ASTM D7041-2004(2010) 1875 Standard Test Method for Determination of Total Sulfur in Light Hydrocarbons Motor Fuels and Oils by Online Gas Chromatography with Flame Photometric Det.pdf

《ASTM D7041-2004(2010) 1875 Standard Test Method for Determination of Total Sulfur in Light Hydrocarbons Motor Fuels and Oils by Online Gas Chromatography with Flame Photometric Det.pdf》由会员分享，可在线阅读，更多相关《ASTM D7041-2004(2010) 1875 Standard Test Method for Determination of Total Sulfur in Light Hydrocarbons Motor Fuels and Oils by Online Gas Chromatography with Flame Photometric Det.pdf（5页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D7041 04 (Reapproved 2010)Standard Test Method forDetermination of Total Sulfur in Light Hydrocarbons, MotorFuels, and Oils by Online Gas Chromatography with FlamePhotometric Detection1This standard is issued under the fixed designation D7041; the number immediately following the design

2、ation indicates 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 dete

3、rmination of total sulfurin liquid hydrocarbons with a final boiling point less than450C by gas chromatography using a flame photometricdetector.1.2 This test method is applicable for total sulfur levels from0.5 to 100 mg S/kg.NOTE 1The pooled limit of quantification (PLOQ) derived from the2002 inte

4、rlaboratory cooperative test program was determined to be 1mgS/kg.NOTE 2Samples can also be tested at other total sulfur levels, but theprecision statements may not apply.1.3 The values stated in SI units are to be regarded asstandard.1.4 This standard does not purport to address all of thesafety co

5、ncerns, 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. For specific hazardstatements see Section 7.2. Referenced Documents2.1 ASTM Sta

6、ndards:2D1298 Test Method for Density, Relative Density (SpecificGravity), or API Gravity of Crude Petroleum and LiquidPetroleum Products by Hydrometer MethodD4052 Test Method for Density, Relative Density, and APIGravity of Liquids by Digital Density MeterD4057 Practice for Manual Sampling of Petro

7、leum andPetroleum ProductsD4177 Practice for Automatic Sampling of Petroleum andPetroleum ProductsE840 Practice for Using Flame Photometric Detectors inGas Chromatography3. Summary of Test Method3.1 The sample is analyzed by gas chromatography with aflame photometric detector. A fixed amount of samp

8、le isinjected into the gas chromatograph where it is vaporized. Theair carrier stream carries the vaporized sample into a hightemperature zone (900C) where the compounds present inthe sample are oxidized. Sulfur compounds are converted tosulfur dioxide (SO2). The carrier stream carries the oxidation

9、components onto a chromatographic column where they areseparated and the SO2is quantified by the flame photometricdetector. Calibration of the detector is achieved by the use of anappropriate external standard.4. Significance and Use4.1 This test method can be used to determine total sulfurlevels in

10、 process feeds and finished products that fall within thescope of this test method.4.2 Low levels of sulfur in process feed stocks can poisonexpensive catalysts used in petroleum refining processes. Thistest method can be used to monitor sulfur levels in thesefeedstocks.5. Apparatus5.1 Gas Chromatog

11、raph, equipped with automatically con-trolled valves, capable of automatic calibration with an exter-nal standard and having a flame photometric detector with anoverall sensitivity to detect at least 0.5 mg/kg of SO2. It mustbe able to automatically control all valve switching times.Although origina

12、lly developed with online analytical measure-ment equipment in an offline mode of operation, suitable onlineor laboratory gas chromatographs may apply this test methodas described. Typical instrument parameters are listed in Table1.5.1.1 Carrier and Detector Gas ControlThe chromato-graph must be equ

13、ipped with flow controllers or pressurecontrollers capable of maintaining a constant supply of carrier1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.03 on Elemental Analysis.Current edition app

14、roved May 1, 2010. Published May 2010. Originallyapproved in 2004. Last previous edition approved in 2004 as D704104. DOI:10.1520/D7041-04R10.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards vol

15、ume 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.gas and detector supply gases. Electronic pressure or flowcontrol is highly recommended.5.1.2 Sample Inj

16、ection SystemAn automatic sample injec-tion device is required. The injector must allow the introduc-tion of small sample sizes (0.1 to 1 L). The sample must beaccurately and repeatably injected into the gas chromatograph.Rotary or stem type liquid injection valves or auto injectors arerecommended.

