pH-responsive intrinsic self-healing coating via in-situ confined solid-liquid transition of hydrogel microdomains

IF 7.5 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Jie Yang, Ting Shen, Jiahong Wei, Chong Chen, Wenkai Cao, Weihua Li
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引用次数: 6

Abstract

Inspired by pH variation in corrosion microenvironment and the emerging solid-liquid composite strategies, this study presents an innovative self-healing coating based on pH-responsive confined solid-liquid transition behavior, with anti-corrosion functionality as a proof of concept. The coating integrates poly (vinyl alcohol) (PVA) crosslinked with boronic acid (BA) through an in-situ solvent exchange process, forming borate ester-based, pH-responsive PVA-BA (AB) hydrogel microdomains within a poly (3-(trimethoxysilyl) propyl methacrylate) (PTPM) network. The AB/PTPM coating achieves healing within 30 min, based on gel-sol transitions of the AB hydrogel microdomains triggered by different pH conditions (pH = 7 and 11). The hydrophobic PTPM network prevents AB hydrogel microdomains from water intrusion. This design balances the fluidity and stability, providing a solution to enhance the durability of protective coatings. The AB/PTPM coating was applied as a topcoat over an epoxy (EP) primer, and the formed bilayer AB/PTPM@EP coating exhibits excellent anti-corrosion restoration properties after self-healing.
基于水凝胶微畴原位固-液过渡的ph响应型自愈涂层
受腐蚀微环境中的pH变化和新兴固液复合策略的启发,本研究提出了一种基于pH响应受限固液转变行为的创新自修复涂层,并将防腐功能作为概念验证。该涂层通过原位溶剂交换工艺将聚乙烯醇(PVA)与硼酸(BA)交联,在聚(3-(三甲氧基硅基)甲基丙烯酸丙酯(PTPM)网络中形成硼酸酯基、ph响应的PVA-BA (AB)水凝胶微域。基于不同pH条件(pH = 7和11)引发的AB水凝胶微域的凝胶-溶胶转变,AB/PTPM涂层在30分钟内实现了愈合。疏水性PTPM网络可以防止AB水凝胶微域被水侵入。这种设计平衡了流动性和稳定性,提供了一种提高保护涂层耐久性的解决方案。将AB/PTPM涂层作为面漆涂在环氧底漆(EP)上,形成的双层AB/PTPM@EP涂层在自愈后表现出优异的抗腐蚀恢复性能。
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来源期刊
npj Materials Degradation
npj Materials Degradation MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
7.80
自引率
7.80%
发文量
86
审稿时长
6 weeks
期刊介绍: npj Materials Degradation considers basic and applied research that explores all aspects of the degradation of metallic and non-metallic materials. The journal broadly defines ‘materials degradation’ as a reduction in the ability of a material to perform its task in-service as a result of environmental exposure. The journal covers a broad range of topics including but not limited to: -Degradation of metals, glasses, minerals, polymers, ceramics, cements and composites in natural and engineered environments, as a result of various stimuli -Computational and experimental studies of degradation mechanisms and kinetics -Characterization of degradation by traditional and emerging techniques -New approaches and technologies for enhancing resistance to degradation -Inspection and monitoring techniques for materials in-service, such as sensing technologies
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