Solubility Measurement and Data Correlation of Isatoic Anhydride in 12 Pure Solvents at Temperatures from 288.15 to 328.15 K

被引:33
|
作者
Tian, Ningning [1 ,2 ]
Yu, Changyou [1 ,2 ]
Du, Shichao [1 ,2 ]
Lin, Bo [1 ,2 ]
Gao, Ye [1 ,2 ]
Gao, Zhenguo [1 ,2 ]
机构
[1] Tianjin Univ, State Key Lab Chem Engn, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[2] Coinnovat Ctr Chem & Chem Engn Tianjin, Tianjin 300072, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
MIXING PROPERTIES; MELTING-POINTS; WATER; ACID; EQUILIBRIUM; PARAMETERS; BENTAZON; ENTROPY;
D O I
10.1021/acs.jced.9b01164
中图分类号
O414.1 [热力学];
学科分类号
摘要
The solid-liquid equilibrium solubility of isatoic anhydride in 12 pure solvents (methanol, ethanol, 1-propanol, isopropyl alcohol, methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, acetone, 2-butanone, acetonitrile, and 1,4-dioxane) at T = 288.15 to 328.15 K was measured by the gravimetric method under atmospheric pressure. Experimental results demonstrate that the mole fraction solubility of isatoic anhydride in these selected solvents increased with the increase of temperature, and the dissolution behavior is affected by multiple factors like polarity, H-bond interaction, cohesive energy density, etc. The modified Apelblat model, the van't Hoff model, the nonrandom two-liquid model, and the lambda h model were used to correlate the experimental solubility data. The maximum values of the relative average deviation and root-mean-square deviation were no more than 4.23 X 10(-2) and 5.31 X 10(-4), respectively. Furthermore, the thermodynamic properties including the mixing Gibbs energy, mixing enthalpy, and mixing entropy were calculated, which indicates that the dissolution of isatoic anhydride was a spontaneous and entropy-favorable process.
引用
收藏
页码:2044 / 2052
页数:9
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