Abstract: A method for gas phase application of chlorine dioxide within an enclosed volume that includes the steps of: climatizing the enclosed volume to achieve a relative humidity (RH) in the range of about 5% to about 56%; generating chlorine dioxide gas; and introducing the chlorine dioxide gas under specified conditions of chlorine dioxide gas concentration and contact time, the specified conditions being effective to eliminate contaminants within the closed volume, and further to mitigate corrosion within the enclosed volume during the gas phase application.

Abstract: Systems and methods to reduce bioburden on at least a portion of a fluid transfer port include supplying a dose of radiation to the portion in optical communication with at least one source of radiation. In an illustrative example, a medical container, such as a vial or IV bag, receives a dose of ultraviolet (UV) energy substantially at a predetermined region of a fluid transfer site. In some examples, such a sanitization process may precede a fluid transfer operation in which a fluid is transferred into or out of the medical container by passing through the sanitized region. Such fluid transfers may be used in automated or semi-automated pharmaceutical processes, such as drug reconstitution. Various embodiments may further include one or more seal assemblies, each seal assembly having an aperture through which the radiation dose is supplied from the source to a controlled region on the fluid transfer port.

Abstract: By a method and a device for preventing corrosion on and in the region of a gas inlet nozzle during nitric acid condensation, contact of the condensing gas with the nozzle and with the surroundings of the nozzle are supposed to be minimized. This is achieved in that the gas inlet nozzle has a sleeve on the inside in the transition region to the interior of the condenser, by which sleeve a gas inlet orifice in the form of an annular gap is formed, whereby the annular space is provided with at least one feed opening for secondary air, so that an enveloping flow of secondary air is produced around the entering NO gas.

Abstract: A dispenser fixture for dispersing aromatic vapors into a facility includes an elongated dispenser chamber bounded by end walls, one containing a motor driven fan and the other wall containing fixtures for supplying and controlling electrical current for powering the fan motor. The chamber, containing trays supporting a replaceable supply of aromatic material, presents the aromatic material to an air flow passing into apertures positioned near or in the other wall such that a carrier arm supporting the fixture orientates the fan motor to discharge air enriched with aromatic vapors in a horizontal direction into the facility. The fixture includes upstanding side walls joining the end walls, a floor wall joining the side walls and the end walls, and a top wall overlying the side and end walls for enclosing the aromatic materials in the chamber. The dispenser fixture may be made of a hard plastic or metal.

Abstract: The present invention relates to a cigar humidor, comprising: a hollow housing; a lid connected to the housing; a germicidal light assembly positioned inside the housing for disinfecting cigars; and a platform transparent to ultraviolet light produced by the assembly.

Abstract: The invention relates to a method for inactivating pathogens such as bacteria and viruses and/or leucocytes in thrombocyte concentrations by irradiation in flexible containers with ultra-violet light using agitation. The blood product is packaged in a flexible bag to permit the intermixing of the fluid by agitation (tilting, rotation, translation). This is also promoted by the filling of the bag to a maximum 30% of the filling capacity.

Abstract: A new, novel and useful disinfection and purification system comprised of organic compounds in synergistic action with selected metal ions and method of manufacture and use. One of the benefits that is derived from this system is the ability to quickly and easily treat a surface, fluid or medium for disinfection of bacteria, fungi, viruses, algae and protozoans, with a non-toxic, non-chlorinated mixture that effectively kills all such organisms in minutes or hours. The disinfection and purification system remains effective for long periods of time maintaining its disinfection capacity making it highly effective for stored or transported mediums such as potable drinking water. The disinfection and purification system may be incorporated with carbon block or membrane filters to disinfect filtered liquids such as water to render it potable.

Abstract: A method and apparatus disinfecting a computer keyboard includes a metal ion treatment applied to the computer keyboard and other user input devices. A further measure taken is the installation of a shutoff mechanism in the link connecting the computer keyboard to the computer system to open the data connections between the keyboard and host system. Another measure is the periodic and reiterated wipedown of the keyboard and ancillary input devices with an antiseptic wipe. The shutoff mechanism is turned off before the wipedown procedure is carried out, to prevent any incidental keyboard entries made during the wipedown process from being transmitted to the host system.

Abstract: An apparatus and method are for disinfection and purification of a liquid, gaseous or solid phase, or a mixture thereof. The apparatus includes: a central electrode, a dielectric layer adjacent to the electrode, a first area adjacent to the dielectric layer, and is configured to introduce a first medium into the first area, a second area adjacent to the first area. The apparatus is also configured to introduce a second medium into the second area, and for creating a plasma in the first medium, while the first medium is present in the first area, by applying a voltage between the first electrode and a second electrode. An injector injects the plasma into the second area, in order to be mixed with the second medium.

Abstract: An apparatus comprising a chamber where a base concentrate common to at least a first flavored food product and a second flavored food product is formed, the first flavored food product having different flavoring than the second flavored food product, the base concentrate having a first temperature. The apparatus also comprises a process line that receives the base concentrate from the chamber, heated liquid from a heated liquid source, and flavoring from either a first flavor source or a second flavor source to form a mixture of base concentrate, heated liquid and flavoring. The mixture has a has second temperature sufficient to achieve a change in the mixture selected from the group consisting of microbial change, chemical change, biochemical change, and enzymatic change, and combinations thereof. A method is also disclosed for change over from forming a first flavored food product to forming a second flavored food product.

