posted on 2002-01-08, 00:00authored byKavita Mistry, Hernan Cortes, David Meunier, Carla Schmidt, Binyamin Feibush, Nelu Grinberg, Ira Krull
In this paper, we report the separations of large, neutral,
synthetic polymers using primarily a nonaqueous mobile
phase without the use of a supporting electrolyte. The
size- exclusion-based mechanism for separation was
achieved on sulfonated polystyrene/divinylbenzene stationary phases. The effect of water, voltage, stationary phase
exchange capacity, and pore size were investigated. The
stationary phase and solvent interactions were studied by
attenuated total reflectance Fourier transform infrared
spectroscopy (ATR FT-IR) and a possible mechanism for
the generation of EOF in the THF/water system is provided. Linear calibration curves were obtained for polystyrenes ranging in MW from 5K to 2M, for columns made
using a combination of high capacity ion exchanger and a
neutral polystyrene/divinylbenzene material of varied pore
sizes. Analysis of polyurethane, polystyrene, and other
polymer samples using CEC correlated well with results
obtained by conventional HPLC. The size exclusion CEC
separations provide an alternative mode for determining
the relative molecular weights of polymers, with reduced
solvent consumption.