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Poly(benzoxazine–co–urea): A Solventless Approach Towards The Introduction of Alternating Urea Linkages In Polybenzoxazine

机译:聚(苯唑嗪-Co -rea):一种无溶剂的方法,用于引入多苯并嗪在多苯唑嗪中引入交替的尿素连接

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摘要

In this paper, an alternative approach towards synthesis of phenolic/urea copolymers has been explored via benzoxazine chemistry. Biobased poly(benzoxazine-co-urea) has been prepared through ring opening polymerisation of a benzoxazine monomer containing urea linkages. The amine co-reactant for the benzoxazine synthesis was derived by the additive rearrangement of 4,4’-methylenebis(phenyl isocyanate) (MDI) with ethylene diamine, which underwent Mannich like condensation with cardanol and paraformaldehyde to yield biobased benzoxazine monomer containing urea linkages. The structure of the amine and the benzoxazine has been characterized by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance spectroscopy (~1H-NMR). Benzoxazine monomer undergoes thermally accelerated ring opening polymerization to form cross-linked networks, which has been demonstrated using rheometry and non-isothermal differential scanning calorimetry (DSC). The presence of alternating urea linkages in the benzoxazine network is expected to improve the adhesive properties of the resin, which was quantified in terms of Lap shear strength. Thermal degradation of the crosslinked copolymer has also been studied by thermogravimetric analysis (TGA).
机译:在本文中,已经通过苯唑嗪化学探索了酚/尿素共聚物合成的另一种方法。生物基聚(苯唑嗪-CO-rea)是通过含有尿素键的苯唑嗪单体的环聚合制备的。苯唑合成的胺共反应是通过与乙二胺的4,4'-甲基苯基(苯基异氰酸苯甲酸苯甲酸苯胺)(MDI)的添加性重排得出的,乙二胺像曼尼奇一样,像耐甲甘氨酸和副甲醇和副甲甲基甲基甲基甲基甲基甲基甲基甲基甲基苯二甲基甲唑烷诺氏菌一样固定。胺和苯唑嗪的结构以傅立叶变换红外光谱(FT-IR)和核磁共振光谱(〜1H-NMR)为特征。苯唑嗪单体经历热加速的环开环聚合以形成交联的网络,已使用流变计和非等温差分扫描量热法(DSC)证明了交联网络。苯并嗪网络中交替的尿素连接的存在有望改善树脂的粘附特性,该特性是根据膝盖剪切强度量化的。还通过热重分析(TGA)研究了交联共聚物的热降解。

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