4.7 Article

Formation of volatile organic sulfur compounds by low thermal maturation of source rocks: A geochemical proxy for natural gas

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MARINE AND PETROLEUM GEOLOGY
卷 158, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.marpetgeo.2023.106531

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Compound specific sulfur isotope analysis; Volatile organic sulfur compounds; Thiols; Thiophenes; Natural gas; Pyrolysis; Hydrogen sulfide

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This study demonstrates the applicability of VOSC as a proxy for gas-source rock correlations and interactions between H2S and other natural gas components. Regardless of the type or lithology of the source rocks, VOSC formation was observed in all experiments. Thiols formation is limited to gas-phase interactions between H2S and hydrocarbons, while thiophenes are not affected by the presence of H2S and preserve the signature of the bulk kerogen.
Volatile organic sulfur compounds (VOSC) are trace components of natural gas that can provide substantial information regarding gas origins, migration, and key processes such as H2S generation and its occurrence in natural gas reservoirs. In the current study we demonstrate the applicability of VOSC as a proxy for gas-source rock correlations and identification of interactions between H2S and other natural gas components. We studied the molecular and isotopic compositions of VOSC formed during low-level thermal maturation (%Ro equivalent = 0.60-0.71) of six different immature source rocks covering a variety of kerogens (types I, II, II-S and III). Anhydrous pyrolysis experiments (300 degrees C, 72h) were performed on all the source rocks studied, and the produced gases were analyzed for their molecular compositions and compound specific sulfur isotopes of the various VOSC formed. The formed gases were either dominated by CH4 (32.2-49.9%) or CO2 (31.9-46.2%) and contained a variety of alkanes in the C2-C5 range. H2S formed in 6 out of 8 experiments at concentrations ranging from 0.6 to 4.3%. The results demonstrated formation of VOSC in all experiments, regardless of kerogen types or source rock lithologies. The formation of thiols (16-121.2 ppm) in the produced gas was restricted to those experiments that contained H2S. This indicates that thiols formation is limited to gas-phase interactions between H2S and hydrocarbons. In contrast, thiophenes formed in all experiments (14.9-1778.8 ppm) regardless of H2S presence. Thiols preserved the delta 34S signal of their associated H2S due to gas-phase interactions between the two, while thiophenes showed no interaction with the associated H2S and instead preserved the delta 34S signature of the bulk kerogen (within 3.5 parts per thousand on average) of each source rock. This work demonstrates the applicability of thiophenes to act as a gas-source rock proxy for natural gas and thiols as a proxy for identification of present or paleointeractions between natural gas and H2S.

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