Abstract

Under hot, deep-basin conditions, hydrogen-to-carbon ratios of residual kerogen are low. Whether ubiquitous water in sedimentary environments contributes hydrogen directly to hydrocarbon gas formation through organic-inorganic interactions is, therefore, critical for natural gas generation. Accordingly, we conducted laboratory experiments on immature to overmature kerogens at 300–600°C and 700 bar to examine the chemical interactions between kerogens and fluid under varying redox states and hydrothermal conditions. Mineral buffers, comprised of magnetite-hematite, nickel‑nickel oxide, cobalt‑cobalt oxide, and molybdenum‑molybdenum trioxide, were added to the experiments to control the redox state of the fluid from geologically reasonable to generally excessive values. The kerogens and mineral buffers were spatially isolated using double-capsule techniques to prevent contact catalysis.Our results indicated that chemical interactions between kerogens and water depended strongly on the kerogen thermal maturity and fluid redox state. The chemical interactions of overmature kerogens with reducing water were stronger than those of immature kerogens, which could be ascribed to the weaker competitive transfer of hydrogen from organics to organics than from water to organics. Unexpectedly high amounts of hydrocarbon gas were generated by incorporating water-derived hydrogen in the pyrolysis of overmature kerogens, and the yields increased under low to high reducing fluid conditions for a given temperature. Along with the increasing thermal maturity, residual kerogen eventually became ineffective for hydrocarbon gas generation through reduction reactions. Demethylation, bridge bond cleavage reaction, aromatic structure ring opening reactions in residual kerogen and subsequent redox reaction of intermediate products with reducing fluids is evidenced as the possible reaction mechanisms. The produced hydrocarbon gas under fH2 level of oilfield water is characterized by high dryness (99 mol%) and more-enriched 13C in CH4 compared with precursors. Natural gas deep within the Sichuan and Appalachian basins with similar characteristics suggests that our simulated organic–inorganic interactions could occur widely under natural conditions. Consequently, a potentially prolific source of natural gas may be formed by the overmature source rocks in the deep basin and fluid redox should be considered for gas potential evaluation of overmature source rocks.

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