MAXIMUM OLEFINS PRODUCTION UTILIZING MULTI-STAGE CATALYST REACTION AND REGENERATION

Abstract

A method and system for increasing olefin production and quality from a hydrocarbon feed comprising a fully integrated multi-stage catalyst regeneration zones with multi-stage reaction zones in series and/or parallel. The multi-stage regeneration with at least one partial and one full burn zone provides an independent control to achieve the lowest possible regenerated catalyst temperature, resulting in highest possible catalyst to oil ratio required to maximize olefins yields through increased catalytic cracking in a multi stage FCC riser/risers.

Claims

1. A method for increasing olefin production from a hydrocarbon feed, said method comprises: a) delivering from a multi-stage catalyst regenerator a fully-regenerated catalyst from at least one catalyst full regeneration zone to a primary riser reactor; b) cracking the hydrocarbon feed in the primary riser reactor to produce a first cracked product, and spent catalyst; c) further cracking the first cracked product in a bed cracking reaction zone atop the primary riser reactor to produce a second cracked product including olefins; d) separating the first cracked product and the second cracked product including olefins from the spent catalyst in a reactor vessel comprising the bed cracking reaction zone; e) recovering the first cracked product and second cracked product including olefins; and f) passing the spent catalyst from the reactor vessel to the multi-stage catalyst regenerator comprising the at least one catalyst full regeneration zone and at least one catalyst partial-regeneration zone, wherein the spent catalyst is partially regenerated in the catalyst partial regeneration zone to provide partially-regenerated catalyst and forwarding the partially-regenerated catalyst to the catalyst full regeneration zone to provide fully regenerated catalyst.

2. The method of claim 1, wherein the multi-stage catalyst regenerator comprises two catalyst regenerator vessels that operate in series with one another.

3. The method of claim 1, wherein the multi-stage catalyst regenerator comprises two catalyst regenerator vessels that operate parallel to one another.

4. The method of claim 1, wherein the multi-stage catalyst regenerator comprises internals and/or packing to provide separate catalyst regeneration zones.

5. The method of claim 1, wherein the portion of the partially-regenerated catalyst that is delivered to the catalyst full regeneration zone has a temperature upon delivery that is less than the temperature of the fully-regenerated catalyst that exits the catalyst full regeneration zone.

6. The method of claim 1, wherein the temperature of the portion of the partially-regenerated catalyst that is delivered to the catalyst full regeneration zone ranges from about 1150 F. to about 1300 F.

7. The method of claim 1, wherein the temperature of the fully-regenerated catalyst that exits the catalyst full regeneration zone ranges from about 1250 F. to about 1500 F.

8. The method of claim 1, wherein the hydrocarbon feed is selected from the group consisting of vacuum gas oils, heavy atmospheric gas oil, atmospheric resid, vacuum resid, coker gas oils, visbreaker gas oils, deashalted oils, hydrocracker bottoms, vegetable oils and heavy conversion product issued from biomass, and any combination thereof or hydrotreated counterparts.

9. The method of claim 1, wherein the cracked product of the riser reactor comprises one or more gaseous product streams comprising C.sub.2 and lighter, C.sub.3 through C.sub.6 light olefins and parafins, C.sub.6-C.sub.8 light FCC gasoline, light cracked naphtha (LCN), intermediate FCC gasoline comprising benzene and C.sub.8-C.sub.9 hydrocarbons, heavy FCC gasoline comprising C.sub.9-C.sub.11 hydrocarbons and other gasoline boiling range products comprising materials boiling in the range C5 to about 430 F., middle distillate boiling in the range from about 330 F. to about 630 F., and uncracked bottoms boiling range from about 650 F. to about 900 F.

10. The method of claim 1, wherein the recycle feed contains at least one product from the group consisting of C.sub.4's, light FCC gasoline (LCN), light cycle oil (LCO), heavy cycle oil product (HCO) and slurry oil.

11. The method of claim 1, wherein recycle feed stream includes hydrocarbons from other refinery and petrochemical units.

12. The method of claim 1, wherein recycle feed stream is coker naphtha.

13. The method of claim 1, wherein the primary riser reactor operates with an outlet temperature of from 840 F. to about 1100 F.

14. The method of claim 1, wherein said spent catalyst is stripped before regeneration.

15. The method of claim 1, wherein the multi-stage catalyst regenerator comprises internals and/or packing.

16. The method of claim 1, wherein the catalyst partial regeneration zone and the catalyst full regeneration zone provide multi stage regeneration of the catalyst.

