Patent Application
20120178655
The disclosed technology relates to lubricants for internal combustion engine, particularly those fueled with biodiesel fuels.
Biodiesel is a general term for fuel-grade materials derived from natural sources such as vegetable oils. They are often fatty acid methyl esters (“FAME”) such as rapeseed methyl ester (“RME”) or soya methyl ester (“SME”). Biodiesel fuels are becoming more prevalent for fueling of diesel engines. The increased use of diesel passenger vehicles in Europe and elsewhere is in part a cause of this increase. Current European diesel standard (EN 590) allows for 5% biodiesel component to be incorporated into fuels, which will soon rise to 7%, with indications that 10% biodiesel content will be introduced by 2012.
Simultaneously, there is continued pressure for reducing particulate matter emissions from diesel engines. Euro 5 requirements, scheduled for implementation in 2009, require reduction in particulate matter to 0.05 g/km. Such levels can only be attained, practically, by use of a diesel particulate filter. These filters require regeneration once they are full of soot, and this is typically achieved by increasing the filter temperature to burn off the soot. The temperature increase is often achieved by post-injection of fuel into the engine cylinder.
However, post-injection of fuel can have the undesirable effect of fuel-dilution of the engine lubricant, as more cylinder wall wetting by the fuel allows more fuel to migrate to and accumulate in the lubricant sump. Biodiesel components are typically less volatile than conventional mineral diesel fuel, and thus concentration of such components in the sump is exacerbated. In fact, use of biodiesel fuel (B05, i.e., containing 5% ester) along with post-injection may result in 40% fuel dilution of the lubricant, and the biodiesel component may account for 50% of the diluent. These high levels of biodiesel in the oil may lead to increased oxidation and deposit formation associated with the lubricant.
U.S. Patent Publication 2008/0182768, Devlin et al, Jul. 31, 2008, discloses a lubricant composition for biodiesel fuel engine applications, containing an oil of lubricating viscosity and a highly grafted, multi-functional olefin copolymer. The lubricating oil may contain a conventional dispersant/inhibitor package, which may contain a detergent such as oil soluble neutral and overbased sulfonates and phenates, among others.
U.S. Patent Publication 2009/0111720, Boffa, Apr. 30, 2009, discloses lubricating oil compositions contaminated with a biodiesel fuel, comprising a base oil of lubricating viscosity an a diarylamine compound. It further comprises at least one additive which may be (among others) detergents. Suitable metal detergents include phenates and sulfonates, among others. Generally the amount of the detergent is from about 0.001 wt. % to about 5 wt %. In an example, a base-line comparison is prepared containing, among other materials, 0.24 wt. % actives of an overbased magnesium sulfonate and 0.65 wt. % actives of an overbased calcium phenate detergent.
U.S. Patent Publication 2009/0111721, Boffa, Apr. 30, 2009, discloses lubricating oil compositions comprising a base oil, a biodiesel fuel, and a detergent. The detergent can be a metal phenate detergent such as alkaline metal phenates. An additional additive or modifier may also be present, including detergents. Suitable metal detergents include phenates and sulfonates. In an example, a baseline formulation contains 0.18 wt. % actives of a low overbased calcium sulfonate detergent.
PCT Publication WO 2009/013275, Jan. 29, 2009, discloses lubricating composition for use in diesel engines compatible with biofuel, containing certain antioxidants. The lubricant may also contain an additives package containing detergent.
The disclosed technology provides a lubricant composition suitable for sump lubricated engines fueled by a liquid fuel which includes a biodiesel component, which exhibits improved oxidation resistance and/or reduced deposit formation in lubricants which contain a portion of the biodiesel component. This is accomplished by the presence of the described sulfonate material.
The disclosed technology provides a method of reducing oxidative degradation of a lubricant composition which contains an oil of lubricating viscosity and at least about 1 percent by weight of a C1-C4 (or C1-C3) alkyl ester of a carboxylic acid of 12 to 24 carbon atoms (that is, the carboxylic acid component of the ester contains 12 to 24 carbon atoms), comprising including within said lubricant composition a sulfonate detergent in an amount sufficient to provide at least 0.2 (or 0.4) percent by weight sulfonate soap to the lubricant composition, wherein the weight ratio of sulfonate soap to phenate soap in the lubricant composition is at least 0.35:1 (or 0.7:1).
Further provided is a method for lubricating a sump-lubricated internal combustion engine fueled by a liquid fuel which comprises a C1-C4 (or C1-C3) alkyl ester of a carboxylic acid of 12 to 24 carbon atoms, comprising supplying to the sump a lubricant comprising an oil of lubricating viscosity and a sulfonate detergent in an amount sufficient to provide at least 0.2 (or 0.4) percent by weight sulfonate soap to the lubricant composition, wherein the weight ratio of sulfonate soap to phenate soap in the lubricant composition is at least 0.35:1 (or 0.7:1).
Also provided is a lubricant composition comprising: (a) an oil of lubricating viscosity; (b) at least about 1 percent by weight of a C1-C4 (or C1-C3) alkyl ester of a carboxylic acid of 12 to 24 carbon atoms; and (c) a sulfonate detergent in an amount sufficient to provide at least about 0.2 (or 0.4) percent by weight sulfonate soap to the lubricant composition, wherein the weight ratio of sulfonate soap to phenate soap in the lubricant composition is at least about 0.35:1 (or 0.7:1). The presence of the ester typically arises from dilution of the lubricant by a liquid fuel.
Various preferred features and embodiments will be described below by way of non-limiting illustration.
