Patent Application
20160281024
The present invention generally relates to an additive package and a lubricant composition that include a seal compatibility additive.
It is known and customary to add stabilizers to lubricant compositions based on mineral or synthetic oils in order to improve their performance characteristics. Some amine compounds are effective stabilizers for lubricants. For example, certain amine compounds may help to disperse soot and maintain the cleanliness of engine components and other amine compounds may help neutralize acids formed during the combustion process. However, these amine compounds may cause detrimental effects on fluoropolymer seals.
It is an object of the present invention to provide new additives that improve the fluoropolymer seal compatibility of lubricant compositions.
The present disclosure provides a method of forming an additive package for a lubricant composition. The method includes the step of providing a base oil and a dispersant. The method further includes the step of heating the base oil and the dispersant to a temperature of from 75 to 115° C. The method further includes the step of combining the base oil and the dispersant to form a first mixture. The method further includes the step of providing a detergent. The method further includes the step of heating the detergent to a temperature of from 50 to 90° C. The method further includes the step of combining the first mixture and the detergent to form a second mixture. The method further includes the step of providing an anti-wear additive and a seal compatibility additive. The method further includes the step of heating the anti-wear additive the seal compatibility additive to a temperature of from 30 to 70° C. The method further includes the step of combining the second mixture, the anti-wear additive, and the seal compatibility additive to form the additive package.
The present disclosure provides another method of forming the additive package for the lubricant composition. The method includes the step of providing the dispersant, the base oil, and the seal compatibility additive. The method further includes the step of heating the dispersant, the base oil, and the seal compatibility additive to a temperature of from 75 to 115° C. The method further includes the step of combining the dispersant, the base oil, and the seal compatibility additive to form a first mixture. The method further includes the step of providing the detergent. The method further includes the step of heating the detergent to a temperature of from 50 to 90° C. The method further includes the step of combining the first mixture and the detergent to form a second mixture. The method further includes the step of providing the anti-wear additive. The method further includes the step of heating the anti-wear additive to a temperature of from 30 to 70° C. The method further includes the step of combining the second mixture and the anti-wear additive to form the additive package.
The present disclosure also provides a lubricant composition that provides improved compatibility with fluoropolymer seals. The lubricant composition includes a first base oil and an additive package. The additive package includes a second base oil and a dispersant combined at a temperature of from 75 to 115° C. The additive package further includes a detergent combined at temperature of from 50 to 90° C. The additive package further includes an antioxidant, an anti-wear additive, and a seal compatibility additive combined at temperature of from 30 to 70° C.
The additive package may be added to conventional lubricant compositions. Both the additive package and the resultant lubricant composition (upon addition of the additive package) are contemplated and described collectively in this disclosure.
The present disclosure provides an additive package for a lubricant composition, and a method of forming the additive package. The additive package includes a seal compatibility additive. The additive package may be added to conventional lubricant compositions. Both the additive package and the resultant lubricant composition (upon addition of the additive package) are contemplated and described collectively in this disclosure.
The additive package may include one or more components to improve various chemical and/or physical properties of the lubricant composition. In addition to the seal compatibility additive, the additive package may further include other components such as amine compounds, polyol esters, dispersants, detergents, anti-wear additives, antioxidants, friction modifiers, base oils and diluents, metal deactivators (or passivators), rust inhibitors, viscosity index improvers, pour point depressors, anti-foam additives, corrosion inhibitors, antifriction additives, or combinations thereof. Each of these components will be described in detail below. These components may be included in various amounts in the additive package. It should be understood that the exemplary mixtures, pre-blends, heating steps, amounts, cooling steps, and order of mixing described below incorporates each and every specific component composition and amount described below.
The additive packages, when formed in the manner described herein, may advantageously possess improved solubility of the seal compatibility additive. For example, at least 50, 60, 70, 80, 85, 90, 95, 97, 99, wt. % of the seal compatibility additive may be dissolved in the ultimately formed additive package. Alternatively, 100 wt. % of the seal compatibility additive may be dissolved in the ultimately formed additive package.
The additive package may be formed by combining one or more of the components introduced above. Further, two or more of the components may be combined separate from the other components of the additive package to form a “pre-blend.” In certain embodiments, the pre-blend may be formed from 2, 3, 4, 5, 6, 7, 8, 9, 10, or greater than 10, components. In other embodiments, the pre-blends consist, or consist essentially of, 2, 3, 4, 5, 6, 7, 8, 9, or 10 components listed above. The pre-blend may be combined with the other components of the additive package, or other pre-blends of components of the additive package. Exemplary pre-blends include, consist of, or consist essentially of: i) the dispersant and the base oil, ii) the dispersant, the base oil, and the seal compatibility additive, iii) the dispersant, the base oil, and the anti-wear additive, iv) the detergent, the base oil, and the seal compatibility additive, v) the seal compatibility additive and the amine compound, vi) the seal compatibility additive and the polyol ester, vii) the seal compatibility additive and the base oil, viii) the detergent and the base oil, ix) the base oil and the anti-wear additive, and x) the dispersant, the detergent, and the base oil.
