Abstract
Four polyimides based on bicyclo[2.2.2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride (BTD), BTD-MIMA, BTD-HFA, BTD-FND, and BTD-TPM, with different rigid substituted diamines were synthesized. The chemical structure of the polyimides was corroborated by 1H NMR spectroscopy. These polyimides were soluble in organic solvents and presented molecular weights (Mn) between 39 and 70 KDa. BTD-MIMA, BTD-HFA, BTD-FND, and BTD-TPM showed thermal stability above 400 °C. These polyimides also presented high glass transition temperatures between 272 and 355 °C. The alicyclic moiety increased solubility compared with other rigid polyimides. Membrane films from BTD-MIMA and BTD-HFA exhibited the highest gas permeability compared to BTD-FND and BTD-TPM. The introduction of ortho-substituents in BTD-MIMA or bulky -CF3 groups in BTD-HFA, in combination with the alicyclic dianhydride fragment, prevented chain packing and enhanced macromolecular chain rigidity. In turn, there was a shift toward higher gas permeability coefficients for BTD-MIMA and BTD-HFA, with a moderate loss of CO2/N2 and CO2/CH4 selectivity, and they presented similar selectivities to those of other reported polyimides with alicyclic BTD moieties containing asymmetric fragments.
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