B01J23/894

Ceria-supported metal catalysts and processes

Provided herein are catalyst materials and processes for processing hydrocarbons. For example, doped ceria-supported metal catalysts are provided exhibiting good activity and stability for commercially relevant DRM process conditions including low temperature and long term operation.

METHODS OF FORMING AND USING METAL ALLOY OXIDATIVE CATALYSTS
20190308175 · 2019-10-10 ·

In a first aspect, the present invention is directed to a process for forming a metal alloy catalyst. Another aspect of the present invention is directed to a process for oxidizing a substrate that includes contacting a substrate with an oxidant in the presence of a metal alloy catalyst to form one or more carboxylic acids. Suitable substrates include sugars, polyols, furfural alcohols, and polyhydroxycarboxylic acids. The oxidation process may use the alloy catalyst formed from the process of the first aspect of the invention.

Perovskite catalysts enhanced combustion on porous media

The effects of different perovskite catalysts, catalytic active materials with a crystal structure of ABO.sub.3, on matrix stabilized combustion in a porous ceramic media are explored. Highly porous silicon carbide ceramics are used as a porous media for a catalytically enhanced matrix stabilized combustion of a lean mixture of methane and air. A stainless steel combustion chamber was designed incorporating a window for direct observation of the flame within the porous media. Perovskite catalytic enhancement of SiC porous matrix with La0.75Sr0.25Fe0.6Cr0.35Ru0.05O3; La0.75Sr0.25Fe0.6Cr0.4O3; La0.75Sr0.25Fe0.95Ru0.05O3; La0.75Sr0.25Cr0.95Ru0.05O3; and LaFe0.95Ru0.05O3, for example, were used to enhance combustion. The flammability limits of the combustion of methane and air were explored using both inert and catalytically enhanced surfaces of the porous ceramic media. By coating the SiC porous media with perovskite catalysts it was possible to lower the minimum stable equivalence ratio.

Direct synthesis method of nanostructured catalyst particles on various supports and catalyst structure produced by the same

Disclosed is a direct synthesis method of nanostructured catalyst particles on surfaces of various supports. In the disclosed synthesis method of a catalyst structure having a plurality of nanostructured catalyst particles dispersed in a support by a one-step process using a high-temperature high-pressure closed reactor, the one-step process includes supplying the support and a catalyst source into the high-temperature high-pressure closed reactor; supplying an atmosphere forming gas of the reactor into the reactor; perfectly sealing the high-temperature high-pressure closed reactor and heating the reactor to produce the catalyst structure in the reactor under self-generated pressure and synthesis temperature conditions, the catalyst structure including the plurality of nanostructured catalyst particles dispersed in the support; removing internal gases of the reactor to allow the reactor to be in a high-temperature, atmospheric pressure state and supplying an inert gas into the reactor to remove unreacted materials and byproducts remaining in the reactor; and cooling the reactor to room temperature while supplying the inert gas to synthesize the catalyst structure.

Catalyst composition for exhaust gas purification and catalyst for exhaust gas purification

The invention relates to a catalyst composition using other metals different from precious metals as a catalytically active component and is to propose a novel catalyst composition for exhaust gas purification which has excellent catalytic activity, in particular, excellent treatment activity of HC even after a thermal durability treatment. The invention is to propose a catalyst composition for exhaust gas purification comprising catalyst particles having a constitution in which Cu and a transition metal A including at least one of Cr, Fe, Mn, Co, Ni, Zr, and Ag are supported on ceria (CeO.sub.2) particles and a catalyst using the same.

NANOSTRUCTURED MIXED METAL OXIDES AS CATALYSTS AND METHOD OF MAKING THEREOF
20190169043 · 2019-06-06 ·

A method of forming a metal oxide material having a rod shape or polyhedral nanostructure includes preparing a first reverse micro-emulsion system comprising an aqueous precipitating agent dispersion and a second reverse micro-emulsion system containing an aqueous metal salt dispersion; combining the micro-emulsions together to initiate a reaction; allowing the reaction to continue to form a product mixture comprising a metal oxide gel and aqueous media; separating the metal oxide gel from the aqueous media; collecting the metal oxide gel; and calcining the metal oxide gel to form the metal oxide material. The metal oxide material corresponds to the chemical formula of La.sub.2M.sub.xNi.sub.1-xO.sub.4, Pr.sub.2-yA.sub.yNiO.sub.4, or La.sub.2-zD.sub.zNiO.sub.4, wherein M is copper, cobalt, iron, manganese, chromium, aluminum, or platinum; A is lanthanum or neodymium; D is calcium, barium or strontium; x ranges from 0 to 1; y ranges from 0 to 2; and z ranges from 0 to 0.25.

