US3717446A - Gasoline anti-icing additives (a) - Google Patents

Gasoline anti-icing additives (a) Download PDF

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US3717446A
US3717446A US00103162A US3717446DA US3717446A US 3717446 A US3717446 A US 3717446A US 00103162 A US00103162 A US 00103162A US 3717446D A US3717446D A US 3717446DA US 3717446 A US3717446 A US 3717446A
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succinimide
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W Howland
W Mallett
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Union Oil Company of California
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/143Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/16Hydrocarbons
    • C10L1/1616Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/222Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/2222(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/234Macromolecular compounds
    • C10L1/238Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/2383Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)

Definitions

  • Carburetor icing occurs in' some vehicles when cruising at speeds of 30-60 mph. Such icing is a considerable problem in the case of certain trucks and cars equipped with carburetors having venturi type fuel-air mixing tubes (emulsion tubes). The ice builds up on the tube and restricts the flow of air, thereby enriching the fuel mixture and reducing efficiency.
  • venturi type fuel-air mixing tubes emulsion tubes
  • the first surfactant additive referred to herein as the succinimideadditive, is a complex condensation product of approximately equal mole-ratios of a relatively low molecular weight alkenyl succinic anhydride with an alkylene polyamine such as diethylene triamine.
  • the second surfactant additive is a long-chain alkyl or alkenyl amine such as oleyl amine.
  • the relative proportion of lubricating oil to the other two additives is not critical within the concentration ranges cited in the Table, for the minimum concentration of 50 pounds per thousand barrels is higher than is needed to induce the desired anti-icing synergism with any of the recited proportions of the other two additives.
  • the lubricating oil is used in these high proportions in order to obtain other desired effects thereof, mainly to effectively reduce intake valve deposits.
  • a premixed package comprising the three additives in the relative proportions discussed above may be conveniently utilized, with or without an added solvent such as toluene, xylenes or other petroleum distillate.
  • a preferred additive package for use herein is composed as follows:
  • the Aliphatic Amine Additive The Aliphatic Amine Additive
  • the aliphatic amines contemplated for use herein comprise those having the formula, RNH wherein R is a straight or branched-chain alkyl or alkenyl radical having from 12 to about 50, preferably 14 to 25 carbon 15 atoms.
  • Suitable exemplary amines include dodecylamine, isododecyl amine, tetradecyl amine, hexadecyl amine, octadecyl amine, octadecenyl amine, oleylamine, tetra-isobutenyl amine, hexa-isobutenyl amine, deca-isobutenyl amine, and the like. Mixtures of any two or more of such amines may also be utilized.
  • These amine additives are well known in the art as carburetor detergents (see e.g., U.S. Pat. No.
  • the Lubricating Oil Additive may be any light, medium or heavy paraffinic lubricating oil of low wax content.
  • it is a solvent dewaxed, distillate oil having a viscosity at 100F. of 200 to 1000 SSU, a viscosity index above 70, and an A.P.I. gravity of about to 32.
  • a typical such oil referred to herein as 300 neutral oil has a viscosity of about 320 SSU at 100F., and at 210F. of about 52.2, a V.l. of about 85, a flash point of 445F. and an A.P.l. gravity of about 28.6.
  • the Succinimide Additive This additive can best be described as a condensation product of one mole of an alkeny] succinic anhydride of the formula:
  • R is an alkenyl group having from eight to about 50, preferably 15-40 carbon atoms
  • R is a lower alkylene radical of about two to eight carbon atoms
  • x is a number from 1 to about 10, preferably 2 to 6.
  • the resulting product is a complex mixture of monomeric and polymeric amides and imides with an average molecular weight normally in the range of about 400 to 800.
  • ethylene diamine is employed as the amine
  • representative reaction products are believed to include compounds such as:
  • the condensation reaction is carried out at temperatures of about l20-250C., preferably 200C., until about one mole of water per mole of alkenyl succinic anhydride employed has been split off.
  • an inert solvent such as toluene or xylene is employed.
  • the reaction is normally complete in about 1-5 hours, depending upon the temperature employed. Suitable condensation procedures are described in more detail in U.S. Pat. No. 2,182,178.
  • Suitable alkenyl succinic anhydride starting materials include compounds wherein R in the above formula is n-octenyl, iso-docecenyl, di-isobutenyl, tri-isobutenyl, tetra-isobutenyl, hexa-isobutenyl, deca-isobutenyl, and the like.
