GB2242438A - Catalytic cracking with quenching - Google Patents

Abstract

Effective quenching is provided in a catalytic cracking process to decrease thermal cracking. For increased product yield, the quench is injected at special locations and a special quench is used. In the illustrated embodiment, the quench is injected into the oil product immediately downstream of a gross cut separator and the quench comprises cycle oil.

Description

1 CATALYTIC CRACKING nil= QUENCHING BACKGROUND OF THE INVENTION is This

invention relates to catalytic cracking and, more particularly, to a process and system for increasing the yield of valuable liquids in a catalytic cracking 5 unit.

Catalytic cracking of oil is an important refinery process which is used to produce gasoline and other hydrocarbons. During catalytic cracking, the feedstock, which is generally a cut or fraction of crude oil, is cracked in a reactor under catalytic cracking temperatures and pressures in the presence of a catalyst to produce more valuable, lower molecular weight hydrocarbons. Gas oil is usually used as a feedstock in catalytic cracking. Gas oil feedstocks typically contain from 55% to 80% gas oil by volume having a boiling range from about 650OF (3430C) to about 1000OF (538OC) and less than 1% RAMS carbon by weight. Gas oil feedstocks also typically contain less than 5% by volume naphtha and lighter hydrocarbons having a boiling temperature below 4300F, from 10% to 30% by volume diesel and kerosene having a boiling range from about 430OF (221OC) to about 650OF (3430C), and less than 10% by volume resid oil having a boiling temperature above 10000F. Resid oil is sometimes present in greater concentrations or added to the gas oil feedstock.

In conventional fluid catalytic cracking units (FCCU), the hot products from the riser reactor continue to undergo thermal cracking reactions above 900OF (482OC) downstream of the riser reactor. These thermal cracking reactions degrade the products, reduce yields, and make excess light gases which often unduly limit the production capability of the catalytic cracking unit.

Furthermore, while it is often desirable to operate a riser reactor at higher temperatures, such as at 10250F (5520C) or higher, to increase gasoline octane and oil and resid conversion, such high temperature cracking have substantially increased the production of ethane and lighter fuel gas. This dramatic Increase of fuel gas production i.

can create an Imbalance in the refinery fuel gas system. lt may also 'Limit the capacity of those FCCUs which have insufficient gas comoression camability to handle the increased load. Therefore, descite incentives for increased gasoline and octane oroduction,.riser temperatures have sometimes been reduced.

OperatIon at higher cracking temperatures produce naphthas which are less stable and are more prone to undergo undesired oxidation reactions which form gums.

Pricr methods for maintaining the stability of cracked naphthas and for maintaining the stability of gasollnes containing craCKed naphthas have in cluded: 1) addItion of antloxidanz cherricals such as Phenylene diamines or hindered phenols; 2) manipulation of the coerating variables of the crackIng process, such as lowering the cracking ter.imerar-u.-e and/or limizIng the amount of resid; or 3) limi-cing the ar.cunt of cracked naphtha blended into th.e fInished gasoline.

Typifying some of %the many prior art cata-lytic crack ers, regenerators. catalystst equipment and refinery proc esses are those shown in U.S. Patents: 2,240,160; 2,382,270; 2,382,382; 2,398,739; 2,398,759; 2,414,002; 2,422,501; 2,425,849; 2,436,927; 2,458,862; 2,669,591; 2,827,422; 2,884,303; 2,901,418; 2,981,676; 2,985,584; 3,004,925; 3,039,953; 3,290,405; 3,338,821; 3,351,548; 3,364,136; 3,513, 087; 3,563,911; 3,59-1,968; 3,661,800; 3,676,519; 3,692,667; 3,81-8,036; 3,844,973; 3,850,742; 3,886,060; 3,907,661; 3,909,392; 4,043,899; 4,218, 300; 4,325,817; 4,331,533; 4,332,674; 4,341,623; 4,341,660; 4,375,021; 4,446,009; 4,478,708; 4,552,645; 4,695,370; 4,764,268; 4,814, 067; 4,824,557; 4,859,310; and European Patent Application Nos. 83307095. 6 (publication no. EPO 113 180 A2), 85307242.9 (publication no. EPO 180 355 A2), and 88309278.5 (publication no. EPO 311 375 Al). These prior art catalytic crackers, regenerazors, catalysts, equipment, and refinery processes have met with varying degrees of success.

1 i 1 It is, therefore, desirable to provide an improved process and system to increase the yield of gasoline (naphtha) in catalytic cracking units and which improves the stability'of gasoline (pet:rol) which contain these 5 naphthas.

SUMMARY OF THE INVENTION

An improved catalytic cracking process and unit are provided which are effective, efficient, and economically attractive.

The novel catalytic cracking process and unit comprises catalytically cracking feed oil, such as gas oil. hydrotrealted oil, and/or resid oil, in a reactor of a catalytic crackIng unit (FCCU) in the presence of a cracking catalyst to produce a catalytically cracked, effluent product stream of upgraded oil and, after catalytic cracking is substantially completed, quenching the product stream externally and downstream of the reactor with a quench line or injector after the catalytically cracked oil has exited and been discharged from the reactor, to increase the yield of naphtha and gasoline (petrol) produce more stable gasoline. Rapid quenching also attains a desIrable shift in coke make and selectivity.

Preferably, the quench has a volumetric expansion on vaporization substantially less than water and steam. In the preferred form, the quench comprises a hydrocarbon stream which has been previously cracked or otherwise processed to remove the most reactive species. Desirably, the quench should have low thermal reactivity. Previously cracked hydrocarbons are very desirable because they are less reactive to thermal quenching than fresh unprocessed virgin feedstocks and hydrotreated stocks.

To this end, the quench can comprise kerosene, light coker gas oil, coke still (coker) distillates (CSD), hydrotreated distillate, or fresh unprocessed virgin feedstocks, such as virgin gas oil, heavy v-4.rg..n naphtha, light virgin naphtha, but preferably comprises light cata- lytic cycle oil (LCCO or LCO), heavy catalytic cycle oil (HCCO or HCO), or heavy catalytic naphtha (T.ICN), or any combination thereof. 'a'.JCCO boils ata lower temperature than HCCO but they have about the same heat of vaporization. For best results, the quench comprises LCCO which has a greater molecular weight than water. HCCO, howevert is also very useful as a quench and less expensIve than LCCO.

Steam and water are generally not desirable as a quench, because they: expand a lot on vaporization, take up a lot of reactor volume, expand in overhead lines, cause pressure disruption, disturb catalyst circulationt adversely affect cyclone operation, and produce substantial quantities of polluted water which have to be puri- fied. Excessive quantities of steam are also required in steam quenching.

Light naphtha (light virgin naphtha, light catalytic naphtha, light coker naphtha, etc.) is also not generally desirable as a quench because it occupies too much volume in the reactor. Furt-ermore, light naphtha is a gasoline blending product and it is not desirable to crack the light naphtha into less valuable hydrocarbons.

Decanted oil (DCO) is not generally desirable as a quench because it has a tendency to coke. Catalyst in the DCO can also erode the interior reactor walls and lines.

Resid is further not desirable as a quench because it has a tendency to coke and plug up lines.

Liquid hydrocarbon quenches are preferred over gas quenches to attain the benefit of:he heat of vaporization of the liquid quench. Desirably, the liquid quench is injected into the product stream in an amount ranging from 2% to 20%, and preferably from 5% to 15% of the volume flow rate of feed oil for best results. Advantageously, quenching decreases the temperature of the product stream and minimizes thermal cracking. Quenching can also increase the conversion of feed oil to upgraded oil and can increase the octane of the gasoline.

i 1 i 1 Kerosene, coker gas oil, and hydrotreated distillates are less advantageous as a quench than are LCCO and qCCO. Liquid nitrogen can be useful as a quench but is very expensive and has an undesirable volumetric expansion.

LCCO and HCCO have a high capacity to absorb heat, enhance operations, and do not materially increase operat ing utility, maintenance,'and waste treatment costs. LCCO and HCCO provide excellent quenches because they are readily available in refineries, economical, stable, have low volume expansion, provide recoverable heat removal and have a low tendency to form coke. Quenching with cycle oil can decrease the amount of coke produced. Cycle oil quenching also 1DermIts high temperature cracking without loss of more valuable hydrocarbons, and without damaging internal cyclones, plenum, or refractory walls. Desirably, cycle oil quenching, substantially decreases fuel gas production.

In the preferred process, the coked catalyst is seParated from the upgraded oil by gross separation in a vapor catalyst separator, such as in a rough cut cyclone, and the upgraded oil is immediately quenched to decrease thermal cracking of the upgraded oil. to less valuable hydrocarbon products and light hydrocarbon gases. Desirably, the quenching occurs downstream of a riser reactor and the vapor product outlet (exit) of the rough cut cyclone of the catalytic cracking unit. It is more efficient and economical to add the quench to the catalytic cracked oil after gross separation of the catalyst from the oil. Required quench volumes and pumping costs are also decreased.

In one of the illustrated embodiments, quenching occurs ur)stream of the disengaging and stripping vessel. in one preferred form of this application, the catalytic cracking unit has an external rough cut cyclone positioned between the riser reactor and the disengaging and stripper vessel and the quench Is injected immediately downstream of the vapor (product) exit of the external rough cut cyclone.

In other illustrated embodiments, the catalytic cracking' unit has a disengaging vessel (disengager) with an internal rough cut separator and the quench is injected into the disengager immediately downstream and in proximity to the vapor (product) exit(s) of the internal rough cut separator. The internal rough cut separator can com prise an internal cyclone or an inverted can.separator.

Ballistic separator and other inertia separators can also be used.

Advantageously, with quenching, the selectivity of coke can be decreased and less coke can be produced in the dilute phase portion of the disengaging and stripping vessel. Spent coked catalyst is regenerated in a regener- ator and is recycled to the riser reactor. Desirably, during the novel quenching process the regeneration temperature of the regenerator is decreased. In the preferred mode, the regenerator is operated in full CO (carbon monoxide) combustion whereby the coked catalyst is regenerated in the presence of a combustion-supporting gas, such as air, comprising excess molecular oxygen in an amount greater than the stoichiometric amount required to completely combust the coke on the coked catalyst to carbon dioxide. The regenerator can also be operated in. partial CO burn. As used in this patent application, the term "conversion" means the relative disappearance of the amount of feed which boils above 430OF (221OC). 30 As used in this application, the term "coke selectivity" means the ratio of coke yield to conversion. A more detailed explanation is provided in the following description and appended claims taken in conjunction with the accompanying drawings.

i 1 1 1 1 1 i i 1 1 t i i t BRIEF.DESCRIPTION OF THE DRAWINGS

Figure 1 is a schematic flow diagram of a catalytic cracking unit with an external cyclone; Figure 2 is a schematic flow diagram of another catalytic cracking unit with an external cyclone; Figure 3 is a schematic flow diagram of part of an oil refinery; Figure 4 is a schematic flow diagram of another part of the oil refinery; Figure 5 Figure 6 schematic flow diagram of a coker unit; schematic flow diagram of a catalytic is a is a cracking unit; and Figures 7 and 8 are charts of-product temperature for various amounts of quenches; is Figure 9 is a chart of quench volume to product volume; Figures 10 and 11 are charts of the effects of initial quench at different catalytic cracking units; Figure 12 is a schematic flow diagram of a catalytic cracking unit with an Internal rough cut separator; Figure 13 is a cross-sectional view of the disengager of Figure 12 taken substantially along lines 13-13 of Figure 12; Figure 14 is an enlarged 'fragmentary cross-sectional view of a disengager with an inverted can and quench lines, taken substantially along lines 14-14 of Figure 15; Figure 15 is a schematic flow diagram of a catalytic cracking unit with a center riser reactor and an internal rough cut separator comprising an inverted can; and 30 Figure 16 is a schematic flow diagram of another catalytic cracking unit with an internal rough cut separator.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS In refining, unrefired, raw, whole crude oil (petroleum) is withdrawn from an aboveground storage tank 10 (Figure 3) by a pump 12 and Dumped through feed line 14 into one or more desalters 16 to remove particulates, such k as sand, salt, and metals, -from the oil. The desalted oil is fed through furnace inlet line 18 into a pipestill furnace 20 where it is heated to a temp erature, such as to 750OF (3990C) at a pressure ranging from 125 to 200 psi (863 to 1380 kPa). The heated oil is removed from the furnace through exit line 22 by a pump 24 and pumped through a feed line 25 to a primary distillation tower 26.

The heated oil enters the flash zone of the primary atmospheric distillation tower, pipestill, or crude oil unit 26 before proceeding to its upper rectifier section or the lower stripper section. The primary tower is preferably operated at a pressure less than 60 psi (414 kPa). In the primary tower, the heated oil is separated into fractions of wet gas, light naphtha, intermediate naphtha, heavy naphtha, kerosene, virgin gas oil, and primary reduced crude.

A portion of the wet gas, naphtha, and kerosene is preferably refluxed (recycled) back to the primary tower to enhance fractionation and efficiency. Wet gas is withdrawn from the primary tower 26 through overhead wet gas line 28. Light naphtha is removed from the primary tower through light naphtha line 29.

