ASTM D2163-2007 Standard Test Method for Determination of Hydrocarbons in Liquefied Petroleum (LP) Gases and Propane Propene Mixtures by Gas Chromatography《用气相色谱法分析液化石油气和丙烯浓缩物的标准试验.pdf

《ASTM D2163-2007 Standard Test Method for Determination of Hydrocarbons in Liquefied Petroleum (LP) Gases and Propane Propene Mixtures by Gas Chromatography《用气相色谱法分析液化石油气和丙烯浓缩物的标准试验.pdf》由会员分享，可在线阅读，更多相关《ASTM D2163-2007 Standard Test Method for Determination of Hydrocarbons in Liquefied Petroleum (LP) Gases and Propane Propene Mixtures by Gas Chromatography《用气相色谱法分析液化石油气和丙烯浓缩物的标准试验.pdf（11页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D 2163 07An American National StandardStandard Test Method forDetermination of Hydrocarbons in Liquefied Petroleum (LP)Gases and Propane/Propene Mixtures by GasChromatography1This standard is issued under the fixed designation D 2163; the number immediately following the designation ind

2、icates 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 (e) indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers the quantitative

3、 determinationof individual hydrocarbons in liquefied petroleum (LP) gasesand mixtures of propane and propene, excluding high-puritypropene in the range of C1to C5. Component concentrationsare determined in the range of 0.01 to 100 volume percent.1.2 This test method does not fully determine hydroca

4、rbonsheavier than C5and non-hydrocarbon materials, and additionaltests may be necessary to fully characterize an LPG sample.1.3 The values stated in SI units are to be regarded as thestandard. The values given in parentheses are for informationonly.1.4 This standard does not purport to address all o

5、f 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:2D 1265 Practice for Sam

6、pling Liquefied Petroleum (LP)Gases, Manual MethodD 1835 Specification for Liquefied Petroleum (LP) GasesD 2421 Practice for Interconversion of Analysis of C5andLighter Hydrocarbons to Gas-Volume, Liquid-Volume, orMass BasisD 2598 Practice for Calculation of Certain Physical Prop-erties of Liquefied

7、 Petroleum (LP) Gases from Composi-tional AnalysisD 3700 Practice for Obtaining LPG Samples Using a Float-ing Piston CylinderD 6729 Test Method for Determination of Individual Com-ponents in Spark Ignition Engine Fuels by 100 MetreCapillary High Resolution Gas ChromatographyE 355 Practice for Gas Ch

8、romatography Terms and Rela-tionshipsE 594 Practice for Testing Flame Ionization Detectors Usedin Gas or Supercritical Fluid ChromatographyE 1510 Practice for Installing Fused Silica Open TubularCapillary Columns in Gas Chromatographs2.2 Canadian General Standards Board Publications:3CAN/CGSB 3.0 No

9、. 14.3 Standard Test Method for theIdentification of Hydrocarbon Components in AutomotiveGasoline Using Gas Chromatography2.3 Gas Processors Association:4GPA Std 2145-03 for hexane3. Terminology3.1 Definitions:3.1.1 Additional terminology related to the practice of gaschromatography can be found in

10、Practice E 355.3.1.2 liquefied petroleum gas (LPG), nhydrocarbon gasesthat can be stored or handled in the liquid phase throughcompression or refrigeration, or both.3.1.2.1 DiscussionLPGs generally consist of C3and C4alkanes and alkenes or mixtures thereof and containing lessthan 10 volume percent o

11、f higher carbon number material.Vapor pressure does not normally exceed 2000 kPa at 40C.3.2 Definitions of Terms Specific to This Standard:3.2.1 propane/propene mixtures, nmixtures primarilycomposed of propane and propene where one of these compo-nents is usually in the concentration range of 30 to

12、85 mass %with the other comprising the majority of the remainder.“Commercial Propane in Specification D 1835 is typically thissort of product mixture.3.2.1.1 DiscussionOther components may be present,usually at less than 10 mass %.1This test method is under the jurisdiction of ASTM Committee D02 onP

13、etroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.D0.03 on Propylene.Current edition approved Dec. 1, 2007. Published February 2008. Originallyapproved in 1963. Last previous edition approved in 1996 as D 216391(1996)which was withdrawn December 2004 and reinstated

14、 in December 2007.2For 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 website.3Available from CGSB, Canadian General Stan

15、dards Board, Gatineau, CanadaK1A 1G6. Visit the CGSB website, www.pwgsc.gc.ca/cgsb/4Available from Gas Processors Association (GPA), 6526 E. 60th St., Tulsa, OK74145, http:/.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.Copyright b

16、y ASTM Intl (all rights reserved); Sun Mar 16 21:58:54 EST 2008Downloaded/printed byGuo Dehua (CNIS) pursuant to License Agreement. No further reproductions authorized.4. Summary of Test Method4.1 An LPG sample is analyzed via either liquid or gassampling valves by gas chromatography and compared to

17、corresponding components separated under identical operatingconditions from a reference standard mixture of known com-position or from use of pure hydrocarbons. The chromatogramof the sample is interpreted by comparing peak retention timesand areas with those obtained for the reference standardmixtu

18、re or pure hydrocarbons.5. Significance and Use5.1 The hydrocarbon component distribution of liquefiedpetroleum gases and propene mixtures is often required forend-use sale of this material. Applications such as chemicalfeed stocks or fuel require precise compositional data to ensureuniform quality.

