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

Identifieur interne : 000168 ( PascalFrancis/Corpus ); précédent : 000167; suivant : 000169

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

Auteurs : Andreea C. Gluhoi ; Nina Bogdanchikova ; Bernard E. Nieuwenhuys

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).

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0920-5861
A02 01      @0 CATTEA
A03   1    @0 Catal. today
A05       @2 113
A06       @2 3-4
A08 01  1  ENG  @1 Total oxidation of propene and propane over gold-copper oxide on alumina catalysts Comparison with Pt/Al2O3
A09 01  1  ENG  @1 Catalysis, Nanomaterials and Environment
A11 01  1    @1 GLUHOI (Andreea C.)
A11 02  1    @1 BOGDANCHIKOVA (Nina)
A11 03  1    @1 NIEUWENHUYS (Bernard E.)
A12 01  1    @1 GARIN (François) @9 ed.
A12 02  1    @1 MAAMACHE (Mustapha) @9 ed.
A12 03  1    @1 SCHMERBER (Guy) @9 ed.
A12 04  1    @1 DEMANGEAT (Claude) @9 ed.
A14 01      @1 Department of Heterogeneous Catalysis and Surface Chemistry, Leiden Institute of Chemistry, Leiden University, P.O. Box 9502 @2 2300 RA Leiden @3 NLD @Z 1 aut. @Z 3 aut.
A14 02      @1 Centro de Ciencias de la Materia Condensada, UNAM, Km. 107, Carretera Tijuana-Ensenada @2 22800 Ensenada, Baja California @3 MEX @Z 2 aut.
A15 01      @1 Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515-CNRS-ULP-ECPM, 25 rue Becquerel @2 67087 Strasbourg @3 FRA @Z 1 aut.
A15 02      @1 Département de Physique, Faculté des Sciences, Université Ferhat Abbas @2 1900 Sétif @3 DZA @Z 2 aut.
A15 03      @1 Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université Louis Pasteur, UMR 7504-CNRS-ULP, 23 rue du Loess, BP 43 @2 67034 Strasbourg @3 FRA @Z 3 aut. @Z 4 aut.
A20       @1 178-181
A21       @1 2006
A23 01      @0 ENG
A43 01      @1 INIST @2 21357 @5 354000142867030060
A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
A45       @0 19 ref.
A47 01  1    @0 06-0371423
A60       @1 P @2 C
A61       @0 A
A64 01  1    @0 Catalysis today
A66 01      @0 NLD
C01 01    ENG  @0 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).
C02 01  X    @0 001C01A03
C03 01  X  FRE  @0 Oxydation @5 01
C03 01  X  ENG  @0 Oxidation @5 01
C03 01  X  SPA  @0 Oxidación @5 01
C03 02  X  FRE  @0 Propène @2 NK @5 02
C03 02  X  ENG  @0 Propene @2 NK @5 02
C03 02  X  SPA  @0 Propeno @2 NK @5 02
C03 03  X  FRE  @0 Propane @2 NK @2 FX @5 03
C03 03  X  ENG  @0 Propane @2 NK @2 FX @5 03
C03 03  X  SPA  @0 Propano @2 NK @2 FX @5 03
C03 04  X  FRE  @0 Or @2 NC @5 04
C03 04  X  ENG  @0 Gold @2 NC @5 04
C03 04  X  SPA  @0 Oro @2 NC @5 04
C03 05  X  FRE  @0 Cuivre oxyde @5 05
C03 05  X  ENG  @0 Copper oxide @5 05
C03 05  X  SPA  @0 Cobre óxido @5 05
C03 06  X  FRE  @0 Alumine @2 NK @5 06
C03 06  X  ENG  @0 Alumina @2 NK @5 06
C03 06  X  SPA  @0 Alúmina @2 NK @5 06
C03 07  X  FRE  @0 Catalyseur sur support @5 07
C03 07  X  ENG  @0 Supported catalyst @5 07
C03 07  X  SPA  @0 Catalizador sobre soporte @5 07
C03 08  X  FRE  @0 Platine @2 NC @5 08
C03 08  X  ENG  @0 Platinum @2 NC @5 08
C03 08  X  SPA  @0 Platino @2 NC @5 08
C03 09  X  FRE  @0 Additif @5 09
C03 09  X  ENG  @0 Additive @5 09
C03 09  X  SPA  @0 Aditivo @5 09
C03 10  X  FRE  @0 Cobalt oxyde @5 10
C03 10  X  ENG  @0 Cobalt oxide @5 10
C03 10  X  SPA  @0 Cobalto óxido @5 10
C03 11  X  FRE  @0 Catalyse hétérogène @5 11
C03 11  X  ENG  @0 Heterogeneous catalysis @5 11
C03 11  X  SPA  @0 Catálisis heterogénea @5 11
C07 01  X  FRE  @0 Métal transition @2 NC @5 12
C07 01  X  ENG  @0 Transition metal @2 NC @5 12
C07 01  X  SPA  @0 Metal transición @2 NC @5 12
C07 02  3  FRE  @0 Métal transition composé @5 13
C07 02  3  ENG  @0 Transition element compounds @5 13
N21       @1 247
N44 01      @1 OTO
N82       @1 OTO
pR  
A30 01  1  ENG  @1 Colloquium on Environment, Materials, Physics and Energy @3 Ouargla DZA @4 2004-12-11

Format Inist (serveur)

