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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Molecular orientation and multilayer formation in the adsorbed film of 1H,1H,10H,10H-perfluorodecane-1,10-diol at the hexane/water interface; Temperature effect on the. adsorption of fluoroalkane-diol
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Molecular orientation and multilayer formation in the adsorbed film of 1H,1H,10H,10H-perfluorodecane-1,10-diol at the hexane/water interface; Temperature effect on the. adsorption of fluoroalkane-diol

机译:1H,1H,10H,10H-全氟癸烷-1,10-二醇在己烷/水界面的分子取向和多层形成;温度对。氟烷二醇的吸附

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摘要

The adsorption of 1H,1H,10H,10H-perfluorodecane-1,10-diol (FC(10)diol) at the hexane/water interface was investigated by the measurement of temperature dependence of interfacial tension and the thermodynamic data analysis in order to know the effect of two hydroxyl groups at both ends of the hydrophobic chain and the rigidity of the hydrophobic chain on the adsorption of fluorocarbon alcohol at the interface. The curves of interfacial tension versus temperature and concentration show break points corresponding to the phase transitions in the adsorbed FC10diol film. The interfacial pressure versus mean area per adsorbed molecule curve shows three kinds of states connected by two discontinuous changes. The area value after the first phase transition is very close to the calculated cross-sectional area of the FC(10)diol molecule along its major axis, and thus the FC(10)diol molecules form a condensed monolayer with molecular orientation parallel to the interface. Another noticeable point is that the value after the second phase transition point decreases furthermore to 0.12 nm(2), which is much smaller than the cross-sectional area of the fluorocarbon chain, 0.28 nm(2), with increasing interfacial pressure. This suggests that FC10diol molecules pile spontaneously and successively form a multilayer above the second phase transition. Furthermore, the partial molar entropy and energy change of adsorption in the expanded and condensed states were evaluated and compared to those of 1H,1H,2H,2H-perfluorodecanol (TFC10OH), which orients almost perpendicular to the interface. In addition to the contact of two hydroxyl groups with hexane in the bulk solution, the results are explained by the dependence of partial molar entropy and energy at the interface on the following factors resulting from the parallel orientation of FC(10)diol at the interface; (a) hydrogen bonding of two hydroxyl groups with water molecules, (b) hydrogen bonding between two hydroxyl groups facing each other, and (c) the fluorocarbon chain-water contact. The adsorbed FC(10)diol film is stabilized by factors a and b, which overwhelm the energetic disadvantage caused by factor c. Furthermore, the entropy change of adsorption Delta s in the multilayer is compared to the Delta s(cal) calculated on the assumption that the condensed monolayer piles to form the multilayer. It was suggested that FC(10)diol molecules are not so densely packed in the multilayer compared to the first condensed monolayer and therefore the multilayer is not simply formed by the piling of condensed monolayers.
机译:通过测量界面张力的温度依赖性和热力学数据分析,研究了1H,1H,10H,10H-全氟癸烷-1,10-二醇(FC(10)diol)在己烷/水界面的吸附。知道疏水链两端的两个羟基以及疏水链的刚性对氟碳醇在界面处的吸附的影响。界面张力与温度和浓度的关系曲线显示了对应于吸附的FC10二醇薄膜中相变的断点。界面压力与每个吸附分子的平均面积的关系曲线显示了通过两种不连续变化而联系在一起的三种状态。第一次相变后的面积值非常接近FC(10)二醇分子沿其长轴的计算横截面面积,因此FC(10)二醇分子形成分子方向平行于FC(10)的缩合单分子层。接口。另一个值得注意的点是,随着界面压力的增加,第二个相变点之后的值进一步减小至0.12 nm(2),该值大大小于碳氟化合物链的横截面积0.28 nm(2)。这表明FC10二醇分子自发地堆积并在第二相变上方连续形成多层。此外,评估了在膨胀和冷凝状态下的部分摩尔摩尔熵和吸附能变化,并将其与几乎垂直于界面取向的1H,1H,2H,2H-全氟癸醇(TFC10OH)进行比较。除了本体溶液中两个羟基与己烷的接触外,结果还通过界面上的部分摩尔熵和能量与以下因素的相关性解释:FC(10)二醇在界面处平行取向; (a)两个羟基与水分子的氢键结合;(b)彼此面对的两个羟基之间的氢键结合;(c)碳氟链与水的接触。吸附的FC(10)二醇薄膜通过因子a和b稳定,这克服了因子c导致的能量不足。此外,将多层中的吸附Δs的熵变与假设冷凝的单层堆积以形成多层的假设所计算的Δs(cal)进行比较。有人提出,与第一个缩合的单分子层相比,FC(10)二醇分子在多层结构中的密度不是很高,因此多层结构不是简单地通过堆叠缩合的单分子层形成的。

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