US2348699A - Method of cracking hydrocarbon vapors - Google Patents

Method of cracking hydrocarbon vapors Download PDF

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US2348699A
US2348699A US394657A US39465741A US2348699A US 2348699 A US2348699 A US 2348699A US 394657 A US394657 A US 394657A US 39465741 A US39465741 A US 39465741A US 2348699 A US2348699 A US 2348699A
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vapors
cracking
granular material
coke
tar
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US394657A
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Malcolm H Tuttle
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Max B Miller & Co Inc
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Max B Miller & Co Inc
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/28Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G11/00Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G11/14Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts

Definitions

  • This invention relates to a method of cracking hydrocarbon vapors and producing such vapors from petroleum residues or the like.
  • petroleum residues or tars are sprayed onto loose, granular material heated to the proper temperature, and the resulting vapors are then passed countercurrent to a stream of the hot granular material.
  • the hot granular material which serves to heat and. crack the vapors in this second stage is then used as a medium on which the petroleum residue or the like is deposited in the first stage in order to distill off vapors and convert the rest of the petroleum residue to coke.
  • the coke-coated catalyst is withdrawn from the coking stage and is burned in a suitable furnace, the hot gases from the furnace being used to preheat the petroleum residue which is fed to the coking stage. In this way, the effectiveness of the catalyst remains constant during the cracking opmethod is illustrated diagrammatically in the accompanying drawing.
  • FIG. III a still which includes a number of shelves ll having openings l2, l3 disposed alternately near the center and near the outside wall of the still.
  • a rotatinghousing M in which is mounted a pipe carrying horizontal arms IS.
  • the pipe 15 is connected through a suitable coupling I! to a pipe l8 through which petroleum residues or tars are supplied.
  • the arms l6 are adapted to spray petroleum residues through ports IS in the rear faces of the arms as they rotate (in a clockwise direction, looking down).
  • the arms l6 also serve as rabble arms, and for this purpose are provided with projections or teeth which agitate the granular material and thus prevent the particles from sticking together. This raking action rearranges the particles so as to obtain maximum surface contact with the tar.
  • the member I4 and arms I6 may be rotated in any convenient manner, for instance by means of a motor 2
  • Granular material 24 is introduced into the still l0 through an opening 25 in the top. This granular material falls onto the upper hearth of the still and is agitated by the rabble arms I 6, which feed it continuously toward the central opening l2 in this hearth, and thence along the other hearths of the furnace.
  • the petroleum residue or the like is sprayed onto the granular material which is hot, preferably between 900 and 1400 F. The heat thus transferred to the petroleum residue or the like converts it into vapors and coke.
  • the granular material coated with coke drops from the last hearth onto the inclined bottom 26 of the furnace Hi. It isthen conveyed by any suitable device, such as a bucket elevator 29, into a furnace 30 to which air is admitted through tuyeres 3
  • the coke is thus burned oif the granular material as in a powdered coal furnace.
  • the hot gases from this furnace may be passed through a tube still 32 in which the petroleum residue, passed from reservoir 33 by pump 34, is preheated.
  • the hot gases then pass to the stack through a suitable outlet 35.
  • the vapors from the top of the cracking tower 35 are passed through condenser 39 into receiver 40.
  • the granular material from which the coke has been burned in the furnace 30 passes into the top of a tower 36 which is provided with suitable bailles 31, for causing the granular material to take a zigzag path through the tower.
  • the vapors from the cokingoperation in the furnace l pass through an elbow 38 into the bottom of the tower 36, and thus rise countercurrent to the descending granularmaterial in the tower.
  • This granular material, as it enters the top of the tower, is so hot that it produces vapor phase cracking of the vapors ascending through the tower.
  • the granular material is introduced at the top of the tower 36 at a temperature of about 1200-1600 F., and enters the furnace It) at a temperature of about 1000-1400 F.
  • heat from a suitable external source may be added to the granular material while it rests on the shelves I l.
  • the petroleum residue may be preheated in the tube still 32 to any desired temperature below coking temperature, for instance to 750 F.
