Serveur d'exploration sur le cobalt au Maghreb

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Effects of support and metal loading on the characteristics of Co based catalysts for selective hydrogenation of citral

Identifieur interne : 000160 ( PascalFrancis/Curation ); précédent : 000159; suivant : 000161

Effects of support and metal loading on the characteristics of Co based catalysts for selective hydrogenation of citral

Auteurs : K. Kouachi [France, Algérie] ; G. Lafaye [France] ; C. Especel [France] ; O. Cherifi [Algérie] ; P. Mardcota [France]

Source :

RBID : Pascal:08-0229737

Descripteurs français

English descriptors

Abstract

Silica-, alumina- and titania-supported Co catalysts with different metal loadings were tested for selective citral hydrogenation in liquid phase. Temperature programmed desorption of hydrogen (H2-TPD) indicated that the catalysts with the highest unsaturated alcohols selectivities present particular H-Co species. Electron diffraction and XRD measurements revealed that these species would be linked to the presence of Co0 hexagonal phase. According to the results obtained by TEM and cyclohexane dehydrogenation, these two properties would be present on large Co particles.
pA  
A01 01  1    @0 1381-1169
A03   1    @0 J. mol. catal., A Chem.
A05       @2 280
A06       @2 1-2
A08 01  1  ENG  @1 Effects of support and metal loading on the characteristics of Co based catalysts for selective hydrogenation of citral
A11 01  1    @1 KOUACHI (K.)
A11 02  1    @1 LAFAYE (G.)
A11 03  1    @1 ESPECEL (C.)
A11 04  1    @1 CHERIFI (O.)
A11 05  1    @1 MARDCOTA (P.)
A14 01      @1 Université de Poitiers, Laboratoire de Catalyse en Chimie Organique, UMR 6503 @2 86022 Poitiers @3 FRA @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 5 aut.
A14 02      @1 Laboratoire de Chimie de Gaz Naturel, Faculté de Chimie, USTHB, BP 32 @2 16111 El Alia, Bab Ezzouar @3 DZA @Z 1 aut. @Z 4 aut.
A20       @1 52-60
A21       @1 2008
A23 01      @0 ENG
A43 01      @1 INIST @2 17107A @5 354000174594710090
A44       @0 0000 @1 © 2008 INIST-CNRS. All rights reserved.
A45       @0 58 ref.
A47 01  1    @0 08-0229737
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of molecular catalysis. A, Chemical
A66 01      @0 NLD
C01 01    ENG  @0 Silica-, alumina- and titania-supported Co catalysts with different metal loadings were tested for selective citral hydrogenation in liquid phase. Temperature programmed desorption of hydrogen (H2-TPD) indicated that the catalysts with the highest unsaturated alcohols selectivities present particular H-Co species. Electron diffraction and XRD measurements revealed that these species would be linked to the presence of Co0 hexagonal phase. According to the results obtained by TEM and cyclohexane dehydrogenation, these two properties would be present on large Co particles.
C02 01  X    @0 001C01A03
C03 01  X  FRE  @0 Support @5 01
C03 01  X  ENG  @0 Support @5 01
C03 01  X  SPA  @0 Soporte @5 01
C03 02  X  FRE  @0 Monoxyde de carbone @2 NK @2 FX @5 02
C03 02  X  ENG  @0 Carbon monoxide @2 NK @2 FX @5 02
C03 02  X  SPA  @0 Carbono monóxido @2 NK @2 FX @5 02
C03 03  X  FRE  @0 Catalyseur @5 03
C03 03  X  ENG  @0 Catalyst @5 03
C03 03  X  SPA  @0 Catalizador @5 03
C03 04  X  FRE  @0 Hydrogénation @5 04
C03 04  X  ENG  @0 Hydrogenation @5 04
C03 04  X  SPA  @0 Hidrogenación @5 04
C03 05  X  FRE  @0 Citral @2 NK @2 FR @5 05
C03 05  X  ENG  @0 Citral @2 NK @2 FR @5 05
C03 06  X  FRE  @0 Cobalt @2 NC @5 06
C03 06  X  ENG  @0 Cobalt @2 NC @5 06
C03 06  X  SPA  @0 Cobalto @2 NC @5 06
C03 07  X  FRE  @0 Silice @2 NK @2 FX @5 08
C03 07  X  ENG  @0 Silica @2 NK @2 FX @5 08
C03 07  X  SPA  @0 Sílice @2 NK @2 FX @5 08
C03 08  X  FRE  @0 Alumine @2 NK @5 09
C03 08  X  ENG  @0 Alumina @2 NK @5 09
C03 08  X  SPA  @0 Alúmina @2 NK @5 09
C03 09  X  FRE  @0 Oxyde de titane @5 10
C03 09  X  ENG  @0 Titanium oxide @5 10
C03 09  X  SPA  @0 Titanio óxido @5 10
C03 10  X  FRE  @0 Catalyseur sur support @5 11
C03 10  X  ENG  @0 Supported catalyst @5 11
C03 10  X  SPA  @0 Catalizador sobre soporte @5 11
C03 11  X  FRE  @0 Catalyse hétérogène @5 12
C03 11  X  ENG  @0 Heterogeneous catalysis @5 12
C03 11  X  SPA  @0 Catálisis heterogénea @5 12
C03 12  X  FRE  @0 Aldéhyde @5 13
C03 12  X  ENG  @0 Aldehyde @5 13
C03 12  X  SPA  @0 Aldehído @5 13
C07 01  X  FRE  @0 Métal transition @2 NC @5 07
C07 01  X  ENG  @0 Transition metal @2 NC @5 07
C07 01  X  SPA  @0 Metal transición @2 NC @5 07
N21       @1 147

