Polymeric Modification of Graphene through Esterification of Graphite Oxide and Poly(vinyl alcohol)

By H. Salavagione, M. A. Gómez, G. Martínez. 2009

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Can nanoparticles really enhance thermal stability of polymers? Part I: An overview on thermal decomposition of addition polymers (2011, background): “In the case of with PVA intercalated in graphite oxide the temperature of maximum degradation rate for the nanocomposites increases more than 100 ◦C, which is a remarkable increase [74].”
Simultaneous in situ reduction, self-alignment and covalent bonding in graphene oxide/epoxy composites (2013, background): “% for thermoplastic polyurethane (TPU) [33] and polymethylmethacrylate (PMMA) [34] and as low as 0.”
A review on the role of interface in mechanical, thermal, and electrical properties of polymer composites (2018, background): “radical traps [233]; and lastly, they are capable of altering the microstructure of the product [4, 222].”
Key Improvements in Interfacial Adhesion and Dispersion of Fibers/Fillers in Polymer Matrix Composites; Focus on PLA Matrix Composites (2021, methodology): “sulfoxide (DMSO) was used as a reaction medium with dimethylcyclohexyl carbodiimide and 4-dimethylaminopyridine (DMAP) [189].”
Graphene and modified graphene-based polymer nanocomposites – A review (2014, background): “Salavagione et al.(80) have reported the synthesis of covalently modified graphene, which was obtained after reduction of modified GO by hydrazine.”