石墨氮化碳
激进的
降级(电信)
化学工程
氧气
碳纤维
材料科学
光化学
羟基自由基
活性氧
化学
光催化
催化作用
有机化学
复合材料
复合数
计算机科学
工程类
电信
生物化学
作者
Jiaqi Hu,Junli Tian,Yue Yang,Shanshan Li,Jinfeng Lu
标识
DOI:10.1016/j.jcis.2024.01.135
摘要
Improving the activation capacity of peroxymonosulfate (PMS) to increase radical and non-radical production is critical for antibiotic degradation. However, how to boost reactive oxygen species (ROS) and speed interfacial charge transfer remains an essential challenge. We report a coupling system of 10 %CNNS/CuBi2O4 photocatalyst and sulfate radical-based advanced oxidation processes (SO4−-AOPs) to enhance the activation of PMS and improve antibiotic degradation. Owing to highly efficient oxygen activation and interfacial charge transfer, the degradation efficiency of the photo-assisted PMS system was as high as 51.6 times and 2.8 times that of photocatalyst and SO4−-AOPs alone, respectively. Importantly, the highly efficient oxygen activation resulted in the production of O2−, which in turn could utilize the excess electrons generated through efficient interfacial charge transfer to convert into non-radical 1O2. The total organic carbon (TOC) elimination effectiveness of the photo-assisted PMS system reached 82 % via the synergy of radicals and non-radicals (O2−, OH, 1O2, SO4−, h+). This system also had excellent potential for reducing the generation and toxicity of disinfection by-products (DBPs), as evidenced through significant reductions in concentrations of trichloromethane (TCM), dichloroacetic acid (DCAA), and trichloronitromethane (TCNM) by 76 %, 64 %, and 35 %, respectively, providing an effective and eco-friendly strategy for antibiotic treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI