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Synthesis of acrolein by oxidative coupling of alcohols over spinel catalysts: microcalorimetric and spectroscopic approaches
Oxidative coupling of methanol and ethanol is becoming a promising alternative to produce sustainable acrolein. In this work, the reaction has been performed in two successive reactors (for oxidation and aldolization respectively) in order to study the role of the acid/base properties of spinel cata...
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Published in: | Catalysis science & technology 2020-01, Vol.1 (6), p.1889-191 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Oxidative coupling of methanol and ethanol is becoming a promising alternative to produce sustainable acrolein. In this work, the reaction has been performed in two successive reactors (for oxidation and aldolization respectively) in order to study the role of the acid/base properties of spinel catalysts with various Al/Mg ratios. The acid/base properties of catalysts were investigated by NH
3
and SO
2
adsorption microcalorimetry. To deeply investigate the adsorption mechanism of the reactants on the catalysts, other adsorption microcalorimetry studies coupled to FTIR were performed using methanol, formaldehyde, acetaldehyde and propionaldehyde. Catalytic results were correlated to FTIR spectra and revealed the disproportionation of formaldehyde. Co-adsorption of aldehydes was also investigated by FTIR showing a preferential adsorption of formaldehyde compared to acetaldehyde. The different species resulting from aldehyde adsorption are discussed.
Oxidative coupling of methanol and ethanol is becoming a promising alternative to produce sustainable acrolein. |
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ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/d0cy00094a |