US2752292A - Shale retorting process - Google Patents
Shale retorting process Download PDFInfo
- Publication number
- US2752292A US2752292A US244620A US24462051A US2752292A US 2752292 A US2752292 A US 2752292A US 244620 A US244620 A US 244620A US 24462051 A US24462051 A US 24462051A US 2752292 A US2752292 A US 2752292A
- Authority
- US
- United States
- Prior art keywords
- gas
- shale
- zone
- retorting
- combustion
- 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
Links
- 238000000034 method Methods 0.000 title claims description 19
- 239000007789 gas Substances 0.000 claims description 49
- 238000002485 combustion reaction Methods 0.000 claims description 26
- 239000007788 liquid Substances 0.000 claims description 8
- 238000003303 reheating Methods 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 3
- 239000000047 product Substances 0.000 description 14
- 239000010880 spent shale Substances 0.000 description 7
- 239000003079 shale oil Substances 0.000 description 5
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000012263 liquid product Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000004058 oil shale Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Images
Classifications
-
- 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
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/02—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by distillation
Definitions
- shale is retorted by contacting it countercurrently with hot fixed gases produced from shale. All of the heat required to effect the conversion of the kerogenic constituents of the shale to liquid and gaseous hydrocarbons is supplied as sensibleheat of the fixed gases.
- the gases are heated by contacting the gases countercurrently with spent shale as it comes from the retort and then burning a portion of them in a combustion zone prior to their introduction into the retort.
- Gas and vaporous products from retort 15 pass through line 14 and conveyor-condenser 12 in countercurrent contact with fresh shale en route to retort 15.
- Liquid shale oil is withdrawn from conveyor-condenser 12 through line 21.
- Shale gas and uncondensed shale vapor is withdrawn from conveyor-condenser 12 at a point intermediate the junction of the conveyor-condenser with lines 21 and 14 through line 22.
- These gases and vapors pass through heat exchanger 23 into liquid gas separator 24.
- Shale oil is withdrawn from liquid gas separator 24 through line 25, and fixed shale gases are withdrawn from the separator through line 26 and pass through pump 27.
- a portion of the fixed shale gases is withdrawn through line 28 as a net gas product, and the remainder is recycled back to the retorting system through line 29 into cooler 18, Where it countercurrently contacts hot shale from retort 15.
- These gases preheated in cooler 18 by contact with the spent shale, pass through line 30 into combustion chamber 31.
- Air is introduced into combustion chamber 31 through line 32 in amount sufiicient to raise the temperature of the total gas stream entering the retort 15 to the temperature required for retorting. This may require the combustion of about 10% of the true make gas of the process.
- the unburned recycle gas and the combustion product are passed from combustion chamber 31 through line 33 into retort 15, where they countercurrently contact the fresh shale in the retort to effect the conversion of its kerogenic components.
- An advantage inherent to the use of a retorting process employing a gas combustion zone separate from the retorting zone is that close control is possible over the temperature of the gas retorting medium, and carbonate decomposition within the retorting zone can thereby be minimized.
- a further advantage associated with separation of the gas combustion process from the retorting process is the fact that close control over the amount of residual oxygen entering the retort with the hot gas stream may be maintained for the purpose of avoiding an oxidizing atmosphere within the retort which would result in lower yields of liquid products.
- the illustrated conveyor condenser 12 may be simplified into a conven tional hopper arrangement located directly above line 14, and shale particles of varying size may be directly fed into the hopper for gravitational loading into the retorting zone.
- the normally liquid and gaseous products may also be taken from the retorting zone 15 in a conventional manner without affecting the retorting process of the invention.
- the vaporized products from the retorting zone may be withdrawn from the upper section of the retorting zone and passed into a condensing or mist agglomeration system.
- the liquid products may be withdrawn from one or more condensers and the product gas accumulated with a distribution into net product gas and recycle gas.
- the basic features of the invention involve a recycle of a portion of the product gas which is introduced into countercurrent contact with the spent shale. After preheating by passage through the spent shale, the preheated recycle gas is withdrawn from contact with the shale and passed through a combustion chamber wherein a suflicient portion thereof is burned in contact with controlled introduction of air or oxygen-containing gas to raise the temperature of the recycle gas to the desired retorting temperature and provide the balance of necessary retorting heat, after which it is brought into contact with fresh shale as the retorting heat carrier medium.
