US1935161A - Treatment of hydrocarbon oils - Google Patents
Treatment of hydrocarbon oils Download PDFInfo
- Publication number
- US1935161A US1935161A US512208A US51220831A US1935161A US 1935161 A US1935161 A US 1935161A US 512208 A US512208 A US 512208A US 51220831 A US51220831 A US 51220831A US 1935161 A US1935161 A US 1935161A
- Authority
- US
- United States
- Prior art keywords
- treatment
- approximately
- distillate
- steam
- sulphur trioxide
- 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
- 238000011282 treatment Methods 0.000 title description 17
- 229930195733 hydrocarbon Natural products 0.000 title description 13
- 150000002430 hydrocarbons Chemical class 0.000 title description 13
- 239000004215 Carbon black (E152) Substances 0.000 title description 12
- 239000003921 oil Substances 0.000 title description 9
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 28
- 229910044991 metal oxide Inorganic materials 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000007670 refining Methods 0.000 description 9
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000005864 Sulphur Substances 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 239000012808 vapor phase Substances 0.000 description 4
- 239000011787 zinc oxide Substances 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 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
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali 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
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- HTUMBQDCCIXGCV-UHFFFAOYSA-N lead oxide Chemical compound [O-2].[Pb+2] HTUMBQDCCIXGCV-UHFFFAOYSA-N 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N lead(II) oxide Inorganic materials [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C10G17/00—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge
- C10G17/09—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge with acid salts
-
- 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
- C10G17/00—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge
- C10G17/02—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge with acids or acid-containing liquids, e.g. acid sludge
Definitions
- the invention embodies a process for refining cracked hydrocarbon oils and comprises subjecting such oils to treatment with sulphur trioxide and steam in the presence of a metallic oxide.
- the invention has'especial application to the refining of the lighter hydrocarbon distillatesin the vapor phase and is particularly useful in the refiningin'the vapor phase of the relatively low boiling products resulting from theconversion of hydrocarbon oils by subjecting the said vapors from the cracking process during or subsequent to fractionation to treatment with sulphur trioxide and steam in the presence of a metallic oxide.
- the usual method of refining cracked distillates is to subject them to treatment with sulphuric acid and alkaline solutions, including plumbite solutions consisting of litharge dissolved in alkaline solutions in various combinations of treatment and subsequently to subject the acid treated product to redistillation' usually in the presence of steam.
- the present invention permits the direct treatment of the hydrocarbon vapors from the cracking process, reducing the cost of reagents and eliminating the redistillation or rerunning operation, although it is within the scope of the invention to revaporize the product in a subsequent operation and subject the vapors to treatment as described. 7
- metallic oxides which may be used and as examples thereof are the following:
- any suitable equipment may be employed which will permit the contacting of the hydrocarbon vapors and the sulphur trioxide and steam treated in the manner described.
- the tower or treating vessel containing the metallic oxides may be introduced directly intothe tower or treating vessel containing the metallic oxides.
- an inert filling material such as Raschig rings, firebrick, crushed rock, gravel, crushed ceramic material, and the like, suitably coated with a metallic oxide, or a mixture of the same may be employed.
- any device which permits the efficient contacting of the vapors undergoing treatment with the metallic oxide may be employed.
- the tower or. treating vessel containing the metallic oxides may be directly connected to a cracking unit or to a rerun, or redistillation unit so that the vapors arising therefrom may be 7 It has been found desirable to neutralize the distillate immediately after condensation either by passing the condensate directly through a body of alkaline material such as a solution of caustic soda or by washing the distillate free of sulphur trioxide with water and/or alkalies, such as a solution of caustic soda, ammonia, or the like.
- the neutralizing agent may also be introduced into the vapor line leading to the condenser or into the condenser itself.
- the amount of sulphur trioxide employed may vary from a fraction of a pound to several pounds,
- temperatures of treatment may be employed, for example, from 250-600 F. more or less, and the pressures may be sub-atmospheric, atmospheric, or superatmospheric. While the results may vary with the temperatures employed, the pressures and temperatures are chosen so that the hydrocarbons are treated substantially in the vapor phase.
- the sulphur trioxide may be admixed with an inert gas such as flue gas, carbon dioxide and the like, and is preferably introduced at various points in the treating tower.
- an inert gas such as flue gas, carbon dioxide and the like
- a mixed Mid-Continent and West Texas cracked distillate when treated in the vapor phase with sulphur trioxide and steam employing iron oxide as a contacting agent gives the following results:
- the untreated distillate shows a gum content of approximately 350 mgs. per 100 ccs. and a light amber color.
