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疏水表面间的 n-醇和水-乙醇混合物的薄液膜中的表面力。

Surface forces in thin liquid films of n-alcohols and of water-ethanol mixtures confined between hydrophobic surfaces.

机构信息

Center for Advanced Separation Technologies, Department of Mining and Minerals Engineering, Virginia Tech, VA 24061, USA.

出版信息

J Colloid Interface Sci. 2012 Aug 1;379(1):114-20. doi: 10.1016/j.jcis.2012.04.032. Epub 2012 Apr 23.

Abstract

An atomic force microscope (AFM) was used to measure the surface forces in thin liquid films (TLFs) confined between gold surfaces hydrophobized by chemisorption of alkylthiols. The measurements were conducted in different H-bonding liquids and in water-ethanol solutions. Attractive forces stronger and longer-ranged than the van der Waals force were observed in water, ethanol, and 1-butanol in a descending order. The attractive force measured in methanol was much weaker. The surface forces measured in ethanol solutions varied with concentration. Initially, the attractive forces decreased rapidly upon ethanol addition, passed through a broad minimum centered around mole fractions in the range of 0.15-0.20, and then increased as the ethanol mole fraction was further increased above ~0.5. Thermodynamic analysis of the data suggests that clusters of water and ethanol may form in TLFs. Thus, the attractive forces may arise from changes in liquid structure. It appears that structuring is a consequence of H-bonding liquid to minimize its free energy in the vicinity of hydrophobic surfaces and in the presence of foreign species in solution.

摘要

原子力显微镜(AFM)被用于测量金表面之间的薄液膜(TLF)中的表面力,这些金表面通过烷基硫醇的化学吸附而疏水化。这些测量是在不同的氢键液体和水-乙醇溶液中进行的。在水、乙醇和 1-丁醇中观察到比范德华力强且作用范围更大的吸引力,顺序递减。在甲醇中测量到的吸引力要弱得多。在乙醇溶液中测量到的表面力随浓度而变化。最初,随着乙醇的加入,吸引力迅速下降,在摩尔分数范围为 0.15-0.20 的中心处通过一个宽的最小值,然后随着乙醇摩尔分数进一步增加到 0.5 以上而增加。对数据的热力学分析表明,水和乙醇的簇可能在 TLF 中形成。因此,吸引力可能来自于液体结构的变化。似乎结构是由于氢键液体为了在疏水表面附近和溶液中存在外来物质的情况下最小化其自由能而产生的。

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