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Surface characterization of alumina-supported catalysts prepared by sol-gel method. Part II.-Surface reactivity with CO

Identifieur interne : 010860 ( Main/Repository ); précédent : 010859; suivant : 010861

Surface characterization of alumina-supported catalysts prepared by sol-gel method. Part II.-Surface reactivity with CO

Auteurs : RBID : Pascal:01-0258335

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Abstract

Surface reactivity toward H2 and CO using a pulse method was investigated for Al2O3, In2O3-Al2O3and Ga2O3-Al2O3. It was found that reduction by either CO or H2 and reoxidation by O2 occurred reversibly on In2O3-Al2O3. Although the surface of Ga2O3-Al2O3 was hardly reduced by H2, CO consumption and CO2 formation was observed on exposure to CO. Mass spectroscopic analysis revealed the formation of H2 from injection of CO pulses on Ga2O3 Al2O3, while small amounts of H2 were detected on In2O3-Al2O3. The formation of H2 on Ga2O3Al2O3 was also evidenced by Fourier transform infrared (FT-IR) spectroscopy. Namely, when Ga2O3-Al2O3 was exposed to CO at elevated temperatures above 573 K, the IR band assignable to Gay+-H species was detected at 1997 cm-1. A reaction model in which the reaction of CO with basic hydroxy groups occurs on the surface of Ga2O3-Al2O3 (CO + OH → CO2 + 1/2H2) is proposed.

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Pascal:01-0258335

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<name sortKey="Hamada, Hideaki" uniqKey="Hamada H">Hideaki Hamada</name>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Alumina</term>
<term>Carbon monoxide</term>
<term>Catalyst activity</term>
<term>Catalytic reaction</term>
<term>Chemical reactivity</term>
<term>Chemical reduction</term>
<term>Experimental study</term>
<term>Gallium oxide</term>
<term>Indium oxide</term>
<term>Infrared spectrometry</term>
<term>Redox catalysis</term>
<term>Supported catalyst</term>
<term>Surface activity</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Etude expérimentale</term>
<term>Réaction catalytique</term>
<term>Réduction chimique</term>
<term>Carbone monoxyde</term>
<term>Catalyseur sur support</term>
<term>Gallium oxyde</term>
<term>Indium oxyde</term>
<term>Alumine</term>
<term>Catalyse redox</term>
<term>Réactivité chimique</term>
<term>Activité catalytique</term>
<term>Activité superficielle</term>
<term>Spectrométrie IR</term>
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<front>
<div type="abstract" xml:lang="en">Surface reactivity toward H
<sub>2</sub>
and CO using a pulse method was investigated for Al
<sub>2</sub>
O
<sub>3</sub>
, In
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
and Ga
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
. It was found that reduction by either CO or H
<sub>2</sub>
and reoxidation by O
<sub>2</sub>
occurred reversibly on In
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
. Although the surface of Ga
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
was hardly reduced by H
<sub>2</sub>
, CO consumption and CO
<sub>2</sub>
formation was observed on exposure to CO. Mass spectroscopic analysis revealed the formation of H
<sub>2</sub>
from injection of CO pulses on Ga
<sub>2</sub>
O
<sub>3</sub>
Al
<sub>2</sub>
O
<sub>3</sub>
, while small amounts of H
<sub>2</sub>
were detected on In
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
. The formation of H
<sub>2</sub>
on Ga
<sub>2</sub>
O
<sub>3</sub>
Al
<sub>2</sub>
O
<sub>3</sub>
was also evidenced by Fourier transform infrared (FT-IR) spectroscopy. Namely, when Ga
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
was exposed to CO at elevated temperatures above 573 K, the IR band assignable to Ga
<sup>y+</sup>
-H species was detected at 1997 cm
<sup>-1</sup>
. A reaction model in which the reaction of CO with basic hydroxy groups occurs on the surface of Ga
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
(CO + OH → CO
<sub>2</sub>
+ 1/2H
<sub>2</sub>
) is proposed.</div>
</front>
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<s0>Surface reactivity toward H
<sub>2</sub>
and CO using a pulse method was investigated for Al
<sub>2</sub>
O
<sub>3</sub>
, In
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
and Ga
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
. It was found that reduction by either CO or H
<sub>2</sub>
and reoxidation by O
<sub>2</sub>
occurred reversibly on In
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
. Although the surface of Ga
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
was hardly reduced by H
<sub>2</sub>
, CO consumption and CO
<sub>2</sub>
formation was observed on exposure to CO. Mass spectroscopic analysis revealed the formation of H
<sub>2</sub>
from injection of CO pulses on Ga
<sub>2</sub>
O
<sub>3</sub>
Al
<sub>2</sub>
O
<sub>3</sub>
, while small amounts of H
<sub>2</sub>
were detected on In
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
. The formation of H
<sub>2</sub>
on Ga
<sub>2</sub>
O
<sub>3</sub>
Al
<sub>2</sub>
O
<sub>3</sub>
was also evidenced by Fourier transform infrared (FT-IR) spectroscopy. Namely, when Ga
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
was exposed to CO at elevated temperatures above 573 K, the IR band assignable to Ga
<sup>y+</sup>
-H species was detected at 1997 cm
<sup>-1</sup>
. A reaction model in which the reaction of CO with basic hydroxy groups occurs on the surface of Ga
<sub>2</sub>
O
<sub>3</sub>
-Al
<sub>2</sub>
O
<sub>3</sub>
(CO + OH → CO
<sub>2</sub>
+ 1/2H
<sub>2</sub>
) is proposed.</s0>
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<s0>Supported catalyst</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Catalizador sobre soporte</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Gallium oxyde</s0>
<s1>ACT</s1>
<s5>07</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Gallium oxide</s0>
<s1>ACT</s1>
<s5>07</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Galio óxido</s0>
<s1>ACT</s1>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Indium oxyde</s0>
<s1>ACT</s1>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Indium oxide</s0>
<s1>ACT</s1>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Indio óxido</s0>
<s1>ACT</s1>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Alumine</s0>
<s1>SUB</s1>
<s2>NK</s2>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Alumina</s0>
<s1>SUB</s1>
<s2>NK</s2>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Alúmina</s0>
<s1>SUB</s1>
<s2>NK</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Catalyse redox</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Redox catalysis</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Catálisis redox</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Réactivité chimique</s0>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Chemical reactivity</s0>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Reactividad química</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Activité catalytique</s0>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Catalyst activity</s0>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Actividad catalítica</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Activité superficielle</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Surface activity</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Actividad superficial</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Spectrométrie IR</s0>
<s5>14</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Infrared spectrometry</s0>
<s5>14</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Espectrometría IR</s0>
<s5>14</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Métal Composé</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>06</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Metal Compounds</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>06</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Metal Compuesto</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>06</s5>
</fC07>
<fN21>
<s1>176</s1>
</fN21>
</pA>
</standard>
</inist>
</record>

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