کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
10244731 47700 2005 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The formation of isocyanic acid during the reaction of NH3 with NO and excess CO over silica-supported platinum, palladium, and rhodium
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
The formation of isocyanic acid during the reaction of NH3 with NO and excess CO over silica-supported platinum, palladium, and rhodium
چکیده انگلیسی
The reaction between NH3 and NO in excess CO over silica-supported platinum, palladium, and rhodium has been investigated for temperatures from 100 to 450 °C. As found previously for the corresponding reactions of H2/NO/CO mixtures, isocyanic acid (HNCO) is produced with each catalyst. With Pd/SiO2, the peak yield when NH3 is used is 46% based on the total nitrogen converted and 55% based on the hydrogen taken from NH3, with the remaining hydrogen converted to water. The reaction over Pt/SiO2 requires a somewhat higher temperature and is more efficient with a maximum HNCO yield of 70% based on nitrogen and 95% on hydrogen. The near-absence of water as a product correlates with the high activity of platinum for the production of HNCO from H2O/NO/CO mixtures, which in turn is driven by activity for the water-gas shift reaction. The peak yield of HNCO from NH3/NO/CO mixtures is much lower with Rh/SiO2 (10% based on nitrogen), and, unlike the yield of the platinum and the palladium catalysts, it is less than that observed during the H2 + NO + CO reaction (30%). In experiments using 15NO and 14NH3, the 15N content of N2, HNCO, and the end nitrogen of N2O are similar, consistent with dissociation of both nitric oxide and ammonia to form a single surface pool of nitrogen atoms. However, neither dissociation is rapidly reversible, since there is little exchange of 14N from ammonia into unreacted 15NO, and significant formation of 15NH3 is confined to Pt/SiO2 at temperatures where it could be formed by hydrolysis of product H15NCO. It is concluded that HNCO is formed by the rapid pick-up of surface hydrogen atoms by metal-bound NCO groups existing in equilibrium with N atoms and surrounding CO molecules. The trends in product distribution and in activity between the three metals can be rationalised in terms of competition between NO and CO for surface sites with CO favoured on Pt, NO favoured on Rh, and Pd exhibiting intermediate characteristics.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Catalysis - Volume 231, Issue 1, 1 April 2005, Pages 201-212
نویسندگان
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