US2624696A - Continuous carbonization of coal and oil mixtures - Google Patents

Continuous carbonization of coal and oil mixtures Download PDF

Info

Publication number
US2624696A
US2624696A US120389A US12038949A US2624696A US 2624696 A US2624696 A US 2624696A US 120389 A US120389 A US 120389A US 12038949 A US12038949 A US 12038949A US 2624696 A US2624696 A US 2624696A
Authority
US
United States
Prior art keywords
coal
coke
line
carbonization
particles
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
US120389A
Inventor
August H Schutte
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.)
CB&I Technology Inc
Original Assignee
Lummus Co
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 Lummus Co filed Critical Lummus Co
Priority to US120389A priority Critical patent/US2624696A/en
Application granted granted Critical
Publication of US2624696A publication Critical patent/US2624696A/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
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B55/00Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material
    • C10B55/02Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material with solid materials
    • C10B55/04Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material with solid materials with moving solid materials
    • C10B55/06Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material with solid materials with moving solid materials according to the "moving bed" type
    • 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
    • Y10S48/00Gas: heating and illuminating
    • Y10S48/04Powdered fuel injection

Definitions

  • This invention relates to an improved method and apparatus for the carbonization of coal in the presence of a continuously moving column of heat-carrying coke.
  • the coke heat-carrying material becomes an ideal circulating medium in which to conduct ccal carbonization, for the petroleum coke has a high density, is substantially non-porous, can be repeatedly recycled with low production of fines, and can be reheated without spalling or other damage. Furthermore, it can be reproduced simultaneously in the system by the mere addition of some residual oil.
  • My invention materially differs from prior attempts to coke coal either by low temperature or by high temperature operations. It it well known that coal when heated passes through a swelling period which has caused objectionable agglomeration and has required tapered vessels, large rams or other extractors, or mechanical agitators for suitable operation. The use of supplementary materials has also been suggested but low temperature coal coke, or char and most forms of petroleum coke are too frangible for effective use.
  • My invention on the other hand is based not only on the use of supplementary coke, but on the use of our previously described dense or equilibrium coke, and in such preponderance that the reaction zone temperatures may be kept closely Within the desired limits to avoid cracking of the vapors.
  • My invention also contemplates ready control of conditions for the optimum yield of valuable products, and the absence of complicated mechanical apparatus heretofore thought necessary to aid the movement of the materials through the reaction zone.
  • the reactor is 2 indicated at Ill. It is an elevated closed vessel which may be structurally mounted on the reheater, a separate sealed vessel indicated at I2. They are connected by transfer line I4 through Vwhich the materials ow by gravity.
  • reheater I 2 At the lower end of reheater I 2 is a line I6 leading to an elevating mechanism I8 which carries material to inlet chamber 20.
  • Line 42 is provided for drawing 01T material from line I6.
  • the elevated material is passed to inlet chamber ZI) which is supplied with an oil inlet line 24 and a coal storage hopper 22.
  • a sealing gas inlet 44 is provided for passing gas to line 23 and valve 25 controls the ow of coal in line 23.
  • Reheater I2 has an upper air or flue gas inlet line 38 and a lower ue gas outlet at 40.
  • the unit is also provided with coke drawofE line 3I leading to separator 33.
  • Product materials from certain operations may be drawn off at 35 while recycled material is passed through line 31, Crusher 39 andline 4I. Suitable valves may be provided in these lines.
  • the unit contains a heat-carrying material, as described in Bowles and Schutte copending application Serial No. 46,168 filed August 25, 1948 which is a rounded, dense, homogeneous petroleum coke produced by the repeated circulation of coke particles through a reactionfchamber similar to that hereinbefore described and to which heavy petroleum residues are applied in liquid form and coked.
