Triblock copolymer based thermoreversible gels .2. Analysis of the sol-gel transition

被引:52
作者
Yu, JM [1 ]
Dubois, P [1 ]
Teyssie, P [1 ]
Jerome, R [1 ]
Blacher, S [1 ]
Brouers, F [1 ]
LHomme, G [1 ]
机构
[1] UNIV LIEGE, CTR EDUC & RES MACROMOLEC, B-4000 LIEGE, BELGIUM
关键词
D O I
10.1021/ma951911+
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Syndiotactic poly(methyl methacrylate) (sPMMA)-polybutadiene (PBD)-sPMMA triblock copolymers of various chemical compositions and different molecular weights have been studied in the presence of o-xylene, which is a selective solvent for the central PBD block. Thermoreversible gels can be formed in a suitable curing temperature range (<35 degrees C) and at a high enough concentration (>1 wt %). The time dependence of the storage (G') and the loss (G '') moduli has been measured in a frequency range of 0.08-1 Hz. The, static and dynamic properties of the gels have been discussed on the basis of the scaling theory. At the gel point, where the loss angle (tan delta(c) = G ''/G') is independent of frequency, typical power laws G'(omega) similar to G ''(omega) similar to omega(Delta) have been observed. The scaling exponent Delta has been found equal to 0.70 +/- 0.02 independently of the PBD and PMMA molecular weight, i.e., 36 000 < <(M)over bar (n)> (PBD) < 100 000 and 20 000 < <(M)over bar (n)> , (PMMA) < 51 000. This exponent is also independent of the copolymer concentration and temperature in the investigated range, i.e., 2-7 wt % and 8-24 degrees C, respectively. This value of Delta agrees with theoretical predictions as well as with experimental values reported for some chemical gels; it is however different from the experimental values published for most physical gels. A PBD-PMMA diblock copolymer also forms a gel in o-xylene, although at higher concentration and lower temperature compared to the parent triblock copolymer. The scaling exponent Delta is then somewhat smaller, i.e., 0.61.
引用
收藏
页码:5384 / 5391
页数:8
相关论文
共 35 条
[1]   EVOLUTION OF STRUCTURE AND VISCOELASTICITY IN AN EPOXY NEAR THE SOL-GEL TRANSITION [J].
ADOLF, D ;
MARTIN, JE ;
WILCOXON, JP .
MACROMOLECULES, 1990, 23 (02) :527-531
[2]  
[Anonymous], 2018, INTRO PERCOLATION TH
[3]   CROSSLINKED BIOPOLYMERS - EXPERIMENTAL-EVIDENCE FOR SCALAR PERCOLATION THEORY [J].
AXELOS, MAV ;
KOLB, M .
PHYSICAL REVIEW LETTERS, 1990, 64 (12) :1457-1460
[4]   LINEAR VISCOELASTICITY AT THE GEL POINT OF A CROSS-LINKING PDMS WITH IMBALANCED STOICHIOMETRY [J].
CHAMBON, F ;
WINTER, HH .
JOURNAL OF RHEOLOGY, 1987, 31 (08) :683-697
[5]  
CHAMBON F, 1985, POLYM BULL, V13, P499
[6]   THE AC ELECTRICAL-CONDUCTIVITY OF BINARY DISORDERED-SYSTEMS, PERCOLATION CLUSTERS, FRACTALS AND RELATED MODELS [J].
CLERC, JP ;
GIRAUD, G ;
LAUGIER, JM ;
LUCK, JM .
ADVANCES IN PHYSICS, 1990, 39 (03) :191-308
[7]   FREQUENCY-DEPENDENCE OF VISCOELASTIC PROPERTIES OF SOME PHYSICAL GELS NEAR THE GEL POINT [J].
CUVELIER, G ;
LAUNAY, B .
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA, 1990, 40 :23-31
[8]  
De Gennes P.-G., 1979, SCALING CONCEPTS POL
[9]  
DEGENNES PG, 1978, CR ACAD SCI B PHYS, V286, P131
[10]   GELATION OF AQUEOUS GELATIN SOLUTIONS .2. RHEOLOGY OF THE SOL-GEL TRANSITION [J].
DJABOUROV, M ;
LEBLOND, J ;
PAPON, P .
JOURNAL DE PHYSIQUE, 1988, 49 (02) :333-343