A mixture of one or more of the components of the additive package and/or the pre-blends of one or more of the components may undergo agitation. Thus, the method of forming the additive package may include the step of agitating the mixture of one or more of the components of the additive package and/or the pre-blends of the components. In certain embodiments, the components and/or the pre-blends of the components are combined under agitation. Examples of suitable methods of agitation include mixing.
The mixture of one or more of the components of the additive package and/or the pre-blends of the components may undergo a resting period before being subsequently mixed with one or more additional components and/or one or more additional pre-blends. The method of forming the additive package may include the step of maintaining at rest the mixture of one or more of the components of the additive package and/or the pre-blends of the components. The resting period may have various durations, including, but not limited to at least, 1 minute, 30 minutes, 1 hour, 8 hours, 24 hours, or 1 week.
One or more of the components of the additive package and/or the pre-blends of the components may be combined at any temperature during a heating step. The method of forming the additive package may include the step of heating one or more of the components of the additive package and/or the pre-blends of the components. The components and/or the pre-blends may be heated prior to, during, and/or after combination of the components and/or the pre-blends. Further, the step of heating may be at a single temperature or at multiple temperatures which follow a temperature profile. The temperature of the heating step may be conducted such that the components or mixtures of components are maintained at a temperature of greater than 20, greater than 30, greater than 40, greater than 50, greater than 60, greater than 70, greater than 80, greater than 90, greater than 100, greater than 110, greater than 120, greater than 130, greater than 140, or greater than 150, ° C.
The method of forming the additive package may include the step of cooling one or more of the components of the additive package and/or the pre-blends of the components. The components and/or the pre-blends may be cooled prior to, during, and/or after combination of the components and/or the pre-blends. Further, the step of cooling may be at a single temperature or at multiple temperatures which follow a temperature profile. The temperature of the cooling step may be conducted such that the components or mixtures of components are maintained at a temperature of less than 150, less than 140, less than 130, less than 120, less than 110, less than 100, less than 90, less than 80, less than 70, less than 60, less than 50, less than 40, less than 30, or less than 20, ° C.
The method of forming the additive package may include the step of maintaining the temperature of one or more of the components of the additive package and/or the pre-blends of the components. The components and/or the pre-blends may have the temperature maintained prior to, during, and/or after combination of the components and/or the pre-blends.
One or more of the components of the additive package and/or the pre-blends of the components may be combined in any order. In some embodiments, the detergent and any other component(s) (e.g., the dispersant) are combined with each other to form one or more mixtures or pre-blends prior to combination with the seal compatibility additive. In other words, in this embodiment, the seal compatibility additive is not combined directly with detergent and the dispersant. In other embodiments, the detergent and any other component(s) (e.g., the dispersant) are combined directly with the seal compatibility additive without initially forming a mixture or a pre-blend. In other words, in this embodiment, the seal compatibility additive is combined directly with detergent and the dispersant.
In one embodiment, the dispersant and the base oil are combined to form a mixture I. The mixture I is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture I is formed at a temperature of from 75 to 115, from 85 to 105, or from 90 to 100, ° C. Next, the detergent is combined with the mixture I to form a mixture II. The mixture II is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture II is formed at a temperature of from 50 to 90, from 60 to 80, or from 65 to 75, ° C. Next, the antioxidant, the anti-wear additive, and the seal compatibility additive are combined with the mixture II to form a mixture III. The mixture III is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture III is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. In this embodiment, the mixture III is the additive package.
In another embodiment, the dispersant, the base oil, and the seal compatibility additive are combined to form a mixture IV. The mixture IV is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture IV is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. Next, the detergent is combined with the mixture IV to form a mixture V. The mixture V is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture V is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. Next, the antioxidant and the anti-wear additive are combined with the mixture V to form a mixture VI. The mixture VI is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture VI is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. In this embodiment, the mixture VI is the additive package.
In another embodiment, the dispersant, the base oil, and the anti-wear additive are combined to form a mixture VII. The mixture VII is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture VII is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. Next, the detergent, the antioxidant, and the seal compatibility additive are combined with the mixture VII to form a mixture VIII. The mixture VIII is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture VIII is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. In this embodiment, the mixture VIII is the additive package.
In another embodiment, the detergent, the base oil, and the seal compatibility additive are combined to form a mixture IX. The mixture IX is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture IX is formed at a temperature of from 40 to 80, from 50 to 70, or from 55 to 65, ° C. Next, the dispersant and the antioxidant are combined with the mixture IX to form a mixture X. The mixture X is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture X is formed at a temperature of from 40 to 80, from 50 to 70, or from 55 to 65, ° C. Next, the anti-wear additive is combined with the mixture X to form a mixture XI. The mixture XI is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture XI is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. In this embodiment, the mixture XI is the additive package.
In another embodiment, the dispersant and the base oil are combined to form a mixture XII. The mixture XII is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture XII is formed at a temperature of from 75 to 115, from 85 to 105, or from 90 to 100, ° C. Next, the detergent is combined with the mixture XII to form a mixture XIII. The mixture XIII is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture XIII is formed at a temperature of from 50 to 90, from 60 to 80, or from 65 to 75, ° C. Next, the seal compatibility additive and the amine compound are combined separate from the mixture XIII to form a mixture XIV. Next, the antioxidant, the anti-wear additive, and the mixture XIV are combined with the mixture XIII to form a mixture XV. The mixture XV is agitated for a period of from 30 to 90, 45 to 75, or 55 to 65, minutes. The mixture XV is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. In this embodiment, the mixture XV is the additive package.
