预聚物
阳离子聚合
光引发剂
乙烯基醚
高分子化学
光致聚合物
材料科学
单体
聚氨酯
固化(化学)
异佛尔酮二异氰酸酯
异氰酸酯
乙醚
胶粘剂
聚合
丙烯酸酯
紫外线固化
三甘醇
多元醇
弹性体
乙烯基聚合物
醋酸乙烯酯
化学工程
活性阳离子聚合
聚合物
乳液聚合
TMPTA公司
有机硅
互穿聚合物网络
三聚氰胺树脂
二甘醇
天然橡胶
作者
Haifeng Gao,Lishuang Lin,Liang Huang,Lixin Wu,Shuqiang Peng,Kehua Lin,Longhui Zheng
标识
DOI:10.1021/acsapm.5c04164
摘要
Conventional radical-based UV-curable acrylic pressure-sensitive adhesives (PSAs) are severely limited by oxygen inhibition, leading to incomplete surface curing and polymerization shrinkage. To address these issues, we report a cationic photopolymerization strategy based on vinyl ether-functionalized polyurethanes for fabricating high-performance optically clear PSAs. A vinyl ether-terminated prepolymer (PUE-BDO) was synthesized by the chain extension of an isocyanate-terminated polyurethane with 1,4-butanediol, followed by end-capping with 4-hydroxybutyl vinyl ether (HBVE). A difunctional vinyl ether monomer (IP-VE) was prepared from HBVE and isophorone diisocyanate. By systematically adjusting the ratios of PUE-BDO, IP-VE, and triethylene glycol divinyl ether (DVE-3), we achieved precise control over the cross-linking network and viscoelastic properties of the materials. The resulting PSAs exhibited exceptional optical clarity, with 99% transmittance and <0.3% haze, alongside rapid strain recovery (<1 s) and a high creep-recovery ratio (∼90%) after 100 loading–unloading cycles at 20% strain. At an optimal composition (50 wt % prepolymer), the PSA demonstrated a 180° peel strength of 18.2 N/25 mm and a loop tack of 17.3 N/25 mm. This study presents a robust and tunable cationic photocuring platform for next-generation flexible display encapsulation that is free from oxygen inhibition and capable of meeting demanding optical and mechanical requirements.
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