US2427173A - Fuel - Google Patents
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- Publication number
- US2427173A US2427173A US528615A US52861544A US2427173A US 2427173 A US2427173 A US 2427173A US 528615 A US528615 A US 528615A US 52861544 A US52861544 A US 52861544A US 2427173 A US2427173 A US 2427173A
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- US
- United States
- Prior art keywords
- lead
- ignition
- compounds
- autoignition
- fuel
- 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.)
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Classifications
-
- 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
- C10L1/14—Organic compounds
- C10L1/26—Organic compounds containing phosphorus
- C10L1/2633—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
- C10L1/2641—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) oxygen bonds only
Definitions
- This invention relates generally to. fuels for high-compression, spark-ignition engines and more particularly to fuels in which there is less tendency to cause autoignition when high compression internal combustion enginesare operated thereon than is the case when present wellknown fuels are used under similar operating conditions. 7
- Autoignition is an ignition of the mixture by some means other than the normal ignition spark. It may occur in advance of the normal flame front after the charge has been ignited by the normal spark or it may occur before the time of normal ignition. In the latter case autoi nition and preignition 'are the same phenomenon.
- Knock does not occur in all explosions because of the so-called ignition lag which is characteristic of all fuel-air mixtures.
- ignition lag is meant the time interval during which a given fuel-air mixture can exist at a given temperature and pressure without undergoing igni.. tion.
- knock may be reduced in intensity or even eliminated entirely "by increasing sumciently the rate of inflammation of the charge.
- the engine emits disagreeable noises and is said to be rough, that is, unless it is especially designed to take extremely heavy loads. In other words, the high pressureswhich develop in extremely short times shock the mechanical system.
- One method of decreasing the time interval during which the fuel-air mixture is subjected to high pressures and temperatures is to ignite the charge at several points simultaneously.
- the number of ignition points vary considerably from one explosion to the other and the rough operation is extremely objectionable. This is because the engine is sufiering from a shock type of excitation that varies erratically in its severity and it is on this account that autoignition is to be avoided even though it occurs after the normal ignition spark.
- the present invention has as its Principal object the reduction or suppression of autoignition in spark-ignition engines.
- this object is accomplished by the use of fuels or gasolines containing addition agents which affect the chemical composition and of the oxidation characteristics of various combustion chamber deposits and of various mixtures of inorganic compounds with carbon.
- fuels or gasolines containing addition agents which affect the chemical composition and of the oxidation characteristics of various combustion chamber deposits and of various mixtures of inorganic compounds with carbon.
- certain compounds of lead commonly found incom- 'bustion chamber deposits have an unusual and unexpected effect uponrthe ignition and burning characteristics of carbon.
- tetraethyl lead being employed commercially.
- Common automotive fuels may "contain up to about 3 cc. of tetraethyl lead per gallon of gasoline.
- Aviation gasolines commonly contain substantially higher concentrations of tetraethyl lead.
- small amounts of various volatile alkyl halides are commonly employed, for example, bromides and chlorides such as ethylene dibromide and ethylene dichloride.
- the Campbell-application discloses and claims use of small amounts of volatile liquid phosphorus compounds in leaded-gasolines for use in internal combustion spark-ignition engines in order to inhibit or prevent the activating effect of lead on ignition of carbon. In this way autoignition is inhibited or prevented.
- phosphorus compounds differ greatly in their effect on the antiknock activity of the tetraethyl lead or other lead alkyl and that most of them tend to depreciate the antiknock activity of tetraethyl lead or other lead alkyl.
- trimethyl phosphate and trimethyl phosphite are particularly advantageous in that they have relatively little effect in depreciating the antiknock value of tetraethyl lead (or other lead alkyl) and at the same time have apowerful effect in preventing autoignition.
- the halide compound and/or compounds normally employed in leadedgasolines may be replaced by the phosphoruscompound or compounds with beneficial eflfect.
- trimethyl phosphate is the better additive for gasolines containing 2 cc. or more of tetramethyl lead per gallon and that trimethyl phosphite is preferable with lower concentrations of lead.
- halides such as ethylene dibromide and/or ethylene dichloride in small amounts on the order of one or two cubic centimeters per gallon of gasoline. I have found that the halide may be eliminated in whole or in part and replaced with the phosphorus compounds with beneficial effect as regards the antiknock activity of the tetraethyl lead.
- a liquid fuel for spark-ignition internal combustion engines consisting of hydrocarbons of the: gasoline boiling range, a small amount of a volatile lead alkyl compound, and at least one of the group consisting of trimethyl phosphate and trimethyl phosphite in amount less than .3%
- a leaded-gasoline containing 1 to 3 cc. per gallon of trimethyl phosphate containing 1 to 3 cc. per gallon of trimethyl phosphate.
