Total oxidation of propene and propane over gold-copper oxide on alumina catalysts Comparison with Pt/Al2O3
Identifieur interne : 000866 ( Main/Exploration ); précédent : 000865; suivant : 000867Total oxidation of propene and propane over gold-copper oxide on alumina catalysts Comparison with Pt/Al2O3
Auteurs : Andreea C. Gluhoi [Pays-Bas] ; Nina Bogdanchikova [Mexique] ; Bernard E. Nieuwenhuys [Pays-Bas]Source :
- Catalysis today [ 0920-5861 ] ; 2006.
Descripteurs français
- Pascal (Inist)
- Wicri :
English descriptors
- KwdEn :
Abstract
Oxidation of propene and propane to CO2 and H2O has been studied over Au/Al2O3 and two different Au/CuO/Al2O3 (4 wt.% Au and 7.4 wt.% Au) catalysts and compared with the catalytic behaviour of Au/Co3O4/Al2O3 (4.1 wt.% Au) and Pt/Al2O3 (4.8 wt.% Pt) catalysts. The various characterization techniques employed (XRD, HRTEM, TPR and DR-UV-vis) revealed the presence of metallic gold, along with a highly dispersed CuO (6 wt.% CuO), or more crystalline CuO phase (12 wt.% CuO). A higher CuO loading does not significantly influence the catalytic performance of the catalyst in propene oxidation, the gold loading appears to be more important. Moreover, it was found that 7.4Au/CuO/Al2O3 is almost as active as Pt/Al2O3, whereas Au/Co3O4/Al2O3 performs less than any of the CuO-containing gold-based catalysts. The light-off temperature for C3H8 oxidation is significantly higher than for C3H6. For this reaction the particle size effect appears to prevail over the effect of gold loading. The most active catalysts are 4Au/CuO/Al2O3 (gold particles less than 3 nm) and 4Au/Co3O4/Al2O3 (gold particles less than 5 nm).
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Total oxidation of propene and propane over gold-copper oxide on alumina catalysts Comparison with Pt/Al<sub>2</sub>
O<sub>3</sub>
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<author><name sortKey="Gluhoi, Andreea C" sort="Gluhoi, Andreea C" uniqKey="Gluhoi A" first="Andreea C." last="Gluhoi">Andreea C. Gluhoi</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Heterogeneous Catalysis and Surface Chemistry, Leiden Institute of Chemistry, Leiden University, P.O. Box 9502</s1>
<s2>2300 RA Leiden</s2>
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<author><name sortKey="Bogdanchikova, Nina" sort="Bogdanchikova, Nina" uniqKey="Bogdanchikova N" first="Nina" last="Bogdanchikova">Nina Bogdanchikova</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Centro de Ciencias de la Materia Condensada, UNAM, Km. 107, Carretera Tijuana-Ensenada</s1>
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<s3>MEX</s3>
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<author><name sortKey="Nieuwenhuys, Bernard E" sort="Nieuwenhuys, Bernard E" uniqKey="Nieuwenhuys B" first="Bernard E." last="Nieuwenhuys">Bernard E. Nieuwenhuys</name>
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<series><title level="j" type="main">Catalysis today</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Additive</term>
<term>Alumina</term>
<term>Cobalt oxide</term>
<term>Copper oxide</term>
<term>Gold</term>
<term>Heterogeneous catalysis</term>
<term>Oxidation</term>
<term>Platinum</term>
<term>Propane</term>
<term>Propene</term>
<term>Supported catalyst</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Oxydation</term>
<term>Propène</term>
<term>Propane</term>
<term>Or</term>
<term>Cuivre oxyde</term>
<term>Alumine</term>
<term>Catalyseur sur support</term>
<term>Platine</term>
<term>Additif</term>
<term>Cobalt oxyde</term>
<term>Catalyse hétérogène</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Propane</term>
<term>Or</term>
<term>Platine</term>
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<front><div type="abstract" xml:lang="en">Oxidation of propene and propane to CO<sub>2</sub>
and H<sub>2</sub>
O has been studied over Au/Al<sub>2</sub>
O<sub>3</sub>
and two different Au/CuO/Al<sub>2</sub>
O<sub>3</sub>
(4 wt.% Au and 7.4 wt.% Au) catalysts and compared with the catalytic behaviour of Au/Co<sub>3</sub>
O<sub>4</sub>
/Al<sub>2</sub>
O<sub>3</sub>
(4.1 wt.% Au) and Pt/Al<sub>2</sub>
O<sub>3</sub>
(4.8 wt.% Pt) catalysts. The various characterization techniques employed (XRD, HRTEM, TPR and DR-UV-vis) revealed the presence of metallic gold, along with a highly dispersed CuO (6 wt.% CuO), or more crystalline CuO phase (12 wt.% CuO). A higher CuO loading does not significantly influence the catalytic performance of the catalyst in propene oxidation, the gold loading appears to be more important. Moreover, it was found that 7.4Au/CuO/Al<sub>2</sub>
O<sub>3</sub>
is almost as active as Pt/Al<sub>2</sub>
O<sub>3</sub>
, whereas Au/Co<sub>3</sub>
O<sub>4</sub>
/Al<sub>2</sub>
O<sub>3</sub>
performs less than any of the CuO-containing gold-based catalysts. The light-off temperature for C<sub>3</sub>
H<sub>8</sub>
oxidation is significantly higher than for C<sub>3</sub>
H<sub>6</sub>
. For this reaction the particle size effect appears to prevail over the effect of gold loading. The most active catalysts are 4Au/CuO/Al<sub>2</sub>
O<sub>3</sub>
(gold particles less than 3 nm) and 4Au/Co<sub>3</sub>
O<sub>4</sub>
/Al<sub>2</sub>
O<sub>3</sub>
(gold particles less than 5 nm).</div>
</front>
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<affiliations><list><country><li>Mexique</li>
<li>Pays-Bas</li>
</country>
</list>
<tree><country name="Pays-Bas"><noRegion><name sortKey="Gluhoi, Andreea C" sort="Gluhoi, Andreea C" uniqKey="Gluhoi A" first="Andreea C." last="Gluhoi">Andreea C. Gluhoi</name>
</noRegion>
<name sortKey="Nieuwenhuys, Bernard E" sort="Nieuwenhuys, Bernard E" uniqKey="Nieuwenhuys B" first="Bernard E." last="Nieuwenhuys">Bernard E. Nieuwenhuys</name>
</country>
<country name="Mexique"><noRegion><name sortKey="Bogdanchikova, Nina" sort="Bogdanchikova, Nina" uniqKey="Bogdanchikova N" first="Nina" last="Bogdanchikova">Nina Bogdanchikova</name>
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