The lubricant as described herein is particularly useful for lubricating diesel engines that are fueled with a liquid fuel that comprises a biodiesel fuel, that is, that contains a certain amount, e.g., at least 2 percent by weight, of a C1-C3 or C1-C4 alkyl ester of a carboxylic acid of 12 to 24 carbon atoms. Such alkyl groups may include methyl, ethyl, 1-propyl, 2-propyl, n-butyl, sec-butyl, isobutyl, or tert-butyl. When the alkyl group is C1-C3, the groups may be methyl, ethyl, 1-propyl, or 2-propyl. In certain embodiments the alkyl group is methyl or ethyl, or alternatively, methyl. The amount of such ester in the liquid fuel may be 2 to 100% by weight, or 4 to 100% or 5 to 100% or 10 to 100%, for instance, 4 to 12% or 5 to 10% or generally 2, 4, 5, 10 or 12% up to 100 or 90 or 80 or 50 or 30%. These percentages are normally calculated on the basis of the liquid fuel excluding any performance additives that may be present. The balance of the fuel may be a petroleum-derived fuel or fraction, such as a middle distillate fuel or other petroleum fuel conventionally used to fuel a diesel engine. The amount of sulfur in the fuel may be less than 300 parts per million by weight for low sulfur fuels, or less than 50 ppm or less than 10 ppm, e.g., 1 to 10 ppm S for ultra-low sulfur fuels. Fuels may also contain higher levels of sulfur, such as up to 1000 ppm or 300 to 500 ppm. Any sulfur which is present may come from the biodiesel component or from a petroleum fraction.
Biodiesel fuels can be derived from animal fats and/or vegetable oils to include biomass sources such as plant seeds as described in U.S. Pat. No. 6,166,231. The esters may thus include, as described above, methyl, ethyl, propyl, or isopropyl esters. The carboxylic acids may be derived from natural or synthetic sources and may contain a relatively pure or single component of acid in terms of chain length, branching, and the like, or they may be mixtures of acids characteristic of acids obtained from animal or, especially, vegetable sources,
Biodiesel fuels thus include esters of naturally occurring fatty acids such as the methyl ester or other lower ester of rapeseed oil which can generally be prepared by transesterifying a triglyceride of a natural fat or oil with an aliphatic alcohol having 1 to 3 or 1 to 4 carbon atoms. Other suitable materials include the methyl esters of soybean oil, sunflower oil, coconut oil, corn oil, olive oil, palm oil, jatropha oil, peanut oil, canola oil, bahassu oil, castor oil, and sesame seed oil. Other materials include used vegetable oils (e.g., used cooking oil) and animal fats. Such materials comprise a mixture of acids most typically of 8 to 24 or 12 to 22 or 16 to 18 carbon atoms, with varying degrees of branching or unsaturation. In one embodiment, the acid is unsaturated. Rapeseed oil, for instance, is believed to comprise largely oleic acid (C18), linoleic acid (C18), linolenic acid (C18), and in some cases erucic acid (C22). Certain amounts of vegetable oils (triglycerides) may also be included in some embodiments.
The lubricant composition described herein comprises an oil of lubricating viscosity. In one embodiment, the oil of lubricating viscosity is an API Group I, Group II, Group III, Group IV, or Group V oil, including a synthetic oil, or mixtures thereof. In another embodiment, the oil is Groups II, III, IV, or V. These are classifications established by the API Base Oil Interchangeability Guidelines. Group III oils contain <0.03 percent sulfur and >90 percent saturates and have a viscosity index of >120. Group II oils have a viscosity index of 80 to 120 and contain <0.03 percent sulfur and >90 percent saturates. Polyalphaolefins are categorized as Group IV. The oil can also be an oil derived from hydroisomerization of wax such as slack wax or a Fischer-Tropsch synthesized wax. Such “Gas-to-Liquid” oils are typically characterized as Group III. Group V is encompasses “all others” (except for Group I, which contains >0.03% S and/or <90% saturates and has a viscosity index of 80 to 120).
The oil of lubricating viscosity, then, can include natural or synthetic lubricating oils and mixtures thereof. Mixture of mineral oil and synthetic oils, particularly polyalphaolefin oils and polyester oils, are often used. Natural oils include animal oils and vegetable oils (e.g. castor oil, lard oil and other vegetable oils) as well as mineral lubricating oils such as liquid petroleum oils and solvent-treated or acid treated mineral lubricating oils of the paraffinic, naphthenic or mixed paraffinic-naphthenic types. Hydrotreated or hydrocracked oils are included within the scope of useful oils of lubricating viscosity.
Oils of lubricating viscosity derived from coal or shale are also useful. Synthetic lubricating oils include hydrocarbon oils and halosubstituted hydrocarbon oils such as polymerized and interpolymerized olefins and mixtures thereof, alkylbenzenes, polyphenyl, (e.g., biphenyls, terphenyls, and alkylated polyphenyls), alkylated diphenyl ethers and alkylated diphenyl sulfides and their derivatives, analogs and homologues thereof. Alkylene oxide polymers and interpolymers and derivatives thereof, and those where terminal hydroxyl groups have been modified by, for example, esterification or etherification, constitute other classes of known synthetic lubricating oils that can be used. Another suitable class of synthetic lubricating oils that can be used comprises the esters of dicarboxylic acids and those made from C5 to C12 monocarboxylic acids and polyols or polyol ethers,
Other synthetic lubricating oils include liquid esters of phosphorus-containing acids, polymeric tetrahydrofurans, silicon-based oils such as the polyalkyl-, polyaryl-, polyalkoxy-, or polyaryloxy-siloxane oils, and silicate oils.
Unrefined, refined and rerefined oils, either natural or synthetic (as well as mixtures of two or more of any of these) of the type disclosed herein-above can be used in the compositions of the present invention. Unrefined oils are those obtained directly from a natural or synthetic source without further purification treatment. Refined oils are similar to the unrefined oils except they have been further treated in one or more purification steps to improve one or more properties. Rerefined oils are obtained by processes similar to those used to obtain refined oils applied to refined oils which have been already used in service. Such rerefined oils often are additionally processed by techniques directed to removal of spent additives and oil breakdown products.
