US2423674A - Process of catalytic cracking of petroleum hydrocarbons - Google Patents
Process of catalytic cracking of petroleum hydrocarbons Download PDFInfo
- Publication number
- US2423674A US2423674A US542005A US54200544A US2423674A US 2423674 A US2423674 A US 2423674A US 542005 A US542005 A US 542005A US 54200544 A US54200544 A US 54200544A US 2423674 A US2423674 A US 2423674A
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- Prior art keywords
- oil
- petroleum
- cracking
- hole
- shale
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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
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/10—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with stationary catalyst bed
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/14—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
- C10G11/16—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "moving bed" method
Definitions
- the present invention relates to a process of catalytic cracking of petroleum hydrocarbons which is characterized by the fact that the hydrocarbons in the liquid and/or vapor phase, in connection with cracking, are brought in contact with a catalyst entirely or at least partly consisting of oil-shape and/or mineral residue of such shale, e. g. residue from distillation or burning thereof, such as shale ashes and the like.
- the catalysts hitherto employed in the cracking of petroleum consisting of metals, oxidic substances and the like, are either too sensitive to so called catalytic poisons, particularly sulfur which frequently occurs in petroleum, or else possess too little catalytic power to be suitable for industrial use without complicated arrangements. It has now been found that catalysts of oil-shale or similar material of the above stated kind, possess valuable properties in these respects.
- the catalyst may from the outset consist of ordinary shale ashes, i. e. ashes obtained in burning or calcining of oil-shale, with or without admixture of other suitable catalytic substances of low sensitivity to sulfur, or the 'catalyst may originally be wholly or partly composed of natural shale.
- the process which comprises pumping crude petroleum oil into a hole drilled in an oil-bearing shale rock formation in contact with said rock while heating the drill hole sufficiently to bring the formation to a temperature within the range of about 250 to600 C. and under a pressure within the range of from atmospheric to 50 atmospheres, withdrawing the resulting products including cracked gases from said hole, passing oil into said hole until the natural oil content of the formation is exhausted, thereafter continuing to pass oil into said hole maintained at said cracking temperature and pressure while utilizing the catalytic properties of the rock to enhance the cracking of said petroleum oil, withdrawing the cracked products including cracked gases from said hole, and recycling said cracked gases to said hole during the cracking process.
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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)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Patented July 8, 1947 PROCESS OF CATALYTIC CRACKING OF PETROLEUM HYDROCARBONS Per Henning Wilhelm Agren, Nynashamn, Sweden, assignor to A. Johnson & 00., New York, N. I[., a company oi Delaware No-Drawing. Application June 24, 1944, Serial No. 542,005. In Sweden August 24, 1942 2 Claims. (Cl 196-52) The present invention relates to a process of catalytic cracking of petroleum hydrocarbons which is characterized by the fact that the hydrocarbons in the liquid and/or vapor phase, in connection with cracking, are brought in contact with a catalyst entirely or at least partly consisting of oil-shape and/or mineral residue of such shale, e. g. residue from distillation or burning thereof, such as shale ashes and the like.
The catalysts hitherto employed in the cracking of petroleum, consisting of metals, oxidic substances and the like, are either too sensitive to so called catalytic poisons, particularly sulfur which frequently occurs in petroleum, or else possess too little catalytic power to be suitable for industrial use without complicated arrangements. It has now been found that catalysts of oil-shale or similar material of the above stated kind, possess valuable properties in these respects. The catalyst may from the outset consist of ordinary shale ashes, i. e. ashes obtained in burning or calcining of oil-shale, with or without admixture of other suitable catalytic substances of low sensitivity to sulfur, or the 'catalyst may originally be wholly or partly composed of natural shale. This alsomakes it possible to carry out the catalytic treatment of petroleum hydrocarbons in contact with naturally occurring oil-shale or its more or less transformed residues, e. g. by pumping crude petroleum into drill holes in oilshale rocks simultaneously with or after a distilling off of the shale oil from the rock by the so called in situ-method, while heating the said drill holes and conveying the oil so that suitable operating conditions are produced. After a short period of operation the oil shale is, of course, free from its naturally occurring oil.
Suitable operating temperatures and pressures, both when treating the petroleum by contacting it in the drill holes with the catalyst forming part of the surrounding rock, and when carrying out the treatment in known petroleum cracking units,
are from 250 to 600 C. and from atmosphericpressure up to 50 atmospheres, under which conditions the catalysts in question have proven to function extremely satisfactory both in regard to yield and to durability. In order to obtain high yields it is suitable to let such gases as are contained in the reaction-mixture, particularly the low-molecular ones, pass over the catalyst several times.
