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Erschienen in: Topics in Catalysis 18-19/2018

04.06.2018 | Original Paper

Carbon-Supported Au Nanoparticles: Catalytic Activity Ruled Out by Carbon Support

verfasst von: Andrea Jouve, Marta Stucchi, Ilaria Barlocco, Claudio Evangelisti, Ferenc Somodic, Alberto Villa, Laura Prati

Erschienen in: Topics in Catalysis | Ausgabe 18-19/2018

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Abstract

The catalytic oxidation of glycerol produces high added value chemical products. Gold-based catalysts showed activity and selectivity depending on particle size and specific preparation method. Moreover, the support plays a fundamental role in modulating the stability of the catalytic system. However, the literature is still lacking of a precise disclosure of these important relationships. Herein, we synthesized two series of gold catalysts on different carbon supports (Vulcan-XC72R, X40S and Norit GSX), the first synthesized by solvated metal atom deposition (SMAD) and the second by Sol Immobilization technique (SOL). First of all, the specific physico-chemical properties of the supports and the synthesis procedure influenced the dispersion and the size of Au NPs making a direct comparison among the different carbon difficult. In particular, on Vulcan-XC72R, AuNPs showed narrow size and good dispersion, whereas on Norit GSX and X40S-Camel a notably wider size distribution has been revealed. XPS analyses showed Au exposure changed accordingly to the presence of oxygen species, lower O content corresponding to lower Au exposure. Unexpectedly however this does not correspond to a lower activity, being the lowest Au/C (%at), the Vulcan ones, the most active catalysts. Comparing SOL and SMAD prepared samples on the same carbon, the SOL ones always result more active.

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Metadaten
Titel
Carbon-Supported Au Nanoparticles: Catalytic Activity Ruled Out by Carbon Support
verfasst von
Andrea Jouve
Marta Stucchi
Ilaria Barlocco
Claudio Evangelisti
Ferenc Somodic
Alberto Villa
Laura Prati
Publikationsdatum
04.06.2018
Verlag
Springer US
Erschienen in
Topics in Catalysis / Ausgabe 18-19/2018
Print ISSN: 1022-5528
Elektronische ISSN: 1572-9028
DOI
https://doi.org/10.1007/s11244-018-1001-7

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