Related Experiment Video
Updated: Aug 6, 2026

A Complete Method for Evaluating the Performance of Photocatalysts for the Degradation of Antibiotics in Environmental Remediation
Published on: October 6, 2022
An oxidation process of tetracycline with low products toxicity by Fe single-atom peroxydisulfate activator from
Qinqin Chen1, Peiyuan Cheng1, Daixi Zhou1
1College of Environment and Climate, Jinan University, Guangzhou 511443, China.
Abstract:
Recently, advanced oxidation processes based on single-atom catalysts have been extensively adopted in water treatments. Although some studies have identified low toxicity in degradation products, the mechanistic understanding remains unclear. In this work, an efficient catalyst named BC-Fe was developed by anchoring atomically dispersed Fe onto biochar (BC) derived from microalgae using a convenient impregnation method. The catalyst of BC-Fe enhanced performance in activating peroxydisulfate (PDS) for the degradation of tetracycline (TC). The BC-Fe/PDS system demonstrated faster TC degradation rate constant of 0.073 min-1. Mechanism investigations revealed that the atomically dispersed Fe-N4 sites activate PDS via efficient electron transfer, generating high-valent metal-oxo (HVMO) species as the primary reactive oxidants. These HVMO species selectively oxidized electron-rich moieties in TC, leading to progressive ring-opening and mineralization into low-toxicity intermediates. Moreover, TC served as an electron donor to the HVMO species, enabling their reduction and forming a favorable cycle of valence states of Fe. This work provides an efficient and environment-benign strategy for the oxidation of antibiotics with minimal secondary pollution.
More Related Videos
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Oxidation of Phenols to Quinones
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
Oxidations of Aldehydes and Ketones to Carboxylic Acids
Aldehydes readily undergo oxidation in strong oxidizing agents such as potassium permanganate and chromic acid. The oxidation can also be carried out using mild oxidizing agents such as silver oxide. In fact, aldehydes can be easily oxidized...
