ASTM D6296-1998(2003)e1 Standard Test Method for Total Olefins in Spark-Ignition Engine Fuels by Multi-dimensional Gas Chromatography《用多维气相色谱法测定火花点火发动机燃料中烯烃总含量的标准试验方法》.pdf

《ASTM D6296-1998(2003)e1 Standard Test Method for Total Olefins in Spark-Ignition Engine Fuels by Multi-dimensional Gas Chromatography《用多维气相色谱法测定火花点火发动机燃料中烯烃总含量的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D6296-1998(2003)e1 Standard Test Method for Total Olefins in Spark-Ignition Engine Fuels by Multi-dimensional Gas Chromatography《用多维气相色谱法测定火花点火发动机燃料中烯烃总含量的标准试验方法》.pdf（8页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D 6296 98 (Reapproved 2003)e1An American National StandardStandard Test Method forTotal Olefins in Spark-ignition Engine Fuels byMultidimensional Gas Chromatography1This standard is issued under the fixed designation D 6296; the number immediately following the designation indicates the

2、 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.e1NOTEWarning notes were editorially moved into the standard t

3、ext in August 2003.1. Scope1.1 This test method provides for the quantitative determi-nation of total olefins in the C4to C10range in spark-ignitionengine fuels or related hydrocarbon streams, such as naphthasand cracked naphthas. Olefin concentrations in the range from0.2 to 5.0 liquid-volume % or

4、mass %, or both, can bedetermined directly on the as-received sample whereas olefinsin samples containing higher concentrations are determinedafter appropriate sample dilution prior to analysis.1.2 This test method is applicable to samples containingalcohols and ethers; however, samples containing g

5、reater than15 % alcohol must be diluted. Samples containing greater than5.0 % ether must also be diluted to the 5.0 % or less level, priorto analysis. When ethyl-tert-butylether is present, only olefinsin the C4to C9range can be determined.1.3 This test method can not be used to determine individual

6、olefin components.1.4 This test method can not be used to determine olefinshaving higher carbon numbers than C10.NOTE 1Precision was determined only on samples containing MTBEand ethanol.1.5 The values stated in SI units are to be regarded as thestandard.1.6 This standard does not purport to address

7、 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 prior to use.2. Referenced Documents2.1 ASTM Standards:D 1319 Test Method

8、 for Hydrocarbon Types in LiquidPetroleum Products by Fluorescent Indicator Adsorption2D 4052 Test Method for Density and Relative Density ofLiquids by Digital Density Meter3D 4307 Practice for Preparation of Liquid Blends for Use asAnalytical Standards3D 4815 Test Method for Determination of MTBE,

9、ETBE,TAME, DIPE, tertiary-Amyl Alcohol and C1to C4Alco-hols in Gasoline by Gas Chromatography3D 5599 Test Method for Determination of Oxygenates inGasoline by Gas Chromatography and Oxygen SelectiveFlame Ionization Detection43. Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 trap

10、, na device utilized to selectively retain specificportions (individual or groups of hydrocarbons or oxygenates)of the test sample and to release the retained components byincreasing the trap temperature.3.2 Acronyms:3.2.1 ETBEethyl-tert-butylether.3.2.2 MTBEmethyl-tertbutylether.4. Summary of Test

11、Method4.1 A reproducible 0.2-L volume of a representativesample, or a dilution thereof, is introduced into a computercontrolled gas chromatographic system5consisting of a seriesof columns, traps, and switching valves operating at varioustemperatures. The valves are actuated at predetermined timesto

12、direct portions of the sample to appropriate columns andtraps. The sample first passes through a polar column thatretains C12+ hydrocarbons, all aromatics, C11+ olefins, andsome alcohols, all of which are subsequently backflushed tovent. The fraction eluting from the polar column, whichcontains C11a

13、nd lower boiling saturated hydrocarbons as wellas decene and lower boiling olefins, enters an ether/alcohol trapwhere the ethers and alcohols are selectively retained and also1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct respo

14、nsibility of SubcommitteeD02.04 on Hydrocarbon Analysis.Current edition approved May 10, 2003. Published August 2003. Originallyapproved in 1998. Last previous edition approved in 1998 as D 629698.2Annual Book of ASTM Standards, Vol 05.01.3Annual Book of ASTM Standards, Vol 05.02.4Annual Book of AST

15、M Standards, Vol 05.03.5The sole source of supply of apparatus known to the committee at this time, theAC FTO Analyzer, is AC Analytical Controls, Inc., 3494 Progress Dr., Bensalem,PA 19020. If you are aware of alternative suppliers, please provide this informationto ASTM Headquarters. Your comments

16、 will receive careful consideration at ameeting of the responsible technical committee,1which you may attend.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.subsequently backflushed. The fraction eluting from the ether/alcohol trap,

