材料科学
胶粘剂
热塑性塑料
粘度
复合材料
机械强度
润湿
共聚物
溶剂
基质(水族馆)
丙烯酸树脂
丙烯酸
热塑性弹性体
降级(电信)
高分子化学
工作(物理)
化学工程
极限抗拉强度
共价键
动态力学分析
艾氏冲击强度试验
耐化学性
作者
Jonas Debuyck,Jeanne Billet,Tim Maiheu,Jolien Beniers,Hannes A. Houck,Filip E. Du Prez
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2026-05-08
卷期号:15 (5): 771-778
标识
DOI:10.1021/acsmacrolett.6c00189
摘要
High Resolution Image Download MS PowerPoint Slide Hot-melt adhesives (HMAs) offer several advantages over solvent-based alternatives, such as lower environmental impact and faster processing, yet their mostly thermoplastic nature often limits mechanical strength and solvent resistance. To address this limitation, poly( n -butyl methacrylate- co -itaconic anhydride) copolymers were designed for facile cross-linking through anhydride ring-opening with alcohols, enabling a dynamic monoester–anhydride exchange within the adhesive. The resulting networks exhibit substantially improved solvent resistance and mechanical performance, resulting in a 10-fold increase in lap-shear strength compared to a thermoplastic reference. Moreover, complex-viscosity measurements reveal a sharp viscosity transition within the typical HMA processing window (120–180 °C), enabling efficient substrate wetting during application while maintaining mechanical integrity at service temperatures. Overall, this work introduces an itaconate-based acrylic platform for dynamically cross-linked HMAs and expands the applicability of reversible anhydride chemistry in adhesive materials.
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