I claim:
1. In the cracking of petroleum oils, the process which comprises passing such an oil into a hole drilled in a natural oil-shale rock formation in contact with said rock and while heating the drill hole to cracking temperatures, passing the oil into said hole until the natural oil content of the formation is exhusted and withdrawing the resulting products from said hole, thereafter continuing to pass oil into said hole and cracking it therein utilizing the catalytic properties of the natural rock formation to enhance the cracking of said petroleum oil, and withdrawing the cracked products from said hole.
2. In the cracking of petroleum oils, the process which comprises pumping crude petroleum oil into a hole drilled in an oil-bearing shale rock formation in contact with said rock while heating the drill hole sufficiently to bring the formation to a temperature within the range of about 250 to600 C. and under a pressure within the range of from atmospheric to 50 atmospheres, withdrawing the resulting products including cracked gases from said hole, passing oil into said hole until the natural oil content of the formation is exhausted, thereafter continuing to pass oil into said hole maintained at said cracking temperature and pressure while utilizing the catalytic properties of the rock to enhance the cracking of said petroleum oil, withdrawing the cracked products including cracked gases from said hole, and recycling said cracked gases to said hole during the cracking process.
PER HENNING WILHELM AGREN.
REFERENCES strap The following references are of record in the file of this patent:
UNITED s'rs'ras PA'I'ENTS Number Name Date 1,458,983 Kirby June 19, 1923 1,475,901 Thompson Nov. 27, 1923 1,707,759 Hampton Apr. 2, 1929 1,868,737 Eglofl July 26, 1932 2,054,725 Greenstreet Sept. 15, 1936 1,614,660 Darlington et al Jan. 18, 1937 2,078,945 Houdry May 4, 1937 1,342,741 Day June 8, 1920 2,265,923 Normand Dec. 9, 1941 1,940,725 Morrell Dec. 26, 1933 1,467,758 Day Sept. 11, 1923 1,917,324 Pier et a1 July 11, 1933 2,382,471 Frey Aug. 14, 1945 1,510,655 Clark Oct. 7, 1924 FOREIGN PATENTS Number Country Date 511,768 Great Britain Aug. 24, 1939 7 OTHER REFERENCES Dunstan et al., fThe Science of Petroleum, vol.
IV, pages 3085 and 3089. Published 1938 by 0xford University Press, New York. (Copy in Division 31.)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE2423674X | 1942-08-24 |
Publications (1)
Publication Number | Publication Date |
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US2423674A true US2423674A (en) | 1947-07-08 |
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US542005A Expired - Lifetime US2423674A (en) | 1942-08-24 | 1944-06-24 | Process of catalytic cracking of petroleum hydrocarbons |
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Cited By (49)
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---|---|---|---|---|
US2623843A (en) * | 1949-08-31 | 1952-12-30 | Standard Oil Dev Co | Refining of liquid or semiliquid carbonaceous materials |
US2733193A (en) * | 1956-01-31 | Haensel | ||
US2871942A (en) * | 1956-11-29 | 1959-02-03 | Texas Co | In situ combustion |
US2939884A (en) * | 1956-11-13 | 1960-06-07 | Texaco Inc | Method for performing chemical reactions, particularly in underground storage cavities |
US3024097A (en) * | 1957-07-22 | 1962-03-06 | Phillips Petroleum Co | Process and arrangement of apparatus for production of mixtures of carbon oxides andhydrogen |
US3061009A (en) * | 1958-01-17 | 1962-10-30 | Svenska Skifferolje Ab | Method of recovery from fossil fuel bearing strata |
US3072187A (en) * | 1960-05-12 | 1963-01-08 | Phillips Petroleum Co | Production and upgrading of hydrocarbons in situ |
US3126957A (en) * | 1964-03-31 | Underground initiated miscible | ||
US3322195A (en) * | 1964-01-20 | 1967-05-30 | Exxon Research Engineering Co | Process and apparatus for recovery of additional fuels from oil and gas wells |
US4193454A (en) * | 1976-03-15 | 1980-03-18 | Mobil Oil Corporation | Super-active clay catalyst and use thereof |
US20030079877A1 (en) * | 2001-04-24 | 2003-05-01 | Wellington Scott Lee | In situ thermal processing of a relatively impermeable formation in a reducing environment |
US20030080604A1 (en) * | 2001-04-24 | 2003-05-01 | Vinegar Harold J. | In situ thermal processing and inhibiting migration of fluids into or out of an in situ oil shale formation |
