US3012962A - Method of bringing a fluidized catalytic cracker-regenerator system on stream - Google Patents

Method of bringing a fluidized catalytic cracker-regenerator system on stream Download PDF

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US3012962A
US3012962A US451519A US45151954A US3012962A US 3012962 A US3012962 A US 3012962A US 451519 A US451519 A US 451519A US 45151954 A US45151954 A US 45151954A US 3012962 A US3012962 A US 3012962A
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regenerator
air
pressure
catalyst
valve
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Justin C Dygert
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Shell USA Inc
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Shell Oil Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G11/00Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G11/14Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
    • C10G11/18Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "fluidised-bed" technique
    • C10G11/185Energy recovery from regenerator effluent gases

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  • the air required for the combustion in the regeneration zone is compressed, passed through the regeneration zone, and is then discharged as flue gas to the stack.
  • the flue gas is generally passed through one or more cyclone separators to remove suspended catalyst particles before being discharged and in some of the earlier plants the cyclone separators were followed by a Cottrell precipitator to improve the recovery of suspended catalyst. It is generally recognized that the cost of compressing the enormous quantities of air required (e.g., to burn tons of coke per hour) represents a major cost item in the catalytic cracking operation.
  • the process of the invention is applicable in fluidized catalyst catalytic cracking systems when the regenerator flue gas is in the usual temperature range and the back pressure available.
  • the regenerator flue gas is in the usual temperature range and the back pressure available.
  • the gas turbine is as low as between 6 and 10 p.s.i.g.
  • the corresponding exit pressures at the .air blower outlet are between about 20 and 26 p.s.i.g., e.g., around 23 p.s.i.g. for an 8.8 p.s.i.g. gas turbine inlet pressure.
  • the gas turbine arrangement In addition to providing a self-sustained operation, the gas turbine arrangement must be capable of bringing the plant on-stream without requiring a large auxiliary system for start-up. If there is adequate compressor capacity and a large auxiliary power source, no particular difliculty is encountered in bringing the plant onstream. However, with a plant which is self-sustained during normal operation with little or no excess power, the normal method of bringing such a plant on-stream cannot be used without such a large auxiliary power supply and even then the bringing of such a plant onstream is a long and costly procedure. It is obviously most desirable to be able to bring the plant on-stream in the minimum time.
  • the apparatus and arrangement of flows are arranged in a novel manner to allow the catalytic cracking system to be brought on-stream in a minimum of time with little or no extra facilities other than the usual starting motor used to start the gas turbine-compressor system.
  • the system and method of the invention allow such a plant to be'brought on-stream in a shorter time than the conventional start-up procedure using the conven tional steam-driven air compressor.
  • FIG. I shows a catalytic cracking system arranged to operate in the manner of the invention.
  • the main pieces of equipment are indicated diagrammatically.
  • FIG. ll illustrates a novel auxiliary combustion tower which may be advantageously substituted for theauxiliary I combustion tower illustrated in FIG. I. ,Like parts are designated by the same reference numbers.
  • the catalytic cracking plant illustrated is designed for low pressure operation.
  • the pressure of the regenerator flue gas at the gas turbine intake is only about 8.8 p.s.i.g.
  • the system comprises a fluid catalyst regenerator l, a fluid catalyst reactor 2, a catalyst storage vessel 3, an air heater 4, an auxiliary combustion tower 5, a gas turbine 6, a low pressure air compressor 7, high pressure air compressors 8 and and a starting motor 10.
  • the compressors 8 and 9 are shown diagrammatically as turbo compressors operating in parallel and driven from the common shaft through gears 37, it will be appreciated that a single second stage compressor may, be substituted if desired.
  • valves 15, 16, 17 and 18, which control the flow of air from the compressors to the auxiliary combustion tower, are opened and valves 11, 19, 40 and 46 are closed.
  • the gas turbine and compressors which may be either of the axial or the radial type, are started with the starting motor 10 and a suitable fuel, e.g., natural gas, is supplied to the auxiliary combustion tower 5 by line 2t).
  • a suitable fuel e.g., natural gas
  • the turbine accelerates as the temperature of the gases in line 21 increases until at a temperature, e.g., about SON-800 E, the system becomes self-sustaining. At this point, the starting motor may be disconnected.
  • the starting motor which may be driven by electricity, gas, gasoline, steam, or the like, may be quite small.
  • a prime mover having a rated horse power of as little as 5% of the normal operating horse power of the gas turbine can be used. In this stage of the start-up all of the high pressure air and low pressure air from the compressors 7, 8, and 9 is cycled to the auxiliary combustion tower.
  • valve 17 controlling the flow of high pressure air to the auxiliary combustion tower is gradually throttled.
  • valve 11 is opened thereby establishing circulation of air through the reactor-regenerator system. Valve 17 is then completely closed.
  • valve 41 may be opened during part of this period and valve 42 may be closed.
  • the hot exhaust from the turbine may be passed by lines 22, 24 and 25 to preheat the regenerator until the back pressure makes it advisable to close valve 41 and open valve 42 thereby passing the hot exhaust gases through the waste heat boiler to the stack. Also some further economy can be gained during this period by burning fuel in the air heater 4 and venting the regenerator exit gases directly to the stack through valve 13.
  • the pressure in the catalytic cracking system will be seen to be intermediate the normal operating pressures.
  • the pressure in the auxiliary combustion tower is above the normal operating pressure, whereas the pressure in the riser 25 is much below the normal operating pressure.
