FTIR study of acetone oxime interaction with H-ZSM-5 and Cu-ZSM-5

Andrey V. Simakov; Evgenii S. Stoyanov; Evgenii V. Rebrov; N. N. Sazonova

doi:10.1117/12.560320

2 August 2004 FTIR study of acetone oxime interaction with H-ZSM-5 and Cu-ZSM-5

Andrey V. Simakov, Evgenii S. Stoyanov, Evgenii V. Rebrov, N. N. Sazonova

Proceedings Volume 5508, Complex Mediums V: Light and Complexity; (2004) https://doi.org/10.1117/12.560320
Event: Optical Science and Technology, the SPIE 49th Annual Meeting, 2004, Denver, Colorado, United States

Abstract

Copper based catalysts are of great importance as catalysts for NO removal from exhaust industrial gases. Earlier authors have shown that NO reaction with acetone oxime (AO) is the rate determining step of NO catalytic reduction by propane over Cu-ZSM-5 catalyst at temperatures below 300oC. Aim of the present work is to clarify the peculiarities of acetone oxime coordination over surface of H-ZSM-5 zeolite and that doped with Cu(II) and Cu(I)-cations. We studied AO coordination in CCl4 solutions and then data obtained were used for analysis of spectra of AO adsorbed on pure zeolite and that dopped with Cu (I) and Cu (II) cations. It was shown that there are monomers and several associates of AO in CCl4 solution differing in size and type of bonding with their own characteristic bands in IR spectra. The spectrum of acetone oxime adsorbed on pure zeolite includes non symmetrical band at 1710 cm-1 due to AO strongly bonded with zeolite surface through H-bond. There are four AO adspecies on zeolite dopped with copper with two different types of AO coordination to Cu(I) or to Cu(II) cations: one with participation of O atom and another one with N atom. Complexes of AO with Cu(I) ions are much more stable then those with Cu(II) ions.

Citation Download Citation

Andrey V. Simakov, Evgenii S. Stoyanov, Evgenii V. Rebrov, and N. N. Sazonova "FTIR study of acetone oxime interaction with H-ZSM-5 and Cu-ZSM-5", Proc. SPIE 5508, Complex Mediums V: Light and Complexity, (2 August 2004); https://doi.org/10.1117/12.560320

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