INVESTIGATIONS ON L(2) PHASE AND CUBIC PHASE IN THE SYSTEM AOT 1-OCTANOL WATER

被引:51
作者
GRADZIELSKI, M
HOFFMANN, H
PANITZ, JC
WOKAUN, A
机构
[1] UNIV BAYREUTH,LEHRSTUHL PHYS CHEM 1,D-95440 BAYREUTH,GERMANY
[2] UNIV BAYREUTH,LEHRSTUHL PHYS CHEM 2,D-95440 BAYREUTH,GERMANY
关键词
D O I
10.1006/jcis.1995.1011
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
The properties of L(2) phase and cubic phase in the ternary system AOT/1-octanol/water have been studied by means of electrical conductivity, NMR self-diffusion experiments, theology, static and dynamic light scattering, SANS, and DSC. L(2) phase and cubic phase are neighboring phases that are both isotropic but vary largely with respect to their macroscopic appearance; i.e., the L(2) phase is of low viscosity, whereas the cubic phase is gel-like. At the phase transition, L(2) phase --> cubic phase, no discontinuities were observed for the electrical conductivity and the self-diffusion coefficient of water; i.e., both phases should structurally be closely related and both are bicontinuous. SANS showed that in the cubic phase the size of the structural units decreases with increasing AOT concentration. The self-diffusion coefficients of both water and octanol/amphiphile are decreasing in parallel with the size of the structural units. At the same time the shear modulus rises with increasing surfactant concentration, which can be explained in terms of a simple network theory, where each structural unit acts as a network point. At high temperatures the cubic phase melts to form the L(2) phase with transition enthalpies of typically 5-250 mJ/g. Finally, it was observed that for not too high AOT content such a phase transition occurs also upon lowering the temperatures; i.e., a reverse melting transition takes place. (C) 1995 Academic Press, Inc.
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页码:103 / 118
页数:16
相关论文
共 63 条
[1]  
[Anonymous], 1952, INT TABLES XRAY CRYS, VI
[2]  
[Anonymous], 2004, SURFACTANTS INTERFAC
[3]   STRUCTURAL SIMILARITIES BETWEEN THE L3 AND BICONTINUOUS CUBIC PHASES IN THE AOT-BRINE SYSTEM [J].
BALINOV, B ;
OLSSON, U ;
SODERMAN, O .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (15) :5931-5936
[4]   OSCILLATORY SHEAR-FLOW MEASUREMENTS ON LIQUID-CRYSTALLINE PHASES WITH HEXAGONAL AND CUBIC STRUCTURES [J].
BOHLIN, L ;
LJUSBERGWAHREN, H ;
MIEZIS, Y .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1985, 103 (01) :294-295
[5]   TRIBLOCK COPOLYMERS IN AQUEOUS-SOLUTION STUDIED BY STATIC AND DYNAMIC LIGHT-SCATTERING AND OSCILLATORY SHEAR MEASUREMENTS - INFLUENCE OF RELATIVE BLOCK SIZES [J].
BROWN, W ;
SCHILLEN, K ;
HVIDT, S .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (14) :6038-6044
[6]   STRUCTURE OF MICROEMULSIONS IN THE BRINE AEROSOL OT/ISOOCTANE SYSTEM AT THE HYDROPHILE LIPOPHILE BALANCE TEMPERATURE STUDIES BY THE SELF-DIFFUSION TECHNIQUE [J].
CARNALI, JO ;
CEGLIE, A ;
LINDMAN, B ;
SHINODA, K .
LANGMUIR, 1986, 2 (04) :417-423
[7]  
CATES ME, 1990, J PHYS-CONDENS MAT, V2, P339
[8]   MICROEMULSION STRUCTURE IN 4-COMPONENT SYSTEMS FOR DIFFERENT SURFACTANTS [J].
CEGLIE, A ;
DAS, KP ;
LINDMAN, B .
COLLOIDS AND SURFACES, 1987, 28 (01) :29-40
[9]   CUBIC PHASES AS STRUCTURES OF DISCLINATIONS [J].
CHARVOLIN, J ;
SADOC, JF .
COLLOID AND POLYMER SCIENCE, 1990, 268 (02) :190-195
[10]  
CHARVOLIN J, 1983, J CHIM PHYS, V1, P80