  • the nonnal operating pressure in the auxiliary combustion tower is about 8.8 p.s.i.g. and the normal operating pressure in the heater '4 is about 23 p.s.i.g.
  • the respective pressures are about 10.0 and 13.1 p.s.i.g.
  • valve 11 may be throttled to maintain the pressure in the auxiliary combustion tower below the discharge pressure of the low pressure compressor 7 whereby the pressure in the regenerator and reactor is gradually increased to the normal operating pressure as measured at or near the heater 4.
  • valve 18 is closed and valve 40 is opened (valve 41 being closed) whereby all of the air is passed through the catalytic cracking system without any appreciable increase in pressure therein.
  • a suitable fuel e.g., natural gas
  • a suitable fuel e.g., natural gas
  • the amount of fuel is adjusted such that the outlet temperature of the heated air is of the order of 1100- 1350 F.
  • heated air is circulated through the cracking system, the auxiliary combustion tower, and the gas turbine to heat the catalytic cracking system while additional heat is supplied by the fuel introduced by line 20.
  • valves in the standpipe lines 32 and 33 may be closed and steam may be injected by line 34 to heat and purge the reactor.
  • the vapors may be vented through valve 14.
  • catalyst is withdrawn from the catalyst storage vessel 3 via line 35 and valve 36 and passed to the regenerator via line 24 and riser 25.
  • this valve is gradually opened as the catalyst is charged.
  • the normal design pressure drop through the catalytic cracking system is maintained by throttling valve 11 and, as the normal pressure drop is imposed by the introduction of catalyst, the pressure drop through valve 13 is decreased thereby providing a smooth transition.
  • valve 40 is closed and valve 18 is opened as catalyst is added such that the pressure at valve 11 remains substantially constant whereas the pressure measured near the preheater 4 gradually increases to overcome the increased pressure drop caused by the catalyst introduced.
  • the heating of the regenerator and catalyst therein is continued with the hot air until the temperature is sufficient to initiate combustion at which time a suitable fuel, e.g., torch oil, is introduced directly to the catalyst bed by lines 27.
  • a suitable fuel e.g., torch oil
  • the temperature in the regenerator increases relatively rapidly to the design operating temperature, e.g., 1100 F. It will usually be necessary to cut back or altogether stop the injection of fuel to the auxiliary combustion tower by line 20 in order to maintain the temperature of the gas in line 21 at the desired turbine inlet temperature, e.g., about 1300 F.
  • the injection of fuel to the air heater 4 is discontinued.
  • circulation of the catalyst through the regenerator and reactor may be started.
  • This catalyst circulation is effected in a normal manner except that steam or natural gas is supplied by line 34 instead of feed oil.
  • oil feed may be injected via line 34 to bring the unit on-stream.
  • the injection of torch oil via lines 27 may then be curtailed or discontinued.
  • the amount of water or steam injected by line 29 is adjusted to prevent the gas phase temperature in the region of the cyclone separators 30 from exceeding about 1150 F.
  • the gases leaving the fluidized bed of catalyst 31 are cooled by the steam injected or produced by vaporization of the water spray in the gas phase above the catalyst bed. If water is injected to affect this cooling, it is preferably condensate Water which is low in mineral matter.
  • the regenerator flue gas leaving the regenerator by line 26 normally contains a small amount of carbon monoxide, e.g., about 6%. This small amount of carbon monoxide is burned in the auxiliary combustion tower 5 and results in an increase in the flue gas temperature.
  • the amount of air introduced through valve 16 is adjusted such that the auxiliary combustion tower exit gas does not exceed the safe maximum turbine temperature. if, for any reason, the carbon monoxide content of the flue gas entering by line 26 is not suflicient to support combustion, a small bleed of natural gas may be introduced by line 20 to give a combustion supporting mixture. This is, however, not necessary when water injection by line 29 is properly adjusted and a normal cracking catalyst is employed in the process.
  • FIG. II illustrates a novel auxiliary combustion tower which may be advantageously substituted for the auxiliary combustion tower illustrated in FIG. I.
  • This tower is provided in the fore-section (in this case the upper section) with an oxidation catalyst such, for example, as the platinum coated ceramic oxidation catalyst sold under the name Oxycat (See The Oil and Gas Journal, June 7, 1954, page 99).
  • the fuel burners are located in the after-section (in this case the lower section).
  • the piping is arranged such that the incoming air may be passed either to the fore-section or to the aftersection, or may be split between these sections by con trolling valves 15 and 16.
  • Suitable intercomunicating ports are provided between the sections, e.g., the ports 44 in the checker brick construction in the lower section, such that the gas entering the tower through valves 11 and 15 passes through the fore-section and then through the after-section, whereas gas introduced through valve 16 passes only through the after-section.
  • valve 15 When bringing the plant on-stream the air stream is split such that at least a part of the air is passed through valve 15. This air passes down through the zone 43 packed with catalyst thereby cooling the catalyst and preventing it from being overheated by heat from the lower combustion zone.
  • this air may be in part introduced through ports 45 in the chamber wall downstream of the flame.
  • the apparatus may be built for upflow of gas with the catalyst in the lower section, or it may be constructed in a horizontal position.
  • the downflow arrangement illustrated affords the least pressure drop between valve 11 and line 21. While it is important to minimize this pressure drop in systems such as in this specific example where the flue gas pressure is of the order of 2 to p.s.i.g., it is less important in applications where the flue gas pressure is higher.
