NO.sub.x control during multistage combustion

BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to a method and apparatus for controlling nitrogen oxide emissions from flue gases generated during multiple stage fluidized bed combustion, and especially during regeneration of spend FCC catalyst.
2. Description of the Prior Art
Catalytic cracking of hydrocarbons is carried out in the absence of externally supplied H.sub.2, in contrast to hydrocracking, in which H.sub.2 is added during the cracking step. An inventory of particulate catalyst is continuously cycled between a cracking reactor and a catalyst regenerator. In the fluidized catalyst cracking (FCC) process, hydrocarbon feed contacts catalyst in reactor at 425.degree. C.-600.degree. C., usually 460.degree. C.-560.degree. C. The hydrocarbons crack, and deposit some carbonaceous coke on the catalyst. The cracked products are separated from the coked catalyst. The coked catalyst is stripped of volatiles, usually with steam, and is then regenerated. In the catalyst regenerator, the coke is burned from the catalyst with oxygen containing gas, usually air. Coke burns off restoring catalyst activity and simultaneously heating the catalyst to, e.g., 500.degree. C.-900.degree. C., usually 600.degree. C.-750.degree. C. Flue gas formed by burning coke in the regenerator may be treated for removal of particulates and for conversion of carbon monoxide, after which the flue gas is normally discharged into the atmosphere.
Most FCc units now use zeolite-containing catalyst having high activity and selectivity. These catalysts work best when the amount of coke on the catalyst after regeneration is relatively low. It is desirable to regenerate zeolite catalyst to as low as residual carbon level as is possible. It is also desirable to burn CO completely within the catalyst regenerator system to conserve heat and to minimize air pollution. Heat conservation is especially important when the concentration of coke on the spent catalyst is relatively low as a result of high catalyst selectivity. Among the ways suggested to decrease the amount of carbon on regenerated catalyst and to burn CO in the regenerator is to add a CO combustion promoter metal in the catalyst or to the regenerator. Metals have been added as an integral component of the cracking catalyst and as a component of a discrete particulate additive, in which the active metal is associated with a support other than the catalyst.
U.S. Pat. No. 2,647,860 proposed adding 0.1-1 weight percent chromic oxide to a cracking catalyst to promote combustion of CO. U.S. Pat. No. 3,808,121, incorporated herein by reference, introduced relatively large-sized particles containing CO combustion-promoting metal into a cracking catalyst regenerator. The small-sized catalyst particles cycle between the cracking reactor and the catalyst regenerator. The large size combustion-promoting particles remain in the regenerator. Oxidation-promoting metals such as cobalt, copper, nickel, manganese, copper-chromite, etc., impregnated on an inorganic oxide such as alumina, are disclosed.
U.S. Pat. Nos. 4,072,600 and 4,093,535, both incorporated by reference, teach use of combustion-promoting metals such as Pt, Pd, Ir, Rh, Os, Ru and Re in cracking catalysts in concentrations of 0.01 to 50 ppm, based on total catalyst inventory.
Some cracking operations using CO combustion promoters generate nitrogen oxides (NO.sub.x) in the regenerator flue gas. It is very difficult in a catalyst regeneration system to completely burn coke and CO in the regenerator without increasing the NO.sub.x content of the regenerator flue gas.
Although many refiners have recognized the problem of NO.sub.x emissions from FCC regenerators, the solutions proposed have not been completely satisfactory. The approaches taken so far have generally been directed to special catalysts which inhibit the formation of NO.sub.x in the FCC regenerator, or to process changes which reduce NO.sub.x emissions from the regenerator.
Recent catalyst patents include U.S. Pat. No. 4,300,997 and its division U.S. Pat. No. 4,350,615, both directed to the use of Pd-Ru CO-combustion promoter, The bi-metallic CO combustion promoter is reported to do an adequate job of converting CO to CO.sub.2 ; while minimizing the formation of NO.sub.x.
Another catalyst development is disclosed in U.S. Pat. No. 4,199,435 which suggests steam treating conventional metallic CO combustion promoter to decrease NO.sub.x formation without impairing too much the CO combustion activity of the promoter.
Process modifications are suggested in U.S. Pat. Nos. 4,413,573 and 4,325,833 directed to two-and three-stage FCC regenerators, which reduce NO.sub.x emissions.
U.S. Pat. No. 4,313,848 teaches countercurrent regeneration of spent FCC catalyst, without backmixing, to minimize NO.sub.x emissions.
U.S. Pat. No. 4,309,309 teaches the addition of a vaporizable fuel to the upper portion of a FCC regenerator to minimize NO.sub.x emissions. Oxides of nitrogen formed in the lower portion of the regenerator are reduced in the reducing atmosphere generated by burning fuel in the upper portion of the regenerator.
