ASTM D5769-2010 6875 Standard Test Method for Determination of Benzene Toluene and Total Aromatics in Finished Gasolines by Gas Chromatography Mass Spectrometry《气相色谱法 质谱分析法测定成品汽油中的.pdf

《ASTM D5769-2010 6875 Standard Test Method for Determination of Benzene Toluene and Total Aromatics in Finished Gasolines by Gas Chromatography Mass Spectrometry《气相色谱法 质谱分析法测定成品汽油中的.pdf》由会员分享，可在线阅读，更多相关《ASTM D5769-2010 6875 Standard Test Method for Determination of Benzene Toluene and Total Aromatics in Finished Gasolines by Gas Chromatography Mass Spectrometry《气相色谱法 质谱分析法测定成品汽油中的.pdf（13页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D5769 10Standard Test Method forDetermination of Benzene, Toluene, and Total Aromatics inFinished Gasolines by Gas Chromatography/MassSpectrometry1This standard is issued under the fixed designation D5769; the number immediately following the designation indicates the year oforiginal ad

2、option 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 determination of benzene,toluene, other sp

3、ecified individual aromatic compounds, andtotal aromatics in finished motor gasoline, including gasolinescontaining oxygenated blending components, by gaschromatography/mass spectrometry (GC/MS).1.2 This test method has been tested for the followingconcentration ranges, in liquid volume percent, for

4、 the follow-ing aromatics: benzene, 0.1 to 4 %; toluene, 1 to 13 %; andtotal (C6 to C12) aromatics, 10 to 42 %. The round-robin studydid not test the method for individual hydrocarbon processstreams in a refinery, such as reformates, fluid catalytic crackednaphthas, and so forth, used in the blendin

5、g of gasolines.1.3 Results are reported to the nearest 0.01 % for benzeneand 0.1 % for the other aromatics by liquid volume.1.4 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

6、 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 its use.2. Referenced Documents2.1 ASTM Standards:2D1298 Test Method fo

7、r Density, Relative Density (SpecificGravity), or API Gravity of Crude Petroleum and LiquidPetroleum Products by Hydrometer MethodD4052 Test Method for Density, Relative Density, and APIGravity of Liquids by Digital Density MeterD4057 Practice for Manual Sampling of Petroleum andPetroleum ProductsD4

8、307 Practice for Preparation of Liquid Blends for Use asAnalytical Standards3. Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 aromaticany hydrocarbon compound containing abenzene or naphthalene ring.3.1.2 calibrated aromatic componentthe individual aro-matic components that have

9、 a specific calibration.3.1.3 cool on-column injectorin gas chromatography,adirect sample introduction system that is set at a temperature ator below the boiling point of solutes or solvent on injection andthen heated at a rate equal to or greater than the column.Normally used to eliminate boiling p

10、oint discrimination oninjection or to reduce adsorption on glass liners within injec-tors, or both. The sample is injected directly into the head ofthe capillary column tubing.3.1.4 open split interfaceGC/MS interface used to main-tain atmospheric pressure at capillary column outlet and toeliminate

11、mass spectrometer vacuum effects on the capillarycolumn. Can be used to dilute the sample entering the massspectrometer to maintain response linearity.3.1.5 reconstructed ion chromatogram (RIC)a limitedmass chromatogram representing the intensities of ion massspectrometric currents for only those io

12、ns having particularmass to charge ratios. Used in this test method to selectivelyextract or identify aromatic components in the presence of acomplex hydrocarbon matrix, such as gasoline.3.1.6 retention gapin gas chromatography, refers to adeactivated precolumn which acts as a zone of low retentionp

13、ower for reconcentrating bands in space. The polarity of theprecolumn must be similar to that of the analytical column.3.1.7 split ratioin capillary gas chromatography, the ratioof the total flow of carrier gas to the sample inlet versus theflow of the carrier gas to the capillary column, expressed

14、by:split ratio 5 S1C!/C (1)where:S = flow rate at the splitter vent, and1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.04.0M on Mass Spectroscopy.Current edition approved May 1, 2010. Published

15、 August 2010. Originallyapproved in 1995. Last previous edition approved in 2004 as D576904. DOI:10.1520/D5769-10.2For 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 th

16、e standards Document Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.C = flow rate at the column outlet.3.1.8 total ion chromatogram (TIC)mass spectrometercomputer output representing either the summed

17、 intensities ofall scanned ion currents or a sample of the current in the ionbeam for each spectrum scan plotted against the correspondingspectrum number. Generally, it can be correlated with a flameionization detector chromatogram.3.1.9 uncalibrated aromatic componentindividual aro-matics for which