When a lubricant is used in connection with a biodiesel fuel, a portion of the ester component of the fuel will typically migrate into the lubricant, as described above. Thus, in some embodiments in which the present invention is employed, the lubricant will contain at least 1 percent by weight or at least 2 or 4 or 5 percent by weight of the ester component. The amount of ester component in the lubricant may be as high as 15 or 20 or 30 or 40 percent or possibly even higher.
The lubricant will contain various additives, including one or more sulfonate detergents. Detergents are generally basic alkali or alkaline earth metal salt of an acidic organic compound, in the present instance, of a sulfonic acid. The detergents may be neutral salts or they may be overbased materials. Overbased materials are single phase, homogeneous Newtonian systems characterized by a metal content in excess of that which would be present according to the stoichiometry of the metal and the particular acidic organic compound reacted with the metal.
The amount of excess metal in an overbased detergent is commonly expressed in terms of metal ratio. The term “metal ratio” is the ratio of the total equivalents of the metal to the equivalents of the acidic organic compound. A neutral metal salt has a metal ratio of 1. A salt having 4.5 times as much metal as present in a normal salt will have metal excess of 3.5 equivalents, or a ratio of 4.5. The basic salts may, for instance, have a metal ratio of 1.5 or 3 or 7, up to 40 or to 25 or to 20. The basicity of the overbased materials may be expressed as total base number (TBN), e.g., ASTM D 4739.
Overbased detergents are typically prepared by reacting an acidic material such as carbon dioxide with a mixture of an acidic organic compound (in the present case, a sulfonic acid), an inert reaction medium comprising at least one inert organic solvent such as mineral oil a stoichiometric excess of a metal base compound, and a promoter.
The acidic organic compounds useful in making overbased compositions, sometimes referred to as the “substrate,” include in a general sense carboxylic acids (such as hydrocarbyl-substituted salicylic acids), sulfonic acids (such as hydrocarbyl-substituted benzenesulfonic acids), phosphorus-containing acids, phenols, and mixtures thereof. In the present technology, the acidic organic compound will include a sulfonic acid.
Illustrative examples of sulfonic acids include mono-, di-, and tri-alkylated benzene and naphthalene (including hydrogenated forms thereof) sulfonic acids. Illustrative of synthetically produced alkylated benzene and naphthalene sulfonic acids are those containing alkyl substituents having 8 or 12 to 30 carbon atoms, such as about 24 carbon atoms. Such acids include di-isododecyl-benzenesulfonic acid. Also included are polyisobutene-substituted benzenesulfonic acids derived from polyisobutene having an
The production of sulfonates from detergent manufactured by-products by reaction with, e.g.. SO3, is well known to those skilled in the art. See, for example, the article “Sulfonates” in Kirk-Othmer “Encyclopedia of Chemical Technology”, Second Edition, Vol. 19, pp. 291 et seq. published by John Wiley & Sons, N.Y. (1969).
The metal compounds useful in making detergents are generally any Group 1 or Group 2 metal compounds (CAS version of the Periodic Table of the Elements). The Group 1 metals of the metal compound include Group I a alkali metals (sodium, potassium, lithium) as well as Group 1b metals such as copper. The Group 2 metals of the metal base include the Group 2a alkaline earth metals (magnesium, calcium, barium) as well as the Group 2b metals such as zinc or cadmium. Generally the metal compounds are delivered as metal salts. The anionic portion of the salt can be hydroxide, oxide, carbonate, borate, or nitrate.
Patents disclosing techniques for making basic salts of the above-described sulfonic acids, as well as carboxylic acids and mixtures thereof include U.S. Pat. Nos. 2,501,731; 2,616,905; 2,616,911; 2,616,925; 2,777,874; 3,256,186; 3,384,585; 3,365,396; 3,320,162; 3,318,809; 3,488,284; and 3,629,109.
The sulfonate may also be a borated complex, or alternatively it may be non-borated. Borated complexes of this type can be prepared by heating a basic metal salt with boric acid at about 50-100° C., the number of equivalents of boric acid being up to roughly equal to the number of equivalents of metal in the salt. U.S. Pat. No. 3,929,650 discloses borated complexes and their preparation.
For purposes of the present invention, the sulfonate, in one embodiment, may be or include an alkali metal detergent, which may be (but need not necessarily be) an overbased alkali metal detergent. The alkali metal may be sodium. The detergent may be an overbased sodium sulfonate detergent. Alternatively, the sulfonate may include an alkaline earth metal detergent, which may be (but need not be) overbased. The alkaline earth metal may be calcium, or, alternatively, magnesium. In one embodiment the detergent is an overbased calcium sulfonate detergent and there may also be present a sodium or magnesium sulfonate detergent. The TBN of any such detergent may be, for instance, 50 to 900 or 100 to 800 or 200 to 750 or 300 to 700 (being calculated on an oil-free basis. The measured TBN will be proportionally lower if the conventional amount of diluent oil is included.
