(166c) Hydrodeoxygenation Or Reforming of Biomass – a DFT Study | AIChE

(166c) Hydrodeoxygenation Or Reforming of Biomass – a DFT Study


Genest, A. - Presenter, Agency for Science, Technology and Research
Roesch, N., Technische Universität München
Basaran, D., Technische Universitaet Muenchen
Chiu, C. C., Agency for Science, Technology and Research

Cost effective conversion of plant and municipal solid waste material (biomass) into materials of higher energy density, to be utilized in the framework of the current carbon-based supply infrastructure, is one of the major challenges for a sustainable future. Aqueous-phase processes proceeding on supported metal catalysts may be a promising approach for the conversion of biomass to alkanes [1], but can also be used for the production of hydrogen [2], along with CO2. These processes and their selectivities are studied for alcohols as model feedstocks to understand mechanisms involved in processing oxygen containing species.

We carried out electronic structure calculations at the DFT level on periodic slab models using VASP. We explored 1- and 2-propanol as models, adsorbed on flat and stepped surfaces of platinum [3-5].

We examined two scenarios generating either H2 or alkanes. On Pt surfaces, hydrogen formation was calculated to be favored over alkane formation, in agreement with experiments [6]. First, we rationalized the experimentally found dissimilar behavior of primary and secondary alcohols in the formation of H2 [3]. After dehydrogenating a primary alcohol in several steps, the C-C bond is cleaved, leading ultimately to carbon dioxide and ethane. Hereby the experimentally observed CO2can be directly released or formed in a subsequent water-gas shift reaction after decarbonylation. Our calculations show that the propensity for C-C bond cleavage depends on the structure of the catalyst surface and on its capability to activate water [4].

The formation of alkanes, involving the cleavage of the alcohol C-O bond on the Pt surface, can proceed by various pathways. For 1-propanol, we present a dehydration-hydrogenation mechanism via propylene as intermediate and a hydrogenolysis mechanism. The former may be able to compete, under acidic conditions, with H2formation [5].


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[2] R. D. Cortright, R. R. Davda, J. A. Dumesic, Nature 2002, 418, 964.

[3] D. Basaran, A. Genest, N. Rösch: J. Catal. 2012, 287, 210.

[4] D. Başaran, A. Genest, J. A. Lercher, N. Rösch, submitted.

[5] C.-c. Chiu, A. Genest, N. Rösch, ChemCatChem 2013, DOI:10.1002/cctc.201300184.

[6] A. Wawrzetz, B. Peng, A. Hrabar, A. Jentys, A. A. Lemonidou, J. A. Lercher, J. Catal. 2010, 269, 411.