US2599338A - Motor fuel - Google Patents

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Publication number
US2599338A
US2599338A US164608A US16460850A US2599338A US 2599338 A US2599338 A US 2599338A US 164608 A US164608 A US 164608A US 16460850 A US16460850 A US 16460850A US 2599338 A US2599338 A US 2599338A
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Prior art keywords
fuel
engine
stalling
furfuryl alcohol
gasoline
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US164608A
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William E Lifson
Gordon W Duncan
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Standard Oil Development Co
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Standard Oil Development Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/185Ethers; Acetals; Ketals; Aldehydes; Ketones
    • C10L1/1852Ethers; Acetals; Ketals; Orthoesters
    • C10L1/1855Cyclic ethers, e.g. epoxides, lactides, lactones

Definitions

  • the present invention relates to a motor fuel composition adapted to provide distinctly improved motor operation under cool moist operating conditions.
  • the motor fuel composition of the present invention comprises a hydrocarbon mixture boiling in the gasoline boiling range which contains as an ingredient a very small percentage of a furfuryl alcohol.
  • the fuel compositions of the present invention may contain solvent oil and other additives such as lead alkyl anti-detonants, dyes, gum inhibitors, oxidation inhibitors, and the like.
  • novel fuel compositions of this invention are primarily intended to overcome certain operational difliculties in connection with automotive, marine, stationary, and airplane engines.
  • the difiiculties referred to result in frequent stalling of the engine under idling conditions. This stalling may be encountered whenever the weather conditions in which the engine is used are such as to provide a relatively high humidity, and a temperature below about 60 F.
  • Table I Number of Complaints of Two Stalls or More (Per 100 Cars) The bare statistics of Table I coupled with the common experience of all automotive .users serves to indicate the magnitude of the problem of engine stalling encountered under cool, humid temperature conditions. However, it is significant to note that this problem has of late become of increased importance due to certain specific factors. First, most post-war cars are now provided without a manual throttle so that car owners are no longer able to increase the idle speed during the warm-up period to prevent stalling. Second, the idle speed of cars with automatic transmissions is rather critical during a warmup and the fastest idle which may be used must not be too fast, increasing the criticality of stalling conditions.
  • a medium volatility fuel was also tested, consisting of a regular grade commercial gasoline havingv ASTM distillation characteristics such that 10% distilled at 121 F., 50% distilled-at 220 F., and 90% distilled at 342 F. The number of stalls encountered with this fuel were 11. Finally a low volatility gasoline was subjected to the same test procedure. The gasoline had ASTM distillation 10, 50, and 90% points, at 126 F., 270 F. and 387 F. It was found that 5 stalls were encountered with this fuel.
  • carburetor icing is related to th volatility of the-fuel employed.
  • the least volatile fuel tested above having a 50% distillation point of 270 F., only resulted in 5 stalls, while the highest volatilityfuel, having a 50% distillation point of 190 F., resulted in 15 stalls.
  • Extrapolating these data as to the volatility of the fuel it appears that a fuel having a volatility such that the ASTM 50% distillation point is 310 F., or higherwould not be subject. to stalling difficulties during warm-up. It must be appreciated, however, that a fuel having ASTM distillation characteristics of this nature would not be desirable as regards warm-up time, cold engine acceleration, economy and crank case dilution.
  • the furfuryl alcohol may be unsaturated and have the formula C4H3OCH2OH.
  • the preferred furfuryl alcohol comprises tetrahydrofurfuryl alcohol (C4H7OCH2OH).
  • the amountof furfuryl alcohol employed should be appreciably less than about 1% by volume based upon the volume of gasoline present.
  • the preferred concentration is in the range from about 05% to .5%, especially in the range from about .1 to 3% by volume.
  • a fuel composition comprising a mixture of hydrocarbons boiling in the gasoline boiling range containing from about .05 to 1% by volume of a tetrahydro furfuryl alcohol.
