US2952637A - Carburetor and engine cleaning composition - Google Patents

Carburetor and engine cleaning composition Download PDF

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US2952637A
US2952637A US731609A US73160958A US2952637A US 2952637 A US2952637 A US 2952637A US 731609 A US731609 A US 731609A US 73160958 A US73160958 A US 73160958A US 2952637 A US2952637 A US 2952637A
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carburetor
engine
oil
carbon atoms
engines
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Ulric B Bray
Harold H Knoch
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Bray Oil Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/06Use of additives to fuels or fires for particular purposes for facilitating soot removal

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  • This invention relates to a composition for cleaning carburetors and internal combustion engines, such as gasoline engines and diesel engines, and particularly for cleaning carburetors and engines which have been fouled in service by deposition of gums and carbonaceous deposits.
  • gasolines also contain non-vaporizable, gummy materials which collect in the small passages of the carburetor and interfere with its action in properly metering fuel and air charged to the engine.
  • the sluggish action of the carburetor may result in an excessively rich fuel mixture thereby aggravating the formation of carbon deposits about the valves and in the cylinders.
  • One object of this invention is to provide a cleaner for the carburetor of gasoline engines which will make unnecessary this expensive overha ng job which sometimes requires replacement of the carburetor by a new carburetor because of the ditficulty of cleaning the fine passages by ordinary means.
  • Our carburetor and engine cleaner is comprised of a combination .ofgngredients which cooperate to, accomknown as the volatile nitrogen bases.
  • the following general and specific formulas show our composition:
  • Example 4 Parts by volume Dipropyleneglycol monobutyl ether Methyl isobutyl carbinol 10 Oleic acid 10 Naphtha-325 F. average boiling point 45 Ammonium hydroxide-28% NH 2.2 Water 25.0
  • Example 5 Parts by volume Methyl isobutyl carbinol 10 Butyl Cellosolve 10 Oleic acid 9 Morpholine 2 Petroleum naphtha-325 F. average boiling point 45 Water 25 wt a 103mm more'wa'erwa-aadathe mixture stll' 1 remained clear.
  • the order of mixing the ingredients in the above formulas is not very important, but we prefer to add the water last.
  • the resulting solution will be brilliantly clear and, when diluted with an equal volume of water, the solution will be an opalescent, white emulsion.
  • the hydrocarbon oil ingredient can be a high flash naphtha, kerosene, olefine polymer, or an aromatic solvent such as xylene or an aromatic petroleum naphtha rich in xylenes, alkyl naphthalenes, etc., such as the solvent extracts from petroleum distillates and the product known as hydroformer bottomsthe fraction from the reforming process boiling above gasoline.
  • aromatic hydrocarbons increases the solvency of the cleaner for varnishes and gums found in the induction system of the engine.
  • hydrocarbon ingredient be a lubricating oil, preferably a distillate oil of 60 seconds Saybolt F.) viscosity and upward,
  • the rust protection can bea'ncreased still further by adding to the composition a small amount of an alkaline earth metal petroleum mahogany sulfonate, preferably about 1 to 3 percent of alkaline earth metal mahogany sulfonate in solution in about 60 percent of oil.
  • an alkaline earth metal petroleum mahogany sulfonate preferably about 1 to 3 percent of alkaline earth metal mahogany sulfonate in solution in about 60 percent of oil.
  • Composition, Parts by Weight General Specific Example 8 Formula Alkoxy alcohol 5 to 10 6.34 butyl Cellosolve. Aliphatic alcohol-4 to 6 carbon atoms 5 to 10 6.34 isobutyl carbinol. Water 15 to 35 26.4 Aromatic naphtha, boiling above 250 F 30 to 40 36.96 350 F. initial B.P. Liquid fatty acid 6 to 12 8.13 oleic acid. Light mineral lubricating oil 10 to 20 12.67 100 pale oil. Petroleum sulionate40% in oil--- 1 to 1.58 calium hsull'ouate as Volatile nitrogen base 1 to 3 1.58 aq. ammonia-28% Composition- Parts by Volume Example Example 9 10 Petroleum naphtha-35/42" API 51.
