US2029748A - Storage of gasoline - Google Patents
Storage of gasoline Download PDFInfo
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- US2029748A US2029748A US598717A US59871732A US2029748A US 2029748 A US2029748 A US 2029748A US 598717 A US598717 A US 598717A US 59871732 A US59871732 A US 59871732A US 2029748 A US2029748 A US 2029748A
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- gasoline
- hydrogen
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- iron
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
Definitions
- This invention relates to the treatment of motor fuel, and reters'more particularly to the treatment of motor fuels produced by cracking. relatively heavier portions of crude petroleum.
- the invention provides a process or method of treatment whereby the deterioration of gasolines during storage with respect to color. gum content, knock rating, et may be substantially prevented, the method of treatment disclosed eliminating the principal causes contributing to the deterioration of the properties of the gasoline above mentioned.
- drawing has been provided which indicates six methods -of generating hydrogen, though other methods than the ones shown may be employed lo as the invention is broad in this respect.
- a simple electrolytic method of generatingv hydrogen is shown.
- a solution of' an electrolyte is maintained below the surface oi! the gasoline in a storage tank and a zinc trameor grid ot suitable type is supported in the electrolyte so that an electric couple is set up between the two metals of different position inthe electro-chemical series, this resulting in the generation of hydrogen at the surface oi.' the iron.
- the latter may comprise various solutions of inorganic acids, bases or salts and may, for example, be a simple solution of sodium chloride. caustic soda or even the natural brine separated v
- the strength of the electrolyte
- tact may be readily adjusted so that hydrogen is generated at a moderately slow rate and no removal 'of spent materials is needed until the gasoline is removed for sale.
- Fig. 2 a modincation. o! the method elm pioyed in Fig. 1 is shown, the electrolysis for the 35 generation of hydrogen being conducted in a pan or series of pans suspended in the gasoline 'at a point near the bottom ot the tank, this method allowing the introduction of new electrolytic materials without removing the gasoline from the 40 tank.
- Vemployed which may. contain materials similar to those employed in so-c'alled dry cells, hydrogen being generated un- I til the materials are spent at which timethe pan may be raised and thedresh charge introduced.
- Fig. 4 a system of hydrogen generation is shown which employs an outside electromotive force to decompose an electrolyte to produce reducing gases.
- a positive eleetromotive torce is impressed onv a carbon or iron electrode of suitimmersed in an electrolyte and insulytes by the thereto.
- the essential reaction is the decomposition of the water in the electrolyte
- the net result will be the release of hydrogen on the second electrode and oxygen on the carbon or other electrode which will result in the formation of oxides so that the reducing atmosphere in this case will consistl of hydrogen or a mixture of the various gases evolved.
- Fig. 5 shows a convenient method of slowly generating hydrogen from wateror aqueous electrointeraction of iron therewith, the rate of reaction being controllably accelerated by incorporating small amounts of copper chloride with the iron particles. This method is of simple and ready application and results in the gradual formation of iron oxide with the simultaneous liberation of equivalent amounts of hydrogen to effect the results desired.
- Fig. 6 shows a method of generating hydrogen somewhat different than the five preceding in that use is made of the sulfur which may be present in some gasolines, particularly those resulting from the cracking of high sulfur charging stocks to produce the necessary amount of hydrogen.
- scrap iron may be added to the gasoline to react slowly with the sulfur compounds with the formation of iron sulildes and the liberation of gaseous hydrogen, the eiciency of the reaction being somewhat promoted by the contact of the iron with the aluminum lining, although the conductivity of the gasoline is of a low value.
- the particular method of hydrogen generation employed and the rate of generation will also depend on a number of other factors such as the temperature of storage and the relative amounts of unsaturated and sulfur compounds present in the gasoline, etcetera. It will be noted that the tanks shown-in the drawing are provided with a vent for the release of excess gas pressure so that they will not be subjected to unsafe internal pressures. Automatic release devices or breathing systems may be employed and if necessary the evolved gases may be subjected to absorption to recover gasoline constituents although in many cases the process has the added advantage of producing a' gradual stabilization or weathering so that the gasoline is thus further improved.
