Hydrolytic decomposition of CF4 over alumina-based binary metal oxide catalysts:: high catalytic activity of gallia-alumina catalyst

被引:38
作者
El-Bahy, ZM [1 ]
Ohnishi, R [1 ]
Ichikawa, M [1 ]
机构
[1] Hokkaido Univ, Ctr Catalysis Res, Kita Ku, Sapporo, Hokkaido 0010021, Japan
关键词
gallia; alumina; CF4; decomposition; acidity; defluorination; hydrolysis; FT-IR of pyridine; TPD-mass;
D O I
10.1016/j.cattod.2004.04.039
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The hydrolytic decomposition of CF4 has been conducted on gallia promoted alumina (Ga-Al oxide) catalysts at 803-903 K and 0.1 MPa. Steady state activity on 20% Ga-Al oxide was 15 times of that on Ce 10%-AlPO4 catalyst, on which the highest activity has been reported. The catalytic activity was further improved by incorporation of sulfate anion in Ga-Al oxide and by applying sol-gel method in preparation of the catalyst. XRD spectra of Ga-Al oxides showed a shift of diffraction peaks assigned to gamma-alumina toward lower angles, indicating the formation of gallia-alumina solid solution. In situ FT-IR of pyridine adsorption spectra of Ga-Al oxides showed peaks solely attributable to Lewis acid (L-acid) sites at 1445-1455, ca. 1495, 1577, ca. 1594, and ca. 1622cm(-1). The steady state catalytic activities increased with increasing peak areas at 1446 or 1622 cm(-1) of Ga-Al oxides with various Ga%, suggesting participation of Lewis acid sites into the reaction. It is demonstrate from surface area measurements of Ga-Al oxide catalyst before and after the reaction that not only higher catalytic activity but also higher catalyst stability were observed on Ga-Al oxide, Ga-Al oxide with sulfate, and Ga-Al oxide prepared by sol-gel method than on their parent oxides of alumina, Ga-Al oxide, and Ga-Al oxide prepared by incipient wetness method, respectively. (C) 2004 Published by Elsevier B.V.
引用
收藏
页码:283 / 290
页数:8
相关论文
共 42 条
[1]   SURFACE CHARACTERIZATION OF AMORPHOUS ALUMINA AND ITS CRYSTALLIZATION PRODUCTS [J].
ABBATTISTA, F ;
DELMASTRO, S ;
GOZZELINO, G ;
MAZZA, D ;
VALLINO, M ;
BUSCA, G ;
LORENZELLI, V ;
RAMIS, G .
JOURNAL OF CATALYSIS, 1989, 117 (01) :42-51
[2]   Surface acidity of MCM-41 by in situ IR studies of pyridine adsorption [J].
Chakraborty, B ;
Viswanathan, B .
CATALYSIS TODAY, 1999, 49 (1-3) :253-260
[3]   Hydrolysis of CF4 over alumina-based binary metal oxide catalysts [J].
El-Bahy, ZM ;
Ohnishi, R ;
Ichikawa, M .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 40 (02) :81-91
[4]   Activity enhancement of SnO2-doped Ga2O3-Al2O3 catalysts by coexisting H2O for the selective reduction of NO with propene [J].
Haneda, M ;
Kintaichi, Y ;
Hamada, H .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1999, 20 (04) :289-300
[5]   Ga2O3/Al2O3 prepared by sol-gel method as a highly active metal oxide-based catalyst for NO reduction by propene in the presence of oxygen, H2O and SO2 [J].
Haneda, M ;
Kintaichi, Y ;
Shimada, H ;
Hamada, H .
CHEMISTRY LETTERS, 1998, (02) :181-182
[6]   Selective reduction of NO with propene over Ga2O3-Al2O3:: Effect of sol-gel method on the catalytic performance [J].
Haneda, M ;
Kintaichi, Y ;
Shimada, H ;
Hamada, H .
JOURNAL OF CATALYSIS, 2000, 192 (01) :137-148
[7]   Adsorption and transformation of halogenated hydrocarbons over zeolites [J].
Hannus, I .
APPLIED CATALYSIS A-GENERAL, 1999, 189 (02) :263-276
[8]   Catalytic hydrolysis of chlorofluorocarbon (CFC-12) over WO3/ZrO2 [J].
Hua, WM ;
Zhang, F ;
Ma, Z ;
Tang, Y ;
Gao, Z .
CATALYSIS LETTERS, 2000, 65 (1-3) :85-89
[9]   DECOMPOSITION OF DICHLORODIFLUOROMETHANE ON TIO2/SIO2 [J].
IMAMURA, S ;
SHIOMI, T ;
ISHIDA, S ;
UTANI, K ;
JINDAI, H .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1990, 29 (09) :1758-1761
[10]   Hydrolytic decomposition of PFCs over AlPO4-Al2O3 catalyst [J].
Jeon, JY ;
Xu, XF ;
Choi, MH ;
Kim, HY ;
Park, YK .
CHEMICAL COMMUNICATIONS, 2003, (11) :1244-1245