RESUMEN
Steroidal hormones such as estriol (E3), are resistant to biodegradation; hence their removal by conventional treatment systems (aerobic and anaerobic) facilities is limited. These substances are detected in surface water, and present risks to the aquatic ecosystem and humans via potential biological activity. Photochemical treatments can be used to remove E3; however, just a few studies have analyzed the kinetics, intermediates, and E3 degradation pathways in natural surface water. In this study, the behavior of E3 under ultraviolet irradiation associated with H2O2, O3 or TiO2 was investigated to determine the degradation potential and the transformation pathways in reactions performed with a natural surface water sample. E3 degradation kinetics (200 ppb) fitted well to the pseudo-first-order kinetics model, with kinetic constant k in the following order: kUV/O3 > kUV/TiO2 > kUV/H2O2 > kUV. The mechanism of degradation using different advanced oxidative processes seemed to be similar and 12 transformation byproducts were identified, with 11 of them being reported here for the first time. The byproducts could be formed by the opening of the aromatic ring and addition of a hydroxyl radical. A possible route of E3 degradation was proposed based on the byproducts identified, and some of the byproducts presented chronic toxicity to aquatic organisms, demonstrating the risks of exposure.
Asunto(s)
Peróxido de Hidrógeno , Agua , Ecosistema , Estriol , Procesos FotoquímicosRESUMEN
The catalytic activity of Mn2O3, FeOOH and CeO2 nanoparticles was evaluated in the treatment of a synthetic petroleum refinery wastewater (SPRW) using O3 in a discontinuous reactor at 25°C and pH 5.5. The mineralization and partial chemical oxidation rates of SPRW using these metal oxides are in the same order of magnitude, and the catalytic activity in the mineralization of SPRW decreased in the order Mn2O3 > CeO2 > FeOOH. The mineralized fraction progressively increased with time in the catalytic process while in the non-catalytic process it remained constant. The effect of the operational conditions on the mineralization and partial chemical oxidation rates using Mn2O3 was investigated in detail. The mineralization rate was found to be lower than the partial oxidation rate due to the formation of partially oxidized by-products, and this is dependent on the solids dosage and pH. An investigation of the mechanism demonstrated that the enhancement effect could be attributed to the introduction of the manganese oxide nanoparticles, which could promote the utilization of O3 and/or enhance the formation of free radicals (â¢OH, â¢O2H and â¢O2-) on the solid surface and further accelerate the degradation of the organic compounds present in the wastewater.
Asunto(s)
Ozono , Petróleo , Contaminantes Químicos del Agua , Catálisis , Oxidación-Reducción , Óxidos , Aguas ResidualesRESUMEN
Four tertiary hybrid treatments to produce high quality reused water, fulfilling Brazilian drinking water regulations, from a slaughterhouse's secondary treated effluent were evaluated. The pilot plant with a capacity of 500 L h(-1) was set up and consisted of these stages: pre-filtration system (cartridge filter 50 micron, activated carbon filter, cartridge filter 10 micron), oxidation (H2O2) or second filtration (ceramic filter, UF) followed by UV radiation (90 L h(-1)). The best combination was T4: pre-filtration followed by H2O2 addition and UV radiation (AOP H2O2/UV). Disinfection kinetics by T4 followed pseudo first-order kinetics: k(T4) = 0.00943 s(-1) or 0.00101 cm2 mJ(-1). Three different zones (A, B, C) were observed in the UV254 degradation kinetics (pseudo-first order kinetics): k' decreased over time (k'(A) > k'(B) > k'(C)).
Asunto(s)
Reciclaje/métodos , Purificación del Agua/métodos , Agua/química , Agua/normas , Proyectos Piloto , Factores de Tiempo , Contaminantes del Agua , Purificación del Agua/normasRESUMEN
In some Brazilian regions, surface water has become scarce, e.g. semi arid climate areas and densely populated and industrial areas, where water over-exploitation and/or fluvial pollution has been more common. Advanced oxidative processes (AOP) provide treated water as a source of reuse water even with the characteristics of drinking water enabling water reuse practices also in food industries. The secondary wastewater of a slaughterhouse was the water source for a tertiary treatment study evaluating the kinetics of the photo-induced degradation of color and UV254 under UV radiation with and without the addition of H2O2. The proximity of the k' values of color and UV254 degradation by UV indicates that the compounds responsible for color may be the same content measured by UV254. The H2O2/UV treatment was 5.2 times faster than simple UV in removing aromatic compounds. The degradation kinetics of aromatic compounds in both treatments followed a pseudo-first order law. The pseudo-first order constant for H2O2/UV and UV treatments were kUV254'=0.0306 min(-1) and kUV254'=0.0056 min(-1), respectively.