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In the context of accelerating geological carbon storage, we present a bio-derived acetic-acid-ligand leaching strategy to enhance mineral carbonation of hematite-rich iron ore tailings. Batch experiments (pH 2, 75 °C) show that biomass-sourced acetic acid, amended with trace ethylenediaminetetraacetic acid (EDTA) or nitrilotriacetic acid (NTA), surmounts the inherently slow dissolution kinetics of Fe2O3, releasing up to 70 % more Fe3⁺ than acetic acid alone. The liberated iron reacts readily with injected CO2 to precipitate siderite (FeCO3), establishing a stable, solid-phase sink for carbon.
Stoichiometric balances indicate that dissolving 70 wt% % of one tonne of pure hematite could immobilize ∼350 kg CO2 at 90 % mineralization efficiency; tailings containing 40 wt% % hematite would still sequester ∼140 kg CO2 per tonne processed. By eliminating chloride and sulphate byproducts and employing renewable acetic acid, this route aligns with life-cycle decarbonization goals while offering a scalable, low-hazard alternative to strong inorganic acids.
The study establishes mechanistic and techno-economic benchmarks for coupling bio-acid leaching with carbon-injection operations and offers transferable insights for other metal-oxide systems relevant to CCUS.