US3004837A - Fuel for two-cycle internal combustion engines - Google Patents

Fuel for two-cycle internal combustion engines Download PDF

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US3004837A
US3004837A US603192A US60319256A US3004837A US 3004837 A US3004837 A US 3004837A US 603192 A US603192 A US 603192A US 60319256 A US60319256 A US 60319256A US 3004837 A US3004837 A US 3004837A
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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
    • C10L1/146Macromolecular compounds according to different macromolecular groups, mixtures thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M3/00Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
    • 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
    • C10L1/16Hydrocarbons
    • C10L1/1625Hydrocarbons macromolecular compounds
    • C10L1/1633Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds
    • C10L1/1641Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds from compounds containing aliphatic monomers
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/198Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
    • C10L1/1985Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/022Ethene
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/024Propene
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/026Butene
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/14Synthetic waxes, e.g. polythene waxes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/105Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/25Internal-combustion engines
    • C10N2040/255Gasoline engines
    • C10N2040/26Two-strokes or two-cycle engines

Definitions

  • the present invention relates to lubricant motor fuels .for two-cycle engines and lubricant additives useful in the formulation of such fuels.
  • the present application is a continuation-in-part of my copending application Serial No. 527,163, filed August 8, 1955, and now U.S. Patent No. 2,896,593.
  • the lubricating oil is mixed directly with the naphtha or other fuel, asdistinguished from other types of gas engines in which the lubricating oil is retained in the crankcase.
  • the mixture consisting of naphtha and a minor proportion of lubricating oil is fed to the combustion chamber, where it is burned.
  • the design and carburetion adjustment of the two-cycle engine is necesgreat deal of difiiculty.
  • a further object of my invention is the provision of a lubricating fuel for two-cycle engines, which will permit storage of the engine with greatly reduced gum formation.
  • a still further object of my invention is the provision of a lubricating fuel for two-cycle engines, which will retain adequate lubricity at greatly elevated temperatures.
  • Still another object of the invention is the provision of a lubricating additive and lubricating fuel for two-cycle engines, which will leave a non-flowing residual inhibitor on heated engine surfaces, thereby to serve as a rust and corrosion preventative.
  • a still further object of the invention is the provision of a lubricating fuel for two-cycle engines, which will leave the engine parts in such condition that they may be easily started when cold.
  • Yet another object of the invention is the provision of a lubricating fuel for two-cycle engines, comprising a homogeneous mixture of mutually miscible components.
  • the present invention contemplates lubricating additives for mixture with two-cycle engine fuel, adapted to fulfill the objects listed above.
  • the lubricating 'oil component of my invention comprises liquid polymers of olefins of which the monomers have not more than five carbon atoms.
  • the operative embodiments are liquid polymers of ethylene, propylene, butylene, isobutylene, and amylene; and particularly preferred is isobutylene. Polymerization of these monomers to the extent necessary to produce a lubricating 'oil may be carried out according to the method of any 3 of US. Patents Numbers 2,278,445, April 7, 1942; 2,301,-
  • the proportion of lubricant additive since the polymeric additive is itself an efficient fuel which gives high horsepower.
  • a cooling effect due to the additive is noted, resulting from the endothermic depolymerization of the additive in the combustion chamber.
  • rich mixtures of additive aid in lowering the temperature and add to the horsepower output of the fuel, they. are obviously somewhat wasteful from an economic standpoint; and hence, it is not anticipated that additive in excess of about 12% byv volume of the whole will be found desirable.
