Structure sensitivity of selective acetylene hydrogenation over the catalysts with shape-controlled palladium nanoparticles
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چکیده
منابع مشابه
Selective Hydrogenation of Acetylene over Palladium in Ultra High Vacuum
Under ultra-high-vacuum conditions, precoverage of a palladium(ll1) surface with hydrogen does not affect either the kinetics or the extent of acetylene uptake at 175 K. The subsequent reactive behavior of the system is however radically altered. Benzene formation is strongly suppressed, the transformation of adsorbed acetylene to another species (@-phase) is enhanced, and the yield of ethylene...
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Pd-Ag shell catalysts impregnated with two different ionic liquids show considerable improvements both in ethylene selectivity and reduced ethane formation in the selective hydrogenation of acetylene under tail-end conditions.
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To explain the unusually high selectivity of copper catalysts toward linolenate, model compounds were hydrogenated (150 C and atmospheric pressure) and the reaction products analyzed. Products varied depending upon location of the double bonds. Monoenes were not reduced by copper chromite except when the double bond was next to a carboxyl group. Dienes with isolated double bonds also were not r...
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A novel TiO2 supported core-shell (Pd@Ag) bimetallic catalyst was fabricated via the sequential photodeposition method. The Ag shell effectively blocks the high coordination sites on the Pd core, and therefore pronouncedly enhances the ethylene selectivity for the catalytic hydrogenation of acetylene in excess ethylene.
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A simple, selective and sensitive derivative spectrophotometric method has been developed for the determination of palladium(II) using a newly synthesised reagent diacetylmonoxime-(p-anisyl)-thiosemicarbazone in acetic acid medium. The molar absorptivity and Sandell’s sensitivity of the coloured species are 3.8 × 10 L mol cm and 2.8 ng cm, respectively. Beer’s law is obeyed between 0.2-2.0 μg m...
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ژورنال
عنوان ژورنال: Kinetics and Catalysis
سال: 2012
ISSN: 0023-1584,1608-3210
DOI: 10.1134/s0023158412020152