B01J37/0045

AN FCC CATALYST COMPOSITION AND A PROCESS FOR ITS PREPARATION

The present disclosure relates to an FCC catalyst composition and a process for preparing the same. In a first aspect, there is provided an FCC catalyst composition comprising 25 to 45 wt % Y-type zeolite, 20 to 40 wt % silicon oxide, 5 to 25 wt % alumina, 5 to 35 wt % of at least one clay and 0.5 to 3 wt % of at least one rare earth oxide. The weight % of each of the component is with respect to the total weight of the composition. The FCC catalyst composition has an average particle size in the range of 45-120μ. In a second aspect, there is provided a process for preparing the FCC catalyst composition, which uses ball milled pseudoboehmite having an average particle size in the range of 1 to 8 micron and the whole process is carried out at a pH value in the range of 6 to 7.

Catalyst With Vanadium Trap
20230072292 · 2023-03-09 ·

This invention provides a catalyst composition characterized in that the catalyst composition comprises one or more rare earth oxophosphorus components.

MATERIALS COMPRISING CARBON-EMBEDDED COBALT NANOPARTICLES, PROCESSES FOR THEIR MANUFACTURE, AND USE AS HETEROGENEOUS CATALYSTS

The present invention relates to catalytically active material, comprising grains of non-graphitizing carbon with cobalt nanoparticles dispersed therein, wherein d.sub.p, the average diameter of cobalt nanoparticles in the non-graphitizing carbon grains, is in the range of 1 nm to 20 nm, D, the average distance between cobalt nanoparticles in the non-graphitizing carbon grains, is in the range of 2 nm to 150 nm, and ω, the combined total mass fraction of metal in the non-graphitizing carbon grains, is in the range of 30 wt % to 70 wt % of the total mass of the non-graphitizing carbon grains, and wherein d.sub.p, D and ω conform to the following relation: 4.5 d.sub.p/ω>D≥0.25 d.sub.p/ω. The present invention, further, relates to a process for the manufacture of material according to the invention, as well as its use as a catalyst.

Particulate Filter
20220316372 · 2022-10-06 ·

A particulate filter disclosed herein includes a wall-flow structure substrate 10 and a wash coat layer 20 held inside a partition 16 of the substrate 10. The wash coat layer 20 includes an inlet layer 22 formed to have predetermined length L.sub.A and thickness T.sub.A from near an end thereof on an exhaust gas inflow side X1, and an outlet layer 24 formed to have predetermined length L.sub.B and thickness T.sub.B from near an end thereof on an exhaust gas outflow side X2. The inlet layer 22 and the outlet layer 24 partially overlap each other. In the particulate filter disclosed herein, the inlet layer 22 contains a precious metal catalyst, while the outlet layer 24 contains substantially no precious metal catalyst. The length L.sub.A of the inlet layer is 50% or more and 75% or less of a total length L of the partition 16. Thus, the particulate filter is capable of achieving both PM collection performance and pressure-drop reduction performance at high levels.

EXHAUST GAS PURIFICATION CATALYST DEVICE

A gas purification catalyst device comprises: a substrate; and one or more catalyst layers on the substrate. Among the one or more catalyst layers, at least one catalyst layer contains both Cu-CHA-type zeolite particles and iron-supporting metal oxide particles in which iron is supported on metal oxide particles.

METHOD FOR PRODUCING A CATALYTICALLY ACTIVE MULTI-ELEMENT OXIDE CONTAINING THE ELEMENTS MO, W, V AND CU

A process for producing a catalytically active multielement oxide comprising the elements Mo, W, V and Cu, wherein at least one source of the elemental constituents W of the multielement oxide is used to produce an aqueous solution, the resultant aqueous solution is admixed with sources of the elemental constituents Mo and V of the multielement oxide, drying of the resultant aqueous solution produces a powder P, the resultant powder P is optionally used to produce geometric shaped precursor bodies, and the powder P is or the geometric shaped precursor bodies are subjected to thermal treatment to form the catalytically active composition, wherein the aqueous solution used for drying comprises from 1.6% to 5.0% by weight of W and from 7.2% to 26.0% by weight of Mo, based in each case on the total amount of aqueous solution.

CATALYST FOR PRODUCTION OF CARBOXYLIC ACID ESTER, METHOD FOR PRODUCING CATALYST FOR PRODUCTION OF CARBOXYLIC ACID ESTER, AND METHOD FOR PRODUCING CARBOXYLIC ACID ESTER
20230146477 · 2023-05-11 · ·

A catalyst for production of carboxylic acid ester, containing: catalyst metal particles; and a support supporting the catalyst metal particles, wherein the catalyst has a hollow particle ratio of 40% or less.

Catalyst composition for oxidative dehydrogenation of alkane

The present invention provides a catalyst composition for the production of olefins from lighter alkanes by oxidative dehydrogenation route and methods of making the dehydrogenation catalyst composites.

Process and catalyst for low temperature non-oxidative dehydrogenation of propane to propylene

A process and catalyst are provided for the non-oxidative dehydrogenation of propane for the production of propylene as petrochemical building blocks. The process provides a direct single-step gas-phase dehydration of propane mixed with nitrogen in the presence and absence of steam/hydrogen over supported bimetallic alumina-silicates zeolites. The catalyst contains no precious metal entities and may contain one metal from group VIB in combination with another metal from group IIIA or IVA supported on FAU, MFI, KFI, BEA type alumina-silicates zeolites. The process provides a propane conversion of 18% to 52% with a propylene yield of 10% to 25%.

Interesterification catalyst and process

A process for the production of an ester product from a mixture of at least two different ester compounds includes the steps of mixing together at least two different starting ester compounds to form a first ester mixture; and contacting the first ester mixture with a catalyst including from 30-60% of calcium oxide and at least one second metal oxide at a temperature of at least 180° C., for a duration of at least one hour, with mixing, to form a second ester mixture having a melting point which is lower than the melting point of the first ester mixture.