The solubilities of He, H-2, N-2, O-2, CO2, CH4, C2H6, C3H8, and n-C4H10 we
re determined at 35 degrees C and pressures up to 27 atmospheres in a syste
matic series of phase separated polyether-polyamide segmented block copolym
ers containing either poly-(ethylene oxide) [PEO] or poly(tetramethylene ox
ide) [PTMEO] as the rubbery polyether phase and nylon 6 [PA6] or nylon 12 [
PA12] as the hard polyamide phase. Sorption isotherms are linear for the le
ast soluble gases (He, H-2, N-2, O-2, and CH4), convex to the pressure axis
for more soluble penetrants (CO2, C3H8, and n-C4H10) and slightly concave
to the pressure axis for ethane. These polymers exhibit high CO2/N-2 and CO
2/H-2 solubility selectivity. This property appears to derive mainly from h
igh carbon dioxide solubility, which is ascribed to the strong affinity of
the polar ether linkages for CO2. As the amount of the polyether phase in t
he copolymers increases, gas solubility increases. The solubility of all ga
ses is higher in polymers with less polar constituents, PTMEO and PA12, tha
n in polymers with more polar PEO and PA6 units. CO2/N-2 and CO2/H-2 solubi
lity selectivity, however, are higher in polymers with higher concentration
s of polar repeat units. The sorption data are complemented with physical c
haracterization (differential scanning calorimetry, elemental analysis, and
wide angle X-ray diffraction) of the various block copolymers. (C) 1999 Jo
hn Wiley & Sons, Inc.