ASTM D4239-2013e1 Standard Test Method for Sulfur in the Analysis Sample of Coal and Coke Using High-Temperature Tube Furnace Combustion《利用高温管式炉燃烧法测定煤和焦炭分析样品中硫含量的标准试验方法》.pdf

《ASTM D4239-2013e1 Standard Test Method for Sulfur in the Analysis Sample of Coal and Coke Using High-Temperature Tube Furnace Combustion《利用高温管式炉燃烧法测定煤和焦炭分析样品中硫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 D4239-2013e1 Standard Test Method for Sulfur in the Analysis Sample of Coal and Coke Using High-Temperature Tube Furnace Combustion《利用高温管式炉燃烧法测定煤和焦炭分析样品中硫含量的标准试验方法》.pdf（6页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4239 131Standard Test Method forSulfur in the Analysis Sample of Coal and Coke Using High-Temperature Tube Furnace Combustion1This standard is issued under the fixed designation D4239; the number immediately following the designation indicates the year oforiginal adoption or, in the ca

2、se 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 Defense.1NOTEFootnote 6 was c

3、orrected editorially in November 2013.1. Scope1.1 This test method covers the determination of sulfur insamples of coal or coke by high-temperature tube furnacecombustion.1.1.1 Two analysis methods are described.1.2 When automated equipment is used, either method canbe classified as an instrumental

4、method.1.3 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.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 establi

5、sh appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D346 Practice for Collection and Preparation of CokeSamples for Laboratory AnalysisD2013 Practice for Preparing Coal Samples for AnalysisD317

6、3 Test Method for Moisture in the Analysis Sample ofCoal and CokeD3176 Practice for Ultimate Analysis of Coal and CokeD3180 Practice for Calculating Coal and Coke Analysesfrom As-Determined to Different BasesD7448 Practice for Establishing the Competence of Labora-tories Using ASTM Procedures in the

7、 Sampling andAnalysis of Coal and CokeD7582 Test Methods for Proximate Analysis of Coal andCoke by Macro Thermogravimetric AnalysisE691 Practice for Conducting an Interlaboratory Study toDetermine the Precision of a Test Method2.2 ISO Standard:3ISO 11722 Solid Mineral Fuels-Hard Coal Determinationof

8、 Moisture in the general analysis test sample by dryingin nitrogen3. Summary of Test Method3.1 Combustion Method A (1350C)A weighed test por-tion of sample is burned in a tube furnace at a minimumcombustion tube operating temperature of 1350C in a streamof oxygen. During combustion at temperatures a

9、bove 1350 C,the sulfur and sulfur compounds contained in the sample aredecomposed and oxidized almost exclusively to gaseous sulfurdioxide, SO2. Moisture and particulates are removed from thegas by filters. The gas stream is passed through a cell in whichsulfur dioxide is measured by an infrared (IR

10、) absorptiondetector. Sulfur dioxide absorbs IR energy at a precise wave-length within the IR spectrum. Energy is absorbed as the gaspasses through the cell body in which the IR energy is beingtransmitted: thus, at the detector, less energy is received. Allother IR energy is eliminated from reaching

11、 the detector by aprecise wavelength filter. Thus, the absorption of IR energy canbe attributed only to sulfur dioxide whose concentration isproportional to the change in energy at the detector. One cell isused as both a reference and a measurement chamber. Totalsulfur as sulfur dioxide is detected

12、on a continuous basis.3.1.1 One procedure for Method A uses coal or cokereference materials to calibrate the sulfur analyzer. A secondprocedure for Method A uses a pure substance, BBOT, tocalibrate the sulfur analyzer.3.2 Combustion Method B (1150C)A weighed test por-tion of sample is burned in a qu

13、artz combustion tube in a1This test method is under the jurisdiction of ASTM Committee D05 on Coaland Coke and is the direct responsibility of Subcommittee D05.21 on Methods ofAnalysis.Current edition approved Oct. 1, 2013. Published October 2013. Originallyapproved in 1983. Last previous edition ap

14、proved in 2012 as D4239 12. DOI:10.1520/D4239-13.2For 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.3Available f

15、rom International Organization for Standardization (ISO), 1, ch. dela Voie-Creuse, Case postale 56, CH-1211, Geneva 20, Switzerland, http:/www.iso.ch.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States1stream of oxygen with an equal or ex

16、cess weight of tungstentrioxide (WO3). Sulfur is oxidized during the reaction of thesample and WO3. The tube furnace is operated at a minimumcombustion tube operating temperature of 1150C and tin (Sn)sample boats are utilized. Moisture and particulates are re-moved from the combustion gas by filters