17. A hydrocarbon cracking system for maximizing olefins production utilizing the method of claim 1 comprising, a multi-stage catalyst regenerator that provides partially-regenerated catalyst and/or fully-regenerated catalyst to a primary riser reactor comprising a first reaction zone and a bed cracking reaction zone atop the primary riser reactor in a reactor vessel to send coked catalyst to the regeneration unit.

18. The method of claim 1, wherein the catalyst full regeneration zone and the catalyst partial regeneration zone are in a single regenerator vessel.

19. A hydrocarbon cracking system for maximizing olefins production utilizing a method of method for increasing olefin production from a hydrocarbon feed, the hydrocarbon cracking system comprising a multi-stage catalyst regenerator that provides partially regenerated catalyst and/or fully regenerated catalyst respectively to a first riser reactor having two reaction zones in series and a secondary riser reactor and each riser reactor receiving a different feed chosen between a hydrocarbon feed and a recycle feed, and a reactor vessel containing one of the reaction zones of the first riser reactor and an area for receiving and sending coked catalyst to the multi-stage catalyst regenerator, said method comprising: a) delivering from a multi-stage catalyst regenerator a partially-regenerated catalyst from at least one catalyst partial regeneration zone to a secondary riser reactor and a fully-regenerated catalyst from at least one catalyst full regeneration zone to a primary riser reactor; b) cracking the hydrocarbon feed in a first reaction zone of the primary riser reactor to produce a first cracked product including olefins and spent catalyst and passing the first cracked product and spent catalyst to a bed cracking reaction zone in a reactor vessel to produce a second cracked product; c) separating the first and second cracked products from the spent catalyst in the reactor vessel; d) recovering the first and second cracked products including olefins and separating an uncracked bottoms and a partially cracked product(s) from the cracked products; e) cracking a recycle feed comprising at least one of the uncracked bottoms, partially cracked, and cracked products of step (d), in the secondary riser reactor to produce a third cracked product and additional spent catalyst; f) separating and recovering the third cracked product comprising olefins from the additional spent catalyst and delivering the additional spent catalyst to the reactor vessel; and g) passing the spent catalyst from the reactor vessel to the multi-stage catalyst regenerator comprising the catalyst partial regeneration zone and the catalyst full regeneration zone, wherein the spent catalyst is partially regenerated to provide the partially-regenerated catalyst and a portion of the partially-regenerated catalyst is delivered to the catalyst full regeneration zone to provide fully regenerated catalyst.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0018] Various embodiments of the overall invention are shown by way of example in the attached Figures, wherein:

[0019] FIG. 1 is a schematic representation of a fluidized catalytic cracking apparatus that includes two-stage catalyst regeneration in series integrated with a riser reactor that provides a first stage reaction zone in the riser and a second stage bed cracking reaction zone.

[0020] FIG. 2 is a schematic representation of a fluidized catalytic cracking apparatus that includes two-stage catalyst regeneration in series integrated with dual riser technology, i.e., a primary and secondary riser reactor, wherein a primary riser reactor provides a first stage reaction zone in the riser and a second stage bed cracking reaction zone, and partially regenerated catalyst is added to the secondary riser reactor.

[0021] FIG. 3 is a schematic representation of a fluidized catalytic cracking apparatus that includes two-stage catalyst regeneration in series integrated with dual riser technology, i.e., a primary and secondary riser reactor, wherein primary riser reactor provides a first stage reaction zone and a second stage bed cracking reaction zone, and fully regenerated catalyst and partially regenerated catalyst are added to the secondary riser reactor.

[0022] FIG. 4 is a schematic representation of a fluidized catalytic cracking apparatus that includes two-stage catalyst regeneration having a single regenerator vessel comprising two catalyst regeneration zones. The apparatus includes dual riser technology, i.e., a primary and secondary riser reactor, wherein the primary riser reactor provides a first stage reaction zone and a second stage bed cracking reaction zone and the secondary riser is in fluid communication with the bed cracking reaction zone of the primary riser reactor.

[0023] FIG. 5 is a schematic representation of a fluidized catalytic cracking apparatus that includes two-stage catalyst regeneration having a single regenerator vessel comprising two catalyst regeneration zones. The apparatus includes dual riser technology, i.e., a primary and secondary riser reactor, wherein the primary riser reactor provides a first stage reaction zone and a second stage bed cracking reaction zone.