In the disclosed technology, the overbased metal sulfonate detergent comprises an oil-soluble neutral metal sulfonate component and a metal carbonate component. By “neutral metal sulfonate” is meant the salt represented by a stoichiometric neutralization of the oil-soluble acidic material, that is, the sulfonic acid, said salt having a metal ratio of 1, regardless of whether such a salt would be strictly neutral or might measure as somewhat acidic or basic by any given test or titration. This material is also referred to as a sulfonate soap. The “amount of neutral sulfonate” or “amount of sulfonate soap” is intended as a measure related to the amount of acidic sulfonate substrate that has been overbased, which will differ from the amount of sulfonate anion by the mass of the neutralizing metal in a manner that may be readily calculated. The amount of the neutral metal sulfonate, or sulfonate soap component, may be readily determined by the person skilled in the art from a knowledge of the total amount of the corresponding detergent present and the extent of overbasing or metal ratio or TBN of the detergent. In one embodiment, the TBN measurement is used to calculate or define the amount of metal sulfonate soap. For example, 1 g (oil free) of an overbased calcium sulfonate detergent having a TBN (oil free) of 517 will contain about 0.46 g CaCO3 ([517 mg KOH/g]×[1 eq KOH/56,100 mg KOH]×[50 g CaCO3/1 eq KOH]). By subtraction, the amount of neutral sulfonate, that is, the sulfonate soap, is about 0.54 g or 54%. (Any inherent residual basicity of the substrate should be discounted from the measured TBN before calculating the amount of neutral soap, as will be apparent to the person skilled in the art.)
The amount of the sulfonate detergent is typically an amount to provide at least 0.2 or 0.3 or 0.4 percent by weight of sulfonate soap to the lubricant composition. Alternative amounts of the sulfonate soap may be 0.5 to 5 weight percent, 0.6 to 3 weight percent, and 0.65 to 2 weight percent sulfonate soap. (These amounts will correspond to approximately the same amounts of sulfonate anion.) The sulfonate soap may also be said to correspond to the total amount of the detergent (on an active chemical basis, without conventional diluents oil) and minus the amount of metal carbonate or other metal salts, but including the amount of metal cation associated with the anion. An alternative approach would also be to also subtract the amount of metal cation associated with the anion. As an example of the latter calculation, a calcium carbonate overbased sulfonate detergent may be available at 53% actives with 47% diluent oil. The overall material may contain 42% sulfonate anion and 4.8% calcium, present predominantly as Ca(CO3)2, as well as the calcium counterion associated with the sulfonate anion. The anion may have a molecular weight of around 600 (being derived from a sulfonic acid having a molecular weight of also around 600, plus the weight of a single acidic proton). Thus if 5 percent by weight of the oil diluted detergent is used, it will supply 2.1 weight percent sulfonate anion. Therefore, if the amount is expressed in terms of sulfonate anion, suitable amounts thereof may include 0.2 or 0.3 or 0.4 or 0.5 to 5 weight percent, 0.6 to 3 weight percent, and 0.65 to 2 weight percent. The present technology may thus provide to 0.8 to 8 percent by weight or 1.2 to 6 percent or 2 to 4 percent of an overbased detergent (oil free basis) in the lubricant, depending on the amount of carbonate salt present, to supply the corresponding amounts of sulfonate soap.
The amount of sulfonate soap or soaps will be at least a significant fraction of the amount of phenate soap or soaps and in some embodiments will exceed the amount of the phenate soap(s), on a weight basis. The weight ratio of sulfonate soap : phenate soap will be at least 0,35:1 or at least 0.5:1 or at least 0.7:1 and may be at least 0.75:1 or 1:1 or 1.2:1. The upper limit of this ratio may be unbounded if there is no phenate detergent present, but if relatively minor amounts are present, upper ratios may be 500:1 or 100:1 or 30:1 or 10:1 or 3:1 or 1.5:1. In one embodiment, the amount of the sulfonate soap is at least 0.4 percent by weight and the weight ratio of sulfonate soap to phenate soap is at least 0.7:1.
In certain embodiments, the total amount of detergents of all types of anions in the lubricant composition (including carbonate component but excluding diluent oil) may be at least 0.5%, or at least 1%, or 1 to 8%, or 1.2 to 5%, or 1.5 to 3%. The detergent or detergents may also be presented in the form of a concentrate for subsequent addition to base oil to form a final lubricant product. In such a concentrate, the amount of detergent will be correspondingly increased, such as 1 to 50 percent or 10 to 30 percent by weight.
Other detergents than sulfonate detergents may optionally also be present in the lubricant, subject to the limitations described above on the amount of phenate detergent. Examples include phenates, salicylates, saligenins, and salixarates, as well as other known types of detergents, e.g., glyoxylates, phosphonates, carboxylates.
The phenols useful in making phenate detergents can be represented by the formula (R1)a—Ar—(OH)b, wherein R1 is an aliphatic hydrocarbyl group of 4 to 400 carbon atoms, or 6 to 80 or 6 to 30 or 8 to 25 or 8 to 15 carbon atoms; Ar is an aromatic group (which can be a benzene group or another aromatic group such as naphthalene); a and b are independently numbers of at least one, the sum of a and b being in the range of two up to the number of displaceable hydrogens on the aromatic nucleus or nuclei of Ar. In one embodiment, a and b are independently numbers in the range of 1 to 4, or 1 to 2. R1 and a are typically such that there is an average of at least 8 aliphatic carbon atoms provided by the R1 groups for each phenol compound. Phenate detergents are also sometimes provided as sulfur-bridged species.
Salicylate detergents may be an alkali metal salt or an alkaline earth metal salt of an alkylsalicylic acid. The salicylic acids may be hydrocarbyl-substituted salicylic acids wherein each substituent contains an average of at least 8 carbon atoms per substituent and 1 to 3 substituents per molecule. The substituents can be polyalkene substituents, where polyalkenes include homopolymers and interpolymers of polymerizable olefin monomers of 2 to 16, or 2 to 6, or 2 to 4 carbon atoms. The olefins may be monoolefins such as ethylene, propylene. 1-butene, isobutene, and 1-octene; or a polyolefinic monomer, such as diolefinic monomer, such 1,3-butadiene and isoprene. In one embodiment, the hydrocarbyl substituent group or groups on the salicylic acid contains 7 to 300 carbon atoms and can be an alkyl group having a molecular weight of 150 to 2000. The polyalkenes and polyalkyl groups (i.e., (polyalkylene)yl groups) are prepared by conventional procedures, and substitution of such groups onto salicylic acid can be effected by known methods. Alkyl salicylates may be prepared from an alkylphenol by Kolbe-Schmitt reaction: alternatively, calcium salicylate can be produced by direct neutralization of alkylphenol and subsequent carbonation. Overbased salicylate detergents and their methods of preparation are disclosed in U.S. Pat. Nos. 4,719,023 and 3,372,116.