U.S. Pat. No. 4,235,704 suggests too much CO combustion promoter causes NO.sub.x formation, and calls for monitoring the NO.sub.x content of the flue gases, and adjusting the concentration of CO combustion promoter in the regenerator based on the amount of NO.sub.x in the flue gas.
The approach taken in U.S. Pat. No. 4,542,114 is to minimize the volume of flue gas by using oxygen rather than air in the FCC regenerator, with consequent reduction in the amount of flue gas produced.
The FCC regenerators shown in U.S. Pat. Nos. 3,893,812 and 4,197,189 are staged regenerators, which emit less NO.sub.x than FCC regenerators using a single dense bed for catalyst regeneration. It is a good regenerator, but still can produce too much NO.sub.x.
All the catalyst and process patents discussed above from U.S. Pat. Nos. 4,300,997 to 4,197,189, are incorporated herein by reference.
In addition to the above patents, there are myriad patents on treatment of flue gases containing NO.sub.x. The flue gas might originate from FCC units, or other units. U.S. Pat. Nos. 4,521,389 and 4,434,147 disclose adding NH.sub.3 to NO.sub.x containing flue gas and catalystically reducing the NO.sub.x to nitrogen.
None of the approaches described above provides the perfect solution. Process approaches which reduce NO.sub.x emissions require extensive rebuilding of the FCC regenerator.
Various catalytic approaches, eg. use of bi-metallic CO combustion promoters, provide some assistance, but the cost and complexity of a bi-metallic combustion promoter is necessary. The reduction in NO.sub.x emissions achieved by catalytic approaches helps some but still may fail to meet the ever more stringent NO.sub.x emissions limits set by local governing bodies. Much of the NO.sub.x formed is not the result of combustion of N.sub.2 within the FCC regenerator, but rather combustion of nitrogen-containing compounds in the coke entering the FCC regenerator. Bi-metallic combustion promoters are probably best at minimizing NO.sub.x formation from N.sub.2.
I have discovered a way to overcome most of the deficiencies of the prior art methods of reducing NO.sub.x emissions from a multistage FCC regenerator. The regenerators of special interest are the "minimum inventory" FCC regenerators which have a dense bed coke combustor, a dilute phase transport riser above the dense bed, and a second dense bed which holds hot, regenerated catalyst for recycle to the FCC reactor and also preferably, to the combustor.
I use conventional CO combustion promoter metals in an unconventional way. By selectively adding most of the CO combustion promoter to the transport riser, or to the top of the second regenerator dense bed I achieved a significant reduction in NO.sub.x emissions while still achieving satisfactory CO combustion. The approach was, in a sense, to turn the teaching of U.S. Pat. No. 3,808,121 upside down. The '121 patent added large-sized particles containing a CO combustion-promoting metal into an FCC regenerator. These particles because of their size and weight congregated at the bottom of the FCC regenerator dense bed. Withdrawal of hot regenerated catalyst occurred from an upper level of the FCC regenerator dense bed, so only the small-sized FCC catalyst cycled back and forth between the reactor.
In my process it is irrelevant whether or not the CO combustion promoter enters the cracking reactor, while it is essential that most coke combustion occur in a reducing atmosphere, with afterburning of CO to CO.sub.2 completed later. Preferably, most afterburning occurs in the dilute phase transport riser or in the upper portion of the second dense bed.
SUMMARY OF THE INVENTION
Accordingly, the present invention provides a fluidized cracking process wherein conventional FCC catalyst contacts conventional FCC feedstocks in a conventional FCC reactor to produce cracked products and coked catalyst which is discharged into a first dense bed coke combustor to which air or an oxygen-containing gas is added to produce at least partially regenerated catalyst and combustion gas which rise from the first dense bed and through a dilute phase transport riser to form a second dense bed of regenerated catalyst and flue gas, and the regenerated catalyst is recycled to the FCC reactor, the improvement comprising selective addition of a CO combustion promoter to the dilute phase transport riser so that there is a greater concentration of CO combustion promoter in the dilute phase transport riser than in the first dense bed.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a simplified representation of one embodiment of a regenerator of the present invention.
FIG. 2 is a simplified diagram of another embodiment of the present invention.
FIG. 3 shows how NO.sub.x emissions vary as a function of relative Pt level on FCC catalyst.
FCC FEED STOCK
Any conventional FCC feed stock can be used. The process of the present invention also makes it possible to use charge stocks which are relatively high in nitrogen content, and which otherwise might result in unacceptable NO.sub.x emissions in conventional FCC units. The feed stocks may range from the typical, such as petroleum distillates or residual stocks, either virgin or partially refined, to the atypical, such as coal oils and shale oils. The feed frequently will contain recycled hydrocarbons, such as light and heavy cycle oils which have already been subjected to cracking.