In another embodiment, the dispersant and the base oil are combined to form a mixture XVI. The mixture XVI is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture XVI is formed at a temperature of from 75 to 115, from 85 to 105, or from 90 to 100, ° C. Next, the detergent is combined with the mixture XVI to form a mixture XVII. The mixture XVII is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture XVII is formed at a temperature of from 50 to 90, from 60 to 80, or from 65 to 75, ° C. Next, the seal compatibility additive and the polyol ester are combined separate from the mixture XVII to form a mixture XVIII. Next, the antioxidant, the anti-wear additive, and the mixture XVIII are combined with the mixture XVII to form a mixture XIX. The mixture XIX is agitated for a period of from 30 to 90, from 45 to 75, or from 55 to 65, minutes. The mixture XIX is formed at a temperature of from 30 to 70, from 40 to 60, or from 45 to 55, ° C. In this embodiment, the mixture XIX is the additive package.
As introduced above, the additive package (or resultant lubricant composition) includes one or more seal compatibility additives. The seal compatibility additive may be a halide seal compatibility additive, an epoxide compound, a boroxine compound, a sulfonate ester, or combinations thereof. The seal compatibility additive can be present in the additive package in various amounts. The seal compatibility additive may be present in the additive package in an amount ranging from 0.1 to 99, from 0.1 to 50, or from 0.1 to 10, wt. %, based on the total weight of the additive package.
In one embodiment, seal compatibility additive is the halide seal compatibility additive. The halide seal compatibility additive includes a halogen compound. The halogen compound minimally includes one or more halogen atoms. However, the halogen compound can take various forms. For example, the halogen compound may comprise a hydrocarbon backbone. More specifically, the halogen compound may comprise an alkyl halide compound, or may comprise a quaternary amine compound having one or more halogen atoms bonded thereto. Alternatively, the halogen compound may be an elemental halogen, such as Cl2, Br2, I2 or F2.
In one or more embodiments, the halogen compound comprises the hydrocarbon backbone and at least one halogen atom bonded to a carbon atom in the hydrocarbon backbone. The halogen compound may be straight or branched. The hydrocarbon backbone may be cyclic or acyclic. The hydrocarbon backbone may also be straight. The hydrocarbon backbone may include from 1 to 30, 2 to 25, 2 to 20, 2 to 15, 9 to 15, or 9 to 12, carbon atoms.
The halogen compound may comprise one or more pendant groups selected from the group of alcohol groups, alkoxy groups, alkenyl groups, alkynyl groups, amine groups, aryl groups, alkylaryl, arylalkyl, heteroaryl groups, alkyl groups, cycloalkyl groups, cycloalkenyl, amide groups, ether groups, ester groups, and combinations thereof, each independently having from 1 to 30, 1 to 20, 1 to 15, or 3 to 12, carbon atoms. Each of these pendant groups may be bonded to a carbon atom positioned in hydrocarbon backbone of the halogen compound. By “unsubstituted,” it is intended that the designated hydrocarbyl group or hydrocarbon group is free from substituent functional groups, such as alkoxy, amide, amine, keto, hydroxyl, carboxyl, oxide, thio, and/or thiol groups, and that the designated hydrocarbyl group or hydrocarbon group is free from heteroatoms and/or heterogroups.
In one embodiment, the halogen compound is cyclic, meaning that the halogen compound includes one or more pendant cyclic groups, that the hydrocarbon backbone, if present, is cyclic, or both. In another embodiment, the halogen compound is acyclic, meaning that the hydrocarbon backbone, if present, is acyclic and the halogen compound is free from pendant cyclic groups.
The hydrocarbon backbone, if present, may include functional groups other than the halogen atom, such as hydroxyl, carboxyl, carbonyl, epoxy, oxide, thio, and thiol groups. These functional groups may be bonded to the carbon atoms which are positioned in the hydrocarbon backbone of the halogen compound. The hydrocarbon backbone, if present, may also comprise one or more heteroatoms, such as oxygen, sulfur, and nitrogen heteroatoms; or one or more heterogroups, such as pyridyl, furyl, thienyl, and imidazolyl.
Alternatively, if present, the hydrocarbon backbone may include no pendant or functional groups bonded to the carbon atoms in the hydrocarbon backbone other than the halogen atom. In addition, or as an alternative, the hydrocarbon backbone may be free from heteroatoms and heterogroups. The hydrocarbon backbone may be saturated or unsaturated.
The halogen compound may include fluorine atoms, bromine atoms, iodine atoms, and combinations thereof. Each of these halogen atoms may be bonded to a carbon atom in the hydrocarbon backbone, a carbon atom in one of the pendant groups of the hydrocarbon backbone, or both. The halogen compound may comprise 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 or more halogen atoms per molecule. It is also contemplated that one or more different halogen atoms may be present in the same molecule of the halogen compound.
