Suspensions of silica particles grafted with concentrated polymer brush: Effects of graft chain length on brush layer thickness and colloidal crystallization

被引:249
作者
Ohno, Kohji [1 ]
Morinaga, Takashi [1 ]
Takeno, Satoshi [1 ]
Tsujii, Yoshinobu [1 ]
Fukuda, Takeshi [1 ]
机构
[1] Kyoto Univ, Inst Chem Res, Kyoto 6110011, Japan
关键词
D O I
10.1021/ma071770z
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We previously reported that monodisperse silica particles (SiPs) afforded with a high-density brush of poly(methyl methacrylate) (PMMA) and suspended in a good solvent for PMMA formed a colloidal crystal in a certain concentration range (Macromolecules 2006, 39, 1245). Here we investigated similar hybrid particles with respect to the influence of graft chain length L-c on their hydrodynamic diameter D-h in dilute suspension and on colloidal crystallization in more concentrated suspension. The average radius r(0) of SiPs was 65 rim, and the surface density sigma(0) of PMMA grafts at the SiP surface was about 0.7 chains/nm(2) (about 36 000 chains per particle). The hydrodynamic thickness of the swollen brush layer h (=D-h/2 - r(0)) was qualitatively interpretable by a modified Daoud-Cotton-type scaling model. Namely, for short graft chains, h obeyed the universal relation, h[1 + (h/2r(0))] - L-c sigma(1/2)(0), applicable to concentrated polymer brushes on flat as well as spherical surfaces, and for chains longer than a critical length, h showed positive deviations from this linear relation, indicating the brush layer getting into the semidilute polymer brush regime. Suspensions of the hybrid particles showed a phase transition from a (disordered) fluid to a fully crystallized system with a narrow fluid/crystal coexisting regime. The critical concentration of crystallization (melting point) decreased with increasing graft chain length, and the nearest-neighbor interparticle distance D-dis in the crystal approached to a micrometer scale as the graft molecular weight reached 500 000. Good correlation was observed between D-h and D-dis such that D-dis = (1.15 +/- 0.05)D-h. Confocal laser scanning microscopic observation suggested that the colloidal crystal generally include both hexagonal close-packed (hcp) and face-centered cubic (fcc) lattice arrangements with the fcc arrangement likely to increase with increasing chain length.
引用
收藏
页码:9143 / 9150
页数:8
相关论文
共 60 条
[1]   STUDIES IN MOLECULAR DYNAMICS .V. HIGH-DENSITY EQUATION OF STATE AND ENTROPY FOR HARD DISKS AND SPHERES [J].
ALDER, BJ ;
HOOVER, WG ;
YOUNG, DA .
JOURNAL OF CHEMICAL PHYSICS, 1968, 49 (08) :3688-&
[2]   ADSORPTION OF CHAIN MOLECULES WITH A POLAR HEAD A-SCALING DESCRIPTION [J].
ALEXANDER, S .
JOURNAL DE PHYSIQUE, 1977, 38 (08) :983-987
[3]   Towards the synthetic all-optical computer:: science fiction or reality? [J].
Arsenault, A ;
Fournier-Bidoz, SB ;
Hatton, B ;
Míguez, H ;
Tétrault, N ;
Vekris, E ;
Wong, S ;
Yang, SM ;
Kitaev, V ;
Ozin, GA .
JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (05) :781-794
[4]   Prediction of absolute crystal-nucleation rate in hard-sphere colloids [J].
Auer, S ;
Frenkel, D .
NATURE, 2001, 409 (6823) :1020-1023
[5]   CONFORMATIONS OF STAR-BRANCHED MACROMOLECULES [J].
BIRSHTEIN, TM ;
ZHULINA, EB .
POLYMER, 1984, 25 (10) :1453-1461
[6]   Controlled growth of hard-sphere colloidal crystals [J].
Cheng, ZD ;
Russell, WB ;
Chaikin, PM .
NATURE, 1999, 401 (6756) :893-895
[7]   From opals to optics: Colloidal photonic crystals [J].
Colvin, VL .
MRS BULLETIN, 2001, 26 (08) :637-641
[8]   POLYMERS TETHERED TO CURVED INTERFACES - A SELF-CONSISTENT-FIELD ANALYSIS [J].
DAN, N ;
TIRRELL, M .
MACROMOLECULES, 1992, 25 (11) :2890-2895
[9]   STAR SHAPED POLYMERS - A MODEL FOR THE CONFORMATION AND ITS CONCENTRATION-DEPENDENCE [J].
DAOUD, M ;
COTTON, JP .
JOURNAL DE PHYSIQUE, 1982, 43 (03) :531-538
[10]   CONFORMATIONS OF POLYMERS ATTACHED TO AN INTERFACE [J].
DEGENNES, PG .
MACROMOLECULES, 1980, 13 (05) :1069-1075