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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)
- Output Control And Ontrol Of Special Type Engine (AREA)
Description
Patented Sept. 9, 1947 Lloyd L. Withrow, Detroit, Mich assignor to General Motors Corporation, Detroit, Mich a corporation of Delaware No Drawing. Application March 29, 1944,
Serial No. 528,615
This invention relates generally to. fuels for high-compression, spark-ignition engines and more particularly to fuels in which there is less tendency to cause autoignition when high compression internal combustion enginesare operated thereon than is the case when present wellknown fuels are used under similar operating conditions. 7
It has long been recognized that there are two distinguishable but related combustion phenomena that act as barriers to the utilization of higher compression ratios in internal combustion spark-ignition engines. By preventing the use of higher compression ratios or higher pressures attained by other means, these two barriers prevent the attainment of fuel economy and efficiency that would otherwise be possible.
These two barriers are: first, knock, and second, autoignition. Substantial progress has been made in the control of knock through the discovery of the antiknock effect of lead alkyls such as tetraethyl lead and through progress in the man- A ufacture of hydrocarbon fuels having high antiknock value. This invention has as its principal object the reduction or suppression of autoigni tion. 1
In order'to make clear the object of this'in vention it is desirable to distinguish between the phenomena of autoignition, preignition and knock. Autoignition as the name implies, is an ignition of the mixture by some means other than the normal ignition spark. It may occur in advance of the normal flame front after the charge has been ignited by the normal spark or it may occur before the time of normal ignition. In the latter case autoi nition and preignition 'are the same phenomenon.
- able form, namely, prior to ignition, the observer hears a sharp, high-pitched sound-knocksimilar to that which might be expected if the spark were advanced far beyond the normal setting.
Autoignition and normal ignition differ from the phenomenon of knock in that these phe- 7 Claims. I (Cl. 44-69) 2 nomena relate to the simultaneous inflammation of relatively small portions of the entire charge and in that theydo not develop local pressures of appreciable magnitudes. The phenomenon of knock, on the other hand, is associated with the development of comparatively high local pressures resulting from the rapid combustion of comparatively large percentages of the charge in the engine. This combustion results from a compression-ignition process occurring in the I unburned fuel-air mixture ahead of the normal flame front, and differs from autoignition in that ignition takes place simultaneously in a relatively large part of the charge eliminating the progressive type of burning process which characterizes normal combustion. In fact, the ignition of the portion of the charge which knocks is so sudden that local pressures develop in this part of the charge and the equalizing of these pressures throughout the combustion space sets up sound waves in the burned charge that are responsible I for the sound of knock.
Knock does not occur in all explosions because of the so-called ignition lag which is characteristic of all fuel-air mixtures. By the term ignition lag is meant the time interval during which a given fuel-air mixture can exist at a given temperature and pressure without undergoing igni.. tion. Obviously then, knock may be reduced in intensity or even eliminated entirely "by increasing sumciently the rate of inflammation of the charge. But, when this is done, the engine emits disagreeable noises and is said to be rough, that is, unless it is especially designed to take extremely heavy loads. In other words, the high pressureswhich develop in extremely short times shock the mechanical system.
One method of decreasing the time interval during which the fuel-air mixture is subjected to high pressures and temperatures is to ignite the charge at several points simultaneously. When engine deposits produce the multiple ignition, the number of ignition points vary considerably from one explosion to the other and the rough operation is extremely objectionable. This is because the engine is sufiering from a shock type of excitation that varies erratically in its severity and it is on this account that autoignition is to be avoided even though it occurs after the normal ignition spark.
The present invention has as its Principal object the reduction or suppression of autoignition in spark-ignition engines. In accordance with the invention, this object is accomplished by the use of fuels or gasolines containing addition agents which affect the chemical composition and of the oxidation characteristics of various combustion chamber deposits and of various mixtures of inorganic compounds with carbon. Of particular significance, it has been found that certain compounds of lead commonly found incom- 'bustion chamber deposits have an unusual and unexpected effect uponrthe ignition and burning characteristics of carbon.
Gasolines used today in automobile engines commonly contain a small amount of a lead alkyl antiknock compound, tetraethyl lead being employed commercially. Common automotive fuels may "contain up to about 3 cc. of tetraethyl lead per gallon of gasoline. Aviation gasolines commonly contain substantially higher concentrations of tetraethyl lead. Along with the tetraethyl lead small amounts of various volatile alkyl halides are commonly employed, for example, bromides and chlorides such as ethylene dibromide and ethylene dichloride. When a gasoline containing lead tetraethyl, and the bromide and/or chloride compounds is used as a fuel in internal combustion engines it is found that the deposits on the walls of the combustion chamber contain carbon and various lead compounds such as lead bromide, basic lead bromide, lead chloride, basic lead chloride, lead sulfate and basic lead sulfate. Lead compounds such as these and also engine deposits from leaded-gasolines exert a catalytic effect and not only lower the ignition temperature of carbon, but they impart to the mixture an ability to continue to burn after the primary source 'of heat is removed that is not had by carbon alone.
