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US2695273A - Lubricating oil compositions - Google Patents

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US2695273A
US2695273A US281226A US28122652A US2695273A US 2695273 A US2695273 A US 2695273A US 281226 A US281226 A US 281226A US 28122652 A US28122652 A US 28122652A US 2695273 A US2695273 A US 2695273A
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lubricating oil
bis
oil
basic
hydrocarbon lubricating
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US281226A
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Edwin O Hook
Jr William D Thomas
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Wyeth Holdings LLC
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American Cyanamid Co
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Priority to US281226A priority patent/US2695273A/en
Priority to GB8050/53A priority patent/GB730738A/en
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    • 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
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • 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
    • C10M2205/22Alkylation reaction products with aromatic type compounds, e.g. Friedel-crafts
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/024Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027Neutral salts 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046Overbased sulfonic acid salts
    • 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
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/02Unspecified siloxanes; Silicones
    • 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
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/06Groups 3 or 13
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/08Groups 4 or 14
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/14Group 7
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/16Groups 8, 9, or 10
    • 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
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • 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
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/042Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
    • 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
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/044Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
    • 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
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/046Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives

Definitions

  • This invention relates to hydrocarbon lubricating oil compositions and to improvement agents to be incorporated therein, and includes methods of producing the same. More particularly, this invention relates to hydrocarbon lubricating oil compositions for use as crankcase oils in passenger automobiles and especially heavy-duty truck, bus, aeroplane, marine and diesel engines which operate for long periods of time at high temperatures.
  • a number of oil-soluble anti-oxidants have been developed to inhibit or retard such oxidational changes to reduce the deterioration of the lubricating oil and obviate these undesirable effects.
  • substituted and unsubstituted alkylidene bis-(4,6-dialkylphenols) have been employed in such a capacity and have greatly improved the resistance of hydrocarbon lubricating oil compositions to oxidational changes and have substantially inhibited or retarded deterioration of the oil and the development of undesirable decomposition products.
  • One consequence of this has been to reduce the corrosion of metallic parts such as alloy bearings in the engine and to thus minimize the deleterious effects of oil deterioration on cylinders, pistons and other relatively moving engine parts.
  • hydrocarbon lubricating oil compositions including alkylidene bis-phenols and their methods of preparation are set forth in U. S. Letters Patent 2,515,906-8 and 2,570,402 and it is a principal purpose of the present invention to improve the operating characteristics of such oil compositions containing the alkylidene bis-phenols set forth therein.
  • alkylidene bis-phenols are listed, primarily for purposes of illustration and such is not to be construed as limitative in any way of the scope of the inventive concept: 2,2'-methylene bis(4-methyl-6-t-butylphenol); 2,2-methylene bis(4-methyl-fi-t-octylphenol);
  • the alkylidene bis-phenols may be used in such pro portions as to stabilize the lubricating oil composition and retard or inhibit the oxidation or deterioration thereof. It has been found that the addition of from about 0.01 up to about 3.0 per cent by weight of these compounds to a lubricating oil subject to oxidational changes will substantially inhibit or greatly retard the formation of objectionable oxidation or decomposition products which are injurious or corrosive to metallic engine parts. The exact amount of inhibitor employed in any particular case, however, will depend upon the nature of the base oil stock used, as well as upon the severity of the operating conditions to which it is intended to be subjected, upon the presence of any other lubricating oil additives which may be utilized in the composition, and so forth.
  • the various oil-soluble basic organic sulfonates which are effective to produce the compositions of the present invention are the basic petroleum or mahogany sulfonates which are well-known products in the oil industry and are produced by methods well-known in the art. These are preferable to use because of their availability and relatively inexpensive nature.
