Abstract:
A single-stage reactor in the form of two concentric tubes and, one acting as a central stack and the other as a wall of reactor, widening out towards the top; a gas diffuser at the bottom of the stack, enabling gas to be injected into the liquid column above the diffuser, while a vesicle remover is located in the upper part of reactor; pipes and for feeding in the reagents, and a pipe for forcing back the gaseous phase at the top of reactor; a connection inclined by over 45.degree. to an extension of the horizontal and establishing direct communication between the bottom of reactor and a decanting chamber; and a vertical degassing tube located between connection and decanting chamber.Application of this arrangement to the reaction between finely divided aluminum, hydrogen and at least one olefin having 2 to 30 carbon atoms, at a temperature of from 100.degree. to 200.degree. and a pressure of 30 to 200 bars, in a perfectly homogeneous medium for the preparation of alkylaluminums.
Abstract:
Tubular reactor for use in polymerization reactions having a design pressure PR of 40-65 barg. The reactor includes a tube with a wall, and at least a portion of the tube is oriented vertically, with at least part of the vertical portion being surrounded by a concentric jacket for the passage of cooling fluid. The design pressure in barg of the jacket PJ is less than 0.0018·PR2.25.
Abstract:
A mixing and metering device for mixing and metering liquid chemicals comprises a circulation pump having a suction port and a pressure port, a pipe coil, the contents volume of which is dimensioned such that the chemicals metered into the device have a residence time sufficient for the chemical reaction, a choke tube which guides the circulation stream exiting from the pipe coil, with formation of a choke point, from the outlet of the pipe coil to a metering conduit which is arranged between the choke tube and the suction port of the circulation pump and at least two metering valves, and also a falling tube which is connected to the choke tube and has a vacuum flange for connection of the mixing and metering device to a vacuum device.
Abstract:
Systems and methods for heating, reacting, and/or treating a stream containing oxidizable matter. Recycle reactor is used alone or in conjunction with plug-flow reactor. Density differences in the recycle reactor facilitate flow within the recycle reactor without substantial external heat exchange.
Abstract:
The invention relates to a method and apparatus for safely producing hydrogen peroxide by injecting dispersed minute bubbles of hydrogen and oxygen into a rapidly flowing liquid medium. The minute bubbles are surrounded by the liquid medium of sufficient volume for preventing an explosive reaction between the hydrogen and oxygen. The liquid medium is formed of an acidic aqueous solution and a Group VIII metal catalyst. Hydrogen is sparged into the flowing medium for dissolution of the hydrogen in the medium. Oxygen bubbles are reacted with the dissolved hydrogen for producing hydrogen peroxide. Preferably, the liquid medium has a velocity of at least 10 feet per second for providing a bubbly flow regime in the reactor. The invention allows the direct combination of oxygen and hydrogen while preventing propagation of an explosive condition within the reactor. The method and apparatus provide for the safe production of hydrogen peroxide with low manufacturing costs.
Abstract:
The invention relates to a method and apparatus for safely producing hydrogen peroxide by injecting dispersed minute bubbles of hydrogen and oxygen into a rapidly flowing liquid medium. The minute bubbles are surrounded by the liquid medium of sufficient volume for preventing an explosive reaction between the hydrogen and oxygen. The liquid medium is formed of an acidic aqueous solution and a Group VIII metal catalyst. Hydrogen is sparged into the flowing medium for dissolution of the hydrogen in the medium. Oxygen bubbles are reacted with the dissolved hydrogen for producing hydrogen peroxide. Preferably, the liquid medium has a velocity of at least 10 feet per second for providing a bubbly flow regime in the reactor. The invention allows the direct combination of oxygen and hydrogen while preventing propagation of an explosive condition within the reactor. The method and apparatus provide for the safe production of hydrogen peroxide with low manufacturing costs.
Abstract:
The invention relates to a method and apparatus for safely producing hydrogen peroxide by injecting dispersed minute bubbles of hydrogen and oxygen into a rapidly flowing liquid medium. The minute bubbles are surrounded by the liquid medium of sufficient volume for preventing an explosive reaction between the hydrogen and oxygen. The liquid medium is formed of an acidic aqueous solution and a Group VIII metal catalyst. Hydrogen is sparged into the flowing medium for dissolution of the hydrogen in the medium. Oxygen bubbles are reacted with the dissolved hydrogen for producing hydrogen peroxide. Preferably, the liquid medium has a velocity of at least 10 feet per second for providing a bubbly flow regime in the reactor. The invention allows the direct combination of oxygen and hydrogen while preventing propagation of an explosive condition within the reactor. The method and apparatus provide for the safe production of hydrogen peroxide with low manufacturing costs.
Abstract:
A continuously flowing fluid is processed by being fed to the top of a hydraulic downdraft column (17) which is of a height such that the pressure at the bottom thereof will approximately be at the pressure necessary to create supercritical water conditions. The fluid is conducted to the bottom of the column (17) and received in a reaction chamber (21) in which the majority of the fluid is recirculated around an annular baffle plate (24). The material in the reaction chamber (21) is heated to a temperature above that necessary to create supercritical water conditions by an independent reaction taking place in a heating chamber (32). The result is that the fluid will undergo chemical reactions at the supercritical temperature and pressure range and will be of a lower specific gravity than the unprocessed fluid. The material not being recirculated in the chamber (21) is fed to one of two updraft columns (30, 31), a start-up column (30) used to preheat the material in the downdraft column (17) during initiation of the process, and a second column ( 31) isolated from the downdraft column (17) so as not to transmit any heat thereto during normal operation of the process. The temperature of the fluid in the downdraft column (17) is thereby controlled to prevent decomposition of the material until the fluid enters the reaction chamber (21) at which time it is abruptly brought up to the supercritical water temperature.