ASTM D6844-2010 6875 Standard Test Method for Silanes Used in Rubber Formulations (bis-(triethoxysilylpropyl)sulfanes) Characterization by High Performance Liquid Chromatography (H.pdf

《ASTM D6844-2010 6875 Standard Test Method for Silanes Used in Rubber Formulations (bis-(triethoxysilylpropyl)sulfanes) Characterization by High Performance Liquid Chromatography (H.pdf》由会员分享，可在线阅读，更多相关《ASTM D6844-2010 6875 Standard Test Method for Silanes Used in Rubber Formulations (bis-(triethoxysilylpropyl)sulfanes) Characterization by High Performance Liquid Chromatography (H.pdf（7页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D6844 10Standard Test Method forSilanes Used in Rubber Formulations(bis-(triethoxysilylpropyl)sulfanes): Characterization by HighPerformance Liquid Chromatography (HPLC)1This standard is issued under the fixed designation D6844; the number immediately following the designation indicates

2、 the year oforiginal adoption or, in 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 covers the characterization of

3、 silanes,or of admixtures of silane and carbon black (see 10.4), of thetype bis-(triethoxysilylpropyl)sulfane by high performanceliquid chromatography.1.2 The values stated in SI units are to be regarded as thestandard. The values given in parentheses are for informationonly.1.3 This standard does n

4、ot 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. Referenced Documents2.1 ASTM Standar

5、ds:2D5297 Test Methods for Rubber Chemical AcceleratorPurity by High Performance Liquid ChromatographyE177 Practice for Use of the Terms Precision and Bias inASTM Test MethodsE682 Practice for Liquid Chromatography Terms and Rela-tionshipsE691 Practice for Conducting an Interlaboratory Study toDeter

6、mine the Precision of a Test Method3. Terminology3.1 Definitions:3.1.1 SxBis-(triethoxysilylpropyl)polysulfane or polysul-fide, (EtO)3SiC3H6SxC3H6Si(OEt)33.1.2 S2Bis-(triethoxysilylpropyl)disulfane or disulfide,(EtO)3SiC3H6S2C3H6Si(OEt)33.1.3 S3Bis-(triethoxysilylpropyl)trisulfane or trisulfide,(EtO

7、)3SiC3H6S3C3H6Si(OEt)33.1.4 S3Bis-(triethoxysilylpropyl)tetrasulfane or tetrasul-fide, (EtO)3SiC3H6S4C3H6Si(OEt)33.1.5 S3Bis-(triethoxysilylpropyl)pentasulfane or penta-sulfide, (EtO)3SiC3H6S5C3H6Si(OEt)33.1.6 S3Bis-(triethoxysilylpropyl)hexasulfane or hexasul-fide, (EtO)3SiC3H6S6C3H6Si(OEt)33.1.7 S

8、3Bis-(triethoxysilylpropyl)heptasulfane or hepta-sulfide, (EtO)3SiC3H6S7C3H6Si(OEt)33.1.8 S3Bis-(triethoxysilylpropyl)octasulfane or octasul-fide, (EtO)3SiC3H6S8C3H6Si(OEt)33.1.9 S3Bis-(triethoxysilylpropyl)nonasulfane or nonasul-fide, (EtO)3SiC3H6S9C3H6Si(OEt)33.1.10 S3Bis-(triethoxysilylpropyl)dec

9、asulfane or deca-sulfide, (EtO)3SiC3H6S10C3H6Si(OEt)33.1.11 average sulfur chain lengththe weighted averageof the sulfur bridge in the polysulfide mixture. Includes S2toS10species.4. Summary of Test Method4.1 A sample of the silane is analyzed by high performanceliquid chromatography to determine am

10、ounts of each compo-nent, the average chain length and the amount of dissolvedelemental sulfur.4.2 Two methods are described: Method A with a constantcomposition of the mobile phase (isocratic), and Method Busing a gradient. Both methods will give similar chromato-grams.5. Significance and Use5.1 Th

11、e average sulfur chain length is an important param-eter in determining the behavior of the silane in a rubbermixture.6. Apparatus6.1 HPLC with UV Detector, operating at 254 nm, InletValve with 5 mm3(L) loop, integrator or data system.6.2 Column C18, 5 m, 4.6 3 250 mm.6.3 Column Oven.6.4 Analytical

