化学
矿化(土壤科学)
草酸
醋酸
电化学
布洛芬
动力学
核化学
降级(电信)
无机化学
电极
有机化学
药理学
物理化学
物理
氮气
电信
医学
量子力学
计算机科学
作者
Lei Xu,Xinyue Cui,Jianbo Liao,Yufeng Liu,Baoyi Jiang,Junfeng Niu
标识
DOI:10.1016/j.cclet.2021.10.065
摘要
Electrochemical degradation performances of three non-steroidal anti-inflammatory drugs (NSAIDs), acetaminophen (ACT), aspirin (ASP) and ibuprofen (IBP), were investigated and compared in their alone and mixture conditions using Ti/SnO2-Sb/La-PbO2. The pseudo-first-order degradation kinetics (k) order was kIBP-A (0.110 min−1) ˃ kASP-A (0.092 min−1) ˃ kACT-A (0.066 min−1) in their alone condition, while that was kACT-M (0.088 min−1) ˃ kASP-M (0.063 min−1) ˃ kIBP-M (0.057 min−1) in their mixture condition. The •OH apparent production rate constant of 5.23 mmol L−1 min−1 m−2 and an electrical energy per order (EEO) value of 6.55 Wh/L could ensure the synchronous degradation of the NSAIDs mixture. The mineralization efficiency of NSAIDs mixture was 86.9% at 240 min with a mineralization current efficiency of 1.67%. Acetic acid and oxalic acid were the main products in the mineralization process for the both conditions. In the mixture condition, there were higher k values at lower initial concentrations and higher current density, while the presence of carbonate and humic acid inhibited their degradation. The results indicated electrochemical advanced oxidation process can effectively and synchronously mineralize NSAIDs mixture in wastewater.
科研通智能强力驱动
Strongly Powered by AbleSci AI