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原位自交联策略用于制备超韧聚乳酸/生物基聚氨酯共混物。

In-situ self-crosslinking strategy for super-tough polylactic acid/ bio-based polyurethane blends.

机构信息

State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, 100029, China.

State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, 100029, China; Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing, 10029, China.

出版信息

Int J Biol Macromol. 2024 Mar;261(Pt 2):129757. doi: 10.1016/j.ijbiomac.2024.129757. Epub 2024 Jan 26.

Abstract

As a bio-based degradable plastic, polylactic acid (PLA) is highly commercialized, but its inherent brittleness limits its widespread use. In-situ polymerization techniques are effective in improving the toughness of PLA. However, the enhancement of the toughening effect in polyurethanes (PUs) through in-situ self-crosslinking still requires improvement and heavily relies on petroleum-derived feedstocks in certain approaches. In this paper, 1,3-polypropanediol (PO3G) of bio-based origin rather than conventional polyols like polyethylene glycol (PEG) and poly propylene glycol (PPG) was used. PLA/PO3G-PU blends were prepared via an in-situ self-crosslinking strategy. With a notch impact and tensile strength of 55.95 kJ/m and 47.77 MPa (a retention rate of 68.9 % compared with pure PLA), respectively, PLA/PO3G-PU blends achieved a better balance between stiffness and toughness. This work provides a new option for PLA to achieve a stiffness-toughness balance and get rid of dependence on petrochemical resources.

摘要

作为一种生物基可降解塑料,聚乳酸(PLA)具有很高的商业价值,但它固有的脆性限制了其广泛应用。原位聚合技术在提高 PLA 的韧性方面非常有效。然而,通过原位自交联来提高聚氨酯(PU)的增韧效果仍需要改进,并且在某些方法中严重依赖石油衍生原料。在本文中,使用了生物基的 1,3-丙二醇(PO3G),而不是传统的多元醇,如聚乙二醇(PEG)和聚丙二醇(PPG)。通过原位自交联策略制备了 PLA/PO3G-PU 共混物。共混物的缺口冲击强度和拉伸强度分别为 55.95kJ/m 和 47.77MPa(与纯 PLA 相比保留率为 68.9%),在刚度和韧性之间达到了更好的平衡。这项工作为 PLA 实现刚度-韧性平衡并摆脱对石化资源的依赖提供了新的选择。

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