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Multi-Layered TiO(2) Films towards Enhancement of Escherichia coli Inactivation
Crystalline TiO(2) has shown its great photocatalytic properties in bacterial inactivation. This work presents a design fabrication of low-cost, layered TiO(2) films assembled reactors and a study of their performance for a better understanding to elucidate the photocatalytic effect on inactivation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456645/ https://www.ncbi.nlm.nih.gov/pubmed/28773930 http://dx.doi.org/10.3390/ma9100808 |
Sumario: | Crystalline TiO(2) has shown its great photocatalytic properties in bacterial inactivation. This work presents a design fabrication of low-cost, layered TiO(2) films assembled reactors and a study of their performance for a better understanding to elucidate the photocatalytic effect on inactivation of E. coli in water. The ability to reduce the number of bacteria in water samples for the layered TiO(2) composing reactors has been investigated as a function of time, while varying the parameters of light sources, initial concentration of bacteria, and ratios of TiO(2) film area and volume of water. Herein, the layered TiO(2) films have been fabricated on the glass plates by thermal spray coating prior to screen printing, allowing a good adhesion of the films. Surface topology and crystallographic phase of TiO(2) for the screen-printed active layer have been characterized, resulting in the ratio of anatase:rutile being 80:20. Under exposure to sunlight and a given condition employed in this study, the optimized film area:water volume of 1:2.62 has shown a significant ability to reduce the E. coli cells in water samples. The ratio of surface area of photocatalytic active base to volume of water medium is believed to play a predominant role facilitating the cells inactivation. The kinetic rate of inactivation and its behavior are also described in terms of adsorption of reaction species at different contact times. |
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