Increased selectivity for allylic oxidation of cyclohexene using TiO2 modified V2O5/MoO3 catalysts

V2O5 and MoO3 mixed oxides supported by SiO2 were studied as the catalysts in the aqueous phase allylic oxidation of cyclohexene to unsaturated alcohol 2-cyclohexene-1-ol and unsaturated ketone 2-cyclohexene-1-one. The additional layer of TiO2 deposited by atomic layer deposition significantly suppr...

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Bibliographic Details
Published inCatalysis communications Vol. 99; pp. 43 - 48
Main Authors Yang, Guoqiang, Huff, Matthew D., Du, Huiyuan, Zhang, Zhibing, Lei, Yu
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.08.2017
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Summary:V2O5 and MoO3 mixed oxides supported by SiO2 were studied as the catalysts in the aqueous phase allylic oxidation of cyclohexene to unsaturated alcohol 2-cyclohexene-1-ol and unsaturated ketone 2-cyclohexene-1-one. The additional layer of TiO2 deposited by atomic layer deposition significantly suppresses the epoxidation pathway and the formation of cyclohexane oxide and cyclohexane-1, 2-diol. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM) were used to study the relationship between the structure of the catalysts and their catalytic performance. The effects on the catalytic activity of different solvent, hydrogen peroxide to cyclohexene ratio, and reusability were investigated. [Display omitted] •V2O5-MoO3 mixed oxides are effective catalysts for selective oxidation of cyclohexene.•Atomic layer deposition was used to precisely deposit a uniform layer of TiO2.•The presence of TiO2 significantly suppressed the formation of byproducts.•The reaction pathways can be controlled by tuning reaction conditions.
ISSN:1566-7367
1873-3905
DOI:10.1016/j.catcom.2017.05.023