B01J35/51

Core-Shell Nanoparticulate Compositions And Methods
20190291092 · 2019-09-26 ·

Core-shell nanoparticulate compositions and methods for making the same are disclosed. In some embodiments core-shell nanoparticulate compositions comprise transition metal core encapsulated by metal oxide shell. Methods of catalysis comprising core-shell nanoparticulate compositions of the invention are disclosed. Compositions comprising core-shell nanoparticles displayed on a metal-oxide support and methods for preparing the same are also disclosed. In some embodiments compositions comprise core-shell nanoparticles displayed as a substantially single layer superposed on a metal oxide support. Methods of catalysis employing the supported core-shell nanoparticles are disclosed.

NANO-CRYSTALLITE BINDER BASED CO COMBUSTION PROMOTER

The present invention relates to catalyst product, a method of making a catalyst and its use in fluid catalytic conversion process. In particular, this invention relates to a process for the preparation of CO-combustion promoter microspheres, comprising a large crystallite low surface area alumina; a composite binder comprising nano-crystallite alumina and dispersant; and platinum or palladium or both. The large crystallite low surface area alumina is bound together by the composite binder in the said particulate composition.

Composition and process for preparation of cracking catalyst suitable for enhancing yields of light olefins

The present invention relates to a fluid catalytic cracking additive composition for cracking of heavy hydrocarbon feed stocks and process for preparing the additive. The additive is suitable for enhancing yields of light olefins such as propylene, isobutylene, LPG and reduces the bottom yields. The invention specifically relates to a fluid catalytic cracking additive composition comprising a pentasil zeolite, zeolites having pore size in a range of 5.4-7.7 , alumina, colloidal silica, kaolin clay, and phosphate, wherein the zeolites having pore size in the range of 5.4-7.7 is present in an amount of 1 to 10 wt % with respect to the total amount of the pentasil zeolite and zeolite having the pore size in the range of 5.4-7.7 .

CATALYST ADDITIVE COMPOSITION FOR REDUCTION OF SULFUR IN GASOLINE

The present invention relates to an improved CuAl.sub.2O.sub.4 spinel based catalyst additive composition having bi-modal pore size for improving gasoline sulfur removal activity by maintaining high gasoline selectivity and maintaining research octane number (RON) while cracking heavier hydrocarbon feedstocks in the fluid catalytic cracking unit. More particularly, present invention relates to a gasoline sulfur reduction (GSR) additive comprising copper aluminate spinel, acidic alumina matrix; and clay, wherein the additive having bimodal pore distribution. Present invention also relates to a process for preparing the gasoline sulfur reduction (GSR) additive.

Coatings

The present invention provides a coating composition suitable for use in forming a coating that can reduce a concentration of pollutant gases in the environment. The coating composition includes from 0.01 to 10 vol.-% of mesoporous titania particles, relative to a total volume of the coating composition, and from 5 to 99.99 vol.-% of a polymeric material, relative to the total volume of the coating composition. The mesoporous titania particles have a continuous exterior convex surface, a particle diameter of ?1 ?m but ? to 50 ?m, a BET specific surface area of from 30 to 350 m.sup.2/g, a modal pore diameter of ?5 nm but ?50 nm, and a pore size distribution so that 85% or more of a total pore volume is associated with pores having a diameter of 10 ?m or less.

Photocatalytic filter, purification device, and purification method

A photocatalytic filter including first photocatalytic particles each of which is a composite of an adsorbent and titanium apatite, second photocatalytic particles each of which is glass coated with titanium apatite, a light source configured to emit ultraviolet rays, and a container accommodating the first photocatalytic particles, the second photocatalytic particles, and the light source.

Catalyst support and related processes

The present invention describes a catalyst support, which is used as an inorganic carrier for a Ziegler-Nata catalyst (ZN), using a modified spray cooling method. Such a catalyst support is prepared from alcoholic solutions of (a) an inorganic compound, in which the inorganic compound is a magnesium compound and (b) an inorganic compound and one or more additives. The solutions are prepared at a temperature below 100 C., carried through a nozzle placed inside a reactor, and sprayed into droplets forming a solid precipitate, which is generally spherical, when in contact with an inert hydrocarbon solvent at low temperature. The obtained catalyst support is reacted with a titanium compound, preferably titanium tetrachloride, in order to produce an active catalyst for olefin polymerization.

Hydrogenation and ethynylation catalysts
10399062 · 2019-09-03 · ·

A process for preparing a catalyst includes impregnating a metal oxide carrier with an aqueous solution to form an impregnated carrier; drying the impregnated carrier to form a dried, impregnated carrier; and heat-treating the dried, impregnated carrier in air to form the catalyst; wherein: the aqueous solution includes a copper salt; and from about 3 wt % to about 15 wt % of a C.sub.3-C.sub.6 multifunctional carboxylic acid; and the catalyst includes from about 5 wt % to about 50 wt % copper oxide.

METHOD FOR MANUFACTURING CRYSTALS OF ALUMINATE OF AT LEAST ONE METAL AND/OR ONE METALLOID AND/OR ONE LANTHANIDE, AND APPLICATIONS OF SAME
20190263672 · 2019-08-29 ·

Disclosed is a method for manufacturing crystals of aluminates of one or more element(s) other than aluminium, referred to as A. The method includes: placing starting reagents, including at least one aluminium element source and a source of the element(s) A that has a degree of oxidation of between 1 and 6, in suspension in a liquid medium, forming a suspension referred to as the starting suspension; milling the starting suspension at 50 C., in a three-dimensional liquid medium ball mill for 5 minutes; recovering, at the outlet of the three-dimensional ball mill, a suspension referred to as the end suspension including the starting reagents in activated form or crystals of aluminate of the element(s) A generally in hydrated form; if required, calcination of the end suspension when it includes the starting reagents in activated form, to obtain generally non-hydrated crystals of aluminate of the element(s) A.

Process for preparation of hydrocarbon fuel from waste rubber

The present disclosure provides a process for preparing a hydrocarbon fuel from waste rubber. The process involves admixing, in a reaction vessel, at least one fluid medium with the waste rubber to obtain a slurry; wherein the concentration of the waste rubber in the slurry ranges from 45% to 70%. A reactor is charged with the slurry and a predetermined amount of at least one catalyst composition to obtain a mixture, followed by introduction of hydrogen to the reactor to attain a predetermined pressure and heating the mixture at a predetermined temperature, to attain an autogenously generated pressure, and for a predetermined time period to obtain a reaction mass comprising the hydrocarbon fuel. This reaction mass comprising the hydrocarbon fuel is then cooled to obtain a cooled reaction mass. The hydrocarbon fuel is then separated from the cooled reaction mass.