Processes for separating CO from CO.sub.2 in flue gas streams from partial oxidation regenerator in FCC processes, as well as reducing the sulfur content of the flue gas stream are described. The processes involve separating the cooled reactor effluent stream into a CO.sub.2 product stream, the CO.sub.2 recycle stream, and a CO product stream. The processes may incorporate either dry sorbent injection (DSI) units or wet gas scrubbing units to remove sulfur compounds. The separation processes can utilize cryogenic fractionation, pressure swing adsorption (PSA) processes including vacuum PSA, and temperature swing adsorption (TSA) processes. The flue gas stream can be used to preheat the CO.sub.2 recycle stream.

Process for preparing a polyolefin polymer comprising the steps of a) forming a particulate polyolefin polymer by polymerizing one or more olefins in the presence of a polymerization catalyst system in a polymerization reactor; b) discharging the formed polyolefin particles from the polymerization reactor; c) degassing the polyolefin particles by a process comprising at least a final step of contacting the polyolefin particles with a nitrogen stream in a degassing vessel; and d) transferring the polyolefin particles from the vessel, in which the contacting of the polyolefin particles with the nitrogen stream is carried out, to a melt mixing device, in which the polyolefin particles are melted, mixed and thereafter pelletized, without passing the particles through a buffering device,
wherein the degassing vessel is only partly filled with polyolefin particles and the empty volume within the degassing vessel is sufficient to take up additional polyolefin particles for at least 3 hours if the transfer of polyolefin particles of step d) from the degassing vessel to the melt mixing device is discontinued and the discharge of polyolefin particles from the polymerization reactor according to step b) is continued with unchanged rate.

The number of small gels that form in polyolefin thin films may be reduced by altering certain production parameters of the polyolefin. In some instances, the number of small gels may be influenced by the melt index of the polyolefin. However, in many instances, melt index is a critical part of the polyolefin product specification and, therefore, is not manipulated. Two parameters that may be manipulated to mitigate small gel count while maintaining the melt index are polyolefin residence time in the reactor and ICA concentration in the reactor.

The present invention relates to a continuous manufacturing apparatus for a carbon nanotube having gas separation units and a continuous manufacturing method for a carbon nanotube using the same. According to the present invention, the present invention has an effect to provide the continuous manufacturing apparatus of the carbon nanotube and continuous manufacturing method using the same, in which it makes possible to perform a rapid processing; has excellent productivity and excellent conversion rate of carbon source; can significantly reduce the cost of production; can reduce energy consumption because a reactor size can be decreased as compared with capacity; and a gas separation unit that not generate a waste gas.

A carbonaceous feed pyrolysis apparatus is provided including two or more hot particle fluidised beds, one of which contains a combustion zone, and one or more positive displacement apparatus for the transfer of hot particles beds. Also provided is a bio-oil production process including two or more fluidised beds, a first combustion zone carried out in one or more combustion fluidised beds in which a particulate material is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which hot particles heated in the combustion zone are used for pyrolysis of bio-mass, the combustion zone being operated at or about atmospheric pressure at a temperature of from 400 C. to 1100 C., and the pyrolysis zone being operated at a pressure of from atmospheric to 100 Barg at a temperature of from 400 C. to 900 C.

The present invention relates to a process for the continuous preparation of a polyolefin in a reactor from one or more -olefin monomers of which at least one is ethylene or propylene, wherein the reactor comprises a fluidized bed, an expanded section located at or near the top of the reactor, a distribution plate located at the lower part of the reactor and an inlet for a recycle stream located under the distribution plate wherein the process comprisesfeeding a polymerization catalyst to the fluidized bed in the area above the distribution platefeeding the one or more -olefin monomers to the reactorwithdrawing the polyolefin from the reactorcirculating fluids from the top of the reactor to the bottom of the reactor, wherein the circulating fluids are compressed using a compressor and subsequently cooled using a heat exchanger to form a cooled recycle stream comprising liquid, and wherein the cooled recycle stream is introduced into the reactor using the inlet for the recycle stream wherein a part of the cooled recycle stream is drawn to form a liquid comprising stream, wherein the liquid comprising stream is introduced into the expanded section during at least part of the polymerization process, and wherein the liquid comprising stream is brought into contact with at least part of the interior surface of the expanded section.

A catalytic reactor may have at least one reactor module and a shell that extends about a reactor center axis. The reactor module may include a gas distribution chamber, a gas collection chamber, and a catalyst. The gas distribution chamber may be connected to a shell-side gas feed. The gas collection chamber may be connected to a shell-side gas discharge. A catalyst bed between the distribution and collection chambers may extend transversely to the reactor center axis. The gas distribution and collection chambers are bounded by the catalyst bed and reactor walls. The gas feed either opens into the gas distribution chamber on the shell side or is connected to a pipe length that extends towards the reactor center axis and opens into the gas distribution chamber in the region of the reactor center axis. A height parallel to the reactor center axis of the gas distribution chamber reduces towards the reactor center axis starting from a mouth of the gas feed in the case of a shell-side connection.

A method is provided of shutting down an operating three-phase slurry bubble column reactor (10) having downwardly directed gas distribution nozzles (30) submerged in a slurry body (19) of solid particulate material suspended in a suspension liquid contained inside a reactor vessel (12), with the gas distribution nozzles (30) being in flow communication with a gas feed line (26) through which gas is fed to the gas distribution nozzles (30) by means of which the gas is injected downwardly into the slurry body (19). The method includes abruptly stopping flow of gas from the gas feed line (26) to the gas distribution nozzles (30) to trap gas in the gas distribution nozzles (30) thereby to inhibit slurry ingress upwardly into the gas distribution nozzles (30).

In a novel process for methanol production from low quality synthesis gas, in which relatively smaller adiabatic reactors can be operated more efficiently, some of the inherent disadvantages of adiabatic reactors for methanol production are avoided. This is done by controlling the outlet temperature in the pre-converter by rapid adjustment of the recycle gas, i.e. by manipulating the gas hourly space velocity in the pre-converter.

The present disclosure relates to a process for production of a monoalkyl aromatic compound by alkylation of alkylatable aromatic compounds with an alkylating agent in a reactor comprising at least a first and a second series-connected alkylation reaction zones and a cooler disposed between the first and the second series-connected alkylation reaction zones. The process comprising a step of cooling at least a portion of an effluent withdrawn from the first alkylation reaction zone before being introduced into the second alkylation reaction zone.