  • the ingredients may be combined in several ways.
  • the volatile base and the fatty acid can be combined to form a soap which is then mixed with the water, butyl Cellosolve and alcohol.
  • the petroleum sulfonate can be dissolved in the light lubricating oil which may be slightly heated to accelerate the solution. This solution can then be diluted with the aromatic naphtha and finally combined with the soap mixture.
  • the volatile base can be ammonia, gaseous or liquid, usually aqua ammonia (28% NH or it can be an organic amine such as butylamine, morpholine, trimethylamine, etc.
  • the amount of the base should be suflicient to neutralize the liquid fatty acid employed. Hydroxyaaaseeaaa Flash Point (co), F- Aniline Percent Aromatic hydrocarbons alkylamines such as the ethanol amines are avoided because of their low volatility and their precipitating action on sludge, causing the sludge to deposit in the ring grooves of the piston.
  • isobutyl carbinol In addition to isobutyl carbinol, other aliphatic alcohols of 4 to 6 carbon atoms can be employed, such as amyl alcohol, Pentasol, cyclohexanol, tertiary butyl carbinol, secondary butyl alcohol, normal butyl alcohol, etc. Methyl isobutyl carbinol is favored because of its pleasant odor.
  • Alkoxy alcohols are ether alcohols in which the alkyl group has from two to five carbon atoms. Examples are ethyl hydroxyethyl ether (ethyl Cellosolve); ethoxy ethoxy ethyl alcohol (ethyl Carbitol); butoxy ethoxy ethyl alcohol (butyl Carbitol); propoxy propyl alcohol and hydroxy ethyl amyl ether. They may contain more than one ether oxygen and usually two or three carbon atoms in the alcohol group. Butyl Cellosolve (butyl' hydroxy ethyl ether) has been found very satisfactory.
  • aromatic naphtha solvent it may be a fraction from coal tar distillate containing xylene or boiling above xylene, but the aromatic naphthas of petroleum origin are preferred because of their low cost. These are usually derived from solvent extracts or from hydroformer or aromatizer distillates. For most purposes, Where odor is not important, it is preferred to use aromatic distillates of upwards of 50% aromatic content having a flash point above about 110 F. (closed cup) and initial boiling point above about 300 F. Two examples of aromatic naphthas suitable for this purpose had the following characteristics:
  • the odor of aromatic petroleum solvents can be improved by a mild treatment with sulfuric acid, for example, 10 p ounds per barrel.
  • sulfuric acid for example, 10 p ounds per barrel.
  • an aromatic distillate boiling in the range of 440 to 590 F. was so treated and neutralized before using in the above formulas.
  • a light lubricating oil When a light lubricating oil is employed in our composition, it is preferably a pale oil having a viscosity the range of about 60 to 150 SSU at 100 F. This may be obtained from any ordinary crude but lubricating distillates from naphthenic or aromatic base crudes are preferred. Heavy lubricating oils can be used in small amounts, however.
  • liquid fatty acids we may use the red of commerce or other liquid fatty acids such as fish oil fatty acid, soy bean fatty acid, tall oil fatty acid, corn oil fatty acid, linseed oil fatty acid, cottonseed fatty acid, coconut fatty acid, rape-seed fatty acid, naphthenic acid and other carboxylic acids of low melting point, below about 35 C. usually having about 12 to 20 carbon atoms.
  • the petroleum sulfonate employed in our composition is the preferentially oil soluble type or mahogany sulfonate obtained by the action of fuming sulfuric acid on petroleum lubricating oils or aromatic alkylates usually within the range of about 100 to 550 SSU viscosity at 100 F.
  • the resulting sulfonic acid after purification to remove inorganic salts is usually concentrated in the oil phase and converted to calcium or barium sulfonate or other polyvalent metal sulfonate.
  • the resulting product in the case of calcium sulfonate having about 8% neutral ash, corresponds to about 40% calcium sulfonate in oil.
  • barium sulfonate is used, the equivalent amount based on the sulfonic acid present is employed and more or less concentrated polyvalent metal sulfonates can be used in equivalent amounts.
