doi:10.1016/j.micromeso.2006.02.004
Copyright © 2006 Elsevier Inc. All rights reserved.
Effect of water on cobalt speciation during solid-state synthesis of Co2+/ZSM5 catalysts: Quantitative study by TPR and XAS
Hanene Ben Boubakera, Mourad Mhamdia, Eric Marceaub,
,
, Sihem Khaddar-Zinea, Abdelhamid Ghorbela, Michel Cheb, c, Younès Ben Taaritd and Françoise Villaine, f
aLaboratoire de Chimie des Matériaux et Catalyse, Université Tunis II-El Manar, 1060 Tunis, Tunisia
bLaboratoire de Réactivité de Surface (UMR 7609 CNRS), Université Pierre et Marie Curie, 4 place Jussieu, 75252 Paris Cedex 05, France
cInstitut Universitaire de France, France
dInstitut de Recherches sur la Catalyse (UPR 5401 CNRS), 2 Avenue Albert Einstein, 69626 Villeurbanne Cedex, France
eLaboratoire de Chimie Inorganique et Matériaux Moléculaires (UMR 7071 CNRS), Université Pierre et Marie Curie, 4 place Jussieu, 75252 Paris Cedex 05, France
fLaboratoire pour l’Utilisation du Rayonnement Electromagnétique (LURE), Centre Universitaire Paris-Sud, BP 34, 91898 Orsay Cedex, France
Received 12 December 2005;
revised 28 January 2006;
accepted 1 February 2006.
Available online 20 March 2006.
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Abstract
The effect of water on cobalt speciation in the synthesis of Co2+/ZSM5 catalysts is quantitatively studied by the combined use of macroscopic and local characterization techniques, TPR and X-ray absorption spectroscopies, respectively. The addition of a small quantity of water to cobalt acetate and zeolite during the preparation of Co2+/ZSM5 by solid-state reaction favors cobalt dispersion and migration into the zeolite. It also inhibits the formation of extraframework phases (Co3O4 particles, cobalt phyllosilicate). Dissociation of solid cobalt acetate upon contact with water is thought to be the driving force for enhanced cobalt migration into the zeolite.
Keywords: Solid-state reaction; TPR; XAS; Speciation; Quantitative analysis
Fig. 1. UV–Visible spectra recorded at room temperature of reference cobalt acetate and sample I1/2 before solid-state reaction.
Fig. 2. TPR thermograms of catalysts A and I.
Fig. 3. Fourier transforms calculated from experimental EXAFS signals, for references Co3O4 and Co2+ ions/ZSM5, catalysts A and catalysts I.
Fig. 4. XANES spectra of samples A1/2 and I, and their simulations by linear combination from reference spectra. Experimental spectra are presented in full lines and simulations based on the values given in Table 2 in dotted lines. Reference spectra are numbered as follows: (1) Co2+ ions/ZSM5 (
); (2) Co3O4 (×); (3) cobalt phyllosilicate (A3/2) (+).
Fig. 5. EXAFS signals of reference compounds and samples A1/2 and I1/2, and their simulations by linear combination from reference spectra. Simulations (“sim”) correspond to the proportions mentioned in Table 3.
Fig. 6. (a) Overall quantification of extra- and intraframework cobalt species as a function of Co weight content. (b) Detailed quantification of cobalt species as a function of Co weight content in catalysts A. (c) Detailed quantification of cobalt species as a function of Co weight content in catalysts I.
Table 1.
Cobalt content and physicochemical characteristics of Co2+/ZSM5 catalysts A and I

Table 2.
Quantification of Co species (%) based on analysis of TPR thermograms

Table 3.
Quantification of Co species (%) as determined by XAS