  • Such compounds are well known in the art, and are normally prepared by reacting the appropriate olefin with maleic anhydride, as described in more detail in e.g. U.S. Pat. Nos. 3,172,892 and 3,443,918.
  • Suitable exemplary alkylene polyamine reactants include ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, pentaethylene hexamine, propylene diamine, dipropylene triamine, di(tetramethylene)triamine, and the like.
  • the succinimide reaction products prepared as described above are fairly effective as carburetor detergent gasoline additives. However, we have found that at concentration levels effective for carburetor detergency, they are almost completely ineffective for de-icing. Strangely enough, at lower concentration levels which are relatively ineffective for carburetor detergency, they appear to function somewhat more effectively for de-icing. But even at these low concentrations they are not as effective as the combination of additives when used at the herein prescribed concentrations.
  • a preferred succinimide additive for use herein is marketed by the American Oil Company under the trade name Amoco 575.
  • the gasoline stocks to which the lubricating oil, succinimide and aliphatic amine may be added with synergistic anti-icing effect include any petroleum fraction boiling in the conventional gasoline range of about 100 to 400F., and preferably having an ASTM 50 percent boiling point between about 180 and 220F.
  • the 50 percent boiling point of a gasoline is a critical indicia of its icing propensity.
  • gasolines with 50 percent boiling points below 180F. are considered severe, such that the surfactant-type additives utilized herein are relatively ineffective; for
  • Typical commercial gasolines which may be utilized herein may comprise e.g., straight run gasolines, cata lytically cracked gasolines, catalytic reformates and alkylates, and blends thereof.
  • the fuel may also contain other conventional additives such as lead alkyls, organic halide lead scavengers, phenolic anti-oxidants,
  • metal deactivators such as disalicylal-ethylene diamine, etc.
  • a spill-type carburetor was used to assure a constant air-fuel ratio.
  • the conventional float and needle valve assembly was removed and a circular weir (overflow drain) installed inside the float chamber.
  • the gasoline flow to the carburetor was adjusted so that a small amount of gasoline would overflow thereby always providing a fixed level of gasoline in the float chamber.
  • An atmosphere of controlled temperature and humidity was supplied to the carburetor by means of an air conditioning unit.
  • a gasoline injection system injecting gasoline into the cylinder was used to fire the cylinder during stabilization periods when the carburetor was without fuel.
  • Test Procedure The actual test procedure consisted in running the engine at constant speed while the throttle was cycled on a fixed time schedule between a cruise and an idle setting. The number of cycles required to develop enough ice to cause a 1" Hg increase in manifold vacuum at the idle setting was taken as an arbitrary stalling condition.
  • succinimide B was identified as a condensation product of one mole of a polyisobutenyl succinic anhydride having an average of approximately 29 carbon atoms in the polyisobutenyl radical, with about 0.75 mole of diethylene triamine.
  • the resulting product was a mixture of amides and imides having a number average molecular weight of about 700, and analyzing 4.9 weight-percent nitrogen.
  • the aliphatic amine was oleylamine sold under the trade name Armeen OD" by Armour and Company.
  • the lubricating oil was the above described 300 neutral oil.
  • Qther exemplary synergistic additive combinations include but are not limited to the following:
  • R-oH-o 0 CHPCQO with about 0.6 to 1.5 moles of an alkylene polyamine of the formula:
  • R is an alkenyl group having from eight to about 50 carbon atoms, R, is a lower alkylene radical of about two to eight carbon atoms, and x is a number from 1 to about and 3. between about 50 and 350 pounds per thousand barrels of a paraffinic lubricating oil;
  • composition as defined in claim 1 wherein said alkylene polyamine is diethylene triamine.
  • a synergistic anti-icing additive for gasoline comprising a paraffinic lubricating oil, and dissolved therein:
  • R is an alkenyl group having from eight to about 50 carbon atoms, R is a lower alkylene radical of about two to eight carbon atoms, and x is a number from 1 to about 10;
  • the weight ratio of component (1) to component (2) being between about 20/ 80 and 60/40.
  • An additive as defined in claim 8 containing about 10-50 volumes of said paraffinic lubricating oil per volume of the combined components l and (2).

