A multilayer supported oxidative coupling of methane (OCM) catalyst composition (alpha-Al.sub.2O.sub.3 support, first single oxide layer, one or more mixed oxide layers, optional second single oxide layer) characterized by formula A.sub.aZ.sub.bE.sub.cD.sub.dO.sub.x/alpha-Al.sub.2O.sub.3; A is alkaline earth metal; Z is first rare earth element; E is second rare earth element; D is redox agent/third rare earth element; the first, second, third rare earth element are not the same; a=1.0; b=0.1-10.0; c=0.1-10.0; d=0-10.0; x balances oxidation states; first single oxide layer (Z.sub.b1O.sub.x1, b1=0.1-10.0; x1 balances oxidation states) contacts alpha-Al.sub.2O.sub.3 support and one or more mixed oxide layers; one or more mixed oxide layers (A.sub.a2Z.sub.b2E.sub.c2D.sub.d2O.sub.x2, a2=1.0; b2=0.1-10.0; c2=0.1-10.0; d2=0-10.0; x2 balances oxidation states; A.sub.aZ.sub.bE.sub.cD.sub.dO.sub.x and A.sub.a2Z.sub.b2E.sub.c2D.sub.d2O.sub.x2 are different) contacts first single oxide layer and optionally second single oxide layer, and second single oxide layer (AO), when present, contacts one or more mixed oxide layers and optionally first single oxide layer.

A method of converting one or more alkanes to one or more alkenes that includes a) providing a first stream containing one or more alkanes and oxygen to an oxidative dehydrogenation reactor; b) converting at least a portion of the one or more alkanes to one or more alkenes in the oxidative dehydrogenation reactor to provide a second stream exiting the oxidative dehydrogenation reactor containing one or more alkanes, one or more alkenes, oxygen, carbon monoxide and optionally acetylene; and c) providing the second stream to a second reactor containing a catalyst that includes a group 11 metal to convert a least a portion of the carbon monoxide to carbon dioxide and reacting the acetylene.

Described herein are heterogeneous materials comprising a mixture of a first n-type semiconductor and a second n-type semiconductor. The first n-type semiconductor may be a single or plural phase TiO.sub.2 material. The second n-type semiconductor includes a metal titanate and/or a noble metal. Upon activation with ultraviolet light, the photocatalytic material mixtures described herein efficiently decompose volatile chemical compounds. Furthermore, the photocatalytic materials disclosed herein are observably more stable, relative to known semiconductor materials, to inactivation by deposition.

The present invention relates generally to the field of exhaust treatment systems for purifying exhaust gas discharged from a lean burn engine. The exhaust treatment system comprises a Diesel Oxidation Catalyst (DOC), a Catalyzed Soot Filter (CSF), a reductant injector, an AEI zeolite based Selective Catalyzed Reduction (SCR) catalyst and an Ammonia Oxidation Catalyst (AMOX) downstream to the AEI zeolite based SCR catalyst.

The exhaust gas purification device includes a substrate, a first catalyst layer, and a second catalyst layer. The substrate includes an upstream end, a downstream end, and a porous partition wall defining a plurality of cells extending between the upstream end and the downstream end. The plurality of cells include an inlet cell opening at the upstream end and sealed at the downstream end, and an outlet cell adjacent to the inlet cell sealed at the upstream end and opening at the downstream end. The first catalyst layer is disposed on a surface of the partition wall in an upstream region. In a downstream region, the second catalyst layer is disposed inside the partition wall, and a second catalyst-containing wall including the partition wall and the second catalyst layer has a porosity of 35% or more.

A ceramic membrane for oxidative coupling of methane can include a perovskite oxide and catalyst material on a surface of the membrane.

A process for coating substrates of motor vehicle exhaust gas catalysts is described, and includes steps of applying a suspension (e.g., washcoat) to a substrate, allowing a shear force to act on the applied washcoat, as in pressure transmitted by gas (e.g., air), and then sucking and/or pressing the washcoat into the substrate. The process in inclusive of providing the suspension (washcoat) containing the catalytic material from above in a metered charge process. An apparatus for carrying out the noted process steps is also featured.

The present invention provides an exhaust gas purification catalyst including an alkaline earth metal supported in a highly dispersed state on a porous carrier. A catalyst layer of the exhaust gas purification catalyst provided by the invention has an alkaline earth metal-supporting region including a porous carrier, a catalyst metal belonging to the platinum group, and a sulfate of at least one type of alkali earth metal supported on the porous carrier. In a cross-section of this region, a Pearson correlation coefficient R.sub.Ae/M is at least 0.5 as calculated using α and β for each pixel obtained by carrying out area analysis by FE-EPMA under conditions of pixel size of 0.34 μm×0.34 μm, and measured pixel number 256×256, and by measuring the characteristic X-ray intensity (α:cps) of the alkaline earth metal element (Ae) and the characteristic X-ray intensity (β:cps) of the main constituent element of the inorganic compound constituting the porous carrier for each pixel.

A modified Y-type molecular sieve having a calcium content of about 0.3-4 wt % calculated on the basis of calcium oxide, a rare earth content of about 2-7 wt % calculated on the basis of rare earth oxide, and a sodium content of no more than about 0.5 wt % calculated on the basis of sodium oxide. The modified Y-type molecular sieve has a total pore volume of about 0.33-0.39 ml/g, a proportion of the pore volume of secondary pores having a pore size of 2-100 nm to the total pore volume of about 10-25%, a lattice constant of about 2.440-2.455 nm, a proportion of non-framework aluminum content to the total aluminum content of no more than about 20%, a lattice collapse temperature of not lower than about 1050° C., and a ratio of B acid to L acid in the total acid content of no less than about 2.30.

Embodiments of the present invention relates to integrated catalyst systems and associated processes that directly converts carbon dioxide or carbohydrate to CO, methane, or other valuable chemicals at room temperature and atmospheric pressure, requiring no extra energy. The integrated catalyst systems are comprised of nitrogenous heterocyclic compounds and at least two metal elements, wherein one metal element needs to be active than the other one. The integrated catalyst systems can be applied to reduce carbon dioxide and carbohydrate at room temperature with considerable conversion efficiency. The reduction process involves the steps of: a) nitrogenous heterocyclic compounds performance as solvent/major catalyst, dual component as reducing agent / co-catalyst; b) introducing the above integrated catalysts into the reactor full of CO.sub.2 or carbohydrate, and keeping stirring the reacting system for 1 to 4 hours, without any illumination or heating; c) CO, methane, or other reduction product is achieved with a conversion efficiency of about 100%; d) the reduction products are gases, which can be directly separated from the system without any additional separation process or involving additional chemicals.