  • Other basic oil-soluble organic sulfonates may be employed- We may use, for example, any basic alkyl or aryl sulfonate, provided it is sufiiciently oil-soluble for its intended purposes and does not contain any chemical group which could react with alkali to prevent the over-neutralization required to supply the required basicity.
  • these oil-soluble surface-active organic sulfonates in the form of their basic metal salts, preferably the basic alkaline earth metal salts.
  • the various metal salts which may be employed are those of the salt forming radicals, calcium, barium, strontium, magnesium, lead and other polyvalent metals such as zinc, cobalt, tin and aluminum.
  • the term basic organic sulfonate includes those sulfonates which are sufficiently overneutralized so as to contain a minimum of 20% metal in excess of the amount theoretically required to form the ordinary neutral organic sulfonate.
  • This excess of metal may be introduced into the sulfonic acid by methods disclosed in U. S. Patent 2,501,7312 and 2,585,520.
  • the desired excess of metal may be introduced and held by the organic sulfonates by employing an alcohol as the carrying medium for the metal in the reaction with the sulfonic acid.
  • methanol may be reacted with barium oxide to form what is believed to be barium methylate or perhaps a hydroxy-methoxy barium compound.
  • This may be reacted with a petroleum sulfonic acid or an oil-soluble organic sulfonic acid to produce a complex containing a substantial amount of barium over and above that which is present in an ordinary neutral sulfonate.
  • barium oxide may be reacted with the methanol in a quantity suflicient to provide at least about 20% of excess barium when reacted with the sulfonic acid to form the final product.
  • the excess of barium must not be lower than about 20%. Therefore, as used herein, the term basic as applied to a petroleum sulfonic acid salt or an oilsoluble organic sulfonic acid salt includes only those sulfonates having at least about 20% or greater excess metal over that found in the corresponding neutral sulfonic acid salt.
  • These basic sulfonates may be used in such proportions as to substantially retard or inhibit the tendency of the oil composition containing the alkylidene bisphenol to form objectionable lacquer-like deposits.
  • the percentages of these inhibiting amounts will naturally depend upon the nature of the base stock used, upon the amount of and the particular alkylidene bisphenol used as an inhibitor therein, upon the severity of the operating conditions to which the oil composition is to be subjected, and so forth.
  • the finished hydrocarbon lubricating oil composition may also contain other additives, such as oiliness and extreme pressure agents such as phosphorus or sulfur containing organic compounds; viscosity index improvers such as high molecular weight resins; pour point depressants such as high molecular weight polymers or waxnaphthalene condensation products; detergents such as metallic sulfonates or phenolates, foam inhibitors such as silicones; and other improvement agents, as desired.
  • oiliness and extreme pressure agents such as phosphorus or sulfur containing organic compounds
  • viscosity index improvers such as high molecular weight resins
  • pour point depressants such as high molecular weight polymers or waxnaphthalene condensation products
  • detergents such as metallic sulfonates or phenolates, foam inhibitors such as silicones
  • foam inhibitors such as silicones
  • the resistance of our improved lubricating oils to varnish and lacquer-like formation was demonstrated by the results of the following tests.
  • the particular alkylidene bis-phenol selected for test purpose was 2,2-methylene bis(4-methyl-6-t-butylphenol) but such was merely for illustrative purposes and is not to be considered limitative of the inventive concept.
  • the particular test procedure employed was a Chevrolet L4 test wherein the engine was operated continuously for 36 hours at 30 horsepower loading with a crankcase temperature of 280 F. and a water jacket outlet temperature of 200 F. The engine was then disassembled and the parts were inspected and rated.
  • the piston varnish ratings are reported on a scale of from 1 to 10, in which 1 means a piston which is very dirty with stuck piston rings and 10 means a perfectly clear piston.
  • the overall rating is reported on a scale from 1 to in which 100 means a clean engine with substantially no sludge deposits and with perfectly clean pistons.
  • the corrosion of the bearings is determined by determining the weights of a pair of whole bearings both before and after the test and then averaging the differences between these values, whereby the average weight loss per Whole bearing is derived.
  • the results of the tests were as follows:
  • a hydrocarbon lubricating oil composition comprismg a ma or proportion of a hydrocarbon lubricating oil, from about 0.01% to about 3% by weight of 2,2-methylene b1s(4-methyl-6-tertiary butyl phenol), and a basic petroleum sulfonate of a metal selected from the group conslstmg of alkaline earth metals and heavy metals in an amount sufficient to reduce the lacquer-forming propensities of the hydrocarbon lubricating oil composition.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