  • an infusible catalytic material such as ground bauxite.
  • bauxite a catalytic material which has a catalytic effeet in the cracking of petroleum hydrocarbons are known.
  • inert granular material such as sand or coke.
  • the temperature of the material in cracking stage should be about 250 F. higher than in the case where a catalytic substance is used. It is also possible to activate such inert materials by absorbing catalytic substances on their surfaces.
  • granular as used herein, 'does not mean that the particles are very fine, but includes material the particles of which range from pea size to -60 mesh. For the cracking step the smaller sizes are advantageous but I prefer to use larger sizes inasmuch as these are better adapted for use in the coking stage of my process.
  • tar as used herein, includes petroleum residues, pressure tars, coal tars, and other similar liquid or liqueflable tarry materials which yield hydrocarbon vapors and coke on heating, whatever their source.
  • My process has a number of advantages: By passing the granular, heat-carrying material countercurrent to the vapors, the vapor phase cracking can be uniformly controlled. When a catalyst is employed its effectiveness does not vary during its contact with the vapors. The process does not have to be interrupted to recondition the catalyst. By operating as described, the granular material may be employed at the desired high temperature during the vapor phase cracking, and the rate of flow may be adJusted so that the desired amount :of heat is supplied to the liquid phase coking stage.” In this manher, the temperatures in the liquid phase treat ment can be controlled so that they are sumciently high to coke the petroleum residue or the like.
  • the method of coking tar and cracking the hydrocarbon vapors produced which comprises continuously passing a granular heating medium countercurrent to such vapors, continuously passing the hot granular heating medium from the previous step onto a bed of such medium, spraying tar onto said bed, agitating the bed to keep it in loose condition, and passing the vapors produced from the tar to the first step recited.
  • Method of treating tar which comprises continuously advancing and agitating a bed of hot granular material, continuously depositing tar on said granular material to coke the tar and produce vapors, withdrawing coke-coated granular material thus produced and burning same, and continuously passing said vapors countercurrent to the thus heated granular material prior to depositing the tar thereon.
  • Method of treating tar which comprises depositing the tar on hot granular catalytic material whereby part of the tar is converted to vapors and part to coke, rabbling the bed to keep it in loose condition, withdrawing catalytic material coated with coke, burning the coke oi! said material, using the hot gases produced in the burning operation to preheat the tar, and passing the hot catalytic material countercurrent to the vapors from the coking operation prior to depositing tar on said catalytic material.
  • the method of coking tar and cracking the vapors thus produced in two stages which comprises heating granular catalytic material to a temperature sufllcient to crack hydrocarbon vspors and well above the temperature necessary to coke tar, feeding said hot catalytic material in a continuous stream onto a bed containing similar material, depositing tar on the hot surface of said bed to convert the tar into vapors and coke, keeping the surface of the bed in a loose condition, cracking the vapors by passing them countercurrent to the stream or hot granular material, condensing the cracked vapors thus produced and withdrawing from the bed catalytic material coated with coke.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Catalysts (AREA)

Description

y 1944- M. H. TUTTLE 2,348,699
METHOD OF CRACKING HYDROGARBQN VAPORS Filed May 22, 1941 INVENTOR ATTORNEY Patented May 9, 1944 METHOD OF CRACKING HYDROCABBON VAPORS Malcolm H. Tuttle, New Rochelle, N. Y., assignor to Max B. Miller & 00., Inc., New York, N. Y., a
corporation of Delaware Application May 22, 1941, Serial No. 394,657
4 Claims.
This invention relates to a method of cracking hydrocarbon vapors and producing such vapors from petroleum residues or the like.
It has heretofore been-proposed to distill petroleum residues and then heat the resulting vapors to high temperature to cause cracking. One of the disadvantages of this method is that carbon forms on the heating surfaces of the cracking apparatus. Moreover, if the distillation is carried too far a crust of carbon builds up in the tubes or on the heating surfaces of the still. This crust is very hard to remove. If the distillation is not carried to completion there remains a heavy tar which is a by-product of low value.
