RESUMEN
The treatment of municipal solid waste landfill leachate in a pilot plant made up of solar compound parabolic collectors, using a solid industrial titanium by-product (WTiO(2)) containing TiO(2) and Fe(III) as a photocatalyst, was investigated. In the study evidence was found showing that the degradation performed with WTiO(2) was mainly due to the Fe provided by this by-product, instead of TiO(2). However, although TiO(2) had very little effect by itself, a synergistic effect was observed between Fe and TiO(2). The application of WTiO(2), which produced coupled photo-Fenton and heterogeneous catalysis reactions, achieved a surprisingly high depuration level (86% of COD removal), higher than that reached by photo-Fenton using commercial FeSO(4) (43%) in the same conditions. After the oxidation process the biodegradability and toxicity of the landfill leachate were studied. The results showed that the leachate biodegradability was substantially increased, at least in the first stages of the process, and again that WTiO(2) was more efficient than FeSO(4) in terms of increasing biodegradability.
Asunto(s)
Minerales/química , Procesos Fotoquímicos , Eliminación de Residuos/métodos , Rayos Ultravioleta , Catálisis , Peróxido de Hidrógeno/química , Residuos Industriales , Hierro/química , Aguas del Alcantarillado/química , Titanio/química , Pruebas de ToxicidadRESUMEN
This work reports on pulp mill wastewater (PMW) tertiary treatment by Fenton (Fe(2+)/H(2)O(2)) and solar photo-Fenton (Fe(2+)/H(2)O(2)/UV) processes in a pilot plant based on compound parabolic collectors (CPCs). Solar photo-Fenton reaction is much more efficient than the respective dark reaction under identical experimental conditions. It leads to DOC mineralisation, COD and total polyphenols (TP) removal higher than 90%. The solar photo-Fenton experiment with 5mg Fe L(-1) reaches 90% of DOC mineralisation with 31kJ L(-1) of UV energy and 50mM of H(2)O(2). The initial non-biodegradability of PMW, as shown by respirometry assays and BOD(5)/COD ratio, can be changed after a solar photo-Fenton treatment. Experiments with 20 and 50mg Fe L(-1) revealed that solar photo-Fenton can reach the same DOC degradation (90%), however, consuming less H(2)O(2) and time. Diluting the initial organic load to 50% also diminishes the dosage of H(2)O(2) and the necessary reaction time to achieve high DOC removals. Accordingly, solar photo-Fenton can be considered an alternative or complementary process to improve the performance of a biologic treatment and, subsequently, achieve legal limits on discharge into natural waters.