The present technology is directed to processes for conversion of synthesis gas in a tubular reactor to produce a synthetic product that utilizes high activity carbon monoxide hydrogenation catalysts and a heat transfer structure that surprisingly provides for higher per pass conversion with high selectivity for the desired synthetic product without thermal runaway.

A turbulent fluidized bed reactor, device and method for preparing para-xylene and co-producing light olefins from methanol and/or dimethyl ether and benzene, resolving or improving the competition problem between an MTO reaction and an alkylation reaction during the process of producing para-xylene and co-producing light olefins from methanol and/or dimethyl ether and benzene, and achieving a synergistic effect between the MTO reaction and the alkylation reaction. By controlling the mass transfer and reaction, competition between the MTO reaction and the alkylation reaction is coordinated and optimized to facilitate a synergistic effect of the two reactions, so that the conversion rate of benzene, the yield of para-xylene, and the selectivity of light olefins are increased. The turbulent fluidized bed reactor includes a first reactor feed distributor and a number of second reactor feed distributors; the first reactor feed distributor and the plurality of second reactor feed distributions are sequentially arranged.

Systems and methods of reducing heat exchanger fouling rate and of producing polyolefins are provide herein. In some aspects, the methods include providing a first gas stream comprising a gas and entrained fine polyolefin particles to a gas outlet line; preferentially removing a portion of the entrained fine polyolefin particles from the gas outlet line to form a bypass stream comprising a higher concentration of the entrained fine polyolefin particles than is present in the first gas stream; providing the bypass stream to a bypass line comprising a bypass line inlet and a bypass line outlet, wherein the bypass line inlet is located upstream of a first heat exchanger, and wherein the bypass line outlet is located downstream of the first heat exchanger; providing at least a portion of the first gas stream to the first heat exchanger, which produces a first cooled gas stream; and combining the bypass stream and a second gas stream at the bypass line outlet to form a combined gas stream comprising one or more olefins or paraffins, wherein a temperature of the combined gas stream is below the dew point of the combined gas stream.

The present invention is directed to a membrane reactor for the hydrogenation of carbon dioxide, said membrane reactor comprising a reaction compartment (2) comprising a catalyst bed, a permeate compartment (4) and a membrane separating the reaction compartment and the permeate compartment, wherein said permeate compartment comprises a condensing surface.

Axial reactor for exothermic or endothermic chemical reactions, comprising at least a first catalytic bed and a second catalytic bed operating in series and at least one heat exchanger between the two catalytic beds, wherein the first catalytic bed has a collector bottom having a box-like structure with flat and parallel walls, which are gas-permeable, and a plurality of parallel channels defined between the walls, wherein a first series of said channels collects the gaseous flow exiting the catalytic bed and passing through the first wall, said gaseous flow is directed towards the heat exchanger, and the flow exiting the exchanger is directed towards the second catalytic bed via a second series of said channels of the collector bottom.

A method of maintaining a backpressure of a fluidic product is provided. The method includes pressurizing a first reservoir to a first predetermined pressure level using compressed air, delivering the fluidic product to the pressurized first reservoir until a current level of the fluidic product in the first reservoir reaches a first predetermined level, pressurizing a second reservoir to a second predetermined pressure level using the compressed air, delivering the fluidic product to the pressurized second reservoir until a current level of the fluidic product in the second reservoir reaches a second predetermined level, and controlling the backpressure of the fluidic product using the first reservoir and the second reservoir such that a discharge flow of the fluidic product is continuous.

Disclosed herein are systems and processes for the conversion of a methane feedstock to C.sub.2+ hydrocarbons.

A multi-stage dehydrogenation process including contacting, in a first stage, a feed stream comprising a hydrocarbon and steam with a dehydrogenation catalyst under dehydrogenation conditions to yield a first stage effluent, heating the first stage effluent, and contacting, in a second stage, the heated first stage effluent with a dehydrogenation catalyst under dehydrogenation conditions to yield a second stage effluent comprising a dehydrogenation product, wherein the first stage includes a first reactor and a second reactor arranged in parallel, and wherein the second stage includes a third reactor connected in series with the first reactor and the second reactor. A multi-stage dehydrogenation system for carrying out dehydrogenation is also provided.

A reactor for conducting exothermic equilibrium reactions, especially for the performance of methanol synthesis by heterogeneously catalysed conversion of synthesis gas, is proposed, which enables readjustment and hence optimization of the reaction conditions along the longitudinal coordinate of the reactor. For this purpose, in accordance with the invention, the reactor is divided into a multitude of series-connected reaction cells, each of which comprises a preheating zone, a cooled reaction zone, one or more cooling zones and a deposition zone for condensable reaction products. In this way, the reaction conditions are adjustable to the respective, local composition of the reaction mixture and variable over the reactor length.

The present technology is directed to processes for conversion of synthesis gas in a tubular reactor to produce a synthetic product that utilizes high activity carbon monoxide hydrogenation catalysts and a heat transfer structure that surprisingly provides for higher per pass conversion with high selectivity for the desired synthetic product without thermal runaway.