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Comparison of different Far-UVC sources with regards to intensity stability, estimated antimicrobial efficiency and potential human hazard in comparison to a conventional UVC lamp
1 , 1 , 2 , 3 , * 1
1  Technische Hochschule Ulm (University of Applied Science), Albert-Einstein-Allee 55, 89081 Ulm (Germany)
2  Zimmer MedizinSysteme GmbH, Junkersstraße 9, 89231 Neu-Ulm (Germany)
3  University Hospital Jena, Am Klinikum 1, 07747 Jena (Germany)
Academic Editor: Ambra Giannetti

Abstract:

The recently much-noticed Far-UVC spectral range offers the possibility of inactivating pathogens without necessarily posing a major danger to humans. Unfortunately, there are various Far-UVC sources that differ significantly in their longer wavelength UVC emission and, subsequently, in their risk potential. Therefore, a simple assessment method for Far-UVC sources is presented here. In addition, the temporal intensity stability of Far-UVC sources was examined in order to reduce possible errors in irradiation measurements. For this purpose, four far-UVC sources and a conventional Hg lamp were each spectrally measured over 60 h and mathematically evaluated for their antimicrobial effect and hazard potential using available standard data. Only two filtered KrCl lamps were found to emit at stable intensity after a warm-up time of 10 min. With regard to the antimicrobial effect, the radiation efficiencies of all examined (Far-) UVC sources were more or less similar. However, the calculated differences in the potential human hazard to eyes and skin were more than one order of magnitude. The two filtered KrCl lamps were the safest, followed by an unfiltered KrCl lamp, a Far-UVC LED and, finally, the Hg lamp. When experimenting with these Far-UVC radiation sources, the irradiance should be checked more than once. If UVC radiation is to be or could be applied in the presence of humans, filtered KrCl lamps are a much better choice than any other available Far-UVC sources.

Keywords: Far-UVC; UVC; long-term stability; risk assessment; threshold limit values, antimicrobial impact

 
 
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