| Résumé | Flue gas is a major source of CO₂ and the development of technologies for its utilization is of utmost interest both by environmental and industrial perspectives. Recently investigated CO₂ valorization processes still face techno-economic challenges for implementation for costs associated with different steps, including CO₂ purification steps. Thus, for the first time in literature, the feasibility of the direct one-step upgrading of real untreated flue gas into syngas is investigated here. For that end, classical alumina-supported catalysts (Ni, Co and Fe) were used for concept validation. The influences of temperature (500–900 °C), metal load (10–15 %), residence time (GHSV = 315–1260 h⁻¹) and the effects of flue gas impurities (NOₓ and SO₂) are reported here. Best CO₂ and H₂O conversion performances (XCO₂ = 53.9 %, XH₂O = 67.0 %) were obtained with the nickel catalyst with 15 wt% Ni at 900 °C and the highest residence time (GHSV = 315 h⁻¹). The highest H₂/CO ratio of the produced syngas was 0.70 and it was obtained with the same 15 wt% Ni catalyst at T = 700 °C, GHSV = 630 h⁻¹. The NOₓ present in the FG was completely removed as part of the one-step upgrading strategy, while SO₂ did not interact with the tested catalysts. Finally, a long-term operation strategy was proposed by supplementing the flue gas with H₂ (H₂/CO₂ = 1.0), which yielded 24 h stable operation with around 40 % CO₂ conversion and a syngas with H₂/CO = 1.2–1.3. The results presented here, for the first time in the literature, demonstrate the feasibility of a novel one-step process for direct valorization of flue gas. The direct upgrading of flue gas would potentially decrease the costs associated with CO₂ purification and valorization. |
|---|
