WO1985001740A1 - A method for catalytically converting residual oils - Google Patents
A method for catalytically converting residual oils Download PDFInfo
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- WO1985001740A1 WO1985001740A1 PCT/US1983/001644 US8301644W WO8501740A1 WO 1985001740 A1 WO1985001740 A1 WO 1985001740A1 US 8301644 W US8301644 W US 8301644W WO 8501740 A1 WO8501740 A1 WO 8501740A1
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- catalyst
- oil
- ultrastable
- zeolite
- boiling
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/02—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils characterised by the catalyst used
- C10G11/04—Oxides
- C10G11/05—Crystalline alumino-silicates, e.g. molecular sieves
Definitions
- Fluid catalytic cracking has undergone many changes since its inception in the early 1940's.
- U.S. Patent No. 4,287,048 particularly identifies an ultrastable "Y" type crystalline zeolite and its method of preparation in the following manner.
- "Stabilized" or ultrastable Y-type zeolites are well-known. They are described, for example, in U.S. Pat Nos. 3,293,192 and 0 3,402,996 and the publication Society of Chemical Engi ⁇ neering (London) Monograph Molecular Sieves, page 186 (1968) by C.V. McDaniel and P.K. Maher, the teachings of which are hereby incorporated by reference.
- ultrastable refers to a Y-type zeolite which is highly 5 resistant to degradation of crystallinity by high tempera- ture and steam treatment and is characterized by a R 2 0 content (wherein R is Na, K or any other alkali metal ion) of less than 4 weight percent, preferably less than 1 weight percent and a unit cell size less than 24.5 Angstroms and a silica to alumina mole ratio in the range of 3.5 to 7 or higher.
- the ultrastable form of Y-type zeolite is obtained primarily by a substantial reduction of the alkali metal ions and the unit cell size reduc ⁇ tion.
- the ultrastable zeolite is identified both by the smaller unit cell and the low alkali metal content in the crystal structure.
- the ultrastable form of the Y-type zeolite can be prepared by successively base exchanging a Y-type zeolite with an aqueous solution of an ammonium salt, such as ammonium nitrate, until the alkali metal content of the Y-type zeolite is reduced to less than 4 weight percent.
- an ammonium salt such as ammonium nitrate
- the base exchanged zeolite is then calcined at a temperature of 1000°F to 1500°F, for up to several hours, cooled and thereafter again successively base exchanged with an aqueous solution of an ammonium salt until the alkali metal content is reduced to less than 1 weight percent, followed by washing and calcination again at a temperature of 1000° to 1500°F to produce an ultrastable zeolite Y.
- the sequence of ion exchange and heat treatment results in the substantial reduction of the alkali metal content of the original zeolite and results in a unit cell shrinkage which is believed to lead to the ultra high stability of the resulting Y-type zeolite.
- the particle size of the zeolites is usually in the range of 0.1 to 10 microns, more particularly in the range of 0.5 to 3 microns.
- Suitable amounts of the ultrastable Y-type zeolite in the catalyst of the present invention include from about 10 to about 80 weight percent, preferably from about 30 to about 50 weight percent, based on the total catalyst.
- the catalytic cracking or conversion of heavy oil feeds comprising atmospheric tower bottoms, vacuum oils plus resid, residual oil, reduced crudes, and topped crudes, shale oil, coal liquefaction oil products and tar sands oil products all of which comprise components boiling above 1000°F or 1050°F are best catalytically converted in a highly vaporized-atomized contact phase of the oil feed with select fluid catalyst particles of a composition herein identified.
- the heat necessary to substantially completely vaporize-atomize all of the high boiling oil feed is contributed by a relatively high regenerator temperature operation of at least about 1350°F and preferably above 1400°F completed in the substantial absence of hydro-thermal damage to the catalyst.
- the more conventional zeolite cracking cata ⁇ lysts comprising relatively large amounts of one or more rare earth exchanged faujasite zeolites are susceptible to considerable hydro-thermal deactivation under high temperature regeneration conditions above about 1400°F and required to remove relatively large amounts of hydrocarbonaceous materials deposited during residual oil cracking operations.
- Cycle oils are liquid products comprising large quanti- ties of condensed ring aromatics.
- the condensed ring aromatics are two, three, four and larger six carbon member rings.
- the cycle oils comprising largely two member rings referred to as light cycle oils (LCO) are commercially marketable as middle distillate.
- Cycle oils comprising largely three and a greater number of con ⁇ densed rings such as found in some heavy cycle oils and particularly slurry oils are of low commercial worth and are usually only marketed as bunker fuel.
- a high surface area crystalline zeolite such as an ultrastable crystal- line zeolite, commercially identified by Davison Chemical Co. as Z-14US, is a highly stable and effective zeolite conversion catalyst at the high regeneration temperatures required when processing high boiling residual oil type feeds despite its relatively low fresh catalyst activity. More importantly, when the processing concepts of this invention are pursued, it is further observed that the
- ultrastable crystalline zeolite contri ⁇ butes to a significant reduction in deposition of hydro ⁇ carbonaceous material, improves light cycle product yield at the expense of heavier cycle oils and provides a product selectivity generally richer in gasoline and gasoline forming components than is achieved with a more conventional rare earth exchanged zeolite such as CREY at comparable fresh feed conversion levels.
- the outer or exterior surface such as provided by a high surface area ultrastable zeolite is found to be very effective in providing accessible and available active cracking sites to effect the now experienced substantial molecular weight reduction of high molecular weight components in a slurry oil to more desirable lower molecular weight components.
- the hydro-thermal stability of an ultrastable crystalline zeolite catalyst prepared as herein identified and briefly discussed is found to be superior to that of a rare earth exchanged "Y" faujasite referred to as CREY and used to form catalyst particles for cracking hydrocarbon feed materials.
- the ultrastable zeolite containing catalysts maintain significantly higher surface area equilibrium catalysts at high rengen- eration temperatures than obtained with a CREY catalyst.
- a matrix or base material with a relatively high amor- phous surface area which provides active cracking sites may be employed with the ultrastable zeolite in lieu of more catalytically inert matrix materials and contribute to the cracking of high boiling cycle oil components obtained in a reduced crude cracking operation.
- the ultrastable hydrogen form of zeolite herein discussed does the desired cracking or conversion of high molecular weight hydrocarbon components with a substantial reduc- tion in coke and gas production. This observed differ ⁇ ence in product selectivity when employing an ultrastable crystalline zeolite in lieu of CREY for reduced crude cracking is unexpected and not previously predictable.
- a high surface area catalyst that can maintain a high surface area exceeding that obtainable with CREY containing catalysts under the conditions of high, above 1400°F, regeneration temperatures.
- a catalyst composition satisfying the above operating parameters and found to be suitable for the specific conversion of high boiling residual oil containing feed stocks is a catalyst comprising an ultrastable crystal ⁇ line zeolite as herein described.
- This particular crystalline zeolite, sieve or crystalline aluminosilicate is industrially referred to as an ultrastable sieve or crystalline zeolite.
- the ultrastable sieve containing catalyst is of a rela ⁇ tively low activity but high surface area catalyst as measured in the fresh catalyst state. This catalyst is described in various patents briefly referred to herein.