  • the coke layers in such case were of the order of 0.001 inch, the density was in excess of 50 lbs. per cu. ft., the crushing strength was approximately 300 lbs. for a 1/2 inch particle, and the particle size range, I find for most effective operation, is from 11g inch major dimension to not above 1%, inch major dimension.
  • hot regenerated heat carrying material such as petroleum coke is passed from the reheating zone by elevating mechanism I8 to inlet chamber 2Q.
  • Simultaneously crushed or ground coal preferably of a size smaller than the average size of the petroleum coke, is passed from hopper 22 through line 23 under the control of valve 25 into inlet chamber 20.
  • Inert sealing gas is passed from line 44 to line 23.
  • the mixing of the coal with preheated circulating coke is done in the free-falling mixing zone 20.
  • the coal is rapidly heated to and passed through its plastic state in this zone of maximum flow turbulence and maximum velocity of motion, thus preventing the formation of harmful agglomerates.
  • Coking of coal as hereinbefore described produces a charred, powdery product. This is separated in, cyclone 38 and is withdrawn through line 32. Vapors are taken oir through line 34.
  • Reheating of the coke of the column is accomplished in the reheater I2 after the coke column passes through transfer line I4 in which it can be purged of all vapors by the use of an inert material such as steam in line 36. Heating may be accomplished by auto-combustion of the coke in which case air or oxygen containing gas is introduced at 38 with the flue gas removed at ⁇ 40. I prefer, however, to use a fuel gas at 38 and radiantly heat the column as it passes through, for usually fuel gas is a less expensive form of heat.
  • 4a petroleum residue may be passed through line 24,- into chamber 20 either simultaneously with the coal orseparately.
  • larger cokeV particles may be produced, which may be used as the heat carrying material.
  • the bed may be built up to any desired size and a constant inventory may be maintained. If it is found that excessive coke is formed, the excess may be drawn Voff at 42.
  • reaction periods of from 30 minutes to several hours may be obtained without excessively high reaction chambers.
  • Such relatively short coking periods may be obtained vbecause the coa-1 is uniformly heated without the necessity for transferring heat through deep layers of coal or coke, as is the case in conventional methods.
  • temperatures in the reactor I are in the order of l000 F. to 1400o F. and I propose to feed from about 2 r up to 6 parts of coke per part of coal feed.
  • the coal may be introduced cold and an excess temperature of the coke will supply all the preheat as well as carbonization heat for the coal.
  • the coal may also be preheated if desirable.
  • high temperature carbonization can also be raccorrrplished in the same apparatus as temperatures of the order of 1800 F. to 21.00 F. can be readily obtained and without damage to the circulating coke.
  • An important feature of my invention is the absence of contaminating ue gas or air in the products of the coal carbonization.
  • the vapors are readily removed from the lower part of reactor I0 through line 28 and passed to a separator such as the cyclone 30 from which char or coal coke is removed in line 32.
  • the vapors leaving at 34 may be condensed in the well known manner to obtain the tars, vapors, etc. characteristic of the carbonization operation.
  • the method of low temperature carbonization ⁇ of volatile coal in the presence of a particle form heated conta-cty mass of granular coke which comprises preheating the particles of saidmass, independently and. simultaneously introducing the coal as particles, said contact coke particles and a liquid oil into a common part of a free-falling zone with intermixing flow turbulence, during which intermiXing the coal is rapidly heated to and passed through its plastic state, thereafter continuously moving the thus intermixed mass in its preheated condition ⁇ downwardly through a reaction zone as an unagitated gravity packed column, mutually adjusting the inlet temperature of said contact particles to the reaction zone, and the rate of introduction of coal and liquid oil to Amaintain a reaction temperature of between about 1000 F.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Coke Industry (AREA)

