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A strong underwater adhesive that totally cured in water

胶粘剂 材料科学 粘附 复合材料 固化(化学) 水溶液 水下 极限抗拉强度 聚二甲基硅氧烷 化学工程 化学 图层(电子) 有机化学 海洋学 地质学 工程类
作者
Yonggan Yan,Jun Huang,Xiaoyong Qiu,Dexuan Zhuang,Hanlian Liu,Chuanzhen Huang,Xunwei Wu,Xin Cui
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:431: 133460-133460 被引量:52
标识
DOI:10.1016/j.cej.2021.133460
摘要

Underwater adhesives have drawn enormous interests for biomedical and engineering applications. In this work, a strong underwater adhesive is developed by addition reaction between bis(3-aminopropyl) terminated polydimethylsiloxane (PDMS) and hexamethylene diisocyanate (HDI). The PDMS-based adhesive was totally cured in aqueous solutions and exhibited strong adhesion with various substrates. The highest underwater adhesion strength of the adhesive on polyethylene terephthalate (PET) substrate reached 2.8 MPa, which is comparable with those commercial glues that cured in air. Such strong underwater adhesion is mainly caused by the combination of chemical crosslinks, hydrogen bonds and other physical interactions. Further study reveals that increasing the curing temperature can decrease the mechanical strength of the adhesive, which leads to a decrease in adhesion strength. Moreover, increasing the salt concentration in aqueous solution would screen the electrostatic charges at the interface and impair the underwater adhesion. Besides, the tensile adhesion tests suggested that the underwater adhesion strength was enhanced by 3 times as the curing time extended from 3 h to 6 h. The increased adhesion is mainly caused by the enhanced mechanical strength of the polymeric adhesive as well as the increased interactions at the adhesive-substrate interface. In addition, the strong adhesion force of the adhesive is also demonstrated from the microscale by employing atomic-force-microscope force measurement. This work provides both practical and fundamental insights into developing underwater adhesives with strong adhesion.
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