Patent Application
20220127539
The disclosed technology relates to a traction fluid containing a base fluid having at least one of cedrene, cedrol, thujopsene or mixtures thereof, preferably provided from cedar oil, as well as a method of lubricating a power transmission apparatus, especially an automotive traction drive, with the traction fluid.
Traction drives are devices in which power or torque is transmitted from an input element to an output element through nominal point or line contact, typically with a rolling action, by virtue of the traction between the contacting elements. Traction drives can be generally used in automotive or industrial machinery for transmitting power between rotating members. They can be used as automatic transmissions and are particularly suitable as a form of continuously variable automatic transmission for use in automobile drivetrains and other applications.
While the working elements of a traction drive are sometimes spoken of as being in contact, it is generally accepted that a fluid film must be provided therebetween. Thus, rather than metal-to-metal rolling contact, a film of fluid is introduced into the load zone, and power is transmitted by shearing of the film, which may become very viscous due to the high pressure at the contact area. The nature and properties of the fluid, therefore, will determine to a large extent the performance and capacity of the traction drive. Traction fluids will preferably have a high shear resistance (often measured as “traction coefficient”) to maximize the power transmission performance. Low viscosity, particularly at low temperatures, is also desirable for efficient operation under cold conditions. The fluid should ideally also exhibit good lubricating properties for and compatibility with other components of the traction drive. Such fluids also serve to remove heat and prevent wear at the contact surfaces and to lubricate bearings and other moving parts associated with the drive.
Traction fluids based on a variety of base fluids are known. For example, U.S. Pat. No. 5,043,497, Muraki et al., Aug. 27, 1991, discloses a lubricating oil for a traction drive, mainly composed of a naphthenic hydrocarbon.
U.S. Pat. No. 3,975,278, Wygant, Aug. 17, 1976, discloses hydrogenated dimers of α-alkyl styrene, which are useful as traction fluids.
U.S. Pat. No. 3,966,624, Duling et al., Jun. 29, 1976, discloses a blended traction fluid containing hydrogenated polyolefin and an adamantane ether.
U.S. Pat. No. 9,156,751, Sekiguchi et al., Oct. 10, 2015, discloses a lubricating composition containing at least 5 mass % longifolene that could be used in a traction drive type continuously variable transmission.
U.S. Pat. No. 7,045,488, Bartley et al., May 16, 2006, discloses a lubricating composition containing a saturated alicyclic hydrocarbon composition comprising molecules containing about 13 to about 33 carbon atoms and containing a ring having at least two geminal methyl groups.
U.S. Pat. No. 8,338,653 to Sekiguchi et al., Dec. 25, 2012 and U.S. Pat. No. 7,402,715 to Yoshida et al., Jul. 22, 2008, both teach fluids containing bicyclo[2.2.1]heptane dimers.
Finding chemistry that combines the required high traction performance (i.e. >0.07 as measured on a mini traction machine) with good low temperature viscometrics, such as a −30° C. Brookfield vis of <20,000 cP is challenging. In addition, suitable candidates must be available and possess reasonable economics. Several commercial traction fluid additives now suffer from poor availability and high cost, or require time consuming purification steps such as distillation, or use tedious processing such as catalytic hydrogenation.
The present invention provides an economical traction fluid or traction fluid component with good traction coefficient and viscometrics. The component can also be used in hydraulic fluids including farm tractor hydraulic fluid, automatic transmission fluid, fluids for push-belt and chain-type continuously variable transmission, and dual clutch transmissions.
The disclosed technology, therefore, solves the problem of lack of reasonably available working traction fluid components by providing a traction fluid containing a base fluid of cedar oil or a major constituent thereof.
In some embodiments, the base fluid can also include a polyolefin polymer and/or a predominantly linear hydrogenated dimer of alpha-alkylstyrene. In an embodiment, the cedar oil comprises at least one of cedrene, cedrol, thujopsene or mixtures thereof. In an embodiment, the traction fluid comprises less than 5 wt. % longifolene.
In another aspect, the technology encompasses a traction fluid containing (A) a base fluid of cedar oil or a major constituent thereof, and (B) at least one lubricant additive for a power transmission apparatus.
The additive package for a power transmission apparatus can include a low-temperature viscosity control agent, such as, a naphthenic oil, a synthetic ester oil, a polyether oil, or mixtures thereof.
The additive package for a power transmission apparatus can include a viscosity modifier, such as, a polymeric viscosity index modifier.
The additive package for a power transmission apparatus can include a dispersant, such as, a succinimide dispersant.
The additive package for a power transmission apparatus can include a detergent, such as, an overbased sulfonate detergent.
The additive package for a power transmission apparatus can include an anti-wear agent, such as, phosphorus-containing acid, salt, or ester thereof.
Another aspect of the technology encompasses a method of lubricating a power transmission apparatus. The method includes employing in the power transmission apparatus a traction fluid as described herein, and operating the power transmission apparatus.
Various preferred features and embodiments will be described below by way of non-limiting illustration.
One aspect of the present technology includes a traction fluid of a base fluid containing cedar oil or a major constituent thereof, and at least one lubricant additive for a power transmission apparatus.
The base fluid will be present in the traction fluid in a “major amount,” meaning at least 50 percent by weight of the traction fluid, that is, 50 to 100 wt %. Preferably the base fluid comprises 70 to 95 percent by weight of the traction fluid, more preferably 75 to 90 percent by weight, and still more preferably 80 to 85 percent by weight.
Cedar oil refers to the oil extracted from a cedar tree, such as its needles, berries, bark or wood. The oil may be extracted, for example, by distillation, such as steam distillation, or in some cases by solvent extraction.
Common types of cedar from which cedar oil may be sourced can include, for example, Cedrus atlantica (also known as Atlas cedar, Atlantic cedar, Moroccan cedar, Lebanon cedar), Cedrus deodara (also known as Himalayan cedar, Deodar cedar), Chamaecyparis lawsoniana (also known as Port Orford cedar, Rose of cedar, Oregon cedar, Lawson's cypress, ginger pine, Port-Orford white cedar, Port-Orford cypress), Chamaecyparis funebris (also known as Chinese cedar, Chinese weeping cypress, Chinese swamp cypress, mourning cypress), Juniperus virginiana (also known as Virginian cedar, Red cedar, eastern red cedar, Virginian juniper, eastern juniper, red juniper, pencil cedar, aromatic cedar), Juniperus ashei (also known as Texas cedar, Mexican cedar, ashe juniper, Ozark white cedar, Mexican juniper, mountain cedar, post cedar, rock cedar), Thuja plicata (also known as Western red cedar, Pacific thuja, canoe cedar, giant cedar, giant arbor-vitae, Pacific red cedar, shinglewood, western arborvitae), Thuja occidentalis (also known as Eastern white cedar, Thuja, arbor-vitae, cedar leaf, white cedar, easter arborvitae, swamp cedar).
Cedar oil can be a mixture of many different hydrocarbons, depending on the species of cedar from which the oil is extracted. Common hydrocarbons contained in some species of cedar oil include, for example, cedrene (in the form of α-cedrene, iso-α-cedrene, and/or β-cedrene), thujopsene, and cedrol.
While cedar oil is the predominant source of cedrene, thujopsene, and cedrol, and in many circumstances the traction fluid will contain cedar oil, of which cedrene, cedrol, thujopsene or mixtures thereof will be constituents, it is anticipated that the traction fluid may contain cedrene, cedrol, thujopsene or mixtures thereof from other sources. By “cedar oil or a major constituent thereof,” it is meant that the base fluid of the traction fluid can contain at least one of cedar oil, cedrene, cedrol, thujopsene, or mixture thereof. In the case that the cedrene, cedrol, thujopsene or mixtures thereof are obtained from a source other than cedar oil, these constituents can be present individually at the “major amounts” mentioned above for the base fluid, or as mixtures according to the percentages listed for the mixtures below.
For example, in one embodiment, the traction fluid can contain a major amount of cedrene, or a major amount of cedrol, or a major amount of thujopsene, whereas in another embodiment, the traction fluid can contain a major amount of a mixture containing 10 to 50 wt % cedrene (α, iso-α and β combined), 10 to 25 wt % cedrol and 20 to 50 wt % thujopsene, or as further elaborated below.
The level of cedrene (from a combination of α-cedrene, iso-α-cedrene and β-cedrene) in a base fluid mixture (generally from cedar oil) can be from about 10 to about 50 wt % of the base fluid, or from about 2 to 32, or from about 12 to 16 wt % of the base fluid, or from about 20 to 38 wt %, or from about 28 to 48 wt % of the base fluid. As individual cedrene components, the level of α-cedrene in a base fluid mixture (generally from cedar oil) can be from about 2 to 40 wt % of the base fluid, or from about 4 to 20 wt %, or from 6 to 14 wt % or from about 20 to 40 wt %, or from about 20 to 32 wt % of the base fluid. The level of β-cedrene in a base fluid mixture (generally from cedar oil) can be from about 5 to 10 or 5 to 9 or 5 to 8 wt % of the base fluid. In some embodiments, the base fluid can be substantially free of or free of β-cedrene. The level of iso-α-cedrene in a base fluid mixture (generally from cedar oil) can be from about 2 to 40 wt % of the base fluid, or from about 12 to 16 wt %, or from about 20 to 40 wt %, or from about 20 to 32 wt % of the base fluid. In some embodiments, the base fluid can be substantially free of or free of iso-α-cedrene. The level of cedrol in a base fluid mixture (generally from cedar oil) can be from about 10 to 25 wt % of the base fluid, or from about 12 to 20 wt % of the base fluid. In some embodiments, the base fluid can be substantially free of or free of cedrol. The level of thujopsene in a base fluid mixture (generally from cedar oil) can be from about 20 to 50 wt %, or 25 to 48, or 20 to 25 wt %. In some embodiments, the base fluid can be substantially free of, or free of thujopsene.
In an embodiment, the cedar oil used as the base fluid can include from about 28 to 36 wt %, or 30 to 34 wt % iso-α-cedrene, from about 1 to 3 wt %, or 1.5 to 2.5 wt % α-cedrene, and from about 20 to 23 wt %, or 21 to 22 wt % thujopsene. In some embodiments, the cedar oil can include from about 10 to 22 wt %, or 12 to 20 wt % cedrol, from about 20 to 32 wt %, or 21 to 31 wt % α-cedrene, from about 0 (i.e., may be substantially free or free of) or 0.5 to 8 wt %, or 0 (i.e., may be substantially free or free of) or 0.5 to 6 wt % β-cedrene, and from about 20 to 50 wt %, or 22 to 48 wt % thujopsene. In some embodiments, the cedar oil can include from about 10 to 24 wt %, or 12 to 23 wt % cedrol, from about 20 to 40 wt %, or 21 to 39 wt % α-cedrene, from about 6 to 12 wt %, or 8 to 10 wt % β-cedrene, and from about 20 to 25 wt %, or 21 to 24 wt % thujopsene.
Some species of cedar oil can also include longifolene. In some embodiments, the traction fluid will contain less than 5 wt % longifolene or less than 4.99 wt %, or less than 4.98 wt % or less than 4.95 wt % longifolene, such as from about 0.01 to 4.99 or 5 wt %, or from 0.1 to 4.95 wt % longifolene. In some embodiments, the traction fluid can be substantially free of or free of longifolene.
