Depletion Interactions: Effects of Added Homopolymer on Ordered Phases Formed by Spherical Block Copolymer Micelles

被引:17
作者
Abbas, Sayeed [1 ]
Lodge, Timothy P. [1 ,2 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
D O I
10.1021/ma8013838
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Three distinct poly(styrene-b-isoprene) (SI) diblock copolymers with molecular weights of 16-16, 38-14, and 50-13 kDa for styrene and isoprene, respectively, formed spherical micelles when dissolved in diethyl phthalate (DEP). Since DEP is a styrene-selective solvent, micelles with polyisoprene in the core and polystyrene in the corona were formed. At block copolymer concentrations of 20%, 16%, and 14% in DEP, the spherical micelles of SI(16-16), SI(38-14), and SI(50-13) pack onto a face-centered cubic (FCC) lattice, a mixture of FCC and body-centered cubic (BCC) lattices, and a BCC lattice, respectively. Polystyrene homopolymers with molecular weights of 4, 48, and 180 kDa were added to these ordered solutions. The following general trends were observed: the FCC phase tended to disorder, and samples that originally behaved like soft solids exhibited liquidlike flow behavior. The effect increased strongly with both the molecular weight and concentration of homopolymer in the solution. Furthermore, the BCC lattice tended to be displaced by the FCC lattice, or to disorder, when homopolymer was added. These results can be explained by invoking depletion interactions, which have been studied extensively in colloid/polymer mixtures. However, the phenomenon differs in certain details from colloidal systems because the addition of homopolymer can
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页码:8895 / 8902
页数:8
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[11]  
Hamley I. W., 2005, BLOCK COPOLYMERS SOL
[12]   A thermally induced transition from a body-centred to a face-centred cubic lattice in a diblock copolymer gel [J].
Hamley, IW ;
Pople, JA ;
Diat, O .
COLLOID AND POLYMER SCIENCE, 1998, 276 (05) :446-450
[13]   Aqueous mesophases of block copolymers of ethylene oxide and 1,2-butylene oxide [J].
Hamley, IW ;
Mai, SM ;
Ryan, AJ ;
Fairclough, JPA ;
Booth, C .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2001, 3 (15) :2972-2980
[14]   Phase behavior of a block copolymer in solvents of varying selectivity [J].
Hanley, KJ ;
Lodge, TP ;
Huang, CI .
MACROMOLECULES, 2000, 33 (16) :5918-5931
[15]   Phase diagrams of hard-core repulsive Yukawa particles [J].
Hynninen, AP ;
Dijkstra, M .
PHYSICAL REVIEW E, 2003, 68 (02) :8
[16]   Static and dynamic structures of spherical nonionic surfactant micelles during the disorder-order transition [J].
Imai, M ;
Yoshida, I ;
Iwaki, T ;
Nakaya, K .
JOURNAL OF CHEMICAL PHYSICS, 2005, 122 (04)
[17]   Phase behavior of styrene-isoprene diblock copolymers in strongly selective solvents [J].
Lai, CJ ;
Russel, WB ;
Register, RA .
MACROMOLECULES, 2002, 35 (03) :841-849
[18]   Direct measurement of the penetration of free chains into a tethered chain layer [J].
Lee, LT ;
Kent, MS .
PHYSICAL REVIEW LETTERS, 1997, 79 (15) :2899-2902
[19]   Effects of mobile polymer concentration and chain length on the structure of tethered chains [J].
Lee, LT ;
Factor, BJ ;
Kent, MS ;
Rondelez, F .
PHYSICA B, 1996, 221 (1-4) :320-324
[20]   STRUCTURE OF TETHERED POLYMER-CHAINS IMMERSED IN A SOLUTION OF MOBILE POLYMER [J].
LEE, LT ;
FACTOR, BJ ;
RONDELEZ, F ;
KENT, MS .
FARADAY DISCUSSIONS, 1994, 98 :139-147