Integrated CO2 capture-fixation chemistry via interfacial ionic liquid catalyst in laminar gas/liquid flow
Simultaneous capture of carbon dioxide (CO 2 ) and its utilization with subsequent work-up would significantly enhance the competitiveness of CO 2 -based sustainable chemistry over petroleum-based chemistry. Here we report an interfacial catalytic reaction platform for an integrated autonomous proce...
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Veröffentlicht in: | Nature communications 2017-03, Vol.8 (1), p.14676-14676, Article 14676 |
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Sprache: | eng |
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Zusammenfassung: | Simultaneous capture of carbon dioxide (CO
2
) and its utilization with subsequent work-up would significantly enhance the competitiveness of CO
2
-based sustainable chemistry over petroleum-based chemistry. Here we report an interfacial catalytic reaction platform for an integrated autonomous process of simultaneously capturing/fixing CO
2
in gas–liquid laminar flow with subsequently providing a work-up step. The continuous-flow microreactor has built-in silicon nanowires (SiNWs) with immobilized ionic liquid catalysts on tips of cone-shaped nanowire bundles. Because of the superamphiphobic SiNWs, a stable gas–liquid interface maintains between liquid flow of organoamines in upper part and gas flow of CO
2
in bottom part of channel. The intimate and direct contact of the binary reagents leads to enhanced mass transfer and facilitating reactions. The autonomous integrated platform produces and isolates 2-oxazolidinones and quinazolines-2,4(1
H
,3
H
)-diones with 81–97% yields under mild conditions. The platform would enable direct CO
2
utilization to produce high-valued specialty chemicals from flue gases without pre-separation and work-up steps.
Microfluidics is an attractive route for synthesis, but can suffer from poor reactivity with gaseous reagents. Here the authors report a microfluidic system catalysing an interfacial reaction between CO
2
and liquid phase reagents by modifying silicon nanowires with immobilized ionic liquid catalysts. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms14676 |