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Bio-Based Composites with Enhanced Matrix-Reinforcement Interactions from the Polymerization of α-Eleostearic Acid

机译:α-硬脂酸聚合具有增强的基体与增强剂相互作用的生物基复合材料

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Vegetable oil-based composites have been proposed as interesting bio-based materials in the recent past. The carbon–carbon double bonds in unsaturated vegetable oils are ideal reactive sites for free radical polymerization. Without the presence of a reinforcement, typical vegetable oil-based polymers cannot achieve competitive thermo-mechanical properties. Compatibilizers have been utilized to enhance the adhesion between resin and reinforcement. This work discusses the antagonist implications of polarity and crosslink density of an unprecedented polar α-eleostearic acid-based resin reinforced with α-cellulose, eliminating the need of a compatibilizer. It is shown that the polar regions of α-eleostearic acid can interact directly with the polar reinforcement. The successful isolation of α-eleostearic acid from tung oil was verified via GC-MS, 1H NMR, Raman, and FT-IR spectroscopies. The optimal cure schedule for the resin was determined by DSC and DEA. The composites’ thermo-mechanical properties were assessed by TGA, DSC, and DMA.
机译:最近,已经提出了基于植物油的复合材料作为有趣的生物基材料。不饱和植物油中的碳-碳双键是自由基聚合的理想反应位。没有增强剂,典型的基于植物油的聚合物就无法获得竞争性的热机械性能。增容剂已被用于增强树脂和增强材料之间的粘合性。这项工作讨论了由α-纤维素增强的前所未有的极性α-硬脂酸基树脂的极性和交联密度的拮抗作用,从而消除了对相容剂的需求。结果表明,α-硬脂酸的极性区域可以直接与极性增强剂相互作用。通过GC-MS,1H NMR,拉曼光谱和FT-IR光谱法验证了从桐油中成功分离出α-硬脂酸。通过DSC和DEA确定树脂的最佳固化时间表。通过TGA,DSC和DMA评估了复合材料的热机械性能。

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