On the nature of nonframework cations in a zeolitic deNOx catalyst -: A synchrotron X-ray diffraction and ESR study of Cu-ferrierite

被引:36
作者
Attfield, MP [1 ]
Weigel, SJ [1 ]
Cheetham, AK [1 ]
机构
[1] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会;
关键词
D O I
10.1006/jcat.1997.1816
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
The location of extra-framework Cu2+ cations in the dehydrated copper ion exchanged zeolite, ferrierite, has been determined from the analysis of synchrotron X-ray powder diffraction data (Cu-0.023(Al0.065Si0.935)O-2; space group Immm, a = 18.8101(2) Angstrom, b = 14.0930(2) Angstrom, c = 7.44527(7) Angstrom, V = 1973.67(6) Angstrom, Z = 36, R-wp = 9.89%, chi(2) = 1.12). One copper site was found towards the side of the 8-ring window at the intersection of the 10- and 8-ring channels. An electron spin resonance (ESR) spectroscopic study indicates the presence of one Cu2+ species in the hydrated sample, which forms two Cu2+ species upon evacuation to 200 degrees C, only one of which remains after evacuation to 360 degrees C. This remaining Cu2+ species has nonaxial symmetry. The low coordination, but high accessibility of the cation site provides a possible explanation for the high activity of ferrierite and its related pentasil family members for nitrogen oxide decomposition. (C) 1997 Academic Press.
引用
收藏
页码:274 / 280
页数:7
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