PHASE-BEHAVIOR OF POLY(VINYL METHYL ETHER)-CROSS-POLYSTYRENE SEMIINTERPENETRATING NETWORKS

被引:4
作者
FELISBERTI, MI
KRIEGER, V
STADLER, R
机构
[1] UNIV MAINZ,INST ORGAN CHEM,JJ BECHER WEG 18-20,W-6500 MAINZ,GERMANY
[2] HERMANN STAUDINGER HAUS,INST MAKROMOLEK CHEM,W-7800 FREIBURG,GERMANY
[3] FREIBURGER MAT FORSCHUNGSZENTRUM,W-7800 FREIBURG,GERMANY
来源
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA | 1990年 / 40卷
关键词
D O I
10.1002/masy.19900400123
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Semi-interpenetrating polymer networks of varying composition are prepared by crosslinking polystyrene containing a small number of maleic anhydride groups (4.8 mol% of MA units) with hexamethylenediamine (HMDA) in the presence of linear poly(vinyl methyl ether) (PVME). Lightly crosslinked samples are homogeneous at room temperature and show a phase behaviour similar to uncrosslinked blends, i.e. lower critical solution temperature (LCST) behaviour. The influence of crosslinking on the phase behaviour has been studied by small angle light scattering (SALS) and turbidity measurements. The cloud point strongly depends on the heating rate. The presence of the network reduces the stable single phase region in agreement to theory. In systems showing spinodal decomposition, it is expected that some concentration fluctuations will grow more rapidly than others resulting in a separated phase system which shows high degree of connectivity with characteristic dimensions. Using temperature jump experiments, SALS can be used to estimate parameters of the phase separation kinetics and the characteristic dimensions of the phases. In temperature jump experiments into the spinodal region a maximum in the scattered light intensity is observed with time at a certain scattering vector. However, the semi-IPN's develop no scattering maximum. This is explained by a damping of the thermodynamical dominant wavelength in spinodal decomposition in the network.
引用
收藏
页码:223 / 235
页数:13
相关论文
共 26 条
[1]   THERMALLY INDUCED PHASE SEPARATION OF POLYSTYRENE-POLY(VINYL METHYL-ETHER) MIXTURES [J].
BANK, M ;
THIES, C ;
LEFFINGW.J .
JOURNAL OF POLYMER SCIENCE PART A-2-POLYMER PHYSICS, 1972, 10 (06) :1097-&
[2]   SMALL-ANGLE NEUTRON-SCATTERING STUDIES OF COMPATIBLE BLENDS OF LINEAR POLYVINYL METHYL-ETHER) AND CROSS-LINKED DEUTERATED POLYSTYRENE [J].
BAUER, BJ ;
BRIBER, RM ;
HAN, CC .
MACROMOLECULES, 1989, 22 (02) :940-948
[3]   PHASE-STABILITY OF WEAKLY CROSSLINKED INTERPENETRATING POLYMER NETWORKS [J].
BINDER, K ;
FRISCH, HL .
JOURNAL OF CHEMICAL PHYSICS, 1984, 81 (04) :2126-2136
[4]   PHASE SEPARATION BY SPINODAL DECOMPOSITION IN ISOTROPIC SYSTEMS [J].
CAHN, JW .
JOURNAL OF CHEMICAL PHYSICS, 1965, 42 (01) :93-+
[5]  
CHEIKH FB, 1986, POLYM COMMUN, V27, P23
[6]   PHASE-TRANSFORMATION IN MIXTURES OF POLYSTYRENE AND POLYVINYL METHYL-ETHER) [J].
DAVIS, DD ;
KWEI, TK .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1980, 18 (12) :2337-2345
[7]   ANGULAR DISSYMMETRY OF THE CRITICAL OPALESCENCE IN LIQUID MIXTURES [J].
DEBYE, P .
JOURNAL OF CHEMICAL PHYSICS, 1959, 31 (03) :680-687
[8]   MECHANICAL RELAXATION IN MISCIBLE POLYMER SYSTEMS - THE GLASS-TRANSITION REGIME IN POLY(VINYLMETHYLETHER) (PVME) CROSS-POLYSTYRENE (PS) SEMIINTERPENETRATING NETWORKS [J].
FELISBERTI, MI ;
FREITAS, LLD ;
STADLER, R .
POLYMER, 1990, 31 (08) :1441-1448
[9]  
FELISBERTI MI, 1990, THESIS FREIBURG
[10]  
FELISBERTI MI, 1990, POLYM MATER SCI ENG, V62, P695