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US2800400A - Motor fuel additive and fuel containing same - Google Patents

Motor fuel additive and fuel containing same Download PDF

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Publication number
US2800400A
US2800400A US400358A US40035853A US2800400A US 2800400 A US2800400 A US 2800400A US 400358 A US400358 A US 400358A US 40035853 A US40035853 A US 40035853A US 2800400 A US2800400 A US 2800400A
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additive
fuel
boric acid
gasoline
amount
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US400358A
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Everett C Hughes
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Standard Oil Co
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Standard Oil 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, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • 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, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/106Liquid carbonaceous fuels containing additives mixtures of inorganic compounds with organic macromolecular compounds
    • 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, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/12Inorganic compounds
    • C10L1/1291Silicon and boron containing compounds
    • 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, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/1822Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
    • C10L1/1824Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
    • 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, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/198Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
    • C10L1/1985Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters

Definitions

  • This'invention relates to a motor 'fuel'additive capable of inhibiting the formation of deposit .in the carburetor and intake manifold of an :internal combustion engine as well as to liquid hydrocarbon motor fuels containing minor concentrations of such an additive.
  • Gum 'deposits may be the cause of serious operational difiiculties, for the accumulation of deposits in the intake passageway diminishesits :size and therefore the maximum air Iflow which the passage iscapable-of deliveringzto the engine. TIlre effects of such deposits on engine performance are, therefore, manifested whenever the engine is operated at or near full throttle as a reductionin power output due directly to the reduction in air flow.
  • a fuel additive which comprises a solution of 'boric'acid'in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound.
  • the solvent mixture of alcohol and polyoxyalkylene is preferably one containing from 20% to 80% alcoholby volume.
  • the additive is preferably prepared by-first dissolving as much boric acid'as possible in the alcohol and then adding the polyoxyalkylene compound to the solution.
  • the alcohol component of thexsolvent'mixture maybe any lower alcohol, such :as methyl, .ethyl-, isopropyl-,
  • butyl-,-or an amyl-alcohol that is soluble in themotor fuel and: is capable of dissolvingboric acid.
  • Methyl alcohol iszpreferre'd.
  • R and R are selected from the group consisting of hydrogen, alkyl and acyl groups having from four to about twenty carbon atoms, R is hydrogen or an alkyl group having from one to about five carbon atoms, n is a variable small whole number from one to about four, preferably two or three, and may vary in this range even in a single long chain molecule, and y represents the number of repeating units in the chain, and may be a whole number from about five to several hundred, depending on the molecular weight.
  • R and R i. e., of the end groups of the chain
  • Gum :solvency properties of these compounds are attributed primarily to the oxyalkylene units which form the chain, and not to the end groups; However, although quite a Wide variety ofthese compounds have gum solvency properties, only those with viscosities in the range of 200 to 1000 SSU at 100 'F. have the necessary 'involatility and gasoline solubility characteristics.
  • the polyoxyalkylene compound be oil-soluble, and have an SSU viscosity at 100 F. of from 200 to 1000.
  • polyoxyalkylene compound-alcohol blends in which the proportion of alcohol is preferably in the range. of 20% .to 80% by volume and which are known to inhibit to an appreciable extent the formation of gummy deposits when ,present intthe'fuel in amounts ranging: from a fraction of 1% to about 5% by volume and preferably about 1% by volume, have-their effectiveness increased still further when small amounts of boric acid are dissolved inthe blend.
  • Test No. 2 indicates that when a stable solution of as little as 0.75% by weight boric acid in polyoxyalkylene compound is added to gasoline, the boric acid forms a precipitate.
  • Tests Nos. 3 and 4 indicate that boric acid dissolved in methanol alone is somewhat less prone to precipitation when the solutions are added to gasoline, but not when the concentration of boric acid in methanol is as high as 1% by weight.
  • test No. 6 shows that the boric acid in a 1% .by weight solution thereof in a blend of polyoxyalkylene compound and alcohol does not precipitate upon addition to gasoline but, unlike in tests Nos. 2 and 4, remains stable as a solute.
