Field theoretical modeling of the coexistence of micelles and vesicles in binary copolymer mixtures

被引:12
|
作者
Li, Feng [1 ,2 ]
Marcelis, Antonius T. M. [2 ]
Sudholter, Ernst J. R. [3 ]
Stuart, Martien A. Cohen [1 ]
Leermakers, Frans A. M. [1 ]
机构
[1] Wageningen Univ, Lab Phys Chem & Colloid Sci, NL-6703 HB Wageningen, Netherlands
[2] Wageningen Univ, Organ Chem Lab, NL-6703 HB Wageningen, Netherlands
[3] Delft Univ Technol, Dept Chem Engn DelftChemTech, Lab Nanoorgan Chem, NL-2628 BL Delft, Netherlands
关键词
AMPHIPHILIC DIBLOCK COPOLYMERS; STATISTICAL THERMODYNAMICS; ASSOCIATION COLLOIDS; BILAYER-MEMBRANES; SURFACTANTS; TRANSITION; ADSORPTION; MECHANICS; LENGTH;
D O I
10.1039/b904525b
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
Using the self-consistent field (SCF) theory for inhomogeneous polymer systems, we elaborate a molecular model on a united atom level and discuss the possibility of coexistence of spherical micelles and small unilamellar vesicles in binary copolymer mixtures in a selective solvent. Our analysis is in line with recent neutron scattering and cryo-TEM results for the mixture of two members of the poly(butylene oxide)-b-poly(ethylene oxide) (referred to as PBnPEm) family, namely the (n, m) (10, 10) and (10, 18) species in water that clearly pointed towards such coexistence. The -PE18 is a micelle forming and the -PE10 a lamellae forming copolymer. Upon increasing concentration of -PE18 the micelle concentration that coexists with the vesicles increases dramatically. In this situation the micelles determine the chemical potentials of the copolymers and with increasing fraction PE18/PE10 the vesicle size becomes dramatically smaller. The selection of vesicle size indicates its thermodynamic stability. The strategy to arrive at thermodynamically stable vesicles with sizes much smaller than 100 nm is of interest for a wide range of applications.
引用
收藏
页码:4173 / 4184
页数:12
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