Abstract: A sterilizing cabinet performs a method of processing a medical device, such as a used medical device or an otherwise non-sterile medical device. The method includes receiving input from a user selecting a sterilization cycle from a plurality of available sterilization cycles. The sterilizing cabinet identifies a biological indicator associated with the selected sterilization cycle. The sterilizing cabinet prompts the user via a touch screen display to place the medical device and the biological indicator into a sterilization chamber of a sterilizing cabinet. The sterilizing cabinet performs load conditioning on the medical device in the sterilization chamber. The sterilizing cabinet then performs the selected sterilization cycle on the medical device in the sterilization chamber after completing the act of load conditioning.

Abstract: A method for sterilizing biological materials is disclosed. A dehydrated biological material is put into a closed container. The closed container is then decompressed under a vacuum. Subsequently, 0.01 g/m3 to 1000 g/m3 of a sterilizing gas, i.e., pure ozone, is introduced into the container for a period of time until the biological material is sterilized.

Abstract: A system and method of sterilization for medical instruments within a hydrogen peroxide sterilization process is provided. A medical instrument is housed in a sterilization tray, wherein the sterilization tray is formed from polypropylene and a glass material. The medical instrument and sterilization tray are subjected to a hydrogen peroxide sterilant.

Abstract: A system and method of abating air pollution and stimulating crop growth. A reagent is introduced to a crop canopy to neutralize air pollutants within said canopy, wherein the reagent induces an oxidation-reduction chemical reaction with the air pollution present throughout the acreage of crops, and by means of the reaction effectually neutralizes the harmful effects of the air pollutants on the crops. The reagent is diluted using a venturi valve or other means. The flow rate of said reagent is regulated using an electronic control unit, based on data collected from at least one type of sensor in the canopy that is in communication with the control unit.

Abstract: Vaporized hydrogen peroxide is used for decontamination of enclosed and sealed areas. It is capable of destroying all forms of microbial life. It is commonly produced from a solution of liquid H2O2 and water, by means of generators specifically designed for the purpose. The present invention provides a combined source for heating steam and vaporized hydrogen peroxide and a method for simultaneously supplying steam and vaporized hydrogen peroxide. A device according to the invention comprises a chamber adapted for receiving water through an inlet and expelling steam through an outlet. A vessel for receiving and vaporizing hydrogen peroxide solution is provided in close contact with the chamber. Heat from the water vapor in the chamber is allowed to supply the required energy for producing hydrogen peroxide vapor in the vessel from an aqueous solution.

Abstract: A preform is easily and speedily sterilized. A number of preforms (1), each having a bottomed tubular shape, are laid on a conveyer (4) in a scraggly overturned manner, these preforms passes inside a chamber (5) together with the conveyer, and hydrogen peroxide water mist is sprayed from both sides of the conveyer in a direction crossing the conveyer in the chamber, thereby adhering the sprayed hydrogen peroxide water to inner and outer surfaces of the preforms (1) on the conveyer (4).

Abstract: A method of sterilizing an article is provided. The method includes providing sterilization wrap system with which to wrap the article to be sterilized. The sterilization wrap system comprises a plurality of wrap units configured in a stack, at least one wrap unit in the stack being detachably attached to at least one other wrap unit in the stack.

Abstract: The present application provides an aqueous, stable, VOC-free microemulsion based antimicrobial disinfectant and/or cleaning concentrate composition capable of inhibiting or killing gram(+), gram(?) and methicillin-resistant Staphylococcus aureus (MRSA) comprising (i) a water-soluble matrix composite made of (a) water-soluble polymer, and (b) water-soluble surfactant; (ii) a blend of antimicrobial agents comprising (a) at least one compound selected from phenols, halogenated phenols, derivatives of phenols, derivatives of halogenated phenols, bis -phenols, cresols, resorcinols, halogenated hydroxyl diphenylethers, anilides or combinations thereof; and (b) at least one compound derived from essential oils; and (iii) optionally, one or more additives. Also, there is described a method of use and process for preparing the composition.

