State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing 100875, China.
State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing 100875, China.
Chemosphere. 2016 May;151:280-8. doi: 10.1016/j.chemosphere.2016.02.089. Epub 2016 Mar 15.
Increasing attention has been paid to environmentally friendly activation methods of peroxymonosulfate (PMS) in advanced oxidation processes (AOPs) for organic pollutant elimination. This work demonstrates that Base can be applied as a novel activator for PMS. The Base/PMS system, at ambient temperature, was able to degrade a variety of organic pollutants, including acid orange 7 (AO7), phenol and bisphenol A. In subsequent experiments with AO7, the decolorization rates for AO7 followed pseudo-first-order kinetics, with rate constant values ranging from 0.0006 to 0.1749 min(-1) depending on the operating parameters (initial PMS, Base, AO7 concentrations and reaction temperature). Furthermore, the mechanism for PMS activation by the Base was elucidated by radical scavenger (tert-butyl alcohol, methanol, sodium azide and p-benzoquinone) and electron spin resonance trapping studies. The results revealed that superoxide anion radical and singlet oxygen other than sulfate radical were the primary reactive oxygen species in the Base/PMS system. The findings of this study present a new pathway for PMS activation and provide useful information for the treatment of wastewater.
越来越多的人关注到过一硫酸盐(PMS)在高级氧化工艺(AOPs)中用于有机污染物消除的环保激活方法。本工作表明,碱可以作为 PMS 的一种新型激活剂。在环境温度下,Base/PMS 体系能够降解多种有机污染物,包括酸性橙 7(AO7)、苯酚和双酚 A。在随后的 AO7 实验中,AO7 的脱色率遵循准一级动力学,其速率常数值范围为 0.0006 到 0.1749 min(-1),取决于操作参数(初始 PMS、Base、AO7 浓度和反应温度)。此外,通过自由基清除剂(叔丁醇、甲醇、叠氮化钠和对苯醌)和电子自旋共振捕获研究阐明了 Base 激活 PMS 的机制。结果表明,超氧阴离子自由基和单线态氧而不是硫酸根自由基是 Base/PMS 体系中的主要活性氧物质。本研究的结果为 PMS 激活提供了一种新途径,并为废水处理提供了有用信息。