[go: up one dir, main page]

US2426848A - Cracking hydrocarbons in the presence of granular coke - Google Patents

Cracking hydrocarbons in the presence of granular coke Download PDF

Info

Publication number
US2426848A
US2426848A US448475A US44847542A US2426848A US 2426848 A US2426848 A US 2426848A US 448475 A US448475 A US 448475A US 44847542 A US44847542 A US 44847542A US 2426848 A US2426848 A US 2426848A
Authority
US
United States
Prior art keywords
bed
coke
hydrocarbons
fractions
cracking
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US448475A
Inventor
Malcolm H Tuttle
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Max B Miller & Co Inc
Original Assignee
Max B Miller & Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Max B Miller & Co Inc filed Critical Max B Miller & Co Inc
Priority to US448475A priority Critical patent/US2426848A/en
Application granted granted Critical
Publication of US2426848A publication Critical patent/US2426848A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S585/00Chemistry of hydrocarbon compounds
    • Y10S585/909Heat considerations
    • Y10S585/911Heat considerations introducing, maintaining, or removing heat by atypical procedure

Definitions

  • This invention relates to the refining of petroleum and aims to provide an improved method of cracking hydrocarbons.
  • Another process which has been used to some extent involves spraying petroleum hydrocarbons upon a bed of coke which is heated from below.
  • the bed upon which the petroleum is deposited becomes, after a time, a dense mass so that it is necessary to discontinue operations in order to remove the bed and'start afresh.
  • the volatile fractions tend to vaporize as soon as they are heated to their boiling points and consequently may fail to reach the high temperature of the coke bed which is necessary for the production of any appreciable quantity of aromatics or unsaturates.
  • hydrocarbons in the vapor phase may be cracked continuously to yield a high percentage of the aromatics and unsaturates.
  • hydrocarbons are introduced into a deep incandescent bed of loose granular coke at a point spaced below the top of the bed so that they are forced to flow through a substantial portion of the bed.
  • the desired temperature of the bed is maintained by burning coke at the bottom of the bed and depletion of the bed is prevented by coking liquid hydrocarbons at the top of the bed.
  • the apparatus illustrated in the drawing includes a tank 4 from which the charging stock is delivered, by means of pump 5 and conduit 6, to heater 1 and thence to flash pot 8 where volatile fractions of the stock are distilled mi.
  • the volatilization of those fractions may be increased by steam delivered to flash pot 8 through pipe 9 controlled by valve II]. It is of importance that this distillation be carried out at a temperature which is less than the coking temperature of the stock, and which may be in the neighborhood of 900 F.
  • the vaporized fractions are introduced into a deep bed It! of loose granular coke contained in chamber I5 and rendered incandescent by burning coke at the bottom of the bed.
  • the supply of coke in chamber I5 is maintained by feeding the liquid fractions I2 to the top of bed I4 where they are coked. If the quantity of the liquid fractions I2 in flash pot 8 should be greater than is required for this coking operation, the excess may be recycled through heater I by means of pump I1 and conduit I8.
  • the chamber I5 is of the type illustrated and described in my co-pending applications, Serial No. 401,701, filed July 10, 1941 (which issued as Patent No. 2,323,501 on July 6, 1943), and Serial No. 407,409, filed August 19, 1941.
  • the walls 20 are composed of a refractory material and are provided with inlets 2I for the admission of air to support combustion at the bottom of the bed I 4.
  • Inlets 22 are provided for the admission of steam or natural gas, or both, to prevent the temperature in the combustion zone from becoming higher than is desired.
  • the liquid fractions I2 are fed to the chamber l5 by means of pump 23 and conduit 24 which communicates with hollow shaft 25.
  • Radial arms 26 are fixed to the hollow shaft 25 and are provided with orifices 21 through which the liquid fractions I2 are fed to the top of bed l4 where they are coked.
  • the shaft 25 is mounted for rotary movement and is driven as by means of pulley 28 and belt 29.
  • are attached to arms 26 and project downwardly into the upper portion of coke bed I4 so that they rake the upper portion of the bed when shaft 25 is rotated and prevent the formation of a crust.
  • the speed of rotation of shaft 25 and the rate at which liquid fractions I2 are fed through orifices 21 are such that the liquid is always sprayed upon a freshly rabbled portion of the surface of bed I4, which is not again rabbled until substantially all of those liquid fractions have been coked.
  • the vaporized fractions from flash pot 8 are introduced into the bed l4 by means of conduit 34 and annular conduit 35 with which a series of inlets 36 communicate. Two of the inlets 36 are shown in the section which is illustrated in the drawing. Those inlets 36 are spaced above the combustion zone and well below the upper portion of bed 14 so that the vaporized hydrocarbons which are introduced into bed l4 through inlets 36 are caused to flow with the hot gases of combustion through a substantial portion of the incandescent bed and through the cokin zone at the top of the bed. Any ash or excess coke which is formed may be discharged from chamber l to car 31 through valve 38.
  • the vapors are withdrawn from the top of chamber l5 through conduit 40 to fractionating column 4
  • the vapors and fixed gases pass through the fractionating column 41 into a condenser 44 and thence into a separator 45 from which the low boiling hydrocarbons and fixed gases are exhausted through a line 46 to a conventional recovery system (not shown) for the separation and recovery of ethylene, butylene, butadiene, etc.
  • the con. densate 41 may be passed to storage by means of pump 48 and line 49 controlled by valve 50, or a portion of it may be returned to the fractionating column 4
  • I start operations by introducing a deep bed of granular coke into the chamber I5.
  • granular coke I mean loose, hard particles of carbonaceous material but I do not mean that the coke is necessarily very fine. I have found that granules ranging in size from /1 inch to /1. inch are very satisfactory.
  • new coke is formed and gradually descends, together with carbon formed during the cracking operation, into the combustion zone and the bed 14 remains open for the passage of gas and vapor.
  • the method of cracking hydrocarbons in the vapor phase which comprises distilling from petroleum stock fractions which volatilize below the coking temperature of the stock, maintaining a deep incandescent bed of loose granular coke by burning coke at the bottom of the bed and coking the liquid residue of said stock at the top of the bed, and introducing the vaporized fractions of said stock into the incandescent bed at a point spaced below its top so that they are caused to flow through a substantial portion of said bed.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Description