Abstract: A method for disinfecting a bottle, in particular a baby bottle, including a bottle jacket which is open on both ends, wherein, in a dispensing position, a bottom cap is fastened to a bottom-side opening and a teat is fastened to a teat-side opening by a fastening ring, the inner periphery of the bottom-side opening being larger than the outer periphery of the fastening ring, wherein, for transfer into a disinfection position, the bottom cap is removed from the bottle jacket, the teat and the fastening ring are placed onto the bottom cap and introduced into the bottle jacket, the bottom cap is attached to the bottom-side opening, a disinfectant is filled into the bottle jacket before the bottle is heated for disinfection.

Abstract: Contaminants are filtered from a fluid flow stream and the filter is regenerated by a process including steps of: providing a filter material comprising both carbon and potassium iodide; passing a contaminated fluid stream in contact with the filter material; adsorbing contaminants from the fluid stream onto surfaces in the filter material; passing an electric current through the filter material with adsorbed contaminant thereon; disassociating contaminant from the surfaces of the filter material; and removing disassociated contaminant from the filter material by carrying away the disassociated contaminant in a fluid flow mass. Separately, a stable, active iodine solution is also provided for numerous deodorizing and disinfecting applications.

Abstract: A system providing a sterile connection between a sensor probe and a fluid processing apparatus (e.g., a bioreactor) includes a first probe receiving element mountable to the fluid processing apparatus and a second probe receiving element having a gas-permeable contaminant barrier material and coupleable to the first probe receiving element. A sensor probe may be mounted to the second probe receiving element, with the combination being sterilized with a sterilant gas such as steam. Following such sterilization, connection between the first and second probe receiving elements is made through matable sterile couplings, and the probe is insertable through the coupled receiving elements to a position in fluid contact with the interior of the fluid processing apparatus.

Abstract: A device for generating a sterilizing gas includes a methanol gas generation device (11) for vaporizing methanol to generate a methanol gas, a tubular part (12) and a catalyst section (13). The tubular section (12) is arranged on top of the methanol gas generation device (11) to provide a flow path for upwardly directing the methanol gas generated by the methanol gas generation device by natural convection. The tubular section also operates to mix the methanol gas with a predetermined proportion of air. The catalyst section (13) is arranged on top of the tubular section (12) for turning the methanol gas mixed with the air at the predetermined proportion in the tubular section (12) into radicals by a catalyzed reaction. The catalyst section (13) is formed by a turn-into-radical reaction catalyst layer (30) obtained on forming a thin metal sheet (35a) to a honeycomb structure.

Abstract: An apparatus for indicating biological content within a container is provided. The apparatus includes a medical sterilization container having a cover removably attached to the medical sterilization container. An enclosable, sterilizable interior compartment is formed by the medical sterilization container and the cover, wherein the interior compartment is sized to house at least one medical instrument. A biological indicator is located at least partially in communication with the interior compartment, wherein the biological indicator provides at least one indication of biological content within the interior compartment after the medical sterilization container and cover are subjected to a sterilization process.

Abstract: A method for disinfecting a volume or surfaces bounding a volume comprising nebulizing a solution comprising a sterilizing agent in a solvent having a lower boiling point than the sterilizing agent to form a nebulant. The nebulant is subjected to energy of a kind and for a duration sufficient to vaporize solvent in preference to sterilizing agent to increase the concentration of the agent in the nebulant particles. Vaporized solvent is removed from the gas stream at or above atmospheric pressure and, if necessary, the nebulant is cooled to below 70° C. The volume or surfaces are exposed to the nebulant for a time sufficient to sterilize said volume or surfaces. Also, apparatus for carrying out the method.

Abstract: Method of disinfecting floors by injecting hot, wet compressed air into the floor, this air being produced by a generator, whether on board or not, consisting of two cylinders of different diameters, one (1) of large diameter into which the atmospheric air is drawn and then compressed in a chamber (11) to a pressure and temperature sufficient to allow almost instantaneous vaporization of a dose of liquid and the other (6), facing the chamber, of smaller diameter in which the charge of humidified compressed air will be partly expanded so as to bring it back to the chosen pressure and temperature for use in order to inject it into the floor.

