Flexible graphene polyimide nanocomposites (0.1-4 wt %) with superior mechanical properties over those of neat polyimide resin have been prepared by solution blending. Imide moieties were grafted to amine-functionalized graphene using a step-by-step condensation and thermal imidization method. The imide-functionalized graphene exhibited excellent compatibility with N-methyl-2-pyrrolidone. The dynamic storage moduli of the graphene polyimide nanocomposites increased linearly with increasing graphene content for both unmodified graphene and imidized graphene. Moduli of the imidized graphene nanocomposites were 25-30% higher than those of unmodified graphene nanocomposites. Both neat polyimide and polyimide nanocomposites exhibited shape memory effects with a triggering temperature of 230 °C. where addition of graphene improved the recovery rate. Addition of graphene improved thermal stability of the polyimide nanocomposites for both graphene and modified graphene.

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The effect of incorporating an organic linking group, 1,6-bis(trimethoxysilyl)hexane (BTMSH), into the underlying silica structure of a styrene cross-linked silica aerogel is examined. Vinyltrimethoxysilane (VTMS) is used to provide a reactive site on the silica backbone for styrene polymerization. Replacement of up to 88 mol % of the silicon from tetramethoxyorthosilicate with silicon derived from BTMSH and VTMS during the making of silica gels improves the elastic behavior in some formulations of the cross-linked aerogels, as evidenced by measurement of the recovered length after compression of samples to 25% strain. This is especially true for some higher density formulations, which recover nearly 100% of their length after compression to 25% strain twice. The compressive modulus of the more elastic monoliths ranged from 0.2 to 3 MPa. Although some of these monoliths had greatly reduced surface areas, changing the solvent used to produce the gels from methanol to ethanol increased the surface area in one instance from 6 to 220 m(2)/g with little affect on the modulus, elastic recovery, porosity, or density.

We describe a three-dimensional core-shell structure where the core is the assembly of nanoparticles that comprises the skeletal framework of a typical silica aerogel, and the shell is polystyrene. Specifically, the mesoporous surfaces of silica were first modified with amines by co-gelation of tetramethylorthosilicate (TMOS) and 3-aminopropyltriethoxysilane (APTES). Next, styrene moieties were attached to the amines by reaction with p-chloromethylstyrene. Finally, dangling styrene moieties were crosslinked by a free-radical polymerization process initiated by AIBN and styrene, p-chloromethylstyrene or 2,3,4,5-pentafluorostyerene introduced in the mesopores. Polystyrene crosslinked aerogels are mechanically strong, lightweight (0.41-0.77 g cm 23 ), highly porous materials (they consist of ca. 63% empty space, with a BET surface areas in the range of 213-393 m 2 g 21 ). Their thermal conductivity (0.041 W m 21 K 21 ) is comparable to that of glass wool. Hydrophobicity, however, is the property that sets the new material apart from analogous polyurea and epoxy crosslinked aerogels. The contact angles of water droplets on disks cut from larger monoliths are >120u. (By comparison, the contact angle with polyurea crosslinked aerogels is only ca. 60u.) Polystyrene crosslinked aerogel monoliths float on water indefinitely, while their polyurea counterparts absorb water and sink within minutes.