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US1954478A - Treatment of hydrocarbon oils - Google Patents

Treatment of hydrocarbon oils Download PDF

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Publication number
US1954478A
US1954478A US428520A US42852030A US1954478A US 1954478 A US1954478 A US 1954478A US 428520 A US428520 A US 428520A US 42852030 A US42852030 A US 42852030A US 1954478 A US1954478 A US 1954478A
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US
United States
Prior art keywords
cracking
hydrocarbon oils
treatment
hydrocarbons
reaction
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
US428520A
Inventor
Egloff Gustav
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.)
Universal Oil Products Co
Original Assignee
Universal Oil Products 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 Universal Oil Products Co filed Critical Universal Oil Products Co
Priority to US428520A priority Critical patent/US1954478A/en
Application granted granted Critical
Publication of US1954478A publication Critical patent/US1954478A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C10G47/00Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
    • C10G47/32Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions in the presence of hydrogen-generating compounds
    • 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
    • C10G47/00Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
    • C10G47/24Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions with moving solid particles
    • 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
    • C10G47/00Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
    • C10G47/24Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions with moving solid particles
    • C10G47/26Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions with moving solid particles suspended in the oil, e.g. slurries

Definitions

  • This invention relates to a process for the treatment of hydrocarbon oils and refers more particularly to a process for the hydrogenation of oils at elevated temperatures.
  • Among the objects of the process is to increase the yield of the lower boiling products made by the thermal decomposition or cracking of higher boiling oils; to saturate in part the more highly unsaturated hydrocarbons, especially those which form gums, polymers, and other undesirable materials in the motor fuel; and to desulphurize in part the hydrocarbons to render them more suitable for motor fuel and to facilitate and reduce the cost of refining.
  • the hydrocarbons treated are the nonvaporized liquid residues of the cracking process.
  • Gasoline which is the major product of the cracking process, contains highly unsaturated hydrocarbons which upon standing polymerize and oxidize to form gums, tars, and other undesirable substances.
  • the presence of sulphur compounds in a motor fuel may result in destructive corrosion of the crank case and other-parts of the motor during combustion and may also result in the destructive corrosion of the cracking or distillation equipment.
  • the hydrocarbons are treated in the liquid state, with especial application to the hydrogenation of the non-vaporized residue from the reaction and flash chamber of the cracking process.
  • the invention may be used in a process well known in the art wherein oil is heated in a continuous coil and discharged in a reaction chamber from which is withdrawn the vaporous products resulting from the distillate and cracking and a non-vaporized residue.
  • the residue from the reaction chamber may be treated according to the present invention by passing same through an insulated pipe or vessel, introducing the finely divided hydride and steam at this stage or preferably by the application of external heat to the residue leaving the reaction chamber while in the presence of steam and the finely divided hydride preferably under pressure.
  • the non-vaporized residue is discharged from the reaction chamber under pressure and is vaporized by its self-contained heat in a vessel at lower pressure
  • I may use those of sodium, potassium, calcium, magnesium, zinc, aluminum, iron, tin and others, including alloys and amalgams.
  • the oxides or metals formed by the reaction with steam have some catalytic 8.0- 3
  • I may also add molecular hydrogen to the materials undergoing reaction in order to assist in the reaction, or I may add gases containing hydrogen such as gases from oil cracking, coke oven gas, producer gas, natural gas, etc.
  • I may make use of any conventional apparatus or equipment suitable for cracking, but preferably I make use of a cracking system consisting of heating tubes or elongated pipe or heating coil in combination with a reaction chamber, dephlegmator or fractionating means and the auxiliary cooling, condensing, and collecting devices.
  • a cracking system consisting of heating tubes or elongated pipe or heating coil in combination with a reaction chamber, dephlegmator or fractionating means and the auxiliary cooling, condensing, and collecting devices.
  • I preferably return the reflux or distillates condensed in the dephlegmating or fractionating ⁇ means to the heating equipment for reconversion as well as auxiliary heating tubes for the mixture of non-vaporized residuum and hydrides and steam. The mixture in? also be returned to the primary heating u es.
  • the oil is heated to a cracking temperature, although my invention contemplates operating the process at lower temperatures also.
  • the process is operated at atmospheric pressure or at super-atmospheric pressure, and may in some cases also be operated at reduced or sub-atmospheric pressures.
  • 2'7 gravity Mid- Continent topped crude when subjected to a cracking temperature of approximately 935 degrees F. and a pressure of approximately 1000' pounds shows an approximate yield of gasoline of 55% in addition to approximately 40% of a practically sludge free fuel oil. About 5% of coke and gas are also produced. The sulphur content of the gasoline produced, which would normally be approximately 0.3%, may be'reduced to approximately 0.1%.
  • a method for hydrogenating' residuum produced in the pressure cracking of hydrocarbon oils which comprises removing the residuum from the cracking process and adding thereto, while still in heated condition, a metallic hydride in 'finely divided form, and subjecting the resultant mixture to hydrogenating conditions of temperature and pressure in the presence of steam.