Abstract: According to the invention a method (and corresponding system) of enhancing application of high intensity acoustic waves is provided, wherein acoustic waves, e.g. ultrasound, and a gaseous medium, e.g. steam, coincide at a treatment zone. This is achieved by a combination of one or more high intensity acoustic generators and/or reflectors. In this way, enhanced efficiency in an area of the gaseous medium (or where the gaseous medium is to affect something) is obtained since a second generator or a reflector is located so that the acoustic waves directly influence the gaseous medium.

Abstract: The present invention provides a method for producing a medical device, preferably an ophthalmic device, more preferably a contact lens, made of a stabilized poly(oxyalkylene)-containing polymeric material. The method of the invention comprises the steps of: curing, in a mold, a composition comprising (a) a prepolymer having at least one poly(oxyalkylene) unit, (b) a biocompatible organic multi-acid or biocompatible salt thereof in an amount sufficient to improve the stability of the poly(oxyalkylene)-containing polymer made from the composition, (c) optionally a photoinitiator or a thermal initiator, and (d) optionally one or more vinylic monomers, to form the medical device being less susceptible to oxidative degradation; and removing the medical device from the mold.

Abstract: The invention relates to a sterilization testing device comprised of a housing with a test chamber, an indicator placed therein, and with a supply for supplying the sterilization medium. According to the invention, the sterilization testing device consists of at least two housing parts that are matched to one another. A supply channel is made inside the housing part and serves to supply the sterilization medium. The supply channel is configured in such a manner that it forms the base body of the test chamber. The test chamber accommodates the indicator that indicates the completion of the sterilization process. Alternatively to this solution, the invention provides a variant, which is very effective with regard to manufacturing and which permits a quantitative statement regarding the sterilization. Webs are formed inside the housing in the at least partially meandering and/or spiral configuration of the supply channel.

Abstract: A method for sterilizing a plastic bottle in an aseptic filling system according to which at least an inner surface or an outer surface of a bottle is sterilized by injecting a heated sterilizing fluid at 65° C.-90° C. while maintaining internal pressure of the bottle at 1 kPa-20 kPa.

Abstract: A steam generation system comprises: an oxygenated water treatment (OWT) sub-system configured to generate water having oxidizing chemistry; a steam generation sub-system configured to convert the water having oxidizing chemistry into steam having oxidizing chemistry; an attemperator or other injection device or devices configured to add an oxygen scavenger to the steam having oxidizing chemistry to generate steam having less oxidizing or reducing chemistry; and a condenser configured to condense the steam having less oxidizing or reducing chemistry into condensed water.

Abstract: The present invention refers to a method of processing a biological fluid which comprises cellular components by heat treatment. The method is particularly useful for preparing biological samples for analyte detection. Further, the invention refers to a processed biological fluid comprising substantially quantitatively disintegrated cellular components.

Abstract: A method for sterilizing a plastic bottle in an aseptic filling system according to which at least an inner surface or an outer surface of a bottle is sterilized by injecting a heated sterilizing fluid at 65° C.-90° C. while maintaining internal pressure of the bottle at 1 kPa-20 kPa.

Abstract: A hydrogel having a floatability where from 40% to 90% of a solution and/or suspension to be thickened are thickened starting from the surface of the liquid and the rest of the solution and/or suspension to be thickened is thickened starting from the bottom of the container, a process for preparing the hydrogel and also its use for absorbing blood and/or body fluids, especially in hygiene articles, or for thickening aqueous solutions and/or suspensions, especially for thickening medical wastes.

Abstract: An integrated process separates salts from salty waters and electrolyzes the salts to produce chlorine products such as chlorine, hypochlorites, chlorates and/or caustic soda.