  • Valves 11, 12, 18, 19, and 42 are open. Valves -15 and/ or 16 are open. No fuel is supplied via line 23 and little if any fuel is supplied by lines 20 or 27. Water is injected by line 29 as needed. Part of the low pressure air from compressor 7 is passed by valves 18 and 15 and/or 16 to the auxiliary combustion tower while the remainder is further compressed by compressors 8 and ,9 and passed through valve 19, line 22, heater 4 (which is no longer in use as a heater), line 24, and riser 25 to the regenerator to supply the needs thereof.
  • the flue gas after passing through the cyclone separators 30, passes via line 26 and valve 11 to the auxiliary combustion tower wherein the residual carbon monoxide is burned in the presence of air introduced through valve 15, and the resulting flue gas, after being tempered with air introduced through valve 16, is passed via line 21 to the turbine 6.
  • the turbine exhaust gases which may be, for example, 200 F. below the turbine inlet gases, are passed through valve 42 to the waste heat broiler 39, which is optional and from there to the stack.
  • the operation of the cracking reactor is not pertinent to the invention and is deemed to be obvious to those skilled in the art; it is therefore not discussed.
  • the improvement which comprises compressing air to an intermediate pressure which is at least equal to the pressure of said flue gas, and with useful work as hereinafter described, combining part of said compressed air with the regenerated flue gas under conditions to combust the carbon monoxide therein, mixing with the combustion gases an additional part of said compressed air in an amount to cool the combustion gases to about 1300" F., passing the cooled combustion gases to a gas expansion engine to generate useful work, utilizing part'of said useful work for aforesaid compression of air to an intermediate pressure, utilizing the remainder of said useful work to compress further a third part of the air which is passed to the regeneration zone to supply'all of the air required for said regeneration.

Description

1961 J c DYGERT 3,012,962
METHOD OF BRINOINC A FLUIDIZED CATALYTIC CRACKER-REGENERATOR SYSTEM ON STREAM Filed Aug. 23, 1954 2 Sheets-Sheet 1 WATER REGENERATOR TO FRACTIONATOR CATALYST STORAGE TO STACK FEED ou AIR HEATER AUXILIARY COMBUSTION TOWER L J HEAT 42 3s 41 BOILER COMPRESSORS F I I INVENTOR JUSTIN c. DYGERT METHOD F BRINGING A FLUIDEZED CATA- LYTIC CRACKER-REGENERATOR SYSTEM 0N STREAM Justin C. Dygert, Walnut Creek, Qalifi, assignor to Shell Oil oxnpany, a corporation of Delaware Filed Aug. 23, 1954, Ser. No. 451,519 3 Claims. (Cl. 208-154) This specification which is directed to those skilled in the arts of catalytic cracking and gas turbine operation, relates to an invention relating to the catalytic cracking of hydrocarbon oils in a self-sustained operation involving the use of a gas turbine, and more particularly to better ways and means for bringing catalytic cracking units on stream and for effecting the regeneration of the catalyst therein.
It will be appreciated by those skilled in the art of catalytic cracking that, in the catalytic cracking of hydrocarbon oils using the fluidized catalyst technique, the used and partially spent powdered catalyst is continuously cycled through a separate regeneration zone wherein the carbonaceous deposits are burned with air. It is the necessary and usual practice to control the temperature during the burning between about 1000 F. and 1200 F. such that the catalyst is not damaged by overheating. For example, in the fluidized catalyst catalytic cracking process the temperature in the regeneration zone is normally maintained at about 1100 F. At temperatures of this order the rate of burning is quite low; consequently, the residence time of the catalyst in the regeneration zone is fairly long and this requires the use of very large vessels containing many tons of catalyst. For example, many fluidized catalyst catalytic cracking plants have regeneration vessels about 40 feet in diameter and such vessels may operate with around 600 tons of catalyst.
In normal operation, the air required for the combustion in the regeneration zone is compressed, passed through the regeneration zone, and is then discharged as flue gas to the stack. In processes using the fluidized catalyst technique the flue gas is generally passed through one or more cyclone separators to remove suspended catalyst particles before being discharged and in some of the earlier plants the cyclone separators were followed by a Cottrell precipitator to improve the recovery of suspended catalyst. It is generally recognized that the cost of compressing the enormous quantities of air required (e.g., to burn tons of coke per hour) represents a major cost item in the catalytic cracking operation.
It will also be appreciated that it has been previously suggested to pass the regenerator fine gas through a gas turbine prior to discharging it to the stack and to utilize the work produced by the turbine to compress air for the regeneration. It is recognized that this would be a desirable end if it could be made to work in practice. In the normal operation the air is compressed by steam power. The boiler requirements at the usual figure of about nine dollars per pound per hour of steam represent a large capital investment. The capital cost of gas turbine facilities is of about the same order of magnitude; therefore, little if anything can be gained by the application of the gas turbine unless the system with the gas turbine is self-sustaining, i.e., the useful work produced by the turbine is capable of pumping all the required air.
It is known that a self-sustained system can be designed provided that the system is operated under a suitable high pressure and such units involving a plurality of small fixed beds of catalyst granules have been built. However, as a practical matter, very important engineer- ;ing problems are encountered in attempts to construct elevated vessels of the large size required in fluidized 3,912,962 Patented Dec. 12, 1961 catalyst catalytic cracking plants when such vessels are intended to operate at temperatures of about 1100 F. under any appreciable pressure. Therefore, in spite of the advantages apparent in a self-sustained fluid catalyst operation, no such operation is in use.
