Pristine and annealed multi-walled C nanotubes are preliminarily tested as catalysts towards the degradation of p-coumaric acid with better performances than the widely used activated carbon. In order to clarify the origin of their different catalytic efficiency, the samples are analysed by means of high-resolution transmission electron microscopy, X-ray photoemission, reflection electron energy loss and micro-Raman spectroscopy. Chemical composition, mass density, bonding configurations and threefold- to fourfold-coordinated carbon bonding ratios are determined. The comparative discussion of the results obtained leads to attribute the higher catalytic activity of the pristine nanotubes to their larger sp2/sp3 carbon bonding fraction and greater amount of oxygen containing functional groups.

Correlation between carbon nanotube microstructure and their catalytic efficiency towards the p-coumaric acid degradation

G. Faggio;Santangelo S
2013-01-01

Abstract

Pristine and annealed multi-walled C nanotubes are preliminarily tested as catalysts towards the degradation of p-coumaric acid with better performances than the widely used activated carbon. In order to clarify the origin of their different catalytic efficiency, the samples are analysed by means of high-resolution transmission electron microscopy, X-ray photoemission, reflection electron energy loss and micro-Raman spectroscopy. Chemical composition, mass density, bonding configurations and threefold- to fourfold-coordinated carbon bonding ratios are determined. The comparative discussion of the results obtained leads to attribute the higher catalytic activity of the pristine nanotubes to their larger sp2/sp3 carbon bonding fraction and greater amount of oxygen containing functional groups.
2013
WET AIR OXIDATION, ENERGY LOSS SPECTRA, SPECTROSCOPY, FILMS
CARBON NANOTUBE, CVD, STRUCTURAL PROPERTIES, X RAY PHOTOEMISSION SPECTROSCOPY, RAMAN SPECTROSCOPY, CATALYSIS
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12318/276
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