ASTM D7057-2009 516 Standard Test Method for Analysis of Isopropylbenzene (Cumene) by Gas Chromatography (External Standard)《气相色谱法分析异丙基苯的标准试验方法》.pdf

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1、Designation: D 7057 09Standard Test Method forAnalysis of Isopropylbenzene (Cumene) by GasChromatography (External Standard)1This standard is issued under the fixed designation D 7057; 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. Scope*1.1 This test method covers the determination of the purityof isopropylbenzene (cumene) by gas chromatograp

3、hy. Cali-bration of the gas chromatography system is done by theexternal standard calibration technique.1.2 This test method has been found applicable to themeasurement of impurities such as nonaromatic hydrocarbons,benzene, toluene, ethylbenzene, phenol, cymenes,t-butylbenzene, n-butylbenzene, n-pr

4、opylbenzene, alpha-methylstyrene, sec-butylbenzene, and diisopropylbenzenes,which are impurities that can be found in isopropylbenzene.The latter impurities can be analyzed over a range of 1 mg/kgto 500 mg/kg by this method (see Table 1). The limit ofdetection for these impurities is summarized in T

5、able 1 as well.1.3 In determining the conformance of the test results usingthis method to applicable specifications, results shall berounded off in accordance with the rounding-off method ofPractice E29.1.4 The values stated in SI units are to be regarded asstandard. No other units of measurement ar

6、e included in thisstandard.1.5 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 p

7、rior to use. For specific hazardstatements, see Section 8.2. Referenced Documents2.1 ASTM Standards:2D 3437 Practice for Sampling and Handling Liquid CyclicProductsD 4307 Practice for Preparation of Liquid Blends for Use asAnalytical StandardsD 4790 Terminology of Aromatic Hydrocarbons and Re-lated

8、ChemicalsD 6809 Guide for Quality Control and Quality AssuranceProcedures for Aromatic Hydrocarbons and Related Ma-terialsE29 Practice for Using Significant Digits in Test Data toDetermine Conformance with SpecificationsE 355 Practice for Gas Chromatography Terms and Rela-tionshipsE 691 Practice for

9、 Conducting an Interlaboratory Study toDetermine the Precision of a Test MethodE 1510 Practice for Installing Fused Silica Open TubularCapillary Columns in Gas Chromatographs2.2 Other Document:OSHA Regulations, 29CFR paragraphs 1910.1000 and1910.120033. Terminology3.1 See Terminology D 4790 for defi

10、nition of terms used inthis test method.4. Summary of Test Method4.1 Cumene (isopropylbenzene) is analyzed by a gas chro-matograph (GC) equipped with a flame ionization detector(FID). A precisely repeatable volume of the sample to beanalyzed is injected onto the gas chromatograph. The peakareas of t

11、he impurities are measured and converted to concen-trations via an external standard methodology. Purity by GC(the Cumene content) is calculated by subtracting the sum ofthe impurities from 100.00, excluding Acetophenone (AP) and2-phenyl-2-propanol (DMPC or DMBA) which are artifacts ofcumene hydrope

12、roxide (CHP) thermal decomposition in theinlet of the GC. Results are reported in weight percent.5. Significance and Use5.1 This test method is suitable for setting specifications onthe materials referenced in 1.2 and for use as an internal qualitycontrol tool where isopropylbenzene is produced or i

13、s used in1This test method is under the jurisdiction of ASTM Committee D16 onAromatic Hydrocarbons and Related Chemicals and is the direct responsibility ofSubcommittee D16.07 on Styrene, Ethylbenzene and C9and C10Aromatic Hydro-carbons.Current edition approved June 1, 2009. Published June 2009. Ori

14、ginallyapproved in 2004. Last previous edition approved in 2004 as D 7057 - 04.2For 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 o

15、nthe ASTM website.3Available from U.S. Government Printing Office Superintendent of Documents,732 N. Capitol St., NW, Mail Stop: SDE, Washington, DC 20401, http:/www.access.gpo.gov.1*A Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive,

16、 PO Box C700, West Conshohocken, PA 19428-2959, United States.a manufacturing process. It may also be used in developmentor research work involving isopropylbenzene.5.2 This test method is useful in determining the purity ofisopropylbenzene with normal impurities present. If extremelyhigh boiling or

17、 unusual impurities are present in the isopropy-lbenzene, this test method would not necessarily detect themand the purity calculation would be erroneous.5.3 Cumene hydroperoxide, if present, will yield thermaldecomposition products, primarily AP and DMPC as stated in4.1, that will elute in the chro

