A multi-stage product gas generation system converts a carbonaceous material, such as municipal solid waste, into a product gas which may subsequently be converted into a liquid fuel or other material. One or more reactors containing bed material may be used to conduct reactions to effect the conversions. Unreacted inert feedstock contaminants present in the carbonaceous material may be separated from bed material using a portion of the product gas. A heat transfer medium collecting heat from a reaction in one stage may be applied as a reactant input in another, earlier stage.

Synthesizing methanol from a synthesis gas and separating an unreacted gas from a reaction mixture obtained by passing through the synthesis step, the method including a synthesis loop having at least two synthesis steps and at least two separation steps; obtaining a first mixed gas by increasing through a circulator a pressure of a residual gas, obtained by removing a purge gas from the final unreacted gas separated from the final reaction mixture subsequent to the final synthesis step, and by mixing the residual gas with a fraction of a make-up gas; synthesizing methanol; separating a first unreacted gas from the first reaction mixture obtained in the synthesizing step; obtaining a second mixed gas by mixing the first unreacted gas and a fraction of the make-up gas; finally synthesizing methanol; and separating the final unreacted gas from the final reaction mixture obtained in the final synthesis step.

An object of the present invention is to suppress performance deterioration of a molybdenum composite oxide-based catalyst at the time of performing gas-phase catalytic partial oxidation with molecular oxygen by using a tubular reactor. The present invention relates to a catalytic oxidation method using a tubular reactor in which a Mo compound layer containing a Mo compound and a composite oxide catalyst layer containing a Mo composite oxide catalyst are arranged in this order from a reaction raw material supply port side and under a flow of a mixed gas containing 75 vol % of air and 25 vol % of water vapor at 440° C., a Mo sublimation amount of the Mo compound is larger than a Mo sublimation amount of the Mo composite oxide catalyst under the same conditions.

The present disclosure relates to a reactor and a method of operation for an exothermal process being catalyzed by a catalytically active material receiving a reactant gas and providing a product gas, in which said exothermal process has a heat development having a potential for thermally degrading said catalytically active material, and which exothermal process operates at a temperature at which the reactants and at least 80% or all of the products are present as gases, said method comprising the steps of a) directing the reactant gas to a first zone of a material catalytically active in the exothermal process producing an first product gas, and b) directing the first product gas to a second zone of a material catalytically active in the exothermal process producing a product gas, with the option of fully or partially by-passing either said first zone or said second zone, while directing a non-condensing gas stream having a temperature at least 50° C. lower than the product gas to said by-passed zone, wherein the choice of by-passing said zone is made based on the time of operation or a process parameter reflecting the catalytic activity of the zone of catalytically active material which is not by-passed with the associated benefit of reducing the extent of thermal deactivation of the catalytically active material, and thus increasing the overall lifetime of the catalytically active material.

A method of forming a hydrocarbon product, the method comprising a first step of enriching a carrier liquid with carbon monoxide and hydrogen and a subsequent step of bringing the enriched carrier liquid into contact with a catalyst in a first reaction zone of a reactor, wherein the catalyst catalyzes reaction of the carbon monoxide and hydrogen to form the hydrocarbon product.

A process for producing 2,3,3,3-tetrafluoropropene comprises the steps: i) in a first adiabatic reactor comprising a fixed bed composed of an inlet and an outlet, bringing 2-chloro-3,3,3-trifluoropropene into contact with hydrofluoric acid in the gas phase in the presence of a catalyst to produce a stream A comprising 2,3,3,3-tetrafluoropropene, HF and unreacted 2-chloro-3,3,3-trifluoropropene; and ii) in a second adiabatic reactor comprising a fixed bed composed of an inlet and an outlet, bringing hydrofluoric acid into contact in the gas phase, optionally in the presence of a catalyst, with at least one chlorinated compound to produce a stream B comprising 2-chloro-3,3,3-trifluoropropene. The stream A obtained in step i) feeds said second reactor. The inlet temperature of the fixed bed of one of said first or second reactors is between 300° C. and 400° C. The longitudinal temperature difference between the inlet and the outlet of the fixed bed in question is less than 20° C.

A reactor design and configuration and a process for the catalytic dehydration of ethanol to ethylene where the reactor train is comprised of a multi-stage single reactor vessel or multiple reactor vessels wherein each stage and/or vessel has different length, internal diameter, and volume than the other stages and/or vessels and in addition the stages and/or reactor vessels are connected in series arrangement, preferably used with an improved means of introducing the ethanol feedstock and a heat carrying inert gas to the improved reactor train. The inert gas is heated in a separate furnace from the ethanol feed and then injected into the ethanol feed to supply the heat of reaction.

Proposed is a process for producing methanol from synthesis gas by means of multi-stage, for example 2-stage, heterogeneously catalyzed methanol synthesis, wherein the methanol product formed in every synthesis stage is removed by condensation and the remaining residual gas is applied to the downstream synthesis stage or after removal of a purge stream recycled to the first synthesis stage as a recycle stream. According to the invention a substream is removed from the synthesis gas fresh gas and introduced into the second methanol synthesis reactor as a bypass stream.

Device for the mixing and distribution of fluids for a catalytic reactor with a downward flow, said device comprising at least one collection zone (A), at least one mixing zone (B) comprising at least one enclosure (15) for the mixing of the fluids, at least one distribution zone (C), characterized in that said mixing zone (B) is situated at the same level as the distribution zone (C) and also comprises at least one enclosure (16) for the exchange of the fluids, connected to, and communicating with, said mixing enclosure (15), said exchange enclosure (16) comprising at least one lateral passage section (17a, 17b) suitable for the passage of the fluids from said exchange enclosure (16) to said distribution zone (C).

A mixing device mounted between two catalyst beds in a multi-bed catalytic reactor with a cylindrical shape. The mixing device has a circular outer rim which corresponds to the inner wall of the reactor, and includes a collecting section for collecting fluid from an up-stream catalytic bed, a mixing section for mixing the collected fluid, and a discharging section for discharging the mixed fluid to a down-stream catalytic bed. The collecting section, the mixing section and the discharging section are disposed outside the center of the circular cross-section of the reactor.