ASTM D7183-2012 2500 Standard Test Method for Determination of Total Sulfur in Aromatic Hydrocarbons and Related Chemicals by Ultraviolet Fluorescence《紫外荧光法测定芳烃和相关化合物中总硫度的标准试验方法》.pdf

《ASTM D7183-2012 2500 Standard Test Method for Determination of Total Sulfur in Aromatic Hydrocarbons and Related Chemicals by Ultraviolet Fluorescence《紫外荧光法测定芳烃和相关化合物中总硫度的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D7183-2012 2500 Standard Test Method for Determination of Total Sulfur in Aromatic Hydrocarbons and Related Chemicals by Ultraviolet Fluorescence《紫外荧光法测定芳烃和相关化合物中总硫度的标准试验方法》.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D7183 12Standard Test Method forDetermination of Total Sulfur in Aromatic Hydrocarbons andRelated Chemicals by Ultraviolet Fluorescence1This standard is issued under the fixed designation D7183; the number immediately following the designation indicates the year oforiginal adoption or,

2、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. Scope*1.1 This test method covers the determination of sulfur inaromatic hydrocarbons, the

3、ir derivatives, and related chemi-cals.1.2 This test method is applicable to samples with sulfurconcentrations from 0.5 to 100 mg/kg.1.3 The following applies for the purposes of determiningthe conformance of the test results using this test method toapplicable specifications, results shall be round

4、ed off in accor-dance with the rounding-off method of Practice E29.1.4 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.5 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It

5、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 9.2. Referenced Documents2.1 ASTM Standards:2D1555 Test Method for Calculation o

6、f Volume and Weightof Industrial Aromatic Hydrocarbons and CyclohexaneD3437 Practice for Sampling and Handling Liquid CyclicProductsD6809 Guide for Quality Control and Quality AssuranceProcedures for Aromatic Hydrocarbons and Related Ma-terialsE29 Practice for Using Significant Digits in Test Data t

7、oDetermine Conformance with SpecificationsE691 Practice for Conducting an Interlaboratory Study toDetermine the Precision of a Test Method2.2 Other DocumentsOSHA Regulations, 29 CFR paragraphs 1910.1000 and1910.120033. Terminology3.1 oxidative pyrolysis, na process in which a sample iscombusted in a

8、n oxygen-rich atmosphere at high temperatureto break down the components of the sample into elementaloxides.3.2 ultraviolet fluorescence, nradiation in the region ofthe electromagnetic spectrum including wavelength from 100to 3900A that excites SO2to (SO2*).4. Summary of Test Method4.1 A specimen is

9、 either directly injected or placed in asample boat. The boat is then inserted into a high temperaturecombustion tube where the sulfur is oxidized to sulfur dioxide(SO2) in an oxygen-rich atmosphere. Water produced duringthe sample combustion is removed and the sample combustiongases are next expose

10、d to ultraviolet (UV) light. The SO2absorbs the energy from the UV light and is converted toexcited sulfur dioxide (SO2*). As it returns to a stable state,light is emitted and detected by a photomultiplier tube and theresulting signal is a measure of the sulfur contained in thespecimen.5. Significan

11、ce and Use5.1 Some process catalysts used in petroleum and chemicalrefining can be poisoned when trace amounts of sulfur-bearingmaterials are contained in the feedstocks. This test method can1This test method is under the jurisdiction of ASTM Committee D16 onAromatic Hydrocarbons and Related Chemica

12、ls and is the direct responsibility ofSubcommittee D16.04 on Instrumental Analysis.Current edition approved Jan. 1, 2012. Published January 2012. Originallyapproved in 2007. Last previous edition approved in 2007 as D7183 - 071. DOI:10.1520/D7183-12.2For referenced ASTM standards, visit the ASTM web

13、site, 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.3Available from U.S. Government Printing Office Superintendent of Documents,732 N. Capitol St., NW, Mail Stop:

14、SDE, Washington, DC 20401, http:/www.access.gpo.gov.1*A Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.be used to determine sulfur in process feeds, sulfur in finishedpro

15、ducts, and can also be used for purposes of regulatorycontrol.6. Interferences6.1 Halogens present in the specimen in concentrationsgreater than 10 % and nitrogen concentrations of 1500 mg/kgor greater can interfere.6.2 Moisture produced during the combustion step caninterfere if not removed prior t

16、o the gas entering the detectorcell.7. Apparatus7.1 Pyrolysis FurnaceAn electric furnace capable ofmaintaining a temperature sufficient to volatilize and pyrolyzeall the sample and oxidize sulfur to SO2. The actual tempera-ture should be recommended by specific instrument manufac-turer.7.2 Quartz Py

