ASTM D4952-2012 Standard Test Method for Qualitative Analysis for Active Sulfur Species in Fuels and Solvents (Doctor Test)《燃料和溶剂中活性硫物质定性分析的标准试验方法(含硫试验)》.pdf

《ASTM D4952-2012 Standard Test Method for Qualitative Analysis for Active Sulfur Species in Fuels and Solvents (Doctor Test)《燃料和溶剂中活性硫物质定性分析的标准试验方法(含硫试验)》.pdf》由会员分享，可在线阅读，更多相关《ASTM D4952-2012 Standard Test Method for Qualitative Analysis for Active Sulfur Species in Fuels and Solvents (Doctor Test)《燃料和溶剂中活性硫物质定性分析的标准试验方法(含硫试验)》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4952 12Standard Test Method forQualitative Analysis for Active Sulfur Species in Fuels andSolvents (Doctor Test)1This standard is issued under the fixed designation D4952; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revisio

2、n, 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.1. Scope*1.1 This test method cove

3、rs and is intended primarily for thedetection of mercaptans in motor fuel, kerosine, and similarpetroleum products. This method may also provide informationon hydrogen sulfide and elemental sulfur that may be present inthese sample types.1.2 The values stated in SI units are to be regarded asstandar

4、d. No other units of measurement are included 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

5、-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Reagent WaterD3227 Test Method for (Thiol Mercaptan) Sulfur in Gaso-line, Kerosine, Aviation Turbine, and Distillate Fuels(Potentiometric Method)2.2 Energy Institute Standards:3IP 30 Det

6、ection of Mercaptans, Hydrogen Sulfide, Elemen-tal Sulfur, and Peroxides Doctor Test Method3. Summary of Test Method3.1 The sample is shaken with sodium plumbite solution, asmall quantity of powdered sulfur added, and the mixtureshaken again. The presence of mercaptans or hydrogen sulfideor both is

7、indicated by discoloration of the sulfur floating at theoil-water interface or by discoloration of either of the phases.4. Significance and Use4.1 Sulfur present as mercaptans or as hydrogen sulfide indistillate fuels and solvents can attack many metallic andnon-metallic materials in fuel and other

8、distribution systems. Anegative result in the doctor test ensures that the concentrationof these compounds is insufficient to cause such problems innormal use.5. Interferences5.1 This test cannot be used if there are more than traceamounts of peroxides in the test sample. Peroxides can give afalse p

9、ositive results where mercaptans are at low level or noteven present.45.2 To check if peroxides are present in sufficient concen-tration to invalidate the test, shake 10 6 0.5 mL of a freshportion of the sample with approximately 2 mL of thepotassium iodide solution, add two drops of the acetic acid

10、solution, and two drops of the starch solution. If the aqueouslayer turns a blue color, this confirms the presence of peroxidesin sufficient quantity to invalidate the test, and the test on thissample should be discontinued. Proceed in accordance with5.4.5.3 Alternatively, one may choose to perform

11、a preliminaryDoctor Test. If a brown precipitate slowly forms, peroxide isprobably present. Proceed in accordance with 5.2 to confirmpresence of peroxides at sufficient quantity to invalidate thetest.5.4 If interference from peroxides is confirmed, proceed tore-sample and retest. Ensure that samplin

12、g and handlingprocedures for the new sample prevent UV light exposures asprescribed in 7.1. None of the normal refinery units or blendingprocesses producing spark ignition motor fuels are known tocreate peroxides under normal operating conditions.6. Reagents and Materials6.1 Purity of ReagentsReagen

13、t grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents conform to the specifications of the Committee on1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of Subcommi

14、tteeD02.03 on Elemental Analysis.Current edition approved April 15, 2012. Published June 2012. Originallyapproved in 1989. Last previous edition approved in 2009 as D495209. DOI:10.1520/D4952-12.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at

15、serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Available from Energy Institute, 61 New Cavendish St., London, WIG 7AR,U.K., http:/www.energyinst.org.4Brooks, B. T., “Sodium Plumbite or Doctor Test of Gasolines,”

16、Industrial andEngineering Chemistry, Vol 16, No. 6, June 1924, p. 588.1*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.Analytical Reagents of the American Chemical Soci

17、ety wheresuch specifications are available.5Other grades may be used,provided it is first ascertained that the reagent is of sufficientlyhigh purity to permit its use without lessening the accuracy ofthe determination.6.2 Purity of WaterUnless otherwise indicated, referencesto water shall be underst

18、ood to mean reagent water as definedby Types II or III of Specification D1193.6.3 Doctor (Sodium Plumbite) Solution(WarningPoisonous and suspect carcinogen.) Dissolve approximately125 g of sodium hydroxide (NaOH) in 1 L of reagent water.Add 60 g of lead monoxide (PbO) and shake vigorously for 15min,

19、 or let stand with occasional shakings for at least one day.Allow to settle and decant or siphon off the clear liquid. If thesolution does not settle clear, filter it through filter paper. Keepthe solution in a tightly sealed bottle and refilter before use ifnot perfectly clear. As an alternative, t

20、he lab may use acommercially prepared solution that meets the requirements ofthe laboratory preparation.NOTE 1Alternate volumes of the solution may be prepared orpurchased, provided the final solution concentration is equivalent.6.4 SulfurPure, sublimed, stored in a closed container.6.5 Potassium Io

21、dide, approximately 100 g/L SolutionDissolve approximately1gofpotassium iodide in approxi-mately 10 mL of water. Prepare fresh for each test.6.6 Acetic Acid, approximately 100 g/L SolutionAddapproximately 10 mL of glacial acetic acid to approximately100 mL water.6.7 Starch Indicator, approximately 5

