ASTM D3703-2007e1 Standard Test Method for Hydroperoxide Number of Aviation Turbine Fuels Gasoline and Diesel Fuels《测定航空涡轮燃料、汽油和柴油燃料中氢过氧化物值的标准试验方法》.pdf

《ASTM D3703-2007e1 Standard Test Method for Hydroperoxide Number of Aviation Turbine Fuels Gasoline and Diesel Fuels《测定航空涡轮燃料、汽油和柴油燃料中氢过氧化物值的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D3703-2007e1 Standard Test Method for Hydroperoxide Number of Aviation Turbine Fuels Gasoline and Diesel Fuels《测定航空涡轮燃料、汽油和柴油燃料中氢过氧化物值的标准试验方法》.pdf（5页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D3703 071Standard Test Method forHydroperoxide Number of Aviation Turbine Fuels, Gasolineand Diesel Fuels1This standard is issued under the fixed designation D3703; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the y

2、ear 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.1NOTEClarified notation of X in Section 13

3、 editorially in November 2009.1. Scope*1.1 This test method covers the determination of the hydro-peroxide content expressed as hydroperoxide number of avia-tion turbine, gasoline and diesel fuels.1.2 The range of hydroperoxide number included in theprecision statement is 0 to 50 mg/kg active oxygen

4、 as hydro-peroxide.1.3 The interlaboratory study to establish the precision ofthis test method consisted of spark-ignition engine fuels(regular, premium and California Cleaner-Burning gasoline),aviation gasoline, jet fuel, ultra low sulfur diesel, and biodiesel.However, biodiesel was not included in

5、 the precision calcula-tion because of the large differences in results within labs andbetween labs.1.4 This test method detects hydroperoxides such as t-butylhydroperoxide and cumene hydroperoxide. It does not detectsterically-hindered hydroperoxides such as dicumyl and di-t-butyl hydroperoxides1.5

6、 Di-alkyl hydroperoxides added commercially to dieselfuels are not detected by this test method.1.6 The values stated in SI units are to be regarded as thestandard. The values given in parentheses are for informationonly.1.7 This standard does not purport to address all of thesafety concerns, if any

7、, associated with its use. It is theresponsibility of the user of this standard to consult andestablish appropriate safety and health practices and deter-mine the applicability of regulatory limitations prior to use.For specific warning statements, see 7.3, 7.6, 9.2, and AnnexA1.2. Referenced Docume

8、nts2.1 ASTM Standards:2D1193 Specification for Reagent WaterD4057 Practice for Manual Sampling of Petroleum andPetroleum ProductsD6447 Test Method for Hydroperoxide Number of AviationTurbine Fuels by Voltammetric Analysis2.2 Other Standards:CRC Report No. 559 Determination of the HydroperoxidePotent

9、ial of Jet Fuels34500-C1 B. Iodometric Method IStandard Methods forthe Examination of Water and Wastewater43. Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 hydroperoxide, norganic peroxide having the gen-eralized formula ROOH.3.1.1.1 DiscussionThis test method detects hydropero

10、x-ides such as t-butyl hydroperoxide (CH3)3COOH and cumenehydroperoxide C6H5C(CH3)2OOH. It does not detectsterically-hindered hydroperoxides such as dicumyl and di-t-butyl hydroperoxides.3.1.2 hydroperoxide number, nan indication of the quan-tity of oxidizing constituents present in certain liquid f

11、uels asdetermined by this test method.3.1.2.1 DiscussionThe higher the quantity of oxidizingconstituents in the fuels, the higher the hydroperoxide number.1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of Subcomm

12、itteeD02.05 on Properties of Fuels, Petroleum Coke and Carbon Material.Current edition approved Dec. 1, 2007. Published January 2008. Originallyapproved in 1978. Last previous edition approved in 2004 as D370399(2004).DOI: 10.1520/D3703-07E01.2For referenced ASTM standards, visit the ASTM website, w

13、ww.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 the Coordinating Research Council, Inc., 219 Perimeter CenterParkway, Atlanta, GA 30346.4Published by

14、the American Health Assoc., the American Water Works Assoc.and Water Environment Federation. Available from American Public HealthPublication Sales, P. O. Box 753, Waldorf, MD 206040753.1*A Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor D

15、rive, PO Box C700, West Conshohocken, PA 19428-2959, United States.4. Summary of Test Method4.1 A quantity of sample dissolved in 2,2,4-trimethylpentane is contacted with aqueous potassium iodidesolution. The hydroperoxides present are reduced by thepotassium iodide. An equivalent amount of iodine i

16、s liberated,which is titrated with an aqueous sodium thiosulfate solution.The results are calculated as milligrams of hydroperoxide perkilogram of sample expressed as hydroperoxide number. (SeeNote 1.)NOTE 1The original standard D3703 was published in 1978 asStandard Test Method for Peroxide Number