FCC CATALYST
Any conventional FCC catalyst may be used. The catalyst can be 100% amorphous, but preferably includes some zeolite in a porous refractory matrix such as silica-alumina, clay, or the like. The zeolite is usually 5-35 wt. % of the catalyst, with the rest being matrix. Conventional zeolites include X and Y zeolites, with ultrastable, or relatively high silica Y zeolites being preferred. Dealuminized Y (DEAL Y) and ultrahydrophobic Y (UHP Y) zeolite may be used. The catalyst may also contain one or more shape selective zeolites, i.e., those having a Constraint Index of 1-12, and typified by ZSM-5, and other materials having a similar crystal structure.
Relatively high silica zeolite based catalyst are preferred for use in the present invention. They withstand the high temperatures usually associated with complete combustion of CO to CO.sub.2 within the FCC regenerator.
The FCC catalyst composition, per se, forms no part of the present invention.
FCC REACTOR CONDITIONS
Conventional FCC reactor conditions may be used. These conditions include catalyst/oil weight ratios of 0.5:1 to 15:1 and preferably 3:1 to 8:1, and a catalyst/oil contact time of 0.5-50 seconds, and preferably 1-20 seconds.
The FCC reactor conditions, per se, are conventional and form no part of the present invention.
MINIMUM INVENTORY FCC REGENERATOR
The starting point of the present invention is a minimum inventory FCC regeneratory such as the disclosed in U.S. Pat. Nos. 3,893,812 or 4,197,189.
In such a design, spent catalyst from an FCC reactor is discharged into a first dense bed. As this regenerator design has several dense beds, the first one is sometimes called a coke combustor, which is a convenient way of labeling the first dense bed by it primary function. Air or other oxygen containing regeneration gas is added, at least partially burning the coke from the catalyst. This coke combustion generates CO, CO.sub.2 and at least partially regenerated catalyst. The CO, CO.sub.2 and partially regenerated catalyst are transported through a dilute phase transport riser where additional CO combustion may occur. Regenerated catalyst, and flue gases containing CO.sub.2 and very little CO, are discharged from the dilute phase transport riser. The regenerated catalyst collects in a second dense bed. Hot regenerated catalyst is recycled to the FCC reactor, although a portion of this hot regenerated catalyst may be recycled to the coke combustor.
These minimum inventory regenerators, so called because they operate with a relatively low inventory of FCC catalyst as compared to earlier designs using only a single dense bed, are good designs for minimizing NO.sub.x emissions. The reasons for the reduced emissions of NO.sub.x from such FCC regenerators is not totally understood, but it is probably due in part to combustion of coke in the generally reducing atmosphere in the coke combustor. The reducing atmosphere is the coke combustor promotes reduction of NO.sub.x to nitrogen. Although the minimum inventory, two dense bed regenerator design is better regards NO.sub.x emissions, there are still some feedstocks containing large amounts of nitrogen, or environmental restrictions, which make further reductions in NO.sub.x emissions desirable.
CO COMBUSTION PROMOTER
Use of a CO combustion promoter is essential for the practice of the present invention, however, these materials are well-known.
U.S. Pat. Nos. 4,072,600 and 4,235,754, the contents of which have been incorporated by reference, disclose operation of an FCC regenerator with minute quantities of a CO combustion promoter. From 0.01 to 50 ppm Pt metal or enough other metal to give the same CO oxidation, may be used with good results.
Very good results are obtained in the "minimum inventory" FCC regenerators with as little as 0.1 to 5 wt. ppm platinum present on the catalyst. Pt can be replaced by other metals, but usually more metal is then required. An amount of promoter which would give a CO oxidation activity equal to 0.3 to 3 wt. ppm of platinum is preferred.
Conventionally, refiners add CO combustion promoter to promote total or partial combustion of CO to CO.sub.2 within the FCC regenerator. More CO combustion promoter can be added without undue bad effect-the primary one being the waste of adding more CO combustion promoter than is needed to burn all the CO.
Preferably, the CO combustion promoter is on a support which is readily segregable from the conventional FCC catalyst. Thus, in one embodiment of the present invention, the CO combustion promoter is on a material with about the same density as the FCC catalyst, but of a smaller particle size than the FCC catalyst, so that it tend to congregate in the upper portion of the FCC regenerator beds.
It is also possible, and preferred, to use Pt (or other CO combustion promoter metal) rich additive on particles as large as or larger than the conventional FCC catalyst. The Pt-rich additive should then have a lower density than the conventional FCC catalyst or be supported by mechanical means in the upper portion of the FCC regenerator dense beds.
A possible mechanical approach is to physically implant the CO combustion promoter within the upper portion of the dense bed of the FCC regenerator. Platinum wires, platinum impregnated honeycombs or rods, could be placed in the upper portion of the FCC regenerator dense bed. Great care should be taken to ensure that such permanently implanted devices do not impair good fluidization within the FCC regenerator. The devices should also be sturdy enough to survive months and even years of operation within the severe erosive environment of an FCC regenerator.
