Sorption, diffusion, and pervaporation separation of water-acetic acid mixtures through the blend membranes of sodium alginate and guar gum-grafted-polyacrylamide
Us. Toti et al., Sorption, diffusion, and pervaporation separation of water-acetic acid mixtures through the blend membranes of sodium alginate and guar gum-grafted-polyacrylamide, J APPL POLY, 83(2), 2002, pp. 259-272
Nonporous homogeneous dense membranes were prepared from the blends of sodi
um alginate (Na-Alg) with guar gum-grafted polyacrylamide (GG-g-PAAm) in th
e ratios of 3:1 and 1:1 and these were tested for the pervaporation separat
ion of water-acetic acid mixtures at 30 degreesC. Blend compatibility was s
tudied in solution by measuring the viscosity and the speed of sound. Membr
anes were crosslinked by glutaraldehyde, The GG-g-PAAm polymer and the cros
slinked blend membranes were characterized by Fourier transform infrared sp
ectra. High separation selectivity was exhibited by the pure Na-Alg membran
e for water-acetic acid (HAc) mixtures containing 20 mass % of water. The p
ermeation flux increased with increasing mass percent of water in the feed
as well as with an increase in the amount of GG-g-PAAm in the blend, but se
paration selectivity decreased. Sorption selectivity was higher for the Na-
Alg membrane than for the blend membranes, but it decreased with increasing
mass percent of GG-g-PAAm in the blends. Diffusion selectivity values vary
systematically with the blend composition, but not with the amount of wate
r in the feed. Diffusion coefficients of the water-HAc mixtures were calcul
ated from Fick's equation using sorption data and compared with those calcu
lated from flux values obtained in pervaporation experiments. The Arrhenius
activation parameters were calculated for the 20 mass % of water in the fe
ed using flux and diffusion data obtained at 30, 40, and 50 degreesC. The d
iffusion and pervaporation results are explained in terms of solution-diffu
sion concepts. (C) 2002 John Wiley & Sons, Inc.