Abstract: A method for subjecting a microorganism to a combination of ozone and irradiation of UV light which has a synergistic effect on the reduction of the microorganism that may be resistant to either ozone or UV light alone. In particular, Adenovirus and Naegleria fowleri, are significantly more reduced when subjected simultaneously to the combination of ozone and UV light than when subjected only to ozone or UV light, respectively.

Abstract: A control system of a surgery autoclave is described, which is capable of establishing a sterilization cycle which includes at least a first evacuation step of a sterilization chamber and of heating of a load and a final drying step. The autoclave includes a device capable of detecting a parameter proportional to the energy used up in a step of the cycle preceding the drying step and the control system establishes at least a reduction of the drying step upon determining that, the parameter of used up energy lies below a preset threshold.

Abstract: Disclosed is a process for reclamation of waste fluids. A conditioning container is employed for receipt of waste material on a continuous flow for treatment within the container by immersible transducers producing ultrasonic acoustic waves in combination with a high level of injected ozone. The treated material exhibits superior separation properties for delivery into a centrifuge for enhanced solid waste removal. The invention discloses a cost efficient and environmentally friendly process and apparatus for cleaning and recycling of flowback, or frac water, which has been used to stimulate gas production from shale formations. The apparatus is mobile and containerized and suitable for installation at the well site.

Abstract: The present invention relates to methods of sanitizing structures, buildings, passenger occupiable vehicles, and other enclosed or enclosable spaces. More particularly, the present invention relates to a method for killing and/or removing pests and their allergens, bacteria, viruses, fungi, molds, volatile organic compounds and other dangerous substances, from such objects or enclosures.

Abstract: A system for collecting and disposing of liquid medical waste includes a fluid collection cart and a draining and cleaning station. The fluid collection cart includes a pair of containers, each of which includes a draining port and a cap. Each cap includes an outer portion having a flushing port and a bore formed therein and an inner portion having vacuum and patient ports formed therein. The inner cap portion is disposable and removably positioned within the bore of the outer cap portion. Liquid level detectors also communicate with each container. The cart also includes a regulator so a low vacuum level may be pulled on one of the containers while a full vacuum level is pulled on the other container. Fluids are collected in the containers via suction tubes connected to the patient ports. The flushing and drain ports of the containers are connected to corresponding flushing and drain connectors on the station when the containers are full so that they may be drained and flushed.

Abstract: An on board monitor for an endoscope reprocessor for monitoring the performance and order of a predetermined set of critical steps for reprocessing an endoscope. The monitor will only allow the overall system to reach the last step indicating successful completion of the process related to the critical steps representing successful reprocessing of an endoscope after the system successfully completes all of the previous critical steps and in the correct order.

Abstract: A chemical vapor sterilization process is enhanced by concentrating a germicide via condensation and re-vaporization thereof, exploiting the difference between the vapor pressures of the germicide and its solvent to extract some of the solvent during the condensation process.

Abstract: An appliance having an enclosure arranged to receive articles to be treated also includes a water container and a steam chamber with a steam outlet. A water dispenser is arranged to dispense water from the water container to the steam chamber. A heating element is thermally associated with the steam chamber. A control is arranged to selectively operate the heating element. A steam path extends between the steam outlet and the enclosure. A chemical dispenser is positioned along the steam path. The heating element heats water in the steam chamber to create steam, and the chemical dispenser adds a chemical to the steam as the steam passes through the steam path.

Abstract: There is provided a packaging container which reserves an acidic beverage having a relatively high acidity and allows spore to remain properly without corrupting and the acidic beverage can be aseptically filled and reserved at a normal temperature with low cost without utilizing a container having high heat-proof property and expensive manufacturing equipment. An interior of a container 2 is sterilized by a sterilizing agent “b” and a heated water “c” so as to allow bacterial spore to be alive but not to allow bacteria vegetative cell, mold and yeast to be alive, and a sterilized content “a” having an acidity of an extent of suppressing germination of the bacteria spore fills the container at a normal temperature or low temperature, and then the container is sealed by a lid 3, thereby providing a packaging container 1.