In order to avoid the deposition of carbon in the cracking apparatus it has been proposed to pass the distilled vapors through a mass of catalytic material retained in a suitable cracking chamber. In this procedure, the aifectiveness of the catalyst is continuously changing as the cracking operation continues. Hence, the rate of feed of the vapors must be varied to make the best use of the catalyst and after a time the catalyst must be reactivated. Although this procedure is an improvement over the previous method of cracking by heat alone, it does not obviate the aforementioned disadvantage in the distillation step.
In accordance with the invention, petroleum residues or tars are sprayed onto loose, granular material heated to the proper temperature, and the resulting vapors are then passed countercurrent to a stream of the hot granular material. The hot granular material which serves to heat and. crack the vapors in this second stage is then used as a medium on which the petroleum residue or the like is deposited in the first stage in order to distill off vapors and convert the rest of the petroleum residue to coke. In order to reheat and revivify the catalyst the coke-coated catalyst is withdrawn from the coking stage and is burned in a suitable furnace, the hot gases from the furnace being used to preheat the petroleum residue which is fed to the coking stage. In this way, the effectiveness of the catalyst remains constant during the cracking opmethod is illustrated diagrammatically in the accompanying drawing.
In the drawing there is shown at III a still which includes a number of shelves ll having openings l2, l3 disposed alternately near the center and near the outside wall of the still. In the center of the still there is a rotatinghousing M in which is mounted a pipe carrying horizontal arms IS. The pipe 15 is connected through a suitable coupling I! to a pipe l8 through which petroleum residues or tars are supplied. The arms l6 are adapted to spray petroleum residues through ports IS in the rear faces of the arms as they rotate (in a clockwise direction, looking down). The arms l6 also serve as rabble arms, and for this purpose are provided with projections or teeth which agitate the granular material and thus prevent the particles from sticking together. This raking action rearranges the particles so as to obtain maximum surface contact with the tar. The member I4 and arms I6 may be rotated in any convenient manner, for instance by means of a motor 2| and bevel gearing 22, 23.
Granular material 24 is introduced into the still l0 through an opening 25 in the top. This granular material falls onto the upper hearth of the still and is agitated by the rabble arms I 6, which feed it continuously toward the central opening l2 in this hearth, and thence along the other hearths of the furnace. The petroleum residue or the like is sprayed onto the granular material which is hot, preferably between 900 and 1400 F. The heat thus transferred to the petroleum residue or the like converts it into vapors and coke. Reference is made to my copending application Serial No. 394,658, filed May 22, 1941, now U. S. Patent No. 2,314,112, issued March 16, 1943, for further details in regard to the coking stage.
The granular material coated with coke drops from the last hearth onto the inclined bottom 26 of the furnace Hi. It isthen conveyed by any suitable device, such as a bucket elevator 29, into a furnace 30 to which air is admitted through tuyeres 3|. The coke is thus burned oif the granular material as in a powdered coal furnace. The hot gases from this furnace may be passed through a tube still 32 in which the petroleum residue, passed from reservoir 33 by pump 34, is preheated. The hot gases then pass to the stack through a suitable outlet 35. The vapors from the top of the cracking tower 35 are passed through condenser 39 into receiver 40.
The granular material from which the coke has been burned in the furnace 30 passes into the top of a tower 36 which is provided with suitable bailles 31, for causing the granular material to take a zigzag path through the tower. The vapors from the cokingoperation in the furnace l pass through an elbow 38 into the bottom of the tower 36, and thus rise countercurrent to the descending granularmaterial in the tower. This granular material, as it enters the top of the tower, is so hot that it produces vapor phase cracking of the vapors ascending through the tower. Advantageously, the granular material is introduced at the top of the tower 36 at a temperature of about 1200-1600 F., and enters the furnace It) at a temperature of about 1000-1400 F. If desired, heat from a suitable external source (not shown) may be added to the granular material while it rests on the shelves I l. The petroleum residue may be preheated in the tube still 32 to any desired temperature below coking temperature, for instance to 750 F. By thus correlating the temperature of the granular material which is introduced into the top of the tower 36 and the rate of vaporization in the still l0, both the coking and cracking operations can be carried out efficiently.
