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基于 2-乙基己基丙烯酸酯的无规共聚物表现出不寻常的玻璃化转变幅度宽和在较宽的组成范围内易于自主自修复。

Random Copolymers Based on 2-Ethylhexyl Acrylate Exhibit Unusual Glass Transition Breadth and Facile Autonomous Self-Healing over a Broad Composition Range.

机构信息

Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL, 60208, USA.

The Dow Chemical Company, 400 Arcola Road, Collegeville, PA, 19426, USA.

出版信息

Macromol Rapid Commun. 2024 Nov;45(22):e2400198. doi: 10.1002/marc.202400198. Epub 2024 Aug 16.

Abstract

Statistical copolymers are commercially important because their properties can be tuned by comonomer selection and composition. Rubbery-state styrene (S)/n-butyl acrylate (nBA) copolymers have previously been reported to exhibit facile, autonomous self-healing over a narrow composition band (47/53 to 53/47 mol%). The need for a narrow composition band is explained by alternating comonomer sequences that accommodate interchain secondary bonding. It is hypothesized that copolymers that achieve interchain secondary bonding without alternating sequences can exhibit facile self-healing over a broad composition range. 2-ethylhexyl acrylate (EHA) is identified as yielding sequence-independent secondary bonding interactions. For these interactions it is tested experimentally by glass transition breadth in rubbery-state S/EHA copolymers, with S/n-hexyl acrylate (nHA) and S/nBA copolymers as controls. The n-alkyl acrylate random copolymers exhibit enhanced glass transition breadths over narrow composition bands that correspond to autonomous self-healing. In contrast, S/EHA copolymers exhibit much greater glass transition breadths than S/nHA and S/nBA copolymers at all compositions tested as well as self-healing of damage over a broad composition range with full tensile-property recovery, often in 3-10 h. Characterization of glass transition breadth may serve as a simple screening tool for identifying copolymers that exhibit broad-composition-range, facile, autonomous self-healing and contribute to polymer resilience and sustainability.

摘要

统计共聚物在商业上很重要,因为它们的性质可以通过共聚单体的选择和组成来调节。先前已经报道过,橡胶态苯乙烯(S)/正丁基丙烯酸酯(nBA)共聚物在很窄的组成范围内(47/53 至 53/47 mol%)表现出易于实现的、自主的自修复能力。需要窄的组成范围是因为交替的共聚单体序列可以适应链间次级键合。据推测,那些不需要交替序列就可以实现链间次级键合的共聚物,可以在很宽的组成范围内表现出易于实现的自修复能力。丙烯酸 2-乙基己酯(EHA)被确定为可以产生序列无关的次级键合相互作用。对于这些相互作用,通过橡胶态 S/EHA 共聚物的玻璃化转变宽度进行了实验测试,同时以 S/正己基丙烯酸酯(nHA)和 S/正丁基丙烯酸酯(nBA)共聚物作为对照。与 S/nHA 和 S/nBA 共聚物相比,这些 n-烷基丙烯酸酯无规共聚物在对应于自主自修复的狭窄组成范围内表现出增强的玻璃化转变宽度。相比之下,在所有测试的组成范围内,S/EHA 共聚物的玻璃化转变宽度都远大于 S/nHA 和 S/nBA 共聚物,并且在很宽的组成范围内可以对损伤进行自修复,同时还可以完全恢复拉伸性能,通常在 3-10 小时内。玻璃化转变宽度的特性可以作为一种简单的筛选工具,用于识别那些在宽组成范围内表现出易于实现的、自主的自修复能力的共聚物,并有助于提高聚合物的弹性和可持续性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f9/11583354/3bedd33ea960/MARC-45-2400198-g010.jpg

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