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Pascal:08-0229737

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<name sortKey="Cherifi, O" sort="Cherifi, O" uniqKey="Cherifi O" first="O." last="Cherifi">O. Cherifi</name>
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<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
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<title level="j" type="main">Journal of molecular catalysis. A, Chemical</title>
<title level="j" type="abbreviated">J. mol. catal., A Chem.</title>
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<term>Aldehyde</term>
<term>Alumina</term>
<term>Carbon monoxide</term>
<term>Catalyst</term>
<term>Citral</term>
<term>Cobalt</term>
<term>Heterogeneous catalysis</term>
<term>Hydrogenation</term>
<term>Silica</term>
<term>Support</term>
<term>Supported catalyst</term>
<term>Titanium oxide</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Support</term>
<term>Monoxyde de carbone</term>
<term>Catalyseur</term>
<term>Hydrogénation</term>
<term>Citral</term>
<term>Cobalt</term>
<term>Silice</term>
<term>Alumine</term>
<term>Oxyde de titane</term>
<term>Catalyseur sur support</term>
<term>Catalyse hétérogène</term>
<term>Aldéhyde</term>
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<term>Cobalt</term>
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<front>
<div type="abstract" xml:lang="en">Silica-, alumina- and titania-supported Co catalysts with different metal loadings were tested for selective citral hydrogenation in liquid phase. Temperature programmed desorption of hydrogen (H
<sub>2</sub>
-TPD) indicated that the catalysts with the highest unsaturated alcohols selectivities present particular H-Co species. Electron diffraction and XRD measurements revealed that these species would be linked to the presence of Co
<sup>0</sup>
hexagonal phase. According to the results obtained by TEM and cyclohexane dehydrogenation, these two properties would be present on large Co particles.</div>
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<s2>86022 Poitiers</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Laboratoire de Chimie de Gaz Naturel, Faculté de Chimie, USTHB, BP 32</s1>
<s2>16111 El Alia, Bab Ezzouar</s2>
<s3>DZA</s3>
<sZ>1 aut.</sZ>
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<s0>Silica-, alumina- and titania-supported Co catalysts with different metal loadings were tested for selective citral hydrogenation in liquid phase. Temperature programmed desorption of hydrogen (H
<sub>2</sub>
-TPD) indicated that the catalysts with the highest unsaturated alcohols selectivities present particular H-Co species. Electron diffraction and XRD measurements revealed that these species would be linked to the presence of Co
<sup>0</sup>
hexagonal phase. According to the results obtained by TEM and cyclohexane dehydrogenation, these two properties would be present on large Co particles.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>001C01A03</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Support</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Support</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Soporte</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Monoxyde de carbone</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Carbon monoxide</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Carbono monóxido</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Catalyseur</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Catalyst</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Catalizador</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Hydrogénation</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Hydrogenation</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Hidrogenación</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Citral</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Citral</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Cobalt</s0>
<s2>NC</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Cobalt</s0>
<s2>NC</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Cobalto</s0>
<s2>NC</s2>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Silice</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Silica</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Sílice</s0>
<s2>NK</s2>
<s2>FX</s2>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Alumine</s0>
<s2>NK</s2>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Alumina</s0>
<s2>NK</s2>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Alúmina</s0>
<s2>NK</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Oxyde de titane</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Titanium oxide</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Titanio óxido</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Catalyseur sur support</s0>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Supported catalyst</s0>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Catalizador sobre soporte</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Catalyse hétérogène</s0>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Heterogeneous catalysis</s0>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Catálisis heterogénea</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Aldéhyde</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Aldehyde</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Aldehído</s0>
<s5>13</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Métal transition</s0>
<s2>NC</s2>
<s5>07</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Transition metal</s0>
<s2>NC</s2>
<s5>07</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Metal transición</s0>
<s2>NC</s2>
<s5>07</s5>
</fC07>
<fN21>
<s1>147</s1>
</fN21>
</pA>
</standard>
</inist>
</record>

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