- column l shows the properties of the gasoline from the fractionator. of the process prior to chemical treatment; column 2 shows the properties after treatment with ten pounds per barrel of sulfuric acid; column 2A shows the properties of this treated gasoline after two months storage; column 3 shows the properties after treatment with four pounds of acid and column 3A shows the properties which this treated gasoline may have after storage during the slow generation of hydrogen beneath its surface.
- the lighter acid treatment producing the gasoline having properties shown in column 3 produced a 29 color which was slightly below the color resulting from a ten pound treatment, which, however, dropped only one point after two months storage so that the nal value was ve points higher than the color of the ten pound treated gasoline after a similar period of storage.
- the lighter acid treatment had noticeably less effect upon the octane number, the value of 74% undergoing no further change upon storage in the reducing atmosphere.
- the gum content underwent substantially no change.
- the method of preventing deterioration of gasoline containing gum and color forming constituents during storage thereof over prolonged and claims is meant a process l time periods, which comprises generating nascent hydrogen beneath the surface of the gasoline in storage, permitting the hydrogen to freely contact with the gasoline. and maintaining an atmosphere of the hydrogen above the surface of the gasoline during the storage period to prevent access of oxidizing gases to the gasoline.
- the method which comprises generating nascent hydrogen beneath the surface of the gasoline in the storagelvessel, permitting the hydrogen to freely contact with the gasoline, and maintaining an atmosphere of the hydrogen in the vessel above the surface of the gasoline during the 'storage period to prevent access of oxidizing gases to the gasoline.
- the method of preventing deterioration of gasoline containing gum and color formingcon-g stituents during storage thereof over prolonged time periods which comprises storing the gasoline in the presence of electrolytic hydrogengenerating means immersed in the body of gasoline. electrolytically generating hydrogen during storage. permitting the hydrogen to freely contact with the gasoline. and maintaining an atmosphere of the hydrogen above the surface of the gasoline.
- the method which comprises reacting upon the sulphur compounds td form hydrogen during storage, permitting the hydrogen to freely contact with the gasoline, and maintaining an atmosphere hydrogen above the surface of the gasoline.
- the method which comprises adding iron to the gasoline and reacting the same with the sulphur compounds to form hydrogen during'storage, permitting the hydrogen to freely contact with the gasoline, and maintaining an atmosphere above the surface of the gasolin 6.
- the method which comprises adding iron to the gasoline and reacting the same in the presence of aluminum with the sulphur compounds to formhydrogen during storage, permitting the hydrogen to freely contact with the gasoline, and maintaining an atmosphere of the hydrogen above the surface of the gasoline.
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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
Feb. 4, 1936.
H. c. WEBER v2,029,748
STORAGE OF GASOLINE Filed March 14, 1932 6450A /A/E @y www@ Patented -Febl 4, 1936 UNITED-A STATESl 2,029,748 STORAGE F GASGLINE Harold c. weber, Milton, Masa.,
versal 0ii Products Com assigner to Unlnany, Chicago. lll.. a..
corporation oi' South lDakota application March 14, iosa-serial No. 593,717
6Claims.
This invention relates to the treatment of motor fuel, and reters'more particularly to the treatment of motor fuels produced by cracking. relatively heavier portions of crude petroleum.
In a more speciiicy sense the invention provides a process or method of treatment whereby the deterioration of gasolines during storage with respect to color. gum content, knock rating, et may be substantially prevented, the method of treatment disclosed eliminating the principal causes contributing to the deterioration of the properties of the gasoline above mentioned.
Gasolines produced from petroleum. and particularly those produced in cracking the heavier portions thereof, contain constituents in minor percentages which are unstable on standing, particularly in the presence of light and air and at times contact with metallic surfaces. which catalyze the reactions. It has been established that the development of color and gums and loss of lmock rating suffered by gasollnes in storage is due to a large extent to the presence of di and'tri been attacked from two general oleilnic hydrocarbons which have a pronounced tendency to polymerize and form high molecular the initial stage in this gum formation being evidently attributable to the initial-formation of the undesirable unstable components to permit' storage over several months without rendering the gasoline unsaleable unless retreated.
