Abstract
Development of novel polymeric materials capable of efficient CO2 capture and separation under ambient conditions is crucial for cost-effective and practical industrial applications. Here we report the facile synthesis of a new CO2-responsive polymer through postpolymerization modification of poly(2-vinyl-4,4-dimethylazlactone) (PVDMA). The reactive pendant azlactone groups of PVDMA are easily modified with 4-(N-methyltetrahydropyrimidine)benzyl alcohol (PBA) without any byproduct formation. FTIR and TGA experiments show the new PBA-functionalized polymer powder can reversibly capture CO2 at room temperature and under atmospheric pressure. CO2 capture was selective, showing a high fixing efficiency even with a mixed gas system (20% CO2, 80% N2) similar to flue gas. CO2 release occurred at room temperature, and release profiles were investigated as a function of temperature. Density functional theory (DFT) calculations coupled with modeling and simulation reveal the presence of two CO2 binding sites in the PBA-functionalized polymer resulting in a two-step CO2 release at room temperature. The ease of material preparation, high fixing efficiency, and robust release characteristics suggest that postpolymerization modification may be a useful route to designing new materials for CO2 capture.
Original language | English |
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Pages (from-to) | 1523-1531 |
Number of pages | 9 |
Journal | Macromolecules |
Volume | 49 |
Issue number | 5 |
DOIs | |
State | Published - Mar 9 2016 |
Funding
This research was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. We also thank European Commission under 7 FP (Project No. PIRSES-GA-2010-269182) and CNMS user project (Proposal No. CNMS2014-033) for sponsoring Ivana Karpisova from Comenius University, Slovakia, to contribute to this work. B.G.S. acknowledges partial support from the Center for Understanding and Control of Acid Gas-Induced Evolution of Materials for Energy (UNCAGE-ME), an Energy Frontier Research Center funded by U.S. Department of Energy, Office of Science, Basic Energy Sciences. S.M.K. acknowledges support from the National Science Foundation (Award # 1133320).