Radiation crosslinking of linear polyethyleneimine‐based nanoparticles grafted to poly(glycidyl methacrylate) via trimethylolpropane triacrylate as potential electronic packaging material

Abstract

AbstractLinear polyethyleneimine (L‐PEI)‐based nanoparticles were synthesized via hydrolysis of poly‐2‐methyl‐2‐oxazoline (PMeOx), which was prepared by cationic ring‐opening polymerization of the oxazoline five‐membered ring. Herein, a kinetic study of the ring‐opening polymerization reaction is discussed. The nuclear magnetic resonance spectrum of PMeOx verified the presence of repeating units and terminal groups in the polymer's structure. Molar ratios of PEI and PMeOx were characterized using size exclusion chromatography with low‐polydispersity polymer chains as the controlled polymerization reaction. PEI and PMeOx exhibited narrow particle size distribution with hydrodynamic radii of 89 and 67 nm, respectively, as determined via dynamic light scattering analysis. In addition, atomic forces and scanning electron microscopy were used to investigate the topography of the PEI thin films. Poly(glycidyl methacrylate) P(GMA) was grafted onto a PEI chain in the presence of trimethylolpropane triacrylate (TMPTA) as the crosslinking agent to synthesize the P(GMA–PEI–TMPTA) tripolymer via free radical polymerization using gamma irradiation. The thermal characterization of the P(GMA–PEI–TMPTA) tripolymer was conducted using thermogravimetric analysis and differential scanning calorimeter. Generally, the thermal stability of the P(GMA–PEI–TMPTA) tripolymer was improved at low‐glycidyl methacrylate concentrations. The prepared tripolymer could be used as effective packaging materials for electronics industries.