scholarly journals Free Volume and Gas Permeation in Anthracene Maleimide-Based Polymers of Intrinsic Microporosity

Membranes ◽  
2015 ◽  
Vol 5 (2) ◽  
pp. 214-227 ◽  
Author(s):  
Muntazim Khan ◽  
Volkan Filiz ◽  
Thomas Emmler ◽  
Volker Abetz ◽  
Toenjes Koschine ◽  
...  
2010 ◽  
Vol 43 (14) ◽  
pp. 6075-6084 ◽  
Author(s):  
Thomas Emmler ◽  
Kathleen Heinrich ◽  
Detlev Fritsch ◽  
Peter M. Budd ◽  
Nhamo Chaukura ◽  
...  

2018 ◽  
Vol 10 (42) ◽  
pp. 36475-36482 ◽  
Author(s):  
Alessio Fuoco ◽  
Bibiana Comesaña-Gándara ◽  
Mariagiulia Longo ◽  
Elisa Esposito ◽  
Marcello Monteleone ◽  
...  

2021 ◽  
Vol 118 (37) ◽  
pp. e2022204118
Author(s):  
Tanner J. Corrado ◽  
Zihan Huang ◽  
Dezhao Huang ◽  
Noah Wamble ◽  
Tengfei Luo ◽  
...  

Polymers of intrinsic microporosity (PIMs) have shown promise in pushing the limits of gas separation membranes, recently redefining upper bounds for a variety of gas pair separations. However, many of these membranes still suffer from reductions in permeability over time, removing the primary advantage of this class of polymer. In this work, a series of pentiptycene-based PIMs incorporated into copolymers with PIM-1 are examined to identify fundamental structure–property relationships between the configuration of the pentiptycene backbone and its accompanying linear or branched substituent group. The incorporation of pentiptycene provides a route to instill a more permanent, configuration-based free volume, resistant to physical aging via traditional collapse of conformation-based free volume. PPIM-ip-C and PPIM-np-S, copolymers with C- and S-shape backbones and branched isopropoxy and linear n-propoxy substituent groups, respectively, each exhibited initial separation performance enhancements relative to PIM-1. Additionally, aging-enhanced gas permeabilities were observed, a stark departure from the typical permeability losses pure PIM-1 experiences with aging. Mixed-gas separation data showed enhanced CO2/CH4 selectivity relative to the pure-gas permeation results, with only ∼20% decreases in selectivity when moving from a CO2 partial pressure of ∼2.4 to ∼7.1 atm (atmospheric pressure) when utilizing a mixed-gas CO2/CH4 feed stream. These results highlight the potential of pentiptycene’s intrinsic, configurational free volume for simultaneously delivering size-sieving above the 2008 upper bound, along with exceptional resistance to physical aging that often plagues high free volume PIMs.


2014 ◽  
Vol 2 (30) ◽  
pp. 11742-11752 ◽  
Author(s):  
Amanda G. McDermott ◽  
Peter M. Budd ◽  
Neil B. McKeown ◽  
Coray M. Colina ◽  
James Runt

X-ray scattering patterns from these high free-volume polymeric glasses contain a feature strongly associated with porosity; it is sensitive to time, temperature and film thickness in a manner consistent with physical aging, which impacts membrane performance in gas separations.


Membranes ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 41 ◽  
Author(s):  
Colin Scholes ◽  
Shinji Kanehashi

Polymers of intrinsic microporosity (PIMs) are a promising membrane material for gas separation, because of their high free volume and micro-cavity size distribution. This is countered by PIMs-based membranes being highly susceptible to physical aging, which dramatically reduces their permselectivity over extended periods of time. Supercritical carbon dioxide is known to plasticize and partially solubilise polymers, altering the underlying membrane morphology, and hence impacting the gas separation properties. This investigation reports on the change in PIM-1 membranes after being exposed to supercritical CO2 for two- and eight-hour intervals, followed by two depressurization protocols, a rapid depressurization and a slow depressurization. The exposure times enables the impact contact time with supercritical CO2 has on the membrane morphology to be investigated, as well as the subsequent depressurization event. The density of the post supercritical CO2 exposed membranes, irrespective of exposure time and depressurization, were greater than the untreated membrane. This indicated that supercritical CO2 had solubilised the polymer chain, enabling PIM-1 to rearrange and contract the free volume micro-cavities present. As a consequence, the permeabilities of He, CH4, O2 and CO2 were all reduced for the supercritical CO2-treated membranes compared to the original membrane, while N2 permeability remained unchanged. Importantly, the physical aging properties of the supercritical CO2-treated membranes altered, with only minor reductions in N2, CH4 and O2 permeabilities observed over extended periods of time. In contrast, He and CO2 permeabilities experienced similar physical aging in the supercritical treated membranes to that of the original membrane. This was interpreted as the supercritical CO2 treatment enabling micro-cavity contraction to favour the smaller CO2 molecule, due to size exclusion of the larger N2, CH4 and O2 molecules. Therefore, physical aging of the treated membranes only had minor impact on N2, CH4 and O2 permeability; while the smaller He and CO2 gases experience greater permeability loss. This result implies that supercritical CO2 exposure has potential to limit physical aging performance loss in PIM-1 based membranes for O2/N2 separation.


Sign in / Sign up

Export Citation Format

Share Document