Abstract

A combination of two known types of surfactant gasoline additives with a non-surfactant lubricating oil additive is found to provide, in addition to good overall carburetor detergency, a synergistic anti-icing effect, as compared to any one or two of the additives alone. One of the surfactant additives is a succinimide condensation product of an alkylene polyamine with an alkenyl succinic anhydride, while the other is a long-chain primary alkyl- or alkenyl amine.

Description

[22] Filed:
United States Patent 11 1 Howland et al.
[54] GASOLINE ANTI-ICING ADDITIVES (A) [75] Inventors: Ward W. Howland, Anaheim; William R. Mallett, Placentia, both of Calif.
[73] Assignee: Union Oil Company of California, Los Angeles, Calif.
Dec. 31, 1910 [21] Appl. No.: 103,162
[52] US. Cl. ..44/58, 44/63, 44/72,
- 44/DIG. i [51] Int. Cl. ..Cl0l 1/18, C101 H22 [58] Field of Search ..44/58, 63, 71, 72, DIG. l
[5 6] References Cited UNITED STATES PATENTS Duncan et al. ..44/72 X 51 Feb. 20, 1973 4/1969 Honnen et al. ..44/72 X 9/1969 Lindstrom et al. ..44/72 X Primary Examiner-Patrick P. Garvin Assistant Examiner,W. J. Shine Attorney-Milton W. Lee, Richard C. Hartman, Lannas S. Henderson, Dean Sandford and Robert E. Strauss 5 7 ABSTRACT alone. One of the surfactant additives is a succinimide condensation product of an alkylene polyamine with an alkenyl succinic anhydride, while the other is a long-chain primary alkylor alkenyl amine.
10 Claims, 1 Drawing Figure GASOLINE ANTI-ICING ADDITIVES (A) BACKGROUND AND SUMMARY OF THE INVENTION A great variety of chemical additives have previously been proposed for use as detergents and/or dispersants in gasolines, for the primary purpose of removing and/or preventing the formation of deposits of dirt, gum, lacquer and the like in the induction system of internal combustion engines, primarily on the internal surfaces of the carburetor throat and associated parts. Some of these detergent additives are known to be effective in varying degrees as anti-icing agents, while others are of little or no value for that purpose. This is not particularly surprising, since the formation and removal of ice from carburetor surfaces bears little apparent analogy to the formation and removal of dirt, gum and lacquer deposits from such surfaces.
As is well known, the operation of carburetor-fed internal combustion engines under cool, humid weather conditions is apt to result in frequent stalling of the engine, especially during the warm-up period. Such stalling is a definite safety hazard as well as a decided inconvenience. It is now recognized that stalling of this nature is attributable to the formation of ice on the throttle plate and the nearby surfaces of the carburetor barrel. The water which forms the ice does not come from the gasoline, but from the air entering the carburetor. As noted above, stalling generally occurs in cool, humid weather when the temperature is between about 35 and 65F., and the relative humidity is above about 65 percent. The most critical conditions are temperatures of about 4060F., and 90-l0O% relative humidity.
As the gasoline evaporates in the carburetor, it reduces the temperature of the surrounding metal surfaces by as much as 4050F. Moisture in the incoming air comes in contact with these parts and begins to build up ice on the throttle plate and in the carburetor barrel. The higher the humidity, the faster is the buildup of ice. Then, when the engine is idling, the throttle plate closes and the ice chokes off the normal flow of air through the small clearance between the throttle plate and the carburetor wall. This causes the engine to stall. The engine can usually be restarted when the heat from the exhaust manifold melts the ice sufficiently. However, stalling will continue until the engine is completely warmed up.
Carburetor icing occurs in' some vehicles when cruising at speeds of 30-60 mph. Such icing is a considerable problem in the case of certain trucks and cars equipped with carburetors having venturi type fuel-air mixing tubes (emulsion tubes). The ice builds up on the tube and restricts the flow of air, thereby enriching the fuel mixture and reducing efficiency.
