氯
化学
高级氧化法
量子产额
羟基自由基
产量(工程)
水处理
降级(电信)
环境化学
反应速率常数
光化学
激进的
环境科学
催化作用
动力学
环境工程
材料科学
有机化学
荧光
物理
冶金
电信
量子力学
计算机科学
作者
Jing Zhao,Chii Shang,Ran Yin
标识
DOI:10.1021/acs.est.3c00255
摘要
Increasing the radical yield and reducing energy consumption would enhance the sustainability and competitiveness of advanced oxidation processes (AOPs) for micropollutant degradation in water. We herein report a novel AOP coupling far-UVC radiation at 222 nm with chlorinated cyanurates (termed the UV222/Cl-cyanurates AOP) for radical generation and micropollutant abatement in water. We experimentally determined the concentrations of HO•, Cl•, and ClO• in the UV222/Cl-cyanurates AOP in deionized water and swimming pool water. The radical concentrations are 10-27 times and 4-13 times, respectively, higher than those in the UV254/Cl-cyanurates AOP and the well-documented UV254/chlorine AOP under comparable conditions (e.g., same UV fluence and oxidant dosing). We determined the molar absorption coefficients and innate quantum yields of two chlorine species and two Cl-cyanurates at 222 nm and incorporated these parameters into a kinetic model. The model enables accurate prediction of oxidant photodecay rates as well as the pH impact on radical generation in the UV222/Cl-cyanurates AOP. We predicted the pseudo-first-order degradation rate constants of 25 micropollutants in the UV222/Cl-cyanurates AOP and demonstrated that many micropollutants can be degraded by >80% with a low UV fluence of 25 mJ cm-2. This work advances the fundamental photochemistry of chlorine and Cl-cyanurates at 222 nm and offers a highly effective engineering tool in combating micropollutants in water where Cl-cyanurates are suitable to use.
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