Interface-modulated morphological transition of biodegradable poly(ε-caprolactone) crystals†

Bingbing Li and Alan R. Esker
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Abstract

Poly(ε-caprolactone)(PCL)-based blends exhibit immense potential for the design of various environmentally friendly disposable or short-lived materials. The degradation of PCL components is determined by their crystallinity and crystal morphology, which is strongly correlated to the laboratory or industrial processing conditions of the blends. By using PCL/poly(t-butyl acrylate) (PtBA) mixed Langmuir monolayers as a model system, this study reports a striking interface-modulated morphological transition of PCL crystals, from highly branched symmetric dendrites, to six-arm dendrites, four-arm dendrites, seaweed-like crystals and distorted rectangular crystals. The results further demonstrate that the PCL chain folding reacts quickly to the change in the degree of undercooling (i.e., surface pressure), which controls the overall crystal morphologies through the interplay of the diffusion coefficient, surface tension, and surface tension anisotropy.

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可生物降解聚(ε-己内酯)晶体的界面调制形态转变†
聚(ε-己内酯)(PCL)基混合物在设计各种环境友好型一次性或短寿命材料方面具有巨大潜力。PCL 成分的降解由其结晶度和晶体形态决定,而结晶度和晶体形态与共混物的实验室或工业加工条件密切相关。本研究以 PCL/聚(丙烯酸叔丁酯)(PtBA)混合朗缪尔单层为模型体系,报告了 PCL 晶体的惊人的界面调制形态转变,从高度支化的对称树枝状晶体到六臂树枝状晶体、四臂树枝状晶体、海藻状晶体和扭曲的矩形晶体。研究结果进一步证明,PCL 链折叠对过冷度(即表面压力)的变化反应迅速,通过扩散系数、表面张力和表面张力各向异性的相互作用控制着整体晶体形态。
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