ASTM D2505-1988(2015) Standard Test Method for Ethylene Other Hydrocarbons and Carbon Dioxide in High-Purity Ethylene by Gas Chromatography《采用气相色谱法测定高纯度乙烯中乙烯 其它烃类和二氧化碳的标准试验方法》.pdf

《ASTM D2505-1988(2015) Standard Test Method for Ethylene Other Hydrocarbons and Carbon Dioxide in High-Purity Ethylene by Gas Chromatography《采用气相色谱法测定高纯度乙烯中乙烯 其它烃类和二氧化碳的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D2505-1988(2015) Standard Test Method for Ethylene Other Hydrocarbons and Carbon Dioxide in High-Purity Ethylene by Gas Chromatography《采用气相色谱法测定高纯度乙烯中乙烯 其它烃类和二氧化碳的标准试验方法》.pdf（7页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D2505 88 (Reapproved 2015)Standard Test Method forEthylene, Other Hydrocarbons, and Carbon Dioxide in High-Purity Ethylene by Gas Chromatography1This standard is issued under the fixed designation D2505; the number immediately following the designation indicates the year oforiginal adop

2、tion 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 carbondioxide, methane, eth

3、ane, acetylene, and other hydrocarbons inhigh-purity ethylene. Hydrogen, nitrogen, oxygen, and carbonmonoxide are determined in accordance with Test MethodD2504. The percent ethylene is obtained by subtracting thesum of the percentages of the hydrocarbon and nonhydrocar-bon impurities from 100. The

4、method is applicable over therange of impurities from 1 to 500 parts per million volume(ppmV).1.2 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 pra

5、ctices and determine the applica-bility of regulatory limitations prior to use. For some specifichazard statements, see Section 6.1.3 The values stated in SI units are to be regarded as thestandard. The values in parentheses are for information only.2. Referenced Documents2.1 ASTM Standards:2D2504 T

6、est Method for Noncondensable Gases in C2andLighter Hydrocarbon Products by Gas ChromatographyD4051 Practice for Preparation of Low-Pressure Gas BlendsE260 Practice for Packed Column Gas ChromatographyF307 Practice for Sampling Pressurized Gas for Gas Analy-sis3. Summary of Test Method3.1 The sample

7、 is separated in a gas chromatograph systemutilizing four different packed chromatographic columns withhelium as the carrier gas. Methane and ethane are determinedby using a silica gel column. Propylene and heavier hydrocar-bons are determined using a hexamethylphosphoramide(HMPA) column. Acetylene

8、is determined by using, in series,a hexadecane column and a squalane column. Carbon dioxideis determined using a column packed with activated charcoalimpregnated with a solution of silver nitrate in ,-oxydipropionitrile. Columns other than those mentioned abovemay be satisfactory (see 5.3). Calibrat

9、ion data are obtainedusing standard samples containing the impurities, carbondioxide, methane, and ethane in the range expected to beencountered. Calibration data for acetylene are obtained as-suming that acetylene has the same peak area response on aweight basis as methane. The acetylene content in

10、 a sample iscalculated on the basis of the ratio of peak area of the acetylenepeak to the peak area of a known amount of methane.Calculations for carbon dioxide, methane, and ethane arecarried out by the peak-height measurement method.4. Significance and Use4.1 High-purity ethylene is required as a

11、feedstock for somemanufacturing processes, and the presence of trace amounts ofcarbon dioxide and some hydrocarbons can have deleteriouseffects. This method is suitable for setting specifications, foruse as an internal quality control tool and for use in develop-ment or research work.5. Apparatus5.1

12、 Any chromatographic instrument with an overall sensi-tivity sufficient to detect 2 ppmV or less of the compoundslisted with a peak height of at least 2 mm without loss ofresolution.5.2 DetectorsThermal ConductivityIf a methanation re-actor is used, a flame ionization detector is also required. Tode

13、termine carbon dioxide with a flame ionization detector, amethanation reactor must be inserted between the column andthe detector and hydrogen added as a reduction gas (see TestMethod D2504, Appendix X1, Preparation of MethanationReactor).1This test method is under the jurisdiction of ASTM Committee

14、 D02 onPetroleum Products, Liquid Fuels, and Lubricantsand is the direct responsibility ofSubcommittee D02.D0.02 on Ethylene.Current edition approved June 1, 2015. Published July 2015. Originally approvedin 1966. Last previous edition approved in 2010 as D2505 88 (2010). DOI:10.1520/D2505-88R15.2For

15、 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.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700,

16、 West Conshohocken, PA 19428-2959. United States15.3 ColumnAny column or set of columns can be usedthat separates carbon dioxide, methane, acetylene and C3andheavier compounds. There may be tailing of the ethylene peakbut do not use any condition such that the depth of the valleysahead of the trace

17、peak is less than 50 % of the trace peakheight. (See Fig. 1 for example.)5.4 RecorderA recorder with a full-scale response of 2 sor less and a maximum rate of noise of 60.3 % of full scale.5.5 Gas-Blending ApparatusA typical gas-blending appa-ratus is shown in Fig. 2. A high-pressure manifold equipp

