. See Section 8.)6.8 Five percent (V/V) Sulfuric Acid SolutionUsing agraduated cylinder, transfer 80 mL of d

23、eionized water to a100-mL volumetric flask. Slowly, carefully, and with stirring,add 5 mL of concentrated sulfuric acid. Cool to room tempera-ture and dilute to the mark with water.6.9 Borate Buffer Solution pH 6.00In a 500 mL beaker,dissolve 5.0 g 6 0.02 g of sodium borate decahydrate and 7.0g 6 0.

24、02 g of boric acid in approximately 300 mL water, withstirring; adjust pH to 6.00 with 5 % sulfuric acid solution.Transfer to a 500-mL volumetric flask, mix, and dilute tovolume with water.7. Preparation of Standard Reagents7.1 Sodium Lauryl Sulfate Solution, 4103NWeighaccurately 1.15 6 0.01 g of so

25、dium lauryl sulfate to 0.1 mg;dissolve in water and dilute to a final volume of 1 L. Calculatethe normality of the solution with the following equation:Normality of sodium lauryl sulfate 5W 3P288.38!100!(1)where:P = purity of the sodium lauryl sulfate, weight %W = weight of sodium lauryl sulfate, g7

26、.2 Keep the solution no longer than 1 month before makinga fresh solution.7.3 Hyamine 1622 Solution,4103NDissolve 1.85 60.5 g of Hyamine 1622 in deionized water. Transfer toa1Lvolumetric flask, and dilute to volume with water.8. Hazards8.1 All reagents and chemicals should be handled with care.Befor

27、e using any chemical, read and follow all safety precau-tions and instructions on the manufacturers label or MSDS(Material Safety Data Sheet).9. Standardization of Hyamine 1622 Solution9.1 This determination must be done in triplicate. Pipet 5.00mL of the standard lauryl sulfate into a 150 mL beaker

28、. Addapproximately 100 mL of deionized water and while stirringadd by pipet 2 mL of the borate buffer.9.2 The electrode should be cleaned between each titration.Asatisfactory procedure is to first rinse it with water, then withalcohol (ethyl alcohol) (Note 5) and again with water followedby wiping t

29、he surface with a soft tissue.NOTE 4The electrode can be quickly washed with ethyl alcohol whenfollowed immediately by a water rinse. Prolonged contact of the electrodewith alcohol or other organic solvent can cause failure of the electrodemembrane.9Metrohm Model EA-440, or equivalent, has been foun

30、d satisfactory. Availablefrom Brinkman Instruments Inc., Cantiague Rd., Westbury, NY 11590.10The Metrohm coaxial adaptor, or equivalent, has been found satisfactory forthis purpose. Available from Brinkman Instruments Inc., Cantiague Rd., Westbury,NY 11590.11Available from Brinkman Instruments Inc.,

31、 Cantiague Rd., Westbury, NY11590.12Available from British Drug House, LTD, or in the U.S. from GallardSchlesinger Manufacturing Corp., 584 Mineola Ave., Carle Place, NY 11514.X= chloride or methyl sulfateR = fatty alkyl groups saturated or unsaturated, normal or branched C8C22FIG. 1 Dialkyl Dimethy

32、l QuaternariesX= usually methyl sulfateR = fatty alkyl groups, saturated or unsaturated, normal or branched C12C18R1= 2-hydroxyethyl,2-hydroxypropylFIG. 2 Diamidoamine Based QuarternariesD5070 90 (2014)29.3 Titrate potentiometrically with Hyamine 1622 and re-cord the titration volume at the endpoint

33、. The endpoint ismarked by the point of inflection on the “S” shaped curve andit is determined by the use of the evaluating ruler.Normality of Hyamine 1622 5N 35.0V(2)where:N = normality of sodium lauryl sulfate standard solution5.0 = sodium lauryl sulfate aliquot taken for titration, mLV = Hyamine

34、1622 solution consumed during, titration,mL10. Procedure for Determination of Dialkyl DimethylQuaternary10.1 Weigh accurately a quantity of sample to the nearest0.1 mg of quaternary ammonium compound active materialinto a 250 ml beaker.10.2 Table 1 may be used as a guide for sample weight,dilution,

35、and aliquot. Dilution of sample must be done inisopropanol using volumetric flask and pipetes as indicated inTable 1.10.3 Add 5 mL of isopropanol. Swirl the beaker until thesample is completely dissolved.Add approximately 150 mL ofdeionized water and stir. While stirring, add, by pipet, 4 mL ofthe b

