Heteroaggregation and Selective Deposition for the Fine Design of Nanoarchitectured Bifunctional Catalysts: Application to Hydroisomerization
In: ACS Catalysis ACS Catalysis, American Chemical Society, 2018, 8 (7), pp.6071-6078. ⟨10.1021/acscatal.8b01461⟩; (2018-05-23)
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Zugriff:
We successfully prepared bifunctional catalysts with the distance between metallic and acid sites tuned at the nanometer scale. Sols of β-zeolite nanoparticles were synthesized and mixed in optimized conditions with a γ-AlOOH boehmite suspension to yield alumina/zeolite aggregates with a nanometer scale intimacy. The composition of the aggregate could be tuned from pure alumina to pure zeolite. Then, by carefully choosing the Pt precursor and the pH conditions, we were able to selectively deposit platinum, either on alumina or in zeolite domains. A subsequent, soft thermo-reduction step was applied that produced well-dispersed Pt nanoparticles either on alumina or in the zeolite nanodomains as confirmed by 3D tomography microscopy experiments. The catalytic properties of the obtained nanostructured catalysts were studied through n-heptane conversion. Comparison of these original bifunctional catalysts with monofunctional or conventional bifunctional catalysts showed the impact of the location of the metal...
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Heteroaggregation and Selective Deposition for the Fine Design of Nanoarchitectured Bifunctional Catalysts: Application to Hydroisomerization
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Autor/in / Beteiligte Person: | Baaziz, Walid ; Tinat, Lionel ; Olfa Ben Moussa ; Blanchard, Juliette ; Jin, Xiaojing ; Durupthy, Olivier ; Sayag, Céline ; Laboratoire de Réactivité de Surface (LRS) ; Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS) ; Matériaux Hybrides et Nanomatériaux (MHN) ; Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP) ; Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS) ; Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS) ; Université de Strasbourg (UNISTRA)-Matériaux et nanosciences d'Alsace (FMNGE) ; Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique ; Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA) ; Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) (LCMCP (site Paris VI)) ; Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP) ; Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS) |
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Quelle: | ACS Catalysis ACS Catalysis, American Chemical Society, 2018, 8 (7), pp.6071-6078. ⟨10.1021/acscatal.8b01461⟩; (2018-05-23) |
Veröffentlichung: | HAL CCSD, 2018 |
Medientyp: | unknown |
ISSN: | 2155-5435 (print) |
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