- the improved method which comprises Withdrawing vapors comprising normally liquid and normally gaseous products from the upper portion of the retorting zone, cooling the vapors to condense shale oil, withdrawing a minor proportion of the uncondensed gas as a product, reheating the major proportion of the uncondensed gas by contacting it with hot spent shale in a reheating zone, withdrawing reheated gas from the reheating zone and passing it into a combustion zone, introducing into the combustion zone a quantity of a free oxygen-containing gas having an oxygen content stoichiometrically suflicient to cause combustion of only a minor proportion of the reheated gas and burning a minor proportion of the reheated gas suf
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
June 26, 1956 J. w. SCOTT, JR 2,752,292
SHALE RETORTING PROCESS Filed Aug. 31, 1951 INVENTOR JOHN w. SCOTT JR.
ATTORNEYS United States Patent 2,752,292 SHALE RETORTING PROCESS John W. Scott, Jr., Berkeley, Calif., assignor to California Research Corporation, ration of Delaware Application August 31, 1951, Serial No. 244,620 2 Claims. (Cl. 202-19) San Francisco, Calif., 21 corpo- This invention relates to an improved process for retorting oil shale and bituminous solids of similar charac- .'ter in order to recover valuable liquid and gaseous hydrocarbon products.
In the process of this invention, shale is retorted by contacting it countercurrently with hot fixed gases produced from shale. All of the heat required to effect the conversion of the kerogenic constituents of the shale to liquid and gaseous hydrocarbons is supplied as sensibleheat of the fixed gases. The gases are heated by contacting the gases countercurrently with spent shale as it comes from the retort and then burning a portion of them in a combustion zone prior to their introduction into the retort.
The process of this invention will be described in detail with reference to the appended drawing, in which fixed gases recovered from the shale are contacted with spent its kerogenic con- Shale particles having a size in the range M1 inch to 2 inches in diameter are passed through line and gastight valve 11 into conveyor-condenser 12. The shale is carried by the conveyor chain 13 into line 14, through which it passes into retort 15. Retorted shale is passed from retort 15 through line 16 and gas-tight valve 17 into cooler 18. Cooled retorted shale is withdrawn from cooler 18 through line 19 and gas-tight valve 20. Gas and vaporous products from retort 15 pass through line 14 and conveyor-condenser 12 in countercurrent contact with fresh shale en route to retort 15. Liquid shale oil is withdrawn from conveyor-condenser 12 through line 21. Shale gas and uncondensed shale vapor is withdrawn from conveyor-condenser 12 at a point intermediate the junction of the conveyor-condenser with lines 21 and 14 through line 22. These gases and vapors pass through heat exchanger 23 into liquid gas separator 24. Shale oil is withdrawn from liquid gas separator 24 through line 25, and fixed shale gases are withdrawn from the separator through line 26 and pass through pump 27. A portion of the fixed shale gases is withdrawn through line 28 as a net gas product, and the remainder is recycled back to the retorting system through line 29 into cooler 18, Where it countercurrently contacts hot shale from retort 15. These gases, preheated in cooler 18 by contact with the spent shale, pass through line 30 into combustion chamber 31. Air is introduced into combustion chamber 31 through line 32 in amount sufiicient to raise the temperature of the total gas stream entering the retort 15 to the temperature required for retorting. This may require the combustion of about 10% of the true make gas of the process. The unburned recycle gas and the combustion product are passed from combustion chamber 31 through line 33 into retort 15, where they countercurrently contact the fresh shale in the retort to effect the conversion of its kerogenic components.
2,752,292 l atht'ed June 26, i 1956 The following table is illustrative of the amounts and temperatures of the process materials involved in typical operation of the process described.
Material Amount S P" Fresh Shale to 2") 500 lb./hr 60 Retortcd Shale (line 16) 414 lb./hr 1, 000 Cooled Shale (line 19)--.. 250 Shale Oil (lines 21 and 25) Shale Gas (line 28) 175 Recycle Gas (line 29) 175 Air (line 32) Recycle Gas (line 33) 249 lb./h 1,050 True Make Gas burned in Combustion 9 percent Chamber 3]. Flue Gas in Make Gas (line 28) 32 percent In the invention described above the combustion of a relatively small proportion of the recycle gas is found to supply suflicient heat to retort the fresh shale. This proportion is ordinarily so small that the net product gas withdrawn from the process through line 28 has a high heat content.
