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本文(ASTM D2887-2008 Standard Test Method for Boiling Range Distribution of Petroleum Fractions by Gas Chromatography《用气相色谱法测定石油馏分的沸点范围分布的试验方法》.pdf)为本站会员(tireattitude366)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM D2887-2008 Standard Test Method for Boiling Range Distribution of Petroleum Fractions by Gas Chromatography《用气相色谱法测定石油馏分的沸点范围分布的试验方法》.pdf

1、Designation: D 2887 08Designation: 406An American National StandardStandard Test Method forBoiling Range Distribution of Petroleum Fractions by GasChromatography1, 2This standard is issued under the fixed designation D 2887; the number immediately following the designation indicates the year oforigi

2、nal 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.This standard has been approved for use by agencies of the Department of Def

3、ense.1. Scope*1.1 This test method covers the determination of the boilingrange distribution of petroleum products. The test method isapplicable to petroleum products and fractions having a finalboiling point of 538C (1000F) or lower at atmosphericpressure as measured by this test method. This test

4、method islimited to samples having a boiling range greater than 55.5C(100F), and having a vapor pressure sufficiently low to permitsampling at ambient temperature.NOTE 1Since a boiling range is the difference between two tempera-tures, only the constant of 1.8F/C is used in the conversion of thetemp

5、erature range from one system of units to another.1.2 This test method is not to be used for the analysis ofgasoline samples or gasoline components. These types ofsamples must be analyzed by Test Method D 3710.1.3 The values stated in SI units are to be regarded asstandard. The inch-pound units give

6、n in parentheses are forinformation only.1.4 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 determine the applica-bility of regulatory

7、 limitations prior to use.2. Referenced Documents2.1 ASTM Standards:3D86 Test Method for Distillation of Petroleum Products atAtmospheric PressureD 1160 Test Method for Distillation of Petroleum Productsat Reduced PressureD 2892 Test Method for Distillation of Crude Petroleum(15-Theoretical Plate Co

8、lumn)D 3710 Test Method for Boiling Range Distribution ofGasoline and Gasoline Fractions by Gas ChromatographyD 4057 Practice for Manual Sampling of Petroleum andPetroleum ProductsD 4626 Practice for Calculation of Gas ChromatographicResponse FactorsD 6708 Practice for Statistical Assessment and Imp

9、rove-ment of Expected Agreement Between Two Test Methodsthat Purport to Measure the Same Property of a MaterialE 260 Practice for Packed Column Gas ChromatographyE 355 Practice for Gas Chromatography Terms and Rela-tionshipsE 516 Practice for Testing Thermal Conductivity DetectorsUsed in Gas Chromat

10、ographyE 594 Practice for Testing Flame Ionization Detectors Usedin Gas or Supercritical Fluid Chromatography3. Terminology3.1 DefinitionsThis test method makes reference to manycommon gas chromatographic procedures, terms, and relation-ships. Detailed definitions of these can be found in PracticesE

11、 260, E 355, and E 594.3.2 Definitions of Terms Specific to This Standard:3.2.1 area slicethe area, resulting from the integration ofthe chromatographic detector signal, within a specified reten-tion time interval. In area slice mode (see 6.3.2), peak detectionparameters are bypassed and the detecto

12、r signal integral isrecorded as area slices of consecutive, fixed duration timeintervals.3.2.2 corrected area slicean area slice corrected for base-line offset, by subtraction of the exactly corresponding areaslice in a previously recorded blank (non-sample) analysis.1This test method is under the j

13、urisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.04.0H on Chromatographic Distribution Methods.Current edition approved Dec. 1, 2008. Published January 2009. Originallyapproved in 1973. Last previous edition approved in 2006 as

14、 D 288706a.2This standard has been developed through the cooperative effort betweenASTM and the Institute of Petroleum, London. The IP and ASTM logos imply thatthe ASTM and IP standards are technically equivalent, but their use does not implythat both standards are editorially identical.3For referen

15、ced 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.1*A Summary of Changes section appears at the end of this standard.Copyri

16、ght ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.3.2.3 cumulative corrected areathe accumulated sum ofcorrected area slices from the beginning of the analysis througha given retention time, ignoring any non-sample area (forexample, solvent).

