CA1291769C - Upgrading diene-containing hydrocarbons - Google Patents
Upgrading diene-containing hydrocarbonsInfo
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Abstract
ABSTRACT
A fluidized bed process for upgrading a diene containing hydrocarbon feed by adding cool feed to relatively hot catalyst.
Preferably an olefinic feed with some C4-C6 diene component is sprayed as a liquid into a fluidized catalyst bed in a lower portion thereof and rapidly atomized and vaporized. The feed is converted to heavier hydrocarbons. Reaction severity preferably is controlled by adjusting catalyst acidity, reactor temperature and/or residence time to produce effluent containing propane:propene in the ratio of 0.2:1 to 200:1. A predominantly liquid product is recovered rich in olefins and/or aromatics.
A fluidized bed process for upgrading a diene containing hydrocarbon feed by adding cool feed to relatively hot catalyst.
Preferably an olefinic feed with some C4-C6 diene component is sprayed as a liquid into a fluidized catalyst bed in a lower portion thereof and rapidly atomized and vaporized. The feed is converted to heavier hydrocarbons. Reaction severity preferably is controlled by adjusting catalyst acidity, reactor temperature and/or residence time to produce effluent containing propane:propene in the ratio of 0.2:1 to 200:1. A predominantly liquid product is recovered rich in olefins and/or aromatics.
Description
917~i9 UPC,RADI~, DIENE-CONTAINI~æ HYD~)CARBONS
This invention relates to a catalytic technique for upgrading olefin streams rich in dienes to heavier hydrocarbons rich in aliphatics and aromatics.
Developments in zeolite catalysis and hydrocarbon conversion processes have created interest in utilizing olefinic feedstocks for produci~g C5 gasoline, diesel fuel, etc. In addition to basic chemical reactions promoted by ZSM-5 type zeolite catalysts, a numbee of discoveries have contributed to the development of new industrial processes. ~hese are safe, environmentally acceptable processes for utilizing feedstocks that contain olefins . Conversion of C2-C4 alkenes and alkanes to produce aromatics-rich liquid hydrocarbon products were found by Cattanach (US 3,760,024) and Yan et al (US 3,845,150) to be effective processes using the ZSM -5 type zeolite catalysts. In U.S. Patents 3,960,978 and 4,021~502, Plank, Rosinski and Givens disclose conversion of C2-C5 olefins, alone or in admixture with paraffinic components, into higher hydrocarbons over crystalline zeolites having controlled acidity. Garwood et al. have also contributed to the understanding of catalytic olefin upqrading techniques and improved processes as in U.S. Patents 4,150,062, 4,211,640 and 4,227,992.
Conversion of olefins, especially propene and butenes, over HZSM-5 is effective at moderately elevated temperatures and pressures. The conversion products are sought as liquid fuels, especially the C5 aliphatic and aromatic hydrocarbons and C4 hydrocarbons, in particular iso-butane. Product distribution for liquid hydrocarbons can be varied by controlling process conditions, such as temperature, pressure and space velocity. Gasoline ~C5-C10) is readily formed at elevated temperature e.g., up to about 700C. and moderate pressure from ambient to about 5500 kPa, preferably about 200 to 2900 kPa. Olefinic gasoline can be produced X.
~91~69 417~+ -2-in good yield and may be recovered as a product or fed to a low severity, high pressure reactor system for further conversion to heavier distillate-range products. Distillate mode operation can be employed to maximize production of Cl0 aliphatics by reacting the lower and intermediate olefins at high pressure and moderate temperature. Operating details for such oligomerization units are disclosed in U.S. Patents 4,456,779; 4,497,968 (~en et al.) and 4,433,185 (Tabak). At moderate temperature and relatively high pressure, the conversion conditions favor distillate-range product having a normal boiling point of at least 165C. (330F.).
Many feedstocks of commercial interest, such as thermal cracking byproduct, etc., contain both mono-olefins and diolefins (e.g. C2-C6 mono-alkenes and C4+ dienes) along with Cl-Cl0 light aliphatics, and a minor amount of aromatics.
Gaseous and liquid streams containing dienes are typically produced in thermal cracking operations. One common example is pyrolysis gasoline, which is produced as ethene (ethylene) byproduct. Such diene-containing streams are often difficult to process due to poor thermal stability and the tendency of dienes to form coke and qum deposits. m is complicates preheating of such streams into the high temperatures required of most catalytic upgrading processes. Prior attempts to upgrade such materials have pretreated the feedstock to hydrogenate the diolefin selectively, as in U.S. Patent No.
4,052,477 (Ireland et al). m e present invention is concerned with providing a safe and low cost technique for catalytically converting diene-rich streams to high value C4+ products It has been found that diene-containing olefinic light hydrocarbons can be upgraded directly to liquid hydrocarbons rich in C5+ aliphatics and aromatics by catalytic _onversion. This technique is particularly useful for upgrading C4+ liquid pyrolysis products, which may contain minor amounts of ethene, propene, C2-C4 paraffins and hydrogen produced in cracking petroleum fractions, such as naphtha, ethane or the like. By upgrading the complex olefinic by-product, gasoline yield and/or ~,91~69 417~+ -3-aromatics production of cracking units can be significantly increased.
Accordingly, the present invention provides a process for upgrading diene-rich liquid olefinic feed comprising at least 1 wt diene and a total C4-C6 olefin content of ahout 5 to 90 wt % to liquid product with a reduced diene content characterized by maintaining a relatively dense phase fluidized bed of zeolite catalyst at 220 to 510C; adding the feed at a temperature lower than the bed temperature into the fluidized bed; and converting a majority of dienes in the feed; and recovering hydrocarbon product containing a major amount of C4+ hydrocarbons and having a C3 to C5 alkane:alkene weight ratio of 0.2:1 to 200:1.
FIG. 1 is a schematic view of a fluidized bed reactor system of the present invention;
FIG. 2 is a vertical cross section view of a liquid-gas feed nozzle which is employed to introduce low temperature diene feed into the feactor bed;
FIG. 3 is an aging plot showing the effect of adding butadiene to a C2-C4 olefinic feed.
FIG. 4 is a schematic view of a fluidized bed reactor and regeneration system of the invention;
FIG. 5 is a process flow sheet for converting olefin feedstock to aromatics-rich product, showing a reactor and effluent separation equipment.
Catalysts Recent developments in zeolite technology have provided a group of medium pore siliceous materials having similar pore geometry. Most prominent among these intermediate pore size zeolites is ZSM-5, which is usually synthesized with Bronsted acid active sites by incorporating a tetrahedrally coordinated metal, such as A1, Ga, B, Fe or mixtures thereof, within the zeolitic framework. m ese medium pore zeolites are favored for acid ~;?..91~
~178+ -4-catalysis; ho~ever, the advantaqes of %SM-5 structures may be utilized by employing highly siliceous materials or cystalline metallosilicate having one or more tetrahedral species havinq varying degrees of acidity. ZSM-5 crystalline structure is readily recognized by its X-ray diffraction pattern, which is described in U.S. Patent No. 3,702,866 (Argauer, et al.).
m e oligomerization catalysts preferred for use herein include the medium pore (i.e., about 5-7A) zeolites having a silica-to-alumina ratio of at least 12, a constraint index of 1 to 12 and acid cracking activity (alpha value) of 10-250, more preferably 10 to ~0 based on total catalyst weight. In the fluidized bed reactor the coked catalyst may have an apparent activity (alpha value) of 10 to 80 under the process conditions to achieve the required degree of reaction severity.
Representative zeolites are ZSM-5, ZSM-ll, ZSM-12, ZSM-22, ZSM-23, ZSM-35, ZSM-38, and ZSM-48. Other suitable zeolites are disclosed in U.S. Patents 3,709,979; 3,832,449; 4,076,979;
3,832,449; 4,076,842; 4,016,245 and 4,046,839; 4,414,423; 4,417,086;
4,517,396 and 4,542,251. While suitable zeolites having a coordinated metal oxide to silica molar ratio of 20:1 to 200:1 or higher may be used, it is advantageous to use ZSM-5 having a silica:alumina molar ratio of about 25:1 to 70:1, suitably modified if desired to adjust acidity and aromatization characteristics.
mese zeolites may be employed in their acid forms, ion exchanged or impregnated with one or more suitable metals, such as Ga, Pd, Zn, Ni, Co and/or other metals of Periodic Groups III to VIII. The zeolite may include a hydrogenation-dehydroqenation component (sometimes eeferred to as a hydrogenation component) which is generally one or more metals of group IB, IIB, IIIB, VA, VIA or VIIIA of the Periodic Table (IUPAC), especially aromatization metals, such as Ga, Pd, etc. Useful hydrogenation components include the noble metals of Group VIIIA, especially platinum, but other noble metals, such as palladium, gold, silver, rhenium or ~ ?.9~7fi9 41~S+ 5 rhodium, may also be used. Rase metal hydrogenation components may also be used, es~eeially nickel, cobalt, molybdenum, tungsten, copper or zinc. The catalyst materials may include two or more catalytic components, such as a metallic oligomerization component (e.g., ionic Ni+2, and a shape-selective medium pore acidic oligomerization catalyst, such as ZSM-5 zeolite) which components may be present in admixture or combined in a unitary bifunctional solid particle. It is possible to utilize an ethene dimerization metal or oligomerization agent to effectively convert feedstock ethene in a continuous reaction zone.
Certain of the ZSM-5 type medium pore shape selective catalysts are sometimes known as pentasils. In addition to the preferred aluminosilicates, the borosilicate, ferrosilicate and "silicalite" materials may be employed.
ZSM-5 type pentasil zeolites are particularly useful in the process because of their regenerability, long life and stability under the extreme conditions of operation. Usually the zeolite crystals have a crystal size from about O.Ol to 2 microns or more.
In order to obtain the desired particle size for fluidization in the turbulent regime, the zeolite catalyst crystals are preferably bound with a suitable inorganic oxide, such as silica, alumina, etc. to provide a zeolite concentration of about 5 to 95 wt. %. It is advantageous to employ ZSM-5 having a silica:alumina molar ratio of 25:1 or greater in a once-through fluidized bed unit to convert 60 to lO0 percent, preferably at least 75 wt ~, of the monoalkenes and dienes in the feedstock. In the description, a 25~ H-ZSM-5 catalyst calcined with 75% silica-alumina matrix binder is employed unless otherwise stated.
~IIlIDIZED BED REP~CTION ZONE
30 It is essential that the diolefin containing feed contact a fluidized bed of catalyst. Fixed catalyst beds will not work in the process of the present invention.