- the ultrastable zeolite containing catalysts have been discussed in the literature for application in the more conventional clean feed gas oil cracking operations but because of its low relative activity compared to rare earth containing zeolites and relatively high cost has not received industry acceptance. However, it has been found that when applied to residual oil cracking opera ⁇ tions, the ultrastable zeolite catalyst becomes a super ⁇ ior catalyst, by providing and producing a profound improvement in cracking selectivity over the state of the art higher activity rare earth exchanged zeolite con- taining catalyst. This is illustrated in the commercial results presented in Table I, wherein cracking data is presented comparing performance of the ultrastable sieve containing catalyst to a rare earth exchanged zeolite containing catalyst.
- the drawing is a graphical representation of the contraction of an ultrastable crystalline zeolite ob ⁇ tained during calcination under different temperature conditions. It is observed that this contraction is substantially less than that obtained when subjecting a CREY catalyst composition to similar conditions.
- a class of zeolite containing catalysts particularly suitable for use in the residual oil conversion process of this invention is once comprising an ultrastable crystalline zeolite commercially identified as Z-14US.
- the preparation of an ultrastable crystalline zeolite discussed above is described in U.S. Patent 4,287,048, and referenced material including U.S. Patents 3,293,192 (1966) and 3,402,966, the subject matter of which is incorporated herein by reference.
- the ultrastable sieve or crystalline zeolite des ⁇ cribed in the above identified reference material and U.S. Patents are characterized by a significant (1-1.5%) decrease in the unit cell dimensions of the parent sodium zeolite. This contraction is caused by extraction of aluminum cations from the crystalline zeolite in the manufacturing process. This has been shown to be true by McDaniel and Maher in their book entitled “Zeolite Chemistry and Catalysis", page 320 by figure 17 and reproduced for inclusion herewith as the drawing. In this drawing the shaded area identifies the unit cell contraction area for ultrastable zeolites of a different silica to alumina ratio.
- the zeolite SiO_/Al 2 0 3 ratio is greater than 3 and the unit cell size or lattice constant is less than 24.65 Angstroms.
- the ultra- stable zeolite will have a Si0 2 /Al 2 0 3 ratio of at least 5 with a unit cell size of about 24.5 Angstroms or less.
- a high sodium content zeolite, matrix components and residual oil feed are known to deactivate a cracking catalyst's zeolite crystalline structure relativity rapidly so it is important to reduce the sodium content of these materials and particularly the finished zeolite sodium content to at least 1 weight percent or less.
- the residual Na 2 0 on the zeolite structure is below 0.5 weight percent.
- other cations may be introduced into the ultrastable zeolite by ion exchange methods well known in the art.
- the ultrastable zeolites useful in the present invention can include any such cation-modified zeolites, e.g. zeolites containing, by exchange, cations from virtually any group of the periodic table except for Group IA. In particular, certain advantages may be obtained by the incorporation of specific cations.
- ultrastable zeolites useful in the practice of the present invention can be modified to include virtually any metal or combination of metals by exchange with the exception of Group IA elements, such as Na, without departing from the spirit of and applica ⁇ bility to the present invention.
- the cracking activity level of an ultrastable crystalline zeolite is less than a rare earth exchanged zeolite such as CREY. Thus it requires considerably more ultrastable zeolite than CREY to form catalyst particles of the same degree of activity. This high addition has been considered heretofore as not suitable for use in hydrocarbon conversion operations of lower regenerator temperatures.
- Modern high activity FCC catalysts are reported to contain in the range of 15-40% of a rare earth type Y zeolite.
- a rare earth zeolite catalyst employed in an FCC unit processing gas oils and operating with regenerator temperatures generally maintained below
- ⁇ mitm 1400°F and more usually not above 1350°F or less requires using for the same activity level an ultrastable crystal ⁇ line zeolite catalyst comprising from 60-160% of the ultrastable zeolite. Obviously, no catalyst could contain more than 100% of any component.
- a catalyst particle of such high zeolite content presents daunting problems to the catalyst suppliers and manufacturers to produce such a catalyst composition with suitable physi ⁇ cal attrition resistant or hardness properties for use in a circulating fluid catalytic cracking system.
- an ultrastable crystal ⁇ line zeolite catalyst obtained as above provided is found to give an equilibrium activity that is equal to or exceeds that of a rare earth type Y sieve (CREY) con ⁇ taining catalyst and provides a higher equilibrium surface area without encountering undersired coke and liquid product selectivity as herein identified.
- CREY rare earth type Y sieve
- Catalysts contained approximately same amount of zeolite promoter (Wt. basis) when new.
- **Z-14US refers to ultra-stable zeolites.
- the large surface area of the ultrastable zeolite is apparently very effective in providing active accessible cracking sites to cause the experienced molecular weight reduction in the slurry oil. Unlike cracking with amorphous cracking catalysts, it is observed that the ultrastable hydrogen zeolites do this cracking with less or a lower coke and gas production.
- Table I clearly indicates that the equilibrium activities of the two catalysts, ultrastable zeolite and rare earth exchanged zeolite, after exposure to regenerator tempera ⁇ tures of about 1400°F, were quite similar in activity even though the CREY catalyst started with 3-4 times the activity of the ultrastable zeolite catalyst. At even higher regenerator temperatures, the benefits obtained by using the ultrastable catalyst are expected to be even greater.
- Ultrastable sieve or crystalline zeolite containing catalysts despite their relatively low fresh catalyst activity equilibrate in a commercial cracking process when cracking residual oil at desired high temperature conditions at acceptable catalyst activity levels and then retain a desired high surface area.
- This high surface area equilibrium leads to desirable cracking selectivity, i.e, high yields of gasoline and gasoline forming components, increased yields of cycle oils containing two member rings produced at the expense of cycle oils containing higher member rings with substan ⁇ tially less coke make and a reduced gas production.
- the ultrastable zeolite may be supported by any one of a different number of support materials or matrices.
- matrices other than an inactive kaoline-clay silicon oxide binder combination can be used to hold or include the ultrastable hydrogen exchanged crystalline zeolite.
- any of the known prior art or conven- tional catalyst matrix materials can be used. Such materials would include synthetic silica-alumina, clay, silica or alumina binders or any combination thereof.
- the finished catalyst will preferably contain not less than 20 wt% or more than 80% of an ultrastable hydrogen form of crystalline zeolite herein identified.
- the ultrastable crystalline "Y" zeolite catalyst preferably employed by this invention for cracking high boiling residual oils may be used however, in conjunction with a metal entrapment material or metals sink for accumulation thereof.
- the finished catalyst will pref ⁇ erably contain not less than 20 wt% or more than 80% of an ultrastable hydrogen form of crystalline zeolite herein identified.
- the catalytic cracking or conversion of high boiling hydrocarbons comprising Conradson carbon producing materials are best catalytically converted in a highly vaporized-atomized condition during contact with the high surface area zeolite containing catalyst herein particu ⁇ larly defined by employing contact temperature conditions provided by hot regenerated catalyst at least equal to the feed pseudo-critical temperature.
- the catalyst regeneration temperature will increase above 1350°F during combustion of deposited carbonaceous material as the residual oil feed Conradson carbon value increases even though the ultrastable zeolite catalyst composition employed in the conversion process of this invention contributes to a reduction in coke make.