  • our composition When used to clean the crankcase of the engine, we may add to our composition a small amount, about 0.1 to 2 percent of an agent to increase film strength, such as tricresyl phosphate, tributyl phosphite, and zinc dimethyl cyclohexyl dithiophosphate.
  • an agent to increase film strength such as tricresyl phosphate, tributyl phosphite, and zinc dimethyl cyclohexyl dithiophosphate.
  • composition can be packaged in convenient containers for distribution and should be maintained sealed at all times to avoid loss of water by evaporation.
  • this combination for cleaning fouledup carburetors and engines, the following procedure is employed:
  • the engine should be warm, for example, about to F.
  • the air cleaner leading to the carburetor should be removed.
  • With the motor running at a fast idle about 300 cc. of the cleaning composition is slowly introduced into the air intake of the carburetor.
  • the speed of the engine is then increased and about 150 cc. more of the cleaning fiuid is poured rapidly into the carburetor, stalling the engine.
  • the ignition is then turned off and the engine allowed to stand for 15 to 30 minutes or longer.
  • the air cleaner is replaced and the engine idled until smoke ceases to be emitted from the exhaust. It is usually desirable to readjust the carburetor after cleaning to compensate for the removal of gums which have interfered with its action.
  • the carburetor and engine cleaning composition of claim 1 containi-ng,,in addition, about 1 to 3% of an oil solution of an alkaline earth metal mahogany sulfonate in 40% concentration.
  • a clear carburetor and engine cleaning composition for removing deposits of gummy materials, carbonaceous matter, and inorganic materials from the carburetor and combustion chambers of internal combustion engines when introduced through the carburetor of said engines,
  • composition consisting essentially of the following ingredients:
  • Petroleum naphtha having an initial boiling point above about 320 F. and containing at least 50 percent of aromatic hydrocarbons 36.96 Aqua anmlonia' (28% NH 1.58 Oleic acid 8.13 100 SSU Viscosity at 100 F. Pale Oil 12.67

Description

, sources. tain tetraethyl lead as an anti-knock agent which burns to form lead oxides and other lead compounds which deposit about the heads of the cylinders and on the valves 1 and spark plugs.
F sult in increasing fuel for smooth operation, usually by about 5 to octane 20,000 miles it becomes 2,952,637 Patented Sept. 13, 1960 CARBURETOR AND ENGINE CLEANING COL [POSITION Ulric B. Bray, Pasadena, and Harold H. Knoch, Whittier, Califi, assignors to Bray Oil Company, Los Angeles, Calif a limited partnership of California No Drawing. Filed Apr. 29, 1958, Ser. No. 731,609 5 Claims. (Cl. 252-118) This invention relates to a composition for cleaning carburetors and internal combustion engines, such as gasoline engines and diesel engines, and particularly for cleaning carburetors and engines which have been fouled in service by deposition of gums and carbonaceous deposits. In the operation of internal combustion engines, particularly of the automotive type, it has been found that there accumulates in the engine and in the fuel induction system, particularly the carburetor, deposits of carbonaceous matter and inorganic materials derived from dust in the annosphere and from materials dissolved in the fuel and/or the lubricating oil or a combinaiton of these Most gasoline motor fuels employed today con- In gasoline engines, these deposits rethe octane rating requirement of the numbers or more.
Many gasolines also contain non-vaporizable, gummy materials which collect in the small passages of the carburetor and interfere with its action in properly metering fuel and air charged to the engine. The sluggish action of the carburetor may result in an excessively rich fuel mixture thereby aggravating the formation of carbon deposits about the valves and in the cylinders.
Begining with a clean engine and carburetor, the undesirable effects of gum and carbon deposition become significant after about 5,000 miles of operating the motor vehicle, and after a period of operation of 10,000 to necessary to overhaul the carburetor and clean out the head of the engine in order to return the engine to its original smooth operating condition and eliminate roughness, excessive knocking, pre-ignition, stalling, etc.