~9~769 4178+ -6-Fluidization is a complex phenomenon. In general terms, suitable fluidized beds include both dense phase beds and dilute phase beds. The lower and uppee limits of fluidization will be discussed.
In an expanded bed, there is enough of an increase in up-flowing gas rate to cause particles to move apart and a few even vibrate and move about in restricted regions. An expanded bed is usually not suitable for use herein.
An ebullating bed represents the lower threshold of fluidization required for use in the present invention. An ebullating bed permits just enough circulation to work. Any gum deposited on the catalyst might deactivate the catalyst near the feed inlet momentarily, but there would be enough gross circulation within the reactor so that incoming feed would see active catalyst.
m e gummed up catalyst could circulate to other portions of the ebullating bed and, in time, the gum components would be cracked and removed, in situ. A portion of the catalyst could also be continuously withdrawn and replaced with fresh or regenerated catalyst.
A conventional dense phase fluidized bed is preferred.
Gas-solid systems in this stage are also called aggregative fluidized beds, a heterogeneously fluidized bed, a bubbling fluidized bed, or simply a gas fluidized bed.
An especially preferred gas-fluidized bed is the turbulent fluidized bed disclosed in US 4,547,616. Such a turbulent fluidized bed is characterized by vigorous solid mixing, and strong interactions between the gas and solid phases.
Dilute phase fluidiæed beds represent an upper limit on fluidization and are also suitable for use herein. This type of 30 fluidized bed is also referred to as a disperse-, dilute-, or lean-phase fluidized bed. Such beds oocur when the superficial vapor velocity in the bed exceeds the terminal velocity of the solids in the bed.
417~+ -7-It is also possible, and may be very beneficial, to combine one or more type of fluidized beds for use in the present invelntion~ Specifically, all or a portion of the feed can be added to a dilute phase riser which discharges into a dense phase bed. In another embodiment liquid feed can be added to a relatively dense phase bed over which is a dilute phase transpoet riser whch discharges into another dense bed of catalyst or into catalyst/product separation means.
In all embodiments, the feed addition means has a low enough temperature/residence time so that plugging of the feed distributor or feed nozzle is avoided, and feed sees an overwhelmin~
amount of hot, active catalyst. Undoubtedly, some dienes form gum on the catalyst, but because the bed is fluidized no plugging of the bed can occur. The very active zeolite catalyst will eventually crack much of the gum, or gum precursor material, to lighter products in the fluidized bed reactor.
Particle size distribution can be a significant factor in fluidization. It is desired to operate the process with particles that will mix well throughout the bed. Larqe particles having a particle size greater than 250 microns should be avoided, and it is advantageous to employ a particle size range consisting essentially of l to 150 microns. Average particle size is usually 20 to lO0 microns, preferably 40 to 80 microns. Particle distribution may be enhanced by having a mixture of larger and smaller particles within the operative range, and it is particularly desirable to have a significant amount of fines. Close control of distribution can be maintained to keep about lO to 25 wt ~ of the total catalyst in the reaction zone in the size range less than 32 microns. This size range of fluidizable particles is classified as Geldart Group A.
m e fluidization regime is preferably controlled to assure operation between the transition velocity and transport velocity, and these fluidization conditions are substantially different from those found in non-turbulent dense beds or transport beds.
~91~9 417~+ -8-In the discussion that follows, percents are by weiqht unless otherwise stated.
Feedstocks - Reaction Conditions Suitable olefinic feedstocks comprise C4-C6 alkenes including conjugated dienes such as 1,3-butadiene, pentadiene isomees, hexadienes, cyclic dienes, or similar C4 aliphatic liquid hydrocarbons having diethylenic conjugated unsaturation.
Aromatics coproduced with the liquid olefinic components may be cofed or sepaeated by solvent extraction prior to conversion of the diene-rich feedstock. Non-deleterious components, such as paraffins and inert gases, may be present. A particularly useful feedstock is a liquid by-product of pyrolysis or thermal cracking units containing typically 40-95 wt ~ C4-C6 total mono-olefins and di-olefins, including about 5-60 wt. % diene, along with varying amounts of C3-C8 paraffins, aromatics and inerts. Specific examples are given in Table 1 below. The process tolerates a wide range of lower alkanes, from 0 to 95%. Preferred pyrolysis feedstocks contain more than 50 wt % C4-C6 lower aliphatic hydrocarbons, and contain sufficient olefins to provide an olefinic partial pressure of at least 50 kPa. ~nder the high severity reaction conditions employed in the present invention, lower alkanes may be partially converted to heavier hydrocarbonds The reaction severity conditions can be controlled to optimize yield of C4-Cg h~drocarbons or of C6-C8 aromatics.
It is understood that aromatics and light paraffin production is promoted by those æeolite catalysts having a high concentration of Bronsted acid reaction sites. Accordingly, an important criterion ` is selecting and maintaining catalyst inventory to provide either fresh or regenerated catalyst having the desired properties.
Typically, acid cracking activity (alpha value) can be maintained from high activity values greater than 100 or 200 to significantly lower values under steady state operation by controlling catalyst X
~J9i7fi9 4178~ ~9~
deactivation and regeneration rates to provide an apparent average alpha value below 100, preferably 10 to 80.
Reaction temperatures and contact time are also significant factors in the reaction severity. The reaction severity index (R.I.) is the weight ratio of propane to propene in reactor effluent. While this index may vary from about 0.2 to 200, it is preferred to operate the steady state fluidized bed unit to hold the R.I. below about 50, with optimum operation at 0.7 to 2 in the substantial absence of added propane. While reaction severity is advantageously determined by the weight ratio of propane:propene in the gaseous phase, it may also be approximated by the analogous ratios of butanes:butenes, pentanes:pentenes, or the average of total reactor effluent alkanes:alkenes in the C3-C5 ranqe.
Accordingly, these alternative expressions may be a more accurate measure of reaction severity conditions when propane is added to the feedstock. m e optimal value will depend upon the exact catalyst composition, feedstock and reaction conditions; however, the typical diene-rich feed mixtures used in the examples herein and additional olefinic feeds can be optimally upgraded to the desired aliphatic-rich gasoline by keeping the R.I. at about 1.
Upgrading of olefins with hydrogen contributors in fluidized bed cracking and oligomerization units is taught by Owen et al in U. S. Patent 4,090,949. This technique is particulatly useful for operation with a pyrolysis cracking unit to increase overall production of liquid product.
m e use of fluidized bed catalysis permits the conversion system to be operated at low pressure drop, which in an economically practical operation can provide a maximum operating pressure only 50 to 200 kPa above atmospheric pressuee. Somewhat higher pressures, up to 2500 kPa may be used to favor aromatics production. Close temperature control is possible by turbulent regime operation. The temperature can be maintained within close tolerances, often less than 5C. Except for a small zone adjacent the bottom gas inlet, ~ ~917~i9 417S~ -10-the midpoint measurement is representative of the entire bed, due to the thorough mixing achieved.
Refereing now to FIG. 1, a reactor vessel 2 is shown provided with heat exchange tube means 4. There may be several separate heat exchange steam generating tube bundles so that temperature control can be separately exercised over the fluid catalyst bed. The bottoms of the tubes are spaced above a feed distributor grid 8 sufficiently to be free of jet action by the charged gas passinq through the small diameter holes in the grid 8.
Although depicted without baffles, the vertical reaction zone can contain open end tubes above the grid for maintaining hydraulic constraints, as disclosed in US Pat. 4,251,484 (Daviduk and Haddad). Optionally, a variety of horizontal baffles may be added to limit axial mixing in the reactor. Heat released from the reaction can be controlled by adjusting feed temperature in a known manner. A large portion of reaction heat can be removed by feedinq cold liquid into the reactor at a temperature below averaqe bed temperature preferably at least 200C below. In the reactor configuration shown the heat exchanger tubes can function to limit mixing in the reactor.
The system provides for withdrawing catalyst from above grid 8 by conduit means 10. This flow line can be provided with control valve means 12 for passage to catalyst regeneration invessel 13, where coked catalyst particles are oxidatively regenerated in contact with air or other regeneration gas at high temperature. The oxidatively regenerated catalyst is then passed to the reactor fluid bed of catalyst by conduit means 14 and flow control valve lfi. The eegenerated catalyst is charged to the catalyst bed sufficiently below the upper interface to achieve good mixing in the fluid bed.
Since the flow of regenerated catalyst passed to the reactor can be relatively small, hot regenerated catalyst does not ordinarily upset the temperature constraints of the reactor operations in a significant amount.
~?~ fi9 417~ -11-Initial fluidization is achieved by forcinq a lift gas upwardly through the catalyst, a light aliphatic C4 gas, with or without diluent or recycle, may be charged through inlet port 20A
at a bottom portion of the reactor in open communication with chamber 24 beneath grid 8. Pressurized feedstock is introduced above reactant distributor grid 8 via supply conduit 21, pump 22 and distributor conduit 23 to one or more spray nozzle means, described and depicted in Fig. 2. The liquid is dispersed into the bed of catalyst thereabove at a velocity sufficient to form a generally upwardly flowing suspension of atomized liquid reactant with the catalyst particles and lift gas.
Advantageously, the liquid diene-containing reactant feed is injected into the catalyst bed by atomizing the pressurized liquid feedstream to form readily dispersible liquid particles having an average size of 300 microns or less. This contributes to rapid vaporization of the liquid at process pressure. ~xothermic conversion provides sufficient heat to vaporize the liquid quickly, thus avoiding deleterious liquid phase reactions of the diene components, which tend to form carbonaceous deposits such as heavy coke, gums, etc.
A plurality of sequentially connected cyclone separator means 30, 32 and 34 provided with diplegs 36, 38 and 40 respectively are positioned in an upper portion of the reactor vessel comprisinq dispersed catalyst phase 28.
The product effluent separated from catalyst particles in the cyclone separating system then passes to a plenum chamber 4~
before withdrawal via conduit 46, operatively connect with effluent separation system 50. The product effluent is cooled and separated to recover C5+ liquid hydrocarbons, gaseous recycle or offgas, along with any byproduct water or catalyst fines carried over.
portion of the light gas effluent fraction may be recycled by compressing to form a motive gas for the liquid feed or via recycle conduit 20B for use as lift gas. The recovered hydrocarbon product comprising C5 olefins and/or ~ aromatics, paraffins and 4178+
naphthenes is thereafter processed as required to provide a desired gasoline or highe~ boiling product.