12、Balance, accuracy 60.1 mg.1This test method is under the jurisdiction of ASTM Committee D11 on Rubberand is the direct responsibility of Subcommittee D11.20 on Compounding Materialsand Procedures.Current edition approved June 1, 2010. Published July 2010. Originally approvedin 2002. Last previous ed

13、ition approved in 2007 as D6844 02 (2007). DOI:10.1520/D6844-10.2For 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 websi

14、te.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.6.5 Hamilton Syringe, 100 mm3(L).6.6 Volumetric Pipet,5cm3.6.7 Volumetric Flasks, 50 and 2000 cm3.6.8 Syringe,3cm3or5cm3.6.9 Glass Bottles,5cm3.6.10 Disposable PTFE Filters, 0.20 m,d

15、=25mm.6.11 Mechanical Flask Shaker.7. Reagents, AR Grade or Equivalent7.1 Reagents for Method A (without gradient):7.1.1 Ethanol, absolute.7.1.2 Methanol.7.1.3 Tetrabutylammoniumbromide.7.1.4 Cyclohexane.7.1.5 Sulfur.7.1.6 Deionised Water.7.2 Reagents for Method B (with gradient):7.2.1 2-Propanol (I

16、PA).7.2.2 Acetonitrile (AcCN).7.2.3 Tetrabutylammoniumbromide.7.2.4 Hexane.7.2.5 Sulfur.7.2.6 Mesitylene.7.2.7 Deionised Water.8. Preparation of Solutions8.1 Tetrabutylammoniumbromide SolutionDissolve 400mg of tetrabutylammoniumbromide in 1000 cm3of deionisedwater.8.2 Mobile Phase:8.2.1 Mobile Phase

17、 for Method A (Isocratic)Transfer 180cm3of tetrabutylammoniumbromide solution and 450 cm3ethanol into a 2000 cm3volumetric flask. Make up to the markwith methanol and mix well.NOTE 1Separation between peaks of the silane species and elementalsulfur can be optimized by carefully varying the amount of

18、 water in themobile phase. In general, higher water content extends retention time,with the silane species being more affected than the elemental sulfur.8.2.2 Mobile Phase for Method B (With Gradient)Thecomposition of the mobile phase is variable:Time (min.) IPA (%) AcCN (%) TBAB (0.04 %)02060 2020

19、50 40 1025 50 40 1028 80 15 530 80 15 532 20 60 20NOTE 2The combination of solvents will affect the retention timesand peak separation efficiency. The above recommendation is one of manypossibilities. The specific solvents and ratios used can be determined bythe technician to fit the needs of the la

20、b. It is important to maintain theseparation of the peaks so they can be unambiguously identified andquantified.8.3 Sulfur StandardWeigh approximately 20 mg of sulfurto the nearest 0.1 mg into a 20 cm3volumetric flask and makeup to the mark with cyclohexane. Stopper the flask and agitateuntil the so

21、lution looks homogeneous. Using a volumetricpipet, transfer 5 cm3of this solution into a 50 cm3volumetricflask, make up to the mark with cyclohexane and mix well.NOTE 3If the test shall be run with an internal standard, 100 mm3(L)of mesitylene may be added to the 50 cm3flask prior to making up withc

22、yclohexane.9. Calibration9.1 Elemental SulfurThe response factor Rsfor convert-ing peak area to weight % sulfur is determined by injecting thesulfur standard into the HPLC unit and making the followingcalculation:Rs5 ms/ As 100 (1)where:ms= mass of sulfur made up to 50 cm3with cyclohexane,andAs= are

23、a of sulfur peak.10. Procedure10.1 Weigh approximately 160 mg of the silane sample tobe analyzed, to the nearest 0.1 mg, into a 50 cm3volumetricflask. Fill the flask to the mark with cyclohexane, stopper andagitate thoroughly to completely dissolve the sample.NOTE 4If the test shall be run with an i

24、nternal standard, 100 mm3(L)of mesitylene may be added to the 50 cm3flask prior to making up withcyclohexane.10.2 Purge the Hamilton syringe once with the solutionbefore injecting 100 mm3(L) into the inlet loop. Take carethat no air bubbles are injected.10.3 Turn the inlet loop into the injection po