  • the concentration of the additive in the gasoline may. range from a significant amount, i. e., as little as about 0.1% by volume, to about 5% by volume. Balancing the amount of improvement obtained against the expense of the additive and of blending it with the gasoline, it is generally preferred that the amount of boric acid in the blend be approximately 1% by weight and that the concentration of the additive in the gasoline be approximately 1% by volume so that the concentration of boric acid in the gasoline will be approximately 0.01% by weight.
  • Example Two fuels were subjected to comparative tests to determine the relative amounts of deposits in the engine fuel induction system.
  • One of these fuels was a motor gasoline containing 1.5 cc./ gal. tetraethyl lead and 1% by volume of an additive consisting of 25% by volume Ucon L-B 285 and 75% by volume methanol.
  • the other fuel was a'sample of the same gasoline containing the same amount of the same additive in which, however, 1% by weight, based on the additive, of boric acid had been dissolved prior to addition of the additive to the gasoline.
  • the first fuel therefore contained no boric acid and the second fuel contained 0.01% by weight boric acid.
  • the procedure used in the tests was as follows: The equipment consisted of a Waukesha single cylinder knock testing engine equipped with a special glass intake manifold. This manifold system incorporated 16% inch long Pyrex tube (22 mm. outside diameter) between the carburetor and the intake port where it was held by two special flanges. A Nichrome coil of 10 ohms resistance was wrapped around the glass manifold about 3 inches from the carburetor end so that the heated area was about 3 /2 inches long. This heating element was controlled by a volt Variac and supplied localized heating to the special manifold.
  • the temperature of the manifold was measured by a surface contact thermocouple located about /2 inch beyond the end of the coil, and the temperature was taken directly from a potentiometer.
  • the intake air was drawn into the carburetor through a preheater consisting of a glow coil heater in the induction system surge.
  • the heater was controlled from the engine panel board. The engine was operated for 10 hours, with the fuel being tested under the following conditions:
  • An additive for use with a gasoline motor fuel which comprises a solution of boric acid in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound having the formula where R and R" are selected from the group consisting of hydrogen and alkyl and acyl groups having from four to about twenty carbon atoms, R is selected from the group consisting of hydrogen and alkyl groups having from one to about five carbon atoms, n is a small whole number having a value within the range from one to about four, and y is a number representing the number of repeating units within the chain to give a viscosity of between 200 and 1000 SSU at 100 F., the amount of alcohol in said solvent mixture ranging from 20% to 80% by volume and the amount of boric acid ranging from an effective amount up to 1% by weight of said solvent mixture.
  • a gasoline motor fuel containing a minor amount within the limits of solubility in the gasoline of an additive comprising a solution of boric acid in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound having the formula where R and R" are selected from the group consisting of hydrogen and alkyl and acyl groups having from four to about twenty carbon atoms, R is selected from the group consisting of hydrogen and alkylgroups having from one to about five carbon atoms, n is a small whole number having a value within the range from one to about four, and y is a number representing the number of repeating units Within the chain to give a viscosity of between 200 and 1000 SSU at 100 F., the concentration by volume of the additive in the fuel ranging from a significant amount up to about 5% and the amount of boric acid ranging from an eifective amount to about 1% by weight of said solvent mixture.
  • An additive for use with a gasoline motor fuel which comprises a solution of boric acid in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound having the formula where R and R" are selected from the group consisting of hydrogen and alkyl and acyl groups having from four to about twenty carbon atoms, R is selected from the group consisting of hydrogen and alkyl groups having from one to about five carbon atoms, n is a small whole number having a value within the range from one to about four, and y is a number representing the number of repeating units within the chain to give a viscosity of between 200 and 1000 SSU at 100 F., the amount of alcohol in said solvent mixture ranging from 20% to by volume and the amount of boric acid ranging from an effective amount up to a minor amount within the limits of solubility of boric acid in the solvent mixture.
  • a gasoline motor fuel containing a minor amount within the limits of solubility in the gasoline of an additive comprising a solution of boric acid in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound having the formula where R and R" are selected from the group consisting of hydrogen and alkyl and acyl groups having from four to about twenty carbon atoms, R is selected from the group consisting of hydrogen and alkyl groups having from one to about five carbon atoms, n is a small whole number having a value within the range from one to about four, and y is a number representing the number of repeating units within the chain to give a viscosity of between 200 and 1000 SSU at F., the concentration by volume of the additive in the fuel ranging from a significant amount up to about 5% and the amount of boric acid ranging from an effective amount up to a minor amount within the limits of solubility of boric acid in the solvent mixture.

