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Synthesis and characterization of acrylonitrile methyl acrylate statistical copolymers as melt processable carbon fiber precursors

机译:作为可熔融加工碳纤维前体的丙烯腈丙烯酸甲酯统计共聚物的合成与表征

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摘要

Statitical (random) copolymers of acrylonitrile (AN) and methyl acrylate (MA) have been synthesized by free radical homogeneous (solution) and heterogeneous (suspension) methods. Selected compositions can be fabricated by environment friendly, solvent-free melt spinning and are of interest as precursors for carbon fibers. The dynamic and steady state melt viscosities of these copolymers were studied as a function of molecular weight and copolymer composition. Melt processability at 200-220 deg C depends on the copolymer composition, and also on the molecular weight, which was controlled by chain transfer agent concentration and reaction temperature. Copolymers of controlled molecular weight containing 10 or more mol% of methyl acrylate show good melt rocessability, which can be further enhanced by stabilizers. This thermoplastic behavior is supported by a significant increase in temperature by the cyclization exotherm. Thermal analysis (differential scanning calorimetry, dynamic mechanical analysis) further illustrates that the comonomers retarded the cyclization, which permits thermoplastic processing.
机译:通过自由基均相(溶液)和非均相(悬浮)方法合成了丙烯腈(AN)和丙烯酸甲酯(MA)的统计(无规)共聚物。所选择的组合物可以通过环境友好的,无溶剂的熔融纺丝来制造,并且作为碳纤维的前体是令人感兴趣的。研究了这些共聚物的动态和稳态熔体粘度与分子量和共聚物组成的关系。在200-220摄氏度下的熔体可加工性取决于共聚物的组成,也取决于分子量,该分子量由链转移剂的浓度和反应温度控制。包含10摩尔%或更多的丙烯酸甲酯的可控制分子量的共聚物显示出良好的熔体加工性能,可以通过稳定剂进一步提高其熔体加工性能。环化放热使温度显着升高,从而支持了这种热塑性行为。热分析(差示扫描量热法,动态力学分析)进一步说明了共聚单体延迟了环化反应,从而允许进行热塑性加工。

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