ASTM D7504-2017a red 5000 Standard Test Method for Trace Impurities in Monocyclic Aromatic Hydrocarbons by Gas Chromatography and Effective Carbon Number《采用气相色谱法和有效碳数测定单环芳烃中微量杂质的标准.pdf

《ASTM D7504-2017a red 5000 Standard Test Method for Trace Impurities in Monocyclic Aromatic Hydrocarbons by Gas Chromatography and Effective Carbon Number《采用气相色谱法和有效碳数测定单环芳烃中微量杂质的标准.pdf》由会员分享，可在线阅读，更多相关《ASTM D7504-2017a red 5000 Standard Test Method for Trace Impurities in Monocyclic Aromatic Hydrocarbons by Gas Chromatography and Effective Carbon Number《采用气相色谱法和有效碳数测定单环芳烃中微量杂质的标准.pdf（16页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D7504 17D7504 17aStandard Test Method forTrace Impurities in Monocyclic Aromatic Hydrocarbons byGas Chromatography and Effective Carbon Number1This standard is issued under the fixed designation D7504; the number immediately following the designation indicates the year oforiginal adopti

2、on 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. Scope*1.1 This test method covers the determination of total nonaromatic hydrocarbo

3、ns and monocyclic aromatic hydrocarbons inbenzene, toluene, ethylbenzene, p-xylene, o-xylene, styrene and mixed xylenes by gas chromatography. The purity of benzene,toluene, ethylbenzene, p-xylene, o-xylene, styrene and mixed xylenes is also calculated. Similar test methods, using the internalstanda

4、rd calibration technique and the external standard calibration technique, are Test Methods D2360, D3797, D4492, D5060,D5135, D5917, and D6563 respectively.1.2 The limit of detection (LOD) is 0.0002 wt % and limit of quantitation (LOQ) is 0.0006 wt % for impurities in toluene, mixedxylenes, p-xylene,

5、 o-xylene, ethylbenzene, benzene, and styrene.1.3 In determining the conformance of the test results using this method to applicable specifications, results shall be roundedoff in accordance with the rounding-off method of Practice E29.1.4 The values stated in SI units are to be regarded as standard

6、. No other units of measurement are included in this standard.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibilityof the user of this standard to establish appropriate safety and health practices and determine the applica

7、bility of regulatorylimitations prior to use.1.6 This international standard was developed in accordance with internationally recognized principles on standardizationestablished in the Decision on Principles for the Development of International Standards, Guides and Recommendations issuedby the Worl

8、d Trade Organization Technical Barriers to Trade (TBT) Committee.2. Referenced Documents2.1 ASTM Standards:2D841 Specification for Nitration Grade TolueneD1555M Test Method for Calculation of Volume and Weight of Industrial Aromatic Hydrocarbons and Cyclohexane MetricD2360 Test Method for Trace Impu

9、rities in Monocyclic Aromatic Hydrocarbons by Gas Chromatography (Withdrawn 2016)3D3437 Practice for Sampling and Handling Liquid Cyclic ProductsD3797 Test Method for Analysis of o-Xylene by Gas Chromatography (Withdrawn 2014)3D4492 Test Method for Analysis of Benzene by Gas ChromatographyD4790 Term

10、inology of Aromatic Hydrocarbons and Related ChemicalsD5060 Test Method for Determining Impurities in High-Purity Ethylbenzene by Gas ChromatographyD5135 Test Method for Analysis of Styrene by Capillary Gas ChromatographyD5136 Specification for High Purity p-XyleneD5211 Specification for Xylenes for

11、 p-Xylene FeedstockD5917 Test Method for Trace Impurities in Monocyclic Aromatic Hydrocarbons by Gas Chromatography and ExternalCalibrationD6229 Test Method for Trace Benzene in Hydrocarbon Solvents by Capillary Gas ChromatographyD6563 Test Method for Benzene, Toluene, Xylene (BTX) Concentrates Anal

