ASTM E1252-1998(2007) Standard Practice for General Techniques for Obtaining Infrared Spectra for Qualitative Analysis《获得定性分析用红外光谱的一般方法的标准规程》.pdf

《ASTM E1252-1998(2007) Standard Practice for General Techniques for Obtaining Infrared Spectra for Qualitative Analysis《获得定性分析用红外光谱的一般方法的标准规程》.pdf》由会员分享，可在线阅读，更多相关《ASTM E1252-1998(2007) Standard Practice for General Techniques for Obtaining Infrared Spectra for Qualitative Analysis《获得定性分析用红外光谱的一般方法的标准规程》.pdf（13页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E 1252 98 (Reapproved 2007)Standard Practice forGeneral Techniques for Obtaining Infrared Spectra forQualitative Analysis1This standard is issued under the fixed designation E 1252; the number immediately following the designation indicates the year oforiginal adoption or, in the case o

2、f 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.1. Scope1.1 This practice covers the spectral range from 4000 to 50cm1and includes techniques that are us

3、eful for qualitativeanalysis of liquid-, solid-, and vapor-phase samples by infraredspectrometric techniques for which the amount of sampleavailable for analysis is not a limiting factor. These techniquesare often also useful for recording spectra at frequencies higherthan 4000 cm1, in the near-infr

4、ared region.1.2 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. Sp

5、ecific precau-tions are given in 6.5.1.2. Referenced Documents2.1 ASTM Standards:2E 131 Terminology Relating to Molecular SpectroscopyE 168 Practices for General Techniques of Infrared Quanti-tative AnalysisE 334 Practice for General Techniques of Infrared Mi-croanalysisE 573 Practices for Internal

6、Reflection SpectroscopyE 932 Practice for Describing and Measuring Performanceof Dispersive Infrared SpectrometersE 1421 Practice for Describing and Measuring Performanceof Fourier Transform Mid-Infrared (FT-MIR) Spectrom-eters: Level Zero and Level One TestsE 1642 Practice for General Techniques of

7、 Gas Chromatog-raphy Infrared (GC/IR) Analysis3. Terminology3.1 DefinitionsFor definitions of terms and symbols, referto Terminology E 131.4. Significance and Use4.1 Infrared spectroscopy is the most widely used techniquefor identifying organic and inorganic materials. This practicedescribes methods

8、 for the proper application of infraredspectroscopy.5. General5.1 Infrared (IR) qualitative analysis is carried out byfunctional group identification (1-3)3or by the comparison ofIR absorption spectra of unknown materials with those ofknown reference materials, or both. These spectra are obtained(4-

9、8) through transmission, reflection, and other techniques,such as photoacoustic spectroscopy (PAS). Spectra that are tobe compared should be obtained by the same technique andunder the same conditions. Users of published referencespectra (9-16) should be aware that not all of these spectra arefully

10、validated.5.1.1 Instrumentation and accessories for infrared qualita-tive analysis are commercially available. The manufacturersmanual should be followed to ensure optimum performanceand safety.5.2 Transmission spectra are obtained by placing a thinuniform layer of the sample perpendicular to the in

11、fraredradiation path (see 9.5.1 for exception in order to eliminateinterference fringes for thin films). The sample thickness mustbe adequate to cause a decrease in the radiant power reachingthe detector at the absorption frequencies used in the analysis.For best results, the absorbance of the stron

12、gest bands shouldbe in the range from 1 to 2, and several bands should haveabsorbances of 0.6 units or more. There are exceptions to thisgeneralization based on the polarity of the molecules beingmeasured. For example, saturated hydrocarbons are nonpolar,and their identifying bands are not strong en

13、ough unless theC-H stretch at 2920 cm1is opaque and the deformation bandsare in the range from 1.5 to 2.0 absorbance units (A) at 1440to 1460 cm1. Spectra with different amounts of sample in theradiation path may be required to permit reliable analysis. Ifspectra are to be identified by computerized

