The hydrogenolysis and the aqueous phase reforming of glycerol have been investigated under mild reaction conditions, using water as the reaction medium and Pd/Fe as the catalyst. The experiments, in the presence of added H-2 or under inert atmosphere, clearly show that the dehydration/hydrogenation route is the key step in the case of C-O bond cleavage (hydrogenolysis) while dehydrogenation is a prerequisite for C-C bond breaking (APR), with the latter favoured at higher reaction temperatures. The temperature dependence of the C-C and C-O bond rupture is discussed by taking into account the bond energies involved in the competitive hydrogenolysis and APR reactions. Finally, the Pd/Fe catalyst was also tested in the hydrogenolysis and APR of ethylene glycol in the same temperature range, with the aim of clarifying the selective cleavage of C-O and C-C bonds in biomass derived C-2-C-3 polyols.

Hydrogenolysis vs. aqueous phase reforming (APR) of glycerol promoted by a heterogeneous Pd/Fe catalyst

VINCI, ALESSANDRO
Secondo
;
ESPRO, Claudia;GUMINA, BIANCA;
2015-01-01

Abstract

The hydrogenolysis and the aqueous phase reforming of glycerol have been investigated under mild reaction conditions, using water as the reaction medium and Pd/Fe as the catalyst. The experiments, in the presence of added H-2 or under inert atmosphere, clearly show that the dehydration/hydrogenation route is the key step in the case of C-O bond cleavage (hydrogenolysis) while dehydrogenation is a prerequisite for C-C bond breaking (APR), with the latter favoured at higher reaction temperatures. The temperature dependence of the C-C and C-O bond rupture is discussed by taking into account the bond energies involved in the competitive hydrogenolysis and APR reactions. Finally, the Pd/Fe catalyst was also tested in the hydrogenolysis and APR of ethylene glycol in the same temperature range, with the aim of clarifying the selective cleavage of C-O and C-C bonds in biomass derived C-2-C-3 polyols.
2015
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3107805
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