4.7 Article

Design and performance evaluation of a photocatalytic reactor for indoor air disinfection

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 28, Issue 19, Pages 23859-23867

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-020-11663-6

Keywords

Bioaerosols; Air purification device; Packed bed; Photocatalysis; Efficiency parameters; Radiation absorption

Funding

  1. Universidad Nacional del Litoral (UNL) [CAI+ D 50020150100020LI, CAI+D 50420150100009LI]
  2. Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) [112 2015 0100093]
  3. Agencia Nacional de Promocion Cientifica y Tecnologica (ANPCyT) [PICT-2014-1020]

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A photocatalytic device for removing airborne microorganisms was developed and tested in this study, showing complete removal of high loads of microorganisms in the air stream in just 1 hour. However, longer irradiation periods were required for inactivating retained bacteria in the reactor bed. Efficiency parameters were calculated to evaluate the influence of irradiation conditions on photocatalytic inactivation of bacteria attached to the coated rings.
Since COVID-19 pandemic, indoor air quality control has become a priority, and the development of air purification devices effective for disinfecting airborne viruses and bacteria is of outmost relevance. In this work, a photocatalytic device for the removal of airborne microorganisms is presented. It is an annular reactor filled with TiO2-coated glass rings and irradiated internally and externally by UV-A lamps. B. subtilis spores and vegetative cells have been employed as model biological pollutants. Three types of assays with aerosolized bacterial suspensions were performed to evaluate distinct purification processes: filtration, photocatalytic inactivation in the air phase, and photocatalytic inactivation over the TiO2-coated rings. The radiation distribution inside the reactor was analysed by performing Monte Carlo simulations of photon absorption in the photocatalytic bed. Complete removal of a high load of microorganisms in the air stream could be achieved in 1 h. Nevertheless, inactivation of retained bacteria in the reactor bed required longer irradiation periods: after 8 h under internal and external irradiation, the initial concentration of retained spores and vegetative cells was reduced by 68% and 99%, respectively. Efficiency parameters were also calculated to evaluate the influence of the irradiation conditions on the photocatalytic inactivation of bacteria attached at the coated rings.

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