The method for catalytic methanation of synthesis gas includes the following steps: 1) feeding the synthesis gas into the bottom of a reactor of an upward concurrent flow transporting bed so as to adequately mix and preheat with methanation catalyst entering the bottom of the reactor until the activation temperature of the catalyst is reached and then the methanation reaction begins; and 2) after the methanation reaction, immediately passing the product gas and the catalyst grains outputted from the transporting bed into a gas-solid separator to perform a rapid separation so as to obtain the product gas.

Systems and methods for producing light olefins wherein a feed stream comprising naphtha is flowed into a reaction unit comprising a fast fluidized bed reactor coupled to and in fluid communication with a riser reactor. The fast fluidized bed reactor comprises baffles therein to minimize backmixing therein to maximize the production of light olefins. The effluent from the fast fluidized bed reactor is further flowed to the riser reactor. The lift gas, which can comprise nitrogen, methane, flue gas, or combinations thereof, is injected in the reaction united via a sparger. Effluent of the riser reactor is separated in a product separation unit to produce a product stream comprising light olefins and spent catalyst. Spent catalyst is further stripped by a stripping gas comprising methane, nitrogen, flue gas, or combinations thereof. Stripped spent catalyst is regenerated to produce regenerated catalyst, which is subsequently flowed to the fast fluidized bed reactor.

A device with annular spouted fluidized bed can be used for carrying out the majority of the technical processes carried out in fluidized bed devices. The reaction chamber of the device has, throughout at least a part of its height, a downwardly tapering funnel shape with step-structured inner surface. The shape of the reaction chamber, together with the tangential admission thereto of fluidized and other gases, makes it possible to create, in the reaction chamber, an adjustable toroidal fluidized bed, in which the rotation rate of the particles of the material undergoing treatment can be adjusted in both horizontal and vertical planes, and also makes it possible to control the dwell time of particles of different sizes in the reaction zone, the intensity with which materials are treated, and other process parameters.

The present invention relates to a method for improving the cooling capacity of a gas solids olefin polymerization reactor by splitting the fluidization gas and returning part of the fluidization gas to the reactor into the bottom zone of the reactor and another part of the fluidization gas directly into the dense phase formed by particles of a polymer of the at least one olefin suspended in an upwards flowing stream of the fluidization gas in the middle zone of the reactor.

The present invention relates to a fluidized bed reactor. The fluidized bed reactor includes: a catalyst bed; a dust collector provided in an upper portion of the fluidized bed reactor collecting catalyst particles in a gas discharged toward the upper portion of the fluidized bed reactor; and a filter portion provided in a region between the dust collector and the catalyst bed, wherein the filter portion includes a filtering screen and a plurality of conical caps coupled to the filtering screen.

A device with annular spouted fluidized bed can be used for carrying out the majority of the technical processes carried out in fluidized bed devices. The reaction chamber of the device has, throughout at least a part of its height, a downwardly tapering funnel shape with step-structured inner surface. The shape of the reaction chamber, together with the tangential admission thereto of fluidized and other gases, makes it possible to create, in the reaction chamber, an adjustable toroidal fluidized bed, in which the rotation rate of the particles of the material undergoing treatment can be adjusted in both horizontal and vertical planes, and also makes it possible to control the dwell time of particles of different sizes in the reaction zone, the intensity with which materials are treated, and other process parameters.

The present invention relates to a fluidized bed reactor. The fluidized bed reactor includes: a catalyst bed; a dust collector provided in an upper portion of the fluidized bed reactor collecting catalyst particles in a gas discharged toward the upper portion of the fluidized bed reactor; and a filter portion provided in a region between the dust collector and the catalyst bed, wherein the filter portion includes a filtering screen and a plurality of conical caps coupled to the filtering screen.

A process for polymerizing olefin monomer(s) in a gas-solids olefin polymerization reactor comprising a top zone; a middle zone, which comprises a top end in direct contact with said top zone and which is located below said top zone, the middle zone having a generally cylindrical shape; and a bottom zone, which is in direct contact with a bottom end of the middle zone and which is located below the middle zone; comprising the following steps: introducing a fluidization gas stream into the bottom zone; polymerizing olefin monomer(s) in the presence of a polymerization catalyst in a dense phase formed by particles of a polymer of the olefin monomer(s) suspended in an upwards flowing stream of the fluidization gas in the middle zone; introducing a jet gas stream through one or more jet gas feeding ports in a jet gas feeding area of the middle zone at the dense phase in the middle zone of the gas-solids olefin polymerization reactor; wherein the kinetic energy (E.sub.JG) input in the reactor by the jet stream is between 1.5 and 50 times higher than the kinetic energy (E.sub.FG) input in the reactor by the fluidization gas stream (FG).

A process and its relating plant for thermal conversion of aluminum chloride hydrate into aluminum oxide and gaseous hydrogen chloride. In a first step, aluminum chloride hydrate is fed into a decomposition reactor where it is heated to a temperature between 120 and 400° C. Afterwards, the partially decomposed aluminum chloride hydrate is finally calcined to aluminum oxide at a temperature between 850 and 1200° C. in a second reactor. The aluminum chloride hydrate is admixed with aluminum oxide in an intensive mixer with a mass ratio between 1:1 and 10:1 aluminum chloride hydrate to aluminum oxide for using a fluidized bed reactor as a decomposition reactor.

A process and its relating plant for thermal conversion of aluminum chloride hydrate into aluminum oxide and gaseous hydrogen chloride. In a first step, aluminum chloride hydrate is fed into a decomposition reactor where it is heated to a temperature between 120 and 400° C. Afterwards, the partially decomposed aluminum chloride hydrate is finally calcined to aluminum oxide at a temperature between 850 and 1200° C. in a second reactor. The aluminum chloride hydrate is admixed with aluminum oxide in an intensive mixer with a mass ratio between 1:1 and 10:1 aluminum chloride hydrate to aluminum oxide for using a fluidized bed reactor as a decomposition reactor.