Abstract

The escalating rate of fossil fuel combustion contributes to excessive CO2 emission and the resulting global climate change has drawn considerable attention. Therefore, tremendous efforts have been devoted to mitigate the CO2 accumulation in the atmosphere. Carbon capture and storage (CCS) strategy has been regarded as one of the promising options for controlling CO2 build-up. However, desorption and compression of CO2 need extra energy input. To circumvent this energy issue, carbon capture and utilization (CCU) strategy has been proposed whereby CO2 can be captured and in situ activated simultaneously to participate in the subsequent conversion under mild conditions, offering valuable compounds. As an alternative to CCS, the CCU has attracted much concern. Although various absorbents have been developed for the CCU strategy, the direct, in situ chemical conversion of the captured CO2 into valuable chemicals remains in its infancies compared with the gaseous CO2 conversion. This review summarizes the recent progress on CO2 capture and in situ catalytic transformation. The contents are introduced according to the absorbent types, in which different reaction type is involved and the transformation mechanism of the captured CO2 and the role of the absorbent in the conversion are especially elucidated. We hope this review can shed light on the transformation of the captured CO2 and arouse broad concern on the CCU strategy.

Highlights

  • The demand for energy of the rapid industrialization results in large-scale combustion of fossil fuel, which causes excessive emissions of carbon dioxide

  • Different CO2 absorbents including inorganic and organic bases, N-heterocyclic carbenes (NHCs), and Nheterocyclic olefins (NHOs), ionic liquids (ILs), frustrated Lewis pairs (FLPs) and polymeric functional materials have been employed in this field

  • Much effort is still desired to explore the potential conversion of the captured CO2

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Summary

Introduction

The demand for energy of the rapid industrialization results in large-scale combustion of fossil fuel, which causes excessive emissions of carbon dioxide. Organic and inorganic bases, N-heterocyclic carbenes (NHCs) and Nheterocyclic olefins (NHOs), ionic liquids (ILs) and frustrated Lewis pairs (FLPs) have already been applied to CO2 capture and in situ conversion. The captured CO2 can be activated simultaneously and the resulting carbamic acid can react with either aziridine or propargyl amine to afford oxazolidinones in the presence of NH4I and AgOAc as a catalyst, respectively (Scheme 4).

Results
Conclusion

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