25、sition and startthe integrator (or data system) immediately. After 40 min,terminate the run and print the chromatogram, including a peaklist.10.4 When analyzing admixtures of silane and carbonblack, weigh approximately 320 mg of the sample to thenearest 0.1 mg into a 50 cm3volumetric flask. Make up

26、to themark with cyclohexane, stopper the flask and shake for 20 minto extract the silane from the black.10.5 Load 2 cm3of the extract from 10.4 intoa3cm3-or5cm3-syringe. Mount the PTFE filter on top of the syringe andtransfer 1.5 cm3of the syringe contents into a waste bottle. Thelast 0.5 cm3are fil

27、tered into a small glass bottle from which100 mm3(L) are used to load the injection loop and analyzedas described in 10.2 and 10.3.11. Calculation11.1 Sulfur Chain DistributionCalculations are per-formed utilizing the response factors for the individual silane(sulfur chain length) species contained

28、in the following table:Sulfur ChainLengthMolecular Massg mol-1Response FactorRS2474.8 31.3S3506.9 8.87S4539.0 4.88S5571.0 3.24S6603.1 2.36S7635.2 1.82S8667.2 1.46S9699.3 1.19S10731.4 1.00D6844 102Si5Ai Ri(i 5 210Ai Ri 100 (2)where:Si= relative amount of silane species with i sulfur atoms in%,Ai= pea

29、k area of silane species with i sulfur atoms, andRi= response factor of silane species with i sulfur atoms.NOTE 5Short-chain silanes may exhibit additional peaks at retentiontimes higher than the one of the S7species. These peaks, due to oligomers,are not taken into consideration when calculating th

30、e sulfur chaindistribution and the average chain length.11.2 Average Chain Length:S 5(i 5 210i Ai Ri/ Mi(i 5 210Ai Ri/ Mi(3)where:S = average sulfur chain length,i = number of sulfur atoms in the silane species, andMi= molecular mass of silane species with i sulfur atoms.11.2.1 Example for calculati

31、on:Species MiRel RFRiResultAiCorrectedArea% SxS2474 31.3 1 407 938 44 068 459 16.8S3506 8.87 8 607 037 763 444 189 29.1S4538 4.88 12 988 212 63 382 475 24.2S5570 3.24 13 083 349 42 390 051 16.2S6602 2.36 8 534 198 20 140 707 7.7S7634 1.82 5 149 428 9 371 959 3.6S8666 1.46 2 815 133 4 110 094 1.6S969

32、8 1.19 1 375 780 1 637 178 0.6S10730 1.00 768 474 768 474 0.3Average Sulfur Chain Length (S-bar) 3.7811.3 Elemental Sulfur:S 5As Rsm(4)where:S = elemental sulfur content in %,As= peak area of elemental sulfur,Rs= response factor for sulfur, andm = mass of silane or admixture in mg in 50 cm3cyclo-hex

33、ane.11.4 Examples for Chromatograms:11.4.1 See Fig. 1.11.4.2 See Fig. 2.FIG. 1 Typical Chromatogram for Method A (Isocratic)D6844 10312. Report12.1 Report the following information:12.1.1 Identification of the silane sample,12.1.2 Average chain length to the nearest 0.01,12.1.3 Sulfur content to the

34、 nearest 0.1 weight %, and12.1.4 Relative amount of silane species with i sulfur atomsin % (optional).13. Precision and Bias313.1 The precision of this test method is based on aninterlaboratory study conducted in 2008. Up to ten laboratoriesparticipated in this study. Each of the labs reported fourr

35、eplicate test results for a variety of analytical parameters, on asingle material. Every “test result” reported represents anindividual determination. Except for the use of only a singlematerial, Practice E691 was followed for the design andanalysis of the data.13.1.1 Repeatability limit (r)Two test

36、 results obtainedwithin one laboratory shall be judged not equivalent if theydiffer by more than the “r” value for that material; “r”istheinterval representing the critical difference between two testresults for the same material, obtained by the same operatorusing the same equipment on the same day