The effect of several lead compounds on ignition temperature is given in table below in which the ignition temperatures of mixtures containing 10 per cent of various substances and 90 per cent of carbon, in the form of carbon black, were t 1 Results obtained by averaging results of four separate determina- As indicated in this table, the halogen compounds of lead are extremely active in promoting the oxidation of carbon. Accordingly, the presence of these compounds in combustion chamber deposits will tend to produce autolgnition when other conditions are favorable.
The Campbell-application, Serial No. 475,003, filed February 6, 1943, discloses and claims use of small amounts of volatile liquid phosphorus compounds in leaded-gasolines for use in internal combustion spark-ignition engines in order to inhibit or prevent the activating effect of lead on ignition of carbon. In this way autoignition is inhibited or prevented.
I have found that phosphorus compounds differ greatly in their effect on the antiknock activity of the tetraethyl lead or other lead alkyl and that most of them tend to depreciate the antiknock activity of tetraethyl lead or other lead alkyl. I have also discovered that trimethyl phosphate and trimethyl phosphite are particularly advantageous in that they have relatively little effect in depreciating the antiknock value of tetraethyl lead (or other lead alkyl) and at the same time have apowerful effect in preventing autoignition. I have also discovered that the halide compound and/or compounds normally employed in leadedgasolines may be replaced by the phosphoruscompound or compounds with beneficial eflfect.
Relatively small amounts of the compounds of phosphorus are all that are required in leadedgasolines in order to correct the tendency toward autoignition. In many instances from 1 to 3 cc. of the phosphorus compound per gallon of gasoline have been used with satisfactory results. In general amounts less than about .3% by volume are employed. The larger amounts tend to cause an excess deposit on the engine valves and this is undesirable.
It appears as a result of my investigations that trimethyl phosphate is the better additive for gasolines containing 2 cc. or more of tetramethyl lead per gallon and that trimethyl phosphite is preferable with lower concentrations of lead.
Ordinary leaded-gasolines contain halides such as ethylene dibromide and/or ethylene dichloride in small amounts on the order of one or two cubic centimeters per gallon of gasoline. I have found that the halide may be eliminated in whole or in part and replaced with the phosphorus compounds with beneficial effect as regards the antiknock activity of the tetraethyl lead.
I claim:
1. A leaded-gasoline containing a small amount of at least one of the group consisting of trimethyl phosphate and trimethyl phosphite.
2. A leaded-gasoline containing a small amount of trimethyl phosphate.
3. A leaded-gasoline containing asmall amount of trimethyl phosphite.
4. A leaded-gasoline containing 1 to 3 cc. per gallon of atleast-one of the group consisting of trimet yl Phosphate and trimethyl phosphite.
5. A liquid fuel for spark-ignition internal combustion engines, consisting of hydrocarbons of the: gasoline boiling range, a small amount of a volatile lead alkyl compound, and at least one of the group consisting of trimethyl phosphate and trimethyl phosphite in amount less than .3%
of the fuel by volume.
