RESUMEN
Conventional municipal wastewater treatment plants are not able to entirely degrade some organic pollutants that end up in the environment. Within this group of contaminants, Emerging Contaminants are mostly unregulated compounds that may be candidates for future regulation. In this work, different advanced technologies: solar heterogeneous photocatalysis with TiO(2), solar photo-Fenton and ozonation, are studied as tertiary treatments for the remediation of micropollutants present in real municipal wastewater treatment plants effluents at pilot plant scale. Contaminants elimination was followed by Liquid Chromatography/Quadrupole ion trap Mass Spectrometry analysis after a pre-concentration 100:1 by automatic solid phase extraction. 66 target micropollutants were identified and quantified. 16 of those contaminants at initial concentrations over 1000 ng L(-1), made up over 88% of the initial total effluent pollutant load. The order of micropollutants elimination efficiency under the experimental conditions evaluated was solar photo-Fenton > ozonation > solar heterogeneous photocatalysis with TiO(2). Toxicity analyses by Vibrio fischeri and respirometric tests showed no significant changes in the effluent toxicity after the three tertiary treatments application. Solar photo-Fenton and ozonation treatments were also compared from an economical point of view.
Asunto(s)
Ozono/química , Fotoquímica/métodos , Eliminación de Residuos Líquidos/métodos , Contaminantes Químicos del Agua/química , Aliivibrio fischeri/efectos de los fármacos , Cromatografía Liquida/métodos , Peróxido de Hidrógeno/química , Espectrometría de Masas/métodos , Fotoquímica/instrumentación , Luz Solar , Titanio/química , Pruebas de Toxicidad , Contaminantes Químicos del Agua/análisis , Contaminantes Químicos del Agua/toxicidadRESUMEN
This study compares two different solar photo-Fenton processes, conventional photo-Fenton at pH3 and modified photo-Fenton at neutral pH with minimal Fe (5 mg L⻹) and minimal initial H2O2 (50 mg L⻹) concentrations for the degradation of emerging contaminants in Municipal Wastewater Treatment Plants effluents in solar pilot plant. As Fe precipitates at neutral pH, complexing agents which are able to form photoactive species, do not pollute the environment or increase toxicity have to be used to keep the iron in solution. This study was done using real effluents containing over 60 different contaminants, which were monitored during treatment by liquid chromatography coupled to a hybrid quadrupole/linear ion trap mass analyzer (LC-QTRAP-MS/MS) operating in selected reaction monitoring (SRM) mode. Concentrations of the selected contaminants ranged from a few ng L⻹ to tens of µg L⻹. It was demonstrated in all cases the removal of over 95% of the contaminants. Photo-Fenton at pH3 provided the best treatment time, but has the disadvantage that the water must be previously acidified. The most promising process was photo-Fenton modified with Ethylenediamine-N,N'-disuccinic acid (EDDS), as the pH remained in the neutral range.
Asunto(s)
Peróxido de Hidrógeno/química , Hierro/química , Oxidantes Fotoquímicos/química , Luz Solar , Aguas Residuales/química , Contaminantes Químicos del Agua/química , Purificación del Agua/métodos , Cromatografía Líquida de Alta Presión , Ciudades , Etilenodiaminas/efectos adversos , Etilenodiaminas/química , Concentración de Iones de Hidrógeno , Quelantes del Hierro/efectos adversos , Quelantes del Hierro/química , Gobierno Local , Concentración Osmolar , Procesos Fotoquímicos , Solubilidad , España , Succinatos/efectos adversos , Succinatos/química , Espectrometría de Masas en Tándem , Contaminantes Químicos del Agua/análisisRESUMEN
Photocatalytic degradation of phenol, nalidixic acid, mixture of pesticides, and another of emerging contaminants in water was mediated by TiO(2) and iron oxide immobilized on functionalized polyvinyl fluoride films (PVF(f)-TiO(2)-Fe oxide) in a compound parabolic collector (CPC) solar photoreactor. During degradation, little iron leaching (<0.2mgL(-1)) was observed. Phenol was efficiently degraded and mineralized at operational pH<5 and nalidixic acid degradation was complete even at pH 7, but mineralization stopped at 35%. Pesticide mixture was slowly degraded (50%) after 150min of irradiation. Degradation of the emergent contaminant mixture was successful for eight compounds and less efficient for six other compounds. The significant reactivity differences between tested compounds were assigned to the differences in structure namely that the presence of complexing or chelating groups enhanced the rates. PVF(f)-TiO(2)-Fe oxide photoactivity gradually increased during 20 days of experiments. X-ray photoelectron spectroscopy (XPS) measurements revealed significant changes on the catalyst surface. These analyses confirm that during photocatalysis mediated by PVF(f)-TiO(2)-Fe oxide, some iron leaching led to enlargement of the TiO(2) surface exposed to light, increasing its synergy with iron oxides and leading to enhanced pollutant degradation.
