Ordered Phases in Aqueous Solutions of Diblock Oxyethylene/Oxybutylene Copolymers Investigated by Simultaneous Small-Angle X-ray Scattering and Rheology

The phase behavior of gels of E40B10 in 0.2 mol dm-3 aqueous K2SO4 was studied as a function of temperature and concentration. E40B10 is a diblock copolymer of poly(oxyethylene) (E) and poly(oxybutylene) (B), where the subscripts denote the number of repeats. The phase of the material was characteri...

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Veröffentlicht in:Macromolecules 1997-09, Vol.30 (19), p.5721-5728
Hauptverfasser: Pople, J. A, Hamley, I. W, Fairclough, J. P. A, Ryan, A. J, Komanschek, B. U, Gleeson, A. J, Yu, G.-E, Booth, C
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Sprache:eng
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Zusammenfassung:The phase behavior of gels of E40B10 in 0.2 mol dm-3 aqueous K2SO4 was studied as a function of temperature and concentration. E40B10 is a diblock copolymer of poly(oxyethylene) (E) and poly(oxybutylene) (B), where the subscripts denote the number of repeats. The phase of the material was characterized by both simultaneous rheology and small-angle X-ray scattering, (SAXS). Depending on polymer volume fraction in the range 23−38% a body-centered cubic (bcc) structure or a face-centered cubic (fcc) structure was observed at low temperature, and at high temperature a hexagonally packed rod structure was formed. The phase transitions were shown to be characterized by discontinuous changes in the values of the dynamic shear moduli. A bcc−fcc transition was observed at high concentration, the corresponding transition temperature increasing with increasing polymer concentration. The effects of reciprocating shear were shown to increase the degree of order, manifested as a sharpening of the diffraction peaks in the SAXS pattern. The dynamic moduli decreased rapidly on the application of oscillatory shear and recovered equally rapidly when the deformation ceased. The decrease in moduli was shown, via the SAXS patterns acquired simultaneously, to be correlated to structural changes within the gel.
ISSN:0024-9297
1520-5835
DOI:10.1021/ma970308j