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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.


ABSTRACT: The UV-induced advanced oxidation processes (AOPs, including UV/Cl2, 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/Cl2  > UV/H2O2  > UV/NH2Cl > 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 (Kobs) 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/Cl2 . Pretreatment of iopamidol by UV/Cl2 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/Cl2 > UV > UV/H2O2 > UV/ClO2 . Among the discussed UV-driven AOPs, UV/Cl2 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.

SUBMITTER: Tian FX 

PROVIDER: S-EPMC7260538 | biostudies-literature | 2020 Oct

REPOSITORIES: biostudies-literature

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Comparison of <i>UV</i>-induced AOPs (<i>UV/Cl<sub>2</sub>, UV/NH<sub>2</sub>Cl, UV/ClO<sub>2</sub></i> and <i>UV/H<sub>2</sub>O<sub>2</sub></i> ) in the degradation of iopamidol: Kinetics, energy requirements and DBPs-related toxicity in sequential disinfection processes.

Tian Fu-Xiang FX   Ye Wen-Kai WK   Xu Bin B   Hu Xiao-Jun XJ   Ma Shi-Xu SX   Lai Fan F   Gao Yu-Qiong YQ   Xing Hai-Bo HB   Xia Wei-Hong WH   Wang Bo B  

Chemical engineering journal (Lausanne, Switzerland : 1996) 20200530


The <i>UV</i>-induced advanced oxidation processes (AOPs, including <i>UV/Cl<sub>2</sub>, UV/NH<sub>2</sub>Cl, UV/ClO<sub>2</sub></i> and <i>UV/H<sub>2</sub>O<sub>2</sub></i> ) 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 <i>UV/Cl<sub>2</  ...[more]

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