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一种用于功能性压敏粘合剂的模块化策略。

A Modular Strategy for Functional Pressure Sensitive Adhesives.

机构信息

Department of Bioengineering, University of California at Berkeley, Berkeley, California 94720, United States.

Department of Chemical Biology, University of California at Berkeley, Berkeley, California 94720, United States.

出版信息

ACS Appl Mater Interfaces. 2021 Jan 20;13(2):3161-3165. doi: 10.1021/acsami.0c19405. Epub 2021 Jan 6.

Abstract

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.

摘要

我们介绍了一种用于合成功能性压敏胶(PSA)的模块化方法,其中通过共聚常见 PSA 单体和 6mol%的甲基丙烯酸缩水甘油酯来合成可修饰的丙烯酸酯 PSA 共聚物,从而允许通过侧挂环氧官能团进行后续的官能团修饰。这种后修饰技术的优点在于,可以安装各种与粘附相关的功能基团,而不会改变分子量。由于候选 PSA 的内聚和粘附性能的比较可能因分子量的差异而变得复杂,因此该策略简化了对功能基团对性能影响的直接比较。作为概念验证,通过将环氧骨架聚合物与巯基改性儿茶酚进行后反应,合成了一种贻贝类启发的儿茶酚 PSA,从而可以在不改变分子量的情况下确定儿茶酚对底层结构-性能关系的影响。通过使用行业标准的 180°剥离和静态剪切测试,将儿茶酚 PSA 的力学性能与相关的对照 PSA 进行比较,结果表明通过儿茶酚修饰可以提高剥离强度。此外,我们观察到 PSA 内聚强度的意外增强归因于儿茶酚的氧化,这不能归因于分子量的差异,分子量的差异是 PSA 内聚强度变化的常见原因。

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