- the treated distillate may be reduced in gum content to approximately 30 mgs. per 100 ccs. and a color of approximately 30 on the Saybolt colorimeter scale.
- the sulphur content may be reduced also.
- a California cracked distillate when treated with approximately two pounds of sulphur trioxide and steam in the presence of copper oxide shows the following results:
- the untreated distillate contains approximately 600 mgs. of gum per 100 ccs.
- the treated distillate may contain approximately 50 mgs. per 100 ccs.
- the untreated distillate is a dark reddish amber in color, and the treated distillate may have a color from 25 to 30 on the Saybolt colorimeter scale.
- the sulphur content is quite appreciably reduced.
- gum per 100 ccs. having a color of approximately 25-30 on the Saybolt calorimeter scale and with an appreciable reduction in sulphur content by treatment with sulphur trioxide and steam employing approximately two pounds per barrel, based on the distillate treated, and using iron oxide as the contacting agent. Similar results may be obtained by employing sulphur trioxide and steam.
- tin oxide gives good results when employed as a contacting agent for the treatment of cracked hydrocarbon vapors with sulphur trioxide and steam. Similar results to those shown for zinc oxide may be obtained, but the results vary in degree.
- the treatment herein described may constitute the sole refining action on the oil, or it may constitute one step in a series of refining steps. It may be preceded by the usual treatments with refining agents such as sulphuric acid, caustic soda, plumbite, filtering earth or the like, and may be succeeded by any combination of the above refining agents, followed, if desired, by distillation.
- refining agents such as sulphuric acid, caustic soda, plumbite, filtering earth or the like
- a step in a process of refining the overhead product of motor fuel boiling range resulting from the cracking of hydrocarbon oil which comprises subjecting said product in a heated vaporous state to treatment with sulphur trioxide and steam in the presence of a metallic oxide.
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 Nov. 14, 1933 mm STA E :1,935,161 1 TREATMENT or HYDROCARBON OILS Jacque C. Morrell and Gustav Egloff, Chicago, 111., assignors to Universal Oil Products Company, Chicago, Dakota No Drawing.
111., a corporation of South Application January 29, 1931 Serial No. 512,208
1 Claim. (01-196 36) This invention relates tothe treatment of hydrocarbon oils, and refers more particularly tov the refining of the relatively low. boiling hydrocarbon distillates. 1
In one of its specific aspects the invention embodies a process for refining cracked hydrocarbon oils and comprises subjecting such oils to treatment with sulphur trioxide and steam in the presence of a metallic oxide. g r The invention has'especial application to the refining of the lighter hydrocarbon distillatesin the vapor phase and is particularly useful in the refiningin'the vapor phase of the relatively low boiling products resulting from theconversion of hydrocarbon oils by subjecting the said vapors from the cracking process during or subsequent to fractionation to treatment with sulphur trioxide and steam in the presence of a metallic oxide.
The usual method of refining cracked distillates is to subject them to treatment with sulphuric acid and alkaline solutions, including plumbite solutions consisting of litharge dissolved in alkaline solutions in various combinations of treatment and subsequently to subject the acid treated product to redistillation' usually in the presence of steam. The present invention permits the direct treatment of the hydrocarbon vapors from the cracking process, reducing the cost of reagents and eliminating the redistillation or rerunning operation, although it is within the scope of the invention to revaporize the product in a subsequent operation and subject the vapors to treatment as described. 7
Among the metallic oxides which may be used and as examples thereof are the following: The
oxides of calcium, magnesium, aluminum, zinc, tin, iron, copper, lead, mercury, cobalt, nickel, chromium, manganese, molybdenum, vanadium, tungsten, and the like. It is within the scope of the present invention to employ mixtures of the metallic oxides.
In applying the process of the invention to practice any suitable equipment may be employed which will permit the contacting of the hydrocarbon vapors and the sulphur trioxide and steam treated in the manner described.
with steam is introduced into the tower.
may be introduced directly intothe tower or treating vessel containing the metallic oxides. In lieu of direct packing of the tower or treating vessel with the metallic oxides an inert filling material such as Raschig rings, firebrick, crushed rock, gravel, crushed ceramic material, and the like, suitably coated with a metallic oxide, or a mixture of the same may be employed. Similarly, any device which permits the efficient contacting of the vapors undergoing treatment with the metallic oxide may be employed.
The tower or. treating vessel containing the metallic oxides may be directly connected to a cracking unit or to a rerun, or redistillation unit so that the vapors arising therefrom may be 7 It has been found desirable to neutralize the distillate immediately after condensation either by passing the condensate directly through a body of alkaline material such as a solution of caustic soda or by washing the distillate free of sulphur trioxide with water and/or alkalies, such as a solution of caustic soda, ammonia, or the like. The neutralizing agent may also be introduced into the vapor line leading to the condenser or into the condenser itself.
