Iodide ion-imprinted chitosan beads for highly selective adsorption for nuclear wastewater treatment applications

环氧氯丙烷 吸附 碘化物 弗伦德利希方程 壳聚糖 化学 核化学 废水 色谱法 无机化学 有机化学 废物管理 工程类
作者
Yassmin Handulle Ismail,Kean Wang,Maryam Al Shehhi,Ali Al Hammadi
出处
期刊:Heliyon [Elsevier BV]
卷期号:10 (3): e24735-e24735 被引量:7
标识
DOI:10.1016/j.heliyon.2024.e24735
摘要

Iodide ions from radioactive iodine isotopes are common contaminants present in nuclear wastewater from nuclear power plants which are considered hazardous contaminants to be released in water sources even at low concentrations due to their association with metabolic disorders, therefore its removal from the nuclear wastewater effluents is necessary. Chitosan beads are natural and cost-efficient adsorbents that have been used for ion removal from wastewater. However, issues of poor selectivity persist in achieving high-efficiency iodide ion removal. In this study, ion-imprinted chitosan beads (IIC) have been synthesized using the phase-inversion method, IIC beads were modified by cross-linking with epichlorohydrin (IIC-EPI) and modified by cross-linking with epichlorohydrin and silicon dioxide nanoparticles (IIC–SiO2-EPI). Through 4 h of batch adsorption experiments, IIC beads achieved a maximum adsorption capacity (Qe) of 0.65 mmol g−1 and showed more preference for the iodide ions compared to the non-imprinted chitosan beads which achieved a maximum adsorption capacity of 0.27 mmol g−1 at pH 7. While the modified beads IIC-EPI and IIC-SiO2-EPI beads have boosted the adsorption capacities to 0.72 mmol g−1 and 0.91 mmol g−1. Scanning electron microscopic cross-sectional images have shown more pores and cavities than the surface images which agrees with the multilayer heterogeneous diffusion suggested by the Freundlich adsorption isotherm, that the experimental data has fitted. Adsorption kinetic data have fitted the Pseudo-second-order model as well as the Weber and Morris intraparticle model, which suggest an intraparticle pore diffusion adsorption mechanism, with the involvement of the physical electrostatic interactions with the cationic chitosan surface.
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