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Characterization of Pt/γ-Al2O3 catalysts deactivated by hexamethyldisiloxane

Karl Arnby (Institutionen för kemi- och bioteknik, Teknisk ytkemi ; Kompetenscentrum katalys (KCK)) ; Mohammad Rahmani ; Mehri Sanati ; Neil Cruise ; Annika Amberntsson Carlsson ; Magnus Skoglundh (Institutionen för kemi- och bioteknik, Teknisk ytkemi ; Kompetenscentrum katalys (KCK))
Applied Catalysis B: Environmental (0926-3373). Vol. 54 (2004), 1, p. 1-7.
[Artikel, refereegranskad vetenskaplig]

The deactivation of alumina supported platinum and iron catalysts by hexamethyldisiloxane (HMDS) exposure has been investigated. Three catalysts (Pt/Al2O3, Fe/Al2O3 and Fe/Pt/Al2O3) were prepared and the influence of short- and long-term deactivation on the activity for oxidation of ethyl acetate was studied. The catalysts were characterized using BET, ICP-AES, XPS, SEM and CO chemisorption. The deactivation was found to proceed by deposition of silicon-species in form of silicate (SixOy) that block the active sites on the surface of the catalysts. The silicon seems to rather attach to platinum and iron sites than to the alumina surface. The Pt/Al2O3 catalyst was moderately deactivated by HMDS even though the silicate was blocking almost the entire platinum surface. Adding iron to the catalyst increased the tolerance towards HMDS as fewer Pt sites were blocked for the Fe/Pt/Al2O3 sample. The deactivation of the two platinum containing samples was reversible since the silicate could partly be removed from the Pt sites by regeneration whereby most of the activity was restored. However, for the Fe/Al2O3 sample the deactivation was more severe and irreversible.

Nyckelord: Silicon, Deactivation, Hexamethyldisiloxane, Ethyl acetate oxidation, Platinum, Iron, Alumina

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Denna post skapades 2006-08-25. Senast ändrad 2017-09-14.
CPL Pubid: 11915


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Institutioner (Chalmers)

Institutionen för kemi- och bioteknik, Teknisk ytkemi (2005-2014)
Kompetenscentrum katalys (KCK)


Nanovetenskap och nanoteknik
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