US3529943A - Gasoline composition containing a metal salt of an azolidinedione - Google Patents

Gasoline composition containing a metal salt of an azolidinedione Download PDF

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US3529943A
US3529943A US824746A US3529943DA US3529943A US 3529943 A US3529943 A US 3529943A US 824746 A US824746 A US 824746A US 3529943D A US3529943D A US 3529943DA US 3529943 A US3529943 A US 3529943A
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gasoline
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composition
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Seymour H Patinkin
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Sinclair Research Inc
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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
    • C10L1/14Organic 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
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/232Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
    • C10L1/233Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring containing nitrogen and oxygen in the ring, e.g. oxazoles
    • 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
    • C10L1/24Organic compounds containing sulfur, selenium and/or tellurium
    • C10L1/2443Organic compounds containing sulfur, selenium and/or tellurium heterocyclic compounds
    • C10L1/2456Organic compounds containing sulfur, selenium and/or tellurium heterocyclic compounds sulfur with oxygen and/or nitrogen in the ring, e.g. thiazoles
    • 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
    • C10L1/26Organic compounds containing phosphorus
    • C10L1/2633Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
    • C10L1/2641Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) oxygen bonds only
    • 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
    • C10L1/30Organic compounds compounds not mentioned before (complexes)
    • C10L1/305Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)
    • C10L1/306Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond) organo Pb compounds

Definitions

  • a gasoline composition consisting essentially of hydrocarbon gasoline, an anti-knock quantity of tetra-loweralkyl lead compound, and a gasoline-soluble metal salt of an azolidinedione having the formula:
  • R is a hydrocarbon radical of up to 30 carbon atoms, R is selected from the group consisting of hydrogen and R; and Z is a chalcogen having an atomic number from 8 to 16.
  • the metal is selected from the group consisting of Groups Ia, Ila, IIIa, Va, 112, Kb, IIIb, IVb, Vb, VIb, VIII), VIII and tin.
  • the invention also contemplates adding an alkali metal salt of an azolidinedione to the gasoline composition in combination with a metal salt of an azolidinedione wherein the metal is one of Groups I IIIa, Va, Ib, IIb, IIIb, IVb, Vb, V117, V111), VIII and tin.
  • the present invention relates to distillate hydrocarbon gasoline compositions which when employed in spark ignition engines lead to improved engine performance.
  • leaded gasolines having added thereto about 0.002 to 0.4 or even 0.8 millimoles or milligram atoms of metal per gallon as certain gasoline-soluble metal salts of azolidinediones exhibit improved engine performance with respect to one or more of lower octane number requirement increase, improved rumble, surface ignition characteristics, reduced piston ring wear and extended exhaust valve life.
  • the metal of the azolidinedione salt can be a metal of Groups IIIa, Va, Ib, IIb, IIIb, IVb, Vb, VIb, VIIb, VIII, tin or a mix ture of two or more of these metals.
  • the invention contemplates adding in combination with the aforementioned metal salt, small amounts of gasoline-soluble alkali metal salts of the azolidinediones of the invention.
  • the preferred alkali metal salts are those of sodium, potassium and lithium.
  • leaded gasolines having added thereto about 0.002 to 0.4 or even 0.8 millimoles or milligram atoms of metal per gallon as gasoline-soluble alkali or alkaline earth metal, i.e. Group Ia or IIa metal salts of azolidinediones exhibit improved engine performance with respect to one or more of lower octane number requirement increase, improved rumble, surface ignition characteristics, reduced piston ring wear and extended exhaust valve life.
  • the preferred alkali metal salts are those of sodium, potassium and lithium, and the preferred alkaline earth metal salts are those of calcium, barium and strontium.
  • azolidinediones sometimes refrred to as azolones, the salts of which constitute the additives of the invention have the following formula:
  • R is a hydrocarbon radical of up to about 30 or more carbon atoms on the average, often at least about 4 and preferable about 8 to 18 carbon atoms
  • R is selected from hydrogen and R
  • Z is a chalcogen having an atomic number from 8 to 16, i.e. oxygen or sulfur.
  • R can be an aliphatic, aromatic or mixed aliphatic-aromatic radical and is preferably non-olefinic and non-acetylenic, i.e. having adjacent carbon atoms no closer than 1.40 A.
  • R can also be substituted with non-interfering groups, if desired.
  • the total number of carbon atoms in a molecule of the azolidinediones is preferably up to about 40 or even up to about 30 and the salts of the azolidinediones are soluble in the gasoline at least to the extent employed in the invention.
  • the salts may contain more or less than the stoichiometric equivalent of the metal and thus the product may contain free azolidinedione or When the metal is polyvalent it may be attached to another group,
  • azolidinediones or azolones from which the metal salts of the invention are made are known compounds, and include, for instance, the 2,4-oxazolidinediones, 2,4- thiazolidinediones, 2-thio-2,4-oxazolidinediones, and 2- thio-2,4-thiazolidinediones, all substituted with at least one hydrocarbon radical having the value designated in the above formula.
  • the preferred R groups include the straight or branch chained alkyl groups, phenyl, and alkyl-substituted phenyls whose alkyl substituents contain a total of up to 18 carbon atoms, and preferably are lower alkyl, especially methyl.
