NaCl interaction with interfacially polymerized polyamide films of reverse osmosis membranes: A solid-state 23Na NMR study

Abstract

23Na nuclear magnetic resonance (NMR) spectroscopy of NaCl-exchanged polyamide (PA) films comparable to those of the active skin layer of many reverse osmosis (RO) membranes provides novel insight into the structural environments and dynamical behavior of Na + in such films. Unsupported PA films were synthesized via interfacial polymerization of trimesoyl chloride in hexane and m-phenylenediamine in aqueous solution, and SEM, FT-IR, and 13C NMR data demonstrate successful thin film polymerization. Compositional data confirm this conclusion and demonstrate equal Na and Cl incorporation during NaCl exchange from aqueous solution. The 23Na NMR spectra for freshly made polymer samples exchanged in 1 M NaCl solution show significant relative humidity (RH) dependence. At near 0% RH, there are resonances for crystalline NaCl and rigidly held Na + in the PA. With increasing RH, a resonance for solution-like dynamically averaged Na + appears and above 51% RH is the only signal observed. The slightly negative chemical shift of this resonance suggests a dominantly hydrous environment with some atomic-scale coordination by atoms of the polymer. The greatly reduced 23Na T 1 relaxation rates for this resonance relative to bulk solution and crystalline NaCl confirm close association with the polymer. Variable temperature 23Na NMR spectra for a sample equilibrated at 97% RH obtained from −80 to 20 °C show the presence of rigidly held Na + in a hydrated environment at low temperatures and replacement of this resonance by the dynamically averaged signal at temperatures above about −20 °C. The results provide support for the solution–diffusion model for RO membranes transport and demonstrate the capabilities of multi-nuclear NMR methods to investigate molecular-scale structure and dynamics of the interactions between dissolved species and RO membranes.