2020
DOI: 10.1134/s199079312004003x
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Tixotropic Properties of Solutions of Some Polysaccharides

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Cited by 4 publications
(4 citation statements)
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“…It is known that the formation of the spatial structure, i.e., the transition of the polymer system from the state of a viscoelastic fluid to an elastic-viscous body (gel) can be judged by the nature of the change in the dependences of the storage moduli, G', and losses, G''. It was previously found that, for an aqueous solution of SCTZ, the transition from the viscoelastic state to the gel occurs at a concentration of 4.0 wt % [23,24]. From the dependences in Fig.…”
Section: Resultsmentioning
confidence: 75%
See 1 more Smart Citation
“…It is known that the formation of the spatial structure, i.e., the transition of the polymer system from the state of a viscoelastic fluid to an elastic-viscous body (gel) can be judged by the nature of the change in the dependences of the storage moduli, G', and losses, G''. It was previously found that, for an aqueous solution of SCTZ, the transition from the viscoelastic state to the gel occurs at a concentration of 4.0 wt % [23,24]. From the dependences in Fig.…”
Section: Resultsmentioning
confidence: 75%
“…One of the ways to create medical materials with controlled sorption, physicochemical, and structuralmechanical (including gel, fiber, and film-forming) properties based on water-soluble polymers is to regulate the processes of aggregation of macromolecules in the initial solutions [23,24]. In the case of PC solutions, the aggregation processes can be controlled not only by changing the concentration mode of the solutions (diluted, semidiluted, and concentrated) but also by changing the ratio of the components of the complex, which affects the conformational-supramolecular state of cooperatively bound macromolecules.…”
Section: Resultsmentioning
confidence: 99%
“…This phenomenon may be due to the formation of strong intermolecular forces among the hydrocolloid chains, since there are a more significant number of junction points among them, allowing for gel structure shaping. In this sense, these intermolecular interactions tend to break during the upward shear rate, and there is not enough time for a partial or total recovery of the gel structure, giving rise to the observed hysteresis [45].…”
Section: Flow Propertiesmentioning
confidence: 99%
“…This phenomenon may be due to the formation of strong intermolecular forces among the hydrocolloid chains, since there are a more significant number of junction points among them, allowing for gel structure shaping. In this sense, these intermolecular interactions tend to break during the upward shear rate, and there is not enough time for a partial or total recovery of the gel structure, giving rise to the observed hysteresis [45]. On the one hand, the experimental data for the descendent flow curves of all the gels were fitted to the Ostwald-de Waele model (power law), with R 2 values between 0.96-0.98 and 0.81-0.92 for the agar-and κ-carrageenan-based gels, respectively.…”
Section: Flow Propertiesmentioning
confidence: 99%