  • composition as defined by claim 2 wherein said composition comprises an aviation motor fuel.
  • Fuel composition comprising a motor fuel having an octane number above about to which has been added from about .05 to 1% of a furfuryl alcohol.
  • Fuel composition comprising a motor fuel having an octane number above about 80 to which has been added from about .05 to 1% of a tetrahydro furfuryl alcohol.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Description

Patented June 3, 11952 V MOTOR FUEL William E. Lifson, Elizabeth, and Gordon W. Duncan, Westfield, N. J assignors to Standard Oil Development Company, a corporation of Delaware No Drawing. Application May 26, 1950, Serial No. 164,608
6 Claims.
The present invention relates to a motor fuel composition adapted to provide distinctly improved motor operation under cool moist operating conditions. The motor fuel composition of the present invention comprises a hydrocarbon mixture boiling in the gasoline boiling range which contains as an ingredient a very small percentage of a furfuryl alcohol. In addition the fuel compositions of the present invention may contain solvent oil and other additives such as lead alkyl anti-detonants, dyes, gum inhibitors, oxidation inhibitors, and the like.
The novel fuel compositions of this invention are primarily intended to overcome certain operational difliculties in connection with automotive, marine, stationary, and airplane engines. The difiiculties referred to result in frequent stalling of the engine under idling conditions. This stalling may be encountered whenever the weather conditions in which the engine is used are such as to provide a relatively high humidity, and a temperature below about 60 F.
While this problem has actually been existent for many years, attention has recently been focused on it due to numerous complaints of car owners particularly in'the northern portion of the United States. These owners report that during cool, wet weather their cars give poor idling performance characterized by a high number of engine stalls. The difiiculty is encountered in all types of cars employing all types of carburetors and utilizing all commercial brands of gasoline.
In order to indicate the magnitude of this difficulty, reference may be made to a survey conducted in the New Jersey area based on the experiences of 300 car owners driving twenty different car models, during the fall and winter period. These cars employed the winter grade of regular and premium commercial gasolines. Table I gives a summary of the results obtained, showing the substantial number of stalls encountered in the operation of the cars under the indicated conditions.
Table I Number of Complaints of Two Stalls or More (Per 100 Cars) The bare statistics of Table I coupled with the common experience of all automotive .users serves to indicate the magnitude of the problem of engine stalling encountered under cool, humid temperature conditions. However, it is significant to note that this problem has of late become of increased importance due to certain specific factors. First, most post-war cars are now provided without a manual throttle so that car owners are no longer able to increase the idle speed during the warm-up period to prevent stalling. Second, the idle speed of cars with automatic transmissions is rather critical during a warmup and the fastest idle which may be used must not be too fast, increasing the criticality of stalling conditions. Third, stalling of a car with automatic transmission frequently does not occur until the driver is ready to accelerate, so that just at this most inconvenient time it is necessary to shift the car to neutral, restart the engine, and shift back into gear; magnifying the inconvenience of frequent stalls. A fourth factor affecting the magnitude of stalling difficulties relates to the volatility of the fuels now provided for automotive use. The volatility of commercial fuels over a period of years has been increased sufficiently to increase stalling difiiculties as will be brought out herein.
On investigating this problem, it has been determined that the cause of repeated engine stalling in cool, humid weather is the formation of ice in the carburetor of the engine. On a cool, moist day, gasoline evaporating in the carburetor exerts suflicient refrigerating effect to condense and freeze moisture present in the air entering the carburetor. Normal fuel vaporization within the carburetor can cause a temperature reduction of the metal parts of the carburetor up to 50 F. below that of the entering air. Consequently, prior to the time of complete engine and radiator warm-up, this drop in temperature may cause formation of ice in the carburetor. Ice formation probably occurs most readily under conditions of light load operation. The result is that after a period of light load operation, when the throttle is closed to the idle position, ice already formed on the throttle plate and adjacent walls, plus ice which then forms, restricts the narrow air openings to cause engine stalling.
