Elsevier

Journal of Membrane Science

Volume 12, Issue 2, December 1982, Pages 195-205
Journal of Membrane Science

Kinetics and equilibria associated with the absorption and desorption of water and lithium chloride in an ethylene—vinyl alcohol copolymer

https://doi.org/10.1016/S0376-7388(00)80182-9Get rights and content

Abstract

Sorption and desorption equilibria and kinetics for LiCl and H2O in an ethylene—vinyl alcohol copolymer film containing 70 mole percent vinyl alcohol were investigated at 25°C. The swelling behavior of water in the polymer was characterized by vapor and liquid sorption experiments over a range of water activities. p]The effects of LiCl content on the water sorption kinetics and equilibria in the films are presented and discussed. The kinetics and mechanism of LiCl sorption have also been studied. The amount of salt sorbed into the polymeric films increases linearly with the salt concentration in the external aqueous solutions. Both the rate and the amount of sorbed water increase significantly as the LiCl content increases. p]The desorption of LiCl, previously sorbed into the polymer, was characterized for different salt loadings. The rate of fractional salt release is independent of LiCl concentration in the film. Initially, the salt release is controlled by the nearly constant-rate absorption of water. The salt release, at long times, lags behind the swelling-controlled water uptake, indicating that the salt release is not completely controlled by the water sorption and that diffusion in the swollen polymer matrix contributes significantly to the long term elution of LiCl. Independent thermal analysis experiments suggest the formation of a metal salt—poly(ethylene—vinyl alcohol) complex.

References (11)

There are more references available in the full text version of this article.

Cited by (18)

  • Towards elucidation of the drug release mechanism from compressed hydrophilic matrices made of cellulose ethers. II. Evaluation of a possible swelling-controlled drug release mechanism using dimensionless analysis

    2010, Journal of Controlled Release
    Citation Excerpt :

    It also implies that the swelling mechanism has to be non-Fickian. This concept was initiated by the early work of Hopfenberg et al. [27–30], which reported on the constant release of a solute dispersed in a hydrophobic polymer placed in an organic solvent, referring to a phase erosion process. In the pharmaceutical field, there were several early reports of anomalous drug transport published [25,31–33].

  • Humidity-induced structural transitions in amylose and amylopectin films

    2001, Carbohydrate Polymers
    Citation Excerpt :

    Tg has also been observed to increase with increasing degrees of crystallinity for linear synthetic polymers with anhydrous crystalline regions (Jin, Ellis & Karasz, 1984). The effect has been explained by a stiffening effect of dispersed microcrystalline cross-links, which leads to less mobility of the chain segments in the connecting amorphous regions (Gaeta, Apicella & Hopfenberg, 1982; Slade & Levine, 1991). The increase in Tg for increasing crystallinity in the amylopectin films also means in practice that, the more crystalline the films were, the less sensitive they were to the surrounding RH, i.e. less sensitive to water.

  • Glass Transitions and Water-Food Structure Interactions

    1995, Advances in Food and Nutrition Research
View all citing articles on Scopus
1

Present address: American Can Co., Barrington Technical Center, Barrington, IL 60010 (U.S.A.).

2

Present address: Istituto di Principi di Ingegneria Chimica, Università di Napoli, Piazzale Tecchio, Naples (Italy).

View full text