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Synthesis of heterogeneous catalysts based on manganese oxides applied for the aerobic oxidation of p-hydroxybenzyl alcohol to p-hydroxybenzaldehyde

Lam Anh Le Viet 1
Thi Xuan Thi Luu 1
Tien Khoa Khoa Le 1, *
  1. Faculty of Chemistry, University of Science, Vietnam National University Ho Chi Minh City, 227 Nguyen Van Cu, District 5, HCMC, Vietnam
Correspondence to: Tien Khoa Khoa Le, Faculty of Chemistry, University of Science, Vietnam National University Ho Chi Minh City, 227 Nguyen Van Cu, District 5, HCMC, Vietnam. Email: ltkhoa@hcmus.edu.vn.
Volume & Issue: Vol. 5 No. 1 (2021) | Page No.: 942-948 | DOI: 10.32508/stdjns.v5i1.942
Published: 2021-01-23

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This article is published with open access by Viet Nam National University Ho Chi Minh City, Viet Nam. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Abstract

In order to synthesize p-hydroxybenzaldehyde from p-hydroxybenzyl alcohol under oxygen atmosphere, we prepared the new heterogeneous catalysts based on manganese oxides by in-situ growth method at different pH values. The crystal structure, phase composition, morphology, and surface groups of catalysts were characterized by powder X-ray diffraction, field emission electron scanning microscopy and Fourier transform infrared spectroscopy. According to the experimental results, the solution pH used for the preparation of the catalysts strongly affected their properties and their catalytic activities. When the pH was increased from 2 to 4, the a-Mn2O3 content increased with the dominant presence of the rod-like particles. The quantity of Mn on the surface also enhanced which might improve the conversion of p-hydroxybenzyl alcohol while maintaining the high selectivity to p-hydroxybenzaldehyde (about 70%). However, when the pH was highr than 4, the quantity of rod-like particles,a-Mn2O3 and surface Mn species decreased which lowered the catalytic activity.

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