Site availability and competitive siting of divalent metal cations in ZSM-5

被引:63
作者
Rice, MJ [1 ]
Chakraborty, AK
Bell, AT
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
D O I
10.1006/jcat.2000.2977
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
Accommodation of divalent cations (M2+) and dimer cations ([MOM](2+)) in zeolites requires the presence of two charge-exchange sites in close proximity to each other. Since each charge-exchange site is associated with a framework Al atom, this constraint requires that 2 Al atoms be located in next-nearest-neighbor T sites. The maximum number of divalent cations that can be accommodated by ZSM-5 as either Z-M(2)(+)Z(-) or Z(-)[MOM](2+)Z(-) (where Z(-) represents a cation-exchange site in the zeolite) has been calculated for a given value of Si/Al, and the results are reported as the maximum value of M/Al. Two cases for the distribution of framework Al atoms are considered: random placement in T sites and placement governed by equilibrium thermodynamics. For both M2+ and [MOM](2+) the maximum value of M/Al is significantly less than 0.5 and 1.0, respectively, because of the required constraints on the Al-Al pairs, and decreases as the Si/Al ratio increases. For M2+ cations the distribution of specific cations (Co2+, Cu2+, Fe2+, Ni2+, Pd2+, Pt2+, and Zn2+) was determined using energies predicted from electronic structure calculations. M2+ cations are preferentially situated in rings containing either five or six T atoms. The manner in which the Al atoms are distributed among T sites affects the distribution of M2+ cations among different types of rings. (C) 2000 Academic Press.
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页码:278 / 285
页数:8
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