Solubilities, partition coefficients, density, and surface tension for imidazoles plus octan-1-ol or plus water or plus n-decane

被引:44
作者
Domanska, U
Kozlowska, MK
Rogalski, M
机构
[1] Warsaw Univ Technol, Fac Chem, Div Phys Chem, PL-00664 Warsaw, Poland
[2] Univ Metz, F-57012 Metz 01, France
关键词
D O I
10.1021/je0103014
中图分类号
O414.1 [热力学];
学科分类号
摘要
The solid-liquid equilibrium (SLE) has been measured from 270 K to the melting temperature of the solid for eight binary mixtures of imidazoles (1H-imidazole, 2-methyl-1H-imidazole, 1,2-dimethylimidazole, benzimidazole, and 2-methylbenzimidazole) with either octan-1-ol or water using a dynamic method. The melting temperature and enthalpy as well as the heat capacity change at the melting temperature were determined using differential scanning calorimetry (DSC). It was observed that the solubility of 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole is much higher in water than in octan-1-ol. The solubility of benzimidazole and 2-methylbenzimidazole is much higher in octan-1-ol. Experimental solubility data were correlated using the Wilson, UNIQUAC ASM, and NRTL 1 models. The solid-solid first-order phase transition has been observed with 2-methyl-1H-imidazole, benzimidazole, and 2-methylbenzimidazole. The best description of the experimental solubility data was obtained by the NRTL I equation. The average root-mean-square deviation on the equilibrium temperatures obtained with solutions of five imidazoles in octan-1-ol is 2.1 K. The solubility data were used to calculate the octan-1-ol/water partition coefficients as a function of temperature. The surface tension of air/octan-1-ol or air/n-decane systems as well as the interfacial tension of octan-1-ol/water or n-decane/water were determined as a function of imidazole concentration at 298.15 K and 308.15 K.
引用
收藏
页码:456 / 466
页数:11
相关论文
共 30 条
[21]   TERNARY LIQUID-LIQUID EQUILIBRIA AND THEIR REPRESENTATION BY MODIFIED NRTL EQUATIONS [J].
NAGATA, I ;
NAKAMIYA, Y ;
KATOH, K ;
KOYABU, J .
THERMOCHIMICA ACTA, 1981, 45 (02) :153-165
[22]   ON THE THERMODYNAMICS OF ALCOHOL-SOLUTIONS - PHASE-EQUILIBRIA OF BINARY AND TERNARY MIXTURES CONTAINING ANY NUMBER OF ALCOHOLS [J].
NAGATA, I .
FLUID PHASE EQUILIBRIA, 1985, 19 (03) :153-174
[23]   ON THE THERMODYNAMICS OF ASSOCIATED SOLUTIONS .2. VAPOR LIQUID EQUILIBRIA OF BINARY-SYSTEMS WITH ONE ASSOCIATING COMPONENT [J].
NATH, A ;
BENDER, E .
FLUID PHASE EQUILIBRIA, 1981, 7 (3-4) :289-307
[24]   A MOLECULAR ORBITAL DESCRIPTION OF PARTITIONING OF AROMATIC COMPOUNDS BETWEEN POLAR AND NONPOLAR PHASES [J].
ROGERS, KS ;
CAMMARATA, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 193 (01) :22-+
[25]  
SANDLER SI, 1993, FLUID PHASE EQUILIBR, V82, P63, DOI 10.1016/0378-3812(93)87129-O
[26]   PHYSICAL PROPERTIES OF HEAVY OXYGEN WATER .1. DENSITY AND THERMAL EXPANSION [J].
STECKEL, F ;
SZAPIRO, S .
TRANSACTIONS OF THE FARADAY SOCIETY, 1963, 59 (482) :331-&
[27]   Investigation of metallodrug-protein interactions by size-exclusion chromatography coupled with inductively coupled plasma mass spectrometry (ICP-MS) [J].
Szpunar, J ;
Makarov, A ;
Pieper, T ;
Keppler, BK ;
Lobinski, R .
ANALYTICA CHIMICA ACTA, 1999, 387 (02) :135-144
[28]   QUASI LATTICE LOCAL COMPOSITION MODEL FOR EXCESS GIBBS FREE-ENERGY OF LIQUID-MIXTURES [J].
VERA, JH ;
SAYEGH, SG ;
RATCLIFF, GA .
FLUID PHASE EQUILIBRIA, 1977, 1 (02) :113-135
[30]  
ZHANG ZY, LANDOLBORNSTEIN NEW, V8