NO : PASCAL 06-0371423 INIST
ET : Total oxidation of propene and propane over gold-copper oxide on alumina catalysts Comparison with Pt/Al2O3
AU : GLUHOI (Andreea C.); BOGDANCHIKOVA (Nina); NIEUWENHUYS (Bernard E.); GARIN (François); MAAMACHE (Mustapha); SCHMERBER (Guy); DEMANGEAT (Claude)
AF : Department of Heterogeneous Catalysis and Surface Chemistry, Leiden Institute of Chemistry, Leiden University, P.O. Box 9502/2300 RA Leiden/Pays-Bas (1 aut., 3 aut.); Centro de Ciencias de la Materia Condensada, UNAM, Km. 107, Carretera Tijuana-Ensenada/22800 Ensenada, Baja California/Mexique (2 aut.); Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515-CNRS-ULP-ECPM, 25 rue Becquerel/67087 Strasbourg/France (1 aut.); Département de Physique, Faculté des Sciences, Université Ferhat Abbas/1900 Sétif/Algérie (2 aut.); Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université Louis Pasteur, UMR 7504-CNRS-ULP, 23 rue du Loess, BP 43/67034 Strasbourg/France (3 aut., 4 aut.)
DT : Publication en série; Congrès; Niveau analytique
SO : Catalysis today; ISSN 0920-5861; Coden CATTEA; Pays-Bas; Da. 2006; Vol. 113; No. 3-4; Pp. 178-181; Bibl. 19 ref.
LA : Anglais
EA : 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).
CC : 001C01A03
FD : Oxydation; Propène; Propane; Or; Cuivre oxyde; Alumine; Catalyseur sur support; Platine; Additif; Cobalt oxyde; Catalyse hétérogène
FG : Métal transition; Métal transition composé
ED : Oxidation; Propene; Propane; Gold; Copper oxide; Alumina; Supported catalyst; Platinum; Additive; Cobalt oxide; Heterogeneous catalysis
EG : Transition metal; Transition element compounds
SD : Oxidación; Propeno; Propano; Oro; Cobre óxido; Alúmina; Catalizador sobre soporte; Platino; Aditivo; Cobalto óxido; Catálisis heterogénea
LO : INIST-21357.354000142867030060
ID : 06-0371423

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Pascal:06-0371423

Le document en format XML

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O
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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
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<title level="j" type="main">Catalysis today</title>
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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>
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<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>
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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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<s1>Department of Heterogeneous Catalysis and Surface Chemistry, Leiden Institute of Chemistry, Leiden University, P.O. Box 9502</s1>
<s2>2300 RA Leiden</s2>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14>
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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>
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<sZ>1 aut.</sZ>
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<s1>Département de Physique, Faculté des Sciences, Université Ferhat Abbas</s1>
<s2>1900 Sétif</s2>
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<sZ>2 aut.</sZ>
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<s1>Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université Louis Pasteur, UMR 7504-CNRS-ULP, 23 rue du Loess, BP 43</s1>
<s2>67034 Strasbourg</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
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<s1>P</s1>
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</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>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
<pR>
<fA30 i1="01" i2="1" l="ENG">
<s1>Colloquium on Environment, Materials, Physics and Energy</s1>
<s3>Ouargla DZA</s3>
<s4>2004-12-11</s4>
</fA30>
</pR>
</standard>
<server>
<NO>PASCAL 06-0371423 INIST</NO>
<ET>Total oxidation of propene and propane over gold-copper oxide on alumina catalysts Comparison with Pt/Al
<sub>2</sub>
O
<sub>3</sub>
</ET>
<AU>GLUHOI (Andreea C.); BOGDANCHIKOVA (Nina); NIEUWENHUYS (Bernard E.); GARIN (François); MAAMACHE (Mustapha); SCHMERBER (Guy); DEMANGEAT (Claude)</AU>
<AF>Department of Heterogeneous Catalysis and Surface Chemistry, Leiden Institute of Chemistry, Leiden University, P.O. Box 9502/2300 RA Leiden/Pays-Bas (1 aut., 3 aut.); Centro de Ciencias de la Materia Condensada, UNAM, Km. 107, Carretera Tijuana-Ensenada/22800 Ensenada, Baja California/Mexique (2 aut.); Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515-CNRS-ULP-ECPM, 25 rue Becquerel/67087 Strasbourg/France (1 aut.); Département de Physique, Faculté des Sciences, Université Ferhat Abbas/1900 Sétif/Algérie (2 aut.); Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université Louis Pasteur, UMR 7504-CNRS-ULP, 23 rue du Loess, BP 43/67034 Strasbourg/France (3 aut., 4 aut.)</AF>
<DT>Publication en série; Congrès; Niveau analytique</DT>
<SO>Catalysis today; ISSN 0920-5861; Coden CATTEA; Pays-Bas; Da. 2006; Vol. 113; No. 3-4; Pp. 178-181; Bibl. 19 ref.</SO>
<LA>Anglais</LA>
<EA>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).</EA>
<CC>001C01A03</CC>
<FD>Oxydation; Propène; Propane; Or; Cuivre oxyde; Alumine; Catalyseur sur support; Platine; Additif; Cobalt oxyde; Catalyse hétérogène</FD>
<FG>Métal transition; Métal transition composé</FG>
<ED>Oxidation; Propene; Propane; Gold; Copper oxide; Alumina; Supported catalyst; Platinum; Additive; Cobalt oxide; Heterogeneous catalysis</ED>
<EG>Transition metal; Transition element compounds</EG>
<SD>Oxidación; Propeno; Propano; Oro; Cobre óxido; Alúmina; Catalizador sobre soporte; Platino; Aditivo; Cobalto óxido; Catálisis heterogénea</SD>
<LO>INIST-21357.354000142867030060</LO>
<ID>06-0371423</ID>
</server>
</inist>
</record>

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