Benzaldehyde hydrogenation over supported nickel catalysts
Identifieur interne : 000218 ( France/Analysis ); précédent : 000217; suivant : 000219Benzaldehyde hydrogenation over supported nickel catalysts
Auteurs : A. Saadi [Algérie] ; R. Merabti [Algérie] ; Z. Rassoul [Algérie] ; M. M. Bettahar [France]Source :
- Journal of molecular catalysis. A, Chemical [ 1381-1169 ] ; 2006.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Nickel.
English descriptors
- KwdEn :
Abstract
The hydrogenation of benzaldehyde over nickel catalysts supported on Al2O3, SiO2, TiO2 and CeO2 was studied at atmospheric pressure in the range temperature of 70-140°C under H2 flow. They were characterized by their BET surface area, XRD spectra, reducibility properties under H2. The obtained products were benzylalcohol, toluene, benzene with yields depending on the nature of the support and reaction temperature. Methylcyclohexane was also produced, mainly at low temperature and on Ni/α-Al2O3 as catalyst. The products of benzaldehyde hydrogenation (benzylalcohol, toluene and methylcyclohexane) and hydrogenolysis (benzene) were preferentially formed at low/ middle and high reaction temperature respectively. The observed selectivities also suggested the existence of bifunctional sites for both the hydrogenation and hydrogenolysis reactions. These sites were believed to be involved as acidic/cationic centers for the adsorption of the oxygenate molecules and metal center for the hydrogenation or hydrogenolysis step.
Affiliations:
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Pascal:06-0425311Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Benzaldehyde hydrogenation over supported nickel catalysts</title>
<author><name sortKey="Saadi, A" sort="Saadi, A" uniqKey="Saadi A" first="A." last="Saadi">A. Saadi</name>
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<country>Algérie</country>
<wicri:noRegion>16111 Bab-Ezzouar</wicri:noRegion>
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<author><name sortKey="Merabti, R" sort="Merabti, R" uniqKey="Merabti R" first="R." last="Merabti">R. Merabti</name>
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<author><name sortKey="Rassoul, Z" sort="Rassoul, Z" uniqKey="Rassoul Z" first="Z." last="Rassoul">Z. Rassoul</name>
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<s3>DZA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
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</affiliation>
</author>
<author><name sortKey="Bettahar, M M" sort="Bettahar, M M" uniqKey="Bettahar M" first="M. M." last="Bettahar">M. M. Bettahar</name>
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<sZ>4 aut.</sZ>
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<series><title level="j" type="main">Journal of molecular catalysis. A, Chemical</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alumina</term>
<term>Benzaldehyde</term>
<term>Catalyst support</term>
<term>Cerium Oxides</term>
<term>Heterogeneous catalysis</term>
<term>Hydrogenation</term>
<term>Nickel</term>
<term>Silica</term>
<term>Supported catalyst</term>
<term>Titanium oxide</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Benzaldéhyde</term>
<term>Hydrogénation</term>
<term>Catalyseur sur support</term>
<term>Catalyse hétérogène</term>
<term>Support catalyseur</term>
<term>Nickel</term>
<term>Alumine</term>
<term>Silice</term>
<term>Titane oxyde</term>
<term>Cérium Oxyde</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Nickel</term>
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<front><div type="abstract" xml:lang="en">The hydrogenation of benzaldehyde over nickel catalysts supported on Al<sub>2</sub>
O<sub>3</sub>
, SiO<sub>2</sub>
, TiO<sub>2</sub>
and CeO<sub>2</sub>
was studied at atmospheric pressure in the range temperature of 70-140°C under H<sub>2</sub>
flow. They were characterized by their BET surface area, XRD spectra, reducibility properties under H<sub>2</sub>
. The obtained products were benzylalcohol, toluene, benzene with yields depending on the nature of the support and reaction temperature. Methylcyclohexane was also produced, mainly at low temperature and on Ni/α-Al<sub>2</sub>
O<sub>3</sub>
as catalyst. The products of benzaldehyde hydrogenation (benzylalcohol, toluene and methylcyclohexane) and hydrogenolysis (benzene) were preferentially formed at low/ middle and high reaction temperature respectively. The observed selectivities also suggested the existence of bifunctional sites for both the hydrogenation and hydrogenolysis reactions. These sites were believed to be involved as acidic/cationic centers for the adsorption of the oxygenate molecules and metal center for the hydrogenation or hydrogenolysis step.</div>
</front>
</TEI>
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<li>France</li>
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<li>Lorraine (région)</li>
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<li>Vandœuvre-lès-Nancy</li>
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<orgName><li>Université Henri Poincaré</li>
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<tree><country name="Algérie"><noRegion><name sortKey="Saadi, A" sort="Saadi, A" uniqKey="Saadi A" first="A." last="Saadi">A. Saadi</name>
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<name sortKey="Merabti, R" sort="Merabti, R" uniqKey="Merabti R" first="R." last="Merabti">R. Merabti</name>
<name sortKey="Rassoul, Z" sort="Rassoul, Z" uniqKey="Rassoul Z" first="Z." last="Rassoul">Z. Rassoul</name>
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<country name="France"><region name="Grand Est"><name sortKey="Bettahar, M M" sort="Bettahar, M M" uniqKey="Bettahar M" first="M. M." last="Bettahar">M. M. Bettahar</name>
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