Abstract
AbstractTo reduce anthropogenic carbon dioxide (CO2) emissions, it is desirable to develop reactions that can efficiently convert low concentrations of CO2, present in exhaust gases and ambient air, into industrially important chemicals, without involving any expensive separation, concentration, compression, and purification processes. Here, we present an efficient method for synthesizing urea derivatives from alkyl ammonium carbamates. The carbamates can be easily obtained from low concentrations of CO2 as present in ambient air or simulated exhaust gas. Reaction of alkyl ammonium carbamates with 1,3-dimethyl-2-imidazolidinone solvent in the presence of a titanium complex catalyst inside a sealed vessel produces urea derivatives in high yields. This reaction is suitable for synthesizing ethylene urea, an industrially important chemical, as well as various cyclic and acyclic urea derivatives. Using this methodology, we also show the synthesis of urea derivatives directly from low concentration of CO2 sources in a one-pot manner.
Publisher
Springer Science and Business Media LLC
Subject
Materials Chemistry,Biochemistry,Environmental Chemistry,General Chemistry
Reference34 articles.
1. Pachauri, R. K. et al. Climate Change 2014: Synthesis Report. Contribution of Working Groups I, II, and III to the fifth assessment report of the Intergovernmental Panel on Climate Change (IPCC, 2014).
2. Leung, D. Y. C., Caramanna, G. & Maroto-Valer, M. M. An overview of current status of carbon dioxide capture and storage technologies. Renew. Sustain. Energy Rev. 39, 426–443 (2014).
3. Bui, M. et al. Carbon capture and storage (CCS): the way forward. Energy Environ. Sci. 11, 1062–1176 (2018).
4. Hunt, A. J., Sin, E. H. K., Marriott, R. & Clark, J. H. Generation, capture, and utilization of industrial carbon dioxide. ChemSusChem 3, 306–322 (2010).
5. Markewitz, P. et al. Worldwide innovations in the development of carbon capture technologies and the utilization of CO2. Energy Environ. Sci. 5, 7281–7305 (2012).
Cited by
32 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献