  • the improvement ofthe present application consists in the addition to the'additive of the earlier application of about 0.5% to about and preferably' about 1%, by weight of the additive, of polypropyleneglycol having an average molecular weight of at least about 600.
  • Polypropylene glycol and naphtha are mutually miscible in all proportions contemplated by the invention.
  • the effect of the polyglycol is twofold.
  • the polyglycol is largely inetfective to produce these results. Above about 10% by weight of the additive, the polyglycol destroys the residual inhibitor film. Inasmuch as polypropylene glycol is hygroscopic,'the destruction of the film by use of excessive polyglycol soon results in rusting and corrosion of the vital engine parts.
  • the polyglycol is largely inelfective to produce the desired results.
  • a preferred average molecular weight is about 1200; and very little, if any, increase in lubricity has been found by the use of higher average molecular weightof about 2000 and more.
  • a waxy solid is ultimately formed; however, this solid is soluble in r the lighter petroleum fractions; and in view of its dilu- -ond, itminimizes the tackiness of the residual inhibitor .tion in the fuel solutions, it is useful as well as the lower molecular weight polymers of average weight at least about 600. Therefore, no maximum upper limit for the average molecular weight of the polyglycol can be found by testing any propylene glycol polymerswhich can be produced by known methods.
  • a suitable method of forming polypropylene glycol is to heat the monomeric (or dimeric, trimerie, etc.) propylene glycol at a temperature of about. 300 to 480 degrees Fahrenheit, preferably 345 to 435 degrees F ahr'enheit; in the presenceof a dehydration catalyst, such as sulphuric acid, phosphoric acid, iodine, hydrogen iodide, etc, with continuous removal of the water of polymerization.
  • a dehydration catalyst such as sulphuric acid, phosphoric acid, iodine, hydrogen iodide, etc, with continuous removal of the water of polymerization.
  • the'glycol is diluted to control the reaction and to form an easily removed azeotrope with the water of polymerization. 7
  • the stability of the polyglycol may be further, improved by' partial amine end-group conversion during, but preferably after polymerization, by heating the amine and polymer in the presence of'a dehydration catalyst,- and preferably in the presence of a solvent.
  • the processes of polymerizing the glycol form no part of my invention. 7
  • straight run naphtha is meant the natural cut having an octane number less than 70, which is obtained from crude oil by ordinary distillation before the remainingfcrude' oil is subjected to cracking for the production of cracked gasolene'.
  • straight run naphtha is sharply distinguished from cracked gasolene, which latter has by contrast a relatively high proportion of wild molecules.
  • Example I As a lubricant additive, a polymer of isobutylene is selected, having a pour point of minus 20 degrees Fahrenheit, a flash point of 215 degrees Fahrenheit, a viscosity at 100 degrees Fahrenheit of 230 Saybolt seconds and a viscosity index at 210 degrees Fahrenheit of 50 Saybolt seconds and a viscosity index of 114.
  • This additive is mixed in the amount of 9% by volume of the whole with a straight run naphtha known as stove and lighting naphtha having a lead content of 0, an octane number of 65, a sulphur content of 0.02%, an A.P.I.
  • Example II Example II Example II Example I is repeated, except that the motor operates for 300 hours, during which the measured temperature of certain bearing surfaces rises to about 575 degrees Fahrenheit, and except that the lubricant additive includes 1% by Weight of the additive of polypropylene glycol having an average molecular weight of 1200.
  • the lubricant additive consists of 99% by weight of polyisobutylene and 1% by weight of polypropylene glycol.
  • a fuel for a two-cycle engine consisting essentially of a major proportion of naphtha and not substantially less than 6% by volume of an additive; the additive comprising a major proportion of liquid polymers of lower olefins having an average molecular weight of at least about 300, and about 0.5% to about 10% by weight of the additive of polypropylene glycol having an average molecular weight of at least about 600*.
  • a lubricating additive for two-cycle engine fuel comprising a major proportion of liquid polymers of lower olefins having an average molecular weight of at least about 3 00 and about 0.5 to about 10% by weight of polypropylene glycol having an average molecular weight of at least about 600.

