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Segmented polyurethane elastomers with liquid crystalline hard segments. 1. Synthesis, characterization and rheology

Conference ·
OSTI ID:126975
; ;  [1]
  1. Univ. of Massachusetts, Amherst, MA (United States); and others

Segmented liquid crystalline polyurethanes (LCPUE) have been studied with hard segments composed of the mesogen 4,4`-bis(6-hydroxyhexoxy)biphenyl, 2,4-tolylene diisocyanate, and 2,6-tolylene diisocyanate and soft segments composed of poly(tetramethylene oxides). Differential scanning calorimetry and wide-angle X-ray scattering experiments show the existence of an enantiotropic mesophase in the hard domains of the elastomer. Compared with nonsegmented polyurethane containing the same mesogen, the isotropization temperature of the mesophase in the elastomer is depressed. This is a result of the oligomeric structure of the hard domains. The endotherm corresponding to the isotropization transition is also broadened, reflecting a lack of uniformity of the hard domains. Furthermore, the mesophase can be oriented by elastic deformation, and it forms a more ordered chain packing during this process. The tensile properties of these segmented polyurethanes are determined by their morphologies and can be manipulated by controlling the hard- and soft-segment concentration ratio. The rheological study indicates a broad transition from a viscoelastic solid to a viscoelastic liquid at the isotropization temperature of the mesophase. Physical gelation studies identify a liquid/solid transition when cooled to 106{degrees}C or below, and show the characteristic, critical behavior at the gel point with a power law relaxation spectrum at low frequencies.

OSTI ID:
126975
Report Number(s):
CONF-950402--
Country of Publication:
United States
Language:
English

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