The present invention relates to a pressure vessel (1) having a pressure vessel wall (1a) which completely surrounds a reaction chamber (2) as a pressure space for the initiation and/or promotion of chemical and/or physical pressure reactions of a sample (P) to be heated which is accommodated in the reaction chamber (2), wherein the pressure vessel wall (1a) has an infrared-permeable high-pressure window (30) which extends away outward in a direction from the reaction chamber (2) and which is supported in the pressure vessel wall (1a) with respect to a pressure in the reaction chamber (2), wherein the pressure vessel (1) furthermore has an infrared to temperature sensor (40) which is situated directly opposite the high-pressure window (30), in order to measure the temperature of a sample (P), accommodated in the reaction chamber (2), during a pressure reaction through the high-pressure window (30).

Alcoholic spirits may be artificially aged under highly pressurized carbon dioxide. The carbon dioxide may form carbonic acid, which may cause various esters to form in the presence of wood as well as to mellow the flavor when no wood is present. Wood may be pretreated with ozone, which may extract lignin which may further convert to vanillin during pressurized CO2 treatment, giving a vanilla note. After processing with pressurized CO2, a post-treatment of ozone may be given to the spirit, which may cause a mild oxidation and further mellowing of the spirit.

Embodiments of a method for reducing unreacted ethylene monomer in a low density polyethylene (LDPE) polymerization process comprises: delivering a monomer feedstock comprising ethylene monomer to a compressor system to produce a pressurized feedstock having a pressure of at least 2000 bar; passing the pressurized feedstock to at least one free radical polymerization reactor to produce a reactor effluent comprising the LDPE and unreacted ethylene monomer; and delivering the reactor effluent to a separation system comprising a first separation vessel, a second separation vessel, and a third separation vessel in series, the third separation vessel having an operating pressure of less than or equal to 0.05 bar, wherein the third separation vessel produces a separation product comprising LDPE and less than or equal to 50 ppm of the unreacted ethylene monomer, wherein there is no stripping agent added upstream of the third separation vessel.

It is provided a process for producing an ethylene copolymer comprising compressing ethylene monomer at a certain pressure; adding a fresh comonomer in liquid form and, optionally, a fresh modifier in liquid form at a certain pressure to the compressed ethylene monomer; introducing the resulting compressed mixture into an autoclave reactor having a first reaction zone and at least one more reaction zone, the first reaction zone having a volume that is greater than 50% of the total reactor volume, and, optionally, at least one additional reactor; adding at least one free radical initiator in order to start a polymerization reaction; and separating the ethylene copolymer from the reaction mixture; wherein all the compressed ethylene monomer or the compressed mixture are introduced into the first reaction zone of the autoclave reactor, and wherein the compressed mixture is introduced into the autoclave reactor and, optionally, into the at least one additional reactor at a temperature from −20° C. to 70° C.

The process and apparatus according to the invention allow the production of chemical compounds without the use of catalysts. For this purpose, the reactants necessary for the desired products are fed to compression reactors. In addition, the reaction conditions are controlled by means of an electronic control device. For this purpose, among other things, the compression reactors are combined with an electric motor, thereby influencing the residence time in the reactors. In addition, it is planned to raise the reactant pressures with the help of a compressor. In addition, the operating conditions are recorded with suitable sensors and/or analysers.

The process and apparatus according to the invention allow the production of hydrocarbons and ammonia without the use of catalysts. For this purpose, waste gases containing CO.sub.2 or N.sub.2 from an upstream process are fed to compression reactors. In addition, hydrogen from an electrolyzer is fed to these reactors to enable hydrogenation of the fed substances. Methane, alcohols and ammonia, for example, can be produced by this process. In order to increase the yield of the process, it is planned to raise the reactant pressure with the aid of a compressor.

A reactor for performing a reaction between two immiscible fluids of different density, comprising an interior formed by a cylindrical, vertically oriented elongate shell, a bottom and a cap, wherein the interior is divided by internals into a backmixed zone, a zone of limited backmixing preferably arranged below the backmixed zone and a plug-flow zone which are at least consecutively traversable by one of the fluids, wherein the backmixed zone comprises at least one inlet and the plug-flow zone comprises an outlet and the backmixed zone comprises at least one mixing apparatus selected from a stirrer, a jet nozzle and means for injecting the fluid of lower density, a first cylindrical internal element which in the interior extends in the longitudinal direction of the reactor, which delimits the zone of limited backmixing from the plug-flow zone and which comprises a first passage to the backmixed zone and a second passage to the plug-flow zone, a second internal element which delimits the backmixed zone from the plug-flow zone such that there is no direct fluid connection between the backmixed zone and the plug-flow zone, and backmixing-preventing third internal elements in the form of random packings, structured packings or liquid-permeable trays arranged in the zone of limited backmixing. The reactor allows an optimal residence time distribution in the reaction of the two immiscible fluids of different density. The invention further relates to a process for performing a continuous reaction in the reactor.

The present invention relates to a pressure vessel (1, 1′), having a lower part (20) and the lid (24) which can be locked to one another, in order, in the state in which they are locked to one another, to surround a reaction chamber (22) on all sides as a pressure space for initiating and/or promoting chemical and/or physical pressure reactions of samples (P) which are received in the reaction chamber (22), and a fluid inlet (FE) with a check valve (4) for feeding a fluid into the reaction chamber (22), the check valve (4) extending at least partially in the lid (24).

A process for synthesis of urea from ammonia and carbon dioxide wherein: the urea synthesis is performed with a stripping process in a synthesis loop including at least a reactor (1), a stripper (2) and a condenser (3); the reactor effluent is treated in the stripper to remove unreacted ammonia and carbon dioxide; the urea solution (14) from the stripper is sent to a low-pressure recovery section (4); the stripper vapours are split into a first portion (151) directed to the reactor and a second portion (152) sent to the condenser; the condenser (3) is a shell-and-tube kettle condenser where condensation of stripper vapours is performed in the tube side (30); a carbamate-containing effluent (20) from the condenser is returned to the reactor.

Alcoholic spirits may be artificially aged under highly pressurized carbon dioxide. The carbon dioxide may form carbonic acid, which may cause various esters to form in the presence of wood as well as to mellow the flavor when no wood is present. Wood may be pretreated with ozone, which may extract lignin which may further convert to vanillin during pressurized CO2 treatment, giving a vanilla note. After processing with pressurized CO2, a post-treatment of ozone may be given to the spirit, which may cause a mild oxidation and further mellowing of the spirit.