As the granular material for use in accordance with the present invention I prefer to employ an infusible catalytic material such as ground bauxite. It will be understood that other catalytic materials may be employed instead of bauxite; many such substances which have a catalytic effeet in the cracking of petroleum hydrocarbons are known. In some cases, satisfactory results may be obtained by the use of inert granular material, such as sand or coke. In this case the temperature of the material in cracking stage should be about 250 F. higher than in the case where a catalytic substance is used. It is also possible to activate such inert materials by absorbing catalytic substances on their surfaces. When an incombustible granular material is employed the deposit of coke on this material results in a material which can be readily burned in ordinary powdered coal furnaces, additional heat being supplied if the coke deposit is insuflicient, when burned, to raise the temperature of the granular material sufliciently for use in the cracking stage. When coke is used as the granular material it is only partially burned in furnace 3|] and any excess not recycled may be withdrawn and sold as a by-product;
The term granular," as used herein, 'does not mean that the particles are very fine, but includes material the particles of which range from pea size to -60 mesh. For the cracking step the smaller sizes are advantageous but I prefer to use larger sizes inasmuch as these are better adapted for use in the coking stage of my process. The term tar, as used herein, includes petroleum residues, pressure tars, coal tars, and other similar liquid or liqueflable tarry materials which yield hydrocarbon vapors and coke on heating, whatever their source.
My process has a number of advantages: By passing the granular, heat-carrying material countercurrent to the vapors, the vapor phase cracking can be uniformly controlled. When a catalyst is employed its effectiveness does not vary during its contact with the vapors. The process does not have to be interrupted to recondition the catalyst. By operating as described, the granular material may be employed at the desired high temperature during the vapor phase cracking, and the rate of flow may be adJusted so that the desired amount :of heat is supplied to the liquid phase coking stage." In this manher, the temperatures in the liquid phase treat ment can be controlled so that they are sumciently high to coke the petroleum residue or the like.
The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention, in the use of such terms and expressions, of excluding any equivalents of the features shown and described, or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed.
What I claim is:
1. The method of coking tar and cracking the hydrocarbon vapors produced which comprises continuously passing a granular heating medium countercurrent to such vapors, continuously passing the hot granular heating medium from the previous step onto a bed of such medium, spraying tar onto said bed, agitating the bed to keep it in loose condition, and passing the vapors produced from the tar to the first step recited.
2. Method of treating tar which comprises continuously advancing and agitating a bed of hot granular material, continuously depositing tar on said granular material to coke the tar and produce vapors, withdrawing coke-coated granular material thus produced and burning same, and continuously passing said vapors countercurrent to the thus heated granular material prior to depositing the tar thereon.
3. Method of treating tar which comprises depositing the tar on hot granular catalytic material whereby part of the tar is converted to vapors and part to coke, rabbling the bed to keep it in loose condition, withdrawing catalytic material coated with coke, burning the coke oi! said material, using the hot gases produced in the burning operation to preheat the tar, and passing the hot catalytic material countercurrent to the vapors from the coking operation prior to depositing tar on said catalytic material.
4. The method of coking tar and cracking the vapors thus produced in two stages which comprises heating granular catalytic material to a temperature sufllcient to crack hydrocarbon vspors and well above the temperature necessary to coke tar, feeding said hot catalytic material in a continuous stream onto a bed containing similar material, depositing tar on the hot surface of said bed to convert the tar into vapors and coke, keeping the surface of the bed in a loose condition, cracking the vapors by passing them countercurrent to the stream or hot granular material, condensing the cracked vapors thus produced and withdrawing from the bed catalytic material coated with coke.
MALCOLM H. TU'I'ILE.
