1、Designation: D3174 12Standard Test Method forAsh in the Analysis Sample of Coal and Coke from Coal1This standard is issued under the fixed designation D3174; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision
2、. 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.1. Scope1.1 This test method covers the determination of the i
3、nor-ganic residue as ash in the analysis sample of coal or coke asprepared in accordance with Practice D2013 or Practice D346.The results obtained can be applied as the ash in the proximateanalysis, Practice D3172, and in the ultimate analysis, PracticeD3176. For the determination of the constituent
4、s in ash,reference is made to Test Methods D3682, D4326 and D6349.Test Method D6357 should be used to prepare ash to be usedfor trace element analysis. See Terminology D121 for defini-tion of ash.1.2 The values stated in SI units are to be regarded asstandard. No other units of measurement are inclu
5、ded in thisstandard.1.3 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 limitations prior to
6、 use.2. Referenced Documents2.1 ASTM Standards:2D121 Terminology of Coal and CokeD346 Practice for Collection and Preparation of CokeSamples for Laboratory AnalysisD388 Classification of Coals by RankD1757 Test Method for Sulfate Sulfur in Ash from Coal andCoke (Withdrawn 2009)3D2013 Practice for Pr
7、eparing Coal Samples for AnalysisD2795 Test Methods for Analysis of Coal and Coke Ash(Withdrawn 2001)3D3172 Practice for Proximate Analysis of Coal and CokeD3173 Test Method for Moisture in the Analysis Sample ofCoal and CokeD3176 Practice for Ultimate Analysis of Coal and CokeD3180 Practice for Cal
8、culating Coal and Coke Analysesfrom As-Determined to Different BasesD3682 Test Method for Major and Minor Elements inCombustion Residues from Coal Utilization ProcessesD4326 Test Method for Major and Minor Elements in Coaland Coke Ash By X-Ray FluorescenceD5016 Test Method for Total Sulfur in Coal a
9、nd CokeCombustion Residues Using a High-Temperature TubeFurnace Combustion Method with Infrared AbsorptionD6349 Test Method for Determination of Major and MinorElements in Coal, Coke, and Solid Residues from Com-bustion of Coal and Coke by Inductively CoupledPlasmaAtomic Emission SpectrometryD6357 T
10、est Methods for Determination of Trace Elements inCoal, Coke, and Combustion Residues from Coal Utiliza-tion Processes by Inductively Coupled Plasma AtomicEmission Spectrometry, Inductively Coupled PlasmaMass Spectrometry, and Graphite Furnace Atomic AbE691 Practice for Conducting an Interlaboratory
11、 Study toDetermine the Precision of a Test Method3. Terminology3.1 For definitions of terms used in this test method, refer toTerminology D121.4. Summary of Test Method4.1 Ash is determined by weighing the residue remainingafter burning the coal or coke under rigidly controlled condi-tions of sample
12、 weight, temperature, time, atmosphere, andequipment specifications.5. Significance and Use5.1 Ash, as determined by this test method, is the residueremaining after burning the coal and coke.Ash obtained differsin composition from the inorganic constituents present in theoriginal coal. Incineration
13、causes an expulsion of all water, theloss of carbon dioxide from carbonates, the conversion of ironpyrites into ferric oxide, and other chemical reactions. Ash, as1This test method is under the jurisdiction of ASTM Committee D05 on Coaland Coke and is the direct responsibility of Subcommittee D05.21
14、 on Methods ofAnalysis.Current edition approved Nov. 1, 2012. Published December 2012. Originallyapproved in 1973. Last previous edition approved in 2011 as D317411. DOI:10.1520/D3174-12.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at servicea
15、stm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3The last approved version of this historical standard is referenced onwww.astm.org.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19
16、428-2959. United States1determined by this test method, will differ in amount from ashproduced in furnace operations and other firing systems be-cause incineration conditions influence the chemistry andamount of the ash. References for correcting ash resultsdetermined by this test method to a minera
17、l-matter-free basisare listed in Classification D388, Section 9.6. Apparatus6.1 Electric Muffle Furnace for Coal or CokeFor deter-mination of ash of coal and coke, the furnace shall have anadequate air circulation and be capable of having its tempera-ture regulated at 500C, 750C, and 950C. The furna
