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Thermosetting Foam with a High Bio-based Content from Acrylated Epoxidized Soybean Oil and Carbon Dioxide

机译:热固性泡沫具有高生物基含量的丙烯酸环氧化大氧化豆油和二氧化碳

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A resilient, thermosetting foam system with a bio-based content of 96% was successfully developed. We implemented a pressurized carbon dioxide foaming process that produces polymeric foams from acrylated epoxidized soybean oil (AESO). A study of the cell dynamics of uncured CO-2/ AESO foams proved useful to optimize cure conditions. During collapse, the foam's bulk density increased linearly with time, and the cell size and cell density exhibited power-law degradation rates. Also, low temperature foaming and cure (i.e. high viscosity) are desirable to minimize structural degradation. The AESO was cured with a free-radical initiator (tert-butyl peroxy-2-ethyl hexanoate, T_ⅰ~60°C). Cobalt naphtenate was used as an accelerator to promote quick foam cure at lower temperature (40-50°C). The foam's density was controlled by the carbon dioxide pressure inside the reactor and by the vacuum applied during cure. The viscosity increased linearly during polymerization. The viscosity was proportional to the extent of reaction before gelation, and the cured foam's structure showed a dependence on the time of vacuum application. The average cell size increased and the cell density decreased with foam expansion at a low extent of cure; however, the foam expansion became limited and unhomogeneous with advanced reaction. When vacuum was applied at an intermediate viscosity, samples with densities ~0.25 g/cm3 were obtained with small (
机译:成功开发了具有生物基含量为96%的弹性的热固性泡沫系统。我们实施了加压二氧化碳发泡过程,其产生来自丙烯酸环氧化大豆油(AESO)的聚合物泡沫。对未固化的CO-2 / Aeso泡沫的细胞动力学的研究证明有助于优化固化条件。在崩溃期间,泡沫的散装密度随时间线性增加,细胞尺寸和细胞密度表现出幂律降解速率。此外,优选低温发泡和固化(即,高粘度)以最小化结构降解。用自由基引发剂(叔丁基过氧-2-己酸己酸酯,T_Ⅰ〜60℃)固化Aeso。萘铵用作促进剂以在较低温度(40-50℃)下促进快速泡沫固化的促进剂。通过反应器内的二氧化碳压力和固化期间的真空来控制泡沫的密度。聚合过程中粘度在线性增加。粘度与凝胶化前反应程度成比例,并且固化的泡沫结构显示对真空施加时间的依赖性。平均细胞尺寸增加,细胞密度随泡沫膨胀的低固化而降低;然而,泡沫膨胀变得有限,对先进的反应无敌。当在中间粘度下施加真空时,用小(

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