TY - JOUR
T1 - Thermodynamic properties of aqueous mixtures of hydrophilic compounds 2. Aminoethanol and its methyl derivatives
AU - Touhara, H.
AU - Okazaki, S.
AU - Okino, F.
AU - Tanaka, H.
AU - Ikari, K.
AU - Nakanishi, K.
N1 - Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1982/2
Y1 - 1982/2
N2 - The vapour pressures of water + 2-aminoethanol, + N-methyl-2-aminoethanol, and + N,N-dimethyl-2-aminoethanol at 298.15 and 308.15 K were measured over the whole composition range by a static method. The excess enthalpies and densities of the same mixtures at 298.15 K were also measured with an isothermal displacement calorimeter and a pyknometer. The thermodynamic excess functions: GE, HE, TSE, and VE were calculated. Except for aminoethanol-rich region in (water + N,N-dimethyl-2-aminoethanol), where GE is slightly positive, the signs and relative magnitudes of molar excess functions were 0 > GE>TSE>HE, VE < 0. These are in accordance with general characteristics of (water + a highly hydrophilic compound). However, hydrophobicity is clearly seen for dilute aqueous solutions where the partial molar volume of aminoethanol exhibits a minimum and the partial molar enthalpy decreases rapidly to a limiting value at infinite dilution. This tendency increases with the introduction of methyl groups into 2-aminoethanol.
AB - The vapour pressures of water + 2-aminoethanol, + N-methyl-2-aminoethanol, and + N,N-dimethyl-2-aminoethanol at 298.15 and 308.15 K were measured over the whole composition range by a static method. The excess enthalpies and densities of the same mixtures at 298.15 K were also measured with an isothermal displacement calorimeter and a pyknometer. The thermodynamic excess functions: GE, HE, TSE, and VE were calculated. Except for aminoethanol-rich region in (water + N,N-dimethyl-2-aminoethanol), where GE is slightly positive, the signs and relative magnitudes of molar excess functions were 0 > GE>TSE>HE, VE < 0. These are in accordance with general characteristics of (water + a highly hydrophilic compound). However, hydrophobicity is clearly seen for dilute aqueous solutions where the partial molar volume of aminoethanol exhibits a minimum and the partial molar enthalpy decreases rapidly to a limiting value at infinite dilution. This tendency increases with the introduction of methyl groups into 2-aminoethanol.
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U2 - 10.1016/0021-9614(82)90026-X
DO - 10.1016/0021-9614(82)90026-X
M3 - Article
AN - SCOPUS:0000903533
SN - 0021-9614
VL - 14
SP - 145
EP - 156
JO - Journal of Chemical Thermodynamics
JF - Journal of Chemical Thermodynamics
IS - 2
ER -