36、orate buffer solution.10.4 Pipet 10 mLof standard solution lauryl sulfate solutionwhile stirring. Transfer the solution to the autotitrator. Titratepotentiometrically with standard Hyamine 1622 solution. Asthe inflection point is approached, reduce the addition rate, andcontinue titrating well past

37、the inflection in the titration curve.(Automatic titrators can be preset to automatically slow downthe addition rate as the inflection point is approached.) Recordthe titration volume at the endpoint. The endpoint is marked bythe point of inflection on the “S” shaped curve and it isdetermined by the

38、 use of the evaluating ruler. Typical titrationcurve of the dialkyl dimethyl ammonium salt is shown in Fig.3.10.5 Calculate the percent dialkyl dimethyl quaternary in-gredient as follows:Dialkyl dimethyl quaternary, weight % (3)5A 3N1! 2 B 3N2!# 3M 3D 3100S 31000 3Awhere:A = standard sodium lauryl s

39、ulfate, mLN1= normality of standard sodium lauryl sulfateB = standard Hyamine 1622 consumed during titration,mLN2= normality of standard Hyamine 1622 solutionM = average equivalent weight of the dialkyl dimethylquaternaryD = dilution of sample, mLS = weight of sample in gramsA = aliquot of sample di

40、lution, mL11. Procedure for Determination of Diamidoamine BasedQuaternary11.1 Weigh accurately a quantity of sample to containapproximately 0.16 meq of quaternary ammonium compoundactive material into a 250 mL beaker (Note 5). Add 5 mL ofisopropanol. Swirl the beaker until sample is completelydissol

41、ved. Add approximately 150 mL of water and stir. Whilestirring, pipet in 2 mL of the borate buffer solution. Titratepotentiometrically with standard sodium lauryl sulfate solu-tion. As the inflection point is approached, reduce the additionrate, and continue titrating well past the inflection in the

42、titration curve. (Automatic titrators can be preset to automati-cally slow down the addition rate as the inflection point isapproached.)NOTE 5To determine the amount of sample needed for an approxi-mately 13.7 mL titration (0.05 meq) use the following equation:TABLE 1 Guide for Sample Weight, Diluti

43、on, and Aliquot to beUsedActiveIngredientsASample, %SampleWeight, gDilution, mL(in Isopropanol)Aliquot, mL2.5 0.565 0.2810 0.1520 4.10 200 230 2.8 200 240 2.1 200 250 1.8 200 160 2.8 200 170 2.4 200 180 2.1 200 190 1.8 200 1AValues are based on an assumed molecular weight of 649 for the dialkyl dime

44、thylquaternary.FIG. 3 Sample: Dihydrogenated-Tallow Dimethyl AmmoniumSulfate, Titrant: 0.00405N Hyamine (back titration ofsodium lauryl sulfate)AAUsing nitrate ion-selective electrodeD5070 90 (2014)3W 50.005 3MD(4)where:W = weight of sample to be taken for analysis, gM = average equivalent weight of

45、 the quaternary ammonium saltpresentD = approximate concentration of the quaternary ammonium saltexpected, weight %11.2 To obtain accurate weights of sample, it is convenientto make up an aqueous solution (for example 250 mL) and takean aliquot corresponding to a known meq of active matter.11.3 Reco

46、rd the titration volume at the end point. Theendpoint is marked by the point of inflection on “S” shapedcurve and it is determined by the use of an evaluating ruler.Typical titration curve of diamidoamine based quaternary isshown in Fig. 4.12. Calculation12.1 Calculate the percent diamidoamine based

47、 quaternaryof the sample as follows:Diamidoamine quaternary, weight % (5)5A 3N 3M 3D 3100S 31000 3Awhere:A = tandard sodium lauryl sulfate solution, mL consumedduring titrationsN = normality of standard sodium lauryl sulfate solutionM = average equivalent weight of the diamidoamine quater-naryD = di

48、lution of samples, mLS = weight of sample, gA = aliquot of sample dilution, mL13. Precision13.1 The following criteria should be used to judge theacceptability of the results (Note 6).13.2 Repeatability (single analyst)The coefficient ofvariation of results (each the average of triplicatedeterminati

49、ons), obtained by the same analyst on differentdays, was estimated to be 1.24 % relative at 20 df. Two suchaverages should be considered suspect (95 % confidence level)if they differ by more than 3.66 % relative.13.3 Reproducibility (multilaboratory)The coefficient ofvariation of results (each the average of duplicate determina-tions) obtained by analysts in different laboratories, has beenestimated to be 2.38 % relative at 9 df. Two such averagesshould be considered suspect (95 % confidence level) if theydiffer by more than 7.62 % relative.13.4 Repor

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