A portion of the cedar oil in the base fluid, from 15 to 85 wt % in some instances, or from 25 to 75 wt % in other instances, can be substituted with either or both of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, and (2) hydrocarbon molecules containing non-aromatic cyclic moieties. That is, the base fluid can include 15 to 85 wt % cedar oil (or its constituents) and from 15 to 85 wt % of at least one of a base fluid of Type (1), Type (2), or a combination thereof.
Suitable base fluids of type (1) include polymers of branched olefins (i.e., polyolefin polymers), preferably isobutylene, particularly those having a number average molecular weight of 180 to 2000, preferably 100 or 200 to 1000 or to 700 as measured by GPC. The polymer is preferably hydrogenated to remove any residual unsaturation. Such materials and their preparation are well known and are described, for instance, in U.S. Pat. No. 3,966,624, as component A, described particularly in column 12 line 32 through column 16 line 11.
The polyolefin polymer may also be non-hydrogenated and in the form of a “conventional” polyolefin or a “high vinylidene” polyolefin. The difference between a conventional polyolefin and a high vinylidene polyolefin can be illustrated by reference to the production of poly(isobutylene) (“PIB”). In a process for producing conventional PIB (a), isobutylene is polymerized in the presence of AlCl3 to produce a mixture of polymers comprising predominantly trisubstituted olefin (III) and tetrasubstituted olefin (IV) end groups, with only a very small amount (for instance, less than 20 percent) of chains containing a terminal vinylidene group (I). In an alternative process, (b), isobutylene is polymerized in the presence of BF3 catalyst to produce a mixture of polymers comprising predominantly (for instance, at least 70 percent) terminal vinylidene groups, with smaller amounts of tetrasubstituted end groups and other structures. The materials produced in the alternative method, sometimes referred to as “high vinylidene PIB,” are also described in U.S. Pat. No. 6,165,235, Table 1.
Typical examples of a polyolefin include polyisobutylene; polypropylene; polyethylene; a copolymer derived from isobutene and butadiene; a copolymer derived from isobutene and isoprene; or mixtures thereof. The polyisobutylene may have a vinylidene double bond content of 5 to 69%, in a second instance of 50 to 69%, and in a third instance of 50 to 95%.
Suitable base fluids of type (2) include a wide variety of cyclic-containing hydrocarbon molecules. Examples of these include di(cyclohexyl)alkanes, cyclohexyl hydrindans and adamantane compounds, as described in U.S. Pat. No. 3,966,624; esters of cyclohexanol and cylohexanecarboxylic acid, as described in U.S. Pat. No. 4,871,476; decalin, cycohexyldecalin, alkyl-substituted decalin, alkyl-substituted cyclohexyldecalin, and mixtures thereof, as described in U.S. Pat. No. 3,803,037; various materials having two cyclohexane rings linked by a methylene group described in U.S. Pat. No. 5,043,497; various hydrocarbon compounds having a bicyclooctane skeleton described in U.S. Pat. No. 5,422,027; hydrogenated products of dimers, trimers, or tetramers of norbornanes and/or norbornenes described in U.S. Pat. No. 5,126,065; hydrogenated dimers, trimers, or polymers of cyclic monoterpenoid monomers described in U.S. Pat. No. 4,975,215; various ter-cyclohexyl compounds disclosed in U.S. Pat. No. 5,850,745; perhydrofluorene derivatives disclosed in U.S. Pat. No. 4,774,013; and preferably linear dimers of hydrogenated α-alkyl styrene, as described in U.S. Pat. No. 3,975,278. Any of the above materials may be used in a hydrogenated form, to assure the removal of carbon unsaturation; indeed, certain hydrogenated styrene derivatives (or cyclohexane derivatives) are inherently hydrogenated species. However, aromatic cyclic structures such as those derived from styrene may also be present in the base fluid, since aromatic cyclic structures are generally considered to be less deleterious than olefinic unsaturation.
The preferred materials for the base fluid of type (2) are predominantly linear dimers of hydrogenated α-alkyl styrene. These dimers are said to be predominantly linear, in contrast to the cyclic dimers which represent another possible structure. Such preferred materials can be represented by the general structure
wherein each R is an alkyl group of 1 to 4 carbon atoms and C6H11 represents a cyclohexyl group. Such materials and their preparation are described in detail in U.S. Pat. No. 3,975,278. Indeed, the base fluid for the present composition preferably contains a major proportion of compounds represented as shown above.
Representative amounts for the makeup of the base fluid can include, for example, 85 wt % cedar oil with 15 wt % of either type (1) or type (2) base fluids, or 75 wt % cedar oil along with 25 wt % of either type (1) or type (2) base fluids, or even 50 wt % cedar oil along with 50 wt % of either type (1) or type (2) base fluids. In some embodiments, the base fluid can include 85 wt % type (1) with 15 wt % either cedar oil, or 75 wt % type (1) along with 25 wt % of cedar oil, or even 50 wt % type (1) along with 50 wt % of cedar oil. In some embodiments, the base fluid can include 85 wt % type (2) with 15 wt % of cedar oil, or 75 wt % type (2) along with 25 wt % of cedar oil, or even 50 wt % type (2) along with 50 wt % of cedar oil. The base fluid can also include an even split of ⅓ cedar oil, ⅓ type (1) base fluid, and ⅓ type (2) base fluid, or 42.5 wt % cedar oil with 42.5 wt % type (1) base fluid and 15 wt % type (2) base fluid, or 42.5 wt % cedar oil with 42.5 wt % type (2) base fluid and 15 wt % type (1) base fluid, or 42.5 wt % type (2) with 42.5 wt % type (1) base fluid and 15 wt % cedar oil.
The base fluid should preferably have a viscosity of greater than 2.5×10−6 m2/s (2.5 cSt) at 100° C. (ASTM D-445), and more preferably a viscosity of at least 3.0×10−6 m2/s (3.0 cSt) or 3.5×10−6 m2/s (3.5 cSt), typically up to 8.0×10−6 m2/s (8.0 cSt) or 7.0×10−6 m2/s (7.0 cSt) or 6.0×10−6 m2/s (6.0 cSt) at 100° C.
In addition to the base fluid, the traction fluid can contain an additive package which can include at least one lubricant additive for a power transmission apparatus. Such additives can include, for example, low-temperature viscosity control agents, dispersants, detergents, antioxidants, anti-wear agents, friction modifiers or mixtures thereof. The amount of the additive package is preferably up to 20 percent by weight of the traction fluid (that is the additive package may not be present, from 0 to 20), or from 5 to 15 percent by weight.
The low-temperature viscosity control agent (which is to be distinguished from a viscosity index modifier, an optional component described below) is selected from among a variety of materials which are known to be useful for this purpose. The low-temperature viscosity control agent is selected from (a) oligomers or polymers of linear alpha olefins of at least 8 carbon atoms, (b) naphthenic oils, (c) synthetic ester oils, (d) polyether oils, and mixtures thereof. These materials are distinguishable from the base fluids, described above, in that they are generally lower viscosity materials than the base fluid, typically exhibiting a viscosity of up to or less than 2.5×10−6 m2/s (2.5 cSt), preferably 1.5 to 2.5, or 1.8 to 2.3×10−6 m2/s (1.5 to 2.5 or 1.8 to 2.3 cSt) at 100° C. These are also materials which typically retain a measure of mobility at low temperatures (e.g., −40° C.) and can serve to reduce the low temperature viscosity of fluids to which they are added. Materials which are of unduly high viscosity or which do not retain mobility at low temperatures do not effectively serve as low-temperature viscosity control agents. Determination of viscosity and low temperature mobility is well within the abilities of those skilled in the art.
Polymers and oligomers of linear α-olefins are well known items of commerce. A typical commercial material is Ethylflo™ 162, a 2×10−6 m2/s (2 cSt) poly α-olefin product of Ethyl Corporation. Preferred materials are those oligomers or polymers of α-olefins containing 8 to 16 carbon atoms, and preferably 10 to 12 carbon atoms. Such materials do not contain a significant fraction of α-olefin monomers of fewer than 8 carbon atoms, that is, less than 5 percent by weight, preferably less than 1 percent by weight, and more preferably substantially no such monomers. Thus common materials such as ethylene-octene polymers, where the ethylene predominates, are excluded from use as low temperature viscosity modifiers in the materials of the present invention. The description “oligomers or polymers” is used since generally low molecular weight materials are desired, and there is otherwise no clear demarcation between an oligomer and a polymer. Materials as low as dimers (a degree of polymerization of 2) are included. Suitable materials for the present invention typically have a molecular weight range of 100 to 1000, preferably 150 to 600, and most preferably 250 to 500 or 250 to 400.
Naphthenic oils are well known items of commerce, commonly derived from petroleum. Preferred materials are hydrogenated naphthenic oils, which are also well known. Examples include Hydrocal™38, from Calumet Lubricants Company and 40 Pale Oil™ from Diamond Shamrock. Synthetic ester oils suitable for use as low temperature viscosity control agents include esters of polyhydroxy compounds and predominantly monocarboxylic acylating agents; esters of predominantly monohydroxy compounds and polycarboxylic acylating agents; esters of monohydroxy compounds and monocarboxylic acylating agents, and mixtures of the foregoing types. The prefix “poly” in this context indicates at least two hydroxy groups or carboxylic groups, as the case may be. The molecular weight of the esters (as of any of the viscosity control agents) should be sufficiently high that the materials are not objectionably volatile so as to be subject to significant evaporative loss under operating conditions, while retaining the above-described viscosities. Certain synthetic ester oils and their methods of preparation are disclosed in PCT publication WO 91/13133. Synthetic ester oils are available as Emery™ synthetic lubricant basestocks, from Henkel Corporation and as Emkarate™ lubricant basestocks from Imperial Chemical Industries PLC.
Polyether oils suitable for use as low temperature viscosity control agent include polyalkylene oxides, and in particular, polyethylene oxides, polypropylene oxides, polybutylene oxides, and mixtures thereof. The polyether oil will typically have a molecular weight in the ranges suitable for maintaining an appropriate viscosity and non-volatility. Such materials are also well known items of commerce and are available as Emkarox™ polyalkylene glycols from Imperial Chemical Industries PLC.
The low temperature viscosity control agent is often a hydrogenated material. Each of these components will preferably contain fewer than 20%, fewer than 15%, or more preferably fewer than 10% molecules containing carbon-carbon unsaturation, and in the most preferred case will be substantially free from carbon-carbon unsaturation, that is to say, retaining at most a low level of unsaturation which does not measurably or significantly affect its performance.
The amount of the low temperature viscosity control agent in the traction fluid is preferably that amount suitable to provide a viscosity at −30° C. of less than or equal to 20,000 cP, such as less than 15,000 cP, preferably less than 10,000 cP. Otherwise expressed, the amount of low temperature viscosity control agent should preferably 1 to 20 percent by weight of the traction fluid, preferably 3 to 15, and more preferably 5 to 10 percent by weight.
