Abstract: Hydrogen peroxide is vaporized (20) and mixed (30) with ammonia gas in a ratio between 1:1 and 1:0.0001. The peroxide and ammonia vapor mixture are conveyed to a treatment area (10) to neutralize V-type, H-type, or G-type chemical agents, pathogens, biotoxins, spores, prions, and the like. The ammonia provides the primary deactivating agent for G-type agents with the peroxide acting as an accelerator. The peroxide acts as the primary agent for deactivating V-type and H-type agents, pathogens, biotoxins, spores, and prions. The ammonia acts as an accelerator in at least some of these peroxide deactivation reactions.

Abstract: A cover assembly for enclosing data connections on a monitor that is mounted to a tubular support arm that has data cables extending therethrough. The cover assembly includes a sleeve surrounding a portion of the tubular support arm. The sleeve defines a passage between the sleeve and the tubular support arm for the cables to extend therethrough. A shield is connected to the second end of the tubular support arm. The shield has an arcuate outer surface with an aperture therethrough. The aperture is dimensioned to receive one end of the sleeve. A cover having an inner arcuate surface mounted to the monitor to be movable therewith. The cover encloses the shield with the arcuate outer surface of the shield facing the arcuate inner surface of the cover. The sleeve extends through a slot in the cover, wherein the monitor is rotatable about a first axis and further is rotatable about a second axis that is perpendicular to the first axis.

Abstract: A method and apparatus for neutralizing biological and/or chemical warfare agents using an ozone-containing solution. The ozone-containing solution is produced by combining ozone-containing gas with an ozone vehicle, such as an organic solution. The ozone-vehicle prolongs the shelf life of the ozone to allow for extended periods of storage. A storage container is used to store the ozone-containing solution and facilitate its transportation to an environment contaminated by the biological and/or chemical warfare agents, or near a potential site for biological or chemical attack. The ozone-containing solution is drawn out of the storage container to apply it to a contaminated environment.

Abstract: A method of treating the surfaces of medical instruments which are contaminated with prions includes contacting the surface with a composition containing a source of peroxide ions, such as hydrogen peroxide, at a molar concentration of at least 1.5M peroxide (equivalent to approximately 5% hydrogen peroxide) and preferably, about 2M peroxide (approximately 7% hydrogen peroxide). The composition is optionally in the form of a gel. The composition is retained in contact with the surfaces for about 1–2 hours until all or substantially all prion contamination is removed.

Abstract: A pulsed electric field system for inactivation of biological agents on a dielectric sheet material. The pulsed electric field (PEF) system includes a dielectric layer located between an active electrode and a ground electrode, wherein said dielectric layer has a uniform surface profile. A pulsed electric field is provided in a gap between the dielectric layer and the active electrode. A transport assembly moves the dielectric sheet material through the gap. In a preferred embodiment, the system also includes sensors for sensing the position of the dielectric sheet material as it passes through the pulsed electric field.

Abstract: A method and apparatus for accelerating charged particles. The charged particles accelerate as they travel through electric fields produced by a plurality of accelerating elements having first and second electrode plates. A magnetic field produced by a pair of magnets causes the charged particles to travel in a generally circular orbit.

Abstract: Almonds are often harvested off the ground from around trees which have been fertilized with manure. Potentially hazardous microbes are transferred from the husk to the shells during the dehusking process. During deshelling, shell dust with attached microbes escapes into the atmosphere and can permeate an entire packaging facility, contaminating previously uncontaminated packaging and food products. A sterile barrier is provided around the packaging facility. As the almonds in the shell are passed through the barrier, their shells are sanitized. After the nutmeats are removed from the shells, the nutmeats are sanitized again and packaged in packaging which has been sanitized.

Abstract: A surface which carries a material which is infected with prions is cleaned with an alkaline cleaning solution to remove as much proteinaceous material as possible from the surface. The cleaning agent is an alkaline cleaning agent which attacks prions remaining on the surface and which attacks prions removed from the surface during the cleaning step. After the cleaning solution is drained, a solution of surfactants, buffers, and heavy metal free corrosion inhibitors is circulated over the surface at 50°–60° C. The surfactants disperse and unclump the prion-contaminated material. A strong oxidant, preferably peracetic acid, is added to the solution to bring the peracetic acid concentration to 1,000–2,500 ppm. The peracetic acid or other strong oxidant attacks the prions, particularly the unclumped prion strands, deactivating the prions. After rinsing and drying, the surface may be wrapped in a microbe impermeable barrier and subjected to terminal sterilization, such as steam autoclaving.

Abstract: A method of forming a microporous fluoropolymer membrane, comprising the steps of: irradiating a sheet of fluoropolymer at a dosage level below the rupture energy of the carbon-to-fluorine (C—F) bonds of the fluoropolymer, but sufficient to rupture carbon-to-carbon (C—C) bonds; and exposing the sheet of fluoropolymer to an etchant for a period of time sufficient to etch away disrupted atoms and molecules, wherein continuous micropassages are formed through the sheet.

