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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (6/6 displayed)

  • 2022Effect of Metal Dopant on the Performance of Ni@CeMeO2 Embedded Catalysts (Me = Gd, Sm and Zr) for Dry Reforming of Methane6citations
  • 2022Effect of Metal Dopant on the Performance of Ni@CeMeO2 Embedded Catalysts (Me = Gd, Sm and Zr) for Dry Reforming of Methane6citations
  • 2021Pt nanoparticles embedded in CeO 2 and CeZrO 2 catalysts for biogas upgrading: Investigation on carbon removal mechanism by oxygen isotopic exchange and DRIFTS11citations
  • 2020Partial oxidation of methane over lanthana-supported catalysts derived from perovskites22citations
  • 2015Selective ring opening of methylcyclohexane and decalin over Rh-Pd supported catalysts: Effect of the preparation method15citations
  • 2010Control of titania nanodomain size as a route to modulate SMSI effect in Pt/TiO2 catalysts20citations

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Chart of shared publication
Noronha, Fabio B.
1 / 1 shared
Neto, Raimundo Crisostomo Rabelo
1 / 1 shared
Marinho, André L. A.
1 / 1 shared
Souza Toniolo, Fabio
2 / 2 shared
Bion, Nicolas
4 / 15 shared
Marinho, André
1 / 1 shared
Toniolo, Fabio
1 / 2 shared
Noronha, Fabio
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Rabelo-Neto, Raimundo
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Bellot Noronha, Fabio
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Marinho, André, L. A.
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Rabelo-Neto, Raimundo, C.
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Marchetti, Sergio Gustavo
1 / 1 shared
Bengoa, José Fernando
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Fonseca, Hilma
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Ruiz, Doris
1 / 1 shared
Do Carmo Rangel, Maria
1 / 1 shared
Dippolito, Silvana A.
1 / 1 shared
Especel, Catherine
2 / 8 shared
Pieck, Carlos L.
1 / 2 shared
Ekou, Tchirioua
1 / 3 shared
Marecot, Patrice
1 / 3 shared
Royer, Sebastien
1 / 16 shared
Samoila, Petrisor
1 / 3 shared
Duprez, Daniel
1 / 8 shared
Bonne, Magali
1 / 9 shared
Chart of publication period
2022
2021
2020
2015
2010

Co-Authors (by relevance)

  • Noronha, Fabio B.
  • Neto, Raimundo Crisostomo Rabelo
  • Marinho, André L. A.
  • Souza Toniolo, Fabio
  • Bion, Nicolas
  • Marinho, André
  • Toniolo, Fabio
  • Noronha, Fabio
  • Rabelo-Neto, Raimundo
  • Bellot Noronha, Fabio
  • Marinho, André, L. A.
  • Rabelo-Neto, Raimundo, C.
  • Marchetti, Sergio Gustavo
  • Bengoa, José Fernando
  • Fonseca, Hilma
  • Ruiz, Doris
  • Do Carmo Rangel, Maria
  • Dippolito, Silvana A.
  • Especel, Catherine
  • Pieck, Carlos L.
  • Ekou, Tchirioua
  • Marecot, Patrice
  • Royer, Sebastien
  • Samoila, Petrisor
  • Duprez, Daniel
  • Bonne, Magali
OrganizationsLocationPeople

article

Selective ring opening of methylcyclohexane and decalin over Rh-Pd supported catalysts: Effect of the preparation method

  • Dippolito, Silvana A.
  • Especel, Catherine
  • Epron, Florence
  • Pieck, Carlos L.
Abstract

International audience ; Bimetallic Rh-Pd catalysts prepared by various impregnation methods were evaluated in the selective ring-opening of decalin and methylcyclohexane (MCH) used as model molecules of hydrogenated aromatics of the Light Cycle Oil fraction. Rh and Pt were deposited on Al2O3 and SiO2-Al2O3 (S40) by coimpregnation (Cl) or successive impregnations (SI) with different orders of metal addition. Catalysts were characterized by H-2 chemisorption, temperature-programmed reduction, temperature-programmed desorption of pyridine, and test reactions of cyclopentane hydrogenolysis and isomerization of 3,3-dimethyl-1-butene. Their catalytic behaviors for the ring-opening reaction were deeply influenced by the acidity of the support, and in a lesser extent by the metal deposition method. On both supports, the CI catalysts, displaying the highest dispersion values, exhibited the best ring opening performances. In the case of the SI catalysts, the addition order of both metals modified in a moderate way the properties of the catalyst. The yield to ring opening products obtained in MCH ring opening with CI catalysts supported on Al2O3 was 39-69% higher than those prepared by SI (conversion = 55-60%) while for the catalysts supported on S40, the yield to ring opening products was 8-48% higher for the CI catalysts compared to SI catalysts (conversion = 72-77%). The conversion of decalin for the bimetallic catalysts supported on Al2O3 was lower than 20% being dehydrogenated compounds the main reaction products regardless the preparation method. The catalyst supported on S40 showed decalin conversion values between 46-53% and yield to ring opening near to 30%. Moreover, the CI catalysts have yield to ring opening 10 to 20% higher than the catalysts prepared by SI. The catalyst prepared by coimpregnation supported on S40 was the most appropriate for opening the MCH and decalin due to an optimal balance between the metal and acid functions.

Topics
  • Deposition
  • dispersion
  • compound
  • chemical ionisation
  • temperature-programmed reduction