Effect of preparation method on the Pt-In modified Mg(Al)O catalysts over dehydrogenation of propane

[Display omitted] •PtIn/Mg(Al)O prepared by the different methods for propane dehydrogenation.•Preparation methods: co-precipitation, co-impregnation, and successive impregnation.•PtIn catalysts greatly enhanced the catalytic performance and stability.•Coke formation was significant reduced, especia...

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Bibliographic Details
Published inCatalysis today Vol. 358; pp. 100 - 108
Main Authors Tolek, Weerachon, Suriye, Kongkiat, Praserthdam, Piyasan, Panpranot, Joongjai
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.12.2020
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Summary:[Display omitted] •PtIn/Mg(Al)O prepared by the different methods for propane dehydrogenation.•Preparation methods: co-precipitation, co-impregnation, and successive impregnation.•PtIn catalysts greatly enhanced the catalytic performance and stability.•Coke formation was significant reduced, especially on the active metal. The Pt-In modified Mg(Al)O catalysts were prepared by co-precipitation, co-impregnation, and successive impregnation methods with Pt and In loading at 0.3 and 0.6 wt.%, respectively. The catalysts were tested in the propane dehydrogenation at 550 °C and atmospheric pressure. Pt loading on In-modified Mg(Al)O support prepared by co-precipitation (Pt/Mg(In)(Al)O) exhibited the highest catalytic performances with initial propane conversion and propylene selectivity of 24.2%.and 98.2%, respectively. As revealed by the H2-TPR and XPS results, the Pt/Mg(In)(Al)O exhibited a stronger metal-support interaction and favorable led to more PtIn alloy formation compared to those obtained by the other methods, which greatly enhanced the catalytic performance and stability. Coke formation was significant reduced on all the prepared bimetallic PtIn catalysts, especially coke on the active metal, which diminished the catalytic deactivation. The catalysts were also characterized by CO chemisorption, transmission electron microscopy (TEM), NH3-temperature program desorption (NH3-TPD).
ISSN:0920-5861
1873-4308
DOI:10.1016/j.cattod.2019.08.047