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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 Apr. 10, 1934 PATENT OFFICE 1,954,478 TREATMENT OF HYDROCARBON OILS Gustav Egloff, Chicago,
Oil Products Company,
tion of South Dakota No Drawing.
Ill., assignor to Universal Chicago, 111., a corpora- Application February 14, 1930,
Serial No. 428,520
1 Claim.
This invention relates to a process for the treatment of hydrocarbon oils and refers more particularly to a process for the hydrogenation of oils at elevated temperatures.
Among the objects of the process is to increase the yield of the lower boiling products made by the thermal decomposition or cracking of higher boiling oils; to saturate in part the more highly unsaturated hydrocarbons, especially those which form gums, polymers, and other undesirable materials in the motor fuel; and to desulphurize in part the hydrocarbons to render them more suitable for motor fuel and to facilitate and reduce the cost of refining.
It is not the purpose of this invention necessarily to completely saturate the hydrocarbons of the olefin series to produce parafiin hydrocarbons, but rather to add hydrogen in regulated amounts. to the more highly unsaturated hydrocarbons for the aforementioned purposes.
In the specific embodiment of the present invention, the hydrocarbons treated are the nonvaporized liquid residues of the cracking process. Gasoline, which is the major product of the cracking process, contains highly unsaturated hydrocarbons which upon standing polymerize and oxidize to form gums, tars, and other undesirable substances. The presence of sulphur compounds in a motor fuel may result in destructive corrosion of the crank case and other-parts of the motor during combustion and may also result in the destructive corrosion of the cracking or distillation equipment.
Among the further objects of my invention is the minimizing of these objectionable features.
In the specific embodiment of the present invention, the hydrocarbons are treated in the liquid state, with especial application to the hydrogenation of the non-vaporized residue from the reaction and flash chamber of the cracking process. For example, the invention may be used in a process well known in the art wherein oil is heated in a continuous coil and discharged in a reaction chamber from which is withdrawn the vaporous products resulting from the distillate and cracking and a non-vaporized residue. The residue from the reaction chamber may be treated according to the present invention by passing same through an insulated pipe or vessel, introducing the finely divided hydride and steam at this stage or preferably by the application of external heat to the residue leaving the reaction chamber while in the presence of steam and the finely divided hydride preferably under pressure.
In one mode of operation the non-vaporized residue is discharged from the reaction chamber under pressure and is vaporized by its self-contained heat in a vessel at lower pressure, the
amount of vaporization depending upon the temsaturated portions including the pitchy and asphaltic material of the oil as well as with sulphur compounds, saturating in part the olefinic hydrocarbons and reducing some of the higher sulphur compounds to hydrogen sulphide which may readily be removed from the final products.
As examples of hydrides, I may use those of sodium, potassium, calcium, magnesium, zinc, aluminum, iron, tin and others, including alloys and amalgams. The oxides or metals formed by the reaction with steam have some catalytic 8.0- 3
tion in promoting the hydrogenation and desulphurization as well as assisting in the cracking. The use of finely divided metals has an additional advantage in that the finer the metal the greater the surface exposure and consequently the greater the velocity or rate of reaction.
In addition to the above i may also add molecular hydrogen to the materials undergoing reaction in order to assist in the reaction, or I may add gases containing hydrogen such as gases from oil cracking, coke oven gas, producer gas, natural gas, etc.
In operating the process of the invention I may make use of any conventional apparatus or equipment suitable for cracking, but preferably I make use of a cracking system consisting of heating tubes or elongated pipe or heating coil in combination with a reaction chamber, dephlegmator or fractionating means and the auxiliary cooling, condensing, and collecting devices. 1100 In the operation of the process I preferably return the reflux or distillates condensed in the dephlegmating or fractionating \means to the heating equipment for reconversion as well as auxiliary heating tubes for the mixture of non-vaporized residuum and hydrides and steam. The mixture in? also be returned to the primary heating u es.
Preferably the oil is heated to a cracking temperature, although my invention contemplates operating the process at lower temperatures also. Preferably the process is operated at atmospheric pressure or at super-atmospheric pressure, and may in some cases also be operated at reduced or sub-atmospheric pressures. Preferably I make use of super-atmospheric pressures ranging from '75 pounds to 3000 pounds, more or less, and at temperatures of from approximately 400 degrees to 1400 degrees F.
As an example of the process, 2'7 gravity Mid- Continent topped crude when subjected to a cracking temperature of approximately 935 degrees F. and a pressure of approximately 1000' pounds shows an approximate yield of gasoline of 55% in addition to approximately 40% of a practically sludge free fuel oil. About 5% of coke and gas are also produced. The sulphur content of the gasoline produced, which would normally be approximately 0.3%, may be'reduced to approximately 0.1%.
The above example is illustrative and is not intended to be fully descriptive of the broad possibilities of the process and hence should not be construed as a limitation upon the process.
I claim as my invention: i
I A method for hydrogenating' residuum produced in the pressure cracking of hydrocarbon oils which comprises removing the residuum from the cracking process and adding thereto, while still in heated condition, a metallic hydride in 'finely divided form, and subjecting the resultant mixture to hydrogenating conditions of temperature and pressure in the presence of steam.
GUSTAV EGLOFF.
US428520A 1930-02-14 1930-02-14 Treatment of hydrocarbon oils Expired - Lifetime US1954478A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3160580A (en) * 1961-10-26 1964-12-08 Degussa Process for desulfurizing and deodorizing hydrocarbons
US3676331A (en) * 1970-06-19 1972-07-11 Phillips Petroleum Co Upgrading of crude oils
US4003824A (en) * 1975-04-28 1977-01-18 Exxon Research And Engineering Company Desulfurization and hydroconversion of residua with sodium hydride and hydrogen
US4007110A (en) * 1975-04-28 1977-02-08 Exxon Research And Engineering Company Residua desulfurization with sodium oxide and hydrogen
US20050135997A1 (en) * 2003-12-19 2005-06-23 Wellington Scott L. Systems and methods of producing a crude product
WO2005061665A3 (en) * 2003-12-19 2006-04-20 Shell Oil Co Systems and methods of producing a crude product
US20100018902A1 (en) * 2003-12-19 2010-01-28 Thomas Fairchild Brownscombe Methods for producing a total product at selected temperatures

