A model is presented to account for inactivation by UV light of microorganisms on the surfaces of solid materials. In the model, the surface is divided into a discrete number of zones, each having a characteristic exposure factor (alpha). This is the ratio of UV intensity actually "seen" by the microorganism to that incident on the surface. Application of the model requires inactivation data obtained under conditions where the surface microorganisms are fully exposed to incident UV (alpha = 1) as well as kinetic inactivation data for the same microorganisms actually present on the surface of interest during UV irradiation. The kinetics in question may apply either to a single species or to the characteristic microflora associated with a particular material. Standard nonlinear programming techniques were used to determine the number of zones among which the microorganisms are distributed, the alpha for each zone, and the fraction of the microbial population present in each zone. The model was applied to data previously published by Gardner and Shama for UV inactivation of Bacillus subtilis spores on the surfaces of filter papers and also to the data of Stermer et al. for UV irradiation of beef. Good representation of the kinetics was obtained, and a maximum of three zones was required to adequately represent the experimental data. One direct application of the model is that it yields quantitative information about the UV fluences necessary to achieve specified reductions in microbial viability.

Inactivation of spores of Bacillus subtilis (ATCC 6633) on two different grades of cellulose filter paper (Whatman Grades 2 and 6), by ultraviolet light (u.v.), at an intensity of approximately 4·5 Wm−2 and at fluences of up to 2 × 103 Jm−2, and u.v. in the presence of hydrogen peroxide, is described in terms of multi‐target and single hit–single target kinetic expressions. Wet spores were inactivated at rates ranging from 6·7 to 10·6 higher than that of dry spores on both grades of filter paper. In addition, spore inactivation was up to 5·6 times more rapid on Grade 2 filter paper. Synergistic inactivation was seen to occur when spores were irradiated in the presence of 1% (w/v) hydrogen peroxide with rates up to 5·3 times higher than with treatment solely by u.v. The results obtained are discussed in general terms with particular reference to surface characteristics which might provide shielding to micro‐organisms from incident u.v. light.

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