US3807974A - Fuels for automotive engines - Google Patents

Fuels for automotive engines Download PDF

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US3807974A
US3807974A US00058155A US5815570A US3807974A US 3807974 A US3807974 A US 3807974A US 00058155 A US00058155 A US 00058155A US 5815570 A US5815570 A US 5815570A US 3807974 A US3807974 A US 3807974A
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ester
composition
gasoline
fuel
phosphate
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R Kerley
A Felt
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Ethyl Corp
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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
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/08Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
    • 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
    • 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
    • C10L1/2608Organic compounds containing phosphorus containing a phosphorus-carbon bond
    • 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

Definitions

  • This invention is concerned with one such problem which, if not eliminated or at least ameliorated, could prove disastrous.
  • This invention provides the means of ameliorating the severity of the foregoing disastrous consequences.
  • a gasoline soluble, engine inductible, fully esterified ester of an oxy-acid ofphosphorus e.g., a phosphate ester, a phosphite ester, etc.
  • the foregoing compositions will normally require gasoline fuels hav ing a'Research Octane Number of at leastabout 90, and preferably, of at least about 95.
  • the gasoline fuel such that it has acontent of aromatic gasoline hydrocarbons ranging from about l to about 60 volume percent, a con tent of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about 80 volume percent, these percentages beingbasedon I the whole fuel.
  • the amounts of the phosphorus esters used in the base fuel will be dependent both on the precise makeup of the gasoline fuel itself and the identity and character of the ester being utilized. As-a generalrule, however, it will be found that theminimum quantity willbe in the orderof at least about 0.02 gramof phosphorus per gallon and thus for general purposes it will generally be sufficient to employ the ester in an amount equivalent to from about 0.02 to about 1.0 gram of phosphorus per gallon although even greater quantities of the additives may be found entirely acceptable. Preferred concentrations fall in the range of from about 0.05 to about 0.5 gram phosphorus per gallon.
  • an unleaded automotive gasoline fuel having a Research Octane Number of at least about 100 and having a content of aromatic gasoline hydrocarbons of at least about 25 volume percent based on the whole fuel and having the tendency of causing an excessive rate of exhaust valve seat wear containing from about 0.05 to about 0.5 gram of phosphorus per gallon of a gasoline soluble, engine inductible, fully esterified ester of an oxy-acid phosphorus having a boiling point at (or extrapolated to) atmospheric pressure of not more than about 425C, the quantity being sufficient to decrease the rate of such wear substantially uniformly from cylinder to cylinder.
  • This invention also provides a method of ameliorating exhaust valve seat wear of automotive vehicular engines operating on an unleaded gasoline which comprises dispensing to such vehicles an unleaded gasoline fuel of sufficiently high octane quality to satisfy the octane requirements of the engines, said fuel containing from about 0.02 to about 1.0 gram of phosphorus per gallon of a gasoline soluble, engine inductible, fully esterified ester of an oxy-acid of phosphorus.
  • Still another embodiment of this invention involves an improvement in the manufacture of finished gasolines for use in automotive fuels, this improvement comprising formulating unleaded gasoline having a Re search Octane Number of at least about 90 and prefer' ablyfrom about 90 to about 104, a content of aromatic gasoline hydrocarbons ranging from about 10 to about .60 volume percent, a content of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about volume percent, said percentages being based on the whole fuel; and incorporating in the finished gasoline from about 0.02 to about 1.0 gram of phosphorus per gallon of a gasoline soluble, engine inductible, fully esterified ester of an oxy-acid of phosphorus so that said finished fuel does not have the tendency of causing an excessive rate of exhaust valve seat wear in the engines of the vehicles in which it is used.
  • octane quality e.g., a Research Octane Number of at least about is best achieved by selecting appropriate blending stocks and blending them in suitable proportions.
  • aromatics e.g., BTX, catalytic reformate or the like
  • alkylate e.g., C -C saturates prepared by reacting C olefin with isobutane using an acid catalyst such as HF or H 80 or blends of both of these hydrocarbon types.
  • the balance of the whole fuel may be made up of other components such as other saturates, olefins, or the like.
  • the olefins are generally formed by using such procedures as thermal cracking, catalytic cracking and polymerization. Dehydrogenation of paraffins to olefins can supplement the gaseous olefins occurring in the refinery to produce feed material for either polymerization or alkylation processes.
  • the saturated gasoline components comprise paraffms and naphthenes. These saturates are obtained from (1) virgin gasoline by distillation (straight run gasoline), (2) alkylation processes (alkylates) and (3) isomerization procedures (conversion of normal paraffins to branched chain paraffins of greater octane quality). Saturated gasoline components also occur in so-called natural gasoline. In addition to the foregoing, thermally cracked stocks, catalytically cracked stocks and catalytic reformates contain saturated components.
  • the motor gasolines used in formulating the improved fuels of this invention generally have initial boiling points ranging from about 80 to about 105F. and final boiling points ranging from about 380 to about 430F. as measured by the standard ASTM distillation procedure (ASTM D-86). Intermediate gasoline fractions boil away at temperatures within these extremes.
  • the olefin content of the fuel will not exceed about volume percent and the most particularly preferred fuels will not contain more than about 5 percent olefins.
  • Table 1 illustrates the hydrocarbon type makeup of a number of particularly preferred fuels for use in this invention.
  • hydrocarbon fuels used in the practice of this invention will be resistant to oxidative degradation on exposure to air.
  • improvements and advances made in refining techniques there is no longer a necessity for relying heavily upon use of catalytically cracked or thermally cracked stocks which tend to be the most oxidatively unstable fuel components.
  • Greater utilization of the more stable components (aromatics and saturates) is now possible and customary.
  • tertiary phosphite esters especially trihydrocarbyl phos- (see US. Pat. No. 3,038,791); and trimethyl phosphate.
  • the volatility of the phosphorus additive used in this invention bears a direct relationship with its engine inductibility. That is to say, the higher its volatility the more inductible the phosphorus ester.
  • a normally liquid, gasoline soluble, engine inductible, fully esterified ester of an oxy-acid of phosphorus which has a volatility essentially equal to, or greater than, that of tricresyl phosphate.
  • esters having a boiling point at, or extrapolated to, atmospheric pressure of not more than about 4255C. is especially recommended.
  • the factory fill oil was drained at the prescribed mileage and a popular 10W-30 motor oil was used during atility is especially advantageous in assuring sufficient uniformity of distribution of the additive among 'the different cylinders of the engine.
  • Self-evidently if the additive does not reach all cylinders of an operating engine in sufficient quantity to inhibit exhaust valve seat wear in each valve train a failure may be rapidly encountered. Just as a chain is only as strong as its weakest link, the proper performance of the engine is only as efficient as its least efficient exhaust valve system. In short, if one exhaust valve seat is excessively worn the vehicle may emit intolerable quantities of atmospheric pollutants even though the remaining exhaust valve mechanisms are working up to designed efficiency.
