Patent classifications
B01J8/04
METHOD FOR PREPARING CHLORINE GAS THROUGH CATALYTIC OXIDATION OF HYDROGEN CHLORIDE
A method for preparing chlorine gas through catalytic oxidation of hydrogen chloride is carried out by one-time hydrogen chloride feeding and multi-stage oxygen feeding, one-time oxygen feeding and multi-stage hydrogen chloride feeding, or both, returning a product gas stream without separation thereof, and optionally carrying out heat insulation means. In the present invention, excessive reaction heat concentration is prevented, therefore, the method of the present invention is a chlorine gas recovery method implemented through the Deacon catalytic oxidation of hydrogen chloride that may be industrialized.
METHOD FOR PREPARING CHLORINE GAS THROUGH CATALYTIC OXIDATION OF HYDROGEN CHLORIDE
A method for preparing chlorine gas through catalytic oxidation of hydrogen chloride is carried out by one-time hydrogen chloride feeding and multi-stage oxygen feeding, one-time oxygen feeding and multi-stage hydrogen chloride feeding, or both, returning a product gas stream without separation thereof, and optionally carrying out heat insulation means. In the present invention, excessive reaction heat concentration is prevented, therefore, the method of the present invention is a chlorine gas recovery method implemented through the Deacon catalytic oxidation of hydrogen chloride that may be industrialized.
CATALYTIC MEMBRANE SYSTEM FOR CONVERTING BIOMASS TO HYDROGEN
A two-reactor catalytic system including a catalytic membrane gasification reactor and a catalytic membrane water gas shift reactor. The catalytic system, for converting biomass to hydrogen gas, features a novel gasification reactor containing both hollow fiber membranes that selectively allow O.sub.2 to permeate therethrough and a catalyst that facilitates tar reformation. Also disclosed is a process of converting biomass to H2. The process includes the steps of, among others, introducing air into a hollow fiber membrane; mixing the O.sub.2 permeating through the hollow fiber membrane and steam to react with biomass to produce syngas and tar; and reforming the tar in the presence of a catalyst to produce more syngas.
METHOD FOR PRODUCING BUTADIENE FROM ETHANOL WITH OPTIMISED IN SITU REGENERATION OF THE CATALYST OF THE SECOND REACTION STEP
The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 4 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing three regeneration loops.
METHOD FOR PRODUCING BUTADIENE FROM ETHANOL WITH OPTIMISED IN SITU REGENERATION OF THE CATALYST OF THE SECOND REACTION STEP
The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 4 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing three regeneration loops.
Process For Recovering Heat At High Temperatures In Plasma Reforming Systems
A heat recovery system for plasma reformers is comprised of a cascade of regenerators and recuperators that are arranged to transfer in stages the heat at high temperatures for storage, transport, and recirculation. Recirculation of heat increases the efficiency of plasma reformers and heat exchanging reduces temperature of the product for downstream applications.
Combined xylene isomerization and transalkylation process unit
The xylene isomerization process unit and the transalkylation process units are combined in the present invention. A fractionation column can be shared by the two units, reducing the capital cost of the complex. In some embodiments, a split shell fractionation column and a split separator can be used.
Combined xylene isomerization and transalkylation process unit
The xylene isomerization process unit and the transalkylation process units are combined in the present invention. A fractionation column can be shared by the two units, reducing the capital cost of the complex. In some embodiments, a split shell fractionation column and a split separator can be used.
Hydrocarbon vapor recovery system with oxygen reduction
A system for reducing dioxygen (O.sub.2) present in vapors from oil storage tanks. The system may include an inlet that receives vapors from the tanks; a heating device coupled with the inlet that heats vapors to a first temperature to form heated vapor; and a vessel coupled receiving heated vapor and containing at least one catalyst to reduce dioxygen from the heated vapor. The catalyst may include palladium, and the vessel may include zinc oxide to remove sulfur from the heated vapor. A compressor may be used to compress the vapors. A controller may be provided to monitor O.sub.2 concentration in heated vapor, and the controller directs flow of heated vapor to a gas pipeline if the O.sub.2 concentration is below a predetermined level; or if the O.sub.2 concentration is unacceptably high, the controller directs flow of vapor to be re-circulated within the system to further reduce O.sub.2 concentration therein.
METHODS, SYSTEMS, AND CATALYSTS FOR THE DIRECT CONVERSION OF SYNGAS TO HIGH-OCTANE HYDROCARBONS
The present disclosure relates to a method that includes converting a gas stream that contains hydrogen (H.sub.2) and carbon monoxide (CO) to a second mixture that contains a hydrocarbon, for example, a hydrocarbon having between 3 and 15 carbon atoms, where the converting is performed using a first catalyst configured to convert H.sub.2 and CO to methanol, a second catalyst configured to convert methanol to dimethyl ether (DME), and a third catalyst configured to convert DME to the hydrocarbon.