Aluminium-rich Beta zeolite-supported platinum nanoparticles for the low-temperature catalytic removal of toluene
The removal of volatile organic compounds is an important aspect of sustainability and environmental protection. Catalytic oxidation is one of the most efficient routes to achieve this. The K super(+) form of an aluminium-rich Beta zeolite-supported Pt nanoparticle (2.2 nm) [Pt/KBeta-seed-directed s...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2015-01, Vol.3 (10), p.5556-5562 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The removal of volatile organic compounds is an important aspect of sustainability and environmental protection. Catalytic oxidation is one of the most efficient routes to achieve this. The K super(+) form of an aluminium-rich Beta zeolite-supported Pt nanoparticle (2.2 nm) [Pt/KBeta-seed-directed synthesis (SDS)] catalyst is very active for the low-temperature catalytic removal of toluene and results in full conversion at a much lower temperature than a conventional KBeta-supported Pt nanoparticle (Pt/KBeta-TEA) catalyst. The higher activity of the Pt/KBeta-SDS catalyst compared with the Pt/KBeta-TEA catalyst is related to the advantages of the higher K super(+) content and fewer terminal silanol defects in the KBeta-SDS catalyst than in the KBeta-TEA catalyst. The higher K super(+) content is helpful for the formation of more Pt super(0) species, and both the higher K super(+) content and the lower number of terminal silanol defects are favourable for the adsorption of toluene, as evidenced by XPS and the toluene-TPD profiles. More importantly, the Pt/KBeta-SDS catalyst shows very stable activities in the presence of H sub(2)O and CO sub(2) in the feed gases. The combination of this extraordinary activity and excellent stability in the catalytic removal of toluene over the Pt/KBeta-SDS catalyst are important for future environment protection. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c4ta06407k |