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. NieuwenhuysSource :
-
Catalysis today [ 0920-5861 ] ; 2006.
RBID : Pascal:06-0371423
Descripteurs français
- Pascal (Inist)
- Oxydation,
Propène,
Propane,
Or,
Cuivre oxyde,
Alumine,
Catalyseur sur support,
Platine,
Additif,
Cobalt oxyde,
Catalyse hétérogène.
English descriptors
- KwdEn :
- Additive,
Alumina,
Cobalt oxide,
Copper oxide,
Gold,
Heterogeneous catalysis,
Oxidation,
Platinum,
Propane,
Propene,
Supported catalyst.
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 |
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A02 | 01 | | | @0 CATTEA |
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A03 | | 1 | | @0 Catal. today |
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A05 | | | | @2 113 |
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A06 | | | | @2 3-4 |
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A08 | 01 | 1 | ENG | @1 Total oxidation of propene and propane over gold-copper oxide on alumina catalysts Comparison with Pt/Al2O3 |
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A09 | 01 | 1 | ENG | @1 Catalysis, Nanomaterials and Environment |
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A11 | 01 | 1 | | @1 GLUHOI (Andreea C.) |
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A11 | 02 | 1 | | @1 BOGDANCHIKOVA (Nina) |
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A11 | 03 | 1 | | @1 NIEUWENHUYS (Bernard E.) |
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A12 | 01 | 1 | | @1 GARIN (François) @9 ed. |
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A12 | 02 | 1 | | @1 MAAMACHE (Mustapha) @9 ed. |
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A12 | 03 | 1 | | @1 SCHMERBER (Guy) @9 ed. |
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A12 | 04 | 1 | | @1 DEMANGEAT (Claude) @9 ed. |
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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. |
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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. |
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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. |
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A15 | 02 | | | @1 Département de Physique, Faculté des Sciences, Université Ferhat Abbas @2 1900 Sétif @3 DZA @Z 2 aut. |
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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. |
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A20 | | | | @1 178-181 |
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A21 | | | | @1 2006 |
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A23 | 01 | | | @0 ENG |
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A43 | 01 | | | @1 INIST @2 21357 @5 354000142867030060 |
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A44 | | | | @0 0000 @1 © 2006 INIST-CNRS. All rights reserved. |
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A45 | | | | @0 19 ref. |
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A47 | 01 | 1 | | @0 06-0371423 |
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A60 | | | | @1 P @2 C |
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A61 | | | | @0 A |
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A64 | 01 | 1 | | @0 Catalysis today |
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A66 | 01 | | | @0 NLD |
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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). |
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C02 | 01 | X | | @0 001C01A03 |
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C03 | 01 | X | FRE | @0 Oxydation @5 01 |
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C03 | 01 | X | ENG | @0 Oxidation @5 01 |
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C03 | 01 | X | SPA | @0 Oxidación @5 01 |
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C03 | 02 | X | FRE | @0 Propène @2 NK @5 02 |
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C03 | 02 | X | ENG | @0 Propene @2 NK @5 02 |
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C03 | 02 | X | SPA | @0 Propeno @2 NK @5 02 |
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C03 | 03 | X | FRE | @0 Propane @2 NK @2 FX @5 03 |
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C03 | 03 | X | ENG | @0 Propane @2 NK @2 FX @5 03 |
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C03 | 03 | X | SPA | @0 Propano @2 NK @2 FX @5 03 |
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C03 | 04 | X | FRE | @0 Or @2 NC @5 04 |
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C03 | 04 | X | ENG | @0 Gold @2 NC @5 04 |
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C03 | 04 | X | SPA | @0 Oro @2 NC @5 04 |
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C03 | 05 | X | FRE | @0 Cuivre oxyde @5 05 |
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C03 | 05 | X | ENG | @0 Copper oxide @5 05 |
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C03 | 05 | X | SPA | @0 Cobre óxido @5 05 |
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C03 | 06 | X | FRE | @0 Alumine @2 NK @5 06 |
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C03 | 06 | X | ENG | @0 Alumina @2 NK @5 06 |
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C03 | 06 | X | SPA | @0 Alúmina @2 NK @5 06 |
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C03 | 07 | X | FRE | @0 Catalyseur sur support @5 07 |
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C03 | 07 | X | ENG | @0 Supported catalyst @5 07 |
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C03 | 07 | X | SPA | @0 Catalizador sobre soporte @5 07 |
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C03 | 08 | X | FRE | @0 Platine @2 NC @5 08 |
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C03 | 08 | X | ENG | @0 Platinum @2 NC @5 08 |
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C03 | 08 | X | SPA | @0 Platino @2 NC @5 08 |
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C03 | 09 | X | FRE | @0 Additif @5 09 |