Description

. 3,004,837 FUEL FOR TWO-CYCLE INTERNAL COMBUSTION ENGINES Lawrence E. Riemenschneider, 175 Park St. Chelsea, Mich- No Drawing. Filed Aug. 9, 1956, Ser. No. 603,192 2 Claims. (Cl. 44-58) The present invention relates to lubricant motor fuels .for two-cycle engines and lubricant additives useful in the formulation of such fuels. The present application is a continuation-in-part of my copending application Serial No. 527,163, filed August 8, 1955, and now U.S. Patent No. 2,896,593.
. In the operation of gas engines of the two-cycle type,
the lubricating oil is mixed directly with the naphtha or other fuel, asdistinguished from other types of gas engines in which the lubricating oil is retained in the crankcase. The mixture consisting of naphtha and a minor proportion of lubricating oil is fed to the combustion chamber, where it is burned. However, the design and carburetion adjustment of the two-cycle engine is necesgreat deal of difiiculty.
V In particular, faulty combustion of the lubricant component of the fuel mixture has heretofore resulted incarbon and sludge deposits which interfere with the exhaust port and cause fouling of the sparkplugs and sticking of the rings. Moreover, excessive carbon deposits have tended to build up on the'head of the piston and in the cylinder head and ring grooves. These difiiculties have led to marked reduction in power delivery and have required frequent disassembly and cleaning of the two-cycle engine. With a new, clean engine, no more than thirty hours of operation before cleaning could heretofore be expected; and upon subsequent operation, the time between plug cleaning has dropped to a fraction of this number of hours and in some cases has fallen to less than one hour.
Apart from the reduction in power and necessity for frequent cleaning resulting from such deposits, a further difiiculty has arisen apart from operation of the engine and as-a result of mere storage of the engine containing fuel mixtures known to the prior art. This difficulty has United States Patent manifested itself in the form of gummy deposits comprising reaction products of the lubricant and certain components of the naphtha, and in the form of deposits forming a coating on metal parts and commonly known inthe art as varnish.
The invention described in my' above-mentioned co-' pending application provided a quite satisfactory solution for the above difficulties in the form of a lubricant additive comprising a small proportion of liquid polymers of olefins of which the monomers have not more than five grees Fahrenheit, which, upon cooling, leaves a thin but tacky film upon the cooled metal surfaces. This film is a non-flowing residual inhibitor which is very desirable in that it acts as a rust and corrosion preventative. While this film is verybeneficial in the prevention of rust and corrosion during the storage of two-cycle motors, it also 3,004,837 Patented Oct. 17, 1961 has a somewhat if only temporarily detrimental effect in that the cold motor is somewhat more diflicult to crank until fresh fuel comes into contact with these sticky surfaces. Then, however, the tackiness disappears almost immediately and is no longer a drag until the motor has again cooled off.
Moreover, a two-cycle engine which is well designed with regard to cooling, essential tolerances for oil films, and coefficients of expansion of bearing members to maintain these tolerances, will not be subject to temperatures at the bearing surfaces in excess of about 500 degrees above 500 degrees Fahrenheit. Frequently, failures of this type are not due to inherent defects of design, but rather are due to misuse, or the failure of the cooling mechanism, or the result of negligence or ignorance on the part of the user-or operator. In any event, even the invention of my earlier application may prove indequate at these higher temperatures, and a shrink fit or seizure may result.
It has now been found that the addition to the additive of my earlier invention of 0.5% to 10% by weight of the additive of polypropylene glycol having an average molecular weight of at least about 600 will raise the temperature tolerance of the lubricant portion of the fuel approximately degrees Fahrenheit, and will also mimmize the tackiness of the residual inhibitor film on the cooled motor surfaces thereby reducing the effort necessary to crank the cold motor.
Accordingly, it is an object of my invention to provide a lubricant motor fuel for two-cycle engines, which will leave no appreciable carbon and sludge'residue upon combustion.
A further object of my invention is the provision of a lubricating fuel for two-cycle engines, which will permit storage of the engine with greatly reduced gum formation.
A still further object of my invention is the provision of a lubricating fuel for two-cycle engines, which will retain adequate lubricity at greatly elevated temperatures.
Still another object of the invention is the provision of a lubricating additive and lubricating fuel for two-cycle engines, which will leave a non-flowing residual inhibitor on heated engine surfaces, thereby to serve as a rust and corrosion preventative.
A still further object of the invention is the provision of a lubricating fuel for two-cycle engines, which will leave the engine parts in such condition that they may be easily started when cold. i
Yet another object of the invention is the provision of a lubricating fuel for two-cycle engines, comprising a homogeneous mixture of mutually miscible components. Finally, the present invention contemplates lubricating additives for mixture with two-cycle engine fuel, adapted to fulfill the objects listed above.
- Other objects and advantages of the present invention will become apparentfromthe following description and examples. j