- regeneration temperatures above 1350°F and up to as high as 1600°F or more can be experienced as carbonaceous deposits increase in response to the feed Conradson carbon content.
- the catalytic conversion operation of this invention is preferably one of relatively short vaporized hydro ⁇ carbon contact with the special catalyst composition comprising from 20 to 80 wt% of ultrastable crystalline zeolite as a dispersed catalyst phase in a riser contact zone wherein the hydrocarbon residence time in contact with catalyst particles can be restricted to within the range of 0.5 to 5 seconds and more usually in the range of 1 to 3 seconds.
- This dispersed catalyst phase- vaporized hydrocarbon contact may be implemented in substantial measure by the use of an atomizing diluent material with the high boiling hydrocarbon feed.
- Diluent materials suitable for this purpose include steam, C0 2 , light normally gaseous hydrocarbons comprising C 3 minus material or a combination thereof in an amount which will reduce the high boiling feed partial pressure and achieve desired atomized-vaporized dispersion contact of hydro ⁇ carbon feed with high temperature catalyst particles. Ato ization of the feed may be substantially implemented by use of appropriate spray nozzles.
- the operating parameters to achieve an optimized contact between feed and catalyst particles also include feed exit velocities in excess of 10 feet per second to achieve atomized spraying of the feed with or without diluent material across a riser reactor cross section for intimate contact with hot catalyst particles charged thereto.
- the above identified operating parameters are intended to also accelerate the mixture relatively uniformly within the feed vaporization section of a riser reactor in a minimum time frame and thus enhance rapid
- the operating conditions and methods for implementing are selected to ensure a relatively dilute phase suspension contact between catalyst parti ⁇ cles and atomized oil feed for vaporized conversion transfer through a riser conversion zone.
- Such dilute catalyst phase operations include catalyst particle concentrations in the range of 2 to 10 pounds per cubic foot and preferably not above about 5 pounds per cubic foot.
- the catalyst hydrocarbon feed suspension formed as above provided is passed through a riser contact zone for a hydrocarbon contact time less than about 5 seconds before discharge therefrom at a temperature sufficiently elevated to maximize recovery of vaporized hydrocarbon material separately from catalyst particles.
- the present invention is directed to the catalytic conversion of high boiling residual oils comprising vacuum gas oils containing high boiling Conradson carbon producing materials employing a special ultrastable crystalline zeolite containing catalyst at a temperature equal to or above the feed pseudo-critical temperature in preferably a riser contact zone for a hydrocarbon residence time in the range of 0.5 to about 5 seconds and more usually not above about 3 seconds.
- the catalyst regeneration temperature generally increase in response to increased deposited carbonaceous material removed by combustion and contributing to high temperature regeneration and conversion of the feed according to the concepts of this invention.
- employing the ultrastable zeolite catalyst provides a lower coke yield than obtained with the rare earth zeolite catalyst thus contributing measur ⁇ ably to the advantages of the processing concepts of this invention as herein described.
- the hydrocarbon conversion operation may be effected at a temperature in the range of 950°F up to about 1400°F or at a temperature equal to or above the feed pseudo-critical temperature employing a reactor pressure from about atmospheric pressure up to about 100 psig but generally not above about 50 psig.
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Abstract
A process for converting residual oil comprising vacuum bottoms in the presence of a cracking catalyst of high surface are and comprising an ultrastable zeolite. More particularly, a conversion process particularly contributing to producing cycle oil and gasoline boiling range products with reduced carbon deposition in combination with a relatively high regeneration temperature operation of at least 1350?oF and above, and a short contact time riser hydrocarbon conversion operation contributing to reducing slurry oil product in favor of lower boiling products is described. A fluid cracking catalyst comprising a special ultrastable crystalline zeolite of high silica to alumina ratio provides hydrothermal stability of acceptable tolerance in the environment employed.
Description
A METHOD FOR CATALYTICALLY CONVERTING RESIDUAL OILS
Background of the Invention
Fluid catalytic cracking has undergone many changes since its inception in the early 1940's. One of the
05 recent process advances in fluid catalytic cracking has been the advent of zeolite catalysts usage which has prompted many process design modifications. Feedstocks, however, have changed very little up to recent years, being comprised of mostly atmospheric and vacuum gas ig oils. However, with the economic need of the industry to process poorer quality crude oils, and a need at the same time to maintain high gasoline yields, the ability to effect conversion of poor quality feed stocks in a FCCU process is now of significant importance. τ_5 The present invention is .directed to extending the processed boiling range of crude oil feedstocks to include substantially all of the atmospheric bottoms, a residual or reduced crude portion thereof and comprising vacuum tower bottoms by catalytically cracking such
2o materials in a selective process more fully discussed below that converts a highly atomized - vaporized mixture of the feed components at a relatively high temperature with an ultrastable crystalline zeolite catalyst herein identified.
25 U.S. Patent No. 4,287,048 particularly identifies an ultrastable "Y" type crystalline zeolite and its method of preparation in the following manner. "Stabilized" or ultrastable Y-type zeolites are well-known. They are described, for example, in U.S. Pat Nos. 3,293,192 and 0 3,402,996 and the publication Society of Chemical Engi¬ neering (London) Monograph Molecular Sieves, page 186 (1968) by C.V. McDaniel and P.K. Maher, the teachings of which are hereby incorporated by reference. In general, "ultrastable" refers to a Y-type zeolite which is highly 5 resistant to degradation of crystallinity by high tempera-
ture and steam treatment and is characterized by a R20 content (wherein R is Na, K or any other alkali metal ion) of less than 4 weight percent, preferably less than 1 weight percent and a unit cell size less than 24.5 Angstroms and a silica to alumina mole ratio in the range of 3.5 to 7 or higher. The ultrastable form of Y-type zeolite is obtained primarily by a substantial reduction of the alkali metal ions and the unit cell size reduc¬ tion. The ultrastable zeolite is identified both by the smaller unit cell and the low alkali metal content in the crystal structure.
As is generally known, the ultrastable form of the Y-type zeolite can be prepared by successively base exchanging a Y-type zeolite with an aqueous solution of an ammonium salt, such as ammonium nitrate, until the alkali metal content of the Y-type zeolite is reduced to less than 4 weight percent. The base exchanged zeolite is then calcined at a temperature of 1000°F to 1500°F, for up to several hours, cooled and thereafter again successively base exchanged with an aqueous solution of an ammonium salt until the alkali metal content is reduced to less than 1 weight percent, followed by washing and calcination again at a temperature of 1000° to 1500°F to produce an ultrastable zeolite Y. The sequence of ion exchange and heat treatment results in the substantial reduction of the alkali metal content of the original zeolite and results in a unit cell shrinkage which is believed to lead to the ultra high stability of the resulting Y-type zeolite. The particle size of the zeolites is usually in the range of 0.1 to 10 microns, more particularly in the range of 0.5 to 3 microns.
Suitable amounts of the ultrastable Y-type zeolite in the catalyst of the present invention include from about 10 to about 80 weight percent, preferably from about 30 to about 50 weight percent, based on the total catalyst.
