Authors
Avery E Baumann, Alice Klapproth, Richard A Mole, Craig M Brown, Christopher M Stafford, Christopher L Soles
Published in
ACS applied polymer materials. Volume 8. Issue 13. Pages 10162-10174. Jul 10, 2026. Epub Jun 22, 2026.
Abstract
Selective facilitated transport membranes are viable technologies for separating dilute CO2 from mixed-gas streams. In this study, we measure the reactivity and transport behavior of two polyallylamine amine polymers that bind CO2 in humid environments. We quantify sorption of CO2 and water components using a tandem quartz crystal microbalance mass sensor coupled with infrared spectroscopy for chemical identification of the sorbed gases and their reaction products. The two high-molecular-mass (glassy) polyallylamine materials, one containing just primary amines and the other containing isopropyl-functionalized secondary amines, react with humid CO2 to form tethered carbamate/carbamic acid groups or bicarbonate ions, respectively. Because our technique allows for the discernment of specific water and CO2 uptake, we also identify that the different reactivities influence the sorbed water content in the polymer films. We further quantify the local or segmental mobility of the dosed polymers with quasielastic neutron scattering measurements on the few nanoseconds to tens of picoseconds time scales, revealing that a classic jump diffusion model describes the dynamics of the polymers and their polymer-sorbate complexes. The resulting jump lengths and residence time between jumps differ based on the polymer chemistry and dosing conditions, with the hindered secondary amine systems generally presenting longer residence times and slightly longer jump distances. This combination study featuring both quasielastic neutron scattering and tandem gravimetric and chemical uptake measurements adds to the broader understanding of amine polymer dynamics and reactivity in CO2 capture applications.
PMID:
42454252
Bibliographic data and abstract were imported from PubMed on 15 Jul 2026.
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