Abstract: An improved air purification adsorbent is disclosed. The air purification adsorbent comprises titanium dioxide (TiO2) impregnated with zinc chloride (ZnCl2). The adsorbent may be used in air purification systems for removing ammonia from air streams. The nanocrystalline (amorphous) structure of the adsorbent results in a higher density of surface defects, higher surface area, and higher reactivity which, when combined with the synergistic effect of ZnCl2 and the nanocrystalline TiO2, provides a significantly longer breakthrough time of ammonia as compared with breakthrough time from unimpregnated nanocrystalline TiO2, the commercial (crystalline) TiO2 impregnated with ZnCl2, pure ZnCL2, and other commercially available adsorbents of ammonia. Other embodiments are described and claimed.

Abstract: To achieve the removal of a broad spectrum of chemical hazards, multiple layers of impregnated activated carbon and nanocrystalline materials are incorporated into the adsorbent bed. For optimum performance using the least amount of material, a two-layer configuration is used. The top layer consists of a homogeneous mixture of an MgO/CaO based nanocrystalline material (e.g., Mg/Ca) and Kureha or other petroleum pitch-based bead shaped activated carbon impregnated treated with phosphoric acid. The bottom layer is comprised of a single layer of Calgon URC carbon. The volume ratios of the components are 9:5:11 Mg/Ca, phosphoric acid treated Kureha carbon, and URC, respectively. The new configuration leads to a 30% reduction in size of the existing NIOSH CBRN CAP 1 cartridge. Other embodiments are disclosed and claimed.

Abstract: An improved air purification adsorbent is disclosed. The air purification adsorbent comprises titanium dioxide (TiO2) impregnated with zinc chloride (ZnCl2). The adsorbent may be used in air purification systems for removing ammonia from air streams. The nanocrystalline (amorphous) structure of the adsorbent results in a higher density of surface defects, higher surface area, and higher reactivity which, when combined with the synergistic effect of ZnCl2 and the nanocrystalline TiO2, provides a significantly longer breakthrough time of ammonia as compared with breakthrough time from unimpregnated nanocrystalline TiO2, the commercial (crystalline) TiO2 impregnated with ZnCl2, pure ZnCL2, and other commercially available adsorbents of ammonia. Other embodiments are described and claimed.

Abstract: To achieve the removal of a broad spectrum of chemical hazards, multiple layers of impregnated activated carbon and nanocrystalline materials are incorporated into the adsorbent bed. For optimum performance using the least amount of material, a two-layer configuration is used. The top layer consists of a homogeneous mixture of an MgO/CaO based nanocrystalline material (e.g., Mg/Ca) and Kureha or other petroleum pitch-based bead shaped activated carbon impregnated treated with phosphoric acid. The bottom layer is comprised of a single layer of Calgon URC carbon. The volume ratios of the components are 9:5:11 Mg/Ca, phosphoric acid treated Kureha carbon, and URC, respectively. The new configuration leads to a 30% reduction in size of the existing NIOSH CBRN CAP 1 cartridge. Other embodiments are disclosed and claimed.

Abstract: Dielectric materials comprising nanocrystalline or nanoparticulate metal oxides or metal carbonates having enhanced dielectric constant values are provided. Specifically, the dielectric materials exhibit high dielectric constant values at low frequencies approaching the DC limit. The dielectric materials also exhibit low dielectric loss factors and high voltage breakdown limits making them well suited for use in capacitors, particularly high energy density capacitors.

Abstract: An improved mixed metal oxide material suitable for use in electrochemical cells is provided. The mixed metal oxide material generally exhibits high surface area and pore volume than conventionally manufactured materials thereby imparting improved electrochemical performance. Batteries manufactured using the mixed metal oxide material are particularly suited for use in implantable medical devices.