We have now discovered that these icing problems can be materially reduced by adding to the gasoline fuel certain minor proportions of two surfactant type additives which have previously been suggested for use individually as carburetor detergents, and a non-surfactant lubricating oil additive which is conventionally used in gasolines to reduce intake valve deposits. Neither of the surfactant additives alone, nor the combination thereof, is particularly effective for anti-icing but surprisingly, when the lubricating oil is added (which in itself is totally inactive as a de-icer), the combination of surfactant additives becomes much more effective for anti-icing. in a sense therefore, the threecomponent additive combination is synergistic over any one component alone, or the two-component surfactant combination.
The first surfactant additive, referred to herein as the succinimideadditive, is a complex condensation product of approximately equal mole-ratios of a relatively low molecular weight alkenyl succinic anhydride with an alkylene polyamine such as diethylene triamine. The second surfactant additive is a long-chain alkyl or alkenyl amine such as oleyl amine.
DETAILED DESCRIPTION Additive Proportions As will be apparent from the data presented hereinafter in the Examples and plotted graphically in the accompanying drawing, the synergistic anti-icing effect is critical to the use of certain minimum proportions of the additives. It is found that the desired synergistic results are obtained when the additives are employed in the following proportions:
TABLE I Pounds per Thousand Barrels of Gasolinel Broad Range Preferred Range Aliphatic Amine 25-20 3-10 Succinimide 6-30 7-15 Lubricating Oil 50-350 -300 l One pound per thousand barrels =4 parts per million In addition, the combined proportion of the amine and succinimide additives should fall within the range of about 1 1-40, preferably 1 15-20 pounds per thousand barrels. (It should be observed that these additives are often supplied commercially as concentrates in an inert solvent; the proportions cited above are on a solvent-free basis.) Preferred synergistic weight ratios of the two additives to each other range between about 20/80 to 60/40 of aliphatic amine to succinimide. The relative proportion of lubricating oil to the other two additives is not critical within the concentration ranges cited in the Table, for the minimum concentration of 50 pounds per thousand barrels is higher than is needed to induce the desired anti-icing synergism with any of the recited proportions of the other two additives. The lubricating oil is used in these high proportions in order to obtain other desired effects thereof, mainly to effectively reduce intake valve deposits.
A premixed package comprising the three additives in the relative proportions discussed above may be conveniently utilized, with or without an added solvent such as toluene, xylenes or other petroleum distillate. A preferred additive package for use herein is composed as follows:
Volume Oleyl Amine succinimide Bl) 2.7 300 Neutral Oill) 54.0 Light Petroleum Solvent 42.0
The Aliphatic Amine Additive The aliphatic amines contemplated for use herein comprise those having the formula, RNH wherein R is a straight or branched-chain alkyl or alkenyl radical having from 12 to about 50, preferably 14 to 25 carbon 15 atoms. Suitable exemplary amines include dodecylamine, isododecyl amine, tetradecyl amine, hexadecyl amine, octadecyl amine, octadecenyl amine, oleylamine, tetra-isobutenyl amine, hexa-isobutenyl amine, deca-isobutenyl amine, and the like. Mixtures of any two or more of such amines may also be utilized. These amine additives are well known in the art as carburetor detergents (see e.g., U.S. Pat. No. 3,011,879), but are in themselves almost completely ineffective for de-icing, either alone or in combination with a lubricating oil. It hence came as a distinct surprise to find that the amine-lubricating oil combination could enhance the effectiveness of the succinimide type additives.
The Lubricating Oil Additive The hydrocarbon oil which is added to the gasoline, and which cooperates with the amine and succinimide additives to reduce icing, may be any light, medium or heavy paraffinic lubricating oil of low wax content. Preferably it is a solvent dewaxed, distillate oil having a viscosity at 100F. of 200 to 1000 SSU, a viscosity index above 70, and an A.P.I. gravity of about to 32. A typical such oil referred to herein as 300 neutral oil has a viscosity of about 320 SSU at 100F., and at 210F. of about 52.2, a V.l. of about 85, a flash point of 445F. and an A.P.l. gravity of about 28.6.
The Succinimide Additive This additive can best be described as a condensation product of one mole of an alkeny] succinic anhydride of the formula:
with about 0.60 to 1.5 moles of an alkylene polyamine of the formula:
wherein R is an alkenyl group having from eight to about 50, preferably 15-40 carbon atoms, R, is a lower alkylene radical of about two to eight carbon atoms, and x is a number from 1 to about 10, preferably 2 to 6. The resulting product is a complex mixture of monomeric and polymeric amides and imides with an average molecular weight normally in the range of about 400 to 800. Where ethylene diamine is employed as the amine, representative reaction products are believed to include compounds such as:
but the presence of other specific amides, imides and amideimides is not to be excluded.
