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Total oxidation of propene and propane over gold-copper oxide on alumina catalysts Comparison with Pt/Al2O3

Identifieur interne : 000155 ( PascalFrancis/Checkpoint ); précédent : 000154; suivant : 000156

Total 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 :

RBID : Pascal:06-0371423

Descripteurs français

English descriptors

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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<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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<name sortKey="Gluhoi, Andreea C" sort="Gluhoi, Andreea C" uniqKey="Gluhoi A" first="Andreea C." last="Gluhoi">Andreea C. Gluhoi</name>
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<name sortKey="Bogdanchikova, Nina" sort="Bogdanchikova, Nina" uniqKey="Bogdanchikova N" first="Nina" last="Bogdanchikova">Nina Bogdanchikova</name>
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<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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<name sortKey="Gluhoi, Andreea C" sort="Gluhoi, Andreea C" uniqKey="Gluhoi A" first="Andreea C." last="Gluhoi">Andreea C. Gluhoi</name>
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<s1>Department of Heterogeneous Catalysis and Surface Chemistry, Leiden Institute of Chemistry, Leiden University, P.O. Box 9502</s1>
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<name sortKey="Bogdanchikova, Nina" sort="Bogdanchikova, Nina" uniqKey="Bogdanchikova N" first="Nina" last="Bogdanchikova">Nina Bogdanchikova</name>
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<s1>Centro de Ciencias de la Materia Condensada, UNAM, Km. 107, Carretera Tijuana-Ensenada</s1>
<s2>22800 Ensenada, Baja California</s2>
<s3>MEX</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Mexique</country>
<wicri:noRegion>22800 Ensenada, Baja California</wicri:noRegion>
</affiliation>
</author>
<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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<s1>Department of Heterogeneous Catalysis and Surface Chemistry, Leiden Institute of Chemistry, Leiden University, P.O. Box 9502</s1>
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<sZ>1 aut.</sZ>
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<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>
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<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Propane</term>
<term>Or</term>
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<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>
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<s1>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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<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
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<sZ>2 aut.</sZ>
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<s2>67034 Strasbourg</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
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<s0>06-0371423</s0>
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<fA60>
<s1>P</s1>
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<fA61>
<s0>A</s0>
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<s0>Catalysis today</s0>
</fA64>
<fA66 i1="01">
<s0>NLD</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>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).</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>001C01A03</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Oxydation</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Oxidation</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Oxidación</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Propène</s0>
<s2>NK</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Propene</s0>
<s2>NK</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Propeno</s0>
<s2>NK</s2>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Propane</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Propane</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Propano</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Or</s0>
<s2>NC</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Gold</s0>
<s2>NC</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Oro</s0>
<s2>NC</s2>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Cuivre oxyde</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Copper oxide</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Cobre óxido</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Alumine</s0>
<s2>NK</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Alumina</s0>
<s2>NK</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Alúmina</s0>
<s2>NK</s2>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Catalyseur sur support</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Supported catalyst</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Catalizador sobre soporte</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Platine</s0>
<s2>NC</s2>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Platinum</s0>
<s2>NC</s2>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Platino</s0>
<s2>NC</s2>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Additif</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Additive</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Aditivo</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Cobalt oxyde</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Cobalt oxide</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Cobalto óxido</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Catalyse hétérogène</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Heterogeneous catalysis</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Catálisis heterogénea</s0>
<s5>11</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Métal transition</s0>
<s2>NC</s2>
<s5>12</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Transition metal</s0>
<s2>NC</s2>
<s5>12</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Metal transición</s0>
<s2>NC</s2>
<s5>12</s5>
</fC07>
<fC07 i1="02" i2="3" l="FRE">
<s0>Métal transition composé</s0>
<s5>13</s5>
</fC07>
<fC07 i1="02" i2="3" l="ENG">
<s0>Transition element compounds</s0>
<s5>13</s5>
</fC07>
<fN21>
<s1>247</s1>
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<fN44 i1="01">
<s1>OTO</s1>
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<s1>OTO</s1>
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<s1>Colloquium on Environment, Materials, Physics and Energy</s1>
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