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Journal ArticleDOI

Kinetics of swelling of gels

Toyoichi Tanaka, +1 more
- 01 Feb 1979 - 
- Vol. 70, Iss: 3, pp 1214-1218
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TLDR
In this article, a theory of the kinetics of the swelling of polyacrylamide gels is presented, which is based on the assumption that the swelling time is determined by the diffusion coefficient of the fluid molecules.
Abstract
We present a theory of the kinetics of the swelling of a gel. The characteristic time of swelling is proportional to the square of a linear dimension of the gel and is also proportional to the diffusion coefficient of the gel network, which is defined as D=E/f where E is the longitudinal bulk modulus of the network, and f is the coefficient of friction between the network and the gel fluid. This constitutes an essential difference between the present theory and the previous theory which is based on the assumption that the swelling time is determined by the diffusion coefficient of the fluid molecules. Experimental data are shown for spheres of 5% polyacrylamide gels and are analyzed using the present theory. The value of the diffusion coefficient obtained from the macroscopic swelling experiments shows excellent agreement with that obtained microscopically using laser light scattering spectroscopy.

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Citations
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Journal ArticleDOI

A modeling analysis for effect of elastic modulus on kinetics of ionic-strength-sensitive hydrogel

TL;DR: In this paper, the influence of elastic modulus on the kinetic performance of smart hydrogels was investigated via a multiphysics transient model, which was developed by the present authors and is known as the multi-effect coupling ionic-strength-stimulus model.
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Fast and Large Shrinking of Thermoresponsive Hydrogels with Phase-Separated Structures.

TL;DR: In this paper, the phase separation of PNIPAAm hydrogels into a PNPAm-rich and a water-rich phase was performed in the presence of NaClO4 salt.
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Deformation of styrene—divinylbenzene copolymers and hypercrosslinked polystyrenes during solvent adsorption and desorption

TL;DR: In this article, an automated procedure was developed for monitoring fast changes in the size of spherical samples of polymers during their contact with a solvent or drying, and the kinetics of bulk deformation in these processes were studied for a series of cross-linked polymers, viz., gel-type and porous styrene.
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Optimizing the Power Production in an Osmotic Engine via Microfluidic Fabricated and Surface Crosslinked Hydrogels Utilizing Fresh and Salt Water

TL;DR: In this article, the authors synthesize poly(acrylic acid-co−sodium acrylate) hydrogels with varying diameters and varying degrees of neutralization (DN = 10−75 mol%) to improve the power of an osmotic engine.
Journal ArticleDOI

Drying Mechanics of Gels

TL;DR: In this paper, a model for the stresses and strains that develop in a gel during drying is presented, where the driving force for shrinkage is assumed to be the interfacial energy, and the gel is considered to be viscoelastic.
References
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Journal ArticleDOI

Statistical-Mechanical Theory of Irreversible Processes : I. General Theory and Simple Applications to Magnetic and Conduction Problems

TL;DR: In this paper, a general type of fluctuation-dissipation theorem is discussed to show that the physical quantities such as complex susceptibility of magnetic or electric polarization and complex conductivity for electric conduction are rigorously expressed in terms of timefluctuation of dynamical variables associated with such irreversible processes.
Journal ArticleDOI

Spectrum of light scattered from a viscoelastic gel

TL;DR: In this paper, the spectrum of light scattered from thermally excited displacement fluctuations in polyacrylamide gels was measured using optical mixing spectroscopy, and the correlation function for the displacements having wave vector q is predicted for these gels to have the form of an exponential decay: exp(− Γt).