Abstract: A device for transport of an electron beam from an accelerator to a product to be irradiated, comprised of a passive plasma channel for forming a low density plasma by ionizing gas molecules in a chamber under low pressure conditions. The device being adjustable in size such that the chamber formed by the device occupies a majority of the distance between the e-beam accelerator and the product to be irradiated.

Abstract: A method and apparatus for monitoring at least one of steam purity and steam quality for steam used in a decontamination process. A capacitor is exposed to the steam, wherein the steam acts as a dielectric between the plates of the capacitor. Permittivity of the dielectric is affected by the purity and/or quality of the steam, and thus a measurement of electrical properties of the capacitor is used to monitor steam purity and/or quality.

Abstract: A system capable of cleaning and disinfecting a filter. A filter element is flushed with a disinfectant solution in a direction opposite to fluid filtration. A filter integrity test checks the integrity of the filter by pressurizing the filter.

Abstract: A system for sterilizing or microbially deactivating instruments and devices. The system includes a circulation system for circulating a microbial deactivation fluid through a chamber for containing the instruments and devices. The chamber forms a portion of the circulation system. The system further includes a fluid over-flow/make-up air assembly. The fluid over-flow/make-up air assembly includes a manifold having an inner cavity that is in fluid communication with the circulation system, an overflow port in the manifold, and an overflow valve assembly disposed in the manifold allowing fluid flow from the cavity to the overflow port when a pressure in the cavity exceeds a pressure in the overflow port by a predetermined amount. A filter assembly is attached to the manifold. The filter assembly has a filter valve assembly in communication with the cavity.

Abstract: A method of microbially decontaminating at least one of a defined area and an item within the defined area. The method includes the steps of (a) inductively heating a block comprising an electrically non-conductive material and an electromagnetically responsive material; (b) passing an atomized liquid into an interior passage defined by the block, wherein the inductively heated block vaporizes the atomized liquid that contacts walls of the passage to form an antimicrobial vapor; and (c) flowing the vapor out of the block to the defined area to microbially decontaminate at least one of the defined area and the item.

Abstract: Food products, such as precooked meats, sausages, and the like are microbially decontaminated in their cooking packages to remove surface microorganism contamination from the packages. The cooking packages are removed and the food products optionally subjected to further processing, such as slicing, and then packaged in aseptic packaging. The microbial decontamination step, further processing and packaging are carried out in a clean room which is maintained to a high level of sterilization or disinfection to minimize or eliminate contamination of the food products with pathogenic microorganisms such as Listeria Monocytogenes. The food products thus leave the packaging plant with a much higher assurance of food safety than is found in a conventional packaging plant.

Abstract: A method and apparatus for monitoring the concentration of metal cations in a chemical solution. In a preferred embodiment, the chemical solution is a solution for derouging or passivating stainless steel. A capacitive sensor provides data indicative of the concentration of chemical components (e.g., iron or chromium) in the chemical solution.

Abstract: A vapor decontamination system for decontaminating a defined region. The system is comprised of a chamber defining a region, and a generator for generating vaporized hydrogen peroxide from a solution of hydrogen peroxide and water. A closed loop circulating system is provided for supplying the vaporized hydrogen peroxide to the region. A destroyer breaks down the vaporized hydrogen peroxide, and a sensor downstream from the destroyer is operable to sense moisture in the system and provide electrical signals indicative thereof. A controller determines the presence of vaporized hydrogen peroxide in the region based upon the electrical signals from the sensor.

Abstract: A chemical concentration detecting system for determining the relative concentration of a chemical component in a gas mixture. The gas mixture may include chemical components that are antimicrobial chemicals, as well as chemical components that are base chemicals, acting as a diluent for the antimicrobial chemical, or as a vehicle or carrier for the antimicrobial chemical. A capacitor is exposed to the gas mixture, wherein the gas mixture acts as a dielectric between the plates of the capacitor. Permittivity of the dielectric is affected by the relative concentrations of the chemical components, and thus a measurement of the capacitance is used to determine the relative concentration levels of the chemical components in the gas mixture.

Abstract: An inflatable seal member for providing a fluid-tight seal. The inflatable seal member is particularly well suited to sealing a processing chamber having pressurized fluids therein. Outward forces (exerted by air pressure) to the inner surfaces of the seal member counteract inward forces (exerted by fluid pressure) to the outer surfaces of the seal member.

Abstract: A BIER vessel evaluates biological indicators for sterilization processes. By flowing gaseous sterilant, such as vaporized hydrogen peroxide, through a chamber (12) before, during, and after introducing the indicators, the indicators are instantaneously exposed to preselected steady state conditions, allowing accurate and reproducible evaluation of the indicator response. A door (32) to an opening (30) in the chamber opens for introducing the indicators to the chamber without appreciably disturbing the steady state conditions therein. After a preselected time, the biological indicators are removed and evaluated for remaining biological activity.