Exploring CO <sub>2</sub> Methanation Using 3D‐Printed Carbon Architectures

To demonstrate for the first time the potential of stereolithography-printed, architected, bio-based carbon-supported Ni catalysts for CO<sub>2</sub> methanation, three honeycomb carbon structures with different textural properties were prepared, impregnated with 15 wt.% of nickel metal particles, and studied to correlate their catalytic performances with their textural properties and surface chemistry. Compared with the non-activated monolith and the steam-activated monolith, the CO<sub>2</sub>-activated monolith achieved a higher CO<sub>2</sub> conversion of 62 % with a CH<sub>4</sub> selectivity of 73 % at 460 °C. Our comparative study demonstrated that the CO<sub>2</sub>-activated carbon support, although having fewer basic sites on the surface, exhibits greater dispersion of the Ni phase, enabling an increase in H<sub>2</sub> chemisorption. These results are of interest for further studies related to the optimization of catalytic performance through the design of the architectural and textural properties of such macrostructures.

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Journal
ChemSusChem
Published
2025-03-17
DOI
https://doi.org/10.1002/cssc.202500303
Citations
1
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
0.52

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article

Exploring CO 2 Methanation Using 3D‐Printed Carbon Architectures

O.S.G.P. Soares, Vanessa Fierro, Nicolas Vincent, Ana Rita Querido et al.
1 citations
ChemSusChem
Catalytic Processes in Materials Science
0.52
article

Exploring CO 2 Methanation Using 3D‐Printed Carbon Architectures

O.S.G.P. Soares, Vanessa Fierro, Nicolas Vincent, Ana Rita Querido, M. Fernando R. Pereira, Pauline Blyweert, Alain Celzard
article en
1 citations

Abstract

To demonstrate for the first time the potential of stereolithography-printed, architected, bio-based carbon-supported Ni catalysts for CO<sub>2</sub> methanation, three honeycomb carbon structures with different textural properties were prepared, impregnated with 15 wt.% of nickel metal particles, and studied to correlate their catalytic performances with their textural properties and surface chemistry. Compared with the non-activated monolith and the steam-activated monolith, the CO<sub>2</sub>-activated monolith achieved a higher CO<sub>2</sub> conversion of 62 % with a CH<sub>4</sub> selectivity of 73 % at 460 °C. Our comparative study demonstrated that the CO<sub>2</sub>-activated carbon support, although having fewer basic sites on the surface, exhibits greater dispersion of the Ni phase, enabling an increase in H<sub>2</sub> chemisorption. These results are of interest for further studies related to the optimization of catalytic performance through the design of the architectural and textural properties of such macrostructures.

ChemSusChemVol. 18(11)
Centre National de la Recherche Scientifique (FR), Universidade do Porto (PT), Institut Universitaire de France (FR), Institut Jean Lamour (FR), Université de Lorraine (FR)
European Regional Development Fund
Openalex Percentile: Top 41%
Catalytic Processes in Materials Science
0.52
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Exploring CO <sub>2</sub> Methanation Using 3D‐Printed Carbon Architectures — O.S.G.P. Soares, Vanessa Fierro, et al. · ChemSusChem (2025) | TGRS Research Map | TGRS