It has now been found that the disadvantages heretofore encountered may be avoided, thereby providing means for a self-sustained operation, in units operating at a low pressure where self-sustained operation would otherwise be impossible. The process of the invention is applicable in fluidized catalyst catalytic cracking systems when the regenerator flue gas is in the usual temperature range and the back pressure available. for the gas turbine is as low as between 6 and 10 p.s.i.g. In normal operation, the corresponding exit pressures at the .air blower outlet are between about 20 and 26 p.s.i.g., e.g., around 23 p.s.i.g. for an 8.8 p.s.i.g. gas turbine inlet pressure.
While the process and arrangement of the apparatus of the invention are particularly suitable for such low pressure catalytic cracking systems, they may also be applied in catalytic cracking systems in which the regenerator exit flue gas pressure is higher, e.g., in the range of 10 to 70 p.s.i.g. i
In addition to providing a self-sustained operation, the gas turbine arrangement must be capable of bringing the plant on-stream without requiring a large auxiliary system for start-up. If there is adequate compressor capacity and a large auxiliary power source, no particular difliculty is encountered in bringing the plant onstream. However, with a plant which is self-sustained during normal operation with little or no excess power, the normal method of bringing such a plant on-stream cannot be used without such a large auxiliary power supply and even then the bringing of such a plant onstream is a long and costly procedure. It is obviously most desirable to be able to bring the plant on-stream in the minimum time.
In the process and apparatus of the invention, the apparatus and arrangement of flows are arranged in a novel manner to allow the catalytic cracking system to be brought on-stream in a minimum of time with little or no extra facilities other than the usual starting motor used to start the gas turbine-compressor system.' In fact, the system and method of the invention allow such a plant to be'brought on-stream in a shorter time than the conventional start-up procedure using the conven tional steam-driven air compressor.
The invention will be described with reference to a particular embodiment. In this description, reference will be had to the accompanying drawing.
FIG. I shows a catalytic cracking system arranged to operate in the manner of the invention. The main pieces of equipment are indicated diagrammatically.
FIG. ll illustrates a novel auxiliary combustion tower which may be advantageously substituted for theauxiliary I combustion tower illustrated in FIG. I. ,Like parts are designated by the same reference numbers.
The catalytic cracking plant illustrated is designed for low pressure operation. Thus, the pressure of the regenerator flue gas at the gas turbine intake is only about 8.8 p.s.i.g. Referring to FIG. I, the system comprises a fluid catalyst regenerator l, a fluid catalyst reactor 2, a catalyst storage vessel 3, an air heater 4, an auxiliary combustion tower 5, a gas turbine 6, a low pressure air compressor 7, high pressure air compressors 8 and and a starting motor 10. While the compressors 8 and 9 are shown diagrammatically as turbo compressors operating in parallel and driven from the common shaft through gears 37, it will be appreciated that a single second stage compressor may, be substituted if desired.
3 with a particular flow of the flue gas and air as will be described in more detail with reference to the operation.
When the plant is shut down for regularly scheduled maintenance, or for other reasons, the catalyst is transferred from the reactor and regenerator to the storage vessel 3. At the start, therefore, the regenerator and reactor are cold, at substantially atmospheric pressure, and empty of catalyst. In starting up, valves 15, 16, 17 and 18, which control the flow of air from the compressors to the auxiliary combustion tower, are opened and valves 11, 19, 40 and 46 are closed. Then the gas turbine and compressors, which may be either of the axial or the radial type, are started with the starting motor 10 and a suitable fuel, e.g., natural gas, is supplied to the auxiliary combustion tower 5 by line 2t). The mixture is ignited by an ignitor (not shown) and valves 15 and 16 are adjusted to maintain a steady combustion. The turbine accelerates as the temperature of the gases in line 21 increases until at a temperature, e.g., about SON-800 E, the system becomes self-sustaining. At this point, the starting motor may be disconnected. The starting motor which may be driven by electricity, gas, gasoline, steam, or the like, may be quite small. Thus, a prime mover having a rated horse power of as little as 5% of the normal operating horse power of the gas turbine can be used. In this stage of the start-up all of the high pressure air and low pressure air from the compressors 7, 8, and 9 is cycled to the auxiliary combustion tower.
When the turbine-compressor system is self-sustaining, and with valves 12, 13 and 14 closed, the temperature of the gases in line 21 is increased by increasing the fuel supplied via lines 20, and valve 19 is opened slightly, thereby forcing a portion of the high pressure air via line 22 to the air heater 4 and from there to the regenerator and reactor vessels. The pressure in the reactorregenerator system is thereby gradually increased. As this pressure increases, valve 17 controlling the flow of high pressure air to the auxiliary combustion tower is gradually throttled. When the pressure in the regenerator reaches substantially the pressure prevailing in the auxiliary combustion tower 5, valve 11 is opened thereby establishing circulation of air through the reactor-regenerator system. Valve 17 is then completely closed. In this second stage of the start-up, part of the high pressure air from compressors 8 and 9 is passed to the closed reactor-regenerator system whereas the remainder of the high pressure air is passed along with the low pressure air to the auxiliary combustion tower. If desired, valve 41 may be opened during part of this period and valve 42 may be closed. Thus, the hot exhaust from the turbine may be passed by lines 22, 24 and 25 to preheat the regenerator until the back pressure makes it advisable to close valve 41 and open valve 42 thereby passing the hot exhaust gases through the waste heat boiler to the stack. Also some further economy can be gained during this period by burning fuel in the air heater 4 and venting the regenerator exit gases directly to the stack through valve 13.