19、 Trace amounts of some hydrocarbon impuri-ties in these materials can have adverse effects on their use andprocessing.5.2 The component distribution data of liquefied petroleumgases and propene mixtures can be used to calculate physicalproperties such as relative density, vapor pressure, and motoroc

20、tane (see Practice D 2598). Precision and accuracy ofcompositional data are extremely important when these dataare used to calculate various properties of these petroleumproducts.6. Apparatus6.1 Gas Chromatograph (GC)Any gas chromatographicinstrument provided with a linear temperature programmableco

21、lumn oven. The temperature control must be capable ofobtaining a retention time repeatability of 0.05 min (3 s)throughout the scope of this analysis.6.2 DetectorA flame ionization detector (FID) having asensitivity of 0.5 ppm (mole) or less for the compounds listedin Table 1 is strongly recommended

22、(see Practice E 594).6.2.1 Other detectors may be used (alone or in series)provided that they have sufficient response, linearity, andsensitivity to measure the components of interest at theconcentration levels required.6.3 Data AcquisitionAny commercial integrator or com-puterized data acquisition

23、system may be used for display ofthe chromatographic detector signal and peak area integration.The device should be capable of calibration and reporting ofthe final response corrected results.6.4 Sample IntroductionWhether liquid or vapor sam-pling, the combination of valve injection size and split

24、ratiomust be selected such that the required sensitivity is achievedand also that no component concentration in a sample is greaterthan the detector upper linearity limit.6.4.1 If capillary columns will be used, then the GC mustinclude a heated splitting type injector that is operated isother-mally.

25、 Split ratios in the range of 5:1 to 200:1, with a typicalvalue of 100:1, will be used dependent upon the sampleinjection volume and sensitivity required. If packed columnswill be used, then a splitting type injector is not required and asuitable packed inlet port may be used.6.4.2 Liquid Sampling (

26、recommended)The GC should beequipped with a liquid sampling valve for introduction of thesample aliquot to the splitting injector. Liquid sampling valveswith an internal fixed sample volume between 0.2 to 0.5 L ora size to provide the minimum detection limits given in 1.1have been used satisfactoril

27、y. The valve shall be rated for atleast 1380 kPa (200 psi) above the vapor pressure of the sampleat the valve operating temperature. A shut-off valve shall beprovided at the exit of the sampling valve waste port. A 2 to 7m packed-screen type filter should be provided at the sampleinlet port of the s

28、ampling valve to remove possible particulatematerial from the sample. The valve shall provide for arepeatability of at least 2% relative sample volume introduc-tion. The sampling valve shall be located at the GC such thatTABLE 1 Expected Retention Order and TimesComponentEstimated Retention Time (mi

29、n)(using typical Al2O3PLOT operating conditions)Estimated Retention Time (min)(using typical 100 m Dimethylpolysiloxanecolumn operating conditions)FID TCDC5Olefin/C6+Composite (backflush) NAA. x xAir Composite (O2,Ar,N2, Co) NAA. . xMethane 1.9 6.5 x xEthane 2.1 6.7 x xPropane 2.7 7.3 x xCyclopropan

30、e 3.4 . x xPropene 3.5 7.2 x x2-Methyl Propane (Isobutane) 4.0 8.4 x xButane 4.2 9.5 x xPropadiene 4.7 . x xEthyne (Acetylene) 5.0 . x xTrans-2-Butene 5.5 9.9 x x1-Butene 5.6 9.2 x x2-Methyl Propene (Isobutene) 5.7 9.1 x x2,2-Dimethylpropane (Neopentane) 5.9 10.1 x xCis-2-Butene 6.2 10.6 x xCyclopen

31、tane 6.7 25.8 x x2-Methyl Butane (Isopentane) 6.8 14.0 x xPentane 7.2 16.9 x x1,3-Butadiene 7.5 9.3 x xPropyne (Methyl Acetylene) 7.9 . x xnC5(Sum C5Olefins and Heavier)B8.1 until end of run . x xANot applicable.BnC5components may be speciated and reported individually.D2163072Copyright by ASTM Intl

32、 (all rights reserved); Sun Mar 16 21:58:54 EST 2008Downloaded/printed byGuo Dehua (CNIS) pursuant to License Agreement. No further reproductions authorized.it can be operated at ambient temperature. The use of floatingpiston sample cylinders is encouraged to minimize or eliminatethe volatilization

