化学
臭氧
矿化(土壤科学)
降级(电信)
甲酸
甲醛
硫酸盐
二甲基亚砜
环境化学
高级氧化法
反应速率常数
无机化学
动力学
有机化学
催化作用
氮气
计算机科学
物理
电信
量子力学
作者
Jerry J. Wu,Manickavachagam Muruganandham,S.H. Chen
标识
DOI:10.1016/j.jhazmat.2007.03.071
摘要
The present study investigates the oxidation of dimethyl sulfoxide (DMSO) by conventional ozonation and the advanced oxidation processes (AOPs). The major degradation products identified were methanesulfinate, methanesulfonate, formaldehyde, and formic acid in ozonation process. The subsequent degradation of intermediates shows that methanesulfonate is more resistance to ozonation, which reduces the mineralization rate of DMSO. The effect of t-butanol addition and ozone gas flow dosage on the degradation rate was evaluated. The rate constant of the reaction of ozone (kD) with DMSO was found to be 0.4162 M−1 S−1. In the second part of this study, DMSO degradation and TOC mineralization were investigated using O3/UV, O3/H2O2 and UV/H2O2 processes. In all theses processes the degradation of target organics is more pronounced than TOC removal. The efficiencies of these processes were evaluated and discussed. The formation of sulfate ion in all AOPs have been identified and compared with other processes. Overall it can be concluded that ozonation and ozone-based AOPs are promising processes for an efficient removal of DMSO in wastewater.
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