37、 in the samelaboratory.13.1.1.1 Repeatability limits are listed in Tables 1-11.13.1.2 Reproducibility limit (R)Two test results shall bejudged not equivalent if they differ by more than the “R” valuefor that material; “R” is the interval representing the criticaldifference between two test results f

38、or the same material,obtained by different operators using different equipment indifferent laboratories.13.1.2.1 Reproducibility limits are listed in Tables 1-11.13.1.3 The above terms (repeatability limit and reproduc-ibility limit) are used as specified in Practice E177.13.1.4 Any judgment in acco

39、rdance with statement 13.1.1or 13.1.2 would have an approximate 95 % probability of beingcorrect.13.2 BiasAt the time of the study, there was no acceptedreference material utilized for determining the bias for this testmethod, therefore no statement on bias is being made.13.3 The precision statement

40、 was determined through sta-tistical examination of the reported results from ten laborato-ries, on one material. Due to the small number of participatinglabs, usually no outliers were removed. However in one case,i.e. for elemental sulfur testing one lab was an extreme outlierand had to be removed

41、from the precision calculation. Thismaterial was described as follows: Material A is a commer-cially available bis-(triethoxysilylpropyl)tetra sulfane.14. Keywords14.1 chain length; chain length distribution; elemental sul-fur; organosilane; silane3Supporting data have been filed at ASTM Internation

42、al Headquarters and maybe obtained by requesting Research Report RR:D11-1104.FIG. 2 Typical Chromatogram for Method B (With Gradient)D6844 104TABLE 1 Elemental Sulfur (%)AMaterial AverageBRepeatabilityStandardDeviationReproducibilityStandardDeviationRepeatabilityLimitReproducibilityLimitx SxSrSRrRA

43、0.32 0.02 0.02 0.02 0.04 0.06AEight labs reported (one outlier lab excluded from calculations).BThe average of the laboratories calculated averages.TABLE 2 Average Chain LengthAMaterial AverageBRepeatabilityStandardDeviationReproducibilityStandardDeviationRepeatabilityLimitReproducibilityLimitx SxSr

44、SRrRA 3.625 0.017 0.007 0.018 0.018 0.051ATen labs reported.BThe average of the laboratories calculated averages.TABLE 3 S2 (relative %)AMaterial AverageBRepeatabilityStandardDeviationReproducibilityStandardDeviationRepeatabilityLimitReproducibilityLimitx SxSrSRrRA 19.7 0.5 0.2 0.5 0.5 1.4ATen labs

45、reported.BThe average of the laboratories calculated averages.TABLE 4 S3 (relative %)AMaterial AverageBRepeatabilityStandardDeviationReproducibilityStandardDeviationRepeatabilityLimitReproducibilityLimitx SxSrSRrRA 31.0 0.8 0.1 0.8 0.3 2.1ATen labs reported.BThe average of the laboratories calculate

46、d averages.TABLE 5 S4 (relative %)AMaterial AverageBRepeatabilityStandardDeviationReproducibilityStandardDeviationRepeatabilityLimitReproducibilityLimitx SxSrSRrRA 23.5 0.3 0.09 0.3 0.2 1.0ATen labs reported.BThe average of the laboratories calculated averages.TABLE 6 S5 (relative %)AMaterial Averag

47、eBRepeatabilityStandardDeviationReproducibilityStandardDeviationRepeatabilityLimitReproducibilityLimitx SxSrSRrRA 14.5 0.2 0.04 0.2 0.1 0.6ATen labs reported.BThe average of the laboratories calculated averages.D6844 105TABLE 7 S6 (relative %)AMaterial AverageBRepeatabilityStandardDeviationReproduci

48、bilityStandardDeviationRepeatabilityLimitReproducibilityLimitx SxSrSRrRA 6.6 0.2 0.1 0.2 0.2 0.5ATen labs reported.BThe average of the laboratories calculated averages.TABLE 8 S7 (relative %)AMaterial AverageBRepeatabilityStandardDeviationReproducibilityStandardDeviationRepeatabilityLimitReproducibi

49、lityLimitx SxSrSRrRA 2.9 0.1 0.04 0.1 0.1 0.3ATen labs reported.BThe average of the laboratories calculated averages.D6844 106ASTM 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 entirely their own responsibility.This standard is subject to revision at any time by the responsible technical