4.7 Article

Comparison of UV-induced AOPs (UV/Cl2, UV/NH2Cl, UV/ClO2 and UV/H2O2) in the degradation of iopamidol: Kinetics, energy requirements and DBPs-related toxicity in sequential disinfection processes

期刊

CHEMICAL ENGINEERING JOURNAL
卷 398, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.125570

关键词

UV-based advanced oxidation processes (AOPs); Degradation; Iopamidol; Electrical energy per order (EE/O); Toxicity; Iodo-trihalomethanes (I-THMs)

资金

  1. Natural Science Foundation of China [51708353]
  2. Shuguang Program [17SG52]
  3. Shanghai Education Development Foundation
  4. Shanghai Municipal Education Commission
  5. Science and Technology Program of Shanghai City of China [16090503500]

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The UV-induced advanced oxidation processes (AOPs, including UV/Cl-2, UV/NH2Cl, UV/ClO2 and UV/H2O2) degradation kinetics and energy requirements of iopamidol as well as DBPs-related toxicity in sequential disinfection were compared in this study. The photodegradation of iopamidol in these processes can be well described by pseudo-first-order model and the removal efficiency ranked in descending order of UV/Cl-2 > UV/H2O2 > UV/NH2(C)l > UV/ClO2 > UV. The synergistic effects could be attributed to diverse radical species generated in each system. Influencing factors of oxidant dosage, UV intensity, solution pH and water matrixes (Cl-, NH4+ and nature organic matter) were evaluated in detail. Higher oxidant dosages and greater UV intensities led to bigger pseudo-first-order rate constants (K-obs) in these processes, but the pH behaviors exhibited quite differently. The presence of Cl-, NH4+ and nature organic matter posed different effects on the degradation rate. The parameter of electrical energy per order (EE/O) was adopted to evaluate the energy requirements of the tested systems and it followed the trend of UV/ClO2 > UV > UV/NH2Cl > UV/ H2O2 > UV/Cl-2. Pretreatment of iopamidol by UV/Cl-2 and UV/NH2Cl clearly enhanced the production of classical disinfection by-products (DBPs) and iodo-trihalomethanes (I-THMs) during subsequent oxidation while UV/ClO2 and UV/H2O2 exhibited almost elimination effect. From the perspective of weighted water toxicity, the risk ranking was UV/NH2Cl > UV/Cl-2 > UV > UV/H2O2 > UV/ClO2. Among the discussed UV-driven AOPs, UV/Cl-2 was proved to be the most cost-effective one for iopamidol removal while UV/ClO2 displayed overwhelming advantages in regulating the water toxicity associated with DBPs, especially I-THMs. The present results could provide some insights into the application of UV-activated AOPs technologies in tradeoffs between cost-effectiveness assessment and DBPs-related toxicity control of the disinfected waters containing iopamidol.

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