Acetaldehyde behavior over platinum based catalyst in hydrogen stream generated by ethanol reforming

Due to the greenhouse effect, hydrogen production from bioethanol reforming is a very important subject in heterogeneous catalysis research. Pt based catalysts are employed in H 2 purification processes and also as electrocatalysts of PEM (“Proton Exchange Membrane”) fuel cells. Hydrogen obtained fr...

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Published inInternational journal of hydrogen energy Vol. 35; no. 24; pp. 13200 - 13205
Main Authors de Lima, Adriana F.F., Colman, Rita C., Zotin, Fátima M.Z., Appel, Lucia G.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.12.2010
Elsevier
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Summary:Due to the greenhouse effect, hydrogen production from bioethanol reforming is a very important subject in heterogeneous catalysis research. Pt based catalysts are employed in H 2 purification processes and also as electrocatalysts of PEM (“Proton Exchange Membrane”) fuel cells. Hydrogen obtained from ethanol reforming may contain, as contaminants, acetaldehyde and small amounts of CO. This aldehyde can be decarbonylated on Pt based catalysts generating carbon monoxide and methane, rendering the hydrogen purification more challenging. Moreover, acetaldehyde might also change the electrocatalyst behavior. Therefore, this contribution aims at studying the acetaldehyde behavior in the presence of platinum based catalysts in hydrogen atmosphere. The Pt/SiO 2, Pt/USY catalysts and an electrocatalyst were characterized by n-butylamine, H 2 and CO 2 adsorption, ATG/DTG measurements and cyclohexane dehydrogenation reaction. It was observed that the acid–basic properties of the supports promote condensation reactions. When in contact with Pt based catalysts, acetaldehyde undergoes C–C and C O bond scissions. The former occurs at a wide range of temperatures, whereas the latter only at low temperatures (<200 °C). The C–C bond scission (decarbonylation) produces methane and CO. The C O bond scission generates carbon residues on the catalyst as well as oxygen species, which in turn is able to eliminate CO from the catalytic surface. The data also show that decarbonylation is not a structure-sensitive reaction.
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ISSN:0360-3199
1879-3487
DOI:10.1016/j.ijhydene.2010.09.030