US1954478A - Treatment of hydrocarbon oils - Google Patents
Treatment of hydrocarbon oils Download PDFInfo
- 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
- Authority
- 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
Links
- 239000003921 oil Substances 0.000 title description 11
- 229930195733 hydrocarbon Natural products 0.000 title description 10
- 150000002430 hydrocarbons Chemical class 0.000 title description 10
- 239000004215 Carbon black (E152) Substances 0.000 title description 4
- 238000000034 method Methods 0.000 description 16
- 238000005336 cracking Methods 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 5
- 150000004678 hydrides Chemical class 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical class [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 239000003502 gasoline Substances 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000001066 destructive effect Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910000497 Amalgam Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
- C10G47/32—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions in the presence of hydrogen-generating compounds
-
- 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
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
- C10G47/24—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions with moving solid particles
-
- 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
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
- C10G47/24—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions with moving solid particles
- C10G47/26—Cracking 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.
Landscapes
- 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.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US428520A US1954478A (en) | 1930-02-14 | 1930-02-14 | Treatment of hydrocarbon oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US428520A US1954478A (en) | 1930-02-14 | 1930-02-14 | Treatment of hydrocarbon oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1954478A true US1954478A (en) | 1934-04-10 |
Family
ID=23699227
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US428520A Expired - Lifetime US1954478A (en) | 1930-02-14 | 1930-02-14 | Treatment of hydrocarbon oils |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1954478A (en) |
Cited By (7)
| 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 |
-
1930
- 1930-02-14 US US428520A patent/US1954478A/en not_active Expired - Lifetime
Cited By (16)
| 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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