The condensation reaction is carried out at temperatures of about l20-250C., preferably 200C., until about one mole of water per mole of alkenyl succinic anhydride employed has been split off. Preferably an inert solvent such as toluene or xylene is employed. The reaction is normally complete in about 1-5 hours, depending upon the temperature employed. Suitable condensation procedures are described in more detail in U.S. Pat. No. 2,182,178.
Suitable alkenyl succinic anhydride starting materials include compounds wherein R in the above formula is n-octenyl, iso-docecenyl, di-isobutenyl, tri-isobutenyl, tetra-isobutenyl, hexa-isobutenyl, deca-isobutenyl, and the like. Such compounds are well known in the art, and are normally prepared by reacting the appropriate olefin with maleic anhydride, as described in more detail in e.g. U.S. Pat. Nos. 3,172,892 and 3,443,918.
Suitable exemplary alkylene polyamine reactants include ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, pentaethylene hexamine, propylene diamine, dipropylene triamine, di(tetramethylene)triamine, and the like.
The succinimide reaction products prepared as described above are fairly effective as carburetor detergent gasoline additives. However, we have found that at concentration levels effective for carburetor detergency, they are almost completely ineffective for de-icing. Strangely enough, at lower concentration levels which are relatively ineffective for carburetor detergency, they appear to function somewhat more effectively for de-icing. But even at these low concentrations they are not as effective as the combination of additives when used at the herein prescribed concentrations.
A preferred succinimide additive for use herein is marketed by the American Oil Company under the trade name Amoco 575.
Base Fuels The gasoline stocks to which the lubricating oil, succinimide and aliphatic amine may be added with synergistic anti-icing effect include any petroleum fraction boiling in the conventional gasoline range of about 100 to 400F., and preferably having an ASTM 50 percent boiling point between about 180 and 220F. The 50 percent boiling point of a gasoline is a critical indicia of its icing propensity. As a rule of thumb, gasolines with 50 percent boiling points below 180F. are considered severe, such that the surfactant-type additives utilized herein are relatively ineffective; for
these highly volatile gasolines freeze point depressants such as alcohols or glycols may be required. Gasolines having a 50 percent point above about 220F. are unlikely to cause icing. Hence, for practical purposes the principal utility of the combined additives of this invention resides in their use in gasolines having a 50 percent boiling point between about 180 and 220F.
Typical commercial gasolines which may be utilized herein may comprise e.g., straight run gasolines, cata lytically cracked gasolines, catalytic reformates and alkylates, and blends thereof. The fuel may also contain other conventional additives such as lead alkyls, organic halide lead scavengers, phenolic anti-oxidants,
metal deactivators such as disalicylal-ethylene diamine, etc.
EXAMPLES gasoline, the blend having an ASTM boiling range substantially as follows:
Percent Overhead F l.B.P. 92 H) 126 20 140 50 196 90 355 95 413 E.P 432 Test Equipment A single cylinder CFR engine coupled to a constant speed dynamometer was used for the tests. The test gasoline was fed to the engine through a special carburetor operating in an atmosphere of controlled temperature and humidity. When carburetor ice formed during a test, the constant speed dynamometer maintained engine speed, so the engine would not stall. The presence and amount of carburetor ice formed was indicated by an increase in manifold vacuum. A vacuum transducer and strip chart recorder were used to provide a record of the variation in manifold vacuum as a test progressed.
A spill-type carburetor was used to assure a constant air-fuel ratio. The conventional float and needle valve assembly was removed and a circular weir (overflow drain) installed inside the float chamber. The gasoline flow to the carburetor was adjusted so that a small amount of gasoline would overflow thereby always providing a fixed level of gasoline in the float chamber.
An atmosphere of controlled temperature and humidity was supplied to the carburetor by means of an air conditioning unit. A gasoline injection system, injecting gasoline into the cylinder was used to fire the cylinder during stabilization periods when the carburetor was without fuel.
Test Procedure The actual test procedure consisted in running the engine at constant speed while the throttle was cycled on a fixed time schedule between a cruise and an idle setting. The number of cycles required to develop enough ice to cause a 1" Hg increase in manifold vacuum at the idle setting was taken as an arbitrary stalling condition.