  • R groups are pentyl, butyl, octyl, isooctyl, Z-ethyI-heptyl, dodecyl, oleyl, octadecyl, tetradecyl, phenyl and alkylated phenyls such as cresyl, xylenyl, propyl phenyl, butyl phenyl, dibutylphenyl, monoamylphenyl, diamyl phenyl, decyl phenyl, dodecyl phenyl, tetradecyl phenyl, hexadecyl phenyl and octadecyl phenyl.
  • phenyl and alkylated phenyls such as cresyl, xylenyl, propyl phenyl, butyl phenyl, dibutylphenyl, monoamy
  • gasoline-soluble phosphorous compound having the formula:
  • R has the value described above with respect to the azolones from which the metal salts of the invention are made;
  • R is hydrogen or R and n is an integer of to 1.
  • R is preferably an aromatic, e.g. phenyl, hydrocarbon radical of 6 to 12 carbon atoms and can be sub stituted as, for instance, with lower alkyl groups say of 1 to 4 carbon atoms.
  • the phosphorous compound can be a mono-, di-, or tri-ester.
  • ester groups is preferably an alkyl phenyl radical, often of about 7 to carbon atoms. See US. Pat. No. 2,889,212 for a further list of the useful phosphates and phosphites.
  • auxiliary phosphate and phosphite additives can be prepared by reacting the appropriate alcohol or aromatic hydroxy compound with phosphoric acid to make the phosphate or with phosphorous trichloride to form the phosphite.
  • the preferred alcohols are alkanols which can be straight or branch chained and alkyl-substituted phenols whose alkyl substituents contain a total of up to 18 carbon atoms, and preferably are lower alkyl, especially methyl.
  • the aromatic hydroxy compounds and aliphatic alcohols may be substituted with non-deleterious groups.
  • Suitable alcohols are pentanol, butanol, octanol, isooctanol, 2-ethyl-heptanol, dodecanol, oleyl alcohol, octadecyl alcohol, tetradecyl alcohol, alcohols prepared by the Oxo process, phenol and alkylated phenols such as cresol, xylenol, propyl phenol, butyl phenol, dibutyl phenol, monoamylphenol, diamyl phenol, decyl phenol, dodecyl phenol, tetradecyl phenol, hexadecyl phenol and octadecyl phenol.
  • Particularly preferred alkyl phenols are ortho, meta and para cresol; 2,4- and 2,5-xylenol; 2,4- dimethyl-6-tertiary butylphenol; octyl and nonylphenols.
  • leaded gasoline to which the additives of the present invention are incorporated is meant hydrocarbon fractions boiling primarily in the gasoline range, usually about 100 to 425 F., having added thereto a small amount, generally between about 1 to 6 cc. per gallon, preferably about 2 to 4 cos. per gallon, of a tetra-loweralkyl lead compound as an anti-knock agent.
  • the gasolines are usually composed of a major amount of a blend of hydrocarbon mineral oil fractions boiling primarily in the aforementioned range and will contain varying proportions of paraflins, olefins, naphthenes and aromatics derived by distillation, cracking and other refining and chemical conversion processes practiced upon crude oil fractions.
  • gasolines derived from cracking gas oil, gasolines or reformate from reforming straight run naphtha over a platinum-alumina catalyst in the presence of hydrogen, etc. are components frequently used in making up a gasoline composition.
  • a typical premium gasoline besides containing a small amount of a tetra-lower-alkyl lead compound as an anti-knock agent may also contain small amounts of other non-hydrocarbon constituents used to impart various properties to the gasoline in its use in internal combustion engines, e.g. halohydrocarbon scavengers, oxidation inhibitors, etc.
  • Such gasolines frequently have a Research Method octane number of about 90 to 105, and a Motor Method octane number of about to 98.
  • the metal salt of the azolones of the invention is incorporated in the leaded gasoline in small amounts sufficient to provide a composition exhibiting an advantage in spark-ignition engines, for instance, with respect to one or more of improved rumble, surface ignition characteristics, lower octane number requirement increase, reduced piston ring wear and longer exhaust valve life.
  • the actual amount of the metal salt additive employed may vary depending upon the particular gasoline used, its lead content, etc. In any event sufiicient of the metal salt is employed to supply 0.002 to 0.4 or even 0.8 preferably 0.025 to 0.3, millimoles or milligram atoms of the metal per gallon of gasoline.
  • the additive will usually provide the gasoline with 0.00004 to 0.008 grams of one or a combination of the metal of the salts per gram of lead, preferably 0.0005 to 0.006 grams of the metal per gram of lead. This often means that about 0.5 to 15 or 30 or more pounds of the metal salt is added, preferably about 2 to 10 pounds, per 1000 barrels of gasoline.
  • the alkali metal salts of the azolones when employed with the metal of the first embodiment, are ordinarily added in an amount of 0.002 to 0.8 millimoles or milligram atoms of metal per gallon of gasoline and the combination of the selected metal salt and alkali metal salt is preferably 0.002 to 0.8 millimoles of metal per gallon of gasoline.
  • auxiliary phosphate or phosphite additive When used, about 0.05 to 0.6 theory, preferably about 0.15 to 0.5 theory, of the auxiliary phosphate or phosphite additive, based on the lead content of the gasoline, is generally employed.
  • theory as applied to the amount of the phosphorous additive means the amount required to react stoichiometrically with the lead so that all of the lead atoms and all of the phosphorous atoms form Pb (PO4).
