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Pyrolysis-gas chromatography/mass spectrometry of fractions separated from a low-temperature coal tar: an attempt to develop a general method for characterising structures and compositions of heavy hydrocarbon liquids

机译:从低温煤焦油中分离出的馏分的热解-气相色谱/质谱:试图开发一种表征重烃液体结构和组成的通用方法

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A low-temperature coal tar has been fractionated by column chromatography into acetonitrile, pyridine and 1-methyl-2-pyrrolidinone- (NMP) solubles. The tar and its fractions have been examined by pyrolysis-gas chromatography/mass spectrometry (GC/MS). Fractionation by planar chromatography was also carried out for purposes of comparison. Molecular masses of the fractions were estimated by size-exclusion chromatography (SEC), and bulk structural characterisation was carried out by C-13-NMR and UV-fluorescence spectrometry. SEC showed that the fractions shifted to progressively shorter elution times (higher apparent masses) with diminishing solubility, i.e. from acetonitrile to NMP solubles. UV-fluorescence spectra showed parallel shifts to longer wavelengths and lower fluorescence quantum yields, indicating increasing sizes of aromatic ring systems and increasingly complex molecules. GC/MS analysis of the tar showed alkanes from C10 to C32 and extensive series of alkylated aromatics, phenols, indenes, naphthalenes, phenanthrenes and fluoranthenes. Pyrolysis-GC/MS results for the acetonitrile solubles closely resembled the data for the tar sample, with extensive series of alkylated benzenes, phenols and naphthalenes as well as alkanes from C16 to C28. The pyridine-soluble fraction showed no significant aromatic pyrolysis products and only relatively weak signals for alkanes between C16 and C27. The NMP-soluble fraction showed even less overall signal, with no significant aromatic components and weak signals for alkanes between C21 and C25, even though C-13-NMR analyses showed that approximately half of the carbon detected was aromatic. The aliphatics are assumed to provide bridging structures between polycyclic aromatic (PCA) ring systems. Copyright (C) 2002 John Wiley Sons, Ltd. [References: 13]
机译:低温煤焦油已通过柱色谱法分离为乙腈,吡啶和1-甲基-2-吡咯烷酮-(NMP)可溶物。焦油及其馏分已通过热解气相色谱/质谱(GC / MS)进行了检查。为了比较的目的,也进行了通过平面色谱的分级分离。通过尺寸排阻色谱法(SEC)估计级分的分子量,并通过C-13-NMR和UV-荧光光谱法进行本体结构表征。 SEC表明,级分转移到逐渐缩短的洗脱时间(较高的表观质量),同时溶解度降低,即从乙腈到NMP可溶物。紫外荧光光谱显示出平行移向更长的波长和更低的荧光量子产率,表明芳香环系统的大小不断增加,分子越来越复杂。焦油的GC / MS分析显示,烷烃的碳原子数为C10至C32,并有大量烷基化的芳族化合物,酚,茚满,萘,菲和芴。乙腈可溶物​​的热解-GC / MS结果与焦油样品的数据非常相似,具有从C16到C28的大量烷基化苯,苯酚和萘以及烷烃。吡啶可溶级分显示没有明显的芳族热解产物,并且对于C16和C27之间的烷烃而言,信号相对较弱。可溶于NMP的馏分显示出更低的总体信号,尽管C-13-NMR分析表明检测到的碳中约有一半是芳烃,但C21和C25之间的烷烃没有明显的芳族组分和微弱信号。假定脂族在多环芳族(PCA)环系统之间提供桥联结构。版权所有(C)2002 John Wiley Sons,Ltd. [引用:13]

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