6533b824fe1ef96bd12815e9

RESEARCH PRODUCT

New Evidence of the Enhanced Elimination of a Persistent Drug Used as a Lipid Absorption Inhibitor by Advanced Oxidation with UV-A and Nanosized Catalysts

Noureddine BarkaLacramioara RusuNarcisa VrinceanuAndrei Ionut SimionRaluca Maria HlihorIldikó Fekete-kertészLidia Favier

subject

pharmaceutic compoundschemistry.chemical_elementtitania catalysts02 engineering and technology010501 environmental scienceslcsh:Chemical technology01 natural sciencesCatalysisCatalysislcsh:Chemistrychemistry.chemical_compoundlcsh:TP1-1185mineralizationPhysical and Theoretical Chemistryemerging water pollutants0105 earth and related environmental sciencesdegradationPollutantQuenching (fluorescence)[SDE.IE]Environmental Sciences/Environmental Engineeringtoxicity[CHIM.CATA]Chemical Sciences/CatalysisMineralization (soil science)021001 nanoscience & nanotechnology6. Clean waterlcsh:QD1-999chemistry13. Climate actionkineticsTitanium dioxidePhotocatalysisDegradation (geology)[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyphotocatalysisNuclear chemistryTitanium

description

This work demonstrates new evidence of the efficient destruction and mineralization of an emergent organic pollutant using UV-A and titanium nanosized catalysts. The target compound considered in this work is the primary metabolite of a lipid regulator drug, clofibrate, identified in many studies as refractory during conventional wastewater treatment. The photocatalytic performance study was carried out in batch mode at laboratory scale, in aqueous suspension. Kinetic data showed that titanium dioxide P25 Aeroxide® exhibits the highest photocatalytic efficiency compared to the other investigated catalysts. Pollutant degradation and mineralization efficiencies strongly increased when decreasing the initial substrate concentration. Target molecules oxidized faster when the catalyst load increased, and the mineralization was enhanced under acidic conditions: 92% of mineralization was achieved at pH 4 after 190 min of reaction. Radical quenching assays confirmed that HO• and ( h vb + ) were the reactive oxygen species involved in the photocatalytic oxidation of the considered pollutant. In addition, further results revealed that the removal efficiency decreased in real water matrices. Finally, data collected through a series of phytotoxicity tests demonstrated that the photocatalytic process considerably reduces the toxicity of the treated solutions, confirming the process’s effectiveness in the removal of persistent and biorefractory emergent organic water pollutants.

10.3390/catal9090761http://dx.doi.org/10.3390/catal9090761