SMALL-ANGLE NEUTRON-SCATTERING NEAR LIFSHITZ LINES - TRANSITION FROM WEAKLY STRUCTURED MIXTURES TO MICROEMULSIONS

被引:192
作者
SCHUBERT, KV
STREY, R
KLINE, SR
KALER, EW
机构
[1] MAX PLANCK INST BIOPHYS CHEM,D-37018 GOTTINGEN,GERMANY
[2] UNIV DELAWARE,DEPT CHEM ENGN,NEWARK,DE 19716
[3] UNIV DELAWARE,DEPT CHEM ENGN,NEWARK,DE 19716
关键词
D O I
10.1063/1.467387
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
We have studied the phase behavior, wetting transitions, and small angle neutron scattering (SANS) of water, n-alkane, and n-alkyl polyglycol ether (C(i)E(j)) systems in order to locate the transition between weakly structured mixtures and microemulsions, and to provide a measure for the transition. We first determined the wetting transition by macroscopic measurements and then measured the location of the Lifshitz lines by SANS. Starting with well-structured mixtures (exhibiting nonwetting middle phases and well-expressed scattering peaks, features that qualify them as microemulsions) the wetting transition was induced by increasing the chain length of the alkane or by changing the oil/water volume ratio, and then the Lifshitz line was crossed. Further, starting with systems past the disorder line (weakly structured mixtures that display wetting middle phases and no scattering peaks), local structure was induced by either increasing the surfactant concentration or decreasing the oil/water volume ratio or the temperature. In each case a Lifshitz line was crossed. Analyzing the scattering experiments quantitatively, allows determination of the amphiphilicity factor, which is a measure of the strength of the surfactant. The results suggest there is a sequence of roughly parallel surfaces within the three-dimensional composition-temperature space. As the amphiphilicity factor increases, first a disorder surface is encountered, then a Lifshitz surface, and finally a wetting transition surface. How and to what extent these surfaces move in the one-phase region toward smaller surfactant concentrations, and intersect there with the body of heterogeneous phases, depends on a number of factors that are discussed in some detail.
引用
收藏
页码:5343 / 5355
页数:13
相关论文
共 63 条
[1]   MICROEMULSIONS - STRUCTURES, SURFACTANT LAYER PROPERTIES AND WETTING TRANSITIONS [J].
ABILLON, O ;
LEE, LT ;
LANGEVIN, D ;
WONG, K .
PHYSICA A, 1991, 172 (1-2) :209-218
[2]  
[Anonymous], 1994, PHASE TRANSITIONS CR
[3]   EVIDENCE FOR ZERO MEAN-CURVATURE MICROEMULSIONS [J].
AUVRAY, L ;
COTTON, JP ;
OBER, R ;
TAUPIN, C .
JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (20) :4586-4589
[4]   FLUID MICROSTRUCTURE TRANSITION FROM GLOBULAR TO BICONTINUOUS IN MIDRANGE MICROEMULSION [J].
BODET, JF ;
BELLARE, JR ;
DAVIS, HT ;
SCRIVEN, LE ;
MILLER, WG .
JOURNAL OF PHYSICAL CHEMISTRY, 1988, 92 (07) :1898-1902
[5]  
CHATENAY D, 1985, ACS SYM SER, V272, P119
[6]   EXPERIMENTAL-STUDY OF INTERFACIAL PHASE-TRANSITIONS IN 3-COMPONENT SURFACTANT SYSTEMS [J].
CHEN, LJ ;
JENG, JF ;
ROBERT, M ;
SHUKLA, KP .
PHYSICAL REVIEW A, 1990, 42 (08) :4716-4723
[7]   WETTING TRANSITIONS AT LIQUID-LIQUID INTERFACES IN 3-COMPONENT WATER PLUS OIL PLUS NONIONIC SURFACTANT SYSTEMS [J].
CHEN, LJ ;
YAN, WJ ;
HSU, MC ;
TYAN, DL .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (07) :1910-1917
[8]  
CHEN SH, 1990, PROG COLL POL SCI S, V81, P30
[9]  
CIACH A, 1992, POLISH J CHEM, V66, P1347
[10]   DECAY OF CORRELATIONS IN LINEAR SYSTEMS [J].
FISHER, ME ;
WIODM, B .
JOURNAL OF CHEMICAL PHYSICS, 1969, 50 (09) :3756-&