Intermediate naphtha is removed from the primary tower through intermediate naphtha line 30. Heavy naphtha is withdrawn from the primary tower 26 through heavy naphtha line 31. Kerosene and oil for producing jet fuel and furnace oil are removed from the primary tower through kerosene line 32. Part of the kerosene andlor heavy naphtha can be fed to the quench line 186 (Figure 1) for use as part of the quench, if desired.

Primary virgin, atmospheric gas oil is removed from the primary tower through primary gas oil line 33 and pumped to the fluid catalytic cracking unit (FCCU) 34 (Figure 4), sometimes via a catalytic feed 1 1 1 9 hydrotreating unit.

Primary reduced crude is discharged from the bottom of the primary tower 26 (Figure 3) through the primary reduced crude line 35. The primary reduced crude in line 35 is pumped by pump 36 into a furnace 38 where it is heated, such as to a temperature from about 520OF (271OC) to about 750OF (3990C). The heated primary reduced crude is conveyed through a furnace discharge line 40 into the flash zone of a pipestill vacuum tower 42 or directly to the FW reactor.

The pipestill vacuum tower 42 (Figure 3) is preferably operated at a pressure ranging from 35 to 50 mm of mercury. Steam can be injected into the bottom portion of the vacuum tower through steam line 44. In the vacuum tower, wet gas or vacuum condensate is withdrawn from the top of the tower through overhead wet gas line 46. Heavy and/or light vacuum gas oil are remove,,. from the middle portion of the vacuum tower through gas oil line 48 and can be fed to a catalytic feed hydrotreating unit (CFHU) 49 (Figure 4) or to the riser reactor. Vacuum-reduced crude is removed from the bottom of the vacuum tower 42 (Figure 3) through a vacuumreduced crude line 50. The vacuum-reduced crude, also referred to as resid or resid oil, typically has an initially boiling point near about 1000OF (5380C).

Some of the resid can be pumped and fed to FCCU 34 (Figure 4) via FCCU resid line 52 or upgraded in a resid hydrotreating unit (RHU) comprising a series of ebullated, expanded bed reactors. Light gas oil (LGO) from the RHU can also be fed to the FCW 34 via an RHU LGO line 54. Some of the resid can be pumped to a coker unit 56 via a coker resid line 58.

A The coker unit 56 (Figure 5) comprises a coker or coke drum 62 and a combined tower 64. In the coker 62, the vacuum tower bottoms are coked at a coking temperature of about 8950F (479OC) to about 915OF (491OC) at a pressure of about 10 psig (69 kPa) to about 50 psig (345 kPa). Coke is withdrawn from the coker 62 a through chute, conduit, or line 66 and transported to a coke storage area for use as solid fuel. Coker product vapors can be withdrawn from the coker 62 through coker vapor line 68 and passed (fed) to a combined coker tower 64. In the combined coker tower 64, the coker product vapor can be separated into fractions of coker gas, coker naphtha, light coker gas oil, coke still distillate (coker distillate) and heavy coker gas oil. Coker gas can be withdrawn from the combined tower 64 through coker gas line 70. Coker naphtha can be withdrawn from the combined tower 64 through coker naphtha line 72. Coke still distillate (coker distillate) can be withdrawn from the combined tower 64 through coke still distillate CSD line 73. Light coker gas oil can be withdrawn from the combined tower 64 through light coker gas line 74 and fed to the FCCU 34 (Figure 4) or the catalytic feed hydro-treater (CFHU) 49. Part of the coke still distillate (coker distillate), light coker gas oil, and/or coker gas can be fed to the quench line 186 for use as part of the quench, if desired. Heavy coker gas oil can be withdrawn from the combined tower 64 (Figure 5) through heavy coker gas oil line 76 and hydrotreated in the catalytic feed hydrotreater (CFHU) 49 (Figure 4) before being catalytically cracked in the catalytic cracker 34 (FCCU).

Heavy coker gas oil from heavy coker gas oil line 76 (Figure 5) and light vacuum gas oil and/or j i i heaving vacuum gas oil from vacuum gas oil line 48 (Figure 3) are conveyed to the riser reactor 100, or alternatively,'to the catalytic feed hydrotreater or catalytic feed hydrotreating unit (CFHU) 49 (Figure 4) where they are hydrotreated with hydrogen from hydrogen feed line 78 at a pressure ranging from atmospheric pressure to 2000 psia (13.8 MPa) preferably from 1000 psia (6.9 MPa) to 1800 psia (12.4 MPa) at a temperature ranging from 650OF (3430C) to 750OF (3990C) in the presence of a hydro-treating catalyst. The hydrotreated gas oil is discharged through a catalytic feed hydrotreater discharge line 80 and fed to the catalytic cracker 34 (FCCU). The catalytic cracking reactor 34 of Figure 1 has an upright elongated vertical riser rector 100 with an upper portion 102 and a lower portion 104. Cracking catalyst and feed oil are mixed in the bottom of the riser reactor 100. The catalytic cracker (riser reactor) 100 catalyt- ically cracks feed oil in the presence of a cracking catalyst under catalytic cracking conditions to produce an upgraded effluent product. Stream of catalytically cracked oil containing particulates of spent coked crack5 ing catalyst.

A gross cut inertia separator comprising an external rough cut cyclone 106 (Figure 1) is connected to and communicates with the upper portion of the riser reactor 100 via a cyclone inlet line 105. The external rough cut cyclone 106 is positioned about and at a similar elevation as the u1DDer portion 102 of the riser reactor 100. The rough cut cyclone makes a gross separation of the coked catalyst from the catalytically cracked oil. Preferably, at least 92% to 98% of the coked catalyst in the oil is removed by the rough cut cyclone 106. Positioned downstream of the external cyclone 106 is an upright disengaging vessel or disengager 108.

The disengaging vessel 108 (Figure 1) disengages and separates a substantial amount of the remaining coked cat- alyst from the catalytically cracked oil. The disengaging vessel 108 operates at a temperature of 9000.7 (482OC) to 975 0 F (5240C). The dlsengaging vessel 108 has an upper dilute phase portion 110 with at least one internal cyclone 112, an effluent product outlet line 113, a lower dense phase portion 114, and a stripping section 116 pro viding a stripper in which volatile hydrocarbons are stripped from the coked catalyst. The stripping section can have baffles or internals 115. Stripping steam lines and injectors 117 can be connected to the stripper 116.

Extending from the upper portion of the external cyclone 106 (Figure 1) is a cyclone outlet line 118 pro viding part of the product stream line 119. The product stream line 118 has an upper horizontal section 118, a vertical intermediate section 120, an intermediate hori zontal section 122, and an elongated vertical section 124 providing a product stream dipleg which extends downwardly through the upper dilute phase portion 110 of the disen- 1 1 - L-6- 1 gaging vessel 108 to the upper section of the dense phase portion 11-4. The product stream dipleg 124 with an inter nal inertia separator providing an outlet 126 located in and communicating with the intermediate section of the upper dilute phase portion of the disengag.ing vessel 108. The product stream line 118 provides a disengaging vessel input line which extends between, connects and communicates with the external cyclone 106 and the upper dilute phase portion 110 of the disengaging vessel 108.

A cyclone outlet spent catalyst line, conduit, and chute provides a catalyst dipleg 128 which extends into the lower dense phase portion 114 adjacent the stripping section 116 of the disengaging vessel 108. The catalyst dipleg 128 has an upper vertical section 130, an interme diate angle section 132, a lower angle section 134, and a vertical dipleg end section 136 with an outlet opening 137. An aeration steam line 138 can be connected to the upper vertical section 130. A fluidizing steam line 139 can be connected to the lower angle section 134.

A regenerator 140 (Figure 1) comprising a regenerator vessel 142 is positioned above the disengaging vessel 108.

The regenerator 140 substantially combusts and regenerates the soent coke catalyst in the presence of a combustion sustaining oxygen-containing gas, such as air. An upright vertical elongated lift pipe 144 provides a spent catalyst riser and line, which extends downwardly from the lower portion of the regeneration vessel 142 through the middle section of the dense phase portion 114 of the disengaging vessel 108 for transporting coked catalyst from the disen- gaging vessel 108 to the overhead regenerator vessel 142. A lift air injector 146 is positioned near the bottom of the lift pipe 144 for injecting air, lifting and transporting the spent catalyst to the regenerator vessel 142 and facilitating combustion of the coked catalyst. The regenerator vessel 142 can have internal cyclones 148 and 150, an upper dilute phase steam ring 152, an overhead -iw_- flue gas line 154 and a lower-dense phase fuel gas ring 156 and line 158.

Regenerated catalyst is discharged through a catalyst discharge line, conduit, and chute 160 (Figure 1) to an overhead withdrawal well and vessel 162 with an optional air ring 164 in its lower portion to offset pressure buildup. A vertical regenerated catalyst standpipe 166 -extends downwardly from the withdrawal well 162 to a slide valve 168. A horizontal regenerated catalyst line 170 is connected to the lower portion 104 of the riser reactor 100 to convey regenerated catalyst to the riser reactor. A fluidization steam -line 171 can be connected to the regenerated catalyst line 170 below the slide valve 168. An aeration air line 172 can be connected to the middle portion of the regenerated catalyst standpipe 166.

An aeration steam line 176 (Figure 1) can also be connected to the lower portion 104 of the riser reactor 100. Injector nozzles 178 (Figure 1) can be positioned in the lower portion 104 of the riser reactor 100 to inject the feed oil into the riser reactor. In the illustrated embodiment, a combined feed oil line 180 is connected to the nozzles 178 and to a fresh feed oill line 33. A recycle oil line 182 can be connected to and communicate with the combined feed oil line 180 to feed heavy catalytic cycle oil (HCCO), decanted oil (DCO) and/or slurry oil, to the riser reactor 100, of up to 40%, preferably at a rate of S% to 10%, by volume of the fresh feed rate in fresh feed oil line 33. The temperature of the regenerator is decreased from about 1OF (0.5.c) to about 20'F (11'C) by cycle oil quenching.

A catalytic cycle oil quench injection line 184, comprising a LCCO injection line and/or an HCCO injection line, with a vertical catalytic cycle oil injector section 186 extends downwardly, connects and communicates with the vertical section 120 of the disengaging vessel input line 118 to inject a light cycle oil (LCCO) quench and/or a heavy catalytic cycle oil (HCCO) quench into the hydrocar- i i - i5_ bon products after the products have exited the external cyclone 106 downstream of the riser reactor 100 and before the products have entered the disengaging vessel 108. The quench minimizes and inhibits substantial thermal cracking of the product stream of catalytically cracked grossly separated oil to less valuable hydrocarbons, such as fuel gas. Cycle oil quenching stops about 75% to 90% of thermal cracking of the product oil and concurrently enhances the yield of naphtha to increase the production of gaso- line. During quenching, the temperature of the product st-rea.n of oil being discharged from the rough cut cyclone 106 is decreased from about 30OF (170C) to about 200OF (111OC), preferably about SOOF (28OC) to about 80OF (440C), such as to a range of 900OF (482OC) to about 930OF (499'C).

Cycle oil quenching enhances the conversion of feed oil to upgraded oil and increases gasoline octane. The injection rate of the quench by volume ranges from 2% to 20%, preferably from 5% to 15%, of the input rate of feed oil in the riser reac:or 100. Advantageously, less coke is produced in the dilute phase portLon 110 of the disengaging vessel 108. Less C 2_ fuel gas is also produced during cycle oil quenching.

Mixing and vaporizatlon of tChe quench can be advanta- geously increased to less than 5 seconds and preferably less than 3 seconds by spraying the quench with one or more atomized quench injectors to provide a quick contact quench and assure rapid mixing. The quench is injected at a downward velocity of 50 to 1.00 ft/sec (15 to 30 m/sec.) at a residence time of 0.1 to 5 seconds, preferably less than 0.2 seconds. Losses of quench should be avoided.

High boiling quench media improves energy recovery. The quench can be preheated, preferably above 212OF (100OC) to enhance heat recovery and minimize heat loss.

Quench is sprayed into the external cyclone vapor exit line 118 to rapidly cool the products before entering the reactor vessel dilute phase.

0 - e, For best results, the quench is injected as soon as the reaction is completed and preferably immediately after the coked catalyst particulates have been grossly separated from the product stream of catalytically cracked oil. Lesser amounts of quench are required after catalyst separation than before catalyst separation.

It was unexpectedly and surprisingly found that the use of cycle oil quench increases the yield of high value naphtha and can improve coke make and selectivity.

It appears that gas oil conversion beyond the riser reactor is substantially completed in the rough cut cyclone where catalyst is present. Excess fuel gas production has previously been associated with long residence time in the dilute phase portion of the disengaging vessel as a result of thermal cracking before the addition of cycle oil quench.