United States Patent LUBRICATING OIL COMPOSITIONS Edwin 0. Hook, New Canaan, and William D. Thomas, Jr., Cos Cob, C0nn., assignors to American Cyanamid Company, New York, N. Y., a corporation of Maine No Drawing. Application April 8, 1952, Serial No. 281,226
4 Claims. (Cl. 25233.4)
This invention relates to hydrocarbon lubricating oil compositions and to improvement agents to be incorporated therein, and includes methods of producing the same. More particularly, this invention relates to hydrocarbon lubricating oil compositions for use as crankcase oils in passenger automobiles and especially heavy-duty truck, bus, aeroplane, marine and diesel engines which operate for long periods of time at high temperatures.
When conventional lubricating oils are subjected to high operating temperatures for extended periods of time, such as in heavy-duty service, they tend to deteriorate with the formation of complex and objectionable oxidation and decomposition products of an acidic nature. These acidic oxidation products which are developed in the oil create serious problems inasmuch as they attack and corrode metallic parts and particularly alloy bearings commonly used in internal combustion engines. As a consequence, alloy bearing-metals, such as copper-lead, silver-cadmium, nickel-cadmium, and the like are corrtgded and require replacement in a relatively short period 0 time.
Additionally, these acidic oxidation and decomposition products tend to polymerize under the high temperature conditions prevailing in an engine to form lacquer-like deposits on the cylinder walls or other stationary parts of the engine and on or between the relatively moving parts of the engine causing them to stick or to wear rapidly. Even larger quantities of these polymerization products remain dispersed in the partially oxidized crankcase oil and are rapidly precipitated to form a heavy mayonnaise-like sludge when the engine cools or when fresh oil is added to the engine. These precipitated sludges become caked on heated metal surfaces and reduce the effective life of the engine by reducing the effectiveness of the lubrication system.
A number of oil-soluble anti-oxidants have been developed to inhibit or retard such oxidational changes to reduce the deterioration of the lubricating oil and obviate these undesirable effects. For example, substituted and unsubstituted alkylidene bis-(4,6-dialkylphenols) have been employed in such a capacity and have greatly improved the resistance of hydrocarbon lubricating oil compositions to oxidational changes and have substantially inhibited or retarded deterioration of the oil and the development of undesirable decomposition products. One consequence of this has been to reduce the corrosion of metallic parts such as alloy bearings in the engine and to thus minimize the deleterious effects of oil deterioration on cylinders, pistons and other relatively moving engine parts.
Although the lubricating oils containing these alkylidene bis-phenols are extremely resistant to oil oxidation and sludge formation under conditions of heavy-duty service, we have found that a lacquer-like formation has developed on metallic engine parts during use of such lubricating oils which has detracted to some extent from the value of the inhibitors and from the satisfactory operation of the engine. Without being bound to any theory on the formation of such a lacquer-like deposit, it is believed that such deposition is a result of decomposition of the inhibitor, alone or with certain components of the oil, rather than that of the lubricating oil alone.
Various compounds which normally have detergent properties have been added to these hydrocarbon lubricating oil compositions containing alkylidene bis-phenols in efforts to improve such conditions but none has here- 2,695,273 Patented Nov. 23, 1954 in which R1 and R2 are substituents selected from the class consisting of aliphatic, cycloaliphatic and aromatic groups and hydrogen; and R3 and R4 are alkyl radicals.
Examples of these hydrocarbon lubricating oil compositions including alkylidene bis-phenols and their methods of preparation are set forth in U. S. Letters Patent 2,515,906-8 and 2,570,402 and it is a principal purpose of the present invention to improve the operating characteristics of such oil compositions containing the alkylidene bis-phenols set forth therein.
Its- R:
Without limiting the scope of the present invention,
the following alkylidene bis-phenols are listed, primarily for purposes of illustration and such is not to be construed as limitative in any way of the scope of the inventive concept: 2,2'-methylene bis(4-methyl-6-t-butylphenol); 2,2-methylene bis(4-methyl-fi-t-octylphenol);
2,2'-methylene bis(4-1nethyl-6-t-dodecylphenol); 2,2-
methylene bis(4-t-octyl-6-methylphenol); 2,2'-methylene bis(4-t-butyl-6-methylphenol); 2,2"-methylene bis(4,6-dit-butylphenol); 2,2-ethylidene bis(4-methyl-6 t octylphenol); 2,2-ethylidene bis(4-methyl-6-t-butylphenol); 2,2-isopropylidene bis(4-t-butyl-6-amylphenol); 2,2'-isopropylidene bis(4-t-butyl-6-methylp'henol); 2,2'-isopropyl idene bis (4,6-di-t-dodecylphenol); 2,2-propylidene bis- (4-methyl-6-t-octylphenol); 2,2-isobutylidene bis(4,6-dimethylphenol); and others set forth in the above mentioned U. S. patents.
The alkylidene bis-phenols may be used in such pro portions as to stabilize the lubricating oil composition and retard or inhibit the oxidation or deterioration thereof. It has been found that the addition of from about 0.01 up to about 3.0 per cent by weight of these compounds to a lubricating oil subject to oxidational changes will substantially inhibit or greatly retard the formation of objectionable oxidation or decomposition products which are injurious or corrosive to metallic engine parts. The exact amount of inhibitor employed in any particular case, however, will depend upon the nature of the base oil stock used, as well as upon the severity of the operating conditions to which it is intended to be subjected, upon the presence of any other lubricating oil additives which may be utilized in the composition, and so forth.
We have now discovered that this lacquer-like formation in hydrocarbon lubricating oil compositions containing alkylidene bis-phenols as anti-oxidants and anticorrosive agents may be substantially inhibited or retarded by the addition to such compositions of a small amount of an oil-soluble basic organic sulfonate.
Among the various oil-soluble basic organic sulfonates which are effective to produce the compositions of the present invention are the basic petroleum or mahogany sulfonates which are well-known products in the oil industry and are produced by methods well-known in the art. These are preferable to use because of their availability and relatively inexpensive nature. Other basic oil-soluble organic sulfonates, however, may be employed- We may use, for example, any basic alkyl or aryl sulfonate, provided it is sufiiciently oil-soluble for its intended purposes and does not contain any chemical group which could react with alkali to prevent the over-neutralization required to supply the required basicity.
