Vanadium-containing ordered mesoporous silicates: Does the silica source really affect the catalytic activity, structural stability, and nature of vanadium sites in V-MCM-41?

Abstract

A series of vanadium-substituted mesoporous materials were synthesized hydrothermally with the use of two commonly used silica sources, fumed silica and tetra ethyl orthosilicate. The extent of mesopore structural ordering was confirmed from X-ray diffraction, N 2 physisorption, SEM, and TEM, and the presence and nature of vanadium species inside the framework of the MCM-41 matrix was confirmed in detail with the use of various characterization techniques like FT-IR, 29Si MAS NMR, DRUV–vis, EPR, 51V MAS NMR, and Raman analysis. It is deduced from the above characterization techniques that, regardless of the silica source, vanadium is incorporated into the silica framework and thereby increases the structural ordering and wall thickness of the mesoporous material. Thermal and hydrothermal studies performed over the V-MCM-41 catalysts show that the Si O Si inorganic backbone from a fumed silica source is more resistant to severe thermal treatments and hydrolysis than the tetraethyl orthosilicate-synthesized catalysts. Spectroscopic characterization reveals the existence of easily accessible isolated tetrahedral vanadium sites on V-MCM-41 catalyst prepared from fumed silica catalyst, whereas the sample obtained from a tetraethyl orthosilicate silica source shows vanadium in more disordered sites. Catalytic results show that both catalysts display excellent activity toward the epoxidation reaction of bulkier olefins, and the exceptional activity of the fumed silica catalyst may arise from the more isolated tetrahedral sites and the complementary textural characteristics, which may facilitate the easy access of substrate to the isolated framework metal sites.