The lubricating 'oil component of my invention comprises liquid polymers of olefins of which the monomers have not more than five carbon atoms. Among the operative embodiments are liquid polymers of ethylene, propylene, butylene, isobutylene, and amylene; and particularly preferred is isobutylene. Polymerization of these monomers to the extent necessary to produce a lubricating 'oil may be carried out according to the method of any 3 of US. Patents Numbers 2,278,445, April 7, 1942; 2,301,-
052, November 3, 1942; 2,318,719, May 11, 1943; 2,329,- 7
714, September 21, l943;'2,345,574, April 4, 1944; or 2,422,443, June 17, 1947. Adequate lubricating properties are obtained when theseliquid polymershave average molecular weights of at least about300, preferably 400 to 500. When polymerization is continued indefinitely, a waxy solid of very much higher average molecular weight is obtained, which, however, is soluble in-the lighter petroleum fractions, and hence is usable because of its dilution in the lighter fractions. However, because of the difiiculty of compounding fuels by the addition of relatively solid olefin polymers, this invention is primarily concerned with the use of liquid olefin polymers.
'Although the operative embodiments of monomers are selected from the lower ethylene series, it will of course .be understood that tiny included amounts of polymers formed from higher monomers will not seriously affect the operativeness of the invention.
Temperatures up to about 500 degrees Fahrenheit are encountered adjacent the crankcase and cylinder walls of two-cycle engines which are properly operated and in good working condition; and the polymers of the lower ethylene'series described above will remain stable somewhat beyond that-temperature range. However, these polymers according to the invention will depolymerize to a gaseous state at around 625 degrees Fahrenheit. Inas- :-much as the temperatures reached during combustion of *by the thorough mechanical mixing of a small "propor- .fiion of polymeric lubricant additive according to the invention with a liquid fuel such as naphtha. The two components are mutually miscible in all proportions contemplated by the invention. A preferred proportion of polymeric lubricant additive is 9% by volume of the whole. A proportion of lubricant additive substantially. smaller than 6% by volume of the whole gives a decreased lubrication effect. There is no true upper limit to the proportion of lubricant additive, since the polymeric additive is itself an efficient fuel which gives high horsepower. Moreover, as the proportion of additive is increased above 6% byv ol'umeof the whole, a cooling effect due to the additive is noted, resulting from the endothermic depolymerization of the additive in the combustion chamber. Thus, while rich mixtures of additive aid in lowering the temperature and add to the horsepower output of the fuel, they. are obviously somewhat wasteful from an economic standpoint; and hence, it is not anticipated that additive in excess of about 12% byv volume of the whole will be found desirable.
As stated above, the improvement ofthe present application consists in the addition to the'additive of the earlier application of about 0.5% to about and preferably' about 1%, by weight of the additive, of polypropyleneglycol having an average molecular weight of at least about 600. Polypropylene glycol and naphtha are mutually miscible in all proportions contemplated by the invention. The effect of the polyglycol is twofold. First,
it elevates the temperature tolerance of the lubricant portion of the fuel approximately 75 degrees Fahrenheit, so that effective lubricity is maintained at temperatures, as high as 575 degrees Fahrenheit or somewhat more; Sec- 4 film, and thus reduces the effort necessary to start the motor when cold.
Below about 0.5% by weight of the additive, the polyglycol is largely inetfective to produce these results. Above about 10% by weight of the additive, the polyglycol destroys the residual inhibitor film. Inasmuch as polypropylene glycol is hygroscopic,'the destruction of the film by use of excessive polyglycol soon results in rusting and corrosion of the vital engine parts.
Below an average molecular weight of about 600, the polyglycol is largely inelfective to produce the desired results. A preferred average molecular weight is about 1200; and very little, if any, increase in lubricity has been found by the use of higher average molecular weightof about 2000 and more. When the polymerization of propylene glycol is continued indefinitely, a waxy solid is ultimately formed; however, this solid is soluble in r the lighter petroleum fractions; and in view of its dilu- -ond, itminimizes the tackiness of the residual inhibitor .tion in the fuel solutions, it is useful as well as the lower molecular weight polymers of average weight at least about 600. Therefore, no maximum upper limit for the average molecular weight of the polyglycol can be found by testing any propylene glycol polymerswhich can be produced by known methods.
A suitable method of forming polypropylene glycol is to heat the monomeric (or dimeric, trimerie, etc.) propylene glycol at a temperature of about. 300 to 480 degrees Fahrenheit, preferably 345 to 435 degrees F ahr'enheit; in the presenceof a dehydration catalyst, such as sulphuric acid, phosphoric acid, iodine, hydrogen iodide, etc, with continuous removal of the water of polymerization. Preferably, the'glycol is diluted to control the reaction and to form an easily removed azeotrope with the water of polymerization. 7
If desired, the stability of the polyglycol may be further, improved by' partial amine end-group conversion during, but preferably after polymerization, by heating the amine and polymer in the presence of'a dehydration catalyst,- and preferably in the presence of a solvent. However, the processes of polymerizing the glycol form no part of my invention. 7