In accordance with the principles of the present invention, we use these oil-soluble surface-active organic sulfonates in the form of their basic metal salts, preferably the basic alkaline earth metal salts. Among the various metal salts which may be employed are those of the salt forming radicals, calcium, barium, strontium, magnesium, lead and other polyvalent metals such as zinc, cobalt, tin and aluminum.
As used herein, the term basic organic sulfonate includes those sulfonates which are sufficiently overneutralized so as to contain a minimum of 20% metal in excess of the amount theoretically required to form the ordinary neutral organic sulfonate. This excess of metal may be introduced into the sulfonic acid by methods disclosed in U. S. Patent 2,501,7312 and 2,585,520. For example, the desired excess of metal may be introduced and held by the organic sulfonates by employing an alcohol as the carrying medium for the metal in the reaction with the sulfonic acid. For example, in the case of the basic barium salt, methanol may be reacted with barium oxide to form what is believed to be barium methylate or perhaps a hydroxy-methoxy barium compound. This, in turn, may be reacted with a petroleum sulfonic acid or an oil-soluble organic sulfonic acid to produce a complex containing a substantial amount of barium over and above that which is present in an ordinary neutral sulfonate. In preparing the barium methylate, barium oxide may be reacted with the methanol in a quantity suflicient to provide at least about 20% of excess barium when reacted with the sulfonic acid to form the final product. If a greater excess is desired, such as up to 100% excess or greater, such may be accomplished by using a greater quantity of barium oxide with respect to the sulfonic acid. However, in order to accomplish the desired objects of the present invention, the excess of barium must not be lower than about 20%. Therefore, as used herein, the term basic as applied to a petroleum sulfonic acid salt or an oilsoluble organic sulfonic acid salt includes only those sulfonates having at least about 20% or greater excess metal over that found in the corresponding neutral sulfonic acid salt.
These basic sulfonates may be used in such proportions as to substantially retard or inhibit the tendency of the oil composition containing the alkylidene bisphenol to form objectionable lacquer-like deposits. We have found that the addition of from about 0.3 up to about 5.0 per cent by weight with respect to the base oil stock containing the customary quantities of alkylidene bis-phenols therein substantially inhibits or greatly reduces the formation of objectionable lacquer-like deposits. The percentages of these inhibiting amounts will naturally depend upon the nature of the base stock used, upon the amount of and the particular alkylidene bisphenol used as an inhibitor therein, upon the severity of the operating conditions to which the oil composition is to be subjected, and so forth. It is also to be noted that these basic sulfonates, when in such combination with hydrocarbon lubricating oil and an alkylidene bisphenol, are not corrosive to silver, copper, or similar metals used in alloy bearings for engines, which is a decided advantage over the usual sulfur-containing inhibitors.
The finished hydrocarbon lubricating oil composition may also contain other additives, such as oiliness and extreme pressure agents such as phosphorus or sulfur containing organic compounds; viscosity index improvers such as high molecular weight resins; pour point depressants such as high molecular weight polymers or waxnaphthalene condensation products; detergents such as metallic sulfonates or phenolates, foam inhibitors such as silicones; and other improvement agents, as desired.
The resistance of our improved lubricating oils to varnish and lacquer-like formation was demonstrated by the results of the following tests. The particular alkylidene bis-phenol selected for test purpose was 2,2-methylene bis(4-methyl-6-t-butylphenol) but such was merely for illustrative purposes and is not to be considered limitative of the inventive concept. The particular test procedure employed was a Chevrolet L4 test wherein the engine was operated continuously for 36 hours at 30 horsepower loading with a crankcase temperature of 280 F. and a water jacket outlet temperature of 200 F. The engine was then disassembled and the parts were inspected and rated.
The piston varnish ratings are reported on a scale of from 1 to 10, in which 1 means a piston which is very dirty with stuck piston rings and 10 means a perfectly clear piston. The overall rating is reported on a scale from 1 to in which 100 means a clean engine with substantially no sludge deposits and with perfectly clean pistons.
The corrosion of the bearings is determined by determining the weights of a pair of whole bearings both before and after the test and then averaging the differences between these values, whereby the average weight loss per Whole bearing is derived. The results of the tests were as follows:
Basic Barium Piston Overall Corrosion Alkyhdene bis phenol Petroleum Varnish Rating (mgms) Sulfonate Basic Lead Piston Overall Alkylidene bis phenol Pseltiffglnitgn Varnish Rating Although we have shown but a few specific examples of our improved hydrocarbon lubricating oil compositions and have set forth the improved test results using a readily available particular alkylidene bis-phenol, we consider our inventive concept not to be limited thereto but to include other compounds of equivalent constitution as set forth in the claims appended hereto. It is understood that any suitable changes, variations and modifications may be made without departing from the spirit and scope of the invention.
We claim:
1. A hydrocarbon lubricating oil composition comprismg a ma or proportion of a hydrocarbon lubricating oil, from about 0.01% to about 3% by weight of 2,2-methylene b1s(4-methyl-6-tertiary butyl phenol), and a basic petroleum sulfonate of a metal selected from the group conslstmg of alkaline earth metals and heavy metals in an amount sufficient to reduce the lacquer-forming propensities of the hydrocarbon lubricating oil composition.
2. The invention as defined in claim 1 wherein the metal is barium.
3. The invention as defined in claim 1 wherein the metal is calcium.
4. The invention as defined in claim 1 wherein the metal is lead.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,570,402 Stevens et al Oct. 9, 1951 2,585,520 Van Ess et al Feb. 12, 1952

