中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A quantitative analysis on thermochemical sulfate reduction products of two model compounds: Implications for reaction mechanism and alteration process of hydrocarbons

文献类型:期刊论文

作者Sun, Zhenyu1,2,3; Chen, Jian2,3; Wang, Qiang2,3; Jia, Wanglu2,3; Peng, Ping'an1,2,3
刊名CHEMICAL GEOLOGY
出版日期2024-09-05
卷号661页码:17
关键词Oxygen-containing compound Low-molecular-weight organic acid Quantitative analysis Reaction mechanism Thermochemical sulfate reduction
ISSN号0009-2541
DOI10.1016/j.chemgeo.2024.122187
英文摘要Thermochemical sulfate reduction (TSR) is an important redox reaction that markedly alters hydrocarbons in deep reservoirs. Although the major achievements that involve reaction mechanism, process, and geochemical characteristics were attained in the last 50 years, a quantitative TSR model that includes major products was not built, which restricts the understanding of the reaction mechanism and the generation process of hydrocarbons in TSR. In this study, two series of thermal simulation experiments of the TSR involving n-octadecane (n-C18) and n-dodecylbenzene (C-12-B) with MgSO4 and H2O in a confined gold-tube system were conducted, and all the major products in different phases, particularly oxygen-containing compounds, were quantitatively analyzed. The results indicated that the high-molecular-weight (HMW) oxygenated compounds in heavy products were predominated by ketones, followed by alcohol and acids, and the low-molecular-weight (LMW) organic acids in water mainly comprised acetic acids, followed by formic acid and propionic acid. Both oxygen-containing compounds prompted the TSR process but in different ways. The accumulation of HMW oxygenated compounds in the non-autocatalytic stages was essential for initiating the catalyzed reaction of TSR. In addition, the oxygenated compounds of hydrocarbons enhance polarity, making hydrocarbons easier to contact with HSO4- or [MgSO4] (CIP). The LMW organic acids possibly prompted the TSR process by acidifying the water and thus facilitating the formation of HSO4- and [MgSO4] (CIP). The oxidation reaction during TSR possibly converted HMW oxygenated compounds to LMW organic acids and CO2. The quantitative analysis of products in TSR revealed that TSR destroyed the hydrocarbons more rapidly but in a different way from thermal cracking and that the generation process of hydrocarbon types in TSR was in the following order: heavy hydrocarbon, gaseous hydrocarbon/light hydrocarbon/solid bitumen, and gaseous hydrocarbon/solid bitumen. Compared with oil cracking, the TSR promoted the oil reservoir to rapidly progress to more mature stages. The hydrocarbon precursor and reaction extent affected the generation process and the character of all products in the TSR. These results can provide an improved understanding of the TSR mechanism and process and be useful in the evaluation of petroleum potential for TSR-altered oils.
WOS研究方向Geochemistry & Geophysics
语种英语
WOS记录号WOS:001249242300001
源URL[http://ir.gig.ac.cn/handle/344008/78375]  
专题有机地球化学国家重点实验室
通讯作者Chen, Jian
作者单位1.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
2.CAS Ctr Excellence Deep Earth Sci, Guangzhou 510640, Peoples R China
3.Chinese Acad Sci, Guangzhou Inst Geochem, State key Lab Organ Geochem, 511 Kehua St, Guangzhou 510640, Peoples R China
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GB/T 7714
Sun, Zhenyu,Chen, Jian,Wang, Qiang,et al. A quantitative analysis on thermochemical sulfate reduction products of two model compounds: Implications for reaction mechanism and alteration process of hydrocarbons[J]. CHEMICAL GEOLOGY,2024,661:17.
APA Sun, Zhenyu,Chen, Jian,Wang, Qiang,Jia, Wanglu,&Peng, Ping'an.(2024).A quantitative analysis on thermochemical sulfate reduction products of two model compounds: Implications for reaction mechanism and alteration process of hydrocarbons.CHEMICAL GEOLOGY,661,17.
MLA Sun, Zhenyu,et al."A quantitative analysis on thermochemical sulfate reduction products of two model compounds: Implications for reaction mechanism and alteration process of hydrocarbons".CHEMICAL GEOLOGY 661(2024):17.

入库方式: OAI收割

来源:广州地球化学研究所

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