Artículo
Autoría
FALCIONI, SEBASTIÁN ARIEL
;
ROHT, YANINA LUCRECIA
;
Drazer, Germán
;
IPPOLITO, IRENE PAULA
Fecha
2024
Editorial y Lugar de Edición
AMER CHEMICAL SOC
Revista
JOURNAL OF PHYSICAL CHEMISTRY B - (Print),
vol. 128
(pp. 9598-9603)
- ISSN 1520-6106
AMER CHEMICAL SOC
AMER CHEMICAL SOC
ISSN
1520-6106
Resumen
Información suministrada por el agente en
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This study examines the swelling kinetics of polyacrylamide hydrogel beads in aqueous glycerin solutions of differentconcentrations. The total absorbed mass of the hydrogel beads remains nearly constant, independent of glycerin concentration, butthe swelling process is markedly slower with increasing glycerin concentration in the aqueous solutions. Absorption capacity curvesexhibit universal kinetics when time is rescaled using a characteristic time proportional to the viscosity of the solution...
This study examines the swelling kinetics of polyacrylamide hydrogel beads in aqueous glycerin solutions of differentconcentrations. The total absorbed mass of the hydrogel beads remains nearly constant, independent of glycerin concentration, butthe swelling process is markedly slower with increasing glycerin concentration in the aqueous solutions. Absorption capacity curvesexhibit universal kinetics when time is rescaled using a characteristic time proportional to the viscosity of the solutions. Additionally,a novel visualization technique is employed to observe the core?shell structure of the hydrogel beads at early times in the swellingprocess. The evolution of the core?shell structure indicates a constant front velocity, which also reveals universal behavior with thesame nondimensional time, suggesting a viscous dominated transport of the solution penetrating the beads.
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Palabras Clave
HYDROGEL BEADSSWELLINGGLICERIN
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