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Thermodynamics of Aqueous Solutions of 18-Crown-6 at 298.15 K: Enthalpy and Entropy Effects

机译:18-Crown-6水溶液在298.15 K时的热力学:焓和熵效应

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We reported previously activity and activity coefficient data for aqueous solutions of 18-crown-6 (18C6) in the concentration range of 0.1–2.0 mol-kg−1 at 298.15 K. The results were interpreted in terms of the binding of four water molecules (two bridged and two singly H-bonded) inside the 18C6 cavity having a D 3d conformation. In this work, we report our thermodynamic analysis of the Gibbs energy and enthalpy data (obtained using enthalpy virial data from literature) in aqueous solutions of 18C6 at 298.15 K. The excess enthalpy and Gibbs energy parameters are computed and further used to obtain excess entropies of solutions as a function of 18C6 concentration. The same data are utilized to compute the partial molar entropies of solvent and solute at finite, as well as at infinite, dilution of 18C6 in water. It is observed that ΔG mix, ΔH mix and TΔS mix values are all negative, whereas ΔG E values show a slightly positive variation as a function of the 18C6 concentration. The partial molar excess entropy of water, ( $(overline{S}_{1}-S_{1}^{circ})^{rm E}$ , decreases (becomes negative) whereas that of 18C6, ( $(overline{S}_2-S_{2}^{circ})^{rm E}$ , increases with a increase in the 18C6 concentration. These results are explained in terms of various effects, which include water structure making, incorporation of water molecules in the crown cavities and crown–crown hydrophobic interactions, which persist even at the lowest concentration studied.
机译:我们报道了先前在298.15 K浓度范围为0.1–2.0 mol-kg-1 的18-crown-6(18C6)水溶液的活度和活度系数数据。在具有D 3d构象的18C6腔内有四个水分子(两个桥连和两个单H键合)。在这项工作中,我们报告了在298.15 K时18C6水溶液中吉布斯能量和焓数据(使用文献中的焓病毒数据获得)的热力学分析。计算了过量的焓和吉布斯能量参数,并进一步用于获得过量的熵溶液浓度与18C6浓度的关系。利用相同的数据来计算在水中有限和无限稀释18C6时溶剂和溶质的部分摩尔熵。可以看出,ΔGmix ,ΔHmix 和TΔSmix 值均为负,而ΔGE 值则随18C6浓度的变化而略有正向变化。水的部分摩尔过量熵($(overline {S} _ {1} -S_ {1} ^ {circ})^ {rm E} $减小(变成负值)而18C6的部分摩尔过量熵($ {S} _2-S_ {2} ^ {circ})^ {rm E} $随18C6浓度的增加而增加,这些结果用各种效应来解释,包括水结构的形成,水分子的掺入。在牙冠腔和牙冠与牙冠之间的疏水性相互作用中,即使在研究的最低浓度下也持续存在。

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