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Molecular Parameters and Their Relation to the Adhesive Performance of Acrylic Pressure-Sensitive Adhesives

机译:分子参数及其与丙烯酸压敏胶黏剂性能的关系

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摘要

Model acrylic pressure-sensitive adhesives (PSAs) based on poly(2-ethyl- hexyl acrylate-stat-acrylic acid) and poly(n-butyl acrylate-stat-acrylic acid) at 97.5/2.5 wt % were s~thesized using semicontinuous emulsion and solution polymerizations. Microgels formed in the lattices retained their discrete network morphology in the film. In contrast, acrylic solution was essentially gel free and crosslinking in the film was provided by the reaction of acrylic acid and post added Al Acetyl Acetonateafter solvent evaporation, which 1ed to continuous network morphology. The difference in film network morphology caused significantly lower shear holding power for the film from emulsion PSA compared with that ofsolvent-bornefilm. Unlike shear holding power, loop tack and peel of acrylic PSAs were mainly controlled by the samesoVgel molecular parameters, regardless of emulsion or solution PSAs. The important molecular param- eters are sol-to-gel ratio, entanglement molecular weight, weight average molecular weight, and to a lesser extent, glass transition temperature.
机译:使用半连续法,以97.5 / 2.5 wt%的比例对基于聚(丙烯酸2-乙基己酯-静态丙烯酸)和聚(丙烯酸正丁酯-静态丙烯酸)的丙烯酸类压敏胶(PSA)进行建模乳液聚合和溶液聚合。在晶格中形成的微凝胶在薄膜中保留了其离散的网络形态。相比之下,丙烯酸溶液基本上是无凝胶的,并且膜的交联是通过丙烯酸与溶剂蒸发后的后添加铝乙酰乙酰丙酮的反应而提供的,这使其具有连续的网络形态。薄膜网络形态的差异导致乳液PSA薄膜的剪切保持力明显低于溶剂型薄膜。与剪切保持力不同,丙烯酸PSA的粘着力和剥离力主要由相同的soVgel分子参数控制,而与乳液或溶液PSA无关。重要的分子参数是溶胶对凝胶的比率,缠结分子量,重均分子量,以及较小程度的玻璃化转变温度。

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