P 1947- M. H. TUTTLE CRACKING HYDROCARBONS IN THE PRESENCE OF GRANULAR COKE Filed June 25, 1942 IN'VENTOR fizzaz/v AK Era ATTO R N EYS \h Elli Patented Sept. 2, 1947 CRACKING HYDROCARBONS IN THE PRES- ENCE F GRANULAR COKE Malcolm H. Tuttle, New Rochelle, N. Y., assignor to Max B. Miller & 00., Inc., New York, N. Y., a corporation of Delaware Application June 25, 1942, Serial No. 448,475
1 Claim. 1
This invention relates to the refining of petroleum and aims to provide an improved method of cracking hydrocarbons.
It is a particular object of my invention to provide a method of cracking hydrocarbons in the vapor phase so that a high yield of aromatics (benzene, toluol and styrene) and of unsaturates (ethylene, butylene and butadiene) is obtained.
In the refining of petroleum is has long been common practice to crack petroleum hydrocarbons, usually under pressure, in stills having metal walls through which heat is supplied. If the cracking be continued to the extent necessary to produce the desired high yield there is deposited on the walls of the still a hard, tenacious crust which builds up in thickness until it becomes necessary to interrupt the cracking operations and remove the crust from the walls of the still. This is a troublesome and expensive operation. When the cracking is not continued to the end point, there remains a by-product of low value commonly known as pressure tar.
Another process which has been used to some extent involves spraying petroleum hydrocarbons upon a bed of coke which is heated from below. The bed upon which the petroleum is deposited becomes, after a time, a dense mass so that it is necessary to discontinue operations in order to remove the bed and'start afresh. Furthermore, the volatile fractions tend to vaporize as soon as they are heated to their boiling points and consequently may fail to reach the high temperature of the coke bed which is necessary for the production of any appreciable quantity of aromatics or unsaturates.
I have discovered that hydrocarbons in the vapor phase may be cracked continuously to yield a high percentage of the aromatics and unsaturates. In accordance with my invention, hydrocarbons are introduced into a deep incandescent bed of loose granular coke at a point spaced below the top of the bed so that they are forced to flow through a substantial portion of the bed. The desired temperature of the bed is maintained by burning coke at the bottom of the bed and depletion of the bed is prevented by coking liquid hydrocarbons at the top of the bed.
Other features, objects and advantages of my invention will in part be pointed out and in part become apparent in connection with the following detailed description of a mode of practicing my invention, reference being made to the accompanying drawing which shows, somewhat diagrammatically, an apparatus for carrying out my method.
The apparatus illustrated in the drawing includes a tank 4 from which the charging stock is delivered, by means of pump 5 and conduit 6, to heater 1 and thence to flash pot 8 where volatile fractions of the stock are distilled mi. The volatilization of those fractions may be increased by steam delivered to flash pot 8 through pipe 9 controlled by valve II]. It is of importance that this distillation be carried out at a temperature which is less than the coking temperature of the stock, and which may be in the neighborhood of 900 F.
The vaporized fractions are introduced into a deep bed It! of loose granular coke contained in chamber I5 and rendered incandescent by burning coke at the bottom of the bed. The supply of coke in chamber I5 is maintained by feeding the liquid fractions I2 to the top of bed I4 where they are coked. If the quantity of the liquid fractions I2 in flash pot 8 should be greater than is required for this coking operation, the excess may be recycled through heater I by means of pump I1 and conduit I8.
The chamber I5 is of the type illustrated and described in my co-pending applications, Serial No. 401,701, filed July 10, 1941 (which issued as Patent No. 2,323,501 on July 6, 1943), and Serial No. 407,409, filed August 19, 1941. The walls 20 are composed of a refractory material and are provided with inlets 2I for the admission of air to support combustion at the bottom of the bed I 4. Inlets 22 are provided for the admission of steam or natural gas, or both, to prevent the temperature in the combustion zone from becoming higher than is desired. The liquid fractions I2 are fed to the chamber l5 by means of pump 23 and conduit 24 which communicates with hollow shaft 25. Radial arms 26 are fixed to the hollow shaft 25 and are provided with orifices 21 through which the liquid fractions I2 are fed to the top of bed l4 where they are coked.
