Integrated biomass-assisted carbothermal reduction and staged hydrometallurgical extraction for selective multi-element recovery from red mud

This study integrated biomass-assisted carbothermal reduction with hydrometallurgical framework to enable comprehensive valorization of red mud. Circumscribed central composite design experiments systematically evaluated the combined effects of temperature (∼600–1000 °C), residence time (∼1–5 h), and red mud-to-biomass ratio (RMB, ∼0.3–1.2) on phase evolution, iron speciation, and magnetic separation performance. Regression analysis supported with XRD-Rietveld refinement and XPS characterizations demonstrated that temperature dominantly governed the Fe³ ⁺→Fe²⁺→Fe⁰ sequence, with hematite transforming to magnetite and subsequently to α-Fe above 850 °C. The RMB regulated reductant-oxide stoichiometry, whereas residence time promoted approach to thermodynamic equilibrium. Coupled TGA-DTG-MS identified three thermal regimes: devolatilization (30–250 °C), intermediate reductive gasification (250–500 °C) associated with partial hematite-to-magnetite conversion, and high-temperature deep reduction (>500 °C), during which sustained CO-rich conditions enabled magnetite metallization and concurrent carbothermal conversion of SiO₂ to SiC-6H. Multi-response optimization uncovered optimal conditions at 954.6 °C, 4.68 h, and RMB = 0.71, achieving ∼90% Fe recovery and ∼89% Fe purity following magnetic separation due to ferromagnetic Fe²⁺ (25%) and Fe⁰ (59%) proportions of total Fe. The non-magnetic tailings were subsequently processed via staged hydrometallurgical extraction: (i) primary acid leaching, (ii) Fe removal using Aliquat 336-based solvent extraction, (iii) selective precipitation of trivalent cations, and (iv) secondary acid leaching to partition transition metals and rare earth elements. This integrated approach recovered 88% Fe, 60% Tb, 55% Cr, and 95% Si into chemically distinct product streams. The combined thermochemical-hydrometallurgical strategy provides an efficient and scalable route for iron metallization and systematic fractionation of valuable elements from red mud. • Integrated carbothermal reduction and hydrometallurgical extraction is studied. • Maximum Fe³ ⁺→Fe⁰ metallization is achieved via statistically optimized reduction. • TGA–DTG–MS links gas evolution with mineral phase transformations. • Magnetic separation yields high-purity Fe concentrate and non-magnetic tailings. • Staged extraction recovers transition and rare earth metals from the tailings.

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Journal
Journal of Analytical and Applied Pyrolysis
Published
2026-05-12
DOI
https://doi.org/10.1016/j.jaap.2026.107841
Primary Topic
Bauxite Residue and Utilization
Type
article
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article

Integrated biomass-assisted carbothermal reduction and staged hydrometallurgical extraction for selective multi-element recovery from red mud

Thoriq Teja Samudra, Hanifrahmawan Sudibyo, Akmal Irfan Majid, Dwi Joko Prasetyo et al.
Journal of Analytical and Applied Pyrolysis
Bauxite Residue and Utilization
article

Integrated biomass-assisted carbothermal reduction and staged hydrometallurgical extraction for selective multi-element recovery from red mud

Thoriq Teja Samudra, Hanifrahmawan Sudibyo, Akmal Irfan Majid, Dwi Joko Prasetyo, Rima Salsabila, Mimbar Sapaat, Ridha C. Oktian, Akmal Argiyanto Pratama, Muslih Anwar
article en

Abstract

This study integrated biomass-assisted carbothermal reduction with hydrometallurgical framework to enable comprehensive valorization of red mud. Circumscribed central composite design experiments systematically evaluated the combined effects of temperature (∼600–1000 °C), residence time (∼1–5 h), and red mud-to-biomass ratio (RMB, ∼0.3–1.2) on phase evolution, iron speciation, and magnetic separation performance. Regression analysis supported with XRD-Rietveld refinement and XPS characterizations demonstrated that temperature dominantly governed the Fe³ ⁺→Fe²⁺→Fe⁰ sequence, with hematite transforming to magnetite and subsequently to α-Fe above 850 °C. The RMB regulated reductant-oxide stoichiometry, whereas residence time promoted approach to thermodynamic equilibrium. Coupled TGA-DTG-MS identified three thermal regimes: devolatilization (30–250 °C), intermediate reductive gasification (250–500 °C) associated with partial hematite-to-magnetite conversion, and high-temperature deep reduction (>500 °C), during which sustained CO-rich conditions enabled magnetite metallization and concurrent carbothermal conversion of SiO₂ to SiC-6H. Multi-response optimization uncovered optimal conditions at 954.6 °C, 4.68 h, and RMB = 0.71, achieving ∼90% Fe recovery and ∼89% Fe purity following magnetic separation due to ferromagnetic Fe²⁺ (25%) and Fe⁰ (59%) proportions of total Fe. The non-magnetic tailings were subsequently processed via staged hydrometallurgical extraction: (i) primary acid leaching, (ii) Fe removal using Aliquat 336-based solvent extraction, (iii) selective precipitation of trivalent cations, and (iv) secondary acid leaching to partition transition metals and rare earth elements. This integrated approach recovered 88% Fe, 60% Tb, 55% Cr, and 95% Si into chemically distinct product streams. The combined thermochemical-hydrometallurgical strategy provides an efficient and scalable route for iron metallization and systematic fractionation of valuable elements from red mud. • Integrated carbothermal reduction and hydrometallurgical extraction is studied. • Maximum Fe³ ⁺→Fe⁰ metallization is achieved via statistically optimized reduction. • TGA–DTG–MS links gas evolution with mineral phase transformations. • Magnetic separation yields high-purity Fe concentrate and non-magnetic tailings. • Staged extraction recovers transition and rare earth metals from the tailings.

Journal of Analytical and Applied PyrolysisVol. 197
Parks Canada (CA), Universitas Gadjah Mada (ID), National Nuclear Energy Agency of Indonesia (ID), National Research and Innovation Agency (ID)
Openalex Percentile: Top 10%
Bauxite Residue and Utilization
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