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  4. Effect of carbon surface functional groups on the synthesis of Ru/C catalysts for supercritical water gasification
 
research article

Effect of carbon surface functional groups on the synthesis of Ru/C catalysts for supercritical water gasification

Peng, Gael
•
Gramm, Fabian
•
Ludwig, Christian  
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2015
Catalysis Science & Technology

A carbon support was treated with HNO3 to create surface functional groups (e.g. -COOH, -OH), which were then characterized by TGA, TPD, CNS elemental analysis, and Boehm titration. HNO3 modified the carbon surface properties by adding a high amount of carboxylic groups, improved the thermal stability of the carbon support, and reduced ca. 50% of the ash. The thermal pre-treatment (723 K under He) following the HNO3 pre-treatment successfully removed the carboxylic groups. 4% Ru/C catalysts were synthesized using the surface-modified carbon supports and characterized by H-2-TPR, CO pulse chemisorption, N-2-physisorption and HAADF-STEM. The Ru dispersion was increased in the presence of the carboxylic groups. Catalytic supercritical water gasification (CSCWG) of 10 wt.% isopropanol over the 4% Ru/C catalysts was carried out at 723 K and 30 MPa for 50 hours to assess the performance of the catalysts. It was found that the Ru/C catalyst prepared involving a pre-treatment with HNO3 did not exhibit a higher catalytic activity than the catalyst whose carbon support was not pre-treated with HNO3. Hence, the activity and the selectivity during CSCWG were not influenced by the pre-treatment of the catalyst support with HNO3.

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Type
research article
DOI
10.1039/c5cy00352k
Web of Science ID

WOS:000356610600024

Author(s)
Peng, Gael
Gramm, Fabian
Ludwig, Christian  
Vogel, Frederic
Date Issued

2015

Publisher

Royal Soc Chemistry

Published in
Catalysis Science & Technology
Volume

5

Issue

7

Start page

3658

End page

3666

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
GR-LUD  
Available on Infoscience
September 28, 2015
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/119139
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