Description

Van. 6,v 1953 A. H. scHUTTE 2,624,696
CONTINUOUS CARBONIZATION OF COAL AND OIL MIXTURES Filed oct. s, 1949 n l f c' I l 1ct-ss one Patented Jan. 6, 1953 UNITED STATES CNTINUOUS CARBONIZATION F COAL AND OIL MIXTURES August H. Schutte, Hastings-on-Hudson, N. Y., assigner to The Lummus Company, New York, N. Y., a corporation of Delaware Application October 8, 1949, Serial No. 120,389
1 Claim. 1
This invention relates to an improved method and apparatus for the carbonization of coal in the presence of a continuously moving column of heat-carrying coke.
In copending application Serial No. 3,747 (now Patent No. 2,561,334), patented July 24, 1951 of which I am a co-inventor, there is disclosed a unique method and apparatus for reducing heavy oil, tars, and other residuum by the use of a continuous gravity packed, gravity moving column of granular coke. The coke may be heated to any desirable reaction temperature without damage and due to its hardness, it withstands attrition very well. Furthermore, due to the large particle size, which may run from inch to 3A, inch, the resultant forces in the column tends to prevent any adherence between particles at the time the oil passes through the sticky stage just before dry coke is formed. No rabbling, agitation, or mechanical force is necessary to maintain the desired continuous ow.
In the present invention, some of the features of the earlier invention are taken advantage of. The coke heat-carrying material becomes an ideal circulating medium in which to conduct ccal carbonization, for the petroleum coke has a high density, is substantially non-porous, can be repeatedly recycled with low production of fines, and can be reheated without spalling or other damage. Furthermore, it can be reproduced simultaneously in the system by the mere addition of some residual oil.
My invention materially differs from prior attempts to coke coal either by low temperature or by high temperature operations. It it well known that coal when heated passes through a swelling period which has caused objectionable agglomeration and has required tapered vessels, large rams or other extractors, or mechanical agitators for suitable operation. The use of supplementary materials has also been suggested but low temperature coal coke, or char and most forms of petroleum coke are too frangible for effective use.
My invention on the other hand is based not only on the use of supplementary coke, but on the use of our previously described dense or equilibrium coke, and in such preponderance that the reaction zone temperatures may be kept closely Within the desired limits to avoid cracking of the vapors. My invention also contemplates ready control of conditions for the optimum yield of valuable products, and the absence of complicated mechanical apparatus heretofore thought necessary to aid the movement of the materials through the reaction zone.
In the attached drawing, illustrative of a preferred embodiment of my invention, such drawing being a schematic elevation of the reactor, reheater, and attached equipment, the reactor is 2 indicated at Ill. It is an elevated closed vessel which may be structurally mounted on the reheater, a separate sealed vessel indicated at I2. They are connected by transfer line I4 through Vwhich the materials ow by gravity.
At the lower end of reheater I 2 is a line I6 leading to an elevating mechanism I8 which carries material to inlet chamber 20. Line 42 is provided for drawing 01T material from line I6. The elevated material is passed to inlet chamber ZI) which is supplied with an oil inlet line 24 and a coal storage hopper 22. A sealing gas inlet 44 is provided for passing gas to line 23 and valve 25 controls the ow of coal in line 23.
In the lower part of reactor II) there is supplied a product outlet line 28 leading to a cyclone 30. The product is withdrawn at 32 while vapors are removed at 34. A gas sealing line 36 is provided for transfer line I 4. Reheater I2 has an upper air or flue gas inlet line 38 and a lower ue gas outlet at 40.
The unit is also provided with coke drawofE line 3I leading to separator 33. Product materials from certain operations may be drawn off at 35 while recycled material is passed through line 31, Crusher 39 andline 4I. Suitable valves may be provided in these lines.
In operation the unit contains a heat-carrying material, as described in Bowles and Schutte copending application Serial No. 46,168 filed August 25, 1948 which is a rounded, dense, homogeneous petroleum coke produced by the repeated circulation of coke particles through a reactionfchamber similar to that hereinbefore described and to which heavy petroleum residues are applied in liquid form and coked. The coke layers in such case were of the order of 0.001 inch, the density was in excess of 50 lbs. per cu. ft., the crushing strength was approximately 300 lbs. for a 1/2 inch particle, and the particle size range, I find for most effective operation, is from 11g inch major dimension to not above 1%, inch major dimension.
In an operating cycle, hot regenerated heat carrying material such as petroleum coke is passed from the reheating zone by elevating mechanism I8 to inlet chamber 2Q. Simultaneously crushed or ground coal, preferably of a size smaller than the average size of the petroleum coke, is passed from hopper 22 through line 23 under the control of valve 25 into inlet chamber 20. Inert sealing gas is passed from line 44 to line 23.
The mixing of the coal with preheated circulating coke is done in the free-falling mixing zone 20. The coal is rapidly heated to and passed through its plastic state in this zone of maximum flow turbulence and maximum velocity of motion, thus preventing the formation of harmful agglomerates. Y
Coking of coal as hereinbefore described produces a charred, powdery product. This is separated in, cyclone 38 and is withdrawn through line 32. Vapors are taken oir through line 34.