At the end of this second stage of the startup, the pressure in the catalytic cracking system will be seen to be intermediate the normal operating pressures. Thus, the pressure in the auxiliary combustion tower is above the normal operating pressure, whereas the pressure in the riser 25 is much below the normal operating pressure.
For example, in the particular case in question the nonnal operating pressure in the auxiliary combustion tower is about 8.8 p.s.i.g. and the normal operating pressure in the heater '4 is about 23 p.s.i.g. At this stage of the startup in the example, the respective pressures are about 10.0 and 13.1 p.s.i.g. These pressure differences afford increased power capacity as well as a large increase in compression capacity which can be used to pump large masses of air through the system and thereby heat it to temperature in the shortest possible time. It is here not a question of preheating the gas but of heating the large masses of equipment.
At this point either of two procedures may be followed. According to the first, valve 11 may be throttled to maintain the pressure in the auxiliary combustion tower below the discharge pressure of the low pressure compressor 7 whereby the pressure in the regenerator and reactor is gradually increased to the normal operating pressure as measured at or near the heater 4. According to the alternative procedure, valve 18 is closed and valve 40 is opened (valve 41 being closed) whereby all of the air is passed through the catalytic cracking system without any appreciable increase in pressure therein.
In either case, a suitable fuel, e.g., natural gas, is introduced into heater 4 via line 23 and ignited as soon as the airflow through the heater is sufficient to support combustion. The amount of fuel is adjusted such that the outlet temperature of the heated air is of the order of 1100- 1350 F. Thus, heated air is circulated through the cracking system, the auxiliary combustion tower, and the gas turbine to heat the catalytic cracking system while additional heat is supplied by the fuel introduced by line 20.
The valves in the standpipe lines 32 and 33 may be closed and steam may be injected by line 34 to heat and purge the reactor. The vapors may be vented through valve 14.
At any desired time after preheating of the cracking system has been initiated, catalyst is withdrawn from the catalyst storage vessel 3 via line 35 and valve 36 and passed to the regenerator via line 24 and riser 25. In the first case mentioned above, where valve 11 is throttled, this valve is gradually opened as the catalyst is charged. Thus, in this case, the normal design pressure drop through the catalytic cracking system is maintained by throttling valve 11 and, as the normal pressure drop is imposed by the introduction of catalyst, the pressure drop through valve 13 is decreased thereby providing a smooth transition. In the second case mentioned above, valve 40 is closed and valve 18 is opened as catalyst is added such that the pressure at valve 11 remains substantially constant whereas the pressure measured near the preheater 4 gradually increases to overcome the increased pressure drop caused by the catalyst introduced.
The heating of the regenerator and catalyst therein is continued with the hot air until the temperature is sufficient to initiate combustion at which time a suitable fuel, e.g., torch oil, is introduced directly to the catalyst bed by lines 27. From this point on the temperature in the regenerator increases relatively rapidly to the design operating temperature, e.g., 1100 F. It will usually be necessary to cut back or altogether stop the injection of fuel to the auxiliary combustion tower by line 20 in order to maintain the temperature of the gas in line 21 at the desired turbine inlet temperature, e.g., about 1300 F. Also, as the regenerator approaches the normal operating temperature the injection of fuel to the air heater 4 is discontinued. At any time during this stage of the startup, circulation of the catalyst through the regenerator and reactor may be started. This catalyst circulation is effected in a normal manner except that steam or natural gas is supplied by line 34 instead of feed oil. When the desired temperature and circulation are achieved, oil feed may be injected via line 34 to bring the unit on-stream. The injection of torch oil via lines 27 may then be curtailed or discontinued.
Also when the temperature in the regenerator ap proaches the desired operating temperature, a fine spray of water or steam is introduced via line 29 into the disengaging space in the top portion of the regenerator above the fluidized bed of catalyst. In fluidized catalyst regenerators of this type, it is found that part of the combustion tends to take place in the gas phase above the catalyst bed. It is essential in the present operation in a low pressure system such as described that combustion in this gas phase zone be curtailed. If combustion takes place in this zone either continuously or at intervals the amount of air passed to the auxiliary combustion tower must be reduced in order to maintain the desired outlet temperature and steady operation of the auxiliary combustion tower becomes diflicult if not impossible. The amount of water or steam injected by line 29 is adjusted to prevent the gas phase temperature in the region of the cyclone separators 30 from exceeding about 1150 F. Thus, in normal operation the gases leaving the fluidized bed of catalyst 31 are cooled by the steam injected or produced by vaporization of the water spray in the gas phase above the catalyst bed. If water is injected to affect this cooling, it is preferably condensate Water which is low in mineral matter.
When operating as described, the regenerator flue gas leaving the regenerator by line 26 normally contains a small amount of carbon monoxide, e.g., about 6%. This small amount of carbon monoxide is burned in the auxiliary combustion tower 5 and results in an increase in the flue gas temperature. The amount of air introduced through valve 16 is adjusted such that the auxiliary combustion tower exit gas does not exceed the safe maximum turbine temperature. if, for any reason, the carbon monoxide content of the flue gas entering by line 26 is not suflicient to support combustion, a small bleed of natural gas may be introduced by line 20 to give a combustion supporting mixture. This is, however, not necessary when water injection by line 29 is properly adjusted and a normal cracking catalyst is employed in the process.
