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强制润湿反应性表面。

Forced wetting of a reactive surface.

机构信息

Laboratory of Surface and Interfacial Physics, University of Mons, 7000 Mons, Belgium.

出版信息

Adv Colloid Interface Sci. 2012 Nov 1;179-182:22-8. doi: 10.1016/j.cis.2012.06.002. Epub 2012 Jun 28.

Abstract

The dynamic wetting of water on gelatin-coated poly(ethylene terephthalate) (GC-PET) has been investigated by forced wetting over a wide speed range and compared with earlier data obtained with unmodified PET. The results were analysed according to the molecular-kinetic theory of dynamic wetting (MKT). Both substrates show complex behaviour, with separate low- and high-speed modes. For the GC-PET, this is attributed to a rapid change in the wettability of the substrate on contact with water, specifically a surface molecular transformation from hydrophobic to hydrophilic. This results in a smooth wetting transition from one mode to the other. For the PET, the bimodal behaviour is attributed to surface heterogeneity, with the low-speed dynamics dominated by interactions with polar sites on the substrate that become masked at higher speeds. In this case, the transition is discontinuous. The study has general ramifications for the investigation of any wetting processes in which a physicochemical transformation takes place at the solid surface on contact with the liquid. In particular, it shows how forced wetting, combined with the MKT, can reveal subtle details of the processes involved. It is unlikely that similar insight could be gained from spontaneous wetting studies, such as spreading drops.

摘要

水在明胶涂覆的聚对苯二甲酸乙二醇酯(GC-PET)上的动态润湿已通过在宽速度范围内强制润湿进行了研究,并与用未改性的 PET 获得的早期数据进行了比较。结果根据动态润湿的分子动力学理论(MKT)进行了分析。两种基底都表现出复杂的行为,具有单独的低速和高速模式。对于 GC-PET,这归因于与水接触时基底润湿性的快速变化,具体而言是表面分子从疏水性到亲水性的转变。这导致从一种模式到另一种模式的平滑润湿转变。对于 PET,双峰行为归因于表面不均匀性,低速动力学主要由与基底上的极性位相互作用主导,在较高速度下这些相互作用被掩盖。在这种情况下,转变是不连续的。该研究对于研究任何润湿过程都具有普遍意义,其中在与液体接触时固体表面发生物理化学转变。特别是,它展示了强制润湿如何结合 MKT 揭示所涉及过程的细微细节。从自发润湿研究(例如扩展的液滴)中获得类似的见解是不太可能的。

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