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Carbon-based electrocatalytic dual-membrane system bolsters singlet oxygen production for ultrafast water decontamination
被引:13
作者:

Yan, Ni
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Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China

Ren, Tengfei
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Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China

Lu, Kechao
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Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China

Gao, Yifan
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Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China

Sun, Meng
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Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China

Huang, Xia
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机构:
Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China

Zhang, Xiaoyuan
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机构:
Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China
机构:
[1] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Advanced wastewater treatment;
Electrocatalytic oxidation;
Singlet oxygen;
Anode-cathode synergy;
Dual-membrane system;
ANODIC-OXIDATION;
PHOTOCATALYTIC DEGRADATION;
MOLECULAR-OXYGEN;
RATE CONSTANTS;
WASTE-WATER;
MINERALIZATION;
POLLUTANTS;
MECHANISM;
OZONATION;
RADICALS;
D O I:
10.1016/j.jhazmat.2023.132787
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Reactive electrochemical membranes (REMs) are promising technologies in treating pharmaceuticals and personal care products (PPCPs) in water. Herein, a novel carbon-based electrocatalytic dual-membrane system was designed to exploit the whole redox process of electrodes, in which the membrane cathode and anode were formed by carbon fibers doped with Fe and metal organic frameworks derived SnO2, respectively. Propranolol (PRO) was used as a representative of PPCPs. The system bolstered singlet oxygen (O-1(2)) production by the synergy of two REM electrodes, further improving the removal rate constant of PRO compared with single-electrode-dominant modes. 97.5 +/- 1.7% of PRO removal was achieved in a single-pass electro-filtration at a residence time of similar to 2.9 s. The generation of O-1(2) and its reaction with pollutants were systematically and thoroughly explored via experiments coupled with theoretical calculation. The toxicity of the decomposition products was predicted to be reduced compared with PRO. These findings suggested that the carbon-based electrocatalytic dual-membrane system could effectively promote O-1(2) production for ultrafast catalytic oxidation of PRO, providing a cost-effective solution for the development of an efficient and stable technology for PPCPs removal.
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页数:11
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