An advantage inherent to the use of a retorting process employing a gas combustion zone separate from the retorting zone is that close control is possible over the temperature of the gas retorting medium, and carbonate decomposition within the retorting zone can thereby be minimized. A further advantage associated with separation of the gas combustion process from the retorting process is the fact that close control over the amount of residual oxygen entering the retort with the hot gas stream may be maintained for the purpose of avoiding an oxidizing atmosphere within the retort which would result in lower yields of liquid products.
In the foregoing specific embodiment of the invention as represented by the appended drawing, it is to be understood that certain modifications in processing techniques and apparatus may be indulged without departing from the basic features of the invention. Thus, the illustrated conveyor condenser 12 may be simplified into a conven tional hopper arrangement located directly above line 14, and shale particles of varying size may be directly fed into the hopper for gravitational loading into the retorting zone. The normally liquid and gaseous products may also be taken from the retorting zone 15 in a conventional manner without affecting the retorting process of the invention. As a conventional modification of the illustrated recovery system, the vaporized products from the retorting zone may be withdrawn from the upper section of the retorting zone and passed into a condensing or mist agglomeration system. The liquid products may be withdrawn from one or more condensers and the product gas accumulated with a distribution into net product gas and recycle gas.
The basic features of the invention involve a recycle of a portion of the product gas which is introduced into countercurrent contact with the spent shale. After preheating by passage through the spent shale, the preheated recycle gas is withdrawn from contact with the shale and passed through a combustion chamber wherein a suflicient portion thereof is burned in contact with controlled introduction of air or oxygen-containing gas to raise the temperature of the recycle gas to the desired retorting temperature and provide the balance of necessary retorting heat, after which it is brought into contact with fresh shale as the retorting heat carrier medium.
This application is a continuation-in-part of application by John W. Scott, Jr., Serial No. 116,260, filed September 17, 1949, now abandoned Obviously many modifications and variations of the invention as hereinabove set forth may be made without departing from the spirit and scope thereof, and only such limitations should be imposed as are indicated in the appended claims.
I claim: I
1. In a process for retorting shale by countercurrently contacting downwardly moving shale particles with hot gas in a retorting zone to decompose the organic constituents of the shale forming shale oil and shale gas, the improved method which comprises Withdrawing vapors comprising normally liquid and normally gaseous products from the upper portion of the retorting zone, cooling the vapors to condense shale oil, withdrawing a minor proportion of the uncondensed gas as a product, reheating the major proportion of the uncondensed gas by contacting it with hot spent shale in a reheating zone, withdrawing reheated gas from the reheating zone and passing it into a combustion zone, introducing into the combustion zone a quantity of a free oxygen-containing gas having an oxygen content stoichiometrically suflicient to cause combustion of only a minor proportion of the reheated gas and burning a minor proportion of the reheated gas sufiicient to raise the temperature of the mixture of combustion products and unburned gas to retorting temperature in the combustion zone, and passing the mixture of combustion products and unburned gas from the combustion zone into the retorting zone.
