DSpace logo

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20199
Title: Role of Breasted Acid Centres for Alkene Double Bond Migration over Alumina at Temperatures above 450 K
Authors: John, Christopher S.
Tada, Akio
Kennedy, Lois V. F.
Keywords: Journal of the Chemical Society : Faraday Transaction - I
Chemistry
Breasted Acid
Alkene
Issue Date: 1978
Publisher: Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (02)
Abstract: Water was added to alumina samples following their activation in vacuo at both 723 and 1023 K. Reactions of [2Ho]propene and of CD2=CH—CH2 were then studied on these catalysts. Adsorption of water (2.7 x 1018 molecule m-2) at ~300 K is molecular and serves only slightly to poison catalytic activity at ~300 K. Adsorption of water at >453 K occurs dissociatively and completely poisons those sites on the fresh catalyst surface which promote reactions at ~300 K. Reaction of propene occurs on such a water poisoned catalyst at ~483 K and proceeds with incorporation of Db (from D2O) through an associative mechanism involving carbonium ions, in contrast to a dissociative mechanism at a reaction temperature of 300 K on an unpoisoned catalyst. Water “ added-back ” to activated alumina at >453 K is therefore effective in producing Bronsted acid centres on the surface and it is suggested that residual hydroxyls, those left following activation, can also participate in carbonium ion formation from propene at >453 K. Therefore, not only is the activity of alumina strongly influenced by its activation temperature but it is also determined by the temperature used for subsequent alkene catalysis.
URI: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20199
Appears in Collections:Journal Articles (before-1995)

Files in This Item:
File Description SizeFormat 
0498-0505.pdf
  Restricted Access
504.47 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.