12、ysis by Gas Chromatography1 This test method is under the jurisdiction of ASTM Committee D16 on Aromatic, Industrial, Specialty and Related Chemicals and is the direct responsibility ofSubcommittee D16.01 on Benzene, Toluene, Xylenes, Cyclohexane and Their Derivatives.Current edition approved April

13、1, 2017June 1, 2017. Published April 2017June 2017. Originally approved in 2009. Last previous edition approved in 20162017 asD7504 16.D7504 17. DOI: 10.1520/D7504-17.10.1520/D7504-17a.2 For referencedASTM standards, visit theASTM website, www.astm.org, or contactASTM Customer Service at serviceastm

14、.org. For Annual Book of ASTM Standardsvolume information, refer to the standards Document Summary page on the ASTM website.3 The last approved version of this historical standard is referenced on www.astm.org.This document is not an ASTM standard and is intended only to provide the user of an ASTM

15、standard an indication of what changes have been made to the previous version. Becauseit may not be technically possible to adequately depict all changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the current versionof the standard as published by

16、 ASTM is to be considered the official document.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States1D6809 Guide for Quality Control and Quality Assurance Procedures for Arom

17、atic Hydrocarbons and Related MaterialsE29 Practice for Using Significant Digits in Test Data to Determine Conformance with SpecificationsE177 Practice for Use of the Terms Precision and Bias in ASTM Test MethodsE260 Practice for Packed Column Gas ChromatographyE355 Practice for Gas Chromatography T

18、erms and RelationshipsE691 Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test MethodE1510 Practice for Installing Fused Silica Open Tubular Capillary Columns in Gas Chromatographs2.2 Other Document:OSHA Regulations, 29 CFR paragraphs 1910.1000 and 1910.1200 43. Ter

19、minology3.1 See Terminology D4790 for definitions of terms used in this test method.4. Summary of Test Method4.1 The specimen to be analyzed is injected into a gas chromatograph equipped with a flame ionization detector (FID) and acapillary column. The peak area of each component is measured and adj

20、usted using effective carbon number (ECN)5 correctionfactors. The concentration of each component is calculated based on its relative percentages of total adjusted peak area andnormalized to 100.0000 %.5. Significance and Use5.1 Determining the type and amount of hydrocarbon impurities remaining fro

21、m the manufacture of toluene, mixed xylenes,p-xylene, o-xylene, ethylbenzene, benzene, and styrene used as chemical intermediates and solvents is often required. This testmethod is suitable for setting specifications and for use as an internal quality control tool where these products are produced o

22、rare used. Typical impurities are: alkanes containing 1 to 10 carbons atoms, benzene, toluene, ethylbenzene (EB), xylenes, andaromatic hydrocarbons containing nine carbon atoms or more.5.2 This method may not detect all components and there may be unknown components that would be assigned inappropri

23、atecorrection factors and thus, the results may not be absolute.6. Interferences6.1 The complete separation of p-xylene from ethylbenzene, or ethylbenzene and m-xylene from p-xylene can be difficult wheneither ethylbenzene or p-xylene is analyzed, respectively. The separation can be considered adequ

24、ate if the distance from thebaseline to the valley between the two peaks is not greater than 50 % of the peak height of lower of the two peaks.4 Available from U.S. Government Printing Office Superintendent of Documents, 732 N. Capitol St., NW, Mail Stop: SDE, Washington, DC 20401, http:/www.access.

