Yavuz Salt

Sorption behavior and preliminary pervaporation results of cross-linked polyvinylalcohol and polydimethylsiloxane membranes prepared for the separation of water-ethylacetate mixtures

Since pervaporation process is the coupling of solution and diffusion mechanisms, a sorption study was carried out with membranes prepared by cross-linking polyvinylalcohol (PVA) and polidimethylsiloxane (PDMS). Tartaric acid (Tac) was used as the cross-linking agent for PVA, and a commercial cross-linking agent was used for PDMS. Sorption experiments were carried out at 30-50°C temperature range in pure water and ethyl acetate using the films prepared. The PVA and PDMS films prepared preferentially sorb water and ethylacetate, respectively. A pervaporation study at 30°C was carried out for pure ethylacetate and pure water, and mixtures of ethylacetate containing 2 and 2.5 wt% water using 100 w m thick PVA membrane. The results indicate that the PVA membrane prepared is extremely selective for water.

DESORPTION OF ETHYL ACETATE-WATER MIXTURE BY USING CROSS-LINKED POLY(VINYLALCOHOL) MEMBRANE AND COMPARISON OF RESULTS WITH PERVAPORATION

In this study using poly(vinylalcohol) (PVOH) membranes cross-linked with tartaric acid (Tac) desorption experiments were performed for selected concentrations of binary ethyl acetate (EtAc)-water mixture at temperatures of 30°, 40°, and 50°C to determine sorption of components. Sorption values measured were compared with those estimated by the Flory-Huggins approach. Additionally, desorption results were compared with pervaporation results of another study in terms of solution-diffusion theory, and the effect of thermodynamic interactions on selective transport of the binary mixture and membrane system was investigated. The results obtained show that selective transport of EtAc-water mixture was influenced by increasing temperature and water content in the feed. It is shown that preferential sorption is more effective for pervaporation selectivity than diffusion selectivity.