Regenerated catalytic cracking catalyst can be fed to the riser reactor 100 (Figure 1) through a regenerated catalyst line 170, respectively.Fresh makeup catalyst can be added to the regenerator 140. In the FCC riser reactor, the hydrocarbon feedstock is vaporized upon being mixed with the hot cracking catalyst and the feedstock is catalytically cracked to more valuable, lower molecular weight hydrocarbons.The temperatures in the riser reactor 100 can range from about 900OF (4820C) to about 1200OF (6490C), preferably from about 950OF (510OC) to about 1040OF (560OC), at a pressure from atmospheric pressure to about 50 psig (345 kPa). Weight hourly space velocity in the riser reactor can range from about 5 to about 200 WHSV. The velocity of the oil vapors in the riser reactor can range from about 5ft/sec (1.5 m/sec) to about 100 ft/sec (30 m/sec).

i - l-f - Suitable cracking catalysts include, but are not limited to, those containing silica and/or alumiha, including the acidic type. The cracking catalyst may contain other refractory metal oxides such as magnesia or zirconia. Preferred cracking catalysts are those containing crystal- -1 %_ line aluminosilicates, zealitest or molecular sieves in an amount sufficient to materially increase the cracking activity of the catalyst, e.g., between about 1 and about 50% by weight. The crystalline aluminosilicates can have silica-to-allumina mole ratios of at least about 2:1, such as from about 2 to 12:1, preferably about 4 to 6:1, for best results. The crystalline aluminosilicates are usually available or made in sodium form, and this component is preferably reduced, for instance, to less.than about 4 or even less than about 1% by weight through exchange with hydrogen ions, hydrogen-precursors such as ammonium ions, or polyvalent metal ions. Suitable polyvalent metals include calcium, strontium, barium, and the rare earth metals such as cerium, lanthanum, neodymium, and/or natur- ally-occurring mixtures of the rare earth metals. Such crystalline materials are able to maintain their pore structure under the high- temperature conditions of cata lyst manufacture, hydrocarbon processing, and catalyst regeneration. The crystalline aluminosilicates often have a uniform pore structure of exceedingly small size with the cross- sectional diameter of the pores being in a size range of about 6 to 20 angstroms, preferably about 10 to 15 angstroms. Silica-alumina based cracking catalysts having a major proportion of silica, e.g., about 60% to 90% by weight silica and about.10% to 40% by weight alumina, are suitable for admixture with the crystalline aluminosilicate or for use as the cracking catalyst. Other cracking catalysts and pore sizes can be used. The cracking catalyst can also contain or comprise a carbon monoxide (C0) burning promoter or catalyst, such as a platinum catalyst, to enhance the combustion of carbon monoxide in the dense phase in the regenerator 140.

Spent catalyst containing deactivating deposits of coke is discharged from the disengaging vessel 108 and lifted uDward through the spent catalyst riser 144 and fed to the bottom portion of the overhead fluidized catalyst regenerator or combustor 140. The riser reactor and 1 i 1 t (pa;eaedas) pa;PUOT;Ovag aq UED siodeA patzsvlg Pup slodeh TTO GT:; ao;puotzoel; UTew at:1 UT dATaATZEula;TY tZouanb a,4z sp asn jo; (1 ajnbij) P9T auTT touanb 11o qú aTOAD atz; o; PaTOA0al aq uco c)DDH lo/pue c)DD1 ag:i go;led 66T auTT 1To pa;ueoap P gbnoaq: zo:euoT:opi; DDi ag: go wO;Oq aq: w039 umPzPq:Tm 5: TTO Pa4URDaC '86T auTT TIO aToAo DiATe;eo AAraq P qbnojq jo;puoT;ova;:)DI aq; wca; UMP3Pq:1TM ST ODDH '96T auTT ITO aTOA0 OT;ATC;P0 96TT OE P qbnoiTz jo;euoi:4oEj; DDj aiz woig umpipM;Tm si oD:)l 4t61 auTI eq;qdeu P qbnoaq: 2oruoi:opi; DDj aql moa; umpapqqlm sT etj;qdeN UT OUTT seb;q5T1 P qbnoit;; ao;euoi;oea; DDi at41 moz; umeapq;lm ale seseb uoqaepoapAM:1q6T1.(0:>C) TIO Pa:URDaP PUP d(C)DDH) TIO aloAD 0-.r4ATLI;LIO AAEa14 d(ODDI) 5Z TTO alOAD oT;ATE;en qbll 1Pq1qdPu dsasPb uOqIR001P4 :1q5TT c;uT (paezedas) paeuoi;opa; aq ueo siodeA paqsel; PUP SJOdeA TTO buTsIldwO:) suoqjEz)oapAt pa)i:)ej:) ATIPoT:Al -e;eO atl:l '061 10:IcuOT;Oel; DD2 al:1 uI '061 201PuOT:OEI; UTM D33 aq:l 0; PaAaAuOO PUP ETT auTT;onpo2d uanl;;a up OZ qbnojq; 901 lassaA 6uTbe5uasip go do; alq; woag umpjpq:;lm ST (TTO PazT;v10M suOqIEDOIPAtl Pa)(0e20 ATTROT;Alr:EO go weajzs;onpoid zuanT;ja atZ 19 eanbij uT umoqs sy -yST auTT seS anT; jo auTT seb-g;o uoT;snq -woo peaqiaAo up qbnoaq; OPT ao:Isnqwoo aq go do aq:ST woag umejpq;Tm ale (seseb enTg) sasvb-ggo uoT;snqwoo ax41 ELT adIdPues;sATE;ED PaElaua5al aq;.Pue OLT auTT sAT -c;eo pa;elauasaj ex; PTA 001 lo;oeal laST1 aq; o; peg PUP 09T aulT:sATP-4RO P@:Plaua5a' q5n01q4 OPT 30;elauaSal atl:

W0JJ pa52Pq05TP ST:SATE;EO paElaUebal aql 10-f0Pal atZ:1 OT uT asn jog;sATe;eo pa;eaeua5aa buTAeal OPT J0;PlauabaJ aq; uT pa;snqwoo ATa'aTdwoo A1TeT:up;sqns si saTOT:ied SATP;eo at uo pauTP:Iuo:5 (a)loo) uoqjEO TenplsaU 2o; -eaauabai aq:l uTq:Tm Alpiemdn ATTRIaua5 saloi42ed;sATE:RO :Iuads at: azTpTnj; o; 9;ea mo,g pup ainssaid P P paoaluT 51 1Te aqI 'PPT jasTi;sATP;ED:luads Pup 9tT au]T 20;JaCUT ITV al; PIA 30:elaUabal eq JO UCT:20d WO:1:10q at:

oluT ATPlemdn pa;oaCuT sT ITV.;Tun buT:opio oT:ATP;ED aq; go s;uauodwoo AjewTad aq; aplAoid aatl;abo; joeaauabaz A-y into: (a) light hydrocarbons, having a boiling temperature less than about 4300F. (221OC), (b) light catalytic cycle oil (LCCO), and (c) decanted oil (DCO). The light hydrocarbons can be withdrawn from the main fractionator through an overhead line and fed to a separator drum. In the separator drum, the light hydrocarbons can be separated into (1) wet gas and (2) C 3 to 430-'F (221-'C) light hydrocarbon material comprising propane, propylene, butane, butylene, and naphtha. The wet gas can be with- drawn from the separator drum through a wet gas line and further processed in a vapor recovery unit (VRU). The C 3 to 430-OF (221-OC) material can be withdrawn from the separator drum through-a discharge.line and passed to the vapor recovery unit (VRU) for further processing. LCCO can be withdrawn from the main fractionator through an LCCO line for use as part of the quench or further refining, processing, or marketing. Decanted oil (DCO) can be withdrawn from the main fractionator through one or more DCO lines for further use. Slurry recycle comprising decanted oil (DCO) can be pumped from the DCO line 199 (Figure 6) at the bottom portion of the main fractionator 190 by a pump through a slurry line 182 (Figure 1) for recycle to the riser reactor 100. The remainder of the DCO can be conveyed through for further use in the refinery.

Spent deactivated (used) coked catalyst discharged from the riser reactor 100 (Figure 1) can be stripped of volatilizable hydrocarbons in the stripper section 116 with a stripping gas, such as with light hydrocarbon gases or steam. The stripped, coked catalyst is passed from the stripper 116 through spent catalyst line 144 into the regenerator 140. Air is injected through air injector line 146 to fluidize and carry the spent coked catalyst into the regenerator 140 via the spent catalyst riser 144 at a rate of about 0.2 ft/sec (0.06 m/sec) to about 4 ft/sec (1.22 m/sec). Preferably, excess air is injected in the regenerator 140 to completely convert the coke on 1 f i 1 i i i i i it- 1 the catalyst to carbon dioxide and steam. The excess air can be from about 2.5% to about 25% greater than the stoi chiometric amount of air necessary for the complete con version of cake to carbon dioxide and steam.

In the regenerator 140 (Figure 1), th.e coke on the catalyst is combusted in the presence of air so that the catalyst contains less than about 0.1% coke by weight.

The coked catalyst is contained in the lower dense phase section of the regenerator, below an upper dilute phase section of the regenerator. Carbon monoxide (C0) can be - combusted in both the dense phase and the dilute phase, although combustion of carbon monoxide predominantly occurs in the dense phase with promoted burning, i.e., the use of a CO burning promoter. The temperature in the dense phase can range from about 1050OF (566'C) to about 1400OF (760OC). The temperature in dilute phase can range from about 1200OF (6490C) to about 1510OF (821OC). The stack gas (combustion gases) exiting the regenerator 140 through overhead flue line 154 preferably contains less than about 0.2% CO by volume (2000 ppm). The major por tion of the heat of combustion of carbon monoxide is pref erably absorbed by the catalyst and is transferred with the regenerated catalyst through the regenerated catalyst line 170 and standpipe 166 riser reactor 100.

In a catalytic cracker (riser reactor) 100, some non- - volatile carbonaceous material, or coke, is deposited on the catalyst particles. Coke comprises highly condensed aromatic hydrocarbons which generally contain 4-10 wt.% hydrogen. As coke builds up on the catalyst, the activity of the catalyst for cracking and the selectivit.y of the catalyst for producing gasoline blending stock diminish.

The catalyst particles can recover a major proportion of their original capabilities by removal of most of the coke from the catalyst by a suitable regeneration process.

Catalyst regeneration is accomplished by burning the coke deposits from the catal st surface with an oxygen y containing gas such as air. The burning of coke deposits -211- from the catalyst requires a large volume of oxygen or air. Oxidation of coke may be characterized in a simplified manner as the oxidation of carbon and may be represented by the following chemical equations:

a. c + 0 2 - C02 b. 2C + 0 2 2C0 C. 2C0 + 0 2 2C0 2 Reactions (a) and (b) both occur at-typical catalyst regeneration conditions wherein the catalyst temperature may range from about 1050'F (56CC) to about 1300OF (704OC) and are exemplary of gas-solid chemical interactions when regenerating catalyst at temperatures within this range. The effect of any increase in temperature is reflected in an increased rate of combustion of carbon and a more complete removal of carbon, or coke, from the cata lyst. particles. As the increased rate of combustIon is accompanied by an increased evolution of heat whenever sufficient oxygen is present, the gas phase reaction (c) may occur. This latter reaction is initiated and propagated by free radicals. Further combustion of CO to C02 is an attractive source of heat energy because reaction (c) is highly exothermic.

The catalytic cracker (catalytic cracking unit) of Figure 2 is generally structurally and functionally simi- lar to the catalytic cracker of Figure 1, except that the light catalytic cycle oil (LCCO) quench line 284 is at an angle of inclination ranging from about 15 degrees to about 45 degrees, preferably about 30 degrees, relative to the vertical to increase the trajectory of the quench and enhance more uniform blending. The regenerator vessel 242 is also positioned laterally away from the disengaging vessel 208. For ease of understanding, the parts, elements, and components of the catalytic cracker of Figure 2 have been given part numbers similar to the corresponding parts, elements, and components of the catalytic cracker of Figure 1, except increased by 100, i.e., in the 200 series, e.g., riser reactor 200, external cyclone 206, 1 i I -ndisengaging vessel 208, stripper 216, regenerator 240, etc. The catalytic cracking reactor preferably comprises a riser.reactor. Some catalytic cracking units can have two riser reactors, two rough cut cyclones, two slide valves, and two standpipes operatively connected to a single regenerator and to a single disengaging vessel.

The catalytic cracker (catalytic cracking unit).of Figures 12 and 13 is generally structurally and functionally similar to the catalytic cracker of Figure 2, except that four internal rough cut inertia separators 306 comprising gross (rough) cut internal cyclones are used in lieu of external cyclones to grossly separate a substantial amount of catalyst from the catalytically cracked oil after the product stream of catalytically cracked oil has been discharged from the riser reactor 300 via horizontal product line 305. Four CCO quench injector lines 384 extend into the interior dilute Dhase portion (zone) 310 is the disengaging vessel (disengager) 308 to locations just above the vapor product exit 318 of the internal gross cut separators _^06 to inject and spray a CCO quench comprising LCCO and/or HCCO into the catalytically cracked oil after most of the coked catalyst has been removed from the oil by the internal gross cut separators 306. The quench injector lines can be positioned at an angle of inclination ranging from about 15 degrees downwardly to about 90 degrees (horizontal) relative to the vertical to minimize backflow of quench.

