ASTM D1840-2007 Standard Test Method for Naphthalene Hydrocarbons in Aviation Turbine Fuels by Ultraviolet Spectrophotometry《紫外线分光光度法测定航空涡轮机燃料中萘烃的标准试验方法》.pdf

《ASTM D1840-2007 Standard Test Method for Naphthalene Hydrocarbons in Aviation Turbine Fuels by Ultraviolet Spectrophotometry《紫外线分光光度法测定航空涡轮机燃料中萘烃的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D1840-2007 Standard Test Method for Naphthalene Hydrocarbons in Aviation Turbine Fuels by Ultraviolet Spectrophotometry《紫外线分光光度法测定航空涡轮机燃料中萘烃的标准试验方法》.pdf（5页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D 1840 07An American National StandardStandard Test Method forNaphthalene Hydrocarbons in Aviation Turbine Fuels byUltraviolet Spectrophotometry1This standard is issued under the fixed designation D 1840; the number immediately following the designation indicates the year oforiginal ado

2、ption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) 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

3、. Scope*1.1 This test method covers the determination, by ultravioletspectrophotometry, of the total concentration of naphthalene,acenaphthene, and alkylated derivatives of these hydrocarbonsin jet fuels. This test method is designed to analyze fuelscontaining not more than 5 % of such components an

4、d havingend points below 315C (600F); however, the range ofconcentrations used in the interlaboratory test programs whichestablished the precision statements for this test method were0.03 to 4.25 volume % for ProcedureA, and 0.08 to 5.6 volume% for Procedure B. This test method determines the maximu

5、mamount of naphthalenes that could be present.1.2 The values stated in SI units are to be regarded as thestandard. The values given in parentheses are for informationonly.1.3 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility

6、 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. For specificwarning statements, see 8.1 and 8.2.2. Referenced Documents2.1 ASTM Standards:2E 131 Terminology Relating to Molecular Spectroscopy

7、E 169 Practices for General Techniques of Ultraviolet-Visible Quantitative AnalysisE 275 Practice for Describing and Measuring Performanceof Ultraviolet, Visible, and Near-Infrared Spectrophotom-eters3. Terminology3.1 Definitions:3.1.1 Definitions of terms and symbols relating to absorp-tion spectro

8、scopy in this test method shall conform to Termi-nology E 131. Terms of particular significance are the follow-ing:3.1.2 radiant energy, nenergy transmitted as electromag-netic waves.3.1.3 radiant power, P, nrate at which energy is trans-ported in a beam of radiant energy.3.2 Definitions of Terms Sp

9、ecific to This Standard:3.2.1 absorbance, A, nthe molecular property of a sub-stance that determines its ability to take up radiant power,expressed byA 5 log101/T! 52log10T (1)where:T = transmittance as defined in 3.2.5.3.2.1.1 DiscussionIt may be necessary to correct theobserved transmittance (indi

10、cated by the spectrophotometer)by compensating for reflectance losses, solvent absorptionlosses, or refraction effects.3.2.2 absorptivity, a, nthe specific property of a substanceto absorb radiant power per unit sample concentration and pathlength, expressed bya 5 A/bc (2)where:A = absorbance define

11、d in 3.2.1,b = sample cell path length, andc = quantity of absorbing substance contained in a unitvolume of solvent.3.2.2.1 DiscussionQuantitative ultraviolet analyses arebased upon the absorption law, known as Beers law. The lawstates that the absorbance of a homogeneous sample containing1This test

12、 method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.04.0F on Absorption Spectroscopic Methods.Current edition approved Nov. 1, 2007. Published December 2007. Originallyapproved in 1961. Last previous edition

13、approved in 2003 as D 1840-03.2For 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.1*A Summary of Changes section

14、appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.Copyright by ASTM Intl (all rights reserved); Tue Mar 24 03:59:39 EDT 2009Downloaded/printed byGuo Dehua (CNIS) pursuant to License Agreement. No furt

15、her reproductions authorized.an absorbing substance is directly proportional to the concen-tration of the absorbing substance at a single wavelength,expressed byA 5 abc (3)where:A = absorbance as defined in 3.2.1,a = absorptivity as defined in 3.2.2,b = sample cell path length, andc = quantity of ab

16、sorbing substance contained in a unitvolume of solvent.3.2.3 concentration, c, nthe quantity of naphthalene hy-drocarbons in grams per litre of isooctane.3.2.4 sample cell path length, b, nthe distance, in centi-metres, measured in the direction of propagation of the beam ofradiant energy, between t

17、he surfaces of the specimen on whichthe radiant energy is incident and the surface of the specimenfrom which it is emergent.3.2.4.1 DiscussionThis distance does not include thethickness of the cell in which the specimen is contained.3.2.5 transmittance, T, nthe molecular property of asubstance that

18、determines its transportability of radiant powerexpressed byT 5 P/Po(4)where:P = radiant power passing through the sample, andPo= radiant power incident upon the sample.4. Summary of Test Method4.1 The total concentration of naphthalenes in jet fuels isdetermined by measurement of the absorbance at

