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Oxidative dehydrogenation of n-butane over transition metal containing hydrotalcite derived catalysts.

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IV International Conference Catalysis and Adsorption in Fuel Processing and Environmental Protection, September 18-21, 2002, Kudowa Zdrój, Poland
Języki publikacji
EN
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EN
Mg-Al layered double hydroxides containing carbonates and nitrates in theinterlayer gallery were used as parent materials for anion exchange. NO-3 and CO2-3 anions were exchanged with oxoanions containing vanadium, chromium, molybdenum and tungsten. Ion-exchange in basic solution led to introduction of V2O 4-7, CrO2-4, MoO2-4 and WO2-4 anions, while V10O286-, Cr2O2-7, Mo7O6-24 and W7O6-24 forms were intercalated in acidic solution. The intercalation was confirmed by X-ray diffraction and FTIR spectroscopy. Oxidative dehydrogenation of n-butane was carried out over hydrotalcite-derived catalysts. The catalysts obtained by thermal decompn. of V2O4-7-contg. Hydrotalcites appeared to be the most active ones in a prodn. of 1,3-butadiene. However, the highest yield of butenes was achieved over Mg-Al-Cr oxides catalyst in the low temp. range (Ł550C).
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  • Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Kraków, Poland
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Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BPW6-0001-0102
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