  • Nickel hexadecyl-2,4-oxazolidinedione is added in an amount of 4 lbs. of the salt per 1000 barrels to a gasoline composed of 37 volume percent light straight run gasoline, 23 volume percent light catalytically cracked gasoline, 13 volume percent heavy catalytically reformed gasoline and 27 volume percent heavy catalytically cracked gasoline containing 3 cc. per gallon of TEL as Motor Mix (TEL Motor Mix contains 59.2% tetraethyl lead, 13.0% ethylene dibromide, 23.9% ethylene dichloride and 3.9% hydrocarbon diluent, dyes, etc.)
  • Evaluation of the resulting composition in a spark ignition engine shows operation of engine to be improved with respect to rumble, surface ignition characteristics, octane number requirement increase, ring wear and exhaust valve life.
  • Evaluation of the resulting composition in a spark i gnition engine shows operation of engine to be improved with respect to rumble, surface ignition characteristics, octane number requirement increase, ring wear and exhaust valve life.
  • the gasoline without the additive of the invention is run for 216 hours and the octane requirement increase noted.
  • the engine is then thoroughly cleaned of all deposits so that it again exhibits the same clean octane requirement and run on an identical cycle, with the same gasoline but containing the additive of the invention.
  • the octane requirement increase is noted and compared with the octane requirement increase found with the gasoline without the additive to determine the extent of improvement.
  • the rumble tendency of an engine after a given time of use is measured by a LIB number.
  • the number represents the percent isooctane (containing 3 cc. TEL/ gallon) required in a blend with benzene (containing 3 cc. TEL/gallon) after a given period of engine operation using the fuel under test, to avoid rumble at a given r.p.m., e.g. 2,000 r.p.m.
  • the test procedure comprises stopping the gasoline to the engine at any given period of engine operation and employing as a fuel to the engine a fuel containing a certain percent of isooctane in an iso octane-benzene blend (containing 3 cc.
  • the piston ring Wear is determined by equipping a single cylinder COT engine with. radioactive rings installed in the grooves of the pistons.
  • the lubricating oil system of the engine is provided with a sealed monitoring well which contains a scintillation counter.
  • the ring wear rate is determined by passing the lubricating oil through the monitoring well and therein detecting the concentration in mg./hour of radioactive iron transported to the oil due to wear of the piston rings.
  • the test to determine the effect of the fuel composition on exhaust valve life involves running an automobile engine at a fixed number of hours at constant or varied speeds and loads depending on the engine used and then noting the number of valves that failed during this period of time.
  • the test used to determine the deposit-induced ignition characteristics of the fuel composition comprises equipping an engine with an L-head cylinder and an electronic Wild ping counter which records the total number of wild pings which have occurred during the test periods. Since deposit-induced ignition is the tendency to ignite the fuelair mixture erratically and to produce uncontrolled combustion noticeable as, for instance, wild ping, the electronic counter which is used in conjunction with an ionization gap, automatically detects and records uncontrolled combustion.
  • a gasoline composition consisting essentially of hydrocarbon gasoline, an anti-knock quantity of tetralower-alkyl lead compound, and a gasoline-soluble metal salt of an azolidinedione having the formula:
  • R is a hydrocarbon radical of up to 30 carbon atoms, R is selected from the group consisting of hydrogen and R; Z is a chalcogen having an atomic number from 8 to 16, said metal being selected from the group consisting of Groups Ia, Ila, IIIa, Va, Ib, IIb, IIIb, IVb Vb, VIb, VIIb, VIII and tin, the :amount of said metal salt being sufficient to provide 0.002 to 0.8 milligram atoms of selected metal of said salt per gallon of gasoline.
  • a gasoline composition consisting essentially of hydrocarbon gasoline, an anti-knock quantity of tetralower-alkyl lead compound, and a gasoline-soluble metal salt of an azolidinedione having the formula:
  • R is a hydrocarbon radical of up to 30 carbon atoms, R is selected from the group consisting of hydrogen and R; Z is a chalcogen having an atomic number from 8 to 16, said metal being selected from the group consisting of Groups IIIa,,Va, Ib, IIb, IIIb, IVb, Vb, VIb, VIIb, VIII and tin, the amount of said metal salt being sufficient to provide 0.002 to 0.8 milligram atoms of selected metal of said salt per gallon of gasoline.
  • composition of claim 2 in which there is also included about 0.05 to 0.6 theory of a gasoline-soluble phosphorous compound having the formula:
  • R is a hydrocarbon radical of up to about 30 carbon atoms on the average, R is selected from the group consisting of hydrogen and R, and n is an integer having a value of to 1.
  • composition of claim 2 wherein the metal is an iron group metal.
  • composition of claim 4 wherein the metal is nickel.
  • composition of claim 3 wherein at least one R in the structure of claim 3 is an alkyl phenyl radical of 7 to 15 carbon atoms.
  • composition of claim 6 wherein the amount of phosphorous compound is about 0.15 to 0.5 theory.
  • composition of claim 6 wherein the selected metal is an iron group metal.
  • composition of claim 8 wherein'the metal is nickel.
  • composition of claim 2 wherein the amount of said metal salt is sufficient to provide about 0.025 to 0.3 millimoles of selected metal per gallon of said gasoline.
