期刊
JOURNAL OF CATALYSIS
卷 352, 期 -, 页码 672-685出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2017.05.015
关键词
Experimental microkinetic; Pt/Al2O3; CO-H-2 co-adsorption; FTIR spectroscopy; Temkin formalism
The present study is dedicated to the development of a Temkin model for competitive chemisorption (denoted Temkin-C) which can be applied in large range of experimental conditions (partial pressures and temperatures). It is based on experimental data from the adsorption/reaction of x% CO/H-2 gas mixtures (x = 1, 10(-2) and 10(-3), total pressure 1 atm.) on a reduced 2.9% Pt/Al2O3 catalyst for two platinum dispersions (D approximate to 0.6 and 0.26) in the temperature range 300-740 K. FTIR spectroscopy (a) shows that three adsorbed CO species: linear, bridged and threefold coordinated CO species (denoted L, B and 3FC respectively) are formed at 300 K and (b) provides the evolution of the coverage of the dominant L CO species (IR band at 2080 cm(-1) at 300 K) for the three CO/H-2 gas mixtures in the 300-740 K temperature range. These data support the rigorous development of a Temkin-C model providing the theoretical coverage of the L CO and hydrogen species in the absence of the CH4 production. The comparison of the theoretical and experimental evolutions of the coverage of the L CO species shows that (a) the L CO species dominates the competitive chemisorption with the hydrogen species and (b) the heats of adsorption of the two species are not significantly modified by their co-adsorption. Moreover, in line with the debate dedicated to the paradox of kinetics on heterogeneous surface (briefly the catalytic activity of a heterogeneous surface can be well represented by assuming an homogeneous surface), the Temkin-C model is compared to models based on the Langmuir formalism currently used in the literature dedicated to kinetic studies. This reveals the clear advantage of the Temkin-C model for the representation of experimental data in large range of experimental conditions. In Part 2, the Temkin-C model is extended by considering that the L CO species is the adsorbed intermediate species of the CH4 formation from the CO/H-2 reaction at T > 500 K. (C) 2017 Elsevier Inc. All rights reserved.
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