Abstract

The extra free volume of glassy, highly permeable 1,2-disubstituted polyacetylenes is associated with the microporous organization of these polymers. In this work, the microporosity of poly(1-trimethylsilyl-1-propyne) (PTMSP) and poly(4-methyl-2-pentyne) (PMP) is investigated by two independent methods—convenient low-temperature Ar sorption and less commonly used small-angle X-ray scattering (SAXS). The Ar sorption data were analyzed in connection with the specific surface area, pore volume, and micropore size distribution. It is shown that the higher specific surface area, total pore volume, and micropore volume of PTMSP than those of PMP are associated with higher gas permeability coefficients. It was found that the Brunauer–Emmett–Teller-specific surface values obtained for PTMSP and PMP from argon sorption isotherms correlate with the specific surface values obtained from the SAXS method. The correlation of the specific surface values obtained from fundamentally different methods makes it possible to evaluate the small-angle scattering method as adequate for assessing the microporosity of polymeric materials. The microporosity of poly(1-trimethylsilyl-1-propyne) (PTMSP) and poly(4-methyl-2-pentyne) (PMP) is investigated by two independent methods—convenient low-temperature Ar sorption and less commonly used small-angle X-ray scattering (SAXS). The Brunauer–Emmett–Teller-specific surface values obtained for PTMSP and PMP from Ar sorption isotherms correlate with the specific surface values obtained from the SAXS method. The correlation of the specific surface values obtained from fundamentally different methods makes it possible to evaluate the small-angle scattering method as adequate for assessing the microporosity of polymeric materials.

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