ASTM D5292-1999(2009) Standard Test Method for Aromatic Carbon Contents of Hydrocarbon Oils by High Resolution Nuclear Magnetic Resonance Spectroscopy《用高裂度核磁共振光谱法测定烃类油中芳香碳含量的标准试验方法.pdf

《ASTM D5292-1999(2009) Standard Test Method for Aromatic Carbon Contents of Hydrocarbon Oils by High Resolution Nuclear Magnetic Resonance Spectroscopy《用高裂度核磁共振光谱法测定烃类油中芳香碳含量的标准试验方法.pdf》由会员分享，可在线阅读，更多相关《ASTM D5292-1999(2009) Standard Test Method for Aromatic Carbon Contents of Hydrocarbon Oils by High Resolution Nuclear Magnetic Resonance Spectroscopy《用高裂度核磁共振光谱法测定烃类油中芳香碳含量的标准试验方法.pdf（7页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D 5292 99 (Reapproved 2009)An American National StandardStandard Test Method forAromatic Carbon Contents of Hydrocarbon Oils by HighResolution Nuclear Magnetic Resonance Spectroscopy1This standard is issued under the fixed designation D 5292; the number immediately following the designa

2、tion indicates the year oforiginal adoption or, in 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.1. Scope1.1 This test method covers the deter

3、mination of the aro-matic hydrogen content (Procedures A and B) and aromaticcarbon content (Procedure C) of hydrocarbon oils usinghigh-resolution nuclear magnetic resonance (NMR) spectrom-eters. Applicable samples include kerosenes, gas oils, mineraloils, lubricating oils, coal liquids, and other di

4、stillates that arecompletely soluble in chloroform at ambient temperature. Forpulse Fourier transform (FT) spectrometers, the detection limitis typically 0.1 mol % aromatic hydrogen atoms and 0.5 mol %aromatic carbon atoms. For continuous wave (CW) spectrom-eters, which are suitable for measuring ar

5、omatic hydrogencontents only, the detection limit is considerably higher andtypically 0.5 mol % aromatic hydrogen atoms.1.2 The reported units are mole percent aromatic hydrogenatoms and mole percent aromatic carbon atoms.1.3 This test method is not applicable to samples containingmore than 1 mass %

6、 olefinic or phenolic compounds.1.4 This test method does not cover the determination of thepercentage mass of aromatic compounds in oils since NMRsignals from both saturated hydrocarbons and aliphatic sub-stituents on aromatic ring compounds appear in the samechemical shift region. For the determin

7、ation of mass or volumepercent aromatics in hydrocarbon oils, chromatographic, ormass spectrometry methods can be used.1.5 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.6 This standard does not purport to address all of thes

8、afety problems, 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. Specific precau-tionary statements are given in 7.2 and 7.3.2. Referenc

9、ed Documents2.1 ASTM Standards:2D 3238 Test Method for Calculation of Carbon Distributionand Structural Group Analysis of Petroleum Oils by then-d-M MethodD 3701 Test Method for Hydrogen Content of AviationTurbine Fuels by Low Resolution Nuclear Magnetic Reso-nance SpectrometryD 4057 Practice for Ma

10、nual Sampling of Petroleum andPetroleum ProductsE 386 Practice for Data Presentation Relating to High-Resolution Nuclear Magnetic Resonance (NMR) Spectros-copy2.2 Energy Institute Methods:IP Proposed Method BD Aromatic Hydrogen and AromaticCarbon Contents of Hydrocarbon Oils by High ResolutionNuclea

11、r Magnetic Resonance Spectroscopy33. Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 aromatic carbon contentmole percent aromatic car-bon atoms or the percentage of aromatic carbon of the totalcarbon:aromatic carbon content 5 100 3aromatic carbon atoms!/total carbon atoms!(1)3.1.

12、1.1 DiscussionFor example, the aromatic carbon con-tent of toluene is 100 3 (6/7) or 85.7 mol % aromatic carbonatoms.3.1.2 aromatic hydrogen contentmole percent aromatichydrogen atoms or the percentage of aromatic hydrogen of thetotal hydrogen:1This test method is under the jurisdiction of ASTM Comm

13、ittee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.04.0F on Absorption Spectroscopic Methods.Current edition approved April 15, 2009. Published July 2009. Originallyapproved in 1992. Last previous edition approved in 2004 as D 529299(2004)1.2For referen

14、ced 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.3Available from Energy Institute, 61 New Cavendish St., London, WIG 7AR,U

15、.K.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.aromatic hydrogen content 5 100 3aromatic hydrogen atoms!/total hydrogen atoms!(2)3.1.2.1 DiscussionFor example, the aromatic hydrogencontent of toluene is 100 3 (5/8) or 62.5 mol %

16、aromatichydrogen atoms.3.2 Definitions of chemical shift (reported in parts permillion (ppm), internal reference, spectral width, and otherNMR terminology used in this test method can be found inPractice E 386.3.3 Chloroform-d refers to chloroform solvent in whichhydrogen is replaced by deuterium, t

