Selective Oxidation of Saturated Hydrocarbons Using Au–Pd Alloy Nanoparticles Supported on Metal–Organic Frameworks

Gold (Au) and palladium (Pd) nanoparticles dispersed on a zeolite-type metal–organic framework (i.e., MIL-101) were prepared via a simple colloidal method. The catalysts were characterized by powder X-ray diffraction, N2 physical adsorption, atomic absorption spectroscopy, transmission electron micr...

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Veröffentlicht in:ACS catalysis 2013-04, Vol.3 (4), p.647-654
Hauptverfasser: Long, Jilan, Liu, Hongli, Wu, Shijian, Liao, Shijun, Li, Yingwei
Format: Artikel
Sprache:eng
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Zusammenfassung:Gold (Au) and palladium (Pd) nanoparticles dispersed on a zeolite-type metal–organic framework (i.e., MIL-101) were prepared via a simple colloidal method. The catalysts were characterized by powder X-ray diffraction, N2 physical adsorption, atomic absorption spectroscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. Au and Pd were mostly in the form of bimetallic alloys on the MIL-101 support. The Au–Pd/MIL-101 was active and selective in the oxidation of a variety of saturated (including primary, secondary, and tertiary) C–H bonds with molecular oxygen. For the liquid-phase oxidation of cyclohexane, cyclohexane conversion exceeding 40% was achieved (TOF: 19 000 h–1) with >80% selectivity to cyclohexanone and cyclohexanol under mild solvent-free conditions. Moreover, the Au–Pd alloy catalyst exhibited higher reactivity than their pure metal counterparts and an Au + Pd physical mixture. The high activity and selectivity of Au–Pd/MIL-101 in cyclohexane aerobic oxidation may be correlated to the synergistic alloying effect of bimetallic Au–Pd nanoparticles.
ISSN:2155-5435
2155-5435
DOI:10.1021/cs300754k