4.8 Article

Solar photocatalytic degradation of persistent pharmaceuticals at pilot-scale: Kinetics and characterization of major intermediate products

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 89, Issue 1-2, Pages 255-264

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcatb.2009.02.013

Keywords

Acetaminophen; Atenolol; Intermediate products; Solar TiO2 photocatalysis; Solar photo-Fenton; UPLC-QqToF-MS

Funding

  1. EU project INNOVA MED [INCO-CT-2006-517728]
  2. MICINN (Spain)
  3. CAPES foundation-Ministry of Education of Brazil [3763-05-6]
  4. ICREA Funding Source: Custom

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The technical feasibility and performance of photocatalytic degradation of anti-inflammatory drug acetaminophen (ACTP) and beta-blocker atenolol (ATL) have been studied in a well-defined system of a pilot-plant scale Compound Parabolic Collectors (CPCs) under natural illumination. Heterogeneous photocatalysis with titanium dioxide (TiO2) and homogeneous photocatalysis by photo-Fenton were investigated with two different matrices: distilled water and synthetic municipal wastewater treatment plant effluent (S.E.). The initial concentrations of the pharmaceuticals studied were 10 mg L-1, whereas the concentrations of the catalysts employed were 200 mg L-1 of TiO2 and 5 mg L-1 of iron. Total disappearance of the parent compounds and discreet mineralization were attained in all experiments. Furthermore, kinetic parameters, release of heteroatoms and formation of carboxylic acids are discussed. The main intermediate products of photocatalytic degradation of atelonol has been structurally elucidated by tandem mass spectrometry (MS2) experiments performed at quadrupole-time of flight (QqToF) mass analyzer coupled to ultra-performance liquid chromatograph (UPLC). Six transformation products were characterized, formed by consecutive attacks of hydroxyl ((OH)-O-center dot) radical in concomitance with the disappearance of the primary compound. The proposed TiO2 and photo-Fenton degradation route of ATL is reported for the first time. (C) 2009 Elsevier B.V. All rights reserved.

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