  • the gasoline used had an RON- (Research Octane Number) of 101, contained. no phosphorus, and was composed of 31.5 volume percent aromatics, 2.0 volume percent olefins and 66.0 volume percent saturates.
  • Exhaust valve seat recession began immediately after the test was started and .continued for 10,500 miles at which point hydrocarbon exhaust emissionswere almost 15 times that found at the beginning of the test. Carbon monoxide emissions had increased about 520 percent and oxides of nitrogen had been reduced about 1.8 percent. Due to the nature of the test schedule, all emission measurements were made using only the hot cycle portion of the Federal Cycle. At the end of the test power had dropped 36.2 percent and fuel economy had been reduced by about 25 percent. lnspection of the cylinder head revealed that exhaust valve seat recession in Cylinder No. 6 had reached 0.077 inch and had caused excessive valve seat run-out which resulted in excessively high exhaust emissions, poor fuel economy and loss in power. Compression pressures were found to be zero in Cylinder 6, and down 23 psi and 25 psi in Cylinders 3 and 5.
  • EXAMPLE ll phosphorus additives pursuant to this invention does A series of tests was conducted using a 1964 model of a popular make of a six-cylinder U.S. automobile engine having a 230 cubic inch displacement. In these tests the engine was operated on a dynamometer under a passenger car cycling schedule of city-suburban operation. This consisted of a 12-hour cycle divided into first an 8-hour period of city-suburban operation, followed by a 4-hour period of turnpike operation. The first 8-hour period was conducted at a basic speed of 2200 rpm (50 miles per hour road load) with 40- second engine idle operation interspersed every three minutes.
  • the four hours of simulated turnpike operation involved one hour at constant speed of 3,200 rpm (75 miles per hour road load), one hour of cycling at speeds from 3,l003,400 rpm, one hour at constant speed of 3,200 rpm. and finally one hour of cycling at reduce the rate of exhaust valve seat wear and thereby extends the period before which a catastrophic failure may be encountered.
  • the tendency of the unleaded fuels of causing an excessive rate of exhaust valve seat wear and consequent emission of excessive quantities of air pollutants via the engine exhaust is decreased although in point of fact, the reduced rates achieved by this invention are still significantly greater than experienced when using conventional leaded gasolines under the same service conditions.
  • Some exemplary phosphorus additives suitable for use in accordance with this invention are triethyl phosphate, dimethylpropyl phosphate, methyldipropyl phosphate, tripropyl phosphate, triisopropyl phosphate, diethylbutyl phosphate, tributyl phosphate, triisobutyl phosphate, triamyl phosphate, triiso'amyl phosphate, triphenyl phosphate, ethyldiphenyl phosphate, phenyldibutyl phosphate, phenyldiethyl phosphate, xylyl diphenyl phosphate, trimethyl phosphite, triethyl phosphite, tripropyl phosphite, triisopropyl phosphite, tributyl phosphite, triisobutyl phosphite, triisoamyl phosphit
  • Antioxidants can be effectively used in the compositions of this invention.
  • Particularly useful materials for this purpose are N,N-di-sec-butyl-p-phenylene diamine, p-N-butylaminophenol, 4-methyl-2,6-di-tertbutyl phenol; 2,6-di-tert-butyl phenol and 2,4-dimethyl-6-tert-butyl phenol.
  • Good results are achieved when these antioxidants are present in the fuels of this invention in concentrations ranging from about 0.5 to about 25 pounds per 1000 barrels.
  • Metal deactivators can also be used to advantage in the compositions of this invention.
  • One very suitable material is N,N-disalcylidene-l,Z-diaminopropane. Generally speaking, concentrations ranging from about 0.l to about 3 pounds per 1,000 barrels arc satisfactory.
  • Additives imparting anti-icing and anti-stalling characteristics can also be used in the fuels of this invention. Preferredfor this purpose are such materials as methanol, isopropanol, or mixtures thereof (concentrations ranging from about 0.5 to about 2 percent by volume are satisfactory); substantially neutral salts formed from primary alkyl amines and alkyl acid orthophosphates (concentrations corresponding to about 2.5 to about 25 pounds per 1,000 barrels are satisfactory and the B-hydroxyethyl ethylenediamine amides of oleic acid (satisfactory concentrations range from about 50 to about 200 parts per million based on the 1 fuel). Some of these additives also confer dete'rgency properties upon the fuels.
  • additives which may be employed in the fuels of this invention are lead-free antiknock agents, dyes, induction system cleanliness agents, topcylinder lubricants, corrosion inhibitors, inert solvents, and the like.
  • composition of claim 1 wherein the ester is a phosphate ester.
  • composition of claim 1 wherein the ester is a phosphite ester.
  • composition of claim 1 wherein the ester is tricresyl phosphate.
  • composition of claim 1 wherein the ester is cresyl diphenyl phosphate.
  • composition of claim 1 wherein the ester is trimethyl phosphate.
  • composition of claim 1 wherein the ester is mixed methyl-phenyl phosphates.
  • composition of claim 1 wherein said ester is present in an amount equivalent to from about 0.02 to about 1.0 gram of phosphorus per gallon.
  • composition of claim I wherein said ester is present in an amount equivalent to from about 0.05 to about 0.5 gram of phosphorus per gallon.
  • composition of claim 1 wherein said ester is present in an amount equivalent to about 0.1 gram of phosphorus per gallon.
  • composition of claim 1 wherein said gasoline fuel has a content of aromatic gasoline hydrocarbons ranging from about 10 to about volume percent, a content of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about volume percent, these percentages being based on the whole fuel, and wherein said ester is a phosphate ester.
  • composition of claim 1 wherein said gasoline fuel has a Research Octane Number of at least about 95.
  • composition of claim '1 wherein said gasoline fuel has a Research Octane Number of about 100.
  • composition of claim 1 wherein said gasoline fuel has a content of aromatic gasoline hydrocarbons ranging from about to about 60 volume percent, a content of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about 80 volume percent, these percentages being based on the whole fuel.
  • An unleaded automotive gasoline fuel having a Research Octane Number of at least about 100 and having a content of aromatic gasoline hydrocarbons of at least about 25 volume percent based on the whole fuel and having the tendency of causing an excessive rate of exhaust valve seat wear containing from about 0.05 to about 0.5 gram of phosphorus per gallon as a gasoline soluble, engine inductible, fully esterified organic ester of an oxy-acid of phosphorus having a boiling point at, or extrapolated to, atmospheric pressure of not more than about 425C, the quantity being sufficient to decrease the rate of such wear substantially uniformly from cylinder to cylinder.
  • composition of claim wherein said ester is a phosphate ester.
