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Emerging investigator series: synthesis of magnesium oxide nanoparticles fabricated on a graphene oxide nanocomposite for CO 2 sequestration at elevated temperatures
Alkaline metal oxides incorporated into porous templates are considered novel chemisorbents for capturing greenhouse gases including CO 2 at elevated temperatures. Thus, magnesium oxide nanoparticles (MONPs) and MONP incorporated graphene oxide (MONP–GO) were synthesized using a sol–gel method. Prep...
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Published in: | Environmental science. Nano 2020-04, Vol.7 (4), p.1225-1239 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Alkaline metal oxides incorporated into porous templates are considered novel chemisorbents for capturing greenhouse gases including CO
2
at elevated temperatures. Thus, magnesium oxide nanoparticles (MONPs) and MONP incorporated graphene oxide (MONP–GO) were synthesized using a sol–gel method. Preparation of these materials was carried out by a three-step facile synthesis route involving: (1) synthesis of magnesium oxide (MO) nanoparticles (MONPs), (2) synthesis of graphene oxide (GO) from commercially available graphene, and (3) incorporation of MONPs on graphene oxide. Both MONP and MONP–GO samples exhibited a significantly high CO
2
uptake of 2.79–3.34 mmol g
−1
at two different elevated temperatures (60 and 120 °C). The increased CO
2
adsorption is due to the presence of terminal OH groups and acid–base pair sites at the magnesium (Mg
2+
–O
2−
) surface in the MONP and MONP–GO materials, respectively, resulting in the formation of hydrogen carbonate species and bidentate carbonate complexes with CO
2
gas. Our composite material also possesses intriguing properties including high thermal and chemical stabilities, low-cost, and environmental benignity along with its enhanced CO
2
sorption making it an excellent candidate for CO
2
capture in fossil fuel-based power plants at elevated temperatures. |
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ISSN: | 2051-8153 2051-8161 |
DOI: | 10.1039/C9EN01442J |