A porous formed body (Y) including a porous formed body (X) that satisfies the following (x-1) to (x-3), and an alkali metal carbonate or an alkali metal bicarbonate, in which a content of the alkali metal carbonate or the alkali metal bicarbonate is in a range of from 1 part by mass to 230 parts by mass, with respect to 100 parts by mass of the porous formed body (X), and a production method thereof, an α-olefin dimerization catalyst and a production method thereof, and a method of producing an α-olefin dimer: requirement (x-1): a volume of pores with a pore diameter in a range of from 0.01 μm to 100 μm is from 0.10 mL/g to 1.00 mL/g; requirement (x-2): a median pore diameter of pores with a pore diameter in a range of from 0.01 μm to 100 μm is from more than 0.01 μm to 10.0 μm; and requirement (x-3): a crushing strength is from 0.7 kgf to 15.0 kgf.

A precursor mixture for producing a porous body, wherein the precursor mixture comprises: (i) milled alpha alumina powder having a particle size of 0.1 to 6 microns, (ii) boehmite powder that functions as a binder of the alpha alumina powders, and (iii) burnout materials having a particle sizes of 1-10 microns. In some embodiments, an unmilled alpha alumina powder having a particle size of 10 to 100 microns is also included in said precursor mixture. Also described herein is a method for producing a porous body in which the above-described precursor mixture is formed to a given shape, and subjected to a heat treatment step in which the formed shape is sintered to produce the porous body.

A precursor mixture for producing a porous body, wherein the precursor mixture comprises: (i) milled alpha alumina powder having a particle size of 0.1 to 6 microns, (ii) boehmite powder that functions as a binder of the alpha alumina powders, and (iii) burnout materials having a particle sizes of 1-10 microns. In some embodiments, an unmilled alpha alumina powder having a particle size of 10 to 100 microns is also included in said precursor mixture. Also described herein is a method for producing a porous body in which the above-described precursor mixture is formed to a given shape, and subjected to a heat treatment step in which the formed shape is sintered to produce the porous body.

A production method comprises the steps of obtaining a mixed slurry by adding an alumina component and at least one selected from an alumina component and a clay mineral to a binder containing a silicon oxide; obtaining a metal trapping precursor by mixing the mixed slurry with a compound of a first metal component and heating the mixed slurry of metal component; and obtaining a metal trapping by drying and calcining the metal trapping precursor. A metal trapping comprises: a binder mainly containing silicon oxide, one or two selected from an alumina component and a clay mineral, and an oxide of a first metal component; having no peak of silicate of the first metal component detected in X-ray diffraction analysis, having an attrition resistance index CAI within a predetermined range. A fluid catalytic cracking catalyst comprises the metal trapping, a zeolite component, a binder component, and a clay mineral component.

A production method comprises the steps of obtaining a mixed slurry by adding an alumina component and at least one selected from an alumina component and a clay mineral to a binder containing a silicon oxide; obtaining a metal trapping precursor by mixing the mixed slurry with a compound of a first metal component and heating the mixed slurry of metal component; and obtaining a metal trapping by drying and calcining the metal trapping precursor. A metal trapping comprises: a binder mainly containing silicon oxide, one or two selected from an alumina component and a clay mineral, and an oxide of a first metal component; having no peak of silicate of the first metal component detected in X-ray diffraction analysis, having an attrition resistance index CAI within a predetermined range. A fluid catalytic cracking catalyst comprises the metal trapping, a zeolite component, a binder component, and a clay mineral component.

The present invention describes a mixture comprising carbonaceous raw material of low value as a fuel and a nanocatalyst. The catalytic mixture comprises from 1% to 50% by weight of a nanocatalyst; and from 99% to 50% by weight of carbonaceous raw material selected from petroleum coke, coal, heavy residual fraction of oil, or a mixture thereof. The nanocatalyst comprises a carbon nanomaterial of between 99.99% and 80% by weight in contents and at least one alkali metal of between 0.01% and 20% by weight in contents, based on the total weight of the nanocatalyst, and the specific surface area of the nanocatalyst ranges between 400 and 1300 m2/g. Furthermore, the present invention also describes a process for gasifying the catalytic mixture which comprises the steps of placing the mixture in a gasifier; heating the mixture in the presence of an oxidizing agent selected from air, pure oxygen, carbon dioxide, water vapor, or a mixture thereof at a temperature ranging between 200 and 1,300° C.; and obtaining a gaseous product comprising H2, CO, CO2, CH4.

The present invention describes a mixture comprising carbonaceous raw material of low value as a fuel and a nanocatalyst. The catalytic mixture comprises from 1% to 50% by weight of a nanocatalyst; and from 99% to 50% by weight of carbonaceous raw material selected from petroleum coke, coal, heavy residual fraction of oil, or a mixture thereof. The nanocatalyst comprises a carbon nanomaterial of between 99.99% and 80% by weight in contents and at least one alkali metal of between 0.01% and 20% by weight in contents, based on the total weight of the nanocatalyst, and the specific surface area of the nanocatalyst ranges between 400 and 1300 m2/g. Furthermore, the present invention also describes a process for gasifying the catalytic mixture which comprises the steps of placing the mixture in a gasifier; heating the mixture in the presence of an oxidizing agent selected from air, pure oxygen, carbon dioxide, water vapor, or a mixture thereof at a temperature ranging between 200 and 1,300° C.; and obtaining a gaseous product comprising H2, CO, CO2, CH4.

An exhaust gas purification catalyst (C), including a three-dimensional structure (10) and a catalyst component layer (20) supported on the three-dimensional structure (10), where the average thickness of the catalyst component layer (20) is 15 μm or more to 200 μm or less, the average particle size of the catalyst component is 2 μm or more to 10 μm or less, and the catalyst component particle size variation coefficient is 10 or more and less than 50. The particle distribution of the catalyst component can be 90% or more to 99.9% or less.

An exhaust gas purification catalyst (C), including a three-dimensional structure (10) and a catalyst component layer (20) supported on the three-dimensional structure (10), where the average thickness of the catalyst component layer (20) is 15 μm or more to 200 μm or less, the average particle size of the catalyst component is 2 μm or more to 10 μm or less, and the catalyst component particle size variation coefficient is 10 or more and less than 50. The particle distribution of the catalyst component can be 90% or more to 99.9% or less.

The present disclosure is generally directed to a new and innovative system, process and method that utilize a new “non-oxygen type of oxidizers” process for methane (CH.sub.4) upgrading to value-added products such as olefins and aromatics (i.e., benzene, toluene and xylene (BTX)) etc. and further removing toxic impurities such as sulphur-containing compounds (i.e. H.sub.2S) by using the sulphur as a source of radical.