As stated above, FIG. II illustrates a novel auxiliary combustion tower which may be advantageously substituted for the auxiliary combustion tower illustrated in FIG. I. This tower is provided in the fore-section (in this case the upper section) with an oxidation catalyst such, for example, as the platinum coated ceramic oxidation catalyst sold under the name Oxycat (See The Oil and Gas Journal, June 7, 1954, page 99). The fuel burners are located in the after-section (in this case the lower section). The piping is arranged such that the incoming air may be passed either to the fore-section or to the aftersection, or may be split between these sections by con trolling valves 15 and 16. Suitable intercomunicating ports are provided between the sections, e.g., the ports 44 in the checker brick construction in the lower section, such that the gas entering the tower through valves 11 and 15 passes through the fore-section and then through the after-section, whereas gas introduced through valve 16 passes only through the after-section.
When bringing the plant on-stream the air stream is split such that at least a part of the air is passed through valve 15. This air passes down through the zone 43 packed with catalyst thereby cooling the catalyst and preventing it from being overheated by heat from the lower combustion zone. The remaining air required for the combustion of the fuel injected by lines 20, as well as that required to cool the combustion gases to a safe tem perature for the gas turbine, is introduced through valve 16. In order to facilitate stabilization of the flame in the after-sectionin the presence of the large excess of air, this air may be in part introduced through ports 45 in the chamber wall downstream of the flame.
It will be appreciated that, while the auxiliary combustion tower described has the catalyst supported in the upper section and operates with downflow of gas, the apparatus may be built for upflow of gas with the catalyst in the lower section, or it may be constructed in a horizontal position. The downflow arrangement illustrated affords the least pressure drop between valve 11 and line 21. While it is important to minimize this pressure drop in systems such as in this specific example where the flue gas pressure is of the order of 2 to p.s.i.g., it is less important in applications where the flue gas pressure is higher.
In the foregoing, the bringing of the catalytic cracking unit on-stream has been described. When the system is on-stream, it is self-sustaining and substantially in balance;
that is the power requirements for the process are satisfied with little, if any, power to spare. The system then operates as follows: Motor 10 is not operating. Valves 13, 14,
17, 36, 40, 41 and 46 are closed. Valves 11, 12, 18, 19, and 42 are open. Valves -15 and/ or 16 are open. No fuel is supplied via line 23 and little if any fuel is supplied by lines 20 or 27. Water is injected by line 29 as needed. Part of the low pressure air from compressor 7 is passed by valves 18 and 15 and/or 16 to the auxiliary combustion tower while the remainder is further compressed by compressors 8 and ,9 and passed through valve 19, line 22, heater 4 (which is no longer in use as a heater), line 24, and riser 25 to the regenerator to supply the needs thereof. The flue gas, after passing through the cyclone separators 30, passes via line 26 and valve 11 to the auxiliary combustion tower wherein the residual carbon monoxide is burned in the presence of air introduced through valve 15, and the resulting flue gas, after being tempered with air introduced through valve 16, is passed via line 21 to the turbine 6. The turbine exhaust gases which may be, for example, 200 F. below the turbine inlet gases, are passed through valve 42 to the waste heat broiler 39, which is optional and from there to the stack. The operation of the cracking reactor is not pertinent to the invention and is deemed to be obvious to those skilled in the art; it is therefore not discussed.
I claim as my invention:
1. In bringing a catalytic cracking plant on-stream, said catalytic cracking plant comprising a fluidized catalyst regenerator and a separate fluidized catalyst reactor, the
combination of steps which comprises closing said regenerator against escape of gas, compressing heated air into said regenerator until the pressure equals substantially the normal operating pressure at the regenerator air inlet whereby the pressure at the regenerator flue gas outlet is substantially above the normal operating pressure, transferring powdered catalyst to said regenerator in suspension in said air, and decreasing the back pressure on the regenerator flue gas outlet as the catalyst is introduced thereby maintaining a substantially constant pressure drop in the air passed through said regenerator.
2. In the catalytic cracking of a hydrocarbon oil with a finely divided cracking catalyst wherein the used catalyst is continuously regenerated in a separate regeneration zone at a temperature of the order of 1000 to 1200 F. by burning carbonaceousdeposits therefrom with air with the production of a flue gas at a low pressure in the range of 6 to 10 p.s.i.g. and containing carbon monoxide, the improvement which comprises compressing air to an intermediate pressure which is at least equal to the pressure of said flue gas, and with useful work as hereinafter described, combining part of said compressed air with the regenerated flue gas under conditions to combust the carbon monoxide therein, mixing with the combustion gases an additional part of said compressed air in an amount to cool the combustion gases to about 1300" F., passing the cooled combustion gases to a gas expansion engine to generate useful work, utilizing part'of said useful work for aforesaid compression of air to an intermediate pressure, utilizing the remainder of said useful work to compress further a third part of the air which is passed to the regeneration zone to supply'all of the air required for said regeneration.
