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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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Molecular thermodynamic analysis for assessing the relationship between reentrant swelling behavior and ternary liquid-liquid equilibrium for poly(N-isopropylacrylamide) nanometer-sized gel particles in a water-tetrahydrofuran cosolvent system.

TL;DR: The influence of phase separation on swelling behavior was investigated based on the thermodynamic framework of reswelling phenomena to determine ternary interaction energy parameters for the liquid-liquid equilibrium of linear poly-NIPA in a water-THF cosolvent system.
Journal ArticleDOI

Influence of the ionic character of a drug on its release rate from hydrogels based on 2-hydroxyethylmethacrylate and acrylamide synthesized by photopolymerization

TL;DR: Higher load- ings and slower release rates of Saf from the hydrolyzed hydrogels were observed, making them particularly suitable for the slow drug-delivery of cationic drugs.
Journal ArticleDOI

Fabrication of pH-degradable supramacromolecular microgels with tunable size and shape via droplet-based microfluidics.

TL;DR: In this article , the authors presented a method to synthesize stimuli-responsive microgels with supramolecular cross-links exhibiting tunable size and shape via droplet-based microfluidics.
Journal ArticleDOI

Effects of microstructure, crosslinking density, temperature and exterior load on dynamic pH-response of hydrolyzed polyacrylonitrile-blend-gelatin hydrogel fibers

Liwei Yu, +1 more
TL;DR: In this paper, a smart hydrogel fiber based on hydrolyzed polyacrylonitrile- blend -gelatin is presented, and the kinetics of the hydrogels fibers in response to pH change is reported.
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Electro-driven polymer gels with biomimetic motility

TL;DR: In this paper, the authors investigated the chemomechanical behavior of weakly crosslinked anionic poly(2-acrylamido-2-methylpropanesulfonic acid) (PAMPS) gel in the presence of the cationic surfactant N-alkylpyridinium chloride (CnPyCl) with various alkyl-chains (n = 4, 8, 10, 12, 16, 18).
References
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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).