ABSTRACT
In this work, the functionalization of graphene nanoplatelets (GNPs) performed by a solvent-free cycloaddition reaction on GNPs with iminodiacetic acid (IDA) and paraformaldehyde (PFA), and the functionality analysis of the resulting functionalized GNPs (f-GNPs) by Boehm titration are introduced. The f-GNPs synthesized at different temperatures were characterized by X-ray diffraction (XRD), Raman spectroscopy and scanning electron microscopy (SEM) for structural and morphological properties. Back titration of the f-GNPs selectively identified 3 types of functional groups on the f-GNP surface, carboxylic, lactonic and phenolic, and suggested that 200 °C gives the highest carboxylic group functionality. With the reaction temperature increasing from 180 to 220 °C, a decrease in the phenolic functionality and an increase in that of lactonic are observed. In the case of 250 °C reactions, it was found that the carboxylic functionality is greatly reduced, while the phenolic functionality showed a significant increase. The f-GNP samples were further characterized by thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS), the results of which showed a good agreement with the titration analysis.
ABSTRACT
Graphene nanoplatelets (GNPs) were functionalized through 1,3-dipolar cycloaddition of azomethine ylide using a solvent-free approach and under different reaction conditions. The yield and the functionality of the carboxyl-terminated pyrrolidine ring attached on the surface of GNPs could be affected by varying the reaction temperature as well as the reactant to GNP weight ratio. The functionalized GNPs were characterized extensively using a range of spectroscopic and microscopy techniques.
