Temperature-dependent solubility of Rebaudioside A in methanol/ethanol and ethyl acetate mixtures: Experimental measurements and thermodynamic modeling

被引:0
|
作者
Liu, Zhenguang [1 ]
Ding, Zexiang [1 ]
Cao, Yifeng [1 ,2 ]
Liu, Baojian [1 ,2 ]
Yang, Qiwei [1 ,2 ]
Zhang, Zhiguo [1 ,2 ]
Ren, Qilong [1 ,2 ]
Bao, Zongbi [1 ,2 ]
机构
[1] Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou,310058, China
[2] Institute of Zhejiang University-Quzhou, Quzhou,324000, China
基金
中国国家自然科学基金;
关键词
Binary mixtures - Entropy - Free energy - Gibbs free energy - Methanol - Organic solvents - Solubility - Temperature;
D O I
10.1016/j.cjche.2024.05.020
中图分类号
学科分类号
摘要
The equilibrium solubility of Rebaudioside A (Reb A) Form II in binary mixtures of methanol/ethanol and ethyl acetate was quantitatively determined within the temperature range of 283.15–328.15 K at ambient pressure. The experimental findings indicate a positive correlation between the solubility of Reb A (Form II) and both the temperature and the methanol/ethanol content in the solvent system. To describe the solubility data, six distinct models were employed: the modified Apelblat equation, the λh model, the combined nearly ideal binary solvent/Redlich–Kister (CNIBS/R–K) model, the van't Hoff-Jouyban-Acree (VJA) model, the Apelblat-Jouyban-Acree (AJA) model, and the non-random two-liquid (NRTL) model. The combined nearly ideal binary solvent/Redlich–Kister model exhibited the most precise fit for solubility in methanol + ethyl acetate mixtures, reflected by an average relative deviation (ARD) of 0.0011 and a root mean square deviation (RMSD) of 12×10−7. Conversely, for ethanol + ethyl acetate mixtures, the modified Apelblat equation provided a superior correlation (ARD = 0.0014, RMSD = 4×10−7). Furthermore, thermodynamic parameters associated with the dissolution of Reb A (Form II), including enthalpy, entropy, and the Gibbs energy change, were inferred from the data. The findings underscore that the dissolution process is predominantly endothermic across the solvent systems examined. Notably, the entropy changes appear to have a significant influence on the Gibbs free energy associated with the dissolution of Reb A (Form II), suggesting that entropic factors may play a pivotal role in the studied systems. © 2024 The Chemical Industry and Engineering Society of China, and Chemical Industry Press Co., Ltd
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页码:164 / 176
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