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   <subfield code="a">On the chemistry of ammonia over oxide catalysts: Fourier transform infrared study of ammonia, hydrazine and hydroxylamine adsorption over iron-titania catalyst</subfield>
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   <subfield code="a">The adsorption and transformation of ammonia over Fe2O3/TiO2 catalyst has been investigated by FT-IR spectroscopy in vacuum at increasing temperature. Ammonia is first coordinated over Lewis sites and later undergoes hydrogen abstraction giving rise either to NH2 amide species or, to its dimeric form N2H4, hydrazine. Other species tentatively identified as imide NH and nitroxyl HNO are produced further. The comparison of the infrared spectra of the species arising from NH3 and N2H4 and NH2OH adsorbed over Fe2O3/TiO2 strongly suggests that N2H4 is an intermediate in NH3 oxidation to N2 over this catalyst. So ammonia is activated in the form of NH2 species for both SCR and SCO. Ammonium ion is detected only in traces at r.t. It seems consequently demonstrated that Brønsted acidity is not necessary for the appearance of SCR and SCO activity.</subfield>
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