17、The valve or injector must be equipped with aheated vaporizer section capable of being heated to at least285C.5.2 Pyrolysis FurnaceA furnace capable of maintaining asufficient temperature (900C) to pyrolyze the entire sampleand oxidize the sulfur compounds to SO2.5.3 Quartz Combustion TubeQuartz tub

18、e capable of with-standing temperatures up to 1200C. The oxidation sectionshall be large enough to ensure complete oxidation of thesample.5.4 ColumnA column that can provide complete separa-tion of SO2from the CO2quench and the other oxidizedcomponents such as H2O.5.5 DetectorAny flame photometric d

19、etector (FPD) canbe used, provided it can detect a minimum peak height twicethat of the baseline noise fora1Linjection of a 0.5 mg S/kgstandard. Detector linearity shall be at least equal to or greaterthan 103. The user is referred to Practice E840 for assistance inoptimizing the operation and perfo

20、rmance of the FPD.5.6 Data Acquisition SystemUse any integrator or com-puterized data acquisition system for peak area integration, aswell as for recording the chromatographic trace. The deviceand software must have the following capabilities:5.6.1 Identification of peak by retention time.5.6.2 Calc

21、ulation and use of response factors.5.6.3 External standard calibration calculation.5.6.4 Graphic presentation of the chromatogram.5.7 Analytical BalanceAny balance capable of accuratelyweighing materials to the nearest 0.01 mg.6. Reagents and Materials6.1 Purity of ReagentsReagent grade chemicals s

22、hall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical Society,where such specifications are available.3Other grades may beused, provided it is first ascertained that

23、the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of the determination.6.2 Carrier-GasZero grade air is recommended.(WarningCompressed air is a gas under high pressure thatsupports combustion.)6.3 HydrogenChromatographic grade recommended,minimum purity 99.995

24、 %. (WarningHydrogen is an ex-tremely flammable gas under high pressure.)6.4 Solvent (Reagent Grade)the solvent chosen should becapable of dissolving the sulfur-containing compound used toprepare the standard. The solvent of choice should have adensity similar to the samples being analyzed and it sh

25、ouldhave sulfur concentrations less than the instrument detectionlimit. Mixed solvents such as an isooctane / toluene mixturecan be used to reach the desired density. (WarningSolventsused as reagents such as toluene and isooctane are flammableand may be harmful or fatal if ingested or inhaled.)6.5 S

26、tandards for Calibration and Peak IdentificationStandards are used for peak identification and retention timedetermination. Also standards of known concentrations arerequired for external standard calibration of the gas chromato-graph.6.5.1 Preparation of Stock Solution (mass/volume), 100 gS/mL (see

27、 Notes 3 and 4). Accurately weigh to the nearest 0.1mg, 0.0456 g of butyl sulfide into a suitable container such asa 100 mL volumetric flask. Dilute to volume with the selectedsolvent. This stock solution can be further diluted to the desiredsulfur concentration. Other sulfur containing compounds su

28、chas thiophene or thianaphthene can be substituted for n-butylsulfide if desired. The concentration of the stock solution canbe calculated as follows:g S/mL 5 M 3 32.06! 3 1 3 106!g/g!/100 mL 3 FW! (1)where:M = exact mass of sulfur reference compound (g), andFW = formula weight of sulfur reference c

29、ompound.NOTE 3Commercial standards can be used provided they are checkedfor accuracy.NOTE 4Stock solutions will have a shelf life of approximately 2 to 3months and should be remixed accordingly.6.5.2 Preparation of Stock Solution: (mass/mass), 100 gS/g (see Notes 3 and 4). Accurately weigh to the ne

30、arest 0.1mg, 0.0456 g of butyl sulfide into a suitable container.Add 100g (accurately weighed to the nearest 0.1 g) of the selectedsolvent. This stock solution can be further diluted to the desiredsulfur concentration. Other sulfur containing compounds such3Reagent Chemicals, American Chemical Socie

31、ty Specifications , AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents notlisted by the American Chemical Society, see Analar Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K. and the United States Pharmacopoeiaand National Formulary, U.S. Pharmaceuti

32、cal Convention, Inc. (USPC), Rockville,MD.TABLE 1 Typical Instrument ParametersCarrier gas Zero airCarrier flow rate 30 mL/minHydrogen flow rate 60 mL/minDetector Flame photometric detectorDetector temperature 120CInjector temperature 285CFurnace temperature 1000CColumn 40 ft by18 in. stainless stee

33、l tubing,12 % polyphenyl ether/1.5 % H3PO4on 40/60 Chromosorb TColumn temperature 115CD7041 04 (2010)2as thiophene or thianaphthene can be substituted for butylsulfide if desired. The concentration of the stock solution canbe calculated as follows:mgS/kg 5 M 3 32.06! 3 1 3 106!mg/kg!/100 g 3 FW! (2)

34、6.6 Butyl SulfideFW 146.29, 21.92 % (m/m) S.6.7 ThiopheneFW 84.14, 38.1 % (m/m) S.6.8 ThianaphtheneFW 134.20, 23.90 % (m/m) S.7. Hazards7.1 Consult current Occupational Safety HealthAdministra-tion (OSHA) regulations, supplier Material Safety Data Sheets,and local regulations for all materials used

