Characterization and mechanism study of aqueous cationic polymerization of p-methylstyrene

Aqueous cationic polymerization has attracted considerable interest as a novel polymerization technique, because it conforms to the green chemistry trend and challenges the concept of traditional cationic polymerization. In this paper, a CumOH/B(C6F5)(3)/Et2O system was used to initiate the aqueous polymerization of p-methylstyrene through suspension and emulsion methods. Several types of surfactants were used, including the cationic surfactant CTAB, non-ionic surfactant NP-40, and anionic surfactant SDBS, and the influences of initiator concentration and temperature on polymerization were investigated. Consistent with previous literature, initiator activity was positively correlated with temperature unlike in traditional cationic polymerization. Gaussian 09W simulation software was used to calculate and optimize changes in the bond lengths and angles of B(C6F5)(3) after ether was added to the system. The addition of ether increased the polarity of B(C6F5)(3), rendering it soluble in water. H-1-NMR was used in identifying the main chain and terminal structures of the polymer, and the mechanism of p-methylstyrene aqueous phase cationic polymerization was proposed.

Automated summary

This paper explores the novel technique of aqueous cationic polymerization and investigates the relationship between initiator activity and temperature, as well as the impact of ether on system polarity through experimentation and simulation. The results suggest that this method has the potential for application in the environmentally friendly field of green chemistry.