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Cited By (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2418890A (en) * 1943-08-13 1947-04-15 Standard Oil Dev Co Stripping of spent catalyst particles in the catalytic conversion of hydrocarbons
US2419519A (en) * 1945-07-27 1947-04-22 Socony Vacuum Oil Co Inc Conversion of hydrocarbons
US2419517A (en) * 1945-07-27 1947-04-22 Socony Vacuum Oil Co Inc Conversion of hydrocarbons
US2425960A (en) * 1943-03-29 1947-08-19 Phillips Petroleum Co Process for hydrocarbon conversion
US2428532A (en) * 1943-05-03 1947-10-07 Phillips Petroleum Co Catalytic hydrocarbon conversion process in the presence of steam
US2432644A (en) * 1943-07-31 1947-12-16 Universal Oil Prod Co Catalytic conversion of hydrocarbons
US2436464A (en) * 1946-06-04 1948-02-24 Edward M Van Dornick Fluid catalytic cracking
US2458109A (en) * 1945-07-27 1949-01-04 Socony Vacuum Oil Co Inc Conversion of hydrocarbons
US2469332A (en) * 1946-06-12 1949-05-03 Socony Vacuum Oil Co Inc Method for conversion of hydrocarbons
US2482138A (en) * 1947-06-24 1949-09-20 Lummus Co Reactor for thermal conversion of hydrocarbons
US2482137A (en) * 1945-02-13 1949-09-20 Lummus Co Process and apparatus for converting hydrocarbons
US2489628A (en) * 1946-01-12 1949-11-29 Socony Vacuum Oil Co Inc Cracking process for the production of olefins from hydrocarbons
US2490975A (en) * 1946-09-19 1949-12-13 Phillips Petroleum Co Catalytic conversion of hydrocarbons
US2499304A (en) * 1946-04-11 1950-02-28 Socony Vacuum Oil Co Inc Method and apparatus for hydrocarbon conversion
US2508292A (en) * 1945-04-21 1950-05-16 Pure Oil Co Sulfur vaporization
US2519340A (en) * 1944-03-23 1950-08-22 Babcock & Wilcox Co Process for the heat-treatment of carbon-containing feed stock
US2526696A (en) * 1946-03-02 1950-10-24 Lummus Co Process for the simultaneous production of coke and gaseous unsaturated hydrocarbonsand apparatus therefor
US2534752A (en) * 1947-06-21 1950-12-19 Sinclair Refining Co Process for the catalytic conversion of hydrocarbons
US2547015A (en) * 1947-11-28 1951-04-03 Houdry Process Corp Process for the conversion of hydrocarbons in the presence of a solid particulate contact material, utilizing a molten metal as the conveying medium
US2561334A (en) * 1948-01-22 1951-07-24 Lummus Co Method of hydrocarbon conversion to lower boiling hydrocarbons and coke
US2561419A (en) * 1945-12-12 1951-07-24 Lummus Co Process for producing gas from oil
US2574489A (en) * 1947-12-19 1951-11-13 Houdry Process Corp Process of converting hydrocarbon material
US2600078A (en) * 1948-08-25 1952-06-10 Lummus Co Heat transfer pebble
US2606861A (en) * 1949-03-10 1952-08-12 Socony Vacuum Oil Co Inc Hydrocarbon conversion process
US2609332A (en) * 1948-08-25 1952-09-02 Lummus Co Hydrocarbon conversion
US2717865A (en) * 1951-05-17 1955-09-13 Exxon Research Engineering Co Coking of heavy hydrocarbonaceous residues
US2735880A (en) * 1956-02-21 Pebble heat exchanger and process
US2798029A (en) * 1952-10-07 1957-07-02 Socony Mobil Oil Co Inc Process for hydrocarbon conversion
US2867580A (en) * 1956-05-11 1959-01-06 Union Oil Co Hydrocarbon conversion process and apparatus
DE974350C (en) * 1945-01-03 1960-12-01 Metallgesellschaft Ag Process for cracking oils, tars or similar hydrocarbons in the gas phase
US20220033714A1 (en) * 2020-07-28 2022-02-03 Saudi Arabian Oil Company Methods and apparatuses for processing hydrocarbons to produce light olefins

