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Abstracts Book - IMRC 2018

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• SF5-O013 Invited Talk<br />

KINETIC STUDIES OF THE PHOTOCATALYTIC DEGRADATION OF<br />

DICLOFENAC<br />

Edgar Moctezuma 1 , Elisa Leyva 1 , Carmen Lara Pérez 1 , Saúl Noriega 1<br />

1 Universidad Autónoma de San Luis Potosí, Facultad de Ciencias Químicas, Mexico.<br />

The photocatalytic oxidation of Diclofenac, which is a non-steroidal antiinflammatory<br />

medication (NSAIDs) 1 , with TiO 2 illuminated with UV light have<br />

been investigated in our laboratories in order to evaluate the effect of initial<br />

reactant concentration on the reaction rate, to identify the most stable<br />

intermediate organic reaction products and to elucidate the mineralization<br />

reaction pathway. The experiments were carried out in a homemade reactor<br />

system which has a Pyrex tube reactor (400 mL) illuminated with four UV-A light<br />

lamps 2 . For each experiment, 250 mL of a Diclofenac water solution were<br />

placed inside the glass reactor and mixed with 0.5 g of TiO 2 . Reaction samples<br />

were analyzed by UV-vis spectroscopy, HPLC, TOC, FTIR, GC-MS and NMR. The<br />

results of the analysis of samples by UV-vis spectroscopy indicate that<br />

Diclofenac degrades slowly and undergoes gradual changes in its structure. The<br />

first noticeable effect at short reaction times corresponds to the insertion of HO•<br />

radicals in the aromatic rings. UV vis spectra also indicated that aromatic<br />

compounds are mineralized via formation of unsaturated carboxylic acids of low<br />

molecular weight. The fraction of reactant transformed into intermediate<br />

organic products was evaluated by a material balance using the results of<br />

analysis of the reaction samples by HPLC and TOC. The organic products and<br />

the remaining reactant were extracted the reaction samples by liquid–liquid<br />

extraction using with ethyl acetate 3 . The chemical structure of those<br />

intermediate organic reaction products was determined by GC-MS, FT-IR and<br />

NMR. Experimental results confirmed that the Diclofenac is efficiently degraded<br />

by photocatalysis via hydroxylation of the aromatic rings to form 2- (2-<br />

hydroxyphenyl) -ethanoic acid and 2,5-dichloroaniline. These organic products<br />

are slowly oxidized to low molecular weight organic acids before being<br />

completely mineralized to CO 2 and water. The kinetic parameters of the LH-HW<br />

reaction rate equation for the photocatalytic degradation of Diclofenac were<br />

calculated by non-linear regression using the experimental results of<br />

concentration as a function of time.<br />

References:<br />

Kanakaraju, B. D. Glass, M. Oelgem, Green Materials for Energy, Products and

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