[0024] FIG. 6A, is a graphic illustration of the effect of regenerator temperature on Catalyst/Oil ratio and propylene yield for a feed having an API of 24.9 and a CCR of 2.4.

[0025] FIG. 6B, is a graphic illustration of the effect of regenerator temperature on Catalyst/Oil ratio and propylene yield for feed having an API of 27.5 and a CCR of 0.05.

[0026] FIG. 6C, is a graphic illustration of the effect of regenerator temperature on Catalyst/Oil ratio and propylene yield for feed having an API of 21.3 and a CCR of 0.2.

DESCRIPTION OF THE INVENTION

[0027] The use of the disclosed multi-stage catalyst regeneration process makes it possible for simultaneous selective processing of high and low boiling components contained in gas oils and residual oils. In the first stage of the presently disclosed regeneration process, catalyst particles, which have hydrocarbonaceous materials such as coke deposited on them, are regenerated under conditions of certain oxygen concentration and temperature ranging from 1150 F. to 1300 F. selected to particularly burn hydrogen associated with hydrocarbonaceous material. These conditions result in a residual level of carbon left on the catalyst and the production of a carbon monoxide (CO) rich flue gas. This relatively mild regeneration serves to limit local catalyst hot spots in the presence of steam formed during hydrogen combustion so that the formed steam will not substantially reduce the catalyst activity. A partially-regenerated catalyst substantially free of hydrogen in the remaining coke and comprising residual carbon is thus recovered from the this catalyst regeneration stage and passed to a second stage higher temperature regenerator where the remaining carbon is substantially completely burned to CO.sub.2 at an elevated temperature up to 1400 F. This second stage regeneration is conducted under conditions and in the presence of sufficient oxygen to burn substantially all residual carbon deposits and to produce CO.sub.2-rich fluid gas.

[0028] The regenerated catalyst is withdrawn from the second stage and charged to the riser reactor at a desired elevated temperature and in an amount sufficient to result in substantially complete vaporization of the hydrocarbon feed. The catalyst particles are typically at a temperature ranging from about 1300 F. to about 1400 F., such that when the hot catalyst comes in contact with the hydrocarbon feed, it is vaporized rapidly followed by subsequent catalytic cracking of the feed.

[0029] According to the embodiment of FIG. 1, a method of cracking a hydrocarbon feed, such as, for example a resid or heavier feedstocks utilizing two-stage regeneration of the catalyst in a multi-stage catalyst regenerator (200), e.g., two regenerator vessels in series. The method operates the first stage regenerator (8) in a partial burn combustion mode to provide a catalyst partial regeneration zone (4), followed by a full burn combustion mode in a catalyst full regeneration zone (5), in a second stage regenerator (9). The first and second regenerators (8, 9) presented in FIG. 1 are integrated in series. However, the regenerators can be utilized in a parallel fashion, which is not shown in FIG. 1. The partial burn regeneration in the first stage regenerator (8) operates in an oxygen deficient environment burning only a portion, typically 50% to 80% of the coke on the catalyst and all the entrained hydrocarbons from the stripper at low regenerator temperatures, ranging from 1150 F. to 1300 F. to minimize hydrothermal deactivation of the catalyst. The carbon on regenerated catalyst CRC for partial burn zone catalyst is typically around 0.3 to 0.9 wt %. The partially-regenerated catalyst from the catalyst partial regeneration zone (4) of the first stage regenerator (8) is then transferred to the catalyst full regeneration zone (5) in the second stage regenerator (9) typically through an internal lift line riser between the two regenerators (8, 9), as shown in FIG. 1, or through external transfer lines. The catalyst is almost completely regenerated in the second stage regenerator (9) operating at about 1300 F. to about 1400 F., in full burn mode with excess oxygen. The carbon on regenerated catalyst CRC for full burn zone catalyst is typically around 0.01 to 0.1 wt %. The two-stage reaction zone comprises a primary or first riser reactor (1) that receives fully regenerated catalyst (6) from a pipe or conduit in fluid communication with a withdraw well (3). The primary riser reactor (1) provides a first stage reaction zone and a second stage reaction zone. The second stage reaction zone comprises a bed cracking reaction zone (2) atop the riser reactor (1) in a reactor vessel (100). The reactor vessel (100) can be, for example a single reactor vessel in which the primary riser reactor's (1) first stage reaction zone is in fluid communication with the bed cracking reaction zone (2) within the reactor vessel (100), as presented in FIG. 1. The bed cracking reaction zone (2) utilizes a bed temperatures about 840 F. to about 1100 F.

