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  • 1
    ISSN: 1572-879X
    Keywords: oxidative dehydrogenation ; ethane ; sulfated zirconia ; lithium chloride
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The oxidative dehydrogenation of ethane over sulfated-zirconia-supported lithium chloride catalysts has been systematically investigated. The optimal experimental parameters were obtained. It is found that sulfation of zirconia increases the catalytic activity. 2–3.5 wt% lithium chloride on sulfated zirconia catalysts exhibit high catalytic activity for oxidative dehydrogenation of ethane, with particularly high activity for ethene production. 70% selectivity to ethene at 98% ethane conversion, giving 68% ethene yield, is achieved over 3.5 wt% LiCl/SZ at 650°C.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-879X
    Keywords: sulfated zirconia ; lithium chloride ; metal oxides ; ethane ; oxidative dehydrogenation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effects of some transition‐ and lanthanide‐metal oxides in LiCl/sulfated‐zirconia (SZ) catalysts on catalytic behavior in the oxidative dehydrogenation of ethane were investigated. It is found that modification of LiCl/SZ by metal oxides significantly improves the catalytic activity and ethene yield. Among those additives, Ni and Nd oxides show the best promoting effect in terms of ethane conversion and ethene yield. 93% ethane conversion with 83% selectivity to ethene has been achieved over the Nd2O3–LiCl/SZ catalyst at 650°C. In addition, those oxide‐promoted LiCl/SZ catalysts are also found to exhibit a longer stability in catalytic performance. Metal‐oxide additives change the chemical structure and surface redox properties, which accounts for the enhancement of activity.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 386 (1971), S. 340-344 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Die Geschwindigkeit der Selbstzersetzung von Fe(OH)2 unter Luftausschluß wurde unter Zusatz von Cu(II) (0-6 Atom-%) bei 30 bis 50°C bestimmt. Das Maximum der Geschwindigkeit und ein Minimum der Aktivierungsenergie tritt bei 1% Cu/Fe auf. Dies wird zwei gleichzeitig wirksamen Einflüssen des Cu zugeschrieben: Erstens der Verzerrung des Koordinationskomplexes durch Cu2+, die die Strukturumwandlung in Magnetit erleichtert, dagegen wirkt negativ der Einfluß des Cu, der zur Vergrößerung der Fe(OH)2-Kristalle führt. Röntgenaufnahmen und elektronenmikroskopische Beobachtungen bestätigen die Annahme.
    Notes: The rate of self-decomposition of iron(II) hydroxide doped with various amounts (0-6 atomic%) of Cu(II) was determined in the absence of oxygen at the temperature range of 30 to 50°C. The maximum rate and the minimum activation energy were observed at 1% Cu/Fe. The result was attributed to the two simultaneous actions of Cu2+, i.e., the distortion effect on coordination complex of Fe2+ by Cu2+ to ease the structural transformation to magnetite and the hindering effect on magnetite formation revealed consequently in the growth of Fe(OH)2 crystals. Both effects were proved by X-ray diffraction and election-microscopic observations.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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