19、285 nm of asolution of the fuel at known concentration.5. Significance and Use5.1 This test method for naphthalene hydrocarbons is one ofa group of tests used to assess the combustion characteristics ofaviation turbine fuels of the kerosene boiling range. Thenaphthalene hydrocarbon content is determ

20、ined because naph-thalenes, when burned, tend to have a relatively larger contri-bution to a sooty flame, smoke, and thermal radiation thansingle ring aromatics.6. Interferences6.1 Interferences add to the apparent naphthalene content.Phenanthrenes, dibenzothiophenes, biphenyls, ben-zothiophenes, an

21、d anthracenes interfere if present. The endpoint limitation of 315C will minimize this interferenceexcept for benzothiophenes and biphenyls. The contribution tomeasured naphthalene content by the presence of 1 % of suchinterfering compounds can be estimated from Table 1.6.2 Saturated hydrocarbons, o

22、lefins, thiophenes, and alkylor cycloalkyl derivatives of benzene will not interfere.7. Apparatus7.1 Spectrophotometer, equipped to measure the absorbanceof solutions in the spectral region 240 to 300 nm with a spectralslit width of 1 nm or less. Wavelength measurements shall berepeatable and known

23、to be accurate within 0.1 nm or less asmeasured by mercury emission line at 253.65 nm or theabsorption spectrum of either holmium oxide glass at 287.5 nmor holmium oxide solution at 287.1 nm. At the 0.4 absorbancelevel in the spectral region between 240 and 300 nm, absor-bance measurements shall be

24、repeatable within 60.5 % orbetter. In the absorbance range encompassing 0.2 to 0.8, thephotometric accuracy shall not differ by more than 60.5 % ofsamples whose absorbance has been established by a standard-izing laboratory.7.1.1 DiscussionMany manufacturers provide secondarystandards, traceable to

25、NIST primary standards, for checkingthe wavelength accuracy and photometric accuracy of spectro-photometers. These materials may be used to verify spectro-photometer performance provided that they have been recali-brated periodically as recommended by the manufacturer.7.2 It shall be initially and t

26、hereafter periodically demon-strated that an instrument can be operated in a manner to givetest results equivalent to those described in 7.1.NOTE 1For recommended methods of testing spectrophotometers tobe used in this test method, refer to Practice E 275. Other preferredalternatives to those in 7.1

27、 are potassium dichromate in perchloric acid(NIST SRM 935 series as described in Practice E 275) for photometricaccuracy and a 20 mg/L high (99 %) purity naphthalene in spectroscopicgrade isooctane for wavelength accuracy. The latter has a minor maximumat 285.7 nm. The naphthalene solution shall not

28、 be used for photometricaccuracy.7.3 Vitreous Silica Cells, two, having path lengths of 1.00 60.005 cm.7.4 Pipets, Class A.7.5 Lens Paper.7.6 Balance, capable of taring or weighing 100 g to thenearest 0.0001 g. The balance shall be accurate to 60.0002 gat a 100-g load.8. Solvents8.1 Spectroscopic 2,

29、2,4 Trimethylpentane (Isooctane).(WarningIsooctane is extremely flammable, harmful if in-haled.)NOTE 2Spectroscopic-grade isooctane is available commercially.Technical-grade isooctane is a satisfactory base stock for the preparationof spectroscopic solvent.Allow about 4 or 5 L of this material to pe

30、rcolatethrough a column of activated silica gel (74 m) 50.8 to 76.2 mm indiameter and 0.6 to 0.9 m in depth. Collect only the portion of the solventthat has a transmission compared to distilled water greater than 90 % overthe entire spectral range from 240 to 300 nm. Store in scrupulously cleanglass

31、-stoppered bottles and always keep covered. In general it will be bestto use a fresh portion of silica gel in preparing a new batch of solvent.However the gel can be reactivated by pouring 500 mL of acetone throughthe column, draining, drying by suction, and heating the gel in thin layersin an oven

32、at 400C until white color is restored. Activated silica gel isstored in closed containers.TABLE 1 Interfering CompoundsType of Interfering CompoundError in Percentage ofNaphthalenes Caused by 1 %Interfering CompoundPhenanthrenes 2Dibenzothiophenes 2Biphenyls 1Benzothiophenes 0.6Anthracenes 0.1D18400

33、72Copyright by ASTM Intl (all rights reserved); Tue Mar 24 03:59:39 EDT 2009Downloaded/printed byGuo Dehua (CNIS) pursuant to License Agreement. No further reproductions authorized.8.2 Solvents for Cleaning CellsAcetone or ethyl alcohol(WarningAcetone and ethyl alcohol are extremely flam-mable and c

34、an be harmful if inhaled), with residue afterevaporation no greater than 10 mg/kg.NOTE 3The 10 mg/kg is the American Chemical Society (ACS)reagent grade maximum specification. An ACS reagent grade solvent maybe used without further testing.9. Calibration and Standardization9.1 Instead of direct cali

35、bration of the spectrophotometerwith known naphthalenes, the average absorptivity of the C10to C13naphthalenes at 285 nm can be taken at 33.7 L/gcm. Thedata used to calculate this average are given in Table 2.10. Procedure ASerial DilutionNOTE 4The user may use alternative Procedure B if preferred.1

