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Phase equilibrium for ternary liquid systems of water + di-(2-ethylhexyl)phosphoric acid plus organic diluents: Thermodynamic study

机译:水+二(2-乙基己基)磷酸与有机稀释剂的三元液体系统的相平衡:热力学研究

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The influences of temperature on equilibrium solubility for the ternary liquid systems of water + di-(2-ethylhexyl)phosphoric acid + organic diluents were investigated by cloud point titration at T = 303.2-333.2 K and atmospheric pressure. Various organic diluents having different dielectric constants of kerosene (n/a), n-heptane (1.9), chlorobenzene (5.6) and 1-octanol (10.3) were designated to observe the polar influence on the solubility. All ternary systems exhibited the type II behavior, and their solubility increased with the polarity and studied temperatures. The tie-line data for each ternary liquid system were also studied and correlated by the Bachman plots. Moreover, the experimental solubility of water in the organic phases were predicted using the modified Apelblat equation, and the results were validated by the relative average deviation (RAD) as shown in a range of 0.01-4.09%. The dissolution thermodynamics of water in the organic phases were studied using the van't Hoff model in order to determine its enthalpy (Delta H-d), entropy (Delta S-d) and Gibbs energy (Delta G(d)). The results indicated that the dissolution of water in the organic phases was endothermic and a non-spontaneous process and driven by entropy. (C) 2015 Elsevier B.V. All rights reserved.
机译:在T = 303.2-333.2 K和大气压下,通过浊点滴定法研究了温度对水+二-(2-乙基己基)磷酸+有机稀释剂三元液体体系平衡溶解度的影响。指定具有不同介电常数的煤油(n / a),正庚烷(1.9),氯苯(5.6)和1-辛醇(10.3)的各种有机稀释剂以观察极性对溶解度的影响。所有三元体系均表现出II型行为,其溶解度随极性和所研究温度的增加而增加。还研究了每个三元液体系统的联系线数据,并通过巴赫曼图进行了关联。此外,使用修正的Apelblat方程预测了水在有机相中的实验溶解度,并通过相对平均偏差(RAD)验证了结果,该相对偏差在0.01-4.09%的范围内显示。为了确定其焓(ΔH-d),熵(ΔS-d)和吉布斯能量(ΔG(d)),使用van't Hoff模型研究了有机相中水的溶解热力学。结果表明,水在有机相中的溶解是吸热的,是非自发过程,受熵驱动。 (C)2015 Elsevier B.V.保留所有权利。

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