Self-assembly in linker-modified microemulsions

被引:58
作者
Acosta, EJ
Harwell, JH
Sabatini, DA
机构
[1] Univ Oklahoma, Inst Appl Surfactant Res, Norman, OK 73019 USA
[2] Univ Oklahoma, Sarkeys Energy Ctr, Dept Chem Engn & Mat Sci, Norman, OK 73019 USA
[3] Univ Oklahoma, Carson Engn Ctr, Coll Engn, Norman, OK 73019 USA
[4] Univ Oklahoma, Carson Engn Ctr, Civil Engn & Environm Sci Dept, Norman, OK 73019 USA
关键词
microemulsion; trichloroethylene; tetrachloroethylene; lipophilic; hydrophilic; linkers; partition; interfacial; tension;
D O I
10.1016/j.jcis.2004.03.037
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
Linker molecules are added to microemulsion systems to enhance the interaction between the surfactant and oil (lipophilic linkers) or water (hydrophilic linkers) phases. Previous results suggest that when lipophilic and hydrophilic linkers are combined they behave as a self-assembled surfactant at the oil/water interface. In this work we investigate this self-assembly phenomenon as a function of surfactant, linker and electrolyte concentration. We find that middle phase microemulsion appears at a specific concentration higher than the critical micelle concentration (CMC), which we denote as the critical middle phase microemulsion concentration (CmuC). When the lipophilic linker dodecanol is added in equimolar ratio to the hydrophilic linker sodium mono- and dimethyl naphthalene sulfonate (SMDNS), the middle phase microemulsion did not appear until the surfactant sodium dihexyl sulfosuccinate (SDHS) concentration was larger than the CmuC of the SDHS-alone system. Dodecanol is shown to segregate near the surfactant tails following a Langmuir-type adsorption process. This segregation is not affected by the electrolyte concentration but is significantly reduced when the surfactant (SDHS) concentration approaches the CmuC. The data suggest that the self-assembly between hydrophilic and lipophilic linkers to form middle phase microemulsions is only possible if a minimum amount of surfactant is present. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:652 / 664
页数:13
相关论文
共 27 条
[1]   Net-average curvature model for solubilization and supersolubilization in surfactant microemulsions [J].
Acosta, E ;
Szekeres, E ;
Sabatini, DA ;
Harwell, JH .
LANGMUIR, 2003, 19 (01) :186-195
[2]   Formulating chlorinated hydrocarbon microemulsions using linker molecules [J].
Acosta, E ;
Tran, S ;
Uchiyama, H ;
Sabatini, DA ;
Harwell, JH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (21) :4618-4624
[3]   The role of hydrophilic linkers [J].
Acosta, E ;
Uchiyama, H ;
Sabatini, DA ;
Harwell, JH .
JOURNAL OF SURFACTANTS AND DETERGENTS, 2002, 5 (02) :151-157
[4]   Coalescence and solubilization kinetics in linker-modified microemulsions and related systems [J].
Acosta, EJ ;
Le, MA ;
Harwell, JH ;
Sabatini, DA .
LANGMUIR, 2003, 19 (03) :566-574
[5]   Sphere-to-rod transitions of micelles in model nonionic surfactant solutions [J].
Al-Anber, ZA ;
Avalos, JB ;
Floriano, MA ;
Mackie, AD .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (08) :3816-3826
[6]  
[Anonymous], 1992, INTERMOLECULAR SURFA
[7]  
AUVRAY L, 1994, MICELLES MEMBRANES M, P347
[8]   INTERFACIAL-TENSIONS AND AGGREGATE STRUCTURE IN C12E5 OIL-WATER MICROEMULSION SYSTEMS [J].
AVEYARD, R ;
BINKS, BP ;
FLETCHER, PDI .
LANGMUIR, 1989, 5 (05) :1210-1217
[9]  
BOURREL M, 1988, MICROMULSIONS RELATE
[10]   IMPROVING SOLUBILIZATION IN MICROEMULSIONS WITH ADDITIVES .1. THE LIPOPHILIC LINKER ROLE [J].
GRACIAA, A ;
LACHAISE, J ;
CUCUPHAT, C ;
BOURREL, M ;
SALAGER, JL .
LANGMUIR, 1993, 9 (03) :669-672