One object of this invention is to provide a cleaner for the carburetor of gasoline engines which will make unnecessary this expensive overha ng job which sometimes requires replacement of the carburetor by a new carburetor because of the ditficulty of cleaning the fine passages by ordinary means.
Another object of the invention is to provide a cleaning composition which will rapidly effect removal of gums and deposits from carburetors and engines without loss of service of the engine and the automotive vehicle involved. Still another object of the invention is to provide a carburetor and engine cleaner which will leave the cleaned parts in such-a .;condition that they are protected against rustand c d frosion resulting from atmospheric moisture, particularly in cases where a freshly cleaned engine is allowed to remain standing idle for a period of time. Still another object of the invention is to provide a liquid cleaner which will not damage or corrode any of the mechanical parts of the engine, particularly the bearings, cylinder walls, valves, valve guides, hydraulic valve lifters,
. Composition, Parts by Volume General Specific Example 1 Formula Alkoxy alcohol 5-12 I 9 butyl Cellosolve. Aliphatic alcohol, 4-6 atoms 5-12 9 methyl, isobutyl carhinol. Hydrocarbon oil 35-55 45 heavy naphtha- 325 F. average boiling point. Liquid fatty acid 612 10 oleic acid. Volatile nitrogen base l-4 2. 1 aqua ammoniai 28% NH:. Water 15-35 v etc., and which will serve to remove from the valve mechanism, gums which cause sluggish valve action or sticking valves.
Numerous cleaners for carburetors and fouled engines have heretofore been tried but they have largely failed to solve the problems encountered. Some have attempted to provide a high solvency action for removal of gummy deposits and have employed for the purpose a volatile solvent mixture. The result has frequently been that the gummy deposit has simply been transferred from one part to another part of the engine, often with disastrous V on the inorganic'deposits oflead and iron salts, metal oxides, dust and dirt which have entered the engine with thecombustionair.
It isthepurpose of our invention to provide a cleaner which will not only dissolve and remove gum deposits in the carburetor and intakepassages, but will also loosen carbonaceous deposits and deposits of inorganic salts, oxides, etc., to such an extentjthat they will be largely swept out of the combustion spaces of the engine during operation. H p
We can also loosen and remove deposits from the crankcase of the engine by withdrawing the lubricating oil and adding the cleaner to the crankcase. Idling the engine serves to circulate the cleaner throughoutthe lubricating system, oil pump and bearings, removing gummy, carbonaceous deposits and loosening stuck rings. The fouled cleaning liquid is withdrawn with dissolved gums and dispersed carbon particles. The crankcase is then recharged with lubricating oil and is ready for further service. I
Our carburetor and engine cleaner is comprised of a combination .ofgngredients which cooperate to, accomknown as the volatile nitrogen bases. The following general and specific formulas show our composition:
The following additional examples illustrate specific compositions with various ingredients falling within the class of materials and proportions set forth in the general formula above:
acids which not onlyv Aromatic naphtha280 F. average boiling point 45 Ammonium hydroxide28% NH 2 Water 35 This product was quite clear and did not become opalescent until the water component was increased to 45 parts.
Example 3 Parts by volume- Cyclohexanol 10 Ethyl Cellosolve 10 Oleic acid 9 Petroleum naphtha-325 F. average boiling point 46 Ammonium hydroxide28% NH; 2 Water 25 This product was clear but clouded on addition of parts more water:
Example 4 Parts by volume Dipropyleneglycol monobutyl ether Methyl isobutyl carbinol 10 Oleic acid 10 Naphtha-325 F. average boiling point 45 Ammonium hydroxide-28% NH 2.2 Water 25.0
Example 5 Parts by volume Methyl isobutyl carbinol 10 Butyl Cellosolve 10 Oleic acid 9 Morpholine 2 Petroleum naphtha-325 F. average boiling point 45 Water 25 wt a 103mm more'wa'erwa-aadathe mixture stll' 1 remained clear.
This product was clear and remained clear after adding 10 parts more water.