  • composition of claim 15 wherein said ester is a phosphite ester.
  • composition of claim 15 wherein said ester is tricresyl phosphate.
  • composition of claim 15 wherein said ester is mixed methyl-phenyl phosphates.
  • composition of claim 15 wherein said fuel has a content of aromatic gasoline hydrocarbons ranging from about 30 to about 60 volume percent based on the whole fuel.
  • a method of ameliorating exhaust valve seat wear of automotive vehicular engines operating on an unleaded gasoline which comprises dispensing to such vehicles an unleaded gasoline fuel of sufficiently high octane quality to satisfy the octane requirements of the engines, said fuel containing from about 0.02 to about 1.0 gram of phosphorus per gallon as a gasoline soluble, engine inductible, fully esterified organic ester of an oxy-acid of phosphorus.

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Abstract

Exhaust valve seat wear of automotive engines operated on unleaded gasoline can be catastrophic under severe operating conditions. This results in severe loss of engine power, marked reduction in fuel economy and sharp increases in exhaust emissions to intolerable levels. This problem may be ameliorated by utilizing high octane gasolines containing suitable quantities of phosphorus esters. Methods of preparing and dispensing the fuels are also described.

Description

United States Patent [191 Kerley et al.
[451 Apr. 30, 1974 1 FUELS FOR AUTOMOTIVE ENGINES [75] lnventors: Robert V. Kerley, Ortonville;
Arthur E. Felt, Farmington, both of Mich.
[73] Assignee: Ethyl Corporation, Richmond, Va.
[22] Filed: July 24, 1970 21 Appl. No.: 58,155
[52] US. Cl 44/58, 44/76, 44/DI G. 4 [51] Int. Cl. C101 1/18, C101 1/26 [58] Field of Search 44/58, 76, DIG. 4
[56] References Cited UNITED STATES PATENTS 3,294,500 12/1966 Zimmerman et al. 44/76 x 3,195,992 7/1965 Olson et a1 44/69 2,897,071 7/1959 Gilbert 44/76 X 2,889,212 6/1959 Yust et a1. 44/76 X 2,851,343 9/1958 Cantrell et a1... 44/76 X 3,077,491 2/1963 Seglin et al. 44/76 X 3,309,431 3/1967 Mark et al. 44/76 X 3,510,281 5/1970 Vermillion et al 44/58 2,256,187 9/1941 Bartram 44/D1G. 4 2,291,442 7/1942 Bass et a1. 44/D1G. 4
2,892,691 6/1959 Howell 44/D1G. 4
2,948,599 8/1960 Orloff et al. 44/D1G. 4
2,965,460 12/1960 Ries 44/D1G. 4
3,038,791 6/1962 Orloff et al. 44/DIG. 4 3,009,790 1 H1961 Pellegrini et a1 44/58 Primary ExaminerDaniel E. Wyman Assistant ExaminerW. J. Shine Attorney, Agent, or Firm-Dona1d L. Johnson; John F. Sieberth ABSTRACT Exhaust valve seat wear of automotive engines operated on unleaded gasoline can be catastrophic under severe operating conditions. This results in severe loss of engine power, marked reduction in fuel economy and sharp increases in exhaust emissions to intolerable levels. This problem may be ameliorated by utilizing high octane gasolines containing suitable quantities of Y phosphorus esters. Methods of preparing and dispensing the fuels are also described.
28 Claims, No Drawings 1 FUELS FOR AUTOMOTIVE ENGINES This invention relates to fuel compositions for spark ignition internal combustion engines. More particularly, this invention is concerned with providing new and useful gasoline fuels to ameliorate certain catastrophic engine failures which might otherwise be encountered in actual service.
BACKGROUND Proposals have been made to require the elimination of alkyllead antiknock agents from gasoline. Implementation of such proposals would, however, create new problems of a serious nature, such as more rapid depletion of natural resources, increased costs to the refiner and the motoring public, and the like.
This invention is concerned with one such problem which, if not eliminated or at least ameliorated, could prove disastrous.
THE INVENTION I It has been discovered that exhaust valve seat wear with unleaded gasoline can be catastrophic under severe operating conditions. For example, using normal passenger car cycling schedules, engine dynamometer tests have shown that such valve seat wear is 25 to 50 times as great as that occurring with normally leaded gasolines. Among the consequences of excessive exhaust valve seat wear are severe loss of engine power, marked reduction in fuel economy and,-perhaps of paramount concern, sharp-increases in exhaust emissions to intolerable levels.
This invention provides the means of ameliorating the severity of the foregoing disastrous consequences.
In accordance with this invention, there is provided an unleaded automotive gasoline fuel of sufficiently high octane'quality to satisfy the octane requirements of automotive engines but having the tendency of causing an excessive rate of exhaust valve seat wear containing a gasoline soluble, engine inductible, fully esterified ester of an oxy-acid ofphosphorus (e.g., a phosphate ester, a phosphite ester, etc.) in an amount sufficient to decrease the ,rate of such wear. The foregoing compositions will normally require gasoline fuels hav ing a'Research Octane Number of at leastabout 90, and preferably, of at least about 95. In addition, it is preferable to formulate the gasoline fuel such that it has acontent of aromatic gasoline hydrocarbons ranging from about l to about 60 volume percent, a con tent of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about 80 volume percent, these percentages beingbasedon I the whole fuel.
The amounts of the phosphorus esters used in the base fuel will be dependent both on the precise makeup of the gasoline fuel itself and the identity and character of the ester being utilized. As-a generalrule, however, it will be found that theminimum quantity willbe in the orderof at least about 0.02 gramof phosphorus per gallon and thus for general purposes it will generally be sufficient to employ the ester in an amount equivalent to from about 0.02 to about 1.0 gram of phosphorus per gallon although even greater quantities of the additives may be found entirely acceptable. Preferred concentrations fall in the range of from about 0.05 to about 0.5 gram phosphorus per gallon.
Among the preferred embodiments of this invention is an unleaded automotive gasoline fuel having a Research Octane Number of at least about 100 and having a content of aromatic gasoline hydrocarbons of at least about 25 volume percent based on the whole fuel and having the tendency of causing an excessive rate of exhaust valve seat wear containing from about 0.05 to about 0.5 gram of phosphorus per gallon of a gasoline soluble, engine inductible, fully esterified ester of an oxy-acid phosphorus having a boiling point at (or extrapolated to) atmospheric pressure of not more than about 425C, the quantity being sufficient to decrease the rate of such wear substantially uniformly from cylinder to cylinder.
This invention also provides a method of ameliorating exhaust valve seat wear of automotive vehicular engines operating on an unleaded gasoline which comprises dispensing to such vehicles an unleaded gasoline fuel of sufficiently high octane quality to satisfy the octane requirements of the engines, said fuel containing from about 0.02 to about 1.0 gram of phosphorus per gallon of a gasoline soluble, engine inductible, fully esterified ester of an oxy-acid of phosphorus.
