首页> 外文期刊>Zeitschrift fur Physikalische Chemie: International Journal of Research in Physical Chemistry and Chemical Physics >Volumetric, Viscosity and Conductance Studies of Solute–Solute and Solute–Solvent Interactions of Some Alkali Metal Chlorides in Aqueous Citric Acid at Different Temperatures
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Volumetric, Viscosity and Conductance Studies of Solute–Solute and Solute–Solvent Interactions of Some Alkali Metal Chlorides in Aqueous Citric Acid at Different Temperatures

机译:在不同温度下含水柠檬酸水溶液中溶溶质和溶质溶剂相互作用的体积,粘度和电导研究

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摘要

The present study aims for the structure-making and structure-breaking behavior of some electrolytes in aqueous citric acid solution. The density, viscosity and conductance of some alkali metal chlorides lithium chloride (LiCl), sodium chloride (NaCl) and potassium chloride (KCl) in 0.01 m aqueous citric acid have been measured in the concentration range 0.01–0.12 m at 303.15, 308.15, 313.15 and 318.15 K. From these measurements, molar volume, viscosity parameters and molar conductance have been deliberated. Debye Hückel limiting law is used for the assessment of the contributions of various types of solute–solvent interactions. Jones–Dole viscosity equation is used to calculate viscosity B-coefficient for these salts in aqueous citric acid, which is known to provide information concerning the solvation of ions and their effects on the structure of the solvent in the near environment of the solute particles. The free energies of activation of viscous flow per mole of solvent, Δμ10?$Delta mu _1^{0ddagger }$ and solute, Δμ20?,$Delta mu _2^{0ddagger },$ have also been evaluated by using viscosity data. Using molar volume, the transfer volume Фvotr has also been computed. The structure making/ breaking behavior of LiCl, NaCl and KCl is inferred from the sign of second derivative of partial molar volume with respect to temperature at constant pressure (d2Φvo/dT2)p, Temperature coefficient of B. dB/dT and temperature coefficient of Walden product i.e. d(Λmoηo)/dT values. It has been found from these studies that LiCl, NaCl and KCl behave as structure-breaker in 0.01 m aqueous citric acid solution. The results have been qualitatively used to explain the molecular interaction and structural changes between the components of these mixtures.
机译:本研究旨在含水柠檬酸水溶液中一些电解质的结构和结构破裂行为。在0.01M柠檬酸中,在303.15,308.15,308.15, 313.15和318.15 K.从这些测量,摩尔体积,粘度参数和摩尔传导已经被审议。 DebyeHückel限制法用于评估各种类型的溶质溶剂相互作用的贡献。 Jones-dole粘度方程用于计算柠檬酸水溶液中这些盐的粘度B系数,这是已知提供关于离子溶解的信息及其对溶质颗粒的接近环境中的溶剂结构的作用。每摩尔溶剂激活粘性流动的自由能量,Δμ10?$ delta mu _1 ^ {0 ddgagger} $ 并溶质,Δμ20?,$ delta mu _2 ^ {0 ddgagger},$ 也通过使用粘度数据进行评估。使用摩尔体积,还计算了转移量фvotr。 LiCl,NaCl和KCl的结构制备/断裂行为是从恒压(D2φVO/ DT2)P,温度系数B.DB / DT和温度系数的温度的第二衍生物的第二衍生物的迹象。 Walden产品IE D(λmoho)/ dt值。从这些研究中发现,LiCl,NaCl和Kcl在0.01M柠檬酸水溶液中表现为结构破碎器。结果已经定性用于解释这些混合物组分之间的分子相互作用和结构变化。

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