OXIDATION WITH NO-REDOX OXIDES - AMMOXIMATION OF CYCLOHEXANONE ON AMORPHOUS SILICAS

Citation
G. Fornasari et F. Trifiro, OXIDATION WITH NO-REDOX OXIDES - AMMOXIMATION OF CYCLOHEXANONE ON AMORPHOUS SILICAS, Catalysis today, 41(4), 1998, pp. 443-455
Citations number
37
Categorie Soggetti
Engineering, Chemical","Chemistry Applied","Chemistry Physical
Journal title
ISSN journal
09205861
Volume
41
Issue
4
Year of publication
1998
Pages
443 - 455
Database
ISI
SICI code
0920-5861(1998)41:4<443:OWNO-A>2.0.ZU;2-N
Abstract
The ammoximation in gas phase of cyclohexanone is a reaction with an o xidation step performed on an insulator oxide such as amorphous silica . Conventional mechanisms for such a kind of reaction are not useful. This paper reviews the efforts carried out to understand the catalytic behavior of the silica and highlights the particular catalytic featur es of the tars, the carbonaceous products formed during the ammoximati on, in the oxidation step of the reaction. The catalytic behavior and the role of the acid sites, of the tars and of the activated forms of molecular oxygen were investigated on several commercial amorphous sil icas and on pure and doped silicas prepared by sol-gel method. The sil ica catalyst shows a bifunctional behavior: acid sites are necessary f or the formation of imine, the intermediate of the reaction, and oxidi zing sites for the formation of oxime. For the first step the presence of silanols of the right acidity results is essential. For the oxidat ive step the carbonaceous products formed during the reaction seem to play an essential role. It has been suggested that the tars are formed by a polymerization reaction which occurs at the silica surface and i nvolves, in the initiation stage, activated oxygen species generated b y the silica surface. The reaction progression with time involves incr easing amounts of the carbonaceous products, with a corresponding decl ine in access to the active sites by pore blockage and, as a consequen ce, with a corresponding decline in the catalytic activity. (C) 1998 E lsevier Science B.V. All rights reserved.