首页> 外文期刊>ACS Omega >Acrylic Functionalization of Cellulose Nanocrystals with 2-Isocyanatoethyl Methacrylate and Formation of Composites with Poly(methyl methacrylate)
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Acrylic Functionalization of Cellulose Nanocrystals with 2-Isocyanatoethyl Methacrylate and Formation of Composites with Poly(methyl methacrylate)

机译:用2-异氰酸酯甲基丙烯酸酯的纤维素纳米晶体丙烯酸官能化和聚(甲基丙烯酸甲酯)的复合材料形成

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Cellulose nanocrystals (CNCs) derived from renewable plant-based materials exhibit strong potential for improving properties of polymers by their dispersal in the polymer matrix as a composite phase. However, the hydrophilicity and low thermal stability of CNCs lead to compromised particle dispersibility in common polymers and limit the processing conditions of polymer–CNC composites, respectively. One route that has been explored is the modification of CNCs to alter surface chemistry. Acrylic materials are used in a broad class of polymers and copolymers with wide commercial applications. Yet, the available methods for adding groups that react with acrylics to enhance dispersion are quite limited. In this work, a versatile chemical modification route is described that introduces acryloyl functional groups on CNCs that can in turn be polymerized in subsequent steps to create acrylic–CNC composites. The hydroxyl group on CNC surfaces was reacted with the isocyanate moiety on 2-isocyanatoethyl methacrylate (IEM), a bifunctional molecule possessing both the isocyanate group and acryloyl group. The resulting modified CNCs (mCNCs) showed enhanced hydrophobicity and dispersibility in organic solvent relative to unmodified CNCs. Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy, solid-state ~(13)C nuclear magnetic resonance (NMR) spectroscopy, and elemental analysis verified the surface modification and allowed an estimation of the degree of modification as high as 0.4 (26.7% surface hydroxyl substitution CNC). The modified CNCs were copolymerized with methyl methacrylate, and the composites had improved dispersion relative to composites with unmodified CNCs and enhanced (104%) tensile strength at 2 wt % CNC when compared to the neat poly(methyl methacrylate) (PMMA), indicating a benefit of the reactive acryloyl groups added to the CNC surface. Overall, the modification strategy was successful in functionalizing CNCs, opening possibilities for their use in organic media and matrices.
机译:衍生自再生植物基材料的纤维素纳米晶(CNC)表现出强大的潜力,以通过它们在聚合物基质中改善聚合物的性质作为复合相。然而,CNCs的亲水性和低热稳定性导致普通聚合物中的颗粒分散性分别限制了聚合物-CNC复合材料的加工条件。已经探索的一条路线是CNC的修改以改变表面化学。丙烯酸材料用于广泛的聚合物和共聚物,具有广泛的商业应用。然而,添加与丙烯酸类反应以增强分散的组的可用方法非常有限。在这项工作中,描述了一种通用的化学改性途径,其在CNC上引入丙烯酰基官能团,其又可以在随后的步骤中聚合以产生丙烯酸类CNC复合材料。 CNC表面上的羟基与甲基丙烯酸二氰酸酯(IEM)上的异氰酸酯部分反应,具有异氰酸酯基团和丙烯酰基的双官能分子。所得改性的CNC(MCNC)在有机溶剂中具有相对于未修饰的CNC的增强的疏水性和分散性。傅里叶变换红外(FTIR)光谱,X射线光电子能谱,固态〜(13)C核磁共振(NMR)光谱和元素分析验证了表面改性,允许估计高达0.4的变形症程度(表面羟基取代26.7%CNC)。用甲基丙烯酸甲酯共​​聚改性的CNC,并且复合材料相对于具有未改性的CNC的复合材料具有改善的分散体,并且与纯多(甲基丙烯酸甲酯)(PMMA)相比,在2wt%CNC中增强(104%)拉伸强度,表示a加入CNC表面的反应性丙烯酰基的益处。总体而言,修改策略在官能高组织的功能化中取得了成功,在有机媒体和矩阵中使用的开放可能性。

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