Speciation of copper in ZSM-48 during NO reduction

被引:37
作者
Huang, YJ
Wang, HP [1 ]
Lee, JF
机构
[1] Natl Cheng Kung Univ, Dept Environm Engn, Tainan 70101, Taiwan
[2] Synchrotron Radiat Res Ctr, Hsinchu, Taiwan
关键词
NO; CO; Cu/ZSM-48; XANES; EXAFS;
D O I
10.1016/S0926-3373(02)00145-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Speciation of copper in ZSM-48 and MCM-41 was studied by in situ extended X-ray absorption fine structural (EXAFS) and X-ray absorption near edge structural (XANES) spectroscopies to reveal the abrupt changes in yields of N2O, NO2 and CO2 from the catalytic reduction of NO with CO at 673 K. Component fitted XANES spectra showed that oxygen was inserted into the metallic copper (Cu(0)) in ZSM-48 and MCM-41 during NO reduction. In the confined channels of ZSM-48, about 91% of total copper was Cu(I) that involved in the catalytic reduction of NO with CO at 673 K. By in situ EXAFS, we found that during the NO reduction process, the oxygen-inserted copper possessed Cu-O, Cu-Cu, and Cu-(O)-Cu bond distances of 1.88, 2.61 and 2.95 Angstrom, respectively, suggesting the possible existence of a linear type cluster with an averaged structure Of Cu2O in ZSM-48. Furthermore, in the channels of ZSM-48, due to the restricted diffusion, NO reduction as well as CO oxidation might primarily occur at the head or end of the clusters. Note that NO could penetrate into ZSM-48 containing the clusters. On the contrary, in the parallel experiment, mainly CuO was observed in the mesopores (similar to32 Angstrom) of MCM-41. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:111 / 118
页数:8
相关论文
共 36 条
[1]   MECHANISM OF THE LEAN NOX REACTION OVER CU/ZSM-5 [J].
ANSELL, GP ;
DIWELL, AF ;
GOLUNSKI, SE ;
HAYES, JW ;
RAJARAM, RR ;
TRUEX, TJ ;
WALKER, AP .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1993, 2 (01) :81-100
[2]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[3]   SELECTIVE CATALYTIC REDUCTION OF NITRIC-OXIDE WITH ETHANE AND METHANE ON SOME METAL EXCHANGED ZSM-5 ZEOLITES [J].
BURCH, R ;
SCIRE, S .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1994, 3 (04) :295-318
[4]   Nitrous oxide formation during the reaction of simulated exhaust streams over rhodium, platinum and palladium catalysts [J].
Cant, NW ;
Angove, DE ;
Chambers, DC .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 17 (1-2) :63-73
[5]   The mechanism of nitrogen oxides reduction by hydrocarbons and in other systems [J].
Cant, NW ;
Cowan, AD .
CATALYSIS TODAY, 1997, 35 (1-2) :89-95
[6]  
Chu P., 1983, US Patent, Patent No. 4397827
[7]   HYDROCRACKING OF VACUUM GAS-OIL ON THE NOVEL MESOPOROUS MCM-41 ALUMINOSILICATE CATALYST [J].
CORMA, A ;
MARTINEZ, A ;
MARTINEZSORIA, V ;
MONTON, JB .
JOURNAL OF CATALYSIS, 1995, 153 (01) :25-31
[8]   The effect of pretreatments on different copper exchanged ZSM-5 for the decomposition of NO [J].
Curtin, T ;
Grange, P ;
Delmon, B .
CATALYSIS TODAY, 1997, 36 (01) :57-64
[9]   No reduction on Cu-ZSM-5 studied by EXAFS [J].
Huang, YJ ;
Wang, HP ;
Lee, JF .
CHEMOSPHERE, 1999, 39 (08) :1347-1356
[10]   Reduction of NO with CH4 effected by copper oxide clusters in the channels of ZSM-5 [J].
Huang, YJ ;
Wang, HP .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (33) :6514-6516