The Pt-rich additive may also be in the form of very large particles which are hollow, such as alumina ping pong balls impregnated with platinum. These exotic CO combustion catalysts would be easy to segregate within the upper portion of the FCC regenerator dense beds, but such an approach may involve extra costs for the unusual support materials. When large particles are used as as support for the CO combustion promoter, the particles are preferably at least 10 times larger in diameter than the average catalyst diameter. When 1/2" diameter particles, with a bulk density of 0.65 g/cc, are used they float on top of a dense phase fluidized bed of FCC catalyst.
FCC REGENERATOR CONDITIONS
The temperatures, pressures, oxygen flow rates, etc., are within the broad ranges of those heretofore found suitable for FCC regenerators, especially those operating with substantially complete combustion of CO to CO.sub.2 within the regeneration zone. In the prior art, suitable and preferred operating conditions in the coke combustor, transport riser, and second dense bed and dilute phase above second dense bed are summarized in Table I below.
TABLE I______________________________________PRIOR ART REGENERATOR CONDITIONS Broad Preferred Most Preferred______________________________________First Dense BedTemperature .degree.C. 590-925 650-760 660-730Density #/FT.sup.3 10-50 15-40 25-30Cat. Residence Time, sec 20-350 30-150 40-100Pressure, atm 1-10 2-5 3-4.5% Stoichiometric O.sub.2 100-150 100-110 100-105Added hereTransport RiserTemperature .degree.C. 590-925 650-760 660-730Density #/FT.sup.3 0.5-10 1-5 2-4Cat. Residence Time, sec 5-100 10-60 20-40Pressure, atm 1-10 2-5 3-4.5% Stoichiometric O.sub.2 0 0 0Added hereSecond Dense BedTemperature .degree.C. 590-925 650-760 660-730Density #/FT.sup.3 10-60 20-50 25-40Cat. Residence Time, sec 10-350 20-150 20-100Pressure, atm 1-10 2-5 3-4.5% Stoichiometric O.sub.2 1-50 1-30 1-10Added hereDilute Phase AboveSecond Dense BedTemperature .degree.C. 570-925 650-760 660-760Density #/FT.sup.3 0.01-10 0.1-2 0.1-1Cat. Residence Time sec 5-100 10-60 10-40Pressure, atm 1-10 2-5 3-4.5% Stoichiometric O.sub.2 0 0 0Added here______________________________________
Temperatures recited above are average temperatures in the region measured. Usually there is a temperature increase going through a minimum inventory regenerator, with the lowest temperatures being where coked catalyst is added to the coke combustor. Intermediate, but higher temperatures are observed in the dilute phase transport riser, with the highest temperatures in the second dense bed.
Depending on the amount of hot regenerated catalyst recycled to the coke combustor, and on the amount of air addition and CO combustion promoter added, it is possible to burn essentially all of the carbon monoxide to CO.sub.2 within the coke combustor. With relatively complete combustion of CO in the first dense bed, or coke combustor, not much temperature rise need be experienced in passing through the dilute phase transport riser, second dense bed or dilute phase above the second dense bed. Most units would not be run this way, with enough hot catalyst recirculation from the second dense bed to the coke combustor to burn all the coke upstream of the transport riser, but it represents on extreme way of operating the unit. Another extreme operation is with a very large temperature rise in the regenerator. This comes about when either coke combustion is incomplete within the combustor, or when significant afterburning occurs in the dilute phase transport riser. Insufficient air in the coke combustor, minimal or no recycle of hot regenerated catalyst to the coke combustor, and little or no CO combustion promoter all favor higher temperature rises within the regenerator. Temperature rises of up to about 100.degree. C. in the transport riser, with further temperature rises in the dilute phase above the second dense bed (due to afterburning) are conceivable. This extreme temperature rise case is not preferred, but it represents an extreme temperature profile which can be seen or generated in such an FCC regenerator.
So far as I know, commercially these regenerators are operated with essentially all of the air addition being to the coke combustor or to the combustor and a riser-mixer upstream of the combustor. In general, FCC operators want to obtain very clean catalyst, because it gives better yields, so all the air that is added is usually added as soon as possible in FCC regenerators. Some of the patent literature shows air injection in various points downstream of the coke combustor, and even fuel injection downstream of the coke combustor, but invariably, commercial units operate with all of the air (or other oxidizing gas such as oxygen) added to the coke combustor.
Commercially, a small amount of fluidizing gas is added to the second dense bed to keep the catalyst fluffed or aerated. The gas used is usually air. The catalyst is hot, and some additional coke combustion will occur here, from a few percent up to perhaps 5 to 15% of total coke removal occurring in the second dense bed.
Typically, all of the air is added to the coke combustor, and none is added higher up in the unit. About 75-95% or more of the coke combustion will occur in the coke combustor, with the remainder occurring in the dilute phase transport riser. Although there is plenty of air around to completely burn CO.sub.2 in the coke combustor, usually much of the CO combustion occurs in the dilute phase transport riser in a non-promoted unit. CO combustion can occur either in the dilute phase or in the coke combustor when CO combustion promoter is present. Usually enough CO combustion promoter is present so that by the time the catalyst leaves the transport riser all CO has been afterburned to CO.sub.2.