Saligenin detergents are commonly overbased magnesium salts which are based on saligenin derivatives. A general example of such a saligenin derivative can be represented by the formula
wherein X is —CHO or —CH2OH, Y is —CH2— or —CH2OCH2—, wherein such —CHO groups typically comprise at least 10 mole percent of the X and Y groups; M represents hydrogen, ammonium, or a metal ion, R1 is a hydrocarbyl group of 1 to 60 carbon atoms, in is 0 to typically 10, and each p is independently 0, 1, 2, or 3. At least one aromatic ring contains an R1 substituent and the total number of carbon atoms in all R1 groups is at least 7. When m is 1 or greater, one of the X groups can be hydrogen. Saligenin detergents are disclosed in greater detail in U.S. Pat. No. 6,310,009.
Salixarate detergents include overbased materials prepared from salicylic acid (which may be unsubstituted) and a hydrocarbyl-substituted phenol, such entities being linked through —CH2— or other alkylene bridges. It is believed that the salixarate derivatives have a predominantly linear, rather than macrocyclic, structure, although both structures are intended to be encompassed by the term “salixarate.” Salixarate derivatives and methods of their preparation are described in greater detail in U.S. Pat. No. 6,200,936 and PCT Publication WO 01/56968.
The sulfonate detergent may be supplied to the lubricant of an engine in a variety of ways. In one embodiment, the sulfonate detergent is added to a concentrate of other lubricant additives that is then blended into a finished lubricant. In another embodiment, the sulfonate detergent is added, as a top-treat, to a finished lubricant containing other lubricant additives. In both of the foregoing methods, the detergent is added directly to the lubricant and is typically present in the lubricant from the beginning of its actual use as a lubricant. That is, in such methods it is not added to the lubricant during the course of the use of the lubricant. However, in yet another embodiment, the sulfonate metal detergent is added to the lubricant in a controlled or slow release method which may be during the course of the use of the lubricant.
The sulfonate detergent (which may be, e.g., an alkali metal detergent or an alkaline earth metal detergent) can thus he part of a slow release lubricant additive package in the form of a lubricant additive gel which is formulated to meet the performance requirements of the system, whereby the slow release of the component of the gelled lubricant additive conditions the fluid. Gels are materials that comprise mixtures of two or more substances and which exist in a semi-solid state more like a solid than a liquid. See, for instance, Parker, “Dictionary of Scientific and Technical Terms,” Fifth Edition, McGraw Hill, 1994, and, Larson, “The Structure and Rheology of Complex Fluids,” Chapter 5, Oxford University Press, New York, N.Y., 1999.
A category of gels suitable for use in accordance with the present invention are those in which gelation occurs through the combination of an overbased detergent and an ashless succinimide dispersant. Examples of this method of supplying an additive to lubricating oil in such a manner can be found in U.S. Pat. Nos. 6,843,916 and 7,000,655 as well as U.S. Patent Application 2005-0085399.
Another means of supplying the sulfonate detergent to the lubricant is by addition thereof to the fuel used to operate an engine, whence it may migrate or leak or be carried into the lubricant system. The detergent may be added to the bulk fuel as part of a concentrate used to provide a finished formulated fuel or as a top treat Examples of providing a benefit to lubricating oil via a fuel additive can be found in U.S. Patent Applications 20050115146 and 2005-0215441. The fuel additive may be a solid additive composition as described in U.S. Patent Application 20060229215.
In one embodiment, the sulfonate detergent can be added to the fuel via contacting the fuel with a gel comprising the detergent, where the gel is appropriately positioned within the fuel system to permit contact with the fuel. The gel can be added also to the fuel by the fuel supplier at a refinery, terminal, or a refueling station by premixing the gel with the fuel. Alternatively, the vehicle operator can add the gel to the fuel tank by dosing the tank during refueling. The gel additive may be dosed to the fuel using a fuel dosing system that provides a controlled level of the additive to the fuel (storage) tank. Examples of additizing fuel by means of contacting the fuel with a gel comprising a fuel or lubricant additive can be found in U.S. Patent Application 20060272597.
The present lubricant compositions may also contain a dispersant such as a nitrogen-containing dispersant. Dispersants are well known in the field of lubricants and include primarily what is known as ashless dispersants and polymeric dispersants. Ashless dispersants are so-called because, as supplied, they do not contain metal and thus do not normally contribute to sulfated ash when added to a lubricant. However they may, of course, interact with ambient metals once they are added to a lubricant which includes metal-containing species. Ashless dispersants are characterized by a polar group attached to a relatively high molecular weight hydrocarbon chain. Typical ashless dispersants include N-substituted long chain alkenyl succinimides, having a variety of chemical structures including typically
where each R1 is independently an alkyl group, frequently a polyisobutylene group derived from polyisobutylene with a molecular weight of 500-5000, and. R2 are alkylene groups, commonly ethylene (C2H4) groups. Such molecules are commonly derived from reaction of an alkenyl acylating agent with a polyamine, and a wide variety of linkages between the two moieties is possible beside the simple imide structure shown above, including a variety of amides and quaternary ammonium salts. Also, a variety of modes of linkage of the R1 groups onto the imide structure are possible, including various cyclic linkages. The ratio of the carbonyl groups of the acylating agent to the nitrogen atoms of the amine may be 1:0.5 to 1:3, and in other instances 1:1 to 1:2.75 or 1:1.5 to 1:2.5. Succinimide dispersants are more fully described in U.S. Pat. Nos. 4,234,435 and 3,172.892.
