Patent classifications
B01J37/0238
Method for preparing supported metal catalyst and supported metal catalyst prepared therefrom
Disclosed is a method for preparing a metal catalyst composite. The method includes pre-treating a carbon support in a reactor, and depositing a metal precursor on the pre-treated carbon support. The pre-treating the carbon support may include exposing the carbon support to a nucleating agent, for example, titanium tetrachloride (TiCl.sub.4), silicon tetrachloride (SiCl.sub.4) and carbon tetrachloride (CCl.sub.4).
METHOD OF FORMING A SELF-CLEANING FILM SYSTEM
A method of forming a self-cleaning film system includes depositing a perfluorocarbon siloxane polymer onto a substrate to form a first layer. The method includes removing a plurality of portions of the first layer to define a plurality of cavities in the first layer and form a plurality of projections that protrude from the substrate. The method includes depositing a photocatalytic material onto the plurality of projections and into the plurality of cavities to form a second layer comprising: a bonded portion disposed in the plurality of cavities and in contact with the substrate, and a non-bonded portion disposed on the plurality of projections and spaced apart from the substrate. The method also includes, after depositing the photocatalytic material, removing the non-bonded portion to thereby form the self-cleaning film system.
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.
Methods for the production of aligned carbon nanotubes and nanostructured material containing the same
Disclosed herein is a scaled method for producing substantially aligned carbon nanotubes by depositing onto a continuously moving substrate, (1) a catalyst to initiate and maintain the growth of carbon nanotubes, and (2) a carbon-bearing precursor. Products made from the disclosed method, such as monolayers of substantially aligned carbon nanotubes, and methods of using them are also disclosed.
Method for adding an organic compound to a porous solid in the gaseous phase
The invention relates to a process for adding an organic compound to a porous solid wherein the porous solid and the organic compound in the liquid state are brought together simultaneously, without physical contact between the solid and the organic compound in the liquid state, at a temperature below the boiling point of the organic compound and under pressure and time conditions such that a fraction of said organic compound is transferred gaseously to the porous solid.
CATALYST WITH A CORE-SHELL STRUCTURE FOR METHANE OXIDATION, METHOD OF PREPARING THE SAME AND METHOD OF OXIDIZING METHANE USING THE SAME
A catalyst with a core-shell structure for methane oxidation, a method of preparing the catalyst, and a method of methane oxidation using the catalyst are disclosed. The catalyst includes a core structure consisting of a nano-support and core nanoparticles; and a shell coating layer coated on the core structure in which the core nanoparticles have a particle diameter smaller than that of the nano-support and are coated on the nano-support to form a core structure. The catalyst has excellent thermal stability during methane oxidation reaction at high temperature and an effect of increasing methane conversion and formaldehyde selectivity.
CATALYTIC PLASMONIC NANOMATERIAL
A method for producing plasmonic nanomaterials that are catalytically or photocatalytically active by fabricating plasmonic nanostructures on substrates using electrodeposition into a nano-template structure and forming a plurality of nanorods in an array, wherein the nanorods are made from materials chosen from the group consisting of materials that are plasmonic and/or catalytic, and materials that are catalytically activated by depositing pure elemental metals, alloys, or alternating layers of different metals or alloys, and producing catalytic plasmonic nanomaterials. Catalytic plasmonic nanomaterials made from the above method. An optical reactor device that utilizes catalytic nanomaterials for photocatalytic synthesis of methanol or ammonia. A method of photocatalytic synthesis of methanol and ammonia by using catalytic plasmonic nanomaterial to convert CO.sub.2 and H.sub.2 to methanol and N.sub.2 and H.sub.2 to ammonia using optical power. A hybrid plasma-plasmonic reactor for the utilization of CO.sub.2 and CH.sub.4 to produce methanol, ethylene, and acetic acid.
Supported catalyst and method of producing fibrous carbon nanostructures
A supported catalyst comprises: a support that is particulate; and a composite layer laminate formed outside the support and including two or more composite layers, wherein each of the composite layers includes a catalyst portion containing a catalyst and a metal compound portion containing a metal compound, the support contains 10 mass % or more of each of Al and Si, and a volume-average particle diameter of the support is 50 μm or more and 400 μm or less.
Bismuth oxide/bismuth subcarbonate/bismuth molybdate composite photocatalyst and preparation method thereof
The present invention discloses a bismuth oxide (Bi.sub.2O.sub.3)/bismuth subcarbonate ((BiO).sub.2CO.sub.3)/bismuth molybdate (Bi.sub.2MoO.sub.6) composite photocatalyst, including a Bi.sub.2MoO.sub.6 photocatalyst, where Bi.sub.2O.sub.3 and (BiO).sub.2CO.sub.3 nanosheets are introduced to a surface of the Bi.sub.2MoO.sub.6 through addition of Na.sub.2CO.sub.3 and roasting. The present invention also discloses a preparation method of the Bi.sub.2O.sub.3/(BiO).sub.2CO.sub.3/Bi.sub.2MoO.sub.6 composite photocatalyst which is specifically implemented by the following steps: step 1: preparing a Bi.sub.2MoO.sub.6 photocatalyst; step 2: introducing Bi.sub.2O.sub.3 and (BiO).sub.2CO.sub.3 nanosheets to a surface of the Bi.sub.2MoO.sub.6 photocatalyst obtained in step 1 through addition of Na.sub.2CO.sub.3 and roasting to obtain the Bi.sub.2O.sub.3/(BiO).sub.2CO.sub.3/Bi.sub.2MoO.sub.6 composite photocatalyst. The photocatalyst of the present invention has no agglomeration, a wide responsive range of visible light, a significantly improved catalytic activity compared with a Bi.sub.2MoO.sub.6 alone, and excellent reusability. Moreover, the preparation method is simple with mild conditions, desired controllability and convenient operation.
METHOD OF SYNTHESIZING HIGH-EFFICIENCY BIFUNCTIONAL ELECTROCATALYSTS
The design of bifunctional catalysts for water splitting by modifying the electronic structure of the catalyst. That bifunctional catalyst that is synthesized is a quaternary FeNi—PSe nanoporous film (FeNi—PSe NF). A self-supported FeNi—PSE NF is synthesized and used as an anode and a cathode in a two-electrode electrolytic cell. The cell is subjected to a water source, and the FeNi—PSe NFs split the water molecules to produce hydrogen fuel. The slightly oxidized FeNi—PSe surface serves as an active site for oxygen evolution reactions, making hydrogen evolution reactions and oxygen evolution reactions well-balanced, thereby improving electrolysis efficiency.