The shaft 25 is mounted for rotary movement and is driven as by means of pulley 28 and belt 29. Rabbling fingers 3| are attached to arms 26 and project downwardly into the upper portion of coke bed I4 so that they rake the upper portion of the bed when shaft 25 is rotated and prevent the formation of a crust. The speed of rotation of shaft 25 and the rate at which liquid fractions I2 are fed through orifices 21 are such that the liquid is always sprayed upon a freshly rabbled portion of the surface of bed I4, which is not again rabbled until substantially all of those liquid fractions have been coked.
The vaporized fractions from flash pot 8 are introduced into the bed l4 by means of conduit 34 and annular conduit 35 with which a series of inlets 36 communicate. Two of the inlets 36 are shown in the section which is illustrated in the drawing. Those inlets 36 are spaced above the combustion zone and well below the upper portion of bed 14 so that the vaporized hydrocarbons which are introduced into bed l4 through inlets 36 are caused to flow with the hot gases of combustion through a substantial portion of the incandescent bed and through the cokin zone at the top of the bed. Any ash or excess coke which is formed may be discharged from chamber l to car 31 through valve 38.
The vapors are withdrawn from the top of chamber l5 through conduit 40 to fractionating column 4| where the higher boiling fractions may be condensed and then recycled through pump 42 and conduit 18 to the heater I where such condensate mixes with the charging stock. The vapors and fixed gases pass through the fractionating column 41 into a condenser 44 and thence into a separator 45 from which the low boiling hydrocarbons and fixed gases are exhausted through a line 46 to a conventional recovery system (not shown) for the separation and recovery of ethylene, butylene, butadiene, etc. The con. densate 41 may be passed to storage by means of pump 48 and line 49 controlled by valve 50, or a portion of it may be returned to the fractionating column 4| through line 5|.
In carrying out my method, I start operations by introducing a deep bed of granular coke into the chamber I5. By granular coke I mean loose, hard particles of carbonaceous material but I do not mean that the coke is necessarily very fine. I have found that granules ranging in size from /1 inch to /1. inch are very satisfactory. As the operations continue, new coke is formed and gradually descends, together with carbon formed during the cracking operation, into the combustion zone and the bed 14 remains open for the passage of gas and vapor.
Operations are conducted so that the temperature in the combustion zone ranges from 2800 to 3200 F.; the temperature at the upper portion of the bed ranges from between 1100" to 1400 F.; and the temperature at the portion of the bed where the vaporized hydrocarbons are admitted ranges from 1400 to 1800 F. The higher temperatures are preferred. The vaporized hydrocarbons flow upwardly through a substantial portion of incandescent bed l4 with the hot gases of combustion which provide a non-oxidizing atmosphere. As a consequence, those hydrocarbons attain the elevated temperatures at which they are cracked to produce a high percentage of arcmatics (benzene, toluol and styrene) and of unsaturates (ethylene, butylene and butadiene).
The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention in th 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:
The method of cracking hydrocarbons in the vapor phase which comprises distilling from petroleum stock fractions which volatilize below the coking temperature of the stock, maintaining a deep incandescent bed of loose granular coke by burning coke at the bottom of the bed and coking the liquid residue of said stock at the top of the bed, and introducing the vaporized fractions of said stock into the incandescent bed at a point spaced below its top so that they are caused to flow through a substantial portion of said bed.
MALCOLM H. TUTILE.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,247,671 Ha11 Nov. 27, 1917 1,357,277 Day Nov. 2, 1940 1,490,862 Smith Apr. 15, 1924 1,643,401 Yard Sept. 27, 1927 1,714,453 Schwarz May 21, 1929 1,832,975 Fairchild Nov. 24, 1931 2,194,574 Snyder Mar. 26, 1940 2,114,416 Donnelly Apr. 19, 1938 2,211,999 Alther Aug. 20, 1940 2,323,501 Tuttle July 6, 1943
US448475A 1942-06-25 1942-06-25 Cracking hydrocarbons in the presence of granular coke Expired - Lifetime US2426848A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US448475A US2426848A (en) 1942-06-25 1942-06-25 Cracking hydrocarbons in the presence of granular coke

