کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4907489 | 1426208 | 2017 | 19 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Understanding the enhanced solubility of 1,3-benzenedicarboxylic acid in polar binary solvents of (acetone + water) at various temperatures
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Understanding solid dissolution in polar binary solvents showing maximum or minimum solubility phenomenon is essential for the design and operation of anti-solvent crystallization process. Solubilities of 1,3-benzenedicarboxylic acid in binary solvents of acetone with water are measured from 278.15 to 323.15Â K using the static equilibrium method, covering the entire range of solvent composition. The solubility always increases with increasing temperature, while, at fixed temperature, a maximum solubility is observed in mixed solvents of certain composition. The experimental temperature-dependent solubility data of 1,3-benzenedicarboxylic acid in cosolvents of different compositions are correlated using the Apelblat model with an average relative deviation (ARD) of 0.18%. Calculations of the derived thermodynamic functions show that the dissolution of 1,3-benzenedicarboxylic acid in the solvent mixtures is endothermic and mainly driven by the enthalpy change. The Simplified Modified Wilson (SMW) model is adopted to reproduce the isothermal solubility data over the entire acetone composition with an overall ARD of 1.41%, with which the maximum mole fraction solubility and the corresponding solvent composition at different temperatures are determined, and are subsequently used to estimate the solubility parameter of 1,3-benzenedicarboxylic acid.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: The Journal of Chemical Thermodynamics - Volume 105, February 2017, Pages 105-111
Journal: The Journal of Chemical Thermodynamics - Volume 105, February 2017, Pages 105-111
نویسندگان
Bingwen Long, Yu Xia, Zhengyuan Deng, Yigang Ding,