Uniaxial elongational behavior of poly(vinyl chloride) physical gel

被引:10
作者
Aoki, Yuji [1 ]
Hirayama, Kentaro [1 ]
Kikuchi, Koji [1 ]
Sugimoto, Masataka [1 ]
Koyama, Kiyohito [1 ]
机构
[1] Yamagata Univ, Dept Polymer Sci & Engn, Yamagata 9928510, Japan
关键词
Poly(vinyl chloride); Plasticizer; Elongational viscosity; Gel elasticity; Stress-strain curve; Neo-Hookean model; RHEOLOGICAL IMAGES; VISCOELASTIC PROPERTIES; LINEAR VISCOELASTICITY; STRAIN BEHAVIOR; SCALING LAW; POLYDIMETHYLSILOXANE;
D O I
10.1007/s00397-010-0483-4
中图分类号
O3 [力学];
学科分类号
08 ; 0801 ;
摘要
A poly(vinyl chloride) di-octyl phthalate (DOP) gel with PVC content of 20 wt.% was prepared by a solvent evaporation method. The dynamic viscoelsticity and elongational viscosity of the PVC/DOP gel were measured at various temperatures. The gel exhibited a typical sol-gel transition behavior with elevating temperature. The critical gel temperature (T-gel) characterized with a power-law relationship between the storage and loss moduli, G(') and G(aEuro3), and frequency omega, , was observed to be 152A degrees C. The elongational viscosity of the gel was measured below the T-gel. The gel exhibited strong strain hardening. Elongational viscosity against strain plot was independent of strain rate. This finding is different from the elongational viscosity behavior of linear polymer solutions and melts. The stress-strain relations were expressed by the neo-Hookean model at high temperature (135A degrees C) near the T-gel. However, the stress-strain curves were deviated from the neo-Hookean model at smaller strain with decreasing temperature. These results indicated that this physical gel behaves as the neo-Hookean model at low cross-linking point, and is deviated from the neo-Hookean model with increasing of the PVC crystallites worked as the cross-linking junctions.
引用
收藏
页码:1071 / 1076
页数:6
相关论文
共 29 条
[1]  
Abe S, 2001, J APPL POLYM SCI, V79, P2146, DOI 10.1002/1097-4628(20010321)79:12<2146::AID-APP1022>3.0.CO
[2]  
2-Q
[3]  
[Anonymous], 1997, ADV POLYM SCI
[4]   A preparation method of thermoreversible poly(vinyl chloride) gels [J].
Aoki, Y .
MACROMOLECULES, 2001, 34 (10) :3500-3502
[5]   Rheological images of poly(vinyl chloride) gels. 5. Effect of molecular weight distribution [J].
Aoki, Y ;
Li, L ;
Uchida, H ;
Kakiuchi, M ;
Watanabe, H .
MACROMOLECULES, 1998, 31 (21) :7472-7478
[6]   Rheological images of poly(vinyl chloride) gels. 6. Effect of temperature [J].
Aoki, Y ;
Li, L ;
Kakiuchi, M .
MACROMOLECULES, 1998, 31 (23) :8117-8123
[7]   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
[8]   VISCOELASTIC BEHAVIOR DURING GELATION OF VARIOUS MOLAR-MASS POLYVINYL-CHLORIDE SOLUTIONS AND POLYMERIZATION TEMPERATURES [J].
DORRESTIJN, A ;
NIJENHUIS, KT .
COLLOID AND POLYMER SCIENCE, 1990, 268 (10) :895-900
[9]   CORRELATION BETWEEN VISCOELASTIC BEHAVIOR AND SMALL-ANGLE X-RAY-SCATTERING OF THERMOREVERSIBLE POLYVINYL-CHLORIDE GELS [J].
DORRESTIJN, A ;
KEIJZERS, AEM ;
NIJENHUIS, KT .
POLYMER, 1981, 22 (03) :305-312
[10]  
Ferry J. D., 1980, VISCOELASTIC PROPERT, V3rd ed.