17、which consists of C11and lower boiling saturatedhydrocarbons and the olefins, enters an olefin trap. The olefinsare selectively retained while the saturated hydrocarbons elute,pass through a nonpolar column, and are detected by a flameionization detector (FID). When the saturated hydrocarbonshave co

18、mpletely eluted to the FID, the nonpolar column ovenis cooled and the olefins, which have been retained on theolefin trap, are desorbed by heating. The desorbed olefins enterand elute from the nonpolar column, which is temperatureprogrammed to separate the olefins by boiling point, and aredetected b

19、y the FID.NOTE 2Separation of olefins by boiling point is necessary for thecalculation of the volume % of the olefins because the density of lowboiling olefins differs from that of high boiling olefins and, therefore, adensity correction must be applied.4.2 Quantitation of the detected olefin peak a

20、reas to providevolume % or mass %, or both, is accomplished through the useof an external standard followed by the application of flameionization detector response factors. The quantitation alsotakes into consideration the baseline compensation, sampledilution, and density corrections.5. Significanc

21、e and Use5.1 The quantitative determination of olefins in spark-ignition engine fuels is required to comply with governmentregulations.5.2 Knowledge of the total olefin content provides a meansto monitor the efficiency of catalytic cracking processes.5.3 This test method provides better precision fo

22、r olefincontent than Test Method D 1319. It also provides data in amuch shorter time, approximately 20 min following calibra-tion, and maximizes automation to reduce operator labor.5.4 This test method is not applicable to M85 or E85 fuels,which contain 85 % methanol and ethanol, respectively.6. Int

23、erferences6.1 Some types of sulfur-containing compounds are irre-versibly absorbed in the olefin and oxygenate traps ultimatelyreducing the trap capacity. However, a variety of spark-ignitionengine fuels have been analyzed without significant perfor-mance deterioration of these traps.6.2 Commercial

24、dyes used to distinguish between gradesand types of spark-ignition engine fuels have not been found tointerfere with this test method.6.3 Commercial detergent additives utilized in spark-ignition engine fuels have not been found to interfere with thistest method.6.4 Dissolved water in spark-ignition

25、 engine fuels has notbeen found to interfere with this test method. Free water mustbe removed using anhydrous sodium sulfate or other dryingagent to permit injection of accurate sample volumes.7. Apparatus7.1 The complete system used to obtain the precision data iscomprised of a computer controlled

26、gas chromatograph, auto-mated sample injector, computer software, and specific hard-ware modifications. These modifications include columns,traps, and valves which are described as follows and in Section8. Fig. 1 illustrates a typical flow diagram and componentconfiguration. Other configurations, co

27、mponents, or conditionsmay be utilized provided they are capable of separating theolefins and producing a precision that is equivalent, or better,than that shown in the table of precision data.7.2 Gas Chromatograph, dual column, temperature pro-grammable over a range from 60 to 160C at approximately

28、20C/min, equipped with heated flash vaporization sampleinlets, a single flame ionization detector, necessary flowcontrollers, and computer control.7.3 Sample Introduction System, manual or automatic, ca-pable of injecting a reproducible 0.2-L injection volume ofliquid. The total injected sample must

29、 be introduced to theFIG. 1 Typical Flow Diagram and Component ConfigurationD 6296 98 (2003)e12chromatographic system, thus excluding the use of split injec-tions or carrier gas purging of the inlet septum. An auto injectoris recommended but optional. The precision data was obtainedusing an automate

30、d sample injector.7.4 Gas Flow and Pressure Controllers, with adequateprecision to provide reproducible flow and pressure of heliumto the chromatographic system, and hydrogen and air for theflame ionization detector. Control of air flow for rapid coolingof specific system components and for automate

31、d valve opera-tion is also required.7.5 Electronic Data Acquisition System, must meet or ex-ceed the following specifications (see Note 3):7.5.1 Capacity for 150 peaks for each analysis,7.5.2 External standard calculation of selected peaks withresponse factors and background correction,7.5.3 Noise a

32、nd spike rejection capability,7.5.4 Sampling rate for fast (5 Hz to give20 points across peak),7.5.5 Peak width detection for narrow and broad peaks, and7.5.6 Perpendicular drop.NOTE 3Standard supplied software is typically satisfactory.7.6 Gas Purifiers, to remove moisture and oxygen fromhelium, mo

33、isture and hydrocarbons from hydrogen, and mois-ture and hydrocarbons from air.7.7 Balance, analytical, capable of weighing 0.0001 g.7.8 Glassware:7.8.1 Vial, autosampler, with caps and including a capcrimper (required when the recommended optional autosam-pler is used).7.8.2 Pipette, Pasteur, dispo

34、sable, with bulb.7.8.3 Pipette, volumetric, graduated in 0.01 mL increments,1- and 2-mL capacity.7.8.4 Pipette, total volume, 1, 3, 5, 10, 20 and 25-mLcapacity.7.9 Septa, polytetrafluoroethylene (PTFE) lined for injector.7.10 Temperature Controllers of System ComponentsTheindependent temperature con