Asunto(s)
Compuestos Férricos/química , Plaguicidas/química , Fotoquímica/métodos , Luz Solar , Titanio/química , Contaminantes Químicos del Agua/química , Catálisis , Concentración de Iones de HidrógenoRESUMEN
This work focuses on the treatment of real effluents from a municipal wastewater treatment plant (RE) with solar photo-Fenton (5 mg and 20 mg L(-1) Fe, pH approximately 3 and 50 mg L(-1) initial H(2)O(2) concentration) at pilot plant scale. In some experiments RE was spiked with 15 different (acetaminophen, antipyrine, atrazine, caffeine, carbamazepine, diclofenac, flumequine, hydroxybiphenyl, ibuprofen, isoproturon, ketorolac, ofloxacin, progesterone, sulfamethoxazole, and triclosan) emerging contaminants (ECs) at 100 and 5 microg L(-1) each which were added directly into RE prior to treatment. All experiments showed successful degradation of ECs in real effluents from different municipal wastewater treatment plants at low iron concentration (5 mg L(-1)). Although the most degradation took place during the Fenton process, photo-Fenton was necessary to degrade all ECs below their limit of detection (LOD). In the case of the RE containing 52 ECs (determined by HPLC-QTRAP-MS), four of them could not be degraded to their LOD and were still present, although at extremely low concentrations (nicotine 47 ng L(-1), cotinine 11 ng L(-1), chlorfenvinphos 99 ng L(-1), and caffeine 8 ng L(-1)). ECs were easily degraded by (*)OH without substantial competition with the organic content of the RE.
Asunto(s)
Contaminación de Medicamentos , Eliminación de Residuos Líquidos/métodos , Purificación del Agua/métodos , Contaminación de Medicamentos/prevención & control , Restauración y Remediación Ambiental/métodos , Peróxido de Hidrógeno , Concentración de Iones de Hidrógeno , Residuos Industriales , Cinética , Límite de Detección , Gobierno Local , Preparaciones Farmacéuticas/análisis , Preparaciones Farmacéuticas/química , España , Contaminantes Químicos del Agua/aislamiento & purificaciónRESUMEN
The degradation of 15 emerging contaminants (ECs) at low concentrations in simulated and real effluent of municipal wastewater treatment plant with photo-Fenton at unchanged pH and Fe=5 mg L(-1) in a pilot-scale solar CPC reactor was studied. The degradation of those 15 compounds (Acetaminophen, Antipyrine, Atrazine, Caffeine, Carbamazepine, Diclofenac, Flumequine, Hydroxybiphenyl, Ibuprofen, Isoproturon, Ketorolac, Ofloxacin, Progesterone, Sulfamethoxazole and Triclosan), each with an initial concentration of 100 microg L(-1), was found to depend on the presence of CO(3)(2-) and HCO(3)(-) (hydroxyl radicals scavengers) and on the type of water (simulated water, simulated effluent wastewater and real effluent wastewater), but is relatively independent of pH, the type of acid used for release of hydroxyl radicals scavengers and the initial H(2)O(2) concentration used. Toxicity tests with Vibrio fisheri showed that degradation of the compounds in real effluent wastewater led to toxicity increase.