差示扫描量热法
催化作用
材料科学
固化(化学)
极限抗拉强度
复合材料
玻璃化转变
傅里叶变换红外光谱
环氧树脂
聚合
放热反应
复合数
抗压强度
化学工程
动态力学分析
催化剂载体
动力学
红外光谱学
活化能
多孔性
聚合物
热分析
作者
Neda Bozorgi,Janitha Jeewantha,Allan C. Manalo,Omar Alajarmeh,Hannah Seligmann,Sean Steed,Stephen Clarke
出处
期刊:Polymers
[Multidisciplinary Digital Publishing Institute]
日期:2026-02-18
卷期号:18 (4): 508-508
标识
DOI:10.3390/polym18040508
摘要
The increasing demand for high-performance composites has driven the need for sustainable alternatives to conventional petroleum-based resins. This research introduces a novel glycerol-derived bio-epoxy resin and investigates the effect of catalyst concentration on its curing behaviour, network structure, and thermomechanical performance. Four catalyst concentrations were evaluated using differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and dynamic mechanical analysis (DMA) combined with tensile, flexural, and compression testing. DSC results revealed that increasing the catalyst concentration significantly lowered the curing activation energy, shifting the exothermic peak temperature from 194.8 °C to 145.2 °C. DMA revealed that the glass transition temperature (Tg), crosslinking density, and stiffness consistently increased up to an optimal catalyst concentration, reaching a maximum Tg of 109.0 °C. Further increases in catalyst content led to slight reductions in Tg and crosslink density due to the formation of a heterogeneous network. The optimal concentration enhanced tensile and compressive strength by 32.8% and 9.3%, respectively. At excessive catalyst concentration, strength properties deteriorated despite increased material rigidity. These findings confirm the critical role of catalyst in governing polymerisation kinetics and network structure, demonstrating that an optimal catalyst percentage is essential for maximising strength and durability, making the bio-epoxy a viable, high-performance alternative for advanced composite manufacturing.
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