共 24 条
Heterogeneously catalyzed persulfate with a CuMgFe layered double hydroxide for the degradation of ethylbenzene
被引:101
作者:
Yan, Jingchun
[1
]
Chen, Yun
[1
,2
]
Qian, Linbo
[1
]
Gao, Weiguo
[1
,2
]
Ouyang, Da
[1
,2
]
Chen, Mengfang
[1
]
机构:
[1] Chinese Acad Sci, Inst Soil Sci, Key Lab Soil Environm & Pollut Remediat, Nanjing 210008, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CuMgFe-LDH;
Persulfate;
Catalysis;
Degradation;
Ethylbenzene;
HYDROGEN-PEROXIDE;
ACTIVATION;
OXIDATION;
MECHANISM;
SULFATE;
GENERATION;
STABILITY;
RADICALS;
REMOVAL;
CUFE2O4;
D O I:
10.1016/j.jhazmat.2017.05.007
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
CuMgFe layered double hydroxide (CuMgFe-LDH) was successfully synthesized and characterized as an efficient catalyst of persulfate (PS) for the degradation of ethylbenzene. Under the conditions of 0.2 g L-1 CuMgFe-LDH and 4.0 mmol L-1 persulfate at pH 7.6, the degradation efficiency of 0.08 mmol L-1 ethylbenzene was 93.7% with TOC removal efficiency of 65.2% in 24 h, and the concentration of Cu leached into the solution was as low as 0.095 mg L-1 after the reaction. The reuse of CuMgFe-LDH showed that the catalyst was highly stable after 5 recycles. Electron Spin Resonance (ESR) test and free radical quenching experiment indicated that SO4 center dot- and (OH)-O-center dot radicals were the dominant species accounted for the degradation of ethylbenzene in the CuMgFe-LDH/persulfate system. Catalytic mechanism of the formation of a complex of equivalent to Cu(II)-O3SOOSO32- and the subsequent redox cycle of Cu(II)/Cu(III) accounted for the generation of radicals was proposed. (C) 2017 Elsevier B.V. All rights reserved.
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页码:372 / 380
页数:9
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