In Figure 12, a vertical outlet spent catalyst line, conduit, and chute 328 depends downwardly from the inter- nal gross cut separators 306 to discharge separated spent coked catalyst into the lower dense phase portion (zone) 314 and stripping section (stripper) 316 of the disengaging vessel 308. The top portion of the upper dilute phase zone 310 of the disengaging vessel 308 can have five secondary internal cyclones 312. The disengaging vessel 308 and secondary internal cyclones 312 above the rough cut separators 306o cooperate to remove the remaining coked a catalyst particles (fines) from the effluent gases and oil vapors. For ease of understanding, the parts, elements, and components of the catalytic cracker of Figures 12 and 13 have been given part numbers similar to the corresponding parts, elements, and components of the. catalytic cracker of Figure 2, riser reactor 3000 internal rough cut cyclone 306, stripper 316; regenerator 340, etc. One of the major design changes implemented on F= 600 unit which is similar to the catalytic cracker of Figures 12 and 13, was the use of HCCO instead of WC0 to quench the disengager. HCCO was selected instead of WC0 to avoid flooding, i.e. exceeding the capacity of the WC0 section of the ftactionator, and to improve overall unit beat recovery, as well as to take advantage of the greater 15 pumping capacity of the HCCO circuit. The HCCO quench nozzles are positioned to maximize quench efficiency by cooling the reaction gases as soon as they exit the cyclone. HCCO quench can cool the disengager by 30OF (170C) to 200OF (1110c), preferably at least about 100OF (z5cc). The catalytic cracker (catalytic cracking unit) of Figures 14 and 15 is generally structurally and functionally similar to the catalytic cracker of Figure 12, except the upright center, central riser reactor 400 25 extends vertically upwardly into the dilute phase portion (zone) 410 of and along the vertical axis of the disengaging vessel (disengager) 408. Coaxially positioned about the upper end 409 of the riser reactor 400 is an internal rough (gross) cut inertia separator 406 comprising an 30 inverted can. The inverted can 406 has: an open bottom end 406a for discharge (egress) of separated coked catalyst into the dense phase portion (zone) 414 and stripper section (stripper) 416 of the disengaging vessel 408; an imperforate solid planar or flat top or ceiling 406b 35 spaced above the upper end 409 of the riser reactor 400 and providing a striker plate upon which the catalyst laden stream of catalytically cracked oil strikes upon 1 l 1 1 1 i i i exiting the upper end 409 of the riser reactor; an upper cylindrical tubular wall 406c which extends downwardly from the top 406b; an intermediate portion providing a hood 406d extending below the upper wall 406c; and a lower cylindrical tubular wall 406e about the open bottom 406a which extends downwardly below the hood 406d.

The hood 406d (Figures 14 and 15) comprises an out wardly flared skirt. The hood 406d has an elongated down wardly diverging upper frustroconical wall 406f, which extends downwardly from the upper wall 406c, and has an downwardly converging frustroconical lower wall 406g, which extends downwardly from wall,406f. The upper frus troconical wall 406f has a pair of diametrically opposite rectangular discharge openings or windows 406h which pro vide outlet ports for egress (exiting) of the effluent product stream of catalytically cracked oil after the oil has been grossly separated from the catalyst.

When the catalyst laden stream of catalytically cracked oil exits the upper end 409 (Figures 14 and 15) of the riser reactor 400, it strikes the top 406b of the internal gross cut separator (inverted can) 406 with suf 1:icient momentum and force to grossly separate a substan tial amount of spent coked catalyst from the catalytically cracked oil. The separated catalyst is discharged in cart by gravity flow through the open bottom 406a of the inverted can 406. The catalytically cracked oil after being grossly separated from the catalyst, is discharged through the windows 406h of the inverted can 406.

A pair of diametrically opposite horizontal quench lines or injectors 484 (Figure 14) extend horizontally into the interior dilute phase portion (zone) 410 of the disengaging vessel 408 at locations in proximity to and in alignment with the windows 406h to inject and spray a quench comprising LCCO and/or qCCO into the catalytically cracked oil. The quench lines 484 can be positioned at a.n.

angle of inclination ranging from about 15 degrees down- j "2& wardly to about 90'degrees (horizontal) relative to the vertical to minimize backflow of quench.

The disengaging vessel 408 (Figure 15) and the secondary internal cyclones 412 at the tor) of the disengaging vessel, above the rough cut separator 406, cooperate to remove the remaining coke cat-alLyst particulates (fines) from the effluent gases and oil vapors. For ease of understanding, the parts, elements, and components of the catalytic cracker of Figures 14 and 15 have been given part numbers similar to the corresponding parts, elements, and components of the catalytic cracker of Figure 12, except in the 400 series, e.g., riser reactor 400, internal rough cut separa-tor 406, stripper 416, regenerator 440, etc.

The catalytic cracker (catalytic cracking unit) of Figure 16 is generally structurally and functionally similar to the catalytic cracker of Figure 12, exceot that the regenerator 540 is positioned below the disengaging vessel (disengager) 508. For ease of understanding, the parts, elements, and components of the catalytic cracker of Figure 16 have been given part numbers s--m-4lar to t-he corresponding parts, elements, and components of the catalytic cracker of Figure 12, except in the 500 series, e.g., riser reactor 506, stripper 51-6, regenerator 540, etc.

In some circumstances, it may be desirable to use a fluid bed reactor or a fluidized catalytic cracking reactor instead of or with a riser reactor.

EXAMPLES

The following examples serve to give specific illustration of the practice of this invention but are not intended in any way to limit the scope oil.' this invention.

ExamDles 11 and 2 7xper.;mental tests were conducted in a catalytic cracking unit (Unit Y) similar to that shown in Figure 1.

1 i 1 i i i i 1 i i 1 -Z- The test of Example 1 provided the base case. Catalytic cracking in Example 1 proceeded without a LCCO quench. Catalytic cracking in the test of Example 2 was conducted with an LCCO quench with a temporary gerry-riq quench line. The operating conditions and test results are shown below. The LCCO quenching test produced unexpected, surprisingly good results since naphtha octanes increased by 0.2 RM/2, conversion increased by 0.64 volume %, naphtha yield increased by 0.5 volume %, heavy catalytic naphtha stability improved, C 2 -gas yield decreased by 23% by weight, and coke selectivity (e.g. coke yield/conversion) improved. The extent, amount, and quality of the products produced during catalytic cracking with LCCO quench were unexpected. Such increase due to LCCO quenching has produced a substantial increase in product value.

1 k 1 -U- Q Example 1 Example 2 Difference Delta Quench, MB/D 0.0 1.5 +1.5 Fresh Feed, MB/D 24.6 24.7 +0.1 Riser, OF (OC) 955.(512.7) 956.(513.3) +1.(+0.5) Rough-Cut Cyclone 951.(511) 903.(484) -48.(-27) Overhead Line, OF (OC) Vapor Line from 940.(504) 903M84) -34.(-20) Disengaging Vessel to Main Fractionator, OF (OC) Temperature Difference 15.(8.3) 53.(29.4) +38.(+21.1 Between Riser Reactor and Disengaging Vessel, OF (OC) Preheated Temperature, OF (OC) 437.(225) 435.(224) -2.(-1) HCOD, Recycle, B/D 710. 790. +80.

Slurry Recycle, B/D 700. 700. 0.

Regen. Bed. Temp., OF (OC) 1312.(711) 1305.(707) -7.(-4) Conversion, Vol % 69.15 69.79 +0.64 Fresh Feed Properties API Gravity 23.9 24.0 +0.1 Nitrogen, Wt % 0.112 0.111 -0.001 Sulfur, Wt % 1.23 1.22 -0.01 Gas Oil, Vol % 97.8 97.6 +0.2 i i Example 1

Difference Example 2 Delta Converslon, Vol% 69.15 69.79 +0.64 TC2-, Wt% 3.34 3.11 -0.23 TC3, Vol% 10.80 10.90 +0.10 C3=/TC3 0.689 0.693 +0.004 TC4, Vol% 13.19 13.52 +0.33 C4=/TC4 0.524 0.513 -0.009 iC4/C4 saturates 0.789 0.785 -0.004 C5/430, Vo1% gasoline 51.83 52.33 +0.50 blending mate:ial, e.g. pentane, oentene LCCO, Vol% 25.54 24.91 -0.63 DCO, Vol% 4.62 4.57 -0.05 Coke, Wt% 5.90 6.16 +0.26 Volume Recovery, Vo-1% 105.99 106.24 +0.24 C5/430 MCL Octane 93.7 93.9 +0.2 RCL Octane 81.4 81.6 +0.2 Example 1

Difference Example 2 Delta LCN induction period, min 25 25 0 RON 94.5 94.5 0 MON 80.2 80.2 0 HCN induction r)er-;od 395 615 +220 RON 92.9 93.4 +1.6 MON 80.9 81.4 +0.5 1 Examples 3 and 4 Bench study tests were performed on kerosene to simulate catalytically cracked oil after the coke catalyst particles'have been removed. In the tests of Examples 3 and 4, the quench rate was 60 grams/hr and the oil producz rate was 125 grams/hour. The quench of Example 3 was HCCO. The quench of Example 4 was LCCO. Quench results of HCCO and LCCO were very similar and are reported below Examole 3 Example 4 Reactor, OF (-c) 1095 (591) 1100 (593) C2- fuel gas (wt%) Isothermal at quenching 14 16+ minutes of cooling 10 9 60 minutes of cooling a 6 Examoles 5 and 6 Experimental tests were conducted in another catalytic cracking unit (FCCU 500) similar to that shown in Figure 2. The test of Example 5 provided a base case without the use of a WC0. Catalytic cracking in the test of Example 6 was performed with a WC0 quench. '."he oil feed rate was 79 MBD. Riser reactor temperature was 1020 0 F ( 549 0 C). Wit-hout LiCCO quench, the reactor llemiDerature at the top of the disengaging vessel was 120F (70e)below the riser reactor. At 5.6 MBD of WC0 quench, the riser reactor temperature decreased 530F (30OC). WC0 quench yielded a desirable decrease in drying gas production by about 16.7% from 1140 114SWH to 980 MSM, sIgnificantly increased gasoline production 4.4% frcm 39.5 MBD to 41.2 MBD, and increased volume recovery by about 1%. WC0 quenching also decreased the production of propane, propylene, and isobutane. The operating conditions and test results a.-e:

i 1 i i LCCO quench rate Riser temperature Disengaging Vessel top temp. Temperature diff. between riser and disengager C2- dry gas c 5 + gasoline Volume % recovery Example 5 Example 6 with No quench LCCO auench 0 MBD 5.6 MBD 1020 0 F (549OC) 1020OF (549OC) 1008 0 F (5420C) 9670F (519OC) +12'F (70C) +530F (30OC) 1140 MSCFH 39.5 MBD 108.9% 980 MSCF1R 41.2 MBD 109.8% Example 5 Example 6 Difference No quench With quench Delta (wt.%) (wt.%) (wt.%) c 2_ dry gas 4.8 4.0 -.8 Propane 2.1 1.8 -.3 Propylene 5.7 5.3 -.4 Isobutane 3.7 3.5 -.2 N-butane 1.2 1.2 - Butenes 6.8 6.7 - C, gasoline 41.2 43.0 + 1.8 LCO/DCO 29.4 29.3 - Coke 5.1 5.2 Examples 7-9

Further experimental tests were conducted at catalytic cracking units with cycle oil quenches. In Example 7, LCCO quench was injected immediately after the product exit of the external rough cut cyclone in a cata- lytic cracking unit (Unit Y) similar to that shown in Figure 1 with a temporary gerry-rig quench line. Example 8, LCCO quench was injected immediately after the product exit of two external rough cut cyclones in another catalytic cracking unit (FCCU 500) similar to that shown in Figure 2. In Example 9, HCCO quench was injected immediately after the product exit-ed four internal rough cut cyclones in a disengager in a catalytic cracking unit sim- ilar to that shown in Figures -12 and 13. Experimental test conditions and results are shown below and in the charts of Figures 10 and 11.

Example 7

Feed Rate 24,700 B/D Riser Outlet Temp. 951coF (511 C) Quench Media LCCO Quench Rate 1500 B/D (6.1%) Vapor Res Time in Disengager 16 sec Fuel Gas Reduction 635 M SCFD K 635 M SCFD 1.61 SW/BBL-Sec is 24.7 M B/D (16 sec) Example 8

Feed Rate Riser Outlet Temp.

Quench Media Quench Rate Vapor Res Time in Disengager Fuel Gas Reduction K = 5,000 M SUD = 7.21 SW/BBL-Sec 77 M B/D (9 seconds) 77,000 B/D 1017 0 F (54TOC) WC0 5500 B/D (7.1%) 9 sec 5 MM SUD 1 i 1 i Examole 9 Feed Rate Riser Outlet Quench Media Quench Rate Vapor Res Time in Disengager Fuel Gas Reduction K 1,500 M SCFD 3.12 SW/BBL-Sec 37 M B/D (13 sec) Examol e-s--- 1J. 0 - 18 37,000 B/D 0 F. (5270C) 980 HCO 3000 B/D (8.1%) 13 sec 1.5 MM SCIF'D is increased reactcr terinerature at or above 940 (504 0 C), but especially above 1000OF (538OC) diminishes the oxidation stability of the naphtha product and gasoline. Also, active matrix octane catalysts (cracking catalysts containing ultrastable-Y zeolite with or without rare earth exchanged into the zeolite, supported on a carrier matrix which exhibits cracking activity independent of the zeolite) will produce a less stable naphtha product and gasoline than will rare earth exchanged Y catalysts, which produce larger volumes of lower octane naphtha.

Furthermore, inclusion of residual oil in the FW feedstock mixture will diminish the stability of the naphtha product and gasoline.