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US448475A US2426848A (en) 1942-06-25 1942-06-25 Cracking hydrocarbons in the presence of granular coke

Publications (1)

Publication Number Publication Date
US2426848A true US2426848A (en) 1947-09-02

Family

ID=23780445

Family Applications (1)

Application Number Title Priority Date Filing Date
US448475A Expired - Lifetime US2426848A (en) 1942-06-25 1942-06-25 Cracking hydrocarbons in the presence of granular coke

Country Status (1)

Country Link
US (1) US2426848A (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2445092A (en) * 1946-08-02 1948-07-13 Socony Vacuum Oil Co Inc Process and apparatus for heat transfer with granular solids
US2526696A (en) * 1946-03-02 1950-10-24 Lummus Co Process for the simultaneous production of coke and gaseous unsaturated hydrocarbonsand apparatus therefor
US2600078A (en) * 1948-08-25 1952-06-10 Lummus Co Heat transfer pebble
US2640019A (en) * 1948-06-01 1953-05-26 Union Oil Co Oil-shale eduction apparatus
US2676909A (en) * 1951-11-05 1954-04-27 Phillips Petroleum Co Pebble heating apparatus for carrying out a plurality of processes concomitantly
US2707148A (en) * 1951-02-08 1955-04-26 Houdry Process Corp Process for pyrolytic cracking of hydrocarbons and gasification of coal
US2707702A (en) * 1949-10-15 1955-05-03 Sinclair Refining Co Art of coking
US2719115A (en) * 1950-05-11 1955-09-27 Sinclair Refining Co Method of coking hydrocarbon oils
US2733194A (en) * 1956-01-31 Method of adding liquid feed to a
US2893950A (en) * 1956-06-29 1959-07-07 Phillips Petroleum Co Method and apparatus for feeding fluid reactants to a moving bed of solid contact particles
US2898292A (en) * 1957-11-05 1959-08-04 Socony Mobil Oil Co Inc Method for distributing a vapor-liquid feed and apparatus therefor
US2976132A (en) * 1958-02-10 1961-03-21 Exxon Research Engineering Co Fixed bed type reactor
US3223616A (en) * 1962-10-01 1965-12-14 Huntington Oil Refining Compan Multivapor petroleum refining and apparatus thereof

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1247671A (en) * 1916-05-03 1917-11-27 William Augustus Hall Distillation of heavy oils, oil residues, and bitumens.
US1357277A (en) * 1918-07-27 1920-11-02 Alfred B Adams Process for treatment of hydrocarbon oils
US1490862A (en) * 1923-03-05 1924-04-15 Vergil T Smith Process for distilling and cracking oils
US1643401A (en) * 1924-03-17 1927-09-27 Willis S Yard Process for manufacturing light hydrocarbon liquids
US1714453A (en) * 1925-03-25 1929-05-21 Coal And Oil Products Corp Oil-cracking process
US1832975A (en) * 1926-01-14 1931-11-24 Universal Oil Prod Co Process for hydrocarbon oil conversion
US2114416A (en) * 1934-03-30 1938-04-19 Joseph F Donnelly Process for pyrolysis of liquid hydrocarbons
US2194574A (en) * 1937-06-14 1940-03-26 Fuel Res Dev Corp Process for producing gasoline and gas
US2211999A (en) * 1936-11-30 1940-08-20 Universal Oil Prod Co Process for hydrocarbon oil conversion
US2323501A (en) * 1941-07-10 1943-07-06 Max B Miller & Co Inc Method of distilling petroleum residues or the like

