Abstract: A method for removing perfluorinated compounds from a fluoropolymer material is provided. The method includes the steps of: (a) providing the fluoropolymer material in a chamber; (b) providing an anaerobic environment in the chamber; and (c) providing a fluorination gas in the chamber, thereby exposing the fluoropolymer material to the fluorination gas. The method results in the removal the perfluorinated compounds from the fluoropolymer material.

Abstract: A method for removing perfluorinated compounds from a fluoropolymer material is provided. The method includes the steps of: (a) providing the fluoropolymer material in a chamber; (b) providing an anaerobic environment in the chamber; and (c) providing a fluorination gas in the chamber, thereby exposing the fluoropolymer material to the fluorination gas. The method results in the removal the perfluorinated compounds from the fluoropolymer material.

Abstract: A method for removing perfluorinated compounds from a fluoropolymer material is provided. The method includes the steps of: (a) providing the fluoropolymer material in a chamber; (b) providing an anaerobic environment in the chamber; and (c) providing a fluorination gas in the chamber, thereby exposing the fluoropolymer material to the fluorination gas. The method results in the removal the perfluorinated compounds from the fluoropolymer material.

Abstract: A method for removing perfluorinated compounds from a fluoropolymer material is provided. The method includes the steps of: (a) providing the fluoropolymer material in a chamber; (b) providing an anaerobic environment in the chamber; and (c) providing a fluorination gas in the chamber, thereby exposing the fluoropolymer material to the fluorination gas. The method results in the removal the perfluorinated compounds from the fluoropolymer material.

Abstract: A method of treating an elastomeric workpiece is provided. The method includes: (a) providing an elastomeric workpiece; and (b) altering a mechanical property of the elastomeric workpiece by fluorinating the elastomeric workpiece in a controlled environment.

Abstract: The current invention provides a series of bicyclic nitroimidazole-substituted phenyl oxazolidinones in which a bicyclic nitroimidazole pharmacophore is covalently bonded to a phenyl oxazolidinone, their pharmaceutical compositions, and the method of use of the compositions for prevention and treatment of bacterial infections. The bicyclic nitroimidazole-substituted phenyl oxazolidinones possess surprising antibacterial activity against wild-type and resistant strains of pathogens, and are therefore useful for the prevention, control and treatment of a number of human and veterinary bacterial infections caused by these pathogens, such as Mycobacterium tuberculosis.

Abstract: The current invention provides a series of bicyclic nitroimidazole-substituted phenyl oxazolidinones in which a bicyclic nitroimidazole pharmacophore is covalently bonded to a phenyl oxazolidinone, their pharmaceutical compositions, and the method of use of the compositions for prevention and treatment of bacterial infections. The bicyclic nitroimidazole-substituted phenyl oxazolidinones possess surprising antibacterial activity against wild-type and resistant strains of pathogens, and are therefore useful for the prevention, control and treatment of a number of human and veterinary bacterial infections caused by these pathogens, such as Mycobacterium tuberculosis.

Abstract: A laminate structure for making a cushioned component for a vehicle interior, such as a seat cushion or head rest, has a high density foam bonded to an interior surface of a seat cover material. After the laminate structure is formed into a desired shape for the cushioned component, it is inserted into a vacuum mold having a mold surface with a shape corresponding with a desired exterior surface shape of the cushioned component. Liquid foam-forming material is injected into the laminate structure within the mold and allowed to cure to form the cushioned component. The high density foam of the laminate structure preferably has a density of at least 4 lbs/ft3 and an air permeability of 5 to 100 ft3/ft2 minute. This high density foam may be created by felting a polyurethane foam.

Abstract: An ester polyurethane foam is prepared by reacting a mixture of one or more polyester polyols with one or more isocyanates and one or more silicone surfactants in the presence of a blowing agent, such as water, and other additives, such as catalysts. The cured foam is chemically treated in a caustic solution to form a hydrophilic ester polyurethane foam having a water absorption rate of at least 20 pounds of water per square foot per minute, preferably at least 25 pounds of water per square foot per minute. The foam also has greater water holding capacity and wet strength than cellulose.

Abstract: Polyurethane foams formed under vacuum (below atmospheric pressure) conditions using toluene diisocyanate or a specific mixture of polyisocyanates with a specific mixture of polyether and graft polyols produces a foam with lower density and better flame retardancy than latex foam, but with equally high resiliency. The foam-forming ingredients are mixed together and foamed under controlled pressures in the range 0.6 to 0.95 bar (absolute), preferably 0.8 to 0.95 bar (absolute). The resulting foam has a ball rebound above about 65 percent.

Abstract: Polyurethane foams formed under vacuum (below atmospheric pressure) conditions using toluene diisocyanate or a specific mixture of polyisocyanates with a specific mixture of polyether and graft polyols produces a foam with lower density and better flame retardancy than latex foam, but with equally high resiliency. The foam-forming ingredients are mixed together and foamed under controlled pressures in the range 0.6 to 0.95 bar (absolute), preferably 0.8 to 0.95 bar (absolute). The resulting foam has a ball rebound above about 65 percent.

