HYDROUS PYROLYSIS OF CRUDE-OIL IN GOLD-PLATED REACTORS

被引:16
作者
CURIALE, JA [1 ]
LUNDEGARD, PD [1 ]
KHARAKA, YK [1 ]
机构
[1] US GEOL SURVEY,MENLO PK,CA 94025
关键词
HYDROUS PYROLYSIS OF OIL; BIOMARKERS; CALIFORNIA OIL; IRAQ OIL; VANADIUM AND NICKEL IN OIL; MOLECULAR MATURITY PARAMETERS; BISNORHOPANE; IN-RESERVOIR OIL MATURITY; GOLD REACTORS;
D O I
10.1016/0146-6380(92)90100-C
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
Crude oils from Iraq and California have been pyrolyzed under hydrous conditions at 200 and 300-degrees-C for time periods up to 210 days, in gold-plated reactors. Elemental (vanadium, nickel), stable isotopic (carbon), and molecular (n-alkanes, acyclic isoprenoids, steranes, terpanes and aromatic steroid hydrocarbons) analyses were made on the original and pyrolyzed oils. Various conventional crude oil maturity parameters, including 20S/(20S + 20R)-24-ethylcholestane ratios and the side-chain-length distribution of aliphatic and aromatic steroidal hydrocarbons, were measured in an effort to assess the modification of molecular maturity parameters in clay-free settings, similar to those encountered in "clean" reservoirs. Concentrations of vanadium and nickel in the Iraq oil decrease significantly and the V/(V + Ni) ratio decreases slightly, with increasing pyrolysis time/temperature. Whole oil carbon isotope ratios remain fairly constant during pyrolysis, as do hopane/sterane ratios and carbon number distribution of 5alpha(H),14alpha(H),17alpha(H),20R steranes. These latter three parameters are considered maturity-invariant. The ratios of short side-chain components to long side-chain components of the regular steranes [C21/(C21 + C29R)] and the triaromatic steroid hydrocarbons [C21/(C21 + C28)] vary systematically with increasing pyrolysis time, indicating that these parameters may be useful as molecular maturity parameters for crude oils in clay-free reservoir rocks. In addition, decreases in bisnorhopane/hopane ratio with increasing pyrolysis time, in a clay-free and kerogen-free environment, suggest that the distribution of these compounds is controlled by either differential thermal stabilities or preferential release from a higher-molecular weight portion of the oil.
引用
收藏
页码:745 / 756
页数:12
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