Redox-state-dependent adsorption of arsenic and antimony on hydrothermally synthesized mesoporous boehmite (γ-AlOOH): mechanistic insights from synchrotron-based spectroscopy
Year: 2026
Type: article
Abstract: Hierarchical mesoporous boehmite (γ-AlOOH) was synthesized via a one-pot hydrothermal method across a wide range of pH, temperature, aging time, and aluminum concentrations to identify optimal formation conditions and elucidate arsenic and antimony adsorption behavior. The optimized sample, which was obtained at pH 4, 150 °C, 24 h aging, and [Al] = 0.1 M, exhibited a plate-stacked spherical morphology with a high surface area (149 m2/g) and large pore volume (0.42 cm3/g). Batch adsorption experiments showed sorption capacities of 66 mg/g for As(III) at pH 9, 38 mg/g for As(V) at pH 5, and 55 mg/g for Sb(V) at pH 5, whereas Sb(III) displayed the lowest uptake (13 mg/g at pH 5). Spectroscopic analyses (synchrotron X-ray absorption spectroscopy, X-ray photoelectron spectroscopy, and Fourier transform infrared) indicated inner-sphere complexation with surface hydroxyls for As(III, V) and Sb(V), whereas Sb(III) bound mainly through weaker outer-sphere interactions, consistent with its negligible Al coordination. Both As(III) and As(V) formed bidentate binuclear corner-sharing complexes on the boehmite surface, whereas Sb(V) adopted both bidentate edge-sharing and corner-sharing geometries. These results show that metal(loid) adsorption strongly depends on anion redox state and highlight that the optimal removal of As and Sb requires solution conditions tailored to each species. Overall, this study provides insights into redox-dependent adsorption and demonstrates that hydrothermally engineered boehmite is a robust, high-capacity adsorbent for metalloid remediation in complex aqueous systems.
Language: English
Subfield: Environmental Chemistry
Field: Environmental Science
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,470
Awards: G3417892827, G6169862286, G944983414
OpenAlex ID: W7155216764