22、 g/L IndicatorSolutionPrepare fresh each time of testing.7. Sampling and Handling of Test Samples7.1 Improper choice of clear glass sample bottles followedby exposure to sunlight or fluorescent lighting emitting UVwavelengths shorter than 550 nm in the laboratory can generateperoxides in cracked gas

23、olines as well as finished batches ofgasolines. Peroxides are generated in proportion to the head-space air volume and time of exposure.6It has been reportedthat peroxides can interfere with the Doctor Testsee 5.1.7.2 It is preferable to collect the field samples using darkbrown/amber bottles or met

24、al cans, or if using clear glassbottles to wrap them in foil or place in a light-tight box toprevent UV light exposure.7.3 The samples should be tested without delay upon receiptin the laboratory before further chemical interactions takeplace.8. Procedure8.1 Shake vigorously together in a test tube

25、10 mL of thesample being tested and 5 mL of sodium plumbite solution forabout 15 s. Add a small amount of pure, sublimed flowers ofsulfur so that practically all of it floats on the interface betweenthe sample and the sodium plumbite solution after shaking.Shake again for 15 s. Allow to settle and o

26、bserve within 2 min.NOTE 2It is important to avoid adding more sulfur than will just coverthe interface. About 20 to 25 mg is the proper quantity, which can beestimated with a little practice. If too much sulfur is added, any possiblediscoloration will be masked by the excess of sulfur.9. Interpreta

27、tion of Results9.1 If the solution is discolored or if the yellow color of thesulfur film is noticeably masked, report the test as positive andconsider the sample as sour. If the sample remains unchangedin color and the sulfur film is bright yellow or only slightlydiscolored with gray or flecked wit

28、h black, report the test asnegative and consider the sample as sweet. If a brownprecipitate slowly forms, peroxide is probably present. Proceedin accordance with 5.2.NOTE 3This examination must be made with extreme care. Some-times the sulfur layer will be only flecked with spots of gray or black, a

29、ndif there is any change in the color of either the sample or the Doctorsolution these spots will be difficult to detect.NOTE 4Strictly speaking, the test will not reject the sample on thebasis of mercaptans only. The primary criterion for rejection is theappearance of the sulfur layer after shaking

30、, and small amounts ofmercaptans will only discolor the sulfur. However, samples which containmercaptans will also normally contain small amounts of sulfur in otherforms which will discolor the layers at the interface. The addition of pure,sublimed flowers of sulfur is required to indicate that a re

31、action ofmercaptan and sodium plumbite has occurred.NOTE 5When the sample contains appreciable amounts of hydrogensulfide, a heavy black precipitate may be formed during the initial shakingand before the addition of the sulfur. If such a precipitate is noted, the testmay be stopped at that point and

32、 the sample reported as “Does not pass.”However, if this observation is at all doubtful, the test should becontinued. If the sample darkens before the addition of sulfur is made, thisindicates that the sample contains mercaptans and an excess of elementalsulfur that is needed to drive the sample rea

33、ction with sodium plumbite.9.1.1 The relationship between the appearance of thesample and the type of sulfur is shown in Table 1.9.2 If the doctor test is positive, mercaptan content may bedetermined using Test Method D3227.10. Precision and Bias10.1 No justifiable values of repeatability, reproduci

34、bility,or bias for this test method can be stated here because the testdetects only the presence or absence of active sulfur species,such as hydrogen sulfide or mercaptan.11. Keywords11.1 doctor test; hydrogen sulfide; kerosine; mercaptans;motor fuel; sulfur5Reagent Chemicals, American Chemical Soci

35、ety 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. Pharmacopei

36、al Convention, Inc. (USPC), Rockville,MD.6Supporting data (Jennings, R., and Kohler, D., “Sunlight and Air ExposureEffects on Octane Number or Cetane Number of Petroleum Product Samples,”April2001) have been filed at ASTM International Headquarters and may be obtained byrequesting Research Report RR

37、:D02-1502.D4952 122SUMMARY OF CHANGESSubcommittee D02.03 has identified the location of selected changes to this standard since the last issue(D495209) that may impact the use of this standard.(1) Added new 2.2.(2) Added new reagents in 6.5-6.7.(3) Added new Section 7 on Sampling and Handling of Tes

38、tSamples and 7.1-7.3.(4) Added new Section 5 on Interferences and precautions tobe taken in interpreting the results in 5.15.4.(5) Revised 9.1.(6) Added new Footnotes 3, 4, and 5.(7) Updated Table 1.ASTM International takes no position respecting the validity of any patent rights asserted in connect

39、ion 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 responsibl

40、e 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 ASTM International Headquarters. Your comments will receive careful cons

41、ideration 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 Standards, at the address shown below.This standard is copyrighted by ASTM International, 100 B

42、arr 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 webs

43、ite(www.astm.org). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).TABLE 1 Relationship Between Sample and SulfurAppearance Type of SulfurFormation of a brown precipitate before addition of sulfur Peroxide is probably present; proceed i

44、n accordance with 5.2Darkening of the sample before addition of sulfur Mercaptans and elemental sulfur present in sampleBlack precipitate before addition of sulfur Appreciable amounts of hydrogen sulfideBlack color of sulfur after shaking Traces of hydrogen sulfideSpots of discoloration in the sulfur layer, plus darkening of thesampleHydrogen sulfide absent; mercaptans or elemental sulfur, or both,presentClear yellow Doctor solution; no discoloration of sulfur Hydrogen sulfide and elemental sulfur absent; traces of mercaptanspresentD4952 123