Referring now to Fig. 4, in which maximum BTX production is sought, liquid feedstock is passed at high pressure via feed conduit 401 for injection into vertical reactor vessel 41~ above a feed distributor grid 412, which provides for distribution of a lift gas passing via conduit 414 throu~h the small diameter holes in the grid 412. Fluidization is effected in the bottom portion of the bed by upwardly flowin~ lift gas introduced via conduit 414. Although depicted without baffles, the vertical reaction zone can contain open end tubes above the grid for maintaining hydraulic constraints, as in US Pat. 4,251,484. Optionally, a variety of horizontal baffles may be added to limit axial mixing in the reactor.
m e~modynamic conditions in the reaction vessel can be controlled by adjusting feed tei~perature, catalyst temperature and rate, or by heat exchange means 16. In the reactor configuration shown the heat exchanger tubes limit mixing in the reactor.
Provision is made for withdeawing catalyst from above grid 412 by conduit means 417 pfovided with flow control valve means to control passage via air lift line 418 to the catalyst regeneration system in vessel 420 where coked catalyst particles are oxidatively regenerated in contact with aif o~ other regeneration gas at high tempeeature. In order to add sufficient heat to the catalytic reaction zone 410, eneegy may be added by combustion of flue gas or othe~ fuel steeam in the regenerator Regenerated catalyst is retufned to the reactor fluid bed 410 through conduit means 422 peovided with flow contfol valve means. The hot regenerated catalyst is charged to the catalyst bed sufficiently below the upper nterface to achieve good mixing in the fluid bed. The rate of flow for eegeneeated catalyst may be adjusted to provide the degree of theemal input fequied fof effecting endothermic conversion, and the fate will depend upon the amount and composition of the alkane components : ::
: ~ :
, ~,91~9 4178~ -13-Initial fluidization is achieved by forcing a lift qas upwardly through the catalyst. A light gas, with or without diluent or recycle, may be charged at a bottom portion of the reaCtQr beneath grid 412. Pressurized liquid feedstock is introduced above reactant distrihutor grid 412, and pumped to one or re spray nozzle means. The liquid is dispersed into the bed of catalyst thereabove at a velocity sufficient to form a generally upwardly flowing suspension of atomized liquid reactant with the catalyst particles and lift gas.
Cyclone separator means may be positioned in an upper portion of the reactor vessel. m e product effluent separated from catalyst particles in the cyclone separatinq system then passes to effluent separation system 430. The product effluent is cooled and separated to recover C5+ liquid hydrocarbons, gaseous recycle or offgas, along with any byproduct water or catalyst fines carried over. A portion of the light gas effluent fraction may be recycled by compressing to form a motive gas for the liquid feed or recycle for use as lift gas. The recovered hydrocarbon product comprising C5 olefins and/or aromatics, paraffins and naphthenes is thereafter processed as described hereafter to provide a desired aromatic product.
In Fig. 5, directed to maximum recovery of BTX, the feedstock stream 501 is injected into reactor vessel 510 containing the fluidized bed of catalyst, along with fluidizing gas stream 514 and recycle streams 516, 518. Reactor effluent is cooled in heat exchanger 520 and partially separated in a series of phase separation drums, HTS 522 (high temperatuee separator) and LTS 524 (low temperature separator). A light gas stream may be recovered from LTS 524, pressurized in compressor 528, and recycled via conduit 5I4 to comprise at least a portion of the lift gas.
Condensed liquid from the separators 522, 5~4 is fed to a debutanizer tower 530, along with a portion of the I.TS overhead vapor. Debutanizer overhead vapor is further fractionated by deethanizer tower 532 from which offgas stream 534 is recovered.
. . ~ ~, .,, i ~.917fi9 417~ 14-m is liqht hydrocarbon stream may be employed as fuel gas in the regenerator vessel. Deethanizer liquid bottoms, rich in C3-C4 LPG
alkanes, may be recovered via line 536 as product or recycled for further conversion via conduit 518 to reactor 510. m e C5+ liquid from the debutanizer 530 is passed to a liquid-liquid extraction unit 540 for recovery of the aromatics components with a selective solvent, such as sulfolane, etc. Following fractionation of the solvent phase, an aromatics product stream 542 is recovered, containing at least 50~ BTX. The C5~ aliphatics components may be recovered as a product gasoline stream; however, it is advantageous to recycle this stream for further conversion to increase the net aromatic product.
Under optimized process conditions the turbulent bed has a superficial vapor velocity of about 0.3 to 2 meters per second (m/sec). At hi~her velocities entrainment of fine particles may become excessive and beyond lO m/sec the entire bed may be transported out of the reaction zone. At lower velocities, the formation of large bubbles or gas voids can be detrimental to conversion. Fven fine particles cannot be maintained effectively in a turbulent bed below about 0.1 m/sec.
A convenient measure of turbulent fluidization is the bed density. A typical turbulent bed has an operating density of about 100 to 500 kg/m3, preferrably 300 to 500, measured at the bottom of the reaction zone, becoming less dense toward the top of the reaction zone due to pressure drop and particle size differentiation. m is density is generally between the catalyst concentration employed in dense beds and the dispersed transport systems. Pressure differential between two vertically spaced points in the reactor column can be measured to obtain the average bed density at such portion of the reaction zone. For instance, in a fluidized bed system employing ZSM-5 particles having a clean apparent density of 1.06 gm/cc and packed density of 0.85, an average fluidized bed density of about 300 to 500 kg/m3 is satisfactory.
~?~91~
4178+ -15-By virtue of the turbulence experienced in the turbulent regime, gas-solid contact in the catalytic reactor is improvedr providing substantially complete conversion, enhanced selectivity and temperature uniformity. One main advantage of this technique is the inherent control of bubble size and characteristic bubble lifetime. Bubbles of the gaseous reaction mixture are small, random and short-lived, thus resulting in goo~ contact between the gaseous reactants and the solid catalyst particles.
A significant difference between the process of this invention and conversion processes of the prior art is that operation in the turbulent fluidization regime is optimized to produce high octane C5 liquid in ~ood yield. The weight hourly space velocity and uniform contact provides a clo~se control of contact time between vapor and solid phases, typically about 3 to 25 seconds. Another advantage of operating in such a mode is the control of bubble size and life span, thus avoiding large scale gas by-passing in the reactor. The process of the present invention does not rely on internal baffles in the reactor for the purpose of bubble size control such as the baffles which are employed in the prior art dense bed processes discussed above.
As the superficial gas velocity is increased in the dense bed, eventually slugging conditions occur and with a further increase in the superficial gas velocity the slug flow breaks down into a turbulent fegime. The transition velocity at which this turbulent regime occurs appears to decrease with particle size. The turbulent regime extends from the transition velocity to the so-called transport velocity, as described by Avidan et al in U.S.
Patent 4,547,616 and by Tabak et al. in U.S. Patent 4,579,999. As the transport velocity is approached, there is a sharp increase in the rate of particle carryover, and in the absence of solid recycle, the bed could empty quickly.
Several useful parameters contribute to fluidization in the turbulent regime in accordance with the process of the present invention. When ~mploying a ZSM-5 type zeolite catalyst in fine X
417S~ ~,9~9 powder form such a catalyst should comprise the zeolite suitably bound or impregnated on a suitable support with a solid density (weight of a representative individual particle divided by its apparent "outside" volume) in the range from 0.6-2 g/cc, preferably 0.9-1.6 g/cc. The catalyst particles can be in a wide range of particle sizes up to about 250 microns, with an average particle size between about 20 and 100 microns, preferably in the range of 10-150 microns and with the average particle size between 40 and 80 microns. When these solid particles are placed in a fluidized bed where the superficial fluid velocity is 0.3-2 m/s, operation in the turbulent regime is obtained. The velocity specified here is for an operation at a total reactor pressure of about 100 to 300 kPa.
Those skilled in the art will appreciate that at higher pressures, a lower gas velocity may be employed to ensure operation in the turbulent fluidization regime.
The reactor can assume any technically feasible configuration, but several important criteria should be considered.
The bed of catalyst in the reactor can be at least about 5-20 meters in height, preferably about 7 meters. Fine particles may be included in the bed, especially due to attrition, and the fines may be entrained in the product gas stream. A typical turbulent bed may have a catalyst carryover rate up to about 1.5 times the reaction zone inventory per hour. If the fraction of fines becomes larqe, a poetion of the carryover can be eemoved from the system and replaced by larger particl~es. It is feasible to have a fine particle separator, such as a cyclone disposed within the reactor shell to recover catalyst carryover and return this fraction continuously to the bottom of the reaction zone for recirculation at a rate of about one catalyst inventory per hour. Optionally, fine Particles carried from the reactor vessel entrained with effluent gas can be recovered by a high operating temperature sintered metal filter.
This process can be used with any process stream which contains sufficient liquid olefins and dienes. Preferably the feed is substantially free of deleterious oxygenates and sulfur X
~?.9~7~.~
4178+ -17-compounds. Because the catalyst can be readily removed and regellerated, or replaced, the process can tolerate a lot of impurities in the feed. Experimental runs are performed using a ZSM-5 catalyst to demonstrate the inventive process. The fluidized bed unit can be operated over a wide range of process variables and catalyst activity.
Reactoe Operation A typical single pass reactor unit employs a temperature-controlled catalyst zone with indirect heat exchange and/or adjustable gas quench, whereby the reaction exotherm can be carefully controlled to prevent excessive temperature above the usual operating range of about 315C to 650C. Preferably average reactor temperature is 340C to 430C to maximize production of gasoline boiling range hydrocarbons. Temperatures of 425-580C
maximize production of aromatics. Heat exchanging hot reactor effluent with feedstock and/or recycle streams will save energy.
Gptional heat exchangers may recover heat from the effluent stream prior to fractionation. It is preferred to operate the olefin conversion reactors at moderate pressure of about 100 to 3000 kPa (atmospheric to about 400 psig) to maximize liquid yields. Higher pressures, to 6000 kPa, favoe aromatics yields.
The weight hourly space velocity (WH5V, based on total olefins in the fresh feedstock is about 0.l-5 WHSV. Typical product fractionation systems are desceibed in U.S. Patents 4,456,779 and 4,504,693 (Cwen, et al.~.
To prevent premature non-catalytic reaction of the dienes, it is desirable to maintain reactant li~uid feedstream temperatu~e below about 180C (350F) until injection into the fluidized bed.
Appropriate thermal insulation or quenching of the feedstream to the injection point can laegely prevent gum and coke formation in the liquid phase prior to catalysis.
, .. .. .
~?.917fi~
4178+ -18-~ tomization of the pressurized liquid reactant feedstream can be achieved by known techniques, such as liquid speay nozzles, motive gas, ultra sonics, etc. A suitable nozzle is shown in Fig.
This invention relates to a catalytic technique for upgrading olefin streams rich in dienes to heavier hydrocarbons rich in aliphatics and aromatics.
