RESUMEN
Photocatalysis has been applied for the elimination or reduction concentration of emerging pollutants in water. One of them, is the moxifloxacin (MOX), a fluoroquinolone that have a potential to develop resistant bacteria and have been present toxicity. The MOX achieves the environment due to inefficient wastewater treatment and incorrect disposal. Aiming to find a sustainable solution for photocatalytic process, compound parabolic concentrator (CPC) reactors have been proposed. In this sense, the present study investigates the application of CPC reactor for the degradation of MOX using sunlight and artificial light (UV-A lamp). In addition, the acute toxicity for L. sativa seeds and A. cepa bulbs, as well as the MOX cytotoxicity and genotoxicity for A. cepa root were investigated before and after treatment. The MOX degradation was around 65% using the sunlight and 44% with the artificial light. This difference was due to the kind of incident radiation (direct and diffuse), as well as the type of radiation (visible and/or ultraviolet) used in the processes. For L. sativa the acute toxicity was eliminated after MOX treatment using sunlight. A. cepa root length increased before the treatment and reduced significantly after it, what can indicate hormesis occurrence. MOX cytotoxicity was not observed. In contrast, genotoxicity assays showed high frequency of chromosomal aberrations for MOX solution, indicating elevated genotoxicity that was eliminated after solar treatment. The transformation products of MOX after CPC reactor solar treatment did not show cytotoxicity and genotoxicity in A. cepa and acute toxicity in L. Sativa. The results indicates that photocatalysis in a CPC solar reactor is efficient for MOX toxicity removal in the treated solutions.
Asunto(s)
Contaminantes Químicos del Agua , Purificación del Agua , Catálisis , Moxifloxacino , Luz Solar , Agua , Contaminantes Químicos del Agua/toxicidadRESUMEN
Glucocorticoids are widely used to treat a variety of diseases. Consequently, these compounds have been found in water and wastewater matrix. Despite studies have proven its toxicity, just a few works investigate techniques to degrade and mineralize them. To solve this issue, this work presents the degradation and mineralization of prednisone (PRED) by electrochemical advanced oxidation (EAO) using a boron-doped diamond supported on niobium (Nb/BDD) anode in synthetic and real wastewater. Cyclic voltammetry (CV) was performed to investigate the PRED oxidation mechanisms. CV suggest that PRED will be oxidized via HO⢠and other oxidants generated from the ions present in the liquid matrix (S2O82-, SO4â¢-, HClO, ClO- etc.). Different EAO conditions as initial pH (3, 7 and 11) and applied current densities (5, 10 and 20 mA cm-2) were evaluated. The best result was obtained at alkaline pH (11) and a current density of 20 mA cm-2, achieving 78% of degradation and 42% of mineralization. Using the best conditions, the EAO was applied as a polishing treatment stage to remove PRED from a biological pre-treated municipal wastewater spiked with PRED. The results indicate that EAO applied in the real matrix provides better results than the synthetic solution, probably associated with the presence of ions that can be electrochemically converted into oxidant species, resulting in higher kinetic constant, mineralization current efficiency and lower energetic consumption. Therefore, the EAO process without the addition of chemicals has proven to be an effective alternative as a tertiary treatment of municipal wastewater contaminated with PRED.
Asunto(s)
Niobio , Prednisona , Contaminantes Químicos del Agua , Boro/química , Diamante/química , Electrodos , Cinética , Modelos Químicos , Niobio/química , Oxidantes , Oxidación-Reducción , Prednisona/química , Aguas Residuales/química , Agua/química , Contaminantes Químicos del Agua/químicaRESUMEN
The environmental detriment due to the presence of emerging contaminants has encouraged the development of advanced oxidation processes. Such methods deal with non-selective chemical reactions. Therefore, toxic byproducts can be generated and distinct post treatment toxicity levels can be expected. The present study investigates the phytotoxicity of 2,4,6-tribromophenol (TBP) to L. sativa seeds and A. cepa bulbs, as well as the TBP phytotoxicity and genotoxicity to A. cepa root. L. sativa seeds and A. cepa bulbs were germinated by being exposed to solutions containing TBP before and after treatment by UV-based processes: direct photolysis (DP), heterogeneous photocatalysis (HP) and photoelectrolysis (PEC). Subsequent analysis of the root length, to determine phytotoxicity, as well as evaluation of chromosomal abnormalities, revealed that the samples treated by DP presented higher phytotoxicity than the untreated ones. On the other hand, samples treated by HP and PEC did not present phytotoxicity. In fact, for the A. cepa assays, phytotoxicity was not observed, including the initial sample. However, genotoxicity assays showed a high frequency of chromosomal aberrations in the initial sample, before the UV-based process treatment. After 140â¯min of treatment by HP, there was a reduction in genotoxicity, while PEC treatment resulted in a sample with no genotoxicity. In contrast, DP presented high levels of phytotoxicity and genotoxicity. Additionally, DP shows similar degradation and debromination values, when compared to the HP and PEC processes, but less mineralization. Therefore, considering that the DP process did not deals with the HO⢠radical, the oxidation pathway can generate byproducts with higher toxicity, which lead to higher levels of phytotoxicity and genotoxicity. These results show that different UV-based oxidation processes are associated to distinct byproducts and toxicity levels. In addition, a toxicity assessment with different organisms should be performed to ensure a safe outcome.