33、of lighter components into the headspace.Common 80% filled LPG storage cylinders should be pressur-ized with an inert gas such as helium to facilitate liquid transferand accurate liquid injections. A minimum pressure of 200 psiabove sample vapor pressure is recommended. A pressuregauge may be used t

34、o make this determination. Before pres-surization, verify that the sample cylinder, transfer lines andvalves are rated to safely contain the pressurized sample. It iscustomary to add a check valve between the helium cylinderand the sample cylinder to prevent contamination in the eventthe sample cyli

35、nder is higher in pressure than the pressurizingcylinder.6.4.3 Vapor Sampling (optional)A six-port gas samplingvalve or a ten-port sampling/column switching valve with1.6 mm (116 in.) fittings and a 200 L fixed sampling loop maybe provided. This valve shall be contained in a heatedenclosure and oper

36、ated at a temperature above the boiling pointof the highest boiling component in the sample. The use of a 2to 7 m frit or packed-screen type filter ahead of the sampleintroduction port is recommended. The valve shall provide fora repeatability of at least 2% relative sample volume introduc-tion.6.5

37、Gas ControlsThe GC shall be provided with suitablefacilities for delivery and control of carrier gas and the detectorgases. This will consist of the appropriate tank and down-stream regulators and supply tubing as well as the mass orpressure controls for the precise regulation of the instrumentopera

38、tion.NOTE 1Most GC suppliers will provide these devices or recommendthe proper supplies.6.6 Column Series/Reversal Switching ValveIf desired, amulti-port valve mentioned may be used to provide the C5olefin/C6+ determination for this analysis. The back-flushconfiguration should be configured accordin

39、g to the manufac-turers recommendations.6.7 ColumnsCondition all columns used according to themanufacturers suggestions prior to use.6.7.1 Analytical ColumnThe recommended analyticalcolumn is a 50 m by 0.53 mm (I.D) Na2SO4deactivated Al2O3porous layer open tubular (PLOT) column. Relative retentionor

40、der is dependent upon the deactivation method for thecolumn. (WarningSpecifically test the column to ensure thatthe column does not adsorb propadiene and butadienes. Thiscondition can exist depending upon the degree of columndeactivation.)6.7.1.1 Routine re-conditioning of the column may berequired

41、to maintain column performance.6.7.1.2 Alternatively, any column(s) that provides the ap-propriate component separations may be used. Columns (100m by 0.25 mm (ID) by 0.5 m film thickness) employed instandard methods Test Method D 6729 and CGSB 3.0 No. 14.3have been successfully used.6.7.2 Pre-colum

42、n (optional)If an initial back flush of theC5olefins or hexane plus (C6+) components, or both, throughthe use of the sequence reversal/back flush valve is desired, asecond column is required. Any pre-column that providesseparation between the components of interest and the com-posite heavier compone

43、nts may be used. Choices may includelengths of column such as a 10 to 30 m section of 0.53 mm(I.D.) 1 m film thickness dimethylpolysiloxane or polyethyl-ene glycol capillary column ora9to15cmsection of the samecolumn material as the analytical column or any pre-columnthat provides the desired retent

44、ion of C5olefins, hexanes, andheavier components. This pre-column acts to keep the heaviercomponents away from the analytical column and to back flushthe heavier components as a composite peak to the detector forquantitation. A pre-column that also has the ability to retainwater and oxygenated hydro

45、carbon compounds is recom-mended to keep those materials from entering the analyticalcolumn.7. Reagents and Materials7.1 Carrier GasesFor carrier gases, it is recommended toinstall commercial active oxygen scrubbers and water dryers,such as molecular sieves, ahead of the instrument to protect thesys

46、tems chromatographic columns. Follow supplier instruc-tions in the use of such gas purifiers and replace as necessary.7.1.1 Hydrogen, 99.995% minimum purity, nC5(C5=and heavier) 0.885ARF values obtained from Test Method D 6729.All response factors are relative to that of methane according to the fol

47、lowing equation:RRFi5 MWi/ NCi! 3 1/MWmethane!where:RRFi= relative response factor of each component with respect to methane,MWi= the molecular weight of the component,NCi= the number of carbon atoms in the component molecule, andMWmethane= the molecular weight of methane.D2163077Copyright by ASTM I

48、ntl (all rights reserved); Sun Mar 16 21:58:54 EST 2008Downloaded/printed byGuo Dehua (CNIS) pursuant to License Agreement. No further reproductions authorized.close cylinder valve, and allow the sample pressure to equili-brate to atmospheric pressure (stopped flow) before introduc-ing the sample in

49、to the carrier gas stream.10.3.1 In a hood, prior to connecting the cylinder, invert thecylinder and purge a small aliquot of the sample through thevalve on the sample cylinder to remove any moisture orparticulate matter which might be present.10.3.2 Attach a secondary sampling vessel, consisting oftwo ball valves joined together and having an internal volumeof approximately one mL to the liquid outlet on the samplevessel.10.3.3 Evacuate the secondary vessel to approximately0.13 kPa (1 mm Hg), including the connection to the liq