RESUMO
Graphene oxide (GO)-incorporated poly(methyl methacrylate) (PMMA) nanocomposites (PMMA-GO) have demonstrated a wide range of outstanding mechanical, electrical, and physical characteristics. It is of interest to review the synthesis of PMMA-GO nanocomposites and their applications as multifunctional structural materials. The attention of this review is to focus on the radical polymerization techniques, mainly bulk and emulsion polymerization, to prepare PMMA-GO polymeric nanocomposite materials. This review also discusses the effect of solvent polarity on the polymerization process and the types of surfactants (anionic, cationic, nonionic) and initiator used in the polymerization. PMMA-GO nanocomposite synthesis using radical polymerization-based techniques is an active topic of study with several prospects for considerable future improvement and a variety of possible emerging applications. The concentration and dispersity of GO used in the polymerization play critical roles to ensure the functionality and performance of the PMMA-GO nanocomposites.
RESUMO
Ionomers are polymers which contain ionic groups that are covalently bound to the main chain. The presence of a small percentage of ionic groups strongly affects the polymer's mechanical properties. Here, we examine a new family of nanostructured ionomer films prepared from core-shell polymer nanoparticles containing acrylonitrile (AN), 1,3-butadiene (Bd) and methacrylic acid (MAA). Three new AN-containing dispersions were investigated in this study. The core-shell nanoparticles contained a PBd core. The shells contained copolymerised Bd, AN and MAA, i.e., PBd-AN-MAA. Three types of crosslinking were present in these films: covalent crosslinks (from Bd); strong physical crosslinks (involving ionic bonding of RCOO(-) and Zn(2+)) and weaker physical crosslinks (from AN). We examined and compared the roles of AN and ionic crosslinking (from added Zn(2+)) on the structure and mechanical properties of the films. The FTIR spectroscopy data showed evidence for RCOOH-nitrile hydrogen bonding with tetrahedral geometry. DMTA studies showed that AN copolymerised within the PBd-AN-MAA phase uniformly. Tensile stress-strain data showed that inclusion of AN increased elasticity and toughness. Analysis showed that about 33 AN groups were required to provide an elastically-effective chain. However, only 1.5 to 2 ionically bonded RCOO(-) groups were required to generate an elastically-effective chain. By contrast to ionic bonding, AN inclusion increased the modulus without compromising ductility. Our results show that AN is an attractive, versatile, monomer for increasing the toughness of nanostructured ionomers and this should also be the case for other nanostructured polymer elastomers.