Abstract: Compositions and methods for destroying chemical and biological agents such as toxins and bacteria are provided wherein the substance to be destroyed is contacted with finely divided metal oxide nanoparticles. The metal oxide nanoparticles are coated with a material selected from the group consisting of surfactants, waxes, oils, silyls, synthetic and natural polymers, resins, and mixtures thereof. The coatings are selected for their tendency to exclude water while not excluding the target compound or adsorbates. The desired metal oxide nanoparticles can be pressed into pellets for use when a powder is not feasible. Preferred metal oxides for the methods include MgO, SrO, BaO, CaO, TiO2, ZrO2, FeO, V2O3, V2O5, Mn2O3, Fe2O3, NiO, CuO, Al2O3, SiO2, ZnO, Ag2O, the corresponding hydroxides of the foregoing, and mixtures thereof.

Abstract: Compositions and methods for destroying chemical and biological agents such as toxins and bacteria are provided wherein the substance to be destroyed is contacted with finely divided metal oxide nanoparticles. The metal oxide nanoparticles are coated with a material selected from the group consisting of surfactants, waxes, oils, silyls, synthetic and natural polymers, resins, and mixtures thereof. The coatings are selected for their tendency to exclude water while not excluding the target compound or adsorbates. The desired metal oxide nanoparticles can be pressed into pellets for use when a powder is not feasible. Preferred metal oxides for the methods include MgO, SrO, BaO, CaO, TiO2, ZrO2, FeO, V2O3, V2O5, Mn2O3, Fe2O3, NiO, CuO, Al2O3, SiO2, ZnO, Ag2O, the corresponding hydroxides of the foregoing, and mixtures thereof.

Abstract: Compositions and methods for destroying chemical and biological agents such as toxins and bacteria are provided wherein the substance to be destroyed is contacted with finely divided metal oxide nanoparticles. The metal oxide nanoparticles are coated with a material selected from the group consisting of surfactants, waxes, oils, silyls, synthetic and natural polymers, resins, and mixtures thereof. The coatings are selected for their tendency to exclude water while not excluding the target compound or adsorbates. The desired metal oxide nanoparticles can be pressed into pellets for use when a powder is not feasible. Preferred metal oxides for the methods include MgO, SrO, BaO, CaO, TiO2, ZrO2, FeO, V2O3, V2O5, Mn2O3, Fe2O3, NiO, CuO, Al2O3, SiO2, ZnO, Ag2O, the corresponding hydroxides of the foregoing, and mixtures thereof.

Abstract: A method for removing at least one contaminant selected from the group consisting of H2S and CO2 from contaminating streams, including the steps of providing an above ground stream comprising hydrocarbon containing the at least one contaminant, and positioning metal-containing nanoparticles having a particle size of less than or equal to about 100 nm in the stream, the metal-containing nanoparticles being selected from the group consisting of metal oxides, metal hydroxides and combinations thereof, whereby the nanoparticles adsorb the contaminants from the stream.

Abstract: Compositions and methods for destroying chemical and biological agents such as toxins and bacteria are provided wherein the substance to be destroyed is contacted with finely divided metal oxide nanoparticles. The metal oxide nanoparticles are coated with a material selected from the group consisting of surfactants, waxes, oils, silyls, synthetic and natural polymers, resins, and mixtures thereof. The coatings are selected for their tendency to exclude water while not excluding the target compound or adsorbates. The desired metal oxide nanoparticles can be pressed into pellets for use when a powder is not feasible. Preferred metal oxides for the methods include MgO, SrO, BaO, CaO, TiO2, ZrO2, FeO, V2O3, V2O5, Mn2O3, Fe2O3, NiO, CuO, Al2O3, SiO2, ZnO, Ag2O, the corresponding hydroxides of the foregoing, and mixtures thereof.

Abstract: A method for removing at least one contaminant selected from the group consisting of H2S and CO2 from hydrocarbon streams, including the steps of providing a stream of hydrocarbon containing the at least one contaminant, and positioning metal-containing nanoparticles in the stream, the metal-containing nanoparticles being selected from the group consisting of metal oxides, metal hydroxides and combinations thereof, whereby the nanoparticles adsorb the contaminants from the stream.