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用于可持续应用的藻酸盐生物聚合物薄膜连续挤出工艺的开发。

Development of a Continuous Extrusion Process for Alginate Biopolymer Films for Sustainable Applications.

作者信息

Eslami Zahra, Elkoun Saïd, Mirzapour Miraidin, Robert Mathieu

机构信息

Center for Innovation in Technological Ecodesign (CITE), University of Sherbrooke, Sherbrooke, QC J1K 2R1, Canada.

Research Center for High-Performance Polymer and Composite Systems (CREPEC), Montreal, QC H3A 0C3, Canada.

出版信息

Polymers (Basel). 2025 Jun 29;17(13):1818. doi: 10.3390/polym17131818.

Abstract

This study presents a novel method for producing extrudable alginate-based films using continuous thermo-mechanical mixing, providing a scalable alternative to conventional solvent-casting techniques. The effects of glycerol concentration (30-50 wt%) and processing temperature (110-120 °C) on the films' thermal, mechanical, and structural properties were systematically investigated. Structural characterization was performed using H NMR and FT-IR, and thermal transitions were analyzed via DSC (Differential Scanning Calorimetry) and DMA (Dynamic Mechanical Analysis). The glass transition temperature (Tg) of the alginate/glycerol/water system was modeled using the Gordon-Taylor equation. Glycerol incorporation significantly reduced Tg-by up to 76 °C with 40 wt% glycerol-and enhanced ductility and toughness, reaching 3.26 MJ/m at the optimal level. The influence of processing temperature was found to depend on plasticizer content: at lower glycerol levels, elevated temperatures decreased Tg and elongation at break, likely due to thermal degradation. However, films with higher glycerol content retained stable mechanical and thermal behavior across both temperature profiles. This work is among the first to explore how processing temperature affects extruded, plasticized pure alginate films. The findings provide key insights into the formulation and scalable production of bio-based packaging materials, highlighting the importance of optimizing both plasticizer concentration and processing parameters.

摘要

本研究提出了一种使用连续热机械混合生产可挤出藻酸盐基薄膜的新方法,为传统溶剂浇铸技术提供了一种可扩展的替代方案。系统研究了甘油浓度(30-50 wt%)和加工温度(110-120°C)对薄膜热性能、力学性能和结构性能的影响。使用核磁共振氢谱(H NMR)和傅里叶变换红外光谱(FT-IR)进行结构表征,并通过差示扫描量热法(DSC)和动态力学分析(DMA)分析热转变。使用戈登-泰勒方程对藻酸盐/甘油/水体系的玻璃化转变温度(Tg)进行建模。加入甘油显著降低了Tg——在甘油含量为40 wt%时降低了76°C之多——并提高了延展性和韧性,在最佳水平下达到3.26 MJ/m。发现加工温度的影响取决于增塑剂含量:在甘油含量较低时,温度升高会降低Tg和断裂伸长率,这可能是由于热降解。然而,甘油含量较高的薄膜在两种温度曲线下都保持了稳定的力学和热性能。这项工作是最早探索加工温度如何影响挤出的、增塑的纯藻酸盐薄膜的研究之一。这些发现为生物基包装材料的配方和可扩展生产提供了关键见解,突出了优化增塑剂浓度和加工参数的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb7/12251756/74c61be3f9e1/polymers-17-01818-g001.jpg

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