Claims (1)

1. A HYDROCARBON LUBRICATING OIL COMPOSITION COMPRISING A MAJOR PROPORTION OF A HYDROCARBON LUBRICATING OIL, FROM ABOUT 0.01% TO ABOUT 3% BY WEIGHT OF 2,2''-METHYLENE BIS(4-METHYL-6-TERTIARY BUTYL PHENOL), AND A BASIC PETROLEUM SULFONATE OF A METAL SELECTED FROM THE GROUP CONSISTING OF ALKALINE EARTH METALS AND HEAVY METALS IN AN AMOUNT SUFFICIENT TO REDUCE THE LACQUER-FORMING PROPENSITIES OF THE HYDROCARBON LUBRICATING OIL COMPOSITION.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2954344A (en) * 1957-12-11 1960-09-27 Exxon Research Engineering Co Heavy duty lubricating oil
US3018248A (en) * 1960-01-20 1962-01-23 California Research Corp Oxidation inhibited mineral oil compositions
US3065178A (en) * 1959-12-21 1962-11-20 Exxon Research Engineering Co Lubricating oil composition
US3920572A (en) * 1973-04-18 1975-11-18 Chevron Res Heat transfer fluids
US3958624A (en) * 1973-04-18 1976-05-25 Chevron Research Company Heat transfer fluids

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2325805A1 (en) * 1973-05-22 1974-12-19 Union Rheinische Braunkohlen LUBRICANT

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2570402A (en) * 1947-12-22 1951-10-09 Gulf Research Development Co Antioxidants for oils and oil compositions containing the same
US2585520A (en) * 1948-12-03 1952-02-12 Shell Dev Lubricating compositions containing highly basic metal sulfonates

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2570402A (en) * 1947-12-22 1951-10-09 Gulf Research Development Co Antioxidants for oils and oil compositions containing the same
US2585520A (en) * 1948-12-03 1952-02-12 Shell Dev Lubricating compositions containing highly basic metal sulfonates

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2954344A (en) * 1957-12-11 1960-09-27 Exxon Research Engineering Co Heavy duty lubricating oil
US3065178A (en) * 1959-12-21 1962-11-20 Exxon Research Engineering Co Lubricating oil composition
US3018248A (en) * 1960-01-20 1962-01-23 California Research Corp Oxidation inhibited mineral oil compositions
US3920572A (en) * 1973-04-18 1975-11-18 Chevron Res Heat transfer fluids
US3958624A (en) * 1973-04-18 1976-05-25 Chevron Research Company Heat transfer fluids

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