Although the use of polymeric lubricant additives in fuel mixtures according to my invention greatly reduces the amount of harmful deposit when used with a naphtha of any type, it'was nevertheless found that some of the deposit was due to the use of generally available gasolenes containing lead and produced by the so-called cracking processes. These 'gasolenes produced by cracking contain a relatively high proportion of unstable molecules'kn'own to the art as'wild molecules which form varnishes on metal surfaces and combine with Inbricant to 'form gums. ,Moreover, certain components of the residues of combustion of cracked gasolene and lubricating 'oil mixtures are electrically conductive at the temperatures encountered in the combustion chamber of a two cycle engine. 'Heretofore, the harmful effect of the residuesa'nd sulphur compounds formed and left by the commonly available gasolenes produced by cracking processes had been completely masked by the greater residues] left by lubricant additives heretofore used.
"Thus, it was found desirable also to provide the further refinement of the composition of fuel mixtures according to'niy invention, comprising the use of lead-free, low sulfur; straight run naphtha as the majorcomponent of the fuel. By straight run naphtha is meant the natural cut having an octane number less than 70, which is obtained from crude oil by ordinary distillation before the remainingfcrude' oil is subjected to cracking for the production of cracked gasolene'. Thus, straight run naphtha is sharply distinguished from cracked gasolene, which latter has by contrast a relatively high proportion of wild molecules.
For the purpose of enabling those skilled in the art 10 Practice the invention, the following exemplary illustr t o sa en:
Example I As a lubricant additive, a polymer of isobutylene is selected, having a pour point of minus 20 degrees Fahrenheit, a flash point of 215 degrees Fahrenheit, a viscosity at 100 degrees Fahrenheit of 230 Saybolt seconds and a viscosity index at 210 degrees Fahrenheit of 50 Saybolt seconds and a viscosity index of 114. This additive is mixed in the amount of 9% by volume of the whole with a straight run naphtha known as stove and lighting naphtha having a lead content of 0, an octane number of 65, a sulphur content of 0.02%, an A.P.I. gravity of 64.5 degrees, and a boiling point range initially at 109 Fahrenheit, 10% at 156 degrees Fahrenheit, at 169 degrees Fahrenheit, at 192 Fahrenheit, at 206 degrees Fahrenheit, at 216 degrees Fahrenheit, at 231 degrees Fahrenheit, at 245 degrees Fahrenheit, at 265 degrees Fahrenheit, at 294 degrees Fahrenheit, and an end boiling point at 339 degrees Fahrenheit. The mixture is burned as fuel in a two-cycle engine; and after 48 hours of operation, no appreciable deposit of residue is noticed in the exhaust port, on the piston head, in the cylinder head, or in the ring groove. Without removal of the fuel from the engine, the engine is permitted to stand for a month; and after the expiration of this latter time, no appreciable deposit of varnish or gum is noticed on any of the parts.
When the motor is started again, there is some degree of difliculty in cranking it; but as soon as fresh fuel comes into contact with the surfaces preserved by the residual inhibitor film, the drag disappears and does not reappear until the motor has again cooled off.
At no time during the above test does the measured temperature of any bearing surface exceed about 500 degrees Fahrenheit.
Example II Example I is repeated, except that the motor operates for 300 hours, during which the measured temperature of certain bearing surfaces rises to about 575 degrees Fahrenheit, and except that the lubricant additive includes 1% by Weight of the additive of polypropylene glycol having an average molecular weight of 1200. Thus, the lubricant additive consists of 99% by weight of polyisobutylene and 1% by weight of polypropylene glycol. After operation, as before, no appreciable deposit of residue is noticed on the parts previously mentioned, and as before, after a month without removal of the fuel, no appreciable deposit of varnish or gum is noticed on any of the parts.
When the motor is again started, it is found to be much easier to crank initially than in the case of Example I.
In both Examples I and II, completely adequate lubricity is maintained even at the highest measured bearing temperatures recited above.
Thus, from a consideration of the foregoing disclosure, it will be obvious that I have achieved all of the initially recited objects of my invention.
Although the present invention has been described in conjunction with preferred embodiments, it is to be understood that modifications and variations may be resorted to without departing from the spirit and scope of the invention, as those skilled in the art will readily understand. Such modifications and variations are considered to be within the purview and scope of the invention and ap pended claims.
I claim:
1. A fuel for a two-cycle engine consisting essentially of a major proportion of naphtha and not substantially less than 6% by volume of an additive; the additive comprising a major proportion of liquid polymers of lower olefins having an average molecular weight of at least about 300, and about 0.5% to about 10% by weight of the additive of polypropylene glycol having an average molecular weight of at least about 600*.
2. A lubricating additive for two-cycle engine fuel, comprising a major proportion of liquid polymers of lower olefins having an average molecular weight of at least about 3 00 and about 0.5 to about 10% by weight of polypropylene glycol having an average molecular weight of at least about 600.
References Cited in the file of this patent UNITED STATES PATENTS 2,049,062 Howard July 28, 1936 2,087,616 Cunradi et a1. July 20, 1937 2,096,218 Voorhees Oct. 19, 1937 2,135,117 Stevens et al Nov. 1, 1938 2,637,720 Schneider et al May 5, 1953 2,807,526 Foreman Sept. 24, 1957 FOREIGN PATENTS 328,587 Great Britain Apr. 22, 1930 399,527 Great Britain Oct. 4, 1933 OTHER REFERENCES Ucon Synthetic Lubricants and Hydraulic Fluids, by I. M. Russ, A.S.T.M. Publication No. 77, Symposium on Synthetic Lubricants, June 16-20, 1947, pages 3, s and 9.

