Abstract:
A catalyst regeneration apparatus for the oxidation of coke from a spent catalyst, said coke being converted to CO, and for the conversion of the CO to CO.sub.2. Hot regenerated catalyst is recycled from a dense bed in the regeneration zone to mix with incoming spent catalyst in a mixer zone. The mixer zone operates in dense phase and is supplied with a relatively small amount of a fluidizing medium, preferably air. After the mixing of spent and fresh catalyst is substantially completed, a relatively large amount of a regenerating gas, preferably air, is admixed with the catalyst mixture, and some coke oxidation occurs. The balance of coke oxidation takes place in a downstream-situated regeneration zone of substantially conventional design. There is a transfer section connecting the mixer zone to the regeneration zone through when the relatively large amount of the regenerating gas is admitted. The transfer section is preferably a substantially horizontal surface having an outside perimeter intermediate the outside perimeters of the regeneration and mixer zones. Regeneration gas addition is made through multiple perforations in the transfer section.
Abstract:
A process for the separation of isobutane from an alkylation reaction zone hydrocarbon effluent stream comprising isobutane, n-butane, propane and alkylate is disclosed. The hydrocarbon effluent stream is charged to an isostripper column. An isobutane vapor stream from the column is condensed in indirect heat exchange with the lower liquid stream from said column comprising n-butane. The lower liquid stream is flashed in indirect heat exchange with said vapor stream at conditions to provide a vapor phase, said vapor phase being compressed and recycled to said column at a temperature to promote vapor formation therein.
Abstract:
A method for operating a fluid catalytic cracking unit comprising a regeneration zone and a reaction zone with a relatively reduced temperature in the regeneration zone while processing a hydrocarbon feedstock having a 50 volume percent distillation temperature greater than about 500.degree. F. which method comprises contacting the feedstock in a reaction zone with a mixture of regenerated fluidizable cracking catalyst and fluidizable low coke make solid particles comprising a refractory inorganic oxide in a ratio of low coke make solid particles to cracking catalyst from about 1:100 to about 10:1, the low coke made solid particles having a surface area of less than about 5 m.sup.2 /g and a coke making capability of less than about 0.2 weight percent coke on the spent low coke make solid particles in the ASTM standard method for testing cracking catalyst by microactivity test (MAT); separating the resulting vaporized hydrocarbon products from the mixture of deactivated fluidizable cracking catalyst and fluidizable low coke made solid particles; recovering the resulting vaporized hydrocarbon products; passing the mixture of cracking catalyst and low coke made solid particles to the regeneration zone for regeneration by removal of coke; and passing the resulting regenerated mixture of cracking catalyst and low coke make solid particles from the regeneration zone to the reaction zone to contact the feedstock as described above whereby the regeneration zone temperature is maintained at a reduced temperature as compared to an equivalent operation without the use of the fluidizable low coke make solid particles while simultaneously not affecting the operation of the reaction zone.
Abstract:
A radial flow reactor design which allows the maintenance of a temperature profile along the height of a catalyst bed which descends through the reactor by gravity flow. Two feed inlet conduits are provided on the inlet side of the annular catalyst bed, with the inlets being divided by a porous flow control and distribution means. The inlet streams have different temperatures and the distribution means produces a changing admixture rate between the two streams along the bed. A preferred form of the distribution means is an open-topped cone located within the centerpipe of the reactor.
Abstract:
An apparatus for regenerating coke-contaminated fluid catalyst is disclosed which comprises a vertical combustion chamber, an inlet to said chamber for spent catalyst and regeneration gas, a heat removal chamber located superadjacent to the combustion chamber and in communication therewith, heat removal means disposed within the heat removal chamber, a catalyst withdrawal conduit connected at one end to the heat removal chamber for withdrawing regenerated fluid catalyst from the heat removal chamber, and a catalyst recycle conduit connecting the withdrawal conduit with the lower portion of the combustion chamber, such that regenerated fluid catalyst can pass from the heat removal chamber to the combustion chamber. There may also be a means and control system for manipulating the extent of immersion of the heat removal means. A control system senses the catalyst temperature at an upper locus of the combustion chamber, formulates an output signal via a temperature control means having an adjustable set point, and regulates the flow rate of regenerated catalyst through the catalyst withdrawal conduit via transmission of said output signal to a flow control means responsive thereto.
