胶粘剂
环氧树脂
单体
固化(化学)
光热治疗
材料科学
组分(热力学)
高分子化学
复合材料
聚合物
纳米技术
图层(电子)
热力学
物理
作者
Shuo Liang,Jingtao Bai,Xiaoyong Peng,Yumei Ji,Xu Han,Zeqian Wang,Feng Liu
标识
DOI:10.1080/00218464.2024.2413016
摘要
One-component epoxy resin adhesives with Ethylamine-boron trifluoride (BF3-MEA) have become popular choices for electronic applications due to their lower curing temperatures and excellent storage stability. However, in the traditional thermal curing process for these adhesives, which relies on the Active Chain End (ACE) mechanism, the formation of cyclic oligomers can compromise their mechanical performance. In this study, we prepared a series of novel one-component adhesives using Diglycidyl-4,5-epoxy-cyclohexane-1,2-dicarboxylate (TDE-85) epoxy resin, Bis [4-(diphenylsulfonio) phenyl] sulfide bis (hexafluoroantimonate) (Photoinitiator 1176), and BF3-MEA through blending, and successfully achieved photothermal dual-curing. We systematically explored various adhesive ratios and curing conditions. Compared to adhesives treated solely by thermal curing, those subjected to photothermal dual-curing exhibited the best shear strength of 13.9 ± 0.7 MPa and a hardness of 88 ± 4 Shore A, representing improvements of 118.2% and 18.9%, respectively. Additionally, the study demonstrated that hydroxyl groups produced by photocuring effectively inhibit the ACE mechanism and promote the Active Monomer (AM) mechanism, which becomes dominant. In summary, the photothermal synergistic curing approach, with the AM mechanism as dominant, prevents the formation of cyclic oligomers and enhances mechanical performance. This study offers a new approach for adhesives used in electronic devices.
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