Developments in zeolite catalysis and hydrocarbon conversion processes have created interest in utilizing olefinic feedstocks for produci~g C5 gasoline, diesel fuel, etc. In addition to basic chemical reactions promoted by ZSM-5 type zeolite catalysts, a numbee of discoveries have contributed to the development of new industrial processes. ~hese are safe, environmentally acceptable processes for utilizing feedstocks that contain olefins . Conversion of C2-C4 alkenes and alkanes to produce aromatics-rich liquid hydrocarbon products were found by Cattanach (US 3,760,024) and Yan et al (US 3,845,150) to be effective processes using the ZSM -5 type zeolite catalysts. In U.S. Patents 3,960,978 and 4,021~502, Plank, Rosinski and Givens disclose conversion of C2-C5 olefins, alone or in admixture with paraffinic components, into higher hydrocarbons over crystalline zeolites having controlled acidity. Garwood et al. have also contributed to the understanding of catalytic olefin upqrading techniques and improved processes as in U.S. Patents 4,150,062, 4,211,640 and 4,227,992.
Conversion of olefins, especially propene and butenes, over HZSM-5 is effective at moderately elevated temperatures and pressures. The conversion products are sought as liquid fuels, especially the C5 aliphatic and aromatic hydrocarbons and C4 hydrocarbons, in particular iso-butane. Product distribution for liquid hydrocarbons can be varied by controlling process conditions, such as temperature, pressure and space velocity. Gasoline ~C5-C10) is readily formed at elevated temperature e.g., up to about 700C. and moderate pressure from ambient to about 5500 kPa, preferably about 200 to 2900 kPa. Olefinic gasoline can be produced X.
~91~69 417~+ -2-in good yield and may be recovered as a product or fed to a low severity, high pressure reactor system for further conversion to heavier distillate-range products. Distillate mode operation can be employed to maximize production of Cl0 aliphatics by reacting the lower and intermediate olefins at high pressure and moderate temperature. Operating details for such oligomerization units are disclosed in U.S. Patents 4,456,779; 4,497,968 (~en et al.) and 4,433,185 (Tabak). At moderate temperature and relatively high pressure, the conversion conditions favor distillate-range product having a normal boiling point of at least 165C. (330F.).
Many feedstocks of commercial interest, such as thermal cracking byproduct, etc., contain both mono-olefins and diolefins (e.g. C2-C6 mono-alkenes and C4+ dienes) along with Cl-Cl0 light aliphatics, and a minor amount of aromatics.
Gaseous and liquid streams containing dienes are typically produced in thermal cracking operations. One common example is pyrolysis gasoline, which is produced as ethene (ethylene) byproduct. Such diene-containing streams are often difficult to process due to poor thermal stability and the tendency of dienes to form coke and qum deposits. m is complicates preheating of such streams into the high temperatures required of most catalytic upgrading processes. Prior attempts to upgrade such materials have pretreated the feedstock to hydrogenate the diolefin selectively, as in U.S. Patent No.
4,052,477 (Ireland et al). m e present invention is concerned with providing a safe and low cost technique for catalytically converting diene-rich streams to high value C4+ products It has been found that diene-containing olefinic light hydrocarbons can be upgraded directly to liquid hydrocarbons rich in C5+ aliphatics and aromatics by catalytic _onversion. This technique is particularly useful for upgrading C4+ liquid pyrolysis products, which may contain minor amounts of ethene, propene, C2-C4 paraffins and hydrogen produced in cracking petroleum fractions, such as naphtha, ethane or the like. By upgrading the complex olefinic by-product, gasoline yield and/or ~,91~69 417~+ -3-aromatics production of cracking units can be significantly increased.
Accordingly, the present invention provides a process for upgrading diene-rich liquid olefinic feed comprising at least 1 wt diene and a total C4-C6 olefin content of ahout 5 to 90 wt % to liquid product with a reduced diene content characterized by maintaining a relatively dense phase fluidized bed of zeolite catalyst at 220 to 510C; adding the feed at a temperature lower than the bed temperature into the fluidized bed; and converting a majority of dienes in the feed; and recovering hydrocarbon product containing a major amount of C4+ hydrocarbons and having a C3 to C5 alkane:alkene weight ratio of 0.2:1 to 200:1.
FIG. 1 is a schematic view of a fluidized bed reactor system of the present invention;
FIG. 2 is a vertical cross section view of a liquid-gas feed nozzle which is employed to introduce low temperature diene feed into the feactor bed;
FIG. 3 is an aging plot showing the effect of adding butadiene to a C2-C4 olefinic feed.
FIG. 4 is a schematic view of a fluidized bed reactor and regeneration system of the invention;
FIG. 5 is a process flow sheet for converting olefin feedstock to aromatics-rich product, showing a reactor and effluent separation equipment.
Catalysts Recent developments in zeolite technology have provided a group of medium pore siliceous materials having similar pore geometry. Most prominent among these intermediate pore size zeolites is ZSM-5, which is usually synthesized with Bronsted acid active sites by incorporating a tetrahedrally coordinated metal, such as A1, Ga, B, Fe or mixtures thereof, within the zeolitic framework. m ese medium pore zeolites are favored for acid ~;?..91~
~178+ -4-catalysis; ho~ever, the advantaqes of %SM-5 structures may be utilized by employing highly siliceous materials or cystalline metallosilicate having one or more tetrahedral species havinq varying degrees of acidity. ZSM-5 crystalline structure is readily recognized by its X-ray diffraction pattern, which is described in U.S. Patent No. 3,702,866 (Argauer, et al.).
m e oligomerization catalysts preferred for use herein include the medium pore (i.e., about 5-7A) zeolites having a silica-to-alumina ratio of at least 12, a constraint index of 1 to 12 and acid cracking activity (alpha value) of 10-250, more preferably 10 to ~0 based on total catalyst weight. In the fluidized bed reactor the coked catalyst may have an apparent activity (alpha value) of 10 to 80 under the process conditions to achieve the required degree of reaction severity.
Representative zeolites are ZSM-5, ZSM-ll, ZSM-12, ZSM-22, ZSM-23, ZSM-35, ZSM-38, and ZSM-48. Other suitable zeolites are disclosed in U.S. Patents 3,709,979; 3,832,449; 4,076,979;
3,832,449; 4,076,842; 4,016,245 and 4,046,839; 4,414,423; 4,417,086;
4,517,396 and 4,542,251. While suitable zeolites having a coordinated metal oxide to silica molar ratio of 20:1 to 200:1 or higher may be used, it is advantageous to use ZSM-5 having a silica:alumina molar ratio of about 25:1 to 70:1, suitably modified if desired to adjust acidity and aromatization characteristics.
mese zeolites may be employed in their acid forms, ion exchanged or impregnated with one or more suitable metals, such as Ga, Pd, Zn, Ni, Co and/or other metals of Periodic Groups III to VIII. The zeolite may include a hydrogenation-dehydroqenation component (sometimes eeferred to as a hydrogenation component) which is generally one or more metals of group IB, IIB, IIIB, VA, VIA or VIIIA of the Periodic Table (IUPAC), especially aromatization metals, such as Ga, Pd, etc. Useful hydrogenation components include the noble metals of Group VIIIA, especially platinum, but other noble metals, such as palladium, gold, silver, rhenium or ~ ?.9~7fi9 41~S+ 5 rhodium, may also be used. Rase metal hydrogenation components may also be used, es~eeially nickel, cobalt, molybdenum, tungsten, copper or zinc. The catalyst materials may include two or more catalytic components, such as a metallic oligomerization component (e.g., ionic Ni+2, and a shape-selective medium pore acidic oligomerization catalyst, such as ZSM-5 zeolite) which components may be present in admixture or combined in a unitary bifunctional solid particle. It is possible to utilize an ethene dimerization metal or oligomerization agent to effectively convert feedstock ethene in a continuous reaction zone.
Certain of the ZSM-5 type medium pore shape selective catalysts are sometimes known as pentasils. In addition to the preferred aluminosilicates, the borosilicate, ferrosilicate and "silicalite" materials may be employed.
ZSM-5 type pentasil zeolites are particularly useful in the process because of their regenerability, long life and stability under the extreme conditions of operation. Usually the zeolite crystals have a crystal size from about O.Ol to 2 microns or more.
In order to obtain the desired particle size for fluidization in the turbulent regime, the zeolite catalyst crystals are preferably bound with a suitable inorganic oxide, such as silica, alumina, etc. to provide a zeolite concentration of about 5 to 95 wt. %. It is advantageous to employ ZSM-5 having a silica:alumina molar ratio of 25:1 or greater in a once-through fluidized bed unit to convert 60 to lO0 percent, preferably at least 75 wt ~, of the monoalkenes and dienes in the feedstock. In the description, a 25~ H-ZSM-5 catalyst calcined with 75% silica-alumina matrix binder is employed unless otherwise stated.
~IIlIDIZED BED REP~CTION ZONE
30 It is essential that the diolefin containing feed contact a fluidized bed of catalyst. Fixed catalyst beds will not work in the process of the present invention.
~9~769 4178+ -6-Fluidization is a complex phenomenon. In general terms, suitable fluidized beds include both dense phase beds and dilute phase beds. The lower and uppee limits of fluidization will be discussed.
In an expanded bed, there is enough of an increase in up-flowing gas rate to cause particles to move apart and a few even vibrate and move about in restricted regions. An expanded bed is usually not suitable for use herein.
An ebullating bed represents the lower threshold of fluidization required for use in the present invention. An ebullating bed permits just enough circulation to work. Any gum deposited on the catalyst might deactivate the catalyst near the feed inlet momentarily, but there would be enough gross circulation within the reactor so that incoming feed would see active catalyst.
m e gummed up catalyst could circulate to other portions of the ebullating bed and, in time, the gum components would be cracked and removed, in situ. A portion of the catalyst could also be continuously withdrawn and replaced with fresh or regenerated catalyst.
A conventional dense phase fluidized bed is preferred.
Gas-solid systems in this stage are also called aggregative fluidized beds, a heterogeneously fluidized bed, a bubbling fluidized bed, or simply a gas fluidized bed.
An especially preferred gas-fluidized bed is the turbulent fluidized bed disclosed in US 4,547,616. Such a turbulent fluidized bed is characterized by vigorous solid mixing, and strong interactions between the gas and solid phases.
Dilute phase fluidiæed beds represent an upper limit on fluidization and are also suitable for use herein. This type of 30 fluidized bed is also referred to as a disperse-, dilute-, or lean-phase fluidized bed. Such beds oocur when the superficial vapor velocity in the bed exceeds the terminal velocity of the solids in the bed.