17、. The gas stream isthen passed through a cell in which sulfur dioxide is measuredby an infrared (IR) absorption detector. Sulfur dioxide absorbsIR energy at a precise wavelength within the IR spectrum.Energy is absorbed as the gas passes through the cell body inwhich the IR energy is being transmitt

18、ed: thus, at the detector,less energy is received. All other IR energy is eliminated fromreaching the detector by a precise wavelength filter. Thus, theabsorption of IR energy can be attributed only to sulfur dioxidewhose concentration is proportional to the change in energy atthe detector. One cell

19、 is used as both a reference and ameasurement chamber. Total sulfur as sulfur dioxide is de-tected on a continuous basis.4. Significance and Use4.1 Sulfur is part of the ultimate analysis of coal and coke.4.2 Results of the sulfur analysis are used for evaluation ofcoal preparation and cleaning, eva

20、luation of potential sulfuremissions from coal and coke combustion or conversionprocesses, and evaluation of coal and coke quality in relation tocontract specifications, as well as for scientific purposes.4.3 The competency of laboratories with respect to use ofthis standard can be established throu

21、gh reference to PracticeD7448.5. Sample5.1 Pulverize the sample to pass No. 60 (250-m) sieve andmix thoroughly in accordance with Practice D2013 or PracticeD346.5.2 Analyze a separate portion of the analysis sample formoisture content in accordance with Test Method D3173,orD7582 or ISO 11722 for cal

22、culations to other than theas-determined basis.5.3 Procedures for calculating as-determined sulfur valuesobtained from the analysis sample to other bases are describedin Practices D3176 and D3180.6. ApparatusCombustion Method A (1350C)6.1 Measurement ApparatusEquipped to combust thesample as describ

23、ed in 3.1 (See Fig. 1).6.2 Tube FurnaceCapable of heating the hot zone or outersurface of the combustion tube, or both (6.3) to at least 1350C.It is normally heated electrically using resistance rods, aresistance wire, or molybdenum disilicide elements. Specificdimensions can vary with manufacturers

24、 design.6.3 Combustion TubeMade of mullite, porcelain, or zirconwith provisions for routing the gases produced by combustionthrough the infrared cell. The tube may have a boat stop madeof reticulated ceramics heated to 1350C that serves to com-plete the combustion of sulfur containing materials.6.4

25、Sample Combustion Boats, made of iron-free materialand of a convenient size suitable for the dimensions of thecombustion tube.6.5 Boat PullerWhere required, a rod of a heat-resistantmaterial with a bent or disk end to insert and remove boatsfrom the combustion tube.Combustion Method B (1150C)6.6 Mea

26、surement ApparatusEquipped to combust thesample as described in 3.2 (See Fig. 2)FIG. 1 Apparatus for the Determination of Sulfur by the Infrared Detection, Method AD4239 13126.7 Tube FurnaceCapable of heating the hot zone or outersurface of the combustion tube, or both (6.8) to at least 1150C.It is

27、normally heated electrically using resistance wire. Specificdimensions can vary with manufacturers design.6.8 Combustion TubeMade of quartz with provisions forrouting the gases produced by combustion through the infraredcell.6.9 Sample Combustion BoatMade of an iron-free tinmaterial and of a conveni

28、ent size suitable for the dimensions ofthe combustion tube.7. Reagents7.1 Purity of ReagentsUse reagent grade chemicals in alltests. Unless otherwise indicated, it is intended that all reagentsconform to the specifications of the Committee on AvailableReagents of the American Chemical Society, where

29、 suchspecifications are available.4Other grades can be used, pro-vided it is first ascertained the reagent is of sufficiently highpurity to permit its use without lessening the accuracy of thedetermination.7.2 Magnesium Perchlorate(WarningMagnesium per-chlorate is a strong oxidizing agent. Do not re

30、generate theabsorbent. Do not allow contact with organic materials orreducing agents.)7.3 Oxygen, 99.5 % PureCompressed gas contained in acylinder equipped with a suitable pressure regulator and aneedle valve to control gas flow. (WarningPure oxygenvigorously accelerates combustion. Verify all regul

31、ators, lines,and valves are free of grease and oil.)7.4 Reference Materials, Reference Material (RM)that arecoal(s) or coke(s) prepared by a national metrology body.Other materials that are coal(s) or coke(s) with documentedtraceability to reference material (CRM) coal(s) or coke(s)prepared by a nat

32、ional metrology body can also be used. Onlyuse material(s) with an assigned value and assigned uncertaintyfor sulfur. The uncertainty expressed as the confidence intervalof the assigned value shall be less than the repeatabilityspecified in the appropriate section on Precision and Bias ofthis test m

33、ethod.7.4.1 To minimize problems with instrument calibration orcalibration verification mix all reference material before re-moving the test portion from the container. Do not use thereference material for calibration or calibration verificationwhen less than 2 g remain in the container. The remaini

