4.7 Article

Solvent nanofiltration through high permeability glassy polymers: Effect of polymer and solute nature

Journal

JOURNAL OF MEMBRANE SCIENCE
Volume 423, Issue -, Pages 65-72

Publisher

ELSEVIER
DOI: 10.1016/j.memsci.2012.07.026

Keywords

PTMSP; PMP; PIM-1; Organic solvent nanofiltration; Effect of solute

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The effect of solute nature on the retention performance of membrane materials based on PTMSP, PMP and PIM-1 has been investigated in ethanol media. Using the examples of PMP and PIM-1, it was shown that membrane swelling could enhance the solvent transport across the membrane, regardless of the initial gas permeability. All polymers show the same level and order of retention for low molecular weight dyes (350 Da) regardless of the difference in polymer nature; in particular, negative retention of the neutral dye Solvent Blue 35 was observed for PTMSP, PMP and PIM-1: -17%, -11% and -4%, respectively. This retention behavior was explained by a blocking effect due to high dye-membrane interaction and comparable size of the solute (V-calc= 685 angstrom(3)) and available free volume elements within the polymer (5-12 angstrom). An increase of dye retention is attributed to a decrease of solute-membrane interaction; for example, PIM-1: Solvent Blue 35 (K=1107; vertical bar delta(PIM) (1)-delta(solute)vertical bar =4.2) < Safranine O (K=47.0; vertical bar delta(PM-1)-delta(solute)vertical bar =6.1) < Orange II (K=3.3; vertical bar delta(PIM-1)-delta(solute)vertical bar =9.7). The retention of higher molecular weight solutes is expected to be limited mainly by free volume size. Thus, it is possible to control nanofiltration parameters by proper selection of the polymer and the variety in the chemical nature of high permeability glassy polymers provides additional flexibility in solvent resistance and further modifications (e.g. cross-linking). A new possible application of PIM-1 as a polymeric sorbent with selectivity towards dissolved neutral compounds is proposed. (c) 2012 Elsevier B.V. All rights reserved.

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