Selective Recovery of n-Butanol from Aqueous Solutions with Functionalized Poly(epoxide ionic liquid)-Based Polyurethane Membranes by Pervaporation

[Image: see text] In this study, hydroxyl-terminated polybutadiene–poly(epoxide ionic liquid)–poly(urethane urea) (HTPB-PEIL-PU) membranes, HTPB-PEIL1-PU and HTPB-PEIL2-PU, were prepared by the reaction of functionalized PEIL, poly(1-methylimidazole-3-methyl-ethyloxy)hexafluorophosphate or poly(1-methylimidazole-3-methyl-ethyloxy)bistrifluoromethanesulfonimidate, respectively, with HTPB using 4,4′-diphenylmethane diisocyanate (MDI) as the chain extender. The HTPB-PEIL-PU and HTPB membranes were investigated for the selective recovery of n-butanol from aqueous solutions by pervaporation. PEIL was confirmed to be successfully embedded in the PU membranes by (1)H NMR, Fourier transform infrared, and differential scanning calorimetry measurements. According to our mechanical measurements, the HTPB-PEIL-PU membranes retain the mechanical properties of the original PU membrane. PEIL was shown to enhance the diffusion rate of n-butanol significantly based on swelling behavior tests. The pervaporation flux through the HTPB-PEIL1-PU membrane increased with increasing feed temperature and feed concentration. In contrast, the separation factor of the HTPB-PEIL1-PU membrane increased with increasing feed temperature but decreased with increasing feed concentration. In addition, the HTPB-PEIL2-PU membrane exhibited an optimal separation factor of up to 29.2 at a feed concentration of 3% and a feed temperature of 70 °C, which is superior to that (22.7) through pure HTPB membranes. Furthermore, the HTPB-PEIL1-PU and HTPB-PEIL2-PU membranes show better long-term stability than other supported ionic liquid membranes.