17、rolysis TubeCapable of withstanding 900 to1200C. The tube should be recommended by the instrumentmanufacturer.7.3 Microlitre SyringeCapable of delivering from 5 to250 L of sample. Check with the instrument manufacturer forrecommendations for specific sample requirements.7.4 Constant Rate Injector Sy

18、stemIf the sample is to beintroduced into the pyrolysis furnace via syringe, use aconstant rate injector or a liquid introduction module.7.5 Liquid Auto-SamplerCapable of injecting 5 to 250 Lof sample.7.6 Automatic Boat Drive SystemIf the instrument isequipped with an inlet system, a device for driv

19、ing the boatinto the furnace at a controlled and repeatable rate is required.7.7 Flow ControlThe instrument must be equipped withflow controllers capable of maintaining a constant supply ofoxygen and carrier gas.7.8 Drier TubeThe instrument must be equipped with amechanism for removal of water vapor

20、.8. Reagents8.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. It is intended that all reagents shall conform tothe specifications of the Committee on Analytical Reagents ofthe American Chemical Society,4where such specifications areavailable, unless otherwise indicated. Other

21、grades may beused, provided it is first ascertained that the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of the determination.8.2 Inert GasEither argon (Ar) or helium (He) may beused. The purity should be no less than 99.99 mol %.8.3 Oxygen GasThe purity sho

22、uld be no less than 99.99mol %.8.4 SolventThe solvent chosen should be capable ofdissolving the sulfur compound. The solvent of choice shouldhave a boiling point similar to the sample being analyzed.Suggested possibilities include, but not limited to methanol,iso-octane, and p-xylene (see Note 1 and

23、 Note 2).NOTE 1A quick screening can be conducted by injecting the solventand sample once or twice and comparing relative area counts.NOTE 2All solvents should have known sulfur content or known to beless than what will interfere with results.8.5 DibenzothiopheneFW184.26, 17.399 % (m/m) Sulfur(see N

24、ote 3).NOTE 3A correction for chemical impurity is required. Normally98 %.8.6 Quartz WoolIf needed.8.7 Sulfur Stock Solution, approximately 870 to 1044 gS/mlThis standard may be purchased if desired. Prepare astock solution by accurately weighing approximately 0.5 to 0.6g of dibenzothiophene to the

25、nearest 0.1 mg into a tared 100mL volumetric flask. Record the weight. Dilute to volume withthe selected solvent. Use Eq 1 to determine the concentrationof stock solution. This stock solution can be further diluted todesired sulfur concentrations (see Note 4 and Note 5). Alter-nate volumes of soluti

26、ons may be prepared so long as thepreparation meets the concentration specified.g S/ml solvent 5gofDBT!3.174!3Purity of DBT!3106!100 ml of Solvent(1)where:DBT = dibenzothiopheneSinDBT = 17.3994 %NOTE 4Working standards should be remixed on a regular basisdepending upon frequency of use and age. Typi

27、cally, stock solutions havea useful life of about 3 months.NOTE 5Check all new calibration standards against the previousstandard.9. Hazards9.1 Consult the current version OSHA regulations, suppli-ers Material Data Sheets, and local regulations for all mate-rials used in this test method.9.2 High te

28、mperature is employed in this test method. Extracare must be exercised when using flammable materials nearthe furnace.9.3 WarningExposure to excessive quantities of ultravio-let light is injurious to health. The operator must avoidexposing any part of their person, especially their eyes, notonly to

29、direct UV light but also to secondary or scatteredradiation that is present.10. Sampling10.1 Consult guidelines for taking samples from bulk con-tainers in accordance with Practice D3437.11. Preparation of Apparatus11.1 Set-up the instrument in accordance with manufactur-ers instructions.11.2 Adjust

30、 gas flows and pyrolysis temperature(s) to theoperating conditions recommended by the manufacturer.4Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For Suggestions on the testing of reagents notlisted by the American Chemical Society, see Analar

31、 Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.D7183 12211.3 The actual operation of injecting a sample will varydepending upon the instrument manufacturer and the t

32、ype ofinlet system used.11.4 An auto-sampler or a constant rate injector must beused when using an instrument equipped with a verticalfurnace.11.5 Prebake the sample boats to be used for the determi-nation.12. Calibration and Standardization12.1 Using the sulfur standard stock solution (see 8.7),mak

33、e a series of calibrations standards covering the range ofexpected sulfur concentration. If the expected levels include 0to 1.0 mg/kg and 1 to 100 mg/kg, then two curves should bemade to cover the entire range, one from 0 to 1.0 mg/kg (lowcurve) and one from 1.0 to 100 mg/kg (high curve).NOTE 6When