[0030] According to the embodiments of FIG. 1 fully regenerated catalyst with the lowest possible temperature is provided through the rejection of carbon monoxide (CO) enriched flue gas port (7) from the catalyst partial regeneration zone (4) in first stage regenerator (8). This ensures the highest possible catalyst circulation from the regenerator for a given riser outlet temperature to maintain same riser heat of cracking requirement, thereby increasing catalyst to oil ratio which further increases catalytic cracking to maximize olefin yields The method provides further increase in propylene and LPG yields from the existing known deep catalytic cracking (DCC) technology, which essentially provides riser plus bed cracking. The increased catalyst circulation leads to increased conversion, propylene yield and Naphtha to LPG conversion due to increased catalytic reaction.

[0031] The claimed method can process various types of feedstocks ranging from light to heavy feed including recycle streams whereas conventional DCC technology, however, is limited to process light feedstocks only.

[0032] FIG. 2 provides an embodiment, utilizing two-stage regeneration in a multi-stage catalyst regenerator (200), e.g., two regenerator vessels in series, integrated with riser reactors and multiple reaction zones in series and parallel, wherein fully regenerated catalyst (6) from catalyst full regeneration zone (5) in the second stage regenerator (9) is fed into a primary riser reactor (1) comprising two-stage reaction zones in series. In this embodiment partially regenerated catalyst (11) from the catalyst partial regeneration zone (4) of the first stage regenerator (8) is fed into a second or secondary riser reactor (10). The catalyst feed to the two risers operating in parallel are from two separate catalyst regenerators (8, 9), allowing for independent control of the catalyst circulation to the primary and secondary riser reactors (1, 10). The primary riser reactor (1) provides a first-stage reaction zone and a second-stage reaction zone comprising a bed cracking reaction zone (2) atop the riser reactor (1) in the single reactor vessel (100). The reactor vessel (100) can be, for example, a single reactor vessel in which the primary riser reactor's (1) first stage reaction zone is in fluid communication with the bed cracking reaction zone (2) within the reactor vessel (100), as presented in FIG. 2. The bed cracking reaction zone (2) utilizes bed temperatures of about 840 F. to about 1100 F. According to the embodiments presented in FIG. 2 the primary riser reactor (1) processes preferably heavier feedstock. Partially-regenerated catalyst (11) from the catalyst partial regeneration zone (4) in the first-stage regenerator (8) is fed into the secondary riser reactor (10), which processes preferably lighter feedstocks and or recycle streams, e.g. uncracked bottoms and partially cracked product streams. The partially cracked product streams include products that have the potential to be reacted or cracked further, such as, for example, gasoline to propylene.

[0033] The feed streams to the primary and secondary risers (1, 10) can be switched, if needed to add more flexibility to attain certain product specifications. Depending upon the feedstocks, catalyst stream to the primary and secondary risers reactors (1, 10) can be reversed, i.e. partially regenerated catalyst to primary riser reactor (1) and fully regenerated catalyst to secondary riser reactor (10). In this embodiment product vapors from the primary riser reactor's (1) reaction zone undergo further reaction the second reaction zone comprising a bed cracking reaction zone (2) atop riser reactor (1) in single reactor vessel (100), for example, to convert naphtha vapors from the primary riser reactor's (1) reaction zone to propylene enriched LPG.

[0034] The vapor residence time in the first riser reactor (1) is typically around 1 to 5 seconds, and more preferably around 2 seconds. The catalyst bed level in bed cracking reaction zone (2) is maintained to receive vapor weight hourly space velocity of around 1 to 10 hr-1 to achieve conversion of naphtha enriched riser vapors to propylene enriched product stream.

[0035] The claimed process utilizing the primary riser reactor (1), which provides a first-stage reaction zone and a second-stage reaction zone comprising a bed cracking reaction zone (2) atop the riser reactor (1) requires a reactor pressure ranging from about 10 psig to 20 psig, preferably 12.5 psig-15 psig and uses steam in riser that is approximately 20-30 wt. % of the feed. By contrast conventional fluidized catalytic cracking apparatus typically operates at a reactor pressure of about 25 psig-40 psig and utilize steam in riser that is approximately 7-8 wt. % of the feed.

[0036] According to an embodiment the catalyst partial regeneration zone (4) is operated at a temperature that is lower than the catalyst full regeneration zone (5). Thus, the cooler catalyst from the catalyst partial regeneration zone (4) to the second riser reactor (10) provides an even higher catalyst to oil ratio for a given reactor outlet temperature (ROT). Further, the degree of partial regeneration of the catalyst in the catalyst partial regeneration zone (4) can be independently controlled, which further controls the catalyst partial regeneration zone's (4) temperature and can be used to increase or decrease the catalyst circulation to the second riser reactor (10).

