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Effect of the basicity created by La2O3 addition on the catalytic properties of Co(O)/SiO2 in CH4 + CO2 reaction

Identifieur interne : 000122 ( PascalFrancis/Curation ); précédent : 000121; suivant : 000123

Effect of the basicity created by La2O3 addition on the catalytic properties of Co(O)/SiO2 in CH4 + CO2 reaction

Auteurs : R. Bouarab [Algérie, France] ; O. Cherifi [Algérie] ; A. Auroux [France]

Source :

RBID : Pascal:06-0041062

Descripteurs français

English descriptors

Abstract

A series of Co(O)/SiO2 catalysts modified by various amounts of La2O3 (5, 10 or 50 wt.%) were synthesized and studied in the reaction of reforming of methane by carbon dioxide to syngas at the temperature of 873 K. The catalysts were prepared by successive incipient wetness impregnation: La2O3-SiO2 supports were first prepared by impregnating silica with La(NO3)3 solutions. After drying and calcining under airflow, samples were then submitted to a second impregnation with Co(NO3)2. The purpose of this work is to study the acid-base property of these catalysts by CO2 adsorption calorimetry at 353 K and to look at their impact on the catalytic property. The amounts of chemisorbed CO2 and the site strength distribution of the basic sites, i.e., the basicity, were shown to be strongly dependent on La2O3 content. The following order of basicity was observed: Co(0)/5 wt.%La2O3-SiO2 < Co(0)/10 wt.%La2O3-SiO2 «Co(O)/50 wt.%La2O3-SiO2. The addition of La2O3 to the Co(O)/SiO2 reference sample revealed a very positive effect on the catalytic stability of catalysts. La2O3 prevented cobalt phase sintering by avoiding particle coalescence.
pA  
A01 01  1    @0 0040-6031
A02 01      @0 THACAS
A03   1    @0 Thermochim. acta
A05       @2 434
A06       @2 1-2
A08 01  1  ENG  @1 Effect of the basicity created by La2O3 addition on the catalytic properties of Co(O)/SiO2 in CH4 + CO2 reaction
A09 01  1  ENG  @1 Calorimetry and Thermal Effects in Catalysis: A Collection of Papers from the Third International Symposium on Calorimetry and Thermal Effects in Catalysis held in Lyon, France, July 6-9, 2004
A11 01  1    @1 BOUARAB (R.)
A11 02  1    @1 CHERIFI (O.)
A11 03  1    @1 AUROUX (A.)
A12 01  1    @1 AUROUX (Aline) @9 ed.
A14 01      @1 Département des Sciences Fondamentales, Ecole Nationale Polytechnique, 10 av. Pasteur @2 El Harrach @3 DZA @Z 1 aut.
A14 02      @1 Institut de Recherches sur la Catalyse, CNRS, 2 av. Einstein @2 69626 Villeurbanne @3 FRA @Z 1 aut. @Z 3 aut.
A14 03      @1 Laboratoire de Chimie de Gaz Naturel, Faculté de Chimie, U.S.T.H.B., BP 32 @2 16111 El Alla, Bah Ezzouar @3 DZA @Z 2 aut.
A15 01      @1 CNRS, Institut de Recherches sur la Catalyse, 2 avenue A. Einstein @2 69626 Villeurbanne @3 FRA @Z 1 aut.
A20       @1 69-73
A21       @1 2005
A23 01      @0 ENG
