“…Supercritical drying in excess of solvent Catalyst support, prepared by previously described procedure, was transferred to the pressure vessel (Autoclave Engineers BTRS-Jr, Division of Snap-title, Inc., Erie, PA, USA) and the vessel was filled with additional 170 ml of ethanol. Such a procedure was necessary to ensure that the pores in the obtained material were always filled with single phase ethanol (liquid, supercritical or gas) thereby avoiding formation of the two phase region (liquid-gas) in the pores [46,47,48]. The vessel was then sealed and heated (heating rate 3.3 C˚/min, total time of heating was 70 min) to the desired temperature and pressure of 100 bars and 528 K. Upon the reaction completion, after half an hour, the system was depressurized to atmospheric pressure followed by gradual temperature decrease to ambient conditions.…”