Mean activity coefficients, phase equilibria of ternary system KCl-KHCO3-H2O at 288.2 and 308.2 K and separation of potassium salts in pesticide imidacloprid production wastewater

被引:0
作者
Feng, Yan [1 ]
Sang, Shi-Hua [1 ]
Zhu, Kuang-Yi [1 ]
Hu, Chun-Tao [1 ]
Tan, Xiao-Tian [1 ]
机构
[1] College of Materials, Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu
基金
中国国家自然科学基金;
关键词
Mean activity coefficient; Phase equilibrium; Pitzer model; Recovery of pesticide wastewater;
D O I
10.1016/j.molliq.2025.127131
中图分类号
学科分类号
摘要
Thermodynamic properties and phase equilibria of aqueous solutions containing potassium salts is of great significance for the resource recovery and utilization of pesticide production wastewater and waste residue. In order to further optimize the mixed ion interaction parameters of electrolyte solution containing HCO32− and recover KCl and KHCO3 from imidacloprid production wastewater, the mean activity coefficients of KCl-KHCO3-H2O mixed electrolyte solutions at 288.2 K and 308.2 K were investigated using the cell potential method, then the phase equilibria of the ternary system KCl-KHCO3-H2O at 288.2 K and 308.2 K was measured experimentally by the isothermal dissolution equilibrium method. In addition, the mixed ion interaction parameters θCl,HCO and ΨK,Cl,HCO in the Pitzer model were solved by combining the mean activity coefficients of KCl in the mixed electrolyte solutions and solubility data of ternary system, and other related thermodynamic parameters were calculated. Furthermore, the solubilities of the ternary system were calculated by using Pitzer model. The calculation results and experimental data are in good agreement. Subsequently, the precipitation amounts of various salts of imidacloprid production wastewater during isothermal evaporation were calculated based on the experimental phase diagrams at 288.2 K and 308.2 K. The process of recovering potassium salts was designed, and the theoretical basis for the separation of potassium salts in wastewater was provided. © 2025 Elsevier B.V.
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