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Abstract: An oscillating capillary rheometer was used to investigate the dynamic viscoelastic and intrinsic viscosity properties of deacetylated xanthan (0.025%), native xanthan (0.025%), guar gum (0.075%), and xanthan–guar mixtures in dilute solutions. Influence of ionic strength on xanthan conformation and interaction with guar gum was elaborated. As the salt concentration increased, a significant (P <0.05) decrease in viscosity (η′) and elasticity (η″) values was observed for both native xanthan–guar mixtures and deacetylated xanthan–guar mixtures. In water and 2mM NaCl solution, the relative viscosity and η″ of both native xanthan–guar mixtures and deacetylated xanthan–guar mixtures were much higher than of those calculated for mixtures assuming no interaction, whereas no pronounced increase was found for polysaccharide mixtures in 40mM NaCl. The intrinsic viscosities of deacetylated xanthan–guar mixtures in water and 2mM NaCl were higher, whereas the intrinsic viscosities of native xanthan–guar mixtures were lower than those calculated from the weight averages of the two individually, assuming no interaction. These results demonstrated that intermolecular interaction has occurred between xanthan and guar mixtures in water and 2mM NaCl, but may not occur in 40mM NaCl, and mutual incompatibility may occur. The results suggest that the degree of disordering of xanthan played a critical role in xanthan–guar interaction and may explain the differences in η′, η″, and intrinsic viscosity measurements between 2 and 40mM NaCl. [Copyright &y& Elsevier]

Abstract: Dynamic viscoelastic and intrinsic viscosity properties of xanthan, guar, and xanthan–guar blends in dilute aqueous solutions were investigated by using an oscillating capillary rheometer. Influence of mixing temperature on xanthan conformation and interaction with guar is discussed. Synergistic interaction occurred at mixing temperatures of 25 and 80°C, but a stronger synergistic interaction was observed at mixing temperature 80°C. The viscous component for all gum solutions was greater than that of the elastic component, which indicated a liquid-like behavior in the dilute regime for the polysaccharide solutions. For both mixing temperatures, the relative viscosities and elasticities of xanthan and guar blends were higher than the relative viscosities and elasticities calculated for blends assuming no interaction. The intrinsic viscosities of xanthan and xanthan–guar blends were higher at 80°C than at 25°C. The intrinsic viscosities of xanthan and guar blends were lower than those calculated from the weight averages of the two, and significantly decreased as the xanthan fraction decreased, indicating that xanthan was crucial in controlling the blend viscosity, and that the molecular binding occurred between xanthan and guar. [Copyright &y& Elsevier]