Flash Flow-Induced Crystallization of Poly(l-lactide) under Elevated Pressure during Industrial-Scale Injection Molding Revealed by Time-Resolved Synchrotron X-ray Scattering

IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Jin Yin, Jie Zhang, Zheng-Yuan Chen, Lu-Feng Deng, De-Zhuang Jia, Hao Lin, Jia-Zhuang Xu, Hua-Dong Huang, Jun Lei, Gan-Ji Zhong, Zhong-Ming Li
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Abstract

Poly(l-lactide) (PLLA) is a promising biodegradable alternative to petroleum-based plastics, but it exhibits slow crystallization kinetics. Understanding flow-induced crystallization under pressure (FICP) during practical polymer processing, such as injection molding, is important to tailor the crystallization and modulate the properties. Compared with the traditional “black-box” research on FICP, understanding the multistep FICP of PLLA during industrial-scale injection molding and the effect of external fields on crystallization via real-time mode is crucial for revealing the underlying mechanism. This work first pays attention to the FICP process of PLLA during industrial-scale injection molding via a homemade in situ investigation platform base-d on a highly brilliant synchrotron X-ray scattering. We find that an initial flash flow (shear time ∼0.1 s) with extremely intense flow (Weissenberg number Wi ≫ 1) induces α/α′-form and β-form precursors in the PLLA melt, and subsequent crystallization around the oriented precursors occurs under quasi-isothermal and residual-pressure conditions. In particular, the elevated packing pressure observably promotes flow-induced oriented precursors and especially the β-form nucleates preferentially, while the segmental diffusion-dominant retardant crystal growth proceeds during the following quasi-isothermal crystallization. Being composed of thicker lamellae with a higher amount, the injection-molded PLLA bars under low pressure exhibit superior mechanical strength and thermomechanical performance. The outcome of this work points out that the pressure field is of great importance in flow-induced crystallization kinetics and the final crystalline morphology, which is valuable for guiding the development of a high-performance PLLA product and expanding its applications.

Abstract Image

时间分辨同步辐射 X 射线散射揭示工业规模注塑成型过程中升压下聚(l-内酰胺)的闪速流动诱导结晶现象
聚乳酸(PLLA)是一种很有前途的可生物降解的石油基塑料替代品,但其结晶动力学缓慢。在注塑成型等实际聚合物加工过程中,了解压力下流动诱导结晶(FICP)对于定制结晶和调节性能非常重要。与传统的 "黑箱 "式 FICP 研究相比,通过实时模式了解聚乳酸在工业规模注塑成型过程中的多步 FICP 以及外部场对结晶的影响,对于揭示其内在机理至关重要。本研究通过基于高亮度同步辐射 X 射线散射的自制原位研究平台,首次关注了聚乳酸在工业规模注塑成型过程中的 FICP 过程。我们发现,初始闪蒸流动(剪切时间∼0.1 秒)和极强流动(魏森伯格数Wi≫1)在聚乳酸熔体中诱导出α/α′形和β形前体,随后在准等温和残压条件下围绕取向前体发生结晶。特别是,在随后的准等温结晶过程中,高堆积压明显促进了流动诱导的取向前体,尤其是β形前体优先成核,而片段扩散主导的阻滞晶体生长则继续进行。低压注塑成型的聚乳酸棒材由较厚的片层组成,且片层数量较多,因此具有优异的机械强度和热机械性能。这项工作的结果表明,压力场对流动诱导结晶动力学和最终结晶形态具有重要影响,这对开发高性能聚乳酸产品和扩大其应用范围具有重要指导意义。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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