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D环芳构化8,14-断藿烷的形成、演化及其地球化学意义
引用本文:卢松年,李伟民,何伟.D环芳构化8,14-断藿烷的形成、演化及其地球化学意义[J].沉积学报,1988,6(3):41-49.
作者姓名:卢松年  李伟民  何伟
作者单位:中国地质大学 北京
摘    要:本文研究了芳烃馏份中D环芳构化8,14-断藿烷和苯并藿烷随深度的变化规律提出作为有机质成熟度的新参数:D环芳构化8,14-断藿烷/(D环芳构化8,14-断藿烷+苯并藿烷)。该参数随深度增加几乎成线性增大,较以往的生物标志物参数更能指示生油岩生油的全过程。引起该参数随深度增大的原因不是两类化合物之间的相互转化,而是他们在形成和消失的时间及速度上存在着差异。辽河西部凹陷下第三系生油门限、生油高峰期该参数值分别为0.3、0.5。

关 键 词:D环芳构化8    14-断藿烷    苯并藿烷    成熟度    辽河油田
收稿时间:1986-08-08

RING D AROMATIZED 8,14-SECOHOPANES IN CRUDE OILS AND SOURCE ROCKSITS GEOCHEMICAL SIGNIFICANCE
Institution:Beijing postgradute School, Wuhan College of Geology
Abstract:Ring D aromatized 8,14-secohopanes ( C29-C30 ) and benzohopanes ( C32-C35 ) have been detected in particular abundance in the aromatic fractions of cru de oils a-nd source rocks from the western depression of Liao-He Basin.The variations of a-mount of both families with depth have been studied and showed that there are more benzohopanes in source rocks shallower than 2800m depth and more ring D aromatized 8,14-secohopanes deeper than 2800m. Both families are thought to be the products formed from bacterial hopanoid p-recursors. Benzohopanes are particularly abundant in immature source rocks. They might be formed directly from the C35 bacterial hopanol by chemical reaction atten-ed by microorganism in the early stage of sedimentation. With increasing tempreu-re, they can be easily destroyed, probably by cleavage of ring C which is unstable, to some of bicyclic terpanes or tricycloditerpanes and alfcylated indanes whitch occurring in crude oils and source rocks. Ring D aromatized 8,14-secohopanes do not appear until threshold. They may be formed from hopanoid precursors by aromatization cleavage of the fragile 8 (14) b-ond on ring C under thermol stress. Until 2800 M their amount is increasing. Fuct-her thermol stress would destroy this family, in particular by cleavage of 11(12) bond and side chain,both are fragile benzylic position,and yield some of bicyclic terpanes and alkylated indanes. The rate of destruction is lower than that of benzohopanes, probably due to the stable molecular structure of ring D aromatized 8,14-secohopanes which has one less 6-membered carbon ring than that of benzohopanes. In short, there are differances in the time and the rate of their formation and destruction. It is difficult to assum from their molecular structure that ring D aromatized 8, 14-secohpanes and benzohopanes can be transformed each other under thermol stress. But the ratio of (C29-C33)ring D aromatized 8, 14-secohopanes/(C29-C33 ring D aromatized 8, 14-secohopanes + C32-C35benzohopanes ) , MAH parameter briefly, can act as a powerful maturation parameter. MAH parameter increases steadily with increasing maturation. because of the differance in the time and the rate of formation and destruction of these two families. In our studied basin, the value of MAH parameter is 0.3-0.5 for upper oil-generating zone and 0.5-1.0 for lower oil-generating zone
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