Abstract: A single-use sterilization container for use in the sterilization of medical instruments is provided. The sterilization container includes a lid having peripheral portion defined by a frangible region. Upon activation of the frangible region, the peripheral portion may be removed rendering the sterilization container inoperable for future use.

Abstract: A collapsible single-use sterilization container for use in the sterilization of medical instruments is provided. The sterilization container includes a lid having central portion defined by a frangible region. Upon activation of the frangible region, the central portion may be removed rendering the sterilization container inoperable for future use.

Abstract: A process for operating a packaging transport system in which objects packed in packaging which is bacteria-impermeable but gas-permeable are sterilized, whereafter the packaging, possibly after removal of some packaging parts, is sterilized again on its outer side in a sterilization chamber which acts as a transfer lock, and then guided into a sterile clean room. The objects involved may, in particular, be syringes having injecting needles, which are filled and sealed in a filling device located in the clean room. Sterilization in the sterilization chamber is accomplished by abruptly applying a vapor mix consisting of water steam and hydrogen peroxide vapor as a condensate layer on the outer side of the transport containers, and immediately removing the condensate layer and the uncondensed vapor mix from the sterilization chamber before any significant amount of hydrogen peroxide is deposited inside the transport containers.

Abstract: An apparatus (200, 300, 400) for generating superheated steam capable of reducing or eliminating microorganisms associated with an item (230) includes a gas heater (10) for heating a gas, a steam generator coupled to the gas heater (10) and having a reservoir (216, 304) for supplying water, wherein the heater (10) heats the gas such that when water is combined therewith, a mixture of superheated steam and gas capable of reducing or eliminating microorganisms is discharged from the apparatus (200, 300, 400). The generation of the steam-gas mixture may be done at one atmosphere of pressure and the mixing may be done prior to expelling the fluid from the apparatus (200, 300, 400). The apparatus (400) may be configured as a hand-held device, A method of treating an item (230) for microorganisms includes generating a superheated steam at approximately one atmosphere of pressure, directing a flow of the steam onto the item (230), and reducing or eliminating microorganisms using the steam.

Abstract: A method of processing waste containing an amount of thermoplastic material and an amount of non-thermoplastic material as constituent materials to produce an output material capable of being used as an ingredient or component in a subsequent manufacturing process, said method comprising the steps of: increasing the temperature of the waste; supplying said waste to a densifier to cause densification of the waste and heat transfer contact between the constituent materials such that the thermoplastic materials soften to at least partially surround said non-thermoplastic materials; and extruding the densified waste to produce an extruded material.

Abstract: A process of purifying air includes selecting a room vapor generator having a housing having a floor mounted therein for generating a stream of air therethrough and having at least one possibly charged probe positioned in the air stream for generating positive ions in the air stream and at least one negatively charged probe positioned in the air stream for generating negative ions in the air stream. The negatively charged probe is spaced from the positively charged probe in the air stream. A liquid storage container is located in the housing and has means for dispersing liquid in the container into the stream of air adding a liquid mixture containing nitrogen, free citrus extract and colloidal silver into the liquid storage container and vaporizing the liquid mixture in the air stream for dispersing the liquid mixture into the surrounding air along with positive and negative ions.

Abstract: A method for increasing a relative humidity in an enclosed space (10) comprising a plurality of graduated steps. The relative humidity is increased from a first relative humidity to a target relative humidity. The method is issued to humidify a chamber (10) wherein a sterilization process using a humidified ozone takes place. The method is carried out by an apparatus for effecting the humidified ozone sterilization comprising a processor programmed to effect humidification in a plurality of gradual steps.

Abstract: The present invention provides a method for producing a medical device, preferably an ophthalmic device, more preferably a contact lens, made of a stabilized poly(oxyalkylene)-containing polymeric material. The method of the invention comprises the steps of: curing, in a mold, a composition comprising (a) a prepolymer having at least one poly(oxyalkylene) unit, (b) a biocompatible organic multi-acid or biocompatible salt thereof in an amount sufficient to improve the stability of the poly(oxyalkylene)-containing polymer made from the composition, (c) optionally a photoinitiator or a thermal initiator, and (d) optionally one or more vinylic monomers, to form the medical device being less susceptible to oxidative degradation; and removing the medical device from the mold.

