Catalytic oxidation of cyclohexane over Ti–Zr–Co catalysts

Ti–Zr–Co alloys have been fabricated and characterized, and their catalytic performance was discussed for the oxidation of cyclohexane with oxygen under solvent-free condition. The icosahedral quasicrystalline phase (I-phase)-forming ability of Ti–Zr–Co alloys with different compositions was discuss...

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Veröffentlicht in:Applied catalysis. A, General General, 2009-10, Vol.368 (1), p.29-34
Hauptverfasser: Hao, Jianmin, Wang, Jinyao, Wang, Qiang, Yu, Yancun, Cai, Shuxia, Zhao, Fengyu
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Sprache:eng
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Zusammenfassung:Ti–Zr–Co alloys have been fabricated and characterized, and their catalytic performance was discussed for the oxidation of cyclohexane with oxygen under solvent-free condition. The icosahedral quasicrystalline phase (I-phase)-forming ability of Ti–Zr–Co alloys with different compositions was discussed, and it was confirmed that I-phase could be formed as a dominating phase at the Ti-rich composition region from Ti 53Zr 27Co 20 to Ti 75Zr 5Co 20 in as-cast alloys. The composition and microstructure of Ti–Zr–Co alloys present crucial influences on its catalytic activity and selectivity in the oxidation of cyclohexane. The influences of some reaction parameters such as temperature, reaction time, and catalyst amounts were also investigated. Ti 70Zr 10Co 20 alloy containing quasicrystal microstructure showed good catalytic performance with a 6.8% conversion of cyclohexane and 90.4% selectivity of cyclohexanol and cyclohexanone. It behaves as an efficient heterogeneous catalyst for the oxidation of cyclohexane and could be recycled five times without loss in activity and selectivity. Ti–Zr–Co alloys have been fabricated and characterized, and their catalytic performance was discussed for the oxidation of cyclohexane with oxygen under solvent-free condition. The composition and microstructure of Ti–Zr–Co alloy present crucial influences on its catalytic activity and selectivity in the oxidation of cyclohexane.
ISSN:0926-860X
1873-3875
DOI:10.1016/j.apcata.2009.08.007