Claims (1)

1. A FUEL FOR A TWO-CYCLE ENGINE CONSISTING ESSENTIALLY OF A MAJOR PROPORTION OF NAPHTHA AND NOT SUBSTANTIALLY LESS THAN 6% BY VOLUME OF AN ADDITIVE, THE ADDITIVE COMPRISING A MAJOR PROPORTION OF LIQUID POLYMERS OF LOWER OLEFINS HAVING AN AVERAGE MOLECULAR WEIGHT OF AT LEAST ABOUT 300, AND ABOUT 0.5% TO ABOUT 10% BY WEIGHT OF THE ADDITIVE OF POLYPROPYLENE GLYCOL HAVING AN AVERAGE MOLECULAR WEIGHT OF AT LEAST ABOUT 600.
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Cited By (12)

* Cited by examiner, † Cited by third party
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JPS493065A (en) * 1972-04-04 1974-01-11
JPS499504A (en) * 1972-05-23 1974-01-28
US3852204A (en) * 1966-02-01 1974-12-03 Cosden Oil & Chem Co Lubricant compositions
JPS5010324B1 (en) * 1968-12-20 1975-04-21
US3901665A (en) * 1972-10-06 1975-08-26 Du Pont Multi-functional fuel additive compositions
US3953179A (en) * 1972-04-04 1976-04-27 Labofina S.A. Lubricating compositions
US4320021A (en) * 1975-10-14 1982-03-16 The Lubrizol Corporation Amino phenols useful as additives for fuels and lubricants
WO1992021736A1 (en) 1991-05-30 1992-12-10 The Lubrizol Corporation Two-cycle lubricant and method of using same
US5234474A (en) * 1991-06-19 1993-08-10 Whewell Christopher J Fuel compositions comprising fullerenes
EP0787790A2 (en) 1996-01-31 1997-08-06 Chevron Chemical Company Lubricant composition suitable for direct fuel injected, crankcase-scavenged two-stroke cycle engines
US6391833B1 (en) 1998-05-15 2002-05-21 Chevron Chemical S.A. Low sulfur lubricant composition for two-stroke engines
US20040116307A1 (en) * 2001-04-02 2004-06-17 Bager Ganemi Lubricant composition