In certain embodiments, the halogen compound comprises the alkyl halide compound and may have a general formula (I):
CnH2n+2−mXm (I)
In general formula (I), n≧1, 1≦m≦(2n+2), and X is a halogen atom. X may be selected from the group including fluorine, bromine, iodine, and combinations thereof. In some embodiments, n may range from 1 to 30, 2 to 25, 2 to 20, 2 to 15, 9 to 15, or 9 to 12; and m may have a value of 1, 2, 3, 4, 5, 6, or more. The alkyl halide compound may be primary, secondary, or tertiary. The alkyl halide compound may be a mono-halide, di-halide, tri-halide, or tetrahalide in some embodiments. It is also contemplated that one or more different halogen atoms may be present in the same alkyl halide compound.
The quaternary halogen compound may be understood as a quaternary amine salt that includes one or more halogen atoms bonded thereto. The halogen atoms may be bonded along the body of the quaternary amine salt or may be bonded to the quaternary amine salt as a halide counter-ion. The quaternary amine compound may include 1, 2, 3, 4, 5, or more nitrogen atoms. The quaternary amine compound may also include 1, 2, 3, 4, 5, or more halogen atoms. It is also contemplated that one or more different halogen atoms may be present in the same quaternary amine compound. The quaternary amine compound may include a variety of different pendent groups, such as alkyl, aryl, alkenyl, alkynyl, cycloalkyl, arylalkyl, or heteroaryl groups, each having from 1 to 30, 1 to 20, 1 to 15, or 3 to 12, carbon atoms, and may be further substituted by one or more amine, imine, hydroxyl, halogen, and/or carboxyl groups. The quaternary amine compound may be cyclic or acyclic.
The halogen compound may have a weight average molecular weight ranging from 30 to 1500, 50 to 1000, 100 to 500, 150 to 500, 200 to 500, or 250 to 500.
The halogen compound may have a boiling point ranging from 50 to 650, 100 to 450, 135 to 450, 140 to 450, 145 to 450, 150 to 450, 155 to 450, or 200 to 400, ° C., at 1 atmosphere. Alternatively, the halogen compound may have a boiling point of at least 100, at least 110, at least 120, at least 130, at least 140, at least 150, or at least 160, ° C., at 1 atmosphere, and less than 450, less than 400, less than 350, less than less than 300, or less than 250, ° C., at 1 atmosphere.
The halogen compound may also be characterized as having a flash point ranging from 10 to 300, 25 to 250, 50 to 250, 75 to 250, or 85 to 200, ° C. Alternatively, the halogen compound may have a flash point of at least 10, at least 15, at least 20, at least 25, at least 30, at least 35, at least 40, at least 45, at least 50, at least 55, at least 60, at least 65, at least 70, at least 75, at least 80, or at least 85, ° C., and a flash point less than 250, less than 225, less than 200, less than 175, less than 150, or less than 125, ° C.
In certain embodiments, the halogen compound is a liquid at a temperature of 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100, ° C., and 1 atmosphere
The halogen compound may be synthesized in a variety of ways. For example, the halogen compound can be prepared by reacting an alkene with a halogen halide, such as hydrogen chloride or hydrogen bromide to yield the corresponding monohalogenated alkene. Alternatively, the halogen compound may be prepared by reacting an alcohol with a hydrogen halide. Alternatively still, the halogen compound may be prepared by reacting an alkyl alcohol with carbon tetra bromide, sodium bromide, and a ruthenium catalyst, all in a dimethylformamide solvent. The carbon tetrabromide may be replaced with other halogen compounds if halogens other than bromide are desired.
Exemplary halogen compounds include tetrabromoethane; ethyliodide; ethylbromide; 1,2-dibromoethane; trifluoro-1,2,2-dibromoethane; 1-fluorooctane; tribromopropane; dibromo cyclohexane; dibromoethane; n-propylbromide; 1-bromo, 4-fluoro cyclohexane; butylbromide; octylbromide; 1-iodododecane; 1-bromododecane; 1,4-di iodobutane; 1,4-dibromobutane; tetrafluoroethane; 3-iodo-1-propanol; 1-bromohexane; 1-iodohexane; 1-bromopropane; and 1-iodopropane.
Conventional uses of the halogen compound involve forming a reaction product of the halogen compound. In such conventional uses, more than 50 wt. % of the halogen compound is typically reacted based on the total weight of the halogen compound before reaction. In certain embodiments, at least 50, at least 60, at least 70, at least 80 or, at least 90, wt. %, of the halogen compound remains unreacted in the additive package and/or lubricant composition based on the total weight of halogen compound utilized to form the additive package and/or the lubricant composition prior to any reaction in the additive package or the lubricant composition. Alternatively, at least 95, at least 96, at least 97, at least 98, or at least 99, wt. %, of the halogen compound remains unreacted in the additive package and/or the lubricant composition based on the total weight of the halogen compound prior to any reaction in the additive package or the lubricant composition.
The term “unreacted” refers to the fact that the unreacted amount of the halogen compound does not react with any components in the additive package or lubricant composition. Accordingly, the unreacted portion of the halogen compound remains in its virgin state when present in the additive package or the lubricant composition before the lubricant composition has been used in an end-use application, such as an internal combustion engine.
The phrase “prior to any reaction” refers to the basis of the amount of the halogen compound in the additive package or lubricant composition. This phrase does not require that the halogen compound reacts with other components in the additive package or the lubricant composition, i.e., 100 wt. % of the halogen compound may remain unreacted in the additive package and/or the lubricant composition based on the total weight of the halogen compound prior to any reaction in the additive package and/or the lubricant composition.
