Meta-cresol degradation by persulfate through UV/O3 synergistic activation: Contribution of free radicals and degradation pathway

过硫酸盐 化学 激进的 对甲酚 降级(电信) 反应速率常数 羟基自由基 臭氧 光化学 甲酚 高级氧化法 动力学 催化作用 有机化学 苯酚 量子力学 计算机科学 电信 物理
作者
Luxi Zou,Yan Wang,Chou Huang,Bingbing Li,Jinze Lyu,Shuo Wang,Hui Lü,Ji Li
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:754: 142219-142219 被引量:39
标识
DOI:10.1016/j.scitotenv.2020.142219
摘要

The kinetic and pathway of meta-cresol (m-cresol) degradation were studied by persulfate oxidation through UV/ozone activation (UV/O3-Na2S2O8) to improve m-cresol removal to eliminate ecological risks. Experimental results showed that the degradation effect of m-cresol with an initial concentration of 50 mg/L was 99.8% in 30 min under the optimization conditions. The reaction kinetic model in the UV/O3-Na2S2O8 system shows that the initial pH value, the respective ozone, and the persulfate dosage were positively correlated with the degradation rate constant value (k). The apparent degradation rate of m-cresol in the UV/O3-Na2S2O8 system was 0.2216 min-1, and the synergy factor (f) was larger than 1, thereby demonstrating a synergistic effect of UV, ozone, and persulfate. The dominant free radicals in the system were sulfate radical (SO- 4·) and hydroxyl radical (·OH), and the contribution ratio of SO- 4· to m-cresol degradation was higher than ·OH. The degradation process of m-cresol by UV/O3 - Na2S2O8 was mainly through the electrophilic addition reaction to substitute the ortho- and para-positions of the hydroxyl group on the benzene ring, followed by the ring-opening reaction and mineralization of the aliphatic compound to achieve the complete degradation of m-cresol.
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