材料科学
异氰酸酯
纳米复合材料
聚氨酯
傅里叶变换红外光谱
聚合物
聚己内酯
高分子化学
单体
化学工程
石墨烯
原位聚合
聚合
氧化物
复合材料
纳米技术
工程类
冶金
作者
Jingjing Bai,Guosheng Hu,Jingting Zhang,Bingxiao Liu,Jingjing Cui,Xiu-Rong Hou,Yu Fan,Zhenzhong Li
标识
DOI:10.1080/00222348.2019.1565102
摘要
Using monomer-functionalized nanofiller to prepare polymeric nanocomposites is a promising strategy toward achieving enhanced performance. In this study toluene-2,4-diisocyanate (TDI), one of the monomers used for synthesizing polyurethane, was covalently functionalized on graphene oxide (GO) and then the functionalized GO (TDI-GO) was polymerized with polycaprolactone diol (PCL) via in-situ polymerization, leading to chemically linked polyurethane nanocomposites through the covalent bonds between the isocyanate groups on GO and the hydroxyl-terminated PCL. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and dispersion experiments of the nanofillers demonstrated that the TDI was successfully grafted onto the GO. The rheological properties were investigated to establish the structure-property relationships of the nanocomposites. The storage moduli (G'), loss moduli (G") and complex viscosity (η*) of the samples increased monotonically with TDI-GO content, which is attributed to the strong polymer-filler interactions and the effective dispersion of the nanofillers. Additionally, the tan δ variation with frequency, the intersection of G' and G", Han plots, van Gurp-Palmen plots and Cole-Cole plots all showed that the incorporation of TDI-GO decreased the degree of microphase separation and improved the elastic properties of the nanocomposites. We suggest this is related to the enhanced interactions between the polymer and nanofillers, which strongly restricted the mobility and relaxation of the polymer chains.
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