Quenching in accordance with this invention can substantially increase the oxidation and storage.stability of the naphtha product and gasoline by reducing the temperature in the dilute phase of the disengaging vessel as quickly as possible followIng the initial gross cut separation of t-he mixture of oil vacor product and catalyst.

Oxidation stabillty tests were conducted at catalytic cracking units wIth and w:.t,l-,out cycle oil quenches.:n Examples 10-13, gas oil feed was catalytically cracked in a catalytIc cracking unit- (Unit Y) similar to that shown 1 in Figure 1 with a temporary gerry-rig quench line, and 1 jected immediately after LWO quench, if indicated, was in the product exit of the external rough cut cyclone. In Examples 14-16, gas oil feed was catalytically cracked in a catalytic cracking unit (FCCU 500) similar to that shown in Figure 2, and LCCO quench, if indicated, was injected immediately after the product exit of two rough cut cyclones. In Examples 17 and 18, gas oil feed was catalytically cracked in a catalytic cracking unit (FCCU 600) similar to that shown in Figures 12 and 13, and HCCO quench, if indicated, was injected -;rrx.iedia"k-ely after the product exited two internal rough cut cyclones in the disengager (disengaging vessel). Experimental test conditions and results are shown below:

i i 1 -3b- EFFECT OF DILUTE PHASE FCU QUENCH ON FCCU NAPETRA OXIDATION STABILITY Ex. Unit Product Strearn Y Y Heavy Catalytic Naphtha Heavy CatalytIc Naphtha 12 Y Light Catalytic Naphtha 13 Y Llcht Catalytic Namhtha 14 F c CU, - 5 0 0 CS-430 is Total Catalytic Naphtha is FCCU-500 CS-430 Total Catalytic Napht-la 16 FCCU-500 CS-430 Total Catalytic Naphtha 17 FCCi-600 MU Wild Gasollne -2045 hrs 1 18 FCC-3-600 FCW Wild Gasoline -2000 hrs 1 k -25G_.

EFFECT OF DILUTE PHASE FM QUENCH ON FCCU NAPHTHA OXIDATION STABILITY Cont'd z; Riser Outlet Dilute Phase QU Ex. Tei p - ature, OF Teature, OF (OC). Fluid 940 (504) 940.(504) None 11 941 (505) 903 (484) 12 940 (504) 940 (504) None 13 941 (505) 903 (484) 14 1019 (548) 999 (537) None is 1020 (549) 940 (504) 16 1019 (548) 939 (504) 17 1020 (549) 990 (532) None 18 1020 (549) 910 (488) HCCO f -W - EFFECT OF DILUTE PHASE FCU QUENCH ON FCCU NAPHTHA OXIDATION STABILITY Cont, d Ex.

Feedstock Composition % Hydrotreated % % HVGO Gas Oil ASTM D-525 Stability, Resid Minutes 10 100 0 0 395 11 100 0 0 615 12 100 0 0 25 is 13 100 0 0 25 14 72 28 0 200 15 78 22 0 225 16 72 28 0 250 17 52 32 16 75 18 52 32 16 125 The preceding Examples 10-18 show the beneficial effects on quench of product stability.

Examples 19-48 Further oxidation stability tests were conducted with cycleoil quenches. T.ICCO quench was injected immediately after the product exit of two rough cut cyclones in a catalytic cracking unit (FCCU 500) similar to Figure 2. HWO quench was inject-ed immediately after the product exited two internal rough cut cyclones in the disengager (disengaging vessel) in a catalytic cracking unit (FCCU 600) similar to that shown in Figures 12 and 13. The Catalyst Complex was comprised of FCCU 500 and FCCU 600. Weighted average riser outlet temperature reflects the reiative flow rates of feed to each unit (FCCU 500 and FCCU 600) and the cracking temperature of each unit (FCCU 500 and FCCU 600). Stabilities of LCN and HCN were measured as received from a sample point in the rundown line. ULR is blended from LCN and HCN which have been treated with an antioxidant additive. Test conditions and results are shown below.

1 i 1 i i 1 i 1 1 i 1 EFFECT OF QUENCHING ON THE OXIDATION STABILITY OF UNLEADED REGULAR (ULR) GASOLINES OF CONTAINING FCCU PRODUCT NAPHTHA Ex.

Percent Riser Outlet Temperatures Resid in F (0c) Feed to Weighted Catalytic F= 500 F= 600 Average Complex 19 970 (521) 980 (527) 974 (523) 4.4 973 (523) 980 (527) 976 (524) 4.0 21 980 (527) 980 (527) 980 (527) 4.2 22 980 (527) 980 (527) 980 (527 4.3 23 980 (527) 980 (527) 980(527) 4.7 Average 977 (525) 980 (527) 978(526) 4.3 Std. Deviation 5 (3) - 3 (2) 0.2 24 980 (527) 981 (527) 980(527) 4.3 983 (528) 983 (528) 983(528) 4.4 26 975 (524) 985 (529) 979(526) 4.4 27 985 (529) 985 (529) 985(529) 4.4 28 985 (529) 985 (529) 985(529) 4. 4 29 985 (529) 985 (529) 985(529) 4.3 985 (529) 985 (529) 985(529) 4.5 Average 983 (528) 984(529) 983(528) 4.4 Std. Deviation 4 (2) 2- (1) 3 (2) 0.1 EFFECT OF QUENCHING ON THE OXIDATION STABILITY OF UNLEADED REGULAR (ULR) GASOLINES OF CONTATNING F= PRODUCT NAPHTHA Cont'd % Total Catalytic % HCN % WN Naphtha Ex. in ULR in ULR in ULR 19 50.3 14.5 64.8 49.8 19.2 69.0 21 56.5 14.0 70.5 22 58.0 14.7 72.7 23 56.0 9.2 65.2 Average 54.1 14.3 68.4 Std. Deviation 3.8 3.5 3.4 24 55.3 13.6 68.9 25 55.6 11.3 66.9 26 54.4 9.5 63.9 27 59.3 14.4 73.7 28 54.3 1-4.7 69.0 29 48.5 1.7.8 66.3 59.0 11.7 70.7 Average 55.2 13.3 68.5 Std. Deviation 3.6 2.7 3.2 j A -Ll- EtTE-CT OF QUENCEING ON THE OX:2AT--ON STAST=TY OF UNLEEADED REGIZAR (ULR) GASOLINES OF FC"U -PRODUCT NAIPH7EA Contd L CCO Ecco ASTM D-525 Quenc..,. Quenc., OxidatIon Stability at at Ex. -U,-P. IMI E C_ FCm-'-? 9,00bFC= 6C0 19 5 3 0 120 225 yes no 535 120 195 yes no 2 1 465 90 20.0 yes no 22 4 'L 5 - - yes no 400 - - yes no Averace 469 110 207 yes no Std. "je,j4.at-on 6 3 L7 16 24 71-0 11-0 >240 yes yes 25 740 135 105 yes yes 26 730 135 >240 yes yes 27 770 105 >300 yes yes 28 710 105 - yes yes 29 825 120 >300 yes yes 3 0 725 - - yes yes Average 744 1i3 yes yes Std. Deviaticn 41. L4 EFFECT OF QUENCHING ON THE OXIDATION STABILITY OF UNLEADED REGULAR (ULR) GASOLINES OF CONTAINING FCCU PRODUCT NAPHTHA Riser Outlet Teweratures Percent OF (OC) Resid in Feed Weighted to Catalytic Ex. F= -500 F= 600 Average lex 31 1010 (543) 1015 (546) 1012 (544) 6.4 32 10110 (543) 1015 (546) 1012 (544) 6.5 33 1010 (543) 1015 (546) 1012 (544Y 6.4 34 1010 (543) 1015 (546) 1012 (544) 6.4 1010 (543) 1015 (546) 1012 (544) 5.8 36 1010 (543) 1015 (546) 1012 (544) 5.5 37 1010 (543) 1015 (546) 1012 (544) 5.4 38 1010 (543) 1015 (546) 1012 (544) 5.4 39 1012 (544) 1015 (546) 1013 (545) 5.5 1012 (544) 1015 (546) 1013 (545) 5.7 41 1013 (545) 1016 (547) 1014 (546) 5.4 Average 1011 (544) 1015 (546) 1012 (544) 5.8 Std. Deviation 1 (0.5) 0.2 (0.1) 1 (0.5) 0.5 42 1010 (543) 1020 (549) 1014 (546) 5.3 43 1010 (543) 1020 (549) 1014 (546) 5.3 44 1010 (543) 1020 (549) 1014 (546) 5.8 1010 (543) 1020 (549) 1014 (546) 6.0 46 1010 (543) 1020 (549) 1014 (546) 6.0 1 -Li3 - EFFECT OF QUENCHING ON THE OXIDATION STABILITY OF UNLEADED REGULAR (ULR) GASOLINES OF CONTAINING FCCU PRODUCT NAPHTHA Cont'd % Total Catalytic % HCN % WN Naphtha Ex. in ULR in ULR in ULR 31 56.0 12.3 68.3 32 56.0 12.6 68.6 33 50.0 15.2 65.2 34 52.0 15.7 67.7 49.0 14.8 63.8 36 56.0 9.0 65.0 37 55.1 12.5 67.6 38 55.1 12.5 67.6 39 54.7 12.7 67.4 56.5 10.5 67.0 41 59.3 13.6 72.9 Average 54.5 12.9 67.3 Std. Deviation 3.0 2.0 2.4 42 52.8 12.3 65.1 43 52.8 12.3 65.1 44 55.8 8.3 64.1 50.0 10.3 60.3 46 50.0 10.3 60.3 0 L EFFECT OF QUENCHING ON THE OXIDATION STARILITY OF UNLEADED REGULAR (ULR) GASOLINES OF CONTAINING F= PRODUCT NAPETRA Cont 1 d Ex.

ASTLM D-525 oxidation Stability ULR LW F1W 31 415 -- - 32 420 >240 >240 33 395 -- - 34 310 340 36 355 37 3 3 5 38 320 - 39 340 90 - 330 105 75 4 1 335 90 135 Average 355 -- - Std. Deviation 36 - 42 720 120 - 43 720 105 >300 44 825 105 >240 710 105 >240 46 710 105 >240 LCCO HCCO Quench Quench at at FC= 500 F== 600 yes no yes no yes no yes no yes no yes no yes no yes no yes no yes no yes no yes no yes yes yes yes yes yes yes yes yes yes Examr)les 49-54 Quenching downstream of the rough cut cyclone also reduces the yield of dlolefins. Diolefins (molecules containing two unsaturated carbon-carbon bonds) are believed to be the pr--d,-,ct of thermal rather than ca,.alyt-,c cracking reactions, and are formed in regions of the FCCU where the temperature is high, or where the resIdence t...me is 1 1 -14.51 long. By reducing the temperature in the disengaging zone, the application of quench will reduce the yield of diolefinic molecules.

C4 diolefins (butadienes, and in particular 1,3,butadiene) are considered detrimental in subsequent processing of FCCU butylenes in an isobutane alkylation unit; they cause a higher than desired dilution of the acid alkylation catalyst.

CS diolefins, including, but not limited to isoprene, 1,3-pentadiene, and cyclopentadiene are considered similarly undesirable in an FCCU product stream. If the CS FCCU product is charged to an isobutane alkylation unit, the CS diolefins contained in this CS hydrocarbon stream can cause a high dilution of the acid alkylation catalyst.

Alternatively, F= product streams containing CS and high molecular weight diolefins may be blended into product gasolines. In gasoline, diolefins are suspected to contribute to product instability. The high reactivity of chemical compounds containing two unsaturated bonds will cause the dialefins to rapidly react with oxygen or other substances, forming undesired gums. Accordingly, a process which produces a lower diolefin yield is to be desired. Quenching of the reactor dilute phase will lower the diolefin yield. The chemical reactions which contribute to instability in gasoline are complex. Diolefins are believed to participate in these reactions, but it is possible that the stability improvements with quenching in Examples 19-48 involve additional molecular compounds other than diolefins as well. 30 An example of the beneficial effect of qu.enching in reducing diolefin yields is given below. CS diolefin yields from the tests are presented. Quenching is expected to change the yield of other diolefins in a similar fashion. 35 Yield tests were performed in a catalytic cracking unit (FCCU 500) similar to Figure 2. Samples of' the total overhead CS-430 naphtha product were obtained from the vapor product line leaving the disengaging vessel.

The samples in Examples 50 and 51 were taken with one riser reactor out of service. Only one riser reactor, discharging through a single external rough cut cyclone into the common disengaging vessel, was operating.

The samples taken in Examples 49 and 52-54 were taken with both riser reactors operating. Gas products from both external rough cut cyclones were quenched immediately downstream of the external rough cut cyclones with LCCO, then both quenched streams entered the common disengaging vessel.