18、ce shallbe equipped with a temperature indicator and means ofcontrolling the temperature within prescribed limits. Meansshall be provided for maintaining air flow at a rate of two tofour changes per minute (see Fig. 1 and Fig. 2). Combustiongases shall be vented from laboratory. Inlet and outlet por
19、tsshall be located and arranged to distribute the air uniformlythroughout the furnace area without the possibility of sweepingsolid particles from the capsules. The temperature over theentire working area of the furnace floor shall be maintainedwithin the specified temperature limits.6.2 Porcelain C
20、apsules, about 22 mm (78 in.) in depth, and44 mm (134 in.) in diameter, or similar shallow dishes orplatinum crucibles.6.3 Balance, sensitive to 0.1 mg.6.4 Crucible Cover, aluminum, porcelain, or similar covers.7. Temperature Calibration7.1 Place a preignited capsule with1gofsand at the centerof the
21、 working area of the furnace, and by the use of apotentiometer and thermocouple or other suitable temperaturemeasuring device, measure the temperature of the sand in thecrucible. The crucible and sand should be at temperatureequilibrium with the furnace. There should be two to four airchanges per mi
22、nute moving throughout the furnace (the airflow may be measured by using a wet-test meter or equivalentcalibrated at standard conditions for air connected to theceramic-pipe exhaust).Adjust the furnace temperature until thepotentiometer reads 750 6 10C and then adjust or read thetemperature on the i
23、ndicating pyrometer. Use this reading asthe proper setting for controlling the furnace.8. Procedure8.1 The sample shall be the material pulverized to pass No.60 (250-mm) sieve in accordance with Practice D2013 orPractice D346.8.2 Transfer approximately 1 g (weighed to the nearest 0.1mg) of the thoro
24、ughly mixed sample to a weighed capsule and(Suggested method for inducing regulated air flow through ashing furnace.)FIG. 1 Air AspiratorD3174 122cover quickly. An alternative way is to use the dried coal fromthe moisture determination in Test Method D3173. Afterremoving the covers, place the capsul
25、e containing the samplein a cold furnace and heat gradually at such a rate that thetemperature reaches 500 6 10C at the end of 1 h.8.3 For coals continue heating the sample until the tempera-ture rises from 500 6 10C to 750 6 15C at the end of 1 hour.For cokes continue heating the sample until the t
26、emperaturerises from 500 6 10C to 950 6 20C at the end of 1 hour.Continue to heat at the final temperature (750C or 950C) foran additional 2 h. Remove the capsule from the muffle furnace,place the cover on the capsule, cool under conditions tominimize moisture pickup, and weigh.8.4 The two-stage ash
27、ing procedure allows pyritic sulfur tobe oxidized and expelled before most metal carbonates aredecomposed. An ample supply of air in the muffle furnace,“two to four volume changes per minute,” must be assured atall times to ensure complete oxidation of the pyritic sulfur andto remove the SO2formed.8
28、.5 While the 4-h incineration interval described is suffi-cient with most coals to reach a condition of complete burn off,certain cokes and nonreactive coals may require additionaltime. If unburned carbon particles are observed, or if duplicateresults are suspect, the samples should be returned to t
29、hefurnace for sufficient time to reach a constant weight (60.001g). The 4-h time limit may be reduced if the sample reaches aconstant weight at 750C to 950C in less than 4 h.8.6 Some samples may be encountered that contain a highamount of carbonates (calcite) or pyrites or both. In such cases,sulfur
30、 retained as sulfates may be both unduly high andnonuniform between duplicate samples. In such cases, sulfatesulfur in the ash can be determined in accordance with TestMethod D5016 and the value properly corrected. If such isCalibration Flowmeter with TubingAmbient AirFor calibration use only, adjus
31、t forced air valve to deliver two to four furnace volume changes per minute (at standardtemperature-pressure conditions.)NOTE 1Flowmeters are usually calibrated for one atmosphere at 70F (760-mm Hg at 21.1C).(Suggested layout for calibration.)FIG. 2 Air AspiratorD3174 123done, the ash value should b
32、e reported and designated bothas-determined and corrected.9. Calculation9.1 Calculate the ash percent in the analysis sample asfollows:Ash in analysis sample, % 5 A 2 B!/C# 3100 (1)where:A = weight of capsule, cover, and ash residue, g,B = weight of empty capsule and cover, g, andC = weight of analy
33、sis sample used, g.10. Report10.1 For reporting analyses to other than as-determinedbasis, refer to Practice D3180.11. Precision and Bias11.1 Precision11.1.1 250 m (No. 60) SamplesThe precision of this testmethod for the determination of ash in the analysis sample ofcoal and coke is shown in Table 1