18、matogram thereby givingincorrect results unless they are excluded as indicated in 4.1.Itis also possible to get erroneous results for trace alpha-methylstyrene present in isopropylbenzene if the inlet hasbecome unduly contaminated with non-volatile foreign sub-stances.5.4 The nonaromatic hydrocarbon

19、s commonly present fromthe isopropylbenzene manufacturing process, particularly anon-zeolitic one, will interfere with the determination ofxylenes (if present).6. Apparatus6.1 Gas ChromatographAny instrument having a flameionization detector that can be operated at the conditions givenin Table 2. Th

20、e system should have sufficient sensitivity toobtain a minimum peak height response for 1 mg/kg benzeneof twice the height of the signal background noise.6.2 ColumnsThe choice of column is based on resolutionrequirements. Any column may be used that is capable ofresolving all significant impurities

21、from isopropylbenzene. Thecolumn described in Table 2 has been used successfully. Unlessthe analyst can be sure of peak identity, for example by gaschromatography-mass spectrometry (GC-MS), the use of thecolumn in Table 2 is strongly recommended.6.3 RecorderElectronic integration is required.6.4 Inj

22、ectorThe specimen must be precisely and repeat-edly injected into the gas chromatograph.An automatic sampleinjection device is highly recommended. Manual injection canbe employed if the precision stated in Table 1, Summary ofPrecision Data, can be reliably and consistently satisfied.7. Reagents and

23、Materials7.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise 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.4Other g

24、rades may beused, provided it is first ascertained that the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of the determination.7.2 GasesHelium, Hydrogen, Nitrogen, or other as Car-rier. Carrier, makeup, and detector gases 99.999 % minimumpurity. Oxygen in carr

25、ier gas less than 1 ppm, less than 0.5 ppmis preferred. Purify carrier, makeup, and detector gases toremove oxygen, water, and hydrocarbons. Purify air to removehydrocarbons and water, and the air used should be zero gradeor better.8. Hazards8.1 Consult current OSHA regulations, suppliers MaterialSa

26、fety Data Sheets, and local regulations for all materials listedin this test method.4Reagent 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

27、 LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.TABLE 1 Summary of Precision Data (mg/kg)Compound Repeatability ReproducibilityRangeStudiedBenzene 1.004+0.006*Benzene 0.924+0.158*B

28、enzene 1.0295Toluene 0.644+0.009*Toluene 1.505+0.069*Toluene 0.2260Ethylbenzene (EB) 1.249+0.022*EB 2.534+0.230*EB 5370n-Propylbenzene (NPB) -0.369+0.015*NPB -6.793+0.214*NPB 180465Phenol (PHE) 1.926+.0095*PHE 3.718+0.207*PHE 1225alpha-methylstyrene(AMS) 1.368+0.057*AMS 21.181+0.976*AMS 6305tert-But

29、ylbenzene(TBB) 1.666+0.011*TBB 4.126+0.086*TBB 2250sec-Butylbenzene(SBB) 0.635+0.010*SBB 0.891+0.090*SBB 2245m-Cymene 0.618+0.011*m-Cymene 1.811+0.181*m-Cymene 5240o-Cymene 0.498+0.012*o-Cymene 1.951+0.156*o-Cymene 1160p-Cymene 0.485+0.019*p-Cymene 1.618+0.097*p-Cymene 2270n-Butylbenzene(NBB) 0.445+

30、0.030*NBB 2.600+0.045*NBB 0.32651,3-diisopropylbenzene(13DIPB) 0.727+0.010*13DIPB 1.570+0.720*13DIPB 12101,4-diisopropylbenzene(14DIPB) 0.435+0.013*14DIPB 1.112+0.040*14DIPB 1285NonAromatics(NA) 0.441+0.242*NA 1.663+0.306*NA 595TABLE 2 Instrumental ParametersDetector flame ionizationInjection Port c

31、apillary splitterColumn A:Tubing fused silicaStationary Phase crosslinked polydimethylsilicone (HP-1, DB-1 or equiv)Film Thickness, m 1.0Length, m 60Diameter, mm 0.32Temperatures:Injector, C 250Detector, C 300Oven, C 85 hold for 13 minRamp 1 = 6C/min to 125C, hold for 2 minRamp 2 = 30C/min to 250C,

32、hold for 7.5 minCarrier Gas HeliumFlow Rate, mls/min 3Split Ratio 60:1Sample Size, L 1.0D70570929. Sampling and Handling9.1 Sample the material in accordance with PracticeD 3437.10. Preparation of Apparatus10.1 Follow manufacturers instructions for mounting andconditioning the column into the chroma