'To more clearly define the problem of engine stalling due to carburetor icing, data were tabulated based on customer reaction surveys, carefully controlled road tests, and laboratory cold room engine performance tests. These tests show that carburetor icing depends primarily upon atmospheric temperature and humidity conditions. The tests show that stalling difficulties due to ice formation in the carburetor are not encountered below about 30 F., norabove about 60 F. when employing fuels having conventional volatility characteristics. Similarly, these tests demonstrate that stalling is only en countered when the humidity is in excess of about 65%.
Another factor having a bearing on the formation of ice in the carburetor, is the volatility. of the fuel employed. To determine this eifect laboratory cold room tests were conducted to evaluate the stalling characteristics duringwarm-up of a number of fuels varying in volatility. In these tests a 1947 Chrysler car was installed in a room equipped with temperature and humidity controls. While the temperature and humidity were maintained at particular levels, the stalling characteristics of the car were determined during the warm-up period. The procedure employed was to start the car and to then immediately raise the engine speed to 1500 R. P. M. This speed was maintained for 30 seconds, afterwhich the engine was allowed to idle for 15 seconds. If the engine stalled before 15 seconds had expired, the car was again started and raised to a speed of 1500 R.-P. M. for 30 seconds, while if stalling did not occur, the speed was immediately increased to 1500B. P. M. after the 15 second idling time. The alternatecycles of. 30 seconds at 1500 R. P. M. followed by 15 seconds at idling were repeated-until the engine was completely warmed up. The number of stalls encountered during this procedure, and up to the time of complete engine warm-up were then recorded. Tests were conducted at 40F. and at a relative humidity of 100% employing. three fuels of varying volatilities. The most volatile fuel was a premium grade of commercial gasoline havinga ASTM distillation point of 110 F., a 50% point of 190 F., and a 90% point of 294 F. It was found that this fuel resulted in about14 or 15 stalls during warm-up. A medium volatility fuel was also tested, consisting of a regular grade commercial gasoline havingv ASTM distillation characteristics such that 10% distilled at 121 F., 50% distilled-at 220 F., and 90% distilled at 342 F. The number of stalls encountered with this fuel were 11. Finally a low volatility gasoline was subjected to the same test procedure. The gasoline had ASTM distillation 10, 50, and 90% points, at 126 F., 270 F. and 387 F. It was found that 5 stalls were encountered with this fuel.
As indicated by these data, carburetor icing is related to th volatility of the-fuel employed. Thus,the least volatile fuel tested above, having a 50% distillation point of 270 F., only resulted in 5 stalls, while the highest volatilityfuel, having a 50% distillation point of 190 F., resulted in 15 stalls. Extrapolating these data as to the volatility of the fuel, it appears that a fuel having a volatility such that the ASTM 50% distillation point is 310 F., or higherwould not be subject. to stalling difficulties during warm-up. It must be appreciated, however, that a fuel having ASTM distillation characteristics of this nature would not be desirable as regards warm-up time, cold engine acceleration, economy and crank case dilution. However, in appreciating the scope of the present invention, it is important to. note that this invention is only of application to gasoline fuels having an ASTM 50% distillation point below about 310 F. At thesame time, as. will be brought out, it is possible to correlate the quantity of additives required to overcome icing problems with the volatility'of the fuel to-be im-- proved. In other. words, smaller proportions of additives may be employed with fuels of relatively low volatility, while higher proportions of additives may be required with fuels of higher volatility.
It has now been discovered that distinctly improved operating conditions are secured with respect to stalling providing a relatively small critical amount of a furfuryl alcohol be employed. The furfuryl alcohol may be unsaturated and have the formula C4H3OCH2OH. However, the preferred furfuryl alcohol comprises tetrahydrofurfuryl alcohol (C4H7OCH2OH).
