基于Aza-Michael加成反应的原始热固性胶膜的合成、表征及在镀锌钢上的粘附。

IF 4.7 3区 工程技术 Q1 POLYMER SCIENCE
Polymers Pub Date : 2025-06-27 DOI:10.3390/polym17131796
Florian Cavodeau, Maurice Brogly, Jean-François Stumbe, Rémi Perrin
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引用次数: 0

摘要

本研究首先通过aza-Michael加成反应合成了原线型二胺预聚物和原胺/丙烯酸酯热固性胶粘剂,然后对其热学、力学和粘附性能进行了表征。aza-Michael加成反应的主要优点是在室温下进行,不需要溶剂,也不需要催化剂。采用aza-Michael加成反应,首次合成了分子量为867 ~ 1882 g mol-1的线性仲二胺预聚物。然后,二胺预聚物与三种不同的丙烯酸酯进行aza-Michael反应,合成了新的胺/丙烯酸酯热固性粘合剂。所有热固性胶粘剂都通过流变学和热分析进行了表征,一旦发生交联aza-Michael反应,就会产生柔软的热固性网络,其玻璃化转变温度范围为-23至-8℃,凝胶点时间范围为40分钟至4小时,表面能的极性成分范围为3至17 mJ m-2。丙烯酸酯的功能直接影响交联速率,交联速率随凝胶点时间的变化呈现递减的主曲线。交联密度受二胺预聚物链长控制。在第二步中,热固性胶粘剂作为薄膜应用于两块镀锌钢板之间,并通过搭剪试验评估粘合性能。结果表明,随着二胺预聚物的动态粘度和分子量的增加,粘接强度也随之增加。增加二胺预聚物链长导致断裂应变增加,剪切模量降低,最大搭剪强度降低。黏结强度随黏结膜厚度的增加而降低。此外,具有高极性和与基材表面能相似的表面能的热固性粘合剂将有利于高附着力和更好的装配粘合强度。最后,丙烯酸酯和二胺预聚物链长度的性质允许调整这些原始软热固性粘合剂的广泛粘合强度和韧性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Characterization, and Adhesion on Galvanized Steel of Original Thermoset Adhesive Films Based on Aza-Michael Addition Reaction.

This study focuses first on the synthesis through an aza-Michael addition reaction of original linear diamine prepolymers and original amine/acrylate thermoset adhesives, and second on their thermal, mechanical and adhesion characterization. The major advantage of the aza-Michael addition reaction is that it takes place at room temperature, without a solvent and without a catalyst. Using the aza-Michael addition reaction, linear secondary diamine prepolymers were first synthesized with a control of the molecular weight, ranging from 867 to 1882 g mol-1. Then, aza-Michael reactions of diamine prepolymers with three different acrylates allowed the synthesis of new amine/acrylate thermoset adhesives. All the thermoset adhesives were characterized by rheology and thermal analysis, leading, once the crosslinking aza-Michael reaction had occurred, to soft thermoset networks with glass transition temperatures ranging from -23 to -8 °C, gel point times ranging from 40 min to 4 h, and a polar component of the surface energy ranging from 3 to 17 mJ m-2. Functionality of the acrylates directly influences the crosslinking rate, and a decreasing master curve is obtained when reporting crosslinking rate versus gel point time. Crosslinking density is controlled by the diamine prepolymer chain length. In a second step, thermoset adhesives were applied as thin films between two galvanized steel plates, and adhesion properties were evaluated through a lap-shear test. Results showed that the adhesive strength increases as the dynamic viscosity and molecular weight of the diamines prepolymer increases. Increasing the diamines prepolymer chain length results in an increase in strain at break, a decrease in the shear modulus, and a decrease in the maximum lap-shear strength. It is also observed that the adhesive strength decreases when the adhesive film thickness increases. Moreover, thermoset adhesives with high polarity and a surface energy similar to the surface energy of the substrate will favor high adhesion and a better adhesive strength of the assembly. Lastly, the nature of the acrylates and diamines prepolymer chain length allow tuning a wide range of adhesive strength and toughness of these original soft thermoset adhesives.

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来源期刊
Polymers
Polymers POLYMER SCIENCE-
CiteScore
8.00
自引率
16.00%
发文量
4697
审稿时长
1.3 months
期刊介绍: Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.
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