Succinimide dispersants employed in the present lubricant composition may be those prepared by the thermal route or by the so-called chlorine route, or mixtures of detergents from both routes. The two types of materials are described in greater detail in US Patent Application 2005-0202981. Briefly, dispersants from the chlorine route are typically prepared by reacting a polymer such as polyisobutylene, less than 20 percent of the chains thereof containing a terminal vinylidene end group, with maleic anhydride in the presence of chlorine and reacting the product with an amine. Typically in such product at least one succinic moiety is attached to the polyisobutene substituent through a cyclic linkage, for instance 85-93 or up to 95 percent or up to 98 percent of such attachments may be cyclic. Dispersants from the thermal “ene” route are typically prepared by reacting a polyisobutylene, at least 70 percent of the chains thereof containing a terminal vinylidene end group, with maleic anhydride in the substantial absence of chlorine and reacting the product with an amine. Typically in such product at least one succinic anhydride moiety is attached to the polyisobutene substituent through a non-cyclic linkage, and, for instance, at least 90 percent or 95 percent or 98 percent of such attachments may be non-cyclic. It is also believed that the product from the chlorine reaction may contain a certain percentage of internal succinic functionality, that is along the backbone of the polymer chain, while such internal succinic functionality is believed to be substantially absent from the thermal “ene” material.
Another class of ashless dispersant is high molecular weight esters. These materials are similar to the above-described succinimides except that they may be seen as having been prepared by reaction of a hydrocarbyl acylating agent and a polyhydric aliphatic alcohol such as glycerol, pentaerythritol, or sorbitol. Such materials are described in more detail in U.S. Pat. No. 3,381,022.
Another class of ashless dispersant is Mannich dispersants. These are materials which are formed by the condensation of a higher molecular weight, alkyl substituted phenol, an alkylene polyamine, and an aldehyde such as formaldehyde, Such materials may have the general structure
(including a variety of isomers and the like) and are described in more detail in U.S. Pat. No. 3,634,515.
Other dispersants include polymeric dispersant additives, which are generally hydrocarbon-based polymers which contain polar functionality to impart dispersancy characteristics to the polymer.
Dispersants can also be post-treated by reaction with any of a variety of agents. Among these are urea, thiourea, dimercaptothiadiazoles, carbon disulfide, aldehydes, ketones, carboxylic acids, hydrocarbon-substituted succinic anhydrides, nitriles, epoxides, boron compounds, and phosphorus compounds. References detailing such treatment are listed in U.S. Pat. No. 4,654,403.
The amount of dispersant, if present in the lubricant, may be 1 to 10 weight percent or 2 to 8 or 4 to 7 weight percent, or correspondingly larger amounts if presented as a concentrate. In certain embodiments the amount of thermal “ene” dispersant in the lubricant is at least 2 or at least 3 percent by weight.
The lubricant may also contain other additives that are known for use in engine lubricants. The lubricant may thus contain a metal salt of a phosphorus acid. Metal salts of the formula
Ξ(R8O)(R9O)P(═S)—S]n-M
where R8 and R9 are independently hydrocarbyl groups containing 3 to 30 carbon atoms, are readily obtainable by heating phosphorus pentasulfide (P2S5) and an alcohol or phenol to form an O,O-dihydrocarbyl phosphorodithioic acid. The alcohol which reacts to provide the R8 and R9 groups may be a mixture of alcohols, for instance, a mixture of isopropanol and 4-methyl-2-pentanol, and in some embodiments a primary alcohol, a secondary alcohol, or a mixture of a secondary alcohol and a primary alcohol, such as isopropanol and 2-ethylhexanol. The resulting acid may be reacted with a basic metal compound to form the salt. The metal M, having a valence n, generally is aluminum, lead, tin, manganese, cobalt, nickel, zinc, or copper, and in many cases, zinc, to form zinc dialkyldithiophosphates. Such materials are well known and readily available to those skilled in the art of lubricant formulation.
The lubricant may also contain a viscosity modifier. Most modern engine lubricants are multigrade lubricants which contain viscosity index improvers to provide suitable viscosity at both low and high temperatures. While the viscosity modifier is sometimes considered a part of the base oil, it is more properly considered as a separate component, the selection of which is within the abilities of the person skilled in the art.
Viscosity modifiers generally are polymeric materials characterized as being hydrocarbon-based polymers generally having number average molecular weights between 25,000 and 500,000, e.g., between 50,000 and 200,000.
Hydrocarbon polymers can be used as viscosity index improvers. Examples include homopolymers and copolymers of two or more monomers of C2 to C30, e.g., C2 to C8 olefins, including both alpha olefins and internal olefins, which may be straight or branched, aliphatic, aromatic, alkyl-aromatic, or cycloaliphatic. Examples include ethylene-propylene copolymers, generally referred to as OCP's, prepared by copolymerizing ethylene and propylene by known processes.
Hydrogenated styrene-conjugated diene copolymers are another class of viscosity modifiers. These polymers include polymers which are hydrogenated or partially hydrogenated homopolymers, and also include random, tapered, star, and block interpolymers. The term “styrene” includes various substituted styrenes. The conjugated diene may contain four to six carbon atoms and may include, e.g., piperylene, 2,3-dimethyl-1,3-butadiene, chloroprene, isoprene, and 1,3-butadiene. Mixtures of such conjugated dienes are useful. The styrene content of these copolymers may be 20% to 70% by weight or 40% to 60%, and the aliphatic conjugated diene content may be 30% to 80% or 40% to 60%. These copolymers can be prepared by methods well known in the art and are typically hydrogenated to remove a substantial portion of their olefinic double bonds.