The dispersants useful as a component in the present fluids include acylated amines, carboxylic esters, Mannich reaction products, hydrocarbyl substituted amines, and mixtures thereof.
Acylated amine dispersants include reaction products of one or more carboxylic acylating agent and one or more amine. The carboxylic acylating agents include C8-30 fatty acids, C14-20 isoaliphatic acids, C18-44 dimer acids, addition dicarboxylic acids, trimer acids, addition tricarboxylic acids, and hydrocarbyl substituted carboxylic acylating agents. Dimer acids are described in U.S. Pat. Nos. 2,482,760, 2,482,761, 2,731,481, 2,793,219, 2,964,545, 2,978,468, 3,157,681, and 3,256,304. The addition carboxylic acylating agents are addition (4+2 and 2+2) products of an unsaturated fatty acid with one or more unsaturated carboxylic reagents. These acids are taught in U.S. Pat. No. 2,444,328. In another embodiment, the carboxylic acylating agent is a hydrocarbyl substituted carboxylic acylating agent. The hydrocarbyl substituted carboxylic acylating agents are prepared by a reaction of one or more of olefins or polyalkenes with one or more of unsaturated carboxylic agents, such as itaconic, citraconic, or maleic acylating agents, typically at a temperature of 160°, or 185° C. up to 240° C., or to 210° C. Maleic acylating agents are the preferred unsaturated acylating agent. The procedures for preparing the acylating agents are well known to those skilled in the art and have been described for example in U.S. Pat. No. 3,412,111; and Ben et al, “The Ene Reaction of Maleic Anhydride With Alkenes”, J. C. S. Perkin II (1977), pages 535-537.
The amines which react with the acylating agents may be known amines, preferably a polyamine, such as an alkylenepolyamine or a condensed polyamine. Polyamines can be aliphatic, cycloaliphatic, heterocyclic or aromatic. Examples of the polyamines include alkylene polyamines, hydroxy containing polyamines, arylpolyamines, and heterocyclic polyamines.
Alkylene polyamines are represented by the formula
wherein n has an average value from 1 or 2 to 10, or to 7, or to 5, and the “Alkylene” group has from 1 or 2 to 10, or to 6, or to 4 carbon atoms. Each R is independently hydrogen, or an aliphatic or hydroxy-substituted aliphatic group of up to 30 carbon atoms. Acylated amines, their intermediates and methods for preparing the same are described in U.S. Pat. Nos. 3,219,666; 4,234,435; 4,952,328; 4,938,881; 4,957,649; 4,904,401; and 5,053,152.
In another embodiment, the dispersant can be a carboxylic ester. The carboxylic ester is prepared by reacting at least one or more carboxylic acylating agents, preferably a hydrocarbyl substituted carboxylic acylating agent, with at least one organic hydroxy compound and optionally an amine. The hydroxy compound may be an alcohol or a hydroxy containing amine.
The alcohols may contain non-hydrocarbon substituents of a type which do not interfere with the reaction of the alcohols with the acid (or corresponding acylating agent) to form the ester. In one embodiment, the alcohols can be polyhydric alcohols, such as alkylene polyols. Preferably, such polyhydric alcohols contain from 2 to 40 carbon atoms, more preferably 2 to 20; and from 2 to 10 hydroxyl groups, more preferably 2 to 6. Polyhydric alcohols include ethylene glycols, including di-, tri- and tetraethylene glycols; propylene glycols, including di-, tri- and tetrapropylene glycols; glycerol; butane diol; hexane diol; sorbitol; arabitol; mannitol; cyclohexane diol; erythritol; and pentaerythritols, including di- and tripentaerythritol; preferably, diethylene glycol, triethylene glycol, glycerol, sorbitol, pentaerythritol and dipentaerythritol. Commercially available polyoxyalkylene alcohol demulsifiers can also be employed as the alcohol component.
The carboxylic ester dispersants may be prepared by any of several known methods. The method which is preferred because of convenience and the superior properties of the esters it produces, involves the reaction of the carboxylic acylating agents described above with one or more alcohol or phenol in ratios from 0.5 equivalent to 4 equivalents of hydroxy compound per equivalent of acylating agent. The preparation of useful carboxylic ester dispersant is described in U.S. Pat. Nos. 3,522,179 and 4,234,435.
The carboxylic ester dispersants may be further reacted with at least one of the above described amines and preferably at least one of the above described polyamines, such as a polyethylenepolyamine, condensed polyamine, or a heterocyclic amine, such as aminopropylmorpholine. The amine is added in an amount sufficient to neutralize any non-esterified carboxyl groups. In one embodiment, the carboxylic ester dispersants are prepared by reacting from 1 to 2 equivalents, or from 1.0 to 1.8 equivalents of hydroxy compounds, and up to 0.3 equivalent, or from 0.02 to 0.25 equivalent of polyamine per equivalent of acylating agent. The carboxylic acid acylating agent may be reacted simultaneously with both the hydroxy compound and the amine. There is generally at least 0.01 equivalent of the alcohol and at least 0.01 equivalent of the amine although the total amount of equivalents of the combination should be at least 0.5 equivalent per equivalent of acylating agent. These carboxylic ester dispersant compositions are known in the art, and the preparation of a number of these derivatives is described in, for example, U.S. Pat. Nos. 3,957,854 and 4,234,435.
In another embodiment, the dispersant may also be a hydrocarbyl-substituted amine. These hydrocarbyl-substituted amines are well known to those skilled in the art. These amines and methods for their preparation are disclosed in U.S. Pat. Nos. 3,275,554; 3,438,757; 3,454,555; 3,565,804; 3,755,433; and 3,822,289. Typically, hydrocarbyl substituted amines are prepared by reacting olefins and olefin polymers, including the above polyalkenes and halogenated derivatives thereof, with amines (mono- or polyamines). The amines may be any of the amines described above, preferably an alkylenepolyamine. Examples of hydrocarbyl substituted amines include ethylenepolyamines such as diethylenetriamine; poly(propylene)amine; N,N-dimethyl-N-poly(ethylene/propylene)amine, (50:50 mole ratio of monomers); polybutene amine; N,N-di(hydroxyethyl)-N-polybutene amine; N-(2-hydroxypropyl)-N-polybutene amine; N-polybutene-aniline; N-polybutenemorpholine; N-poly(butene)-ethylenediamine; N-poly(propylene)trimethylenediamine; N-poly(butene)-diethylenetriamine; N′,N″-poly(butene)tetraethylenepentamine; and N,N-dimethyl-N′-poly(propylene)-1,3-propylenediamine.
In another embodiment, the dispersant may also be a Mannich dispersant. Mannich dispersants are generally formed by the reaction of at least one aldehyde, such as formaldehyde and paraformaldehyde, at least one of the above described amines, preferably a polyamine, such as a polyalkylenepolyamine, and at least one alkyl substituted hydroxyaromatic compound. The amounts of the reagents is such that the molar ratio of hydroxyaromatic compound to formaldehyde to amine is in the range from (1:1:1) to (1:3:3). The hydroxyaromatic compound is generally an alkyl substituted hydroxyaromatic compound. This term includes the above described phenols. The hydroxyaromatic compounds are those substituted with at least one, and preferably not more than two, aliphatic or alicyclic groups having from 6 to 400, or from 30 to 300, or from 50 to 200 carbon atoms. These groups may be derived from one or more of the above described olefins or polyalkenes. In one embodiment, the hydroxyaromatic compound is a phenol substituted with an aliphatic or alicyclic hydrocarbon-based group having an
The dispersant can also be a dispersant which has been treated or reacted with any of a variety of common agents. In one embodiment, the boron compound is a borated dispersant. Typically, a borated dispersant contains 0.1% to 5%, or 0.5% to 4%, or 0.7% to 3% by weight boron. In one embodiment, the borated dispersant is a borated acylated amine, such as a borated succinimide dispersant. Borated dispersants are described in U.S. Pat. Nos. 3,000,916; 3,087,936; 3,254,025; 3,282,955; 3,313,727; 3,491,025; 3,533,945; 3,666,662 and 4,925,983. Borated dispersant are prepared by reaction of one or more dispersant with one or more boron compounds such as an alkali or mixed alkali metal and alkaline earth metal borate. These metal borates are generally a hydrated particulate metal borate which are known in the art. Alkali metal borates include mixed alkali and alkaline metal borates. These metal borates are available commercially.
Dispersants can also be treated by or reacted with other agents to produce well-known variants. Such agents include sulfurizing agents such as elemental sulfur or CS2 and dimercaptothiadiazoles. Reactions of dispersants with a dimercaptothiadiazole is taught, for example, in U.S. Pat. No. 4,136,043.
The amount of the dispersant in the traction fluid composition is preferably 1 to 10 weight percent, preferably 1.5 to 7 weight percent, and more preferably 2 to 3 weight percent.
The additive package for the traction fluid can also contain one or more detergents, which are normally salts, and specifically overbased salts. Overbased salts, or 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 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 one. 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 of the present invention have a metal ratio of 1.5, more preferably 3, more preferably 7, up to 40, preferably 25, more preferably 20.
The basicity of the overbased materials of the present invention generally is expressed in terms of a total base number. A total base number is the amount of acid (perchloric or hydrochloric) needed to neutralize all of the overbased material's basicity. The amount of acid is expressed as potassium hydroxide equivalents (mg KOH per gram of sample). Total base number is determined by titration of one gram of overbased material with 0.1 Normal hydrochloric acid solution using bromophenol blue as an indicator. The overbased materials of the present invention generally have a total base number of at least 20, preferably 100, more preferably 200. The overbased materials generally have a total base number up to 600, preferably 500, more preferably 400.
The overbased materials are prepared by reacting an acidic material (typically an inorganic acid or lower carboxylic acid, preferably carbon dioxide) with a mixture comprising an acidic organic compound, a reaction medium comprising at least one inert, organic solvent (such as mineral oil, naphtha, toluene, xylene) for said acidic organic material, a stoichiometric excess of a metal base, and a promoter.
The acidic organic compounds useful in making the overbased compositions of the present invention include carboxylic acids, sulfonic acids, phosphorus-containing acids, phenols or mixtures thereof. Preferably, the acidic organic compounds are carboxylic acids or sulfonic acids with sulfonic and salicylic acids more preferred. Reference to acids, such as carboxylic, or sulfonic acids, is intended to include the acid-producing derivatives thereof such as anhydrides, lower alkyl esters, acyl halides, lactones and mixtures thereof unless otherwise specifically stated.
The carboxylic acids useful in making the overbased salts (A) of the invention can be aliphatic or aromatic, mono- or polycarboxylic acid or acid-producing compounds. These carboxylic acids include lower molecular weight carboxylic acids (e.g., carboxylic acids having up to 22 carbon atoms such as acids having 4 to 22 carbon atoms or tetrapropenyl-substituted succinic anhydride) as well as higher molecular weight carboxylic acids. The carboxylic acids of this invention are preferably oil-soluble. Usually, in order to provide the desired oil-solubility, the number of carbon atoms in the carboxylic acid should be at least 8, more preferably at least 18, more preferably at least 30, more preferably at least 50. Generally, these carboxylic acids do not contain more than 400 carbon atoms per molecule.