Still another embodiment of this invention involves an improvement in the manufacture of finished gasolines for use in automotive fuels, this improvement comprising formulating unleaded gasoline having a Re search Octane Number of at least about 90 and prefer' ablyfrom about 90 to about 104, a content of aromatic gasoline hydrocarbons ranging from about 10 to about .60 volume percent, a content of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about volume percent, said percentages being based on the whole fuel; and incorporating in the finished gasoline from about 0.02 to about 1.0 gram of phosphorus per gallon of a gasoline soluble, engine inductible, fully esterified ester of an oxy-acid of phosphorus so that said finished fuel does not have the tendency of causing an excessive rate of exhaust valve seat wear in the engines of the vehicles in which it is used.
The above and other embodiments, features, advantages, and characteristics of this invention will become still further apparent from the ensuing description and appended claims.
ADDITIONAL CONSIDERATIONS RELATIVE TO THE BASE FUEL In formulating the fuels of this invention the requisite octane quality (e.g., a Research Octane Number of at least about is best achieved by selecting appropriate blending stocks and blending them in suitable proportions. In accordance with present refinery technology the achievement of these high octane levels is most readily accomplished by employing aromatics (e.g., BTX, catalytic reformate or the like) or alkylate (e.g., C -C saturates prepared by reacting C olefin with isobutane using an acid catalyst such as HF or H 80 or blends of both of these hydrocarbon types. The balance of the whole fuel may be made up of other components such as other saturates, olefins, or the like. The olefins are generally formed by using such procedures as thermal cracking, catalytic cracking and polymerization. Dehydrogenation of paraffins to olefins can supplement the gaseous olefins occurring in the refinery to produce feed material for either polymerization or alkylation processes. The saturated gasoline components comprise paraffms and naphthenes. These saturates are obtained from (1) virgin gasoline by distillation (straight run gasoline), (2) alkylation processes (alkylates) and (3) isomerization procedures (conversion of normal paraffins to branched chain paraffins of greater octane quality). Saturated gasoline components also occur in so-called natural gasoline. In addition to the foregoing, thermally cracked stocks, catalytically cracked stocks and catalytic reformates contain saturated components.
The classification of gasoline components into aromatics, olefins and saturates is well recognized in the art. Procedures for analyzing gasolines and gasoline components for hydrocarbon composition have long been known and used. Commonly used today is the FIA analytical method involving fluorescent indicator adsorption techniques. These are based on selective adsorption of gasoline components on an activated silica gel column, the components being concentrated by hydrocarbon type in different parts of the column. Special fluorescent dyes are added to the-test sample and are also selectively separated with the sample fractions to make the boundaries of the aromatics, olefins and saturates clearly visible under ultraviolet light. Further details concerning this method can be found in 1969 Book of ASTM Standards, Jan. 1969 Edition, under ASTM Test Designation D 13l9-66T.
The motor gasolines used in formulating the improved fuels of this invention generally have initial boiling points ranging from about 80 to about 105F. and final boiling points ranging from about 380 to about 430F. as measured by the standard ASTM distillation procedure (ASTM D-86). Intermediate gasoline fractions boil away at temperatures within these extremes.
From the standpoint of minimizing atmospheric pollution to the greatest extent possible, it is best to keep the olefin content of the fuel as low as can be economically achieved as olefins reportedly give rise to smogforming emissions, especially from improperly adjusted vehicular engines. Accordingly, in the preferred base stocks of this invention the olefin content will not exceed about volume percent and the most particularly preferred fuels will not contain more than about 5 percent olefins. Table 1 illustrates the hydrocarbon type makeup of a number of particularly preferred fuels for use in this invention.
TABLE I Hydrocarbon Blends of Particularly Preferred Base Fuels Volume Percentage It is also desirable to utilize base fuels having a low sulfur content as the oxides of sulfur tend to contribute an irritating and choking character to smog and other forms of atmospheric pollution. Therefore to the extent it is economically feasible the fuel will contain not more than about 0.1 weight percent of sulfur in the form of conventional sulfur-containing impurities. Fuels in which the sulfur content is no more than about 0.02 weight percent are especially preferred for use in this invention.
Utilization of non-hydrocarbon blending stocks or components in formulating the fuels of this invention is feasible and in some instances may actually be desirable. Thus, use may be made of methanol, tertiary butanol and other inexpensive, abundant and nondeleterious oxygen-containing fuel components.
It will of course be understood that the hydrocarbon fuels used in the practice of this invention will be resistant to oxidative degradation on exposure to air. Through improvements and advances made in refining techniques there is no longer a necessity for relying heavily upon use of catalytically cracked or thermally cracked stocks which tend to be the most oxidatively unstable fuel components. Greater utilization of the more stable components (aromatics and saturates) is now possible and customary. Nevertheless, in any instance where the base fuel has insufficient storage stability in the presence of air, use will be made of an ap- ADDITIONAL CONSIDERATIONS RELATIVE TO THE PHOSPHORUS ESTER In choosing the phosphorus additives to be employed in the practice of this invention the essential requirements to be observed are, as already indicated, that they be soluble in the gasoline and that they be engine inductible. As a general rule the greater the gasoline solubility of the phosphorus ester, the greater the likelihood it will have sufficient engine inductibility. For this reason one should choose phosphorus esters which are either infinitely soluble or at least very highly soluble in the gasoline base stock being used. A vast amount of information is already available on the suitability of numerous phosphorus esters for use in preparing gasolinetype fuels by virtue of the fact that such phosphorus additives have long been known to have the properties of cooperating effectively with alkyllead antiknock agents in order to alleviate such problems as spark plug fouling, surface ignition, and rumble. Thus, phosphorus esters of the type described for such usage will generally be found satisfactory. See for example the disclosures of US. Pat. Nos. 2,405,560; 2,427,173; 2,765,220; 2,860,958; 2,870,186; 2,889,212; 2,897,071; 2,911,431; 2,948,599; 2,948,600; 3,000,709; 3,004,838; and 3,038,791, all disclosures of which are incorporated herein as if fully set forth in this specification.
From the cost effectiveness standpoint the use of tertiary phosphite esters, especially trihydrocarbyl phos- (see US. Pat. No. 3,038,791); and trimethyl phosphate.