14、 curve matching,the absorbance of the strongest band should be less than 1;1This practice is under the jurisdiction of ASTM Committee E13 on MolecularSpectroscopy and Separation Science and is the direct responsibility of Subcom-mittee E13.03 on Infrared and Near Infrared Spectroscopy.Current editio

15、n approved Dec. 1, 2007. Published December 2007. Originallyapproved in 1988. Last previous edition approved in 2002 as E 1252 98 (2002).2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume i

16、nformation, refer to the standards Document Summary page onthe ASTM website.3The boldface numbers in parentheses refer to a list of references at the end ofthe text.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.Copyright by ASTM In

17、tl (all rights reserved); Wed Jan 21 22:33:01 EST 2009Downloaded/printed byGuo Dehua (CNIS) pursuant to License Agreement. No further reproductions authorized.otherwise, the effect of the instrument line shape function willcause errors in the relative intensities of bands in spectrameasured by dispe

18、rsive spectrometers and by FT-IR spectrom-eters with certain apodization functions (specially triangular).5.2.1 Techniques for obtaining transmission spectra varywith the sample state. Most samples, except free-standing thinfilms, require IR transparent windows or matrices containingthe sample. Tabl

19、e 1 gives the properties of IR windowmaterials commonly employed. Selection of the window ma-terial depends on the region of the IR spectrum to be used foranalysis, on the absence of interference with the sample, andadequate durability for the sample type.5.3 Spectra obtained by reflection configura

20、tions commonlyexhibit both reflection and absorption characteristics and areaffected by the refractive indices of the media and the inter-faces. Spectral interpretation should be based on references rununder the same experimental conditions. In particular, it shouldbe realized that the spectrum of t

21、he surface of a samplerecorded by reflection will often differ from the spectrum of thebulk material as recorded by transmission spectroscopy. This isbecause the chemistry of the surface often differs from that ofthe bulk, due to factors such as surface oxidation, migration ofspecies from the bulk t

22、o the surface, and possible surfacecontaminants. Some surface measurements are extremely sen-sitive to small amounts of materials present on a surface,whereas transmission spectroscopy is relatively insensitive tothese minor components.5.3.1 Reflection spectra are obtained in four configurations:5.3

23、.1.1 Specular reflectance (7.5),5.3.1.2 Diffuse reflectance (7.6),5.3.1.3 Reflection-absorption (7.7),5.3.1.4 Internal reflection (7.9). Refer to Practices E 573.This technique is also called Attenuated Total Reflection(ATR), and5.3.1.5 Grazing angle reflectance.5.4 Photoacoustic IR spectra (11.2).5

24、.5 Emission spectroscopy (11.4).TEST METHODS AND TECHNIQUES6. Analysis of Liquids6.1 Fixed CellsA wide range of liquid samples of low tomoderate viscosity may be introduced into a sealed fixed-pathlength cell. These are commercially available in a variety ofmaterials and path lengths. Typical path l

25、engths are 0.01 to 0.2mm. See 5.2 for considerations in selection of cell materialsand path lengths.6.2 Capillary FilmsSome liquids are too viscous to forceinto or out of a sealed cell. Examination of viscous liquids isaccomplished by placing one or more drops in the center of aflat window. Another

26、flat window is then placed on top of theliquid. Pressure is applied in order to form a bubble-freecapillary film covering an area large enough that the entireradiation beam passes through the film. The film thickness isregulated by the amount of pressure applied and the viscosityof the liquid. A cap

27、illary film prepared in this manner has apath length of about 0.01 mm. Volatile and highly fluidmaterials may be lost from films prepared in this manner.Demountable spacers can be used when a longer path length isrequired to obtain a useful spectrum.6.3 Internal Reflection Spectroscopy (IRS)Viscous

28、mate-rials can be smeared on one or both sides of an internalreflection element (IRE). See Practices E 573 for detailedinformation on this technique.6.4 Disposable IR Cards4These can be used to obtainspectra of non-volatile liquids. A very small drop, usually lessthan 10 L of the liquid, is applied

29、near the edge of the sampleapplication area. If the sample does not easily flow across thesubstrate surface, it may be spread using an appropriate tool.The sample needs to be applied in a thin layer, completelycovering an area large enough that the entire radiation beampasses through the sample. Not

