Sustainable leaching of nickel and cobalt from asbestos waste using deep eutectic solvents: Kinetic modeling and recovery performance

• Asbestos waste valorized via ligand-functionalized deep eutectic solvent. • Selective Ni/Co recovery (>72%) with <8% Fe/Mg/Si co-dissolution achieved. • Leaching mechanism scrutinized by FTIR, 1 H NMR, and kinetic modeling. • Autocatalytic Prout–Tompkins kinetics confirmed by R 2 > 0.99. • Diffusion-limited process evidenced by low E a (13.7–15.7 kJ/mol). A sustainable hydrometallurgical route was developed for the selective recovery of nickel and cobalt from asbestos production waste using a novel deep eutectic solvent (DES) composed of ethylene glycol and hydroxylamine hydrochloride. Magnetic separation yielded a Ni–Co-enriched fraction with a 10–12-fold increase in target metal content relative to the raw waste, as confirmed by WD-XRF, SEM/EDS, and chemical analysis. Under optimized conditions (80 °C, 4 h, L/S = 4:1), leaching efficiencies of 72.4% for Ni and 79.6% for Co were achieved, while co-dissolution of Fe, Mg, and Si remained below 8%, demonstrating exceptional selectivity. Kinetic analysis revealed a dual-control mechanism: the excellent fit to the Prout–Tompkins model (R 2 > 0.99) reflects autocatalytic, ligand-assisted surface reactions driven by Ni 2+/ Co 2+ coordination with DES components, whereas the low activation energies (15.73 kJ/mol for Ni, 13.68 kJ/mol for Co) and strong agreement with the Jander diffusion model indicate that mass transfer through the evolving porous residue governs the overall rate. Critically, 1 H NMR spectroscopy of the spent DES shows pronounced signal broadening and attenuation due to paramagnetic Ni 2+/ Co 2+ ions, providing direct, solution-phase evidence of metal - ligand complexation - a key advancement over indirect FTIR data alone. Complementary SEM and XRD analyses confirm selective phase dissolution without bulk matrix degradation. These results establish the DES as an environmentally benign, ligand-functionalized leaching medium that enables the valorization of hazardous asbestos waste into a secondary source of critical metals, aligning with green and circular hydrometallurgical principles.

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Publication Details

Journal
Journal of Hazardous Materials Advances
Published
2025-11-20
DOI
https://doi.org/10.1016/j.hazadv.2025.100948
Citations
2
Primary Topic
Metal Extraction and Bioleaching
Type
article
Field-Weighted Citation Impact
1.35
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article

Sustainable leaching of nickel and cobalt from asbestos waste using deep eutectic solvents: Kinetic modeling and recovery performance

Galymzhan Maldybayev, Mohamad Ibrahim, Rustam Sharipov, Omirserik Baigenzhenov et al.
2 citations
Journal of Hazardous Materials Advances
Metal Extraction and Bioleaching
1.35
article

Sustainable leaching of nickel and cobalt from asbestos waste using deep eutectic solvents: Kinetic modeling and recovery performance

Galymzhan Maldybayev, Mohamad Ibrahim, Rustam Sharipov, Omirserik Baigenzhenov, Tiancheng Mu, A.T. Dagubayeva
article en
2 citations

Abstract

• Asbestos waste valorized via ligand-functionalized deep eutectic solvent. • Selective Ni/Co recovery (>72%) with <8% Fe/Mg/Si co-dissolution achieved. • Leaching mechanism scrutinized by FTIR, 1 H NMR, and kinetic modeling. • Autocatalytic Prout–Tompkins kinetics confirmed by R 2 > 0.99. • Diffusion-limited process evidenced by low E a (13.7–15.7 kJ/mol). A sustainable hydrometallurgical route was developed for the selective recovery of nickel and cobalt from asbestos production waste using a novel deep eutectic solvent (DES) composed of ethylene glycol and hydroxylamine hydrochloride. Magnetic separation yielded a Ni–Co-enriched fraction with a 10–12-fold increase in target metal content relative to the raw waste, as confirmed by WD-XRF, SEM/EDS, and chemical analysis. Under optimized conditions (80 °C, 4 h, L/S = 4:1), leaching efficiencies of 72.4% for Ni and 79.6% for Co were achieved, while co-dissolution of Fe, Mg, and Si remained below 8%, demonstrating exceptional selectivity. Kinetic analysis revealed a dual-control mechanism: the excellent fit to the Prout–Tompkins model (R 2 > 0.99) reflects autocatalytic, ligand-assisted surface reactions driven by Ni 2+/ Co 2+ coordination with DES components, whereas the low activation energies (15.73 kJ/mol for Ni, 13.68 kJ/mol for Co) and strong agreement with the Jander diffusion model indicate that mass transfer through the evolving porous residue governs the overall rate. Critically, 1 H NMR spectroscopy of the spent DES shows pronounced signal broadening and attenuation due to paramagnetic Ni 2+/ Co 2+ ions, providing direct, solution-phase evidence of metal - ligand complexation - a key advancement over indirect FTIR data alone. Complementary SEM and XRD analyses confirm selective phase dissolution without bulk matrix degradation. These results establish the DES as an environmentally benign, ligand-functionalized leaching medium that enables the valorization of hazardous asbestos waste into a secondary source of critical metals, aligning with green and circular hydrometallurgical principles.

Journal of Hazardous Materials AdvancesVol. 21
Universiti Sains Malaysia (MY), Kazakh-British Technical University (KZ), Satbayev University (KZ), National Nuclear Center of the Republic of Kazakhstan (KZ), National Center on Complex Processing of Mineral Raw Materials of the Republic of Kazakhstan, Renmin University of China (CN)
Openalex Percentile: Top 17%
Metal Extraction and Bioleaching
1.35
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