Issue 10, 2015

Efficient mineralization of benzoic and phthalic acids in water by catalytic ozonation using a nickel oxide catalyst

Abstract

Organic acids (OAs) are usually used as refractory model compounds that require prolonged reaction time for their mineralization by different treatments. In this study, benzoic and phthalic acids in aqueous solution were significantly degraded and mineralized by catalytic ozonation in the presence of nickel oxide (NiO). For instance, only 42% mineralization was obtained by direct reaction with molecular ozone, while by catalytic ozonation 98% was achieved. These surprising results led to study in depth the role of NiO in the catalytic ozonation of both organic acids. With the aim of identifying the surface species responsible for the high activity of NiO, X-ray photoelectron spectroscopy (XPS) and high performance liquid chromatography (HPLC) were used as the main analytical tools. According to the results, the mineralization of both organic acids was directly influenced by the organic groups adsorbed onto the NiO surface. Therefore, NiO plays a relevant role as a catalyst forming complex surface compounds which are subsequently decomposed increasing the mineralization efficiency. In addition, a simplified kinetic study was conducted to characterize the effect of NiO concentration on the removal efficiency of both organic acids and the accumulation and degradation of the main byproduct (oxalic acid). These results were explained in terms of a combination of two reaction mechanisms such as conventional ozonation and indirect reaction based on ˙OH radicals.

Graphical abstract: Efficient mineralization of benzoic and phthalic acids in water by catalytic ozonation using a nickel oxide catalyst

Article information

Article type
Paper
Submitted
01 Jun 2015
Accepted
23 Jul 2015
First published
23 Jul 2015

New J. Chem., 2015,39, 7839-7848

Author version available

Efficient mineralization of benzoic and phthalic acids in water by catalytic ozonation using a nickel oxide catalyst

D. Magallanes, J. L. Rodríguez, T. Poznyak, M. A. Valenzuela, L. Lartundo and I. Chairez, New J. Chem., 2015, 39, 7839 DOI: 10.1039/C5NJ01385B

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