The amountof furfuryl alcohol employed should be appreciably less than about 1% by volume based upon the volume of gasoline present. The preferred concentration is in the range from about 05% to .5%, especially in the range from about .1 to 3% by volume.
It is appreciated that it has heretofore been suggested that relatively large quantities of furfuryl alcohol be employed in motor gasolines in order 'to improve their antidetonant character istics. In order tofsecure this result it has. been necessary, as stated; to use relatively-large quantities, as for example, in the range from'about 1% to 10% and higher of the furfuryl alcohol. If quantities less than this be employed, no anti detonant efiect is secured. Furthermore, in. the prior art if furfuryl alcohol were employed, it was necessary that the'base fuel have a relatively low octane number value, otherwise-the furfuryl alcohol wouldactually have an adverse antidetonant effect. Thus, nowhere in the'art has it been taught or disclosed to use furfuryl alcohol particularly tetrahydrofurfurylalcohol' in conjunction with fuels havingclear-octane numbers above about 80..
The present invention maybe more fully appreciated by thefollowing examples illustrating the same.
various concentrations in'twogasolines; a premium grade automotive gasolineand an aviation 0 gasoline. The antieknock'quality of the blends was comparedv with the same quality of the original gasolines according to the test methods appropriate for each type of gasoline. The results secured are as follows 4. Aviation Gasoline 103.2 132.2 5. No. 4 with 1.0 vol. percent t-h'f.
alcohol 101. 2 125. 7
1 ASTM Motor Method D-357-47.
'- ASTM Research Method D-908-47T.
3 ASTM Aviation Method D-6l4-47l.
4 ASTM Supercharge Method D-909-47l.
From :the above it is :evident that the tetrahydrof urfuryl alcohol-x didnot improve the anti-.
Performance Performance No. No.
knock quality and actually decreased the antiknock quality of these high octane number gasolines.
EXAMPLE II Additional operations were conducted wherein a motor fuel having the following inspections:
Engler distillation Initial ..F 100 15% F 130 30% F 158 60% F. 212 93% ..F 302 Reid V. P lbs 12 was run in a gasoline engine as described. Various quantities of blending agents were used with the following results:
AUTOMOTIVE CAR-BUBETOR ICING Tnsrs Efiect of addition agents on icing severity [1947 Chrysler; 40 F. and 100% relative humidity gyro matic transmission; Sisson automatic choke] From the above it is apparent that tetrahydro furfuryl alcohol is particularly efiective, especially when employed in a concentration from .2 to 5% by volume.
EXAMPLE 111 Additional operations were conducted using an aviation fuel of the following inspections:
Engler distillation Initial .F 100 50% ..F 200 Final F 325 Reid V. P lbs '1 The initial engine speed (Fixed Throttle) was 1750 R. P. M. The loss in speed after 3 minutes was determined when using various blends. The results secured are as follows:
GARBURETOR ICING IN CONTINENTAL ENGINE ANTI- ICING ADDITIVE EFFECTIVENESS Initial engine speed (fixed throttle), 1750 R. P.
M.; intake air, 50 F., 97 .-.':3% relative hamidity; air surrounding carburetor, 50 F.
[Amount of carburetor ice accumulated is reflected in magnitude of speed loss] From the above it is apparent that tetrahydro furfuryl alcohol is particularly effective.
Having described the invention, it is claimed:
1. A fuel composition comprising a mixture of hydrocarbons boiling in the gasoline boiling range containing from about .05 to 1% by volume of a tetrahydro furfuryl alcohol.
2. Composition as defined by claim 1 wherein the concentration of the tetrahydro furfuryl alcohol is in the range from .2 to .5%.
3. Composition as defined by claim 2 wherein said composition comprises an aviation motor fuel.
4. Fuel composition comprising a motor fuel having an octane number above about to which has been added from about .05 to 1% of a furfuryl alcohol. v
5. Fuel composition comprising a motor fuel having an octane number above about 80 to which has been added from about .05 to 1% of a tetrahydro furfuryl alcohol.
