ASTM D4937-1996(2012) Standard Test Method for p-Phenylenediamine Antidegradants Purity by Gas Chromatography《用气相色谱法测定对苯二胺抗降解剂纯度的标准试验方法》.pdf

《ASTM D4937-1996(2012) Standard Test Method for p-Phenylenediamine Antidegradants Purity by Gas Chromatography《用气相色谱法测定对苯二胺抗降解剂纯度的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D4937-1996(2012) Standard Test Method for p-Phenylenediamine Antidegradants Purity by Gas Chromatography《用气相色谱法测定对苯二胺抗降解剂纯度的标准试验方法》.pdf（7页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4937 96 (Reapproved 2012)Standard Test Method forp-Phenylenediamine Antidegradants Purity by GasChromatography1This standard is issued under the fixed designation D4937; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision,

2、 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 determination of the purityof Class I, II, and III p-phenylenediamine (PPD) a

3、ntidegradantsas described in Classification D4676 by gas chromatography(GC) detection and area normalization for data reduction.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 not purport to address a

4、ll 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 Standards:2D3853 Terminology R

5、elating to Rubber and RubberLaticesAbbreviations for Chemicals Used in Com-poundingD4483 Practice for Evaluating Precision for Test MethodStandards in the Rubber and Carbon Black ManufacturingIndustriesD4676 Classification for Rubber Compounding MaterialsAntidegradantsE260 Practice for Packed Column

6、 Gas Chromatography2.2 ISO Standard:3ISO 6472 Rubber Compounding IngredientsAbbreviations3. Terminology3.1 Definitions:3.1.1 area normalization, na method of calculating thepercent composition by measuring the area of each observedpeak and dividing each peak area by the total area. Thisassumes that

7、all peaks are eluted and that each component hasthe same detector response.3.1.2 lot sample, na production sample representative of astandard production unit, normally referred to as the sample.3.1.3 specimen, nthe actual material used in the analysis.It must be representative of the lot sample.3.2

8、AbbreviationsThe following abbreviations are in ac-cordance with Terminology D3853 and ISO 6472:3.2.1 77PDN,N8bis-(1,4-dimethylpentyl)-p-phenylenedi-amine.3.2.2 DTPDN,N8-ditolyl-p-phenylenediamine.3.2.3 IPPDN-isopropyl-N8-phenyl-p-phenylenediamine.3.2.4 PPDp-phenylenediamine.3.2.5 6PPDN-(1,3 dimethy

9、lbutyl)-N8-phenyl-p-phenylenediamine.4. Summary of Test Method4.1 The analysis is performed by temperature programmedGC utilizing either a packed column (Procedure A) or acapillary column (Procedure B). Quantification is achieved byarea normalization using a peak integrator or laboratory datasystem.

10、5. Significance and Use5.1 This test method is designed to assess the relative purityof production PPDs. These additives are primarily used asantiozonants for tires and other rubber or polymeric products.5.2 Since the results of this test method are based on areanormalization, it assumes that all co

11、mponents are eluted fromthe column and each component has the same detector re-sponse. Although this is not strictly true, the errors introducedare relatively small and much the same for all samples; thus,they can be ignored since the intent of the test method is toestablish relative purity.5.3 Alth

12、ough trace amounts of “low boilers” are present inproduction samples, they are disguised by the solvent peakwhen using packed columns (Procedure A).6. Interferences6.1 Utilizing the chromatographic conditions prescribedthere are no significant co-eluting peaks; however, degradationof column performa

13、nce could result in interference problems.1This test method is under the jurisdiction of ASTM Committee D11 on Rubberand is the direct responsibility of Subcommittee D11.11 on Chemical Analysis.Current edition approved May 1, 2012. Published July 2012. Originally approvedin 1989. Last previous editi

14、on approved in 2006 as D4937 96 (2006)1. DOI:10.1520/D4937-96R12.2For 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 webs

15、ite.3Available from the American National Standards Institute, 25 W. 43rd St., 4thFloor, New York, NY 10036.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.Thus, when using the packed column it is essential that thetotal system be ca

16、pable of 5000 theoretical plates before beingused for this analysis. The evaluation of system efficiency isdescribed in 7.4.7. Apparatus7.1 Gas Chromatograph:7.1.1 Procedure A: Packed ColumnAny high-quality tem-perature programmed gas chromatograph equipped with athermal conductivity detector (see N

17、ote 1) is sufficient for thisanalysis. Refer to Practice E260 for general gas chromatogra-phy practices.NOTE 1Although a thermal conductivity detector is recommended, aflame ionization detector can be used if appropriate adjustment is made forflow rate and specimen size. Since this probably would in

18、volve using asmaller diameter column, the adjustment in flow and injection volumeshould be proportional to the cross-sectional area of the column. Aprocedure for this calculation is included at the end of Section 9.7.1.2 Procedure B: Capillary ColumnA temperature pro-grammable unit with flame ioniza

