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Renewable N-doped active carbons as efficient catalysts for direct synthesis of cyclic carbonates from epoxides and CO2
[Display omitted] •Direct carbonation epoxides with CO2 using N-doped carbons.•Activity originates from pyridinic, pyridonic, and quaternary N-sites.•Correlation between surface textural properties and catalyst poisoning.•Kinetically controlled reaction (activation energy 39.6 kJ/mol and 43.3 kJ/mol...
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Published in: | Applied catalysis. B, Environmental Environmental, 2019-02, Vol.241, p.41-51 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Direct carbonation epoxides with CO2 using N-doped carbons.•Activity originates from pyridinic, pyridonic, and quaternary N-sites.•Correlation between surface textural properties and catalyst poisoning.•Kinetically controlled reaction (activation energy 39.6 kJ/mol and 43.3 kJ/mol).
In the spirit of green chemistry and greenhouse gas mitigation, we explore herein the chemical utilization of CO2 upon synthesis of cyclic carbonates over N-doped activated carbons. The N-doped carbocatalysts were obtained from inexpensive N-rich bio-waste precursors and characterized by standard techniques (N2 physisorption, chemisorption, XPS, SEM, TEM, XRD, FT-IR and Micro-Raman spectroscopy). The materials exhibited excellent catalytic activity for direct carbonation of epoxides with CO2 to cyclic carbonates (yields upto 99%) under solvent free, moderate temperature (100–150 °C) and low CO2 pressure (5–50 bar) conditions. The observed catalytic activity of the N-doped carbocatalysts was attributed to the Lewis basic sites originating from pyridinic, pyridonic, and quaternary N-sites capable of activating the CO2 molecule. While control experiments with multiwalled carbon nanotubes (MWCNT) or commercial activated carbon, failed to produce cyclic carbonates due to lack of active (basic) sites. In terms of the catalytic performance, the N-doped carbocatalysts presenting a high porosity (634–1316 m2/g) and high levels of pyridinic (33%) and quaternary N-doping (30%), (i.e. CA500 and MA500), exhibited the highest activity and selectivity (TOF, conversion and cyclic carbonate yields upto 99% in 5–15 h). Most importantly, these materials demonstrated good operational stability and reusability. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2018.09.019 |