Alternatively, the percentage of the halogen compound that remains unreacted is determined after all of the components which are present in the additive package or lubricant composition reach equilibrium with one another. The time period necessary to reach equilibrium in the additive package or lubricant composition may vary widely. For example, the amount of time necessary to reach equilibrium may range from a single minute to many days, or even weeks. In certain embodiments, the percentage of the halogen compound that remains unreacted in the additive package or lubricant composition is determined after 1 minute, 1 hour, 5 hours, 12 hours, 1 day, 2 days, 3 days, 1 week, 1 month, 6 months, or 1 year.
In one aspect, the halide seal compatibility additive is an iodide seal compatibility additive. The iodide seal compatibility additive includes at least iodine atom. Beyond that, the iodide seal compatibility additive may take many forms. For example, the iodide seal compatibility additive may include a hydrocarbon backbone. Furthermore, the iodide seal compatibility additive may be an alkyl iodide compound, or may be a quaternary amine compound having at least one iodine atom bonded thereto. Alternatively still, the iodide seal compatibility additive may be elemental iodine (I2).
In one or more embodiments, the iodide seal compatibility additive includes a hydrocarbon backbone and at least one iodine atom bonded to a carbon atom in the hydrocarbon backbone. In certain embodiments, the iodide seal compatibility additive includes the hydrocarbon backbone and at least one iodine atom. The iodide seal compatibility additive may be straight or branched. The hydrocarbon backbone may be cyclic or acyclic. The hydrocarbon backbone may include from 1 to 30, 2 to 25, 2 to 20, 2 to 15, 9 to 15, or 9 to 12, carbon atoms. As used herein, the term “acyclic” is intended to refer to hydrocarbon backbones which are free from any cyclic structures and to exclude aromatic structures.
In some aspects, the iodide seal compatibility additive may include at least one pendant group. In some embodiments, the at least one pendant group is selected from alcohol groups, alkoxy groups, alkenyl groups, alkynyl groups, amine groups, aryl groups, alkylary groups, arylalkyl groups, heteroaryl groups, alkyl groups, cycloalkyl groups, cycloalkenyl, amide groups, ether groups, ester groups, and combinations thereof, each having from 1 to 30, 1 to 20, 1 to 15, or 3 to 12, carbon atoms. Each of these pendant groups may be bonded to a carbon atom positioned in the hydrocarbon backbone of the iodide seal compatibility additive.
In one embodiment, the iodide seal compatibility additive is cyclic, meaning that the iodide seal compatibility additive includes the hydrocarbon backbone and that the hydrocarbon backbone includes at least one pendant cyclic group, that the hydrocarbon backbone is cyclic, or both. In another embodiment, the iodide seal compatibility additive is acyclic, meaning that the hydrocarbon backbone is acyclic and that the iodide seal compatibility additive is free from pendant cyclic groups. Alternatively, the hydrocarbon backbone of the iodide seal compatibility additive may be free of pendant and/or functional groups bonded to the carbon atoms in the hydrocarbon backbone other than the iodine atom.
The hydrocarbon backbone of the iodide seal compatibility additive may include functional groups, such as hydroxyl, carboxyl, carbonyl, epoxy, oxide, thio, and thiol groups. One or more of these functional groups may be bonded to hydrocarbon backbone of the iodide seal compatibility additive. The hydrocarbon backbone of the iodide seal compatibility additive may also include at least one heteroatom, such as oxygen, sulfur, and nitrogen heteroatoms; or at least one heterogroup, such as pyridyl, furyl, thienyl, and imidazolyl. In addition, or as an alternative, the hydrocarbon backbone may be free from heteroatoms and heterogroups. For example, the hydrocarbon backbone may be free from oxygen hetero atoms. The hydrocarbon backbone may be saturated or unsaturated.
The iodide seal compatibility additive may additionally include fluorine atoms, chlorine atoms, bromine atoms, and combinations thereof. Each of these halogen atoms may be bonded to a carbon atom in the hydrocarbon backbone of the iodide seal compatibility additive or a carbon atom in one of the pendant groups of the hydrocarbon backbone of the iodide seal compatibility additive. The iodide seal compatibility additive may include 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more halogen atoms per molecule. It is also contemplated that two or more different, or that two or more of the same, halogen atoms may be present in the same iodide seal compatibility additive. For example, the iodide seal compatibility additive may include at least one iodine atom and at least one bromine atom.
As described above, the iodide seal compatibility additive may be an alkyl iodide compound. The alkyl iodide compound may have a general formula:
CnH2n+2−mIm (II).
In formula (II), n≧1, and 1≦m≦(2n+2). In some embodiments, n may range from 1 to 30, 2 to 25, 2 to 20, 2 to 15, 9 to 15, or 9 to 12; and m may have a value of 1, 2, 3, 4, 5, 6, or more. The alkyl iodide compound may be primary, secondary, or tertiary. It is also contemplated that two or more different, or two or more of the same, halogen atoms may be present in the same alkyl iodide compound. For example, the iodide seal compatibility additive may include 1,4 diiodobutane or 1-iodo-4-bromobutane.
