Physical Aging, Plasticization and Their Effects on Gas Permeation in "rigid" Polymers of Intrinsic Microporosity

Abstract

Long-term physical aging and plasticization, two mobility-based phenomena that are counterintuitive in the context of "rigid" polymers of intrinsic microporosity (PIMs), were evaluated using pure- and mixed-gas permeation data for representative ladder and semiladder PIMs. PIMs between 1 and 4 years old retained from 10- to 1000-fold higher H 2 and O 2 permeabilities than commercial membrane materials with similar or higher selectivities. A triptycene-based ladder polymer (TPIM-1) exhibited very large selectivity gains outweighing permeability losses after 780 days, resulting in unprecedented performance for O 2 /N 2 (P(O 2) = 61 Barrer, α(O 2 /N 2) = 8.6) and H 2 /N 2 (P(H 2) = 1105 Barrer, α(H 2 /N 2) = 156) separations. Interestingly, TPIM-1 aged more and faster than its more flexible counterpart, PIM-1, which exhibited P(O 2) = 317 Barrer and α(O 2 /N 2) = 5.0 at 1380 days. Additionally, the more "rigid" TPIM-1 plasticized more significantly than PIM-1 (i.e., TPIM-1 endured ∼93% increases in mixed-gas CH 4 permeability over pure-gas values compared to ∼60% for PIM-1). A flexible 9,10-bridgehead (i.e., TPIM-2) mitigated the enhancements induced by physical aging but reduced plasticization. Importantly, intra-chain rigidity alone, without consideration of chain architecture and ultra-microporosity, is insufficient for designing aging- and plasticization-resistant gas separation membranes with high permeability and high selectivity