Understanding how the structure of carbonaceous materials changes upon oxidation at mild temperature as a function of the graphitic order is of great importance for the development of clean combustion technologies, such as carbon fuel cells. The micro- and nanostructures of a range of carbon materials at room temperature and upon mild oxidation at 300 °C have been analysed by means of mercury porosimetry, Nitrogen adsorption, X-Ray Diffraction, Raman spectroscopy and Electron Paramagnetic Resonance. The samples included carbons with increasing level of graphitic order: three chars derived from two bituminous coals and a lignite, a synthetic carbon and a graphitized coke. The experimental characterization allows to classify the materials according to different structural parameters, including porosity, surface area, degree of graphitization and paramagnetic activation of the carbonaceous surface. A correlation with the rank of the analysed materials is observed. For the graphitized coke, oxidation leads to more crystalline order and enhancement of the paramagnetic signal. A similar increase in the paramagnetic activity is observed for the Lignite char. On the other hand, for the higher rank, bituminous and synthetic chars, mild oxidation leads to a slight expansion of the amorphous carbon and loss of paramagnetic activity. The differences are rationalized in terms of formation of new carbon-oxygen complexes on the graphitized coke and on the Lignite char, and redistribution of already existing complexes for the higher-rank coals. This investigation complements previous X-ray photoelectron spectroscopy measurements.

On how mild oxidation affects the structure of carbons: Comparative analysis by different techniques

Luciano Cortese;Osvalda Senneca
2020

Abstract

Understanding how the structure of carbonaceous materials changes upon oxidation at mild temperature as a function of the graphitic order is of great importance for the development of clean combustion technologies, such as carbon fuel cells. The micro- and nanostructures of a range of carbon materials at room temperature and upon mild oxidation at 300 °C have been analysed by means of mercury porosimetry, Nitrogen adsorption, X-Ray Diffraction, Raman spectroscopy and Electron Paramagnetic Resonance. The samples included carbons with increasing level of graphitic order: three chars derived from two bituminous coals and a lignite, a synthetic carbon and a graphitized coke. The experimental characterization allows to classify the materials according to different structural parameters, including porosity, surface area, degree of graphitization and paramagnetic activation of the carbonaceous surface. A correlation with the rank of the analysed materials is observed. For the graphitized coke, oxidation leads to more crystalline order and enhancement of the paramagnetic signal. A similar increase in the paramagnetic activity is observed for the Lignite char. On the other hand, for the higher rank, bituminous and synthetic chars, mild oxidation leads to a slight expansion of the amorphous carbon and loss of paramagnetic activity. The differences are rationalized in terms of formation of new carbon-oxygen complexes on the graphitized coke and on the Lignite char, and redistribution of already existing complexes for the higher-rank coals. This investigation complements previous X-ray photoelectron spectroscopy measurements.
2020
Istituto di Scienze e Tecnologie per l'Energia e la Mobilità Sostenibili - STEMS
Inglese
1-4
100006
12
https://doi.org/10.1016/j.jaecs.2020.100006
Sì, ma tipo non specificato
milod oxidation
structure
porosity
xrd
epr
raman
La rivista è Applications in energy and combustion science, sister journal di Progress in energy and combustion science, ma non rieco a caricare il nome corretto della rivista, dato che è nuova. In seguito si deve modificare ISSN: 2666-352X
5
info:eu-repo/semantics/article
262
Levi, Gianluca; Causà, Mauro; Cortese, Luciano; Salatino, Piero; Senneca, Osvalda
01 Contributo su Rivista::01.01 Articolo in rivista
open
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/442024
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