17、he heavier isotope ofhydrogen. Chloroform-d is available from a variety of chemi-cal and isotope suppliers.4. Summary of Test Method4.1 Hydrogen (1H) nuclear magnetic resonance (NMR)spectra are obtained on solutions of the sample inchloroform-d, using a CW or pulse FT high-resolution NMRspectrometer

18、. Carbon (13C) NMR spectra are obtained onsolutions of the sample in chloroform-d using a pulse FThigh-resolution NMR spectrometer. Tetramethylsilane is pre-ferred as an internal reference in these solvents for assigningthe 0.0 parts per million (ppm) chemical shift position inboth1H and13C NMR spec

19、tra.4.2 The aromatic hydrogen content of the sample is mea-sured by comparing the integral for the aromatic hydrogenband in the1H NMR spectrum (5.0 to 10.0 ppm chemical shiftregion) with the sum of the integrals for both the aliphatichydrogen band (0.5 to 5.0 ppm region) and the aromatichydrogen ban

20、d (5.0 to 10.0 ppm region).4.3 The aromatic carbon content of the sample is measuredby comparing the integral for the aromatic carbon band inthe13C spectrum (100 to 170 ppm chemical shift region) withthe sum of the integrals for both the aliphatic carbon band (10to 70 ppm region) and the aromatic ca

21、rbon band (100 to 170ppm region).4.4 The integral of the aromatic hydrogen band must becorrected for the NMR absorption line due to residual chloro-form (7.25 ppm chemical shift) in the predominantlychloroform-d solvent.4.5 The integrals of the aliphatic hydrogen band and of thealiphatic carbon band

22、 must be corrected for the NMR absorp-tion line due to the internal chemical shift reference tetrameth-ylsilane (0.0 ppm chemical shift in both1H and13C spectra).5. Significance and Use5.1 Aromatic content is a key characteristic of hydrocarbonoils and can affect a variety of properties of the oil i

23、ncluding itsboiling range, viscosity, stability, and compatibility of the oilwith polymers.5.2 Existing methods for estimating aromatic contents usephysical measurements, such as refractive index, density, andnumber average molecular weight (see Test Method D 3238)orinfrared absorbance4and often dep

24、end on the availability ofsuitable standards. These NMR procedures do not requirestandards of known aromatic hydrogen or aromatic carboncontents and are applicable to a wide range of hydrocarbon oilsthat are completely soluble in chloroform at ambient tempera-ture.5.3 The aromatic hydrogen and aroma

25、tic carbon contentsdetermined by this test method can be used to evaluate changesin aromatic contents of hydrocarbon oils due to changes inprocessing conditions and to develop processing models inwhich the aromatic content of the hydrocarbon oil is a keyprocessing indicator.6. Apparatus6.1 High-Reso

26、lution Nuclear Magnetic ResonanceSpectrometerA high-resolution continuous wave (CW) orpulse Fourier transform (FT) NMR spectrometer capable ofbeing operated according to the conditions in Table 1 and Table2 and of producing peaks having widths less than the frequencyranges of the majority of chemica

27、l shifts and coupling con-stants for the measured nucleus.6.1.11H NMR spectra can be obtained using either CW orpulse FT techniques but13C measurements require signalaveraging and, therefore, currently require the pulse FT tech-nique. Low resolution NMR spectrometers and procedures arenot discussed

28、in this test method (see Test Method D 3701 foran example of the use of low resolution NMR).6.2 Tube TubesUsuallya5or10mmoutside diametertube compatible with the configuration of the CW or pulse FTspectrometer.7. Reagents and Materials7.1 Purity of ReagentsReagent grade chemicals shall beused in all

29、 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 Society,where such specifications are available.5Other grades may be4Brandes, G., “The Structural Groups of Petroleum Fractions. I

30、. StructuralGroupAnalysis With the Help of Infrared Spectroscopy,” Brennstoff-Chemie Vol 37,1956, p. 263.5“Reagent Chemicals, American Chemical Society Specification.” AmericanChemical Society, Washington, D.C. For suggestions on the testing of reagents notlisted by the American Chemical Society, se

31、e “Analar Standards for LaboratoryU.K. Chemicals,” BDH Ltd., Poole, Dorset, and the “United States Pharmacopeia.”TABLE 1 Sample and Instrument Conditions for ContinuousWave (CW) Measurements of1H NMR SpectraSolvent Chloroform-dSample concentration Up to 50 % v/v for distillable oilsSample temperatur

32、e Instrument ambientInternal lock NoneSample spinning rate As recommended by manufacturer, typically 20 Hzr-f Power level As recommended by instrument manufacturerSignal to noise level A minimum of 5:1 for the maximum height of thesmaller integrated absorption bandChemical shift reference Preferably

33、 tetramethylsilane (0.0 ppm) at nogreater than 1 vol % concentrationIntegration Integrate over the range 0.5 to 5.0 ppm for thealiphatic band and 5.0 to 10.0 ppm for the aromaticbandD 5292 99 (2009)2used, provided it is first ascertained that the reagent is ofsufficiently high purity to permit its u

34、se.7.2 Chloroform-dFor1H NMR, chloroform-d must con-tain less than 0.2 vol % residual chloroform. Care must betaken not to contaminate the solvent with water and otherextraneous materials. (WarningHealth hazard. Highly toxic.Cancer suspect agent. Can be fatal when swallowed andharmful when inhaled.

