Agnieszka Lipke, Agnieszka Sawicka, Bartosz Płaska, Mariusz Trytek, Grzegorz Wójcik, Diana Vistorskaja, Denis Sokol, Agnieszka Gładysz-Płaska, Marek Majdan, Aivaras Kareiva
Multimetallic layered double hydroxides (LDHs) are promising oxyanion sorbents, but their practical use requires evaluation of sorption efficiency and chemical stability. This study examined how introducing Cu2+ and Zn2+ into the LDH structure affects As(V) sorption, comparing binary Mg3Al1 and four-component Mg2Cu0.5Zn0.5Al1 in carbonate and chloride forms. The materials were synthesised by the co-precipitation method and characterised using XRD, FTIR, SEM, BET, and XPS, while their layer metal composition was determined by ICP-OES. The sorption studies were supplemented by chemical stability analysis (pH 4-11) and As(V) desorption experiments. Equilibrium data were evaluated using the Redlich-Peterson isotherm model. The four-component LDH showed higher As(V) sorption capacity than the conventional MgAl system, with the best performance observed for chloride forms: 37.5 mg/g for MgCuZnAl-LDH and 22.5 mg/g for MgAl-LDH. The sorption kinetics are well described by the pseudo-second-order and Elovich models, indicating a significant contribution from chemisorption. The results suggest that As(V) removal involves the combined action of anion exchange, electrostatic interactions and inner-sphere complex formation, controlled by the composition of the LDH layer and the type of interlayer anion. The introduction of Cu2+ and Zn2+ promoted additional active sites and stronger As(V) surface interactions. The results indicate that MgCuZnAl-LDH, particularly in the chloride form, exhibits promising As(V) sorption performance under model conditions involving a single solute.