25、gpo.gov.5 Scanlon, J. T. and Willis, D. E., “Calculation of Flame Ionization Detector Relative Response Factors Using the Effective Carbon Number Concept,” Journal ofChromatographic Science, Vol. 23, August 1985, pp. 333339.TABLE 1 Recommended Method ParametersInlet SplitTemperature, C 270Column:Tub

26、ing fused silicaLength, m 60Internal diameter, mm 0.32Stationary phase crosslinked polyethyleneglycolFilm thickness, m 0.25Column temperature programInitial temperature, C 60Initial time, min 10Programming rate, C/min 5Final, C 150Time 2, min 10Carrier gas helium or hydrogenLinear velocity, cm/s at

27、145C 20 helium or 45 hydrogenSplit ratio 100:1Sample size, L 0.6Detector: flame ionizationTemperature, C 300Analysis time, min 38D7504 17a27. Apparatus7.1 Chromatographic data system is required.7.2 ColumnsThe choice of column is based on resolution requirements.Any column may be used that is capabl

28、e of resolvingall significant impurities from the major component. The column and conditions described in Table 1 have been used successfullyand shall be used as a referee in cases of dispute.7.3 Gas ChromatographAny instrument having a flame ionization detector and a splitter injector suitable for

29、use with a fusedsilica capillary column may be used, provided the system has sufficient sensitivity, linearity, and range to determine 0.0001 wt %,while not exceeding the full scale of either the detector or the electronic integration for the major component. It shall have a splitinjection system th

30、at will not discriminate over the boiling range of the samples analyzed. The system should be capable ofoperating at conditions given in Table 1.7.4 InjectorThe specimen must be precisely and repeatably injected into the gas chromatograph. An automatic sampleinjection devise is highly recommended.7.

31、5 Syringechromatographic, capable of delivering appropriate L volumes.8. Reagents and Materials8.1 Purity of ReagentReagent grade chemicals shall be used in all tests. Unless otherwise indicated, it is intended that allreagents shall conform to the specifications of the Committee on Analytical Reage

32、nts of the American Chemical Society,6 wheresuch specifications are available. Reagents with an establish purity greater than ACS reagent grade may be used.8.2 Carrier Gas, Makeup Gas and Detector Gases 99.999 % Pure. Oxygen in carrier gas less than 1 ppm, less than 0.5 ppmis preferred. Purify carri

33、er, makeup and detector gases to remove oxygen, water, and hydrocarbons.8.3 Air for the FID should contain less than 0.1 ppm total hydrocarbon.8.4 Calibration Equipment Set-up Check Standard.Sample This standard may be purchased if desired.8.4.1 High Purity p-Xylene (99.99 wt.% or greater purity)Mos

34、t p-xylene is available commercially at a purity less than 99.9wt. %, but can be purified by recrystallization. To prepare 2 qt. of high-purity p-xylene, begin with approximately 1 gal ofreagent-grade p-xylene and cool in an explosion-proof freezer at between 10 C to +10 C until approximately 12 to

35、34 of thep-xylene has frozen. Remove the sample and decant the liquid portion. Allow the p-xylene to thaw and repeat the crystallizationstep on the remaining sample until the p-xylene is free of contamination (no peaks detected other than p-xylene) as indicated bygas chromatography.8.4.2 Fill a 100

36、mL volumetric flask approximately 34 full of the high purity p-xylene.8.4.3 Add 0.1 mL m-xylene.8.4.4 Add 0.01 mL of toluene, ethylbenzene, cumene, o-xylene, styrene, alpha methylstyrene, and phenylacetylene.8.4.5 Add 0.001 mL benzene and 1, 4-dioxane.8.4.6 Dilute to volume with high purity para-xyl

37、ene.8.4.7 Impurities that are not present in the samples being analyzed may be omitted from the check sample.8.4.8 The purpose of the set-up check sample is to help determine the retention time of the various components and that thepara-xylene and meta-xylene are adequately separated. This sample sh

38、ould not be used for calibration.9. Hazards9.1 Consult current OSHA regulations, suppliers Safety Data Sheets, and local regulations for all materials used in this testmethod.10. Sampling10.1 Sample the material in accordance with Practice D3437.11. Preparation of Apparatus11.1 Follow manufacturers

