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Oxidation Stability of Multiwalled Carbon Nanotubes for Catalytic Applications

MPG-Autoren
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Frank,  Benjamin
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Rinaldi,  Ali
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Blume,  Raoul
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Su,  Dang Sheng
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Zitation

Frank, B., Rinaldi, A., Blume, R., Schlögl, R., & Su, D. S. (2010). Oxidation Stability of Multiwalled Carbon Nanotubes for Catalytic Applications. Chemistry of Materials, 22(15), 4462-4470. Retrieved from http://dx.doi.org/10.1021/cm101234d.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0010-F54C-5
Zusammenfassung
The oxidation of multiwalled carbon nanotubes (CNTs) was investigated with regard to a detailed prediction of the lifetime of this material as a catalyst for oxidative dehydrogenations. A power-law kinetics is found to be adequate for the description of CO2 formation in the temperature range of 623−823 K and under O2 partial pressures of 0.025−0.6 bar. The stability against oxidation can be enhanced by passivation with B2O3 or P2O5 and by high temperature treatment. The progress of oxidative degradation was monitored by TEM and Raman spectroscopy. A mechanistic study supported by high pressure XPS and SSITKA reveals full agreement with the established model of the oxidation of conventional carbon materials; however, the theory of sequential layer degradation as observed for single crystal graphite is not transferable to a technical grade CNT material, and instead, various modes of propagation of combustion sites are identified.