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A novel dual-collimation batch reactor for determination of ultraviolet inactivation rate constants for microorganisms in aqueous suspensions.
Martin-SB Jr.; Shogren-ES; Blum-DH; Kremer-PA; Bahnfleth-WP; Freihaut-JD
Proceedings of the 10th International Conference on Healthy Buildings, July 8-12, 2012, Brisbane, Australia. Santa Cruz, CA: International Society of Indoor Air Quality and Climate, 2012 Jul; 1:322-327
We developed, characterized, and tested a new dual-collimation aqueous UV reactor to improve the accuracy and consistency of aqueous k-value determinations. This new system is unique because it collimates UV energy from a single lamp in two opposite directions. The design provides two distinct advantages over traditional single-collimation systems: 1) realtime UV dose (fluence) determination; and 2) simple actinometric determination of the Reactor Factor (RF = 1.06) that relates measured irradiance levels to actual irradiance levels experienced by the microbial suspension. This RF replaces three of the four typical correction factors required for single-collimation reactors. Using this dual-collimation reactor, Bacillus subtilis spores demonstrated inactivation following the classic multi-hit model with k=0.1395 cm 2/mJ. Aspergillus niger spores exhibited two-stage decay with a shoulder, with the resistant fraction of the population (f) of 0.251, k 1=0.1968 cm2/mJ, k2=0.0426 cm2/mJ.
Aqueous-solutions; Ultraviolet-light; Reaction-rates; Microbial-test-systems; Microorganisms; Bacteria; Fungi; Author Keywords: Collimated-beam reactor; Ultraviolet germicidal irradiation; Chemical actinometry
Proceedings of the 10th International Conference on Healthy Buildings, July 8-12, 2012, Brisbane, Australia
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