B01J8/38

Stator-rotor vortex chamber for mass and/or heat transfer processes

A device for bringing a target medium into contact with a carrier fluid comprises a chamber comprising a circumferential wall, a bottom wall and a top wall forming an enclosure for containing the target medium while contacting the carrier fluid, the chamber being substantially rotationally symmetric with respect to an axis of symmetry and adapted for remaining mechanically static in operation of the device. The device comprises a fluid inlet for injecting the carrier fluid into the chamber in a substantially tangential direction with respect to an inner surface of the circumferential wall, and an outlet. The device comprises a fluid distributor in the chamber for enabling the injected carrier fluid to pass through the distributor in a substantially inward radial direction, the distributor being substantially rotationally symmetric and adapted for rotating around the axis when driven by a transfer of momentum between the injected carrier fluid and the distributor.

Methods and apparatuses for energy storage device electrode fabrication

An apparatus for forming an electrode film mixture can have a first source including a polymer dispersion comprising a liquid and a polymer, a second source including a second component of the electrode film mixture, and a fluidized bed coating apparatus including a first inlet configured to receive from the first source the dispersion, and a second inlet configured to receive from the second source the second component.

PROCESS AND PLANT FOR THERMAL DECOMPOSITION OF ALUMINIUM CHLORIDE HYDRATE INTO ALUMINIUM OXIDE

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.

PROCESS AND PLANT FOR THERMAL DECOMPOSITION OF ALUMINIUM CHLORIDE HYDRATE INTO ALUMINIUM OXIDE

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.

Process and apparatus for fluidizing a catalyst bed
11260357 · 2022-03-01 · ·

A process and apparatus for fluidizing a catalyst cooler with fluidization gas fed to the cooler below the catalyst bed is disclosed. Fluidization headers extend through an outlet manifold and deliver fluidization gas through distributors protruding through an outlet tube sheet defining said outlet manifold. The outlet manifold collects heated water vapor from the catalyst cooler and discharges it from the catalyst cooler.

SYSTEM TO MAXIMIZE CO FROM FLUID CATALYTIC CRACKING (FCC) PROCESS BY COKE OXIDATION WITH METAL OXIDES
20220056357 · 2022-02-24 ·

Provided is a process capable of converting the cokes on spent catalysts in a fluid catalytic cracking (FCC) process into synthesis gas. The produced synthesis gas contains high concentrations of CO and H.sub.2 and may be utilized in many downstream applications such as syngas fermentation for alcohol production, hydrogen production and synthesis of chemical intermediates. A reducer/regenerator reactor for a fluid catalytic process comprising a chemical looping system to produce synthesis gas is also described.

NAPHTHA CATALYTIC CRACKING CATALYST, CATALYTIC CRACKING METHOD AND REACTION DEVICE

A method for catalytic cracking of naphtha is provided. Naphtha is catalytically cracked under the action of a catalyst. The catalyst includes aluminosilicate, alkali metal oxide, alkaline earth metal oxide, TiO.sub.2, iron oxide, vanadium oxide and nickel oxide. On the other hand, a rapid separation component is arranged in a disengager of a catalytic cracking reaction device, so that a transport disengaging height is greatly reduced without changing a gas flow and a diameter of the disengager. In addition, the separation efficiency of oil gas and the catalyst is improved.

System and method for preventing catalyst from overheating

A system for preventing a catalyst from overheating is provided. The system includes: a first reactor filled with a catalyst at least in part and configured to receive reaction gas and produce product gas; and a second reactor configured to cool a catalyst discharged from the first reactor. The catalyst is circulated between the first reactor and the second reactor by injecting the catalyst cooled in the second reactor into the first rector.

Methods and apparatuses for energy storage device electrode fabrication

An apparatus for forming an electrode film mixture can have a first source including a polymer dispersion comprising a liquid and a polymer, a second source including a second component of the electrode film mixture, and a fluidized bed coating apparatus including a first inlet configured to receive from the first source the dispersion, and a second inlet configured to receive from the second source the second component.

Systems and Methods for Measuring Particle Accumulation on Reactor Surfaces
20170320034 · 2017-11-09 · ·

Systems and methods for monitoring a particle/fluid mixture are provided. The method can include flowing a mixture comprising charged particles and a fluid past a particle accumulation probe. The method can also include measuring electrical signals detected by the probe as some charged particles pass the probe without contacting the probe while other charged particles contact the probe. The measured electrical signals can be manipulated to provide an output. The method can also include determining from the output if the charged particles contacting the probe have, on average, a different charge than the charged particles that pass the probe without contacting the probe.