Browsing by Subject "Electrochemical sensors"

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    Characterization of niobium-zirconium mixed oxide as a novel catalyst for selective catalytic reduction of NO x
    (2009) Cayirtepe, I.; Naydenov, A.; Ivanov, G.; Kantcheva, M.
    The performance of mixed niobium-zirconium oxide in the SCR of NO x with propene in excess oxygen has been studied. The mixed oxide is prepared by impregnation of hydrated zirconia with acidic solution (pH 0.5) of peroxoniobium(V) complex, [Nb2(O2)3] 4+, ensuring ZrO2:Nb2O5 mole ratio of 6:1. The calcined sample (denoted as 25NbZ-P) has the structure of Zr 6Nb2O17. According to the catalytic test, the conversion of NO x over the 25NbZ-P catalyst passes through a maximum at 220 °C. Based on the in situ FT-IR results, a reaction mechanism is proposed with nitroacetone and NCO species as the key reaction intermediates. The results of the investigation show that the catalytic properties of the Zr6Nb2O17 solid solution could be of interest regarding the development of low-temperature catalyst for the SCR of NO x with hydrocarbons. © 2009 Springer Science+Business Media, LLC.
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    Gold catalysts supported on ceria doped by rare earth metals for water gas shift reaction: influence of the preparation method
    (2009) Andreeva, D.; Ivanov, I.; Ilieva, L.; Abrashev, M. V.; Zanella, R.; Sobczak, J. W.; Lisowski, W.; Kantcheva, M.; Avdeev, G.; Petrov, K.
    Gold catalysts based on ceria, doped by various RE metals (La, Sm, Gd, Yb, Y) were studied. The influence of the preparation methods on structure, properties and catalytic activity in the WGS reaction was investigated. The catalysts' supports were prepared using two different methods: co-precipitation (CP) and mechanochemical activation (MA). The catalysts were tested in a wide temperature interval without and after reactivation. All samples were characterized using a combination of X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), Raman spectroscopy (RS) and X-ray photoelectron spectroscopy (XPS) and TPR. It was found that the catalytic activity of MA catalysts is higher than CP ones. The gold catalysts based on ceria doped by Yb and Sm exhibited the highest activity. After reactivation in air the MA samples almost kept the WGS activity same, while the CP catalysts increased it. The catalysts of a single- and double-phase structure are formed as a result of CP and MA preparation, respectively. There are no big differences in the gold particles size (2-3 nm) depending on dopants and on the preparation techniques. The RS spectra analysis indicates that most probably the oxygen vacancies are adjacent to Me3+ dopant and the ceria structure seems to be better ordered than in the case of alumina as a dopant. There is no distinct correlation between reducibility and WGS activity. The XPS analysis disclose positively charged gold particles in addition to metallic gold within a surface region of fresh samples and only metallic gold on the samples after catalytic processing. There is no simple correlation between the concentration of Ce3+ in the samples and their WGS activity.