Decision support in disinfection technologies for treated wastewater reuse

The environmental and social impact derived from treated wastewater reuse is an intrinsically complex multidimensional process, which involves multiple criteria and multiple stakeholders. This paper presents the use of multicriteria decision through the TOPSIS method, applied to six different methodologies concerning the disinfection of treated wastewater before reusing. Results have shown that the best disinfection technique for treated wastewater has been chlorination with 4 ppm, if this water is to be destined to an urban, agricultural or industrial use, due to a large weight given to cost and environmental criteria. Conversely, in recreational and environmental uses, the alternative of ultraviolet light disinfection was the chosen alternative. Economic criteria showed priority in the most entrepreneurial uses of the water, although social and political cost had a greater weight in the case of environmental or recreational uses. The inclusion of environmental and social assessment in the disinfection technique decision support clearly provides a cleaner and more sustainable production.     

Light-induced transformations of aza-aromatic pollutants adsorbed on models of atmospheric particulate matter: Acridine and 9(10-H) acridone

The effect of the characteristics of the surface on the phototransformation of acridine, one of the most abundant azapolycyclic compounds encountered in urban atmospheres, and of one of its principal photoproducts, acridone, was studied when adsorbed onto models of the atmospherice particulate matter. For this purpose, relative photodegradation rates were determined from absorption or emission intensities as a function of irradiation times, and some products were isolated and characterized. The relative photodegradation rates of adsorbed acridine show the tendency (NH(4))(2) SO(4) > MgO > Al(2)O(3) >SiO(2). In general, the rates decrease as the fraction of protonated acridine species on the surface increases in MgO, Al(2)O(3), and SiO(2), except for (NH(4))(2) SO(4) where a fast surface reaction occurs. Oxygen reduces the photodestruction rates by as much as 40 to 60% when compared to an inert atmosphere, implying the participation of an acrideine triplet state in the transformation processes on all surfaces except on (NH(4))(2)SO(4). Acridone, a major product, undergoes a photoinduced tautomerization to 9-hydroxy acridine. The formation of a dihydrodiol, another photoproduct of acridine, is suggested by comparison to reported spectral properties of these compounds. This is formed through a singlet oxygen reaction. Photoproducts showing the absence of the narrow absorption band of 250 nm, characteristic of the pi -->pi* transition in tricyclic aromatics, were detected in small yields but not identified. These results suggest possible photochemical transformation pathways that could lead to the ultimate fate of these pollutants in the environment.