Study of intermediate by-products and mechanism of the photocatalytic degradation of ciprofloxacin in water using graphitized carbon nitride nanosheets

• Published in: Chemosphere (Oxford) 2020-05, Vol.247, p.125910-125910, Article 125910
• Main Authors: Jiménez-Salcedo, Marta, Monge, Miguel, Tena, María Teresa
• Format: Article
• Language: English
• Subjects: Accurate-mass spectrometry; Anti-Bacterial Agents - chemistry; By-products; Carbon - chemistry; Catalysis; Chromatography, Liquid; Ciprofloxacin; Ciprofloxacin - chemistry; Degradation pathway; g-C3N4 nanosheets; Graphite - chemistry; Kinetics; Light; Nitrogen Compounds - chemistry; Oxidation-Reduction; Photocatalysis; Tandem Mass Spectrometry; Water Pollutants, Chemical - analysis; Water Pollutants, Chemical - chemistry
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2020.125910

The photocatalytic degradation of the antibiotic ciprofloxacin in water was carried out with nanosheets of graphitic carbon nitride (g-C3N4) as catalyst and visible light irradiation using low-power (4 × 10 W) white light LEDs. The aim of this study was to identify the intermediate by-products formed during the degradation and to propose a pathway for CIP degradation. To achieve this goal, photocatalytically degraded CIP solutions were analysed by liquid chromatography coupled to high-resolution mass spectrometry using a QTOF instrument. The accurate mass and the MS/MS data of the detected ions allowed us to determine the elementary composition of eight by-products and to propose the chemical structures for seven of them. Three of these by-products have been reported for the first time and the elementary composition of a fourth one that had been wrongly reported in the literature was accurately established. CIP degradation followed a pseudo-first order kinetics with a pseudo-first order kinetic constant of 0.035 min−1. In addition, a study of the influence of several scavengers showed that only the presence of triethanolamine dramatically reduced the pseudo-first order kinetic constant (0.00072 min−1), pointing out that the reactive species were the holes produced in the catalyst. Finally, the main pathway of CIP degradation seems to be the attack to the piperazine group by ·OH radicals, following heterocycle breakup and the subsequent loss of two of its carbon atoms as CO2 molecules, and then defluorination, oxidation and cleavage of the cycles of this intermediate. [Display omitted] •Ciprofloxacin photocatalytically degraded with g-C3N4 nanosheet and visible light.•Tentative identification of byproducts by accurate-mass spectrometry LC-MS/MS.•Eight intermediates detected and their elementary composition provided.•Piperazinyl moiety is attacked by ·OH radicals, formed from VB holes and OH−.•Four ciprofloxacin by-products reported for the first time in photocatalysis.