The aluminated sepiolite, obtained by alkaline treatment with KAlO2, a
s well as the silver-exchanged aluminated sepiolite were tested in eth
anol conversion. The reactions were performed at 280 degrees C and wit
h 50 Torr of ethanol in He. After the alumination through KAlO2, ethan
ol dehydrogenation and ethanol dehydration resulted from the Lewis aci
dity. The dispersion of silver led to a bifunctional catalytic system
and the overall catalytic activity and the selectivity towards the ace
taldehyde production increased. As a result of the Prins reaction, a s
ignificant yield in butadiene was observed.