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浅析长侧链正烷基二氢化茚、烷基噻吩类化合物的地质意义

Geological significance of novel long side chain indanes and thiophenes

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【作者】 周文吴庆余盛国英王睿勇戴金彪刘志礼

【Author】 ZHOU Wen1, WU Qing- yu2, SHENG Guo- ying3, WANG Rui- yong1, DAI Jin- biao2, LIU Zhi- li1 (1. Department of Biological and Biotechnology, Nanjing University, Nanjing 210093, China; 2. Department of Biological and Biotechnology, Tsinghua University, Beijin

【机构】 南京大学生物科学与技术系!江苏南京210093清华大学生物科学与技术系!北京100084中国科学院广州地球化学研究所!广东广州510640

【摘要】 从颗石藻、球等辫金藻300℃热模拟产物中检测出长侧链正烷基二氢化茚、烷基噻吩类化合物。二氢化茚类化合物碳数分布范围为C13~C25,nC14烷基二氢化茚的相对含量最高。没检测到茚类化合物,说明二氢化茚和茚可以源自不同的先质,生活于咸水环境的低等生物是二氢化茚类化合物的母质之一。在300℃热解产物中检测出以m/z111和125为基峰的两个系列的长侧链烷基噻吩,表明在中—高盐度环境下,藻类将无机硫转化为有机硫的生物化学作用,成为岩石抽提物和原油中的含硫化合物形成的又一途径。

【Abstract】 Novel long side chain n- alkylindanes and n- alkylthiophoenes were found in 300 ℃ pyrolysates of Isocrysis galbana, Emiliania huxleyi and Gephyrocapsa oceanica. The carbon numbers of indanes range from 13 to 25, with the maximum at C23. No indene was found, clearly showing that indanes and indenes may originate from different precursors, and algae lived in saltwater are important contributors to the indanes. Two novel series of alkylthiophenes, with base peak m/z 111 and 125, respectively, show that biochemistry function of algae, through which inorganic sulphur was transformed into organic sulphur under the condition of high to medium salinity, is another origin of sulphur- bearing organic matter in sediments and petroleums.

【关键词】 二氢化茚噻吩长侧链烷基藻类热模拟
【Key words】 indanethiophenelong side chain n- alkylalgaepyrolysis
【基金】 国家杰出青年基金!(49525205);有机地球化学国家重点实验室基金
  • 【分类号】P593
  • 【被引频次】1
  • 【下载频次】131
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