Reheating of the coke of the column is accomplished in the reheater I2 after the coke column passes through transfer line I4 in which it can be purged of all vapors by the use of an inert material such as steam in line 36. Heating may be accomplished by auto-combustion of the coke in which case air or oxygen containing gas is introduced at 38 with the flue gas removed at `40. I prefer, however, to use a fuel gas at 38 and radiantly heat the column as it passes through, for usually fuel gas is a less expensive form of heat.
If it is desired to produce a more agglomerated product, 4a petroleum residue may be passed through line 24,- into chamber 20 either simultaneously with the coal orseparately. Thus larger cokeV particles may be produced, which may be used as the heat carrying material. In this manner, the bed may be built up to any desired size and a constant inventory may be maintained. If it is found that excessive coke is formed, the excess may be drawn Voff at 42.
Alternatively if large amounts of oi1 are admitted at 24 it is possible to control the agglomerati'on and to produce a larger product which maybe removed through line 3l and passed to separator 33. Here the product may be taken off through line 35 and the remainder passed through line 3l to a crusher, if desired, to be recycled through line 4l to the reheater l2.
As the coke is hard and dry and of relatively large size,V and the coal is in crushed or ground sizes, the gravity Ipacked column will move solely by gravity through reactor I9, transfer line ld and reheater l2 `under control of valve 2S at the bottom.
The rate of movement will depend on the coal characteristics but with regulated gravity ow, reaction periods of from 30 minutes to several hours may be obtained without excessively high reaction chambers. Such relatively short coking periods may be obtained vbecause the coa-1 is uniformly heated without the necessity for transferring heat through deep layers of coal or coke, as is the case in conventional methods.
For low temperature carbonization, temperatures in the reactor I are in the order of l000 F. to 1400o F. and I propose to feed from about 2 r up to 6 parts of coke per part of coal feed. The coal may be introduced cold and an excess temperature of the coke will supply all the preheat as well as carbonization heat for the coal. The coal may also be preheated if desirable.
It is of course to be understood that high temperature carbonization can also be raccorrrplished in the same apparatus as temperatures of the order of 1800 F. to 21.00 F. can be readily obtained and without damage to the circulating coke.
An important feature of my invention is the absence of contaminating ue gas or air in the products of the coal carbonization. The vapors are readily removed from the lower part of reactor I0 through line 28 and passed to a separator such as the cyclone 30 from which char or coal coke is removed in line 32. The vapors leaving at 34 may be condensed in the well known manner to obtain the tars, vapors, etc. characteristic of the carbonization operation.
Generally the products of carbonization will correspond with well known practice and they depend on the types of coal treated. However, with more uniform and hence, lower reactor temperatures, there is less tendency for vapor cracking.
Under some conditions, it may be found possible to coke the tar yielded by the coal, particularly with the relatively low temperature operations. In such case the only other products will be the char removed at 32 and the volatile material removed at 34.
While I have shown and described a preferred form of embodiment of my invention, I am aware that modifications may be made thereto which come within the scope and spirit of the description herein and of the claim appended hereinafter.
I claim:
The method of low temperature carbonization `of volatile coal in the presence of a particle form heated conta-cty mass of granular coke, which comprises preheating the particles of saidmass, independently and. simultaneously introducing the coal as particles, said contact coke particles and a liquid oil into a common part of a free-falling zone with intermixing flow turbulence, during which intermiXing the coal is rapidly heated to and passed through its plastic state, thereafter continuously moving the thus intermixed mass in its preheated condition `downwardly through a reaction zone as an unagitated gravity packed column, mutually adjusting the inlet temperature of said contact particles to the reaction zone, and the rate of introduction of coal and liquid oil to Amaintain a reaction temperature of between about 1000 F. and about 1400 F. in said reaction zone below the free-falling zone of intermixing, retaining the coke contact particles with the admixed coal and oil in said column of said reaction zone and without other addition of heat for a time sufficient to complete conversion of the coal and oil to vapors and non-agglomerating particles of dry coke, withdrawing the coke contact particles from the reaction zone by a controlled gravity flow without agitation or application of mechanical force, removing the said vapors and dry coke particles from the lower part of sai-d column prior to the withdrawal of the coke :Contact particles from the reaction zone, sealing the removal of the coke contact particles from the reaction zone against loss of vapors therefrom, passing said vcoke contact particles through a reheating zone, subjecting said coke contact particles to reheating in the presence of products of combustion, and reintroducing said reheated coke contact parti-cles to the reaction zone, thereby maintaining a substantially uniform column level therein.
AUGUST H. SCHUTTE.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,826,007 Loebel1 Oct. 6, 1931 1,899,887 Thiele Feb. 28, 1933 2,105,156 Morgan Jan. l1, 1938 2,339,932 Kuhl Jan. 25, 1944 2,362,270 Hemminger Nov. 7, 1944 2,462,366 Davies et al Feb. 22, 1949 2,482,137 Schutte Sept. 20, 1949 2,509,019 Simpson et al May 23, 1950 FOREIGN PATENTS Number Country Date 419,444 Great Britain Nov. 8, 1934
US120389A 1949-10-08 1949-10-08 Continuous carbonization of coal and oil mixtures Expired - Lifetime US2624696A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US120389A US2624696A (en) 1949-10-08 1949-10-08 Continuous carbonization of coal and oil mixtures

