US1804451A - Process of treating petroleum - Google Patents
Process of treating petroleum Download PDFInfo
- Publication number
- US1804451A US1804451A US35476A US3547625A US1804451A US 1804451 A US1804451 A US 1804451A US 35476 A US35476 A US 35476A US 3547625 A US3547625 A US 3547625A US 1804451 A US1804451 A US 1804451A
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- US
- United States
- Prior art keywords
- alcohol
- oil
- distillation
- residue
- petroleum
- 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
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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
- C10G19/00—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment
-
- 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
- C10G53/00—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes
- C10G53/02—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes plural serial stages only
Definitions
- the lubricating oil fraction from such etroleums may contain considerable quantities of saponifiable constituents which may range from one-half to three percent by weight of the oil, and that these compounds, ifpresent in the oil during the subsequent acidvtreating, will frequently cause difiiculty by the formation of refractory emulsions.
- the alkali may be supplied during the distillation of" the crude-oil or the lubricating oil fraction may be redistilled in the'presence of alkaline material, but in either case, the resulting lubricatin oil fraction after such treatment is practice 1y free from sap'onifiable constituents and is in proper condition for refining with acid.
- alkali salts are formed which are comparatively non-volatile and which are thereby concentrated in the distillation residues, and it is a particular object of this invention to concentrate the saponifiable constituents of petroleum by subjecting the oil to distillation in the presence of alkaline material, thus aiding in the subsequent recovery of these constituents.
- the distillation residue or still bottoms resulting from the distillation of petroleum'in the presence of alkaline material, such for example as causticsoda, is treated with alcohol in any suitable container or vessel.
- the residue may constitute from 2 to 25 percent by volume of the original crude oil a d may contain up to from 30 to 40 percent of the alkali salts of the saponifiable material.
- the treatment with alcohol is more effective when carried out under the influence of heat and is best carried out in a closed vessel fittedwith steam coils or jacket'for heating and supplied with a reflux condenser to. revent loss of alcohol from volatilization. cans for agitating and stirring thecontents of the vessel will aid materially in reducing quired in the extraction process.
- the mixture is allowed to cool somewhat and to separate into two layers, the upper layer consisting of the alkali salts in alcoholic solution while the lower layer consists of the heavy hydrocarbon oil portion, of the still residue.
- the alcohol layer is drawn off and may then be subjected to distillation for the removal of the alcohol from the alkali salts dissolved therein.
- the alcohol thus recovered may be used again in extracting a fresh portion of the distillation residue.
- the hydrocarbon portion of the distillation residue may be used as a fuel either alone or in mixture with lighter oils or for any other suitable purpose.
- the alcohol used in the extraction of the alkali salts may vary in purity and may contain some water and, although the best results have been obtained from the use of 95% ethyl alcohol, satisfactory extraction may be accomplished with as low as 80% solutions of ethyl alcohol'in water.
- the usual denaturants contained in denatured ethyl alcohol do not affect its extraction properties to an appreciable degree and in general denatured ethyl alcohol is a satisfactory solvent for this purpose.
- ethyl alcohol is not the only alcohol suitable for extracting the alkaline.
- salts of saponifiable constituents of petroleum, and methyl, isopropyl, or other of the lower molecular weight aliphatic alcohols maybe satisfactoril used in the proo ess, although it is prefera le to use the cheapest' solvent which will accomplish the desired separation.
- a typical crude petroleum from the Gulf coastal fields is distilled by the aid of heat and'steam in the usual manner, yielding approximately 35 percent by volume of a fraction suitable for the manufacture of lubricating oil.
- This fraction is then redistilled in the presence of caustic soda, using a slight excess of caustic over and above that required for complete reaction with the saponifiable constituents of the oil, and the distillation is continued until about 5 percent of the lubricating fraction remains in the still.
- This distillation residue while hot enough to remain in a fluid condition is drawn into the extraction vessel and is then treated with approximately its own weight of 95% ethyl alcohol, the mixture being thoroughly stirred while the temperature is maintained at about 170 F. After stirring for one hour, the
- a method of treating naphthenic base crude petroleums for the recovery of naphthenic acids therefrom which comprises, separating the crude oil by distillation into three major portions, consisting essentially of a light oil distillate, an intermediate lubricating oil distillate containing a substantial quantity of naphthenic acids and a heavy still residue, redistilling the lubricating oil distillate in thepresence of alkali to reduce redistilled lubricating oils substantia 1y free from naphthenic acids and a small still residue containing in concentrated condition the alkali salts of the naphthenic acid content of the original lubricating oil distillate, treating this still residue with alcohol to dissolve the alkali salts, and separating the alcoholic solution of the alkali salts from the residual hydrocarbon oil.
