The moisture-resistant catalyst for air pollution remediation is a catalyst with moisture-resistant properties, and which is used for removing nitrogen compound pollutants, such as ammonia (NH.sub.3), from air. The moisture-resistant catalyst for air pollution remediation includes at least one metal oxide catalyst, at least one inorganic oxide support for supporting the at least one metal oxide catalyst, and a porous framework for immobilizing the at least one metal oxide catalyst and the at least one inorganic oxide support, where the porous framework is moisture-resistant. As non-limiting examples, the at least one metal oxide catalyst may be supported on the at least one inorganic oxide support by precipitation, impregnation, dry milling, ion-exchange or combinations thereof. The at least one metal oxide catalyst supported on the at least one inorganic oxide support may be physically embedded in the porous framework.

A honeycomb-structured catalyst for decomposing an organic substance, which includes a catalyst particle. The catalyst particle contains a perovskite-type composite oxide represented by A.sub.xB.sub.yM.sub.zO.sub.w, where the A contains at least of Ba and Sr, the B contains Zr, the M is at least one of Mn, Co, Ni, and Fe, y+z=1, 1.001≤x≤1.05, 0.05≤z≤0.2, and w is a positive value that satisfies electrical neutrality. The toluene decomposition rate is greater than 90% when toluene is decomposed using the honeycomb-structured catalyst subjected to a heat treatment at 1200° C. for 48 hours and a gas that contains 50 ppm toluene, 80% nitrogen, and 20% oxygen as a volume concentration as a target at a space velocity of 30,000/h and a catalyst temperature of 400° C.

The disclosure discloses a catalyst capable of simultaneously removing COS and H.sub.2S in garbage gasification and a preparation method thereof, and belongs to the technical field of preparation of desulfurization catalysts. The method includes the following steps: pretreating an SBA-15 molecular sieve with a templating agent unremoved, which primarily includes the steps of removing the templating agent and introducing halogen atoms to modify the molecular sieve; then synthesizing an active component solution; and finally introducing active components into channels of the pretreated molecular sieve via surface tension by adopting an impregnation method, performing washing and drying, and performing calcining under an N.sub.2 atmosphere, so as to obtain the catalyst. The catalyst prepared according to the present disclosure can load the active components in fixed positions inside and outside the channels, and the components are easy to obtain, thereby having the advantages of low cost and good desulfurization effects.

The disclosure is directed to an air purifier and an automobile air conditioner with an air purifier. The air purifier includes a reactor, a column, an air guider and a plurality of light emitting elements. The reactor includes an air inlet and an air outlet. The column is disposed in the reactor, and the column has a N-side walls. The air guider is disposed on the column, and the air guider is coated with a photocatalyst. The light emitting elements are placed on the N side walls of the column configured to irradiate on the photocatalyst, where each of the light emitting elements has an emitting angle of θ and θ*N>360°.

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 supported catalyst for decomposing an organic substance that includes a support and a catalyst particle supported on the support. The catalyst particle contains a perovskite-type composite oxide represented by A.sub.xB.sub.yM.sub.zO.sub.w, where the A contains at least one selected from Ba and Sr, the B contains Zr, the M is at least one selected from Mn, Co, Ni and Fe, y+z=1, x≥0.995, z≤0.4, and w is a positive value satisfying electrical neutrality. A film thickness of a catalyst-supporting film supported on the support and containing the catalyst particle is 5 μm or more, or a supported amount as determined by normalizing a mass of the catalyst particle supported on the support by a volume of the support is 45 g/L or more.

A muffler includes a muffler housing having an exhaust gas inlet port adapted for securing to an exhaust pipe of an automobile so that exhaust gases from an internal combustion engine of the automobile are directed through the muffler housing from the exhaust gas inlet to an exhaust gas outlet. The muffler housing includes a plurality of rigid surfaces that form an exhaust gas pathway including a plurality of turns and lead from the exhaust gas inlet port to the exhaust gas outlet port. A photocatalyst coating is secured to an area of the rigid surfaces, and a light source is secured to the muffler housing and positioned to direct light onto the photocatalyst coating. The exhaust gases come into contact with the photocatalyst coating and reactive species generated by the photocatalyst coating decompose one or more pollutants in the exhaust gas.

The present invention relates to a methane combustion catalyst including platinum and iridium supported on a tin oxide carrier for combusting methane in a combustion exhaust gas containing sulfur oxide. In the methane combustion catalyst, a ratio R.sub.TO of platinum oxides to metal platinum is 8.00 or more, wherein the ratio R.sub.TO is based on existence percentages of the metal platinum (Pt) and the platinum oxides (PtO and PtO.sub.2) obtained from a platinum 4f spectrum analyzed and measured by X-ray photoelectron spectroscopy (XPS) and calculated in accordance with the following expression. In the following expression, R.sub.Pt is an existence percentage of the metal platinum (Pt), R.sub.Pto is an existence percentage of PtO, and R.sub.Pto2 is an existence percentage of PtO.sub.2.

R.sub.TO=(R.sub.PtO+R.sub.PtO2)/R.sub.Pt  [Expression 1]

Catalytic articles having a high porosity substrate containing platinum, palladium or a mixture thereof, in walls of the high porosity substrate and an SCR catalyst coating on a wall of the high porosity substrate are disclosed. The platinum, palladium or mixture thereof can be present in the wall of the high porosity support as a metal, or as a supported platinum, palladium or a mixture thereof. The catalytic articles are useful for selective catalytic reduction (SCR) of NOx in exhaust gases and in reducing the amount of ammonia slip. Methods for producing such articles are described. Methods of using the catalytic articles in an SCR process, where the amount of ammonia slip is reduced, are also described.

The invention describes a process for the photocatalytic reduction of carbon dioxide carried out in the liquid phase and/or in the gas phase under irradiation employing a photocatalyst of microporous crystalline metal sulfide type, said process being carried out by bringing a charge containing the CO.sub.2 and at least one sacrificial compound into contact with said photocatalyst, then by irradiating the photocatalyst by at least one irradiation source producing at least one wavelength lower than the bandgap width of said photocatalyst, so as to reduce the CO.sub.2 and to oxidize the sacrificial compound, so as to produce an effluent containing, at least in part, C.sub.1 or more carbon-based molecules other than CO.sub.2.