Highly tough graphene oxide/ cis ‐1,4‐polyisoprene films enabled by ionic liquid‐enhanced chemical Interface interaction

石墨烯 材料科学 氧化物 离子液体 接口(物质) 离子键合 复合材料 化学工程 氧化石墨烯纸 纳米技术 离子 有机化学 冶金 接触角 催化作用 化学 工程类 坐滴法
作者
Liyun Guo,Haichang Zhang,Jing Hua
出处
期刊:Polymer Composites [Wiley]
卷期号:46 (15): 13774-13789
标识
DOI:10.1002/pc.30023
摘要

Abstract To better substitute natural rubber latex (NRL) with cis ‐1,4‐polyisoprene latex (IRL), and thus fundamentally solve the problem of allergies induced by NRL products in humans, a novel latex compounding method was devised. This method aimed to enhance the mechanical properties of IRL films by non‐covalently modifying graphene oxide (GO) with ionic liquids (IL), which significantly improved the dispersion of GO in water. The interaction between IL and GO was thoroughly investigated. Subsequently, IL‐GO/IRL composite latexes featuring a fine dispersion of IL‐GO were successfully developed. An extensive investigation into the properties and morphology of the IL‐GO/IRL latex revealed their stability, excellent film‐forming abilities, and superior mechanical characteristics, rendering them ideal for dipping processes. The resulting thickness‐adjustable IL‐GO/IRL composite films exhibited remarkable mechanical properties. Notably, the tensile strength of the 1.5IL‐GO/IRL vulcanized film surpassed that of GO/IRL films by 2.75 times and NRL films by 10.49%. Additionally, the crosslinking density of the IL‐GO/IRL vulcanized films was improved. Further analysis of the interaction between IL‐GO and polyisoprene macromolecules was also conducted. The composite films are poised to find applications in high‐end medical and artificial intelligence fields. Highlights Mechanical performance of IRL was enhanced by introducing IL‐GO. Fine GO dispersed composite latexes were ideal for the dipping process. Composite films boast superior mechanical properties surpassing NRL films. Resulting composite film was thickness‐adjustable and ultra‐thin. CC bonds in IL and IR formed covalent linkages, boosting GO‐IR chain interaction.
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