Patent classifications
B01J2208/00415
DIRECT ELECTRICAL HEATING OF CATALYTIC REACTIVE SYSTEM
Methods of heating a reactor system by providing electrical energy are described. A reactor system comprising at least one reactor tube having a catalyst disposed therein and comprises at least one electrically conductive surface is heated by providing electrical energy to the at least one electrically conductive surface on the reactor tube and adjusting a current level of the electrical energy provided to the at least one electrically conductive surface to control the temperature of the reactor tube and the catalyst disposed therein. The reactor tube may be electrically isolated from other electrically conductive components of the reactor system.
Reactor and Method for Carrying Out a Chemical Reaction
A reactor includes a reactor vessel and one or more reaction tubes A number of tube sections of the one or more reaction tubes in each case run between a first region and a second region in the reactor vessel. For the electrical heating of the tube sections, the tube sections in the first region can be electrically connected to (a) current connection(s) of a current source. In the first region, current feed arrangements are provided; in each case one or in each case one group of the tube sections are electrically connected, and each comprise (a) contact passage(s) that in each case adjoin(s) at least one of the tube sections in the first region. A wall of the contact passages in each case is connected to a current feed element that has a rod-shaped section that runs at a wall passage through a wall of the reactor vessel.
Reactor and Method for Carrying Out a Chemical Reaction
A reactor for carrying out a chemical reaction, which has a reactor vessel and one or more reaction tubes, wherein power input elements for electrical heating of the reaction tube(s) are guided into the reactor vessel. It is provided that the power input elements each have a rod-shaped section that, in each case, runs at a wall passage through a wall of the reactor vessel in such a way that a connection chamber into which the rod-shaped sections project is arranged outside the reactor vessel and adjacently to the wall of the reactor vessel through which the rod-shaped sections run at their wall passages, and that cooling panels through which a cooling fluid can flow are provided in the connection chamber and are arranged between at least two or between at least two groups of the rod-shaped sections that project into the connection chamber.
INTERNAL CONFIGURATION FOR REDOX-BASED HEAT STORAGE SYSTEMS
The invention is directed to a system for energy storage comprising a chemical combustion reactor comprising a reactor segment that comprises at least two porous active fixed beds that are separated by an inactive insulating layer which are at least partially surrounded by an insulating mantle. The active beds comprise a metal and/or oxide thereof.
PRODUCTION OF N-PENTANAL FROM LOW-BUTENE FEEDSTOCK MIXTURES
The invention is concerned with the issue of how to produce n-pentanal by hydroformylation from feedstock mixtures comprising a small proportion of n-butene and a large proportion of n-butane. Specifically, solutions for further optimizing established processes for hydroformylation of such low-butene mixtures in terms of material utilization are sought. The present invention has for its object to enhance the material utilization of the feedstock mixture in the production of n-pentanal from feedstock mixtures having a small proportion of n-butene and a large proportion of n-butane. The process shall be capable of economic operation on an industrial scale. In particular an existing oxo plant shall be honed to achieve better raw material utilization. This object is achieved by a combination of a hydroformylation and a dehydrogenation, wherein said combination has the special feature that the dehydrogenation is arranged after the hydroformylation in the downstream direction and is thus markedly smaller than conventional dehydrogenations provided upstream. A skillful product removal effectively removes contaminants formed in the process.
Processes and systems for the conversion of acyclic hydrocarbons to cyclopentadiene
This invention relates to processes and systems for converting acyclic hydrocarbons to alkenes, cyclic hydrocarbons and/or aromatics, for example converting acyclic C.sub.5 hydrocarbons to cyclopentadiene in a reactor system. The process includes heating an electrically-conductive reaction zone by applying an electrical current to the first electrically-conductive reaction zone; and contacting a feedstock comprising acyclic hydrocarbons with a catalyst material in the electrically-conductive reaction zone under reaction conditions to convert at least a portion of the acyclic hydrocarbons to an effluent comprising alkenes, cyclic hydrocarbons, and/or aromatics.
Method for producing trifluoroethylene
A method to stably produce trifluoroethylene with a high selectivity by reacting 1,1,1,2-tetrafluoroethane with a solid reactant and suppressing the formation of by-products such as polymer carbon is provided. In the method, a material gas containing 1,1,1,2-tetrafluoroethane passes through a layer consisting of a particulate solid reactant having an average particle size of from 1 μm to 5,000 μm to bring the solid reactant and 1,1,1,2-tetrafluoroethane into contact with each other in a state where the layer consisting of the solid reactant is fluidized.
C-11 cyanide production system
A method for providing .sup.11C-labeled cyanides from .sup.11C labeled oxides in a target gas stream retrieved from an irradiated high pressure gaseous target containing O.sub.2, wherein .sup.11C labeled oxides are reduced with H.sub.2 in the presence of a nickel catalyst under a pressure and a temperature sufficient to form a product stream comprising at least about 95% .sup.11CH.sub.4, the .sup.11CH.sub.4 is then combined with an excess of NH.sub.3 in a carrier/reaction stream flowing at an accelerated velocity and the combined .sup.11CH4 carrier/reaction stream is then contacted with a platinum (Pt) catalyst particulate supported on a substantially-chemically-nonreactive heat-stable support at a temperature of at least about 900° C., whereby a product stream comprising at least about 60% H.sup.11CN is provided in less than 10 minutes from retrieval of the .sup.11C labeled oxide.
Catalyst Support, Recycle Reactor and Method for Releasing Hydrogen
A catalyst support may be provided that comprises: an inner core, which includes at least one phase change material; a coating layer around the inner core, which includes at least one metal oxide; a catalytically active layer, which is positioned in interstices of the coating layer and/or lying on the coating layer, wherein at least one catalytically active substance is included in the catalytically active layer; and a supporting layer which is positioned under the coating layer. A recycle reactor may be provided comprising a reservoir for accommodating a chemical hydrogen storage substance; the catalyst support; a screw conveyor for input and transport of the catalyst support; and a heating device with which the catalyst support can be heated. A method for releasing hydrogen from a chemical hydrogen storage substance may be provided.
Systems and methods for processing solid materials using shockwaves produced in a supersonic gaseous vortex
Solid materials may be processed using shockwaves produced in a supersonic gaseous vortex. A high-velocity stream of gas may be introduced into a reactor. The reactor may have a chamber, a solid material inlet, a gas inlet, and an outlet. The high-velocity stream of gas may be introduced into the chamber of the reactor through the gas inlet. The high-velocity stream of gas may effectuate a supersonic gaseous vortex within the chamber. The reactor may be configured to facilitate chemical reactions and/or comminution of solid feed material using tensive forces of shockwaves created in the supersonic gaseous vortex within the chamber. Solid material may be fed into the chamber through the solid material inlet. The solid material may be processed within the chamber by nonabrasive mechanisms facilitated by the shockwaves within the chamber. The processed material that is communicated through the outlet of the reactor may be collected.