18、 a calibration is not available. These compo-nents are estimated from the calibration of several calibratedaromatic components.3.1.10 wall coated open tubular (WCOT)a type of capil-lary column prepared by coating or bonding the inside wall ofthe capillary with a thin film of stationary phase.4. Summ

19、ary of Test Method4.1 A gas chromatograph equipped with a dimethylpolysi-loxane WCOT column is interfaced to a fast scanning massspectrometer that is suitable for capillary column GC/MSanalyses. The sample is injected either through a capillarysplitter port or a cool-on-column injector capable of in

20、troduc-ing a small sample size without overloading the column. Thecapillary column is interfaced directly to the mass spectrometeror by way of an open split interface or other appropriate device.4.2 Calibration is performed on a mass basis, using mixturesof specified pure aromatic hydrocarbons. Volu

21、me percent datais calculated from the densities of the individual componentsand the density of the sample. A multipoint calibration consist-ing of at least five levels and bracketing the expected concen-trations of the specified individual aromatics is required.Specified deuterated hydrocarbons are

22、used as the internalstandards, for example, d6-benzene for quantitating benzene.Unidentified aromatic hydrocarbons present that have not beenspecifically calibrated for are quantitated using the calibrationof an adjacent calibrated compound and summed with the otheraromatic components to obtain a to

23、tal aromatic concentrationof the sample.4.3 Specified quality control mixture(s), such as syntheticquality control mixtures must be analyzed to monitor theperformance of the calibrated GC/MS system. Analysis of agasoline as a reference material is strongly recommended.5. Significance and Use5.1 Test

24、 methods to determine benzene and the aromaticcontent of gasoline are necessary to assess product quality andto meet fuel regulations.5.2 This test method can be used for gasolines that containoxygenates (alcohols and ethers) as additives. It has beendetermined that the common oxygenates found in fi

25、nishedgasoline do not interfere with the analysis of benzene and otheraromatics by this test method.6. Apparatus6.1 Gas Chromatography:6.1.1 System equipped with temperature-programmable gaschromatograph suitable for split injections with WCOT columnor cool-on-column injector that allows the injecti

26、on of small(for example, 0.1 L) samples at the head of the WCOTcolumn or a retention gap.An autosampler is mandatory for theon-column injections.6.1.2 WCOT column containing dimethylpolysiloxanebonded stationary phase, meeting the specification in thefollowing table. For on-column injections, a colu

27、mn containinga thicker film of stationary phase, such as 45 m, is recom-mended to prevent column sample overload.Resolution R between 1,3,5-trimethylbenzene and 1-methyl-2-ethylbenzene at the 3 mass % leveleach must be equal to or greater than2.0R 52t1t2!1.699y2 1 y1!t2 = retention time of 1,3,5-tri

28、methylbenzenet1 = retention time of 1-methyl-2-ethylbenzeney2 = peak width at half height of 1,3,5-trimethylbenzeney1 = peak width at half height 1-methyl-2-ethyl benzene6.2 Mass Spectrometry:6.2.1 Mass spectrometer capable of producing electronimpact spectra at 70, or higher, electron volts or equi

29、valent, andcapable of scanning the range of the specified quantitationmasses or m/e. The mass scan range shall cover the masses ofinterest for quantitation and should yield at least 5 scans acrossthe peak width at half peak width fora1to3mass percenttoluene and cover the masses of interest for quant

30、itation. Ascan range of 41 to 200 daltons is adequate.6.2.2 The mass spectrometer must be capable of beinginterfaced to a gas chromatograph and WCOT columns. Theinterface must be at a high enough temperature to preventcondensation of components boiling up to 220C, usually 20Cabove the final column t

31、emperature is adequate. Direct columninterface to the mass spectrometer can be used. An open splitinterface with computer controlled programmable flow control-ler(s) can also be used, particularly with cool on-columninjections, to maintain all aromatic components within thelinearity of the mass spec

32、trometer and at the same timemaintain detectability of lower concentration aromatic compo-nents. For example, a higher open-split-interface make-up gasflow can be used for the high concentration components, suchas toluene and xylenes, and a lower make-up gas flow rate maybe used during the elution o

33、f the lower concentration benzeneand C9+ components. Other interfaces may be used providedthe criteria specified in Sections 9 and 10 are met.6.2.3 A computer system shall be interfaced to the massspectrometer to allow acquisition of continuous mass scans ortotal ion chromatogram (TIC) for the durat

34、ion of the chromato-graphic program and be able to analyze repeatedly 0.01 masspercent 1,4-diethylbenzene with the specified signal/noise ratioof 5. Software must be available to allow searching anyGC/MS run for specific ions or reconstructed ions and plottingthe intensity of the ions with respect t