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C03 | 09 | X | ENG | @0 Additive @5 09 |
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C03 | 09 | X | SPA | @0 Aditivo @5 09 |
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C03 | 10 | X | FRE | @0 Cobalt oxyde @5 10 |
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C03 | 10 | X | ENG | @0 Cobalt oxide @5 10 |
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C03 | 10 | X | SPA | @0 Cobalto óxido @5 10 |
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C03 | 11 | X | FRE | @0 Catalyse hétérogène @5 11 |
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C03 | 11 | X | ENG | @0 Heterogeneous catalysis @5 11 |
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C03 | 11 | X | SPA | @0 Catálisis heterogénea @5 11 |
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C07 | 01 | X | FRE | @0 Métal transition @2 NC @5 12 |
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C07 | 01 | X | ENG | @0 Transition metal @2 NC @5 12 |
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C07 | 01 | X | SPA | @0 Metal transición @2 NC @5 12 |
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C07 | 02 | 3 | FRE | @0 Métal transition composé @5 13 |
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C07 | 02 | 3 | ENG | @0 Transition element compounds @5 13 |
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N21 | | | | @1 247 |
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N44 | 01 | | | @1 OTO |
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N82 | | | | @1 OTO |
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pR |
A30 | 01 | 1 | ENG | @1 Colloquium on Environment, Materials, Physics and Energy @3 Ouargla DZA @4 2004-12-11 |
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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 |
Links to Exploration step
Pascal:06-0371423
Le document en format XML
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O<sub>3</sub>
</title>
<author><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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<s2>2300 RA Leiden</s2>
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<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
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<author><name sortKey="Bogdanchikova, Nina" sort="Bogdanchikova, Nina" uniqKey="Bogdanchikova N" first="Nina" last="Bogdanchikova">Nina Bogdanchikova</name>
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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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<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>
</title>
<author><name sortKey="Gluhoi, Andreea C" sort="Gluhoi, Andreea C" uniqKey="Gluhoi A" first="Andreea C." last="Gluhoi">Andreea C. Gluhoi</name>
<affiliation><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>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Bogdanchikova, Nina" sort="Bogdanchikova, Nina" uniqKey="Bogdanchikova N" first="Nina" last="Bogdanchikova">Nina Bogdanchikova</name>
<affiliation><inist:fA14 i1="02"><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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</affiliation>
</author>
<author><name sortKey="Nieuwenhuys, Bernard E" sort="Nieuwenhuys, Bernard E" uniqKey="Nieuwenhuys B" first="Bernard E." last="Nieuwenhuys">Bernard E. Nieuwenhuys</name>
<affiliation><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>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Catalysis today</title>
<title level="j" type="abbreviated">Catal. today</title>
<idno type="ISSN">0920-5861</idno>
<imprint><date when="2006">2006</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Catalysis today</title>
<title level="j" type="abbreviated">Catal. today</title>
<idno type="ISSN">0920-5861</idno>
</seriesStmt>
</fileDesc>
<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>
</textClass>
</profileDesc>
</teiHeader>
<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>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0920-5861</s0>
</fA01>
<fA02 i1="01"><s0>CATTEA</s0>
</fA02>
<fA03 i2="1"><s0>Catal. today</s0>
</fA03>
<fA05><s2>113</s2>
</fA05>
<fA06><s2>3-4</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><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>
</s1>
</fA08>
<fA09 i1="01" i2="1" l="ENG"><s1>Catalysis, Nanomaterials and Environment</s1>
</fA09>
<fA11 i1="01" i2="1"><s1>GLUHOI (Andreea C.)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>BOGDANCHIKOVA (Nina)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>NIEUWENHUYS (Bernard E.)</s1>
</fA11>
<fA12 i1="01" i2="1"><s1>GARIN (François)</s1>
<s9>ed.</s9>
</fA12>
<fA12 i1="02" i2="1"><s1>MAAMACHE (Mustapha)</s1>
<s9>ed.</s9>
</fA12>
<fA12 i1="03" i2="1"><s1>SCHMERBER (Guy)</s1>
<s9>ed.</s9>
</fA12>
<fA12 i1="04" i2="1"><s1>DEMANGEAT (Claude)</s1>
<s9>ed.</s9>
</fA12>
<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>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="02"><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>
</fA14>
<fA15 i1="01"><s1>Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515-CNRS-ULP-ECPM, 25 rue Becquerel</s1>
<s2>67087 Strasbourg</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
</fA15>
<fA15 i1="02"><s1>Département de Physique, Faculté des Sciences, Université Ferhat Abbas</s1>
<s2>1900 Sétif</s2>
<s3>DZA</s3>
<sZ>2 aut.</sZ>
</fA15>
<fA15 i1="03"><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>
</fA15>
<fA20><s1>178-181</s1>
</fA20>
<fA21><s1>2006</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>21357</s2>
<s5>354000142867030060</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2006 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>19 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>06-0371423</s0>
</fA47>
<fA60><s1>P</s1>
<s2>C</s2>
</fA60>
<fA64 i1="01" i2="1"><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>
</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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