  • composition of claim 10 in which there is also included about 0.05 to 0.6 theory of a gasolinesoluble phosphorous compound having the formula:
  • RO OR i RO o wherein R is a lower alkyl phenyl radical of 7 to carbon atoms and R is selected from the group consisting of phenyl and R.
  • composition of claim 10 wherein the selected metal is an iron group metal.
  • composition of claim 12 wherein the metal is nickel.
  • composition of claim 13 wherein the phosphorous compound is cresyl diphenyl phosphate.
  • a gasoline composition consisting essentially of hydrocarbon gasoline, an anti-knock quantity of tetralower-alkyl lead compound, and a gasoline-soluble metal salt of an azolidinedione having the formula:
  • R is a hydrocarbon radical of up to carbon atoms, R is selected from the group consisting of hydrogen and R; Z is a chalcogen having an atomic number from 8 to 16, said metal being selected from the group consisting of alkali and alkaline earth metals and the amount of said metal salt being suflicient to provide 0.002 to 0.8 milligram atoms of metal of said metal salt per gallon of gasoline.
  • composition of claim 15 in which there is also included about 0.05 to 0.6 theory of a gasoline-soluble phosphorous compound having the formula:
  • RO OR RO/ wherein R is a hydrocarbon radical of up to about 30 carbon atoms on the average, R is selected from the group consisting of hydrogen and R, and n is an integer having a value of 0 to 1.
  • composition of claim 16 wherein at least one R in the structure of claim 16 is an alkyl phenyl radical of 7 to 15 carbon atoms.
  • composition of claim 17 wherein the amount of phosphorous compound is about 0.15 to 0.5 theory.
  • composition of claim 15 wherein the metal is an alkaline earth metal.
  • composition of claim 15 wherein the metal is an alkali metal.
  • composition of claim 15 wherein the amount of said metal salt is sufiicient to provide about 0.025 to 0.3 millimole of selected metal per gallon of said gasoline.
  • composition of claim 21 in which there is also included about 0.05 to 0.6 theory of a gasoline-soluble phosphorous compound having the formula:
  • RO 0R RO/ o wherein R is a lower alkyl phenyl radical of 7 to 15 carbon atoms and R is selected from the group consisting of phenyl and R.
  • composition of claim 22 wherein the metal is an alkali metal.
  • composition of claim 23 wherein the phosphorous compound is cresyl diphenyl phosphate.

Description

United States Patent 3,529,943 GASOLINE COMPOSITION CONTAINING A METAL SALT OF AN AZOLIDINEDIONE Seymour H. Patinkin, Chicago, Ill., assignor to Sinclair Research Inc., New York, N.Y., a corporation of Delaware No Drawing. Continuation of application Ser. No. 645,524, June 12, 1967. This application May 7, 1969, Ser. No. 824,746
Int. Cl. Cl 1/22 US. Cl. 44-63 24 Claims ABSTRACT OF THE DISCLOSURE A gasoline composition consisting essentially of hydrocarbon gasoline, an anti-knock quantity of tetra-loweralkyl lead compound, and a gasoline-soluble metal salt of an azolidinedione having the formula:
wherein R is a hydrocarbon radical of up to 30 carbon atoms, R is selected from the group consisting of hydrogen and R; and Z is a chalcogen having an atomic number from 8 to 16. The metal is selected from the group consisting of Groups Ia, Ila, IIIa, Va, 112, Kb, IIIb, IVb, Vb, VIb, VIII), VIII and tin. The invention also contemplates adding an alkali metal salt of an azolidinedione to the gasoline composition in combination with a metal salt of an azolidinedione wherein the metal is one of Groups I IIIa, Va, Ib, IIb, IIIb, IVb, Vb, V117, V111), VIII and tin.
This application is a continuation of application Ser. No. 645,524, filed June 12, 1967, which, in turn, was a continuation in part of applications Ser. Nos. 399,391 and 399,392, filed Sept. 25, 1964, all now abandoned.
The present invention relates to distillate hydrocarbon gasoline compositions which when employed in spark ignition engines lead to improved engine performance.
One of the chief disadvantages attending the use of known additives to lessen abnormal combustion of gasoline in, for instance, automobile engines is that they adversely affect the nature and increase the amount of deposits in the combustion space. These effects manifest themselves in a variety of ways particularly in the case of the higher compression engines. For instance, a fuel having an octane number appropriate to the designed engine compression ratio is unable to give the same antiknock performance after the formation of extensive deposits. To obtain the intended anti-knock performance requires a fuel of higher octane number, and this effect has become known as the octane requirement increase or ORI of the engine. Modern engines also evidence a tendency to rumble, an objectionable shuddering noise, apparently caused by flexing of the crankshaft due to deposit-induced abnormal combustion. Surface ignition induced by deposits also often creates abnormalities such as pre-ignition, autoignition and Wild ping. Combustion chamber deposits are known to cause piston ring Wear and to reduce exhaust valve life. All of these facets of combustion abnormalities can lead to engine damage and/or loss in power and efliciency.
Various commonly employed gasoline additives as, for example, phosphate compounds such as tricresyl phosphate, cresyl diphenyl phosphate, etc., are known to im- Patented Sept. 22, 1970 prove engine operation with respect to certain of the problems presented by deposit-induced ignition. Relatively large amounts of these compounds are needed, however, to effectively combat the combustion abnormalities, particularly rumble.