The quaternary halogen compound may be understood as a quaternary amine salt that includes at least one iodine atom bonded thereto. The iodine atom may be bonded along the body of the quaternary amine salt or may be bonded to the quaternary amine salt as a iodide counter-ion. The quaternary amine compound may include 1, 2, 3, 4, 5, or more nitrogen atoms. The quaternary amine compound may also include 1, 2, 3, 4, 5, or more iodine atoms. The quaternary amine compound may include a variety of different pendent groups, such as alkyl, aryl, alkenyl, alkynyl, cycloalkyl, arylalkyl, or heteroaryl groups, each having from 1 to 30, 1 to 20, 1 to 15, or 3 to 12, carbon atoms, and may be further substituted by at least one amine, imine, hydroxyl, halogen, and/or carboxyl group. The quaternary amine compound may be cyclic or acyclic.
Exemplary iodide seal compatibility additives include:
The iodide seal compatibility additive may have a weight average molecular weight ranging from 50 to 1500, 50 to 1000, 100 to 500, 150 to 500, 200 to 500, or 250 to 500.
The iodide seal compatibility additive may have a boiling point ranging from 50 to 650, 100 to 450, 135 to 450, 140 to 450, 145 to 450, 150 to 450, 155 to 450, or 200 to 400, ° C., at 1 atmosphere. Alternatively, the iodide seal compatibility additive may have a boiling point of at least 100, at least 110, at least 120, at least 130, at least 140, at least 150, or at least 160, ° C., at 1 atmosphere, and less than 450, less than 400, less than 350, less than less than 300, or less than 250, ° C., at 1 atmosphere.
The iodide seal compatibility additive may also be characterized as having a flash point ranging from 10 to 300, 25 to 250, 50 to 250, 75 to 250, or 85 to 200, ° C. Alternatively, the iodide seal compatibility additive may have a flash point of at least 10, at least 15, at least 20, at least 25, at least 30, at least 35, at least 40, at least 45, at least 50, at least 55, at least 60, at least 65, at least 70, at least 75, at least 80, or at least 85, ° C., and a flash point less than 250, less than 225, less than 200, less than 175, less than 150, or less than 125, ° C.
In certain embodiments, the iodide seal compatibility additive is a liquid at a temperature of 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100, ° C., and 1 atmosphere.
The iodide seal compatibility additive may be synthesized in a variety of ways. For example, the iodide seal compatibility additive can be prepared by reacting an alkene with hydrogen iodide to yield the corresponding monohalogenated alkane. Alternatively, the iodide seal compatibility additive may be prepared by reacting an alcohol with a hydrogen iodide.
In the context of the additive package, the halide seal compatibility additive, such as the iodide seal compatibility additive, can be present in an amount ranging from 0.1 to 99, 5 to 50, or 10 to 40, wt. %, based on the total weight of the additive package. In the context of a lubricant composition, the halide seal compatibility additive, such as the iodide seal compatibility additive, can be present in an amount ranging from 0.01 to 10, 0.05 to 5, 0.01 to 3, 0.01 to 2, 0.01 to 1.5, 0.01 to 1, 0.01 to 0.75, 0.01 to 0.5, 0.01 to 0.25, or 0.01 to 0.1, wt. %, based on the total weight of the lubricant composition.
In another embodiment, the seal compatibility additive is an epoxide compound. In certain embodiments, the epoxide compound may be represented by general formula (III):
In general formula (III), each R1 is independently a hydrogen atom or a hydrocarbyl group. Multiple groups designated by R1 may be bonded together to form a cyclic structure.
The term “cyclic” is intended to refer to compounds that include any molecules having at least three atoms joined together to form a ring. In some embodiments, the term “cyclic” does not include aromatic compounds.
The epoxide compound may include one or more oxirane ring. The oxirane ring may be a terminal oxirane ring or an internal oxirane ring. The term “terminal oxirane ring” means that one of the carbon atoms which form the oxirane ring must contain two hydrogen atoms, or that two carbons which form the oxirane ring also form part of a cyclic ring. The term “internal oxirane ring” means that neither of the carbon atoms which form the oxirane ring is bonded to more than one hydrogen atom. The epoxide compound may be free from internal oxirane rings, or may include fewer than 4, 3, 2, or 1, internal oxirane rings. Alternatively, the epoxide compound may include 1, 2, 3, 4, or more internal oxirane rings. Alternatively still, the epoxide compound may include at least 1, at least 2, at least 3, at least 4 terminal oxirane rings. In certain embodiments, at least one, or at least two, oxirane rings may be terminal and may be cyclic, i.e., the carbons of the oxirane rings are part of a cyclic ring.
Each hydrocarbyl group designated by R1 may independently be substituted or unsubstituted, straight or branched, alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, alkylaryl, arylalkyl group, or combinations thereof. Each hydrocarbyl group designated by R1 may independently include from 1 to 100, 1 to 50, 1 to 40, 1 to 30, 1 to 20, 1 to 15, 1 to 10, 1 to 6, or 1 to 4, carbon atoms. Alternatively, each hydrocarbyl group designated by R1 may independently include less than 20, less than 15, less than 12, or less than 10, carbon atoms.
