Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Faria, Jimmy

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University of Twente

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2022Elasto-Raman scattering: Arsenic optical phonon as a probe of nematicity in Ba Fe 2 As 22citations
  • 2022Enhanced catalytic activity and stability of nanoshaped Ni/CeO2 for CO2 methanation in micro-monoliths22citations
  • 2018Interplay of support chemistry and reaction conditions on copper catalyzed methanol steam reforming38citations

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Colson, Dorothée
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Forget, Anne
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Philippe, Jean-Côme
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Sacuto, Alain
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Gallais, Yann
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Cazayous, Maximilien
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Houver, Sarah
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Navarro, Juan Carlos
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García-Moncada, Nuria
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Odriozola, José Antonio
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Lefferts, Leon
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Serrano-Ruiz, Juan Carlos
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Díaz-Pérez, Manuel Antonio
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Moya, Javier
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2022
2018

Co-Authors (by relevance)

  • Colson, Dorothée
  • Forget, Anne
  • Philippe, Jean-Côme
  • Sacuto, Alain
  • Gallais, Yann
  • Cazayous, Maximilien
  • Houver, Sarah
  • Navarro, Juan Carlos
  • García-Moncada, Nuria
  • Odriozola, José Antonio
  • Lefferts, Leon
  • Serrano-Ruiz, Juan Carlos
  • Díaz-Pérez, Manuel Antonio
  • Moya, Javier
OrganizationsLocationPeople

article

Enhanced catalytic activity and stability of nanoshaped Ni/CeO2 for CO2 methanation in micro-monoliths

  • Faria, Jimmy
  • Navarro, Juan Carlos
  • García-Moncada, Nuria
  • Odriozola, José Antonio
  • Lefferts, Leon
Abstract

<p>Coupling inherently fluctuating renewable feedstocks to highly exothermic catalytic processes, such as CO<sub>2</sub> methanation, is a major challenge as large thermal swings occurring during ON- and OFF- cycles can irreversible deactivate the catalyst via metal sintering and pore collapsing. Here, we report a highly stable and active Ni catalyst supported on CeO<sub>2</sub> nanorods that can outperform the commercial CeO<sub>2</sub> (octahedral) counterpart during CO<sub>2</sub> methanation at variable reaction conditions in both powdered and μ-monolith configurations. The long-term stability tests were carried out in the kinetic regime, at the temperature of maximal rate (300 °C) using fluctuating gas hourly space velocities that varied between 6 and 30 L h<sup>−1</sup>·g<sub>cat</sub><sup>−1</sup>. Detailed catalyst characterization by μ-XRF revealed that similar Ni loadings were achieved on nanorods and octahedral CeO<sub>2</sub> (c.a. 2.7 and 3.3 wt. %, respectively). Notably, XRD, SEM, and HR-TEM-EDX analysis indicated that on CeO<sub>2</sub> nanorods smaller Ni-Clusters with a narrow particle size distribution were obtained (∼ 7 ± 4 nm) when compared to octahedral CeO<sub>2</sub> (∼ 16 ± 13 nm). The fast deactivation observed on Ni loaded on commercial CeO<sub>2</sub> (octahedral) was prevented by structuring the reactor bed on μ-monoliths and supporting the Ni catalyst on CeO<sub>2</sub> nanorods. FeCrAlloy® sheets were used to manufacture a multichannel μ-monolith of 2 cm in length and 1.58 cm in diameter, with a cell density of 2004 cpsi. Detailed catalyst testing revealed that powdered and structured Ni/CeO<sub>2</sub> nanorods achieved the highest reaction rates, c.a. 5.5 and 6.2 mmol CO<sub>2</sub> min<sup>−1</sup>·g<sub>Ni</sub><sup>−1</sup> at 30 L h<sup>−1</sup>·g<sub>cat</sub><sup>−1</sup> and 300 °C, respectively, with negligible deactivation even after 90 h of fluctuating operation.</p>

Topics
  • density
  • impedance spectroscopy
  • pore
  • cluster
  • scanning electron microscopy
  • x-ray diffraction
  • transmission electron microscopy
  • Energy-dispersive X-ray spectroscopy
  • sintering
  • X-ray fluorescence spectroscopy