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Adsorption and decomposition of isopropyl alcohol over zinc oxide. Infrared and kinetic study

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TLDR
In this article, the adsorption of isopropyl alcohol and acetone on zinc oxide was studied by an infrared technique, which revealed that the alcohol is dissociatively adsorbed at room temperature to form zinc alcoholate and hydroxyl group on the surface, while the acetone takes place in its enolic form.
Abstract
The adsorption of isopropyl alcohol and acetone on zinc oxide was studied by an infrared technique which revealed that isopropyl alcohol is dissociatively adsorbed at room temperature to form zinc alcoholate and hydroxyl group on the surface, while the adsorption of acetone takes place in its enolic form. When adsorbed isopropyl alcohol was heated to 363 K, the zinc alcoholate species changed gradually to acetone adsorbed in its enolic form, which further desorbed at higher temperatures as acetone, being replaced by the attacking isopropyl alcohol.The behaviour of the adsorbed species during decomposition of isopropyl alcohol on zinc oxide was studied in more detail, leading to the overall reaction mechanism described by eqn (V).

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Base catalysis by alkali-modified zeolites: I. Catalytic activity

TL;DR: In this paper, isopropanol is reacted over alkali-exchanged X and Y zeolites in the presence and absence of occluded exchange salts at 350 °C and atmospheric pressure.
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Investigation of the surface structure and basic properties of calcined hydrotalcites

TL;DR: In this paper, the influence of preparation method, calcination temperature, and Mg : Al atomic ratio on the basic properties of calcined hydrotalcites was investigated.
Journal ArticleDOI

Isopropanol oxidation by pure metal oxide catalysts: number of active surface sites and turnover frequencies

TL;DR: In this paper, the number of active surface sites and their nature, redox or acidic, for bulk metal oxide catalysts using isopropanol as a chemical probe molecule was determined.
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Base catalysis by alkali-modified zeolites: II. Nature of the active site

TL;DR: Recherche de la nature du site basique forme par la decomposition de l'acetate de cesium dans CsNaY as discussed by the authors, et.
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