Hydrothermally improved natural manganese-containing catalytic materials to degrade 4-chlorophenol
Natural manganese-containing mineral (NMM) was used as a catalyst in heterogeneous catalytic ozonation for 4-chlorophenol (4-CP) degradation. The surface and structural properties of NMM were modified by the hydrothermal aging process and called H-NMM. The catalytic activity of NMM and H-NMM were ev...
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Veröffentlicht in: | Environmental research 2023-06, Vol.226, p.115641-115641, Article 115641 |
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Sprache: | eng |
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Zusammenfassung: | Natural manganese-containing mineral (NMM) was used as a catalyst in heterogeneous catalytic ozonation for 4-chlorophenol (4-CP) degradation. The surface and structural properties of NMM were modified by the hydrothermal aging process and called H-NMM. The catalytic activity of NMM and H-NMM were evaluated for the catalytic ozonation process (COP). The synergistic effect of NMM and H-NMM in ozonation processes for 4-CP degradation under optimal conditions (pH of 7, 1 g/L of NMM and H-NMM, 0.85 mg/min of O3, and 15 min of reaction time) was measured by 3.04 and 4.34, respectively. During the hydrothermal process, Mn4+ and Fe2+ were converted to Mn2+ and Fe3+, which caused better performance of the H-NMM than the NMM. During the catalytic ozonation process, Mn2+ is completely oxidized, which increases the production of Hydroxyl radical (•OH). The reactive oxygen species (ROS) generated in the system were identified using radical scavenging experiments. •OH, superoxide radical (•O2−), and singlet oxygen (1O2) represented the dominant reactive species for 4-CP degradation. The O3/H-NMM process indicated a powerful ability in the mineralization of 4-CP (66.31% of TOC degradation). H-NMM exhibited excellent stability and reusability in consecutive catalytic cycles, and the NMM exhibited desirable performance. This study offers NMM and H-NMM as effective, stable, and competitive catalysts for hastening and enhancing the ozonation process to mitigate environmentally related pollutants of high concern. |
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ISSN: | 0013-9351 1096-0953 |
DOI: | 10.1016/j.envres.2023.115641 |