34、ngmaterial can be used for instrument conditioning.7.5 BBOT (2,5-di(5-tert-butylbenzoxazol-2-yl)thiophene,C26H26N2O2S)A pure substance and certified reference ma-terial for sulfur (7.47 % sulfur).7.6 Tungsten Oxide (WO3)A combustion promoter and afluxing agent. (WarningTungsten Oxide is a strong oxi

35、diz-ing agent.)8. Procedure8.1 Instrument PreparationPerform apparatus set up sys-tem checks in accordance with manufacturers instructions.8.1.1 Balance CalibrationCalibrate the instrument bal-ance in accordance with manufacturers instructions.8.2 Calibration of the Infrared Detection SystemIf thein

36、strument has been previously calibrated in accordance withthe section on instrument calibration, proceed to the AnalysisProcedure, otherwise carry out a calibration as specified in thefollowing section.8.2.1 Calibration with Coal and Coke Certified ReferenceMaterialsSelect reference materials (7.4),

37、 in the range of thesamples to be analyzed. Use at least three such referencematerials, for each range of sulfur values to be tested. Selectone reference material containing at least as much sulfur as thehighest level of sulfur expected. Select two additional refer-ence materials, one approximately

38、at the mid-point of the rangeand one below the lowest level of sulfur expected.8.2.1.1 Use a mass of material recommended by the appa-ratus manufacturer to carry out a minimum of three determi-nations to condition the equipment before calibration. Use amaterial with a sulfur value near the mid point

39、 of the expectedcalibration range.8.2.1.2 For each reference coal or coke employed forcalibration, use the as-determined sulfur value previouslycalculated from the certified dry-basis sulfur value and residualmoisture determined using either Test Methods D3173 or4Reagent Chemicals, American Chemical

40、 Society 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 Pharmacopeiaand National Formulary, U.S. Pharm

41、acopeial Convention, Inc. (USPC), Rockville,MD.FIG. 2 Apparatus for the Determination of Sulfur by the Infrared Detection, Method BD4239 1313D7582 or ISO 11722. Use a mass of material and thecalibration procedure recommended by the apparatus manufac-turer. Weigh to at least the nearest 1 mg and even

42、ly spread thetest portion of the reference material into the sample combus-tion boat (6.4). Position the sample in the hot zone of thefurnace until the instrument returns to baseline as indicatedaccording to settings recommended by the manufacturer. If theanalysis time exceeds the maximum analysis t

43、ime recom-mended by the manufacturer take corrective action as recom-mended by the manufacturer.8.2.2 Calibration with BBOTTo meet the precision re-quirements of this method, six calibration points are requiredfor a linear fit and eight calibration points are required for anonlinear fit. A calibrati

44、on point consists of a determination ona single test portion of calibration material. Select test portionsof the calibrant that have at least as much sulfur as the highestlevel of sulfur expected, test portions of the calibrant that haveas much sulfur as the lowest level of sulfur expected and testp

45、ortions spread evenly in between the highest and lowest levelsof sulfur.8.2.2.1 The mass of the calibrant needed can be calculatedusing the following equation: (Note 1).MC5MT3 SAD!SC(1)WhereMC= Mass of calibrantMT= Mass normally used for test samplesSAD= Percent sulfur (as-determined) in the test sa

46、mpleSC= Percent sulfur in the pure substance calibrantNOTE 1In the interlaboratory study that yielded the data for theprecision statement for this method, the mass of BBOT used forcalibration ranged from about 15 mg to over 80 mg. Some analyzers mayuse larger amounts. Amounts less than 15 mg BBOT sh

47、ould only bemeasured on a five-place analytical balance.8.2.3 Calibration VerificationCarry out a minimum ofthree determinations to condition the equipment before cali-bration verification (see 8.2.1.1). Verify the instrument calibra-tion prior to analyzing test samples, upon completion of all tests

48、amples and as needed to meet quality control requirements.Analyze a test portion of reference material(s) (7.4) using theapparatus conditions employed for instrument calibration(8.2.1). Use a mass that does not exceed the maximum massused for instrument calibration and with a sulfur value withinthe

49、range of the instrument calibration. If the value determinedfor each reference material employed for verification is notwithin the specified uncertainty for the assigned sulfur valuerepeat the instrument calibration in accordance with 8.2.1.Repeat all samples analyzed since the last successful calibra-tion verification.8.3 Combustion Method A (1350C)Set up the apparatus(see 8.1) and verify the calibration (see 8.2.3).8.3.1 Raise the furnace temperature as recommended by themanufacturer to at least 1350C. Weigh a mass of the samp