A novel aspect on structural formation of physical gels

被引:19
作者
Chou, CM [1 ]
Hong, PD [1 ]
机构
[1] Natl Taiwan Univ Sci & Technol, Dept Polymer Engn, Taipei 10607, Taiwan
关键词
D O I
10.1021/ma025831z
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
By using the time-resolved small angle light scattering (TRSALS) technique, we present the first real-time measurement of the physical gelation process for a crystalline polymer. The finding is that the light scattering patterns show a unique feature in the H-v and the V-v scattering for PVDF gel electrolytes. More significant is the fact that the initial H-v scattering pattern with a four-leaf-clover shape gradually turns into a final pattern with 2-fold structure, composed of an X-type and a four-crescent-moon shape at low and high q ranges, respectively. The experimental results are noteworthy in that they show the characteristics of the special birefingent transition, i.e., the anisotropic-to-isotropic transition in the gelation process. Our observations illustrate a novel aspect in the structural formation of physical gels. During the course of the gelation we observed the existence of three distinct time regimes: (i) a nucleation and growth stage, where the droplet formation can be interpreted in terms of the simultaneous formation of crystallites or fibril texture with the growth of the birefringent droplets and the crystallites or the fibrils act as junction points in the droplets, leading to approximate dispersion of the hard spheres in the solutions; (ii) the dynamic cluster-to-percolation transition stage, where the large-scale concentration fluctuation is triggered by the hard spheres diffusion and aggregation to form the macroscopic percolation structures and where this main characteristics of the process is simultaneously accompanied by the anisotropic-to-isotropic transition; (iii) a ripening process in the late stage of gelation that causes the arrangement and growth of microstructures such as crystallites or fibrils to be highly concentrated. It is clear that these experimental results are entirely different from previous understandings of spinodal gels. We may proceed from these results to conclude that the formation of the birefringent droplets and the colloid aggregation dominate the physical gelation process in the present work.
引用
收藏
页码:7331 / 7337
页数:7
相关论文
共 43 条
[11]   A DYNAMIC SCALING ASSUMPTION FOR PHASE-SEPARATION [J].
FURUKAWA, H .
ADVANCES IN PHYSICS, 1985, 34 (06) :703-750
[12]   CRYSTALLIZATION AND MELTING OF AQUEOUS GELATIN [J].
GODARD, P ;
BIEBUYCK, JJ ;
DAUMERIE, M ;
NAVEAU, H ;
MERCIER, JP .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1978, 16 (10) :1817-1828
[13]   SPATIAL ORDERING AND STRUCTURE FACTOR SCALING IN THE SIMULATIONS OF COLLOID AGGREGATION [J].
GONZALEZ, AE ;
RAMIREZSANTIAGO, G .
PHYSICAL REVIEW LETTERS, 1995, 74 (07) :1238-1241
[14]   SPONTANEOUS PINNING OF DOMAIN GROWTH DURING SPINODAL DECOMPOSITION OF OFF-CRITICAL POLYMER MIXTURES [J].
HASHIMOTO, T ;
TAKENAKA, M ;
IZUMITANI, T .
JOURNAL OF CHEMICAL PHYSICS, 1992, 97 (01) :679-689
[15]   Phase separation and gelation behaviors in poly(vinylidene fluoride)/tetra(ethylene glycol) dimethyl ether solutions [J].
Hong, PD ;
Chou, CM .
POLYMER, 2000, 41 (23) :8311-8320
[16]   Effects of phase separation on structural characteristics of poly(vinyl chloride) physical gels [J].
Hong, PD ;
Chou, CM .
MACROMOLECULES, 2000, 33 (26) :9673-9681
[17]  
KELLER A, 1995, FARADAY DISCUSS, V110, P1
[18]   THE KINETICS OF PRECIPITATION FROM SUPERSATURATED SOLID SOLUTIONS [J].
LIFSHITZ, IM ;
SLYOZOV, VV .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 1961, 19 (1-2) :35-50
[19]   Structure evolution during gelation at later stages of spinodal decomposition in gelatin/maltodextrin mixtures [J].
Lorén, N ;
Altskär, A ;
Hermansson, AM .
MACROMOLECULES, 2001, 34 (23) :8117-8128
[20]   SMALL-ANGLE POLARIZED-LIGHT SCATTERING FROM AMORPHOUS SPHERES [J].
MEETEN, GH ;
NAVARD, P .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1984, 22 (12) :2159-2163