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3160580A (en) * 1961-10-26 1964-12-08 Degussa Process for desulfurizing and deodorizing hydrocarbons
US3676331A (en) * 1970-06-19 1972-07-11 Phillips Petroleum Co Upgrading of crude oils
US4003824A (en) * 1975-04-28 1977-01-18 Exxon Research And Engineering Company Desulfurization and hydroconversion of residua with sodium hydride and hydrogen
US4007110A (en) * 1975-04-28 1977-02-08 Exxon Research And Engineering Company Residua desulfurization with sodium oxide and hydrogen
US20050135997A1 (en) * 2003-12-19 2005-06-23 Wellington Scott L. Systems and methods of producing a crude product
US20050133406A1 (en) * 2003-12-19 2005-06-23 Wellington Scott L. Systems and methods of producing a crude product
US20050145538A1 (en) * 2003-12-19 2005-07-07 Wellington Scott L. Systems and methods of producing a crude product
US20050155906A1 (en) * 2003-12-19 2005-07-21 Wellington Scott L. Systems and methods of producing a crude product
US20050167322A1 (en) * 2003-12-19 2005-08-04 Wellington Scott L. Systems and methods of producing a crude product
WO2005061665A3 (en) * 2003-12-19 2006-04-20 Shell Oil Co Systems and methods of producing a crude product
WO2005061664A3 (en) * 2003-12-19 2006-05-11 Shell Oil Co Systems and methods of producing a crude product
US7413646B2 (en) 2003-12-19 2008-08-19 Shell Oil Company Systems and methods of producing a crude product
US20080272029A1 (en) * 2003-12-19 2008-11-06 Scott Lee Wellington Systems and methods of producing a crude product
US7625481B2 (en) 2003-12-19 2009-12-01 Shell Oil Company Systems and methods of producing a crude product
US20100018902A1 (en) * 2003-12-19 2010-01-28 Thomas Fairchild Brownscombe Methods for producing a total product at selected temperatures
US7879223B2 (en) 2003-12-19 2011-02-01 Shell Oil Company Systems and methods of producing a crude product

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