The lower molecular weight monocarboxylic acids contemplated for use in this invention include saturated and unsaturated acids. Examples of such useful acids include dodecanoic acid, decanoic acid, oleic acid, stearic acid, linoleic acid, and tall oil acid. Monocarboxylic acids include isoaliphatic acids, often containing a principal chain having from 14 to 20 saturated, aliphatic carbon atoms and at least one but usually no more than four pendant acyclic lower alkyl groups. Specific examples of isoaliphatic acids include 10-methyltetradecanoic acid, 3-ethylhexadecanoic acid, and 8-methyloctadecanoic acid.
High molecular weight carboxylic acids can also be used in the present invention. These acids have a substituent group derived from a polyalkene. The polyalkene is characterized as containing at least 30 carbon atoms, preferably at least 35, more preferably at least 50, and up to 300 carbon atoms, preferably 200, more preferably 150. In one embodiment, the polyalkene is characterized by an
Illustrative carboxylic acids include palmitic acid, stearic acid, myristic acid, oleic acid, linoleic acid, behenic acid, hexatriacontanoic acid, tetrapropylenyl-substituted glutaric acid, polybutenyl-substituted succinic acid derived from a polybutene (
In another embodiment, the carboxylic acids are aromatic carboxylic acids. A group of useful aromatic carboxylic acids are those of the formula
wherein R1 is an aliphatic hydrocarbyl group of preferably 4 to 400 carbon atoms, a is a number of zero to 4, usually 1 or 2, Ar is an aromatic group, each X is independently sulfur or oxygen, preferably oxygen, b is a number of 1 to 4, usually 1 or 2, c is a number of zero to 4, usually 1 to 2, with the proviso that the sum of a, b and c does not exceed the number of valences of Ar. Preferably, R1 and a are such that there is an average of at least 8 aliphatic carbon atoms provided by the R1 groups. Examples of aromatic carboxylic acids include substituted and non-substituted benzoic, phthalic and salicylic acids or anhydrides.
Examples of the aromatic groups that are useful herein include the polyvalent aromatic groups derived from benzene, naphthalene, and anthracene, preferably benzene. Specific examples of Ar groups include phenylenes and naphthylene, e.g., methylphenylenes, ethoxyphenylenes, isopropylphenylenes, hydroxyphenylenes, and dipropoxynaphthylenes.
Within this group of aromatic acids, a useful class of carboxylic acids are those of the formula
wherein R1 is defined above, a is zero to 4, preferably 1 to 2; b is 1 to 4, preferably 1 to 2, c is zero to 4, preferably 1 to 2, and more preferably 1; with the proviso that the sum of a, b and c does not exceed 6. Preferably, R1 and a are such that the acid molecules contain at least an average of 12 aliphatic carbon atoms in the aliphatic hydrocarbon substituents per acid molecule. Preferably, b and c are each one and the carboxylic acid is a salicylic acid.
The sulfonic acids useful in making the overbased salts of the invention include the sulfonic and thiosulfonic acids. Generally they are salts of sulfonic acids. The sulfonic acids include the mono- or polynuclear aromatic or cycloaliphatic compounds. The oil-soluble sulfonates can be represented for the most part by one of the following formulae: R2-T-(SO3−)a and R3—(SO3−)b, wherein T is a cyclic nucleus such as, for example, benzene, naphthalene, anthracene, diphenylene oxide, diphenylene sulfide, or petroleum naphthenes; R2 is an aliphatic group such as alkyl, alkenyl, alkoxy, or alkoxyalkyl; (R2)+T contains a total of at least 15 carbon atoms; and R3 is an aliphatic hydrocarbyl group containing at least 15 carbon atoms. Examples of R3 are alkyl, alkenyl, alkoxyalkyl, and carboalkoxyalkyl. Specific examples of R3 are groups derived from petrolatum, saturated and unsaturated paraffin wax, and the above-described polyalkenes. The groups T, R2, and R3 in the above Formulae can also contain other inorganic or organic substituents in addition to those enumerated above such as, for example, hydroxy, mercapto, halogen, nitro, amino, nitroso, sulfide, and disulfide. In the above Formulae, a and b are at least 1. In one embodiment, the sulfonic acids have a substituent (R2 or R3) which is derived from one of the above-described polyalkenes.
Illustrative examples of these sulfonic acids include monoeicosanyl-substituted naphthalene sulfonic acids, dodecylbenzene sulfonic acids, didode-cylbenzene sulfonic acids, dinonylbenzene sulfonic acids, dilauryl betanaphthalene sulfonic acids, the sulfonic acid derived by the treatment of polybutene having a number average molecular weight (
Another group of sulfonic acids are 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 from 8 to 30 carbon atoms, preferably 12 to 30 carbon atoms, and advantageously about 24 carbon atoms. Such acids include di-isododecylbenzene sulfonic acid, polybutenyl-substituted benzenesulfonic acid, polypropylenyl-substituted benzenesulfonic acids derived from polypropene having an
Dodecyl benzene “bottoms” sulfonic acids can also be used. These are the material leftover after the removal of dodecyl benzene sulfonic acids that are used for household detergents. These materials are generally alkylated with higher oligomers. The bottoms may be straight-chain or branched-chain alkylates with a straight-chain dialkylate preferred.
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 phosphorus-containing acids useful in making the basic metal salts (A) of the present invention include any phosphorus acids such as phosphoric acid or esters; and thiophosphorus acids or esters, including mono and dithiophosphorus acids or esters. Preferably, the phosphorus acids or esters contain at least one, preferably two, hydrocarbyl groups containing from 1 to 50 carbon atoms, typically 1 to 30, preferably 3 to 18, more preferably 4 to 8.
In one embodiment, the phosphorus-containing acids are dithiophosphoric acids which are readily obtainable by the reaction of phosphorus pentasulfide (P2S5) and an alcohol or a phenol. The reaction involves mixing at a temperature of 20° C. to 200° C. four moles of alcohol or a phenol with one mole of phosphorus pentasulfide. The oxygen-containing analogs of these acids are conveniently prepared by treating the dithioic acid with water or steam which, in effect, replaces one or both of the sulfur atoms with oxygen.
In another embodiment, the phosphorus-containing acid is the reaction product of a polyalkene and phosphorus sulfide. Useful phosphorus sulfide-containing sources include phosphorus pentasulfide, phosphorus sesquisulfide, and phosphorus heptasulfide.
The phenols useful in making the basic metal salts (A) of the invention can be represented by the formula (R1)a—Ar—(OH)b, wherein R1 is defined above; Ar is an aromatic group; 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. Preferably, a and b are independently numbers in the range of 1 to 4, more preferably 1 to 2. R1 and a are preferably such that there is an average of at least 8 aliphatic carbon atoms provided by the R1 groups for each phenol compound.
While the term “phenol” is used herein, it is to be understood that this term is not intended to limit the aromatic group of the phenol to benzene. Accordingly, it is to be understood that the aromatic group as represented by “Ar”, as well as elsewhere in other formulae in this specification and in the appended claims, can be mononuclear such as a phenyl, a pyridyl, or a thienyl, or polynuclear. The polynuclear groups can be of the fused type wherein an aromatic nucleus is fused at two points to another nucleus such as found in naphthyl or anthranyl. The polynuclear group can also be of the linked type wherein at least two nuclei (either mononuclear or polynuclear) are linked through bridging linkages to each other. These bridging linkages can be chosen from the group consisting of alkylene linkages, ether linkages, keto linkages, sulfide linkages, polysulfide linkages of 2 to 6 sulfur atoms, or a direct carbon-carbon linkage between the groups without any intervening atoms.
The acid to be overbased can be present as the acid itself, or it can be supplied in the form of an alternative source for such acid, that is, another material which will react under the conditions of the overbasing to produce the desired overbased product, possibly by means of forming the actual acid as an intermediate in situ. Thus, for example, suitable acid sources include the acids themselves as well as esters, amides, anhydrides, and salts of the acids. A preferred acid source is the vegetable oil based on the acid, e.g., palm oil, or coconut oil. The source can likewise be a hydrogenated vegetable oil, derived from an unsaturated vegetable oil. Vegetable oils are generally triglycerides. In the alkaline environment of the overbasing reaction, the oils are believed to be saponified to form the salt, which is then overbased, although the present invention is not intended to be limited by any such theoretical explanation.
The metal compounds useful in making the basic metal salts 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 1a alkali metals (e.g., sodium, potassium, lithium) as well as Group 1b metals such as copper. The Group 1 metals are preferably sodium, potassium, lithium and copper, more preferably sodium or potassium, and more preferably sodium. The Group 2 metals of the metal base include the Group 2a alkaline earth metals (e.g., magnesium, calcium, barium) as well as the Group 2b metals such as zinc or cadmium. Preferably the Group 2 metals are magnesium, calcium, barium, or zinc, preferably magnesium or calcium, more preferably calcium. Generally the metal compounds are delivered as metal salts. The anionic portion of the salt can be, e.g., hydroxide, oxide, carbonate, borate, or nitrate.
An acidic gas is employed to accomplish the formation of the overbased metal salt. The acidic gas is preferably carbon dioxide or sulfur dioxide, and is most preferably carbon dioxide.
A promoter is a chemical employed to facilitate the incorporation of metal into the basic metal compositions. The promoters are quite diverse and are well known in the art, as evidenced by the cited patents. A particularly comprehensive discussion of suitable promoters is found in U.S. Pat. Nos. 2,777,874, 2,695,910, and 2,616,904. These include the alcoholic and phenolic promoters, which are preferred. The alcoholic promoters include the alkanols of one to twelve carbon atoms such as methanol, ethanol, amyl alcohol, octanol, isopropanol, and mixtures of these. Phenolic promoters include a variety of hydroxy-substituted benzenes and naphthalenes a particularly useful class of phenols are the alkylated phenols of the type listed in U.S. Pat. No. 2,777,874, e.g., heptylphenols, octylphenols, and nonylphenols. Mixtures of various promoters are sometimes used.
Patents specifically describing techniques for making basic salts of the above-described sulfonic acids, carboxylic acids, and mixtures of any two or more of these 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 amount of the overbased material, that is, the detergent, is preferably 0.05 to 5 percent by weight of the traction fluid, more preferably 0.05 to 3 percent, 0.1 to 1.5 percent, or most preferably 0.2 to 1 percent by weight.
Preferably both a dispersant and a detergent are included in the composition; preferably a succinimide dispersant and a calcium overbased sulfonate detergent.
The traction fluid can also contain a polymeric viscosity index modifier, preferably in limited amounts, that is, up to 10 percent by weight of the composition. Preferably the amount of this component is 0 to 1 percent by weight, and in one embodiment the traction fluids are substantially free from polymeric viscosity index modifiers.
Polymeric viscosity index modifiers (VMs) are extremely well known in the art and most are commercially available. Hydrocarbon VMs include polybutenes, poly(ethylene/propylene) copolymers, and hydrogenated polymers of styrene with butadiene or isoprene. Ester VMs include esters of styrene/maleic anhydride polymers, esters of styrene/maleic anhydride/acrylate terpolymers, and polymethacrylates. The acrylates are available from RohMax and from The Lubrizol Corporation; polybutenes from Ethyl Corporation and Lubrizol; ethylene/propylene copolymers from Exxon and Texaco; hydrogenated polystyrene/isoprene polymers from Shell; styrene/maleic esters from Lubrizol, and hydrogenated styrene/butadiene polymers from BASF.
