A method for synthesis of PtNi smooth surface core/shell particles or Nano cages and porous nanocages from segregated nanoparticles.

The present invention deals with catalysts for the conversion of CO by the shifting reaction of high temperature water gas, free from chromium and iron, consisting of alumina promoted by potassium, by zinc and copper oxides and in a second embodiment also additionally nickel. The catalysts thus prepared maintain high CO conversion activity, not having the environmental limitations or operating limitations with low excess steam in the process, which exist for catalysts in accordance with the state of the art. Such catalysts are used in the hydrogen or synthesis gas production process by the steam reforming of hydrocarbons, allow the use of low steam/carbon ratios in the process, exhibiting high activity and stability to thermal deactivation and lower environmental restrictions for production, storage, use and disposal, than the industrially used catalysts based on iron, chromium, and copper oxides.

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.

This disclosure relates to red mud compositions. This disclosure also relates to methods of making red mud compositions. This disclosure additionally relates to methods of using red mud compositions.

Provided is a method for producing bio-aromatic compounds from glycerol. The method uses a primary alcohol, secondary alcohol or a combination thereof as a mixing medium in converting glycerol into an aromatic compound, and thus overcomes the high viscosity of glycerol and improves the problem of rapid catalytic deactivation, thereby increasing the yield of aromatic compounds and improving the stability of catalyst. In addition, the method for producing bio-aromatic compounds uses a zeolite-based catalyst that is a kind of solid acid catalysts, and suggests optimum reaction conditions, and thus imparts a high added value to glycerol produced as a byproduct in a biodiesel production process and increases the cost-efficiency of process.

The principles and embodiments of the present invention relate generally to systems and methods for applying a catalytic coating to the outwardly facing edges of the cell walls of a catalytic substrate to reduce the amount of soot that accumulates at the entrances of the substrate cells that can increase back pressure and reduce the flow of exhaust gases through the substrate.

The invention concerns a synthesis process of a compound of the following formula (I) or one of the salts thereof,

##STR00001## wherein R represents a COOH, CH.sub.2OH or CHO group, comprising the step according to which the but-3-ene-1,2-diol (BDO) is subjected to an oxidation in the presence of a catalyst, said catalyst comprising an active phase based on at least one noble metal selected from palladium, gold, silver, platinum, rhodium, osmium, ruthenium and iridium, and a support containing alkaline sites.

The invention also concerns the application of this reaction to the preparation of bioavailable compounds of methionine used, in particular, in animal nutrition.

A method of selectively catalysing the reduction of oxides of nitrogen (NO.sub.x) including nitrogen monoxide in an exhaust gas of a stationary source of NO.sub.x emissions also containing oxides of sulfur (SO.sub.x) comprising the steps of passively oxidising nitrogen monoxide to nitrogen dioxide (NO.sub.2) over an oxidation catalyst comprising a platinum group metal so that a NO.sub.2/NO.sub.x content is from 40-60%; introducing a nitrogenous reductant into the exhaust gas; and contacting exhaust gas having the 40-60% NO.sub.2/NO.sub.x content and containing the nitrogenous reductant with a selective catalytic reduction (SCR) catalyst comprising an aluminosilicate zeolite promoted with copper.

Systems and methods are provided for conversion of a combined feed of oxygenates (such as methanol or dimethyl ether) and olefins to a high octane naphtha boiling range product with a reduced or minimized aromatics content. The oxygenate conversion can be performed under conditions that reduce or minimize hydrogen transfer. Optionally, a catalyst that further facilitates formation of branched paraffins can be used, such as a catalyst that has some type of 12-member ring site available on the catalyst surface.

There is disclosed a highly crystalline, small crystal, ferrierite zeolite prepared from a gel containing a source of silica, alumina, alkali metal and a combination of two templating agents. The resulting material includes ferrierite crystals having a particle size of about or less than about 200 nm. The desired crystal size can be achieved by using a specific composition of the gel. The purity of the material and the crystal size was determined by using X-ray powder diffraction and scanning electron microscopy. The material has excellent surface area and micropore volume as determined by nitrogen adsorption.