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Abstract

Summary

The hydrogenation of CO into renewable fuels is a particularly promising utilization pathway, in which thermocatalytic CO hydrogenation is regarded as the most viable and scalable technology. In-situ shale conversion operates at temperatures between 300 and 500 °C, which aligns closely with the reaction conditions required for thermocatalytic CO hydrogenation to methanol. This similarity suggests that integrating thermocatalytic CO hydrogenation into in-situ shale conversion could reduce CO emissions while enhancing the economic value of shale oil production. Therefore, by leveraging both CO hydrogenation with H₂ and CO reduction with HS, in-situ shale conversion has the potential not only to mitigate self-generated CO, H, and HS but also to address CO-included waste gases from human activities on the surface. In this study, we successfully demonstrate the thermocatalytic hydrogenation and reduction of CO during in-situ shale conversion by heating simulations. This work shows extremely large carbon capture and utilization (CCU) potential, with initial projections of 15 m3 of CO conversion and utilization per tonne of shale oil produced. Further estimates indicate that the recoverable resources of this in-situ conversion shale oil in the Ordos Basin (China) alone exceed 70 billion tons, corresponding to a potential CCU of ∼1,050 billion cubic meters.

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2025-09-01
2026-02-08
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References

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