6. A leaded-gasoline containing 1 to 3 cc. per gallon of trimethyl phosphate.
7. A leaded-gasoline containing 1 to 3 cc. per gallon of trimethyl phosphite.
LLOYD L. WITHROW.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US528615A US2427173A (en) | 1944-03-29 | 1944-03-29 | Fuel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US528615A US2427173A (en) | 1944-03-29 | 1944-03-29 | Fuel |
Publications (1)
Publication Number | Publication Date |
---|---|
US2427173A true US2427173A (en) | 1947-09-09 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US528615A Expired - Lifetime US2427173A (en) | 1944-03-29 | 1944-03-29 | Fuel |
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Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2543514A (en) * | 1948-01-10 | 1951-02-27 | Thompson Prod Inc | Supplementary fuel |
US2764866A (en) * | 1953-01-02 | 1956-10-02 | Exxon Research Engineering Co | Use of phosphorus compounds in leaded gasoline |
US2860958A (en) * | 1956-08-10 | 1958-11-18 | Ethyl Corp | Antiknock compositions |
US2862801A (en) * | 1953-11-05 | 1958-12-02 | Ethyl Corp | Gasoline fuels |
US2866753A (en) * | 1956-07-17 | 1958-12-30 | Pure Oil Co | Process for removing free sulfur with an organic phosphite |
US2876246A (en) * | 1955-10-07 | 1959-03-03 | Fmc Corp | Tris (phenyl chloroethyl) phosphite |
US2881202A (en) * | 1955-10-07 | 1959-04-07 | Fmc Corp | Gasoline ignition control additives |
US2889212A (en) * | 1952-07-22 | 1959-06-02 | Shell Dev | Lead scavenger compositions |
US2899387A (en) * | 1959-08-11 | Process for preventing corrosion during | ||
US2899386A (en) * | 1959-08-11 | Process for removing mercaptan sulfur | ||
US2938776A (en) * | 1955-04-26 | 1960-05-31 | Standard Oil Co | Distillate fuel composition |
US2948599A (en) * | 1954-07-26 | 1960-08-09 | Ethyl Corp | Gasoline fuel compositions |
US2979523A (en) * | 1956-03-06 | 1961-04-11 | Gulf Oil Corp | Addition products of dialkyl acid orthophosphate and olefin oxides |
US2999740A (en) * | 1956-11-27 | 1961-09-12 | Tidewater Oil Company | Surface ignition suppression |
US3000709A (en) * | 1956-10-24 | 1961-09-19 | Ethyl Corp | Antiknock gasoline compositions |
US3009790A (en) * | 1957-04-05 | 1961-11-21 | Gulf Research Development Co | Fuel for spark ignition engines |
US3070430A (en) * | 1958-12-29 | 1962-12-25 | Exxon Research Engineering Co | Combustion chamber deposit modifiers for leaded gasolines |
DE980064C (en) * | 1950-06-10 | 1970-07-09 | Shell Res Ltd | Fuel for combustion engines |
US4752374A (en) * | 1987-04-20 | 1988-06-21 | Betz Laboratories, Inc. | Process for minimizing fouling of processing equipment |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2256187A (en) * | 1935-07-17 | 1941-09-16 | Monsanto Chemicals | Mineral oil product and process of treating the same |
US2301370A (en) * | 1941-02-26 | 1942-11-10 | American Cyanamid Co | Stabilization of tetraethyl lead |
US2405560A (en) * | 1943-02-06 | 1946-08-13 | Gen Motors Corp | Fuel |
-
1944
- 1944-03-29 US US528615A patent/US2427173A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2256187A (en) * | 1935-07-17 | 1941-09-16 | Monsanto Chemicals | Mineral oil product and process of treating the same |
US2301370A (en) * | 1941-02-26 | 1942-11-10 | American Cyanamid Co | Stabilization of tetraethyl lead |
US2405560A (en) * | 1943-02-06 | 1946-08-13 | Gen Motors Corp | Fuel |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2899387A (en) * | 1959-08-11 | Process for preventing corrosion during | ||
US2899386A (en) * | 1959-08-11 | Process for removing mercaptan sulfur | ||
US2543514A (en) * | 1948-01-10 | 1951-02-27 | Thompson Prod Inc | Supplementary fuel |
DE980064C (en) * | 1950-06-10 | 1970-07-09 | Shell Res Ltd | Fuel for combustion engines |
US2889212A (en) * | 1952-07-22 | 1959-06-02 | Shell Dev | Lead scavenger compositions |
US2764866A (en) * | 1953-01-02 | 1956-10-02 | Exxon Research Engineering Co | Use of phosphorus compounds in leaded gasoline |
US2862801A (en) * | 1953-11-05 | 1958-12-02 | Ethyl Corp | Gasoline fuels |
US2948599A (en) * | 1954-07-26 | 1960-08-09 | Ethyl Corp | Gasoline fuel compositions |
US2938776A (en) * | 1955-04-26 | 1960-05-31 | Standard Oil Co | Distillate fuel composition |
US2876246A (en) * | 1955-10-07 | 1959-03-03 | Fmc Corp | Tris (phenyl chloroethyl) phosphite |
US2881202A (en) * | 1955-10-07 | 1959-04-07 | Fmc Corp | Gasoline ignition control additives |
US2979523A (en) * | 1956-03-06 | 1961-04-11 | Gulf Oil Corp | Addition products of dialkyl acid orthophosphate and olefin oxides |
US2866753A (en) * | 1956-07-17 | 1958-12-30 | Pure Oil Co | Process for removing free sulfur with an organic phosphite |
US2860958A (en) * | 1956-08-10 | 1958-11-18 | Ethyl Corp | Antiknock compositions |
US3000709A (en) * | 1956-10-24 | 1961-09-19 | Ethyl Corp | Antiknock gasoline compositions |
US2999740A (en) * | 1956-11-27 | 1961-09-12 | Tidewater Oil Company | Surface ignition suppression |
US3009790A (en) * | 1957-04-05 | 1961-11-21 | Gulf Research Development Co | Fuel for spark ignition engines |
US3070430A (en) * | 1958-12-29 | 1962-12-25 | Exxon Research Engineering Co | Combustion chamber deposit modifiers for leaded gasolines |
US4752374A (en) * | 1987-04-20 | 1988-06-21 | Betz Laboratories, Inc. | Process for minimizing fouling of processing equipment |
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