The order of mixing the ingredients in the above formulas is not very important, but we prefer to add the water last. The resulting solution will be brilliantly clear and, when diluted with an equal volume of water, the solution will be an opalescent, white emulsion. For cleaning engines, removing carbon deposits, etc., greater effectiveness is obatined by limiting the amount of water to about 35% The hydrocarbon oil ingredient can be a high flash naphtha, kerosene, olefine polymer, or an aromatic solvent such as xylene or an aromatic petroleum naphtha rich in xylenes, alkyl naphthalenes, etc., such as the solvent extracts from petroleum distillates and the product known as hydroformer bottomsthe fraction from the reforming process boiling above gasoline. The use of aromatic hydrocarbons increases the solvency of the cleaner for varnishes and gums found in the induction system of the engine.
We prefer that a minor proportion of the hydrocarbon ingredient be a lubricating oil, preferably a distillate oil of 60 seconds Saybolt F.) viscosity and upward,
the purpose of which is to leave a non-volatile film of oil on exposed metal surfaces in the engine, providing lubrication and preventing rust. The rust protection can bea'ncreased still further by adding to the composition a small amount of an alkaline earth metal petroleum mahogany sulfonate, preferably about 1 to 3 percent of alkaline earth metal mahogany sulfonate in solution in about 60 percent of oil. Formulas of such a composition are presented below:
Composition, Parts by Weight General Specific Example 8 Formula Alkoxy alcohol 5 to 10 6.34 butyl Cellosolve. Aliphatic alcohol-4 to 6 carbon atoms 5 to 10 6.34 isobutyl carbinol. Water 15 to 35 26.4 Aromatic naphtha, boiling above 250 F 30 to 40 36.96 350 F. initial B.P. Liquid fatty acid 6 to 12 8.13 oleic acid. Light mineral lubricating oil 10 to 20 12.67 100 pale oil. Petroleum sulionate40% in oil--- 1 to 1.58 calium hsull'ouate as Volatile nitrogen base 1 to 3 1.58 aq. ammonia-28% Composition- Parts by Volume Example Example 9 10 Petroleum naphtha-35/42" API 51. 68 Petroleum naphthaodorless-347 409 "3.: 28 6:4 81 Pnnfasnl O. 71 Water 23.6 23 Oleic acid I 7. 92 7. Calcium mahogany sulfonate 1. 48 1. Ammonium hydroxide28% N H; 1. 81 1. Distillate lubricating oil-60 pale oil 12.
In making up these compositions, the ingredients may be combined in several ways. Thus, the volatile base and the fatty acid can be combined to form a soap which is then mixed with the water, butyl Cellosolve and alcohol. The petroleum sulfonate can be dissolved in the light lubricating oil which may be slightly heated to accelerate the solution. This solution can then be diluted with the aromatic naphtha and finally combined with the soap mixture.
It is sometimes convenient, in commercial practice, to first mix all the ingredients except the volatile base, for example, ammonia, which is added last with thorough mixing. Agitation with air or mechanically in a tank for a period of 15 to 30 minutes is usually sufficient. Part of the mineral lubricating oil can be withheld to follow the addition of volatile base to insure complete addition of the latter when pumping through a line. The product is a clear, stable solution which can be kept in closed containers indefinitely without separation. Inasmuch as p the water and naphtha are present in the form of a transparent emulsion, the product has a powerful wetting and penetrating action for either oil-wet or water-wet surfaces which enables the liquid to loosen deposits from surfaces where they are accumulated.
The volatile base can be ammonia, gaseous or liquid, usually aqua ammonia (28% NH or it can be an organic amine such as butylamine, morpholine, trimethylamine, etc. The amount of the base should be suflicient to neutralize the liquid fatty acid employed. Hydroxyaaaseeaaa Flash Point (co), F- Aniline Percent Aromatic hydrocarbons alkylamines such as the ethanol amines are avoided because of their low volatility and their precipitating action on sludge, causing the sludge to deposit in the ring grooves of the piston.
In addition to isobutyl carbinol, other aliphatic alcohols of 4 to 6 carbon atoms can be employed, such as amyl alcohol, Pentasol, cyclohexanol, tertiary butyl carbinol, secondary butyl alcohol, normal butyl alcohol, etc. Methyl isobutyl carbinol is favored because of its pleasant odor.