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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)
  • Inorganic Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Description

MOTOR FUEL ADDITIVE AND 'FUEL CONTAINING SAME Everett C. Hughes, Shaker Heights, Ohio, assignor to The Standard Oil Company, Cleveland, Ohio, a corporation of Ohio 7 I No Drawing. Application December 24, 1953, Serial No. 400,358
12 Claims. (CI. 44-56) This'invention relates to a motor 'fuel'additive capable of inhibiting the formation of deposit .in the carburetor and intake manifold of an :internal combustion engine as well as to liquid hydrocarbon motor fuels containing minor concentrations of such an additive.
Fuels derived from petroleum, and particularly cracked gasoline fuels, normally contain from 10 to 60% olefins which tend to polymerize upon standing .to form potential'gum. "This gum is readily decomposed during combustion of the fuel in the engine .to-formadhering deposits on the valves and intheintakeisystem.
Gum 'depositsmay be the cause of serious operational difiiculties, for the accumulation of deposits in the intake passageway diminishesits :size and therefore the maximum air Iflow which the passage iscapable-of deliveringzto the engine. TIlre effects of such deposits on engine performance are, therefore, manifested whenever the engine is operated at or near full throttle as a reductionin power output due directly to the reduction in air flow.
.The art has been aware that if there were incorporated in the .fuel'an additive which has .a high solvent power for the gummy :residue and which is also a non-volatile liquid at combustion temperatures, it would remain with the residue 'on the metal parts, such as valve stems, dissolve thegum, and then drain from the parts. Thus it would remove and prevent deposition .of residue 'on such parts. Numerous materials of this type, such as torch oil, have therefore previously been blended with motor fuels. In .additionto havinga high solventpowerfor the gummy residue and substantial non-volatility,.however,
such substances must also be relatively stable to oxidation and decompose into volatiledecompositionsproducts. Those materials used heretofore .haVeLbeen deficient in one or more of these properties.
.It has now been found that'the'formation of fuel gum deposits can be inhibited with surprising effectiveness through the utilizationof a fuel additive which comprises a solution of 'boric'acid'in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound.
The solvent mixture of alcohol and polyoxyalkylene is preferably one containing from 20% to 80% alcoholby volume. The additive ispreferably prepared by-first dissolving as much boric acid'as possible in the alcohol and then adding the polyoxyalkylene compound to the solution.
The alcohol component of thexsolvent'mixturemaybe any lower alcohol, such :as methyl, .ethyl-, isopropyl-,
butyl-,-or an amyl-alcohol, that is soluble in themotor fuel and: is capable of dissolvingboric acid. Methyl alcoholiszpreferre'd.
The oil=soluble polyoxyalkylene compounds forming "a component of =-the solvent mixture in :the additive of the invention are old compounds, well knownto those skilled in the art, and therefore form no part perse of-the presited States Patent .2 v ent invention. They are characterized by having the following general formula:
in which R and R are selected from the group consisting of hydrogen, alkyl and acyl groups having from four to about twenty carbon atoms, R is hydrogen or an alkyl group having from one to about five carbon atoms, n is a variable small whole number from one to about four, preferably two or three, and may vary in this range even in a single long chain molecule, and y represents the number of repeating units in the chain, and may be a whole number from about five to several hundred, depending on the molecular weight.
For the purposes of the invention the character of R and R, i. e., of the end groups of the chain, is not critical. Gum :solvency properties of these compounds are attributed primarily to the oxyalkylene units which form the chain, and not to the end groups; However, although quite a Wide variety ofthese compounds have gum solvency properties, only those with viscosities in the range of 200 to 1000 SSU at 100 'F. have the necessary 'involatility and gasoline solubility characteristics.
