The preparation of a new amorphous mesoporous silica-titania (MST) is here reported. Following a modification of the standard procedure employed in the preparation of TS-1, a material showing a narrow pore size distribution in the mesopore region (approximate to 30 A mean pore diameter) is obtained. The catalytic features, tested in the epoxidation of a series of unsaturated terpenic alcohols, were compared with those of an ordered mesoporous material as Ti-containing MCM-41. MST displayed mainly a higher activity than [Ti]-MCM-41 and a progressive increase in epoxidation rate was observed passing from bishomoallylic to allylic alcohols. Under these conditions, a global improvement in alkene conversion was achieved using methylacetate as solvent, without a remarkable loss in epoxide selectivity. During repeated recycles no significant changes in both catalytic performances and active metal content were recorded.
A comparison between [Ti]-MCM-41 and amorphous mesoporous silica-titania as catalysts for the epoxidation of bulky unsaturated alcohols / Berlini, C.; Ferraris, G.; Guidotti, M.; Moretti, Giuliano; Psaro, R.; Ravasio, N.. - In: MICROPOROUS AND MESOPOROUS MATERIALS. - ISSN 1387-1811. - 44-45:(2001), pp. 595-602. [10.1016/s1387-1811(01)00239-6]
A comparison between [Ti]-MCM-41 and amorphous mesoporous silica-titania as catalysts for the epoxidation of bulky unsaturated alcohols
MORETTI, GIULIANO;
2001
Abstract
The preparation of a new amorphous mesoporous silica-titania (MST) is here reported. Following a modification of the standard procedure employed in the preparation of TS-1, a material showing a narrow pore size distribution in the mesopore region (approximate to 30 A mean pore diameter) is obtained. The catalytic features, tested in the epoxidation of a series of unsaturated terpenic alcohols, were compared with those of an ordered mesoporous material as Ti-containing MCM-41. MST displayed mainly a higher activity than [Ti]-MCM-41 and a progressive increase in epoxidation rate was observed passing from bishomoallylic to allylic alcohols. Under these conditions, a global improvement in alkene conversion was achieved using methylacetate as solvent, without a remarkable loss in epoxide selectivity. During repeated recycles no significant changes in both catalytic performances and active metal content were recorded.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.