Esters obtained by copolymerizing styrene and maleic anhydride in the presence of a free radical initiator and thereafter esterifying the copolymer with a mixture of C4-18 alcohols also are useful as viscosity modifying additives in motor oils, Likewise, polymethacrylates (PMA) are used as viscosity modifiers. These materials are typically prepared from mixtures of methacrylate monomers having different alkyl groups, which may be either straight chain or branched chain groups containing 1 to 18 carbon atoms.
When a small amount of a nitrogen-containing monomer is copolymerized with alkyl methacrylates, dispersancy properties are incorporated into the product. Thus, such a product has the multiple function of viscosity modification, pour point depressancy and dispersancy and are sometimes referred to as dispersant-viscosity modifiers. Vinyl pyridine, N-vinyl pyrrolidone and N,N dimethylaminoethyl methacrylate are examples of nitrogen-containing monomers. Polyacrylates obtained from the polymerization or copolymerization of one or more alkyl acrylates also are useful as viscosity modifiers. Dispersant viscosity modifiers may also be interpolymers of ethylene and propylene which are grafted with an active monomer such as maleic anhydride and then derivatized with an alcohol or an amine or grafted with nitrogen compounds.
The lubricant may also comprise an antioxidant. Antioxidants encompass phenolic antioxidants, which may be of the general the formula
wherein R4 is an alkyl group containing 1 to 24, or 4 to 18, carbon atoms and a is an integer of 1 to 5 or I to 3, or 2. The phenol may be a butyl substituted phenol containing 2 or 3 t-butyl groups, such as
The para position may also be occupied by a hydrocarbyl group or a group bridging two aromatic rings. In certain embodiments the para position is occupied by an ester-containing group, such as, for example, an antioxidant of the formula
wherein R3 is a hydrocarbyl group such as an alkyl group containing, e.g., 1 to 18 or 2 to 12 or 2 to 8 or 2 to 6 carbon atoms; and t-alkyl can be t-butyl. Such antioxidants are described in greater detail in U.S. Pat. No. 6,559,105.
Antioxidants also include aromatic amines, such as those of the formula
wherein R5 can be an aromatic group such as a phenyl group, a naphthyl group, or a phenyl group substituted by R7, and R6 and R7 can be independently a hydrogen or an alkyl group containing 1 to 24 or 4 to 20 or 6 to 12 carbon atoms. In one embodiment, an aromatic amine antioxidant can comprise an alkylated diphenylamine such as nonylated diphenylamine of the formula
or a mixture of a di-nonyl amine and a mono-nonyl amine.
Antioxidants also include sulfurized olefins such as mono-, or disulfides or mixtures thereof. These materials generally have sulfide linkages having 1 to 10 sulfur atoms, for instance, 1 to 4, or 1 or 2. Materials which can be sulfurized to form the sulfurized organic compositions of the present invention include oils, fatty acids and esters, olefins and polyolefins made thereof, terpenes, or Diels-Alder adducts. Details of methods of preparing some such sulfurized materials can be found in U.S. Pat. Nos. 3,471,404 and 4,191,659.
Molybdenum compounds can also serve as antioxidants, and these materials can also serve in various other functions, such as friction modifiers and antiwear agents. The use of molybdenum and sulfur containing compositions in lubricating oil compositions as antiwear agents and antioxidants is known. U.S. Pat. No. 4,285,822, for instance, discloses lubricating oil compositions containing a molybdenum and sulfur containing composition prepared by (1) combining a polar solvent, an acidic molybdenum compound and an oil-soluble basic nitrogen compound to form a molybdenum-containing complex and (2) contacting the complex with carbon disulfide to form the molybdenum and sulfur containing composition.
Typical amounts of antioxidants will, of course, depend on the specific antioxidant and its individual effectiveness, but illustrative total amounts can be 0.01 to 5 percent by weight or 0.15 to 4.5 percent or 0.2 to 4 percent.
Titanium compounds of various types may also be present, and they may serve as deposit control agents and filterability improvers as well as antioxidants. Examples of titanium compounds in lubricants, and their preparation, are described in greater detail in U.S. patent publication 2006-01217271, Sep. 28, 2006. Examples of titanium compounds include titanium (IV) alkoxides such as titanium methoxide, titanium ethoxide, titanium propoxide, titanium isopropoxide, titanium butoxide; and other titanium compounds or complexes including titanium phenates; titanium carboxylates such as titanium (IV) 2-ethyl-1.3-hexanedioate or titanium citrate or titanium oleate; titanium (IV) 2-ethylhexoxide; and titanium (IV) (triethanolaminato)-isopropoxide. Other forms of titanium include the reaction product of titanium compounds with various acid materials to form salts, especially oil-soluble salts. In another embodiment, the titanium can be supplied as a Ti-modified dispersant, such as a succinimide dispersant. Such materials may be prepared by forming a titanium mixed anhydride between a titanium alkoxide and a hydrocarbyl-substituted succinic anhydride, such as an alkenyl- (or alkyl) succinic anhydride. In another embodiment, the titanium can be supplied as a tolyltriazole oligomer salted with and/or chelated to titanium. Other forms of titanium can also be provided, such as surface-modified titanium dioxide nanoparticles. The amount of titanium present in the lubricant may typically be 1 to 1000 parts per million by weight (ppm), alternatively 10 to 500 ppm or 10 to 150 ppm or 20 to 500 ppm or 20 to 300 ppm or 30 to 100 ppm or, again, alternatively, 50 to 500 ppm.