18、edwith a gage capable of accurately measuring ethylene pressuresup to 3.4 MNm2gage (500 psig) is required. Other types ofgas-blending equipment, such as described in Practice D4051,can be used.NOTE 1 Practice E260 contains information that will be helpful tothose using this method.6. Reagents and Ma

19、terials6.1 Copper or Aluminum, or Stainless Steel Tubing, 6.4 mm(14 in. ) outside diameter, and nylon tubing, 3.2 mm (18-in.)outside diameter.6.2 Solid SupportsCrushed firebrick or calcined diatoma-ceous earth, such as Chromosorb P,335 mesh to 80 mesh and80 mesh to 100 mesh. Other supporting materia

20、ls or meshsieves can be satisfactory.6.3 Active SolidsActivated carbon, 30 mesh to 40 mesh,4silica gel, 100 to 200-mesh.5Other sizes may be satisfactory.6.4 Liquid PhasesHexamethylphosphoramide (HMPA6),hexadecane.6Squalene,6silver nitrate, and ,-oxydipropionitrile.7Other liquid phases may be satisfa

21、ctory.(WarningCombustible solvents. See A1.7.) (WarningHMPAmay be harmful if inhaled. Causes irritation.Apotentialcarcinogen (lungs). See A1.5.)6.5 Helium. ( WarningCompressed Gas, Hazardous Pres-sure. See A1.2.)6.6 Hydrogen. ( WarningFlammable Gas, HazardousPressure. See A1.6.)6.7 Acetone. ( Warnin

22、gExtremely Flammable. SeeA1.1.)6.8 Gases for CalibrationPure or research grade carbondioxide, methane, ethane, acetylene, ethylene, propane, and3The sole source of supply of the apparatus is available from the Celite Division,Johns Mansville Co., New York, NY. If you are aware of alternative supplie

23、rs,please provide this information to ASTM International Headquarters. Your com-ments will receive careful consideration at a meeting of the responsible technicalcommittee1, which you may attend.4A fraction sieved in the laboratory to 30 to 40 mesh from medium activitycharcoal, 20 to 60 mesh, sold b

24、y Central Scientific Co., 1700 Irving Park Road,Chicago, IL 60613, has been found satisfactory for this purpose. If you are aware ofalternative suppliers, please provide this information to ASTM InternationalHeadquarters. Your comments will receive careful consideration at a meeting of theresponsibl

25、e technical committee1, which you may attend.5The sole source of supply of the apparatus known to the committee at this timeis Silica gel Code 923 available from the Davison Chemical Co., Baltimore, Md.21203. If you are aware of alternative suppliers, please provide this information toASTM Internati

26、onal Headquarters. Your comments will receive careful consider-ation at a meeting of the responsible technical committee1, which you may attend.6The sole source of supply of the apparatus known to the committee at this timeis available from the Fisher Scientific Co., St. Louis, MO. If you are aware

27、ofalternative suppliers, please provide this information to ASTM InternationalHeadquarters. Your comments will receive careful consideration at a meeting of theresponsible technical committee1, which you may attend.7,-oxydipropionitrile, sold by Distillation Products Industries, Division ofEastman K

28、odak Co., Rochester, NY, has been found to be satisfactory. If you areaware of alternative suppliers, please provide this information to ASTM Interna-tional Headquarters. Your comments will receive careful consideration at a meetingof the responsible technical committee1, which you may attend.FIG. 1

29、 Typical Chromatogram for PropyleneFIG. 2 Gas-Blending ManifoldD2505 88 (2015)2propylene. Certified calibration blends are commercially avail-able from numerous sources and may be used. (WarningFlammable Gases, Hazardous Pressure. See A1.2 and A1.3.)6.9 Methanol. ( WarningFlammable.Vapor Harmful. Se

30、eA1.4.)NOTE 2The use of copper tubing is not recommended with samplescontaining acetylene as this could lead to the formation of potentiallyexplosive copper acetylide.7. Sampling7.1 Samples should be supplied to the laboratory in highpressure sample cylinders, obtained using the proceduresdescribed

31、in Practice F307, or similar methods.8. Preparation of Apparatus8.1 Silica Gel ColumnDry the silica gel in an oven at204 C (400 F) for 3 h, cool in a desiccator, and store inscrew-cap bottles. Pour the activated silica gel into a 0.9 m(3 ft) length of 6.4 mm (14 in.) outside diameter copper oralumin

32、um tubing plugged with glass wool at one end. Tap orvibrate the tube while adding the silica gel to ensure uniformpacking and plug the top end with glass wool. Shape thecolumn to fit into the chromatograph.8.2 Silver Nitrate,-OxydipropionitrileActivated Car-bon ColumnWeigh 10 g of ,-oxydipropionitri

33、le into abrown 125 mL (4 oz) bottle. Add 5 g of silver nitrate (AgNO3)crystals. With occasional shaking, dissolve as much AgNO3aspossible, and allow the bottle to stand overnight to ensuresaturation. Prepare this solution fresh, as required. Withoutdisturbing the crystals at the bottom of the bottle