Alternatively, each hydrocarbyl group designated by R1 may be independently substituted, and include one or more heteroatoms, such as oxygen, nitrogen, sulfur, chlorine, fluorine, bromine, or iodine, and/or one or more heterogroups, such as pyridyl, furyl, thienyl, and imidazolyl. Alternatively, or in addition to including heteroatoms and heterogroups, each hydrocarbyl group designated by R1 may independently include one or more substituent groups selected from alkoxy, amide, amine, carboxyl, epoxy, ester, ether, hydroxyl, keto, metal salt, sulfuryl, and thiol groups. Alternatively, each hydrocarbyl group designated by R1 may be independently unsubstituted.
Exemplary alkyl groups include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, 2-ethylhexyl, octyl and dodecyl groups. Exemplary cycloalkyl groups cyclopropyl, cyclopentyl and cyclohexyl groups. Exemplary aryl groups include phenyl and naphthalenyl groups. Exemplary arylalkyl groups include benzyl, phenylethyl, and (2-naphthyl)-methyl.
As described above with respect to general formula (III), the hydrocarbyl group designated by R1 may include one or more epoxy groups. These hydrocarbyl epoxy groups may be represented by the general formula (IV):
In general formula (IV), R2 is a divalent hydrocarbon group and each R3 may independently be a hydrogen atom or a hydrocarbyl group. The divalent hydrocarbon group designated by R2 may be substituted or unsubstituted, straight or branched, alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, alkylaryl, arylalkyl group, or combinations thereof. Each hydrocarbon group designated by R2 may independently include from 1 to 100, 1 to 50, 1 to 40, 1 to 30, 1 to 20, 1 to 15, 1 to 10, 1 to 6, or 1 to 4, carbon atoms. Alternatively still, each hydrocarbyl group designated by R2 may independently include less than 20, less than 15, less than 12, or less than 10, carbon atoms. Alternatively, each hydrocarbon group designated by R2 may be independently substituted, and include one or more heteroatoms, such as oxygen, nitrogen, sulfur, chlorine, fluorine, bromine, or iodine, and/or one or more heterogroups, such as pyridyl, furyl, thienyl, and imidazolyl. Alternatively, or in addition to including heteroatoms and heterogroups, each hydrocarbon group designated by R2 may independently include one or more substituent groups selected from alkoxy, amide, amine, carboxyl, epoxy, ester, ether, hydroxyl, keto, metal salt, sulfuryl, and thiol groups. The hydrocarbyl groups designated by R3 may have the same meaning as R1 as described above with respect to general formula (III). Multiple groups designated by R3 may be bonded together to form a cyclic structure.
Referring again to general formula (III), if at least one R1 is a hydrocarbyl group including an amide group, exemplary epoxide compounds include N-methyl 2,3-epoxypropionamide, N-ethyl 2,3-epoxypropionamide, N-propyl 2,3-epoxypropionamide, N-isopropyl 2,3-epoxypropionamide, N-butyl 2,3-epoxypropionamide, N-isobutyl 2,3-epoxypropionamide, N-tert-butyl 2,3-epoxypropionamide, N-hexyl 2,3-epoxypropionamide, N-octyl 2,3-epoxypropionamide, N-(2-ethylhexyl)-2,3-epoxypropionamide, and N-dodecyl 2,3-epoxypropanionamide.
In certain embodiments, the epoxide compound of general formula (III) may be an alkyl epoxide compound. The alkyl epoxide compound may be exemplified by 1,2-epoxybutane, 2-methyl 2,3-epoxy butane, 1,2-epoxypentane, 1,2-epoxyhexane, 1,2-epoxyheptane, 1,2-epoxyoctane, 1,2-epoxynonane, 1,2-epoxydecane, 1,2-epoxyundecane, 1,2-epoxydodecane, 1,2-epoxytridecane, 1,2-epoxytetradecane, 1,2-epoxypentadecane, 1,2-epoxyhexadecane, 1,2-epoxyheptadecane, 1,1-,2-epoxyoctadecane, 1,2-epoxynonadecane, and 2,3-epoxy pentane.
Alternatively, in other embodiments, the epoxide compound of general formula (III) may be an alkyl glycidyl ether compound. The alkyl glycidyl ether compound may be exemplified by decyl glycidyl ether, undecyl glycidyl ether, dodecyl glycidyl ether, tridecyl glycidyl ether, tetradecyl glycidyl ether, 2-ethylhexyl glycidyl ether, neopentyl glycol diglycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol tetraglycidyl ether, 1,6-hexane diol diglycidyl ether, sorbitol polyglycidyl ether, polyalkylene glycol monoglycidyl ether, and polyalkylene glycol diglycidyl ether.
Exemplary epoxide compounds also include glycidol, glycidol derivatives, glycidyl, glycidyl derivatives, allyl 2,3-epoxypropyl ether, isopropyl 2,3-epoxypropyl ether, (tert-butoxymethyl)oxirane, and [[(2-ethylhexyl)oxy]methyl]oxirane.
In some embodiments, the epoxide compound may be an epoxide ester compound. The epoxide ester compound may be represented by general formula (V):
In general formula (V), each group designated by R4 is independently a hydrogen atom or a hydrocarbyl group, and wherein at least one group designated by R4 is an epoxy group or is a hydrocarbyl group substituted with an epoxy group. Alternatively, in certain embodiments, each group designated by R4 is an epoxy group or a hydrocarbyl group substituted with at least one epoxy group. Further still, at least one of the groups designated by R4 in general formula (V) may designate a cyclic hydrocarbyl group where two carbons of the oxirane ring are part of the cyclic ring. The hydrocarbyl groups designated by R4 may independently have the same meaning as R1 described above with respect to general formula (III).