It has now been found that leaded gasolines having added thereto about 0.002 to 0.4 or even 0.8 millimoles or milligram atoms of metal per gallon as certain gasoline-soluble metal salts of azolidinediones, exhibit improved engine performance with respect to one or more of lower octane number requirement increase, improved rumble, surface ignition characteristics, reduced piston ring wear and extended exhaust valve life. The metal of the azolidinedione salt can be a metal of Groups IIIa, Va, Ib, IIb, IIIb, IVb, Vb, VIb, VIIb, VIII, tin or a mix ture of two or more of these metals. Among these metals it is preferred to use aluminum, antimony bismuth, cop per, zinc, cadmium, mercury, scandium, titanium, zirconium, vanadium, nobium, chromium, molybdenum, tungsten, manganese, the iron group metals (iron, cobalt and nickel) and tin. Nickel and cobalt are especially preferred. The Groups of the Periodic Chart mentioned above are as designat edon the inside front cover of the Merck Index, Seventh Edition, Merck & Co., Inc., Rahway, N.J., 1960. As another embodiment, the invention contemplates adding in combination with the aforementioned metal salt, small amounts of gasoline-soluble alkali metal salts of the azolidinediones of the invention. The preferred alkali metal salts are those of sodium, potassium and lithium.
It has also been found that leaded gasolines having added thereto about 0.002 to 0.4 or even 0.8 millimoles or milligram atoms of metal per gallon as gasoline-soluble alkali or alkaline earth metal, i.e. Group Ia or IIa metal salts of azolidinediones exhibit improved engine performance with respect to one or more of lower octane number requirement increase, improved rumble, surface ignition characteristics, reduced piston ring wear and extended exhaust valve life. The preferred alkali metal salts are those of sodium, potassium and lithium, and the preferred alkaline earth metal salts are those of calcium, barium and strontium.
The azolidinediones, sometimes refrred to as azolones, the salts of which constitute the additives of the invention have the following formula:
wherein R is a hydrocarbon radical of up to about 30 or more carbon atoms on the average, often at least about 4 and preferable about 8 to 18 carbon atoms, R is selected from hydrogen and R, and Z is a chalcogen having an atomic number from 8 to 16, i.e. oxygen or sulfur. R can be an aliphatic, aromatic or mixed aliphatic-aromatic radical and is preferably non-olefinic and non-acetylenic, i.e. having adjacent carbon atoms no closer than 1.40 A. R can also be substituted with non-interfering groups, if desired. The total number of carbon atoms in a molecule of the azolidinediones is preferably up to about 40 or even up to about 30 and the salts of the azolidinediones are soluble in the gasoline at least to the extent employed in the invention. Also the salts may contain more or less than the stoichiometric equivalent of the metal and thus the product may contain free azolidinedione or When the metal is polyvalent it may be attached to another group,
, 3 for instance, the inorganic anion of the metal compound used to form the azolidinedione salt.
The azolidinediones or azolones from which the metal salts of the invention are made are known compounds, and include, for instance, the 2,4-oxazolidinediones, 2,4- thiazolidinediones, 2-thio-2,4-oxazolidinediones, and 2- thio-2,4-thiazolidinediones, all substituted with at least one hydrocarbon radical having the value designated in the above formula.
The preferred R groups include the straight or branch chained alkyl groups, phenyl, and alkyl-substituted phenyls whose alkyl substituents contain a total of up to 18 carbon atoms, and preferably are lower alkyl, especially methyl. Illustrative of suitable R groups are pentyl, butyl, octyl, isooctyl, Z-ethyI-heptyl, dodecyl, oleyl, octadecyl, tetradecyl, phenyl and alkylated phenyls such as cresyl, xylenyl, propyl phenyl, butyl phenyl, dibutylphenyl, monoamylphenyl, diamyl phenyl, decyl phenyl, dodecyl phenyl, tetradecyl phenyl, hexadecyl phenyl and octadecyl phenyl.
In order to provide leaded gasolines of further enhanced characteristics, for instance, as to preignition, spark plug fouling and even, in at least some cases, rumble, there can be included in the gasoline composition of the invention a gasoline-soluble phosphorous compound having the formula:
B On
wherein R has the value described above with respect to the azolones from which the metal salts of the invention are made; R is hydrogen or R and n is an integer of to 1. R is preferably an aromatic, e.g. phenyl, hydrocarbon radical of 6 to 12 carbon atoms and can be sub stituted as, for instance, with lower alkyl groups say of 1 to 4 carbon atoms. Thus, the phosphorous compound can be a mono-, di-, or tri-ester. We also prefer to employ a phenyl, alkyl-phenyl or a mixed phenyl-alkyl phenyl ester of phosphorous. Thus, one or more of the ester groups is preferably an alkyl phenyl radical, often of about 7 to carbon atoms. See US. Pat. No. 2,889,212 for a further list of the useful phosphates and phosphites.
These auxiliary phosphate and phosphite additives can be prepared by reacting the appropriate alcohol or aromatic hydroxy compound with phosphoric acid to make the phosphate or with phosphorous trichloride to form the phosphite.