The accomplishment of this end has thus far standpoints, the rst being' to remove the trouble-making components by suitable chemical treatments which lIihe present process is distinct from these two general methods stated,v and in one specic eml bodiment consists in providing a reducing atmosstored gasolines, thus from crude oil. Y the amount of aine used and the emciency of coninherent in the raw gasoline or treatment with sulfuric-acid or- The net result of these re- It is preferred to employ hydrogen as areducing atmosphere, and the invention further comprises the generation of hydrogen in contact with the gasoline, this being possible of accomplishment by a number of methods which may readily l To illustrate some of the the attached be applied in practice. methods which may be employed, drawing has been provided which indicates six methods -of generating hydrogen, though other methods than the ones shown may be employed lo as the invention is broad in this respect. Referring to Flg. 1 of the drawing, a simple electrolytic method of generatingv hydrogen is shown. A solution of' an electrolyte is maintained below the surface oi! the gasoline in a storage tank and a zinc trameor grid ot suitable type is supported in the electrolyte so that an electric couple is set up between the two metals of different position inthe electro-chemical series, this resulting in the generation of hydrogen at the surface oi.' the iron. which return serves the twotold purpose oi' providing a reducing atmosphere for the gasoline'and preventing corrosion or the iron. (The latter may comprise various solutions of inorganic acids, bases or salts and may, for example, be a simple solution of sodium chloride. caustic soda or even the natural brine separated v The strength of the electrolyte,
tact may be readily adjusted so that hydrogen is generated at a moderately slow rate and no removal 'of spent materials is needed until the gasoline is removed for sale. l l
In Fig. 2 a modincation. o! the method elm pioyed in Fig. 1 is shown, the electrolysis for the 35 generation of hydrogen being conducted in a pan or series of pans suspended in the gasoline 'at a point near the bottom ot the tank, this method allowing the introduction of new electrolytic materials without removing the gasoline from the 40 tank.
In` Fig. 3 a'pan is again Vemployed which may. contain materials similar to those employed in so-c'alled dry cells, hydrogen being generated un- I til the materials are spent at which timethe pan may be raised and thedresh charge introduced.
, In Fig. 4 a system of hydrogen generation is shown which employs an outside electromotive force to decompose an electrolyte to produce reducing gases. A positive eleetromotive torce is impressed onv a carbon or iron electrode of suitimmersed in an electrolyte and insulytes by the thereto. Assuming that the essential reaction is the decomposition of the water in the electrolyte, the net result will be the release of hydrogen on the second electrode and oxygen on the carbon or other electrode which will result in the formation of oxides so that the reducing atmosphere in this case will consistl of hydrogen or a mixture of the various gases evolved.
Fig. 5 shows a convenient method of slowly generating hydrogen from wateror aqueous electrointeraction of iron therewith, the rate of reaction being controllably accelerated by incorporating small amounts of copper chloride with the iron particles. This method is of simple and ready application and results in the gradual formation of iron oxide with the simultaneous liberation of equivalent amounts of hydrogen to effect the results desired.
Fig. 6 shows a method of generating hydrogen somewhat different than the five preceding in that use is made of the sulfur which may be present in some gasolines, particularly those resulting from the cracking of high sulfur charging stocks to produce the necessary amount of hydrogen. By employing an aluminum lined tank which is resistant to the corrosive action of hydrogen sulfide and homologous sulfur compounds, scrap iron may be added to the gasoline to react slowly with the sulfur compounds with the formation of iron sulildes and the liberation of gaseous hydrogen, the eiciency of the reaction being somewhat promoted by the contact of the iron with the aluminum lining, although the conductivity of the gasoline is of a low value.
