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Enhancing acid orange II degradation in ozonation processes with CaFe(2)O(4) nanoparticles as a heterogeneous catalyst

This study used CaFe(2)O(4) nanoparticles as a catalyst for ozonation processes to degrade Acid Orange II (AOII) in aqueous solution. The study compared heterogeneous catalytic ozonation (CaFe(2)O(4)/O(3)) with ozone treatment alone (O(3)) at different pH values (3–11), catalyst dosages (0.25–2.0 g...

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Autores principales: Van, Huu Tap, Hoang, Van Hung, Luu, Thi Cuc, Vi, Thuy Linh, Nga, Luong Thi Quynh, Marcaida, Gio Serafin Ivan Jimenez, Pham, Truong-Tho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543647/
https://www.ncbi.nlm.nih.gov/pubmed/37790093
http://dx.doi.org/10.1039/d3ra04553f
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author Van, Huu Tap
Hoang, Van Hung
Luu, Thi Cuc
Vi, Thuy Linh
Nga, Luong Thi Quynh
Marcaida, Gio Serafin Ivan Jimenez
Pham, Truong-Tho
author_facet Van, Huu Tap
Hoang, Van Hung
Luu, Thi Cuc
Vi, Thuy Linh
Nga, Luong Thi Quynh
Marcaida, Gio Serafin Ivan Jimenez
Pham, Truong-Tho
author_sort Van, Huu Tap
collection PubMed
description This study used CaFe(2)O(4) nanoparticles as a catalyst for ozonation processes to degrade Acid Orange II (AOII) in aqueous solution. The study compared heterogeneous catalytic ozonation (CaFe(2)O(4)/O(3)) with ozone treatment alone (O(3)) at different pH values (3–11), catalyst dosages (0.25–2.0 g L(−1)), and initial AOII concentrations (100–500 mg L(−1)). The O(3) alone and CaFe(2)O(4)/O(3) systems nearly completely removed AOII's color. In the first 5 min, O(3) alone had a color removal efficiency of 75.66%, rising to 92% in 10 min, whereas the CaFe(2)O(4)/O(3) system had 81.49%, 94%, and 98% after 5, 10, and 20 min, respectively. The O(3) and CaFe(2)O(4)/O(3) systems degrade TOC most efficiently at pH 9 and better with 1.0 g per L CaFe(2)O(4). TOC removal effectiveness reduced from 85% to 62% when the initial AOII concentration increased from 100 to 500 mg L(−1). The study of degradation kinetics reveals a pseudo-first-order reaction mechanism significantly as the solution pH increased from 3 to 9. Compared to the O(3) alone system, the CaFe(2)O(4)/O(3) system has higher k values. At pH 9, the k value for the CaFe(2)O(4)/O(3) system is 1.83 times higher than that of the O(3) alone system. Moreover, increasing AOII concentration from 100 mg L(−1) to 500 mg L(−1) subsequently caused a decline in the k values. The experimental data match pseudo-first-order kinetics, as shown by R(2) values of 0.95–0.99. AOII degradation involves absorption, ozone activation, and reactive species production based on the existence of CaO and FeO in the CaFe(2)O(4) nanocatalyst. This catalyst can be effectively recycled multiple times.
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spelling pubmed-105436472023-10-03 Enhancing acid orange II degradation in ozonation processes with CaFe(2)O(4) nanoparticles as a heterogeneous catalyst Van, Huu Tap Hoang, Van Hung Luu, Thi Cuc Vi, Thuy Linh Nga, Luong Thi Quynh Marcaida, Gio Serafin Ivan Jimenez Pham, Truong-Tho RSC Adv Chemistry This study used CaFe(2)O(4) nanoparticles as a catalyst for ozonation processes to degrade Acid Orange II (AOII) in aqueous solution. The study compared heterogeneous catalytic ozonation (CaFe(2)O(4)/O(3)) with ozone treatment alone (O(3)) at different pH values (3–11), catalyst dosages (0.25–2.0 g L(−1)), and initial AOII concentrations (100–500 mg L(−1)). The O(3) alone and CaFe(2)O(4)/O(3) systems nearly completely removed AOII's color. In the first 5 min, O(3) alone had a color removal efficiency of 75.66%, rising to 92% in 10 min, whereas the CaFe(2)O(4)/O(3) system had 81.49%, 94%, and 98% after 5, 10, and 20 min, respectively. The O(3) and CaFe(2)O(4)/O(3) systems degrade TOC most efficiently at pH 9 and better with 1.0 g per L CaFe(2)O(4). TOC removal effectiveness reduced from 85% to 62% when the initial AOII concentration increased from 100 to 500 mg L(−1). The study of degradation kinetics reveals a pseudo-first-order reaction mechanism significantly as the solution pH increased from 3 to 9. Compared to the O(3) alone system, the CaFe(2)O(4)/O(3) system has higher k values. At pH 9, the k value for the CaFe(2)O(4)/O(3) system is 1.83 times higher than that of the O(3) alone system. Moreover, increasing AOII concentration from 100 mg L(−1) to 500 mg L(−1) subsequently caused a decline in the k values. The experimental data match pseudo-first-order kinetics, as shown by R(2) values of 0.95–0.99. AOII degradation involves absorption, ozone activation, and reactive species production based on the existence of CaO and FeO in the CaFe(2)O(4) nanocatalyst. This catalyst can be effectively recycled multiple times. The Royal Society of Chemistry 2023-10-02 /pmc/articles/PMC10543647/ /pubmed/37790093 http://dx.doi.org/10.1039/d3ra04553f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Van, Huu Tap
Hoang, Van Hung
Luu, Thi Cuc
Vi, Thuy Linh
Nga, Luong Thi Quynh
Marcaida, Gio Serafin Ivan Jimenez
Pham, Truong-Tho
Enhancing acid orange II degradation in ozonation processes with CaFe(2)O(4) nanoparticles as a heterogeneous catalyst
title Enhancing acid orange II degradation in ozonation processes with CaFe(2)O(4) nanoparticles as a heterogeneous catalyst
title_full Enhancing acid orange II degradation in ozonation processes with CaFe(2)O(4) nanoparticles as a heterogeneous catalyst
title_fullStr Enhancing acid orange II degradation in ozonation processes with CaFe(2)O(4) nanoparticles as a heterogeneous catalyst
title_full_unstemmed Enhancing acid orange II degradation in ozonation processes with CaFe(2)O(4) nanoparticles as a heterogeneous catalyst
title_short Enhancing acid orange II degradation in ozonation processes with CaFe(2)O(4) nanoparticles as a heterogeneous catalyst
title_sort enhancing acid orange ii degradation in ozonation processes with cafe(2)o(4) nanoparticles as a heterogeneous catalyst
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543647/
https://www.ncbi.nlm.nih.gov/pubmed/37790093
http://dx.doi.org/10.1039/d3ra04553f
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