Alkoxy alcohols are ether alcohols in which the alkyl group has from two to five carbon atoms. Examples are ethyl hydroxyethyl ether (ethyl Cellosolve); ethoxy ethoxy ethyl alcohol (ethyl Carbitol); butoxy ethoxy ethyl alcohol (butyl Carbitol); propoxy propyl alcohol and hydroxy ethyl amyl ether. They may contain more than one ether oxygen and usually two or three carbon atoms in the alcohol group. Butyl Cellosolve (butyl' hydroxy ethyl ether) has been found very satisfactory.
In our preferred composition employing aromatic naphtha solvent, it may be a fraction from coal tar distillate containing xylene or boiling above xylene, but the aromatic naphthas of petroleum origin are preferred because of their low cost. These are usually derived from solvent extracts or from hydroformer or aromatizer distillates. For most purposes, Where odor is not important, it is preferred to use aromatic distillates of upwards of 50% aromatic content having a flash point above about 110 F. (closed cup) and initial boiling point above about 300 F. Two examples of aromatic naphthas suitable for this purpose had the following characteristics:
Sample 1 Gravity, API
Distillation:
initial point The odor of aromatic petroleum solvents can be improved by a mild treatment with sulfuric acid, for example, 10 p ounds per barrel. Thus, an aromatic distillate boiling in the range of 440 to 590 F. was so treated and neutralized before using in the above formulas.
When a light lubricating oil is employed in our composition, it is preferably a pale oil having a viscosity the range of about 60 to 150 SSU at 100 F. This may be obtained from any ordinary crude but lubricating distillates from naphthenic or aromatic base crudes are preferred. Heavy lubricating oils can be used in small amounts, however. For the liquid fatty acids, we may use the red of commerce or other liquid fatty acids such as fish oil fatty acid, soy bean fatty acid, tall oil fatty acid, corn oil fatty acid, linseed oil fatty acid, cottonseed fatty acid, coconut fatty acid, rape-seed fatty acid, naphthenic acid and other carboxylic acids of low melting point, below about 35 C. usually having about 12 to 20 carbon atoms.
The petroleum sulfonate employed in our composition is the preferentially oil soluble type or mahogany sulfonate obtained by the action of fuming sulfuric acid on petroleum lubricating oils or aromatic alkylates usually within the range of about 100 to 550 SSU viscosity at 100 F. The resulting sulfonic acid after purification to remove inorganic salts, is usually concentrated in the oil phase and converted to calcium or barium sulfonate or other polyvalent metal sulfonate. The resulting product in the case of calcium sulfonate having about 8% neutral ash, corresponds to about 40% calcium sulfonate in oil. If barium sulfonate is used, the equivalent amount based on the sulfonic acid present is employed and more or less concentrated polyvalent metal sulfonates can be used in equivalent amounts. We may also employ the basic alkaline earth metal sulfonates in the same manner, having, for example, alkali values of 10 to 60 mg. KOH per gram.
When used to clean the crankcase of the engine, we may add to our composition a small amount, about 0.1 to 2 percent of an agent to increase film strength, such as tricresyl phosphate, tributyl phosphite, and zinc dimethyl cyclohexyl dithiophosphate.
