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Adsorption of Alkanes on Isomerisation Catalysts

MPS-Authors
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Wrabetz,  Sabine
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Yang,  Xiaobo
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Ahmad,  Rafat
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Hahn,  Alexander H. P.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Jentoft,  Friederike C.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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wrabetzetal_setaram_2002_edoc.pdf
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Citation

Wrabetz, S., Yang, X., Ahmad, R., Hahn, A. H. P., & Jentoft, F. C. (2002). Adsorption of Alkanes on Isomerisation Catalysts. Poster presented at SETARAM Calvet Calorimeters Users Club, Berlin.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-14D0-3
Abstract
Zirconia modified with sulfate is a potential catalyst for the isomerization of n-butane to i-butane. The number of adsorption sites for small alkanes and the respective differential heats of adsorption on zirconia samples are thus of interest. In order to study the adsorption of propane, n-butane, and i-butane on a series of zirconia catalysts including partially deactivated samples, SETARAM MS-70 calorimeters were coupled with a volumetric system. At 313 K and an equilibrium pressure of 5 mbar, typically 10 to 100 µmol alkane per g catalyst were adsorbed. The majority of the sites on the materials were similar, with heats of adsorption between 40-60 kJ mol-1, only a small number of sites at coverages < 2 µmol g-1 was different. A number of interesting phenomena occurred: 1. For particularly active catalysts, the heats of adsorption of i-butane and n-butane increased with increasing coverage. 2. The adsorption was occasionally followed by secondary reactions. 3. After hours of constant pressure, a spontaneous, but slow uptake of sorptive with considerable heat evolution was observed.

Methods: BET, GC, Microcalorimetry
Elements: Fe, O, S, Zr