Preferred VMs include acrylate- or methacrylate-containing copolymers or copolymers of styrene and an ester of an unsaturated carboxylic acid such as styrene/maleic ester (typically prepared by esterification of a styrene/maleic anhydride copolymer). Preferably the viscosity modifier is a polymethacrylate viscosity modifier. Polymethacrylate viscosity modifiers are prepared from mixtures of methacrylate monomers having different alkyl groups. The alkyl groups may be either straight chain or branched chain groups containing from 1 to 18 carbon atoms. When a small amount of a nitrogen-containing monomer is copolymerized with alkyl methacrylates, dispersancy properties are also incorporated into the product. Thus, such a product has the multiple function of viscosity modification, pour point dispersancy and dispersancy. Such products have been referred to in the art as dispersant-type viscosity modifiers or simply 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. It is preferred that the viscosity modifier of the present invention is a dispersant viscosity modifier.
In one embodiment a dispersant viscosity modifier is prepared by polymerizing 57.5 parts methyl methacrylate, 12.7 parts butyl methacrylate, 226.5 parts each of C9-11 methacrylate and C12-15 methacrylate, 114.8 parts C16-18 methacrylate and 11.7 parts N-(3-(dimethylamino)propyl) methacrylamide in a staged addition process. Details of the preparation of these and related polymers are found in European Patent Application 750,031, published Dec. 27, 1996.
The copolymers described above typically have a weight average molecular weight (
Another optional component of the traction fluids is an antiwear agent. Anti-wear agents are well known to those of skill in the art. One particular anti-wear agent that may be employed in the traction fluids includes a phosphorus acid, a phosphorus acid salt, a phosphorus ester, or mixtures thereof. The phosphorus acid or ester can be of the formula (R1X)(R2X)P(X)nXmR3 or a salt thereof, where each X is independently an oxygen atom or a sulfur atom, n is 0 or 1, m is 0 or 1, m+n is 1 or 2, and R1, R2, and R3 are hydrogen or hydrocarbyl groups, and preferably at least one of R1, R2, or R3 is hydrogen. This component thus includes phosphorous and phosphoric acids, thiophosphorous and thiophosphoric acids, as well as phosphite esters, phosphate esters, thiophosphite esters, and thiophosphate esters. It is noted that certain of these materials can exist in tautomeric forms, and that all such tautomers are intended to be encompassed by the above formula and included within the present invention. For example, phosphorous acid and certain phosphite esters can be written in at least two ways:
differing merely by the placement of the hydrogen. Each of these structures is intended to be encompassed by the present invention.
The phosphorus-containing acids can be at least one phosphate, phosphonate, phosphinate or phosphine oxide. These pentavalent phosphorus derivatives can be represented by the formula
wherein R1, R2 and R3 are as defined above. The phosphorus-containing acid can be at least one phosphite, phosphonite, phosphinite or phosphine. These trivalent phosphorus derivatives can be represented by the formula
wherein R1, R2 and R3 are defined as above. Generally, the total number of carbon atoms in R1, R2 and R3 is at least 8, and in one embodiment at least 12, and in one embodiment at least 16. Examples of useful R1, R2 and R3 groups include hydrogen, t-butyl, isobutyl, amyl, isooctyl, decyl, dodecyl, oleyl, C18 alkyl, eicosyl, 2-pentenyl, dodecenyl, phenyl, naphthyl, alkylphenyl, alkylnaphthyl, phenylalkyl, naphthylalkyl, alkylphenylalkyl, and alkylnaphthylalkyl groups.
In another embodiment, the phosphorus acid or ester is characterized by at least one direct carbon-to-phosphorus linkage such as those prepared by the treatment of an olefin polymer, such as one or more of the above polyalkenes (e.g., polyisobutene having a molecular weight of 1000) with a phosphorizing agent such as phosphorus trichloride, phosphorus heptasulfide, phosphorus pentasulfide, phosphorus trichloride and sulfur, white phosphorus and a sulfur halide, or phosphorothioic chloride.
It is preferred that at least two of the X atoms in the above structure are oxygen, so that the structure will be (R1O)(R2O)P(X)nXmR3, and more preferably (R1O)(R2O)P(X)nXmH. This structure can correspond, for example, to phosphoric acid when R1, R2, and R3 are hydrogen. Phosphoric acid exists as the acid itself, H3PO4 and other forms equivalent thereto such as pyrophosphoric acid and anhydrides of phosphoric acid, including 85% phosphoric acid (aqueous), which is the commonly available commercial grade material. The formula can also correspond to a mono- or dialkyl hydrogen phosphite such as dibutyl hydrogen phosphite (a phosphite ester) when one or both of R1 and R2 are alkyl, respectively and R3 is hydrogen, or a trialkyl phosphite ester when each of R1, R2, and R3 is alkyl; in each case where n is zero, m is 1, and the remaining X is O. The structure will correspond to phosphoric acid or a related material when n and m are each 1; for example, it can be a phosphate ester such as a mono-, di- or trialkyl monothiophosphate when one of the X atoms is sulfur and one, two, or three of R6, R7, and R8 are alkyl, respectively.
Phosphoric acid and phosphorus acid are well-known items of commerce. Thiophosphoric acids and thiophosphorous acids are likewise well known and are prepared by reaction of phosphorus compounds with elemental sulfur or other sulfur sources. Processes for preparing thiophosphorus acids are reported in detail in Organic Phosphorus Cornpounds, Vol. 5, pages 110-111, G. M. Kosolapoff et al., 1973.
Salts of the above phosphorus acids are well known. Salts include ammonium and amine salts as well as metal salts. Zinc salts, such as zinc dialkyldithiophosphates, are useful in certain applications.
The amount of the above phosphorus acid, salt, or ester in the traction fluid of the present invention is preferably an amount sufficient to provide at least 0.01 percent by weight of phosphorus to the fluids (calculated as P), preferably 0.01 to 0.1 percent, and more preferably 0.03 to 0.06 or 0.05 percent by weight.
Other materials that may be used as antiwear agents include tartrate esters, tartramides, and tartrimides. Examples include oleyl tartrimide (the imide formed from oleylamine and tartaric acid) and oleyl diesters (from, e.g., mixed C12-16 alcohols). Other related materials that may be useful include esters, amides, and imides of other hydroxy-carboxylic acids in general, including hydroxy-polycarboxylic acids, for instance, acids such as tartaric acid, citric acid, lactic acid, glycolic acid, hydroxy-propionic acid, hydroxyglutaric acid, and mixtures thereof. These materials may also impart additional functionality to a lubricant beyond antiwear performance. These materials are described in greater detail in US Publication 2006-0079413 and PCT publication WO2010/077630. Other anti-wear agents include borate esters (including borated epoxides), dithiocarbamate compounds, molybdenum-containing compounds, and sulfurized olefins, and they may be present in comparable amounts. Such other antiwear agents may typically be present in the traction fluid in an amount of 0.1 weight % to 5 weight %, or 0.2 weight % to 3 weight %, or greater than 0.2 weight % to 3 weight %.
Another component may be an antioxidant. Antioxidants encompass phenolic antioxidants, which may be hindered phenolic antioxidants, one or both ortho positions on a phenolic ring being occupied by bulky groups such as t-butyl. 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 antioxidants are described in greater detail in U.S. Pat. No. 6,559,105.
Antioxidants also include aromatic amines. In one embodiment, an aromatic amine antioxidant can comprise an alkylated diphenylamine such as nonylated diphenylamine or a mixture of a dinonylated and a mono-nonylated diphenylamine, or an alkylated phenylnaphthylamine, or mixtures thereof.
Antioxidants also include sulfurized olefins such as mono- or disulfides or mixtures thereof. These materials generally have sulfide linkages of 1 to 10 sulfur atoms, e.g., 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 antiwear agents or friction modifiers. U.S. Pat. No. 4,285,822 discloses lubricating oil compositions containing a molybdenum- and sulfur-containing composition prepared by combining a polar solvent, an acidic molybdenum compound and an oil-soluble basic nitrogen compound to form a molybdenum-containing complex and contacting the complex with carbon disulfide to form the molybdenum- and sulfur-containing composition.
Other materials that may serve as antioxidants include titanium compounds. U.S. Patent Application Publication 2006-0217271 discloses a variety of titanium compounds, including titanium alkoxides and titanated dispersants, which materials may also impart improvements in deposit control and filterability. Other titanium compounds include titanium carboxylates such as neodecanoate.
Typical amounts of antioxidants will 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 weight percent.
Another optional, but preferred, species in the traction fluids of the present invention is one or more friction modifiers. Friction modifiers include alkoxylated fatty amines, borated fatty epoxides, fatty phosphites, fatty epoxides, fatty amines, borated alkoxylated fatty amines, metal salts of fatty acids, fatty acid amides, glycerol esters, borated glycerol esters, and fatty imidazolines.
As one preferred example of a friction modifier, zinc salts of fatty acids are well known materials. Fatty acids are generally hydrocarbon-based carboxylic acids, both synthetic and naturally occurring, preferably aliphatic acids, although acids containing aromatic functionality are also included. Occasional heteroatom substitution can be permitted in the hydrocarbyl portion of the fatty acid, consistent with the definition of “hydrocarbyl,” below. Preferably the acid contains 14 to 30 carbon atoms, more preferably 16-24 carbon atoms, and preferably about 18 carbon atoms. The acid can be straight chain (e.g. stearic) or branched (e.g., isostearic). The acid can be saturated or it can contain olefinic unsaturation. A preferred acid is oleic acid, and the correspondingly preferred salt is zinc oleate, a commercially available material, the preparation of which is well known and is within the abilities of the person skilled in the art.
The zinc salt can be a neutral salt, that is, in which one equivalent of zinc is reacted with one equivalent of acid such as oleic acid. Alternatively, the zinc salt can be a slightly basic salt, in which one equivalent of a zinc base is reacted with somewhat less than one equivalent of acid. An example of such a material is a slightly basic zinc oleate, that is, Zn4Oleate6O1.
Alkyl-substituted imidazolines are also well known friction modifying materials. They can generally be formed by the cyclic condensation of a carboxylic acid with a 1,2 diaminoethane compound. They generally have the structure
where R is an alkyl group and R1 is a hydrocarbyl group or a substituted hydrocarbyl group, including —(CH2CH2NH)n—H groups. Among the numerous suitable carboxylic acids useful in preparing the imidazoline are oleic acid, stearic acid, isostearic acid, tall oil acids, and other acids derived from natural and synthetic sources. Specially preferred carboxylic acids are those containing 12 to 24 carbon atoms including the 18 carbon acids such as oleic acid, stearic acid, and isostearic acid. Among suitable 1,2 diaminoethane compounds are compounds of the general structure R—NH—C2H4—NH2, where R is a hydrocarbyl group or a substituted hydrocarbyl group (e.g., hydroxyhydrocarbyl or aminohydrocarbyl). A preferred diamine is N-hydroxyethyl-1,2-diaminoethane, HOC2H4NHC2H4NH2.