The invention will now be described in more detail with reference to the two figures, after which the regenerator conditions used in the present invention will be discussed.

DETAILED DESCRIPTION
FIG. 1 is a simplified flow diagram of one embodiment of the present invention as incorporated in an FCC regenerator consisting of a coke combuster, a dilute phase transport riser and a second dense bed for collection of regenerated catalyst. CO combustion promoter concentrates in catalyst fines which are collected and recycled, via the cyclone and its dipleg, to the dilute phase transport riser.
In FIG. 2, directed to a preferred embodiment, CO combustion promoter is preferentially added to the dilute phase transport riser. The CO combustion promoter is contained to a great extent on relatively large, low density, floating particles. Controlled lifting of the low density particles from the first dense bed or coke combustor to the second or outer dense bed containing hot regenerated catalyst may occur. The air velocity in the riser part of the regenerator may not be high enough to entrain many of the large particles. Each embodiment will be discussed in more detail below.
In FIG. 1, spent catalyst from an FCC reactor is charged via line 1 to a coke combustor 14. Combustor 14 contains a relatively dense bed of catalyst. Combustion air is added via line 3, while optional hot recycled catalyst is preferably added via line 17 and flow control means 17. Recycle of hot catalyst via line 7 is optional but preferred. Catalyst recycle acts as kindling to help light the fire in combustor 14 to promote rapid combustion of coke into carbon monoxide.
In lieu of, or as a supplement to, hot catalyst recycle via line 7 preheating of air or of spent catalyst in line 1 will increase the temperature in coke combuster 14 to promote rapid coke combustion.
Catalyst accumulates in combustor 14 and as it reaches the upper limits of combustor 14 catalyst enters the dilute phase transport riser 24. The narrowed cross-sectional area available for fluid low increases the vertical gas velocity, resulting in a transition from dense phase operation to dilute phase operation in the upper portion 20 of the transport riser. Traditionally most of the CO combustion to COhd 2, also known as afterburning, occurred in the dilute phase transport riser. Additional oxygen-containing gas, preferably air, may be added to dilute phase transport riser 24 by means not shown in the drawing. Addition of more air to the transport riser, and less to combustor 14, will promote CO after burning in the transport riser, and create a more reducing atmosphere in combustor 14.
In addition to air addition via lines 3 and 33, air may also be added via lines 133 and 233, as shown in FIG. 1.
Regenerated catalyst exits the transport riser via outlet 32 and is collected in a second dense bed 44. Hot regenerated catalyst is recycled to the FCC reactor via line 5 while another portion of hot regenerated catalyst is preferably recycled via line 7 to the combustor 14. Preferably, additional combustion air is added to the second dense bed via air inlets 33. The additional air helps remove the last traces of coke that may be on the catalyst, and also creates a more oxidizing atmosphere which promotes combustion of CO to CO.sub.2.
Flue gas and catalyst fines are removed from the upper containment vessel 40 via two stages of cyclone separators which removed catalyst fines from flue gas. Flue gas enters primary cyclone 52 via inlet 51. Catalyst fines are discharged via dipleg 56 into transport riser 24. Exhaust gas from a primary cyclone 52 enters secondary cyclone 50, where additional catalyst fines are recovered and discharged via dipleg 54 into dilute phase transport riser 24. Flue gas, substantially free of catalyst fines and promoter, is removed via line 60.
Operating conditions in each portion of the regenerator are discussed in more detail hereafter.
In the present invention, in combustor 14, the operating conditions are
______________________________________ Most Suitable Preferred Preferred______________________________________Temperature .degree.C. 590 to 925 650 to 760 660 to 730Pressure, atm 1 to 10 1 to 5 3 to 4.5Air/Coke lb/lb 5 to 25 10 to 20 12 to 17Stoichiometric Air 50 to 120 75 to 110 80 to 105Added, %Average Catalyst Size, 30 to 200 40 to 100 50 to 80MicronsRecycled/Spent Catalyst .05 to 2.0 0.1 to 1.0 0.15 to 0.7% Coke on Spent Catalyst .2 to 2.0 0.3 to 1.5 0.3 to 1.0wt % Coke on Catalyst 0 to 0.7 0.01 to 0.03 0.001 to 0.2Leaving Combustor______________________________________
In dilute phase transport riser 24, the conditions are
______________________________________Conditions Acceptable Preferred Most Preferred______________________________________Temperature, .degree.C. 590-925 650-760 660-730Density #/Ft.sup.3 0.5-10 1-5 2-4g/cc 0.008-0.16 0.016-0.080 0.032-0.064Catalyst VerticalVelocityfps 0.5-20 0.5-15 0.56-10m/s 0.15-6.0 0.15-4.5 0.15-3.0% CO Combustion 50-100 70-100 90-100% Total Air Addition 0-100 0-40 0-20% Coke on catalyst 0-0.7 0.01-0.3 0.01-0.2@ riser outletMole % CO, inlet 0-10 0-5 0-3Mole % C0, outlet 0-5 0-3 0-2______________________________________
In the dilute phase transport riser 24 a small amount of additional coke is removed from the catalyst, but that is not the primary purpose of transport riser 24. Preferably, enough additional air is added to the transport riser, or is present in gases leaving the coke combustor, to complete combustion of CO to CO.sub.2 within the dilute phase of the transport riser. Ideally, enough CO combustion promoter is preferentially added to the dilute phase transport riser to rapidly convert all of the CO to CO.sub.2 before the catalyst and gases exit the riser.