The preferred alcohols are alkanols which can be straight or branch chained and alkyl-substituted phenols whose alkyl substituents contain a total of up to 18 carbon atoms, and preferably are lower alkyl, especially methyl. The aromatic hydroxy compounds and aliphatic alcohols may be substituted with non-deleterious groups. Illustrative of suitable alcohols are pentanol, butanol, octanol, isooctanol, 2-ethyl-heptanol, dodecanol, oleyl alcohol, octadecyl alcohol, tetradecyl alcohol, alcohols prepared by the Oxo process, phenol and alkylated phenols such as cresol, xylenol, propyl phenol, butyl phenol, dibutyl phenol, monoamylphenol, diamyl phenol, decyl phenol, dodecyl phenol, tetradecyl phenol, hexadecyl phenol and octadecyl phenol. Particularly preferred alkyl phenols are ortho, meta and para cresol; 2,4- and 2,5-xylenol; 2,4- dimethyl-6-tertiary butylphenol; octyl and nonylphenols.
By the term leaded gasoline to which the additives of the present invention are incorporated is meant hydrocarbon fractions boiling primarily in the gasoline range, usually about 100 to 425 F., having added thereto a small amount, generally between about 1 to 6 cc. per gallon, preferably about 2 to 4 cos. per gallon, of a tetra-loweralkyl lead compound as an anti-knock agent. The gasolines are usually composed of a major amount of a blend of hydrocarbon mineral oil fractions boiling primarily in the aforementioned range and will contain varying proportions of paraflins, olefins, naphthenes and aromatics derived by distillation, cracking and other refining and chemical conversion processes practiced upon crude oil fractions. ,Straight run gasolines, gasolines derived from cracking gas oil, gasolines or reformate from reforming straight run naphtha over a platinum-alumina catalyst in the presence of hydrogen, etc., are components frequently used in making up a gasoline composition. A typical premium gasoline, besides containing a small amount of a tetra-lower-alkyl lead compound as an anti-knock agent may also contain small amounts of other non-hydrocarbon constituents used to impart various properties to the gasoline in its use in internal combustion engines, e.g. halohydrocarbon scavengers, oxidation inhibitors, etc. Such gasolines frequently have a Research Method octane number of about 90 to 105, and a Motor Method octane number of about to 98.
The metal salt of the azolones of the invention is incorporated in the leaded gasoline in small amounts sufficient to provide a composition exhibiting an advantage in spark-ignition engines, for instance, with respect to one or more of improved rumble, surface ignition characteristics, lower octane number requirement increase, reduced piston ring wear and longer exhaust valve life. The actual amount of the metal salt additive employed may vary depending upon the particular gasoline used, its lead content, etc. In any event sufiicient of the metal salt is employed to supply 0.002 to 0.4 or even 0.8 preferably 0.025 to 0.3, millimoles or milligram atoms of the metal per gallon of gasoline. The additive will usually provide the gasoline with 0.00004 to 0.008 grams of one or a combination of the metal of the salts per gram of lead, preferably 0.0005 to 0.006 grams of the metal per gram of lead. This often means that about 0.5 to 15 or 30 or more pounds of the metal salt is added, preferably about 2 to 10 pounds, per 1000 barrels of gasoline. The alkali metal salts of the azolones, when employed with the metal of the first embodiment, are ordinarily added in an amount of 0.002 to 0.8 millimoles or milligram atoms of metal per gallon of gasoline and the combination of the selected metal salt and alkali metal salt is preferably 0.002 to 0.8 millimoles of metal per gallon of gasoline.
When used, about 0.05 to 0.6 theory, preferably about 0.15 to 0.5 theory, of the auxiliary phosphate or phosphite additive, based on the lead content of the gasoline, is generally employed. The term theory as applied to the amount of the phosphorous additive means the amount required to react stoichiometrically with the lead so that all of the lead atoms and all of the phosphorous atoms form Pb (PO4 The following examples are given to illustrate the advantages provided leaded gasolines by the additives of the present invention.
EXAMPLE I Nickel hexadecyl-2,4-oxazolidinedione, calculated as 8.25% by weight nickel, is added in an amount of 4 lbs. of the salt per 1000 barrels to a gasoline composed of 37 volume percent light straight run gasoline, 23 volume percent light catalytically cracked gasoline, 13 volume percent heavy catalytically reformed gasoline and 27 volume percent heavy catalytically cracked gasoline containing 3 cc. per gallon of TEL as Motor Mix (TEL Motor Mix contains 59.2% tetraethyl lead, 13.0% ethylene dibromide, 23.9% ethylene dichloride and 3.9% hydrocarbon diluent, dyes, etc.)
Evaluation of the resulting composition in a spark ignition engine shows operation of engine to be improved with respect to rumble, surface ignition characteristics, octane number requirement increase, ring wear and exhaust valve life.
Similar results can be obtained by adding to the same gasoline containing TEL Motor Mix and GDP the following additives in the designated amounts.