6. Composition as defined by claim 5 wherein the concentration of the tetrahydro furfuryl alcohol is in the range from .2 to .5% by volume.
WILLIAM E. LIFSON. GORDON W. DUNCAN.
REFERENCES CITED UNITED STATES PATENTS Name Date Magruder et a1. Jan. 21, 1941 Number

Claims (1)

1. A FUEL COMPOSITION COMPRISING A MIXTURE OF HYDROCARBONS BOILING IN THE GASOLINE BOILING RANGE CONTAINING FROM ABOUT .05 TO 1% BY VOLUME OF A TETRAHYDRO FURFURYL ALCOHOL.
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Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2786745A (en) * 1950-10-17 1957-03-26 California Research Corp Fuel oil
US2826037A (en) * 1951-11-09 1958-03-11 Phillips Petroleum Co Polycyclic aldehydes as hypergolic fuels
US2857255A (en) * 1954-02-19 1958-10-21 Socony Mobil Oil Co Inc Gasoline composition
US2857254A (en) * 1955-03-14 1958-10-21 Sun Oil Co Motor fuel
US2876750A (en) * 1954-01-21 1959-03-10 Phillips Petroleum Co Fuel containing anti-icing additives
US2883276A (en) * 1954-01-21 1959-04-21 Phillips Petroleum Co Fuel containing anti-icing additives
US2889213A (en) * 1954-01-06 1959-06-02 Phillips Petroleum Co Engine fuel containing anti-icing additives
US2917378A (en) * 1955-12-08 1959-12-15 American Cyanamid Co Liquid fuel compositions
US2919684A (en) * 1954-01-21 1960-01-05 Phillips Petroleum Co Fuel containing anti-icing additive
US2952969A (en) * 1955-05-26 1960-09-20 Exxon Research Engineering Co Aviation turbo fuel
US3036902A (en) * 1958-03-03 1962-05-29 Standard Oil Co Motor fuel composition
US3061420A (en) * 1955-02-11 1962-10-30 Exxon Research Engineering Co Motor fuel
US3144750A (en) * 1951-12-10 1964-08-18 Phillips Petroleum Co Polycyclic alcohols as hypergolic fuels
US4339245A (en) * 1980-10-24 1982-07-13 Phillips Petroleum Company Motor fuel
US4405335A (en) * 1982-09-27 1983-09-20 Ethyl Corporation Diesel fuel composition
US4405333A (en) * 1982-09-27 1983-09-20 Ethyl Corporation Diesel fuel composition
US4406665A (en) * 1982-08-16 1983-09-27 Ethyl Corporation Diesel fuel composition
DE3502802A1 (en) * 1985-01-29 1986-07-31 Ernst 7504 Weingarten Kirchgässner Process for improved and environmentally sounder utilisation of motor fuels
US5891202A (en) * 1996-03-15 1999-04-06 Shell Oil Company Gasoline composition
US5925152A (en) * 1996-03-15 1999-07-20 Shell Oil Company Gasoline composition
US5948126A (en) * 1996-03-15 1999-09-07 Shell Oil Company Gasoline composition
EP1188812A1 (en) * 2000-09-15 2002-03-20 Institut Francais Du Petrole Compositions of diesel fuels containing oxygenates derived from tetrahydrofurfuryl
WO2009141166A1 (en) 2008-05-19 2009-11-26 Furanix Technologies B.V. Fuel composition
EP2128227A1 (en) 2008-05-19 2009-12-02 Furanix Technologies B.V Monosubstituted furan derivatives via decarboxylation and use thereof as (aviation) fuel

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2229215A (en) * 1938-02-23 1941-01-21 Carter Carburetor Corp Antifreeze substance for fuel tanks

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2229215A (en) * 1938-02-23 1941-01-21 Carter Carburetor Corp Antifreeze substance for fuel tanks