In prior art units, much CO would be afterburned to CO.sub.2 within the transport riser, but severe oxidizing conditions existed in both the coke combustor and transport riser. In the present invention, severe oxidation conditions may be present in the transport riser and must be avoided in the coke combustor.
In the second dense bed 44, the conditions are
______________________________________Conditions Acceptable Preferred Most Preferred______________________________________Temperature 590-925 650-760 660-730Density #/FT.sup.3 10-60 20-50 25-40g/cc 0.16-0.96 0.32-0.80 0.64______________________________________
Very little combustion occurs here, so little CO combustion or coke removal occurs. The second dense bed is a good place to clean up the FCC catalyst. There is almost no water of combustion, or residual steam from steam stripping, so little hydrothermal deactivation occurs. Most of the coke (and NO.sub.x precursors have already been removed, so severe regeneration conditions can be used to remove residual coke without forming much NO.sub.x.
In the dilute phase above second dense bed 44, the conditions are
______________________________________ MostConditions Acceptable Preferred Preferred______________________________________Temperature 590-925 650-760 660-760Mole % O.sub.2 0-20 0-10 0-5% CO 50-100 70-100 90-100CombustionDensity #/FT.sup.3 0.01-10 0.1-2 0.1-1g/cc 0.00016-0.16 0.0016-0.032 0.0016-0.016______________________________________
Although it is possible to operate with only a single cyclone separator discharging catalyst fines rich in CO combustion promoter into the dilute phase transport riser, operation with at least two stages of cyclones separation, as shown in the drawing, is preferred. Depending on plant conditions, it may be most cost efficient to allow the primary cyclone to discharge directly into the second dense bed 44, while the second stage cyclone discharged into dilute phase transport riser 24. Although not shown in the drawing, the diplegs of the cyclones discharging into the dilute phase transport riser 24 preferably have flapper valves, seal pots or other means which prevent reverse flow of gas of the diplegs of the cyclones. The diplegs also may discharge into catalyst distributors, such as trough and weir distributions to promote better mixing of promoter rich fines with CO rich gas in the dilute phase transport riser 24.
Although the cyclone diplegs discharge directly down into transport riser 24, in practice it may be easier to connect the diplegs to the sides or to transition section 25. Such an approach keeps the diplegs out of the severe erosive environment present in the fully developed dilute phase flow in the upper portions of the dilute phase transport riser, and minimizes to some extent the problems of back flow up the dipleg.
The FCC catalyst used is conventional.
The CO combustion promoter is not conventional. It floats. It may be concentrated in the catalyst fines. This means that either a relatively low density promoter, with the same or larger particle size than the FCC catalyst, is used or that a CO combustion promoter of smaller particle size is used. In the past, refiners avoided use of CO combustion promoter which congregated in the catalyst fines, as this would lead to relatively rapid loss of the expensive CO combustion promoter with catalyst fines.
FIG. 2 shows another embodiment of the present invention with preferential recycle of CO combustion promoter to the dilute phase transport riser 24. In FIG. 2, like elements have the same figure numerals in FIG. 1. In the FIG. 2 embodiment, conventional cyclones are used, but the CO combustion promoter is present as a relatively low density (floating) material which congregates in the upper portion 42 of dense bed 44. The floating CO combustion promoter is preferentially removed from the second dense bed via funnel 2, line 70, and flow control means 72 and discharged via line 74 into dilute phase transport riser 24, after which is passes up through the riser 24 to the top portion 30 of the riser.
Dense bed 14, within vessel 10, functions in the FIG. 2 embodiment as in the FIG. 1 embodiment.
The primary and second cyclones 52 and 50 respectively operate in a more conventional manner in that they merely return catalyst fines, and any floating CO combustion promoter present, to the second dense bed 44.
Preferably, the floating CO promoter is a relatively large size, strong, and light material which readily segregates to form a relatively low density dense bed 42, forming an interface 46 with relatively heavier dense bed 44.