30、e that any volatile componentsof a mixture will be lost in this process, which may make theuse of a disposable card a poor choice for such systems.6.5 Solution Techniques:6.5.1 Analysis of Materials Soluble in Infrared (IR) Trans-parent Solvent: The Split Solvent TechniqueMany solid andliquid sample

31、s are soluble in solvents that are transparent inparts of the infrared spectral region. A list of solvents com-monly used in obtaining solution spectra is given in Table 2.The selection of solvents depends on several factors. Thesample under examination must have adequate solubility, itmust not reac

32、t with the solvent, and the solvent must haveappropriate transmission regions that enable a useful spectrumto be obtained. Combinations of solvents and window materi-als can often be selected that will allow a set of qualitativesolution-phase spectra to be obtained over the entire IR region.One exam

33、ple of this “split solvent” technique utilizes carbontetrachloride (CCl4) and carbon disulfide (CS2) as solvents.NOTE 1Warning: Both CCl4and CS2are toxic; keep in a wellventilated hood. Use of these solvents is prohibited in many laboratories.In addition, CS2is extremely flammable; keep away from ig

34、nition sources,even a steam bath. Moreover, CS2is reactive (sometimes violently) withprimary and secondary aliphatic amines and must not be used as a solventfor these compounds. Similarly, CCl4reacts with aluminum metal.Depending on conditions such as temperature and particle size, thereaction has b

35、een lethally violent.6.5.1.1 Absorption by CCl4is negligible in the region 4000to 1330 cm1and by CS2in the region 1330 to 400 cm1incells of about 0.1 mm thickness. (Other solvents can be used.)Solutions are prepared, usually in the 5 to 10 % weight/volumerange, and are shaken to ensure uniformity. T

36、he solutions aretransferred by clean pipettes or by syringes that have beencleaned with solvent and dried to avoid cross-contaminationwith a previous sample. If the spectrum of a 10 % solutioncontains many bands that are too deep and broad for accuratefrequency measurement, thinner cells or a more d

37、ilute solutionmust be used.NOTE 2New syringes should be cleaned before use. Glass is thepreferred material. If plastic is used as containers, lids, syringes, pipettes,and so forth, analytical blanks are necessary as a check against contami-nation.4The 3M disposable IR Card is manufactured by 3M Co.,

38、 Disposable ProductsDivision.E 1252 98 (2007)2Copyright by ASTM Intl (all rights reserved); Wed Jan 21 22:33:01 EST 2009Downloaded/printed byGuo Dehua (CNIS) pursuant to License Agreement. No further reproductions authorized.TABLE 1 Properties of Window Materials (in order of long-wavelength limit)W

39、indow MaterialChemicalCompositionCutoff RangeAUseful Transmission RangeWaterSolubilityRefractiveIndexat(;m)Remarks(m) (cm1) (m) (cm1)Glass SiO2+ ;2.5 ;4000 0.352 28 5705000 insoluble 1.51.9 HF, alkaliBQuartz (fused) SiO2;3.5 ;2857 0.24 50 0002500 insoluble 1.43 4.5 HFBSIlicon Nitrate Si3N40.34.5 33

40、0002200Silicon Carbide SiC 0.65 16 6002000Calcite CaCO30.25 50 0002000 1.65, 1.5 0.589CReacts with acidsSapphire Al2O3;5.5 ;1818 0.25.5 50 0001818 insoluble 1.77 0.55 Good strength, no cleavageALON 9AI2O3.5AIN 0.25.5 50 0001700 1.8 0.6Spinel MgAI2O40.26 50 0001600 1.68 0.6Strontium Titanate SrTiO30.

