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The "directâ[euro] synthesis of trialkoxysilanes: New data for understanding the processes of the copper-containing active sites formation during the activation of the initial silicon based contact mass

Display Omitted * The process of the copper-containing active sites formation was studied. * Topochemical and heterogeneous chemical reactions take part in this process. * A new mechanism of the activation of the contact mass was formulated. The paper presents comprehensive studies on the process of...

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Bibliographic Details
Published in:Journal of catalysis 2016-06, Vol.338, p.143
Main Authors: Adonin, Nicolay Yu, Prikhod'ko, Sergey A, Shabalin, Anton Yu, Prosvirin, Igor P, Zaikovskii, Vladimir I, Kochubey, Dmitry I, Zyuzin, Dmitry A, Parmon, Valentin N, Monin, Evgeny A, Bykova, Irina A, Martynov, Petr O, Rusakov, Sergey L, Storozhenko, Pavel A
Format: Article
Language:English
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Summary:Display Omitted * The process of the copper-containing active sites formation was studied. * Topochemical and heterogeneous chemical reactions take part in this process. * A new mechanism of the activation of the contact mass was formulated. The paper presents comprehensive studies on the process of the copper-containing active sites formation which are needed for the "directâ[euro] synthesis of trialkoxysilanes at the interaction of alcohols with a silicon-based contact mass. These sites are formed during a two step consequent pretreatment of the initial contact mass by hydrogen and argon flow. The so activated samples of contact mass were investigated using HAADF-STEM EDX, EXAFS, XPS and XRD methods. The role of each step of the activation is disclosed. Participation of topochemical and heterogeneous chemical reactions as well as processes of diffusion and sorption-desorption during the active sites formation was found. Based on the retrieved data a new mechanism for the formation of the active sites on the surface of silicon during the activation of the contact mass for the "directâ[euro] synthesis of trialkoxysilanes is suggested.
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2016.03.012