34、, weigh 2.5 gof supernatant AgNO3solution into a 250 mL beaker and add50 mL of methanol. While stirring this mixture, slowly add22.5 g of activated carbon. Place the beaker on a steam bath toevaporate the methanol. When the impregnated activatedcarbon appears to be dry, remove the beaker from the st

35、eambath and finish drying in an oven at 100 C to 110 C for 2 h.Plug one end of a 4 ft (1.2 m) length of 6.4 mm (14 in.) outsidediameter aluminum or stainless steel tubing with glass wool.Hold the tubing vertically with the plugged end down and pourfreshly dried column packing into it, vibrating the

36、columnduring filling to ensure uniform packing. Plug the top end withglass wool and shape the tubing so that it may be mountedconveniently in the chromatograph.8.3 Hexamethylphosphoramide Column (HMPA)Dry the35 mesh to 80 mesh inert support at 204 C (400 F). Weigh75 g into a wide-mouth 500 mL (16 oz

37、) bottle. Add 15 g ofHMPA to the inert support and shake and roll the mixture untilthe support appears to be uniformly wet with the HMPA. Pourthe packing into a 6 m (20 ft) length of 6.4 mm (14 in.) outsidediameter copper of aluminum tubing plugged at one end withglass wool. Vibrate the tubing while

38、 filling to ensure moreuniform packing. Plug the top end of the column with glasswool and shape the column to fit into the chromatograph.8.4 Hexadecane-Squalane ColumnDissolve 30 g of hexa-decane into approximately 100 mL of acetone. Add 70 g of80 mesh to 100 mesh inert support. Mix thoroughly and p

39、ourthe mixture into an open pan for drying. The slurry should bestirred during drying to ensure uniform distribution. When theacetone has evaporated, add a portion of the packing to a 7 m(25 ft) length of 3.2 mm (18 in.) outside diameter nylon tubingwhich has been plugged at one end with glass wool.

40、 Vibrate thecolumn while filling to ensure more uniform packing. Fill thecolumn with packing to only 4 m (15 ft) of the length of thecolumn. Fill the remainder of the column with squalanepacking prepared in the same manner as the hexadecanepacking. Plug the open end of the tubing with glass wool and

41、shape the column to fit into the chromatograph with thehexadecane portion of the column at the front end of thecolumn. The column shall be purged under test conditions (nosample added) until a constant baseline is obtained.NOTE 3Columns made with liquid phases listed above were usedsatisfactorily in

42、 cooperative work. Other columns may be used (see 5.3).9. Calibration9.1 Preparation of Standard Mixtures:9.1.1 Preparation of ConcentratePrepare a concentrate ofthe impurities expected to be encountered. A certified calibra-tion blend containing the expected impurities can be obtainedand used as th

43、e concentrate. An example of a satisfactoryconcentrate is given in Table 1. The concentrate can beprepared using the gas blending manifold as shown in Fig. 2 orusing a similar apparatus as follows: Evacuate the apparatusand add the components in the order of increasing vaporpressure; that is, propyl

44、ene, carbon dioxide, ethane and meth-ane. Record the increase in pressure on the manometer as eachcomponent is added. Close the reservoir and evacuate themanometer after each addition.9.1.2 Dilution of ConcentrateDilute the concentrate withhigh-purity ethylene in a ratio of approximately 1:4000. Thi

45、scan be done by adding the calculated amount of the concentrateand high purity ethylene to an evacuated cyclinder using thegas-blending apparatus (Fig. 2). Use a source of high-pressure,high-purity ethylene equipped with a needle valve and apressure gage capable of accurately measuring the pressure

46、ofthe blend as the ethylene is added to the cylinder containing theconcentrate. Add the calculated amount of ethylene; warm oneend of the cylinder to ensure mixing of the blend. Allow thetemperature to reach equilibrium before recording the finalpressure on the cylinder. Prepare at least three calib

47、rationsamples containing the compounds to be determined over therange of concentration desired in the products to be analyzed.9.2 Calculation of Composition of Standard MixturesCalculate the exact ratio of the concentrate dilution withethylene by correcting the pressure of the ethylene added forthe

48、compressibility of ethylene (Table 2). Multiply the dilutionratio or factor by the percentage of each component present inthe original concentrate (Table 1). These calculations give theTABLE 1 Suggested Composition of a Concentrate of ImpuritiesUsed in Preparing Standard Mixtures for Calibration Pur

49、posesComponent PercentCarbon dioxide 10Methane 45Ethane 25Propylene 20D2505 88 (2015)3amount of each component that has been added to thehigh-purity ethylene blend stock.The actual composition of thefinal blend must be ascertained by making corrections for theimpurities present in the high-purity ethylene used for theblend stock.The amount of correction is determined by makingchromatograph runs on the high-purity ethylene and measuringthe peak heights of the impurities. These peak heights will beused in adjusting the calibrat