4.7 Article

Oxygen vacancies enhancing performance of Mg-Co-Ce oxide composite for the selective catalytic ozonation of ammonia in water

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 436, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2022.129000

Keywords

Ammonia; Wastewater treatment; Catalytic ozonation; Oxygen vacancy; Metal oxide

Funding

  1. Science and Technology Major Project of the Bureau of Science and Technology of Xiamen, China [3502Z20191012]
  2. Quanzhou City Sciences & Technology Program of China, China [2018C082R]
  3. Natural Sci-ence Foundation of China, China [51678255, 51178117]

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This study investigated the catalytic ozonation of ammonia in water using MgO/Co3O4/CeO2 catalyst. The optimized catalyst exhibited excellent performance in selectively converting ammonia to gaseous nitrogen, indicating its potential application in ammonia removal.
Catalytic ozonation based on heterogeneous metal oxides is a promising approach to removing ammonia as gaseous nitrogen from water. Herein, MgO/Co3O4/CeO2 was prepared for catalytic ozonation of ammonia in an aqueous solution. The influence of various reaction conditions was systematically investigated and optimized, in which the reaction kinetics was also analyzed. After doping Ce, the catalyst with Mg-Co-Ce molar ratio of 4:1:1 and calcined at 700 C for 3 h, has abundant surface oxygen vacancies and exhibited excellent performance for the selective catalytic oxidation of ammonia to gaseous nitrogen by ozone. It was found that the catalytic activity of catalysts was positively related to oxygen vacancies concentration on the composites surface, which might play a vital role in selective catalytic ozonation. Under the optimal conditions, the ammonia removal rate in MgO/Co3O4/CeO2 catalytic system was 0.03328 min(-1) (R-2 = 0.99942), about 2.1 times greater than that of MgO/Co3O4 (0.01597 min(-1), R-2 = 0.99813), and the selectivity was further enhanced from 73.57% to 86.94%. Moreover, the evolution of nitrogen and chlorine species was determined to discuss the mechanism of selective oxidation of ammonia in the low chlorine-containing solution. This study might promote the understanding of catalytic ozonation of ammonia to gaseous nitrogen selectively.

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