The catalytic activity of a ZrO2/SO4 catalyst in the isomerization of n-butane at 423 K is reversibly suppressed by addition of CO. IR analysis of the adsorption of CO indicates that the only σ-coordination of CO onto coordinatively unsaturated surface Zr4+ cations occurs in the 300-473 K interval. © 1994 J.C. Baltzer AG, Science Publishers.

Isomerization of n-butane on sulfated zirconia: Evidence for the dominant role of Lewis acidity on the catalytic activity

PINNA, Francesco;SIGNORETTO, Michela;STRUKUL, Giorgio;
1994-01-01

Abstract

The catalytic activity of a ZrO2/SO4 catalyst in the isomerization of n-butane at 423 K is reversibly suppressed by addition of CO. IR analysis of the adsorption of CO indicates that the only σ-coordination of CO onto coordinatively unsaturated surface Zr4+ cations occurs in the 300-473 K interval. © 1994 J.C. Baltzer AG, Science Publishers.
1994
26
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/21296
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