The catalytic performance of alkali (K+ and Na+)-promoted Pt/Al2O3 catalysts for the complete oxidation of ethanol present in trace amounts (500 ppm) in air has been investigated. Pure alumina acts mainly as an acidic catalyst producing diethyl ether and ethylene, while complete oxidation of ethanol to CO2 requires temperatures higher than 400 degrees C. Addition of alkalis in alumina neutralizes its acidic sites and suppresses the formation of diethylether and ethylene. Ethanol oxidation over the Pt/Al2O3 catalyst results in the formation of partially oxidized compounds, such as acetaldehyde and acetic acid, as well as CO2 at higher temperatures. Alkali-promoted catalysts do not produce acetic acid and are significantly more active than un-promoted Pt/Al2O3, especially when they have been pre-reduced. The most effective catalyst was Pt/Al2O3 (K/Al = 0.10), in which complete oxidation of ethanol to CO2 was achieved at similar to 220 degrees C, while complete oxidation of ethanol over the un-promoted catalyst was obtained at 280 degrees C. (c) 2006 Elsevier B.V. All rights reserved.
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Univ Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, FranceUniv Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, France
Blasin-Aubé, V
Belkouch, J
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Univ Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, FranceUniv Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, France
Belkouch, J
Monceaux, L
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Univ Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, FranceUniv Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, France
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Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, SwedenRoyal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Ferrandon, M
Ferrand, B
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机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Ferrand, B
Björnbom, E
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机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Björnbom, E
Klingstedt, F
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机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Klingstedt, F
Neyestanaki, AK
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机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Neyestanaki, AK
Karhu, H
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机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Karhu, H
Väyrynen, IJ
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机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
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Univ Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, FranceUniv Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, France
Blasin-Aubé, V
Belkouch, J
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Univ Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, FranceUniv Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, France
Belkouch, J
Monceaux, L
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Univ Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, FranceUniv Technol Compiegne, Genie Procedes Ind UMR 6067, F-60206 Compiegne, France
机构:
Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, SwedenRoyal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Ferrandon, M
Ferrand, B
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机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Ferrand, B
Björnbom, E
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h-index: 0
机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Björnbom, E
Klingstedt, F
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h-index: 0
机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Klingstedt, F
Neyestanaki, AK
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h-index: 0
机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Neyestanaki, AK
Karhu, H
论文数: 0引用数: 0
h-index: 0
机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden
Karhu, H
Väyrynen, IJ
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机构:Royal Inst Technol, Dept Chem Engn & Technol, Div Chem React Engn, SE-10044 Stockholm, Sweden