Cale. Amount of adpercent ditive, lbs./ 1,000 E x. Additive metal bbls. gasoline II Al salt of ditetra-decyl-2,4-thiazo- 1. 74 5 lidinedione. III Sb salt of octyIbenzene-2,4-th1azo- 12.0 5
lidinedione. IV Cu salt of hexadecyl-2,4-thiazoli- 8.45 4
dinedione. V Zn salt of octadecyl-2-thi0-2,4-thi- 7.70 4
azolidinedione. VI Sc salt of tetradeeyl-2-thio-2A 4. 84 3 thiazolidinedione. VII..." Ti salt of dodecylbenzene-2-thio- 3.08 10 2,4-thiazolidinedione. VIII- Zr salt of hexadeey1-2-th1o2A- 6.02 11 thiazolidenedione. IX V salt of dideeyl-2-thio-2,4-thiaz- 3.96 5
olidinedione. X Cr salt of dodecyl-2A-oxazoh- 6.08 3
dinedione. XI S of tetradecyl-Zflwxazoh- 9.1 4
dinedione. XII Sn salt of octadecy1' A-oxazol1- 7.7 8
dinedione. XIII--- Mn salt of dioetyl-be11zene-2,4-ox- 5.4
azolidine-dione. XIV..-- N3 salt of didecyl-2,4-thiazolidine- 5.4 1
lone. Ni salt of hexadecyl-2,4-oxazoli- 8.25 2
dinedrone EXAMPLE XV Sodium didecyl-Z,4-thiazolidinedione, calculated as 5.4% by weight sodium, is added in an amount of 2 lbs. of the salt per 1000 barrels to a gasoline composed of 37 volume percent light straight run gasoline, 23 volume percent light catalytically cracked gasoline, 13 volume percent heavy catalytically reformed gasoline and 27 volume percent heavy catalytically cracked containing 3 cc. per gallon of TEL as Motor Mix (TEL Motor Mix contains 59.2% tetraethyl lead, 13.0% ethylene dibromide, 23.9% ethylene dichloride and 3.9% hydrocarbon diluent, dyes, etc.) and 0.2 theory cresyl diphenyl phosphate (CDP).
Evaluation of the resulting composition in a spark i gnition engine shows operation of engine to be improved with respect to rumble, surface ignition characteristics, octane number requirement increase, ring wear and exhaust valve life.
EXAMPLE XVI ment of a 327 cubic inch 10.1:1 compression ratio engine,
the gasoline without the additive of the invention is run for 216 hours and the octane requirement increase noted. The engine is then thoroughly cleaned of all deposits so that it again exhibits the same clean octane requirement and run on an identical cycle, with the same gasoline but containing the additive of the invention. After 216 hours use, the octane requirement increase is noted and compared with the octane requirement increase found with the gasoline without the additive to determine the extent of improvement.
The rumble tendency of an engine after a given time of use is measured by a LIB number. The number represents the percent isooctane (containing 3 cc. TEL/ gallon) required in a blend with benzene (containing 3 cc. TEL/gallon) after a given period of engine operation using the fuel under test, to avoid rumble at a given r.p.m., e.g. 2,000 r.p.m. The test procedure comprises stopping the gasoline to the engine at any given period of engine operation and employing as a fuel to the engine a fuel containing a certain percent of isooctane in an iso octane-benzene blend (containing 3 cc. TEL/ gallon), manually opening the throttle at a given rate and recording the r.p.m. at which rumble occurs, if any in fact occurs. The faster one is able to run the engine with the lowest percent of isooctane in the blend the better the rumble resistance of the engine. Thus, the lower the LIB number the better the rumble characteristics of the engine. The gasoline with and without the additive of the invention is tested in this manner and the LIB numbers obtained with each are compared.
The piston ring Wear is determined by equipping a single cylinder COT engine with. radioactive rings installed in the grooves of the pistons. The lubricating oil system of the engine is provided with a sealed monitoring well which contains a scintillation counter. The ring wear rate is determined by passing the lubricating oil through the monitoring well and therein detecting the concentration in mg./hour of radioactive iron transported to the oil due to wear of the piston rings.
The test to determine the effect of the fuel composition on exhaust valve life involves running an automobile engine at a fixed number of hours at constant or varied speeds and loads depending on the engine used and then noting the number of valves that failed during this period of time.
The test used to determine the deposit-induced ignition characteristics of the fuel composition comprises equipping an engine with an L-head cylinder and an electronic Wild ping counter which records the total number of wild pings which have occurred during the test periods. Since deposit-induced ignition is the tendency to ignite the fuelair mixture erratically and to produce uncontrolled combustion noticeable as, for instance, wild ping, the electronic counter which is used in conjunction with an ionization gap, automatically detects and records uncontrolled combustion.
It is claimed:
1. A gasoline composition consisting essentially of hydrocarbon gasoline, an anti-knock quantity of tetralower-alkyl lead compound, and a gasoline-soluble metal salt of an azolidinedione having the formula:
wherein R is a hydrocarbon radical of up to 30 carbon atoms, R is selected from the group consisting of hydrogen and R; Z is a chalcogen having an atomic number from 8 to 16, said metal being selected from the group consisting of Groups Ia, Ila, IIIa, Va, Ib, IIb, IIIb, IVb Vb, VIb, VIIb, VIII and tin, the :amount of said metal salt being sufficient to provide 0.002 to 0.8 milligram atoms of selected metal of said salt per gallon of gasoline.
2. A gasoline composition consisting essentially of hydrocarbon gasoline, an anti-knock quantity of tetralower-alkyl lead compound, and a gasoline-soluble metal salt of an azolidinedione having the formula:
wherein R is a hydrocarbon radical of up to 30 carbon atoms, R is selected from the group consisting of hydrogen and R; Z is a chalcogen having an atomic number from 8 to 16, said metal being selected from the group consisting of Groups IIIa,,Va, Ib, IIb, IIIb, IVb, Vb, VIb, VIIb, VIII and tin, the amount of said metal salt being sufficient to provide 0.002 to 0.8 milligram atoms of selected metal of said salt per gallon of gasoline.