The amount of sulphur trioxide employed may vary from a fraction of a pound to several pounds,
based on a barrel of hydrocarbon distillate treated.
Various temperatures of treatment may be employed, for example, from 250-600 F. more or less, and the pressures may be sub-atmospheric, atmospheric, or superatmospheric. While the results may vary with the temperatures employed, the pressures and temperatures are chosen so that the hydrocarbons are treated substantially in the vapor phase.
In order to reduce the intensity of the reaction the sulphur trioxide may be admixed with an inert gas such as flue gas, carbon dioxide and the like, and is preferably introduced at various points in the treating tower.
As specific examples of the operation of the 'process of my invention and of the results obtained, at California cracked distillate of approximately motor fuel boiling range is vaporized and subjected to treatment with sulphur trioxide and steam in the presence of zinc oxide. The vapors are passed at a suitable rate through the tower containing the zinc oxide and approximately one pound per barrel of sulphur trioxide together The untreated product shows a gum content of approximately 450 mgs. per 100 cos. and is a reddish brown color. The sulphur content was approximately 0.25. The treated product shows a gum content of approximately 18 mgs. per 100 ccs. and has a color of plus 25 on the Saybolt colorimeter scale. The sulphur content is reduced to approximately 0.16. The gum determinations are made by the copper dish method.
When the zinc oxide is distributed over pumice stone similar results to those just described were obtained.
A mixed Mid-Continent and West Texas cracked distillate when treated in the vapor phase with sulphur trioxide and steam employing iron oxide as a contacting agent gives the following results: The untreated distillate shows a gum content of approximately 350 mgs. per 100 ccs. and a light amber color. The treated distillate may be reduced in gum content to approximately 30 mgs. per 100 ccs. and a color of approximately 30 on the Saybolt colorimeter scale. The sulphur content may be reduced also.
A California cracked distillate when treated with approximately two pounds of sulphur trioxide and steam in the presence of copper oxide shows the following results: The untreated distillate contains approximately 600 mgs. of gum per 100 ccs. The treated distillate may contain approximately 50 mgs. per 100 ccs. The untreated distillate is a dark reddish amber in color, and the treated distillate may have a color from 25 to 30 on the Saybolt colorimeter scale. The sulphur content is quite appreciably reduced.
With a Mid-Continent distillate containing approximately 350 mgs. of gum per 100 ccs. and having a dark yellow color one may obtain a product containing approximately 25 mgs. of
gum per 100 ccs. having a color of approximately 25-30 on the Saybolt calorimeter scale and with an appreciable reduction in sulphur content by treatment with sulphur trioxide and steam employing approximately two pounds per barrel, based on the distillate treated, and using iron oxide as the contacting agent. Similar results may be obtained by employing sulphur trioxide and steam.
The use of tin oxide gives good results when employed as a contacting agent for the treatment of cracked hydrocarbon vapors with sulphur trioxide and steam. Similar results to those shown for zinc oxide may be obtained, but the results vary in degree.
The above examples are only illustrative and should not be construed as restrictions or limitations on the broad scope of the invention.
The treatment herein described may constitute the sole refining action on the oil, or it may constitute one step in a series of refining steps. It may be preceded by the usual treatments with refining agents such as sulphuric acid, caustic soda, plumbite, filtering earth or the like, and may be succeeded by any combination of the above refining agents, followed, if desired, by distillation.
We claim as our invention:
A step in a process of refining the overhead product of motor fuel boiling range resulting from the cracking of hydrocarbon oil, which comprises subjecting said product in a heated vaporous state to treatment with sulphur trioxide and steam in the presence of a metallic oxide.
JACQUE C. MORRELL. GUSTAV EGLOFF.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US512208A US1935161A (en) | 1931-01-29 | 1931-01-29 | Treatment of hydrocarbon oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US512208A US1935161A (en) | 1931-01-29 | 1931-01-29 | Treatment of hydrocarbon oils |
Publications (1)
Publication Number | Publication Date |
---|---|
US1935161A true US1935161A (en) | 1933-11-14 |
Family
ID=24038143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US512208A Expired - Lifetime US1935161A (en) | 1931-01-29 | 1931-01-29 | Treatment of hydrocarbon oils |
Country Status (1)
Country | Link |
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US (1) | US1935161A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2418374A (en) * | 1943-11-20 | 1947-04-01 | Texas Co | Process for the production of alkadienes |
-
1931
- 1931-01-29 US US512208A patent/US1935161A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2418374A (en) * | 1943-11-20 | 1947-04-01 | Texas Co | Process for the production of alkadienes |
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