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US120389A US2624696A (en) 1949-10-08 1949-10-08 Continuous carbonization of coal and oil mixtures

Publications (1)

Publication Number Publication Date
US2624696A true US2624696A (en) 1953-01-06

Family

ID=22389954

Family Applications (1)

Application Number Title Priority Date Filing Date
US120389A Expired - Lifetime US2624696A (en) 1949-10-08 1949-10-08 Continuous carbonization of coal and oil mixtures

Country Status (1)

Country Link
US (1) US2624696A (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2709676A (en) * 1951-05-05 1955-05-31 Exxon Research Engineering Co Production of coke agglomerates
US2736690A (en) * 1954-05-13 1956-02-28 Exxon Research Engineering Co Integrated process for coking, agglomerating and calcining hydrocarbon oil
US2742410A (en) * 1951-03-10 1956-04-17 Lummus Co Continuous coking process
US2768938A (en) * 1954-05-24 1956-10-30 Exxon Research Engineering Co Method of coking and grinding coke
US2829956A (en) * 1955-03-29 1958-04-08 Koppers Co Inc Process for conversion of liquid hydrocarbons in horizontal chamber ovens
US2874095A (en) * 1956-09-05 1959-02-17 Exxon Research Engineering Co Apparatus and process for preparation of seed coke for fluid bed coking of hydrocarbons
US3018227A (en) * 1957-01-22 1962-01-23 Consolidation Coal Co Preparation of formcoke
US3022246A (en) * 1954-10-07 1962-02-20 Exxon Research Engineering Co Seed coke production in fluid coking systems
US3129164A (en) * 1961-06-30 1964-04-14 Cameron And Jones Inc Method of treating and pipelining of crude shale oil-coal slurries
US3505201A (en) * 1967-01-27 1970-04-07 Alberta Res Council Separation of coal-oil suspensions
US4786368A (en) * 1985-09-30 1988-11-22 Amoco Corporation Static mixer retorting of oil shale
US9631553B2 (en) * 2012-12-29 2017-04-25 Institute Of Engineering Thermophysics, Chinese Academy Of Sciences Process and equipment for coal gasification, and power generation system and power generation process thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1826007A (en) * 1923-12-07 1931-10-06 Henry L Doherty Apparatus for manufacturing combustible gas
US1899887A (en) * 1928-05-14 1933-02-28 Ernest w
GB419444A (en) * 1933-04-08 1934-11-08 John Stanley Morgan Process of heating coal
US2105156A (en) * 1933-04-08 1938-01-11 Morgan John Stanley Apparatus for heating coal
US2339932A (en) * 1941-04-10 1944-01-25 Standard Oil Dev Co Chemical process
US2362270A (en) * 1940-11-01 1944-11-07 Standard Oil Dev Co Viscosity reducing
US2462366A (en) * 1944-01-21 1949-02-22 Consolidation Coal Co Heating of granular materials
US2482137A (en) * 1945-02-13 1949-09-20 Lummus Co Process and apparatus for converting hydrocarbons
US2509019A (en) * 1943-09-21 1950-05-23 Socony Vacuum Oil Co Inc Method and apparatus for conversion of hydrocarbons with moving bed of solids

