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The Formation of isocyanic acid and ammonia during the reduction of NO over supported platinum group metals

Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.14/40576

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Title: The Formation of isocyanic acid and ammonia during the reduction of NO over supported platinum group metals
Related: Catalysis today, Vol. 93-95, p.761-768
DOI: 10.1016/j.cattod.2004.06.068
Publisher: Elsevier Science
Date: 2004
FoR/RFCD Code(s): 030601 Catalysis and Mechanisms of Reactions
Author/Creator: Cant, Noel W
Author/Creator: Chambers, Dean C
Author/Creator: Liu, Irene O. Y
Description: The formation of isocyanic acid (HNCO) by reaction of NO and CO with sources of hydrogen has been investigated along with its subsequent hydrolysis on oxides. High HNCO yields are possible with H₂ itself using Pt/SiO₂ and Pd/SiO₂ with Rh/SiO₂ less effective. The H₂ forms NH₃ and H₂O initially but they are recycled to HNCO as the temperature is increased. The NH₃+NO+CO reaction is equally as effective as a generator of HNCO. Oxides other than silica catalyse complete hydrolysis of HNCO to NH₃ and CO₂. The combination of HNCO formation from NH₃ and subsequent hydrolysis back to NH₃ allows the amplification of ammonia by a factor of 3 when using a combination of Pd/SiO₂ followed by CeO₂–SiO₂. Multiplication by 6 is possible with Pt/SiO₂ ahead of CeO₂–SiO₂ since additional HNCO is generated on Pt by the reaction of NO and CO with surface hydrogen derived through the water-gas shift reaction. The reaction of a H₂O/NO/CO mixture over a Pt/Al₂O₃ catalyst forms NH₃ with >80% yield in this way.
Description: 8 page(s)
Subject Keyword: 030601 Catalysis and Mechanisms of Reactions
Subject Keyword: isocyanic acid
Subject Keyword: NO reduction by CO and H₂
Subject Keyword: Pt/SiO₂
Subject Keyword: Pd/SiO₂
Subject Keyword: Rh/SiO₂
Subject Keyword: Pt/Al₂O₃
Subject Keyword: ammonia formation
Resource Type: journal article
Organisation: Macquarie University. Dept. of Chemistry and Biomolecular Sciences

Identifier: http://hdl.handle.net/1959.14/40576
Identifier: ISSN:1873-4308
Identifier: mq-rm-2004020570
Language: eng
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