Abstract
Thermocatalytic conversion of CO2 into liquid fuels and chemicals is a promising approach to mitigate global warming. Although, the CO2 conversion and long-chain hydrocarbon selectivity are highly dependent on the choice of metal-oxide promoter, but role of the promoter remains unclear. Herein, the role of MgO as a promoter for an Fe-based catalyst was investigated. Bimetallic Na-FeMgOx catalyst exhibited a high C5+ yield of 25.1% with a CO2 conversion of 49.1% at the early stage of the reaction. The presence of MgO facilitates the reduction of Fe oxides and formation of oxygen vacancies by transferring electrons to Fe-based phases. In addition, at the early stage of reaction, the decoration of the Mg oxide surface with nanosized χ-Fe5C2 enhances the C5+ yield. However, the progressive transformation of MgO to MgCO3 during CO2 conversion deactivates the Na-FeMgOx catalyst. A detailed deactivation mechanism is also discussed.
| Original language | English |
|---|---|
| Article number | 123052 |
| Journal | Applied Catalysis B: Environmental |
| Volume | 338 |
| DOIs | |
| State | Published - 5 Dec 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 13 Climate Action
Keywords
- CO hydrogenation
- Deactivation
- Fe catalyst
- Fischer–Tropsch synthesis
- Mg promotor
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