17、of Aviation Turbine Fuels.This test method originally used carbon tetrachloride (CCl4), which wasdetermined to be carcinogenetic. CCl4was later replaced with 1,1,2-trichloro-1,2,2 trifluoroethane. 1,1,2-trichloro-1,2,2-trifluoroethane is anozone depleting substance. The use of an ozone depleting sub

18、stanceprecludes its use by many operators.5. Significance and Use5.1 The magnitude of the hydroperoxide number is anindication of the quantity of oxidizing constituents present.Deterioration of the fuels results in the formation of hydrop-eroxides and other oxygen-carrying compounds. The hydrop-erox

19、ide number measures those compounds that will oxidizepotassium iodide.5.2 The determination of the hydroperoxide number ofaviation turbine fuels, gasoline and diesel is significant becauseof the adverse effect of hydroperoxide upon certain elastomersin the fuel systems.5.3 The determination of hydro

20、peroxide number of gasolineis significant because hydroperoxides have been demonstratedto decrease both Research and Motor Octane Numbers. Inaddition, hydroperoxides have adverse effects on certain fuelsystem components.5.4 The determination of hydroperoxide number of dieselfuel is significant becau

21、se hydroperoxides have been demon-strated to increase the Cetane Number. In addition, hydroper-oxides have adverse effects on certain fuel system components.6. Apparatus6.1 Iodine Number Flask, 250 mL, glass-stoppered.6.2 Burettes, 10-mL, 25-mL, Class A with polytetrafluoro-ethylene (PTFE) stop cock

22、.6.3 Volumetric Flasks, 100-mL and 1000-mL, 2000 mLClass A with PTFE stoppers.6.4 Mixing Cylinders, 100 mL and 500-mL, glass-stoppered.6.5 Microburet, 10-mL, Class A.6.6 Analytical Balance, capable of weighing to the nearestmilligram.6.7 Brown Bottles, 100-mL, 300-mL, 1000-mL with screwcaps with ine

23、rt inserts.6.8 Measuring Cylinders, 25-mL and 100-mL.7. Reagents7.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical S

24、ociety,where such specifications are available.5Other 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.7.1.1 Commercially available solutions already preparedmay be used in place of

25、 laboratory preparations, if they meetthe method requirements.7.2 Purity of WaterUnless otherwise indicated, referencesto water shall be understood to mean reagent water that meetsthe requirement of Type I, II, or III of Specification D1193.7.3 Acetic Acid SolutionMix 4 mL of concentrated hydro-chlo

26、ric acid (HCl, sp gr 1.19) with 996 mL of glacial aceticacid (CH3COOH). (WarningPoison. Corrosive. Combus-tible. Can be fatal if swallowed. Causes severe burns. Harmfulif inhaled. See A1.2).7.4 Nitrogen Gas, 99.9995% Minimum purity7.5 Carbon Dioxide, 99.9995% Minimum purity7.6 2,2,4-trimethylpentane

27、 (iso-octane),(WarningFlammable, dangerous fire risk. Toxic by injection and inha-lation. See A1.1.)7.7 Potassium Dichromate Solution, Standard (0.1 N), ACSreagent grade. Dissolve 2.452 g of the dried potassium dichro-mate (K2Cr2O7) in water and dilute to 500 mL in a volumetricflask. This solution i

28、s 0.1 N. As an alterative, the lab may usecommercially prepared solution.7.8 Potassium Dichromate Solution, Standard (0.01 N),(WarningAvoid contact with eyes and skin and avoidbreathing of dust)Dilute 100 mL of 0.1 N K2Cr2O7solutionwith water to 1000 mL in a volumetric flask.)7.9 Potassium Iodide So

29、lution, Dissolve 120 g of potassiumiodide (KI) in 100 mL of water. Larger quantities of solutionmay be prepared, provided the concentration of KI in water isequivalent. Protect the solution from sunlight by storing inbrown bottles and blanketed with nitrogen or carbon dioxide.Discharge any color fro

30、m this solution by placing 1 mL of KIsolution, 50 mL of water, and 5 mL of starch solution in a300-mL flask and blanketing with nitrogen or carbon dioxide.If a blue color develops, add 0.005 N Na2S2O3solution from amicroburet until color just disappears. Add a sufficient quantityof Na2S2O3solution,

31、thus determined, to the main KI solutionto convert all free iodine to iodide. When properly prepared, 1mL of KI solution should not turn blue when starch solution isadded, but with starch plus one drop of 0.01 N K2Cr2O7solution plus two drops of HCl, the blue color should develop.Store this solution

32、 under nitrogen or carbon dioxide.7.10 Sodium Thiosulfate Solution, Standard (0.1 N), Dis-solve 12.5 g of sodium thiosulfate (Na2S2O35H2O) plus 0.1 gof sodium carbonate (Na2CO3) in 500 mL of water (theNa2CO3is added to stabilize the Na2S2O3solution). Let thissolution stand a week or more before usin

33、g. Standardize5Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For Suggestions on the testing of reagents notlisted by the American Chemical Society, see Annual Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United Sta

