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  • 1
    ISSN: 1572-879X
    Keywords: hydrogen cyanide ; NO reduction ; isobutane ; Fe‐MFI
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract FTIR analysis of the gaseous products of the selective catalytic reduction of NO by isobutane over a Fe‐MFI catalyst made by solid‐state ion exchange shows, for the first time, that HCN can be a substantial product. Under dry conditions the amounts formed can exceed that of N2 for temperatures up to 280°C and NO conversions of 25% with a maximum HCN concentration of∼150 ppm formed at 315°C. However, introduction of 0.7% water causes the subsequent conversion of about one‐half the HCN to N2, probably through hydrolysis to NH3 and the NH3‐SCR reaction which is very rapid on Fe‐MFI. The steps through which HCN forms remain to be established.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-9028
    Keywords: isocyanic acid ; nitrogen oxides ; Pt/SiO2 ; hydrolysis ; nitromethane ; deactivation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Reactions which can produce and consume isocyanic acid (HNCO) over two types of catalysts active for the reduction of nitrogen oxides have been investigated. More than 1000 ppm HNCO can be produced by the reduction of 3000 ppm NO with H2/CO mixtures over a Pt/SiO2 catalyst. Complete hydrolysis of HNCO to ammonia and carbon dioxide occurs if even weakly catalytic materials, such as CeO2/SiO2 and BaO/SiO2, are placed downstream. Isocyanic acid is also involved as an intermediate in the reaction of nitromethane over Co‐ZSM5 and Cu‐ZSM5 under the conditions of hydrocarbon SCR. In the initial stages of reaction there is complete conversion through to N2 with Cu‐ZSM5 but the process stops at ammonia with Co‐ZSM5 at temperatures below 350°C. In both cases, but especially with Co‐ZSM5, isocyanic acid becomes observable as the catalyst deactivates during continuous exposure at temperatures below about 290°C. In situ FTIR measurements indicate that deactivation is due to a reaction between isocyanic acid and ammonia which generates cyclic s‐triazine compounds.
    Type of Medium: Electronic Resource
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