A simplified solution–diffusion theory in pervaporation: the total solvent volume fraction model

Abstract A simplified solution–diffusion model called total solvent volume fraction model is developed for the description of the permeant transport through highly selective membranes in pervaporation. It is based on the assumption that the diffusion coefficient is the product of a limit diffusivity and an analytic function depending only on the total volume fraction of all the solvent species in the membrane. The equations developed for binary liquid mixtures in the particular case where the analytical functions are the same for both permeant species were checked with the experimental data obtained from the pervaporation of water–ethanol mixtures through a PVA-based membrane. The three computed parameters obtained by fitting were successfully used to predict the variations of the partial fluxes with the downstream pressure, particularly the maximum in the ethanol flux, and the inversion of the membrane selectivity. The model appears to be also valid for a moderately selective membrane, the cellulose acetate membrane, in the pervaporation of water–ethanol mixtures.

[1]  P. Schaetzel,et al.  Sorption of organic solvents into dense silicone membranes. Part 2.—Development of a new approach based on a clustering hypothesis for associated solvents , 1993 .

[2]  P. Schaetzel Ideal and non-ideal diffusion through polymers: Application to pervaporation , 2001 .

[3]  Takeshi Matsuura,et al.  Predictability of transport equations for pervaporation on the basis of pore-flow mechanism , 1992 .

[4]  P. Schaetzel The solution–diffusion model: Order of magnitude calculation of coupling between the fluxes in pervaporation , 2001 .

[5]  Q. Nguyen,et al.  Influence of downstream pressure on the pervaporation of water—tetrahydrofuran mixtures through a regenerated cellulose membrane (Cuprophan)☆ , 1986 .

[6]  S. Doong,et al.  Prediction of flux and selectivity in pervaporation through a membrane , 1995 .

[7]  C. A. Smolders,et al.  ON THE MECHANISM OF SEPARATION OF ETHANOL/WATER MIXTURES BY PERVAPORATION I. CALCULATIONS OF CONCENTRATION PROFILES* , 1984 .

[8]  E. Thompson,et al.  Dependence of diffusive permeation rates and selectivities on upstream and downstream pressures : V. Experimental results for the hexane/heptane (ideal) and toluene/ethanol (nonideal) systems☆ , 1986 .

[9]  J. Brun,et al.  Modelling of the pervaporation of binary mixtures through moderately swelling, non-reacting membranes , 1985 .

[10]  Takeshi Matsuura,et al.  A new transport model for pervaporation , 1991 .

[11]  E. Thompson,et al.  Dependence of diffusive permeation rates and selectivities on upstream and downstream pressures : IV. Computer simulation of nonideal systems , 1984 .

[12]  Y. Cohen,et al.  Ceramic-supported polymer membranes for pervaporation of binary organic/organic mixtures , 2003 .

[13]  E. Thompson,et al.  Dependence of diffusive permeation rates on upstream and downstream pressures , 1977 .

[14]  P. Schaetzel,et al.  Permselective properties of PVA-PAA blended membrane used for dehydration of fusel oil by pervaporation , 1997 .

[15]  M. D. Pinho,et al.  Mass transfer in radiation-grafted pervaporation membranes , 1990 .

[16]  P. Schaetzel,et al.  Mass transfer analysis of pervaporation through an ion exchange membrane , 1993 .