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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Oscillation of interfacial tension at a liquid/liquid interface composed of di(2-ethylhexyl) phosphoric acid and calcium chloride
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Oscillation of interfacial tension at a liquid/liquid interface composed of di(2-ethylhexyl) phosphoric acid and calcium chloride

机译:由二(2-乙基己基)磷酸和氯化钙组成的液/液界面上的界面张力振荡

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摘要

Nonlinear oscillation of interfacial tension was found for a liquid/liquid interface composed of di(2-ethylhexyl) phosphoric acid-heptane/calcium chloride/water. The range of the oscillations was over several millineutons per meter, with the longest one continuing over a few hours. A wide variety of oscillation patterns was observed, but they were classified into two groups. One group showed that the power spectrum was proportional to f(-2), with f being the frequency, and the distribution function of the amplitudes followed a Gaussian distribution function. This type of oscillation, type A, became slightly weaker with decreasing temperature and looked like a random process which may be associated with thermal energy. Another type, type B, was entirely different from type A. The power spectrum approximately followed a scaling law. The scaling index was almost unity; however, the scaling law was not perfect compared to that of type A. The distribution function of the amplitudes was not a Gaussian distribution. An increase in temperature made the average amplitude smaller. This type of oscillation required a higher interfacial tension than that for type A. Further, a quasi-periodic change of interfacial tension was sometimes observed. Those changes suggested that type B oscillation was caused by an attractive interaction between surfactant molecules. It introduced an unstable region in the interfacial pressure-interfacial area isotherm which caused type B oscillation. A simple model was proposed to explain type B oscillations, which could capture some experimental trends. [References: 23]
机译:对于由二(2-乙基己基)磷酸/正庚烷/氯化钙/水组成的液/液界面,发现了界面张力的非线性振荡。振荡的范围超过每米几毫牛顿,最长的一次持续数小时。观察到各种各样的振荡模式,但是将它们分为两组。一组表明功率谱与f(-2)成正比,其中f为频率,并且振幅的分布函数遵循高斯分布函数。随着温度的降低,这种类型的振荡(A型)变得略微减弱,并且看起来像一个随机过程,可能与热能有关。另一类B型与A型完全不同。功率谱大致遵循比例定律。缩放指数几乎是统一的。但是,与A型相比,定标定律并不完美。振幅的分布函数不是高斯分布。温度升高使平均幅度变小。这种类型的振动比A型振动需要​​更高的界面张力。此外,有时观察到界面张力的准周期变化。这些变化表明,B型振荡是由表面活性剂分子之间的吸引相互作用引起的。它在界面压力-界面面积等温线中引入了一个不稳定区域,导致B型振荡。提出了一个简单的模型来解释B型振荡,它可以捕获一些实验趋势。 [参考:23]

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