39、instructions for mounting and conditioning the column into the chromatograph and adjusting theinstrument to the conditions described in Table 1, allowing sufficient time for the equipment to reach equilibrium. See PracticesE260, E355, and E1510 for additional information on gas chromatography practi

40、ces and terminology.12. Calibration12.1 Prior to implementation of the ECN method, a laboratory should demonstrate that acceptable precision and bias can beobtained using a synthetic mixture the equipment is set up properly using an equipment set-up check sample. This sample should6 Reagent Chemical

41、s, American Chemical Society Specifications, American Chemical Society, Washington, DC. For Suggestions on the testing of reagents not listed bythe American Chemical Society, see Analar Standards for Laboratory Chemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeia and National

42、Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville, MD.D7504 17a3be used to: determine retention times of each component, and that the separation of knownmeta composition-xylene from(Calibrationpara check sample).-xylene is satisfactory. See 6.1 for the definition of an adequate separa

43、tion.13. Procedure13.1 Bring the sample to room temperature.13.2 Check the chromatography performance to make sure that the column is properly resolving peaks.13.3 Inject an appropriate amount of sample into the instrument.13.4 Review the chromatographic data system result. Measure the area of all p

44、eaks. The non-aromatics fraction includes allpeaks up to ethylbenzene except for the peaks assigned to benzene and toluene. Sum together all the non-aromatic peaks as a totalarea. When either benzene or toluene is analyzed and 1,4-dioxane is required to be reported, the non-aromatic fraction does no

45、tinclude the peak assigned to 1,4-dioxane.NOTE 1A poorly resolved peak, such as p-xylene from high purity ethylbenzene or m-xylene from high purity p-xylene, will often require a tangentskim from the neighboring peak.13.5 See Figs. 1-8 for representative chromatograms.14. Calculation or Interpretati

46、on of Results14.1 Using the ECN weight correction factors listed in Table 2, calculate the concentration of each component as follows:Ci 51003Ai 3Ri!/(i51nAi 3Ri! (1)TABLE 2 Effective Carbon Number Correction Factors andDensityComponentECNCorrectionFactorADensity at 20CNon Aromatics 1.0000 0.7255 (a

47、verage)BBenzene 0.9100 0.8780CBenzene 0.9095 0.8780CToluene 0.9200 0.8658CToluene 0.9195 0.8658CEthylbenzene 0.9275 0.8658CEthylbenzene 0.9271 0.8658Cp-Xylene 0.9275 0.8597Cp-Xylene 0.9271 0.8597Cm-Xylene 0.9275 0.8630Cm-Xylene 0.9271 0.8630Co-Xylene 0.9275 0.8786Co-Xylene 0.9271 0.8786CCumene 0.933

48、3 0.8605CCumene 0.9329 0.8605C1,4-Dioxane 3.0800 1.0329D1,4-Dioxane 3.0774 1.0329DC9 + Aromatics 0.9333 0.8715E averageC9 + Aromatics 0.9329 0.8715E averageStyrene 0.9215 0.9048CStyrene 0.9210 0.9048CC10 Aromatics 0.938 0.8694E averageC10 Aromatics 0.9376 0.8694E averagep-diethylbenzene(PDEB)0.938 0

49、.8620Ep-diethylbenzene(PDEB)0.9376 0.8620EPhenylacetylene 0.8296 0.9300FAlpha-methylstyreneAMS0.9276 0.9077FA Correction factors are relative to n-heptane.B DS # 4A Physical Constants of Hydrocarbons C1 through C10, ASTM, 1971.Average of hexane, methylcyclopentane, methylcyclohexane, heptane, andethylcyclopentane.C Test Method D1555M.D Keith, L. H., Walters, D B., Compendium of Safety Data Sheets for Research andIndustrial Chemicals, Part II, VCH Publishers, Deerfield Beach, p. 726, 1985.E CRC Handbook of Chemistry and Physics, David R. Lide, 88t