4.7 Article

Eliminating tetracycline antibiotics matrix via photoactivated sulfate radical-based advanced oxidation process over the immobilized MIL-88A: Batch and continuous experiments

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 431, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.133213

Keywords

Metal-organic frameworks; Sulfate radical-advanced oxidation process; Tetracycline antibiotics; DFT calculations; Wastewater treatment

Funding

  1. National Natural Science Foundation of China [22176012, 21806008]
  2. Beijing Natural Science Foundation [8202016]
  3. Great Wall Scholars Training Program Project of Beijing Municipality Universities [CITTCD20180323]
  4. Beijing Talent Project [2020A27]
  5. Science and Technology General Project of Beijing Municipal Education Commission [KM202110016010]
  6. JST-ERATO Yamauchi Materials Space-Tectonics Project [JPMJER2003]
  7. Fundamental Research Funds for Beijing University of Civil Engineering and Architecture [X20147, X20141, X20135, X20146]
  8. King Saud University, Riyadh, Saudi Arabia [RSP-2021/261]

Ask authors/readers for more resources

This study demonstrates the successful immobilization of MIL-88A(Fe) MOF on cotton fibers to fabricate MIL-88A (Fe)/cotton fibers (MC) using an eco-friendly method. The prepared MC effectively activates peroxydisulfate to eliminate tetracycline antibiotics in simulated wastewater under UV-light irradiation. The study also investigates the degradation pathways of the antibiotics and demonstrates the long-term operation possibility of the MC in a continuous photoactivated SR-AOP system using a self-designed fixed bed reactor. The findings highlight the potential use of MOFs in large-scale wastewater treatment.
This work demonstrates the successful immobilization of MIL-88A(Fe) MOF on cotton fibers to fabricate MIL-88A (Fe)/cotton fibers (MC) by an eco-friendly method. The prepared MC is used to activate peroxydisulfate for eliminating multiple tetracycline antibiotics, such as oxytetracycline (OTC), tetracycline (TTC), and chlortetracycline (CTC) in simulated wastewater under UV-light irradiation. The photoactivated sulfate radical-advanced oxidation processes (SR-AOPs) towards the removal of tetracycline antibiotics matrix (initial concentration of 10.0 mg/L) using MC were initially investigated using a batch method. The results reveal that 97.5% OTC, 95.2% TTC, and 100.0% CTC can be degraded in the MC/UV/PDS system in the presence of 2 g/L of MC and 1 mM of PDS. The degradation pathways of OTC, TTC, and CTC were clarified via liquid chromatography-mass spectrometry analysis and DFT calculations. The quantitative structure-activity relationship analysis shows that the tetracycline antibiotics are transformed into their corresponding intermediates with lower toxicity within 8.0 min. A self-designed fixed bed reactor, in which the MC was packed into the annular channel, was adopted to test the long-term operation possibility of the MC in the continuous photoactivated SR-AOP system. The findings demonstrate that the whole antibiotics matrix can be removed completely within 22 h. This work is the first to demonstrate the use of MOFs as catalysts for SR-AOP to achieve continuous purification of simulated wastewater. The findings highlight a new possibility for the use of MOFs in large-scale wastewater treatment over.

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