Influence of metal-support interactions on the stability of Ni/SiO2 catalysts during cyclic oxidation-reduction treatments

Mario Montes, Jean Bruno Soupart, Myriam De Saedeleer, Benjamin K. Hodnett, Bernard Delmon

Research output: Contribution to journalArticlepeer-review

Abstract

Ni/SiO2 catalysts prepared by impregnation and deposition-precipitation have been subjected to cyclic treatments in hydrogen at 500 °C and oxygen at 450 °C to test their resistance to sintering. The activity of the catalysts in benzene hydrogenation was tested after each cycle. The resulting behaviour was found to depend upon the method of preparation and whether the initial treatment of the precursor was reducing or oxidizing. For a catalyst prepared by impregnation and reduced initially, a strong reduction in catalytic activity was recorded as the number of cycles was increased; this behaviour is ascribed to facile sintering which occurs in the absence of an interaction between metal particles and the support. When the same precursor was calcined initially large NiO crystallites were formed on the external surface of the support; subsequent reduction-oxidation cycles acted to change their texture, making them more irregular or porous and resulting in an increased metallic surface area and catalytic activity. Catalysts prepared by deposition-precipitation were very resistant to sintering owing to strong interactions between the metal and support; at the precursor stage, a nickel hydrosilicate was formed which had a turbostratic morphology. Direct reduction of this compound gave rise to finely divided particles of metallic nickel trapped between the SiO2 support which retained its turbostratic morphology. Calcination of this precursor caused some nickel to enter the support, further anchoring the active phase and rendering it very resistant to sintering.

Original languageEnglish
Pages (from-to)3209-3220
Number of pages12
JournalJournal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases
Volume80
Issue number11
DOIs
Publication statusPublished - 1984
Externally publishedYes

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