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从中试规模生产的解聚天然木质素制备基于生物的环氧热固性聚合物。

Toward Bio-Based Epoxy Thermoset Polymers from Depolymerized Native Lignins Produced at the Pilot Scale.

机构信息

Chemical Engineering Program, Notre Dame University-Louaize, P.O. Box 72, Zouk Mikael, 1211 Zouk Mosbeh, Lebanon.

Scion, Private Bag 3020, Rotorua 3046, New Zealand.

出版信息

Biomacromolecules. 2020 Apr 13;21(4):1548-1559. doi: 10.1021/acs.biomac.0c00108. Epub 2020 Mar 30.

Abstract

Producing the next generation of thermoset polymers from renewable sources is an important sustainability goal. Hydrogenolysis of pinewood lignin was scaled up for the first time from lab scale to a 50 L pilot-scale reactor, producing a range of depolymerized lignin oils under different conditions. These lignin hydrogenolysis oils were glycidylated, blended with bisphenol A diglycidyl ether, and cured to give epoxy thermoset polymers. The thermal and mechanical properties of the epoxy polymers were assessed by differential scanning calorimetry, thermogravimetric analysis, flexural testing, and dynamic mechanical thermal analysis. Replacing up to 67% of the bisphenol A epoxy with the lignin oil epoxies resulted in cured epoxy polymers with improvements of up to 25% in flexural stiffness and strength. Considerable scope exists in simplifying and scaling up the hydrogenolysis process to produce depolymerized lignins that can substitute established petrochemicals in the quest for renewable high-performance thermoset polymers.

摘要

从可再生资源中生产下一代热固性聚合物是一个重要的可持续性目标。松木木质素的氢解首次从实验室规模扩大到 50L 中试规模反应器,在不同条件下产生了一系列解聚木质素油。这些木质素氢解油进行了缩水甘油化,与双酚 A 二缩水甘油醚混合,并进行固化以得到环氧热固性聚合物。通过差示扫描量热法、热重分析、弯曲测试和动态力学热分析评估了环氧聚合物的热性能和机械性能。用木质素油环氧树脂替代高达 67%的双酚 A 环氧树脂,可使固化的环氧聚合物在弯曲刚度和强度方面提高高达 25%。在简化和扩大氢解过程以生产可替代现有石化产品的解聚木质素方面,有很大的空间可用于寻找可再生的高性能热固性聚合物。

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