共查询到16条相似文献,搜索用时 46 毫秒
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应用离子选择性电极法测定混合电解质溶液中离子活度系数,由实验结果对该方法的可行性和混合电解质水溶液活度系数随温度和浓度的变化关系进行了讨论,并对单一电解质溶液和混合电解质溶液中离子的活度系数进行了对比分析。结果表明,该方法快速、简便、灵活、成本低,是测定混合电解质溶液离子活度系数的有效方法。 相似文献
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The simple equation relating the activity coefficient of each solute in mixed electrolyte solution to its value in binary solutions under isopiestic equilibrium was tested by comparison with the experimental data for the 18 electrolyte solutions consisting of 1:1, 1:2, and 1:3 electrolytes. The isopiestic measurements were made on the quaternary system BaCl2-NH4Br-NaI-H2O and its ternary subsystems NaI-NH4Br-H2O, NaI-BaCl2-H2O, and NH4Br-BaCl2-H2O at 298.15K. The results were used to test the applicability of the Zdanovskii's rule to the mixed electrolyte solutions which contain no common ions, and the agreement is excellent. The activity coefficients of the solutes in the above quaternary and ternary systems calculated from the above-mentioned simple equation are in good agreement with the Pitzer's equation. 相似文献
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Farzad Deyhimi Mojgan Sabzehzari Zohreh Karimzadeh 《Chemical Engineering Communications》2013,200(12):1654-1665
The mean activity coefficients for NaCl in a ternary electrolyte system were determined by the potentiometric method, at 25°C, using a solvent polymeric (PVC) sodium-selective membrane electrode (Na+ ISE), containing N,N′-dibenzyl-N,N′-diphenyl-1,2-phenylenedioxydiacetamide as ionophore, and combined with an Ag/AgCl electrode. The potentiometric measurements were performed at the same ionic strengths in different series of mixed salt solutions, each characterized by a fixed salt molal ratio r (where r = m1/m2 = 1, 10, 50, 100). The nonideal behavior of the ternary NaCl(m1) + LiCl(m2) + H2O electrolyte system was described based on the Pitzer ion-interaction model for mixed salts over the ionic strength ranging from 0.01 up to about 4 mol/kg. Two- and three-particle Pitzer interaction parameters for a mixed electrolyte system were determined based on potentiometric data, and the critical role of potentiometric selectivity coefficient (K 12) of ISE as limiting factor in the potentiometric measurements was analyzed. 相似文献
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Farzad Deyhimi Mojgan Sabzehzari Zohreh Karimzadeh 《Chemical Engineering Communications》2007,194(12):1654-1665
The mean activity coefficients for NaCl in a ternary electrolyte system were determined by the potentiometric method, at 25°C, using a solvent polymeric (PVC) sodium-selective membrane electrode (Na+ ISE), containing N,N'-dibenzyl-N,N'-diphenyl-1,2-phenylenedioxydiacetamide as ionophore, and combined with an Ag/AgCl electrode. The potentiometric measurements were performed at the same ionic strengths in different series of mixed salt solutions, each characterized by a fixed salt molal ratio r (where r = m1/m2 = 1, 10, 50, 100). The nonideal behavior of the ternary NaCl(m1) + LiCl(m2) + H2O electrolyte system was described based on the Pitzer ion-interaction model for mixed salts over the ionic strength ranging from 0.01 up to about 4 mol/kg. Two- and three-particle Pitzer interaction parameters for a mixed electrolyte system were determined based on potentiometric data, and the critical role of potentiometric selectivity coefficient (K12) of ISE as limiting factor in the potentiometric measurements was analyzed. 相似文献
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近年来,电解质溶液理论的研究日益活跃^[1]。因为理论模型能反映微观粒子参数与溶液结构和性质间的关系,参数物理意义明确,预测功能强。电解质溶液的原始模型中,忽略了离子-溶剂和溶剂-溶剂相互作用,而只考虑在溶剂平均场中离子之间的相互作用。这类模型不能反映溶液的本质和溶质-溶剂间的真实相互作用,因此很难推广到混合溶剂电解质溶液。用微扰理论研究电解质溶液的状态方程已经取得很大进展^[2]。硬球离子流体^[3]和离子-偶极^[4]模型流体的微扰理论处理结果已经成功地用于构筑实际电解质溶液的状态方程^[5]。作者采用微扰理论研究了电解质溶液的密度性质^[6],本文将进一步研究活度系数的计算问题。 相似文献
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A. Kumar 《Chemical Engineering Communications》1988,66(1):201-205
An alternate method to use the McKay-Perring equation for estimating the activity coefficients in aqueous mixed electrolyte solutions is suggested. The predicted activity coefficients are in good agreement with the experimental ones. 相似文献
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本文研究了竹红菌素HA,HB以及13-SO_3Na-DDHA在DMF-H_2O(体积分数=1)混合体系中的电化学氧化还原性质。结果表明,它们都为两步单电子还原过程,反应机理为:油溶性.水溶性13-SO3Na-DDHA:(第一步)(质子化);(第二步).并且,HA,HB的单电子还原半醒自由基非常稳定,而13-SO_3Na-DDHA单电子还原半醌自由基存在歧化反应,其速率常数k_f=0.408。 相似文献