化学
过氧二硫酸盐
过氧化氢
激进的
碳酸氢盐
反应速率常数
光降解
降级(电信)
腐植酸
砷
硫酸盐
无机化学
动力学
核化学
光化学
高级氧化法
环境化学
催化作用
光催化
有机化学
计算机科学
肥料
量子力学
电信
物理
作者
Lu Chen,Hongchao Li,Jieshu Qian
标识
DOI:10.1016/j.jhazmat.2020.124558
摘要
Organoarsenicals such as roxarsone (ROX) pose a great threat to the eco-environment and human health. Herein, the degradation of ROX via UV-based advanced oxidation processes (AOPs) including UV/hydrogen peroxide (UV/H2O2), UV/peroxydisulfate (UV/PDS), and UV/peroxymonosulfate (PMS) processes are comparatively investigated. The removal efficiency of ROX in the UV-based AOPs follows the order of UV/H2O2 > UV/PDS > UV/PMS at pH 7.0, while UV/PDS is the most effective process in reducing the total organic carbon (TOC). The second-order rate constants of ROX with hydroxyl radicals (•OH) and sulfate radicals (SO4•−) are determined to be (2.71 ± 0.27) × 109 and (7.68 ± 0.37) × 108 M−1 s−1, respectively. The degradation of ROX obeys the pseudo-first-order kinetics model, and the apparent rate constants (k) linearly increase with increasing the oxidants dosage from 0.10 to 1.0 mM. The solution pH (5.0–11.0) exhibits a limited effect on the oxidation of ROX in UV/H2O2 and UV/PDS processes, but a great enhancement is observed at pH 11.0 in UV/PMS process. Humic acid and bicarbonate obviously suppress the photodegradation of ROX. In addition, arsenic in ROX is mainly converted to As(V) in the three UV-based AOPs. Overall, this study provides essential information for the degradation of ROX via the traditional UV-based AOPs.
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