The lubricants may also include antiwear agents other than or in addition to those materials mentioned above that may have antiwear properties. Examples of anti-wear agents include phosphorus-containing antiwear/extreme pressure agents such as phosphorus acids, metal thiophosphates, phosphoric acid esters and salts thereof, phosphorus-containing carboxylic acids, esters, ethers, and amides; and phosphites. The phosphorus acids include phosphoric, phosphonic, phosphinic, and thiophosphoric acids including dithiophosphoric acid as well as monothiophosphoric acids, thiophosphinic acids, and thiophosphonic acids. Non-phosphorus-containing anti-wear agents include borated esters, molybdenum-containing compounds (already described), and sulfurized olefins.
Other additives that may optionally be used in the lubricating oils of this invention include pour point depressing agents, extreme pressure agents, anti-wear agents, color stabilizers and anti-foam agents.
The lubricant may also contain a certain amount of the fatty esters described above as biodiesel fuels. These may or may not be intentionally included in the lubricant composition, but, as discussed above, lubricants in diesel engines burning biodiesel-containing fuels will typically accumulate a certain amount of the esters in the sump along with the rest of the lubricant, The lubricants of the present invention, containing the alkali metal detergent, show superior performance when the lubricant contains the long chain ester, compared to the same lubricants without the alkali metal detergent.
Fully formulated lubricant samples are prepared containing conventional components as well as certain sulfonate, phenate, and/or salixarate detergents, as reported in the Table below. Each lubricant is prepared in a mineral base oil containing a viscosity modifier to provide a 5W-40 viscosity grade. Each also contains (on an oil free basis) 0.9% antioxidants. 0.8% zinc dialkyldithio-phosphates, 3.2% succinimide dispersant, and a trace of antifoam agent.
The lubricants are subjected to a biodiesel oil oxidation and deposit test. This test simulates oxidation of engine oils in the presence of fuel dilution by biodiesel fuel, in this case 100% rapeseed methyl ester. A 100 mL sample of the lubricant is additized with 75 ppm iron naphthenate and with 5 mL of the biodiesel fuel and placed into a glass tube with an air inlet. The tube is immersed in a bath at 170° C. and air is blown through the tube at 5 L/hr. Samples, 10 mL, are removed for viscosity analysis (100° C.) at 72, 96, 120, 144, and 168 hours. The time required for the viscosity of the sample to reach 60 mm2/s (cSt) is estimated by interpolation from the measured values and is set as the time for the oil to fail. Longer times represent improved stability of the sample. Also reported are the measured viscosities at 72, 96, and 120 hours (lower values are better).
The results show that increasing sulfonate soap level leads to improved performance. Lower amount of phenate soap also correlates with improved performance.
As used herein, the term “hydrocarbyl substituent” or “hydrocarbyl group” is used in its ordinary sense, which is well-known to those skilled in the art. Specifically, it refers to a group having a carbon atom directly attached to the remainder of the molecule and having predominantly hydrocarbon character. Examples of hydrocarbyl groups include:
hydrocarbon substituents, that is, aliphatic (e.g., alkyl or alkenyl), alicyclic (e.g., cycloalkyl, cycloalkenyl) substituents, and aromatic-, aliphatic-, and alicyclic-substituted aromatic substituents, as well as cyclic substituents wherein the ring is completed through another portion of the molecule (e.g., two substituents together form a ring);
substituted hydrocarbon substituents, that is, substituents containing non-hydrocarbon groups which, in the context of this invention, do not alter the predominantly hydrocarbon nature of the substituent (e.g., halo (especially chloro and fluoro), hydroxy, alkoxy, mercapto, alkylmercapto, nitro, nitroso, and sulfoxy);
hetero substituents, that is, substituents which, while having a predominantly hydrocarbon character, in the context of this invention, contain atoms other than carbon in a ring or chain otherwise composed of carbon atoms. Heteroatoms include sulfur, oxygen, nitrogen, and encompass substituents as pyridyl, furyl, thienyl and imidazolyl. In general, no more than two, or no more than one, non-hydrocarbon substituent will be present for every ten carbon atoms in the hydrocarbyl group; typically, there will be no non-hydrocarbon substituents in the hydrocarbyl group.
It is known that some of the materials described above may interact in the final formulation, so that the components of the final formulation may be different from those that are initially added. For instance, metal ions (of, e.g., a detergent) can migrate to other acidic or anionic sites of other molecules. The products formed thereby, including the products formed upon employing the composition of the present invention in its intended use, may not be susceptible of easy description. Nevertheless, all such modifications and reaction products are included within the scope of the present invention; the present invention encompasses the composition prepared by admixing the components described above.
Each of the documents referred to above is incorporated herein by reference. The mention of any document is not an admission that such document qualifies as prior art or constitutes the general knowledge of the skilled person in any jurisdiction. Except in the Examples, or where otherwise explicitly indicated, all numerical quantities in this description specifying amounts of materials, reaction conditions, molecular weights, number of carbon atoms, and the like, are to be understood as modified by the word “about.” Unless otherwise indicated, each chemical or composition referred to herein should be interpreted as being a commercial grade material which may contain the isomers, by-products, derivatives, and other such materials which are normally understood to be present in the commercial grade. However, the amount of each chemical component is presented exclusive of any solvent or diluent oil, which may be customarily present in the commercial material, unless otherwise indicated. It is to be understood that the upper and lower amount, range, and ratio limits set forth herein may be independently combined. Similarly, the ranges and amounts for each element of the invention can be used together with ranges or amounts for any of the other elements. As used herein, the expression “consisting essentially of permits the inclusion of substances that do not materially affect the basic and novel characteristics of the composition under consideration.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US10/39401 | 6/22/2010 | WO | 00 | 3/27/2012 |
| Number | Date | Country | |
|---|---|---|---|
| 61220626 | Jun 2009 | US |