Each test was preceded by a careful purge and restabilization procedure. During the purge period an auxiliary air heater mounted in the carburetor inlet tube was energized. This added heat dried out moisture condensed during the preceding test and brought the carburetor throttle body back to test conditions more quickly. The temperature of the throttle body dropped to about 25F. during each test. After the throttle body was heated to 50F., the auxiliary heater was turned off and the engine was stabilized for an additional three minutes with fuel supplied directly to the cylinder by the injection system. Fuel flowed through the carburetor only during the actual test period.
Additives The succinimide additive (Succinimide B) was identified as a condensation product of one mole of a polyisobutenyl succinic anhydride having an average of approximately 29 carbon atoms in the polyisobutenyl radical, with about 0.75 mole of diethylene triamine. The resulting product was a mixture of amides and imides having a number average molecular weight of about 700, and analyzing 4.9 weight-percent nitrogen.
The aliphatic amine was oleylamine sold under the trade name Armeen OD" by Armour and Company.
The lubricating oil was the above described 300 neutral oil.
The results of the various runs were as follows:
TABLE 2 concentration, anti-icing rating, Run No. Additive Lbs/M Bbll) cycles to stall 1 None 6 2 None 6 3 Succinimide B 7.0 8 4 Succinimide B 7.0 8 5 Succinimide B 7.0 8 6 Succinimide B 7.0 9 7 Succinimide B 14 7 8 Succinimide B 14 7 9 Succinimide B 14 7 l0 Succinimide B 14 7 l l Succinimide B 14 7 l2 Succinimide B 14 7 l3 oleylamine 7 7 l4 oleylamine l0 7 l 5 oleylamine 20 7 l 6 oleylamine 20 7 l7 (oleylamine 3 .5) (Succinimide B 9.05) 8 18 Repeat of Run 17 9 l9 (oleylamine 2.5) 6
(Succinimide B 3.5) (Neutral Oil 20 Repeat of Run 19 6 2l (oleylamine 3.5 l l (Succinimide B 9.05) (Neutral Oil 155 22 Repeal of Run 21 ll 23 Repeat of Run 21 ll l) Solvent-free basis.
The foregoing data is plotted graphically in the accompanying drawing, and it is evident from the graph that the three-component additive of runs 21-23 represents a synergistic improvement over the additives of runs 3-18. It is further evident from runs 19 and 20 that these synergistic results are critical to the use of certain minimum proportions of the surfactant additives.
Qther exemplary synergistic additive combinations include but are not limited to the following:
Concentration in Gasoline,
Lbs/M Barrels Additive succinimide Cl) n-Dodecylarnine Neutral Oil (300 SSU/ 100F) 200 Succinimide DZ) 6.0 Hexaisobutenylamine 10.0 Neutral Oil (500 SSU/lOO F) 400.0 succinimide E3) 10.0 Tetraisobutenylamine 8.0 Neutral Oil (300 SSU/IOO F) 80.0
(1) A condensation product of 0.8 moles of propylene diamine with one mole of 11,625 Av. molecular weight polyisobutenyl succinic anhydride.
(2) A condensation product of 0.9 mole of tetraethylene pentamine with one mole of a 350 Av. molecular weight polyisobutenyl succinic anhydride.
(3) A condensation product of 1.2 moles of dipropylene triamine with one mole of a 550 Av. molecular weight polyethylene succinic anhydride.
mole of an alkenyl succinic anhydride of the formula:
R-oH-o= 0 CHPCQO with about 0.6 to 1.5 moles of an alkylene polyamine of the formula:
wherein R is an alkenyl group having from eight to about 50 carbon atoms, R, is a lower alkylene radical of about two to eight carbon atoms, and x is a number from 1 to about and 3. between about 50 and 350 pounds per thousand barrels of a paraffinic lubricating oil;
and wherein the combined proportion of components (l) and (2) in the gasoline is between about 1 1 and 40 pounds per thousand barrels. 2. A composition as defined in claim 1 wherein the 5 weight ratio of component (1) to component (2) is between about 20/ 80 and 60/40.
