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A response to the chemical or biological contamination of aircraft requires the use of a suitable decontaminant. Among possible chemical decontaminants, vapour phase hydrogen peroxide appears to be a likely candidate in terms of a combination of efficacy, low environmental impact and potential for materials compatibility. The present paper examines the effect of hydrogen peroxide, both in the vapour phase and as a liquid concentrate on two common structural materials used in aviation, namely 2024 and 7075 age hardenable aluminium alloys and on 304 austenitic stainless steel, the latter as employed in galley and lavatory surfaces. The present paper characterises both the effects of hydrogen peroxide on the microstructure of the materials and the impact that decontamination has on the tensile properties and corrosion resistance of these materials. Microstructural effects are both relatively small in magnitude and confined to a region immediately beside the exposed surface. No systematic effect is found on either the tensile properties or the post-exposure corrosion resistance of the three alloys examined. These observations are encouraging in terms of the use of vapour phase hydrogen peroxide for decontamination applications.

Austenitic stainless steels, widely used in food processing, undergo microstructural changes during welding, resulting in three distinctive zones: weld metal, heat-affected zone, and base metal. This research was conducted to determine the attachment of Listeria monocytogenes in these three zones before and after exposure to a corrosive environment. All experiments were done with tungsten inert gas welding of type 304 stainless steel. The four welding treatments were large or small beads with high or low heat. After welding, all surfaces were polished to an equivalent surface finish. A 10-microl droplet of an L. monocytogenes suspension was placed on the test surfaces. After 3 h at 23 degrees C, the surfaces were washed and prepared for scanning electron microscopy, which was used to determine attachment of L. monocytogenes by counting cells remaining on each test surface. In general, bacteria were randomly distributed on each surface type. However, differences in surface area of inoculum due to differences in interfacial energy (as manifested by the contact angle) were apparent and required normalization of bacterial count data. There were no differences (P > 0.05) in numbers of bacteria on the three surface zones. However, after exposure to the corrosive medium, numbers of bacteria on the three zones were higher (P < 0.05) than those on the corresponding zones of noncorroded surfaces. For the corroded surfaces, bacterial counts on the base metal were lower (P < 0.05) than those on heat-affected and weld zones.