Abstract
Air pollution by nitrogen oxides, NOx, is a major problem, and new capture and abatement technologies are urgently required. Here we report a metal-organic framework (MFM-520: MFM = Manchester Framework Material) that can efficiently confine dimers of NO2, resulting in a high adsorption capacity of 4.2mmol/g (298K, 0.01bar) with full reversibility and no loss of capacity over 125 cycles. Treatment of NO2@MFM-520 with water in air leads to quantitative
conversion of the captured NO2 into HNO3, an important feedstock for fertilizer production, and fully regenerates MFM-520. The confinement of N2O4 inside nano-pores has been established at a molecular level, and dynamic breakthrough experiments using both dry and humid NO2 gas streams verify the excellent stability and selectivity of MFM-520, and confirm its potential for precious-metal-free deNOx technologies.
conversion of the captured NO2 into HNO3, an important feedstock for fertilizer production, and fully regenerates MFM-520. The confinement of N2O4 inside nano-pores has been established at a molecular level, and dynamic breakthrough experiments using both dry and humid NO2 gas streams verify the excellent stability and selectivity of MFM-520, and confirm its potential for precious-metal-free deNOx technologies.
| Original language | English |
|---|---|
| Pages (from-to) | 1085-1090 |
| Journal | Nature Chemistry |
| Volume | 11 |
| DOIs | |
| Publication status | Published - 22 Nov 2019 |
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EPSRC National Research Facility for Electron Paramagnetic Resonance
Collison, D. (Academic lead), Mcinnes, E. (Academic lead), Tuna, F. (Academic lead), Bowen, A. (Academic lead), Shanmugam, M. (Senior Technical Specialist), Brookfield, A. (Technical Specialist), Fleming, E. (Other) & Cliff, M. (Core Facility Lead)
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