3. In the catalytic cracking of a hydrocarbon with a finely divided cracking catalyst wherein the used catalyst is continuously regenerated in a separate regeneration.
zone at a temperature of the order of 1000" to 1200 F. by burning carbonaceous deposits therefrom with air with the production of a flue gas at a low pressure in the range of 6 to 10 p.s.i.g. and containing carbon monoxide, the
improvement which comprises passing said flue gas at said pressure to an auxiliary combustion zone underconditions to burn the carbon monoxide therein to heat the flue gas to a temperature of about 1300 F., passing the heated gas to a gas expansion engine to generate useful work, utilizing part of said useful work to compress air to an vsure of said flue gas, passing a portion of said air at intermediate pressure to the auxiliary combustion zone, utilizing the remainder of said useful work to compress further the remainder of the air from the intermediate pressure to a final pressure above the pressure of the flue gas and passing the air at said final pressure to the regeneration zone as all of the air required for regeneration.
Vose Aug. 1, 1939 Ramseyer Nov. 27, 1945 8, 2,391,366 Tyson Dec. 18, 1945 2,449,096 Wheeler Sept. 14, 1948 2,758,979 Guthrie Aug. 14, 1956 5 FOREIGN PATENTS 973,589 France Feb. 12, 1951 OTHER REFERENCES Arden et al.: Disposal of Refinery Waste Gases, Oil
and Gas Journal, pages 99 to 101, page 109, June 7, 1954.

Claims (1)

1. IN BRINGING A CATALYTIC CRACKING PLANT ON-STREAM, SAID CATALYTIC CRACKING PLANT COMPRISING A FLUIDIZED CATALYST REGENERATOR AND A SEPARATE FLUIDIZED CATALYST REACTOR, THE COMBINATION OF STEPS WHICH COMPRISES CLOSING SAID REGENERATOR AGAINST ESCAPE OF GAS, COMPRESSING HEATED AIR INTO SAID REGENERATOR UNTIL THE PRESSURE EQUALS SUBSTANTIALLY THE NORMAL OPERATING PRESSURE AT THE REGENERATOR AIR INLET WHEREBY THE PRESSURE AT THE REGENERATOR FLUE GAS OUTLET IS SUBSTANTIALLY ABOVE THE NORMAL OPERATING PRESSURE, TRANSFERRING POWDERED CATALYST TO SAID REGENERATOR IN SUSPENSION IN SAID AIR, AND DECREASING THE BACK PRESSURE ON THE REGENERATOR FLUE GAS OUTLET AS THE CATALYST IS INTRODUCED THEREBY MAINTAINING A SUBSTANTIALLY CONSTANT PRESSURE DROP IN THE AIR PASSED THROUGH SAID REGENERATOR.
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US3166381A (en) * 1961-12-26 1965-01-19 Ingersoll Rand Co Air feed system
US3264209A (en) * 1962-10-22 1966-08-02 Phillips Petroleum Co Simultaneously coking iron ore and cracking hydrocarbons
US3537977A (en) * 1968-07-08 1970-11-03 Chevron Res Refinery utilizing hydrogen produced from a portion of the feed
US3795485A (en) * 1971-06-28 1974-03-05 Fluor Corp Synthesis gas generation apparatus
US4006075A (en) * 1975-01-06 1977-02-01 Exxon Research And Engineering Company Method of regenerating a cracking catalyst with substantially complete combustion of carbon monoxide
US4010094A (en) * 1974-03-14 1977-03-01 Standard Oil Company Combusting flue gas in a cracking catalyst regeneration process
US4273565A (en) * 1978-05-05 1981-06-16 Exxon Research & Engineering Co. Cyclone support
US4904372A (en) * 1988-11-18 1990-02-27 Stone & Webster Engineering Corporation Process and apparatus for recovering heat energy from catalyst regenerator flue gases
US5102628A (en) * 1987-05-21 1992-04-07 The University Of Western Ontario Riser simulator
US5114682A (en) * 1988-11-18 1992-05-19 Stone & Webster Engineering Corporation Apparatus for recovering heat energy from catalyst regenerator flue gases
EP0859752A1 (en) * 1995-06-06 1998-08-26 Mobil Oil Corporation Integration of steam reforming unit and cogeneration power plant
EP1935966A1 (en) 2006-12-21 2008-06-25 Uop Llc System and method of reducing carbon dioxide emissions in a fluid catalytic cracking unit
EP1939269A1 (en) 2006-12-21 2008-07-02 Uop Llc Preheating process and apparatus for FCC regenerator
EP2022837A1 (en) * 2007-08-01 2009-02-11 Uop Llc Process and apparatus for recovering power from fcc product
US20090159496A1 (en) * 2007-12-21 2009-06-25 Uop Llc Method and system of heating a fluid catalytic cracking unit for overall co2 reduction
US20090163351A1 (en) * 2007-12-21 2009-06-25 Towler Gavin P System and method of regenerating catalyst in a fluidized catalytic cracking unit
US20090158662A1 (en) * 2007-12-21 2009-06-25 Towler Gavin P System and method of increasing synthesis gas yield in a fluid catalytic cracking unit
US20090158661A1 (en) * 2007-12-21 2009-06-25 Uop Llc Method and system of recovering energy from a fluid catalytic cracking unit for overall carbon dioxide reduction
CN101497811A (en) * 2007-12-21 2009-08-05 Bp北美公司 Method and system of heating a fluid catalytic cracking unit having a regenerator and a reactor
US20130041195A1 (en) * 2011-08-11 2013-02-14 Kellogg Brown & Root Llc Systems And Methods For Controlling Transport Reactors
US20180058334A1 (en) * 2016-08-30 2018-03-01 General Electric Company System and method to vary exhaust backpressure on gas turbine

