Accelerating effect of ZrO2 doping on catalytic performance and thermal stability of CeO2-CrOx mixed oxide for 1,2-dichloroethane elimination

被引:59
作者
Yang, Peng [1 ]
Yang, Shanshan [1 ]
Shi, Zhinan [1 ]
Tao, Fei [1 ]
Guo, Xiaolin [1 ]
Zhou, Renxian [1 ]
机构
[1] Zhejiang Univ, Inst Catalysis, Hangzhou 310028, Zhejiang, Peoples R China
关键词
CeO2-ZrO2-CrOx; ZrO2; doping; Thermal stability; Catalytic oxidation; 1,2-Dichloroethane; OXYGEN STORAGE CAPACITY; VOLATILE ORGANIC-COMPOUNDS; DEEP OXIDATION; CHLORINATED VOCS; SOLID-SOLUTIONS; COMBUSTION; CERIA; CE; TRICHLOROETHYLENE; CHLOROBENZENE;
D O I
10.1016/j.cej.2015.10.025
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A series of CeO2-ZrO2-CrOx mixed oxides with different Ce/Zr molar ratios were synthesized by co-precipitation method and tested for deep catalytic oxidation of 1,2-dichloroethane (DCE), as one of the typical chlorinated VOCs pollutants. The results show that the addition of proper amount of ZrO2 significantly improves the catalytic activity of CeO2-CrOx, and only very slight C2H3Cl is detected as the sole byproduct in the oxidation process, due to the relative concentration of oxygen vacancies and Cr6+ species on the catalysts being increased. Moreover, though aged at 700 degrees C for 4 h, the catalytic performances and the thermal stability of the aged CeO2-ZrO2-CrO5 catalysts can be maintained to a large extent, especially for the CZCr catalyst (atom molar ratio Ce:Zr:Cr = 2:2:1). It may be related to that smaller Zr and Cr ions are embedded into CeO2 lattice to form solid solution and thus the structure stability being maintained. Besides, the catalysts exhibit good durability for 1,2-dichloroethane oxidation during the long-term continuous test, whether in dry air or in the existence of water and non-chlorinated VOCs, indicating that the CeO2-ZrO2-CrOx catalysts deserve more attention and may be potential for industrial application. (C)2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:544 / 553
页数:10
相关论文
共 48 条
[1]   Mesoporous magnesium oxide and its composites: Preparation, characterization, and removal of 2-chloroethyl ethyl sulfide [J].
Anh-Tuan Vu ;
Jiang, Shunbo ;
Ho, Keon ;
Lee, Joong Beom ;
Lee, Chang-Ha .
CHEMICAL ENGINEERING JOURNAL, 2015, 269 :82-93
[2]   State of the art in catalytic oxidation of chlorinated volatile organic compounds [J].
Aranzabal, Asier ;
Pereda-Ayo, Benat ;
Pilar Gonzalez-Marcos, M. ;
Gonzalez-Marcos, Jose A. ;
Lopez-Fonseca, Ruben ;
Gonzalez-Velasco, Juan R. .
CHEMICAL PAPERS, 2014, 68 (09) :1169-1186
[3]   Role of yttrium loading in the physico-chemical properties and soot combustion activity of ceria and ceria-zirconia catalysts [J].
Atribak, I. ;
Bueno-Lopez, A. ;
Garcia-Garcia, A. .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2009, 300 (1-2) :103-110
[4]   Electrical and oxygen storage/release properties of nanocrystalline ceria-zirconia solid solutions [J].
Boaro, M ;
Trovarelli, A ;
Hwang, JH ;
Mason, TO .
SOLID STATE IONICS, 2002, 147 (1-2) :85-95
[5]   Fractional-hydrolysis-driven formation of nonuniform dopant concentration catalyst nanoparticles of Cr/CexZr1-xO2 and their catalysis in oxidation of NO [J].
Cai, Wei ;
Zhong, Qin ;
Zhang, Shule ;
Zhao, Wei .
CHEMICAL ENGINEERING JOURNAL, 2014, 236 :223-232
[6]   CHEMICAL MODIFICATION OF CATALYST SUPPORT FOR ENHANCEMENT OF TRANSIENT CATALYTIC ACTIVITY - NITRIC-OXIDE REDUCTION BY CARBON-MONOXIDE OVER RHODIUM [J].
CHO, BK .
JOURNAL OF CATALYSIS, 1991, 131 (01) :74-87
[7]   On the mechanism of the catalytic destruction of 1,2-dichloroethane over Ce/Zr mixed oxide catalysts [J].
de Rivas, Beatriz ;
Lopez-Fonseca, Ruben ;
Gonzalez-Velasco, Juan R. ;
Gutierrez-Ortiz, Jose I. .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2007, 278 (1-2) :181-188
[8]  
Erlt G., 2008, HDB HETEROGENEOUS CA, P2385
[9]   Thermal ageing of Pt on low-surface-area CeO2-ZrO2-La2O3 mixed oxides:: Effect on the OSC performance [J].
Fan, Jun ;
Wu, Xiaodong ;
Wu, Xiaodi ;
Liang, Qing ;
Ran, Rui ;
Weng, Duan .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2008, 81 (1-2) :38-48
[10]   Mechanism of catalytic destruction of 1,2-dichloroethane and trichloroethylene over γ-Al2O3 and γ-Al2O3 supported chromium and palladium catalysts [J].
Feijen-Jeurissen, MMR ;
Jorna, JJ ;
Nieuwenhuys, BE ;
Sinquin, G ;
Petit, C ;
Hindermann, JP .
CATALYSIS TODAY, 1999, 54 (01) :65-79