Asunto(s)
Fenoles/toxicidad , Contaminantes Químicos del Agua/toxicidad , Daño del ADN , Oxidación-Reducción , Fenoles/química , Fotólisis , Pruebas de Toxicidad , Contaminantes Químicos del Agua/químicaRESUMEN
The photoelectrocatalytic (PEC) degradation of 4-nonylphenol ethoxylate (NP4EO) using a low, moderate, or high UV photon flux in different treatment times was investigated. The byproducts were verified using gas chromatography with flame ionization detection (GC-FID) and gas chromatography with quadrupole mass analyzer (GC-qMS). The GC results showed that the use of a low (2.89 µmol m(-2)s(-1)) or a high (36.16 µmol m(-2)s(-1)) UV photon flux reaching the anode surface was associated to the production of alcohols and the toxic byproduct nonylphenol (NP), leading to the same degradation pathway. Meanwhile, the use of a moderate UV photon flux (14.19 µmol m(-2)s(-1)) reaching the anode surface did not produce alcohols or the NP toxic byproduct. This study demonstrates that different UV photon fluxes will have an influence in the degradation of NP4EO with or without generation of toxic byproducts. Furthermore, it is concluded that, after the determination of the UV photon flux able to degrade NP4EO without NP formation, the treatment time is essential in removal of NP4EO, since increasing the treatment time of 4 to 10 h, when using the PEC best conditions (moderate UV photon flux), implies in a higher treatment efficiency.
Asunto(s)
Disruptores Endocrinos/química , Fenoles/química , Fotones , Rayos Ultravioleta , Eliminación de Residuos Líquidos/métodos , Contaminantes Químicos del Agua/química , Electrólisis , Disruptores Endocrinos/efectos de la radiación , Ionización de Llama , Cromatografía de Gases y Espectrometría de Masas , Fenoles/efectos de la radiación , Fotólisis , Factores de Tiempo , Contaminantes Químicos del Agua/efectos de la radiaciónRESUMEN
Four different oxidation process, namely direct photolysis (DP) and three advanced oxidation processes (heterogeneous photocatalysis - HP, eletrochemical oxidation - EO and photo-assisted electrochemical oxidation - PEO) were applied in the treatment of wastewater containing nonylphenol ethoxylate (NPnEO). The objective of this work was to determine which treatment would be the best option in terms of degradation of NPnEO without the subsequent generation of toxic compounds. In order to investigate the degradation of the surfactant, the processes were compared in terms of UV/Vis spectrum, mineralization (total organic carbon), reaction kinetics, energy efficiency and phytotoxicity. A solution containing NPnEO was prepared as a surrogate of the degreasing wastewater, was used in the processes. The results showed that the photo-assisted processes degrade the surfactant, producing biodegradable intermediates in the reaction. On the other hand, the electrochemical process influences the mineralization of the surfactant. The process of PEO carried out with a 250W lamp and a current density of 10mA/cm(2) showed the best results in terms of degradation, mineralization, reaction kinetics and energy consumption, in addition to not presenting phytotoxicity. Based on this information, this process can be a viable alternative for treating wastewater containing NPnEO, avoiding the contamination of water resources.
Asunto(s)
Disruptores Endocrinos , Glicoles de Etileno , Tensoactivos , Rayos Ultravioleta , Eliminación de Residuos Líquidos/métodos , Contaminantes Químicos del Agua , Carbono/análisis , Supervivencia Celular/efectos de los fármacos , Electroquímica , Disruptores Endocrinos/química , Disruptores Endocrinos/efectos de la radiación , Disruptores Endocrinos/toxicidad , Glicoles de Etileno/química , Glicoles de Etileno/efectos de la radiación , Glicoles de Etileno/toxicidad , Lactuca/efectos de los fármacos , Lactuca/genética , Lactuca/crecimiento & desarrollo , Pruebas de Mutagenicidad , Cebollas/efectos de los fármacos , Cebollas/genética , Cebollas/crecimiento & desarrollo , Oxidación-Reducción , Fotólisis , Raíces de Plantas/efectos de los fármacos , Raíces de Plantas/genética , Raíces de Plantas/crecimiento & desarrollo , Tensoactivos/química , Tensoactivos/efectos de la radiación , Tensoactivos/toxicidad , Contaminantes Químicos del Agua/química , Contaminantes Químicos del Agua/efectos de la radiación , Contaminantes Químicos del Agua/toxicidadRESUMEN
In this work the photoelectrooxidation (PEO) was applied in the treatment of a solution containing nonylphenol ethoxylate surfactant (NP4EO). The use of different lamps (125 and 250 W), current density (5 and 10 mA cm(-2)) and treatment time (0, 60, 120, 180 and 240 min) were investigated. The samples were characterized by UV/Vis, total organic carbon (TOC), gas chromatography associated to mass spectroscopy (GC/MS) and ecotoxicity. The reaction kinetics were calculated and the light flux and pH were measured. The results of analysis by UV/Vis show that there is degradation of nonylphenol ethoxylated in the treatment time of 240 min for all configurations, and the configurations that used a 250 W lamp and a current density of 10 mA cm(-2) obtained better results, with a reduction of 83% in TOC, indicating a high mineralization of the surfactant. It was further found in the GC/MS that the configurations that used the 125 W lamp promoted a smaller incident light flux on the solution, and, regardless of the applied current density, it was generated the reaction intermediate nonylphenol, more toxic than the parent compound. The opposite can be observed when a 250 W lamp was used, which produced a higher incident light flux. Based on the degradation products detected, a simplified mechanism for degradation of nonylphenol ethoxylate was proposed. Although a treatment time of 240 min with photoelectrooxidation with different configurations was not effective in the complete mineralization of the compound, a promising process was developed with the treatment using a lamp of 250 W and a current density of 10 mA cm(-2), which generated a solution with less toxicity than the original one.