Solid-liquid phase behavior of binary mixture of tetraethylene glycol decyl ether and water

被引:18
作者
Nibu, Y [1 ]
Inoue, T [1 ]
机构
[1] Fukuoka Univ, Fac Sci, Dept Chem, Fukuoka 81480, Japan
关键词
tetraethylene glycol decyl ether; nonionic surfactant; surfactant/water mixture; phase behavior; phase diagram; phase compound; surfactant-water interaction; differential scanning calorimetry; Fourier transform infrared spectroscopy;
D O I
10.1006/jcis.1998.5615
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solid-liquid phase behavior of binary mixture of nonionic surfactant, tetraethylene glycol decyl ether (C10E4), and water was examined by means of differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR), polarized optical microscopy (POM), and visual observation in the temperature range -40-70 degrees C. The DSC experiments allowed us to determine many phase boundaries among various phases appearing in this mixture system, including mesomorphic phases. The T-X phase diagram for fluid phases of C10E4/H2O mixture constructed from the results of DSC and visual observation was in good agreement with that previously reported by Lang and Morgan for the same mixture system except for the occurrence of a dilute lamellar phase (Lang, J. C. and Morgan, R. D., J. Chem. Phys., 73, 5849 (1980). The FT-IR spectra obtained for the mixture in a solid state demonstrated that the phase compound expressed by C10E4 . 6H(2)O is formed in the solid phase, which indicates that there is a strong interaction in the solid state between water and the hydrophilic polyoxyethylene chain of the surfactant. The FT-IR results also suggested that the strength of the hydrogen bond between water and the polyoxyethylene chain of C10E4 differs among the phase states of the mixture, and increases in the order L-2 < L-1 < L-alpha approximate to H-1 < solid, where L-2 refers to the inverted micellar phase, L-1 the normal micellar phase, L-alpha the lamellar phase, and H-1 the normal hexagonal phase. (C) 1998 Academic Press.
引用
收藏
页码:231 / 240
页数:10
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