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- Publisher
- Springer Journals
- Copyright
- Copyright
- Subject
- Chemistry; Catalysis; Industrial Chemistry/Chemical Engineering; Organometallic Chemistry; Physical Chemistry
- ISSN
- 1011-372X
- eISSN
- 1572-879X
- DOI
- 10.1007/BF00808332
- Publisher site
- See Article on Publisher Site
Abstract
The N2O decomposition over an [Fe]-ZSM-5 and an Fe-HZSM-5 zeolite was studied. We found that framework incorporated iron species were much more active than Fe(III) introduced as framework charge countercations by ion exchange (TOF at 0.1 vol% N2O:1.47 × 10−4 at 280°C for [Fe]-ZSM-5 vs. 2.58 × 10−4 at 468°C for Fe-HZSM-5). The higher activity of [Fe]-ZSM-5 was attributed to the uniqueness of framework iron species. Both [Fe]-ZSM-5 and Fe-HZSM-5 zeolites showed enhanced activity in the presence of excess oxygen. This is in sharp contrast to ruthenium exchanged zeolites which showed strong oxygen inhibiting effect on the rate of N2O decomposition.
Journal
Catalysis Letters – Springer Journals
Published: Nov 28, 2004