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Chemical reduction of graphite oxide (GO) to produce graphene nanosheets often results in irreversible agglomeration and precipitation. Herein, stable well-dispersed graphene sheets in solvents were obtained by simultaneous functionalization and reduction of GO under alkaline conditions, in the presence of sodium borohydride and imidazolium ionic liquids (Imi-ILs) containing two vinyl-benzyl groups. In this case, positively charged imidazolium groups of Imi-ILs underwent ion-exchange with negatively charged GO sheets and were linked to their edges, while Imi-ILs were non-covalently attached onto the large surfaces of graphene through p-p and/or cation-p stacking interactions. The vinyl-benzyl reactive sites were then copolymerized in situ with methyl methacrylate to fabricate graphene/poly(methyl methacrylate) (PMMA) composites. Functionalized graphene sheets were uniformly dispersed in the PMMA matrix and contributed to large increases in storage modulus (+58.3%) and glass transition temperature (+19.2 C) at 2.08 vol.% loading. High electrical conductivity was also achieved at graphene loading levels beyond 1 vol.% (ca. 2.55 Sm À1 ) with a low percolation threshold (0.25 vol.%) for the composites. Hence, a general methodology which facilitates the development of a multifunctional advanced material has been successfully established. This can be extended to other vinyl polymer-based composites containing graphene.

Multiwalled carbon nanotube (MWCNT)/carbon fiber (CF)/vinyl ester (VE) laminate composites have been fabricated in this study. Pristine MWCNTs were treated with acid solution, which formed numerous oxygen-containing functional groups onto their surface, resulting in COOH-MWCNTs. Thereafter, acrylic functional groups were grafted onto the COOH-MWCNTs to generate acryl-MWCNTs. Three types of MWCNTs (pristine MWCNTs, COOH-MWCNTs, and acryl-MWCNTs) were used to reinforce the CF/VE-based composites. The dispersion of MWCNTs in the VE matrix and the interfacial interaction between MWCNTs and the VE matrix were investigated. Thereafter, the individual reinforcement efficiencies of these MWCNTs are compared. The flexural strength of the MWCNT/CF/VE composite with 1.0 phr acryl-MWCNTs content is 29.8% greater than that of neat CF/VE composites, and the flexural modulus of the MWCNT/CF/VE composite is 9.9% higher than that of neat CF/VE composites. Compared with neat CF/VE composites, 1.0 phr acryl-MWCNT/CF/VE composites exhibit an approximately 19.9 °C increase in glass transition temperature (Tg). The coefficients of thermal expansion significantly decreased from 47.2 ppm/°C of the neat CF/VE composites to 35.6 ppm/°C of the acryl-MWCNTs/CF/VE composites with 1 phr acryl-MWCNT content. This study provides a method for developing acryl-MWCNT/CF/VE composites with good dispersion of MWCNTs in VE matrix and strong interfacial interaction between the MWCNTs and VE matrix for enhancing the stress transfer from VE matrix to CF reinforcement.

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