- a method of treating naphthenic base crude petroleums for the recovery of naphthenic acids therefrom which comprises, distilling from'the crude petroleum a lubricating oil distillate consisting of thirty to forty per cent of the crude oil and containing a substantial quantity of naphthenic acids, rcdistilling the major portion of the lubricating oil distillate in the presence of alkali to produce redistilled lubricating oils substantially free from naphthenic acids and a small still residue containing in concentrated condition the alkali salts of the naphthenic acid content of the original lubricating oil distillate, treating this still residue with eighty to ninety per cent ethyl alcohol, and separatee a-151 3 ing the alcoholic solution of the alkali salts from the residual hydrocarbon oil.
- a method of treating naphthenic base crude petroleums for the recovery of naph- 5 thenic acids therefrom which comprises, separating bydistillation from the crude petroleum a fraction for the manufacture of lubrieating oil containing a substantial quantity of naphthenic acids, redistilling said fraction in the presence of caustic soda to produce redistilled lubricatin oils substantially free from naphthenic acids and a small still residue said residue having approximately five per cent of the volume of said fraction, treating this undistilled residue with alcohol to dissolve the alkali salts, and separating the alcoholic solution of the alkali salts from the residual hydrocarbon oil.
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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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
' 1T0 Drawing.
Patented May 12, I931 um'rao s'rA'rss PATENT; oFri-ci:
TROY M. ANDREWS AND CAB-L E. LAUEB, OF PORT ARTHUR, "13BX43, ASSIGNOBS,- BY MESNE ASSIGNMENTS, TO THE TEXASiCOMPN-Y, OF NEW YORK, N. Y., A CORPORA- rron or pnnawn'nn PROCESS OF TREATING PETROLEUM This invention relates to the treatment of petroleum and comprises a process whereby saponifiable constituents are extracted and recovered from distillation residues'obtained are ordinarily used. The crude oils of this type are usually comparatively heavy oils containing only a small quantity of the lighter hydrocarbons such as gasoline or naphtha. However, upon distillation, these crudes yield large quantities of fractions suitable as raw stock for the manufacture of high grade lubricating oils, as much as to ercent of the crude usually being suitable for this the oil is roughly separated into three major portions consisting of a lighter portion such as gas oil, an intermediate portion which is the lubricating oil distillate, and the heavy tarry still residues. The intermediate portion is further refined by treatment with sulfuric acid filtration and the like toyield stable products of merchantable grade.
It has been found that the lubricating oil fraction from such etroleums may contain considerable quantities of saponifiable constituents which may range from one-half to three percent by weight of the oil, and that these compounds, ifpresent in the oil during the subsequent acidvtreating, will frequently cause difiiculty by the formation of refractory emulsions. A preferred method of removing these saponifiable compounds from 1925. Serial .No. 35,478.
presence of an alkaline material. The alkali may be supplied during the distillation of" the crude-oil or the lubricating oil fraction may be redistilled in the'presence of alkaline material, but in either case, the resulting lubricatin oil fraction after such treatment is practice 1y free from sap'onifiable constituents and is in proper condition for refining with acid.
As a result of the reaction between the saponifiable constituents and the alkaline material during distillation, alkali salts are formed which are comparatively non-volatile and which are thereby concentrated in the distillation residues, and it is a particular object of this invention to concentrate the saponifiable constituents of petroleum by subjecting the oil to distillation in the presence of alkaline material, thus aiding in the subsequent recovery of these constituents.
Now we have found that by treating the residues resulting from the distillation of petroleum in the presence of alkaline material with alcohol, the alkali salts which are formed during the distillation by the reaction between the saponifiable constituents and the alkaline materials are dissolved and may thus be separated from the heavy hydrocarbon portion of the residue which is relatively insoluble in alcohol.
In the practice ofthe invention a preferable procedure is as follows:
The distillation residue or still bottoms resulting from the distillation of petroleum'in the presence of alkaline material, such for example as causticsoda, is treated with alcohol in any suitable container or vessel. The residue may constitute from 2 to 25 percent by volume of the original crude oil a d may contain up to from 30 to 40 percent of the alkali salts of the saponifiable material. The treatment with alcohol is more effective when carried out under the influence of heat and is best carried out in a closed vessel fittedwith steam coils or jacket'for heating and supplied with a reflux condenser to. revent loss of alcohol from volatilization. cans for agitating and stirring thecontents of the vessel will aid materially in reducing quired in the extraction process.
the time re- After thoroughly stirring the still bottomsand alcohol while under the influence of heat,
the mixture is allowed to cool somewhat and to separate into two layers, the upper layer consisting of the alkali salts in alcoholic solution while the lower layer consists of the heavy hydrocarbon oil portion, of the still residue. During the period of settling, boiling of the alcohol is to be avoided as this would result in the prevention of a clean separation of the oil and alcohol layers. After the separation of the two layers is substantially complete the alcohol layer is drawn off and may then be subjected to distillation for the removal of the alcohol from the alkali salts dissolved therein. The alcohol thus recovered may be used again in extracting a fresh portion of the distillation residue. The hydrocarbon portion of the distillation residue may be used as a fuel either alone or in mixture with lighter oils or for any other suitable purpose. 7 V 1 The alcohol used in the extraction of the alkali salts may vary in purity and may contain some water and, although the best results have been obtained from the use of 95% ethyl alcohol, satisfactory extraction may be accomplished with as low as 80% solutions of ethyl alcohol'in water. The usual denaturants contained in denatured ethyl alcohol do not affect its extraction properties to an appreciable degree and in general denatured ethyl alcohol is a satisfactory solvent for this purpose. However, ethyl alcohol is not the only alcohol suitable for extracting the alkaline. salts of saponifiable constituents of petroleum, and methyl, isopropyl, or other of the lower molecular weight aliphatic alcohols maybe satisfactoril used in the proo ess, although it is prefera le to use the cheapest' solvent which will accomplish the desired separation.
