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High performance aliphatic polyurea films reinforced using nonfunctionalized multiwalled carbon nanotubes

机译:高性能脂族聚脲膜使用非功能化多壁碳纳米管增强

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Polyurea nanocomposites appear to be a recent advanced elastomer with high robustness. This study shows that without chemical surface functionalism, multiwalled carbon nanotubes (MWCNTs) can significantly increase the tensile strength of aliphatic polyurea nanocomposites which are cured at room temperature. This is achieved via ultrasonic dispersion techniques which prevent agglomeration and the role of MWCNTs as physical crosslink sites, encouraging the formation of hydrogen bonds, thus entangling the polymer chains in the polyurea matrix and restricting chain movement. The incorporation of MWCNT drastically increases the tensile strength of the nanocomposite by 1000%, from 2.16 +/- 0.24 MPa to 21.7 +/- 4.4 MPa. The thermal and chemical properties of samples are investigated using dynamic mechanical analysis (DMA), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FTIR), and acetone swelling tests. In this study, we showed that polyurea films reinforced with MWCNTs have high swelling resistance compared to the pure polyurea films. Aliphatic polyurea is also known to have high UV stability. The tensile properties achieved by the nanocomposite in this study are comparable to the aliphatic and aromatic polyurea products in the market and can make these films suitable products for rolling and coating applications.
机译:聚脲纳米复合材料似乎是最近具有高稳健性的先进弹性体。本研究表明,没有化学表面功能主义,多壁碳纳米管(MWCNT)可以显着提高在室温下固化的脂族聚脲纳米复合材料的拉伸强度。这是通过超声波分散技术实现的,防止MWCNT作为物理交联位点的聚集和作用,促进氢键的形成,从而缠绕聚合物链中的聚合物链并限制链运动。 MWCNT的掺入大大增加了纳米复合材料的拉伸强度1000%,从2.16 +/- 0.24MPa达到21.7 +/- 4.4MPa。使用动态机械分析(DMA),热重分析(TGA),差示扫描量热法(DSC),傅里叶变换红外光谱(FTIR)和丙酮溶胀试验来研究样品的热和化学性质。在这项研究中,我们表明,与纯聚脲膜相比,用MWCNT加强的聚脲膜具有高溶胀性。还已知脂族聚脲具有高紫外线稳定性。本研究中纳米复合材料实现的拉伸性能与市场上的脂族和芳族聚脲产品相媲美,可以使这些薄膜适用于轧制和涂层应用的产品。

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