The foregoing composition can be packaged in convenient containers for distribution and should be maintained sealed at all times to avoid loss of water by evaporation. When using this combination for cleaning fouledup carburetors and engines, the following procedure is employed:
The engine should be warm, for example, about to F. The air cleaner leading to the carburetor should be removed. With the motor running at a fast idle, about 300 cc. of the cleaning composition is slowly introduced into the air intake of the carburetor. The speed of the engine is then increased and about 150 cc. more of the cleaning fiuid is poured rapidly into the carburetor, stalling the engine. The ignition is then turned off and the engine allowed to stand for 15 to 30 minutes or longer. The air cleaner is replaced and the engine idled until smoke ceases to be emitted from the exhaust. It is usually desirable to readjust the carburetor after cleaning to compensate for the removal of gums which have interfered with its action. Tests on engines cleaned in this manner have shown an increase in maximum horsepower upward of 5 to 10 HR Under some conditions, it has beenfoundgthat ethylene glycol antifreeze in the cooling system has gained access to the crankcase through a leaking gasket and, being insoluble in lubricating oil, it remained in the crankcase when the oil was drained. Our cleaner has the power Parts by weight Alkoxy alcohol containing 2-5 carbon atoms in the alkyl group 5-10 Aliphatic alcohol having 4-6 carbon atoms 5-10 Aromatic naphtha boiling above 300 F. 30-40 Liquid fatty acid of 12 to 20 carbon atoms 6-12 Volatile nitrogen base selected from the class consisting of ammonia, butylamine, morpholine, and
trimethylamine 1- 3 Water 15-35 2. The carburetor and engine cleaning composition of claim 1 to'which is added 10-20 parts by weight of a hydrocarbon distillate lubricating oil having a viscosity above 60 seconds Saybolt at 100 F.
3. The carburetor and engine cleaning composition of claim 1 containi-ng,,in addition, about 1 to 3% of an oil solution of an alkaline earth metal mahogany sulfonate in 40% concentration.
4. A clear carburetor and engine cleaning composition for removing deposits of gummy materials, carbonaceous matter, and inorganic materials from the carburetor and combustion chambers of internal combustion engines when introduced through the carburetor of said engines,
7 said composition consisting essentially of the following ingredients:
Parts by weight Alkoxy alcohol containing 2-5 carbons in the alkyl group 5 to Aliphatic alcohol having 4 to 6 carbon atoms 5 to 10 Water to Aromatic naphtha boiling above about 320 F.
comprising at least aromatic hydrocarbons Y 30 to 40 Oleicacid a 1 6to 12 Light mineral lubricating oil of -3150 SSU @F. '10 to20 Petroleum mahogany sulfonate of an alkaline earth metal 1' to 3 Aqua ammonia ...-'.';..I V' I 1 to 3 5. A carburetor and engine cleanereomprising a substantially transparent emulsion consisting essentially of the following ingredients in parts by weight:
Butyl hydroxy ethyl ether 6.34 Isobutyl carbinol 6.34 Water 26.4
Petroleum naphtha having an initial boiling point above about 320 F. and containing at least 50 percent of aromatic hydrocarbons 36.96 Aqua anmlonia' (28% NH 1.58 Oleic acid 8.13 100 SSU Viscosity at 100 F. Pale Oil 12.67
Calcium mahogany sulfonate having 8% neutral ash 1.58
References Cited in the file of this patent UNITED STATES PATENTS 2,128,685 Yates Aug. 30, 1938 2,355,591 Flaxman Aug. 8, 1944 2,559,574 Weissberg July 3, 1951 2,672,450 Pearsa'll Mar. 16, 1954

Claims (1)

1. A CLEAR CARBURETOR AND ENGINE CLEANING COMPOSITION FOR REMOVING DEPOSITS OF GUMMY MATERIALS, CARBONACEOUS MATTER AND INORGANIC SUBSTANCES FROM THE CARBURETOR AND COMBUSTION CHAMBERS OF INTERNAL COMBUSTION ENGINES WHEN INTRODUCED THROUGH THE CARBURETOR OF SAID ENGINES WHILE IDLING, SAID COMPOSITION CONSISTING ESSENTIALLY OF THE FOLLOWING INGREDIENTS: PARTS BY WEIGHT ALKOXY ALCOHOL CONTAINING 2-5 CARBON ATOMS IN THE ALKYL GROUP --------------------------------- 5-10 ALIPHATIC ALCOHOL HAVING 4-6 CARBON ATOMS ------- 5-10 AROMATIC NAPHTHA BOILING ABOVE 300*F. ----------- 30-40 LIQUID FATTY ACID OF 12 TO 20 CARBON ATOMS ------ 6-12 VOLATILE NITROGEN BASE SELECTED FROM THE CLASS CONSISTING OF AMMONIA, BUTYLAMINE, MORPHOLINE, AND TRIMETHYLAMINE --------------------------------- 1-3 WATER ------------------------------------------- 15-35