34、looking for levels of sulfur below 1 mg/kg make acalibration curve using an auto-sampler or constant rate injector andstandards, made from the sulfur stock solution, to cover the expectedrange of samples. Follow manufacturers recommendations for construct-ing the curve.NOTE 7When looking for concent

35、rations from 1 mgS/kg to 100mgS/kg, follow manufacturers recommendations for constructing thecurve.12.2 The sample size can be determined either volumetri-cally, by syringe or by mass.12.3 Volumetric measurement can be utilized by filling thesyringe with standard, carefully eliminating all bubbles,

36、andpushing the plunger to a calibrated mark on the syringe, andrecording the volume of liquid in the syringe. After injectingthe standard, read the volume remaining in the syringe. Thedifference between the two volume readings is the volume ofstandard injected. This test method requires the known or

37、measured density, to the third decimal place.12.4 Alternatively, the syringe may be weighed before andafter the injection to determine the weight of the sampleinjected. This technique provides greater precision than thevolume delivery method, provided a balance with a precisionof 60.0001 g is used.1

38、2.5 Follow the instrument manufacturers recommendationfor introducing samples into the instrument.12.6 If there are any problems with the calibration standardsfollow the instrument manufacturers recommendations tocorrect.12.7 Construct a linear regression curve (g S versus Area)using as many points

39、as recommended by the instrumentmanufacturer.12.8 The linear regression curve should have a minimum of0.99 correlation coefficient. If it does not, examine each pointon the curve to determine which point or points are out. Correctthe problem and run new Standards.13. Procedure13.1 Obtain a test spec

40、imen using the procedure describedin Section 10. The sulfur concentration in the test specimenmust be less than the concentration of the highest standard andgreater than the concentration of the lowest standard used inthe calibration.13.2 Follow the instrument manufacturers recommenda-tions for samp

41、le size.13.3 Follow the instrument manufacturers recommenda-tions for introducing samples into the instrument.13.4 Determine the sulfur concentration, by the average ofthree determinations, calculated by the instrument software.Make sure replicates are repeatable.14. Calculation14.1 All calculations

42、 are performed by the software, andresults are displayed and printed out in ppm (mg/kg) asappropriate. The density is input during sample data entry andis used by the instrument to convert from wt./vol. to wt./wt.14.2 Use Test Method D1555 for measurements utilizingvolume and known density in millig

43、rams per kilograms asfollows:Sulfur, mg/kg 5MB!V 3 D(2)14.3 Measurement utilizing weight of sample:sulfur, mg/kg 5M2B!w(3)where:M = measured sulfur value, gB = blank measured sulfur value, gV = sample injection volume, mLD = density of sample g/mLw = weight of sample, g15. Report15.1 Report the sulf

44、ur results as (mg/kg ) of the sample tothe nearest 0.01 mg/kg for samples less than 1 mg/kg. Reportto the nearest .1 for sample greater than 1 mg/kg.16. Precision and Bias516.1 The precision of this test method is based on guidelinesof Practice E691, an interlaboratory study determination ofTotal Su

45、lfur in Aromatic Hydrocarbons and Related Chemicalsby Ultraviolet Fluorescence, conducted in 2004. Each of 19laboratories tested 5 different materials for sulfur concentra-tions between 0.05 and 0.9 mg/kg (Table 1). Results formaterials containing 0.05 and 0.1 mg/kg were dropped due tohigh variabili

46、ty. In a corresponding effort, 25 laboratoriesjoined in the evaluation of 3 materials with sulfur concentra-tions between 15 and 90 mg/kg (Table 2). Each test result wasaverage of 3 individual determinations. Participating laborato-ries reported 3 replicate test results for each material. Allsamples

47、 were prepared from high purity p-xylene with knownquantities of sulfur added.16.1.1 RepeatabilityTwo test results obtained within onelaboratory shall be judged not equivalent if they differ by morethan the “r” value for that material; “r” is the intervalrepresenting the critical difference between

48、two test results for5Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Research Report RR:D16-1035.D7183 123the same material, obtained by the same operator using thesame equipment on the same day in the same laboratory.16.1.2 ReproducibilityTwo test

49、 results should be judgednot equivalent if they differ by more than the “R” value for thatmaterial; “R” is the interval representing the difference be-tween two test results for the same material, obtained bydifferent operators using different equipment in different labo-ratories.16.1.3 Any judgement in accordance with these two state-ments would have an approximate 95 % probability of beingcorrect.16.2 BiasAt this time of the study, no accepted referencematerial suitable for determining the bias for this test methodwas utilized,