35、trol of two columns and two traps,column switching valves, and sample lines is required. Allsystem components that contact the sample must be heated toa temperature that will prevent condensation of any samplecomponent. Table 1 lists the system components and operatingtemperature (see Note 4). Some

36、of the components requireisothermal operation, some require rapid heating and cooling,while one requires reproducible temperature programming.The indicated temperatures are typical; however, the controlsystems utilized must have the capability of operating attemperatures 620 of those indicated to ac

37、commodate specificsystems. Temperature control may be by any means that willmeet the requirements of Table 1.NOTE 4The system components and temperatures listed in Table 1and Section 8 are specific to the analyzer used to obtain the precision data.Other columns and traps that can adequately perform

38、the requiredseparations are also satisfactory but may require different temperatures.7.11 Valves, Column, and Trap Switchingautomated6-port rotary valves are recommended. The valves must beintended for gas chromatographic usage and meet the follow-ing requirements:7.11.1 The valves must be capable o

39、f continuous operationat operating temperatures that will prevent sample condensa-tion.7.11.2 The valves must be constructed of materials that arenonreactive with the sample under analysis conditions. Stain-less steel, PFA, and Vespel6are satisfactory.7.11.3 The valves must have a small internal vol

40、ume butoffer little restriction to carrier gas flow under analysis condi-tions.7.12 Valves, Air, to control pressurized air for ether/alcoholand olefin trap cooling; 3-port automated valves are recom-mended.NOTE 5New valves, tubing, columns, traps, and other materials thatcontact the sample or gasse

41、s may require conditioning prior to operationin accordance with the manufacturers instructions.8. Reagents and Materials8.1 Air, compressed, 10 mg/kg each of total hydrocarbonsand H2O. (WarningCompressed gas under high pressurethat supports combustion.)8.2 Helium, 99.999 % pure, 0.1 mg/kg H2O(Warnin

42、gCompressed gas under high pressure.)8.3 Hydrogen, 99.999 % pure, 0.1 mg/kg H2O(WarningExtremely flammable gas under high pressure.)8.4 2,2,4-trimethylpenane (isooctane), 99.99 % pure(WarningFlammable. Harmful if inhaled.)8.5 Columns and Traps (System Components)This testmethod requires the use of t

43、wo chromatographic columns andtwo traps (see Note 4). Each system component is indepen-dently temperature controlled as described in 7.10 and Table 1.Refer to Fig. 1 for the location of the components in thesystem. The following list of columns and traps containsguidelines that are to be used to jud

44、ge suitability.8.5.1 Polar ColumnAt a temperature of 160C, thiscolumn must retain all aromatic components in the sample andelute all nonaromatic components boiling below 200C, whichincludes decene and lower boiling olefins, within 2 min aftersample injection.8.5.1.1 This column must elute all aromat

45、ics and othercomponents retained from 8.5.1 within 8 min of when it isbackflushed.8.5.2 Ether/Alcohol TrapAt a temperature of 140C, thistrap must retain alcohols and ethers and elute all non-oxygenates boiling below 200C within 4.5 to 5.0 min aftersample injection.6PFA and Vespel are trade marks of

46、E.I. DuPont de Nemours and Co.TABLE 1 Temperature Control Ranges of System ComponentsTypical OperatingComponentTemperatureRange, CHeating Time, min,maxCooling Time, min,maxPolar column 60 to 160 temperatureNonpolar column 60 to 160 programmed, ; 20C/minEther/alcohol trap 120 to 280 1 5Olefin trap 15

47、5 to 280 1 5Column switching 100 isothermalValvesSample lines 100 isothermalD 6296 98 (2003)e138.5.2.1 At a temperature of 280C, this trap must elute allretained components.8.5.3 Olefin TrapWithin a temperature range from 140 to165C, this trap must quantitatively retain (trap) all olefins inthe C4to

48、 C10range for at least 10 min after sample injectionwhile eluting all non-olefin components boiling below 200C.8.5.3.1 At a temperature of 280C, this trap must quantita-tively elute all trapped olefins.8.5.4 Nonpolar ColumnAt a temperature of 160C, thiscolumn must elute paraffins and naphthenes thro

49、ugh C11within2 min.8.5.4.1 This column must distribute the C4through C10olefins by carbon number when temperature programmed from60 to 160C at approximately 20C/min.8.6 Set Up MixturesTwo qualitative synthetic mixturescontaining isooctane and ethers are required to verify that allinstrument components, temperatures, and cut times are satis-factory to produce accurate analyses and to aid in makingoperating adjustments as columns and traps age. The compo-sition of these mixtures and approximate component concen-trations are shown in Table 2. The