The foregoing examples of methods for producing reducing atmospheres essential to the preservation of desirable properties in gasoline are merely illustrative of many different methods that may be employed. The rate of generation of the gas may be controlled in a variety of ways, and in general will be maintained only at a point sufiicient to prevent the depreciation of properties in any particular gasoline being stored. It has been found that with gasolines of fairly good stability that the amount of hydrogen necessary is very small, and in some cases it is suillcient merely to provide enough for the initial displacement of oxidizing gases in the storage tank, while in others the generation of hydrogen must be maintained at a higher rate to insure effective inhibiting action.
The particular method of hydrogen generation employed and the rate of generation will also depend on a number of other factors such as the temperature of storage and the relative amounts of unsaturated and sulfur compounds present in the gasoline, etcetera. It will be noted that the tanks shown-in the drawing are provided with a vent for the release of excess gas pressure so that they will not be subjected to unsafe internal pressures. Automatic release devices or breathing systems may be employed and if necessary the evolved gases may be subjected to absorption to recover gasoline constituents although in many cases the process has the added advantage of producing a' gradual stabilization or weathering so that the gasoline is thus further improved.
As an example of the results which may be obtained by the application oi.' the process, the case of storage of a gasoline made by cracking heavy Mid-Continent residuum may be cited. To suillciently stabilize the gasoline produced from the process so that it may be stored for two monthswithout undue depreciation in properties may necessitate the use of 8 to 10 pounds of 66 B.
ving at the same time from 20 to 55 mgs.
sulfuric acid per barrel of gasoline. By maintaining a reducing atmosphere in the gasoline, the amount of acid necessary for producing a saleable product before and after storage may be reduced to four pounds per barrel.
The following tabulation shows in column l the properties of the gasoline from the fractionator. of the process prior to chemical treatment; column 2 shows the properties after treatment with ten pounds per barrel of sulfuric acid; column 2A shows the properties of this treated gasoline after two months storage; column 3 shows the properties after treatment with four pounds of acid and column 3A shows the properties which this treated gasoline may have after storage during the slow generation of hydrogen beneath its surface.
Gravity, A. P. 1....,.-. 56.1 56. 2 55.8 56.3 56
End point, F. 410 415 417 412 411 Color, Sayb t 10 +30 23 29 28 Gums, copper dish 340 20 55 30 25 Total sulfur, per cent.-. 0. 28 0. 11 0.11 0. 13 0. l2
Octane number 76 7l 69 74 74 Consideration of the figures in the preceding tabulation will make the advantages of the process readily apparent. It willbe observed that while the color produced in the ten pound acid treatment was +30, that the color dropped after two months storage to 23, the gum content ris- Furthermore, the relatively heavy acid treatment reduced the octane number 4%, this dropping still further on storage to a nal value of 69%.
The lighter acid treatment producing the gasoline having properties shown in column 3 produced a 29 color which was slightly below the color resulting from a ten pound treatment, which, however, dropped only one point after two months storage so that the nal value was ve points higher than the color of the ten pound treated gasoline after a similar period of storage. The lighter acid treatment had noticeably less effect upon the octane number, the value of 74% undergoing no further change upon storage in the reducing atmosphere. The gum content underwent substantially no change.
The preceding description of the invention and the examples of results obtainable by its use will serve to define its character and show its advantages, but neither is to be construed as imposing limitations thereon.
By the .term electrolytic means as used in the specification which not only includes the use of electric current for generating hydrogen, but also the use of metals or other substances in conjunctionwith a medium whereby a diierence in electromotive potential exists between two or more of the substances, and as a result hydrogen is generated.
The expression storage over prolonged time periods", used in the claims, is intended to differentiate from the customary refining of oil wherein the time of contact between the oil and rening agents in treating apparatus is only of relatively short duration as compared with .the customary long time periods during which oil is kept in storage vessels while awaiting disposal.
