Patent classifications
B01J23/48
Gold nanoparticle superlattice embedded in porous silica and method for manufacturing same
The present invention relates to a catalyst composition comprising a gold nanoparticle superlattice embedded in hierarchical porous silica and a method for manufacturing the same. The catalyst composition comprising a gold nanoparticle superlattice embedded in hierarchical porous silica according to the present invention comprises micropores and mesopores in the superlattice, so that these pores are channelized to allow the rapid access of reactants to surfaces of gold nanoparticles, and the catalyst composition is very structurally stable and has excellent catalytic activity, and thus has an effect of exhibiting a CO conversion rate of 100% at room temperature.
Gold nanoparticle superlattice embedded in porous silica and method for manufacturing same
The present invention relates to a catalyst composition comprising a gold nanoparticle superlattice embedded in hierarchical porous silica and a method for manufacturing the same. The catalyst composition comprising a gold nanoparticle superlattice embedded in hierarchical porous silica according to the present invention comprises micropores and mesopores in the superlattice, so that these pores are channelized to allow the rapid access of reactants to surfaces of gold nanoparticles, and the catalyst composition is very structurally stable and has excellent catalytic activity, and thus has an effect of exhibiting a CO conversion rate of 100% at room temperature.
Method of manufacturing catalyst ink free of eluted transition metal for fuel cell
Disclose is a method of manufacturing catalyst ink for a fuel cell, and particularly the method includes removing eluted transition metal from a noble-metal/transition-metal alloy catalyst.
Kirigami derived metal catalysts
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.
Nitrogen oxide sorbent and exhaust gas cleaning catalyst
A nitrogen oxide storage material comprising: Mg.sub.1-yAl.sub.2O.sub.4-y, wherein y is a number satisfying 0≤y≤0.2, a noble metal, an oxide of a metal other than the noble metal, and a barium compound, the noble metal, the oxide, and the barium compound being loaded on Mg.sub.1-yAl.sub.2O.sub.4-y. The metal oxide comprises at least one metal oxide selected from zirconium oxide, praseodymium oxide, niobium oxide, and iron oxide.
METHODS OF SULFURIZING METAL CONTAINING PARTICLES
Methods of sulfurizing metal containing particles in the absence of hydrogen are described. One method includes contacting a bed of metal containing particles with a gaseous stream comprising hydrogen sulfide and inert gas under reaction conditions sufficient to produce sulfided metal containing particles. The gaseous stream is introduced into a vertical reactor at an inlet positioned at the bottom portion of the reactor and any unreacted hydrogen sulfide and inert gas is removed at an outlet positioned above the inlet. The sulfided metal containing particles can be removed from the reactor and stored.
METHOD FOR PRODUCING CATALYST FIBROUS STRUCTURE
A catalyst fibrous structure having a catalyst metal carried on a fibrous structure, wherein (a) a Log differential micropore volume distribution curve thereof obtained by measurement using a mercury intrusion technique has a peak having a maximum micropore diameter in the range of from 0.1 μm to 100 μm; (b) a Log differential micropore volume at the peak is 0.5 mL/g or more; and (c) an amount of a catalyst metal compound and a binder carried per unit volume is 0.05 g/mL or more. A production method for producing a catalyst fibrous structure having: (1) mixing a catalyst metal compound or a catalyst precursor, and an inorganic binder and a solvent; (2) grinding the mixture to obtain a coating material of the catalyst metal compound or the catalyst precursor having a median particle diameter of 2 μm or less and a viscosity of from 10 mPa.Math.s to 200 mPa.Math.s; (3) impregnating a fibrous structure with the coating material to fill up voids of the fibrous structure with the coating material of the catalyst metal compound or the catalyst precursor; (4) heating and drying the fibrous structure, directly as it is, at a temperature not lower than the boiling point of the solvent; and (5) heating and calcination the dried fibrous structure at a temperature not lower than the dehydration temperature of the inorganic binder to obtain a catalyst fibrous structure.
Synthesis of Colloidal Precious Metals Nanoparticles with Controlled Size And Morphology
The present invention relates to colloidal dispersions comprising a plurality of precious group nanoparticles, wherein about 90% or more of the precious group metal is in fully reduced form; a dispersion medium comprising a polar solvent; a water-soluble polymer suspension stabilizing agent; and a reducing agent, wherein the nanoparticle concentration is at least about 2 wt. % of the colloidal dispersion, wherein the nanoparticles have an average particle size of about 1 to about 6 nm and at least 95% of the nanoparticles have a particle size within this range; and further wherein the colloidal dispersion is substantially free of halides, alkali metals, alkaline earth metals and sulfur compounds. Methods of preparing, further processing, and using such colloidal dispersions are also provided herein.
PHOTOCATALYTIC HYDROGEN PRODUCTION FROM WATER OVER CATALYSTS HAVING P-N JUNCTIONS AND PLASMONIC MATERIALS
A photocatalyst and a method for producing hydrogen and oxygen from water by photocatalytic electrolysis are disclosed. The photocatalyst includes a photoactive material and metal or metal alloy material (15)—e.g. pure particles or alloys of Au, Pd and Ag—capable of having plasmon resonance properties deposited on the surface of the photoactive material. The photoactive material includes a p-n junction (17) formed by contact of a n-type semiconductor material (10), such as mixed phase TiO2 nano particles (anatase to rutile ratio of 1.5 to 1 or greater), and a p-type semiconductor material (16), such as CoO or Cu2O.
PHOTOCATALYTIC HYDROGEN PRODUCTION FROM WATER OVER CATALYSTS HAVING P-N JUNCTIONS AND PLASMONIC MATERIALS
A photocatalyst and a method for producing hydrogen and oxygen from water by photocatalytic electrolysis are disclosed. The photocatalyst includes a photoactive material and metal or metal alloy material (15)—e.g. pure particles or alloys of Au, Pd and Ag—capable of having plasmon resonance properties deposited on the surface of the photoactive material. The photoactive material includes a p-n junction (17) formed by contact of a n-type semiconductor material (10), such as mixed phase TiO2 nano particles (anatase to rutile ratio of 1.5 to 1 or greater), and a p-type semiconductor material (16), such as CoO or Cu2O.