FeVO4 nanorods decorated natural sepiolite as highly efficient peroxymonosulfate catalyst for tetracycline degradation
Yu-bo Wang , Xiao-long Hu , Rui Li , Long Zhang , Jun-ying Song , Li Wang , Qing-bin Guo , Deng-zheng Gao , Peng Huang , Qing Lu , Wen-bing Zhang
Journal of Central South University ›› 2025, Vol. 32 ›› Issue (10) : 3876 -3894.
FeVO4 nanorods decorated natural sepiolite as highly efficient peroxymonosulfate catalyst for tetracycline degradation
Developing a low-cost stable and high-performance peroxymonosulfate (PMS) catalyst to degrade refractory organic pollutants is still an urgent problem. Herein, this study reported FeVO4 nanorods decorated sepiolite (FeVO4/sepiolite) through simple hydrothermal method as an adsorptive-catalyst for PMS activation to degrade tetracycline (TC). Benefiting from the introduction of sepiolite support, FeVO4 nanorods could be uniformly immobilized onto fibrous sepiolite surface. As a result, FeVO4/sepiolite composite was endowed with excellent adsorption properties, rich surface hydroxyl groups, more reaction active sites, and the stable redox cycle of Fe3+/Fe2+ and V5+/V4+. Therefore, higher TC degradation efficiency (91.19% within 40 min) and larger reaction rate constant (0.1649 min−1) were obtained in FeVO4/sepiolite/PMS system than in FeVO4/PMS system. Besides, the composite presented good stability and reusability, and the effects of application parameters on TC degradation were investigated in detail. Through quenching experiment and electron paramagentic resonance (EPR) test, it was found that both radical and non-radical species participates in TC degradation, and 1O2 were the main active species. The PMS activation mechanism was proposed, and the possible degradation pathway was also analyzed according to the high performance liquid chromatography-mass spectrometry (HPLC-MS) results. Overall, this work provides meaningful insights for designing natural mineral based PMS activators to effectively remediate antibiotic wastewater.
FeVO4 / sepiolite / peroxymonosulfate / tetracycline
| [1] |
|
| [2] |
|
| [3] |
|
| [4] |
|
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
|
| [9] |
|
| [10] |
|
| [11] |
|
| [12] |
|
| [13] |
|
| [14] |
|
| [15] |
|
| [16] |
|
| [17] |
|
| [18] |
|
| [19] |
|
| [20] |
|
| [21] |
|
| [22] |
|
| [23] |
|
| [24] |
|
| [25] |
|
| [26] |
|
| [27] |
|
| [28] |
|
| [29] |
|
| [30] |
|
| [31] |
|
| [32] |
|
| [33] |
|
| [34] |
|
| [35] |
|
| [36] |
|
| [37] |
|
| [38] |
|
| [39] |
|
| [40] |
|
Central South University
/
| 〈 |
|
〉 |