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.
引用
收藏
页码:372 / 380
页数:9
相关论文
共 24 条
[1]   Copper(II)/H2O2-mediated DNA cleavage:: Involvement of a copper(III) species in H-atom abstraction of deoxyribose units [J].
Amine, A ;
Atmani, Z ;
El Hallaoui, A ;
Giorgi, M ;
Pierrot, M ;
Réglier, M .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (01) :57-60
[2]   Assessment of bimetallic and trimetallic iron-based systems for persulfate activation: Application to sulfamethoxazole degradation [J].
Ayoub, Ghada ;
Ghauch, Antoine .
CHEMICAL ENGINEERING JOURNAL, 2014, 256 :280-292
[3]   THE KINETICS AND MECHANISM OF THE DECOMPOSITION OF CAROS ACID .1. [J].
BALL, DL ;
EDWARDS, JO .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1956, 78 (06) :1125-1129
[4]   OXIDATION OF SOME PHENOLIC COMPOUNDS WITH CU(III) [J].
CHANDRA, S ;
YADAVA, KL .
MICROCHEMICAL JOURNAL, 1970, 15 (01) :78-&
[5]   Selective Removal of Copper(II) from Natural Waters by Nanoporous Sorbents Functionalized with Chelating Diamines [J].
Chouyyok, Wilaiwan ;
Shin, Yongsoon ;
Davidson, Joseph ;
Samuels, William D. ;
Lafemina, Nikki H. ;
Rutledge, Ryan D. ;
Fryxell, Glen E. ;
Sangvanich, Thanapon ;
Yantasee, Wassana .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2010, 44 (16) :6390-6395
[6]   Mechanism of Base Activation of Persulfate [J].
Furman, Olha S. ;
Teel, Amy L. ;
Watts, Richard J. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2010, 44 (16) :6423-6428
[7]   Insights into the mechanism of heterogeneous activation of persulfate with a clay/iron-based catalyst under visible LED light irradiation [J].
Gao, Yaowen ;
Zhang, Zhuoyue ;
Li, Simiao ;
Liu, Jin ;
Yao, Linyu ;
Li, Yixi ;
Zhang, Hui .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2016, 185 :22-30
[8]   Ibuprofen removal by heated persulfate in aqueous solution: A kinetics study [J].
Ghauch, Antoine ;
Tuqan, Al Muthanna ;
Kibbi, Nadine .
CHEMICAL ENGINEERING JOURNAL, 2012, 197 :483-492
[9]   The reactions of SO3 with HO2 radical and H2O•••HO2 radical complex. Theoretical study on the atmospheric formation of HSO5 and H2SO4 [J].
Gonzalez, Javier ;
Torrent-Sucarrat, Miquel ;
Anglada, Josep M. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2010, 12 (09) :2116-2125
[10]   Mesoporous Layer-by-Layer Ordered Nanohybrids of Layered Double Hydroxide and Layered Metal Oxide: Highly Active Visible Light Photocatalysts with Improved Chemical Stability [J].
Gunjakar, Jayavant L. ;
Kim, Tae Woo ;
Kim, Hyo Na ;
Kim, In Young ;
Hwang, Seong-Ju .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (38) :14998-15007