33、tograph and adjustingthe instrument to the conditions described in Table 2 allowingsufficient time for the equipment to reach equilibrium. SeePractices E 1510 and E 355 for additional information on gaschromatography practices and terminology.11. Calibration11.1 Prepare a synthetic mixture of high p

34、urity cumenecontaining impurities at concentrations representative of thoseexpected in the samples to be analyzed in accordance withPractice D 4307. The weight of each hydrocarbon impuritymust be measured to the nearest 0.1 mg. Because the avail-ability of stock cumene with a purity higher than 99.9

35、7 % isproblematic, the method of standard additions may be requiredfor impurities such as tert-butylbenzene and n-propylbenzene,as well as for a number of the other impurities listed in 1.2 thatare commonly present.11.2 Inject the resulting solution from 11.1 into the gaschromatograph, collect and p

36、rocess the data. A typical chro-matogram is illustrated in Fig. 1 based on the conditions listedin Table 2.11.3 Determine the response factor for each impurity in thecalibration mixture as follows:Rfi 5 Ci/Ai (1)where:Rfi = response factor for impurity i,Ci = concentration of impurity i in the calib

37、ration mixture,andAi = peak area of impurity i.FIG. 1 Typical Chromatogram using Conditions in Table 2D705709311.4 Initially analyze the calibration solution a minimum ofthree times and calculate an average Rfi. Subsequent calibra-tions may be a single analysis as long as the response factorsfor all

38、 components of interest are within 65 % of the initialvalidation response factors. A “rolling” average as defined bymost modern chromatographic software may also be used. Theresponse factor for tert-butylbenzene is used for unknowns andnon-aromatics quantification.12. Procedure12.1 Inject into the g

39、as chromatograph an appropriateamount of sample as previously determined according to 6.1and start the analysis.12.2 Obtain a chromatogram and peak integration report.Fig. 1 illustrates a typical analysis of cumene using the columnand conditions outlined in Table 2.13. Calculations13.1 Calculate the

40、 concentration of each impurity as fol-lows:Ci 5 Ai! Rfi! (2)where:Ci = concentration of component i in mg/kg,Ai = peak area of component i, andRfi = response factor for component i,13.2 Calculate the total concentration of all impurities inwt % (excluding AP and DMBA as per 5.3) as follows:Ct5(Ci/1

41、0000 (3)where:Ct= total concentration of all impurities.13.3 Calculate the purity of isopropylbenzene as follows:Cumene, weight percent 5 100.00 2 Ct(4)14. Report14.1 Report the individual impurities to the nearest mg/kg.14.2 Report the purity of isopropylbenzene to the nearest0.01 wt %.15. Precisio

42、n and Bias515.1 The criteria in Table 1 should be used to judge theacceptability at the 95 % probability level of the resultsobtained by this test method. The criteria were derived from anInterlaboratory study of five samples analyzed in triplicate byfive laboratories. The results were derived using

43、 the protocolset forth in Practice E 691.15.2 RepeatabilityResults in the same laboratory shouldnot be considered suspect unless they differ by more than theamounts calculated from the appropriate equations in Table 1.15.3 ReproducibilityResults submitted by two laborato-ries should not be considere

44、d suspect unless they differ bymore than the amounts calculated from the appropriate equa-tions in Table 1.15.4 BiasSince there is no accepted reference materialsuitable for determining the bias for the procedure in this testmethod for measuring isopropylbenzene purity, bias has notbeen determined.1

45、6. Quality Guidelines16.1 Refer to Guide D 6809 for suggested QA/QC activitiesthat can be used as a part of this method. It is recommendedthat the operator of this method select and perform relevantQA/QC activities like the ones in Guide D 6809 to help ensurethe quality of data generated by this met

46、hod.17. Keywords17.1 alpha-methylstyrene; analysis by gas chromatography;benzene; butylbenzene; cumene; cymene; diisopropylbenzene;ethylbenzene; isopropylbenzene; methyl cumene; nonaromatichydrocarbons; propylbenzene; tolueneSUMMARY OF CHANGESCommittee D16 has identified the location of selected cha

47、nges to this standard since the last issue(D 7057 - 04) that may impact the use of this standard. (Approved June 1, 2009.)(1) Reference to SI units added in Scope.(2) Minor changes to verbiage in other sections to be consis-tent with updated D16 Editorial Guidelines.5Supporting data are available fr

48、om ASTM International Headquarters. RequestRR:D161033.D7057094ASTM 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

49、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, 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 attend. If y

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