Non-thermal plasma irradiated polyaluminum chloride for the heterogeneous adsorption enhancement of Cs+ and Sr2+ in a binary system

Abstract

The natural ecosystem will continually deteriorate for decades by the leakage of Cs and Sr isotopes. The exploration of the new materials or techniques for the efficient treatment of radioactive wastewater is critically important. In this study, a dielectric barrier discharge (DBD) configuration was constructed to operate the non-thermal plasma (NTP). The NTP was incorporated into the synthesis of polyaluminum chloride (PAC) in two different procedures to intensify the synthesis of PAC (NTP-PAC) and enhance the further removal of Cs and Sr from wastewater. The employment of NTP in two procedures both had significantly changed the physicochemical characteristics of PAC materials, which facilitated the further adsorption application of NTP-PAC on the treatment of Cs⁺ and Sr²⁺. Different molecular, morphological, and adsorption characteristics were confirmed to the NTP-PAC materials. The heterogeneous adsorption of the NTP-PAC can be appropriately fitted by both the pseudo-first-order kinetic model and the Elovich model. Both physisorption and chemisorption reaction mechanisms were ensured for the heterogeneous adsorption of the NTP-PAC material towards Cs⁺ and Sr²⁺, which guaranteed the excellent adsorption performance of NTP-PAC materials compared to PAC. The electron collisions caused by NTP with alum pulp created highly reactive growth precursors and intensified the nucleation and hydrolysis polymerization of PAC. The employment of NTP explicitly broadens the reaction pathways between PAC and cationic contaminants in the aqueous environment, which expands the application area of PAC materials in environmental sustainability.

Keywords: A dielectric barrier discharge configuration; Binary equilibrium adsorption; Contamination of Cs(+) and Sr(2+); Non-thermal plasma; Optimization; Polyaluminum chloride.