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New polyurethanes based on 4,4′‐diphenylmethane diisocyanate and 1,4:3,6 dianhydrosorbitol, 2. Synthesis and properties of segmented polyurethane elastomers
Author(s) -
CognetGeorjon Estelle,
Méchin Francoise,
Pascault JeanPierre
Publication year - 1996
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.1996.021971109
Subject(s) - elastomer , materials science , polybutadiene , polyurethane , diphenylmethane , polymer chemistry , diol , condensation polymer , glass transition , phase (matter) , composite material , polymer , chemistry , organic chemistry , copolymer , catalysis
1,4:3,6‐Dianhydrosorbitol (DAS) was used as chain extender in the preparation of new segmented polyurethane elastomers, based on polyoxytetramethylene or hydrogenated polybutadiene soft segments and 4,4′‐diphenylmethane diisocyanate (MDI). These materials exhibit a two‐phase microstructure, due to the thermodynamic immiscibility between hard and soft segments, which results in an elastomeric behavior over a wide temperature range. The thermal and dynamic mechanical properties of various formulations were then examined and related to the complex morphology of the corresponding (often semi‐crystalline) materials. DAS leads to particularly stiff hard segments and provides longer rubbery plateaux, compared with a classical diol such as 1,4‐butanediol. Phase separation is favored by longer and less polar soft segments. In any case, the structure of the materials strongly depends on the composition and synthesis procedure (bulk polycondensation leads to more heterogeneous samples), and most of all on the thermal history of the samples. This latter behavior is related to the existence of a possible order‐disorder transition (ODT) which explains the change‐over from a two‐phase to a one‐phase system after specific annealing experiments.