USE OF POSITRON-EMITTING N-13 FOR STUDIES OF THE SELECTIVE REDUCTION OF NO BY NH3 OVER VANADIA-TITANIA CATALYST AT VERY-LOW REACTANT CONCENTRATIONS

Citation
U. Baltensperger et al., USE OF POSITRON-EMITTING N-13 FOR STUDIES OF THE SELECTIVE REDUCTION OF NO BY NH3 OVER VANADIA-TITANIA CATALYST AT VERY-LOW REACTANT CONCENTRATIONS, Journal of physical chemistry, 97(47), 1993, pp. 12325-12330
Citations number
31
Categorie Soggetti
Chemistry Physical
ISSN journal
00223654
Volume
97
Issue
47
Year of publication
1993
Pages
12325 - 12330
Database
ISI
SICI code
0022-3654(1993)97:47<12325:UOPNFS>2.0.ZU;2-J
Abstract
Positron-emitting (NO)-N-13 molecules produced with a cyclotron were u sed to investigate the selective catalytic reduction (SCR) of NO by NH 3 over vanadia/titania at very low reactant concentrations. The (NO)-N -13 concentration was on the order of 5 x 10(-9) ppm, which is more th an 11 orders of magnitude lower than the usually used concentrations. Catalyst samples were pretreated with H-2 or NH3, without adding these reagents during the conversion experiments. Under these conditions th e vanadia/titania catalyst pretreated with NH3 kept its full activity for at least 5 h. At the low NO concentrations present, 50% conversion was already achieved at 80-degrees-C, with complete conversion at 150 -degrees-C. The reaction rate at 92-degrees-C was 1.9 x 10(-18) mol of NO (g of catalyst)-1 s-1. This value is in good agreement with the va lue expected from measurements with a similarly prepared catalyst assu ming a first-order reaction in NO. The activation energy was calculate d to be 37 kJ mol-1, which compares fairly well with the one measured on a similarly prepared catalyst under usual reactant concentrations ( 43 kJ mol-1). In contrast, vanadia/titania pretreated with H2 did not show any NO conversion. These results indicate that NH3 is necessary f or NO conversion and that one N atom of the formed N2 originates from NH3. Using a thermochromatographic apparatus, adsorption enthalpies (a t zero coverage) for NO and NO2 on various oxides were determined. Val ues of -21 +/- 2 and -33 +/- 3 kJ mol-1 were found for NO and NO2, res pectively, independent of the material.