These compounds are prepared by condensation of the corresponding oxides, or oxide mixtures, such as ethylene or 1,2-propylene oxide, or mixtures thereof, as is set forth more 'fully in -U. S. Patents Nos. 2,425,755 to Roberts et al., issued August 19, 1947; 2,425,845 to 'Toussaint et. al., issued August 19, 1947; 2,448,664 to Fife et al., issued September7, 1948, and 2,457,139 to Fife et al., issued December 28, 1948. If R or R" is alkyl, an aliphatic alcohol is incorporated in the reaction mixture, and if R or R is acyl, an aliphatic carboxylic acid is incorporated in the reaction mixture.
Compounds in accordance with the above general formula are available commercially under the trade name from the Carbide and Carbon Chemicals Corporation. The compounds available commercially may have a hydroxyl group at one end of the chain and an alkyl ether or ester group at the other end of the chain, such as those of Patent Nos. 2,425,755, 2,448,664 and 2,457,139 but it will be understood that for the purpose of the instant invention compounds having two terminal hydroxyl groups at each end of the chain, such as those ,of Patent No. 2,425,845, or having two terminal alkyl ether or ester groups at each end of the chain are suitable as well. All three types of these compounds are intended to be covered-by the generic term polyoxyalkylene compound as employed in the specification and claims.
It isessential that the polyoxyalkylene compound be oil-soluble, and have an SSU viscosity at 100 F. of from 200 to 1000. Compounds having a viscosity of less than 200 SSUare too volatile to serve as gum solvents, while those havinga viscosity of over 1000 SSU are too insoluble in gasoline fuels to be suitable.
Itis surprising that polyoxyalkylene compound-alcohol blends, in which the proportion of alcohol is preferably in the range. of 20% .to 80% by volume and which are known to inhibit to an appreciable extent the formation of gummy deposits when ,present intthe'fuel in amounts ranging: from a fraction of 1% to about 5% by volume and preferably about 1% by volume, have-their effectiveness increased still further when small amounts of boric acid are dissolved inthe blend. lt is also surprising that a given concentration of b'oricacid dissolved in the blend will remaindissolved in thepresence of a motor fuel such as gasoline'inasmuchas thesame concentration of boric acid 3 mine the solubility in gasoline, of Ucon L-B 285, a monobutyl poly-1,2-oxypropylene glycol having a viscosity of 285 SSU at 100 F., a viscosity index of 146, a pour point of -40 F., arefractive index 11 9 of 1.448 and a density of 0.975 g./cc.:at 100-F.,.methanol, and of boric acid dissolved in the Ucon compound alone, the methanol alone and in blends thereof. The results of these tests are tabulated immediately below:
Additive in Gaso- Boric Acid, Perline, Percent by cent by Weight Test Volume I Solubility of Boric N 0. Acid in Gasoline- 7 Solvent Mixture Ucon Methanol in in L-B 285 Additive Gasoline I l Soluble. 2 5 0.75 0.0375 Borie Acid precipitates.
3 5 0.75 0.0375 Soluble. 4 5 1.0 0. 05 Boric Acid precipitates. 5 1. 25 3. 75 0. 75 0. 0375 Soluble. 6 0.25 0. 75 1.0 0.01 Do. 7 0. 25 O. 75 1. 25 0.0125 Btzritc Acid precipia es.
1 A monobutyl 'pohi-lfl-oxypropylene glycol having a viscosity of 285 ssU at 100 F.
Test No. 2 indicates that when a stable solution of as little as 0.75% by weight boric acid in polyoxyalkylene compound is added to gasoline, the boric acid forms a precipitate. Tests Nos. 3 and 4 indicate that boric acid dissolved in methanol alone is somewhat less prone to precipitation when the solutions are added to gasoline, but not when the concentration of boric acid in methanol is as high as 1% by weight. As contrast, test No. 6 shows that the boric acid in a 1% .by weight solution thereof in a blend of polyoxyalkylene compound and alcohol does not precipitate upon addition to gasoline but, unlike in tests Nos. 2 and 4, remains stable as a solute.