The rates to each riser reactor in in Examples 49, 52, and 54 were identical but were reasonably split, roughly 50/50. For Example 53, the fiow rate of quench was 2500 b/d to the A outlet, 4100 b/d to the 3 outlet, giving a total of 6600 b/d. f The following results were obtained:

Tests Performed Without Quench Fresh WC0 CS Diolefin Cracking Feed Quench Volume Ex. Temp B/D B/D of Fresh Feed 49 1016'F (547'C) 73,500 0 0.21 10270F (553OC) 48,900 0 0.22 51 10270F (5530C) 48,900 0 0.17 Tests Performed With LCCO Quench IL c c 0 CS Diclefin Cracking Fresh Quench Volume Ex. Temo B/D B/D of 7.reshFeed 52 10090 F (5430C) 80,600 7,000 0.08 53 101-9 0 F (548OC) 76,500 6,600 0.11 54 10200 F (5490C) 74,600 6,300 0.11 i 41- 1 At substantially the same cracking temperature, CS diolefin yields were reduced approximately 35-50% by the application of AriCCO quenching.

Quench Selection In general, the quench should have a boiling point of 125 0 F (520C), preferably at least 430OF (221OC) in order to have a sufficient heat capacity to effectively cool the catalytically cracked oil product to minimize thermal cracking of the oil product as well as to allow heat recovery at the bottom rather than the top of the fractionator. Desirably, the quench should have a molecular weight over 90 to limit the total volumetric expansion of the quench and oil product upon vaporization to 100% to 120%, preferably 103% to 105% or less, of the volume of the oil products without the quench, i.e., the volumetric expansion of the quench should be from 0 to 20%, preferably 3% to 5% or less of the volume of the catalytically cracked oil. Furthermore, the quench should be inactive and inert to thermal cracking at 900'F (482'C) to 1100'F (5930C) for a residence time of 1-30 seconds in the dilute phase zone of the disengaging vessel. Previously cracked hydrocarbons, such as LCCO, HCCO, HCN, coker gas oil and coker distillates, are very desirable as quenches since they are less reactive to thermal cracking than fresh unprocessed virgin stocks, such as virgin gas oil and virgin naphtha, and hydrotreated stocks, such as hydrotreated gas oil and hydrotreated distillates. Moreover, the quench preferably has a boiling point under 900OF (482OC) to completely vaporize in the dilute phase of the disengager in order provide effective cooling of the catalytically cracked oil product and avoid coking of the walls and lines of the refinery equipment.

It is also desirable that the quench decrease C2 fuel gas production in order to allow higher operating temperatures at the cat- alytic cracking unit.

-410d- I i The properties of various quenches are shown in Table A. LCCO in this patent application also includes intermediate reflux on tower pump arounds with a boiling range, Al gravity, and molecular weight similar to that 5 shown for LCCO in Table A.

i 1 1 is 1 i i 1 i 1 t 4 Table A

Properties of Quenches Nominal Average Nominal API Molecular Boiling Point Gravity Wt.

Light Catalytic 430-650OF 11-30 200-300 Cycle oil (221-343OC) 20 avg 215 avg (LCCO) Heavy Catalytic 650-850OF.2-25 250-350 Cycle Oil (343-454 0 C) 10 avg (HCCO) Heavy Catalytic 300-430 0 F 20-50 100-250 Naphtha (149-221OC) 35-40 avg (HCN) Light Coker 500-650 0 F 30-35 210-300 Gas Oil 5260F avg 34 avg (:,CGO) (260-3430C 274 0 C avg) Coker Still 430-650 0 F 30-40 200-250 Distillates 504 0 F avg 35 215 avg (221-3430C 2620C avg) Kerosene 320-530 0 F 35-45 150-200 400-450OF avg 41 avg 175 (1.60-277 0 c 204-2320C avg) - Rr-l- Table A (úcnt'd.) Nominal Average Nominal API Molecular Boiling Poil-t- Gravitv Wt.

Hydrotreated 430-650OF 35-45 225-265 Distillate 560OF avg 39.5 avg 230 (221-3430C 293 0 C avg) Virgin Gas Oil 650-1000OF 21-32 300-400 (VGO) (343-538)OC 25 avg 350 avg Heavy Virgin 300-350 0 F 40-60 100-250 Naphtha 3250F avg 50 150 (HVN) (149-177 0 C 1630C avg) Light Virgin 125-175 0 F 60-80 70-150 Naphtha 150OF avg 70 125 (LVN) ( 52-790C 66 z C avg) Hydrotreated 650-10000 F 24-35 300-400 Gas Oil (343-5358 0 C) 29 avg 350 avg (HGO) Decanted Oil 700-1200OF -4 to +1.0 400-600 (DCO) 900 0 F avg +2 avg 500 avg ( 371-6490C 4820C avg) Resid 1000-1600 3 7 1 0-20 300-1000 (538-871 0 C) 12 avg 700 avg Water 212OF 10 avg 18 (F. 2 0) (100,C) I -5) - Quenching involves injecting a fluid, preferably a liquid, into the catalytic cracking unit, preferably immediate downstream of the gross cut separator (cyclone), to stop the reactions.

Generally, a superior quench process:

1) Will provide maximum economic benefits by effectively reducing the loss of valuable products to the thermal reactions that occur after catalytic cracking is substantially completed.

2. Will have minimum adverse effects on operations.

3. Will minimally affect utility costs.

Although it is quite clear that a number of fluids could be used as quench, because the requirements of a quenching process are complex, the selection of a quench material and implementation of quenching are neither simple nor obvious. A fluid that is outstanding in one aspect may be unacceptable in another.

The quench fluid cools and dilutes the FCC riser products and so reduces the yield of thermal products. Figures 7 and 8 show, i.e., the ability of various quenches to cool the product stream, i.e., show the relative cooling capacities of different fluids. Quenched product temperature is plotted as a function of the amount of quench addition. The LCCO/CAT in Figure 7 means that LCCO quench was injected into the oil product before the catalyst was grossly separated from the oil product. The quench addition, expressed as a percentage, is the ratio of the weight of quench fluid to the -,Taight of the product stream. The heat capacity of the quench fluid and its heat of vaporization (if a liquid) influence the cooling capacity. Water is very effective and cools at 20OF (11OC) per 1 wt% addition. Hydrocarbons 5L.

are also effective and provide cooling at approximately 70F%(40C) per 1 wt% addition. Less effective is steam (40F (20C) per 1 wt%) because it is already vaporized. Cooling the products before removing catalyst requires tremendous amounts of quench fluid because the catalyst holds large quantities of heat and there is so much catalyst present (typically 6 times the i i 1 i 1 C3- weight of oil). Although water provides good cooling, has drawbacks that offset this advantace.

Table 3

RelatIve Quench Thermal Molecular Crack- Wt. abilitv C,I Product Quench Fuel Gas Con- Con- Reduction centration cent:ation Wt.% Water is 0.00 0.737 0.263 78.0 Eydro- carbons 106 0.36 0.846 0.1154 69.4 114 0.59 0.856 0.144 68.0 1.20 1.37 0.871 0.1129 64.4 201. 0.65 0.913 0.087 65.7 216 1.06 0.913 0.082 64.0 245 2.46 0.927 0.073 60.8 339 1.05 0.946 0.054 63.L 365 1.71 0.950 0.050 62.1 414 3.96 0.956 0.044 59.1 Adding a quench fluid reduces the fuel gas by 25- de=easing the temperature of the product dilutIng the concentration of riser products. The rate of thermal degradation of the riser products (and also the hydrocarbon auenc") depends upon the temreratu.-e, the residence t-..me in the system, the cancentratIon of vapor, and the inherent reactIvity (thern.al crackability) of the material. Reducing the concentration of rIser products slows the rate a.' degradation provided that the quench fluid iltsell-1 has a lower thermal crackability than the riser product. Table 3 gives the re-lative molar concentrations of riser mrcducz ar 10007 (538OC) and queric.n fluid fcr var-Jjus quenc-.,.Iiuids of different molecular weights injected at a ratio of about 15% by weight of the 1 -5t- product. In Table 3 and the following tables the C2-fuel gas reduction is relative to the instantaneous cooling of the hydrocarbon products from 1000'F (538'C) to 900'F (482OC),iith a residence time of about 13 seconds. The quench fluids (injected as liquids) expand to different volumes depending on the molecular weights. The lowest molecular weights provide the maximum expansion and, therefore, the maximum dilution of the riser product. Table 3 also provides an estimate of the reduction in C2- fuel gas production based on laboratory tests and includes the relative thermal reactivity of the quench fluids. Quench fluids that have low molecular weights give the maximum reduction in C2-fuel gas production since C2-fuel provided measures the extent of thermal degradation, pro- vided that the quench fluid itself has a low susceptibility to thermal cracking.

Stability of the quench is important. -A quench material that is unstable will require excessive replacement and will itself contribute to the C2yield. Table 3 includes the thermal stability of the various fluids. The thermal stability (crackability) was determined from laboratory tests of various quench fluids. The values In the table are relative to the thermal stability of heavy catalytIc nar)htha, which will have properties similar to riser products. Of course, the non-hydrocarbon, wall-er, does not crack, so its performance establishes a target for the hydrocarbons. Hydrocarbons with low crackability give satisfactory performance.

Mixing time is also an important factor in quenching.

When the quench fluid is injected into the hot product stream, the quench and product streams must mix as quickly as possible in order to get the maximum rate of cooling. Inefficient mixing of the two streams allows extra time for the thermal reactions to proceed. By using atomizing nozzles to.;"-ect the auench fluid, very small- droplets are formed that disperse and vaporize quickly.

i i 1 - The effect of mixing time on the reduction in thermal products is indicated in Table C, based on laboratory results for LCCO quench:

Table C

Effects of Cooling Time on C2 Fuel Gas Reduction for LCCO Quench Cooling Product Time Wt% of Quench C2-Fuel Gas Temperature sec to Product Reduction % 1000'F (538'C) i is 92.4 1000OF (5380C) 5 15 64.0 1200'F (649'C) 1 60 92.4 1200 0 F (649'C) 5 60 68.5 Vapor expansion is an important factor in selecting the proper quench. Vaporized quench enters the product recovery system and must be compatible with the process equipment and control. improper selection of the quench fluid can lead to upsets in the riser discharge flow, in the seoaration of catalyst from the product vapors, and can cause interference with the efficient operation of the product fractionator. In order to minimize these disruptions, the quench fluid should give the minimum expansion to the vapor so that erratic and extreme pressure levels are avoided. Figure 9 shows the ratio of the volume of "-.he quenched product stream to the product stream alone as a function of temperature drop upon quenching 'for various quench fluids. The legend WCO/CAT in Figure 9 means Chat LCCO quench was injected into the oil product before the catalyst was grossly separated from the oil product. The gases, steam and propane, have the largest increases because substantial quantities must be added to cool the stream, and the low molecular weight -AG- gives large volumes of gas.;Jater also has a substantial vapor expansion. A water-quenched stream will have almost 20% more volume than the product stream alone. This magnitude of expansion can affect operations adversely and should be avoided. On the other hand, the liquid hydrocarbons exhibit a nearly neutral volume change. For the liquid hydrocarbons, the molecular weight is typically high enough so that the volume of gas is much less than for water. Also, the expansion of the hydrocarbon is offset by the contraction of the cooled product so that a nearly constant volumetric flow rate is achieved. This criterion is in contrast to the benefit of low molecular weight di'Luting the product vapor.

There are practical limits on the amount of quench that is used. The benefits diminish as the amount of quench increases. Also, the benefits are greatest the higher the riser product temperature. Table D illustrates this. Each pair of conditions in the table correspond to two levels of quench addition. At 1000OF (538OC) doublIng the amount of quench reduces the C2-yield by only 45%. At 1200OF (6490C) increasing quench by a factor of 4 brings on-ly a 30% improvement.

1 i 1 1 1 1 1 i 1 i i t i Table D

Pre- Post- C2 s Quench Pre- Quench Post Ratio of Fuel Ga Time, Quench Time, Quench Quench to Reduc- seconds Temp. seconds Temp. Feed % tion, % Quench:

is S Water 1 1000OF 12 950OF 2.33 71.2 (5380C) (5100c) Water 1 1000OF 12 900OF 5 99.3+ (538'C) (482'C) LCCO 1 1000 0 F 12 950OF 7 64.0 (538'C) (5100c) LCCO 1 1000OF 12 900OF is 92.4 (5380C) (482'C) LCCO 5 1000 0 F 8 950,F 7 43.9 (53SOC) (5100c) LCCO 5 1000 F 8 900 0 F is 64.0 (538 C) (482'C) -U- Table D (Cont'd.) J.

is PreQuench Pre- Time, Quench seconds Temp.

Quench:

PO S t - C2 Quench Post Ratio of Fuel Gas Time, Quench Quench toReducseconds Tem1D. Feed % tion, % Water 1 1200OF 12 1100OF 5 74.3 (649'C) (5930C) Water 1 1200'F 12 900 0 F 20 97.5 (6490C) (482OC) 0 LCCO 1 1200OF 2 1100 F 15 67.2 (649OC) (593OC) LCCO 1 1200 0 F 12 900 0 F 60 92.4 (6490C) (4820C) 0 LCCO 5 1200'F 8 i100 F 15 45.8 (6490C) (593'C) 0 0 LCCO 5 1200 F 8 900 60 -68.5 (6490C) (4820C) Caking is another important criteria in determining the proper quench. A high tendency to form coke is detrimental to a quench fluid. Coke deposits can restrict process flows that could force a shutdown. Excessive coke in the regenerator could adversely affect the unit's heat balance and economics. On the other hand, a quench fluid that reduces coke by interaction with catalyst in the dilute zone of the disengager vessel improves the unit's coke selectivity and economics.