3. A composition as defined in claim 1 wherein said alkylene polyamine is diethylene triamine.
4. A composition as defined in claim 1 wherein said aliphatic amine js oleylamine.
. A composition as defined U1 claim 1 wherein the combined proportion of said components (1) and (2) in the gasoline is between about 11.5 and 20 pounds per thousand barrels.
6. A composition as defined in claim 1 wherein said base gasoline has a 50 percent boiling point between about 180 and 220F.
7. A composition as defined in claim 1 wherein the weight-ratio of component (1) to component (2) is between about 20/80 and 60/40; said alkylene polyamine is diethylene triamine; said aliphatic amine is oleylamine; the combined proportion of said components (1) and (2) in the gasoline is between about 1 1.5 and 20 pounds per thousand barrels; and wherein said base gasoline has a 50 percent boiling point between about 180 and 220F.
8. A synergistic anti-icing additive for gasoline comprising a paraffinic lubricating oil, and dissolved therein:
1. an aliphatic amine of the formula RNl-l wherein R is an alkyl or alkenyl radical having from 12 to about 50 carbon atoms; and
2. a succinimide condensation product of one mole of an alkenyl succinic anhydride of the formula:
O GHQ-0:0
with about 0.6 to 1.5 moles of an alkylene polyamine of the formula:
H N(R,NH H,
wherein R is an alkenyl group having from eight to about 50 carbon atoms, R is a lower alkylene radical of about two to eight carbon atoms, and x is a number from 1 to about 10;
the weight ratio of component (1) to component (2) being between about 20/ 80 and 60/40.
9. An additive as defined in claim 8 wherein said aliphatic amine is oleylamine and said alkylene polyamine is diethylene triamine.
10. An additive as defined in claim 8 containing about 10-50 volumes of said paraffinic lubricating oil per volume of the combined components l and (2).
t i i

Claims (14)

1. an aliphatic amine of the formula RNH2, wherein R is an alkyl or alkenyl radical having from 12 to about 50 carbon atoms; and
1. between about 2.5 and 20 pounds per thousand barrels of an aliphatic amine of the formula RNH2, wherein R is an alkyl or alkenyl radical having from 12 to about 50 carbon atoms;
1. An anti-icing gasoline composition comprising a base gasoline boiling substantially in the range of about 100*-400*F., and dissolved therein:
2. A composition as defined in claim 1 wherein the weight ratio of component (1) to component (2) is between about 20/80 and 60/40.
2. between about 6 and 30 pounds per thousand barrels of a succinimide condensation product of one mole of an alkenyl succinic anhydride of the formula: with about 0.6 to 1.5 moles of an alkylene polyamine of the formula: H2N(R1NH)xH, wherein R is an alkenyl group having from eight to about 50 carbon atoms, R1 is a lower alkylene radical of about two to eight carbon atoms, and x is a number from 1 to about 10; and
2. a succinimide condensation product of one mole of an alkenyl succinic anhydride of the formula: with about 0.6 to 1.5 moles of an alkylene polyamine of the formula: H2N(R1NH)xH, wherein R is an alkenyl group having from eight to about 50 carbon atoms, R1 is a lower alkylene radical of about two to eight carbon atoms, and x is a number from 1 to about 10; the weight ratio of component (1) to component (2) being between about 20/80 and 60/40.
3. A composition as defined in claim 1 wherein said alkylene polyamine is diethylene triamine.
3. between about 50 and 350 pounds per thousand barrels of a paraffinic lubricating oil; and wherein the combined proportion of components (1) and (2) in the gasoline is between about 11 and 40 pounds per thousand barrels.
4. A composition as defined in claim 1 wherein said aliphatic amine is oleylamine.
5. A composition as defined in claim 1 wherein the combined proportion of said components (1) and (2) in the gasoline is between about 11.5 and 20 pounds per thousand barrels.
6. A composition as defined in claim 1 wherein said base gasoline has a 50 percent boiling point between about 180* and 220*F.
7. A composition as defined in claim 1 wherein the weight-ratio of component (1) to component (2) is between about 20/80 and 60/40; said alkylene polyamine is diethylene triamine; said aliphatic amine is oleylamine; the combined proportion of said components (1) and (2) in the gasoline is between about 11.5 and 20 pounds per thousand barrels; and wherein said base gasoline has a 50 percent boiling point between about 180* and 220*F.
