journal article·2001-03-01

Determination of the Heat of Adsorption of Ammonia on Zeolites from Temperature-Programmed Desorption Experiments

Jean-Pierre Joly, Alain Perrard

Langmuir· Volume 17· Issue 5
Publisher page

Abstract

A general equation, obtained from the classical TPD theory and statistical thermodynamics, has been designed for determining the enthalpy of adsorption, Δ H, from a series of temperature-programmed desorption (TPD) runs carried out with various sample masses, heating rates, or inert gas flow rates. This equation applies to TPD performed either under vacuum or under an inert gas stream, provided that readsorption occurs freely during the experiments. It has been applied to ammonia TPD (under vacuum) from HY zeolite samples of different masses. The pressure of ammonia over the sample was in the range 1 × 10 - 4 −15 Pa. The value of Δ H obtained is −136 kJ/mol. Results showed that the molecule of ammonia in the gas phase completely loses its translational motion when it is adsorbed. Finally, a simple experimental method has been proposed to rapidly investigate whether readsorption occurs during the TPD runs. It has been found that, under our experimental conditions, free readsorption effectively takes place at temperatures under 750 K but that desorption is irreversible above this temperature.
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Research context

OpenAlex topics: Catalytic Processes in Materials Science · Zeolite Catalysis and Synthesis · Carbon Dioxide Capture Technologies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Laboratoire d'Application de la Chimie à l'Environnement (LACE), UMR 5634 CNRS, Université Claude Bernard Lyon 1, 43 Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex, France, and Institut de Recherches sur la Catalyse-CNRS, UPR 5401, 2 Avenue Albert Eintein, 69626 Villeurbanne Cedex, France

References (15)

Show source-provided references
1. Sharma S. B. · Appl. Catal., A · 1993 · 102 · 25310.1016/0926-860X(93)80232-F ↗
2. Karge H. G. · J. Phys. Chem. · 1990 · 94 · 76510.1021/j100365a047 ↗
3. Hashiguchi, T.; Sakai, S. InAcid-Base Catalysis; Tanabe, K., Hattori, H., Yamagushi, T., Tanaka, T., Eds.; Kodansha: Tokyo, 1989; p 191.
4. Corma A. · Zeolites · 1987 · 7 · 55910.1016/0144-2449(87)90098-4 ↗
5. Höchtl M. · Microporous Mesoporous Mater. · 1999 · 31 · 27110.1016/S1387-1811(99)00078-5 ↗
6. Gang L. · J. Catal. · 1999 · 186 · 10010.1006/jcat.1999.2524 ↗
7. Cvetanovic R. J. · Adv. Catal. · 1967 · 17 · 10310.1016/S0360-0564(08)60686-0 ↗
8. Sawa M. · Zeolites · 1990 · 10 · 30710.1016/0144-2449(94)90147-3 ↗
9. Kapustin J. I. · Appl. Catal. · 1988 · 42 · 23910.1016/0166-9834(88)80005-8 ↗
10. Kauzman W. · 1966
11. Joly J. P. · Appl. Catal., A · 1993 · 96 · 35510.1016/0926-860X(90)80022-7 ↗
12. Auroux A. · J. Phys. Chem. · 1990 · 94 · 637110.1021/j100379a041 ↗
13. Gorte R. J. · J. Catal. · 1982 · 75 · 16410.1016/0021-9517(82)90131-2 ↗
14. Kräger, J.; Ruthven, D. M.Diffusion in zeolites; John Wiley and Sons Inc. New York, 1992; p 459.
15. Hagelstein, M.; Hatje, U.; Förster, H.; Ressler, T.; Metz, W. InStudies in Surface Science and Catalysis. Zeolites and Related MicroporousMaterials: State of Art 1994; Weitkamp, J., Karge, H. G., Pfeifer, H., Hölderich, W., Eds.; Elsevier: Amsterdam, 1994; Vol. 84, p 1217.10.1016/S0167-2991(08)63660-5 ↗