TRANSPORT RESISTANCES DURING PERVAPORATION THROUGH A COMPOSITE MEMBRANE - EXPERIMENTS AND MODEL-CALCULATIONS

Authors
Citation
E. Bode et C. Hoempler, TRANSPORT RESISTANCES DURING PERVAPORATION THROUGH A COMPOSITE MEMBRANE - EXPERIMENTS AND MODEL-CALCULATIONS, Journal of membrane science, 113(1), 1996, pp. 43-56
Citations number
30
Categorie Soggetti
Engineering, Chemical","Polymer Sciences
Journal title
ISSN journal
03767388
Volume
113
Issue
1
Year of publication
1996
Pages
43 - 56
Database
ISI
SICI code
0376-7388(1996)113:1<43:TRDPTA>2.0.ZU;2-Z
Abstract
For an investigation of transport resistances of a GFT PVA-PAN Pervap 1000 type membrane the pervaporation flux of pure water was measured a s a function of downstream pressure, with the membrane oriented in nor mal and in reverse position (= PVA layer facing the feed or the permea te). Assuming equilibrium across all interfaces, it was possible to br eak up the total resistance into (a) a support layer resistance part, and (b) an active layer resistance part. (a) Support layer resistance part = resistance of the support excluding its upstream skin: A model of liquid water transported by capillary forces through small pores, a nd of vapor by Poiseuille and Knudsen flow and eventually by surface d iffusion along pore walls is presented for describing the 3 transport regimes observed experimentally. The support layer was found to consum e up to 80% of the total resistance. (b) Active layer resistance part = resistances of the PVA layer and the slightly porous PAN skin: 3 mod els describing the influence of the PAN skin are discussed and judged in detail. Then the skin resistance is estimated and used to derive th e permeability of water in PVA as a function of water activity or 'equ ivalent partial pressure' EPP in the polymer which is then compared to vapor permeation, vapor sorption and diffusivity data published by He intz and Lichtenthaler. Strong discrepancies are found and discussed i n terms of possible interface resistances, of free and bound water and of cluster formation which would mean that in cases like this diffusi vities can be derived from stationary state pervaporation but not from non-stationary state kinetic sorption experiments.