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Solar-driven photocatalytic chlorine activation for the simultaneous degradation of pharmaceuticals and personal care products and the inactivation of Escherichia coli in drinking water
被引:6
作者:
Lung, Cheuk Wai
[1
]
Zheng, Zexiao
[1
]
Lo, Irene M. C.
[1
,2
]
机构:
[1] Hong Kong Univ Sci & Technol, Dept Civil & Environm Engn, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Inst Adv Study, Hong Kong, Peoples R China
来源:
关键词:
Chlorine activation;
Disinfection;
Photocatalysis;
Pharmaceuticals and personal care products;
degradation;
TIO2;
PHOTOLYSIS;
RADICALS;
REMOVAL;
ROLES;
PPCPS;
NOM;
D O I:
10.1016/j.chemosphere.2022.137019
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Removal of pharmaceuticals and personal care products (PPCPs) is often inefficient during conventional water treatment, posing threats to human health. Herein, we have developed a novel solar/TiO2/chlorine system upgraded from chlorine disinfection for the simultaneous degradation of PPCPs and the inactivation of Escherichia coli from drinking water. The addition of 100 mu M of chlorine to the photocatalytic process considerably enhanced the degradation efficiency of PPCPs and demonstrated excellent disinfecting abilities, as confirmed by a 4.7 x increase in the carbamazepine degradation rate constant coupled with a 3.2-log (99.94%) reduction of E. coli cells within 1 min. Photoinduced charge pairs (h(VB)(+) and e(CB)(-) were identified for reactive species generation, and HO center dot and ClO center dot were the primary contributors to PPCPs degradation. The process exhibited satisfactory carbamazepine degradation efficiency in different water matrices and the cycling tests showed the TiO2 photocatalyst to be highly stable and reusable. Overall, our solar/TiO2/chlorine system is a potentially effective alternative to conventional drinking water treatment using chlorination.
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页数:11
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