8. A synergistic anti-icing additive for gasoline comprising a paraffinic lubricating oil, and dissolved therein:
9. An additive as defined in claim 8 wherein said aliphatic amine is oleylamine and said alkylene polyamine is diethylene triamine.
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Cited By (14)

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US4039300A (en) * 1974-06-03 1977-08-02 Atlantic Richfield Company Gasoline fuel composition and method of using
US4069023A (en) * 1975-05-01 1978-01-17 Exxon Research & Engineering Co. Carboxylate esters of 1-aza-3,7-dioxabicyclo[3.3.0] oct-5-yl methyl alcohols, their preparation and use as additives for oleaginous compositions
US4325708A (en) * 1977-09-09 1982-04-20 Phillips Petroleum Company Fuel detergent compositions containing lubricating oil
US4645515A (en) * 1985-04-12 1987-02-24 Chevron Research Company Modified succinimides (II)
EP0251419A1 (en) * 1983-12-30 1988-01-07 Ethyl Corporation Fuel composition and additive concentrates, and their use in inhibiting engine coking
EP0376578A1 (en) * 1988-12-30 1990-07-04 Mobil Oil Corporation Polyalkylene succinimide deposit control additives and fuel compositions containing same
US4973336A (en) * 1988-06-10 1990-11-27 Gheysens Jean Louis G Fuel additives
US5114435A (en) * 1988-12-30 1992-05-19 Mobil Oil Corporation Polyalkylene succinimide deposit control additives and fuel compositions containing same
US5242469A (en) * 1990-06-07 1993-09-07 Tonen Corporation Gasoline additive composition
US5393309A (en) * 1991-09-13 1995-02-28 Chevron Research And Technology Company Fuel additive compositions containing polyisobutenyl succinimides
US5697988A (en) * 1991-11-18 1997-12-16 Ethyl Corporation Fuel compositions
WO2018073544A1 (en) 2016-10-21 2018-04-26 Total Marketing Services Combination of fuel additives
FR3057877A1 (en) * 2016-10-21 2018-04-27 Total Marketing Services COMBINATION OF FUEL ADDITIVES
RU2719587C2 (en) * 2016-10-21 2020-04-21 Тоталь Маркетин Сервис Combination of fuel additives

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4039300A (en) * 1974-06-03 1977-08-02 Atlantic Richfield Company Gasoline fuel composition and method of using
US4069023A (en) * 1975-05-01 1978-01-17 Exxon Research & Engineering Co. Carboxylate esters of 1-aza-3,7-dioxabicyclo[3.3.0] oct-5-yl methyl alcohols, their preparation and use as additives for oleaginous compositions
US4325708A (en) * 1977-09-09 1982-04-20 Phillips Petroleum Company Fuel detergent compositions containing lubricating oil
EP0251419A1 (en) * 1983-12-30 1988-01-07 Ethyl Corporation Fuel composition and additive concentrates, and their use in inhibiting engine coking
US4645515A (en) * 1985-04-12 1987-02-24 Chevron Research Company Modified succinimides (II)
US4973336A (en) * 1988-06-10 1990-11-27 Gheysens Jean Louis G Fuel additives
EP0376578A1 (en) * 1988-12-30 1990-07-04 Mobil Oil Corporation Polyalkylene succinimide deposit control additives and fuel compositions containing same
US5114435A (en) * 1988-12-30 1992-05-19 Mobil Oil Corporation Polyalkylene succinimide deposit control additives and fuel compositions containing same
US5242469A (en) * 1990-06-07 1993-09-07 Tonen Corporation Gasoline additive composition
US5393309A (en) * 1991-09-13 1995-02-28 Chevron Research And Technology Company Fuel additive compositions containing polyisobutenyl succinimides
US5697988A (en) * 1991-11-18 1997-12-16 Ethyl Corporation Fuel compositions
WO2018073544A1 (en) 2016-10-21 2018-04-26 Total Marketing Services Combination of fuel additives
FR3057877A1 (en) * 2016-10-21 2018-04-27 Total Marketing Services COMBINATION OF FUEL ADDITIVES
RU2719587C2 (en) * 2016-10-21 2020-04-21 Тоталь Маркетин Сервис Combination of fuel additives
US10767126B2 (en) 2016-10-21 2020-09-08 Total Marketing Services Combination of fuel additives

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