A43 01      @1 INIST @2 14753 @5 354000131483590110
A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
A45       @0 14 ref.
A47 01  1    @0 06-0041062
A60       @1 P @2 C
A61       @0 A
A64 01  1    @0 Thermochimica acta
A66 01      @0 NLD
C01 01    ENG  @0 A series of Co(O)/SiO2 catalysts modified by various amounts of La2O3 (5, 10 or 50 wt.%) were synthesized and studied in the reaction of reforming of methane by carbon dioxide to syngas at the temperature of 873 K. The catalysts were prepared by successive incipient wetness impregnation: La2O3-SiO2 supports were first prepared by impregnating silica with La(NO3)3 solutions. After drying and calcining under airflow, samples were then submitted to a second impregnation with Co(NO3)2. The purpose of this work is to study the acid-base property of these catalysts by CO2 adsorption calorimetry at 353 K and to look at their impact on the catalytic property. The amounts of chemisorbed CO2 and the site strength distribution of the basic sites, i.e., the basicity, were shown to be strongly dependent on La2O3 content. The following order of basicity was observed: Co(0)/5 wt.%La2O3-SiO2 < Co(0)/10 wt.%La2O3-SiO2 «Co(O)/50 wt.%La2O3-SiO2. The addition of La2O3 to the Co(O)/SiO2 reference sample revealed a very positive effect on the catalytic stability of catalysts. La2O3 prevented cobalt phase sintering by avoiding particle coalescence.
C02 01  X    @0 001C01A03B
C03 01  X  FRE  @0 Basicité @5 01
C03 01  X  ENG  @0 Alkalinity @5 01
C03 01  X  SPA  @0 Alcalinidad @5 01
C03 02  X  FRE  @0 Lanthane oxyde @5 02
C03 02  X  ENG  @0 Lanthanum oxide @5 02
C03 02  X  SPA  @0 Lantano óxido @5 02
C03 03  X  FRE  @0 Silice @1 ACT @2 NK @2 FX @5 03
C03 03  X  ENG  @0 Silica @1 ACT @2 NK @2 FX @5 03
C03 03  X  SPA  @0 Sílice @1 ACT @2 NK @2 FX @5 03
C03 04  X  FRE  @0 Carbone dioxyde @2 NK @2 FX @5 04
C03 04  X  ENG  @0 Carbon dioxide @2 NK @2 FX @5 04
C03 04  X  SPA  @0 Carbono dióxido @2 NK @2 FX @5 04
C03 05  X  FRE  @0 Méthane @2 NK @2 FX @5 05
C03 05  X  ENG  @0 Methane @2 NK @2 FX @5 05
C03 05  X  SPA  @0 Metano @2 NK @2 FX @5 05
C03 06  X  FRE  @0 Reformage @5 06
C03 06  X  ENG  @0 Reforming @5 06
C03 06  X  SPA  @0 Reformación @5 06
C03 07  X  FRE  @0 Catalyseur @5 07
C03 07  X  ENG  @0 Catalyst @5 07
C03 07  X  SPA  @0 Catalizador @5 07
C03 08  X  FRE  @0 Additif @5 08
C03 08  X  ENG  @0 Additive @5 08
C03 08  X  SPA  @0 Aditivo @5 08
C03 09  X  FRE  @0 Cobalt Oxyde @1 ACT @2 NC @2 NA @5 09
C03 09  X  ENG  @0 Cobalt Oxides @1 ACT @2 NC @2 NA @5 09
C03 09  X  SPA  @0 Cobalto Óxido @1 ACT @2 NC @2 NA @5 09
C03 10  X  FRE  @0 Activité catalytique @5 10
C03 10  X  ENG  @0 Catalyst activity @5 10
C03 10  X  SPA  @0 Actividad catalítica @5 10
N21       @1 016
pR  
A30 01  1  ENG  @1 International Symposium on Calorimetry and Thermal Effects in Catalysis @2 3 @3 Lyon FRA @4 2004-07-06

