A method of manufacturing a catalyst article, the method comprising: providing a complex of a maleic acid-containing polymer and a PGM; providing a support material; applying the complex to the support material to form a loaded support material; disposing the loaded support material on a substrate; and heating the loaded support material to form nanoparticles of the PGM on the support material.

The invention generally relates to a process for purifying a hydrogen gas for use in a fuel cell. The process involves taking a hydrogen feed stream from a high-pressure tank and passing it through a purifier comprising an adsorbent to provide a purified hydrogen stream which is sent to a fuel cell. A particular adsorbent which can be used is a metal-organic framework composition. The adsorbent can be housed in a device such as a canister or cartridge having an inlet and outlet port.

A filter media can include a fiber coated with a barrier coating that is substantially non-reactive to reactive species, and a photocatalytic coating disposed on the barrier coating, wherein the photocatalytic coating generates reactive species in response to illumination with optical radiation.

Methods and systems for separating liquid components are disclosed. A vessel is provided containing a solids conveyance device. At least a first portion of the vessel acts as an indirect-contact heat exchanger and a second portion of the vessel contains a filter. A process liquid stream, containing a first component and a second component, is passed into the first portion of the vessel. A portion of the second component is frozen and entrained in the first portion of the vessel into the process liquid stream, resulting in a process slurry stream. The process slurry stream is passed into a second portion of the vessel by the solids conveyance device. The process slurry stream is separated into a solid product stream and a primary liquid product stream by passing the primary liquid product stream through the filter and out of the vessel while separately removing the solid product stream out of the vessel.

A compressor assembly for a portable oxygen concentrator includes a first compressor chamber having a first connector, a second compressor chamber having a second connector, and a tube having a first end having a first connection interface configured to connect to the first connector and a second end having a second connection interface configured to connect to the second connector. The first connection interface is shaped to maintain the connection between the first connector and the first connection interface in a fixed orientation and the second connection interface is shaped to maintain the connection between the second connector and the second connection interface in a fixed orientation. One or more of the first connector, the second connector, and the tube are compliant.

A gas treatment method includes: a process (a) of allowing gas to be treated in which a target substance to be treated is mixed with air to pass through inside a housing, the target substance to be treated exhibiting volatility at room temperature and belonging to at least one substance selected from a group consisting of carbon compounds, nitrogen compounds, and sulfur compounds; a process (b) of introducing ozone into a space through which the gas to be treated flows inside the housing at 200° C. or lower; a process (c) of stirring the gas to be treated after the process (b); and a process (d) of heating the gas to be treated to 300° C. or higher after executing the process (c).

An integrated waste gas treatment system includes an adsorption/desorption device that receives a waste gas that includes an organic compound and an organic nitrogen compound exhausted from a semiconductor manufacturing facility, where the adsorption/desorption device adsorbs the organic compound and the organic nitrogen compound and concentrates and desorbs the organic compound and the organic nitrogen compound, and a catalytic decomposition device disposed adjacent to the adsorption/desorption device, where the catalytic decomposition device includes a catalytic chamber that provides a gas passage through which a gas desorbed from the adsorption/desorption device flows and an oxidation-reduction catalyst disposed in the gas passage that removes the organic compound and the organic nitrogen compound from the desorbed gas. The organic compound and the organic nitrogen compound are subjected to an oxidation treatment by the oxidation-reduction catalyst, and nitrogen oxides generated by the oxidation treatment are removed by a selective reduction reaction.

A process is provided using a concentrated sodium bicarbonate solution as a solubilizer mixed with a calcium hydroxide to chemically produce an insoluble calcium carbonate and produce an alkaline liquid solution, then passing the alkaline liquid solution through detrimental gases in a scrubber to produce an enhanced sodium bicarbonate which regenerates the sodium bicarbonate thus creating a continuous closed loop. The process can also produce a sodium phosphate (trisodium phosphate) by mixing the alkaline liquid solution with a phosphoric acid.

The present invention belongs to the technical field of functional organic macromolecule composite catalysts and involves the preparation of a nitrogen-doped lattice macromolecule composite loaded with an efficient denitrification and sulfur resistance catalyst, firstly using the method of adding metal salts to make a large amount of Ce.sup.3+, Ce.sup.4+, Sn.sup.3+ and Sn.sup.4+ ions accumulate around the cyanuric acid molecule. Afterwards, 2,4,6-triaminopyrimidine and cytosine were added to graft with the cyanuric acid to produce the N-doped macromolecule in the first stage. After that, potassium permanganate was used as the oxidizing agent, and redox reaction occurred on the surface of N-doped macromolecules, so that the manganese cerium tin catalyst was grown in situ on the surface of N-doped macromolecules, and finally calcined at once to cross-link the N-doped macromolecules to generate catalyst composites. The catalysts described in this invention have higher efficient NOx reduction and sulfur resistance performance.

A method for making a titania-polymer nanocomposite by simultaneously forming TiO.sub.2 nanoparticles in situ from a TiO.sub.2 precursor in the presence of urea and interfacially polymerizing polyamide precursors thereby producing a titania-polymer nanocomposite. A titania-polymer nanocomposite made by this method. A method for removing a dye or metal from water comprising contacting contaminated water with the titania-polymer nanocomposite.