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2786745A (en) * 1950-10-17 1957-03-26 California Research Corp Fuel oil
US2826037A (en) * 1951-11-09 1958-03-11 Phillips Petroleum Co Polycyclic aldehydes as hypergolic fuels
US3144750A (en) * 1951-12-10 1964-08-18 Phillips Petroleum Co Polycyclic alcohols as hypergolic fuels
US2889213A (en) * 1954-01-06 1959-06-02 Phillips Petroleum Co Engine fuel containing anti-icing additives
US2876750A (en) * 1954-01-21 1959-03-10 Phillips Petroleum Co Fuel containing anti-icing additives
US2883276A (en) * 1954-01-21 1959-04-21 Phillips Petroleum Co Fuel containing anti-icing additives
US2919684A (en) * 1954-01-21 1960-01-05 Phillips Petroleum Co Fuel containing anti-icing additive
US2857255A (en) * 1954-02-19 1958-10-21 Socony Mobil Oil Co Inc Gasoline composition
US3061420A (en) * 1955-02-11 1962-10-30 Exxon Research Engineering Co Motor fuel
US2857254A (en) * 1955-03-14 1958-10-21 Sun Oil Co Motor fuel
US2952969A (en) * 1955-05-26 1960-09-20 Exxon Research Engineering Co Aviation turbo fuel
US2917378A (en) * 1955-12-08 1959-12-15 American Cyanamid Co Liquid fuel compositions
US3036902A (en) * 1958-03-03 1962-05-29 Standard Oil Co Motor fuel composition
US4339245A (en) * 1980-10-24 1982-07-13 Phillips Petroleum Company Motor fuel
US4406665A (en) * 1982-08-16 1983-09-27 Ethyl Corporation Diesel fuel composition
US4405335A (en) * 1982-09-27 1983-09-20 Ethyl Corporation Diesel fuel composition
US4405333A (en) * 1982-09-27 1983-09-20 Ethyl Corporation Diesel fuel composition
DE3502802A1 (en) * 1985-01-29 1986-07-31 Ernst 7504 Weingarten Kirchgässner Process for improved and environmentally sounder utilisation of motor fuels
US5891202A (en) * 1996-03-15 1999-04-06 Shell Oil Company Gasoline composition
US5925152A (en) * 1996-03-15 1999-07-20 Shell Oil Company Gasoline composition
US5948126A (en) * 1996-03-15 1999-09-07 Shell Oil Company Gasoline composition
EP1188812A1 (en) * 2000-09-15 2002-03-20 Institut Francais Du Petrole Compositions of diesel fuels containing oxygenates derived from tetrahydrofurfuryl
FR2814173A1 (en) * 2000-09-15 2002-03-22 Inst Francais Du Petrole DIESEL FUEL COMPOSITIONS CONTAINING TETRAHYDROFURFURYL OXYGEN COMPOUNDS
US6537336B2 (en) 2000-09-15 2003-03-25 Institut Français du Pétrole Diesel fuel compositions containing oxygenated compounds derived from tetrahydrofurfuryl
WO2009141166A1 (en) 2008-05-19 2009-11-26 Furanix Technologies B.V. Fuel composition
EP2128227A1 (en) 2008-05-19 2009-12-02 Furanix Technologies B.V Monosubstituted furan derivatives via decarboxylation and use thereof as (aviation) fuel
EP2128226A1 (en) 2008-05-19 2009-12-02 Furanix Technologies B.V Fuel component
US20110107659A1 (en) * 2008-05-19 2011-05-12 Furanix Technologies B.V. Fuel composition
US8435313B2 (en) 2008-05-19 2013-05-07 Furanix Technologies, B.V. Fuel composition
US9145526B2 (en) 2008-05-19 2015-09-29 Furanix Technologies B.V. Process for preparing fuel compositions

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