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首页> 外文期刊>Journal of Molecular Liquids >Composition-dependent dynamical structures of monohydric alcohol-water mixtures studied by microwave dielectric analysis
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Composition-dependent dynamical structures of monohydric alcohol-water mixtures studied by microwave dielectric analysis

机译:微波介电分析研究一元醇-水混合物的成分依赖动力学结构

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Dielectric relaxation measurements on methanol (MA)-water, ethanol (EA)-water, and 1-propanol (1PA)-water mixtures were carried out using TDR (Time Domain Reflctometry) for the entire concentration range of 0less than or equal toX(molar fraction of alcohol)less than or equal to1.0 up to 25GHz at 20degreesC-30degreesC. We have calculated the excess activation free energy, enthalpy, and entropy of these mixtures, DeltaG(E), DeltaH(E),and DeltaS(E), and the excess partial molar quantities for alcohol, DeltaG(A)(E), DeltaH(A)(E), and DeltaS(A)(E) (A=MA, EA, and 1PA) and those for water, DeltaG(W)(E), DeltaH(W)(E), and DeltaS(W)(E) from the temperature-dependent relaxation times. There exists,boundary above and below which behaviors of the partial molar quantities are quite different. If we call the concentration corresponding to the boundary X-b, X(b)similar to0.30, 0.18, and 0.14 for methanol-water, ethanol-water, and 1-propanol-water, respectively. In the region of Xgreater than or equal toX(b), DeltaH(A)(E) and DeltaS(A)(E) are nearly zero. This means that, in terms of the activation enthalpy and entropy, alcohol molecules in the mixtures find themselves in not a very different environment from that in pure liquid. In water-rich region, DeltaH(A)(E) and DeltaS(A)(E) exhibit two maxima at X-1 and X-2 where X(1)similar to0.045, 0.04, and 0.03, and X(2)similar to0.12, 0.08, and 0.06, for methanol-water, ethanol-water, and 1-propanol-water, respectively. This is clearly attributed to hydrophobic hydration. Detailed analysis of the behavior of Delta(A)(E) and DeltaS(A)(E) (A=MA, EA, and 1PA) suggests the formation of two kinds of saturated hydration structures and their transition; the clathrate hydration shells with tetrahededral local arrangements of water moleculres around Xsimilar toX(1), and non-clathrate shells with large cavities with three-coordinated local arrangements around Xsimilar toX(2). [References: 36]
机译:使用TDR(时域反射法)在甲醇(MA)-水,乙醇(EA)-水和1-丙醇(1PA)-水混合物上进行介电弛豫测量,整个浓度范围为0小于或等于X(在20°C至30°C的25 GHz频率下小于或等于1.0的酒精摩尔分数。我们已经计算出这些混合物DeltaG(E),DeltaH(E)和DeltaS(E)的过量活化自由能,焓和熵,以及酒精的过量部分摩尔量DeltaG(A)(E), DeltaH(A)(E)和DeltaS(A)(E)(A = MA,EA和1PA)以及水,DeltaG(W)(E),DeltaH(W)(E)和DeltaS( W)(E)取决于温度的弛豫时间。在上下边界存在,部分摩尔量的行为有很大不同。如果我们称对应于边界X-b的浓度,则X(b)分别类似于甲醇-水,乙醇-水和1-丙醇-水的0.30、0.18和0.14。在Xgreater大于或等于X(b)的区域中,DeltaH(A)(E)和DeltaS(A)(E)几乎为零。这意味着,就活化焓和熵而言,混合物中的醇分子所处的环境与纯液体中的环境相差无几。在富水地区,DeltaH(A)(E)和DeltaS(A)(E)在X-1和X-2处显示两个最大值,其中X(1)类似于0.045、0.04和0.03,而X( 2)分别类似于甲醇,水,乙醇和1-丙醇的水,分别为0.12、0.08和0.06。显然这归因于疏水水合。对Delta(A)(E)和DeltaS(A)(E)(A = MA,EA和1PA)的行为进行的详细分析表明,两种饱和水合结构的形成及其过渡。 X到X(1)周围具有四分子局部水分子的笼形水合壳,X到X(2)周围具有大腔体的三配位非笼形水合壳。 [参考:36]

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