Patent classifications
B01J35/51
PORE-ENCAPSULATED CATALYSTS FOR SELECTIVE HYDROGENOLYSIS OF PLASTIC WASTE
Disclosed herein is a catalyst which comprises a silica core having an outer surface and a mesoporous silica shell having an outer surface and an inner surface with the inner surface being inside the outer surface of said mesoporous silica shell proximate to and surrounding the outer surface of said silica core. Wherein the outer surface of the mesoporous silica shell has openings leading to pores within the mesoporous silica shell which extend toward the outer surface of said silica core. The catalyst also includes catalytically active metal nanoparticles positioned within the pores proximate to said core, wherein the catalytic metal nanoparticles comprise about 0.0001 wt % to about 1.0 wt % of the catalyst. Also disclosed are methods of making the catalyst and using it to carry out a process for catalytically hydrogenolysizing a polyolefinic polymer.
CATALYST CARRIER AND CATALYST COMPRISING SAME
The present application relates to a catalyst carrier for use in the synthesis of dialkyl oxalates by gas-phase catalytic coupling of carbon monoxide comprising microscopic fine pores and one or more macroscopic large pores running through the catalyst carrier, wherein the ratio of the average pore diameter of each macroscopic large pore to the average diameter of the catalyst carrier is 0.2 or more. The present application also relates to a catalyst, comprising the catalyst carrier, an active component and an optional auxiliary, supported on the catalyst carrier. The catalyst according to the present invention not only catalyze effectively coupling of carbon monoxide in a gas phase to form dialkyl oxalate, but also improves heat dissipation, reduces pressure drop, reduces the amount applied of precious metal such as palladium, thereby reducing the use cost of the catalyst and production cost of dialkyl oxalate and then facilitating industrial mass production of dialkyl oxalate.
Methods of synthesizing nano-sized tungsten particles by sol-gel process and method of preparing light oil from extra-heavy oil using the synthesized nano-sized tungsten particles
Disclosed is a method of synthesizing nano-sized tungsten-silica core-shell particles by a silica-based sol-gel process. According to the method, tungsten-silica nanoparticles are very easy to synthesize by a simple process at ambient pressure and temperature. In addition, tungsten oxide-silica (WO.sub.x@SiO.sub.2) nanoparticles including tungsten in a stable oxidation state can be synthesized. In the tungsten oxide-silica nanoparticles, the size of the tungsten protected with the silica shell can be maintained in the nanometer range without further processing. Also disclosed is a method of synthesizing nano-sized tungsten oxide (WO.sub.x) and tungsten carbide (WC) particles by further processing of the tungsten-silica core-shell particles.
Aluminum based metallic glass powder for efficient degradation of AZO dye and other toxic organic chemicals
The present invention provides amorphous bi-functional catalytic aluminum metallic glass particles having an aluminum metallic glass core and 2 or more transition metals disposed on the surface of the aluminum metallic glass core to form amorphous bi-functional aluminum metallic glass particles with catalytic activity.
Nanocomposite hollow sphere as a photocatalyst and methods thereof
A photocatalytic nanocomposite hollow sphere comprising a shell surrounding a hollow core, and the shell comprising zirconium dioxide, hydroxyapatite, and platinum, as well as a method for producing the nanocomposite hollow sphere and a method employing the nanocomposite hollow sphere in reducing an aromatic nitro compound to an aromatic amine compound under visible light are disclosed.
SAPO-34/ZSM-5@KAOLIN MICROSPHERE COMPOSITE CATALYTIC MATERIAL AND ITS PREPARATION AND USE
The present invention relates to a composite catalytic material of SAPO-34/ZSM-5@kaolin microspheres and its preparation and use, the method comprises the steps of: 1) processing kaolin into kaolin microspheres, and baking them to obtain activated kaolin microspheres; 2) mixing the activated kaolin microspheres obtained in step 1), water, a phosphorus source, and a template agent to prepare a gel; 3) mixing the gel obtained in step 2) and a ZSM-5 molecular sieve, and carrying out aging, crystallization, and separation to obtain a composite material of SAPO-34/ZSM-5@kaolin; 4) subjecting the composite material obtained in step 3) to ammonium exchange treatment and baking, to obtain the composite catalytic material of SAPO-34/ZSM-5@kaolin microspheres. The present invention not only greatly shortens the preparation route for the catalyst and reduces the cost of catalyst preparation, but also allows adjustment of the fractions of SAPO-34 and ZSM-5 molecular sieves in the composite material by adjustment of the synthesis conditions.
ZINC OXIDE PARTICLE PREPARATION AND METHODS OF USE
A method of using ZnO particles for the treatment of colon cancer and a method of using the particles for reducing the concentration of an organic contaminant in an aqueous solution is described. The ZnO particles are substantially spherical and may have nanopetals that provide a nanoflower morphology. The synthesis and characterization of the ZnO particles is also discussed.
Method For Treating Reverse Osmosis Concentrated Water
A method for treating reverse osmosis concentrated water, comprises adding a precipitant and oxidant to reverse osmosis concentrated water for treatment, filtering to obtain clear liquid, and adding catalyst for water treatment to clear liquid for catalytic oxidation to obtain a first-stage treated water. Optionally, the liquid may be subjected after catalytic oxidation to an adsorption treatment; performing reverse osmosis treatment on first-stage treated water to obtain second-stage reverse osmosis product water and second-stage reverse osmosis concentrated water; and adding oxidant to second-stage reverse osmosis concentrated water for oxidation treatment to obtain directly discharged effluent water. The obtaining of effluent water may further comprise subjecting liquid after oxidation treatment to adsorption treatment. The above method can recycle 75-85 wt % of water, and operates easily. Thereby, improvement to overall utilization rate of water, and treatment of little remaining water is met to effluent standard for reduction of environmental pollution and economic investment.
Supported Catalyst Used For Synthesizing Polyether Amine, And Manufacturing Method
A supported catalyst used for synthesizing a polyether amine, and a manufacturing method of the catalyst. The catalyst comprises: a porous oxide as a support; Ni, Cu, Pd, and Rh as active components; and one or more of any of Zr, Cr, Mo, Fe, Zn, Sn, Bi, Ce, La, Hf, Sr, Sb, Mg, Be, Re, Ta, Ti, Sc, Ge and related metals as an auxiliary agent. The catalyst can be used in an amination reaction for a large molecular weight polyether polyol, and is particularly active and selective for an amination reaction of a low molecular weight polyether polyol. The catalyst has a simple and economic manufacturing technique and good potential for future applications.
CATALYST SYSTEM FOR OXIDATIVE DEHYDROGENATION, REACTOR FOR OXIDATIVE DEHYDROGENATION INCLUDING CATALYST SYSTEM, AND METHOD OF PERFORMING OXIDATIVE DEHYDROGENATION USING REACTOR
Provided is a catalyst system for oxidative dehydrogenation, a reactor for oxidative dehydrogenation including the catalyst system, and a method of performing oxidative dehydrogenation using the reactor. In the catalyst system, a fixed-bed reactor is filled with a catalyst for oxidative dehydrogenation in an n-stage structure (n being an integer of 2 or more), wherein each stage of the n-stage structure satisfies Equations 1 and 2 as claimed so that the concentration of an active ingredient included in the catalyst gradually increases in the direction in which reactants are fed into the reactor. Heat generated inside the reactor may be effectively controlled during oxidative dehydrogenation, thereby improving conversion rate, selectivity, and yield. In addition, catalyst deterioration may be reduced, thereby improving long-term stability of the catalyst.