Oxidation of cyclohexene with H2O2 catalyzed by vanadium based polyoxometalates doped modified clays as green catalysts

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Abstract

The catalytic performance of supported heteropolyacids in various liquid-solid and gas-solid heterogeneous reactions may be affected by the choice of support and/or the method of heteropolyacid deposition. Vanadium substituted polyphosphomolybdate with the Keggin structure H4[PVMo11O40]13H2O (PVMo) was dispersed throughout acid activated bentonite (clay from Hammam Boughrara, Maghnia, Algeria). A series of catalysts were prepared via modified impregnation. Modified preparation method employed ultrasonication as a means of the dispersion homogenization, followed by freeze-drying. The catalysts were characterized by the Brunauer-Emmett-Teller, the Fourier transform infrared, and 31P solid-state magic angle spinning-NMR spectroscopy. The catalytic performance of PVMo/Hmont was evaluated in the oxidation of cyclohexene. Intact Keggin anions were preserved on Hmont after deposition aided by ultrasonication. The obtained results showed that a better catalytic activity can be obtained with PVMo/bentonite (98% of conversion and 89% of cyclohexene oxide), by drop addition of H2O2, for 3 h.

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APA

Boudjema, S., Rabah, H., & Choukchou-Braham, A. (2017). Oxidation of cyclohexene with H2O2 catalyzed by vanadium based polyoxometalates doped modified clays as green catalysts. In Acta Physica Polonica A (Vol. 132, pp. 469–472). Polish Academy of Sciences. https://doi.org/10.12693/APhysPolA.132.469

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