δ13C of free and macromolecular aromatic structures in the Murchison meteorite

被引:118
作者
Sephton, MA [1 ]
Pillinger, CT [1 ]
Gilmour, I [1 ]
机构
[1] Open Univ, Planetary Sci Res Inst, Milton Keynes MK7 6AA, Bucks, England
关键词
D O I
10.1016/S0016-7037(98)00108-2
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Analyses of the organic compounds in the Murchison meteorite have led to a greater understanding of the nature of extraterrestrial organic materials. However, the relationship between low and high molecular weight material remains poorly understood. To investigate this relationship, untreated Murchison was subjected to supercritical fluid extraction (SFE) to obtain the free organic components in the meteorite. Toluene and other volatile aromatic hydrocarbons dominated the extract, and the carbon isotopic composition of these molecules was determined by gas chromatography-isotope ratio-mass spectrometry (GCIRMS). delta(13)C values of the aromatic hydrocarbons ranged from -28.8 to -5.8 parts per thousand. These compounds displayed a (13)C-enrichment with increasing carbon number suggesting an origin by cracking. The high molecular weight organic material in the meteorite was isolated and subjected to hydrous pyrolysis. This procedure produced a number of aromatic products, the majority of which were volatile aromatic hydrocarbons, particularly toluene. SFE was used to extract and successfully retain them. This enabled the first carbon isotopic analysis of this poorly understood material to be performed at the molecular level by GCIRMS. delta(13)C values for aromatic pyrolysis products occupied a range from -24.6 to -5.6 parts per thousand. The trend of (13)C-enrichment with increasing carbon number, observed in the free compounds, was also evident in the macromolecular fragments. Furthermore, the organic fragments of the macromolecular material were consistently (13)C-enriched when compared to structurally identical free molecules. This suggested that the free aromatic hydrocarbons in Murchison were produced by the preterrestrial degradation of the organic macromolecular material. This natural degradation event was extended by the hydrous pyrolysis experiment. Copyright (C) 1998 Elsevier Science Ltd.
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页码:1821 / 1828
页数:8
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