Pd-graphites were prepared by reduction of PdCl2-graphite intercalation com
pounds (PdCl2-GICs). Transmission electron microscope (TEM) measurements on
the samples indicated that Pd nanoparticles with a wide size distribution
were formed, mostly encapsulated inside the graphite host. The quasi-two-di
mensional character of the Pd nanoparticles was confirmed by H-2 sorption s
tudies, which revealed the absence of P-hydride formation over a broad rang
e of pressure. Although the structures of the three Pd-graphites studied we
re very similar, differences were found between them in terms of their cata
lytic performance in the gas-phase reactions of 1-butene, cis-2-pentene and
cyclohexene. It was established that the transformations of both 1-butene
and cis-2-pentene took place in the interlamellar space of the graphite, wh
ereas, in consequence of the the non-planar character of the substrate, the
diffusion of cyclohexene between the graphite layers was sterically hinder
ed. This molecular sieving effect implies that the Pd-graphites may be rega
rded as shape-selective catalysts. Pretreatment at 473 K was found to lower
the catalytic activities considerably. The experimental evidence indicated
that restructuring of the Pd crystallites resulted in a moderate aggregati
on of the active Pd-particles available for the reactant molecules. (C) 200
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