We present a novel approach to the fabrication of advanced polymeric nanocomposites from poly(vinyl alcohol) (PVA) by incorporation of PVA-grafted graphene oxide. In this work, we have synthesized PVA-grafted graphene oxide (PVA-g-GO) for the strong interfacial adhesion of graphene oxide (GO) to the PVA matrix. It was found that the mechanical properties of PVA were greatly improved by incorporating PVA-g-GO. For example, the tensile strength and Young's modulus of the PVA nanocomposite films containing 1 wt % net GO in the PVA-g-GO significantly increased by 88 and 150%, respectively, as compared to unfilled PVA. The elongation at break was also increased by 22%, whereas the GO/PVA nanocomposite containing 1 wt % pristine GO was decreased by 15%. Therefore, the presence of the PVA-g-GO in the PVA matrix could make the PVA not only stronger but also tougher. The strong interfacial adhesion between PVA-g-GO and the PVA matrix was attributed to the good compatibility between PVA-g-GO and the matrix PVA as well as the hydrogen-bonding between them.

Carbon nanomaterials such as multiwalled carbon nanotubes (MWCNTs) and graphene oxide (GO) have been functionalized by highly hydrophilic and biocompatible poly(vinyl alcohol) (PVA) for loading and delivery of an anticancer drug, camptothecin (CPT). For the first time, CPT was loaded onto MWCNT-PVA and GO-PVA through π-π interactions and its capability to kill human breast and skin cancer cells was investigated.

A novel approach to chemically functionalize multiwalled carbon nanotubes (MWCNTs) for making advanced polymeric nanocomposites with liquid crystalline polymers (LCPs) is presented. In this approach, two types of chemical moieties (i.e., carboxylic and hydroxyl benzoic acid groups) are selectively introduced onto the sidewalls of the MWCNTs. Fourier transform IR and Raman spectroscopy are used to examine the interaction between the functionalized MWCNTs and the LCP. The strong interaction between the functionalized MWCNTs and the LCP greatly improved the dispersion of MWCNTs in the polymer matrix as well as the interfacial adhesion. The dispersion of the MWCNTs in the LCP matrix is observed by optical microscopy and field‐emission scanning electron microscopy. As a result, the addition of 1 wt% MWCNTs in the LCP resulted in the significant improvement (41 and 55%) in the tensile strength and modulus of the LCP.

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