Abstract: Disclosed is a method of controlling a real-time oxidation-reduction potential in a hot water system to inhibit corrosion in the hot water system. The method includes defining one or more operational protective zones in the hot water system. One or more of the operational protective zones includes an oxidation-reduction potential probe that is operable to measure a real-time oxidation-reduction potential in the hot water system at operating temperature and pressure. The probe transmits the measured real-time potential to the controller, which assesses and interprets the transmitted potential to determine whether it conforms to an oxidation-reduction potential setting. If the measured potential does not conform the oxidation-reduction potential setting, the controller is operable to feed one or more active chemical species into the hot water system.

Abstract: A germicidal system and method for deactivating pathogens on the surface of a bodily extremity protected by a prophylactic covering substantially opaque to UV-C radiation. The device includes an enclosure having one or more openings through which the extremity can be inserted. The enclosure contains a radiation source configured to produce germicidal radiation having a wavelength of about 253.7 nm. The openings are configured relative to the radiation source such that the inserted extremity is in close proximity to the radiation source. The prophylactic covered extremity is preferably a gloved hand thereby sanitizing the surface of the glove. The extremity inserted is preferably exposed for a predetermined period of time to ensure a desired level of sanitization. Optionally, the device can include an orientation detector to determine the position of the user's hand and the spread of the user's fingers, and a surface detector to determine whether the user's hand is covered by a glove.

Abstract: The invention relates to the use of a cleaning agent that contains surfactants and has a pH value of at least 11 when diluted in an aqueous solution and ready for use. Said cleaning agent is used to destabilize prions during mechanical and manual cleaning and/or disinfection of medical and/or surgical instruments and appliances. It has been recognized that this combination enables a reliable destabilization of prions during the mechanical reconditioning of surgical instruments.

Abstract: An autoclave for the sterilization of clinical dental instruments is described, of the type comprising a sterilization chamber (1) equipped with a series of appliance fittings (4) for the inflow and outflow of fluids, and apt to contain a load of instruments onto which to carry through a sterilization cycle, characterized in that said appliance fittings (4) are gathered on at least one connection body or partition (3), with which a reducing container (7) is quickly able to be engaged and disengaged, which container has a volume apt to contain at least one instrument to be sterilized, the inner volume of such container (7) communicating with said appliance fittings (4) and said container (7) being apt to be entirely contained within said sterilization chamber (1). The small-volume container for said autoclave is further described, as well as a full treatment system employing said container.

Abstract: The present invention is directed to a chemical oxygen generator to produce cool oxygen gas comprising: a. a charge housing, b. a solid but porous charge contained in the said housing, the charge being made of a chemical mixture that generates oxygen upon decomposition and that will undergo a self-sustained exothermal decomposition after initiation, the said charge containing at most 3.0 wt. % of binder material, the said porous charge allows the generated oxygen to pass through the charge without damaging the virgin material and without creating volumetric burning, the said charge is mounted in the housing in such a way that the generated oxygen passes through the charge and under the pressure difference flows from the moving decomposition front towards the vent, c. an ignition device mounted at one end of the cartridge in such a way that it is capable to initiate a self-sustained decomposition of the charge at the charge surface adjacent to the initiator, d.

Abstract: A sterile device immersed in a sterile buffer and a method for providing same. The sterile device may be a medical device such as a biosensor having a biomolecule as a sensing element such as, for example, a glucose oxidase enzyme. The buffer may be a bicarbonate solution. Both the device and the buffer may be packaged and stored over long term while maintaining sterilization. The sterilization method may comprise a combination of gaseous, liquid and light sterilization.

Abstract: In an exemplary embodiment, the present invention includes at least one reservoir with a delivery mechanism in communication therewith. The delivery mechanism draws an air treatment material from the reservoir and provides the air treatment material in response to a decreased level of active air treatment material or the detection of a malodor. Additionally, the delivery mechanism includes a control system and a detection system. The control system activates the detection system at a timed interval or in response to a change in one or more ambient conditions (e.g., motion, temperature, light, humidity, etc.). Once activated, the detection system samples the environment for either the level of active air treatment material or the quality of the environment.

Abstract: An air sanitization system including a reactive oxygen species generator, a variable speed fan, a pathogen sensor and a controller. The reactive oxygen species generator generates reactive oxygen species from an oxygen-containing gas and discharges the reactive oxygen species to a conditioned space. The variable speed fan directs the oxygen-containing gas to the reactive oxygen species generator at a controlled speed. The pathogen sensor senses a level of airborne pathogens in the conditioned space and generates a signal indicative of the level of pathogens sensed. The controller receives the signal from the pathogen sensor and varies the speed of the variable speed fan in response to the signal to decrease a speed of the variable speed fan in response to an increase in the level of airborne pathogens sensed by the pathogen sensor.

Abstract: The disclosure is directed to a sterilized medical device including a non-polymerized blend including a silicone matrix material and a radiation resistant component.

Abstract: A reusable container for the sterile transfer of pharmaceutical recipients, in particular of syringe bodies. The container comprises an outer case and a sterilizable interior, wherein the interior is microbially isolated from the environment of the container. The interior has at least one holder for accommodating at least one nest for storing a plurality of pharmaceutical recipients. The nest can be removably accommodated in the holder. The container further has at least one container door for removing or introducing the nest into the interior and at least one lock for coupling the container to a sterile space. The lock is configured in such a way that, after coupling to the sterile space, it is possible to open the container door without substantially suspending sterility.