ASTM D6729-2004(2009) 402 Standard Test Method for Determination of Individual Components in Spark Ignition Engine Fuels by 100 Metre Capillary High Resolution Gas Chromatography《采.pdf

1、Designation: D 6729 04 (Reapproved 2009)Standard Test Method forDetermination of Individual Components in Spark IgnitionEngine Fuels by 100 Metre Capillary High Resolution GasChromatography1This standard is issued under the fixed designation D 6729; the number immediately following the designation i

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

3、on of individualhydrocarbon components of spark-ignition engine fuels andtheir mixtures containing oxygenate blends (MTBE, ETBE,ethanol, and so forth) with boiling ranges up to 225C. Otherlight liquid hydrocarbon mixtures typically encountered inpetroleum refining operations, such as blending stocks

4、 (naph-thas, reformates, alkylates, and so forth) may also be analyzed;however, statistical data was obtained only with blendedspark-ignition engine fuels.1.2 Based on the cooperative study results, individual com-ponent concentrations and precision are determined in therange of 0.01 to approximatel

5、y 30 mass %. The procedure maybe applicable to higher and lower concentrations for theindividual components; however, the user must verify theaccuracy if the procedure is used for components with concen-trations outside the specified ranges.1.3 The test method also determines methanol, ethanol,t-but

6、anol, methyl t-butyl ether (MTBE), ethyl t-butyl ether(ETBE), t-amyl methyl ether (TAME) in spark ignition enginefuels in the concentration range of 1 to 30 mass %. However,the cooperative study data provided sufficient statistical datafor MTBE only.1.4 Although a majority of the individual hydrocar

7、bonspresent are determined, some co-elution of compounds isencountered. If this test method is utilized to estimate bulkhydrocarbon group-type composition (PONA) the user of suchdata should be cautioned that some error will be encountereddue to co-elution and a lack of identification of all componen

8、tspresent. Samples containing significant amounts of olefinic ornaphthenic (for example, virgin naphthas), or both, constitu-ents above n-octane may reflect significant errors in PONAtype groupings. Based on the gasoline samples in the inter-laboratory cooperative study, this procedure is applicable

9、 tosamples containing less than 25 mass % of olefins. However,some interfering coelution with the olefins above C7is pos-sible, particularly if blending components or their higherboiling cuts such as those derived from fluid catalytic cracking(FCC) are analyzed, and the total olefin content may not

10、beaccurate.1.4.1 Total olefins in the samples may be obtained orconfirmed, or both, if necessary, by Test Method D 1319(volume %) or other test methods, such as those based onmultidimensional PONA type of instruments.1.5 If water is or is suspected of being present, its concen-tration may be determi

11、ned, if desired, by the use of TestMethod D 1744, or equivalent. Other compounds containingoxygen, sulfur, nitrogen, and so forth, may also be present, andmay co-elute with the hydrocarbons. If determination of thesespecific compounds is required, it is recommended that testmethods for these specifi

12、c materials be used, such as TestMethods D 4815 and D 5599 for oxygenates, and D 5623 forsulfur compounds, or equivalent.1.6 Annex A1 of this test method compares results of thetest procedure with other test methods for selected compo-nents, including olefins, and several group types for severalinte

13、rlaboratory cooperative study samples. Although benzene,toluene, and several oxygenates are determined, when doubtfulas to the analytical results of these components, confirmatoryanalyses can be obtained by using specific test methods.1.7 The values stated in SI units are to be regarded as thestanda

14、rd. The values given in parentheses are provided forinformation purposes only.1.8 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 deter

15、mine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D 1319 Test Method for Hydrocarbon Types in LiquidPetroleum Products by Fluorescent Indicator Adsorption1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and

16、 Lubricants and is the direct responsibility of SubcommitteeD02.04.0L on Gas Chromatography Methods.Current edition approved April 15, 2009. Published July 2009. Originallyapproved in 2001. Last previous edition approved in 2004 as D 6729041.2For referenced ASTM standards, visit the ASTM website, ww

17、w.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.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.D 17

18、44 Standard Test Method for Determination of Water inLiquid Petroleum Products by Karl Fischer Reagent3D 4815 Test Method for Determination of MTBE, ETBE,TAME, DIPE, tertiary-Amyl Alcohol and C1to C4Alco-hols in Gasoline by Gas ChromatographyD 5599 Test Method for Determination of Oxygenates inGasol