A preferred alkyl-substituted imidazoline is 1-hydroxyethyl-2-heptadecenyl imidazoline.
Another type of friction modifier includes borated epoxides, which are described in detail in U.S. Pat. No. 4,584,115, and are generally prepared by reacting an epoxide, preferably a hydrocarbyl epoxide, with boric acid or boron trioxide. The epoxide can be expressed by the general formula
wherein each R is independently hydrogen or a hydrocarbyl group containing 8 to 30 carbon atoms, at least one of which is hydrocarbyl. Also included are materials in which any two of the R groups together with the atoms to which they are attached, for a cyclic group, which can be alicyclic or heterocyclic. Preferably one R is a hydrocarbyl group of 10 to 18 carbon atoms and the remaining R groups are hydrogen. More preferably the hydrocarbyl group is an alkyl group. The epoxides can be commercial mixtures of C14-16 or C14-18 epoxides, which can be purchased from ELFATOCHEM or Union Carbide and which can be prepared from the corresponding olefins by known methods. Purified epoxy compounds such as 1,2-epoxyhexadecane can be purchased from Aldrich Chemicals. Alternatively this material can be a reactive equivalent of an epoxide. By the term “reactive equivalent of an epoxide” is meant a material which can react with a boronating agent (described below) in the same or a similar manner as can an epoxide to give the same or similar products. An example of a reactive equivalent of an epoxide is a diol. Another example of a reactive equivalent to epoxides is the halohydrins. Other equivalents will be apparent to those skilled in the art. Other reactive equivalents include materials having vicinal dihydroxy groups which are reacted with certain blocking reagents. The borated compounds are prepared by blending the boron compound and the epoxide and heating them at a suitable temperature, typically 80° to 250° C., until the desired reaction has occurred. Boronating agents include the various forms of boric acid (including metaboric acid, HBO2, orthoboric acid, H3BO3, and tetraboric acid, H2B4O7), boric oxide, boron trioxide, and alkyl borates of the formula (RO)xB(OH)y wherein X is 1 to 3 and y is 0 to 2, the sum of x and y being 3, and where R is an alkyl group containing 1 to 6 carbon atoms. The molar ratio of the boronating agent to the epoxide or reactive equivalent thereof is generally 4:1 to 1:4. Ratios of 1:1 to 1:3 are preferred, with 1:2 being an especially preferred ratio. An inert liquid can be used in performing the reaction. The liquid may be, for example, toluene, xylene, or dimethylformamide. Water is formed and is typically distilled off during the reaction. Alkaline reagents can be used to catalyze the reaction. A preferred borated epoxide is the borated epoxide of a predominantly 16 carbon olefin.
Other friction modifiers include diethoxylated long chain amines such as N,N-bis-(2-hydroxyethyl)-tallowamine. Certain phosphorus-containing materials, described above, can also serve as friction modifiers, in particular, dialkylphosphites having alkyl groups of 12 to 24 carbon atoms.
The amount of friction modifier or modifiers is preferably 0.01 to 2 percent by weight of the traction fluid composition. More preferably it is 0.05 to 1.2 percent, and most preferably 0.1 to 1 percent by weight.
The traction fluid may, in some instances, also contain a minor amount of an oil of lubricating viscosity, also referred to as a base oil. The base oil may be selected from any of the base oils in Groups I-V of the American Petroleum Institute (API) Base Oil Interchangeability Guidelines (2011), namely
Groups I, II and III are mineral oil base stocks. Other generally recognized categories of base oils may be used, even if not officially identified by the API: Group II+, referring to materials of Group II having a viscosity index of 110-119 and lower volatility than other Group II oils; and Group III+, referring to materials of Group III having a viscosity index greater than or equal to 130. The oil of lubricating viscosity can include natural or synthetic oils and mixtures thereof. Mixture of mineral oil and synthetic oils, e.g., polyalphaolefin oils and/or polyester oils, may be used. In one embodiment the oil of lubricating viscosity has a kinematic viscosity at 100° C. by ASTM D445 of 1.5 to 7.5, or 2 to 7, or 2.5 to 6.5, or 3 to 6 mm2/s. In one embodiment the oil of lubricating viscosity comprises a poly alpha olefin having a kinematic viscosity at 100° C. by ASTM D445 of 1.5 to 7.5 or any of the other aforementioned ranges.
Another aspect of the present invention is a method for lubricating a power transmission apparatus. The method includes supplying to the power transmission apparatus the traction fluid described above and operating the apparatus.
The power transmission apparatus in question can be any of a variety of power transmission device, such as, for example, automotive transmissions such as automatic transmissions or toroidal transmissions, push-belt and chain-type continuously variable transmission, and dual clutch transmissions. The power transmission apparatus can also include devices that are not operated via gears, belts, pulleys or other mechanical drive, but rather rely on the traction fluid for transmission of power. A type of transmission device particularly envisioned is a traction drive. Traction drives are devices in which power or torque is transmitted from an input element to an output element through nominal point or line contact, typically with a rolling action, by virtue of the traction between the contacting elements. Traction drives can be generally used in automotive or industrial machinery for transmitting power between rotating members. They can be used as automatic transmissions and are particularly suitable as a form of continuously variable automatic transmission for use in automobile drivetrains and other applications.
While the working elements of a traction drive are sometimes spoken of as being in contact, it is generally accepted that a fluid film must be provided therebetween. Thus, rather than metal-to-metal rolling contact, a film of fluid is introduced into the load zone, and power is transmitted by shearing of the film, which may become very viscous due to the high pressure at the contact area. The nature and properties of the fluid, therefore, will determine to a large extent the performance and capacity of the traction drive. Traction fluids will preferably have a high shear resistance (often measured as “traction coefficient”) to maximize the power transmission performance. Low viscosity, particularly at low temperatures, is also desirable for efficient operation under cold conditions. The fluid should ideally also exhibit good lubricating properties for and compatibility with other components of the traction drive. Such fluids also serve to remove heat and prevent wear at the contact surfaces and to lubricate bearings and other moving parts associated with the drive.
The power transmission apparatus can also be a hydraulically operated device, such as those found in a farm tractor.
A common method of measuring a traction fluid's shear resistance is by superimposing sliding on a rolling elasto-hydrodynamically (“EHD”) lubricated contact. The resultant resistance to shear of the fluid is measured and the larger it is the higher the traction coefficient and ability of the fluid to transmit torque across the EHD film. A measure of the ability of a fluid to transmit torque is the traction coefficient and represented by the equation:
Traction coefficients are measured with a mini traction machine (MTM) where a highly loaded contact is formed between a polished steel ball and the surface of a disc. Slide/roll motion between the ball and the disc is controlled by independent motors driving the ball and the disc. Traction coefficient is impacted by pressure, temperature and slide to roll ratio. It increases with pressure and decreases with temperature. As the slide to roll ratio increases, traction coefficient increases rapidly before reaching a maximum asymptotic value. It is highly desirable to have a rapidly increasing traction coefficient and lowest possible slide to roll ratio. Slide to roll ratio is defined as:
Traction coefficient is a bulk property of the base fluid with additives only making minor positive or negative contributions to the overall traction of the formulation. If the amount of additive, viscosity modifier or base oil is increased with low traction properties, the resulting fluid traction would be lower.
In an embodiment, the traction fluid can provide a traction coefficient measured with an MTM machine at the following conditions:
of greater than 0.05, or greater than 0.06 or even greater than 0.07.
Along with a high MTM coefficient, potential traction fluids also must have excellent low temperature viscometrics similar to current automatic or manual transmission fluids.
In an embodiment, the traction fluid can provide a Brookfield viscosity measured according to ASTM 2983 at −30° C. of less than 20,000 cP, or less than 15,000 cP, or even less than 10,000 cP.
In embodiments, the traction fluid can provide an MTM traction coefficient of greater than 0.05. In embodiments, the traction fluid can provide an MTM traction coefficient measured per the above stated conditions of greater than 0.05 and a Brookfield viscosity measured per the above stated conditions of less than 20,000 cP. In embodiments, the traction fluid can provide an MTM traction coefficient measured per the above stated conditions of greater than 0.06 and a Brookfield viscosity measured per the above stated conditions of less than 15,000 cP. In embodiments, the traction fluid can provide an MTM traction coefficient measured per the above stated conditions of greater than 0.07 and a Brookfield viscosity measured per the above stated conditions of less than 15,000 cP. In embodiments, the traction fluid can provide an MTM traction coefficient measured per the above stated conditions of greater than 0.07 and a Brookfield viscosity measured per the above stated conditions of less than 15,000 cP. In embodiments, the traction fluid can provide an MTM traction coefficient measured per the above stated conditions of greater than 0.07 and a Brookfield viscosity measured per the above stated conditions of less than 10,000 cP.
As used herein, the term “condensation product” is intended to encompass esters, amides, imides and other such materials that may be prepared by a condensation reaction of an acid or a reactive equivalent of an acid (e.g., an acid halide, anhydride, or ester) with an alcohol or amine, irrespective of whether a condensation reaction is actually performed to lead directly to the product. Thus, for example, a particular ester may be prepared by a transesterification reaction rather than directly by a condensation reaction. The resulting product is still considered a condensation product.
The amount of each chemical component described is presented exclusive of any solvent or diluent oil, which may be customarily present in the commercial material, that is, on an active chemical basis, unless otherwise indicated. However, unless otherwise indicated, each chemical or composition referred to herein should be interpreted as being a commercial grade material which may contain the isomers, byproducts, derivatives, and other such materials which are normally understood to be present in the commercial grade.
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 other than carbon in a ring or chain otherwise composed of carbon atoms and encompass substituents as pyridyl, furyl, thienyl and imidazolyl. Heteroatoms include sulfur, oxygen, and nitrogen. 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; alternatively, there may 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.
As used herein, the term “about” means that a value of a given quantity is within ±20% of the stated value. In other embodiments, the value is within ±15% of the stated value. In other embodiments, the value is within ±10% of the stated value. In other embodiments, the value is within ±5% of the stated value. In other embodiments, the value is within ±2.5% of the stated value. In other embodiments, the value is within ±1% of the stated value.
Additionally, as used herein, the term “substantially” means that a value of a given quantity is within ±10% of the stated value. In other embodiments, the value is within ±5% of the stated value. In other embodiments, the value is within ±2.5% of the stated value. In other embodiments, the value is within ±1% of the stated value. The term “substantially free,” means that some concentration of the noted element may be present, but at such a level as not to make a meaningful contribute to the composition. Substantially free may encompass, for example, 5% of the minimum concentration described for the noted element, or 4%, or 3% or even 2% or 1% of the minimum concentration or even ½%. In contrast to “substantially free,” the term “free” means the noted element is completely missing; that is, there is 0% of the noted element.
The invention herein is useful for lubricating a power transmission apparatus, which may be better understood with reference to the following examples.
Sample 1—Santotrac-50, a hydrogenated α-methylstyrene dimer.