Other parameters which should be considered in choosing the phosphorus ester for use in this invention include its stability, its water solubility and its volatility. Stability of the phosphorus additive is of course important as it must not rapidly deteriorate into sludge or other insoluble precipitates. As a general proposition,
the vast majority of the phosphorus oxy-acid esters referred to in the above patents will be found to satisfy this stability parameter. Water solubility may assume significance in the event of prolonged storage or shipment of finished fuels in contact with water. Obviously if the additive is preferentially dissolved in the water it will no longer remain present in the fuel in order to exert the exhaust valve seat wear inhibiting characteristics for which it is intended pursuant to this invention. Here again, the vast majority of the phosphorus oxyacid esters referred to in the above patents fulfill the requirement of being at most no more than slightlysoluble in water.
The volatility of the phosphorus additive used in this invention bears a direct relationship with its engine inductibility. That is to say, the higher its volatility the more inductible the phosphorus ester. To achieve the best results possible from this invention one should utilize a normally liquid, gasoline soluble, engine inductible, fully esterified ester of an oxy-acid of phosphorus which has a volatility essentially equal to, or greater than, that of tricresyl phosphate. Thus the use of esters having a boiling point at, or extrapolated to, atmospheric pressure of not more than about 4255C. is especially recommended. Besides insuring that the additive is well inducted into the engine and thus doesnot contribute to excessive induction system deposits, this vol- Prior to the start of the program, the following m'ea- EXAMPLE 1 A brand new 1970 model four-door sedan made by a well known U.S. automobile manufacturer with a sixcylinder, 230 cubic inch engine and an automatic transmission was chosen to represent an inexpensive family car. After making sure all adjustments in the engine were set to manufacturers specifications and a 500 mile break-in run completed, the car was loaded with sufficient weight to equal that of a family of two adults and three children. Turnpike operation was chosen to simulate a vacation-trip. The car was equipped with a car top carrier and some weight was added to the trunk.
surements were made:
1. Exhaust valve stem tip height.
- 2. Exhaust emissions using the hot cycle portion of the Federal Cycle (see Federal Register, Volume 33, Number 108, Tuesday, June 4, 1968).
3. Maximum rear wheel power at 50 miles per hour.
4. Constant speed fuel consumption at 50 miles per hour, road load (beam reading of 8 horsepower).
Each day during the test, measurements were made of Items 1-4 above.
Each day the vehicle was driven an average of 883 miles in turnpike operation at an average speed of about 66 miles per hour. After each four hours of driving the car was refueled with the same gasoline from the same storage tank.
The factory fill oil was drained at the prescribed mileage and a popular 10W-30 motor oil was used during atility is especially advantageous in assuring sufficient uniformity of distribution of the additive among 'the different cylinders of the engine. Self-evidently, if the additive does not reach all cylinders of an operating engine in sufficient quantity to inhibit exhaust valve seat wear in each valve train a failure may be rapidly encountered. Just as a chain is only as strong as its weakest link, the proper performance of the engine is only as efficient as its least efficient exhaust valve system. In short, if one exhaust valve seat is excessively worn the vehicle may emit intolerable quantities of atmospheric pollutants even though the remaining exhaust valve mechanisms are working up to designed efficiency. It will be seen therefore that it is especially desirable to use suitably volatile phosphorus esters in the practice of this invention-clearly phosphorus-containing salts or other non-volatileforms of phosphorus are unsuitable as they have insufficient engine inductibility and are incapable of adequate distribution among the cylinders of the engine.
'The following examples illustrate the gravity of the problem and the extent to which it may be ameliorated by means of this invention.
the remainder of the test run.
The gasoline used had an RON- (Research Octane Number) of 101, contained. no phosphorus, and was composed of 31.5 volume percent aromatics, 2.0 volume percent olefins and 66.0 volume percent saturates.
Exhaust valve seat recession began immediately after the test was started and .continued for 10,500 miles at which point hydrocarbon exhaust emissionswere almost 15 times that found at the beginning of the test. Carbon monoxide emissions had increased about 520 percent and oxides of nitrogen had been reduced about 1.8 percent. Due to the nature of the test schedule, all emission measurements were made using only the hot cycle portion of the Federal Cycle. At the end of the test power had dropped 36.2 percent and fuel economy had been reduced by about 25 percent. lnspection of the cylinder head revealed that exhaust valve seat recession in Cylinder No. 6 had reached 0.077 inch and had caused excessive valve seat run-out which resulted in excessively high exhaust emissions, poor fuel economy and loss in power. Compression pressures were found to be zero in Cylinder 6, and down 23 psi and 25 psi in Cylinders 3 and 5.
The results obtained are further summarized in the following Table.
TABLE 11' Exhaust Emissions, ppm
Maximum Rear Fuel Consumption Exhaust Valve Federal Cycle Wheel Power A! 50 mph Stem Tip-Height r;r---a uorcyasomy Y mph mad toad cTage', tress;
Miles HC co NOx HP MPG W TABLE 11-- Continued After replacement of the excessively worn engine parts the test was repeated using a different batch of i the same 101 RON fuel which analyzed 46.5, 4.0, and 49.5 volume percent aromatics, olefms and saturates, respectively. This fuel, however, was blended so that it contained 0.11 gram of phosphorus as mixed methylphenyl phosphates (marketed by Ethyl Corporation as Ethyl Ignition Control Compound 3). With this phosphorus-containing fuel the test was conducted for 10,498 miles under the same conditions as described above. Valve seat wear averaged 0.009 inches with a maximum of 0.01 5 inch. Emissions increased more regularly than on the unleaded fuel without phosphorus, from 75 ppm hydrocarbons to 126 ppm. A fuller summary of the data from this test is presented in Table 111.
TABLE ni ree Gasoline Exhaust limissionm ppm Maximum Rear Fuel Consumption Exhaust Valve Federal Cycle 7 Wheel Power At 50 mph Ste m Tip-Height lest Cle on] At 50 mph Road 1.5511 Change. lnches Miles (1 CO NOx HP MPG Avg. Max.
speeds from 3,100 4,400 rpm.
In each test of this series a non-leaded fuel blend of 75 volume percent aviation alkylate plus volume percent toluene was employed. This fuel blend had a Research Octane Number of approximately 100. In one test the engine was operated on the above cycling schedule on this base fuel blend which did not contain any phosphorus additive. 1n the other two tests a phosphorus additive was incorporated in the same base fuel blend so that the effect of the additive on exhaust valve seat wear could be directly ascertained. In each of these tests the same crank case lubricating oil (a well known brand) was employed. The results of these tests are summarized in the following Table.
It can be seen from the above results that the use of Results of Highway Operation on Unleaded, Phosphorus-Containing Gasoline Exhaust Emissions. ppm Maximum Rear Fuel Consumption Exhaust Valve Federal Cycle Wheel Power At mph Stem Tip-Height Test Q HotCycle n y "ATS'UTrTph iTad Load Cliifiil'lnc'hes Miles HC CO NOx Fl P MPG Avg. Max.
TABLE IV Results of Operation under a Passenger Car Cycling Schedule Exhaust Valve Seat Wear, Inches per 100 Hours Test Duration, Test Fuel Composition Hours Max. Cyl. Avg. Cyl.
