ASTM D5263-1993(2008)e1 Standard Test Method for Determining the Relative Degree of Oxidation in Bituminous Coal by Alkali Extraction《碱萃取时烟煤中氧化过程相对等级测定的标准试验方法》.pdf

《ASTM D5263-1993(2008)e1 Standard Test Method for Determining the Relative Degree of Oxidation in Bituminous Coal by Alkali Extraction《碱萃取时烟煤中氧化过程相对等级测定的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D5263-1993(2008)e1 Standard Test Method for Determining the Relative Degree of Oxidation in Bituminous Coal by Alkali Extraction《碱萃取时烟煤中氧化过程相对等级测定的标准试验方法》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D5263 93 (Reapproved 2008)1Standard Test Method forDetermining the Relative Degree of Oxidation in BituminousCoal by Alkali Extraction1This standard is issued under the fixed designation D5263; the number immediately following the designation indicates the year oforiginal adoption or, i

2、n 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.1NOTEEq 1 was editorially corrected in November 2010.1. Scope1.1 This colorimetric test method

3、 describes the determina-tion of the relative degree of oxidation by alkali extraction ofcoals that are high volatile A bituminous to low volatilebituminous in rank.1.2 This test cannot be sensitive to thermally oxidized coal.It is intended for coals that may be oxidized as a result ofweathering.1.3

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 establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.1.4 The values sta

5、ted in SI units shall be regarded asstandard.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Reagent WaterD4621 Guide for Quality Management in an OrganizationThat Samples or Tests Coal and Coke33. Terminology3.1 There are no terms in this standard that require new orother than di

6、ctionary definitions.4. Summary of Test Method4.1 Humic acids, which are present in oxidized coals, areextracted from the coal with sodium hydroxide solution. Thedegree of oxidation is determined by colorimetrically measur-ing the transmittance of the alkali extract solution at 520 nm.The intensity

7、of the color produced by the humic acids is afunction of the degree of oxidation.5. Significance and Use5.1 This test method is a relative measure of the degree ofoxidation present in coal. It does not determine the quantitativeamount of oxidized coal present. It is only intended to serve asa guide

8、to the supplier, buyer, and user for selecting coals formetallurgical use.NOTE 1The values shown in Table 1 are based on the transmittanceobtained using the original procedure4(wavelength at 520 nm, 17-mmlight path, 2 to 3-min boiling time, dilution of the extract to 80 mL). Atthese conditions, coal

9、s that had transmittance values greater than 90 %were considered to be unoxidized, coals less than 80 % were consideredto be oxidized, and coals between 80 and 90 % were considered suspect.As this procedure becomes accepted as the standard and more experimen-tal data are gathered, modifications to t

10、hese cutoff values are expected.Note that lower rank bituminous coals are more easily extracted thanhigher rank coal.6. Apparatus6.1 Transmission SpectrophotometerSingle-beam, gratingspectrophotometer having a wavelength range of 340 to 900nm.6.2 Glass Test Tubes/Cuvettes, with light paths ranging f

11、rom10 to 17 mm may be used. Test tubes with an inside diameterof 17 6 0.3 mm are commonly used.6.3 Analytical Balance, sensitive to 0.001 g.6.4 Hot Plate, capable of bringing aqueous solutions to aboil.6.5 Thermometer, capable of measuring up to 100C with asensitivity of 60.5C.6.6 Filter Papers, Typ

12、e II, Class F and G.6.7 Timer, capable of measuring 30 min to the nearestsecond.6.8 Graduated Cylinder, 100-mL capacity.1This test method is under the jurisdiction of ASTM Committee D05 on Coaland Coke and is the direct responsibility of Subcommittee D05.15 on MetallurgicalProperties of Coal and Cok

13、e.Current edition approved Feb. 1, 2008. Published April 2008. Originallypublished approved in 1992. Last previous edition approved in 2001 asD5263 93(2001). DOI: 10.1520/D5263-93R08E01.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceas

14、tm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Withdrawn. The last approved version of this historical standard is referencedon www.astm.org.4Lowenhaupt, D. E., and Gray, R. J., International Journal of Coal Geology,1980,

15、 Vol 1, pp. 6373.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.6.9 Beakers, 400-mL capacity.7. Reagents7.1 Sodium Hydroxide Solution (certified 1N).7.2 Octylphenoxypolyethoxyethanol Nonionic SurfactantWetting agent.7.2.1 Wetting ag