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US2049062A (en) * 1935-08-03 1936-07-28 Standard Oil Dev Co Motor fuel containing olefine polymers and method of making the fuel
US2087616A (en) * 1932-07-22 1937-07-20 Ig Farbenindustrie Ag Operating internal combustion engines
US2096119A (en) * 1936-04-13 1937-10-19 Lensch Rudolph Metal spray gun
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US2637720A (en) * 1949-09-30 1953-05-05 Standard Oil Dev Co Method of polymerizing isobutylene in the presence of nu-butenes and ether
US2807526A (en) * 1950-10-04 1957-09-24 Standard Oil Co Additive for motor fuels and fuel compositions containing the same

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GB399527A (en) * 1928-05-10 1933-10-04 Ig Farbenindustrie Ag A process for improving oils, especially lubricating oils
GB328587A (en) * 1928-12-22 1930-04-22 Ig Farbenindustrie Ag Improvements in the manufacture and production of motor fuels
US2087616A (en) * 1932-07-22 1937-07-20 Ig Farbenindustrie Ag Operating internal combustion engines
US2049062A (en) * 1935-08-03 1936-07-28 Standard Oil Dev Co Motor fuel containing olefine polymers and method of making the fuel
US2096119A (en) * 1936-04-13 1937-10-19 Lensch Rudolph Metal spray gun
US2135117A (en) * 1936-11-17 1938-11-01 Gulf Research Development Co Polymerization of olefines
US2637720A (en) * 1949-09-30 1953-05-05 Standard Oil Dev Co Method of polymerizing isobutylene in the presence of nu-butenes and ether
US2807526A (en) * 1950-10-04 1957-09-24 Standard Oil Co Additive for motor fuels and fuel compositions containing the same

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3852204A (en) * 1966-02-01 1974-12-03 Cosden Oil & Chem Co Lubricant compositions
JPS5010324B1 (en) * 1968-12-20 1975-04-21
JPS493065A (en) * 1972-04-04 1974-01-11
US3953179A (en) * 1972-04-04 1976-04-27 Labofina S.A. Lubricating compositions
JPS5134953B2 (en) * 1972-04-04 1976-09-29
JPS5734317B2 (en) * 1972-05-23 1982-07-22
JPS499504A (en) * 1972-05-23 1974-01-28
US3901665A (en) * 1972-10-06 1975-08-26 Du Pont Multi-functional fuel additive compositions
US4320021A (en) * 1975-10-14 1982-03-16 The Lubrizol Corporation Amino phenols useful as additives for fuels and lubricants
WO1992021736A1 (en) 1991-05-30 1992-12-10 The Lubrizol Corporation Two-cycle lubricant and method of using same
US5234474A (en) * 1991-06-19 1993-08-10 Whewell Christopher J Fuel compositions comprising fullerenes
EP0787790A2 (en) 1996-01-31 1997-08-06 Chevron Chemical Company Lubricant composition suitable for direct fuel injected, crankcase-scavenged two-stroke cycle engines
US5866520A (en) * 1996-01-31 1999-02-02 Chevron Chemical Company Lubricant composition suitable for direct fuel injected, crankcase-scavenged two-stroke cycle engines
US6040279A (en) * 1996-01-31 2000-03-21 Chevron Chemical Company Llc Lubricant composition suitable for direct fuel injected, crankcase-scavenged two-stroke cycle engines
US6391833B1 (en) 1998-05-15 2002-05-21 Chevron Chemical S.A. Low sulfur lubricant composition for two-stroke engines
US20040116307A1 (en) * 2001-04-02 2004-06-17 Bager Ganemi Lubricant composition

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