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Coprecipitated iron based catalysts for hydrotreatingHellgardt, Klaus January 1996 (has links)
No description available.
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Studies of the Pt/oxide systems : characterisation and reactivity for the oxidation of propaneKaur, Prabhjot January 1993 (has links)
No description available.
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Computer simulation of fluids in zeolitesWoods, Gary B. January 1989 (has links)
No description available.
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The statistical aspects of the analysis and design of enzyme kinetic studiesAllcock, Gillian C. January 2001 (has links)
No description available.
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X-ray crystallographic studies of organometallic complexes and the determination of the structure of nickel (II) insulinReid, Amanda Julietta January 1993 (has links)
No description available.
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Synthesis, structure and catalytic activity of cationic zirconium and hafnium alkyl complexesLancaster, Simon John January 1995 (has links)
No description available.
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Catalytic enantioselective tandem carbonyl ylide formation-cycloadditionStupple, Paul Anthony January 1999 (has links)
No description available.
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Studies on new diiminodiphosphine-type ligands and their metal complexesVei, Ino C. January 2002 (has links)
No description available.
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A comparative study of molybdenum and iron phosphate-based catalysts in n-hexane activation.Mncwabe, Zibuyile. January 2009 (has links)
A comparative study of the activation of n-hexane over the 12-molybdophopshoric acid (H3PMo12O40
or HPA), its Fe3+ doped salt (Fe0.69H0.93PMo12O40 or Fe doped HPA) and the iron phosphate catalyst
(P/Fe = 1.22) was carried out. It was found that the Fe doped HPA catalyst is thermally more stable
and less acidic that the HPA catalyst. The HPA and the Fe doped HPA catalysts were more reactive
that the iron phosphate catalyst. Both the HPA and Fe doped HPA catalytically produced 2,5-
dimethyltetrahydrofuran and 2,5-hexadione (oxygenates), with the Fe doped HPA catalyst selectively
producing more oxygenates than the HPA catalyst. This implied that the Fe3+ cation promoted the
oxygen insertion reactions. The iron phosphate catalyst catalytically produced cis-2-hexene and 1-
hexene but did not produce oxygenates, which means that the iron phosphate catalyst promotes
oxidative dehydrogenation but does not promote oxygen insertion reactions. At 349 oC, the HPA
catalyst played a role in initiating benzene formation. At isoconversion, the iron phosphate catalyst
produced the highest yield of benzene (5.8 % at 8.1 % hexane conversion), which may have formed
through both catalytic and non-catalytic reactions. The Fe doped HPA catalyst produced a lower
benzene yield (1.4 % at 6 % hexane conversion) than the HPA catalyst (3.6 % at 8.3 % hexane
conversion) at almost isoconversion and isothermal conditions. / Thesis (M.Sc.)-University of KwaZulu-Natal, Westville, 2009.
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Heterocycle carbonyl pyrazolyl palladium(II) complexes :synthesis, ethylene oligomerisation and polymerisation catalysis.Ojwach, Stephen Otieno January 2004 (has links)
No abstract available.
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