ORGANIC INORGANIC HYBRID MATERIALS .2. COMPARED STRUCTURE OF POLYDIMETHYLSILOXANE AND HYDROGENATED POLYBUTADIENE BASED CERAMERS

被引:56
作者
SURIVET, F
LAM, TM
PASCAULT, JP
MAI, C
机构
[1] INST NATL SCI APPL,MAT MACROMOLEC LAB,CNRS,URA 507,20 AVE ALBERT EINSTEIN,F-69621 VILLEURBANNE,FRANCE
[2] CTR RECH CORNING EUROPE,F-77211 AVON,FRANCE
[3] INST NATL SCI APPL,GEMPPM,CNRS,URA 341,F-69621 VILLEURBANNE,FRANCE
关键词
D O I
10.1021/ma00047a027
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Different ceramer networks were successfully prepared in bulk or in solution. High transparency was observed for all the samples based on hydrogenated polybutadiene (H-PBD) and polydimethylsiloxane (PDMS) oligomers. These materials are microphase-separated materials due to the thermodynamic incompatibility between the different constitutive units. A similar microstructure exists in both types of samples: silicate clusters (or more precisely, polysiloxane clusters) including the cross-link points are dispersed in the oligomer-rich phase. In the case of PDMS ceramers, the three types of constitutive units are immiscible, so the morphology of such materials may be described by a three-phase system including the soft phase, practically pure in PDMS, the silicate clusters, and an interfacial region containing the urethane-urea units. The structure of the polymer obliged this mixed phase to be between the soft and the hard segments. For H-PBD ceramers, the soft segments and the urethane-urea units are miscible, and a two-phase model may schematize the H-PBD ceramer structure. In every case, good correlation was observed between the clusters separation distances and the end-to-end distance of the oligomers. These schematic models are consistent with our experimental results: they explain the existence of a periodicity in the networks and the fact that the correlation distance increases with increasing oligomer length.
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页码:5742 / 5751
页数:10
相关论文
共 30 条
[1]   STRUCTURE PROPERTY BEHAVIOR OF SOL-GEL DERIVED HYBRID MATERIALS - EFFECT OF A POLYMERIC ACID CATALYST [J].
BRENNAN, AB ;
WILKES, GL .
POLYMER, 1991, 32 (04) :733-739
[3]   SYNTHESIS AND PROPERTIES OF POLYURETHANES BASED ON POLYOLEFIN .1. RIGID POLYURETHANES AND AMORPHOUS SEGMENTED POLYURETHANES PREPARED IN POLAR-SOLVENTS UNDER HOMOGENEOUS CONDITIONS [J].
CUVE, L ;
PASCAULT, JP ;
BOITEUX, G ;
SEYTRE, G .
POLYMER, 1991, 32 (02) :343-352
[4]   SCATTERING BY AN INHOMOGENEOUS SOLID [J].
DEBYE, P ;
BUECHE, AM .
JOURNAL OF APPLIED PHYSICS, 1949, 20 (06) :518-525
[5]   TIME TEMPERATURE TRANSFORMATION (TTT) CURE DIAGRAM - MODELING THE CURE BEHAVIOR OF THERMOSETS [J].
ENNS, JB ;
GILLHAM, JK .
JOURNAL OF APPLIED POLYMER SCIENCE, 1983, 28 (08) :2567-2591
[6]  
FUJITA M, 1989, POLYM COMMUN, V30, P200
[7]   SI-29 SOLID-STATE NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY OF COMPOSITE INTERFACES [J].
HOH, KP ;
ISHIDA, H ;
KOENIG, JL .
POLYMER COMPOSITES, 1990, 11 (02) :121-125
[8]  
Huang H., 1987, POLYM PREPR AM CHEM, V28, P434
[9]  
HUANG HH, 1987, POLYM BULL, V18, P455
[10]   STRUCTURE PROPERTY BEHAVIOR OF HYBRID MATERIALS INCORPORATING TETRAETHOXYSILANE WITH MULTIFUNCTIONAL POLY(TETRAMETHYLENE OXIDE) [J].
HUANG, HH ;
WILKES, GL ;
CARLSON, JG .
POLYMER, 1989, 30 (11) :2001-2012