US20030100451A1 (en) * | 2001-04-24 | 2003-05-29 | Messier Margaret Ann | In situ thermal recovery from a relatively permeable formation with backproduction through a heater wellbore |
US6581684B2 (en) | 2000-04-24 | 2003-06-24 | Shell Oil Company | In Situ thermal processing of a hydrocarbon containing formation to produce sulfur containing formation fluids |
US6588504B2 (en) | 2000-04-24 | 2003-07-08 | Shell Oil Company | In situ thermal processing of a coal formation to produce nitrogen and/or sulfur containing formation fluids |
US20030155111A1 (en) * | 2001-04-24 | 2003-08-21 | Shell Oil Co | In situ thermal processing of a tar sands formation |
US20030173081A1 (en) * | 2001-10-24 | 2003-09-18 | Vinegar Harold J. | In situ thermal processing of an oil reservoir formation |
US20030173085A1 (en) * | 2001-10-24 | 2003-09-18 | Vinegar Harold J. | Upgrading and mining of coal |
US20030196801A1 (en) * | 2001-10-24 | 2003-10-23 | Vinegar Harold J. | In situ thermal processing of a hydrocarbon containing formation via backproducing through a heater well |
US6698515B2 (en) | 2000-04-24 | 2004-03-02 | Shell Oil Company | In situ thermal processing of a coal formation using a relatively slow heating rate |
US6715546B2 (en) | 2000-04-24 | 2004-04-06 | Shell Oil Company | In situ production of synthesis gas from a hydrocarbon containing formation through a heat source wellbore |
US6715548B2 (en) | 2000-04-24 | 2004-04-06 | Shell Oil Company | In situ thermal processing of a hydrocarbon containing formation to produce nitrogen containing formation fluids |
US20050269077A1 (en) * | 2004-04-23 | 2005-12-08 | Sandberg Chester L | Start-up of temperature limited heaters using direct current (DC) |
US7011154B2 (en) | 2000-04-24 | 2006-03-14 | Shell Oil Company | In situ recovery from a kerogen and liquid hydrocarbon containing formation |
US7073578B2 (en) | 2002-10-24 | 2006-07-11 | Shell Oil Company | Staged and/or patterned heating during in situ thermal processing of a hydrocarbon containing formation |
US7090013B2 (en) | 2001-10-24 | 2006-08-15 | Shell Oil Company | In situ thermal processing of a hydrocarbon containing formation to produce heated fluids |
US7096953B2 (en) | 2000-04-24 | 2006-08-29 | Shell Oil Company | In situ thermal processing of a coal formation using a movable heating element |
US7104319B2 (en) | 2001-10-24 | 2006-09-12 | Shell Oil Company | In situ thermal processing of a heavy oil diatomite formation |
US7121342B2 (en) | 2003-04-24 | 2006-10-17 | Shell Oil Company | Thermal processes for subsurface formations |
US7165615B2 (en) | 2001-10-24 | 2007-01-23 | Shell Oil Company | In situ recovery from a hydrocarbon containing formation using conductor-in-conduit heat sources with an electrically conductive material in the overburden |
US20070045267A1 (en) * | 2005-04-22 | 2007-03-01 | Vinegar Harold J | Subsurface connection methods for subsurface heaters |
US20070095536A1 (en) * | 2005-10-24 | 2007-05-03 | Vinegar Harold J | Cogeneration systems and processes for treating hydrocarbon containing formations |
US20070108201A1 (en) * | 2005-04-22 | 2007-05-17 | Vinegar Harold J | Insulated conductor temperature limited heater for subsurface heating coupled in a three-phase wye configuration |
US20080035348A1 (en) * | 2006-04-21 | 2008-02-14 | Vitek John M | Temperature limited heaters using phase transformation of ferromagnetic material |
US20080128134A1 (en) * | 2006-10-20 | 2008-06-05 | Ramesh Raju Mudunuri | Producing drive fluid in situ in tar sands formations |
US20090071652A1 (en) * | 2007-04-20 | 2009-03-19 | Vinegar Harold J | In situ heat treatment from multiple layers of a tar sands formation |
US20090189617A1 (en) * | 2007-10-19 | 2009-07-30 | David Burns | Continuous subsurface heater temperature measurement |
US20090260823A1 (en) * | 2008-04-18 | 2009-10-22 | Robert George Prince-Wright | Mines and tunnels for use in treating subsurface hydrocarbon containing formations |
US20100089586A1 (en) * | 2008-10-13 | 2010-04-15 | John Andrew Stanecki | Movable heaters for treating subsurface hydrocarbon containing formations |
US20100155062A1 (en) * | 2007-07-24 | 2010-06-24 | Boone Thomas J | Use Of A Heavy Petroleum Fraction As A Drive Fluid In The Recovery of Hydrocarbons From A Subterranean Formation |
US20100258309A1 (en) * | 2009-04-10 | 2010-10-14 | Oluropo Rufus Ayodele | Heater assisted fluid treatment of a subsurface formation |