19、tion detector (FID) equippedfor capillary columns. When utilizing the full capillary col-umns (0.25 mm), a split injection system is required; howevera “cold on-column” injector is preferred for the wide bore(0.53 mm) capillaries. The FID should have sufficient sensitiv-ity to give a minimum peak he

20、ight response of 30 V for 0.1mass % of 6PPD when operated at the stated conditions.Background noise at these conditions is not to exceed 3 V.7.2 Gas Chromatographic Columns:7.2.1 Packed Column for Procedure A1.828 m 3 6.35mm (6 ft 314 in.) outside diameter 3 4 mm (0.16 in.) insidediameter glass colu

21、mns packed with 10 % methyl silicone fluid(100 %) on 80/100 mesh acid washed and silanized diatomitesupport. The column should be conditioned with a helium flowof approximately 20 cm3/min by programming from ambienttemperature to 350C at the rate of 2 to 3C/min and holdingat 350C overnight with the

22、detector disconnected.7.2.2 Capillary Column for Procedure B(1)30m3 0.25mm ID fused silica capillary, internally coated to a filmthickness of 0.25 m (bonded) with methyl silicone; (2)15m 3 0.53 mm fused silica (megabore) capillary with 3.0 mbonded film of 5 % phenyl silicone, HP-5 or equivalent.7.3

23、Integrator/Data System, capable of determining therelative amount of each component by means of integration ofthe detector output versus time. When using capillary columns(Procedure B) the device must integrate at a sufficiently fastrate so that narrow peaks (one second peak width) can beaccurately

24、measured.7.4 When using a packed column, a minimum of 5000theoretical plates, as measured from the 6PPD peak, with thechromatographic conditions stated in 9.1 is required for analy-sis. Theoretical plates (TP) are determined by the followingformula:TP 5 5.5 XR!/Y0/5!#2(1)where:X(R) = retention time

25、measured from the injection pointto the apex of the 6PPD peak (adjust theattenuation to keep peak on scale), mm, andY (0.5) = 6PPD band width at half-height, mm.8. Calibration and Standardization8.1 When using the conditions described for Procedure A(packed column), the detector response of 6PPD for

26、 injectionsof 500 to 5000 g was found to be somewhat nonlinear (seeX1.3). However, over the more limited range, 750 to 2500 g,the response was nearly linear (see X1.4). As a result, it issuggested that the samples be prepared so that 1250 to 1500 ginjections are made.8.2 Chromatograms from typical s

27、pecimens run on thepacked columns according to the prescribed procedure aregiven in Appendix X1.9. Procedure9.1 Procedure AChromatographic Conditions:Helium flow rate 50 cm3/minInjection port temperature 300CInitial column temperature 100CHeating rate 8C/minFinal Temperature 350CDetector temperature

28、 350CDetector: TC attenuation 89.1.1 Integrator/data system parameters are presented inX1.2.9.1.2 Specimen PreparationTo ensure specimen homoge-neity, lot samples of 6PPD should be ground with a mortar andpestle prior to weighing the test unit. In the case of liquid 6PPDwhere partial crystallization

29、 may have occurred resulting infractionation, the lot sample should be melted in a 50 to 60Coven with occasional stirring, prior to weighing the test unit.9.2 Procedure AAnalysis:9.2.1 Weigh 2.5 to 3.0 g specimen (to the nearest milligram)intoa10cm3volumetric flask, dilute to volume with methyl-ene

30、chloride, and shake well to dissolve.9.2.2 When the instrument has equilibrated at the initialconditions described in 9.1, inject 5.0 mm3(L) of samplesolution and initiate the temperature program and data collec-tion.9.2.3 When the run is complete, inspect the chromatogramand output data for proper

31、appearance and peak identification(see X1.1).9.2.4 Repeat the run described in 9.2.2 on the same speci-men.NOTE 2Specimen size and carrier gas flow rates should be adjusted inaccordance with the cross-sectional area of the column utilized. Forexample, if a nominal18 in. outside diameter column (1.87

32、 mm insidediameter) is used rather than a14 in. outside column (3.54 mm insidediameter), the adjustment would be as follows: The ratio of cross-sectionalareas is 3.54/1.87 squared, which equals 3.6. Thus, the sample size andhelium carrier flow rate should be decreased by this factor; that is, the fl

33、owrate of 50/3.6 or 14 cm3/min and sample size to 5/3.6 or 1.4 mm3(L).9.3 Procedure B: Chromatographic ConditionsThe sug-gested operating conditions for the analysis using a capillarycolumn are given in Table 1. Column (1) is for a standardcapillary and Column (2) is for a megabore capillary.9.4 Pro

34、cedure BSample Analysis:D4937 96 (2012)29.4.1 Prepare the sample as in 9.1.2 and the test specimenaccording to Table 1.9.4.2 When the instrument has equilibrated at the initialconditions described in Table 1, inject the indicated amount ofdiluted test specimen and immediately start the recorder,inte