1 Base Fuel NO P 107 0.106 0.082 2 Base Fuel plus 0.095 g. P/gal. 200 0.015 0.008 3 Base Fuel plus 0.189 g. P/gal. 200 0.014 0.009
Mixed methyl-phenyl phosphates. Trimethyl phosphate.
EXAMPLE ll phosphorus additives pursuant to this invention does A series of tests was conducted using a 1964 model of a popular make of a six-cylinder U.S. automobile engine having a 230 cubic inch displacement. In these tests the engine was operated on a dynamometer under a passenger car cycling schedule of city-suburban operation. This consisted of a 12-hour cycle divided into first an 8-hour period of city-suburban operation, followed by a 4-hour period of turnpike operation. The first 8-hour period was conducted at a basic speed of 2200 rpm (50 miles per hour road load) with 40- second engine idle operation interspersed every three minutes. The four hours of simulated turnpike operation involved one hour at constant speed of 3,200 rpm (75 miles per hour road load), one hour of cycling at speeds from 3,l003,400 rpm, one hour at constant speed of 3,200 rpm. and finally one hour of cycling at reduce the rate of exhaust valve seat wear and thereby extends the period before which a catastrophic failure may be encountered. Thus, the tendency of the unleaded fuels of causing an excessive rate of exhaust valve seat wear and consequent emission of excessive quantities of air pollutants via the engine exhaust is decreased although in point of fact, the reduced rates achieved by this invention are still significantly greater than experienced when using conventional leaded gasolines under the same service conditions.
lnasmuch as the phosphorus esters used in the practice of this invention are consumed in the engine combustion process so that their function is properly attributable to the elemental phosphorus content of the additive, the remainder of the phosphorus molecule is of significance only insofar as it contributes to the proper physical properties needed for an efficient and effective gasoline additive. Thus, as pointed out above, use may be made of a very large variety of fully esterified esters of oxy-acids of phosphorus so long as they are capable of being introduced in each cylinder of the engine in sufficient quantities so that on combustion the exhaust valve seat wear inhibiting action of the phosphorus will be manifested. Some exemplary phosphorus additives suitable for use in accordance with this invention are triethyl phosphate, dimethylpropyl phosphate, methyldipropyl phosphate, tripropyl phosphate, triisopropyl phosphate, diethylbutyl phosphate, tributyl phosphate, triisobutyl phosphate, triamyl phosphate, triiso'amyl phosphate, triphenyl phosphate, ethyldiphenyl phosphate, phenyldibutyl phosphate, phenyldiethyl phosphate, xylyl diphenyl phosphate, trimethyl phosphite, triethyl phosphite, tripropyl phosphite, triisopropyl phosphite, tributyl phosphite, triisobutyl phosphite, triisoamyl phosphite, diphenylpropyl phosphite, diphenylbutyl phosphite, triphenyl phosphite, tricresyl phosphite, dimethyl methane phosphonate, triethyl methane phosphonate, di-m-tolyl methane phosphonate, di-p-tolyl methane phosphonate, diethyl ethane phosphonate, dibutyl ethane phosphonate, diethylpropane phosphonate, dipropylpropane phosphonate, diethylbutane phosphonate, dibutylbutane phosphonate,
diethyl-n-hexane phosphonate, dibutyl-n-octane phosfying other types of suitable additives for use in the 7 practice of this invention. As pointed out above, particularly preferred additives because of their cost effectiveness, good physical properties and long history of successful commercial service in leaded gasoline are tricresyl phosphate, cresyldiphenyl phosphate, tri-' methyl phosphate, and mixed methyl-phenyl phosphates. it is worth noting that unlike the situation existing in leaded gasolines the utilization of phosphorus additives in an unleaded fuel would not involve some of the problems encountered in finding suitable phosphorus additives for use in leaded fuel. When employing a phosphorus additive inleaded gasoline it was essential to avoid excessive destruction of the antiknock effectiveness contributed by the alkyllead antiknock compound. ln the present situation such a problem would not be encountered as there would be no interaction between lead and its deposits, and the phosphorus additive.
Antioxidants can be effectively used in the compositions of this invention. Particularly useful materials for this purpose are N,N-di-sec-butyl-p-phenylene diamine, p-N-butylaminophenol, 4-methyl-2,6-di-tertbutyl phenol; 2,6-di-tert-butyl phenol and 2,4-dimethyl-6-tert-butyl phenol. Good results are achieved when these antioxidants are present in the fuels of this invention in concentrations ranging from about 0.5 to about 25 pounds per 1000 barrels.
Metal deactivators can also be used to advantage in the compositions of this invention. One very suitable material is N,N-disalcylidene-l,Z-diaminopropane. Generally speaking, concentrations ranging from about 0.l to about 3 pounds per 1,000 barrels arc satisfactory.
Additives imparting anti-icing and anti-stalling characteristics can also be used in the fuels of this invention. Preferredfor this purpose are such materials as methanol, isopropanol, or mixtures thereof (concentrations ranging from about 0.5 to about 2 percent by volume are satisfactory); substantially neutral salts formed from primary alkyl amines and alkyl acid orthophosphates (concentrations corresponding to about 2.5 to about 25 pounds per 1,000 barrels are satisfactory and the B-hydroxyethyl ethylenediamine amides of oleic acid (satisfactory concentrations range from about 50 to about 200 parts per million based on the 1 fuel). Some of these additives also confer dete'rgency properties upon the fuels.
Among the other additives which may be employed in the fuels of this invention are lead-free antiknock agents, dyes, induction system cleanliness agents, topcylinder lubricants, corrosion inhibitors, inert solvents, and the like.
We claim:
1. An unleaded automotive gasoline fuel'having a Research Octane Number of at least about 90 to satisfy the octane requirements of automotive engines but having the tendency of causing an excessive rate of exhaust valve seat wear containing a gasoline soluble, engine inductible, fully esterified organic ester of an oxyacid of phosphorus in an amount sufficient to decrease the rate of such wear.
2. The composition of claim 1 wherein the ester is a phosphate ester.
3. The composition of claim 1 wherein the ester is a phosphite ester.
4. The composition of claim 1 wherein the ester is tricresyl phosphate.
5. The composition of claim 1 wherein the ester is cresyl diphenyl phosphate.
6. The composition of claim 1 wherein the ester is trimethyl phosphate.
7. The composition of claim 1 wherein the ester is mixed methyl-phenyl phosphates.
8. The composition of claim 1 wherein said ester is present in an amount equivalent to from about 0.02 to about 1.0 gram of phosphorus per gallon.
9. The composition of claim I wherein said ester is present in an amount equivalent to from about 0.05 to about 0.5 gram of phosphorus per gallon.
