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: Disclosed is a composition for forming or treating reverse osmosis (RO), forward osmosis (FO), microfiltration (MF), or nanofiltration (NF) membranes, which includes a stable liquid blend of two of the following polymers: an oxygen polymer, a nitrogen polymer, and a sulfur polymer, where each polymer in a blend have matched solubility parameters; provided, that a nitrogen polymer can be in the form of a powder; where the weight ratio of polymers in each blend can range from 1:99 to 99:1; where each polymer optionally can be halogenated; where any polymer can be dispersed in a solvent for forming the blend.

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: A tobacco product comprising nanocrystalline particles and methods of reducing the levels of undesirable compounds in tobacco smoke are provided. The nanocrystalline particles are effective sorbents of numerous toxic compounds released by burning tobacco and may be incorporated into the tobacco itself, incorporated into a filter element, or incorporated into the fibers of a wrapping paper.

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: Composites for destroying chemical and biological agents such as toxins and bacteria, and methods of preparing and using those composites are provided. According to the invention, the substance to be destroyed is contacted with the inventive composites which comprise finely divided metal oxide nanoparticles at least partially coated with carbon. Advantageously, the composites 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 oxide nanoparticles include MgO, SrO, BaO, CaO, TiO2, ZrO2, FeO, V2O3, V2O5, Mn2O3, Fe2O3, NiO, CuO, Al2O3, SiO2, ZnO, Ag2O, and mixtures thereof.

Abstract: Composites for destroying chemical and biological agents such as toxins and bacteria, and methods of preparing and using those composites are provided. According to the invention, the substance to be destroyed is contacted with the inventive composites which comprise finely divided metal oxide nanoparticles at least partially coated with carbon. Advantageously, the composites 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 oxide nanoparticles include MgO, SrO, BaO, CaO, TiO2, ZrO2, FeO, V2O3, V2O5, Mn2O3, Fe2O3, NiO, CuO, Al2O3, SiO2, ZnO, Ag2O, 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.