41、396 25 0001700 insoluble 2.4 HFBTitanium Dioxide TiO20.426 24 0001700 insoluble 2.62.9 H2SO4and AlkaliBLithium Fluoride LiF ;6.0 ;1667 0.27 50 0001429 slightly 1.39 1.39 AcidBZirconia ZrO20.367 27 0001500 insoluable 2.15 HF and H2SO4BSilicon Si 1.57 and10FIR66001430 insoluble 3.4 11.0 Reacts with HF

42、, alkaliDYttria Y20.258 40 0001250 1.9 0.6Yttria (La-doped) 0.09La2O3-0.91Y2O30.258 40 0001250 1.8 0.6IRTRAN IEMgF228 5 0001 250 slightly 1.3 6.7 HNO3BMagnesium Oxide MgO 0.48 25 0001300 insoluble 1.6 5 Acid and NH4saltsBFluorite CaF2;8.0 ;1250 0.210 50 0001000 insoluble 1.40 8.0 Amine salt and NH4s

43、altsBStrontium Fluoride SrF20.1311 77 000909 slightly 1.4IRTRAN IIIECaF20.211 50 000909 insoluble 1.34 5.0 Polycrystalline, no cleavageGallium PhosphideGaPGaP 0.511 20 000910Lead Fluoride PbF20.312 3450833 1.7 1ServofraxFAs2S3112 10 000833 insolubleslightly (hot)2.59 0.67 AlkaliB, softens at 195CBar

44、ium Fluoride BaF2;11 ;909 0.213 50 000769 insoluble 1.45 5.1AMTIR GeAsSe Glass 0.914 11 000725 insoluble 2.5 10 Hard, brittle, attacked by alkali, goodATR materialIRTRAN IIEZnS 114 10 000714 insoluble 2.24 5.5 Insoluble in most solventsIndium Phosphide InP 114 10 000725Potassium Floride KF 0.1615 62

45、 500666 soluble 1.3 0.3 Extremely deliquescent: notrecommended for routine useRock salt NaCl ;16 ;625 0.216 50 000625 soluble 1.52 4.7 Soluble in glycerineGCadmium Sulfide CdS 0.516 20 000625Arsenic Triselenide As2Se30.817 12 500600 slightly 2.8 Soluble in basesGallium Arsenide GaAs 117 10 000600 in

46、soluble 3.14 Slightly soluable in acids and basesGermanium Ge 220 5 000500 insoluble 4.0 13.0Sylvite KCl 0.321 33 333476 soluble 1.49 0.5 Soluble in glycerineGIRTRAN IVEZnSe 121 10 000476 insoluble 2.5 1.0 PolycrystallineSodium Bromide NaBr 0.223 50 000435 Soluble 1.7 0.35Sodium Iodide NaI 0.2525 40

47、 000400 Soluble 1.7 0.5Silver Chloride AgCl ;22 ;455 0.625 16 6667400 insoluble 2.0 3.8 Soft, darkens in lightHreacts withmetalsPotassium Bromide KBr ;25 ;400 0.227 50 000370 soluble 1.53 8.6 Soluble in alcohol; fogsCadmium Telluride CdTe ;28 ;360 0.528 20 000360 insoluble 2.67 10 Acids, HNO3BThalli

48、um ChlorideTICI0.430 25 000330 slightly 2.2 0.75 ToxicKRS-6 Tl2CIBr 0.432 25 000310 slightly 2.02.3 0.624 ToxicSilver Bromide AgBr ;35 ;286 235 5 000286 insoluble Soft, darkens in lightH, reacts withmetalsKRS-5 Tl2Brl ;40 ;250 0.738 14 286263 slightly 2.38 4.0 Toxic, soft, soluble in alcohol, HNO3BC

49、esium Bromide CsBr ;35 ;286 0.340 33 333250 soluble 1.66 8.0 Soft, fogs, soluble alcoholsPotassium Iodide Kl 0.1545 66 600220Thallium Bromide TIBr 0.4545 22 000220 slightly 2.3 0.625 ToxicCesium Iodide CsI ;52 ;192 0.350 33 330220 soluble 1.74 8.0Low-densitypolyethylene(CH2CH2)n 20220 50045 insoluble 1.52 Very soft, organic liquids penetrateinto polymer at ambienttemperatureType 61I(CH2CH2)n 2220 5 00045 insoluble 1.52 Softens at 90CType 62I(CF2CF2)nJ222