35、Can produce toxic vapors whenburned.)7.3 Tetramethylsilane, American Chemical Society (ACS)reagent internal chemical shift reference for1H and13C NMRspectra. (WarningFlammable liquid.)7.4 Chromium (III) 2,4-Pentanedionate, relaxation reagentfor13C NMR spectra, typically 97 % grade.8. Sampling8.1 It

36、is assumed that a representative sample acquired by aprocedure of Practice D 4057 or equivalent has been receivedin the laboratory. If the test is not to be conducted immediatelyupon receipt of the sample, store in a cool place until needed.8.2 A minimum of approximately 10 mL of sample isrequired f

37、or this test method. This should allow duplicatedeterminations, if desired.8.3 All samples must be homogeneous prior to subsam-pling. If any suspended particles present are attributable toforeign matter such as rust, filter a portion of the sample to betested through a small plug of glass wool, cont

38、ained in a cleansmall funnel, into a clean and dry vial or NMR sample tubecontaining chloroform-d.8.4 If the sample contains waxy materials, heat the samplein the container to approximately 60C and mix with ahigh-shear mixer prior to sampling. It may be necessary totransfer a portion of the sample t

39、o an NMR tube containingchloroform-d by means of a pipet which has been heated toapproximately 60C to maintain the homogeneity of thesample.8.5 For a valid test result, samples must be completelysoluble in chloroform-d. Check to ensure that the final solutionis homogeneous and free of undissolved pa

40、rticles.9. Procedures9.1 Three different procedures are described in this sectionfor determining the aromatic hydrogen content, (see 9.6)Procedures A and B (see 9.7), and the aromatic carbon contentof hydrocarbon oils, Procedure C (see 9.8).9.2 The procedure selected by the analyst will depend on th

41、eavailable NMR instrumentation and on whether an aromatichydrogen or aromatic carbon content is of greater value inevaluating the characteristics of the hydrocarbon oil.9.3 Appendix X1 and Practice E 386 should be used inconjunction with the NMR spectrometer manufacturers in-structions in order to e

42、nsure optimum performance of the NMRinstrument in the application of these procedures.9.4 If tetramethylsilane is used as an internal chemical shiftstandard, prepare a 1 % v/v TMS in solvent solution by addingtetramethylsilane to chloroform-d solvent. Since TMS is veryvolatile, this solution should

43、be refrigerated or replaced if thecharacteristic absorption due to TMS is no longer evident inthe1Hor13C NMR spectrum.9.5 If it is inconvenient to prepare the test solution directlyin the NMR sample tube as suggested in the followingprocedures, the test solution can be prepared in a small vial andtr

44、ansferred into the NMR sample tube after solvent additionand sample dissolution. Care should be exercised to ensure thatthe final solution concentrations are not different from thoseindicated in the procedures and that no contamination occursduring the transfer process.9.6 Procedure A1H NMR Measurem

45、ents Using a Con-tinuous Wave (CW) NMR Spectrometer:TABLE 2 Sample and Instrument Conditions for Pulse FourierTransform Measurements of1H and13C NMR SpectraSolvent:1H NMR Chloroform-d13C NMR Chloroform-dSample concentration:1H NMR Must be optimized for the instrument in use butmay be as high as 5 %

46、v/v13C NMR Up to 50 % v/v for petroleum distillates and 30 %v/v for coal liquidsRelaxation agent Chromium (III) 2,4-pentanedionate recommendedfor13C NMR solutions only. Where used, a 20 mMsolution (about 10 mg per mL)Sample temperature Instrument ambientInternal lock Deuterium (when chloroform-d is

47、used for1H NMR)Sample spinning rate As recommended by manufacturer, typically 20 Hz1H Decoupling Only for13C NMR. Broadband over the whole ofthe1H frequency range, gated on during13C dataacquisition only with a decoupler rise time lessthan2m/sPulse flip angle Approximately 30Sequence delay time:1HNM

48、R10s13CNMR3swithand 60 s without relaxationagentMemory size foracquisition:Choose to give a minimum digitizing rate of 0.5Hz/point for1H and 1.2 Hz/point for13C NMR. Ifnecessary, increase memory size and zero fillSpectral width:1H NMR At least 15 ppm in frequency and centered, asclose as possible, t

49、o the 5 ppm chemical shiftvalue13C NMR At least 250 ppm in frequency and centered, asclose as possible, to the 100 ppm chemical shiftvalueFilter bandwidth Set to be equal to or greater than the spectralwidth and as permitted by the instruments filterhardwareExponential linebroadeningSet at least equal to the digitizing rateSignal to noise levels:1H NMR A minimum of 20:1 for the maximum height of thesmaller integrated band13C NMR A minimum of 60:1 for the maximum height of thechloroform-d resonance appearing between 75 and80 ppm on the chemical shift scaleChe