417~+ -7-It is also possible, and may be very beneficial, to combine one or more type of fluidized beds for use in the present invelntion~ Specifically, all or a portion of the feed can be added to a dilute phase riser which discharges into a dense phase bed. In another embodiment liquid feed can be added to a relatively dense phase bed over which is a dilute phase transpoet riser whch discharges into another dense bed of catalyst or into catalyst/product separation means.
In all embodiments, the feed addition means has a low enough temperature/residence time so that plugging of the feed distributor or feed nozzle is avoided, and feed sees an overwhelmin~
amount of hot, active catalyst. Undoubtedly, some dienes form gum on the catalyst, but because the bed is fluidized no plugging of the bed can occur. The very active zeolite catalyst will eventually crack much of the gum, or gum precursor material, to lighter products in the fluidized bed reactor.
Particle size distribution can be a significant factor in fluidization. It is desired to operate the process with particles that will mix well throughout the bed. Larqe particles having a particle size greater than 250 microns should be avoided, and it is advantageous to employ a particle size range consisting essentially of l to 150 microns. Average particle size is usually 20 to lO0 microns, preferably 40 to 80 microns. Particle distribution may be enhanced by having a mixture of larger and smaller particles within the operative range, and it is particularly desirable to have a significant amount of fines. Close control of distribution can be maintained to keep about lO to 25 wt ~ of the total catalyst in the reaction zone in the size range less than 32 microns. This size range of fluidizable particles is classified as Geldart Group A.
m e fluidization regime is preferably controlled to assure operation between the transition velocity and transport velocity, and these fluidization conditions are substantially different from those found in non-turbulent dense beds or transport beds.
~91~9 417~+ -8-In the discussion that follows, percents are by weiqht unless otherwise stated.
Feedstocks - Reaction Conditions Suitable olefinic feedstocks comprise C4-C6 alkenes including conjugated dienes such as 1,3-butadiene, pentadiene isomees, hexadienes, cyclic dienes, or similar C4 aliphatic liquid hydrocarbons having diethylenic conjugated unsaturation.
Aromatics coproduced with the liquid olefinic components may be cofed or sepaeated by solvent extraction prior to conversion of the diene-rich feedstock. Non-deleterious components, such as paraffins and inert gases, may be present. A particularly useful feedstock is a liquid by-product of pyrolysis or thermal cracking units containing typically 40-95 wt ~ C4-C6 total mono-olefins and di-olefins, including about 5-60 wt. % diene, along with varying amounts of C3-C8 paraffins, aromatics and inerts. Specific examples are given in Table 1 below. The process tolerates a wide range of lower alkanes, from 0 to 95%. Preferred pyrolysis feedstocks contain more than 50 wt % C4-C6 lower aliphatic hydrocarbons, and contain sufficient olefins to provide an olefinic partial pressure of at least 50 kPa. ~nder the high severity reaction conditions employed in the present invention, lower alkanes may be partially converted to heavier hydrocarbonds The reaction severity conditions can be controlled to optimize yield of C4-Cg h~drocarbons or of C6-C8 aromatics.
It is understood that aromatics and light paraffin production is promoted by those æeolite catalysts having a high concentration of Bronsted acid reaction sites. Accordingly, an important criterion ` is selecting and maintaining catalyst inventory to provide either fresh or regenerated catalyst having the desired properties.
Typically, acid cracking activity (alpha value) can be maintained from high activity values greater than 100 or 200 to significantly lower values under steady state operation by controlling catalyst X
~J9i7fi9 4178~ ~9~
deactivation and regeneration rates to provide an apparent average alpha value below 100, preferably 10 to 80.
Reaction temperatures and contact time are also significant factors in the reaction severity. The reaction severity index (R.I.) is the weight ratio of propane to propene in reactor effluent. While this index may vary from about 0.2 to 200, it is preferred to operate the steady state fluidized bed unit to hold the R.I. below about 50, with optimum operation at 0.7 to 2 in the substantial absence of added propane. While reaction severity is advantageously determined by the weight ratio of propane:propene in the gaseous phase, it may also be approximated by the analogous ratios of butanes:butenes, pentanes:pentenes, or the average of total reactor effluent alkanes:alkenes in the C3-C5 ranqe.
Accordingly, these alternative expressions may be a more accurate measure of reaction severity conditions when propane is added to the feedstock. m e optimal value will depend upon the exact catalyst composition, feedstock and reaction conditions; however, the typical diene-rich feed mixtures used in the examples herein and additional olefinic feeds can be optimally upgraded to the desired aliphatic-rich gasoline by keeping the R.I. at about 1.
Upgrading of olefins with hydrogen contributors in fluidized bed cracking and oligomerization units is taught by Owen et al in U. S. Patent 4,090,949. This technique is particulatly useful for operation with a pyrolysis cracking unit to increase overall production of liquid product.
m e use of fluidized bed catalysis permits the conversion system to be operated at low pressure drop, which in an economically practical operation can provide a maximum operating pressure only 50 to 200 kPa above atmospheric pressuee. Somewhat higher pressures, up to 2500 kPa may be used to favor aromatics production. Close temperature control is possible by turbulent regime operation. The temperature can be maintained within close tolerances, often less than 5C. Except for a small zone adjacent the bottom gas inlet, ~ ~917~i9 417S~ -10-the midpoint measurement is representative of the entire bed, due to the thorough mixing achieved.
Refereing now to FIG. 1, a reactor vessel 2 is shown provided with heat exchange tube means 4. There may be several separate heat exchange steam generating tube bundles so that temperature control can be separately exercised over the fluid catalyst bed. The bottoms of the tubes are spaced above a feed distributor grid 8 sufficiently to be free of jet action by the charged gas passinq through the small diameter holes in the grid 8.
Although depicted without baffles, the vertical reaction zone can contain open end tubes above the grid for maintaining hydraulic constraints, as disclosed in US Pat. 4,251,484 (Daviduk and Haddad). Optionally, a variety of horizontal baffles may be added to limit axial mixing in the reactor. Heat released from the reaction can be controlled by adjusting feed temperature in a known manner. A large portion of reaction heat can be removed by feedinq cold liquid into the reactor at a temperature below averaqe bed temperature preferably at least 200C below. In the reactor configuration shown the heat exchanger tubes can function to limit mixing in the reactor.
The system provides for withdrawing catalyst from above grid 8 by conduit means 10. This flow line can be provided with control valve means 12 for passage to catalyst regeneration invessel 13, where coked catalyst particles are oxidatively regenerated in contact with air or other regeneration gas at high temperature. The oxidatively regenerated catalyst is then passed to the reactor fluid bed of catalyst by conduit means 14 and flow control valve lfi. The eegenerated catalyst is charged to the catalyst bed sufficiently below the upper interface to achieve good mixing in the fluid bed.
Since the flow of regenerated catalyst passed to the reactor can be relatively small, hot regenerated catalyst does not ordinarily upset the temperature constraints of the reactor operations in a significant amount.
~?~ fi9 417~ -11-Initial fluidization is achieved by forcinq a lift gas upwardly through the catalyst, a light aliphatic C4 gas, with or without diluent or recycle, may be charged through inlet port 20A
at a bottom portion of the reactor in open communication with chamber 24 beneath grid 8. Pressurized feedstock is introduced above reactant distributor grid 8 via supply conduit 21, pump 22 and distributor conduit 23 to one or more spray nozzle means, described and depicted in Fig. 2. The liquid is dispersed into the bed of catalyst thereabove at a velocity sufficient to form a generally upwardly flowing suspension of atomized liquid reactant with the catalyst particles and lift gas.
Advantageously, the liquid diene-containing reactant feed is injected into the catalyst bed by atomizing the pressurized liquid feedstream to form readily dispersible liquid particles having an average size of 300 microns or less. This contributes to rapid vaporization of the liquid at process pressure. ~xothermic conversion provides sufficient heat to vaporize the liquid quickly, thus avoiding deleterious liquid phase reactions of the diene components, which tend to form carbonaceous deposits such as heavy coke, gums, etc.
A plurality of sequentially connected cyclone separator means 30, 32 and 34 provided with diplegs 36, 38 and 40 respectively are positioned in an upper portion of the reactor vessel comprisinq dispersed catalyst phase 28.
The product effluent separated from catalyst particles in the cyclone separating system then passes to a plenum chamber 4~
before withdrawal via conduit 46, operatively connect with effluent separation system 50. The product effluent is cooled and separated to recover C5+ liquid hydrocarbons, gaseous recycle or offgas, along with any byproduct water or catalyst fines carried over.
portion of the light gas effluent fraction may be recycled by compressing to form a motive gas for the liquid feed or via recycle conduit 20B for use as lift gas. The recovered hydrocarbon product comprising C5 olefins and/or ~ aromatics, paraffins and 4178+
naphthenes is thereafter processed as required to provide a desired gasoline or highe~ boiling product.
Referring now to Fig. 4, in which maximum BTX production is sought, liquid feedstock is passed at high pressure via feed conduit 401 for injection into vertical reactor vessel 41~ above a feed distributor grid 412, which provides for distribution of a lift gas passing via conduit 414 throu~h the small diameter holes in the grid 412. Fluidization is effected in the bottom portion of the bed by upwardly flowin~ lift gas introduced via conduit 414. Although depicted without baffles, the vertical reaction zone can contain open end tubes above the grid for maintaining hydraulic constraints, as in US Pat. 4,251,484. Optionally, a variety of horizontal baffles may be added to limit axial mixing in the reactor.
m e~modynamic conditions in the reaction vessel can be controlled by adjusting feed tei~perature, catalyst temperature and rate, or by heat exchange means 16. In the reactor configuration shown the heat exchanger tubes limit mixing in the reactor.
Provision is made for withdeawing catalyst from above grid 412 by conduit means 417 pfovided with flow control valve means to control passage via air lift line 418 to the catalyst regeneration system in vessel 420 where coked catalyst particles are oxidatively regenerated in contact with aif o~ other regeneration gas at high tempeeature. In order to add sufficient heat to the catalytic reaction zone 410, eneegy may be added by combustion of flue gas or othe~ fuel steeam in the regenerator Regenerated catalyst is retufned to the reactor fluid bed 410 through conduit means 422 peovided with flow contfol valve means. The hot regenerated catalyst is charged to the catalyst bed sufficiently below the upper nterface to achieve good mixing in the fluid bed. The rate of flow for eegeneeated catalyst may be adjusted to provide the degree of theemal input fequied fof effecting endothermic conversion, and the fate will depend upon the amount and composition of the alkane components : ::
: ~ :
, ~,91~9 4178~ -13-Initial fluidization is achieved by forcing a lift qas upwardly through the catalyst. A light gas, with or without diluent or recycle, may be charged at a bottom portion of the reaCtQr beneath grid 412. Pressurized liquid feedstock is introduced above reactant distrihutor grid 412, and pumped to one or re spray nozzle means. The liquid is dispersed into the bed of catalyst thereabove at a velocity sufficient to form a generally upwardly flowing suspension of atomized liquid reactant with the catalyst particles and lift gas.
