2003
DOI: 10.1016/s0021-9517(02)00035-0
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Hydrogenation/dehydrogenation reactions: isopropanol dehydrogenation over copper catalysts

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Cited by 135 publications
(52 citation statements)
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“…9), and they can be deconvoluted into four contributions: 284.8 eV (C-C bonds), 286.2 eV (C-OH or C-O-C bonds), 287.2 eV (C = O bonds) and 288.7 eV (O-C = O bonds). In this sense, according to the study of several authors on the adsorption heats of FUR, FOL and MF in Cu-based catalysts, it can be assumed that that FOL and mainly FUR are strongly adsorbed on active sites [31,45]. Therefore, the band observed between 286.2 and 288.7 eV can be attributed to the adsorption of reactants and products on the catalyst surface.…”
Section: Catalytic Testsmentioning
confidence: 99%
“…9), and they can be deconvoluted into four contributions: 284.8 eV (C-C bonds), 286.2 eV (C-OH or C-O-C bonds), 287.2 eV (C = O bonds) and 288.7 eV (O-C = O bonds). In this sense, according to the study of several authors on the adsorption heats of FUR, FOL and MF in Cu-based catalysts, it can be assumed that that FOL and mainly FUR are strongly adsorbed on active sites [31,45]. Therefore, the band observed between 286.2 and 288.7 eV can be attributed to the adsorption of reactants and products on the catalyst surface.…”
Section: Catalytic Testsmentioning
confidence: 99%
“…The dehydrogenation of alcohols to aldehydes or ketones is a well-known industrial process, and these reactions are primarily carried out on copper catalysts because of their high selectivity to the dehydrogenation product [27]. Catalytic dehydrogenation of alcohols plays a key role in the chemical industry particularly in the synthesis of various pharmaceuticals and fine chemicals apart from bulk chemicals.…”
Section: Dehydrogenation Of Alcoholsmentioning
confidence: 99%
“…(7). Copper chromite catalysts possess high selectivity and satisfactory activity [27,100] for isopropyl alcohol dehydrogenation (eqn. 11):…”
Section: Dehydrogenation Of Alcoholsmentioning
confidence: 99%
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“…4, where the trend of IPA disappearance was found closely to match that of acetone generation. It is believed that this dehydrogenation involves the abstraction of hydrogen atoms by • OH free radicals from the hydroxyl group ( OH) of IPA (CH 3 COH CH 3 ) molecules to form the corresponding acetone (CH 3 COCH 3 ) molecules [31,32]. Although IPA disappearance rates in both modes were much faster than those of acetone ( Figs.…”
Section: Catalytic Effects Of Gacmentioning
confidence: 99%