Abstract: A fuel reservoir for a liquid fuel cell particularly useful for portable electronic devices or for a reformer, includes (a) a container defining a volume for holding a liquid fuel; (b) a wicking structure positioned within the volume and into which at least one portion of the liquid fuel wicks and from which said liquid fuel subsequently may be metered, such as by pumping; (c) a retainer to hold the wicking structure in a desired orientation within the container; and (d) an outlet for the liquid fuel that is in communication with the wicking structure. A method of dispensing liquid fuel and a method of assembling a fuel cartridge are also disclosed.

Abstract: A gas diffusion layer for a fuel cell is formed from a porous material, which porous material comprises a solid matrix and interconnected pores or interstices therethrough that has at least one external surface and internal surfaces, wherein at least a portion of the at least one external surface is coated with one or more layers of at least one electrically conductive material. The electrically conductive material preferably has a resistivity less than 20 ohm-cm. Exemplary electrically conductive materials used for coating are metals, such as nickel, gold, platinum, cobalt, chromium, copper, indium, aluminum, titanium, zirconium, metal alloys of such materials, salts of such materials, and mixtures thereof, and amorphous carbon or graphite. A single or a series of multiple discrete conductive coating layers may be applied to the foam strands using coating methods such as electroplating, electroless plating, plasma vapor deposition, sputtering, arc forming, dipping and painting.

Abstract: A laminate structure for making a cushioned component for a vehicle interior, such as a seat cushion or head rest, has a high density foam bonded to an interior surface of a seat cover material. After the laminate structure is formed into a desired shape for the cushioned component, it is inserted into a vacuum mold having a mold surface with a shape corresponding with a desired exterior surface shape of the cushioned component. Liquid foam-forming material is injected into the laminate structure within the mold and allowed to cure to form the cushioned component. The high density foam of the laminate structure preferably has a density of at least 4 lbs/ft3 and an air permeability of 5 to 100 ft3/ft2 minute. This high density foam may be created by felting a polyurethane foam.

Abstract: An ester polyurethane foam is prepared by reacting a mixture of one or more polyester polyols with one or more isocyanates and one or more silicone surfactants in the presence of a blowing agent, such as water, and other additives, such as catalysts. The cured foam is chemically treated in a caustic solution to form a hydrophilic ester polyurethane foam having a water absorption rate of at least 20 pounds of water per square foot per minute, preferably at least 25 pounds of water per square foot per minute. The foam also has greater water holding capacity and wet strength than cellulose.

Abstract: A fuel delivery system for a liquid fuel cell particularly useful for portable electronic devices includes (a) a container defining a volume for holding a liquid fuel; (b) a reservoir structure positioned within the volume and into which at least a portion of the liquid fuel wicks and from which said liquid fuel subsequently may be metered, such as by pumping. The reservoir structure is formed from a material with a free rise wick height greater than at least one half of the longest dimension of the reservoir structure. Among materials with such wicking capability are foams, bundled fibers and nonwoven fibers, including particularly felted and unfelted reticulated polyurethane foams. The container may have a generally flat and thin profile, formed as a pouch or envelope with substantially planar top and bottom faces of flexible film material, such that the container holding the reservoir structure and filled with liquid fuel can be bent or shaped.

Abstract: Water recovery in direct liquid fuel cells, particularly direct methanol fuel cells, is accomplished by incorporating a reservoir structure composed of a wicking material, which may be a composite material, adjacent to the cathode. The wicking material has a free rise wick height of at least one half its longest dimension. The wicking materials may be selected from foams, bundled fibers and nonwoven fibers. In one embodiment, holes or perforations are formed through the thickness of the sheet, and a conductive layer is adjacent to, adhered to or coated on at least one surface of the wicking material. To recycle water, a second reservoir structure of wicking material is incorporated adjacent to the anode, and a liquid flow path is provided between the first and second reservoir structures. The absorbed water flows through the liquid flow path, is mixed with fuel and introduced to the second reservoir structure adjacent to the anode.

Abstract: Copolymer DMC-catalyzed polyoxypropylene polyols which exhibit processing latitude similar to base-catalyzed copolymer analogs and base-catalyzed homopolyoxypropylene analogs may be prepared by oxyalkylation with a mixture of propylene oxide and ethylene oxide such that a finite ethylene oxide content is maintained in the oxyalkylation reactor for the most substantial part of the oxyalkylation, the polyoxypropylene polyol having randomly distributed oxyethylene moieties which constitute 1.5 weight percent or more of the polyol product.

Abstract: Molded polyurethane seating foams exhibiting low resonant frequencies and low ball rebound are produced by reacting an isocyanate-terminated prepolymer prepared from a polyol component comprising in major part one or more low intrinsic unsaturation substantially polyoxypropylene polyols and/or polymer polyols with a blowing/chain extending stream comprising water and optionally amines and alkanolamines.

Abstract: Copolymer DMC-catalyzed polyoxypropylene polyols which exhibit processing latitude similar to base-catalyzed copolymer analogs and homopolyoxypropylene analogs may be prepared by oxyalkylation with a mixture of propylene oxide and ethylene oxide such that a finite ethylene oxide content is maintained in the oxyalkylation reactor for the most substantial part of the oxyalkylation, the polyoxypropylene polyol having randomly distributed oxyethylene moieties which constitute 1.5 weight percent or more of the polyol product. Block copolymer polyols having external blocks containing lesser oxyethylene content than internal blocks and bicompositional compositions containing discrete multimodal and dissimilar and optionally multimodal polyols produced by a continuous addition of starter process are useful as polyols exhibiting greater processing latitude.