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Direct degradation of methylene blue by unactivated peroxymonosulfate: reaction parameters, kinetics, and mechanism

化学 亚甲蓝 反应速率常数 降级(电信) 碳酸氢盐 腐植酸 氯化物 动力学 核化学 污染物 无机化学 催化作用 光催化 有机化学 电信 肥料 物理 量子力学 计算机科学
作者
Xu Zuo,Jianxin Nie,Beier Jiang,Aijun Jiang,Shiyang Zou,Junrong Wu,Bingquan Ding,Xue hui Wang,Yang Liu
出处
期刊:Environmental Science and Pollution Research [Springer Nature]
卷期号:29 (50): 75597-75608 被引量:5
标识
DOI:10.1007/s11356-022-21197-8
摘要

Advanced oxidation processes (AOPs) are efficient methods for water purification. However, there are few studies on using peroxymonosulfate (PMS) to remove pollutants directly. In this study, about 76% of methylene blue (MB) was removed by PMS directly within 180 min through a non-radical pathway, verified by scavenging tests, electron paramagnetic resonance and kinetic calculations. Additionally, the effects of PMS dosage, MB concentration, temperature, initial pH and competitive anions were determined. High PMS dosage, temperature and pH promoted MB degradation (from 76 to 98%) while MB concentration showed no effect on MB removal. Besides, MB degradation followed pseudo-first-order kinetic with rate constants of 0.0082 to 0.3912 min−1. The second-order rate constant for PMS reaction with MB was 0.08 M−1 s−1 at pH 3–6, but increased dramatically to 4.68 M−1 s−1 at pH 10.50. Chlorine could be catalysed by PMS at high concentration Cl− and degradation efficiency reached 98% within 90 min. High concentration of bicarbonate accelerated MB removal due to the high pH value while humic acid showed a marginal effect on MB degradation. Furthermore, TOC removal rate of MB in the presence of chloride reached 45%, whereas PMS alone caused almost no mineralisation. This study provides new insights into pollutant removal and an additional strategy for water purification.
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