摘要:

Wastewater treatment plants simultaneously emit greenhouse gases and rely on external carbon sources, presenting both a challenge and an opportunity for carbon circularity. We develop a comprehensive life-cycle assessment of 32 Waste-to-Chemical pathways that integrate thermochemical and electrochemical conversions in sequential or parallel architectures to convert CH4 and CO2 into reusable carbon sources for in-plant utilization. Sequential thermochemical-electrochemical coupling consistently delivers the strongest climate benefit, with formate identified as the optimal product, reducing emissions up to ~35% reduction relative to direct-emission baselines. We further validate this pathway experimentally using commercially available Pd/Al2O3 catalysts for CH4 thermochemical oxidation and Bi2O3 catalysts for CO2 electroreduction in a porous solid electrolyte reactor. Residual heat generated during CH4 oxidation enhances downstream CO2 electroreduction, enabling 97.2 ± 1.2% Faradaic efficiency toward separation-free formate at 150 mA cm−2 and 45 °C. These results validate that commercially relevant catalysts and thermally coupled operation can deliver experimentally validated performance aligned with system-level projections. This framework establishes a scalable strategy for embedding carbon circularity into wastewater infrastructure and transforming wastewater treatment plants into distributed platforms for low-carbon chemical production.

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