10. The composition of claim 1 wherein said ester is present in an amount equivalent to about 0.1 gram of phosphorus per gallon.
11. The composition of claim 1 wherein said gasoline fuel has a content of aromatic gasoline hydrocarbons ranging from about 10 to about volume percent, a content of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about volume percent, these percentages being based on the whole fuel, and wherein said ester is a phosphate ester.
12. The composition of claim 1 wherein said gasoline fuel has a Research Octane Number of at least about 95.
13. The composition of claim '1 wherein said gasoline fuel has a Research Octane Number of about 100.
14. The composition of claim 1 wherein said gasoline fuel has a content of aromatic gasoline hydrocarbons ranging from about to about 60 volume percent, a content of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about 80 volume percent, these percentages being based on the whole fuel.
15. An unleaded automotive gasoline fuel having a Research Octane Number of at least about 100 and having a content of aromatic gasoline hydrocarbons of at least about 25 volume percent based on the whole fuel and having the tendency of causing an excessive rate of exhaust valve seat wear containing from about 0.05 to about 0.5 gram of phosphorus per gallon as a gasoline soluble, engine inductible, fully esterified organic ester of an oxy-acid of phosphorus having a boiling point at, or extrapolated to, atmospheric pressure of not more than about 425C, the quantity being sufficient to decrease the rate of such wear substantially uniformly from cylinder to cylinder.
16. The composition of claim wherein said ester is a phosphate ester.
17. The composition of claim 15 wherein said ester is a phosphite ester.
l8.'The composition of claim 15 wherein said ester is tricresyl phosphate.
19. The composition of claim 15 wherein said ester is cresyl diphenyl phosphate.
20. The composition of claim 15 wherein said ester is trimethyl phosphate.
21. The composition of claim 15 wherein said ester is mixed methyl-phenyl phosphates.
22. The composition of claim 15 wherein said fuel has a content of aromatic gasoline hydrocarbons ranging from about 30 to about 60 volume percent based on the whole fuel.
23. A method of ameliorating exhaust valve seat wear of automotive vehicular engines operating on an unleaded gasoline which comprises dispensing to such vehicles an unleaded gasoline fuel of sufficiently high octane quality to satisfy the octane requirements of the engines, said fuel containing from about 0.02 to about 1.0 gram of phosphorus per gallon as a gasoline soluble, engine inductible, fully esterified organic ester of an oxy-acid of phosphorus.
24. The method of claim 23 wherein the fuel dispensed has a Research Octane Number. in the range of from about to about 104.
25. The method of claim 23 wherein said ester is tricresyl phosphate.
26. The method of claim 23 wherein said ester is cresyl diphenyl phosphate.
27. The method of claim 23 wherein said ester is trimethyl phosphate.
28. The method of claim 23 wherein said ester is mixed'methyl-phenyl phosphates.
22 3 UNITED STATES PATENT OFFICE I ERTIFICATE OF CORRECTION Patent No. 5, 7, 97" Dated April 5 97" Inventor(s) Robert V. Kerley and Arthur E. Felt It is certifiedthat error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below;
Column 8, line 5 of TABLE IV, the heading "Inches per 100 Hours" should appear directly under "Exhaust Valve Seat Wear,
Signed and sealed this 1st day of October 1974.
(SEAL) Attest:
MCCOY M. GIBSON JR. 7 C. MARSHALL DANN Attesting Officer Commissioner of Patents

Claims (27)

  1. 2. The composition of claim 1 wherein the ester is a phosphate ester.
  2. 3. The composition of claim 1 wherein the ester is a phosphite ester.
  3. 4. The composition of claim 1 wherein the ester is tricresyl phosphate.
  4. 5. The composition of claim 1 wherein the ester is cresyl diphenyl phosphate.
  5. 6. The composition of claim 1 wherein the ester is trimethyl phosphate.
  6. 7. The composition of claim 1 wherein the ester is mixed methyl-phenyl phosphates.
  7. 8. The composition of claim 1 wherein said ester is present in an amount equivalent to from about 0.02 to about 1.0 gram of phosphorus per gallon.
  8. 9. The composition of claim 1 wherein said ester is present in an amount equivalent to from about 0.05 to about 0.5 gram of phosphorus per gallon.
  9. 10. The composition of claim 1 wherein said ester is present in an amount equivalent to about 0.1 gram of phosphorus per gallon.
  10. 11. The composition of claim 1 wherein said gasoline fuel has a content of aromatic gasoline hydrocarbons ranging from about 10 to about 60 volume percent, a content of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about 80 volume percent, these percentages being based on the whole fuel, and wherein said ester is a phosphate ester.
  11. 12. The composition of claim 1 wherein said gasoline fuel has a Research Octane Number of at least about 95.
  12. 13. The composition of claim 1 wherein said gasoline fuel has a Research Octane Number of about 100.
  13. 14. The composition of claim 1 wherein said gasoline fuel has a content of aromatic gasoline hydrocarbons ranging from about 10 to about 60 volume percent, a content of olefinic gasoline hydrocarbons ranging from 0 to about 30 volume percent and a content of saturated gasoline hydrocarbons ranging from about 40 to about 80 volume percent, these percentages being based on the whole fuel.
  14. 15. An unleaded automotive gasoline fuel having a Research Octane Number of at least about 100 and having a content of aromatic gasoline hydrocarbons of at least about 25 volume percent based on the whole fuel and having the tendency of causing an excessive rate of exhaust valve seat wear containing from about 0.05 to about 0.5 gram of phosphorus per gallon as a gasoline soluble, engine inductible, fully esterified organic ester of an oxy-acid of phosphorus having a boiling point at, or extrapolated to, atmospheric pressure of not more than about 425*C., the quantity being sufficient to decrease the rate of such wear substantially uniformly from cylinder to cylinder.
  15. 16. The composition of claim 15 wherein said ester is a phosphate ester.
  16. 17. The composition of claim 15 wherein said ester is a phosphite ester.
  17. 18. The composition of claim 15 wherein said ester is tricresyl phosphate.
  18. 19. The composition of claim 15 wherein said ester is cresyl diphenyl phosphate.
  19. 20. The composition of claim 15 wherein said ester is trimethyl phosphate.
  20. 21. The composition of claim 15 wherein said ester is mixed methyl-phenyl phosphates.
  21. 22. The composition of claim 15 wherein said fuel has a content of aromatic gasoline hydrocarbons ranging from about 30 to about 60 volume percent based on the whole fuel.
  22. 23. A method of ameliorating exhaust valve seat wear of automotive vehicular engines operating on an unleaded gasoline which comprises dispensing to such vehicles an unleaded gasoline fuel of suFficiently high octane quality to satisfy the octane requirements of the engines, said fuel containing from about 0.02 to about 1.0 gram of phosphorus per gallon as a gasoline soluble, engine inductible, fully esterified organic ester of an oxy-acid of phosphorus.