2. Method substantially as described in claim 1, wherein about 10% of the reheated gas is burned in the combustion zone;
References Cited in the file of this patent UNITED STATES PATENTS 1,551,956 Hubmann Sept. 1, 1925 1,805,109 Runge et a1 May 12, 1931 1,937,552 Davis Dec. 5, 1933 2,014,212 Seguy Sept. 10, 1935 2,289,917 Lambiotte July 14, 1942 2,396,036 Blanding Mar. 5, 1946 2,406,810 Day Sept. 3, 1946 2,448,223 Lantz Aug. 31, 1948 2,501,153 Bery Mar. 21, 1950 2,578,357 Hyslop Dec. 11, 1951 FOREIGN PATENTS 147,117 Great Britain June 2, 1921 283,259 Great Britain Jan. 2, 1928 107,907 Australia July 5, 1939
Claims (1)
1. IN A PROCESS FOR RETORTING SHALE BY COUNTERCURRENTLY CONTACTING DOWNWARDLY MOVING SHALE PARTICLES WITH HOT GAS IN A RETORTING ZONE TO DECOMPOSE THE ORGANIC CONSTITUENTS OF THE SHALE FORMING SHALE OIL AND SHALE GAS, THE IMPROVED METHOD WHICH COMPRISES WITHDRAWING VAPORS COMPRISING NORMALLY LIQUID AND NORMALLY GASEOUS PRODUCTS FROM THE UPPER PORTION OF THE RETORTING ZONE, COOLING THE VAPORS TO CONDENSE SHALE OIL, WITHDRAWING A MINOR PROPORTION OF THE UNCONDENSED GAS AS A PRODUCT, REHEATING THE MAJOR PROPORTION OF THE UNCONDENSED GAS BY CONTACTING IT WITH HOT SPEND SHALE IN A REHEATING ZONE, WITHDRAWING REHEATED GAS FROM THE REHEATING ZONE AND PASSING IT INTO A COMBUSTION ZONE, INTRODUCING INTO THE COMBUSTION ZONE A QUANTITY OF A FREE OXYGEN-CONTAINING GAS HAVING AN OXYGEN CONTENT STOICHIOMETRICALLY SUFFICIENT TO CAUSE COMBUSTION OF ONLY A MINOR PROPORTION OF THE REHEATED GAS AND BURNING A MINOR PROPORTION OF THE REHEATED GAS SUFFICIENT TO RAISE THE TEMPERATURE OF THE MIXTURE OF COMBUSTION PRODUCTS AND UNBURNED GAS TO RETORTING TEMPERATURE IN THE COMBUSTION ZONE, AND PASSING THE MIXTURE OF COMBUSTION PRODUCTS AND UNBURNED GAS FROM THE COMBUSTION ZONE INTO THE RETORTING ZONE.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US244620A US2752292A (en) | 1951-08-31 | 1951-08-31 | Shale retorting process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US244620A US2752292A (en) | 1951-08-31 | 1951-08-31 | Shale retorting process |
Publications (1)
Publication Number | Publication Date |
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US2752292A true US2752292A (en) | 1956-06-26 |
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ID=22923478
Family Applications (1)
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US244620A Expired - Lifetime US2752292A (en) | 1951-08-31 | 1951-08-31 | Shale retorting process |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2966446A (en) * | 1956-06-04 | 1960-12-27 | Union Oil Co | Shale retorting process |
US3617466A (en) * | 1968-12-06 | 1971-11-02 | Atlantic Richfield Co | Gas combustion retort process |
US4148710A (en) * | 1977-06-13 | 1979-04-10 | Occidental Oil Shale, Inc. | Fluidized bed process for retorting oil shale |
US4395309A (en) * | 1980-11-03 | 1983-07-26 | Esztergar Ernest P | Fractional distillation of hydrocarbons from coal |
US4439307A (en) * | 1983-07-01 | 1984-03-27 | Dravo Corporation | Heating process gas for indirect shale oil retorting through the combustion of residual carbon in oil depleted shale |
US4490237A (en) * | 1983-07-01 | 1984-12-25 | Dravo Corporation | Process for recovering heat from the combustion of residual carbon in oil depleted shale |
US10829693B2 (en) | 2017-08-30 | 2020-11-10 | Pyro Dynamics LLC | Apparatus, system, and method for shale pyrolysis |
US11111440B1 (en) | 2020-02-27 | 2021-09-07 | Pyro Dynamics, Llc | Apparatus, system, and method for shale pyrolysis |
US11866649B2 (en) | 2020-02-27 | 2024-01-09 | Pyro Dynamics, Llc | Apparatus, system, and method for shale pyrolysis |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB147117A (en) * | 1918-06-29 | 1921-06-02 | Meyer Paul | Improvements in or relating to a process and a device for carbonizing solid fuels in a circulating current of gas |
US1551956A (en) * | 1924-05-22 | 1925-09-01 | American Lurgi Corp | Process of distilling wet combustible material |