17、3.2.4 final boiling point (FBP)the temperature (corre-sponding to the retention time) at which a cumulative correctedarea count equal to 99.5 % of the total sample area under thechromatogram is obtained.3.2.5 initial boiling point (IBP)the temperature (corre-sponding to the retention time) at which

18、a cumulative correctedarea count equal to 0.5 % of the total sample area under thechromatogram is obtained.3.2.6 slice ratethe time interval used to integrate thecontinuous (analog) chromatographic detector response duringan analysis. The slice rate is expressed in hertz (for example,integrations or

19、 slices per second).3.2.7 slice timethe time associated with the end of eachcontiguous area slice. The slice time is equal to the slicenumber divided by the slice rate.3.2.8 total sample areathe cumulative corrected area,from the initial area point to the final area point, where thechromatographic s

20、ignal is considered to have returned tobaseline after complete sample elution.3.3 Abbreviations:3.3.1 Acommon abbreviation of hydrocarbon compounds isto designate the number of carbon atoms in the compound. Aprefix is used to indicate the carbon chain form, while asubscripted suffix denotes the numb

21、er of carbon atoms (forexample, normal decane = n-C10; isotetradecane = i-C14).4. Summary of Test Method4.1 The boiling range distribution determination by distilla-tion is simulated by the use of gas chromatography. A nonpolarpacked or open tubular (capillary) gas chromatographic col-umn is used to

22、 elute the hydrocarbon components of the samplein order of increasing boiling point. The column temperature israised at a reproducible linear rate and the area under thechromatogram is recorded throughout the analysis. Boilingpoints are assigned to the time axis from a calibration curveobtained unde

23、r the same chromatographic conditions by ana-lyzing a known mixture of hydrocarbons covering the boilingrange expected in the sample. From these data, the boilingrange distribution can be obtained.5. Significance and Use5.1 The boiling range distribution of petroleum fractionsprovides an insight int

24、o the composition of feedstocks andproducts related to petroleum refining processes. The gaschromatographic simulation of this determination can be usedto replace conventional distillation methods for control ofrefining operations. This test method can be used for productspecification testing with t

25、he mutual agreement of interestedparties.5.2 Boiling range distributions obtained by this test methodare essentially equivalent to those obtained by true boilingpoint (TBP) distillation (see Test Method D 2892). They arenot equivalent to results from low efficiency distillations suchas those obtaine

26、d with Test Method D86or D 1160.6. Apparatus6.1 ChromatographThe gas chromatograph used musthave the following performance characteristics:6.1.1 DetectorEither a flame ionization or a thermalconductivity detector may be used. The detector must havesufficient sensitivity to detect 1.0 % dodecane with

27、 a peakheight of at least 10 % of full scale on the recorder underconditions prescribed in this test method and without loss ofresolution as defined in 9.3.1. When operating at this sensitiv-ity level, detector stability must be such that a baseline drift ofnot more than 1 % of full scale per hour i

28、s obtained. Thedetector must be capable of operating continuously at atemperature equivalent to the maximum column temperatureemployed. Connection of the column to the detector must besuch that no temperature below the column temperature exists.NOTE 2It is not desirable to operate a thermal conducti

29、vity detector ata temperature higher than the maximum column temperature employed.Operation at higher temperature generally contributes to higher noiselevels and greater drift and can shorten the useful life of the detector.6.1.2 Column Temperature ProgrammerThe chromato-graph must be capable of lin

30、ear programmed temperatureoperation over a range sufficient to establish a retention time ofat least 1 min for the IBP and to elute compounds up to aboiling temperature of 538C (1000F) before reaching theupper end of the temperature program. The programming ratemust be sufficiently reproducible to o

31、btain retention timerepeatability of 0.1 min (6 s) for each component in thecalibration mixture described in 7.8.6.1.3 Cryogenic Column CoolingColumn starting tem-peratures below ambient will be required if samples with IBPsof less than 93C (200F) are to be analyzed. This is typicallyprovided by add

32、ing a source of either liquid carbon dioxide orliquid nitrogen, controlled through the oven temperature cir-cuitry. Excessively low initial column temperature must beavoided to ensure that the stationary phase remains liquid. Theinitial temperature of the column should be only low enough toobtain a

33、calibration curve meeting the specifications of themethod.6.1.4 Sample Inlet SystemThe sample inlet system mustbe capable of operating continuously at a temperature equiva-lent to the maximum column temperature employed, or providefor on-column injection with some means of programming theentire colu