Summary of the Invention
The catalytic cracking or conversion of heavy oil feeds comprising atmospheric tower bottoms, vacuum oils plus resid, residual oil, reduced crudes, and topped crudes, shale oil, coal liquefaction oil products and tar sands oil products all of which comprise components boiling above 1000°F or 1050°F are best catalytically converted in a highly vaporized-atomized contact phase of the oil feed with select fluid catalyst particles of a composition herein identified. The heat necessary to substantially completely vaporize-atomize all of the high boiling oil feed is contributed by a relatively high regenerator temperature operation of at least about 1350°F and preferably above 1400°F completed in the substantial absence of hydro-thermal damage to the catalyst. The more conventional zeolite cracking cata¬ lysts comprising relatively large amounts of one or more rare earth exchanged faujasite zeolites are susceptible to considerable hydro-thermal deactivation under high temperature regeneration conditions above about 1400°F and required to remove relatively large amounts of hydrocarbonaceous materials deposited during residual oil cracking operations.
It is observed through commercial experience of catalytically cracking heavier and heavier feed stocks that there is a marked tendency for the regenerator temperature to rise to higher levels as the quality of the fed stock deteriorates. (Heavier and lower quality feed stocks for the purposes of this discussion refers to the inclusion of high boiling residual oils of high Conradson carbon in the feed) .
It is also observed that if the regenerator tempera¬ ture is restrained by means not usually employed in conventional gas oil cracking such as providing steam coils in the regenerator, external catalyst coolers and/or other means employed by some operators, the
selectivity of the hydrogen conversion reaction shifts in the direction of producing undesirable large amounts of coke and liquid products referred to as "cycle oils". Cycle oils are liquid products comprising large quanti- ties of condensed ring aromatics. The condensed ring aromatics are two, three, four and larger six carbon member rings. The cycle oils comprising largely two member rings referred to as light cycle oils (LCO) are commercially marketable as middle distillate. Cycle oils comprising largely three and a greater number of con¬ densed rings such as found in some heavy cycle oils and particularly slurry oils are of low commercial worth and are usually only marketed as bunker fuel.
On the other hand, it is observed in commercial catalytic cracking of the heavier feed stocks comprising residual oils that if the tendency for the regenerator temperature to rise to a higher level is not restrained then the undesirable reaction to selectivity described above does not occur. That is, at higher regenerator temperatures and at temperatures generally above those employed commercially for gas oil cracking, above 1350°F, coke production is equal to or lower than that observed in conventional gas oil cracking, and the production of condensed ring aromatics larger than two member rings is discouraged.
It is observed in a study of catalysts suitable for converting high boiling residual oils, that contrary to many of the teachings in the prior art, a high surface area crystalline zeolite such as an ultrastable crystal- line zeolite, commercially identified by Davison Chemical Co. as Z-14US, is a highly stable and effective zeolite conversion catalyst at the high regeneration temperatures required when processing high boiling residual oil type feeds despite its relatively low fresh catalyst activity. More importantly, when the processing concepts of this invention are pursued, it is further observed that the
'
high surface area ultrastable crystalline zeolite contri¬ butes to a significant reduction in deposition of hydro¬ carbonaceous material, improves light cycle product yield at the expense of heavier cycle oils and provides a product selectivity generally richer in gasoline and gasoline forming components than is achieved with a more conventional rare earth exchanged zeolite such as CREY at comparable fresh feed conversion levels.
It is further observed that the commercially availa- ble high activity zeolitic catalysts comprising rare earth exchanged zeolites, experience a serious surface area decline. This surface area decline is viewed to be due to hydro-thermal instability under the conditions of the preferred unit operating mode. As the surface area progressively decays, it is further observed that product selectivity shifts in the direction of increased heavy cycle oil production and particularly cycle oils of ring structures greater than 2 member rings, increased gas production comprising H~, C, *s and C2*s and more i por- tantly reduced gasoline production.
The outer or exterior surface such as provided by a high surface area ultrastable zeolite is found to be very effective in providing accessible and available active cracking sites to effect the now experienced substantial molecular weight reduction of high molecular weight components in a slurry oil to more desirable lower molecular weight components. The hydro-thermal stability of an ultrastable crystalline zeolite catalyst prepared as herein identified and briefly discussed is found to be superior to that of a rare earth exchanged "Y" faujasite referred to as CREY and used to form catalyst particles for cracking hydrocarbon feed materials. The ultrastable zeolite containing catalysts maintain significantly higher surface area equilibrium catalysts at high rengen- eration temperatures than obtained with a CREY catalyst. A matrix or base material with a relatively high amor-
phous surface area which provides active cracking sites may be employed with the ultrastable zeolite in lieu of more catalytically inert matrix materials and contribute to the cracking of high boiling cycle oil components obtained in a reduced crude cracking operation. However, unlike cracking with an amorphous cracking catalyst, the ultrastable hydrogen form of zeolite herein discussed does the desired cracking or conversion of high molecular weight hydrocarbon components with a substantial reduc- tion in coke and gas production. This observed differ¬ ence in product selectivity when employing an ultrastable crystalline zeolite in lieu of CREY for reduced crude cracking is unexpected and not previously predictable. Thus the cracking of high boiling residual oils co - prising metallo-organic components boiling above 1025°F benefits in several significant ways herein identified when employing the ultrastable form of crystalline zeolites in catalyst compositions providing high surface area particle compositions. It is, therefore, concluded that to more success¬ fully crack high boiling range feed stocks comprising residual oil of high Conradson carbon value and to obtain desired product selectivity requires at least two funda¬ mental operation conditions: 1. High regenerator temperatures which means a high catalyst temperature at the point of oil catalyst contact.
2. A high surface area catalyst that can maintain a high surface area exceeding that obtainable with CREY containing catalysts under the conditions of high, above 1400°F, regeneration temperatures.
A catalyst composition satisfying the above operating parameters and found to be suitable for the specific conversion of high boiling residual oil containing feed stocks is a catalyst comprising an ultrastable crystal¬ line zeolite as herein described. This particular
crystalline zeolite, sieve or crystalline aluminosilicate is industrially referred to as an ultrastable sieve or crystalline zeolite. Compared to the state of the art rare earth exchanged zeolite (CREY) containing catalyst, the ultrastable sieve containing catalyst is of a rela¬ tively low activity but high surface area catalyst as measured in the fresh catalyst state. This catalyst is described in various patents briefly referred to herein. The ultrastable zeolite containing catalysts have been discussed in the literature for application in the more conventional clean feed gas oil cracking operations but because of its low relative activity compared to rare earth containing zeolites and relatively high cost has not received industry acceptance. However, it has been found that when applied to residual oil cracking opera¬ tions, the ultrastable zeolite catalyst becomes a super¬ ior catalyst, by providing and producing a profound improvement in cracking selectivity over the state of the art higher activity rare earth exchanged zeolite con- taining catalyst. This is illustrated in the commercial results presented in Table I, wherein cracking data is presented comparing performance of the ultrastable sieve containing catalyst to a rare earth exchanged zeolite containing catalyst. The drawing is a graphical representation of the contraction of an ultrastable crystalline zeolite ob¬ tained during calcination under different temperature conditions. It is observed that this contraction is substantially less than that obtained when subjecting a CREY catalyst composition to similar conditions.
Discussion of Specific Embodiments
A class of zeolite containing catalysts particularly suitable for use in the residual oil conversion process of this invention is once comprising an ultrastable crystalline zeolite commercially identified as Z-14US.
