4.7 Article

Switch to love, switch to kill- The interaction of Co-doped La(OH)3 and peroxymonosulfate achieved highly efficient As(III) removal in water

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 473, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.145410

Keywords

Arsenic; Adsorption; Lanthanum oxides; Oxidation; Peroxymonosulfate

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A bifunctional Co-doped La(OH)(3) composite with catalytic and adsorption active sites was synthesized and demonstrated excellent performance in removing As(III) from water. The Co-La/PMS system achieved nearly 100% As(III) removal within 10 minutes. The combined system showed significantly higher removal capacity and faster kinetics compared to Co-La adsorption alone. The enhanced performance was attributed to the production of reactive oxygen species and the generation of new adsorption sites. The Co-La/PMS system offers a promising approach for purifying arsenic-contaminated water.
Materials combing catalytic and adsorption dual active sites are very important for arsenite (As(III)) due to its high mobility in water. Therefore, in this study, a bifunctional walnut-like Co-doped La(OH)(3) composites (Co-La) with independent catalytic sites and post-formed adsorption sites were synthesized via a simple hydrothermal method. Nearly 100% As(III) removal can be achieved in Co-La and peroxymonosulfate interaction systems (Co-La/PMS) within 10 min at the molar ratio of PMS to As(III) of 1.2. The results indicate that the combined Co-La adsorption system demonstrated superior performance compared to the Co-La adsorption alone. Precisely, the maximum removal capacity of the system was measured at 243.90 mg center dot g(-1), and the pseudo-first-order kinetic rate constant (k(1)) was determined to be 1.0771 min(-1). These values were significantly greater than those observed for Co-La adsorption alone. Notably, the kinetic rate constant was 239 times faster, and the removal capacity was 4.6 times higher in the combined system. The fast kinetics of As(III) elimination can be elucidated by the production of reactive oxygen species (ROS) such as SO4 center dot-, center dot OH, O-2(center dot-) and O-1(2), which expedite the conversion of As(III) into arsenate (As(V) in this particular system. Meanwhile, the increase in adsorption capacity is ascribed to the fact that PMS can drive La(OH)(3) of Co-La to transform into transition states La2SO4(OH)(4), thus generating a new exchangeable adsorption site for As(V). A fixed membrane reactor assembled with Co-La was utilized to achieve a near-complete removal of As(III) within 3 min. The Co-La/PMS systems demonstrate exceptional effectiveness in eliminating arsenic from water across diverse real-water metrics, offering a unique perspective and technological progress in purifying water contaminated with arsenic.

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