Cited By (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2735880A (en) * 1956-02-21 Pebble heat exchanger and process
US2425960A (en) * 1943-03-29 1947-08-19 Phillips Petroleum Co Process for hydrocarbon conversion
US2428532A (en) * 1943-05-03 1947-10-07 Phillips Petroleum Co Catalytic hydrocarbon conversion process in the presence of steam
US2432644A (en) * 1943-07-31 1947-12-16 Universal Oil Prod Co Catalytic conversion of hydrocarbons
US2418890A (en) * 1943-08-13 1947-04-15 Standard Oil Dev Co Stripping of spent catalyst particles in the catalytic conversion of hydrocarbons
US2519340A (en) * 1944-03-23 1950-08-22 Babcock & Wilcox Co Process for the heat-treatment of carbon-containing feed stock
DE974350C (en) * 1945-01-03 1960-12-01 Metallgesellschaft Ag Process for cracking oils, tars or similar hydrocarbons in the gas phase
US2482137A (en) * 1945-02-13 1949-09-20 Lummus Co Process and apparatus for converting hydrocarbons
US2508292A (en) * 1945-04-21 1950-05-16 Pure Oil Co Sulfur vaporization
US2458109A (en) * 1945-07-27 1949-01-04 Socony Vacuum Oil Co Inc Conversion of hydrocarbons
US2419519A (en) * 1945-07-27 1947-04-22 Socony Vacuum Oil Co Inc Conversion of hydrocarbons
US2419517A (en) * 1945-07-27 1947-04-22 Socony Vacuum Oil Co Inc Conversion of hydrocarbons
US2561419A (en) * 1945-12-12 1951-07-24 Lummus Co Process for producing gas from oil
US2489628A (en) * 1946-01-12 1949-11-29 Socony Vacuum Oil Co Inc Cracking process for the production of olefins from hydrocarbons
US2526696A (en) * 1946-03-02 1950-10-24 Lummus Co Process for the simultaneous production of coke and gaseous unsaturated hydrocarbonsand apparatus therefor
US2499304A (en) * 1946-04-11 1950-02-28 Socony Vacuum Oil Co Inc Method and apparatus for hydrocarbon conversion
US2436464A (en) * 1946-06-04 1948-02-24 Edward M Van Dornick Fluid catalytic cracking
US2469332A (en) * 1946-06-12 1949-05-03 Socony Vacuum Oil Co Inc Method for conversion of hydrocarbons
US2490975A (en) * 1946-09-19 1949-12-13 Phillips Petroleum Co Catalytic conversion of hydrocarbons
US2534752A (en) * 1947-06-21 1950-12-19 Sinclair Refining Co Process for the catalytic conversion of hydrocarbons
US2482138A (en) * 1947-06-24 1949-09-20 Lummus Co Reactor for thermal conversion of hydrocarbons
US2547015A (en) * 1947-11-28 1951-04-03 Houdry Process Corp Process for the conversion of hydrocarbons in the presence of a solid particulate contact material, utilizing a molten metal as the conveying medium
US2574489A (en) * 1947-12-19 1951-11-13 Houdry Process Corp Process of converting hydrocarbon material
US2561334A (en) * 1948-01-22 1951-07-24 Lummus Co Method of hydrocarbon conversion to lower boiling hydrocarbons and coke
US2600078A (en) * 1948-08-25 1952-06-10 Lummus Co Heat transfer pebble
US2609332A (en) * 1948-08-25 1952-09-02 Lummus Co Hydrocarbon conversion
US2606861A (en) * 1949-03-10 1952-08-12 Socony Vacuum Oil Co Inc Hydrocarbon conversion process
US2717865A (en) * 1951-05-17 1955-09-13 Exxon Research Engineering Co Coking of heavy hydrocarbonaceous residues
US2798029A (en) * 1952-10-07 1957-07-02 Socony Mobil Oil Co Inc Process for hydrocarbon conversion
US2867580A (en) * 1956-05-11 1959-01-06 Union Oil Co Hydrocarbon conversion process and apparatus
US20220033714A1 (en) * 2020-07-28 2022-02-03 Saudi Arabian Oil Company Methods and apparatuses for processing hydrocarbons to produce light olefins

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