Abstract

The concurrent disposal of industrial lithium slag (LS) and the remediation of heavy-metal-contaminated water remain critical environmental imperatives. Herein, industrial lithium slag was successfully upcycled into a high-capacity geopolymer via alkali activation to systematically evaluate its Pb(II) removal mechanisms. Synthesized under optimal conditions (11 mol/L alkali concentration, 0.616 solid-to-liquid ratio), the geopolymer showed exceptional Pb(II) capture, achieving ~99% removal efficiency within 120 min for a 100 mg/L Pb(II) solution at pH 6.0. The adsorption kinetics obeyed the pseudo-first-order model, yielding a remarkable theoretical equilibrium capacity of 284 mg/g. Thermodynamic results reveal a spontaneous (ΔG < 0), endothermic (ΔH = 17.66 kJ/mol) process with increased interfacial randomness (ΔS > 0). Integrating macroscopic performance with characterizations and density functional theory (DFT) computations elucidated a site-specific chemisorption mechanism and the precipitation of PbSO4 caused by Pb(II) and SO42− in LS. Ultimately, this work provides a sustainable paradigm for the value-added upcycling of industrial solid waste.

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