Cyclone separator means may be positioned in an upper portion of the reactor vessel. m e product effluent separated from catalyst particles in the cyclone separatinq system then passes to effluent separation system 430. The product effluent is cooled and separated to recover C5+ liquid hydrocarbons, gaseous recycle or offgas, along with any byproduct water or catalyst fines carried over. A portion of the light gas effluent fraction may be recycled by compressing to form a motive gas for the liquid feed or recycle for use as lift gas. The recovered hydrocarbon product comprising C5 olefins and/or aromatics, paraffins and naphthenes is thereafter processed as described hereafter to provide a desired aromatic product.
In Fig. 5, directed to maximum recovery of BTX, the feedstock stream 501 is injected into reactor vessel 510 containing the fluidized bed of catalyst, along with fluidizing gas stream 514 and recycle streams 516, 518. Reactor effluent is cooled in heat exchanger 520 and partially separated in a series of phase separation drums, HTS 522 (high temperatuee separator) and LTS 524 (low temperature separator). A light gas stream may be recovered from LTS 524, pressurized in compressor 528, and recycled via conduit 5I4 to comprise at least a portion of the lift gas.
Condensed liquid from the separators 522, 5~4 is fed to a debutanizer tower 530, along with a portion of the I.TS overhead vapor. Debutanizer overhead vapor is further fractionated by deethanizer tower 532 from which offgas stream 534 is recovered.
. . ~ ~, .,, i ~.917fi9 417~ 14-m is liqht hydrocarbon stream may be employed as fuel gas in the regenerator vessel. Deethanizer liquid bottoms, rich in C3-C4 LPG
alkanes, may be recovered via line 536 as product or recycled for further conversion via conduit 518 to reactor 510. m e C5+ liquid from the debutanizer 530 is passed to a liquid-liquid extraction unit 540 for recovery of the aromatics components with a selective solvent, such as sulfolane, etc. Following fractionation of the solvent phase, an aromatics product stream 542 is recovered, containing at least 50~ BTX. The C5~ aliphatics components may be recovered as a product gasoline stream; however, it is advantageous to recycle this stream for further conversion to increase the net aromatic product.
Under optimized process conditions the turbulent bed has a superficial vapor velocity of about 0.3 to 2 meters per second (m/sec). At hi~her velocities entrainment of fine particles may become excessive and beyond lO m/sec the entire bed may be transported out of the reaction zone. At lower velocities, the formation of large bubbles or gas voids can be detrimental to conversion. Fven fine particles cannot be maintained effectively in a turbulent bed below about 0.1 m/sec.
A convenient measure of turbulent fluidization is the bed density. A typical turbulent bed has an operating density of about 100 to 500 kg/m3, preferrably 300 to 500, measured at the bottom of the reaction zone, becoming less dense toward the top of the reaction zone due to pressure drop and particle size differentiation. m is density is generally between the catalyst concentration employed in dense beds and the dispersed transport systems. Pressure differential between two vertically spaced points in the reactor column can be measured to obtain the average bed density at such portion of the reaction zone. For instance, in a fluidized bed system employing ZSM-5 particles having a clean apparent density of 1.06 gm/cc and packed density of 0.85, an average fluidized bed density of about 300 to 500 kg/m3 is satisfactory.
~?~91~
4178+ -15-By virtue of the turbulence experienced in the turbulent regime, gas-solid contact in the catalytic reactor is improvedr providing substantially complete conversion, enhanced selectivity and temperature uniformity. One main advantage of this technique is the inherent control of bubble size and characteristic bubble lifetime. Bubbles of the gaseous reaction mixture are small, random and short-lived, thus resulting in goo~ contact between the gaseous reactants and the solid catalyst particles.
A significant difference between the process of this invention and conversion processes of the prior art is that operation in the turbulent fluidization regime is optimized to produce high octane C5 liquid in ~ood yield. The weight hourly space velocity and uniform contact provides a clo~se control of contact time between vapor and solid phases, typically about 3 to 25 seconds. Another advantage of operating in such a mode is the control of bubble size and life span, thus avoiding large scale gas by-passing in the reactor. The process of the present invention does not rely on internal baffles in the reactor for the purpose of bubble size control such as the baffles which are employed in the prior art dense bed processes discussed above.
As the superficial gas velocity is increased in the dense bed, eventually slugging conditions occur and with a further increase in the superficial gas velocity the slug flow breaks down into a turbulent fegime. The transition velocity at which this turbulent regime occurs appears to decrease with particle size. The turbulent regime extends from the transition velocity to the so-called transport velocity, as described by Avidan et al in U.S.
Patent 4,547,616 and by Tabak et al. in U.S. Patent 4,579,999. As the transport velocity is approached, there is a sharp increase in the rate of particle carryover, and in the absence of solid recycle, the bed could empty quickly.
Several useful parameters contribute to fluidization in the turbulent regime in accordance with the process of the present invention. When ~mploying a ZSM-5 type zeolite catalyst in fine X
417S~ ~,9~9 powder form such a catalyst should comprise the zeolite suitably bound or impregnated on a suitable support with a solid density (weight of a representative individual particle divided by its apparent "outside" volume) in the range from 0.6-2 g/cc, preferably 0.9-1.6 g/cc. The catalyst particles can be in a wide range of particle sizes up to about 250 microns, with an average particle size between about 20 and 100 microns, preferably in the range of 10-150 microns and with the average particle size between 40 and 80 microns. When these solid particles are placed in a fluidized bed where the superficial fluid velocity is 0.3-2 m/s, operation in the turbulent regime is obtained. The velocity specified here is for an operation at a total reactor pressure of about 100 to 300 kPa.
Those skilled in the art will appreciate that at higher pressures, a lower gas velocity may be employed to ensure operation in the turbulent fluidization regime.
The reactor can assume any technically feasible configuration, but several important criteria should be considered.
The bed of catalyst in the reactor can be at least about 5-20 meters in height, preferably about 7 meters. Fine particles may be included in the bed, especially due to attrition, and the fines may be entrained in the product gas stream. A typical turbulent bed may have a catalyst carryover rate up to about 1.5 times the reaction zone inventory per hour. If the fraction of fines becomes larqe, a poetion of the carryover can be eemoved from the system and replaced by larger particl~es. It is feasible to have a fine particle separator, such as a cyclone disposed within the reactor shell to recover catalyst carryover and return this fraction continuously to the bottom of the reaction zone for recirculation at a rate of about one catalyst inventory per hour. Optionally, fine Particles carried from the reactor vessel entrained with effluent gas can be recovered by a high operating temperature sintered metal filter.
This process can be used with any process stream which contains sufficient liquid olefins and dienes. Preferably the feed is substantially free of deleterious oxygenates and sulfur X
~?.9~7~.~
4178+ -17-compounds. Because the catalyst can be readily removed and regellerated, or replaced, the process can tolerate a lot of impurities in the feed. Experimental runs are performed using a ZSM-5 catalyst to demonstrate the inventive process. The fluidized bed unit can be operated over a wide range of process variables and catalyst activity.
Reactoe Operation A typical single pass reactor unit employs a temperature-controlled catalyst zone with indirect heat exchange and/or adjustable gas quench, whereby the reaction exotherm can be carefully controlled to prevent excessive temperature above the usual operating range of about 315C to 650C. Preferably average reactor temperature is 340C to 430C to maximize production of gasoline boiling range hydrocarbons. Temperatures of 425-580C
maximize production of aromatics. Heat exchanging hot reactor effluent with feedstock and/or recycle streams will save energy.
Gptional heat exchangers may recover heat from the effluent stream prior to fractionation. It is preferred to operate the olefin conversion reactors at moderate pressure of about 100 to 3000 kPa (atmospheric to about 400 psig) to maximize liquid yields. Higher pressures, to 6000 kPa, favoe aromatics yields.
The weight hourly space velocity (WH5V, based on total olefins in the fresh feedstock is about 0.l-5 WHSV. Typical product fractionation systems are desceibed in U.S. Patents 4,456,779 and 4,504,693 (Cwen, et al.~.
To prevent premature non-catalytic reaction of the dienes, it is desirable to maintain reactant li~uid feedstream temperatu~e below about 180C (350F) until injection into the fluidized bed.
Appropriate thermal insulation or quenching of the feedstream to the injection point can laegely prevent gum and coke formation in the liquid phase prior to catalysis.
, .. .. .
~?.917fi~
4178+ -18-~ tomization of the pressurized liquid reactant feedstream can be achieved by known techniques, such as liquid speay nozzles, motive gas, ultra sonics, etc. A suitable nozzle is shown in Fig.
2, ~herein a concentric feed liquid projection device lO0 is depicted in vertical cross section view. Pressurized liquid 1OWS
through a supply conduit 123. The nozzle is mounted onto the vessel internal steucture by screw cap means 130 or similar attachment means. A motive Eluid supplied under pressure through conduit 12 drives the pressurized liquid flowing from the nozzle orifice 140 for injection into the reaction vessel at sufficient velocity to induce a fine vertically directed spray of atomized liquid having an average particle size up to about 300, preferably about 50 microns.
The number and arrangement of nozzles will depend upon the cross sectional area of the fluidized bed and fluidization characteristics of the gas-solid-liquid mixture. The atomized stream from a pressurized nozzle can be made to effect penetration into the bed at a depth and/or lateral radius of a meter or more. The mixture fluid may be an inert material, nitrogen, lower aliphatic gas, stream, etc.
Thermal insulation of the liquid diene-containing feedstream from the hot reaction medium in the reaction vessel can be achieved by applying to the liquid feed conduit a layer of thermal insulation, such as a ceramic shield or the like. Jacketed conduits with heat adsorbing fluid may also be suitable.
In the present example a C4+ liquid stream is converted to aromatics-rich gasoline in the fluidized bed reactor employing acid ZS~1-5 powder catalyst having a fresh alpha value of about 80 at an average conversion temperature of about 425C (800F) and total pressure of about 275 kPa (25 psig).
The liquid pyrolysis gasoline feedstock contains about 22 wt. % C4 mono-alkenes, 27% C4+ dienes (mainly 1,3-butadiene), 49% C4 paraffins, 2% aromatics and naphthenes, and less than 1% C3 aliphatics.
