Paula Cimavilla-Román, Pablo Álvarez-Zapatero, Suset Barroso-Solares, Anja Vananroye, Paula Moldenaers, Miguel Ángel Rodriguez-Pérez
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引用次数: 0
Abstract
The viscoelastic properties development during the reactive foaming of four standard polyurethane formulations was monitored using a flooded parallel plate rheometer. The measurements in situ demonstrated how foams of low catalyst content took longer than 10 min to increase their viscosity from 1 to 103 Pa s, while foams with higher catalysts reached this modulus in less than 4 min. This polymerization speed deeply impacted the evolution of the cellular structure during foaming, which was demonstrated through in situ x-ray imaging and computer simulation. Foams with high catalyst stabilized in their final cell size in 4–5 min, concurring with the stage of largest viscosity buildup. In contrast, the foams of low catalyst content underwent strong degeneration as a result of the slow gelification and stiffening of the matrix. Simulation results also revealed that stabilization of the cellular structure happens faster when the catalyst and blowing agent contents are increased.
使用浸没式平行板流变仪监测了四种标准聚氨酯配方在反应发泡过程中粘弹性能的变化。现场测量结果表明,催化剂含量低的泡沫需要 10 分钟以上的时间才能将粘度从 1 Pa s 提高到 103 Pa s,而催化剂含量高的泡沫在不到 4 分钟的时间内就能达到这一模量。这种聚合速度对发泡过程中蜂窝结构的演变产生了深刻影响,这一点已通过现场 X 射线成像和计算机模拟得到证实。使用高催化剂的泡沫在 4-5 分钟内就稳定了最终的细胞大小,这与粘度积累最大的阶段相吻合。相反,催化剂含量低的泡沫则由于基质凝胶化和硬化缓慢而发生强烈退化。模拟结果还显示,当催化剂和发泡剂含量增加时,蜂窝结构的稳定速度更快。
期刊介绍:
The Journal of Applied Polymer Science is the largest peer-reviewed publication in polymers, #3 by total citations, and features results with real-world impact on membranes, polysaccharides, and much more.