[0037] The second riser reactor (10) utilizes FCC catalyst to supply heat to the reaction. Appropriate catalysts for use secondary riser reactor include, for example, ZSM-5, which provides for the conversion of naphtha to propylene. ZSM-5's use as a fluid catalytic cracking additive is found to carry very little delta coke and requires very little regeneration. Operating the secondary riser reactor on partially regenerated catalyst from 1st stage regenerator is more efficient.

[0038] The presently claimed methods and apparatus optimize separate catalyst feeds from two catalyst regenerators to parallel riser reactors that provides independent control of catalyst circulation to the riser reactors. Further, the inventive process decreases load on the lift line, i.e. transfer line connecting the first stage regenerator (8) to the second stage regenerator (9). As such, a portion of the partially regenerated catalyst (11) from the catalyst partial regeneration zone (4) in the first-stage regenerator (8) is fed into the second riser reactor (10) and the rest of the partially regenerated catalyst in the catalyst partial regeneration zone (4) in the first-stage regenerator (8) is transferred to the catalyst full regeneration zone (5) in the second stage regenerator (9) for full combustion and full regeneration of the catalyst.

[0039] According to another embodiment as presented in FIG. 3 fully regenerated catalyst (6) from the catalyst full regeneration zone (5) in the second stage regenerator (9) is fed into a primary riser reactor (1), via withdraw well (3). The primary riser reactor (1) contains two-stage reaction zone comprising the primary riser reactor (1) that provides a first stage reaction zone and a second stage bed cracking reaction zone (2) atop riser reactor (1) in single reactor vessel (100). According to this embodiment the principal riser processes heavier feedstock, and partially regenerated catalyst (11) from catalyst partial regeneration zone (4) in first-stage regenerator (8) as well as fully regenerated catalyst (6a) is fed into a secondary riser reactor (10), i.e., second riser reactor (10). The secondary riser reactor (10) preferably processes lighter feedstocks and/or recycle streams. Depending upon the feedstocks, catalyst stream to the principal and secondary risers can be reversed, i.e. partially and fully regenerated catalyst to principal riser and fully regenerated catalyst to secondary riser. The embodiments of FIG. 3 provides fully regenerated catalyst (6) to first riser reactor (1) and fully and partially regenerated catalyst (6a, and 11) to the second riser reactor (10). Adding a proportion of fully and partially regenerated catalyst (6a, and 11) to the second riser reactor (10) provides the flexibility to vary delta coke on catalyst i.e., the difference between coke on spent catalyst (at stripper outlet) and coke on regenerated catalyst, expressed as a weight percent of catalyst, required to optimize heat balance and cracking potential for second riser reactor (10) operation

[0040] In FIG. 2 and FIG. 3, it should be noted that vapors from secondary riser (10) can terminate either into (not shown, see e.g., FIG. 4) and undergo further reaction in a second stage bed cracking reaction zone (2) above the first stage reaction, or above the bed cracking reaction zone (2), as shown.

[0041] In the prior art FCC two-stage regeneration processes all the catalyst from the first stage regeneration is transferred to the second-stage regeneration. In the presently disclosed methods less air is required in the second stage regenerator (9) because less coke is transferred from first stage regenerator (8) to the second stage regenerator (9), and there is an overall reduction in air required to burn the coke. The inventive methods provide for a reduction in the size of the second stage regenerator (9) and its internals reducing equipment costs. Combining fully and partially regenerated catalyst streams (6a, and 11) to second riser reactor (10) optimizes the secondary riser reactor (10) operation to a full extent.

