儿茶酚
胶粘剂
材料科学
环氧化物
共聚物
聚合物
单体
甲基丙烯酸酯
抗剪强度(土壤)
复合材料
甲基丙烯酸缩水甘油酯
高分子化学
化学工程
有机化学
图层(电子)
催化作用
化学
土壤水分
土壤科学
工程类
环境科学
作者
Kyueui Lee,Brylee David B. Tiu,Valentin Martchenko,K. Mai,Goun Lee,Matthias Gerst,Phillip B. Messersmith
标识
DOI:10.1021/acsami.0c19405
摘要
A modular approach to synthesizing functional pressure sensitive adhesives (PSAs) was introduced, wherein a modifiable acrylic PSA copolymer was synthesized by copolymerizing common PSA monomers with 6 mol % glycidyl methacrylate, allowing for subsequent functional group modification via the pendant epoxide functionality. This postmodification technique has the advantage of allowing the installation of a variety of functional groups relevant to adhesion, without variation of molecular weight. Because comparisons of cohesive and adhesive performance of candidate PSAs can be complicated by molecular weight differences, this strategy simplifies direct comparisons of the effects of functional groups on performance. As a proof of concept, a mussel-inspired catecholic PSA was synthesized by postreaction of the epoxide scaffold polymer with a thiol-modified catechol, allowing the effect of catechol on underlying structure–property relationships to be determined without variation in molecular weight. The mechanical performance of catecholic PSA was compared to relevant control PSAs by using industry-standard 180° peel and static shear tests, revealing an increase in peel strength achieved through catechol modification. Moreover, we observed an unexpected enhancement in PSA cohesive strength attributed to oxidation of catechol, which cannot be attributed to differences in molecular weight, a common source of changes in PSA cohesive strength.
科研通智能强力驱动
Strongly Powered by AbleSci AI