X
~X917fi~
4178+ -19-Typical olefinic pyrolysis byproduct streams are shown in Table 1.
Following initial heating and fluidization of the powdered catalyst with a heated lift gas (e.g. C2 hydrocarbon), the feedstream is preheated and maintained below 180C prior to injection into the bed. After achieving steady state operation at a reaction severity index tR.I.) of about 1, the effluent conversion product (less any lift gas components) comprises 82 wt. % C5~
liquid gasoline havin~ a research octane rating of 94 (RON). The total aromatics content is 18 wt. %, including 1% benzene (B), 5%
toluene (T), 6% xylenes (X) and ethyl benzene, 4~ Cg aromatics isomers and 10% C10 isomers, mainly durene. The predominant nonaromatic fraction (65~) contains mainly mono-olefins, paraffins and naphthenes, and the light gas C4 fraction is 17% of the conversion product.
~?.917fi9 4178+ -20-Example of Diene-Rich Feedstock (ethane cracker byproduct) Component Vol.
C3 1.0 i-butene 0.08 1,3-butadiene 0.51 t.2,butene 0.1 c.2,butene 0.15 1,2 butadiene 0.14 3m 1 butene 0.45 isopentane 5-44 1,4 pentadiene 0.6 l-pentene 0.63 n-pentane 1.92 isoprene 2.3 c,2,pentene 0.35 2m2butene 0 45 t,l,3, pentadiene 1.5 c,l,3,pentadiene 1.0 20 cyclopentadiene 13.7 cyclopentene 1.7 2,3 d.m. butane 1.7 3moentene 0.85 hexane 0.95 unknown C6 1.04 cyclohexane 3.06 benzene 34 4 unknown C8 3-47 Toluene 10.1 vinyleydohexene 0.19 ethylbenzene 1.29 xylene 1.01 styrene 0 3 unknown Cg+ ~ 6.9 ~L?291~fi~
4178+ -21-The above diene-rich stream example contains C6 aromatic hydrocarbons which can be separated before feeding to the reactor. Typical ranges of diene-rich pyrolysis gasoline streans comprised of mainly C4-C6 hydrocarbons are:
Vol. %
Cienes 5-60 Mono-alkenes 5-30 Aromatics 1-5*
Alkanes 20-60 Naphthenes 1-5 *can be as high as 60% if C6~ fraction is not separated.
.
1?~917fi~
417~+ -2~-A series of continuous olefin conversion runs are conducted using H-2SM-5 (65%) catalyst having an alpha value of about 175 at the beginning of the aging runs made under oligomerization conditions without regeneration to upgrade mixtures of ethene, propene and butadiene and to determine the effects of diene concentration on catalyst aging. The control feedstock (Example 2) is compared with diene-containing feeds in Table 1.
Example 2 Example 3 Example 4 Ethene 0 0.7 1.8 Propene 26.8 28.1 22.9 Butenes 35.7 31.9 31.7 1,3 Butadiene O (control) û.8 5.1 Alkanes (C4 ) 37.5 38.5 38.5 Recycle (mol/mol olefin) 2.5:1 2.5:1 2.5:1 ~X91~6~
4178+ -23-The conversion unit is a single bed isothermal reactor using HZSM-S having a crystal size less than 0.5 microns, together with 35% alumina binder and having a fresh alpha value of 175. The continuous runs are conducted at about 6600 kPa and weight hourly space velocity (wHSV) of about 0.8 parts olefin feed per part by weight of catalyst per hour. The conversion runs are started at 205C (400F) and the temperature is increased to compensate for coke deposition, while maintaining total olefin conversion of at least 80~, preferably over 90X. Results of the aging studies are plotted in Fig. 3, with all conversion rates being normalized to 80%
to 166C+ (330F+) product for comparison purposes. Selectivity of the conversion product to heavier hydrocarbons is shown in Table 3.
Example 2 Example 3 Example 4 Total Liquid Product, 50~ pt, C (F) 261/(501) 259/(498) 244/(472) ~istillate Species (As Cut) 5 wt. ~, C (F) 232/(434) 250/(483) 297(477) 95 wt. % C (F) 369/(697) 383/(722) 379(715) Gravity, API 44.3 41.2 38.9 Aniline Point 177 184 172 .~ .
. . .
~9i~
4178-~ -24-While the aromatics product content of the control runs averaged about 2-5~, the 5.1% butadiene feed (Example 4) is upgraded to an aromatics content of 15.5 wt. %, more than 3 times the diene input. The average paraffin content is less than 14% and the liquid dominant product is 70% + olefins and naphthenes.
m ese results indicate butadiene, at levels of 1 wt. %
or less, do not cause siqnificantly increased catalyst aginq or lower peoduct selectivity. It was surprising that adding diene would increase the a~omatics yield, and surprisinq that such larqe aromatics yields could be achieved at reactor temperatures just above 200C. Typical FCC C3/C4 olefins from a depropanizer feed stream contain n.3-0.6 wt. % butadiene which is less than the 0.8 wt. % butadiene concentration that was used in this study. Even at the 5.1 wt. % butadiene level, though catalyst aging was increased, product selectivity to heavier hydrocarbons r~mained relatively high.
In the present high severity example a C4 liquid stream is converted to aromatics-rich gasoline in the fluidized bed reactor employing acid ZSM-5 powder catalyst having a fresh alpha value of about 175 at an average conversion temperature of about 480C (900F) and total pressure of about 275 kPa (25 psiq).
The liquid feed was the same as used in example 1.
Following initial heating and fluidization of the powde~ed catalyst with a heated lift gas (e.g. C2 hydrocarbon), the feedstream is preheated and maintained below 180C prior to injection into the bed. After achieving steady state operation at a reaction severity index (R.I.) of about 2, the effluent conversion product (less any lift gas components) has an aromatics content of 34.4 wt. %, including 4.9% benzene (B), 11.8% toluene (T), 14~
xylenes (X) and 0.9% ethyl benzene, 2.3% Cg aromatics isomers and 0.5% C10 isomers. The nonaromatic fraction contains mainly t ?.91~6~?
4178+ -25-mono-olefins, paraffins and naphthenes, and the light gas C4 fraction is 13.5% of the conversion product.
Comparative effluent streams for high severity and low severity conversion runs under steady state reactor conditions are shown in Table 4. High severity operation means a reactor temperature of 600C. Low severity operation was run at 425C
reactor temperature, at a RI of 2. ~oth were run at 0.87 WHSV, 1 bar (100 kPa) over HZSM-5.
~?.,9176~t 4178+ -25-Products EXAMPLE 5A EXAMPLE 5B
Yi High Severity Low Severitv H2, wt. ~ 3.0 1.3 Cl 13.5 2.6 C2 10.3 6.1 C3 3.8 3.4 c4 2.0 1.4 C5 Non-Aromatic - 50.3 Benzene 22.1 4.9 Toluene 21.9 11.8 Ethyl Benzene 0.9 0.9 Xylene 15.6 14.0 C9 Aromatics 2.7 2.3 C10 3.2 0.5 Coke 1.0 0.5 100. 0 100. 0 ~.917~i~
4178~ -27-The flexibility of the fluid bed operating parameters for controlling the reactor temperature under exothermic reaction conditions allows an easy adjustment for achieving the optimal yield structure.
Fither C5~ liquid yield, or BTX yield may be optimized when temperatures of 315-650C are used in the reactor. The net yield o~ aromatics can comprise over 3C~o of the olefins in the feed. The propane:propene ratio will usually be 0.7:1 to 5:1 to maximize aromatics.
To fluidize the catalyst at the bottom of the reactor prior to injection of the liquid feed stream, a lift gas may be employed.
This can be an inert diluent or recyled light gas, such as methane, ethane, ethene, propane, etc. Recycle of C3 light hydrocarbons may also be desirable under certain circumstances, for instance with unreacted aliphatics which requiure further conversion or for dilution of highly exothermic feedstocks.
The thermodynamic balance of exothermic olefin oligomerization and endothermic paraffin reactions can have significant impact on the reaction severity conditions.
The use of a fluid-bed reactor in this process offers several advantages over a fixed-bed reactor. Due to continuous catalyst regeneration, fluid-bed reactor operation need not be adversely affected by oxygenate, sulfur and/or nitrogen containing contaminants present in the pyrrolysis byproduct.
through a supply conduit 123. The nozzle is mounted onto the vessel internal steucture by screw cap means 130 or similar attachment means. A motive Eluid supplied under pressure through conduit 12 drives the pressurized liquid flowing from the nozzle orifice 140 for injection into the reaction vessel at sufficient velocity to induce a fine vertically directed spray of atomized liquid having an average particle size up to about 300, preferably about 50 microns.
The number and arrangement of nozzles will depend upon the cross sectional area of the fluidized bed and fluidization characteristics of the gas-solid-liquid mixture. The atomized stream from a pressurized nozzle can be made to effect penetration into the bed at a depth and/or lateral radius of a meter or more. The mixture fluid may be an inert material, nitrogen, lower aliphatic gas, stream, etc.
Thermal insulation of the liquid diene-containing feedstream from the hot reaction medium in the reaction vessel can be achieved by applying to the liquid feed conduit a layer of thermal insulation, such as a ceramic shield or the like. Jacketed conduits with heat adsorbing fluid may also be suitable.
In the present example a C4+ liquid stream is converted to aromatics-rich gasoline in the fluidized bed reactor employing acid ZS~1-5 powder catalyst having a fresh alpha value of about 80 at an average conversion temperature of about 425C (800F) and total pressure of about 275 kPa (25 psig).
The liquid pyrolysis gasoline feedstock contains about 22 wt. % C4 mono-alkenes, 27% C4+ dienes (mainly 1,3-butadiene), 49% C4 paraffins, 2% aromatics and naphthenes, and less than 1% C3 aliphatics.
X
~X917fi~
4178+ -19-Typical olefinic pyrolysis byproduct streams are shown in Table 1.
Following initial heating and fluidization of the powdered catalyst with a heated lift gas (e.g. C2 hydrocarbon), the feedstream is preheated and maintained below 180C prior to injection into the bed. After achieving steady state operation at a reaction severity index tR.I.) of about 1, the effluent conversion product (less any lift gas components) comprises 82 wt. % C5~
liquid gasoline havin~ a research octane rating of 94 (RON). The total aromatics content is 18 wt. %, including 1% benzene (B), 5%
toluene (T), 6% xylenes (X) and ethyl benzene, 4~ Cg aromatics isomers and 10% C10 isomers, mainly durene. The predominant nonaromatic fraction (65~) contains mainly mono-olefins, paraffins and naphthenes, and the light gas C4 fraction is 17% of the conversion product.