[0042] In FIG. 4 and FIG. 5 the multi stage catalyst regenerator is incorporated into a single regenerator vessel (200a) and the catalyst feed to a first or primary riser reactor (1) and a second or secondary riser reactor (10) are from the catalyst partial regeneration zone(s) and catalyst full regeneration zone(s) that lie within the single regenerator vessel (200a). Internals/packing (12), such as structured packing as shown in FIGS. 4 and 5 can be used to achieve catalyst partial regeneration zone (4a) above the packing (12) and catalyst full regeneration zone (5a) below the packing (12). In the single regenerator vessel (200a) packing (12) separates the catalyst bed into an upper catalyst partial regeneration zone or partially regenerated catalyst zone (4a) and a lower catalyst full regeneration zone or fully regenerated catalyst zone (5a), and reduces back mixing to achieve O.sub.2 enriched environment in the lower fully regenerated catalyst zone (5a) section, as well as an O.sub.2 deficient environment in the upper partially regenerated catalyst zone (4a). The upper zone temperature will be lower due to colder stream of spent catalyst added to the upper zone and due to partial combustion, i.e. incomplete CO combustion. Injection of low temperature air or oxygen or mixture of air and oxygen above the packing (12) will reduce the effect of hot flue gas coming from the lower section. The low temperature partially regenerated catalyst in an upper catalyst partial regeneration zone (4a) provides high catalyst circulation in the second riser (10). As such, the catalyst partial regeneration zone (4a) operating in partial burn mode is always at lower temperature than the catalyst full regeneration zone (5a). Feeding partially-regenerated catalyst (11) to second riser reactor (10) provides higher catalyst circulation, which is required to crack lighter feedstock and maximize propylene and LPG yields. If necessary, the single regenerator vessel's (200a) conditions can be changed to provide the catalyst full regeneration zone or fully regenerated catalyst zone (5a) above the packing and the catalyst partial regeneration zone (4a) to be placed below the packing.

[0043] FIG. 4 and FIG. 5 present two different embodiments as an example of how vapors from secondary riser (10) can terminate either into or above the bed cracking reaction zone (2). In FIG. 5 the product vapors from the secondary riser reactor (10) do not undergo further reaction in a second stage bed cracking reaction zone (2) above the first stage reaction zone

[0044] According the embodiment presented in FIG. 4 fully-regenerated catalyst (6) from the lower catalyst full regeneration zone (5a) section of the single regenerator vessel (200a) below the packing/internals (12) is fed into the primary riser reactor (1) for the processing of medium to heavier feedstock. Partially regenerated catalyst (11) from the upper catalyst partial regeneration zone (4a) in the top section of the single regenerator vessel (200a) above the packing/internals (12) is fed into the secondary riser reactor (10) for the processing of lighter feedstocks and/or recycle streams.

[0045] According to the embodiment presented in FIG. 4 catalyst streams from the single regenerator vessel (200a) utilizing separate regeneration zones within the single regenerator vessel (200a) are fed to parallel riser reactors, i.e., first or primary riser reactor (1) and second or secondary riser reactor (10). Depending upon the feedstocks, catalyst stream to the riser reactors (1) and (10) can be reversed, e.g., partially-regenerated catalyst (11) to primary riser reactor (1) and fully-regenerated catalyst (6) to secondary riser reactor (10). According to this embodiment product vapors from the primary riser reactor (1) undergo further reaction in a second stage bed cracking reaction zone (2) in single reactor vessel (100) above the first stage reaction zone of riser reactor (1) the products from secondary riser (10) terminate into the bed cracking reaction zone (2) to maximize olefin yields.

[0046] Similar to the embodiments of FIG. 3 utilization of the single regeneration vessel (200a) as presented in FIGS. 4 and 5 can be adapted to feed partially and fully regenerated catalyst to the secondary riser (10) and fully regenerated catalyst to the principal riser reactor (1), as well as, fully and partially regenerated catalyst to the primary riser reactor (1) and fully regenerated catalyst to secondary riser (10).

[0047] The embodiments of FIG. 4 and FIG. 5 are beneficial to process light to heavier, preferably medium feedstocks to further maximize olefins and reduce regenerator air utilization, reduce size and lower cost.

[0048] FIGS. 6A, 6B and 6C graphically illustrate three examples of the presently claimed processes based on three different feedstocks ranging from light to heavy. As discussed, the disclosed process provides the flexibility to control the regenerated catalyst temperature as well as attain lowest possible overall temperature, resulting in highest possible catalyst to oil ratio required to maximize olefins, specifically propylene, compared to prior technology. The examples illustrate an effect of reducing the overall regenerator temperature on overall catalyst circulation, i.e. catalyst to oil ratio and propylene yields. The graphs in FIGS. 6A-6C shows increase in catalyst circulation and propylene yields as the overall temperature reduces in reference to where existing FCC technologies are operating compare to the present processes.

[0049] The above description and examples are merely illustrative of the invention and should not be construed as limiting the scope of the invention. Various modifications will become apparent to the skilled artisan in view of the foregoing disclosure. It is intended that all such modifications coming within the scope and spirit of the appended claims should be embraced thereby.