36、0.1 For recommended techniques, refer to Practices E 169.Check carefully sections on handling and cleaning of cells andglassware, instrument adjustments, and method of absorbancemeasurement.10.2 Prepare three dilutions of the sample as follows:10.2.1 First DilutionIf the sample is more volatile than

37、isooctane, add 10 to 15 mL of spectroscopic isooctane to aclean, dry, glass-stoppered, 25 mL volumetric flask. Weigh outapproximately1gofsample in the flask, dilute to volume withspectroscopic solvent, and mix thoroughly. If the sample is lessvolatile than isooctane, weigh out approximately1gofsampl

38、ein the flask, dilute to volume with spectroscopic solvent, andmix thoroughly.10.2.2 Second DilutionPipet 5.00 mL of the first dilutioninto a 50-mLglass-stoppered volumetric flask, dilute to volumewith spectroscopic isooctane, and mix thoroughly.10.2.3 Third DilutionDilute 5.00 mL of second dilution

39、 to50 mL in the same manner as in 10.2.2.10.3 Determination of Cell CorrectionMeasure andrecord the absorbance of the spectroscopic isooctane-filledsample cell as compared to the spectroscopic isooctane-filledsolvent cell.10.4 Measurement of AbsorbanceTransfer portions of thefinal dilution into the

40、sample cell of the spectrophotometer.Cover the cells immediately to prevent transfer of aromatichydrocarbons from the sample cell to the solvent cell. Checkthe windows of the absorption cells and make certain they areclean. Measure the absorbance as recommended in PracticesE 169. Record the absorban

41、ce of the sample as compared tospectroscopic isooctane at 285 nm.NOTE 5The dilution of the sample should be controlled so thatabsorbance readings fall within a range of 0.2 to 0.8 for maximumreproducibility of results. To accomplish this it may be necessary to use analternative third dilution than t

42、he one specified in 10.2.3, such as 10 mLof the second dilution to 25 mL with solvent.11. Procedure BAlternative 100-mL Dilution11.1 DiscussionThe incorporation of the single dilutionprocedure has been included as an alternative procedure toreduce: test time, glassware, cleaning, and dilution errors

43、.11.2 For recommended techniques, refer to Practices E 169.Check carefully sections on handling and cleaning of cells andglassware, instrument adjustments, and method of absorbancemeasurement.11.3 Sample PreparationAdd an appropriate weight ofsample to a clean, dry, tared 100-mL volumetric flask. Re

44、cordthe weight to the nearest 0.0001 g. Dilute to the mark withspectroscopic grade isooctane, stopper, and mix thoroughly.11.3.1 Refer to Table 3 for lists of sample weights associ-ated with naphthalene(s) concentrations that give 0.2 to 0.8absorbance readings as directed in Note 7. A 60-mg samplewi

45、ll be appropriate for typical jet fuels in the range of 0.8 to3.0 % volume naphthalenes.NOTE 6A micropipette is a convenient tool for adding an appropriatevolume. If the fuel density is not known at the time of sample preparation,use 0.8 as an approximation.11.4 Determination of Cell CorrectionProce

46、ed as writtenin 10.3.11.5 Measurement of AbsorbanceProceed as written in10.4.12. Calculations12.1 Calculate the mass percentage of naphthalenes in thesample as follows:Naphthalenes, mass % 5 A 3 K!/33.7 3 W!# 3 100 (5)where:A = corrected absorbance (observed absorbance minus cellcorrection) of the d

47、ilution measured,TABLE 2 Data Issued by API Research Project 44CompoundAPI SerialNumberL/gcmNaphthalene 605 28.51-methyl Naphthalene 539 32.02-methyl Naphthalene 572 22.91,2-dimethyl Naphthalene 215 37.31,3-dimethyl Naphthalene 216 36.41,4-dimethyl Naphthalene 217 43.51,5-dimethyl Naphthalene 218 54

48、.01,6-dimethyl Naphthalene 219 36.41,7-dimethyl Naphthalene 220 36.01,8-dimethyl Naphthalene 221 46.02,3-dimethyl Naphthalene 222 22.02,6-dimethyl Naphthalene 226 21.32,7-dimethyl Naphthalene 224 23.51-isopropyl Naphthalene 203 31.7TABLE 3 Estimated Sample Weight and Volume to Take for theVolume % N

49、aphthalene Content of the Sample in the SingleDilution Procedure to Keep the Absorption Values Between 0.2and 0.8 Units (Assuming a Density of 0.8)SampleVolume(mL)SampleWeight(mg)Volume % Naphthalenesfor Expected Absorbanceof 0.2 unitsVolume % Naphthalenesfor Expected Absorbanceof 0.8 units0.050 40 1.2 4.80.075 60 0.8 3.20.100 80 0.6 2.40.150 120 0.4 1.60.200 160 0.3 1.20.300 240 0.2 0.8D1840073Copyright by ASTM Intl (all rights reserved); Tue Mar 24 03:59:39 EDT 2009Downloaded/printed byGuo Dehua (CNIS) pursuant to License Agreement. No fu