Accelerated Pollutant Degradation by UV/H2O2 at the Air-Water Interface of Microdroplets

被引:0
|
作者
Liu, Xiaochen [1 ]
Pan, Yishuai [1 ]
Yao, Yu [1 ]
Chen, Shuxuan [1 ]
Chen, Baoliang [1 ]
Chu, Chiheng [1 ]
机构
[1] Zhejiang Univ, Dept Environm Sci, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
water treatment; UV/H2O2; system; air-waterinterface; interfacial reaction; hydroxyl radical; ADVANCED OXIDATION; HYDROXYL RADICALS; QUANTUM YIELD; PHARMACEUTICALS; TRANSFORMATION; CARBAMAZEPINE; UV/CHLORINE; GENERATION; PHOTOLYSIS; PPCPS;
D O I
暂无
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ultraviolet light-induced homolysis of hydrogen peroxide (UV/H2O2) can generate powerful hydroxyl radicals ((OH)-O-center dot) for sustainable water purification. However, the efficiency of the conventional bulk-phase UV/H2O2 system is limited by the low yield and utilization of (OH)-O-center dot, in turn necessitating high UV energy input and long purification period. In this study, we present an innovative UV/H2O2 microdroplet system for enhanced pollutant degradation. The degradation of pollutants in sprayed microdroplets was accelerated by 8.5-63.3-fold compared to those in bulk water, demonstrating universal effectiveness across a range of pollutant types and diverse aqueous matrices. This enhancement stems from elevated (OH)-O-center dot production at the air-water interface due to the enhanced UV absorbance of H2O2. The production of (OH)-O-center dot in the microdroplet system was 45-fold higher than that in bulk water, facilitating rapid (OH)-O-center dot-mediated pollutant degradation. Moreover, pollutants accumulate at the air-water interface, where (OH)-O-center dot is concentrated, leading to higher utilization of (OH)-O-center dot for mediating pollutant degradation before quenching. Our findings provide a solution to overcome the bottlenecks in (OH)-O-center dot production and utilization, offering insights for improving the efficiency of UV/H2O2 water treatment systems.
引用
收藏
页码:5406 / 5414
页数:9
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