The use of quench increase utilities costs. A superior quencn fluid mininrizes those costs. Costs that are associated with the following: replacement of lost quench 1 i i i I i is _Effi - fluid; pumping the quench fluid; incomplete heat recovery and losses; water requirements for cooling and as boiler feed; and treatment of dirty process water.

Some hydrocarbon quench materials can thermally degrade. C2-fuel gas is produced by the degradation. Table E presents computer model predictions on the effects of various quench medium properties on the gross reduction in C2-. A quench fluid that degrades the products shows a lower C2-fuel gas reduction. 10 Table E

Effects of Quench Material Properties on Predicted Performance Avg Boiling Relative Concen- C2 Pt Thermal tration Fuel Gas Spec ABP Molecular Crackof Reduc- Gravity OF (0 c) t ability Quench tion, 0.825 300 (149) 130 1.38 0.129 91.3 0.825 575 (301) 245 2.46 0.073 89.5 0.825 800 (426) 414 4.00 0.044 88.6 0.93 300 (149) 114 0.59 0.144 94.5 0.93 575 (301) 216 1.06 0.082 92.4 0.93 800 (426) 365 1.72 0.050 91.4 0.99 300 (149) 106 0.37 0.154 95.6 0.99 575 (301) 201 0.66 0.087 93.4 0.99 800 (426) 339 1.06 0.054 92.4 There are not any or very 3Little additional process 35 water cost associated with the use of hydrocarbon fluids as quench material. Process water must be obtained when water is the quench material. The use of process water -<0(>- has additional cost. Water becomes contaminated when it goes through the process and must be treated to meet Pol lution control regulations.

Heat recovery is another important factor in select ing the proper quenchp Substantial-quantities of heat are absorbed by the quench material. This heat must be recov erable in a usable form if the quench process is to be practical. Generally, the higher the temperature at which heat is available, the more easily it can be recovered.

Therefore, quench fluids that boil at h igher temperatures will enable better heat recovery. In the FCC catalytic cracking unite the heat recovery is integrated into the product fractionator system. Low temperature energy in the fractionator system is typically lost to cooling water. Energy in streams below approximately 212OF (1000c) to 350'F (1770C) is not recovered. Therefore, water is a poor quench medium from an energy recovery standpoint since it condenses at 212OF (100OC) at atmospheric pressure and since most of its energy is released when it condenses. A fluid that boils just below the target quench temperature will provide the maximum heat recovery.

In Table F, the enthalpies of some candidate quench fluids (LCCO, HCCO, HVGO Gas Oil, Water) are given that correspond to the temperatures in the table. The heats, Q1, Q2, Q3, 04r are shown which are the heats absorbable above (a) 625OF (329C), (b) between 625OF (3290C) and 475OF (2460C), (c) between 4750F (2460C) and 325OF (163OC), (d) and between 3250F (1630C) and 60OF (160C), respectively. Materials that absorb large amounts of heat at high temperatures (e.g.e high Q1) are preferred, and those that absorb heat at low temperature (e.g., high Q4) are not preferred. For the materials in Table F, the order of preference as a quench medium is (1) HCCO, (2) LCCO, (3) Gas Oil, and lastly Water. The quenched product temperature a,-,d QI upper limit for each quench was i j at 900'F (482'C). The enthalpies were determined at a pressu.re of 20 psig (238 kPa).

is i TABLE F

ENTHALPIES OF FCCU PRODUCT QUENCH FLUIDS AND AVAILABLE HEATS WC0 HCCO Available Available Teinp. BTUILB Heat BTUILB Temp. BWILB Heat BMILB CIF (OC) (Jlgm) (jIgm) OF (OC) (Jlgrm) (Jlgrm) 1200 (649) 866.2 (2015) Maximum 1200 (649) 811.5 (1888) Maxi= 1174 (634) 846.9 (1970) Product 1174 (634) 793.3 (1845) Product 1125 (607) 810.5 (1885) Temp. 1125- (607) 758.9 (1765) Temp.

1050 (566) 756.1 (1759) 1050 (566) 707.7 (1646) 975 (524) 703.3 (1636) 975 (524)657.8 (1530) 900 (482) 652.1 (1517) 900 (482)609.5 (1418) 825 (441) 602.7 (1402) 825 (441) 562.9 (1309) 750 (399) 555.1 (1291) 750 (399) 433.0 (1007) Liquid 675 (357) 508.4 (1183) 675 (357) 384.0(893) 625 (329) 417.9 (972)Ql= 234.2 (545) 625 (329) 353.7 (823)Q1=255.8 (595) 600 (316) 372.6 (867) Liquid 600 (316) 338.6 (788) 525 (274) 325.9 (758) 525 (274) 295.5 (687) 475 (246) 296.4 (689)Q2= 121.4 (282) 475 (246) 268.3 (624)Q2=85.4 (199) 450 (232) 281.7 (655) 450 (232) 254.7 (592) 375 (191) 239.9 (558) 375 (191) 216.4 (503) 325 (163) 213.8 (497)Q3= 82.7 (192) 325 (163) 192.7 (448)Q3=75.6 (176) 300 (149) 200.7 (467) 300 (149) 180.9 (421) 225 (107) 164.5 (383) 225 (107) 148.4 (345) (66) 131.3 (305) 150 (66) 119.3 (277) (24) 101.8 (237) 75 (24) 94.0 (219) (16) 95.9 (225)Q4= 117.9 (274) 60 (16) 88.9 (207)Q4=103.8(240) 32 (0) 84.9 (197) 32 (0) 79.5 (185) i 1 1 TABLE F (cont'd.) ENTHALPIES OF FCCU PRODUCT QUENCH FLUIDS AND AVAILABLE HEATS Feed Oil (ENM) Gas Oil water I= Available Available BTUlLB Heat BTUJLB Temp. BTU/LB Heat BTUlLB OF (0c) W (Jlgm) CF (0c) (Jlgm) (i/grm) 1200 (649) 925.6 (2153) Maximum 1200 (649) 1639 (3812) Maximum 1174 (634) 904.5 (2103) Product 1174 (634) 1626 (3782) Product 1125 (607) 864.8 (2011) Temp. 1125 (607) 1600 (3721) Temp.

1050 (566) 805.3 (1873) 1050 (566) 1560 (3629) 975 (524) 747.2 (1738) 975 (524) 1522 (3540) 900 (482) 678.6 (1578) 900 (482) 1483 (3449) 825 (441) 566.8 (1318) Liquid 825 (441) 1445 (3361) 750 (399) 509.6 (1185) 750 (399) 1408 (3275) 675 (357) 454.5 (1057) 675 (357) 1371 (3189) 625 (329) 419.2 (975) Q1=259.4 (603) 625 (329) 1347 (3133)Q1=136.15(317 600 (316) 401.5 (934) 600 (316) 1335 (3105) 525 (274) 350.7 (816) 525 (274) 1299 (3021) 475 (246) 318.4 (741) Q2=100.8 (234) 475 (246) 1275 (2966)Q2=72 (167) 450 (232) 302.2 (702) 450 (232) 1263 (2938) 375 (191) 256.3 (596) 375 (191) 1227 (2854) 325 (163) 227.5 (529) Q3=90.9 (211) 325 (163) 1203 (2798)Q3=72 (167) 300 (149) 213.1 (496) 300 (149) 1191 (2770) 225 (107) 173.0 (402) 225 (107) 193 (449) (66) 136.3 (317) 150 (66) 118 (274) (24) 103.5 (241) 75 (24) 45 (105) Liquid (16) 96.9 (225) Q4=130.6 (304) 60 (16) 20 (47)Q4=1175 (2733 32 (0) 84.7 (197) 32 (0) 0 (0) Quench Material Selection: Some quench fluids are evaluated in Table G. Different refineries may use different quench materials to meet specific requirements or to take advantage of special opportunities. Among the fluids examined below, LCCO is best and HCCO is second best. Water has some serious shortcomings. The remaining.materials have certain characteristics that can reduce their attractiveness as a quench fluid.

t t Table G

Evaluation of Candidate Quench Materials Quench Water Steam Propane HCN LCCO HCCO Cooling Capacity Product Dilution Stability 20 Volume Expansion Coking Tendency Pumping/ Transporting Heat Recovery 25 Water Use Waste Disposal E E E p E p p A A A A G G G G E E G F A E E E 1 E E p E E E p I i G A E E G p p p F F A p p F p E E E p E E E A 1 Key:

P: Poor F: Fair A: Average G:

Good E: Excellent -165- 1 Table G (cont'd.) Evaluation of Candidate Quench Materials Hydro- Hydro (HVG0) treated treated Quench DCO GasOil Kerosene GasOil LCCO Cooling Capacity A A A A A Product Dilution F F A F AStability G A A A A volume Expansion E E I" E E Coking Tendency p G E E E Pumping/ Transporting A A A A A Heat Recovery E G G G G Water Use E E E E E waste Disposal E E E E E Key:

P: Poor F: Fair A: Average G: Good E: Excellent Among the many advantages of the novel catalytic cracking and quenching process and system are:

1. Enhanced product values and quality.

2. Greater yield of more valuable hydrocarbons.

3. Production of more naphtha and finished gaso line.

4. Higher throughput.

5. Better throughput and oxidation stability of product naphCha.

_Y,_L_ %6nw.o- 6.

7. 8. 9.

Decreased thermal cracking and product degradation thereby minimizing overcrack.ing of gasoline into ethane and light fuel gas. Lower pentadiene content in the naphtha product. Less low value fuel gas production. Increased octane number of naphtha and finished gasoline.

10. Economical 11. Efficient 12. Effective.

Although embodiments of the invention have been shown and described, it is to be understood that various modifications and substitutions, as well as rearrangements of process steps, can be made by those skilled in the art without departing from the novel spirit and scope of the invention.

i j i i i i i 1

Claims (25)

1. CLAIMS:-

   28:CATA.BRIT A process for catalytically cracking feed oil, in which the feed oil is catalytically cracked in the presence of a cracking catalyst and at an elevated cracking temperature to produce a product stream comprising cracked feed oil, the product stream is cooled to a temperature below said cracking temperature by contact with a quench fluid to deter further cracking of the cracked feed oil to light hydrocarbon gases, and wherein directly after separation of Catalyst from the product stream following said catalytic cracking, the quench fluid is delivered into said product stream to mix intimately therewith and thereby rapidly cool the product stream.
2. A catalytic cracking process, comprising the steps of: catalytically cracking feed oil in a reactor of a catalytic cracking unit in the presence of a cracking catalyst to produce a catalytically cracked effluent product stream of upgraded oil; and quenching said product stream externally and downstream of said reactor with a quench comprising at least one member selected from the group consisting of light catalytic cycle oil, heavy catalytic cycle oil, heavy catalytic naphtha, kerosene, coker distillates, light coker gas oil, hydrotreated distillate, fresh unprocessed virgin gas oil, and fresh unprocessed virgin naphtha.
3. 3. A catalytic cracking process in accordance with claim 2 wherein: said feed oil comprises gas oil; and said quenching further includes decreasing the temperature of said product 1 stream, and minimising thermal cracking of said product stream; and said quench is injected into said product stream in an amount ranging from about 2% to about 20% per barrel of feed oil.
4. 4. with claim 2 or 3, wherein: said reactor comprises a riser reactor; said product stream is quenched after said catalytic cracking is substantially completed; and said quench contacts said product stream in an amount ranging from about 5% to about 15% per barrel of feed oil.

   1 1 A catalytic cracking process in accordance
5. 5. steps of:

   A catalytic cracking process, comprising the catalytically cracking feed oil in the presence of a cracking catalyst; and cooling said catalytically cracked feed oil after said catalytic cracking is substantially completed to substantially minimise thermal cracking of said catalytically cracked oil to fuel gas by contacting said catalytically cracked oil with a hydrocarbon liquid quench having a boiling point greater than water, a molecular weight over 90, and a volumetric expansion less than about 20% of the volume of said catalytically cracked oil.
6. 6. A catalytic cracking process in accordance with claim 5 wherein: said quench is substantially inert to thermal cracking at about 4820C to about 5930C; said feed oil is catalytically cracked in a 1 f i I i i i i C - Q91 reactor; said quench is selected from the group consisting of previously cracked hydrocarbons, fresh unprocessed virgin feedstock, and hydrotreated hydrocarbons; and said catalytically cracked oil is cooled by said quench by an amount ranging from about 170C to about 1110C.
7. 7. A catalytic cracking process in accordance with claim 5 or 6, wherein: said volumetric expansion of said quench is less than about 5%; said quench improves the oxidation stability of the naphtha product and gasoline; a substantial portion of said quench has a boiling point of at least about 2210C and below about 4820C and substantially completely vaporises in the dilute phase.

   2 5'
8. 8. A catalytic cracking process in accordance with claim 5, 6 or 7, wherein said quench is selected from the group consisting of light catalytic cycle oil, heavy catalytic cycle oil, heavy catalytic naphtha, coker gas oil, and coker distillates.
9. 9. A catalytic cracking process in accordance with any one of claims 5 to 8, including substantially separating said catalyst from said catalytically cracked oil in a gross cut separator having a vapor exit providing a product outlet and injecting said quench into said catalytically cracked oil after said separating in proximity to said product outlet of said gross cut separator.