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Cited By (13)

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US3146207A (en) * 1961-05-23 1964-08-25 Rosenfeld Myer Solvent degreasing self-emulsifying cleaning composition
US3222213A (en) * 1962-12-28 1965-12-07 Union Carbide Corp Rinsing formulation
US3717590A (en) * 1970-12-17 1973-02-20 R Fetty Liquid water-soluble detergent compositions
US3882038A (en) * 1968-06-07 1975-05-06 Union Carbide Corp Cleaner compositions
US4302365A (en) * 1980-02-11 1981-11-24 American Grease Stick Company Engine degreaser composition
JPS61268854A (en) * 1985-05-22 1986-11-28 Honda Motor Co Ltd Washing of carburetor
US4774015A (en) * 1986-02-28 1988-09-27 Cherokee Chemical Co., Inc. Carburetor cleaner
US4921628A (en) * 1986-10-17 1990-05-01 Integrated Chemistries, Incorporated Cleaning composition for removal of PCBs
US5391316A (en) * 1992-03-06 1995-02-21 Lever Brothers Company, Division Of Conopco, Inc. Low-foaming, liquid cleaning compositions containing paraffin and fatty acid salt
US5407453A (en) * 1993-03-19 1995-04-18 The Lubrizol Corporation Deposit cleaning composition for internal combustion engines
US20120125445A1 (en) * 2010-11-19 2012-05-24 Chevron Oronite Company Llc Method for cleaning deposits from an engine fuel delivery system
US8809248B2 (en) 2009-06-01 2014-08-19 3M Innovative Properties Company Engine cleaning composition and method for cleaning the engine
US20180002645A1 (en) * 2015-01-30 2018-01-04 The Lubrizol Corporation Composition for cleaning gasoline engine fuel delivery systems, air intake systems, and combustion chambers

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Cited By (16)

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US3146207A (en) * 1961-05-23 1964-08-25 Rosenfeld Myer Solvent degreasing self-emulsifying cleaning composition
US3222213A (en) * 1962-12-28 1965-12-07 Union Carbide Corp Rinsing formulation
US3882038A (en) * 1968-06-07 1975-05-06 Union Carbide Corp Cleaner compositions
US3717590A (en) * 1970-12-17 1973-02-20 R Fetty Liquid water-soluble detergent compositions
US4302365A (en) * 1980-02-11 1981-11-24 American Grease Stick Company Engine degreaser composition
JPH0562234B2 (en) * 1985-05-22 1993-09-08 Honda Motor Co Ltd
JPS61268854A (en) * 1985-05-22 1986-11-28 Honda Motor Co Ltd Washing of carburetor
US4774015A (en) * 1986-02-28 1988-09-27 Cherokee Chemical Co., Inc. Carburetor cleaner
US4921628A (en) * 1986-10-17 1990-05-01 Integrated Chemistries, Incorporated Cleaning composition for removal of PCBs
US5391316A (en) * 1992-03-06 1995-02-21 Lever Brothers Company, Division Of Conopco, Inc. Low-foaming, liquid cleaning compositions containing paraffin and fatty acid salt
US5407453A (en) * 1993-03-19 1995-04-18 The Lubrizol Corporation Deposit cleaning composition for internal combustion engines
US8809248B2 (en) 2009-06-01 2014-08-19 3M Innovative Properties Company Engine cleaning composition and method for cleaning the engine
US20120125445A1 (en) * 2010-11-19 2012-05-24 Chevron Oronite Company Llc Method for cleaning deposits from an engine fuel delivery system
US8632638B2 (en) * 2010-11-19 2014-01-21 Chevron Oronite Company Llc Method for cleaning deposits from an engine fuel delivery system
US20180002645A1 (en) * 2015-01-30 2018-01-04 The Lubrizol Corporation Composition for cleaning gasoline engine fuel delivery systems, air intake systems, and combustion chambers
US10781411B2 (en) * 2015-01-30 2020-09-22 The Lubrizol Corporation Composition for cleaning gasoline engine fuel delivery systems, air intake systems, and combustion chambers

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