Premium
Relationships between synthesis and mechanical properties of new polyurea materials
Author(s) -
Samson Nathalie,
Mechin Françoise,
Pascault JeanPierre
Publication year - 1997
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/(sici)1097-4628(19970919)65:12<2265::aid-app2>3.0.co;2-7
Subject(s) - polyurea , molar mass , condensation polymer , materials science , elastomer , polymer chemistry , polymer , monomer , molar ratio , crystallization , reactivity (psychology) , molding (decorative) , composite material , chemical engineering , catalysis , chemistry , organic chemistry , polyurethane , medicine , alternative medicine , pathology , engineering
New segmented polyureas were prepared from 4,4′‐diisocyanato dicyclohexylmethane and amino terminated polyoxypropylene. Different cycloaliphatic and aromatic diamines were used as chain extenders as well as to synthesize the corresponding model hard segments (HSs). The competition between polycondensation and HS crystallization requires a sufficiently fast reaction (e.g., cycloaliphatic diamines associated with a catalyst, if necessary in solution), although low reactivity monomers would be necessary to avoid demanding processing techniques such as reaction injection molding; otherwise, materials with isolated (i.e., not chemically linked) HS are obtained and they display poor mechanical properties. In contrast, when an appropriate synthesis procedure is used, elastomers with high molar masses and narrow molar mass distributions can be obtained. These characteristics, associated with the high melting temperature of the hard domains, result in very good mechanical behavior, up to high enough temperatures (∼ 180–190°C). The presence of low molar masses can be responsible for a rather low but continuous energy dissipation between the relaxations of the soft and hard domains (and particularly at room temperature), but can be well limited by a short thermal treatment at high temperature. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65: 2265–2280, 1997