Karaca F, Morgan T J, George A, Bull I D, Herod A A, Millan M, Kandiyoti R
Department of Chemical Engineering, Marmara University, Goztepe Campus, 34722 Kadikoy, Istanbul, Turkey.
Rapid Commun Mass Spectrom. 2009 Jul;23(13):2087-98. doi: 10.1002/rcm.4104.
A coal tar pitch was fractionated by solvent solubility into heptane-solubles, heptane-insoluble/toluene-solubles (asphaltenes), and toluene-insolubles (preasphaltenes). The aim of the work was to compare the mass ranges of the different fractions by several different techniques. Thermogravimetric analysis, size-exclusion chromatography (SEC) and UV-fluorescence spectroscopy showed distinct differences between the three fractions in terms of volatility, molecular size ranges and the aromatic chromophore sizes present. The mass spectrometric methods used were gas chromatography/mass spectrometry (GC/MS), pyrolysis/GC/MS, electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICRMS) and laser desorption time-of-flight mass spectrometry (LD-TOFMS). The first three techniques gave good mass spectra only for the heptane-soluble fraction. Only LDMS gave signals from the toluene-insolubles, indicating that the molecules were too involatile for GC and too complex to pyrolyze into small molecules during pyrolysis/GC/MS. ESI-FTICRMS gave no signal for toluene-insolubles probably because the fraction was insoluble in the methanol or acetonitrile, water and formic acid mixture used as solvent to the ESI source. LDMS was able to generate ions from each of the fractions. Fractionation of complex samples is necessary to separate smaller molecules to allow the use of higher laser fluences for the larger molecules and suppress the formation of ionized molecular clusters. The upper mass limit of the pitch was determined as between 5000 and 10,000 u. The pitch asphaltenes showed a peak of maximum intensity in the LDMS spectra at around m/z 400, in broad agreement with the estimate from SEC. The mass ranges of the toluene-insoluble fraction found by LDMS and SEC (400-10,000 u with maximum intensity around 2000 u by LDMS and 100-9320 u with maximum intensity around 740 u by SEC) are higher than those for the asphaltene fraction (200-4000 u with maximum intensity around 400 u by LDMS and 100-2680 u with maximum intensity around 286 u by SEC) and greater than values considered appropriate for petroleum asphaltenes (300-1200 u with maximum intensity near 700 u).
通过溶剂溶解度将煤焦油沥青分离为庚烷可溶物、庚烷不溶物/甲苯可溶物(沥青质)和甲苯不溶物(前沥青质)。这项工作的目的是通过几种不同技术比较不同馏分的质量范围。热重分析、尺寸排阻色谱法(SEC)和紫外荧光光谱法显示,这三种馏分在挥发性、分子尺寸范围和存在的芳香发色团尺寸方面存在明显差异。所使用的质谱方法有气相色谱/质谱联用(GC/MS)、热解/GC/MS、电喷雾电离傅里叶变换离子回旋共振质谱(ESI-FTICRMS)和激光解吸飞行时间质谱(LD-TOFMS)。前三种技术仅对庚烷可溶馏分给出了良好的质谱图。只有激光解吸质谱(LDMS)能给出甲苯不溶物的信号,这表明这些分子对于气相色谱来说挥发性太低,且在热解/GC/MS过程中过于复杂而无法热解成小分子。ESI-FTICRMS未给出甲苯不溶物的信号,可能是因为该馏分不溶于用作ESI源溶剂的甲醇或乙腈、水和甲酸的混合物。LDMS能够从每种馏分中产生离子。对复杂样品进行分馏对于分离较小分子是必要的,以便对较大分子使用更高的激光能量密度,并抑制电离分子簇的形成。沥青的质量上限确定为5000至10000 u之间。沥青质在LDMS光谱中显示出最大强度峰出现在m/z约400处,与SEC的估计大致相符。通过LDMS和SEC发现的甲苯不溶馏分的质量范围(LDMS为400 - 10000 u,最大强度约为2000 u;SEC为100 - 9320 u,最大强度约为740 u)高于沥青质馏分(LDMS为200 - 4000 u,最大强度约为400 u;SEC为100 - 2680 u,最大强度约为286 u),且大于认为适用于石油沥青质的值(300 - 1200 u,最大强度接近700 u)。