It has been found by further tests that surprisingly small concentrations of additive containing dissolved boric acid will have an appreciable effect in inhibiting the formation of gummy deposits in the fuel distribution system of an internal combustion engine. While it is preferred to dissolve in the additive and therefore incorporate into the fuel as much boric acid as will form a stable solution with the solvent blends, appreciable effects are also produced when the amount of boric acid in the fuel is considerably below 0.01% by weight and the amount thereof in the additive is considerably below 0.75%. Inasmuch as the maximum amount of boric acid capable of stable dissolution in the solvent blend is about 1% by weight, as shown by the data from test No. 7 in the table, the concentration of boric acid in the gasoline may range from an extremely small but effective amount, e. g., about 0.001% by weight, to about 0.05% by weight and. the concentration of the additive in the gasoline may. range from a significant amount, i. e., as little as about 0.1% by volume, to about 5% by volume. Balancing the amount of improvement obtained against the expense of the additive and of blending it with the gasoline, it is generally preferred that the amount of boric acid in the blend be approximately 1% by weight and that the concentration of the additive in the gasoline be approximately 1% by volume so that the concentration of boric acid in the gasoline will be approximately 0.01% by weight.
The utility of the additive and motor fuel blend of the invention will become further apparent from the following example:
Example Two fuels were subjected to comparative tests to determine the relative amounts of deposits in the engine fuel induction system. One of these fuels was a motor gasoline containing 1.5 cc./ gal. tetraethyl lead and 1% by volume of an additive consisting of 25% by volume Ucon L-B 285 and 75% by volume methanol. The other fuel was a'sample of the same gasoline containing the same amount of the same additive in which, however, 1% by weight, based on the additive, of boric acid had been dissolved prior to addition of the additive to the gasoline. The first fuel therefore contained no boric acid and the second fuel contained 0.01% by weight boric acid.
The procedure used in the tests was as follows: The equipment consisted of a Waukesha single cylinder knock testing engine equipped with a special glass intake manifold. This manifold system incorporated 16% inch long Pyrex tube (22 mm. outside diameter) between the carburetor and the intake port where it was held by two special flanges. A Nichrome coil of 10 ohms resistance was wrapped around the glass manifold about 3 inches from the carburetor end so that the heated area was about 3 /2 inches long. This heating element was controlled by a volt Variac and supplied localized heating to the special manifold. The temperature of the manifold was measured by a surface contact thermocouple located about /2 inch beyond the end of the coil, and the temperature was taken directly from a potentiometer. The intake air was drawn into the carburetor through a preheater consisting of a glow coil heater in the induction system surge. The heater was controlled from the engine panel board. The engine was operated for 10 hours, with the fuel being tested under the following conditions:
R. P. M 600. Coolant temperature 210 F. Oil temperature Approximately F. Air temperature:
Intake at carburetor 95 5. /2 beyond the coil 5. Approximate fuel consumption" 1.2 lbs/hr. (1.8 gal./
10 hrs.)
The glass manifold was weighed both before and after each test run. It was found that whereas the test with the gasoline containing no boric acid deposited an average of 0.0180 gram in the glass manifold after 10 hours of operation, the gasoline containing 0.01% by weight of boric acid deposited an average of only 0.0088 gram under the same conditions, i. e., less than half the amount of gum deposited in the other test. These results show the remarkable eifectiveness of the small concentrations of boric acid in a polyoxyalkylene compound alcohol blend.
It is to be understood that many modifications and alterations will occur to those skilled in the art upon reading this description. All such modifications and alterations are intended to be included within the scope of the invention as defined in the appended claims.
I claim: 7
1. An additive for use with a gasoline motor fuel which comprises a solution of boric acid in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound having the formula where R and R" are selected from the group consisting of hydrogen and alkyl and acyl groups having from four to about twenty carbon atoms, R is selected from the group consisting of hydrogen and alkyl groups having from one to about five carbon atoms, n is a small whole number having a value within the range from one to about four, and y is a number representing the number of repeating units within the chain to give a viscosity of between 200 and 1000 SSU at 100 F., the amount of alcohol in said solvent mixture ranging from 20% to 80% by volume and the amount of boric acid ranging from an effective amount up to 1% by weight of said solvent mixture.