I claim as my invention:
1, The method of preventing deterioration of gasoline containing gum and color forming constituents during storage thereof over prolonged and claims is meant a process l time periods, which comprises generating nascent hydrogen beneath the surface of the gasoline in storage, permitting the hydrogen to freely contact with the gasoline. and maintaining an atmosphere of the hydrogen above the surface of the gasoline during the storage period to prevent access of oxidizing gases to the gasoline.
2. In the storage over prolonged time periods df gasoline con gum and color forming constituents, the method which comprises generating nascent hydrogen beneath the surface of the gasoline in the storagelvessel, permitting the hydrogen to freely contact with the gasoline, and maintaining an atmosphere of the hydrogen in the vessel above the surface of the gasoline during the 'storage period to prevent access of oxidizing gases to the gasoline.
3. The method of preventing deterioration of gasoline containing gum and color formingcon-g stituents during storage thereof over prolonged time periods, which comprises storing the gasoline in the presence of electrolytic hydrogengenerating means immersed in the body of gasoline. electrolytically generating hydrogen during storage. permitting the hydrogen to freely contact with the gasoline. and maintaining an atmosphere of the hydrogen above the surface of the gasoline.
4. In the st'drage over prolonged time periods of gasoline gum and color forming constituents, the method which comprises reacting upon the sulphur compounds td form hydrogen during storage, permitting the hydrogen to freely contact with the gasoline, and maintaining an atmosphere hydrogen above the surface of the gasoline.
5. In the storage over prolonged time periods of gasoline containing sulphur compounds and gum and color forming constituents, the method which comprises adding iron to the gasoline and reacting the same with the sulphur compounds to form hydrogen during'storage, permitting the hydrogen to freely contact with the gasoline, and maintaining an atmosphere above the surface of the gasolin 6. In the storage over prolonged time periods of gasoline containing sulphur compounds and gum and color forming constituents, the method which comprises adding iron to the gasoline and reacting the same in the presence of aluminum with the sulphur compounds to formhydrogen during storage, permitting the hydrogen to freely contact with the gasoline, and maintaining an atmosphere of the hydrogen above the surface of the gasoline.
. HAROLD C. WEBER.
containing sulphur compounds and of the of the hydrogen
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Application Number | Priority Date | Filing Date | Title |
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US598717A US2029748A (en) | 1932-03-14 | 1932-03-14 | Storage of gasoline |
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US598717A US2029748A (en) | 1932-03-14 | 1932-03-14 | Storage of gasoline |
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US2029748A true US2029748A (en) | 1936-02-04 |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2728716A (en) * | 1952-03-28 | 1955-12-27 | Exxon Research Engineering Co | Adsorption process |
US2779712A (en) * | 1953-10-23 | 1957-01-29 | Standard Oil Co | Continuous process for the removal of mercaptans from hydrocarbons and apparatus therefor |
US2909486A (en) * | 1954-07-13 | 1959-10-20 | Eugene L Colichman | Inhibiting the polymerization of nuclear coolants |
US4017268A (en) * | 1975-02-12 | 1977-04-12 | Gilley E Gene | Hydrocarbon fuel containing dispersed hydrogen and method of use thereof |
US4233132A (en) * | 1979-03-19 | 1980-11-11 | Randall Carr | Method and apparatus for producing hydrogen |
-
1932
- 1932-03-14 US US598717A patent/US2029748A/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2728716A (en) * | 1952-03-28 | 1955-12-27 | Exxon Research Engineering Co | Adsorption process |
US2779712A (en) * | 1953-10-23 | 1957-01-29 | Standard Oil Co | Continuous process for the removal of mercaptans from hydrocarbons and apparatus therefor |
US2909486A (en) * | 1954-07-13 | 1959-10-20 | Eugene L Colichman | Inhibiting the polymerization of nuclear coolants |
US4017268A (en) * | 1975-02-12 | 1977-04-12 | Gilley E Gene | Hydrocarbon fuel containing dispersed hydrogen and method of use thereof |
US4233132A (en) * | 1979-03-19 | 1980-11-11 | Randall Carr | Method and apparatus for producing hydrogen |
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