Abstract

Poly(methyl methacrylate- co-glycidyl methacrylate–tris(hydroxymethyl)aminomethane) (PMGT) copolymers were obtained by copolymerization of methyl methacrylate (MMA) and a chelating monomer, glycidyl methacrylate–tris(hydroxymethyl)aminomethane (GMA–Tris), with potassium persulfate as an initiator. The glass transition temperature ( T g) and the proton spin-lattice relaxation time in the rotating frame ( T 1 ρ H ) substantiated the formation of random copolymers. Borate-loaded PMGT (BPMGT) complexes were prepared by mixing PMGT and boric acid solution. The formation of coordination bond between PMGT and borate was studied using differential scanning calorimetry, infrared and 13C solid-state nuclear magnetic resonance spectroscopy. A single composition dependent T g was obtained for the PMGT copolymers. The T g value of BPMGT complex was much higher than that of PMGT copolymer with the same composition. The T 1 ρ H of the main chains in the PMGT copolymers and BPMGT complexes had one value, and that in the complexes was higher than that in the copolymers. The apparent activation energy ( E a) of the thermo-oxidative degradation of Tris units in complexes was larger than that in copolymers, whereas the E a value of the MMA–GMA matrix was reversed.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call