Characterization reveals that chitosan and Aliquat 336 significantly improve gold recovery in membranes, indicating potential for resource management.
Abstract The efficient recovery of gold from acidic aqueous solutions is vital for sustainable resource management and high-value metal recycling. In this work, poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) polymer inclusion membranes (PIMs) incorporating chitosan (CS) nanoparticles (0–2.0 wt.%) and Aliquat 336 as the ionic carrier were fabricated via solvent casting and comprehensively characterized. FTIR analysis confirmed intermolecular interactions between CS and PVDF-HFP through hydrogen bonding, while SEM revealed that moderate CS loading (1.5 wt.%) enhanced surface roughness and pore uniformity, whereas excessive loading (2.0 wt.%) induced nanoparticle aggregation. Contact angle and water uptake measurements showed progressively improved hydrophilicity with CS incorporation, correlating with increased aqueous phase accessibility. Thermogravimetric analysis and Coats–Redfern modelling indicated a slight reduction in thermal stability and activation energy with increasing CS content, attributed to thermally unstable CS functional groups and disruption of PVDF-HFP crystallinity. Gold adsorption experiments analyzed by ICP-OES demonstrated consistently high removal efficiencies for all membranes, with a maximum of 99.92% at 2.0 wt.% CS. Kinetic analysis revealed excellent fitting of both pseudo-first-order (PFO) and pseudo-second-order (PSO) models (R² ≥ 0.981). The highest adsorption rate constants were observed at 1.5 wt.% CS, confirming rapid uptake dominated by a chemisorption mechanism. Overall, moderate CS incorporation (1.5 wt.%) provided the optimal balance between enhanced hydrophilicity, ion-binding capacity, and structural integrity, offering valuable insights for the design of sustainable, bio-based PIMs for efficient precious metal recovery.
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Lim et al. (2025) studied this question.
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