35、grator, and column temperature programming sequence.9.4.3 When the run is complete, inspect the chromatogramand output data for proper appearance and peak identification.Typical chromatograms on the 0.53 mm megabore capillary isshown in Figs. X2.1-X2.4 (6PPD) respectively.9.4.4 Repeat the run descri

36、bed in 9.4.2 on the same speci-men.10. Calculation10.1 Calculate the relative area percent of 6PPD and theother identified components as follows:A 5 AC/AT! 3 100 % (2)where:A = area of 6PPD, %,AC= area of component, andAT= total area.11. Report11.1 Report the following information:11.1.1 The combine

37、d area of all unidentified peaks aspercent other,11.1.2 All results to the nearest 0.1 %, and11.2 The final report should include proper identification ofthe specimen and the data from the two individual injectionsplus their average.12. Precision and BiasProcedure A12.1 This precision and bias secti

38、on has been prepared inaccordance with Practice D4483. Refer to Practice D4483 forterminology and other statistical details.12.1.1 The precision results in this precision and biassection give an estimate of the precision of this test methodwith the materials (antidegradants) used in the particularin

39、terlaboratory programs as described below. The precisionparameters should not be used for acceptance/rejection testingof any group of materials without documentation that they areapplicable to those particular materials and the specific testingprotocols that include this test method.12.2 A Type 1 (i

40、nterlaboratory) precision was evaluated in1987. Both repeatability and reproducibility are short term. Aperiod of a few days separates replicate test results.Atest resultis the mean value, as specified by this test method, obtained ontwo determinations or measurements of the property or param-eter i

41、n question.12.3 Four different materials were used in the interlabora-tory program. These were tested in four laboratories on twodifferent days.12.4 The results of the precision calculations for repeatabil-ity and reproducibility are given in Table 2, in ascending orderof material average or level,

42、for each of the materials evalu-ated.12.5 The precision of this test method may be expressed inthe format of the following statements which use an “appro-priate value” or r, R,(r), or (R), that is, that value to be used indecisions about test results (obtained with the test method).TABLE 1 Procedure

43、 BChromatographic ConditionsColumn (1) 30 m 3 0.25 mm (2) 15 m 3 0.53 mmStationary Phase bonded methyl silicone bonded 5 % phenylsiliconeFilm thickness 0.25 m 3.0 mCarrier gas (helium) (helium)Linear velocity at 100C 0.34 m/sec NAFlow rate 1.0 cm3/min 30.0 cm3/minHead pressure 60 kPa, gauge (9 psig)

44、 NADetector FID FIDDetector Temperature 300C 300CInjection Port Temperature 300C oven trackingHydrogen Flow RateA30 cm3/min 30 cm3/minAir Flow RateA300 cm3/min 300 cm3/minMakeup Gas Nitrogen or Helium Nitrogen or HeliumMakeup Flow RateA29 cm3/min 10 cm3/minSplit Ratio 180:1 (no split)Column Temperat

45、ureProgramRamp A Ramp BInitial temperature 42C 35C 240CProgram rate 9C/min 15C/min 8C/minFinal temperature 300C 240C 290CTime at finaltemperature22 min 3 min 17 minSample Size 0.4 mm3(L) 1 mm3(L)Solvent methylene chloride methylene chlorideSample Concentration 10 mg/cm33 mg/cm3AConsult the manufactu

46、rers manual for optimum selection of flow rates ondifferent instruments.TABLE 2 GC Purity of PPDS, Percent (Procedure A)Material AverageWithin LaboratoryABetween LaboratoryASrr (r) SRR (R)M1-6PPD 97.09 0.1651 0.4673 0.481 1.926 5.45 5.61M2-IPPD 96.05 0.2792 0.7900 0.822 1.239 3.50 3.65M3-77PD 96.05

47、0.1121 0.3172 0.330 1.382 3.91 4.07M4-DTPD 94.85 0.2894 0.8191 0.864 2.080 5.88 6.20Pooled valuesB96.01 0.2301 0.6512 0.678 1.6588 4.6943 4.889ASr= repeatability standard deviation.r = repeatability = 2.83 times the square root of the repeatability variance.(r) = repeatability (as a percent of mater

48、ial average).SR= reproducibility standard deviation.R = reproducibility = 2.83 times the square root of the reproducibility variance.(R) = reproducibility (as a percent of material average).BNo values omitted.D4937 96 (2012)3The appropriate value is that value of r or R associated with amean level i

49、n Table 2 closest to the mean level underconsideration at any given time, for any given material, inroutine testing operations.12.6 RepeatabilityThe repeatability, r, of this test methodhas been established as the appropriate value tabulated in Table1. Two single test results, obtained under normal test methodprocedures, that differ by more than this tabulated r (for anygiven level) must be considered as derived from different ornonidentical sample populations.12.7 ReproducibilityThe reproducibility, R, of