35、in this test method.7.2 High temperatures are used in this method; extra pre-caution should be exercised when working with flammablematerials near the pyrolysis furnace.8. Sampling8.1 General Requirements:8.1.1 Collect samples in accordance with Practice D4057 orD4177.8.1.2 To prevent the loss of vo

36、latile components, which maybe present in some samples, protect samples from excesstemperatures prior to testing. This can be done by storage in anice bath or refrigerator.8.1.3 Analyze samples as soon as possible to prevent loss ofsulfur components or contamination.8.1.4 Do not store samples in pla

37、stic containers, sincevolatile materials may diffuse through the walls of the con-tainer.8.1.5 Do not test samples stored in leaky containers. Discardand obtain a new sample if leaks in the containers are detected.9. Preparation of Apparatus9.1 Place in service in accordance with the manufacturersin

38、structions. Typical instrument parameters are listed in Table1.9.2 Set gas flows and temperatures to the desired operatingconditions, in accordance with the manufacturers instructions.9.3 Ignite the flame photometric detector according to themanufacturers procedure.9.4 Prepare the sample introductio

39、n accessories, if required,according to the manufacturers instructions.9.5 Load a sulfur standard (see 6.5) into the injection valveor auto injector and inject into the gas chromatograph. Deter-mine the retention time of the SO2peak.9.6 Set-up a chromatographic analysis method according tothe manufa

40、cturers instructions.10. Calibration10.1 Choose which type of calibration method is required(mass/volume or mass/mass) and prepare a calibration standardfrom the stock solution (see 6.5.1 or 6.5.2) by volumetricdilution or mass dilution (see Note 3). The concentration of thecalibration standard shou

41、ld be approximately 50 % of thefull-scale concentration range of the test samples to be ana-lyzed.10.1.1 Load calibration standard into injection valve or autoinjector.10.1.2 Inject the calibration standard into the gas chromato-graph. See Table 2 for recommended injection volumes.10.1.3 Analyze the

42、 calibration standard and obtain a chro-matogram. Calculate the relative response factor for the SO2peak:RFS5 Cn/ AS! (3)where:RFS= relative response factor of SO2,Cn= sulfur concentration (mgS/kg) of the compound inthe calibration mixture, andAS= peak area of the SO2component.11. Procedure11.1 Obta

43、in a test sample using the procedure outlined inSection 8.11.2 Sample injection volumes can range from 0.1 to 1 L.Experience dictates the best sample volume. The injectionvolume must be the same as used in the calibration procedure.Typical injection volumes are listed in Table 2.11.3 Load the sample

44、 into the injection valve or autoinjector according to the manufacturers recommended proce-dure.11.4 Inject the sample into the chromatograph by startingthe chromatographic method, in accordance with the manufac-turers instructions.11.5 Record concentration reading from gas chromatograph.See Fig. 1

45、for a typical chromatogram.11.6 Density values needed for the calculations are to betested using Test Methods D1298, D4052, or equivalent, at thetemperature at which the sample specimen was taken foranalysis by this test method.12. Calculation12.1 If the analyzer was calibrated on a mass/volume basi

46、sthen calculate the sulfur content of the test sample in parts permillion by mass (mg/kg) as follows:sulfur, ppm g/g, mg/kg! 5 CSv/DS(4)where:CSv= concentration reading from analyzer (g/mL), andDS= density of sample (g/mL).12.1.1 If the analyzer was calibrated on a mass/mass basisthen calculate the

47、sulfur content of the test sample in parts permillion by mass (mg/kg) as follows:sulfur, ppm mg/g, mg/kg! 5 CSm!DC!/DS(5)where:CSm= concentration reading from analyzer (mg/kg),DC= density of calibration standard (g/mL), andDS= density of sample (g/mL).TABLE 2 Suggested Injection VolumeSulfur, mg/kg

48、Sample Size, LLess than 1 0.5 to 11 to 100 up to 0.5Greater than 100 0.1 to 0.25D7041 04 (2010)313. Report13.1 Report the total sulfur concentration in parts permillion by mass (mg/kg) to the nearest 0.1 mgS/kg.14. Precision and Bias4,514.1 PrecisionThe precision of this test method as deter-mined b

49、y statistical examination of interlaboratory test resultsare as follows:NOTE 5The following precision data were developed in a 2002interlaboratory cooperative test program. Nine participants analyzedsample sets of blind duplicates of 16 types of hydrocarbons andhydrocarbon-oxygenate blends. The sample set consisted of eight gasolinesamples and eight diesel samples. For the gasoline sample set, theconcentration range was approximately from 3 to 100 mgS/kg and for thediesel sample set, approximately between 2 to 85 mgS/