Abstract
Various samples of nanosized V2O5 (2–20 wt%)/TiO2 catalytic systems (of particle sizes ranged between 5 and 50 nm were characterized. The effect of addition of MoO3 (3–9 wt%), in different sequences, was followed up in view of competing interactions with titania surface. Characterization was performed through XRD, FTIR, BET, and TEM techniques. Catalytic activity of prepared samples was tested in redox-initiated polymerization of methyl methacrylate, in presence of NaHSO3 cocatalyst. The proposed polymerization mechanism indicated participation of radicals, primarily generated on a TiO2 surface, with V5+/V4+ and/or Mo6+/Mo5+ redox pairs to form active radical species with the monomer. In all cases, extremely high yields of reasonably high molecular weight polymers, of syndiotactic-structure, were functions of catalyst nanosized nature, rapid redox-initiation steps, and mode of MoO3 addition.
Notes
a I: isotacticity, H: heterotacticity and S: syndiotacticity (ratios in %).