34、tes Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.D3703 0712against 0.1 N K2Cr2O7solution, using any appropriate tech-nique, such as the one indicated in 4500-C1 B. Standardize atintervals frequent enough to detect changes of 0.0005 innormality.7.11 Sod

35、ium Thiosulfate Solution, Standard (0.005 N), Pre-pare a twenty-fold dilution of the 0.1 N Na2S2O3solutionprepared in 7.10, using a volumetric flask. One way toaccomplish this is to dilute 100 mL of 0.1 N Na2S2O3solutionswith water to 2000 mL in a volumetric flask. Prepare thissolution fresh with re

36、standardized 0.1 N Na2S2O3solutionwhen any change of 0.0005 or over in normality is detected.7.12 Starch Solution, Make a paste of6gofarrowrootstarch or soluble iodometric starch with cold water. Pour thepaste into 1 L of boiling water. Add 20 g of potassiumhydroxide (KOH), mix thoroughly, and allow

37、 to stand forapproximately 2 h. Add 6 mL of glacial acetic acid. Mixthoroughly and then add sufficient HCl (sp gr 1.19) to adjustthe pH value of the solution to 4.0. Store in a glass-stopperedbottle. Starch solution prepared in this manner can remainchemically stable for up to one year.7.13 t-Butyl

38、Hydroperoxide, (CH3)3COOH, 90% minimumpurity, Make working standards with iso-octane to cover therange of the expected results.8. Sampling8.1 Samples shall be taken in accordance with the proce-dures described in Practice D4057.8.2 If samples cannot be tested immediately, they should bestored in a r

39、efrigerator at a temperature between 1 and 4C (35and 40F). Bring the sample to room temperature beforetesting.9. Procedure9.1 Select the appropriate weight of sample from the fol-lowing table:Estimated Peroxide Number,mg/kgSample Mass, g0to10 5011 to 30 3531 to 50 2551 to 80 (Note 2)181 to 100 5NOTE

40、 2The precision statement was based up to 50 mg/kg oxygen.The precision might not apply for samples greater than 50 mg/kg.9.2 Weigh the sample, accurate to 1 mg, into a 250-mLiodine flask that has been flushed with nitrogen or carbondioxide. With a measuring cylinder, add 25 mL of 2,2,4-trimethylpen

41、tane (WarningSee A1.1). Pass a vigorous flowof nitrogen or carbon dioxide through the solvent for at least 1min; then, without stopping the gas flow, add 20 mL of aceticacid solution and reduce the flow of gas so that the rate is onebubble per second. Add 2 mL of KI solution and mixvigorously for 30

42、 6 1 s. Set the flask aside to stand for 5 min6 3s.9.3 At the end of the reaction period, add 100 mL of waterand stop the gas flow. Add 5 mL of starch solution. Titrate with0.005N Na2S2O3solution to the disappearance of the bluecolor.9.4 Titrate a reagent blank just prior to each set of unknowndeter

43、minations, following the same procedure as described in9.1-9.3. (See Note 3.)NOTE 3This end point is of the returning type. The end point intendedin this method is the disappearance of the blue color for 30 s or longer. Ifthere is no blue color upon the addition of the starch solution, there is node

44、tectable hydroperoxide and therefore there is no need to titrate thesolution with Na2S2O3solution.10. Quality Control10.1 Confirm the performance of the test procedure byanalyzing a known hydroperoxide such ast-butylhydroperoxide or cumyl hydroperoxide.11. Calculation11.1 Calculate the peroxide numb

45、er as follows:Hydroperoxide number, mg/kg 5 A 2 B!N 3 1000 3 8/S (1)where:X = measured hydroperoxide number,A = millilitres of Na2S2O3solution required for titration ofthe sample,B = millilitres of Na2S2O3solution required for titration ofthe blank,N = normality of the Na2S2O3solution,8 = milliequiv

46、alent of hydroperoxide number, andS = grams of sample used, accurate to 0.001 g.12. Report12.1 Report the result calculated in 11.1 to three (3) signifi-cant figures.12.2 If there is no detectable hydroperoxide (see Note 3),report “None Detected.”13. Precision and Bias613.1 PrecisionThe precision of

47、 this method was deter-mined from an interlaboratory study (ILS). The study con-tained thirteen (13) fuel samples which were tested in nine (9)laboratories in duplicate. The fuel types in the study were:regular and premium gasoline, ultra low sulfur diesel, Jet A,and isooctane blank. A biodiesel fue

48、l was also included in thestudy but was not used in calculating the precision statementbecause of the variabilities between laboratories.13.1.1 RepeatabilityThe difference between two succes-sive test results, obtained by the same operator with the sameapparatus under constant operating conditions o

49、n identical testmaterial would, in the long run, in the normal and correctoperation of the test method, exceed the following values onlyin one case in twenty:Repeatability 5 0.2829*X 1 0.0001! 0.6596 mg/kg (2)where:X = measured hydroperoxide number in Eq 1.13.1.2 ReproducibilityThe difference between two singleand independent results obtained by different operators work-ing in different laboratories on identical test material would, in6Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Research Repo