Institution: | International Centre for Pure and Applied Chemistry, Area di Ricerca, Padriciano 99, I-34012, Trieste, Italy Dipartimento di Biochimica, Biofisica e Chimica delle Macromolecole, Università di Trieste, 1, I-34127, Trieste, Italy Cavendish Laboratory, University of Cambridge, Madingley Road, Cambridge CB3 0HE, UK |
Abstract: | The viscoelastic properties of aqueous solutions of the exocellular polysaccharide of Cyanospira capsulata have been studied, over a wide range of polymer concentrations, using small deformation oscillatory, steady and transient shear methods. The viscoelastic spectra generally resemble those of an entangled network, although notable deviations can be observed in the low frequency dependence of G′ and G″. At higher polymer concentrations, the viscoelastic spectrum shows solid-like behaviour over a wide range of frequencies. The superposition of η*(ω) and η(
) curves occurs only at low frequencies, at higher frequencies the slope of η*(ω) is lower than that of η(
). By studying the time evolution of shear stress after the inception of a steady shear rate (stress overshoot), the recovery of non-linear properties after steady shearing flow is seen to occur after times of c. 103 s (in the case of 1·1% w/v solutions). The overall viscoelastic properties appear original in comparison with those of the two structurally limiting types of polysaccharide, the ‘ordered’ chain xanthan and the ‘random coil’ guar. A rationale for this ‘anomalous’ viscoelastic behaviour can be tentatively proposed in terms of flickering intermolecular cross-interactions between semi-flexible segments, which occur in addition to the usual topological constraints. |