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薄水膜在疏水化金表面之间受限的过剩热力学性质。

Excess thermodynamic properties of thin water films confined between hydrophobized gold surfaces.

机构信息

Center for Advanced Separation Technologies, Virginia Tech, Blacksburg, VA 24061, USA.

出版信息

J Colloid Interface Sci. 2011 Dec 1;364(1):257-63. doi: 10.1016/j.jcis.2011.08.027. Epub 2011 Aug 19.

Abstract

Surface forces between gold surfaces were measured in pure water at temperatures in the range of 10-40 °C using an atomic force microscope (AFM). The surfaces were hydrophobized by self-assembly of alkanethiols (C(n)SH) with n=2 and 16 in ethanol solutions. The data were used to determine the changes in excess free energies (ΔG(f)) of the thin water films per unit area by using the Derjaguin approximation [1]. The free energy data were then used to determine the changes in excess film entropy (ΔS(f)) and the excess film enthalpy (ΔH(f)) per unit area. The results show that both ΔS(f) and ΔH(f) decrease with decreasing film thickness, suggesting that the macroscopic hydrophobic interaction involves building some kind of structures in the intervening thin films of water. It was found that |ΔH(f)|>|TΔS(f)|, which is a necessary condition for an attractive force to appear when the enthalpy and entropy changes are both negative. That macroscopic hydrophobic interaction is enthalpically driven is contrary to the hydrophobic interactions at molecular scale. The results obtained in the present work are used to discuss possible origins for the long-range attractions observed between hydrophobic surfaces.

摘要

使用原子力显微镜(AFM)在 10-40°C 的温度范围内测量了纯水中金表面之间的表面力。通过将烷硫醇(C(n)SH)与 n=2 和 16 在乙醇溶液中自组装,使表面疏水化。使用 Derjaguin 近似[1],通过使用 Derjaguin 近似[1],使用这些数据确定单位面积的薄水膜的过剩自由能(ΔG(f))的变化。然后,使用自由能数据确定单位面积的过剩膜熵(ΔS(f))和过剩膜焓(ΔH(f))的变化。结果表明,随着膜厚度的减小,ΔS(f)和ΔH(f)都减小,这表明宏观疏水相互作用涉及在 intervening 水薄膜中构建某种结构。发现 |ΔH(f)|>|TΔS(f)|,这是当焓和熵变化均为负时出现吸引力的必要条件。宏观疏水相互作用是由焓驱动的,这与分子尺度上的疏水相互作用相反。本工作获得的结果用于讨论在疏水表面之间观察到的长程吸引力的可能起源。

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