   - to - ( 1
10. 10. steps of: catalytically cracking feed oil in a catalytic cracking unit comprising a regenerator and at lest one catalytic cracking reactor selected from the group consisting of a riser reactor and a fluidised bed rector, in the presence of a cracking catalyst to produce upgraded oil leaving coked catalyst; making a gross-cut separation of said coked catalyst from said upgraded oil and substantially immediately thereafter; quenching said upgraded oil to substantially decrease thermal cracking of said upgraded oil to less valuable hydrocarbon products and light hydrocarbon gases; regenerating said coked catalyst in a regenerator; and recycling said regenerated catalyst to said catalytic cracking reactor.

    1 5 A catalytic cracking process, comprising the
11. 11. A catalytic cracking process in accordance with claim 10 wherein; said upgraded oil is quenched with about 2% to about 15% of said quench per volume of said feed oil; said quench is selected from the group consisting of light cycle oil, heavy cycle oil, heavy catalytic naphtha, and combinations thereof; and said quenching occurs downstream of said riser reactor.
12. 12. steps of:

    A catalytic cracking process, comprising the catalytically cracking feed oil in a reactor I i i - +1 - of a.catalytic cracking unit in the presence of a cracking catalyst to produce a catalytically cracked effluent stream of upgraded oil containing catalyst; substantially separating said catalyst from said upgraded oil in an external gross cut separator and in a disengaging vessel; quenching said upgraded oil downstream of said external gross cut separator and upstream of said disengaging vessel with a quench comprising at least one member selected from the group consisting of light catalytic cycle oil, heavy catalytic cycle oil, heavy catalytic naphtha, kerosene, coker distillates, light coker gas oil, hydrotreated distillate, fresh unprocessed virgin gas oil, and fresh unprocessed virgin naphtha; and said quench is injected into said stream in an amount ranging from about 2% to about 20% by volume per barrel of feed oil.

    -
13. 13. steps of:

    crude oil; A catalytic cracking process, comprising the substantially desalting petroleum comprising heating said desalted crude oil in a furnace; pumping said heated crude oil to a primary distillation tower; separating said heated crude oil in said primary distillation tower into streams of naphtha, primary gas oil, and primary reduced crude; pumping said primary reduced crude oil to a pipestill vacuum tower; separating said primary reduced crude oil in said pipestill vacuum tower into streams of wet gas, heavy gas oil, and vacuum reduced crude oil providing resid oil; conveying a feed oil comprising said primary gas oil from said primary distillation tower to an upright elongated riser reactor of a catalytic cracking unit; feeding fresh and regenerated crystalline cracking catalyst to said riser reactor; catalytically cracking said feed'oil in said riser reactor in the presence of said cracking catalyst under catalytic cracking conditions to produce an upgraded effluent product stream of catalytically cracked oil containing spent coked catalyst; separating a substantial amount of said spent coked catalyst from said product stream in an external rough cut separator downstream of said riser reactor to make a gross separation of said coked catalyst from said product stream; injecting and quenching said product stream soon after said product stream exits said external separator with a cycle oil quench for substantially minimising thermal cracking of said product stream to less valuable hydrocarbons and concurrently enhancing the yield of naphtha to substantially increase the production of gasoline, said quench comprising a cycle oil selected from the group consisting of light catalytic cycle oil and heavy catalytic cycle oil, said quench being injected into said product stream in an amount ranging from about 5% to about 15% by volume per barrel of feed oil; conveying said quenched product stream into an upper dilute phase portion of a disengaging vessel; disengaging and separating a substantial amount of the remaining spent coked catalyst fines i 1 i 1 I 1 1 i from said quenched product stream in at least one internal cyclone in said dilute phase portion of said disengaging ves'sel; stripping volatile hydrocarbons from said coked catalyst in a stripping section of said disengaging vessel; passing said stripped coked catalyst to a regenerator of said catalytic cracking unit; injecting air into said regenerator; regenerating said spent catalyst by substantially combusting coke on,said spent catalyst in the presence of air in said regenerator; recycling said regenerated catalyst to said riser reactor; separating said cracking oil in a fractionator into streams of light hydrocarbon gases, catalytic naphtha, catalytic cycle oil including light catalytic cycle oil, and decanted oil; and recycling said light catalytic cycle oil from said fractionator to a quench injection line located between said external cyclone and said fluidised bed reactor for use as said quench.
14. 14. steps of: catalytically cracking feed oil in a rector of a catalytic cracking unit in the presence of a cracking catalyst to produce a catalytically cracked effluent stream of upgraded oil containing catalyst; substantially separating said catalyst from said upgraded oil in an internal gross cut separator in a disengaging vessel, said internal gross cut separator comprising an inertia separator selected from the group consisting of an internal cyclone and A catalytic cracking process, comprising the 1 -713 r - an inverted can separator; and quenching said upgraded oil downstream of said internal gross cut separator in said disengaging vessel with a quench comprising at least one member selected from the group consisting of light catalytic cycle oil, heavy catalytic cycle oil, heavy catalytic naphtha, kerosene, coker distillates, light coker"gas oil, hydrotreated distillate, fresh unprocessed virgin gas oil, and fresh unprocessed virgin naphtha, said quench being injected into said stream in an amount raging from about-2% to about 20% by volume per barrel of feed oil.
15. 15. steps of:

    crude oil; A catalytic cracking process, comprising the substantially desalting petroleum comprising heating said desalted crude oil in a furnace; pumping said heated crude oil to a primary distillation tower; separating said heated crude oil in said primary distillation tower into streams of naphtha, primary gas oil, and primary reduced crude; pumping said primary reduced crude oil to a pipestill vacuum tower; separating said primary reduced crude oil in said pipestill vacuum tower into streams of wet gas, heavy gas oil, and vacuum reduced crude oil providing resid oil; conveying a feed oil comprising said primary gas oil from said primary distillation tower to an upright elongated riser reactor of a catalytic cracking unit; feeding fresh and regenerated crystalline i i t i i 1 cracking catalyst to said riser reactor; catalytically cracking said feed oil in said riser reactor in the presence of said cracking catalyst under catalytic cracking conditions to produce an upgraded effluent product stream of catalytically cracked oil containing spent coked catalyst; separating a substantial amount of said spent coked catalyst from said product stream in an internal rough cut separator in the dilute phase portion of a disengaging vessel located downstream of said riser reactor to make a gross separation of said coked catalyst from said product stream; injecting and quenching said product stream soon after said product stream exits said internal separator with-a cycle oil quench for substantially minimising thermal cracking of said product stream to less valuable hydrocarbons and concurrently enhancing the yield of naphtha to substantially increase the production of gasoline, said quench comprising a cycle oil selected from the group consisting of light catalytic cycle oil and heavy catalytic cycle oil, said quench being injected into said product stream in an amount ranging from about 5% to about 15% by volume per barrel of feed oil; disengaging and separating a substantial amount of the remaining spent coked catalyst fines from said quenched product stream in at least one internal cyclone in said dilute faze portion of said disengaging vessel; stripping volatile hydrocarbons from said coked catalyst in a stripping section of said disengaging vessel; passing said stripped coked catalyst to a regenerator of said catalytic cracking unit; -7r is injecting air into said regenerator; regenerating said spent catalyst by substantially combusting coke on said spent catalyst in the presence of air in said regenerator; recycling said regenerated catalyst to said riser reactor; separating said quenched catalytically cracked oil in a fractionator into streams of light hydrocarbon gases, catalytic naphtha, catalytic cycle oil including light catalytic cycle oil, and decanted oil; and recycling said light catalytic cycle oil from said fractionator to said disengaging vessel for use as said quench.
16. 16. A catalytic cracking process in accordance with claims 13 or 15 including feeding some of said resid oil to said riser reactor for use as part of said feed oil and said quench comprises heavy catalytic cycle oil.
17. 17. A catalytic cracking process in accordance with claims 13 or 15 wherein light catalytic cycle oil is injected into said feed oil as at least part of said quench.
18. 18. A catalytic cracking process in accordance with claim 15 wherein: said separating includes impinging said effluent product stream upon exiting said riser reactor against a striker plate of an inverted can separator, discharging said separated catalyst through the open bottom of said inverted can separator, and passing said separated catalytically cracked oil through at least one window comprising a product lb 1 i 1 outlet of said inverted can separator; and said quenching comprises spraying said cycle oil in proximity to said window of said inverted can separator.

    - 20.
19. 19. A catalytical cracking unit comprising: an upright riser reactor for catalytically cracking feed oil in the presence of a cracking catalyst to produce an upgraded effluent product stream of catalytically cracked oil, separating means connected to the riser reactor for separating said product stream from catalyst and having an outlet for catalyst and another outlet for the separated product stream, and means arranged to deliver in to said separated product stream issuing through said other outlet a fluid quench to reduce the temperature of the stream to deter thermal cracking of the catalytically cracked oil.
20. A catalytic cracking unit, comprising: an upright elongated riser reactor for or catalytically cracking feed oil in the presence of a cracking catalyst to produce an upgraded effluent product stream of catalystically cracked oil leaving coked catalyst, said riser reactor having an upper portion and a lower portion; an external rough cut separator connected to and communicating with said upper portion of said riser reactor and being spaced from, positioned about and at a substantially similar elevation as said upper portion of said riser reactor for making a gross separation of said coked catalyst from said catalytically cracked oil; an upright disengaging vessel for substantially disengaging and separating a substantial - '75 - Y is amount of remaining coked catalyst from said catalytically cracked oil, said disengaging vessel having an upper dilute phase zone with at least one internal separator, a lower dense phase zone, and a stripping section providing a stripper; product line extending between and connecting said external separator and said upper diluate phase portion of said vessel; a spent catalyst line extending between and connecting said external separator and said dense phase portion of said disengaging vessel; a regenerator comprising a vessel an upright elongated lift pipe for transporting coked catalyst to regenerator, an air injector communicating with said lift pipe for injecting air and facilitating combustion of said coked catalyst, and a regenerated catalyst line connected to said riser reactor for conveying regenerated catalyst to said riser reactor; and a cycle oil quench injection line connected to and communicating with said input line for injecting a quench comprising cycle oil selected from the group consisting of light catalytic cycle oil and heavy catalytic cycle oil, into said catalytically cracked oil after said catalytically cracked oil has exited said external separator downstream of said riser reactor and has been grossly separated from said catalyst and before said catalytically cracked oil enters said disengaging vessel for enhancing the yield of naphtha and substantially decreasing thermal cracking of said product stream of oil, said cycle oil quench line including a substantial vertical light cycle oil injector for injecting said quench substantially vertically downwardly into said input 1 r, 1 k 7q line or being at an angle of inclination ranging from about.15 degrees to about 45 degrees relative to a vertical reference line for increasing mixing of said quench with said products.
21. 21. -A catalytic cracking unit, comprising:

    an upright elongated riser reactor for catalytically cracking feed oil in the presence of a cracking catalyst to produce an upgraded effluent product stream of catalytically cracked oil leaving coked catalyst, said riser reactor having an upper portion and a lower portion; an upright disengaging vessel communicating with said riser reactor for substantially disengaging and separating a substantial amount of coked catalyst from said catalytically cracked oil, said disengaging vessel having an upper dilute phase zone with at least one internal cyclone, a lower dense phase zone, and a stripping section providing a stripper; an internal gross cut separator positioned in said dilute phase zone of said disengaging vessel for making a gross separation of said coked catalyst from said catalytically cracked oil, said internal gross cut separator defining a vapor port providing an oil outlet and having a lower portion providing a catalyst outlet; a regenerator comprising a vessel, an upright elongated lift pipe for transporting coked catalyst from said disengaging vessel to said regenerator, an air injector communicating with said lift pipe for injecting air and facilitation combustion of said coked catalyst, and a regenerating catalyst line connected to said so - 1 riser reactor for conveying regenerated catalyst to said riser reactor; and at least one cycle oil quench injection line extending into the interior of said disengaging vessel and substantially aligned in registration with said oil outlet of said internal gross cut separator for injecting-a quench comprising cycle oil selected from the group consisting of.light catalytic cycle oil and heaving catalytic cycle oil, into said catalytically cracked oil after said catalytically cracked oil has exited said oil outlet of said internal gross cut separator and has- been grossly separated from said catalyst for substantially enhancing the yield of naphtha and substantially decreasing thermal cracking of said product stream of oil.

    is
22. 22. A catalytic cracking unit in accordance with claim 21 wherein said cycle oil quench line is at an angle of inclination ranging from about 15 degrees to about 90 degrees relative to a vertical reference line extending through said disengager for substantially minimising backflow of said quench.
23. 23. A catalytic cracking unit in accordance with claim 21 wherein said regenerator is located below said disengaging vessel and said catalytic cracking unit includes a substantially horizontal conduit extending between and connecting the top portion of said riser reactor to said internal gross cut cyclone.
24. 24. A catalytic cracking process substantially as herein described.
25. 25. A catalytic cracking unit substantially as herein described with reference to the accompanying drawings.

    Published 1991 at The Patent Office- Concept House. Cardiff Road. Newport. Gwent NP9 I RH. Further copies may be obtained from Sales Branch 1:nit 6_ Nine Mile Point. C%A-mfelinfach. Cross Keys. Newport. NPI 7HZ. Printed by Multiplex techniques lid. St Mary Cray. Kent.

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