461658 New Poly(alkyl imines) for CO2 Capture from Ambient Air

Wednesday, November 16, 2016: 9:10 AM
Cyril Magnin I (Parc 55 San Francisco)
Simon H. Pang1, Li-Chen Lee1, Ryan P. Lively1 and Christopher W. Jones1,2, (1)School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, (2)School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA

Research efforts in CO2 capture technologies have dramatically increased due to interest in reducing the effect of anthropogenic emissions on atmospheric CO2 concentrations. Much of this research has focused on capture from large point sources such as flue gas. Direct capture of CO2 from ambient air is proposed as a complementary technology that has the advantage of not needing a flue gas feed stream and thus is more versatile in its deployment. However, at an ultradilute concentration of 400 ppm, the driving force for adsorption is low, necessitating the development of adsorbents that may be different from those used in flue gas capture. Additionally, these adsorbents must be stable under oxidizing conditions due to the presence of oxygen in the feed stream.

In this work, we present work towards the development of a series of new poly(alkyl imines) as well-defined branched molecules for CO2 capture. By changing the structure and flexibility of the adsorbent aminopolymer, we show that the CO2 capture capacity and efficiency can be readily tuned. These materials represent a departure from the traditionally-studied poly(ethylenimine) (PEI) for CO2 capture by using a well-defined molecular species with controlled and varied alkyl linker length. Additionally, these structures only contain primary and tertiary amines, which impart high capture capacity under ultradilute conditions and stability against oxidative degradation.

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