3. The composition of claim 2 in which there is also included about 0.05 to 0.6 theory of a gasoline-soluble phosphorous compound having the formula:
wherein R is a hydrocarbon radical of up to about 30 carbon atoms on the average, R is selected from the group consisting of hydrogen and R, and n is an integer having a value of to 1.
4. The composition of claim 2 wherein the metal is an iron group metal.
5. The composition of claim 4 wherein the metal is nickel.
6. The composition of claim 3 wherein at least one R in the structure of claim 3 is an alkyl phenyl radical of 7 to 15 carbon atoms.
7. The composition of claim 6 wherein the amount of phosphorous compound is about 0.15 to 0.5 theory.
8. The composition of claim 6 wherein the selected metal is an iron group metal.
9. The composition of claim 8 wherein'the metal is nickel.
10. The composition of claim 2 wherein the amount of said metal salt is sufficient to provide about 0.025 to 0.3 millimoles of selected metal per gallon of said gasoline.
11. The composition of claim 10 in which there is also included about 0.05 to 0.6 theory of a gasolinesoluble phosphorous compound having the formula:
RO OR i RO o wherein R is a lower alkyl phenyl radical of 7 to carbon atoms and R is selected from the group consisting of phenyl and R.
12. The composition of claim 10 wherein the selected metal is an iron group metal.
13. The composition of claim 12 wherein the metal is nickel.
14. The composition of claim 13 wherein the phosphorous compound is cresyl diphenyl phosphate.
15. A gasoline composition consisting essentially of hydrocarbon gasoline, an anti-knock quantity of tetralower-alkyl lead compound, and a gasoline-soluble metal salt of an azolidinedione having the formula:
wherein R is a hydrocarbon radical of up to carbon atoms, R is selected from the group consisting of hydrogen and R; Z is a chalcogen having an atomic number from 8 to 16, said metal being selected from the group consisting of alkali and alkaline earth metals and the amount of said metal salt being suflicient to provide 0.002 to 0.8 milligram atoms of metal of said metal salt per gallon of gasoline.
16. The composition of claim 15 in which there is also included about 0.05 to 0.6 theory of a gasoline-soluble phosphorous compound having the formula:
RO OR RO/ wherein R is a hydrocarbon radical of up to about 30 carbon atoms on the average, R is selected from the group consisting of hydrogen and R, and n is an integer having a value of 0 to 1.
17. The composition of claim 16 wherein at least one R in the structure of claim 16 is an alkyl phenyl radical of 7 to 15 carbon atoms.
18. The composition of claim 17 wherein the amount of phosphorous compound is about 0.15 to 0.5 theory.
19. The composition of claim 15 wherein the metal is an alkaline earth metal.
20. The composition of claim 15 wherein the metal is an alkali metal.
21. The composition of claim 15 wherein the amount of said metal salt is sufiicient to provide about 0.025 to 0.3 millimole of selected metal per gallon of said gasoline.
22. The composition of claim 21 in which there is also included about 0.05 to 0.6 theory of a gasoline-soluble phosphorous compound having the formula:
RO 0R RO/ o wherein R is a lower alkyl phenyl radical of 7 to 15 carbon atoms and R is selected from the group consisting of phenyl and R.
23. The composition of claim 22 wherein the metal is an alkali metal.
24. The composition of claim 23 wherein the phosphorous compound is cresyl diphenyl phosphate.
References Cited UNITED STATES PATENTS 2,737,932 3/1956 Thomas 44-6*8 X 3,146,203 8/1964 Frew 44-68 X 3,231,347 1/1966 Revukas 4468 X DANIEL E. WYMAN, Primary Examiner W. I. SHINE, Assistant Examiner U.S. Cl. X.R. 44-68, 69
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4380456A (en) * 1981-07-30 1983-04-19 Taylor William H Gasoline fuel additive composition
WO2002088244A2 (en) * 2001-04-27 2002-11-07 Nikolai Ivanovich Butenko Composite additive for liquid fuels

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2737932A (en) * 1956-03-13 thomas
US3146203A (en) * 1961-11-20 1964-08-25 Shell Oil Co Ocatane requirement increase reducing fuel and lubricant compositions
US3231347A (en) * 1961-07-31 1966-01-25 Cities Service Oil Co Gasolene composition containing organometallic orthophosphates

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2737932A (en) * 1956-03-13 thomas
US3231347A (en) * 1961-07-31 1966-01-25 Cities Service Oil Co Gasolene composition containing organometallic orthophosphates
US3146203A (en) * 1961-11-20 1964-08-25 Shell Oil Co Ocatane requirement increase reducing fuel and lubricant compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4380456A (en) * 1981-07-30 1983-04-19 Taylor William H Gasoline fuel additive composition
WO2002088244A2 (en) * 2001-04-27 2002-11-07 Nikolai Ivanovich Butenko Composite additive for liquid fuels
WO2002088244A3 (en) * 2001-04-27 2003-05-08 Nikolai Ivanovich Butenko Composite additive for liquid fuels

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