Preparation method of Cu—Pd—CeO2/?—Al2O3@NP catalyst and synthesis method of benzopyrazine compounds

A preparation method of CuPdCeO.sub.2/?-Al.sub.2O.sub.3@NP catalyst and a synthesis method of benzopyrazine compounds. The preparation method of the CuPdCeO.sub.2/?-Al.sub.2O.sub.3@NP catalyst comprises the following steps: (1) preparing a CeO.sub.2/?-Al.sub.2O.sub.3 carrier; (2) preparing a CeO.sub.2/?-Al.sub.2O.sub.3@NP carrier; (3) preparing the CuPdCeO.sub.2/?-Al.sub.2O.sub.3@NP catalyst by impregnation method. A one-pot method for synthesizing benzopyrazine compounds of formula (III) includes using an o-nitroaniline compound of formula (I) and an aliphatic diol compound of formula (II) as raw materials, carrying out the one-pot synthesis of the benzopyrazine compound of formula (III) under solvent-free condition and under the combined action of the CuPdCeO.sub.2/?-Al.sub.2O.sub.3@NP catalyst prepared by the method and an alkali. The CuPdCeO.sub.2/?-Al.sub.2O.sub.3@NP catalyst increases the number of basic sites by doping N and P, and meanwhile loads CeO.sub.2 to assist in the extraction of protons, thereby improving the dehydrogenation activity and product selectivity.

VISIBLE LIGHT-SENSITIVE PHOTOCATALYST COMPOSITION AND A VISIBLE LIGHT-SENSITIVE PHOTOCATALYST FILM COMPRISING THE SAME
20240198322 · 2024-06-20 · ·

The present invention relates to a visible light-sensitive photocatalyst composition and a visible light-sensitive photocatalyst film comprising the same, and more particularly, to a visible light-sensitive photocatalyst composition and a visible light-sensitive photocatalyst film comprising the same, which has catalytic properties of oxidizing and decomposing organic matter in the air in not only ultraviolet rays but also visible rays, sunlight and indoor lights, and is capable of removing harmful substances, deodorizing, sterilizing, etc., and can provide visibility.

NANOCATALYSTS, PREPARATION METHODS AND APPLICATIONS FOR REFORMING CARBON DIOXIDE AND METHANE TO SYNGAS

The catalyst in this present application includes a support and an active component dispersed on/in the support; wherein the support is at least one selected from inorganic oxides and the support contains macropores and mesopores; and the active component includes an active element, and the active element contains an iron group element. As a high temperature stable catalyst for methane reforming with carbon dioxide, the catalyst can be used to produce syngas, realizing the emission reduction and recycling utilization of carbon dioxide. Under atmospheric pressure and at 800 C., the supported metal catalyst with hierarchical pores shows excellent catalytic performance. In addition to high activity and good selectivity, the catalyst has high stability, high resistance to sintering and carbon deposition.

Highly active and thermally stable coated gasoline particulate filters
10265684 · 2019-04-23 · ·

Coated gasoline particulate filters (cGPFs) that are produced according to varied material compositions and catalyst configurations are disclosed. The cGPFs include FeCe (rich)-activated Rh compositions that provide greater catalytic functionality. These cGPFs are incorporated within engine systems as components of TWC systems for controlling and reducing engine exhaust emissions. The conversion performance of these TWC systems is assessed and compared employing worldwide harmonized light duty test cycle (WLTC) protocol within a gasoline fueled internal combustion engine. These TWC systems exhibit a significant catalytic performance when compared with the catalytic performance of a PGM-based Original Equipment Manufacturer (OEM) catalyst employed in TWC applications. Further, TWC catalysts are produced including Fe-activated Rh layers comprising dopant elements. The catalytic performance of the TWC catalysts is evaluated by performing light-off and standard isothermal oxygen storage capacity oscillating tests. The TWC catalysts exhibit improved catalytic performance and significant oxygen storage capacity.