19、ine by Gas Chromatography and Oxygen SelectiveFlame Ionization DetectionD 5623 Test Method for Sulfur Compounds in Light Petro-leum Liquids by Gas Chromatography and Sulfur Selec-tive DetectionE 355 Practice for Gas Chromatography Terms and Rela-tionships3. Terminology3.1 DefinitionsThis test method

20、 makes reference to manycommon gas chromatographic procedures, terms, and relation-ships. Detailed definitions can be found in Practice E 355.4. Summary of Test Method4.1 Representative samples of the petroleum liquid areintroduced into a gas chromatograph equipped with an opentubular (capillary) co

21、lumn coated with the specified stationaryphase. Helium carrier gas transports the vaporized samplethrough the column, in which it is partitioned into individualcomponents which are sensed with a flame ionization detectoras they elute from the end of the column. The detector signalis recorded digital

22、ly by way of an integrator or integratingcomputer. Each eluting component is identified by comparingits retention time to that established by analyzing referencestandards or samples under identical conditions. The concen-tration of each component in mass % is determined bynormalization of the peak a

23、reas after correction of selectedcomponents with detector response factors. The unknowncomponents are reported individually and as a summary total.5. Significance and Use5.1 Knowledge of the specified individual component com-position (speciation) of gasoline fuels and blending stocks isuseful for r

24、efinery quality control and product specification.Process control and product specification compliance for manyindividual hydrocarbons may be determined through the use ofthis test method.6. Apparatus6.1 Gas Chromatograph, a gas chromatograph equippedwith cryogenic column oven cooling and capable of

25、 producingrepeatable oven ramps from 0 to at least 300C is required.The following features are useful during the sample analysisphase: electronic flow readout, electronic sample split-ratioreadout, and electronic pneumatic control of flow. Though theiruse is not required, careful review of this test

26、 method willdemonstrate the usefulness of a gas chromatograph equippedwith these features. These features will replace the need tocarry out the manual calculations that must be performed aslisted in 8.1 and 8.2.6.2 Inleta capillary split/splitless inlet system operated inthe split mode is recommende

27、d. It must be operated in its linearrange. Refer to 8.4 to determine the proper split ratio.6.2.1 Carrier Gas Pneumatic ControlConstant carrier gaspressure control was used by all cooperative study participants.This may be either direct pressure to the inlet (injector) or byusing a total flow/back p

28、ressure system.6.2.2 Pneumatic Operation of the ChromatographTheuse of constant pressure was the mode of operating the gaschromatography used by the participants in the interlaboratorycooperative study. Other carrier gas control methods such asconstant flow (pressure programming) may be used, but th

29、ismay change the chromatography elution pattern unless thetemperature programming profile is also adjusted to compen-sate for the flow differences.6.2.3 Temperature ControlThe injector operated in thesplit mode shall be heated by a separate heating zone andheated to temperatures of 200 to 275C.6.3 C

30、olumn, a fused silica capillary column, 100 m in lengthby 0.25 mm inside diameter, coated with a 0.5 m film ofbonded dimethylpolysiloxane. The column must meet theresolution requirements expressed in 8.3. Columns from twodifferent commercial sources were used in the interlaboratorycooperative study.

31、6.4 Data System, a computer based chromatography datasystem capable of accurately and repeatedly measuring theretention time and areas of eluting peaks. The system shall beable to acquire data at a rate of at least 10 Hz.Although it is notmandatory, a data system which calculates column resolution(R

32、) is extremely useful as it will replace the need to carry outthe manual calculations which must be performed as listed in8.3.6.4.1 Electronic Integrators, shall be capable of storing upto 400 components in the peak table and shall be able toacquire the data at 10 Hz or faster speeds. They shall bec

33、apable of integrating peaks having peak widths at half heightwhich are 1.0s wide. The integrator must be capable ofdisplaying the integration mode of partially resolved peaks. Inaddition, these integrators should be able to download acommonly readable format of data (that is, ASCII) to acomputer in

34、order to facilitate data processing.6.5 Sample IntroductionSample introduction by way of avalve, automatic injection device, robotic arm or other auto-matic means is highly recommended. An automatic sampleintroduction device is essential to the reproducibility of theanalysis. Manual injections are n

35、ot recommended. All of thereproducibility data reported by this test method for thesamples analyzed were gathered using automatic injectiondevices.6.6 Flame Ionization Detector (FID)The gas chromato-graph should possess a FID having a sensitivity of 0.005coulombs/g for n-butane. The linear dynamic r

