...
首页> 外文期刊>Organic Geochemistry: A Publication of the International Association of Geochemistry and Cosmochemistry >High-temperature GC evidence for the early formation of C40+ n-alkanes in coals
【24h】

High-temperature GC evidence for the early formation of C40+ n-alkanes in coals

机译:煤中C40 +正构烷烃早期形成的高温GC证据

获取原文
获取原文并翻译 | 示例
           

摘要

High-temperature GC analyses were performed on a coal-sourced waxy oil from the Toka-1 well in the Taranaki Basin and on three bitumens, extracted ultrasonically with boiling toluene, from coals from the Tara-1 well in the Great South Basin, New Zealand. The coals represent an evolutionary trend from immature to post oil expulsion. In all samples the C40+ alkanes were characterised by dominant straight-chain members up to about C-65, which decreased significantly in abundance in bitumen with increasing maturity. They are present at an early stage of maturity, prior to the main phase of n-alkane generation, and may be liberated from cutan/cutin sources within kerogen by thermal decarboxylation of esters or have an earlier origin in the bitumen inherited from diagenesis. An odd-over-even predominance in the C40+ n-alkanes was most marked in the C51-C57 range and decreased with increasing maturity, suggesting that minor amounts of C40+ n-alkanes with a CPI approaching 1 are also generated during catagenesis. However, the observed C40+ n-alkane distributions may be affected to a degree by decreasing efficiency of solvent extraction with increasing n-alkane molecular weight, and by further long-chain n-alkanes generated during catagenesis being partially inaccessible to solvent extraction. (C) 2000 Elsevier Science Ltd. All rights reserved. [References: 30]
机译:对塔拉纳基盆地Toka-1井的煤制蜡质油和新沸腾甲苯超声提取的三个沥青(新南大盆地Tara-1井的煤)进行了高温GC分析。西兰。煤代表了从未成熟到驱油后的演变趋势。在所有样品中,C40 +烷烃的特征是占支配地位的直链成员,最高可达约C-65,随着成熟度的增加,沥青中的丰度显着降低。它们存在于正构烷烃主要阶段之前的成熟早期,可通过酯的热脱羧作用从干酪根中的角质/角质中释放出来,或起源于成岩作用的沥青中起源较早。在C51 + C57范围内,C40 +正构烷烃的奇数偶占优势最为明显,并且随着成熟度的增加而降低,这表明在催化作用期间还会产生少量的CPI接近1的C40 +正构烷烃。但是,观察到的C40 +正构烷烃分布可能会受到一定程度的影响,原因是随着正构烷烃分子量的增加,溶剂萃取效率降低,并且在催化作用期间生成的其他长链正构烷烃部分无法进入溶剂萃取。 (C)2000 Elsevier ScienceLtd。保留所有权利。 [参考:30]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号