  23. 24. The method of claim 23 wherein the fuel dispensed has a Research Octane Number in the range of from about 90 to about 104.
  24. 25. The method of claim 23 wherein said ester is tricresyl phosphate.
  25. 26. The method of claim 23 wherein said ester is cresyl diphenyl phosphate.
  26. 27. The method of claim 23 wherein said ester is trimethyl phosphate.
  27. 28. The method of claim 23 wherein said ester is mixed methyl-phenyl phosphates.
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3895925A (en) * 1974-06-10 1975-07-22 Texaco Inc Motor fuel composition
US4225449A (en) * 1979-04-19 1980-09-30 Edwin Cooper, Inc. Lubricating oil and fuel compositions
US4435186A (en) 1982-05-03 1984-03-06 Texaco Inc. Alcohol fuels containing wear-inhibiting amounts of reaction products of amines and phosphate esters of phosphonic acids
US4588415A (en) * 1985-09-20 1986-05-13 Ethyl Corporation Fuel compositions
US4720288A (en) * 1986-03-27 1988-01-19 Union Oil Company Of California Gasoline fuel composition
US4752374A (en) * 1987-04-20 1988-06-21 Betz Laboratories, Inc. Process for minimizing fouling of processing equipment
US5055625A (en) * 1990-02-06 1991-10-08 Fred Neidiffer Gasoline additive composition and method for using same
US5114436A (en) * 1987-04-20 1992-05-19 Betz Laboratories, Inc. Process and composition for stabilized distillate fuel oils
US5344468A (en) * 1991-06-14 1994-09-06 Ethyl Petroleum Additives, Inc. Organic phosphates and their use as wear inhibitors
US6746495B2 (en) * 2000-10-24 2004-06-08 Exxonmobil Research And Engineering Company Method for controlling deposit formation in gasoline direct injection engine by use of a fuel having particular compositional characteristics

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2256187A (en) * 1935-07-17 1941-09-16 Monsanto Chemicals Mineral oil product and process of treating the same
US2291442A (en) * 1938-11-22 1942-07-28 Lubri Zol Corp Upper cylinder lubricant
US2851343A (en) * 1955-01-17 1958-09-09 Gulf Oil Corp Gasoline fuel compositions
US2889212A (en) * 1952-07-22 1959-06-02 Shell Dev Lead scavenger compositions
US2892691A (en) * 1952-04-28 1959-06-30 Exxon Research Engineering Co Motor fuels and motor fuel additives
US2897071A (en) * 1953-06-30 1959-07-28 Ethyl Corp Gasoline fuels
US2948599A (en) * 1954-07-26 1960-08-09 Ethyl Corp Gasoline fuel compositions
US2965460A (en) * 1955-02-17 1960-12-20 Standard Oil Co Distillate hydrocarbon compositions
US3009790A (en) * 1957-04-05 1961-11-21 Gulf Research Development Co Fuel for spark ignition engines
US3038791A (en) * 1959-07-16 1962-06-12 Ethyl Corp Phenyl phosphate compositions
US3077491A (en) * 1959-10-26 1963-02-12 Fmc Corp Preparation of triarylphosphates
US3195992A (en) * 1959-03-27 1965-07-20 California Research Corp Gasoline composition containing lead compounds
US3294500A (en) * 1954-05-15 1966-12-27 Bayer Ag Fuel for internal combustion engines
US3309431A (en) * 1962-12-31 1967-03-14 Monsanto Co Method for the preparation of tritertiary alkyl phosphites
US3510281A (en) * 1964-09-17 1970-05-05 Texaco Inc Jet fuel composition

Patent Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2256187A (en) * 1935-07-17 1941-09-16 Monsanto Chemicals Mineral oil product and process of treating the same
US2291442A (en) * 1938-11-22 1942-07-28 Lubri Zol Corp Upper cylinder lubricant
US2892691A (en) * 1952-04-28 1959-06-30 Exxon Research Engineering Co Motor fuels and motor fuel additives
US2889212A (en) * 1952-07-22 1959-06-02 Shell Dev Lead scavenger compositions
US2897071A (en) * 1953-06-30 1959-07-28 Ethyl Corp Gasoline fuels
US3294500A (en) * 1954-05-15 1966-12-27 Bayer Ag Fuel for internal combustion engines
US2948599A (en) * 1954-07-26 1960-08-09 Ethyl Corp Gasoline fuel compositions
US2851343A (en) * 1955-01-17 1958-09-09 Gulf Oil Corp Gasoline fuel compositions
US2965460A (en) * 1955-02-17 1960-12-20 Standard Oil Co Distillate hydrocarbon compositions
US3009790A (en) * 1957-04-05 1961-11-21 Gulf Research Development Co Fuel for spark ignition engines
US3195992A (en) * 1959-03-27 1965-07-20 California Research Corp Gasoline composition containing lead compounds
US3038791A (en) * 1959-07-16 1962-06-12 Ethyl Corp Phenyl phosphate compositions
US3077491A (en) * 1959-10-26 1963-02-12 Fmc Corp Preparation of triarylphosphates
US3309431A (en) * 1962-12-31 1967-03-14 Monsanto Co Method for the preparation of tritertiary alkyl phosphites
US3510281A (en) * 1964-09-17 1970-05-05 Texaco Inc Jet fuel composition

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3895925A (en) * 1974-06-10 1975-07-22 Texaco Inc Motor fuel composition
US4225449A (en) * 1979-04-19 1980-09-30 Edwin Cooper, Inc. Lubricating oil and fuel compositions
US4435186A (en) 1982-05-03 1984-03-06 Texaco Inc. Alcohol fuels containing wear-inhibiting amounts of reaction products of amines and phosphate esters of phosphonic acids
US4588415A (en) * 1985-09-20 1986-05-13 Ethyl Corporation Fuel compositions
US4720288A (en) * 1986-03-27 1988-01-19 Union Oil Company Of California Gasoline fuel composition
US4752374A (en) * 1987-04-20 1988-06-21 Betz Laboratories, Inc. Process for minimizing fouling of processing equipment
US5114436A (en) * 1987-04-20 1992-05-19 Betz Laboratories, Inc. Process and composition for stabilized distillate fuel oils
US5055625A (en) * 1990-02-06 1991-10-08 Fred Neidiffer Gasoline additive composition and method for using same
US5344468A (en) * 1991-06-14 1994-09-06 Ethyl Petroleum Additives, Inc. Organic phosphates and their use as wear inhibitors
US6746495B2 (en) * 2000-10-24 2004-06-08 Exxonmobil Research And Engineering Company Method for controlling deposit formation in gasoline direct injection engine by use of a fuel having particular compositional characteristics

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