2. The additive defined in claim 1 wherein the amount Lil of boric acid is about 1% by weight of the solvent mixture.
3. The additive defined in claim 1 wherein the oilsoluble polyoxyalkylene compound has a viscosity of 285 SSU at 100 F.
4. The additive defined in claim 1 wherein lower alcohol is methanol.
5. The additive defined in claim 1 wherein lower alcohol is isopropanol.
6. A gasoline motor fuel containing a minor amount within the limits of solubility in the gasoline of an additive comprising a solution of boric acid in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound having the formula where R and R" are selected from the group consisting of hydrogen and alkyl and acyl groups having from four to about twenty carbon atoms, R is selected from the group consisting of hydrogen and alkylgroups having from one to about five carbon atoms, n is a small whole number having a value within the range from one to about four, and y is a number representing the number of repeating units Within the chain to give a viscosity of between 200 and 1000 SSU at 100 F., the concentration by volume of the additive in the fuel ranging from a significant amount up to about 5% and the amount of boric acid ranging from an eifective amount to about 1% by weight of said solvent mixture.
7. The motor fuel defined in claim 5 wherein the amount of boric acid present in the fuel is about 0.01% by weight.
8. The motor fuel defined in claim 5 wherein the oilsoluble polyoxyalkylene compound has a viscosity of 285 SSU at 100 F.
9. The motor fuel defined in claim 5 wherein lower alcohol is methanol.
10. The motor fuel defined in claim 5 wherein lower alcohol is isopropanol.
11. An additive for use with a gasoline motor fuel which comprises a solution of boric acid in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound having the formula where R and R" are selected from the group consisting of hydrogen and alkyl and acyl groups having from four to about twenty carbon atoms, R is selected from the group consisting of hydrogen and alkyl groups having from one to about five carbon atoms, n is a small whole number having a value within the range from one to about four, and y is a number representing the number of repeating units within the chain to give a viscosity of between 200 and 1000 SSU at 100 F., the amount of alcohol in said solvent mixture ranging from 20% to by volume and the amount of boric acid ranging from an effective amount up to a minor amount within the limits of solubility of boric acid in the solvent mixture.
12. A gasoline motor fuel containing a minor amount within the limits of solubility in the gasoline of an additive comprising a solution of boric acid in a solvent mixture consisting essentially of a lower alcohol and an oil-soluble polyoxyalkylene compound having the formula where R and R" are selected from the group consisting of hydrogen and alkyl and acyl groups having from four to about twenty carbon atoms, R is selected from the group consisting of hydrogen and alkyl groups having from one to about five carbon atoms, n is a small whole number having a value within the range from one to about four, and y is a number representing the number of repeating units within the chain to give a viscosity of between 200 and 1000 SSU at F., the concentration by volume of the additive in the fuel ranging from a significant amount up to about 5% and the amount of boric acid ranging from an effective amount up to a minor amount within the limits of solubility of boric acid in the solvent mixture.
References Cited in the file of this patent UNITED STATES PATENTS 2,151,432 Lyons Mar. 21, 1939 2,460,700 Lyons Feb. 1, 1949 2,563,101 Colwell Aug. 7, 1951 2,614,985 Cook Oct. 21, 1952 UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 2,800,400 July 23, 1957 Everett 0. Hughes It is hereby certified that error appears .in the printed specification of the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 3, line 33, for "As contrast" read In contrast column 4, line 32, for beyond the coil" read beyond the coil column 5, lines 17 and 49, and column 6, line 22, after the closing bracket in the formulae, insert sub y", ineach occurrence.
Signed and sealed this 10th dey of September 1957.
(SEAL) Attest:
KAR H. AXLINE ROBERT C. WATSON Atteeting Officer Conmissioner of Patents