Sample 2—a 400 molecular weight conventional, unhydrogenated polyisobutylene
Sample 3—Panalane L14E, a 400 molecular weight hydrogenated polyisobutylene.
Sample 4—cedar oil extracted from Juniperus ashei, having from about 14 to about 18 wt % α-cedrene content, from about 2 to about 4 wt % β-cedrene content, from about 38 to about 42 wt % thujopsene content, and from about 24 to about 26 wt % cedrol content.
Sample 5—cedar oil extracted from Juniperus virginiana, having from about 10 to about 12 wt % α-cedrene content, from about 2 to about 4 wt % β-cedrene content, from about 38 to about 42 wt % thujopsene content, and from about 28 to about 32 wt % cedrol content.
Sample 6—cedar oil extracted from Juniperus virginiana, having from about 28 to about 32 wt % α-cedrene content, from about 5 to about 7 wt % β-cedrene content, from about 23 to about 25 wt % thujopsene content, and from about 23 to about 25 wt % cedrol content.
Sample 7—cedar oil extracted from Juniperus ashei, having from about 8 to about 10 wt % α-cedrene content, from about 2 to about 4 wt % β-cedrene content, from about 45 to about 47 wt % thujopsene content, and from about 24 to about 26 wt % cedrol content.
Sample 8—cedar oil extracted from Cedrus deodara, without detectable amounts of cedrene, thujopsene, or cedrol.
Sample 9—cedar oil extracted from Cedrus atlantica, without detectable amounts of cedrene, thujopsene, or cedrol.
Sample 10—2-(6,6-dimethyl-2-bicyclo[3.1.1]hept-2-enyl)ethanol; also known as Nopol.
Sample 11—a mixture of 25 wt % of the cedar oil of Sample 5 with 75 wt % of Sample 2.
Sample 12—a mixture of 50 wt % of the cedar oil of Sample 5 with 50 wt % of Sample 2.
Sample 13—a mixture of 75 wt % of the cedar oil of Sample 5 with 25 wt % of Sample 2.
Sample 14—a mixture of 25 wt % of the cedar oil of Sample 7 with 75 wt % of Sample 2.
Sample 15—a mixture of 50 wt % of the cedar oil of Sample 7 with 50 wt % of Sample 2.
Sample 16—a mixture of 75 wt % of the cedar oil of Sample 7 with 25 wt % of Sample 2.
Sample 17—a mixture of 50 wt % of the cedar oil of Sample 4 with 50 wt % of Sample 1.
Sample 18—a mixture of 25 wt % of the cedar oil of Sample 4 with 50 wt % of Sample 1 and 25 wt % Sample 3.
Sample 19—a mixture of 25 wt % of the cedar oil of Sample 9 with 50 wt % Sample 1 and 25 wt % Sample 3.
Sample 20—a mixture of ⅓ by weight of the cedar oil of Sample 6 with ⅓ by weight of Sample 1 and ⅓ by weight Sample 3.
Each of the documents referred to above is incorporated herein by reference, including any prior applications, whether or not specifically listed above, from which priority is claimed. 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.” 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 transitional term “comprising,” which is synonymous with “including,” “containing,” or “characterized by,” is inclusive or open-ended and does not exclude additional, un-recited elements or method steps. However, in each recitation of “comprising” herein, it is intended that the term also encompass, as alternative embodiments, the phrases “consisting essentially of” and “consisting of,” where “consisting of” excludes any element or step not specified and “consisting essentially of” permits the inclusion of additional un-recited elements or steps that do not materially affect the essential or basic and novel characteristics of the composition or method under consideration.
Provided is a traction fluid comprising (A) a base fluid comprising cedar oil or a major constituent thereof, and (B) at least one lubricant additive for a power transmission apparatus.
The traction fluid of the preceding paragraph, wherein the cedar oil comprises at least one of cedrene, cedrol, thujopsene or mixtures thereof.
The traction fluid of any previous paragraph wherein the traction fluid comprises less than 5 wt. % longifolene.
The traction fluid of any previous paragraph wherein the base fluid further comprises a polyolefin polymer.
The traction fluid of any previous paragraph, wherein the base fluid further comprises a predominantly linear hydrogenated dimer of alpha-alkyl styrene.
The traction fluid of any previous paragraph, wherein the additive package for a power transmission apparatus comprises at least one of a low-temperature viscosity control agent, viscosity modifier, dispersant, detergent, antioxidant, anti-wear agent, friction modifier or mixtures thereof.
The traction fluid of any previous paragraph, wherein the low-temperature viscosity control agent comprises a naphthenic oil.
The traction fluid of any previous paragraph, wherein the low-temperature viscosity control agent comprises a synthetic ester oil.
The traction fluid of any previous paragraph, wherein the low-temperature viscosity control agent comprises a polyether oil
The traction fluid of any previous paragraph wherein said additive package includes a succinimide dispersant.
The traction fluid of any previous paragraph comprising an overbased sulfonate detergent.
The traction fluid of any previous paragraph wherein said fluid contains up to about 10 percent by weight of a polymeric viscosity index modifier.
The traction fluid of any previous paragraph wherein said antiwear agent comprises at least one phosphorus-containing acid, salt, or ester in an amount to contribute about 0.005 to about 0.06% phosphorus to the traction fluid.
The traction fluid of any previous paragraph further comprising about 0.01 to about 2 percent by weight of a friction modifier.
A method of lubricating a power transmission apparatus, comprising employing therein the traction fluid of any previous paragraph and operating the power transmission apparatus.
A traction fluid comprising (A) a base fluid comprising cedar oil.
A traction fluid comprising (A) a base fluid comprising at least one of cedrene, cedrol, thujopsene or mixtures there
The traction fluid of any previous paragraph, further comprising (B) at least one lubricant additive for a power transmission apparatus.
The traction fluid of any previous paragraph wherein the cedar oil comprises at least one of cedrene, cedrol, thujopsene or mixtures thereof.
The traction fluid of any previous paragraph, wherein the base fluid is present in a major amount.
The traction fluid of any previous paragraph, wherein the base fluid is present at greater than 50 wt % of the traction fluid.
The traction fluid of any previous paragraph, wherein the base fluid is present at from 50 to 100 wt % of the traction fluid.
The traction fluid of any previous paragraph, wherein the base fluid is present at from 70 to 95 wt % of the traction fluid.
The traction fluid of any previous paragraph, wherein the base fluid is present at from 75 to 90 wt % of the traction fluid.
The traction fluid of any previous paragraph, wherein the base fluid is present at from 80 to 85 wt % of the traction fluid.
The traction fluid of any previous paragraph, wherein the cedar oil is selected from the group consisting of Cedrus atlantica, Cedrus deodara, Chamaecyparis lawsoniana, Chamaecyparis funebris, Juniperus virginiana, Juniperus ashei, Thuja plicata, Thuja occidentalis, and mixtures thereof.
The traction fluid of any previous paragraph, wherein the cedar oil is selected from the group consisting of Chamaecyparis funebris, Juniperus virginiana, Juniperus ashei, and mixtures thereof.
The traction fluid of any previous paragraph, wherein the base fluid comprises from about 10 to about 50 wt % cedrene.
The traction fluid of any previous paragraph, wherein the base fluid comprises from about 2 to 32 wt % cedrene.
The traction fluid of any previous paragraph, wherein the base fluid comprises from about 12 to 16 wt % cedrene
The traction fluid of any previous paragraph, wherein the base fluid comprises from about 20 to 38 wt % cedrene
The traction fluid of any previous paragraph, wherein the base fluid comprises from about 28 to 48 wt % cedrene.
The traction fluid of any previous paragraph, wherein the base fluid comprises α-cedrene at from about 2 to 40 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises α-cedrene at from about 4 to 20 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises α-cedrene at from about 20 to 40 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises α-cedrene at from about 20 to 32 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises β-cedrene at from about 5 to 10 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises β-cedrene at from about 5 to 9 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises β-cedrene at from about 5 to 8 wt %.
The traction fluid of any previous paragraph, wherein the base fluid is substantially free or completely free of β-cedrene.
The traction fluid of any previous paragraph, wherein the base fluid comprises iso-α-cedrene at from about 2 to 40 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises iso-α-cedrene at from about 12 to 16 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises iso-α-cedrene at from about 20 to 40 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises iso-α-cedrene at from about 20 to 32 wt %.
The traction fluid of any previous paragraph, wherein the base fluid is substantially free or completely free of iso-α-cedrene.
The traction fluid of any previous paragraph, wherein the base fluid comprises cedrol at from about 10 to 25 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises cedrol at from about 12 to 20 wt %.
The traction fluid of any previous paragraph, wherein the base fluid is substantially free or completely free of cedrol.
The traction fluid of any previous paragraph, wherein the base fluid comprises thujopsene at from about 20 to 50 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises thujopsene at from about 25 to 48 wt %.
The traction fluid of any previous paragraph, wherein the base fluid comprises thujopsene at from about 20 to 25 wt %.
The traction fluid of any previous paragraph, wherein the base fluid is substantially free or completely free of thujopsene.
The traction fluid of any previous paragraph, wherein the base fluid comprises cedar oil comprising from about 28 to 36 wt % iso-α-cedrene, from about 1 to 3 wt % α-cedrene, and from about 20 to 23 wt % thujopsene.
The traction fluid of any previous paragraph, wherein the base fluid comprises cedar oil comprising from about 30 to 34 wt % iso-α-cedrene, from about 1.5 to 2.5 wt % α-cedrene, and from about 21 to 22 wt % thujopsene.
The traction fluid of any previous paragraph, wherein the base fluid comprises cedar oil comprising from about 10 to 22 wt % cedrol, from about 20 to 32 wt % α-cedrene, from about 0 or 0.5 to 8 wt % β-cedrene, and from about 20 to 50 wt % thujopsene.
The traction fluid of any previous paragraph, wherein the base fluid comprises cedar oil comprising from about 12 to 20 wt % cedrol, from about 21 to 31 wt % α-cedrene, from about 0.5 to 6 wt % β-cedrene, and from about 22 to 48 wt % thujopsene.
The traction fluid of any previous paragraph, wherein the base fluid comprises cedar oil comprising from about 10 to 24 wt % cedrol, from about 20 to 40 wt % α-cedrene, from about 6 to 12 wt % β-cedrene, and from about 20 to 25 wt % thujopsene.
The traction fluid of any previous paragraph, wherein the base fluid comprises cedar oil comprising from about 12 to 23 wt % cedrol, from about 21 to 39 wt % α-cedrene, from about 8 to 10 wt % β-cedrene, and from about 21 to 24 wt % thujopsene.
The traction fluid of any previous paragraph wherein the traction fluid comprises less than 5 wt. % longifolene.
The traction fluid of any previous paragraph wherein the traction fluid comprises less than 4.99 wt. % longifolene.
The traction fluid of any previous paragraph wherein the traction fluid comprises less than 4.98 wt. % longifolene.
The traction fluid of any previous paragraph wherein the traction fluid comprises less than 4.95 wt. % longifolene.
The traction fluid of any previous paragraph wherein the traction fluid comprises from about 0.01 to 4.99 wt. % longifolene.