In order that the invention may be more fully understood, the following specific example of the operation of the process will be described.
A typical crude petroleum from the Gulf coastal fields is distilled by the aid of heat and'steam in the usual manner, yielding approximately 35 percent by volume of a fraction suitable for the manufacture of lubricating oil. This fraction is then redistilled in the presence of caustic soda, using a slight excess of caustic over and above that required for complete reaction with the saponifiable constituents of the oil, and the distillation is continued until about 5 percent of the lubricating fraction remains in the still. This distillation residue while hot enough to remain in a fluid condition, is drawn into the extraction vessel and is then treated with approximately its own weight of 95% ethyl alcohol, the mixture being thoroughly stirred while the temperature is maintained at about 170 F. After stirring for one hour, the
mixture is allowed to settle for three hours during which time stratification of the oil and alcohol layers takes place. The alcohol layer is then withdrawn from the vessel and the alcohol is distilled from the dissolved equally adapted for the recovery of similar constituents from the alkali distillation residues from any petroleum oil which may contain saponifiable constituents.
Obviously many modifications and variations of the invention, as hereinbefore set forth, may be made without departing from the spirit and scope thereof, and therefore, only such limitation should be imposed as are indicated in the appended claims.
We claim:
1. A method of treating naphthenic base crude petroleums for the recovery of naphthenic acids therefrom, which comprises, separating the crude oil by distillation into three major portions, consisting essentially of a light oil distillate, an intermediate lubricating oil distillate containing a substantial quantity of naphthenic acids and a heavy still residue, redistilling the lubricating oil distillate in thepresence of alkali to reduce redistilled lubricating oils substantia 1y free from naphthenic acids and a small still residue containing in concentrated condition the alkali salts of the naphthenic acid content of the original lubricating oil distillate, treating this still residue with alcohol to dissolve the alkali salts, and separating the alcoholic solution of the alkali salts from the residual hydrocarbon oil.
2. A method of treating naphthenic base crude petroleums for the recovery of naphthenic acids therefrom which comprises, distilling from'the crude petroleum a lubricating oil distillate consisting of thirty to forty per cent of the crude oil and containing a substantial quantity of naphthenic acids, rcdistilling the major portion of the lubricating oil distillate in the presence of alkali to produce redistilled lubricating oils substantially free from naphthenic acids and a small still residue containing in concentrated condition the alkali salts of the naphthenic acid content of the original lubricating oil distillate, treating this still residue with eighty to ninety per cent ethyl alcohol, and separatee a-151 3 ing the alcoholic solution of the alkali salts from the residual hydrocarbon oil.
3. A method of treating naphthenic base crude petroleums for the recovery of naph- 5 thenic acids therefrom which comprises, separating bydistillation from the crude petroleum a fraction for the manufacture of lubrieating oil containing a substantial quantity of naphthenic acids, redistilling said fraction in the presence of caustic soda to produce redistilled lubricatin oils substantially free from naphthenic acids and a small still residue said residue having approximately five per cent of the volume of said fraction, treating this undistilled residue with alcohol to dissolve the alkali salts, and separating the alcoholic solution of the alkali salts from the residual hydrocarbon oil.
In witness whereof we have hereunto set our hands this 27th day of May, 1925.
TROY M. ANDREWS. CARL E. LAUER.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US35476A US1804451A (en) | 1925-06-06 | 1925-06-06 | Process of treating petroleum |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US35476A US1804451A (en) | 1925-06-06 | 1925-06-06 | Process of treating petroleum |
Publications (1)
Publication Number | Publication Date |
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US1804451A true US1804451A (en) | 1931-05-12 |
Family
ID=21882914
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US35476A Expired - Lifetime US1804451A (en) | 1925-06-06 | 1925-06-06 | Process of treating petroleum |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2477190A (en) * | 1945-07-09 | 1949-07-26 | Union Oil Co | Naphthenic acid production |
US2966456A (en) * | 1957-01-02 | 1960-12-27 | Sun Oil Co | Removing acids from petroleum |
-
1925
- 1925-06-06 US US35476A patent/US1804451A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2477190A (en) * | 1945-07-09 | 1949-07-26 | Union Oil Co | Naphthenic acid production |
US2966456A (en) * | 1957-01-02 | 1960-12-27 | Sun Oil Co | Removing acids from petroleum |
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