Angela-Guiovana Rincón
École Polytechnique Fédérale de Lausanne
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Featured researches published by Angela-Guiovana Rincón.
Applied Catalysis B-environmental | 2003
Angela-Guiovana Rincón; Cesar Pulgarin
A detrimental effect on the survival of bacteria Escherichia coli KI2 was observed after photocatalytic exposure. The reactions have been carried out in a batch photoreactor using mainly titanium dioxide (TiO2) P-25 Degussa as a catalyst. Illumination was produced by a Hanau Suntest lamp. Some parameters, such as light intensity, extend of continuous irradiation, catalyst concentration and temperature have a positive effect on disinfection. Intermittent illumination results in an increase in the time required for E. coli inactivation. No bacterial growth was observed after illumination of a contaminated TiO2 suspension. In contrast, without catalyst, illuminated bacteria recovered its initial concentration after 3 h in the dark. Bacterial inactivation in the absence of catalyst was more affected than that with catalyst when increasing light intensity from 400 to 1000 W/m(2). TiO2 concentrations higher than 1 g/l do not significantly increase the initial inactivation rate for both intensities. However, at 1000W/m(2) a modification of TiO2 concentration ranging between 0.25 and 1.5g/l did not affect the total inactivation time, as with 400 W/m(2). Water turbidity negatively affects the photocatalytic inactivation of bacteria. TiO2 immobilized on Nafion((R)) membranes inactivates E. coli with efficiencies close to those observed for bacterial suspension containing the same concentration of suspended TiO2. For fixed TiO2 on glass, the dose (W min/m(2)) necessary for the total inactivation decreases by increasing the fixed TiO2 amount. Fixed TiO2 P-25 was more active to photocatalytic inactivation when compared with immobilized rutile and anatase. However fixed rutile enhances E. coli inactivation as anatase. The effect of temperature and turbidity were made using wastewater sample
Journal of Solar Energy Engineering-transactions of The Asme | 2007
Angela-Guiovana Rincón; Cesar Pulgarin
Background. In recent years, there has been a growing interest in the development of new processes for water disinfection since the traditional processes, such as chlorination, can lead to the production of toxic disinfection by-products. Sunlight has been used as a method of water disinfection and heliophotocatalysis by titanium dioxide (TiO2) has been recently considered as a new approach to improve the conventional solar water disinfection. This paper discusses the effect of the chemical composition of water on the E. coli photo inactivation. Method of Approach. Ten types of water having a different chemical composition were contaminated by E. coli K12 and exposed to a simulated solar irradiation in the absence of TiO2 (photolysis) and in presence of TiO2 (photocatalysis). Bacteria were monitored by plate count. The durability of disinfection was assessed in terms of the effective disinfection time (EDT) in a subsequent dark period of 24 h (EDT24). Natural water from the Leman Lake (LLW), milli-Q water (MQW), MQW containing a mixture of NO3-, PO4-3, SO4-2, Cl− and HCO3-, phosphate buffered saline water, water from the outlet of a biological wastewater treatment plant (WW); MQW containing a mixture of KCl-NaCl and commercial bottled drinking water (CBW) where used to suspend E. coli at laboratory scale. Field scale experiments using solar irradiation in a compound parabolic concentrator (CPC) with E. coli suspended in LLW were also carried out. Results. The sensitivity of bacteria to the phototreatment depends on the nature of the water. Moreover, experiments systematically performed under the solar simulator showed that the order of E. coli inactivation rate and the EDT24 are different for each system. In photolytic systems, E. coli solar inactivation rate is accelerated by the presence in water of NO3- and HCO3- when compared to that observed in MQW. EDT24 was reached at 3 h of irradiation for only 3 (WLL, WW1, and CBW) of the ten studied waters. In the presence of TiO2, the rate of the solar disinfection generally increased. However, a negative effect of chemical substances present in water on the E. coli photocatalytic inactivation was observed in waters when compared to MQW. This effect was especially important in the presence of phosphate, and carbonate. EDT24 was less than 2 h for the majority of the water types. In the presence of TiO2, a “residual disinfection effect” was observed for samples even when bacterial culturability below the detection limit was not reached after photocatalytic treatment. Solar irradiation in a CPC photoreactor indicates that the presence of TiO2 accelerates the detrimental action of sunlight. The EDT24 was reached before 3 h, in photocatalytic experiments but not in those in the absence of TiO2. The influence of TiO2 surface characteristics and charge, as well as the postirradiation events observed in heliophototreated water, in an optimal growth medium are also discussed. Conclusions. The presence of NO3-, HCO3-, PO4-3, SO4-2, Cl−, and HCO3- greatly affects the photolytic and photocatalytic disinfection processes. The natural ions and organic matter affect the solar disinfection of water in the presence and absence of TiO2 and influences the post irradiation events after sunlight illumination. Antagonistic effect in several conditions or synergistic effects in others can be expected when inorganic and/or organic substances are present in phototreated water sources. EDT24 is useful tool for standardization of solar water disinfection. EDT24 values depend on parameters such as the chemical composition of water, light intensity, initial bacterial concentration, and TiO2 concentration.
Applied Catalysis B-environmental | 2004
Angela-Guiovana Rincón; Cesar Pulgarin
Applied Catalysis B-environmental | 2004
Angela-Guiovana Rincón; Cesar Pulgarin
Solar Energy | 2004
Angela-Guiovana Rincón; Cesar Pulgarin
Solar Energy | 2006
D. Gumy; Angela-Guiovana Rincón; R. Hajdu; Cesar Pulgarin
Journal of Photochemistry and Photobiology A-chemistry | 2006
T. Yuranova; Angela-Guiovana Rincón; Cesar Pulgarin; D. Laub; N. Xantopoulos; H. J. Mathieu; J. Kiwi
Applied Catalysis B-environmental | 2006
Angela-Guiovana Rincón; Cesar Pulgarin
Catalysis Today | 2005
Angela-Guiovana Rincón; Cesar Pulgarin
Catalysis Today | 2007
Angela-Guiovana Rincón; Cesar Pulgarin