Claims (1)

  1. 6. A GASOLINE MOTOR FUEL CONTAINING A MINOR AMOUNT WITHIN THE LIMITS OF SOLUBILITY IN THE GASOLINE OF AN ADDITIVE COMPRISING A SOLUTION OF BORIC ACID IN A SOLVENT MIXTURE CONSISTING ESSENTIALLY OF A LOWER ALCOHOL AND AN OIL-SOLUBLE POLYOXYALKYLENE COMPOUND HAVING THE FORMULA
US400358A 1953-12-24 1953-12-24 Motor fuel additive and fuel containing same Expired - Lifetime US2800400A (en)

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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2929695A (en) * 1954-09-27 1960-03-22 Standard Oil Co Boric acid-diol-alcohol additive and liquid leaded motor fuel containing same
US2938777A (en) * 1956-04-19 1960-05-31 Tidewater Oil Company Gasoline fuel composition
US3030939A (en) * 1958-07-10 1962-04-24 Standard Oil Co Method of operating spark-ignition combustion engine
DE1144971B (en) * 1957-10-11 1963-03-07 Texaco Development Corp Hydrocarbon fuel from the gasoline boiling range
US3232876A (en) * 1961-07-21 1966-02-01 Gulf Research Development Co Boron-containing copolymers and lubricating oils containing them
US4298352A (en) * 1977-11-29 1981-11-03 Berol Kemi Ab Diesel fuel comprising methanol and a methanol-soluble polyoxyalkylene compound
US4541837A (en) * 1979-12-11 1985-09-17 Aeci Limited Fuels
US5366519A (en) * 1992-12-18 1994-11-22 Chevron Research And Technology Company Fuel additive compositions containing poly(oxyalkylene) hydroxyaromatic esters and poly(oxyalkylene) amines
US5427591A (en) * 1992-12-18 1995-06-27 Chevron Chemical Company Poly(oxyalkylene) hydroxyaromatic esters and fuel compositions containing the same
US5462567A (en) * 1992-12-28 1995-10-31 Chevron Chemical Company Fuel additive compositions containing poly(oxyalkylene)hydroxyaromatic esters and aliphatic amines
DE4421329A1 (en) * 1994-06-17 1995-12-21 Metallgesellschaft Ag Tri:functional alcohol for use as anti-sedimentation fuel additive

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2151432A (en) * 1937-07-03 1939-03-21 Leo Corp Method of operating internal combustion engines
US2460700A (en) * 1947-07-01 1949-02-01 Leo Corp Method of operating an internal-combustion engine
US2563101A (en) * 1948-03-08 1951-08-07 Thompson Prod Inc Fuel charge for internalcombustion engines
US2614985A (en) * 1951-10-25 1952-10-21 Shell Dev Lubricating composition containing boric acid

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2151432A (en) * 1937-07-03 1939-03-21 Leo Corp Method of operating internal combustion engines
US2460700A (en) * 1947-07-01 1949-02-01 Leo Corp Method of operating an internal-combustion engine
US2563101A (en) * 1948-03-08 1951-08-07 Thompson Prod Inc Fuel charge for internalcombustion engines
US2614985A (en) * 1951-10-25 1952-10-21 Shell Dev Lubricating composition containing boric acid

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2929695A (en) * 1954-09-27 1960-03-22 Standard Oil Co Boric acid-diol-alcohol additive and liquid leaded motor fuel containing same
US2938777A (en) * 1956-04-19 1960-05-31 Tidewater Oil Company Gasoline fuel composition
DE1144971B (en) * 1957-10-11 1963-03-07 Texaco Development Corp Hydrocarbon fuel from the gasoline boiling range
US3030939A (en) * 1958-07-10 1962-04-24 Standard Oil Co Method of operating spark-ignition combustion engine
US3232876A (en) * 1961-07-21 1966-02-01 Gulf Research Development Co Boron-containing copolymers and lubricating oils containing them
US4298352A (en) * 1977-11-29 1981-11-03 Berol Kemi Ab Diesel fuel comprising methanol and a methanol-soluble polyoxyalkylene compound
US4541837A (en) * 1979-12-11 1985-09-17 Aeci Limited Fuels
US5366519A (en) * 1992-12-18 1994-11-22 Chevron Research And Technology Company Fuel additive compositions containing poly(oxyalkylene) hydroxyaromatic esters and poly(oxyalkylene) amines
US5427591A (en) * 1992-12-18 1995-06-27 Chevron Chemical Company Poly(oxyalkylene) hydroxyaromatic esters and fuel compositions containing the same
US5462567A (en) * 1992-12-28 1995-10-31 Chevron Chemical Company Fuel additive compositions containing poly(oxyalkylene)hydroxyaromatic esters and aliphatic amines
DE4421329A1 (en) * 1994-06-17 1995-12-21 Metallgesellschaft Ag Tri:functional alcohol for use as anti-sedimentation fuel additive
DE4421329C2 (en) * 1994-06-17 1998-02-26 Metallgesellschaft Ag Use of trifunctional alcohols as fuel additive

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