~?.917fi9 4178+ -20-Example of Diene-Rich Feedstock (ethane cracker byproduct) Component Vol.
C3 1.0 i-butene 0.08 1,3-butadiene 0.51 t.2,butene 0.1 c.2,butene 0.15 1,2 butadiene 0.14 3m 1 butene 0.45 isopentane 5-44 1,4 pentadiene 0.6 l-pentene 0.63 n-pentane 1.92 isoprene 2.3 c,2,pentene 0.35 2m2butene 0 45 t,l,3, pentadiene 1.5 c,l,3,pentadiene 1.0 20 cyclopentadiene 13.7 cyclopentene 1.7 2,3 d.m. butane 1.7 3moentene 0.85 hexane 0.95 unknown C6 1.04 cyclohexane 3.06 benzene 34 4 unknown C8 3-47 Toluene 10.1 vinyleydohexene 0.19 ethylbenzene 1.29 xylene 1.01 styrene 0 3 unknown Cg+ ~ 6.9 ~L?291~fi~
4178+ -21-The above diene-rich stream example contains C6 aromatic hydrocarbons which can be separated before feeding to the reactor. Typical ranges of diene-rich pyrolysis gasoline streans comprised of mainly C4-C6 hydrocarbons are:
Vol. %
Cienes 5-60 Mono-alkenes 5-30 Aromatics 1-5*
Alkanes 20-60 Naphthenes 1-5 *can be as high as 60% if C6~ fraction is not separated.
.
1?~917fi~
417~+ -2~-A series of continuous olefin conversion runs are conducted using H-2SM-5 (65%) catalyst having an alpha value of about 175 at the beginning of the aging runs made under oligomerization conditions without regeneration to upgrade mixtures of ethene, propene and butadiene and to determine the effects of diene concentration on catalyst aging. The control feedstock (Example 2) is compared with diene-containing feeds in Table 1.
Example 2 Example 3 Example 4 Ethene 0 0.7 1.8 Propene 26.8 28.1 22.9 Butenes 35.7 31.9 31.7 1,3 Butadiene O (control) û.8 5.1 Alkanes (C4 ) 37.5 38.5 38.5 Recycle (mol/mol olefin) 2.5:1 2.5:1 2.5:1 ~X91~6~
4178+ -23-The conversion unit is a single bed isothermal reactor using HZSM-S having a crystal size less than 0.5 microns, together with 35% alumina binder and having a fresh alpha value of 175. The continuous runs are conducted at about 6600 kPa and weight hourly space velocity (wHSV) of about 0.8 parts olefin feed per part by weight of catalyst per hour. The conversion runs are started at 205C (400F) and the temperature is increased to compensate for coke deposition, while maintaining total olefin conversion of at least 80~, preferably over 90X. Results of the aging studies are plotted in Fig. 3, with all conversion rates being normalized to 80%
to 166C+ (330F+) product for comparison purposes. Selectivity of the conversion product to heavier hydrocarbons is shown in Table 3.
Example 2 Example 3 Example 4 Total Liquid Product, 50~ pt, C (F) 261/(501) 259/(498) 244/(472) ~istillate Species (As Cut) 5 wt. ~, C (F) 232/(434) 250/(483) 297(477) 95 wt. % C (F) 369/(697) 383/(722) 379(715) Gravity, API 44.3 41.2 38.9 Aniline Point 177 184 172 .~ .
. . .
~9i~
4178-~ -24-While the aromatics product content of the control runs averaged about 2-5~, the 5.1% butadiene feed (Example 4) is upgraded to an aromatics content of 15.5 wt. %, more than 3 times the diene input. The average paraffin content is less than 14% and the liquid dominant product is 70% + olefins and naphthenes.
m ese results indicate butadiene, at levels of 1 wt. %
or less, do not cause siqnificantly increased catalyst aginq or lower peoduct selectivity. It was surprising that adding diene would increase the a~omatics yield, and surprisinq that such larqe aromatics yields could be achieved at reactor temperatures just above 200C. Typical FCC C3/C4 olefins from a depropanizer feed stream contain n.3-0.6 wt. % butadiene which is less than the 0.8 wt. % butadiene concentration that was used in this study. Even at the 5.1 wt. % butadiene level, though catalyst aging was increased, product selectivity to heavier hydrocarbons r~mained relatively high.
In the present high severity example a C4 liquid stream is converted to aromatics-rich gasoline in the fluidized bed reactor employing acid ZSM-5 powder catalyst having a fresh alpha value of about 175 at an average conversion temperature of about 480C (900F) and total pressure of about 275 kPa (25 psiq).
The liquid feed was the same as used in example 1.
Following initial heating and fluidization of the powde~ed catalyst with a heated lift gas (e.g. C2 hydrocarbon), the feedstream is preheated and maintained below 180C prior to injection into the bed. After achieving steady state operation at a reaction severity index (R.I.) of about 2, the effluent conversion product (less any lift gas components) has an aromatics content of 34.4 wt. %, including 4.9% benzene (B), 11.8% toluene (T), 14~
xylenes (X) and 0.9% ethyl benzene, 2.3% Cg aromatics isomers and 0.5% C10 isomers. The nonaromatic fraction contains mainly t ?.91~6~?
4178+ -25-mono-olefins, paraffins and naphthenes, and the light gas C4 fraction is 13.5% of the conversion product.
Comparative effluent streams for high severity and low severity conversion runs under steady state reactor conditions are shown in Table 4. High severity operation means a reactor temperature of 600C. Low severity operation was run at 425C
reactor temperature, at a RI of 2. ~oth were run at 0.87 WHSV, 1 bar (100 kPa) over HZSM-5.
~?.,9176~t 4178+ -25-Products EXAMPLE 5A EXAMPLE 5B
Yi High Severity Low Severitv H2, wt. ~ 3.0 1.3 Cl 13.5 2.6 C2 10.3 6.1 C3 3.8 3.4 c4 2.0 1.4 C5 Non-Aromatic - 50.3 Benzene 22.1 4.9 Toluene 21.9 11.8 Ethyl Benzene 0.9 0.9 Xylene 15.6 14.0 C9 Aromatics 2.7 2.3 C10 3.2 0.5 Coke 1.0 0.5 100. 0 100. 0 ~.917~i~
4178~ -27-The flexibility of the fluid bed operating parameters for controlling the reactor temperature under exothermic reaction conditions allows an easy adjustment for achieving the optimal yield structure.
Fither C5~ liquid yield, or BTX yield may be optimized when temperatures of 315-650C are used in the reactor. The net yield o~ aromatics can comprise over 3C~o of the olefins in the feed. The propane:propene ratio will usually be 0.7:1 to 5:1 to maximize aromatics.
To fluidize the catalyst at the bottom of the reactor prior to injection of the liquid feed stream, a lift gas may be employed.
This can be an inert diluent or recyled light gas, such as methane, ethane, ethene, propane, etc. Recycle of C3 light hydrocarbons may also be desirable under certain circumstances, for instance with unreacted aliphatics which requiure further conversion or for dilution of highly exothermic feedstocks.
The thermodynamic balance of exothermic olefin oligomerization and endothermic paraffin reactions can have significant impact on the reaction severity conditions.
The use of a fluid-bed reactor in this process offers several advantages over a fixed-bed reactor. Due to continuous catalyst regeneration, fluid-bed reactor operation need not be adversely affected by oxygenate, sulfur and/or nitrogen containing contaminants present in the pyrrolysis byproduct.
Claims (9)
1. A process for upgrading diene-rich liquid olefinic feed comprising at least 1 wt % diene and a total C4-C6 olefin content of about 5 to 90 wt % to liquid product with a reduced diene content characterized by maintaining a fluidized bed of zeolite catalyst at 220 to 510°C;
adding the feed at a temperature lower than the bed temperature into the fluidized bed and converting a majority of dienes in the feed;
and recovering hydrocarbon product containing a major amount of C4+ hydrocarbons and having a C3 to C5 alkane:alkene weight ratio of 0.2:1 to 200:1.
adding the feed at a temperature lower than the bed temperature into the fluidized bed and converting a majority of dienes in the feed;
and recovering hydrocarbon product containing a major amount of C4+ hydrocarbons and having a C3 to C5 alkane:alkene weight ratio of 0.2:1 to 200:1.
2. The process of claim 1 further characterized in that a single, relative dense phase fluidized bed is used and the fluidized bed density is 100 to 500 kg/m3, measured at the bottom of the bed, and the bed is maintained as a turbulent fluidized bed.
3. The process of claim 1 further characterized in that the fluidized bed is a dilute phase fluidized bed.
4. The process of claim 1 further characterized in that the catalyst comprises 5 to 90 wt. % of a siliceous metallo-silicate acid zeolite having the structure of ZSM-5, an alpha activity of 10 to 250, and containing at least 10 to 25 wt. % particles having a particle size less than 32 microns.
5. The process of claim 4 further characterized in that the feed is added as an atomized stream of finely divided liquid.
6. The process of claim 1, 2, 3, 4 or 5 further characterized in that the superficial feed vapor velocity is 0.3-2 m/sec; the bed temperature is 315 to 510°C; the weight hourly feedstock space velocity (based on total olefin) is 0.1 to 5; the propane:propene weight ratio of reactor effluentis 0.7:1 to 2:1; and the average fluidized bed density measured at the reaction zone bottom is 300 to 500 kg/m3.
7. The process of claim 1, 2, 3, 4 or 5 further characterized in that a C3-hydrocarbon gas is added to the feed.
8. The process of claim 1, 2, 3, 4 or 5 further characterized in that a portion of light hydrocarbon gas is recovered from reactor effluent and recycled to a lower portion of the reactor as a fluidizing lift gas added to the reactor below the liquid feed.
9. The process of claim 1, 2, 3, 4 or 5 further characterized in that the catalyst contains a hydrogenation-dehydrogenation metal component to increase aromatics production.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/006,399 US4751338A (en) | 1987-01-23 | 1987-01-23 | Conversion of diene-containing light olefins to aromatic hydrocarbons |
| US006,408 | 1987-01-23 | ||
| US07/006,408 US4778661A (en) | 1987-01-23 | 1987-01-23 | Upgrading diene-containing light olefins in a fluidized bed reactor |
| US006,399 | 1987-01-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1291769C true CA1291769C (en) | 1991-11-05 |
Family
ID=26675578
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000557021A Expired - Lifetime CA1291769C (en) | 1987-01-23 | 1988-01-21 | Upgrading diene-containing hydrocarbons |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA1291769C (en) |
-
1988
- 1988-01-21 CA CA000557021A patent/CA1291769C/en not_active Expired - Lifetime
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