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<term>Catalyst activity</term>
<term>Cobalt Oxides</term>
<term>Lanthanum oxide</term>
<term>Methane</term>
<term>Reforming</term>
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<term>Méthane</term>
<term>Reformage</term>
<term>Catalyseur</term>
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<div type="abstract" xml:lang="en">A series of Co(O)/SiO
<sub>2</sub>
catalysts modified by various amounts of La
<sub>2</sub>
O
<sub>3</sub>
(5, 10 or 50 wt.%) were synthesized and studied in the reaction of reforming of methane by carbon dioxide to syngas at the temperature of 873 K. The catalysts were prepared by successive incipient wetness impregnation: La
<sub>2</sub>
O
<sub>3</sub>
-SiO
<sub>2</sub>
supports were first prepared by impregnating silica with La(NO
<sub>3</sub>
)
<sub>3</sub>
solutions. After drying and calcining under airflow, samples were then submitted to a second impregnation with Co(NO
<sub>3</sub>
)
<sub>2</sub>
. The purpose of this work is to study the acid-base property of these catalysts by CO
<sub>2</sub>
adsorption calorimetry at 353 K and to look at their impact on the catalytic property. The amounts of chemisorbed CO
<sub>2</sub>
and the site strength distribution of the basic sites, i.e., the basicity, were shown to be strongly dependent on La
<sub>2</sub>
O
<sub>3</sub>
content. The following order of basicity was observed: Co(0)/5 wt.%La
<sub>2</sub>
O
<sub>3</sub>
-SiO
<sub>2</sub>
< Co(0)/10 wt.%La
<sub>2</sub>
O
<sub>3</sub>
-SiO
<sub>2</sub>
«Co(O)/50 wt.%La
<sub>2</sub>
O
<sub>3</sub>
-SiO
<sub>2</sub>
. The addition of La
<sub>2</sub>
O
<sub>3</sub>
to the Co(O)/SiO
<sub>2</sub>
reference sample revealed a very positive effect on the catalytic stability of catalysts. La
<sub>2</sub>
O
<sub>3</sub>
prevented cobalt phase sintering by avoiding particle coalescence.</div>
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<s1>Effect of the basicity created by La
<sub>2</sub>
O
<sub>3</sub>
addition on the catalytic properties of Co(O)/SiO
<sub>2</sub>
in CH
<sub>4</sub>
+ CO
<sub>2</sub>
reaction</s1>
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</fA66>
<fC01 i1="01" l="ENG">
<s0>A series of Co(O)/SiO
<sub>2</sub>
catalysts modified by various amounts of La
<sub>2</sub>
O
<sub>3</sub>
(5, 10 or 50 wt.%) were synthesized and studied in the reaction of reforming of methane by carbon dioxide to syngas at the temperature of 873 K. The catalysts were prepared by successive incipient wetness impregnation: La
<sub>2</sub>
O
<sub>3</sub>
-SiO
<sub>2</sub>
supports were first prepared by impregnating silica with La(NO
<sub>3</sub>
)
<sub>3</sub>
solutions. After drying and calcining under airflow, samples were then submitted to a second impregnation with Co(NO
<sub>3</sub>
)
<sub>2</sub>
. The purpose of this work is to study the acid-base property of these catalysts by CO
<sub>2</sub>
adsorption calorimetry at 353 K and to look at their impact on the catalytic property. The amounts of chemisorbed CO
<sub>2</sub>
and the site strength distribution of the basic sites, i.e., the basicity, were shown to be strongly dependent on La
<sub>2</sub>
O
<sub>3</sub>
content. The following order of basicity was observed: Co(0)/5 wt.%La
<sub>2</sub>
O
<sub>3</sub>
-SiO
<sub>2</sub>
< Co(0)/10 wt.%La
<sub>2</sub>
O
<sub>3</sub>
-SiO
<sub>2</sub>
«Co(O)/50 wt.%La
<sub>2</sub>
O
<sub>3</sub>
-SiO
<sub>2</sub>
. The addition of La
<sub>2</sub>
O
<sub>3</sub>
to the Co(O)/SiO
<sub>2</sub>
reference sample revealed a very positive effect on the catalytic stability of catalysts. La
<sub>2</sub>
O
<sub>3</sub>
prevented cobalt phase sintering by avoiding particle coalescence.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>001C01A03B</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Basicité</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Alkalinity</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Alcalinidad</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Lanthane oxyde</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Lanthanum oxide</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Lantano óxido</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Silice</s0>
<s1>ACT</s1>
<s2>NK</s2>
<s2>FX</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Silica</s0>
<s1>ACT</s1>
<s2>NK</s2>
<s2>FX</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Sílice</s0>
<s1>ACT</s1>
<s2>NK</s2>
<s2>FX</s2>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Carbone dioxyde</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Carbon dioxide</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Carbono dióxido</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Méthane</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Methane</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Metano</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Reformage</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Reforming</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Reformación</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Catalyseur</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Catalyst</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Catalizador</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Additif</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Additive</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Aditivo</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Cobalt Oxyde</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Cobalt Oxides</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Cobalto Óxido</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Activité catalytique</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Catalyst activity</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Actividad catalítica</s0>
<s5>10</s5>
</fC03>
<fN21>
<s1>016</s1>
</fN21>
</pA>
<pR>
<fA30 i1="01" i2="1" l="ENG">
<s1>International Symposium on Calorimetry and Thermal Effects in Catalysis</s1>
<s2>3</s2>
<s3>Lyon FRA</s3>
<s4>2004-07-06</s4>
</fA30>
</pR>
</standard>
</inist>
</record>

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   |texte=   Effect of the basicity created by La2O3 addition on the catalytic properties of Co(O)/SiO2 in CH4 + CO2 reaction
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