The bulk physical properties of the preferred low density floating CO combustion promoter are
Broad
0.1-0.7 g/cm.sup.3
0.1-1.4 inch diameter
0.25-3.5 cm diameter
Preferred
0.3-0.6 g/cm.sup.3
0.25-1.0"0 diameter
0.75-2.5 cm diameter
The embodiments shown in FIG. 1 and FIG. 2 can be merged to some extent by using a CO combustion promoter which congregates in the upper portion of a dense bed. Such promoters will also be found in relatively high concentration in catalyst fines present in cyclone dip legs. The inverse funnel 2 shown in FIG. 2 can be used to preferentially recycle the CO promoter-rich upper portion of the second dense bed to the transport riser, if the dip legs of at least some of the cyclones discharge into the inlet of funnel 2. The net effect will be preferential recycle of CO combustion promoter into the transport riser 24. This permits CO combustor 14 to operate relatively lean in CO combustion promoter, resulting in a reducing atmosphere in CO combustor 14. This promotes reduction of NO.sub.x formed in CO combustor 14 to nitrogen.
Although not shown in the drawing, reverse flow of CO promoter, from the top of the dense bed in combustor 14 to the top of the second dense bed, 42 is possible. An ivnerted funnel can be placed in the upper portion of combustor 14, to withdraw catalyst and CO promoter which can then be discharged, using a lift gas, into, or above, the second dense bed.
ILLUSTRATIVE EMBODIMENT
The following illustrative embodiment shows what results are expected when processing a feedstock in an FCC regenerator incorporating the improvements of either FIG. 1 or FIG. 2. The results shown are estimates based upon commercial data from a single dense bed FCC regenerator.
FEEDSTOCK PROPERTIES
20 .degree.API
1600 ppm Nitrogen
650.degree.-1000.degree. F. nominal boiling range
FCC REACTOR CONDITIONS
5 second catalyst residence time
35 psig pressure
975.degree. F. Top Temperature
REGENERATOR OPERATING CONDITIONS
The FCC regenerator operated with a single dense bed having an average dense bed temperature of 1280.degree. F. There was 1.0 volume % of O.sub.2 in the regenerator flue gas. Tests were conducted in a commercial FCC unit, operating with a single dense bed of catalyst in the regenerator. The CO combustion catalyst was uniformly distributed within the regenerator. The flue gas contained 2100 mg/Nm.sup.3 NO.sub.x and 70 ppm CO, with 7 ppm Pt on catalyst. Other tests were conducted with different levels of Pt to generate the data represented by FIG. 3. FIG. 3 shows how NO.sub.x content of the flue gas depends on Pt concentration in the dense bed.
By segregation the Pt in the top of the dense bed, the Pt content in the portion of the bed where the NO.sub.x is formed will approach 0 and, according to the graph, NO.sub.x emissions will decrease. For example, reducing the Pt content in the bottom of the bed from 7 ppm to 3 ppm will decrease NO.sub.x from 2100 mg/Nm.sup.3 to 900 mg/Nm.sup.3. This is much more Pt, and much more NO.sub.x than would typically be emitted from a minimum inventory FCC unit. The relative changes in NO.sub.x level with changes in Pt level are expected to be the same in both types of regenerators.
The CO combustion promoter is a Pt on alumina additive with the properties shown in Table II. These additives, and many more, are commercially available.
TABLE II______________________________________Conventional Co Oxidation Promoters A B______________________________________Real Density, g/cc 2.718 2.718Particle Density, g/cc 1.597 1.619MSA Particle Size Distribution, % wt0-20 microns 2.4 0.020-40 microns 12.2 13.240-60 microns 31.7 34.260-80 microns 29.3 31.580+ microns 24.4 21.1Average Particle Size, microns 62.1 61.3Platinum Promoter Level, ppm 101 431Co Oxidation TestPromoter, g 0.0240 0.0096Conventional catalyst, g 19.9760 19.9904Platinum, ppm of mix 0.121 0.207______________________________________
Similar relative decreases in NO.sub.x emissions in a 2-stage or minimum inventory regenerator can be achieved when the promoter downstream of the combustor 14. By floating the promoter on top of the first dense bed in coke combustor 14, or recycling a promoter rich fines to transport riser 24, essentially complete CO combustion can still be achieved without exceeding temperature limits of the exit cyclones.
Preferential recycle of CO combustion-rich promoter to the dilute phase transport riser 24, without adjusting any other conditions in the FCC regenerator will not significantly change the regenerator operation, except to reduce NO.sub.x emissions. Essentially all of the heat from the CO combustion will be transferred to the catalyst so the heat balance in the unit will be the same.
Combustor 14 may be slightly cooler, when the Pt combustion promoter is in the recycled fines. A slight increase in recycle of hot regenerator catalyst to the coke combustor will counteract this.
Operation with preferential recycle of catalyst fines, via cyclone separation, to transport riser 24, coupled with a cutback in air addition to CO-combustor 14, and supplemental air addition to second dense bed 44 via lines 33, will significantly reduce NO.sub.x emissions.
