形成网络的聚合物溶液的凝结时间,具有可变多重性的可逆交叉连接连接
1Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Kyoto 615-8510, Japan.
Gels (Basel, Switzerland)
|May 26, 2023
概括
这项研究理论上计算了结合分子的溶液的凝时间 (tg),揭示了它取决于分子性质和交联动力学. 这些发现使得可以从宏观凝测量中估计微观参数.
科学领域:
- 聚合物化学 聚合物化学
- 物理化学 物理化学
- 材料科学 材料科学 材料科学
背景情况:
- 了解凝动态对于控制材料特性至关重要.
- 现有的模型往往简化了交联反应的复杂动力学.
研究的目的:
- 理论上计算功能性 (关联) 分子溶液的凝时间 (tg).
- 建立宏观凝行为和微观反应参数之间的关系.
主要方法:
- 逐步交联反应的动力方程.
- 凝时间分解为放松时间 (tR) 和热力学因子 (Q).
- 对尺度度 (x) 的分析及其与关联常数 (λ(T)) 的关系.
主要成果:
- 凝时间 (tg) 是放松时间 (tR) 和热力学因子 (Q) 的乘积,两者都取决于缩放度 (x).
- 叠加原理与 λ (T) 作为度转移因子保持一致.
- 凝结时间遵循高度区域的功率定律,指数与交叉连接倍数 (k) 相关.
- 由于交叉链接可逆性的延迟效应被计算出来,有助于优化凝加工.
结论:
- 交联反应的微观参数可以从宏观凝时间测量中估计.
- 热力学因子 (Q) 在平衡凝点呈现奇点,而放松时间 (tR) 保持连续.
- 这项研究为理解和控制可逆交叉链接系统中的凝提供了一个框架,适用于像疏水改性水溶性聚合物这样的材料.
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