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1247671A (en) * 1916-05-03 1917-11-27 William Augustus Hall Distillation of heavy oils, oil residues, and bitumens.
US1357277A (en) * 1918-07-27 1920-11-02 Alfred B Adams Process for treatment of hydrocarbon oils
US1490862A (en) * 1923-03-05 1924-04-15 Vergil T Smith Process for distilling and cracking oils
US1643401A (en) * 1924-03-17 1927-09-27 Willis S Yard Process for manufacturing light hydrocarbon liquids
US1714453A (en) * 1925-03-25 1929-05-21 Coal And Oil Products Corp Oil-cracking process
US1832975A (en) * 1926-01-14 1931-11-24 Universal Oil Prod Co Process for hydrocarbon oil conversion
US2114416A (en) * 1934-03-30 1938-04-19 Joseph F Donnelly Process for pyrolysis of liquid hydrocarbons
US2211999A (en) * 1936-11-30 1940-08-20 Universal Oil Prod Co Process for hydrocarbon oil conversion
US2194574A (en) * 1937-06-14 1940-03-26 Fuel Res Dev Corp Process for producing gasoline and gas
US2323501A (en) * 1941-07-10 1943-07-06 Max B Miller & Co Inc Method of distilling petroleum residues or the like

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2733194A (en) * 1956-01-31 Method of adding liquid feed to a
US2526696A (en) * 1946-03-02 1950-10-24 Lummus Co Process for the simultaneous production of coke and gaseous unsaturated hydrocarbonsand apparatus therefor
US2445092A (en) * 1946-08-02 1948-07-13 Socony Vacuum Oil Co Inc Process and apparatus for heat transfer with granular solids
US2640019A (en) * 1948-06-01 1953-05-26 Union Oil Co Oil-shale eduction apparatus
US2600078A (en) * 1948-08-25 1952-06-10 Lummus Co Heat transfer pebble
US2707702A (en) * 1949-10-15 1955-05-03 Sinclair Refining Co Art of coking
US2719115A (en) * 1950-05-11 1955-09-27 Sinclair Refining Co Method of coking hydrocarbon oils
US2707148A (en) * 1951-02-08 1955-04-26 Houdry Process Corp Process for pyrolytic cracking of hydrocarbons and gasification of coal
US2676909A (en) * 1951-11-05 1954-04-27 Phillips Petroleum Co Pebble heating apparatus for carrying out a plurality of processes concomitantly
US2893950A (en) * 1956-06-29 1959-07-07 Phillips Petroleum Co Method and apparatus for feeding fluid reactants to a moving bed of solid contact particles
US2898292A (en) * 1957-11-05 1959-08-04 Socony Mobil Oil Co Inc Method for distributing a vapor-liquid feed and apparatus therefor
US2976132A (en) * 1958-02-10 1961-03-21 Exxon Research Engineering Co Fixed bed type reactor
US3223616A (en) * 1962-10-01 1965-12-14 Huntington Oil Refining Compan Multivapor petroleum refining and apparatus thereof

Similar Documents

Publication Publication Date Title
US2426848A (en) Cracking hydrocarbons in the presence of granular coke
US2348699A (en) Method of cracking hydrocarbon vapors
GB617284A (en) Process for producing volatile hydrocarbons from hydrocarbonaceous solids
US2323501A (en) Method of distilling petroleum residues or the like
US2901418A (en) Improved quench oil for high temperature coking of residua
US2852440A (en) Production of aromatics and unsaturated hydrocarbons
US2495613A (en) Method of and apparatus for cracking tarry materials
US2179080A (en) Coking of hydrocarbon oils
US2364492A (en) Method of coking and cracking petroleum residues or the like
US2114416A (en) Process for pyrolysis of liquid hydrocarbons
US1974295A (en) Treatment of hydrocarbon oils
US1568018A (en) Treatment of hydrocarbons
US2366218A (en) Catalytic combination process
US3440163A (en) Coke binder oils from dealkylated condensed aromatic tars
US2899376A (en) Liquid phase - boo
US2005118A (en) Conversion process
US2101641A (en) Method of producing coke
US2073367A (en) Conversion and coking of carbonaceous materials
US2098033A (en) Conversion and coking of hydrocarbons
US2140276A (en) Continuous coking of hydrocarbon oils
US2233951A (en) Process of producing low boiling hydrocarbons
US2255060A (en) Treatment of hydrocarbon and other residues
US2075599A (en) Conversion and coking of hydrocarbon oils
US2108649A (en) Treatment of hydrocarbon oils
US2237414A (en) Process and apparatus for coking hydrocarbon oils