By practicing the present invention, there will usually be a slight increase in CO combustion within the riser in the regenerator. This is because instead of trying to eliminate CO wherever it can be found in the regenerator, CO production is tolerated and indeed even encouraged in coke combustor 14. Addition of sufficient CO combustion promoter to transport riser 24 enables a refiner to burn substantially all of the CO to CO.sub.2 within the transport riser before the catalyst is discharged to form second dense bed 44. Achieving substantially complete CO combustion within the transport riser minimizes afterburning in the dilute phase above dense bed 44.
The "minimum inventory" FCC regenerators as shown in FIG. 1 make less NO.sub.x than conventional single bed regenerators. These NO.sub.x emissions are significantly reduced by selective addition of CO combustion promoter to the dilute phase transport riser. Even further reductions are possible, where very low NO.sub.x emission limits must be met. This can be achieved by tolerating a significant amount of afterburning within the dilute phase space 84. Such afterburning will result in higher temperatures of the CO promoter-rich additive. This "super-heated" additive will be very efficient at promoting CO combustion within the dilute phase transport riser and will reduce slightly the average temperature of the FCC catalyst inventory in the regenerator. The benefits of this regime of operation are most apparent in reference to FIG. 2, i.e., CO combustor 14 could be operated with perhaps only 50 to 90% of the total air needed to completely burn all of the coke on the catalyst to carbon dioxide. Conditions in second dense bed 44, and the amount of air added to the second dense bed via line 33, may be adjusted so that the desired coke burn is obtained, while leaving a significant amount of CO present in the flue gas. This CO can be completely combusted to CO.sub.2 in region 42, a region characterized by a dense bed of relatively low density floating particles containing CO combustion promoter. Complete CO combustion can occur here, resulting in very high temperatures which could be deleterious to normal FCC cracking catalyst but need not damage CO combustion catalyst. The heat of CO combustion would be transferred to the floating CO combustion promoter contained in dense bed 42, and this material recycled via Funnel 2 and line 70 and 74 into the dilute phase transport riser for heat recovery by direct contact heat exchange of floating particles with conventional FCC catalyst.
The operation discussed immediately above permits optimization of each part of the FCC regenerator. CO combustor 14 can be viewed as a carbon monoxide generator which removes most of the coke from the catalyst, but need not remove all of it. Completion of coke removal, and complete CO combustion, will usually occur in transport riser 24.
Second dense bed 44 can be used to remove the amount of coke from catalyst needed to achieve the desired coke level on regenerated catalyst, but need not achieve complete combustion of CO to CO.sub.2. Floating dense bed 42, and to a lesser extent the dilute phase above it, may function to remove substantially all of the carbon monoxide from the flue gas. Conditions in bed 42, and in the dilute phase, can be optimized solely for maximum CO combustion. Conditions of very high temperature and high oxygen concentration can be easily tolerated as the floating CO combustion material need not have any FCC cracking activity, preferably it never gets to the FCC reactor. Other benefits flow from such an operation, namely, that the average temperature of the FCC catalyst inventory in the regenerator is decreased, and the time that the catalyst spends in a relatively steam rich atmosphere at high temperature is also reduced. This is because coke combustor 14 will form most of the H.sub.2 O that is going to form in the regenerator at the lowest temperature in the regenerator. H.sub.2 O of combustion formed in combustor 14 will not enter second dense bed 44. The temperature in second dense bed 44 will be higher than in combustor 14, but most of the hydrocarbonaceous coke will have been removed from the catalyst prior to its entry into dense bed 44, so further combustion occurring therein will not lead to formation of H.sub.2 O. This should lead to a significant increase in FCC catalyst life.
Another advantage of the process of the present invention is that is provides refiners for the first time with the opportunity to selectively promote, or hinder, coke combustion and CO afterburning in several placed in the FCC regenerator. If NO.sub.x emissions are not a problem then coke combustion and CO afterburning may be optimized by adding excess air to the coke combustor 14. If NO.sub.x emissions are a severe problem, coke combustion in combustor 14 can be restricted to perhaps 50% of normal, creating a CO rich reducing atmosphere which will aid in minimizing NO.sub.x emissions. Coke combustion can be completed in the transport riser or even in the second dense bed.
The very gentle regeneration possible with three stages of coke removal also minimizes local overheating on catalyst particles, and also reduces the average catalyst temperature.

Number	Name	Date
3808121	Wilson, Jr.	Apr 1974
3893812	Conner et al.	Jul 1975
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4151121	Gladrow	Apr 1979
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4204944	Flanders et al.	May 1980
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4356082	Gross	Oct 1982
4430201	Castagnos, Jr. et al.	Feb 1984
4541921	Gross et al.	Sep 1985
4542114	Hegarty	Sep 1985

NO.sub.x control during multistage combustion

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