34、. The precision characterizedby repeatability (Sr,r)and reproducibility (SR,R)is describedin Table A1.1 and Table A1.2 in Annex A1.11.1.1.1 Repeatability Limit (r)The value below which theabsolute difference between two test results calculated to a drybasis (Practice D3180) of separate and consecuti
35、ve testdeterminations, carried out on the same sample of 250 m (No.60) coal and coke in the same laboratory, by the same operator,using the same apparatus on samples taken at random from asingle quantity of homogeneous material, may be expected tooccur with a probability of approximately 95 %.11.1.1
36、.2 Reproducibility Limit (R)The value below whichthe absolute difference between two test results calculated to adry basis (Practice D3180), carried out in different laboratories,using samples of 250 m (No. 60) coal and coke taken atrandom from a single quantity of material that is as homoge-neous a
37、s possible, may be expected to occur with a probabilityof approximately 95 %.11.1.2 2.36 mm (No. 8) Samples4The precision of this testmethod for the determination of ash in the analysis sample ofcoal and coke is shown in Table 2.11.1.2.1 Repeatability Limit (r)The value below which theabsolute diffe
38、rence between two test results calculated to a drybasis (Practice D3180) of separate and consecutive testdeterminations, carried out on the same sample, using the sameriffle, determined on a single test specimen of two separate 2.36mm (No. 8) test units of coal reduced entirely to 250 m (No.60) and
39、prepared from the same bulk sample coal in the samelaboratory, by the same operator, using the same apparatus onsamples taken at random from a single quantity of homoge-neous material, may be expected to occur with a probability ofapproximately 95 %.11.1.2.2 Reproducibility Limit (R)The value below
40、whichthe absolute difference between two test results calculated to adry basis (Practice D3180), carried out in different laboratories,using samples of 2.36 mm (No. 8) coal reduced entirely to 250m (No. 60), taken at random from a single quantity of materialthat is as homogeneous as possible, may be
41、 expected to occurwith a probability of approximately 95 %.11.2 BiasSince this is an empirical test method, the degreeof absolute bias cannot be determined.12. Keywords12.1 ash; coal; coke4An interlaboratory study, designed consistent with Practice E691, was con-ducted in 1989. Eight laboratories pa
42、rticipated in this study. Supporting data areavailable from ASTM Headquarters. Request Report RR:D05-1015. In addition,information for coke was calculated per Practice E691 using 48 sets of data for 24coke samples for a commercially available interlaboratory proficiency test program.The cokes used i
43、n this study included furnace coke, foundry coke and coke breeze.Details and supporting information are given in RR:D05-1039TABLE 1 Determination of Ash in the Analysis Sample of Coaland CokeRange RepeatabilityLimit,rReproducibilityLimit,RCoal 2.68 to17.86 %0.22 0.32Coke 5.73 to11.75 %0.10 0.20TABLE
44、 2 Range and Limits for Repeatability and Reproducabilityfor the Detrmination of Ash in Coal and CokeCoal Range RepeatabilityLimit,rReproducibilityLimit,RBituminous 5.0 to15.0 %0.30 % 0.49 %Subbituminous-Lignite4.5 to30.0 %0.33 % 0.47 %D3174 124ANNEX(Mandatory Information)A1. PRECISION STATISTICS 25
45、0 m (No. 60) SAMPLESA1.1 The precision of this test method, characterized byrepeatability (Sr,r) and reproducibility (SR,R) has beendetermined for the following materials as listed in Table A1.1and Table A1.2.A1.2 Repeatability Standard Deviation (Sr)The standarddeviation of test results obtained un
46、der repeatability condi-tions.A1.3 Reproducibility Standard Deviation (SR)The stan-dard deviation of test results obtained under reproducibilityconditions.TABLE A1.1 Repeatability (Sr,r) and Reproducibility (SR,R)Parameters Used for Calculation of Precision Statement for CoalSamplesMaterial Average
47、SrSRrR912 lvb 6.86364 0.049024 0.072788 0.13717 0.20366911 hvAb 2.68068 0.047123 0.055633 0.13185 0.15566915 hvAb 10.0873 0.065132 0.080675 0.18224 0.22573894 hvCb 10.475 0.075743 0.121383 0.21193 0.33963914 hvCb 12.515 0.071347 0.082831 0.19963 0.23176901 subB 16.7593 0.07752 0.1306 0.2169 0.365428
48、97 subA 8.81705 0.06302 0.10659 0.17633 0.29824916 subA 11.0723 0.061279 0.083981 0.17146 0.23498896 subC 13.5182 0.127066 0.194514 0.35553 0.54425Lignite 17.865 0.103367 0.163095 0.28922 0.45634D3174 125ASTM International takes no position respecting the validity of any patent rights asserted in co
49、nnection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standardsand should be addressed to AST