The preparation of an ultrastable crystalline zeolite discussed above is described in U.S. Patent 4,287,048, and referenced material including U.S. Patents 3,293,192 (1966) and 3,402,966, the subject matter of which is incorporated herein by reference.
The ultrastable sieve or crystalline zeolite des¬ cribed in the above identified reference material and U.S. Patents are characterized by a significant (1-1.5%) decrease in the unit cell dimensions of the parent sodium zeolite. This contraction is caused by extraction of aluminum cations from the crystalline zeolite in the manufacturing process. This has been shown to be true by McDaniel and Maher in their book entitled "Zeolite Chemistry and Catalysis", page 320 by figure 17 and reproduced for inclusion herewith as the drawing. In this drawing the shaded area identifies the unit cell contraction area for ultrastable zeolites of a different silica to alumina ratio.
To be a suitable ultrastable crystalline zeolite component of the catalyst for use in the process of this invention, the zeolite SiO_/Al203 ratio is greater than 3 and the unit cell size or lattice constant is less than 24.65 Angstroms. In a particular embodiment, the ultra- stable zeolite will have a Si02/Al203 ratio of at least 5 with a unit cell size of about 24.5 Angstroms or less. A high sodium content zeolite, matrix components and residual oil feed are known to deactivate a cracking catalyst's zeolite crystalline structure relativity rapidly so it is important to reduce the sodium content of these materials and particularly the finished zeolite sodium content to at least 1 weight percent or less. Various techniques for achieving this low sodium content are discussed in the literature. Preferably the residual Na20 on the zeolite structure is below 0.5 weight percent. As set forth in the patents referred to hereinbefore and incorporated by reference, other cations may be
introduced into the ultrastable zeolite by ion exchange methods well known in the art. As will be known and understood by those skilled in the art, the ultrastable zeolites useful in the present invention can include any such cation-modified zeolites, e.g. zeolites containing, by exchange, cations from virtually any group of the periodic table except for Group IA. In particular, certain advantages may be obtained by the incorporation of specific cations. For example, ion exchange with rare earth elements, i.e. those of atomic numbers 57 to 71, may increase the activity and strengthen or increase the stability of the ultrastable zeolites. Similarly, incorporation of magnesium and/or elements from the chromium group (Cr, Mo and W) may be useful to promote burning. Magnesium and calcium may advantageously be incorporated as SO gathering agents and the metals of Group IVA and VA may be useful to passivate metals, such as nickel. In general, the ultrastable zeolites useful in the practice of the present invention can be modified to include virtually any metal or combination of metals by exchange with the exception of Group IA elements, such as Na, without departing from the spirit of and applica¬ bility to the present invention.
The cracking activity level of an ultrastable crystalline zeolite is less than a rare earth exchanged zeolite such as CREY. Thus it requires considerably more ultrastable zeolite than CREY to form catalyst particles of the same degree of activity. This high addition has been considered heretofore as not suitable for use in hydrocarbon conversion operations of lower regenerator temperatures.
Modern high activity FCC catalysts are reported to contain in the range of 15-40% of a rare earth type Y zeolite. In a conventional rare earth zeolite catalyst employed in an FCC unit processing gas oils and operating with regenerator temperatures generally maintained below
^mitm
1400°F and more usually not above 1350°F or less requires using for the same activity level an ultrastable crystal¬ line zeolite catalyst comprising from 60-160% of the ultrastable zeolite. Obviously, no catalyst could contain more than 100% of any component. A catalyst particle of such high zeolite content presents formidable problems to the catalyst suppliers and manufacturers to produce such a catalyst composition with suitable physi¬ cal attrition resistant or hardness properties for use in a circulating fluid catalytic cracking system.
At relatively high regenerator temperatures in the range of 1350°F - 1600°F and required in the high temper¬ ature conversion of residual oils an ultrastable crystal¬ line zeolite catalyst obtained as above provided is found to give an equilibrium activity that is equal to or exceeds that of a rare earth type Y sieve (CREY) con¬ taining catalyst and provides a higher equilibrium surface area without encountering undersired coke and liquid product selectivity as herein identified. It has also been found that at a high oil feed—catalyst sus¬ pension mix temperatures at least equal to the pseudo- critical temperature of the feed and characterized by regenerated catalyst temperatures at or above 1350°F the heavy or high boiling multi ring components in the oil feed are more readily converted thermally and catalyti¬ cally to lower boiling desired products by the high surface area ultrastable zeolite catalyst in modern catalytic cracking facilities.
A commercial test of the ultrastable hydrogen form of crystalline zeolite containing catalyst herein identi¬ fied provides the data shown in Table I. In this opera¬ tion where the regenerator was operating over 1400°F, the ultrastable zeolite containing catalyst actually out¬ performed a CREY catalyst. That is, lower coke yields were observed and there is a substantial drop in the heavy cycle oil yield and its gravity. Extra light cycle
°
oil and gasoline is produced at the expense of coke and heavy cycle oil with liquid C3 plus yield increased significantly and all factors resulting in economic gain.
TABLE I
COMMERCIAL CRACKING PERFORMANCE
Type Zeolite in Catalyst* Z-14US** C-RE-Y
CAT ADDN's #/Bbl. FEED .34 .4
FEED RATE, B/D 18,070 18,000
FEED CON. CARBON, Wt.% 2.5 2.5
RX. TEMP. °F 982 974
REGEN. DENSE PHASE TEMP. °F 1,413 1,402
CONVERSION VOL.% 80.8 80.1
C2 - YIELD, SCFB 312 324
ALKY FEED, VOL.% (C3 - C4) 26.7 26.1
GASOLINE, VOL.% 58.1 55.7
LCO, VOL.% 12.8 10.1
SLURRY, VOL.% 6.4 9.8
TOTAL LIQUID YIELD C-j + VOL.% 104.0 101.7
COKE, Wt.% 5.6 6.4
MICRO ACTIVITY 60 70
CATALYST SURFACE AREA M2/gm 105 65
*Catalysts contained approximately same amount of zeolite promoter (Wt. basis) when new.
**Z-14US refers to ultra-stable zeolites.
_OM r- v i"
The reduction in heavy cycle oil product and increase in light cycle oil product obtained as above-identified was surprisingly unexpected when compared to the results obtained with a rare earth exchanged crystalline zeolite (CREY) containing catalyst. Both forms of zeolite catalysts were supported by a relatively inactive matrix material. The increase in equilibrium surface area indicates that substantially more zeolite is present in the equilibrium catalyst comprising the ultrastable hydrogen form zeolite containing catalyst.
TABLE II
Catalyst Sieve Type US RE-Y
Matrix Type Low Surface Area/Activity
Equil. S.A. 105 65
The large surface area of the ultrastable zeolite is apparently very effective in providing active accessible cracking sites to cause the experienced molecular weight reduction in the slurry oil. Unlike cracking with amorphous cracking catalysts, it is observed that the ultrastable hydrogen zeolites do this cracking with less or a lower coke and gas production. The data provided in Table I clearly indicates that the equilibrium activities of the two catalysts, ultrastable zeolite and rare earth exchanged zeolite, after exposure to regenerator tempera¬ tures of about 1400°F, were quite similar in activity even though the CREY catalyst started with 3-4 times the activity of the ultrastable zeolite catalyst. At even higher regenerator temperatures, the benefits obtained by using the ultrastable catalyst are expected to be even greater.
