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COULOMBIC AND NON-COULOMBIC CONTRIBUTIONS TO THE CRITICALITY OF IONIC FLUIDS - AN EXPERIMENTAL APPROACH

机译:库仑和非库仑对离子流体临界性的贡献-一种实验方法

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The recent discovery of liquid-liquid phase separations in electrolyte solutions with critical points near room temperature enables the systematic study of the critical behavior of ionic fluids. Depending on the nature of the molecular interactions, either sharp mean-field or Ising behavior is obtained in the temperature range down to t=(T-T-c)/T-c=10(-4) or less. Mean-field-like criticality is obtained with systems which in the framework of a simple corresponding states model are fairly close to the critical point of the ''restricted primitive model'' (RPM) of equally-sized charged spheres in a dielectric continuum. In these cases the phase separation is driven by the Coulombic forces (so-called Coulombic phase separations). This type of unmixing occurs for 1:1 electrolytes in solvents of low dielectric constant. Simple mechanisms for unmixing suggested in the literature are discussed in relation to the available data. Some evidence for departures from the simple RPM prediction is found. The presence of additional short-range interactions leads to sharp Ising behavior. Examples are solutions of tetraalkylammonium salts in water and other highly structured solvents, where phase separation results from the peculiar solvophobic nature of ions (solvophobic phase separations). Previous speculations that this type of unmixing shows the tendency toward closed loops are confirmed by the first direct observation of a lower consolute point in an aqueous solution of propyl-tributylammonium iodide. By light scattering studies and measurements of the coexistence curve near the upper and lower consolute points Ising criticality is confirmed. A new mechanism for phase separation is reported for the system ethylammonium nitrate + octanol, where ion pairs are stabilized by hydrogen bonding beyond what is expected from the RPM. This comparatively subtle additional interaction (so-called stricky ions) already changes the behavior of otherwise RPM-like systems from mean-field to Ising criticality. The results are discussed with particular emphasis on their implications for possible scenarios for explaining a mean-field critical point or crossover from mean-field to Ising behavior beyond the accessible temperature range. [References: 84]
机译:电解质溶液中具有接近室温的临界点的液-液相分离的最新发现使系统研究离子流体的临界行为成为可能。取决于分子相互作用的性质,在低至t =(T-T-c)/ T-c = 10(-4)或更低的温度范围内,可获得清晰的平均场或Ising行为。在简单的对应状态模型的框架内,系统非常接近均值场临界,该系统非常接近电介质连续体中大小相等的带电球的“受限原始模型”(RPM)的临界点。在这些情况下,相分离是由库仑力驱动的(所谓的库仑相分离)。对于低介电常数溶剂中的1:1电解质,会发生这种类型的混合。结合现有数据讨论了文献中提出的简单的分解机制。找到了一些偏离简单RPM预测的证据。其他短程相互作用的存在导致尖锐的伊辛行为。实例是四烷基铵盐在水和其他高度结构化的溶剂中的溶液,其中相分离是由离子的独特的疏溶剂性引起的(疏溶剂相分离)。以前的推测是,这种分解是显示出趋向于闭环的趋势,这是通过首先直接观察到丙基三丁基碘化铵水溶液中的较低固溶点来证实的。通过光散射研究和对上下共点附近共存曲线的测量,可以确定伊辛临界值。据报道系统乙基硝酸铵+辛醇有一种新的相分离机理,其中离子对通过氢键稳定,超出了RPM的预期范围。这种相对微妙的附加相互作用(所谓的强离子)已经将原本类似于RPM的系统的行为从平均场变为伊辛临界。对结果进行了讨论,并特别强调了其对可能情况的影响,这些情况可能用于解释超出可访问温度范围的平均场临界点或从平均场到Ising行为的交叉。 [参考:84]

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