Abstract:
A catalyst regeneration process and apparatus for the oxidative removal of coke from a coke-contaminated fluid catalyst. The process utilizes a high temperature coke combustion zone and a catalyst disengagement zone. A mixture of coke-contaminated catalyst, and oxygen-containing gas are contacted in the combustion zone and from there, the regenerated catalyst and flue gas mixture passes to the catalyst disengagement zone. There are one or more diplegs through which regenerated catalyst flows from the disengagement zone to the combustion zone. The diplegs are sized so as to ensure a low maximum accumulation of catalyst in the disengagement zone. The temperature at a lower locus of the combustion zone may be controlled by control of the catalyst inventory in the reactor-regenerator system.
Abstract:
Alkylaromatic hydrocarbons are dehydrogenated in admixture with steam, with the dehydrogenation zone effluent being condensed to form a water stream which is purified in a stripping column. The stripping column is reboiled by indirect heat exchange against the effluent of the dehydrogenation zone. The steam-rich overhead vapor stream of the stripping column is mixed directly into the dehydrogenation zone feed stream without intermediate condensation or pressurization.
Abstract:
Methods of control and control systems for a catalyst regeneration process and apparatus for the oxidative removal of coke from a coke-contaminated fluid catalyst. Simultaneous production of hot regenerated catalyst and a relatively-cooler flue gas is provided. The process comprises a high temperature coke combustion zone, and a lower temperature heat removal zone. Coke contaminated catalyst, oxygen containing gas and regenerated catalyst from the heat removal zone are contacted in the high temperature combustion zone, the temperature of which is controlled by adjusting the rate at which catalyst is recycled from the heat removal zone. Catalyst maybe withdrawn from the top of the combustion zone and sent to the reaction zone at the controlled combustion zone temperature, the remainder of the catalyst and the hot flue gas pass to the upper heat removal zone, where both gas and catalyst are cooled, preferably by utilizing the catalyst as a heat transfer medium in a dense-phase heat exchange system. The optimum temperature may be achieved by mixing regenerated catalyst from the two zones, and 0-100% of regenerated catalyst may be withdrawn from either of the two zones. The extent of heat removal in the upper zone can be adjusted by changing the level of the dense bed in the heat removal zone, and this would be used for making gross changes in the quantity of the heat removed from the process.
Abstract:
A catalyst regeneration process and apparatus for the oxidative removal of coke from a coke-contaminated fluid catalyst. Simultaneous production of hot regenerated catalyst and a relatively-cooler flue gas is provided. The process comprises a high temperature coke combustion zone, and a lower temperature heat removal zone. Coke contaminated catalyst, oxygen containing gas and regenerated catalyst from the heat removal zone are contacted in the high temperature combustion zone, the temperature of which is controlled by adjusting the rate at which catalyst is recycled from the heat removal zone. Catalyst may be withdrawn from the top of the combustion zone and sent to the reaction zone at the controlled combustion zone temperature, the remainder of the catalyst and the hot flue gas pass to the upper heat removal zone, where both gas and catalyst are cooled, preferably by utilizing the catalyst as a heat transfer medium in a dense-phase heat exchange system. The optimum temperature may be achieved by mixing regenerated catalyst from the two zones, and 0-100% of regenerated catalyst may be withdrawn from either of the two zones. The temperature in the upper zone can be adjusted by changing the level of the dense bed in the heat removal zone, and this would be used for making gross changes in the quantity of the heat removed from the process.
Abstract:
A catalyst regeneration process and apparatus for the oxidative removal of coke from a coke-contaminated fluid catalyst. Simultaneous production of hot regenerated catalyst and a relatively-cooler flue gas is provided. The process comprises a high temperature coke combustion zone, and a lower temperature heat removal zone. Coke contaminated catalyst, oxygen containing gas and regenerated catalyst from the heat removal zone are contacted in the high temperature combustion zone, the temperature of which is controlled by adjusting the rate at which catalyst is recycled from the heat removal zone. Catalyst may be withdrawn from the top of the combustion zone and sent to the reaction zone at the controlled combustion zone temperature, the remainder of the catalyst and the hot flue gas pass to the upper heat removal zone, where both gas and catalyst are cooled, preferably by utilizing the catalyst as a heat transfer medium in a dense-phase heat exchange system. The optimum temperature may be achieved by mixing regenerated catalyst from the two zones, and 0-100% of regenerated catalyst may be withdrawn from either of the two zones. The temperature in the upper zone can be adjusted by changing the level of the dense bed in the heat removal zone, and this would be used for making gross changes in the quantity of the heat removed from the process.