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Synthesis and properties of near IR induced self-healable polyurethane/graphene nanocomposites

机译:近红外诱导的自修复聚氨酯/石墨烯纳米复合材料的合成与性能

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A series of self-healable polyurethane (SHPU)/modified graphene (MG) nanocomposites were synthesized from poly(tetramethylene glycol) (PTMG) and 4,4'-methylene diphenyl diisocyanate (MDI) with minute amounts (0-1 wt%) of MG which was chemically modified graphene oxide (GO) with phenyl isocyanate and reduced in the presence of phenylhydrazine. MG gave dual effects of reinforcing filler and light absorption medium. That is, SHPU/MG nanocomposites showed significantly enhanced Young's modulus and near infrared (NIR) absorption along with increased glass transition temperature (T_g). However, break strength and break strain decreased at high GO contents (MG075, MG100) implying that MG disturbs chain orientations. The self-healing behavior of nanocomposites was done by intermolecular diffusion of polymer chains which was accelerated by thermal energy generated by NIR absorptions. The self-healing effect was most pronounced with 0.75 wt% MG (MG075) where the elastic strain energy was even greater than the fresh material up to over 200% strain. Further addition of MG (MG100) induced more light absorption, but physically disturbed the interchain diffusion to reduce the self-healing efficiency.
机译:由聚四亚甲基二醇(PTMG)和4,4'-亚甲基二苯基二异氰酸酯(MDI)微量合成了一系列自修复聚氨酯(SHPU)/改性石墨烯(MG)纳米复合材料(0-1 wt%) MG,其是用异氰酸苯酯化学改性的氧化石墨烯(GO),并在苯肼存在下还原的。 MG具有增强填料和光吸收介质的双重作用。也就是说,SHPU / MG纳米复合材料显示出显着增强的杨氏模量和近红外(NIR)吸收,同时玻璃化转变温度(T_g)升高。但是,在高GO含量(MG075,MG100)下,断裂强度和断裂应变降低,这表明MG干扰了链的取向。纳米复合材料的自我修复行为是通过聚合物链的分子间扩散来完成的,该扩散由近红外吸收产生的热能加速。 0.75 wt%MG(MG075)的自修复效果最为明显,在高达200%以上的应变下,其弹性应变能甚至比新鲜材料还大。进一步添加MG(MG100)会引起更多的光吸收,但会物理干扰链间扩散,从而降低自愈效率。

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