16、ent shall not be diluted (100 % concentra-tion).8. Calibration and Standardization8.1 Optical light filters with known absorbance/transmissionshall be used to check wavelength accuracy and linearity of thespectrophotometer. Solutions with accurate absorbance valuescan be found in published literatur

17、e.58.2 A blank solution consisting of 100 mL of 1N sodiumhydroxide is prepared by following the procedure outlined inSection 9, except coal is not used.9. Procedure9.1 Activate the spectrophotometer and set at 520-nm wave-length; allow sufficient time for the instrument to stabilize (30min).9.2 Weig

18、h out1g(60.01 g) of the 250-m (No. 60 U.S.Standard Sieve Series) coal sample.9.3 Transfer the coal to a standard 400-mL beaker.9.4 Add 100 mL of NaOH solution and one drop of wettingagent (100 % concentration) to the coal. Place a glass stirringrod into the beaker.9.5 Place beaker(s) onto a preheate

19、d hot plate and place athermometer in the beaker.9.6 Bring temperature of the contents to 98C (208F). Itshall take 3 to 4 min to reach a boil, depending on the numberof beakers on the hot plate.When measuring the temperature ofthe blank solution or test solution, or both, suspend thethermometer in a

20、 manner such that the temperature of thesolution and not the temperature of the beaker resting on top ofthe hot plate is being measured.9.7 At the time the blank solution or test solution, or both,in the beakers reaches the temperature of 98C (208F), set thetimer for 3 min. Allow the solution to boi

21、l for 3 min, stirringthe contents for at least 5 s for each 1-min interval.9.8 After the 3-min boil, carefully remove hot beakers andallow to cool under ambient conditions for 30 min. This is alsodetermined by using a timer.9.9 Filter (by gravity) the entire blank solution or testsolution, or both,

22、on a stack of one Type II Class F filter paperon top of one Type II Glass G filter paper. Filter the slurry intoa 100-mL graduated cylinder, making sure funnel and gradu-ated cylinder are dry before each test. After filtration, adddeionized (distilled) water (Type II, Specification D1193)tothe cylin

23、der to bring the solution to 80 mL and stir with a glassrod.NOTE 2The beaker should not be rinsed onto the filter paper. It is notsignificant if some coal remains in the beaker.9.10 Adjust the 0 and 100 % transmittance levels of thespectrophotometer.9.10.1 Adjust the spectrophotometer to read zero b

24、y closingthe lid of the sample/tube holder assembly of the instrument.9.10.2 Fill cuvette/test tube with the blank solution andinsert into the spectrophotometer.9.10.3 Adjust the spectrophotometer to read 100 % trans-mittance by inserting the blank solution (see 8.2).9.11 Place the cuvette/test tube

25、 containing the test solutioninto the spectrophotometer; measure and record the percenttransmittance of each test solution.NOTE 3Use only cuvette/test tubes for the test solution that yield thesame transmittance values as the cuvettes/test tubes used with the blanksolutions.NOTE 4Periodically during

26、 the analysis, check the span (0 and 100 %transmittance) to be sure that the instrument has not drifted.10. Calculation10.1 Since the light path is a variable in this test, resultsmust be adjusted to a common basis to make comparisons. A17-mm light path will be used. Thus, if the test was performedu

27、sing any other light path than 17 mm, the result must beadjusted to the 17-mm light path using Beers law.10.2 Adjust results as follows:Ax5 LogSTx100D(1)A175 Ax17 mm/bx! (2)T175 102A17! 3 100 (3)where:Tx= transmittance obtained by analysis, %;Ax= absorbance corresponding to Tx;bx= test light path, m

28、m;A17= absorbance at 17-mm light path; andT17= transmittance (calculated) at 17-mm light path.11. Report11.1 Report the value T17(obtained in Section 9).11.2 All accountability and quality control aspects of GuideD4621 apply to this test method.12. Precision and Bias12.1 PrecisionThe relative precis

29、ion of this test methodfor the determination of the degree of oxidation of bituminouscoal covers the range (percent transmittance) from 55 to 98 %.5Mellon, M. G., Analytical Absorption Spectroscopy , John Wiley alkali extraction; colorimetric; humic ac-ids; oxidation (weathering); transmittanceASTM

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32、 should be addressed to ASTM International Headquarters. Your comments will receive careful consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on

33、 Standards, at the address shown below.This standard is copyrighted by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).D5263 93 (2008)13