Abstract: The invention relates to an improvement in a method for sterilizing an article in a sterilizing chamber by exposing the article to humidified ozone in at least two consecutive sterilizing cycles, the improvement comprising, after the first of said consecutive sterilizing cycles and before the second of said consecutive sterilizing cycles, removing from the sterilizing chamber any condensed water present.

Abstract: A chemical vapor sterilization process is enhanced by concentrating a germicide via exploitation of the difference between the vapor pressures of the germicide and its solvent. A diffusion restriction can be placed into the diffusion path to assist this process and the path then opened to provide rapid diffusion of the thus concentrated germicide. The path through the diffusion restriction can be closed to allow the pressure in a sterilization chamber to be lowered prior to receiving the concentrated germicide.

Abstract: A sterilizable pouch having both internal and external sterilization record indicators to indicate whether attempted steam sterilization of the pouch and contents was successful or unsuccessful. The pouch preferably has one indicium in each indicator responsive to multi-parameter sterilization by steam, and another indicium in each indicator responsive to gas sterilization, such as using ethylene oxide.

Abstract: A method for sterilizing at least one item in a chamber, comprising the steps of: disposing the at least one item in the chamber; pumping the atmosphere from the chamber until the atmosphere of the chamber has a pressure of less than ten torr; adding water vapor and ozone to the chamber; and generating electrical discharge in the chamber, such that the electrical discharge produces OH radicals from the water vapor and the ozone so as to contribute to sterilization of at least part of the at least one item.

Abstract: A method and apparatus for removing soil from an inner surface of a lumen wall of a medical instrument are disclosed. A carrier gas entrains particles capable of sublimation at room temperature and transports the particles into and through the lumen. As the particles collide with the soil attached to the inner surface of the lumen wall, and as the particles sublime, the soil is removed from the inner surface of the lumen wall and transported out an exit of the lumen.

Abstract: A method for operating a cleaning device or a cleaning system is proposed. In this case, the cleaning device is set up for carrying out a process for cleaning an article with a germicidal action. The method includes the following steps: information on a target germ with which the article could be contaminated is received; at least one process parameter of the cleaning process is selected according to the target germ in such a way that the target germ is killed with a high degree of probability during the cleaning process; and the cleaning process is carried out with the process parameter.

Abstract: A pseudo-plastic or thixotropic carrier having anti-malodorous components dissolved or suspended therein is sprayed on the internal surfaces of an ostomy bag or pouch. The viscoelastic properties of the carrier allow the composition to be conveniently dispensed from a spray bottle into the ostomy bag and retained on the inner walls thereof without being displaced therefrom by incoming waste during use of the ostomy bag. This allows the composition to continue to deodorize the ostomy bag headspace even after waste material begins to fill the bag.

Abstract: The present invention relates to the field of sterilization of items that are sensitive to e.g. temperature, pH, positive or negative pressure, radiation or oxidation. More particularly, the invention concerns a method, the use of this method and an apparatus for sterilization or disinfection, comprising the steps of contacting one or more item or part of an item with (a) a water-based fluid containing at least one enzyme, and (b) a substantially water-free environment with a gas having oxidative properties, where said step (a) precedes said step (b). According to the invention, items can be sterilized that are otherwise impaired by conventional sterilization procedures, such as laboratory items, medical items, dental items, military items, biological items, and food processing-related items.

Abstract: A free radical sterilization system having a chamber defining a region, and a generator for generating free radical reach effluent from a free radical electric generator and/or a vaporizer. A closed loop circulating system without a free-radical destroyer is provided for supplying the mixture of free radicals from the electric generator mixed with the hydrogen peroxide solution in the form of the effluent to the chamber. The free-radical sterilization system is used in sterilizing items in the chamber and, with an open-bottomed wound chamber, in treating wounds on a body.