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Influence of preparation method on catalytic properties of mixed calcium-cobalt orthophosphates

Identifieur interne : 001136 ( Main/Merge ); précédent : 001135; suivant : 001137

Influence of preparation method on catalytic properties of mixed calcium-cobalt orthophosphates

Auteurs : A. Legrouri [Maroc] ; S. S. Romdhane ; J. Lenzi [France] ; M. Lenzi [France] ; G. Bonel [France]

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RBID : Pascal:96-0276914

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Abstract

Mixed calcium-cobalt orthophosphates of the formula Ca3-xCOx(PO4)2, with 0 ≤ x ≤ 1.1, were prepared by coprecipitation and solid-state reaction. Structural characterization showed that, in both cases, the solids obtained resulted from substitution of some Ca2+ ions by Co2+ ions in the β-Ca3(PO4)2 structure. The solubility limit of cobalt in this structure corresponded to x = 0.31. The morphology of these compounds was investigated by surface-area measurements and scanning electron microscopy. When tested in the 2-propanol decomposition reaction, the maximum activity in dehydrogenation was obtained with the compound corresponding to cobalt maximum solubility in β-Ca3(PO4)2 structure. Higher activities were obtained for samples prepared by coprecipitation.

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Pascal:96-0276914

Le document en format XML

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<name sortKey="Romdhane, S S" sort="Romdhane, S S" uniqKey="Romdhane S" first="S. S." last="Romdhane">S. S. Romdhane</name>
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<term>Calcium Phosphates</term>
<term>Catalyst activity</term>
<term>Cobalt Phosphates</term>
<term>Coprecipitation</term>
<term>Preparation</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Activité catalytique</term>
<term>Préparation</term>
<term>Coprécipitation</term>
<term>Cobalt Phosphate</term>
<term>Calcium Phosphate</term>
<term>Ca3-xCox(PO4)2</term>
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<front>
<div type="abstract" xml:lang="en">Mixed calcium-cobalt orthophosphates of the formula Ca
<sub>3-x</sub>
CO
<sub>x</sub>
(PO
<sub>4</sub>
)
<sub>2</sub>
, with 0 ≤ x ≤ 1.1, were prepared by coprecipitation and solid-state reaction. Structural characterization showed that, in both cases, the solids obtained resulted from substitution of some Ca
<sup>2+</sup>
ions by Co
<sup>2+</sup>
ions in the β-Ca
<sub>3</sub>
(PO
<sub>4</sub>
)
<sub>2</sub>
structure. The solubility limit of cobalt in this structure corresponded to x = 0.31. The morphology of these compounds was investigated by surface-area measurements and scanning electron microscopy. When tested in the 2-propanol decomposition reaction, the maximum activity in dehydrogenation was obtained with the compound corresponding to cobalt maximum solubility in β-Ca
<sub>3</sub>
(PO
<sub>4</sub>
)
<sub>2</sub>
structure. Higher activities were obtained for samples prepared by coprecipitation.</div>
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