Subject of the invention is an exhaust gas purification system for a gasoline engine, comprising in consecutive order the following devices: a first three-way-catalyst (TWC1), a gasoline particulate filter (GPF) and a second three-way-catalyst (TWC2), wherein the oxygen storage capacity (OSC) of the GPF is greater than the OSC of the TWC2, wherein the OSC is determined in mg/l of the volume of the device. The invention also relates to methods in which the system is used and uses of the system.

A high surface area to mass catalyst is formed by a method that includes a Kirigami mapped cutting of a flat three metal laminate composite formed on a deposition support. Kirigami derived catalyst has a shape that provides a high surface to mass ratio and promotes the flow of a fluid containing a reagent for a reaction catalyzed by the exterior metal catalyst films of the three metal laminate composite. Structural integrity of the Kirigami derived catalyst results from a support metal film residing between two metal catalyst films. The shaping to the Kirigami derived structure involves cutting the flat three metal laminate composite to that of a Kirigami map, imposing stress on the cut structure to force a non-planar deformation, and delaminating the Kirigami derived catalyst from the deposition support.

A three-way catalyst article, and its use in an exhaust system for internal combustion engines, is disclosed. The catalyst article for treating exhaust gas comprising: a substrate comprising an inlet end and an outlet end with an axial length L; a first catalytic region comprising a first platinum group metal (PGM) component and a first oxygen storage capacity (OSC) material, wherein the first OSC material has a fresh specific surface area (SSA) of at least 10 m.sup.2/g; and wherein the first OSC material has an SSA difference of no more than 30 m.sup.2/g between the fresh first OSC material and the aged first OSC material.

Provided is a method capable of industrially efficiently producing acetic acid yielding a good potassium permanganate test result, without costing much. In the acetic acid production method, (1) by-produced acetaldehyde is industrially advantageously removed from a process stream, and (2) a crotonaldehyde concentration in an acetic acid stream from a light ends column is controlled to a specific level or lower, and/or a reflux ratio at a second distillation column is controlled to 0.1 or more. In addition, (3) the method includes the step of subjecting at least one of an aqueous phase and an organic phase of a light ends column overhead condensate to distillation in a crotonaldehyde-removing column; the light ends column is operated at a reflux ratio of 2 or more (when the aqueous phase is refluxed); and the crotonaldehyde-removing column is operated so as to meet a specific condition(s).

A process for ring hydrogenation of dialkyl terephthalates having C.sub.3- to C.sub.16-alkyl groups can be performed in a hydrogenation unit composed of two reaction units in series. In the process, a suitable process parameter in relation to the first reaction unit is adjusted so that a certain reaction conversion is achieved.

A precious metal-supported eggshell catalyst with a preparation method and an application are provided. The precious metal-supported eggshell catalyst includes a carrier, a precious metal and a promoter. As an active component, the precious metal and the promoter are evenly distributed on surface of the carrier, wherein the promoter includes one or more than two of a precious metal, an alkaline earth metal, a transition metal lanthanide series metal, an actinium series metal and/or a metal oxide thereof. With a highly utilization of the precious metal, the precious metal-supported eggshell catalyst showed high conversion, good selectivity and excellent stability, and the precious metal-supported eggshell catalyst is used more than 300 hours with no obvious loss of activity in preparing 1,3-propanediol through hydrogenation of 3-hydroxypropionaldehyde aqueous solution. Furthermore, with large particles the precious metal-supported eggshell catalyst is easily separated from reaction products.

Proposed is a catalyst complex having high activity for carbon dioxide conversion reaction that converts carbon dioxide to useful compounds through reaction of carbon dioxide and hydrocarbon containing at least one hydroxyl group, and a carbon dioxide conversion process using the same, wherein the catalyst complex includes, as an active metal in the catalyst complex, at least one of noble metals and at least one of transition metals other than noble metals, thereby having high activity for the carbon dioxide conversion reaction.

The present invention relates to a process for preparing liquid hydrocarbons by the Fischer-Tropsch process integrated into refineries, in particular comprising recycling streams from the steam reforming hydrogen production process as the feedstock for the Fischer-Tropsch process.

A process for the catalytic oxidation of ammonia, comprising: passing an ammonia-containing gas, in the presence of oxygen, over a catalyst contained in a reactor, obtaining a process gas containing nitrogen oxides, and cooling said process gas with a heat exchanger accommodated in the reactor, wherein a portion of said process gas, located in the shell side, bypasses the heat exchanger and forms a hot current which mixes with cooled gas downstream the heat exchanger, and the bypass is regulated on the basis of a target outlet temperature of the mixed process gas.

The present disclosure provides methods for producing a regenerated hydrogenation catalyst from a fouled hydrogenation catalyst having a total surface area and at least one associated impurity. The method can include maintaining contact between the fouled hydrogenation catalyst and a flushing medium that comprises water, oxygen, and an inert or diluent gas at a regeneration temperature and a regeneration pressure sufficient to remove at least a portion of the at least one impurity from the hydrogenation catalyst to produce the regenerated hydrogenation catalyst, where the regenerated hydrogenation catalyst is characterized as retaining at least 70% of the activity of the hydrogenation catalyst.