34、mn, including the point of sample introduction, up tothe maximum temperature required. Connection of the columnto the sample inlet system must be such that no temperaturebelow the column temperature exists.6.1.5 Flow ControllersThe gas chromatograph must beequipped with mass flow controllers capable

35、 of maintainingcarrier gas flow constant to 61 % over the full operatingtemperature range of the column. The inlet pressure of thecarrier gas supplied to the gas chromatograph must be suffi-ciently high to compensate for the increase in column back-pressure as the column temperature is raised. An in

36、let pressureof 550 kPa (80 psig) has been found satisfactory with thepacked columns described in Table 1. For open tubularcolumns, inlet pressures from 10 to 70 kPa (1.5 to 10 psig)have been found to be suitable.D28870826.1.6 MicrosyringeA microsyringe is needed for sampleintroduction.NOTE 3Automati

37、c sampling devices or other sampling means, such asindium encapsulation, can be used provided: the system can be operatedat a temperature sufficiently high to completely vaporize hydrocarbonswith atmospheric boiling points of 538C (1000F), and the samplingsystem is connected to the chromatographic c

38、olumn avoiding any coldtemperature zones.6.2 ColumnAny column and conditions may be used thatprovide separation of typical petroleum hydrocarbons in orderof increasing boiling point and meet the column performancerequirements of 9.3.1 and 9.3.3. Successfully used columnsand conditions are given in T

39、able 1.6.3 Data Acquisition System:6.3.1 RecorderA 0 to 1 mV range recording potentiom-eter or equivalent, with a full-scale response time of2sorlessmay be used.6.3.2 IntegratorMeans must be provided for determiningthe accumulated area under the chromatogram. This can bedone by means of an electroni

40、c integrator or computer-basedchromatography data system. The integrator/computer systemmust have normal chromatographic software for measuring theretention time and areas of eluting peaks (peak detectionmode). In addition, the system must be capable of convertingthe continuously integrated detector

41、 signal into area slices offixed duration. These contiguous area slices, collected for theentire analysis, are stored for later processing. The electronicrange of the integrator/computer (for example, 1 V, 10 V) mustbe within the linear range of the detector/electrometer systemused. The system must

42、be capable of subtracting the area sliceof a blank run from the corresponding area slice of a samplerun.NOTE 4Some gas chromatographs have an algorithm built into theiroperating software that allows a mathematical model of the baselineprofile to be stored in memory. This profile is automatically sub

43、tractedfrom the detector signal on subsequent sample analyses to compensate forany baseline offset. Some integration systems also store and automaticallysubtract a blank analysis from subsequent analytical determinations.7. Reagents and Materials7.1 Purity of ReagentsReagent grade chemicals shall be

44、used in all tests. Unless otherwise indicated, it is intended thatall reagents conform to the specifications of the Committee onAnalytical Reagents of the American Chemical Society wheresuch specifications are available.4Other grades may be used,provided it is first ascertained that the reagent is o

45、f sufficientlyhigh purity to permit its use without lessening the accuracy ofthe determination.7.2 Liquid Phase for ColumnsMethyl silicone gums andliquids provide the proper chromatographic hydrocarbon elu-tion characteristics for this test method.7.3 Solid Support for Packed ColumnsChromatographicg

46、rade diatomateous earth solid support material within aparticle size range from 60 to 100 sieve mesh size is recom-mended.7.4 Carrier GasHelium or nitrogen of high purity.(WarningHelium and nitrogen are compressed gases underhigh pressure.) Additional purification is recommended by theuse of molecul

47、ar sieves or other suitable agents to removewater, oxygen, and hydrocarbons. Available pressure must besufficient to ensure a constant carrier gas flow rate (see 6.1.5).7.5 HydrogenHydrogen of high purity (for example, hy-drocarbon free) is used as fuel for the flame ionization detector(FID). (Warni

48、ngHydrogen is an extremely flammable gasunder high pressure.)7.6 AirHigh purity (for example, hydrocarbon free) com-pressed air is used as the oxidant for the flame ionizationdetector (FID). (WarningCompressed air is a gas under highpressure and supports combustion.)7.7 Column Resolution Test Mixtur

49、eFor packed columns,a nominal mixture of 1 mass % each of n-C16and n-C184Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For Suggestions on the testing of reagents notlisted by the American Chemical Society, see Annual Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.TABLE 1 Typical Operating ConditionsPacked Columns 1 2 3 4 Open Tubular Columns 5 6 7Column

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