Isomerization of n-hexane over silica-supported heteropoly acids promoted by the reduced Ce-Ni oxides
Identifieur interne : 000A25 ( Main/Exploration ); précédent : 000A24; suivant : 000A26Isomerization of n-hexane over silica-supported heteropoly acids promoted by the reduced Ce-Ni oxides
Auteurs : WENXING KUANG [France] ; Alain Rives [France] ; BOUCHTA OULED BEN TAYEB [France, Maroc] ; Michel Fournier [France] ; Robert Hubaut [France]Source :
- Journal of colloid and interface science [ 0021-9797 ] ; 2002.
Descripteurs français
- Pascal (Inist)
- Isomérisation, Hexane, Silice, Hétéropolyacide, Cérium Oxyde, Nickel Oxyde, Réduction chimique, Catalyseur modifié, Catalyseur sur support, Promoteur, Hydrocarbure, Alcane, Spectrométrie Raman, Coke, Désactivation, Catalyse hétérogène, Tungstosilicique acide, Tungstophosphorique acide, Tungstoborique acide.
- Wicri :
- topic : Hydrocarbure, Coke.
English descriptors
- KwdEn :
Abstract
The structure and catalytic properties of silica-supported heteropoly acids promoted by the reduced Ce-Ni oxides are first studied by using chemical analysis XRD, FT-Raman, XPS, EPR, TG, surface area measurements, and microreactor test. It is found that silica-supported heteropoly acids have isomerization activity, but are very easy to deactivate by coke deposition. With the promotion of the reduced Ce-Ni oxides, however, the better activity and the higher selectivity to isomers could be obtained, suggesting that the reduced Ce-Ni oxides really have hydrogenating/dehydrogenating functions. Moreover, it is found that the presence of the reduced Ce-Ni oxides is not only beneficial for eliminating the coke deposition, but also effective for maintaining the structure of silica-supported heteropoly acids during reaction. The effect of the composition of the mechanical mixtures of silica-supported heteropoly acids and the Ce-Ni oxides on the catalytic properties has been explored.
Affiliations:
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Le document en format XML
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<term>Cerium Oxides</term>
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<term>Deactivation</term>
<term>Heterogeneous catalysis</term>
<term>Heteropolyacid</term>
<term>Hexane</term>
<term>Hydrocarbon</term>
<term>Isomerization</term>
<term>Modified catalyst</term>
<term>Nickel Oxides</term>
<term>Promoter</term>
<term>Raman spectrometry</term>
<term>Silica</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Isomérisation</term>
<term>Hexane</term>
<term>Silice</term>
<term>Hétéropolyacide</term>
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<term>Nickel Oxyde</term>
<term>Réduction chimique</term>
<term>Catalyseur modifié</term>
<term>Catalyseur sur support</term>
<term>Promoteur</term>
<term>Hydrocarbure</term>
<term>Alcane</term>
<term>Spectrométrie Raman</term>
<term>Coke</term>
<term>Désactivation</term>
<term>Catalyse hétérogène</term>
<term>Tungstosilicique acide</term>
<term>Tungstophosphorique acide</term>
<term>Tungstoborique acide</term>
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<front><div type="abstract" xml:lang="en">The structure and catalytic properties of silica-supported heteropoly acids promoted by the reduced Ce-Ni oxides are first studied by using chemical analysis XRD, FT-Raman, XPS, EPR, TG, surface area measurements, and microreactor test. It is found that silica-supported heteropoly acids have isomerization activity, but are very easy to deactivate by coke deposition. With the promotion of the reduced Ce-Ni oxides, however, the better activity and the higher selectivity to isomers could be obtained, suggesting that the reduced Ce-Ni oxides really have hydrogenating/dehydrogenating functions. Moreover, it is found that the presence of the reduced Ce-Ni oxides is not only beneficial for eliminating the coke deposition, but also effective for maintaining the structure of silica-supported heteropoly acids during reaction. The effect of the composition of the mechanical mixtures of silica-supported heteropoly acids and the Ce-Ni oxides on the catalytic properties has been explored.</div>
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