GB283259A (en) * | 1926-10-02 | 1928-01-02 | Carlshuette Ag Fuer Eisengiess | Improvements relating to the distillation of carbonaceous substances |
US1805109A (en) * | 1925-03-12 | 1931-05-12 | Internat Coal Carbonization Co | Processing of coal |
US1937552A (en) * | 1928-08-15 | 1933-12-05 | Nat Aniline & Chem Co Inc | Process and apparatus for carbonizing powdered coal |
US2014212A (en) * | 1932-04-30 | 1935-09-10 | Universal Oil Prod Co | Coking hydrocarbon oils |
US2289917A (en) * | 1942-07-14 | Process of continuous carbonization | ||
US2396036A (en) * | 1943-11-10 | 1946-03-05 | Standard Oil Dev Co | Shale distillation |
US2406810A (en) * | 1944-03-18 | 1946-09-03 | Universal Oil Prod Co | Treatment of hydrocarbonaceous solids |
US2448223A (en) * | 1936-06-30 | 1948-08-31 | Azote & Prod Chim | Low-temperature distillation of fuels by direct contact with reheated distillate vapors |
US2501153A (en) * | 1947-01-21 | 1950-03-21 | Union Oil Co | Shale oil eduction |
US2578357A (en) * | 1949-06-18 | 1951-12-11 | Consolidation Coal Co | Method for treating granular solids |
-
1951
- 1951-08-31 US US244620A patent/US2752292A/en not_active Expired - Lifetime
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2289917A (en) * | 1942-07-14 | Process of continuous carbonization | ||
GB147117A (en) * | 1918-06-29 | 1921-06-02 | Meyer Paul | Improvements in or relating to a process and a device for carbonizing solid fuels in a circulating current of gas |
US1551956A (en) * | 1924-05-22 | 1925-09-01 | American Lurgi Corp | Process of distilling wet combustible material |
US1805109A (en) * | 1925-03-12 | 1931-05-12 | Internat Coal Carbonization Co | Processing of coal |
GB283259A (en) * | 1926-10-02 | 1928-01-02 | Carlshuette Ag Fuer Eisengiess | Improvements relating to the distillation of carbonaceous substances |
US1937552A (en) * | 1928-08-15 | 1933-12-05 | Nat Aniline & Chem Co Inc | Process and apparatus for carbonizing powdered coal |
US2014212A (en) * | 1932-04-30 | 1935-09-10 | Universal Oil Prod Co | Coking hydrocarbon oils |
US2448223A (en) * | 1936-06-30 | 1948-08-31 | Azote & Prod Chim | Low-temperature distillation of fuels by direct contact with reheated distillate vapors |
US2396036A (en) * | 1943-11-10 | 1946-03-05 | Standard Oil Dev Co | Shale distillation |
US2406810A (en) * | 1944-03-18 | 1946-09-03 | Universal Oil Prod Co | Treatment of hydrocarbonaceous solids |
US2501153A (en) * | 1947-01-21 | 1950-03-21 | Union Oil Co | Shale oil eduction |
US2578357A (en) * | 1949-06-18 | 1951-12-11 | Consolidation Coal Co | Method for treating granular solids |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2966446A (en) * | 1956-06-04 | 1960-12-27 | Union Oil Co | Shale retorting process |
US3617466A (en) * | 1968-12-06 | 1971-11-02 | Atlantic Richfield Co | Gas combustion retort process |
US4148710A (en) * | 1977-06-13 | 1979-04-10 | Occidental Oil Shale, Inc. | Fluidized bed process for retorting oil shale |
US4395309A (en) * | 1980-11-03 | 1983-07-26 | Esztergar Ernest P | Fractional distillation of hydrocarbons from coal |
US4439307A (en) * | 1983-07-01 | 1984-03-27 | Dravo Corporation | Heating process gas for indirect shale oil retorting through the combustion of residual carbon in oil depleted shale |
US4490237A (en) * | 1983-07-01 | 1984-12-25 | Dravo Corporation | Process for recovering heat from the combustion of residual carbon in oil depleted shale |
US10829693B2 (en) | 2017-08-30 | 2020-11-10 | Pyro Dynamics LLC | Apparatus, system, and method for shale pyrolysis |
US11111440B1 (en) | 2020-02-27 | 2021-09-07 | Pyro Dynamics, Llc | Apparatus, system, and method for shale pyrolysis |
US11834612B2 (en) | 2020-02-27 | 2023-12-05 | Pyro Dynamics, Llc | Apparatus, system, and method for shale pyrolysis |
US11866649B2 (en) | 2020-02-27 | 2024-01-09 | Pyro Dynamics, Llc | Apparatus, system, and method for shale pyrolysis |
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