Removal of phenol from wastewater by high-gravity intensified heterogeneous catalytic ozonation with activated carbon
In this study, the high-gravity technique is used to intensify the heterogeneous catalytic ozonation with activated carbon (AC) as the catalyst for removal of phenol from wastewater in a rotating packed bed (RPB), and the effects of high-gravity factor, inlet O 3 concentration, liquid–gas ratio, and...
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Veröffentlicht in: | Environmental science and pollution research international 2022-05, Vol.29 (23), p.34830-34840 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this study, the high-gravity technique is used to intensify the heterogeneous catalytic ozonation with activated carbon (AC) as the catalyst for removal of phenol from wastewater in a rotating packed bed (RPB), and the effects of high-gravity factor, inlet O
3
concentration, liquid–gas ratio, and initial pH on the degradation and mineralization of phenol at room temperature are investigated. It is revealed that the degradation rate of phenol reaches 100% at 10 min and the removal rate of total organic carbon (TOC) reaches 91% at 40 min under the conditions of high-gravity factor
β
= 40, inlet O
3
concentration = 90 mg·L
−1
, liquid flow rate = 80 L·h
−1
, and initial pH = 11. Compared with the bubbling reactor (BR)/O
3
/AC and RPB/O
3
systems, the mineralization rate of phenol by the RPB/O
3
/AC system is increased by 24.78% and 34.77%, respectively. Free radical quenching experiments are performed using tertiary butanol (TBA) and benzoquinone (BQ) as scavengers of ·OH and O
2
−
, respectively. It is shown that the degradation and mineralization of phenol are attributed to the direct ozonation and the indirect oxidation by ·OH generated from the decomposition of O
3
adsorbed on AC surface, respectively. ·OH and O
2
·−
are also detected by electron paramagnetic resonance (EPR). Thus, it is concluded that AC-catalyzed ozonation and high-gravity technique have a synergistic effect on ·OH initiation, which in turn can significantly improve the degradation and mineralization of organic wastewater. |
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ISSN: | 0944-1344 1614-7499 |
DOI: | 10.1007/s11356-021-18093-y |