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2167698A (en) * 1936-01-17 1939-08-01 Houdry Process Corp Method for regenerating catalytic masses
US2389636A (en) * 1943-10-19 1945-11-27 Brassert & Co Cracking hydrocarbon gases and vapors
US2391366A (en) * 1943-06-15 1945-12-18 Standard Oil Dev Co Chemical reactions
US2449096A (en) * 1945-03-29 1948-09-14 Standard Oil Co Power recovery from catalytic conversion systems employing fluidized solids
FR973589A (en) * 1951-02-12
US2758979A (en) * 1952-03-28 1956-08-14 Exxon Research Engineering Co Method for regenerating catalyst by combustion

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR973589A (en) * 1951-02-12
US2167698A (en) * 1936-01-17 1939-08-01 Houdry Process Corp Method for regenerating catalytic masses
US2391366A (en) * 1943-06-15 1945-12-18 Standard Oil Dev Co Chemical reactions
US2389636A (en) * 1943-10-19 1945-11-27 Brassert & Co Cracking hydrocarbon gases and vapors
US2449096A (en) * 1945-03-29 1948-09-14 Standard Oil Co Power recovery from catalytic conversion systems employing fluidized solids
US2758979A (en) * 1952-03-28 1956-08-14 Exxon Research Engineering Co Method for regenerating catalyst by combustion

Cited By (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3166381A (en) * 1961-12-26 1965-01-19 Ingersoll Rand Co Air feed system
US3264209A (en) * 1962-10-22 1966-08-02 Phillips Petroleum Co Simultaneously coking iron ore and cracking hydrocarbons
US3537977A (en) * 1968-07-08 1970-11-03 Chevron Res Refinery utilizing hydrogen produced from a portion of the feed
US3795485A (en) * 1971-06-28 1974-03-05 Fluor Corp Synthesis gas generation apparatus
US4010094A (en) * 1974-03-14 1977-03-01 Standard Oil Company Combusting flue gas in a cracking catalyst regeneration process
US4098680A (en) * 1975-01-06 1978-07-04 Exxon Research & Engineering Co. Method of regenerating a cracking catalyst
US4006075A (en) * 1975-01-06 1977-02-01 Exxon Research And Engineering Company Method of regenerating a cracking catalyst with substantially complete combustion of carbon monoxide
US4273565A (en) * 1978-05-05 1981-06-16 Exxon Research & Engineering Co. Cyclone support
US5102628A (en) * 1987-05-21 1992-04-07 The University Of Western Ontario Riser simulator
US4904372A (en) * 1988-11-18 1990-02-27 Stone & Webster Engineering Corporation Process and apparatus for recovering heat energy from catalyst regenerator flue gases
US5114682A (en) * 1988-11-18 1992-05-19 Stone & Webster Engineering Corporation Apparatus for recovering heat energy from catalyst regenerator flue gases
EP0859752A1 (en) * 1995-06-06 1998-08-26 Mobil Oil Corporation Integration of steam reforming unit and cogeneration power plant
EP0859752A4 (en) * 1995-06-06 1999-04-21 Mobil Oil Corp Integration of steam reforming unit and cogeneration power plant
EP1939269A1 (en) 2006-12-21 2008-07-02 Uop Llc Preheating process and apparatus for FCC regenerator
EP1935966A1 (en) 2006-12-21 2008-06-25 Uop Llc System and method of reducing carbon dioxide emissions in a fluid catalytic cracking unit
EP2022837A1 (en) * 2007-08-01 2009-02-11 Uop Llc Process and apparatus for recovering power from fcc product
CN101497811A (en) * 2007-12-21 2009-08-05 Bp北美公司 Method and system of heating a fluid catalytic cracking unit having a regenerator and a reactor
US20090163351A1 (en) * 2007-12-21 2009-06-25 Towler Gavin P System and method of regenerating catalyst in a fluidized catalytic cracking unit
US20090158662A1 (en) * 2007-12-21 2009-06-25 Towler Gavin P System and method of increasing synthesis gas yield in a fluid catalytic cracking unit
US20090158661A1 (en) * 2007-12-21 2009-06-25 Uop Llc Method and system of recovering energy from a fluid catalytic cracking unit for overall carbon dioxide reduction
US20090159496A1 (en) * 2007-12-21 2009-06-25 Uop Llc Method and system of heating a fluid catalytic cracking unit for overall co2 reduction
US7699975B2 (en) * 2007-12-21 2010-04-20 Uop Llc Method and system of heating a fluid catalytic cracking unit for overall CO2 reduction
US7811446B2 (en) 2007-12-21 2010-10-12 Uop Llc Method of recovering energy from a fluid catalytic cracking unit for overall carbon dioxide reduction
US7921631B2 (en) 2007-12-21 2011-04-12 Uop Llc Method of recovering energy from a fluid catalytic cracking unit for overall carbon dioxide reduction
US7932204B2 (en) 2007-12-21 2011-04-26 Uop Llc Method of regenerating catalyst in a fluidized catalytic cracking unit
US7935245B2 (en) 2007-12-21 2011-05-03 Uop Llc System and method of increasing synthesis gas yield in a fluid catalytic cracking unit
US20130041195A1 (en) * 2011-08-11 2013-02-14 Kellogg Brown & Root Llc Systems And Methods For Controlling Transport Reactors
US8980195B2 (en) * 2011-08-11 2015-03-17 Kellogg Brown & Root Llc Systems and methods for controlling transport reactors
US20180058334A1 (en) * 2016-08-30 2018-03-01 General Electric Company System and method to vary exhaust backpressure on gas turbine

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