The following conclusions are reached in view of the above with respect to the fluid catalytic cracking of
OMP
residual oil with an ultrastable crystalline zeolite catalyst.
1. High catalyst temperatures at point of oil catalyst contact, vis-a-vis, high regenerator tempera- tures are necessary to more completely vaporize the high boiling residual oil feed stock.
2. Failure to adequately vaporize-atomize the feed encourages poor cracking selectivity, i.e., encourages high coke make, high cycle oil production, particularly cycle oils rich in ring structures greater than 2 member rings, high gas make and low gasoline production. The poor performance attributed when the feed is inadequately vaporized is likely due to the "coke shut off" of the active catalyst sites by the portion of the feed not vaporized.
3. As the residual oil content of the feed stock increases the catalyst high temperature at point of oil contact (vis-a-vis high regenerator temperature) must be permitted to rise to a higher optimum level in order to encourage more nearly complete vaporization of the feed if undesirable cracking selectivity is to be avoided.
4. Utilization of catalysts containing rare earth exchanged zeolites is inconsistent with high temperature regeneration despite their inherent relatively high initial activity, because of rapid surface area decay and rapid loss of activity in high temperature regeneration environment.
5. Ultrastable sieve or crystalline zeolite containing catalysts despite their relatively low fresh catalyst activity equilibrate in a commercial cracking process when cracking residual oil at desired high temperature conditions at acceptable catalyst activity levels and then retain a desired high surface area. This high surface area equilibrium leads to desirable cracking selectivity, i.e, high yields of gasoline and gasoline forming components, increased yields of cycle oils
containing two member rings produced at the expense of cycle oils containing higher member rings with substan¬ tially less coke make and a reduced gas production. The ultrastable zeolite may be supported by any one of a different number of support materials or matrices. For example, matrices other than an inactive kaoline-clay silicon oxide binder combination can be used to hold or include the ultrastable hydrogen exchanged crystalline zeolite. In fact, any of the known prior art or conven- tional catalyst matrix materials can be used. Such materials would include synthetic silica-alumina, clay, silica or alumina binders or any combination thereof. The finished catalyst will preferably contain not less than 20 wt% or more than 80% of an ultrastable hydrogen form of crystalline zeolite herein identified.
The ultrastable crystalline "Y" zeolite catalyst preferably employed by this invention for cracking high boiling residual oils may be used however, in conjunction with a metal entrapment material or metals sink for accumulation thereof. The finished catalyst will pref¬ erably contain not less than 20 wt% or more than 80% of an ultrastable hydrogen form of crystalline zeolite herein identified.
The catalytic cracking or conversion of high boiling hydrocarbons comprising Conradson carbon producing materials are best catalytically converted in a highly vaporized-atomized condition during contact with the high surface area zeolite containing catalyst herein particu¬ larly defined by employing contact temperature conditions provided by hot regenerated catalyst at least equal to the feed pseudo-critical temperature. Thus the catalyst regeneration temperature will increase above 1350°F during combustion of deposited carbonaceous material as the residual oil feed Conradson carbon value increases even though the ultrastable zeolite catalyst composition employed in the conversion process of this invention
contributes to a reduction in coke make. Thus when processing vacuum gas oils comprise the resid portion of the crude oil, regeneration temperatures above 1350°F and up to as high as 1600°F or more can be experienced as carbonaceous deposits increase in response to the feed Conradson carbon content.
The catalytic conversion operation of this invention is preferably one of relatively short vaporized hydro¬ carbon contact with the special catalyst composition comprising from 20 to 80 wt% of ultrastable crystalline zeolite as a dispersed catalyst phase in a riser contact zone wherein the hydrocarbon residence time in contact with catalyst particles can be restricted to within the range of 0.5 to 5 seconds and more usually in the range of 1 to 3 seconds. This dispersed catalyst phase- vaporized hydrocarbon contact may be implemented in substantial measure by the use of an atomizing diluent material with the high boiling hydrocarbon feed. Diluent materials suitable for this purpose include steam, C02, light normally gaseous hydrocarbons comprising C3 minus material or a combination thereof in an amount which will reduce the high boiling feed partial pressure and achieve desired atomized-vaporized dispersion contact of hydro¬ carbon feed with high temperature catalyst particles. Ato ization of the feed may be substantially implemented by use of appropriate spray nozzles. Thus the operating parameters to achieve an optimized contact between feed and catalyst particles also include feed exit velocities in excess of 10 feet per second to achieve atomized spraying of the feed with or without diluent material across a riser reactor cross section for intimate contact with hot catalyst particles charged thereto.
The above identified operating parameters are intended to also accelerate the mixture relatively uniformly within the feed vaporization section of a riser reactor in a minimum time frame and thus enhance rapid
'-ξJREAl O PI
heat transfer from hot catalyst particles to charged feed preferably atomized and thus prevent localized enhanced catalyst to oil ratios contributing to a dense catalyst bed phase. That is, the operating conditions and methods for implementing are selected to ensure a relatively dilute phase suspension contact between catalyst parti¬ cles and atomized oil feed for vaporized conversion transfer through a riser conversion zone. Such dilute catalyst phase operations include catalyst particle concentrations in the range of 2 to 10 pounds per cubic foot and preferably not above about 5 pounds per cubic foot.
The catalyst hydrocarbon feed suspension formed as above provided is passed through a riser contact zone for a hydrocarbon contact time less than about 5 seconds before discharge therefrom at a temperature sufficiently elevated to maximize recovery of vaporized hydrocarbon material separately from catalyst particles.
In a more particular and specific aspect, the present invention is directed to the catalytic conversion of high boiling residual oils comprising vacuum gas oils containing high boiling Conradson carbon producing materials employing a special ultrastable crystalline zeolite containing catalyst at a temperature equal to or above the feed pseudo-critical temperature in preferably a riser contact zone for a hydrocarbon residence time in the range of 0.5 to about 5 seconds and more usually not above about 3 seconds.
Thus, as the end boiling point of the hydrocarbon feed or the Conradson carbon level thereof increases so also will the catalyst regeneration temperature generally increase in response to increased deposited carbonaceous material removed by combustion and contributing to high temperature regeneration and conversion of the feed according to the concepts of this invention. However, as discussed above, employing the ultrastable zeolite
catalyst provides a lower coke yield than obtained with the rare earth zeolite catalyst thus contributing measur¬ ably to the advantages of the processing concepts of this invention as herein described. Depending on the feed hydrocarbon to be converted, its boiling range and Conradson carbon contributing factor, the hydrocarbon conversion operation may be effected at a temperature in the range of 950°F up to about 1400°F or at a temperature equal to or above the feed pseudo-critical temperature employing a reactor pressure from about atmospheric pressure up to about 100 psig but generally not above about 50 psig.
The riser cracking operation of this invention may be employed in conjunction with the catalyst regeneration arrangement of copending application serial number
169,086, filed July 15, 1980, the subject matter of which is incorporated herein by reference thereto. That is the apparatus and operating concepts of the above identified application and the methods of implementation except as particularly modified by employing an ultrastable crystal¬ line zeolite containing catalyst as herein provided may be employed with considerable advantage in protecting the activity's electrical characteristics of the ultrastable crystalline zeolite catalyst particularly when reducing residual coke on the ultrastable zeolite catalyst to less than about 0.25 wt%.