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1826007A (en) * 1923-12-07 1931-10-06 Henry L Doherty Apparatus for manufacturing combustible gas
US1899887A (en) * 1928-05-14 1933-02-28 Ernest w
GB419444A (en) * 1933-04-08 1934-11-08 John Stanley Morgan Process of heating coal
US2105156A (en) * 1933-04-08 1938-01-11 Morgan John Stanley Apparatus for heating coal
US2362270A (en) * 1940-11-01 1944-11-07 Standard Oil Dev Co Viscosity reducing
US2339932A (en) * 1941-04-10 1944-01-25 Standard Oil Dev Co Chemical process
US2509019A (en) * 1943-09-21 1950-05-23 Socony Vacuum Oil Co Inc Method and apparatus for conversion of hydrocarbons with moving bed of solids
US2462366A (en) * 1944-01-21 1949-02-22 Consolidation Coal Co Heating of granular materials
US2482137A (en) * 1945-02-13 1949-09-20 Lummus Co Process and apparatus for converting hydrocarbons

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2742410A (en) * 1951-03-10 1956-04-17 Lummus Co Continuous coking process
US2709676A (en) * 1951-05-05 1955-05-31 Exxon Research Engineering Co Production of coke agglomerates
US2736690A (en) * 1954-05-13 1956-02-28 Exxon Research Engineering Co Integrated process for coking, agglomerating and calcining hydrocarbon oil
US2768938A (en) * 1954-05-24 1956-10-30 Exxon Research Engineering Co Method of coking and grinding coke
US3022246A (en) * 1954-10-07 1962-02-20 Exxon Research Engineering Co Seed coke production in fluid coking systems
US2829956A (en) * 1955-03-29 1958-04-08 Koppers Co Inc Process for conversion of liquid hydrocarbons in horizontal chamber ovens
US2874095A (en) * 1956-09-05 1959-02-17 Exxon Research Engineering Co Apparatus and process for preparation of seed coke for fluid bed coking of hydrocarbons
US3018227A (en) * 1957-01-22 1962-01-23 Consolidation Coal Co Preparation of formcoke
US3129164A (en) * 1961-06-30 1964-04-14 Cameron And Jones Inc Method of treating and pipelining of crude shale oil-coal slurries
US3505201A (en) * 1967-01-27 1970-04-07 Alberta Res Council Separation of coal-oil suspensions
US4786368A (en) * 1985-09-30 1988-11-22 Amoco Corporation Static mixer retorting of oil shale
US9631553B2 (en) * 2012-12-29 2017-04-25 Institute Of Engineering Thermophysics, Chinese Academy Of Sciences Process and equipment for coal gasification, and power generation system and power generation process thereof

Similar Documents

Publication Publication Date Title
US1983943A (en) Process for carbonizing carbonaceous materials
US2543884A (en) Process for cracking and coking heavy hydryocarbons
US2709675A (en) Treatment of agglomerative carbonaceous solids
US2608526A (en) Coking of carbonaceous fuels
US4199432A (en) Staged turbulent bed retorting process
US2605215A (en) Conversion of heavy carbonaceous oils to motor fuels, fuel gas, and synthesis gas
US2485315A (en) Controlled severity fluid coking
US2624696A (en) Continuous carbonization of coal and oil mixtures
US2602019A (en) Process for promoting endothermic reactions at elevated temperatures
US2582711A (en) Fluidized carbonization process
US3316155A (en) Coking process
US2432135A (en) Distillation of oil shale in fluidized condition with simultaneous combustion of spent shale
US2396036A (en) Shale distillation
US2709676A (en) Production of coke agglomerates
US2776935A (en) Heat treating fluid coke compactions
US4099933A (en) Process for the multiple zone gasification of coal
US2560357A (en) Production of solid fuel agglomerates
US2561334A (en) Method of hydrocarbon conversion to lower boiling hydrocarbons and coke
US3117918A (en) Production of low sulfur formcoke
US3951856A (en) Process for making activated carbon from agglomerative coal
US2805189A (en) Method of heating and fluidizing for a carbonization process
US3843559A (en) Process for making activated carbon from agglomerative coal with water injection temperature control in a fluidized oxidation stage
US2627499A (en) Catalytic distillation of shale
US2268094A (en) Catalytic process for treating hydrocarbon oils
US2701758A (en) Thermal processes