Hydrogen production from formic acid vapour over a Pd/C catalyst promoted by potassium salts: evidence for participation of buffer-like solution in the pores of the catalyst
Doping a 1 wt.% Pd/C catalyst with alkali metal carbonates has a very significant promotional effect on its activity in hydrogen production from the decomposition of formic acid vapour (2 vol.%, 1 bar), potassium and caesium carbonates giving the largest effects. The K carbonate species present on the fresh catalysts react with formic acid to form formate ions, these being dissolved in a formic acid/water solution condensed in the pores of the support. The steady-state activities of the samples containing formate ions were 1-2 orders of magnitude greater than those of the unpromoted Pd/C and CO content was lower than 30 ppm. The activation energies for the reaction increased with doping from 66 to 88-99 kJ mo1-1, relatively independent of the cation of the dopant. Similar but lesser effects were found with unsupported Pd nanocrystals doped with K carbonate. The rate-determining step for the promoted samples appears to be the decomposition of formate ions on the Pd surface. (C) 2014 Elsevier B.V. All rights reserved.
History
Publication
Applied Catalysis B: Environmental;160-161, pp. 35-43
Publisher
Elsevier
Note
peer-reviewed
Other Funding information
SFI, Chinese Scholarship Council, Irish Government’s Programme for Research in Third Level Institutions, Cycle 4
Rights
This is the author’s version of a work that was accepted for publication in Applied Catalysis B: Environmental. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Applied Catalysis B: Environmental, 160-161, pp. 35=43, http://dx.doi.org/10.1016/j.apcatb.2014.05.004