Having thus generally described the method and concepts of this invention and discussion of specific embodiments in support thereof, it is to be understood that no undue restrictions are to be imposed by reasons thereof except as defined by the following claims.
Claims
1. A method for upgrading crude oil boiling above 600°F which comprises, contacting the crude oil boiling above 600°F with a catalyst comprising ultrastable crystalline zeolite up to about 80 wt% at an elevated catalyst conversion temperature of at least 950°F for a time providing high yields of gasoline boiling range products, and recovering said gasoline boiling range product.
2. The method of Claim 1 wherein said crude oil boiling above 600°F is a reduced crude comprising metallo- organic compounds.
3. The method of Claim 1 wherein the catalyst comprises at least 20 wt.% of ultrastable crystalline zeolite.
4. The method of Claim 1 wherein the conversion of the crude oil is accomplished at a temperature within the range of 950°F to 1400°F for a hydrocarbon residence time in contact with catalyst particles less than 5 seconds.
5. The method of Claim 1 wherein the products of said conversion operation particularly include light cycle, oil, gasoline boiling range material and gaseous components readily convertible to gasoline boiling range components.
6. A method for upgrading residual oils to products boiling below about 600°F which comprises contacting a residual oil comprising components boiling above 1025°F, with a relatively low activity ultrastable crystalline zeolite catalyst of substantial surface area greater than a rare earth exchanged zeolite at an elevated catalyst conversion temperature of at least 950°F, and recovering a product of said catalyst conversion operation comprising gasoline boiling range products.
7. A method for converting a reduced crude to light cycle oil and lower boiling products which comprise contacting said reduced crude at an elevated cracking temperature with a high surface area ultrastable crystal¬ line zeolite catalyst comprising Na-0 in an amount less than 1.0 wt.%, and recovering a product of said cracking operation comprising light cycle oil and lower boiling products comprising gasoline.
OMPI ^ >, WIPO '%NAT
8. A method for upgrading hydrocarbons boiling above 600°F and comprising metallo-organic compounds which comprises contacting said hydrocarbons boiling above 600°F with a catalyst comprising an ultrastable crystalline zeolite in an amount within the range of 20 to 80 wt.% at a temperature above 950°F thereby deacti¬ vating the catalyst with deposited hydrocarbonaceous material, removing deposited hydrocarbonaceous materials with oxygen by combustion at a temperature of at least 1350°F to provide a regenerated catalyst comprising less than 0.25 wt.% residual carbon, and recycling catalyst thus regenerated to the hydrocarbon conversion step.
9. A method for upgrading high boiling hydro¬ carbons comprising vacuum bottoms to produce lower boiling products comprising cycle oils, gasoline and gasoline forming components which comprises contacting said high boiling hydrocarbons with an ultrastable crystalline zeolite catalyst of equilibrium surface area greater than a rare earth exchanged zeolite and a unit * cell size less than about 24.65 Angstroms, said con¬ tacting effected at a temperature in the range of about 950° to about 1150°F for a hydrocarbon residence time less than 5 seconds in contact with said ultrastable catalyst particles, and recovering high yields of products comprising cycle oils and lower boiling gasoline component materials.
10. The method of Claim 8 wherein removal of deposited hydrocarbon material is accomplished in at least one dense fluid catalyst bed regenerator operation.
11. The method of Claim 8 wherein removal of deposited hydrocarbonaceous material is accomplished in a plurality of sequentially arranged dense fluid catalyst bed regeneration operations.
12. The method of Claim 8 wherein removal of deposited hydrocarbonaceous material is accomplished in the combination of dense fluid catalyst bed and dispersed catalyst phase regeneration operations.
13. A method for catalytically converting high boiling residual oils comprising gas oils and higher boiling Conradson carbon producing materials which comprises, catalytically converting a residual oil comprising vacuum gas oil and higher boiling materials with a high surface area catalytically active ultrastable zeolite containing catalyst of lower initial activity than a catalyst comprising a rare earth exchanged crystal¬ line zeolite of lower surface area for a hydrocarbon residence time in a reaction zone in the range of 0.5 to about 5 seconds at a temperature above the pseudo- critical temperatures of the residual oil feed, and recovering a product of said catalytic conversion opera¬ tion substantially reduced in multi ring components in favor of mono and dicyclic ring components.
14. The method of Claim 13 wherein lower boiling product selectivity is improved at the expense of a molecular weight reduction in the slurry oil product of the operation.
15. The method of Claim 13 wherein less coke and gas production is obtained with the high surface area ultrastable zeolite containing catalyst than is obtain¬ able with a lower surface area catalyst comprising rare earth exchanged crystalline zeolite.
16. A method for catalytically converting high boiling oil material boiling above 600°F comprising one or more materials selected from the group consisting of atmospheric tower bottoms, vacuum gas oils plus resid, a residual oil, a residual crude, a topped crude, shale oil, coal liquefaction oil products and tar sands oil products all of which materials comprise components boiling above 1000°F which comprises, contacting said high boiling oil material at a temperature at least equal to the pseudo-critical temperature thereof with a catalyst comprising from 20 to 80 wt% of an ultrastable crystalline zeolite of high surface area of less than 1 wt% alkali metal ion, a unit cell less than 24.5 Angstroms and a silica to alumina mole ratio in the range of 3.5 to about 7, said contacting between said oil material and said catalyst accomplished in a confined, relatively dilute suspension traversing a reaction zone for a hydrocarbon residence time less than 5 seconds, and recovering vaporous hydrocarbon conversion products separately from catalyst particles comprising carbona¬ ceous deposits following traverse of said reaction zone.
17. The method of Claim 16 wherein the recovered vaporous hydrocarbon conversion products are charac¬ terized by a product selectivity of improved light cycle oil and generally richer in gasoline and gasoline forming components than is achieved with a rare earth exchanged zeolite catalyst at comparable fresh oil feed conversion levels.
18. A method for upgrading a residual oil portion of crude oil boiling above 600°F comprising metallo- organic compounds which comprises contacting said residu¬ al portion of crude oil boiling above 600°F with a catalyst consisting of from 20 to 80 weight percent of an ultrastable faujasite crystalline zeolite dispersed in a silica-clay matrix for a time at a temperature particu¬ larly selective for conversion of the residual portion of crude oil to products of gasoline, light cycle oil and gasoline forming gaseous components, and recovering said products comprising gasoline and light cycle oil.
19. The method of Claim 18 wherein the cycle oil comprises two member rings produced at the expense of producing of cycle oils of higher member rings.
20. The method of Claim 18 wherein the ultrastable faujasite zeolite of a 0.5-3 microns size is distributed in a matrix material selected from; a kaolin clay-silicon oxide binder material; silica-alumina, clay, silica, alumina and a high surface area amorphous material providing active cracking sites.
21. The method of Claim 18 wherein the catalyst comprises the ultrastable faujasite crystalline zeolite in an amount within the range of 30 to 50 weight percent.
22. The method of Claim 18 wherein the ultrastable crystalline zeolite component of the catalyst is prepared under conditions to provide a high surface area material, a silica/alumina ratio of at least 3 and a unit cell size less than 24.65 Angstroms.
