离子液体
润湿
涂层
差示扫描量热法
化学工程
粘附
结冰
介电谱
材料科学
化学
有机化学
复合材料
电化学
物理化学
工程类
催化作用
物理
热力学
气象学
电极
作者
Saba Goharshenas Moghadam,Gelareh Momen,Ehsan Bakhshandeh,Reza Jafari
标识
DOI:10.1016/j.cej.2024.149696
摘要
The demand for anti-icing coatings to endure extremely low temperatures is substantial. Despite the innovative pioneering research on the anti-icing potential of ionic liquids (ILs), the development of such coatings is still in its infancy. Our study investigates how matrix hydrophobicity influences mobility of ILs at subzero temperatures and, consequently, their anti-icing behavior. Wettability results highlight the key role of IL anion hydrophobicity. Dielectric spectroscopy distinguishes ion mobility in the coatings at low temperatures. We also investigate how varying crosslink density affects ion mobility by measuring the water absorbency. Higher mobility of released ILs from the coatings at subzero was confirmed by their presence in water solutions, validated with UV–vis spectroscopy, and resulted in increased ionic conductivity. Differential scanning calorimetry and experimental setups were employed to assess ice formation temperature, time, and ice adhesion strength. Notably, surfaces containing IL exhibited a remarkable reduction in ice formation temperature to –23.5 ℃ and achieved an exceptionally low ice adhesion strength (∼15 kPa), attributed to the formation of a quasi-liquid layer (QLL). Solid-state NMR spectroscopy provided confirmation of the existence of QLL at the interface. Ice adhesion strength of coatings was examined against accelerated weathering, icing/de-icing cycles, as well as endurance against frost formation under freeze–thaw. Our findings underscore the significance of selecting the right matrix with regards to hydrophobicity and ILs when designing coatings for subfreezing applications.
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