36、ange of thedetector should be 106or better. The detector is heated to300C.7. Reagents and Materials7.1 Calibrating Standard MixtureA spark ignition enginefuel standard of known composition and concentration by masscan be used. In order to corroborate the identification of the3Withdrawn. The last app

37、roved version of this historical standard is referencedon www.astm.org.D 6729 04 (2009)2sample, a typical chromatogram (Fig. 1) was obtained fromreference sample ARC96OX.47.2 Gas Chromatograph GasesAll of the following gasesshall have a purity of 99.999 % (V/V) or greater.NOTE 1Warning: Gases are co

38、mpressed. Some are flammable and allgases are under high pressure.7.2.1 HeliumThe test data was developed with helium asthe carrier gas. It is possible that other carrier gases may beused for this test method.At this time, no data is available fromthis test method with other carrier gases.7.2.2 Air,

39、 Hydrogen and Make-up Gas (Helium or Nitro-gen), shall have a purity of 99.999 % (V/V) or greater.8. Instrument Check Out Prior to Analysis8.1 Setting:8.1.1 Linear Gas VelocityIf the gas chromatograph isequipped with an electronic flow readout device, set the flow to1.8 mL/min. This is achieved by s

40、etting the carrier gas flowrate by injection of methane or natural gas at 35C. Ensure thatthe retention time is 7.00 6 0.05 min. This corresponds to alinear velocity of 25 to 26 cm/s. This is equivalent to retentiontimes of methane at 0C ranging from 6.5 to 6.8 min.8.1.2 If the gas chromatograph is

41、not equipped with anelectronic flow readout device, calculate the linear gas velocityin cm/s using Eq 1.linear gas velocity 5 V 5column length cm!retention time of methanes!(1)8.1.3 The typical retention times for methane and linear gasvelocity for helium are 6.5 to 6.8 and 24 to 26 cm/s,respectivel

42、y.8.2 Setting the Split RatioIf the gas chromatograph isequipped with an electronic split-ratio readout device, set thesplit ratio to a sample split of 200:1. If the gas chromatographis not equipped with an electronic split-ratio readout device,one must first calculate column flow rate and then proc

43、eed tocalculating split ratio using Eq 2 and 3.column flow rate 5 F 560 p r2! LTref! 2Pi Po!T!3Pref!Pi2 Po2!(2)where:F = flow rate as calculated by using the equation,r = column radius, cm,L = column length, cm,Pi= inlet pressure,Po= outlet pressure,Pref= reference pressure, 1 atm,T = temperature of

44、 the column oven,Tref= temperature at the column outlet, and = linear velocity, cm/s.split ratio 5 S 5split vent flow 1 FF(3)8.2.1 The column flow rate is calculated by the use of Eq 2.Use the results obtained from Eq 3 to adjust the split flow untila split flow of approximately 200:1 is achieved.8.

45、3 Evaluation of Column Performance:8.3.1 Prior to using the column described in Table 1,measure the resolution of the column under the conditions ofTable 2. Check that the resolution for the following pairs ofcomponents is obtained using Eq 4 to calculate the resolutionof a pair of components:R 52tR

46、2 tR1!1.699 Wh11 Wh2!(4)where:R = resolution,tR2= retention time of the first member of the pair,tR1= retention time of the second member of the pair,Wh1= peak width at half height of the first member of thepair, andWh2= peak width at half height of the second member ofthe pair.8.3.1.1 Column resolu

47、tion should be checked frequently byexamining the resolution of these compounds.8.3.2 Evaluation of the BaselineCarry out a blank base-line run utilizing no solvent injection, by setting the GC inaccordance with the conditions of Table 1.8.3.3 Subtract the baseline from a sample chromatogramand veri

48、fy that the residual signal at the beginning of thechromatogram does not differ from the end of the chromato-gram by more than 2 %.8.4 Evaluation of Splitter LinearityUsing the referencegasoline sample, inject this sample according to the schedulelisted in Table 3.8.4.1 Select from the chromatogram

49、about 10 to 15 compo-nents, which have concentrations in the range of .01 to 30weight %. Tabulate for each split ratio the concentrations of the10 to 15 components. Verify that for each component selected,its concentration does not vary by more than 3 %.9. Procedure9.1 Set the operating conditions of the gas chromatograph asshown in Table 1. These conditions will elute all componentsup to and including pentadecane (nC15).9.2 All of the parameters in Table 1 can be marginallychanged to optimize for sample types and optimize for char-acteristics o