1887

Abstract

Summary

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 FeO, releasing up to 70 % more Fe3⁺ than acetic acid alone. The liberated iron reacts readily with injected CO to precipitate siderite (FeCO), 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 CO at 90 % mineralization efficiency; tailings containing 40 wt% % hematite would still sequester ∼140 kg CO 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.

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/content/papers/10.3997/2214-4609.202521128
2025-10-27
2026-01-16
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References

  1. Hong, S. et al., Metal recovery from iron slag via pH swing-assisted carbon mineralization with various organic ligands. Journal of CO2 Utilization, 2023. 69: p. 102418.
    [Google Scholar]
  2. Hammad, E.N., et al.Environmental impacts of ecofriendly iron oxide nanoparticles on dyes removal and antibacterial activity. Applied Biochemistry and Biotechnology, 2022. 194(12): p. 6053–6067.
    [Google Scholar]
  3. Tao, Z. et al., Iron oxide nanoparticles in the soil environment: Adsorption, transformation, and environmental risk. Journal of Hazardous Materials, 2023: p. 132107.
    [Google Scholar]
  4. Panias, D. et al., Mechanisms of dissolution of iron oxides in aqueous oxalic acid solutions. Hydrometallurgy, 1996. 42(2): p. 257–265.
    [Google Scholar]
  5. McAnena, A. et al., Iron isotope fractionation during sulfide-promoted reductive dissolution of iron (oxyhydr) oxide minerals. Geochimica et Cosmochimica Acta, 2024. 369: p. 17–34.
    [Google Scholar]
  6. Hemmelmann, J.C., H.Xu, and W.Krumm, Empirical modeling of iron oxide dissolution in sulphuric and hydrochloric acid. Metallurgical and Materials Transactions B, 2013. 44: p. 1232–1235.
    [Google Scholar]
  7. Schwertmann, U., Solubility and dissolution of iron oxides. Plant and soil, 1991. 130: p. 1–25.
    [Google Scholar]
  8. Bigham, J., R.W.Fitzpatrick, and D.Schulze, Iron oxides. Soil mineralogy with environmental applications, 2002. 7: p. 323–366.
    [Google Scholar]
  9. Martín-Espejo, J.L., et al., Sustainable routes for acetic acid production: Traditional processes vs a low-carbon, biogas-based strategy. Science of The Total Environment, 2022. 840: p. 156663.
    [Google Scholar]
  10. Pal, P. and J.Nayak, Acetic acid production and purification: critical review towards process intensification. Separation & Purification Reviews, 2017. 46(1): p. 44–61.
    [Google Scholar]
  11. Miller, W.P., L.W.Zelazny, and D.Martens, Dissolution of synthetic crystalline and noncrystalline iron oxides by organic acids. Geoderma, 1986. 37(1): p. 1–13.
    [Google Scholar]
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