The traction fluid of any previous paragraph wherein the traction fluid comprises from about 0.1 to 4.95 wt. % longifolene.
The traction fluid of any previous paragraph wherein from 15 to 85 wt % of the cedar oil or major constituents thereof in the base fluid are substituted by (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, (2) hydrocarbon molecules containing non-aromatic cyclic moieties, or combinations of (1) and (2).
The traction fluid of any previous paragraph wherein from 25 to 75 wt % of the cedar oil or major constituents thereof in the base fluid are substituted by (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, (2) hydrocarbon molecules containing non-aromatic cyclic moieties, or combinations of (1) and (2).
The traction fluid of any previous paragraph wherein the base fluid comprises 15 to 85 wt % cedar oil or major constituents thereof, and from 15 to 85 wt % of at least one of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, (2) hydrocarbon molecules containing non-aromatic cyclic moieties, or combinations of (1) and (2).
The traction fluid of any previous paragraph wherein the base fluid comprises 25 to 75 wt % cedar oil or major constituents thereof, and from 25 to 75 wt % of at least one of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, (2) hydrocarbon molecules containing non-aromatic cyclic moieties, or combinations of (1) and (2).
The traction fluid of any previous paragraph wherein the polymers of at least one olefin which contains 3 to 5 carbon atoms comprises a branched polyolefin polymer.
The traction fluid of any previous paragraph, wherein the branched polyolefin polymer is hydrogenated.
The traction fluid of any previous paragraph wherein the branched polyolefin polymer comprises a polyisobutylene of from 100 to 1000 Mn measured by GPC.
The traction fluid of any previous paragraph wherein the branched polyolefin polymer comprises a polyisobutylene of from 200 to 1000 Mn measured by GPC.
The traction fluid of any previous paragraph wherein the branched polyolefin polymer comprises a polyisobutylene of from 180 to 2000 Mn measured by GPC.
The traction fluid of any previous paragraph wherein the branched polyolefin polymer comprises a polyisobutylene of from 100 to 700 Mn measured by GPC.
The traction fluid of any previous paragraph wherein the branched polyolefin polymer comprises a polyisobutylene of from 200 to 700 Mn measured by GPC.
The traction fluid of any previous paragraph, wherein the hydrocarbon molecules containing non-aromatic cyclic moieties comprises a predominantly linear hydrogenated dimer of alpha-alkylstyrene.
The traction fluid of any previous paragraph, wherein the predominantly linear hydrogenated dimer of alpha-alkylstyrene is represented by the general structure
The traction fluid of any previous paragraph wherein the base fluid comprises 85 wt % cedar oil with 15 wt % of at least one of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, (2) hydrocarbon molecules containing non-aromatic cyclic moieties, or (3) combinations of (1) and (2).
The traction fluid of any previous paragraph wherein the base fluid comprises 75 wt % cedar oil with 25 wt % of at least one of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, (2) hydrocarbon molecules containing non-aromatic cyclic moieties, or (3) combinations of (1) and (2).
The traction fluid of any previous paragraph wherein the base fluid comprises 50 wt % cedar oil with 50 wt % of at least one of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, (2) hydrocarbon molecules containing non-aromatic cyclic moieties, or (3) combinations of (1) and (2).
The traction fluid of any previous paragraph wherein the base fluid comprises 85 wt % (1) polymers of at least one olefin which contains 3 to 5 carbon atoms with 15 wt % cedar oil.
The traction fluid of any previous paragraph wherein the base fluid comprises 75 wt % (1) polymers of at least one olefin which contains 3 to 5 carbon atoms with 25 wt % cedar oil.
The traction fluid of any previous paragraph wherein the base fluid comprises 50 wt % (1) polymers of at least one olefin which contains 3 to 5 carbon atoms with 50 wt % cedar oil.
The traction fluid of any previous paragraph wherein the base fluid comprises 85 wt % (2) hydrocarbon molecules containing non-aromatic cyclic moieties with 15 wt % cedar oil.
The traction fluid of any previous paragraph wherein the base fluid comprises 75 wt % (2) hydrocarbon molecules containing non-aromatic cyclic moieties with 25 wt % cedar oil.
The traction fluid of any previous paragraph wherein the base fluid comprises 50 wt % (2) hydrocarbon molecules containing non-aromatic cyclic moieties with 50 wt % cedar oil.
The traction fluid of any previous paragraph wherein the base fluid comprises ⅓ cedar oil, ⅓ of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, and ⅓ of (2) hydrocarbon molecules containing non-aromatic cyclic moieties.
The traction fluid of any previous paragraph wherein the base fluid comprises 42.5 wt % cedar oil, 42.5 wt % of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, and 15 wt % of (2) hydrocarbon molecules containing non-aromatic cyclic moieties.
The traction fluid of any previous paragraph wherein the base fluid comprises 42.5 wt % cedar oil, 15 wt % of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, and 42.5 wt % of (2) hydrocarbon molecules containing non-aromatic cyclic moieties.
The traction fluid of any previous paragraph wherein the base fluid comprises 15 wt % cedar oil, 42.5 wt % of (1) polymers of at least one olefin which contains 3 to 5 carbon atoms, and 42.5 wt % of (2) hydrocarbon molecules containing non-aromatic cyclic moieties.
The traction fluid of any previous paragraph, further comprising a minor amount of oil of lubricating viscosity.
The traction fluid of any previous paragraph, wherein the additive package for a power transmission apparatus comprises at least one of a low-temperature viscosity control agent, viscosity modifier, dispersant, detergent, antioxidant, anti-wear agent, friction modifier or mixtures thereof.
The traction fluid of any previous paragraph, wherein the low-temperature viscosity control agent comprises oligomers or polymers of linear alpha olefins of at least 8 carbon atoms.
The traction fluid of any previous paragraph wherein said alpha olefins contain about 10 to about 12 carbon atoms.
The traction fluid of any previous paragraph, wherein said oligomer or polymer has a molecular weight of about 250 to about 400.
The traction fluid of any previous paragraph, wherein the low-temperature viscosity control agent comprises a naphthenic oil.
The traction fluid of any previous paragraph, wherein the low-temperature viscosity control agent comprises a synthetic ester oil.
The traction fluid of any previous paragraph wherein the synthetic ester oil is selected from the group consisting of: (i) esters of polyhydroxy compounds and predominantly monocarboxylic acylating agents, (ii) esters of predominantly monohydroxy compounds and polycarboxylic acylating agents, and (iii) esters of monohydroxy compounds and monocarboxylic acylating agents, or (iv) mixtures of (i) through (iii).
The traction fluid of any previous paragraph, wherein the low-temperature viscosity control agent comprises a polyether oil
The traction fluid of any previous paragraph, wherein said polyether oil is selected from the group consisting of polyethylene oxides, polypropylene oxides, polybutylene oxides, and mixtures thereof.
The traction fluid of any previous paragraph wherein said additive package includes a succinimide dispersant.
The traction fluid any previous paragraph wherein the amount of said dispersant is about 1 to about 10 percent by weight of the traction fluid.
The traction fluid any previous paragraph comprising an overbased sulfonate detergent.
The traction fluid of any previous paragraph wherein said overbased sulfonate detergent is a calcium overbased sulfonate detergent.
The traction fluid of any previous paragraph wherein the amount of said detergent is about 0.05 to about 5 percent by weight of the traction fluid.
The traction fluid of any previous paragraph wherein said fluid contains up to about 10 percent by weight of a polymeric viscosity index modifier.
The traction fluid of any previous paragraph wherein said fluid contains 0 to about 1 percent by weight of the polymeric viscosity index modifier.
The traction fluid of any previous paragraph wherein said fluid is substantially free from polymeric viscosity index modifiers.
The traction fluid of any previous paragraph wherein said antiwear agent comprises at least one phosphorus-containing acid, salt, or ester in an amount to contribute about 0.005 to about 0.06% phosphorus to the traction fluid.
The traction fluid of any previous paragraph wherein said phosphorus-containing acid, salt, or ester comprises dibutyl hydrogen phosphite.
The traction fluid of any previous paragraph further comprising about 0.01 to about 2 percent by weight of a friction modifier.
A method of lubricating a power transmission apparatus, comprising employing therein the traction fluid of any previous paragraph, and operating the power transmission apparatus.
The method of any previous paragraph wherein said power transmission apparatus drive is an automatic transmission.
The method of any previous paragraph wherein said automatic transmission is a continuously variable transmission.
The method of any previous paragraph wherein said power transmission apparatus is a traction/drive.
The method of any previous paragraph wherein said power transmission apparatus is a push-belt continuously variable transmission.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides a mini traction machine (“MTM”) coefficient of friction as measured on an MTM at a pressure of 1.25 GPa, temperature of 100° C., speed of 3 m/s and slide/roll ratio of 5% of greater than 0.05.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides a mini traction machine (“MTM”) coefficient of friction as measured on an MTM at a pressure of 1.25 GPa, temperature of 100° C., speed of 3 m/s and slide/roll ratio of 5% of greater than 0.06.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides a mini traction machine (“MTM”) coefficient of friction as measured on an MTM at a pressure of 1.25 GPa, temperature of 100° C., speed of 3 m/s and slide/roll ratio of 5% of greater than 0.07.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides a Brookfield viscosity as measured according to ASTM 2983 at −30° C. of less than 20,000 cP.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides a Brookfield viscosity as measured according to ASTM 2983 at −30° C. of less than 15,000 cP.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides a Brookfield viscosity as measured according to ASTM 2983 at −30° C. of less than 10,000 cP.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides an mini traction machine (“MTM”) coefficient of friction as measured on an MTM at a pressure of 1.25 GPa, temperature of 100° C., speed of 3 m/s and slide/roll ratio of 5% of greater than 0.05 and a Brookfield viscosity as measured according to ASTM 2983 at −30° C. of less than 20,000 cP.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides an mini traction machine (“MTM”) coefficient of friction as measured on an MTM at a pressure of 1.25 GPa, temperature of 100° C., speed of 3 m/s and slide/roll ratio of 5% of greater than 0.06 and a Brookfield viscosity as measured according to ASTM 2983 at −30° C. of less than 15,000 cP.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides an mini traction machine (“MTM”) coefficient of friction as measured on an MTM at a pressure of 1.25 GPa, temperature of 100° C., speed of 3 m/s and slide/roll ratio of 5% of greater than 0.07 and a Brookfield viscosity as measured according to ASTM 2983 at −30° C. of less than 15,000 cP.
The traction fluid or method of any previous paragraph, wherein the traction fluid provides an mini traction machine (“MTM”) coefficient of friction as measured on an MTM at a pressure of 1.25 GPa, temperature of 100° C., speed of 3 m/s and slide/roll ratio of 5% of greater than 0.07 and a Brookfield viscosity as measured according to ASTM 2983 at −30° C. of less than 10,000 cP.
While certain representative embodiments and details have been shown for the purpose of illustrating the subject invention, it will be apparent to those skilled in this art that various changes and modifications can be made therein without departing from the scope of the subject invention. In this regard, the scope of the invention is to be limited only by the following claims.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2020/013278 | 1/13/2020 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62793496 | Jan 2019 | US |