US20130161008A1 (en) * | 2011-12-22 | 2013-06-27 | Argonne National Laboratory | Preparation and use of nano-catalysts for in-situ reaction with kerogen |
US8631866B2 (en) | 2010-04-09 | 2014-01-21 | Shell Oil Company | Leak detection in circulated fluid systems for heating subsurface formations |
US8701768B2 (en) | 2010-04-09 | 2014-04-22 | Shell Oil Company | Methods for treating hydrocarbon formations |
US8820406B2 (en) | 2010-04-09 | 2014-09-02 | Shell Oil Company | Electrodes for electrical current flow heating of subsurface formations with conductive material in wellbore |
US9016370B2 (en) | 2011-04-08 | 2015-04-28 | Shell Oil Company | Partial solution mining of hydrocarbon containing layers prior to in situ heat treatment |
US9033042B2 (en) | 2010-04-09 | 2015-05-19 | Shell Oil Company | Forming bitumen barriers in subsurface hydrocarbon formations |
US9309755B2 (en) | 2011-10-07 | 2016-04-12 | Shell Oil Company | Thermal expansion accommodation for circulated fluid systems used to heat subsurface formations |
US10047594B2 (en) | 2012-01-23 | 2018-08-14 | Genie Ip B.V. | Heater pattern for in situ thermal processing of a subsurface hydrocarbon containing formation |
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Cited By (441)
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---|---|---|---|---|
US2733193A (en) * | 1956-01-31 | Haensel | ||
US3126957A (en) * | 1964-03-31 | Underground initiated miscible | ||
US2623843A (en) * | 1949-08-31 | 1952-12-30 | Standard Oil Dev Co | Refining of liquid or semiliquid carbonaceous materials |
US2939884A (en) * | 1956-11-13 | 1960-06-07 | Texaco Inc | Method for performing chemical reactions, particularly in underground storage cavities |
US2871942A (en) * | 1956-11-29 | 1959-02-03 | Texas Co | In situ combustion |
US3024097A (en) * | 1957-07-22 | 1962-03-06 | Phillips Petroleum Co | Process and arrangement of apparatus for production of mixtures of carbon oxides andhydrogen |
US3061009A (en) * | 1958-01-17 | 1962-10-30 | Svenska Skifferolje Ab | Method of recovery from fossil fuel bearing strata |
US3072187A (en) * | 1960-05-12 | 1963-01-08 | Phillips Petroleum Co | Production and upgrading of hydrocarbons in situ |
US3322195A (en) * | 1964-01-20 | 1967-05-30 | Exxon Research Engineering Co | Process and apparatus for recovery of additional fuels from oil and gas wells |
US4193454A (en) * | 1976-03-15 | 1980-03-18 | Mobil Oil Corporation | Super-active clay catalyst and use thereof |
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US7017661B2 (en) | 2000-04-24 | 2006-03-28 | Shell Oil Company | Production of synthesis gas from a coal formation |
US7011154B2 (en) | 2000-04-24 | 2006-03-14 | Shell Oil Company | In situ recovery from a kerogen and liquid hydrocarbon containing formation |
US6581684B2 (en) | 2000-04-24 | 2003-06-24 | Shell Oil Company | In Situ thermal processing of a hydrocarbon containing formation to produce sulfur containing formation fluids |
US6997255B2 (en) | 2000-04-24 | 2006-02-14 | Shell Oil Company | In situ thermal processing of a hydrocarbon containing formation in a reducing environment |
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US20110088904A1 (en) * | 2000-04-24 | 2011-04-21 | De Rouffignac Eric Pierre | In situ recovery from a hydrocarbon containing formation |
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US6959761B2 (en) | 2000-04-24 | 2005-11-01 | Shell Oil Company | In situ thermal processing of a coal formation with a selected ratio of heat sources to production wells |
US6953087B2 (en) | 2000-04-24 | 2005-10-11 | Shell Oil Company | Thermal processing of a hydrocarbon containing formation to increase a permeability of the formation |
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US6913078B2 (en) | 2000-04-24 | 2005-07-05 | Shell Oil Company | In Situ thermal processing of hydrocarbons within a relatively impermeable formation |
US6910536B2 (en) | 2000-04-24 | 2005-06-28 | Shell Oil Company | In situ thermal processing of a hydrocarbon containing formation using a natural distributed combustor |
US6607033B2 (en) | 2000-04-24 | 2003-08-19 | Shell Oil Company | In Situ thermal processing of a coal formation to produce a condensate |
US6902004B2 (en) | 2000-04-24 | 2005-06-07 | Shell Oil Company | In situ thermal processing of a hydrocarbon containing formation using a movable heating element |
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