23. The method of Claim 18 wherein conversion of the residual portion of the crude oil is accomplished for a time less than 3 seconds at an elevated temperature sufficient to achieve substantially instantaneous vaporiza¬ tion of the charged residual oil in atomized condition upon contact with high temperature catalyst particles.
24. The method of Claim 23 wherein the temperature of the catalyst is at least equal to the feed pseudo- critical temperature and residual oil feed comprises metallo-organic components boiling above 1025°F.
25. The method of Claim 24 wherein the catalyst elevated temperature achieved by burning hydrocarbona¬ ceous deposits of said residual oil conversion increases in response to the feed Conradson carbon content at catalyst regeneration temperatures in the range of 1350 to 1600°F.
26. The method of Claim 18 wherein the ultrastable faujasite crystalline zeolite is prepared to provide high surface area zeolite with a silica/alumina ratio of at least 5 and a unit cell size of about 24.5 Angstroms or less.
27. The method of Claim*18 wherein an atomizing diluent material is used with the residual oil feed comprising one or more materials selected from steam, C02, light normally gaseous hydrocarbons comprising C, minus materials in cooperation with atomizing spray nozzles.
28. The method of Claim 27 wherein the conditions are selected to insure a relatively dilute phase sus¬ pension contact between catalyst particles and atomized oil feed for vaporized conversion transfer through a riser conversion zone as a particle concentration in the range of 2 to 10 pounds per cubic foot and a vapor residence time within the range of 0.5 to 3 seconds.
29. The method of Claim 18 wherein the residual oil portion of crude oil comprises high boiling Conradson carbon producing materials and metal contaminants.
30. The method of Claim 18 wherein the residual oil conversion operation is effected at a temperature in the range of about 950°F up to about 1400°F and at a tempera¬ ture equal to or above the feed pseudo-critical tempera¬ ture.
OMH
^ ATI
31. A method for catalytically converting residual oils comprising vacuum bottoms which comprises, converting said residual oil with a catalyst con¬ sisting of about 30-50 weight percent of ultrastable faujasite crystalline zeolite dispersed in a matrix material of clay and silica binder providing active cracking sites, said catalytic conversion effected at said residual oil pseudo-critical temperature for a time in the range of 0.5 to 3 seconds in a riser reaction zone, and recovering a product selectively of said catalytic conversion particularly comprising gasoline and light cycle oils comprising largely two member rings separately from catalyst particles comprising hydrocarbonaceous deposits of said conversion.
32. The method of Claim 31 wherein the separated catalyst comprising hydrocarbonaceous deposits is re¬ generated in a sequence of separate catalyst regeneration zones of increasing temperatures in the direction of catalyst flow permitting effecting the residual oil conversion at a temperature in the range of 950 to 1400°F.
33. The method of Claim 32 wherein the sequence of catalyst regeneration steps removes residual carbon on the catalyst to below 0.25 weight percent.
34. The method of Claim 31 wherein the zeolite comprises less than 0.5 weight percent a20 and a higher surface area than a rare earth exchanged faujasite crystalline zeolite.
35. A method of Claim 18 wherein the ultrastable faujasite crystalline zeolite contains at least one element selected from the group consisting of Cr, Mo and W.
36. A method of Claim 18 wherein the ultrastable faujasite crystalline zeolite contains at least one element selected from the group consisting of magnesium and calcium.
37. A method of Claim 18 wherein the ultrastable faujasite crystalline zeolite contains at least one element selected from the group consisting of the metals of Group IVA and VA.
- RE j
OMPI
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU22631/83A AU573554B2 (en) | 1983-10-20 | 1983-10-20 | Catalytically converting resids |
JP58503731A JPS61500316A (en) | 1983-10-20 | 1983-10-20 | Catalytic conversion method of residual oil |
GB08510127A GB2159535B (en) | 1983-10-20 | 1983-10-20 | A method for catalytically cracking residual oils |
BR8307756A BR8307756A (en) | 1983-10-20 | 1983-10-20 | PROCESSES TO IMPROVE THE DEGREE OF EBULICATION OF CRU OIL, TO BENEFIT OIL WASTE, TO CONVERT REDUCED CRUISE OIL INTO LIGHT OIL, TO BENEFIT HYDROCARBONES, TO BENEFIT FROM ELEVATED HYDROELICATE, EVERYTHING TO ELEPHIC, A PORTION OF RESIDUAL OIL FROM RAW OIL AND TO CATALLY CONVERT PETROLEUM WASTE |
PCT/US1983/001644 WO1985001740A1 (en) | 1983-10-20 | 1983-10-20 | A method for catalytically converting residual oils |
DE3390537T DE3390537C2 (en) | 1983-10-20 | 1983-10-20 | Catalytic cracking of residual oils |
NL8320358A NL8320358A (en) | 1983-10-20 | 1983-10-20 | PROCESS FOR THE CATALYTIC CONVERSION OF RESIDUE OIL FRACTIONS. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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PCT/US1983/001644 WO1985001740A1 (en) | 1983-10-20 | 1983-10-20 | A method for catalytically converting residual oils |
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WO1985001740A1 true WO1985001740A1 (en) | 1985-04-25 |
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PCT/US1983/001644 WO1985001740A1 (en) | 1983-10-20 | 1983-10-20 | A method for catalytically converting residual oils |
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AU (1) | AU573554B2 (en) |
BR (1) | BR8307756A (en) |
DE (1) | DE3390537C2 (en) |
GB (1) | GB2159535B (en) |
NL (1) | NL8320358A (en) |
WO (1) | WO1985001740A1 (en) |
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WO1986002889A1 (en) * | 1984-11-05 | 1986-05-22 | Francis Patrick Zikan | Steering and anti-theft device for vehicles |
JP5258281B2 (en) * | 2007-12-18 | 2013-08-07 | 日揮触媒化成株式会社 | Catalyst composition for catalytic cracking of hydrocarbon and process for producing the same |
BRPI0800236B1 (en) * | 2008-01-24 | 2019-05-14 | Petroleo Brasileiro S.A. - Petrobras | FLUID CATALYTIC CRACKING PROCESS AND EQUIPMENT FOR THE PRODUCTION OF LOW AROMATIC MEDIUM DISTILLED |
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- 1983-10-20 JP JP58503731A patent/JPS61500316A/en active Granted
- 1983-10-20 AU AU22631/83A patent/AU573554B2/en not_active Expired
- 1983-10-20 NL NL8320358A patent/NL8320358A/en active Search and Examination
- 1983-10-20 WO PCT/US1983/001644 patent/WO1985001740A1/en active Application Filing
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Also Published As
Publication number | Publication date |
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GB2159535B (en) | 1988-06-29 |
DE3390537T1 (en) | 1986-09-18 |
DE3390537C2 (en) | 1995-08-10 |
GB2159535A (en) | 1985-12-04 |
JPH0412754B2 (en) | 1992-03-05 |
JPS61500316A (en) | 1986-02-27 |
AU573554B2 (en) | 1988-06-16 |
NL8320358A (en) | 1985-09-02 |
GB8510127D0 (en) | 1985-05-30 |
BR8307756A (en) | 1985-08-27 |
AU2263183A (en) | 1985-05-07 |
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