The silver-hafnium phosphate (AgHf2(PO4)(3)), belonging to the Nasicon-type
structure, was synthesized by a sol-gel method and characterized by severa
l techniques. The Ag+ cations were found to be, as in zeolite frameworks, e
asy to reduce to metallic silver. This reduction was investigated by STEM/E
DX which showed that, under an intense electron beam, the Ag+ ions diffuse
toward the surface of the sample and form metallic particles of sizes varyi
ng from 3 to 15 nm, The X-ray diffraction patterns confirmed that the reduc
tion does not damage the phosphate structure, The Ag+ ions were replaced in
the structure by protons giving rise to (PO-H) acid groups.
The catalytic behavior of AgHf2(PO4)(3) was studied in butan-2-ol conversio
n. In the absence of O-2, the reaction leads to an abrupt decrease of the d
ehydrogenation activity and a dehydration reaction that reaches a pseudo-st
ationary state. Concomittantly, the Ag+ cations are reduced to Ag-0. In the
presence of O-2, the dehydrogenation reaction undergoes a complex transito
ry state which can be decomposed into two steps. During the first one, the
activity decreases in concert with the reduction of Ag+ ions. Tn the second
step it increases as the amount of oxidized silver species (AgxOy), which
are the active sites for the alcohol dehydrogenation, increases.
UV-VIS characterization of AgHf2(PO4)(3) in dynamic conditions similar to t
hose used in the catalytic tests confirmed that butan-2-ol reduces Ag+ ions
to metallic silver which, in the presence of O-2 in the reaction mixture,
are oxidized to (AgxOy). (C) 2001 Elsevier Science B.V. All rights reserved
.