35、o time or scan number.The ability to integrate the area under a specific ion plot peakis essential for quantitation. The quantitation software mustallow linear least squares or quadratic nonlinear regression andquantitation with multiple internal standards. It is also recom-mended that software be a

36、vailable to automatically perform theidentification of aromatic components as specified in 13.1.1.D5769 1027. Reagents and Materials7.1 Carrier GasHelium and hydrogen have been usedsuccessfully. The recommended minimum purity of the carriergas used is 99.999 mol percent. Additional purification usin

37、gcommercially available scrubbing reagents may be necessaryto remove trace oxygen, which may deteriorate the perfor-mance of the GC WCOT. (WarningHelium and hydrogenare supplied under high pressure. Hydrogen can be explosiveand requires special handling. Hydrogen monitors that auto-matically shut of

38、f supply to the GC in case of serious leaks areavailable from GC supply manufacturers.)7.2 Dilution SolventsReagent grade 2,2,4-trimethylpentane (iso-octane), n-heptane, n-nonane, cyclohex-ane, or toluene, or a combination thereof, used as a solvent inthe preparation of the calibration mixtures. (Wa

39、rningThegasoline samples and solvents used as reagents such asiso-octane, cyclohexane, n-heptane, n-octane, and toluene, areflammable and may be harmful or fatal if ingested or inhaled.Benzene is a known carcinogen. Use with proper ventilation.Safety glasses and gloves are required while preparing s

40、amplesand standards. Samples should be kept in well ventilatedlaboratory areas.)NOTE 1Toluene should be used as a solvent only for the preparationof C9+ components and shall be free from interfering aromatics.7.3 Internal StandardsDeuterated analogs of benzene,ethylbenzene, and naphthalene, as speci

41、fied in Table 1, shall beused as internal standards because of their similar chromato-graphic characteristics as the components analyzed. The use ofa fourth internal standard toluene-d8 is recommended. Deuter-ated naphthalene is hygroscopic and should be stored awayfrom high humidity.7.4 Standards f

42、or Calibration and IdentificationAromatichydrocarbons used to prepare standards should be 99 % orgreater purity (see Table 1). If reagents of high purity are notavailable, an accurate assay of the reagent shall be performedusing a properly calibrated GC or other techniques. Theconcentration of the i

43、mpurities that overlap the other calibra-tion components shall be known and used to correct theconcentration of the calibration components. The use of onlyhigh purity reagents is strongly recommended because of theerror that may be introduced from impurity corrections. Stan-dards are used for calibr

44、ation as well as for establishing theidentification by retention time in conjunction with massspectral match (see 13.1.1). Naphthalene is hygroscopic andshould be stored away from high humidity.8. Sampling8.1 Every effort should be made to ensure that the sample isrepresentative of the fuel source f

45、rom which it is taken. Followthe recommendations of Practice D4057, or its equivalent,when obtaining samples from bulk storage or pipelines. Sam-pling to meet certain regulatory specifications may require theuse of specific sampling procedures. Consult appropriate regu-lations.8.2 Appropriate steps

46、should be taken to minimize the lossof light hydrocarbons from the gasoline sample while samplingand during analyses. Upon receipt in the laboratory, chill thesample in its original container to between 0 to 5C before andafter a sample aliquot is removed for analysis.8.3 After the sample is prepared

47、 for analysis with internalstandard(s), chill the sample and fill the autosampler vial toapproximately 90 % of its volume. The remainder of thesample should be re-chilled immediately and protected fromevaporation for further analyses, if necessary. To preventevaporation of the sample, the autosample

48、r vials should bestored at 0 to 5C until ready for loading on the autosampler.9. Calibration9.1 Preparation of Calibration StandardsMulti-component calibration standards using all the compounds listedin Table 1 are prepared by mass according to Practice D4307.TABLE 1 Mass Spectrometer Quantitation I

49、ons for Sample Components and Internal StandardsCompound CASNo.Primary Ion(Dalton)Internal Standard(ISTD)ISTD ION(Dalton)Benzene 71-43-2 78 Benzene-d6 84 + 83Toluene 108-88-3 92 Ethylbenzene-d10 ortoluene-d8116 + 115 or 100 + 99Ethylbenzene 100-41-4 106 Ethylbenzene-d10 116 + 1151,3-Dimethylbenzene 108-38-3 106 Ethylbenzene-d10 116 + 1151,4-Dimethylbenzene 106-42-3 106 Ethylbenzene-d10 116 + 1151,2-Dimethylbenzene 95-47-6 106 Ethylbenzene-d10 116 + 115(1-Methylethyl)-benzene 98-82-8 120 Ethylbenzene-d10 116 + 115Propyl-benzene 103-65-1 120 Ethylbenzene-d1