Issue 29, 2019

A comparison study between V-SBA-15 and V-KIT-6 catalysts for selective oxidation of diphenylmethane

Abstract

Vanadium incorporated mesoporous SBA-15 and KIT-6 catalysts were prepared by a direct hydrothermal method under mild acidic reaction conditions. The structural features of the catalysts have been thoroughly investigated by using various characterization techniques including N2-physisorption, X-ray diffraction, 51V NMR spectroscopy, Raman spectroscopy, H2-TPR, and XPS. The characterization results revealed that under hydrated conditions, the incorporated vanadium was highly dispersed on the surface of SBA-15 and KIT-6 catalysts with octahedral coordination. However, the various spectral analyses manifest that the local environment of vanadium is entirely different for SBA-15 and KIT-6 supports. The influence of the supports and their catalytic activity for the diphenylmethane oxidation reaction are investigated. The efficiency of the catalysts was compared in terms of a constant level of vanadium loading on both the catalysts, and it was observed that the V-KIT-6 catalyst exhibited better catalytic activity than V-SBA-15. The enhanced activity of the V-KIT-6 catalyst was mainly attributed to the presence of a large portion of vanadium on the external walls with the V5+ oxidation state. The deactivation study was performed on both catalysts and it was found that both catalysts exhibited a similar level of conversion and selectivity under identical experimental conditions. In addition, the catalytic activity was directly correlated with various characterization results.

Graphical abstract: A comparison study between V-SBA-15 and V-KIT-6 catalysts for selective oxidation of diphenylmethane

Supplementary files

Article information

Article type
Paper
Submitted
18 Apr 2019
Accepted
18 Jun 2019
First published
04 Jul 2019

New J. Chem., 2019,43, 11554-11563

A comparison study between V-SBA-15 and V-KIT-6 catalysts for selective oxidation of diphenylmethane

D. Santhanaraj, C. Suresh, A. Selvamani and K. Shanthi, New J. Chem., 2019, 43, 11554 DOI: 10.1039/C9NJ02007A

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