The epoxide ester compound of general formula (V) may be exemplified by methyl 2,3-epoxypropionate, ethyl 2,3-epoxypropionate, propyl 2,3-epoxypropionate, isopropyl 2,3-epoxypropionate, butyl 2,3-epoxypropionate, isobutyl 2,3-epoxypropionate, hexyl 2,3-epoxypropionate, octyl 2,3-epoxypropionate, 2-ethylhexyl 2,3-epoxypropionate, and dodecyl 2,3-epoxypropionoate.
In certain embodiments, the epoxide ester compound of general formula (V) may be more specifically represented by general formula (VI):
In general formula (VI), each group designated by R5 may be a hydrogen atom or a hydrocarbyl group. The hydrocarbyl group designated by R5 may have the same meaning as R1 described above with respect to general formula (III). The epoxide ester compound of general formula (II) may be exemplified by glycidyl-2,2-dimethyl octanoate, glycidyl benzoate, glycidyl-tert-butyl benzoate, glycidyl acrylate, and glycidyl methacrylate.
In certain embodiments, the epoxide compound is a cyclic epoxide compound. The cyclic epoxide compound may be represented by general formula (VII):
In general formula (VII), Z represents the type and number of atoms necessary to complete the cyclic ring of general formula (VII). The ring designated by Z may include from 2 to 20, 3 to 15, 5 to 15, carbon atoms. For example, the ring designated by Z may include 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbons, not accounting for the number of carbon atoms in any substituent groups. Z may be a substituted or unsubstituted, branched or unbranched, divalent hydrocarbon group that may include one or more heteroatoms, such as oxygen, nitrogen, sulfur, chlorine, fluorine, bromine, or iodine, or one or more heterogroups, such as pyridyl, furyl, thienyl, and imidazolyl. In addition to, or alternatively to, including heteroatoms and/or heterogroups, the ring designated by Z may include one or more hydrocarbyl substituent groups, such as those described for R2 in general formula (III). The divalent hydrocarbon group designated by Z may be aliphatic or aromatic. In some embodiments, the divalent hydrocarbon group designated by Z may be exemplified by: cyclopropyl, cyclopentyl, cyclohexyl, phenyl, naphthalenyl, benzyl, phenylethyl, and (2-naphthyl)-methyl groups. It should be appreciated that the heteroatoms, heterogroups, and/or substituent groups described above may be bonded to various atoms in the ring designated by Z; for example, the hydrocarbyl substituent groups may be bonded directly to one or more carbons in the ring designated by Z that form part of the oxirane ring. Alternatively, the substituent groups, heterogroups, and heteroatoms may be bonded to other carbon atoms in the hydrocarbon group, such as carbons that are not part of the oxirane ring. In some embodiments, the cyclic epoxide compound of general formula (VII) may be a cycloaliphatic epoxide compound having at least two terminal oxirane rings.
The cyclic epoxide compound of general formula (VII) may be exemplified by 1,2-epoxycyclohexane, 1,2-epoxycyclopentane, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate, bis(3,4-epoxy cyclohexylmethyl) adipate, bis(3,4-epoxy-6-methylcyclohexylmethyl) adipate, and 4-epoxyethyl-1,2-epoxycyclohexane.
As should be appreciated from general formulas (III), (IV), (V), (VI), and (VII) described above, the epoxide compound may be a monoepoxide, or a polyepoxide compound, such as a diepoxide. The polyepoxide compound includes at least two oxirane rings. Furthermore, in some embodiments, the polyepoxide compound may include fewer than 10, fewer than 8, fewer than 5, fewer than 4, or fewer than 3, oxirane rings per molecule.
The polyepoxide compound may include one or more substituted or unsubstituted, branched or unbranched, hydrocarbyl or divalent hydrocarbon groups, such alkyl, alkenyl, cycloalkyl, alkylcycloalkyl, aryl, alkylaryl group, arylalkyl groups, and combinations thereof. Each hydrocarbyl or divalent hydrocarbon group included in the polyepoxide compound may independently be substituted with one or more heteroatoms, such as oxygen, nitrogen, sulfur, chlorine, bromine, fluorine, or iodine, and/or may independently include one or more heterogroups, such as pyridyl, furyl, thienyl, and imidazolyl. Each hydrocarbyl or divalent hydrocarbon group in the polyepoxide compound may include one or more substituent groups selected from alkoxy, amide, amine, carboxyl, epoxy, ester, ether, hydroxyl, keto, metal salt, sulfuryl, and thiol groups. Each of the hydrocarbyl or divalent hydrocarbon groups in the polyepoxide compound may independently include from 1 to 100, 1 to 50, 1 to 40, 1 to 30, 1 to 20, 1 to 10, 1 to 6, or 1 to 4, carbon atoms. The hydrocarbyl or divalent hydrocarbon groups may be bonded to one another or to one or more carbon atoms of the oxirane rings to form the polyepoxide compound.
In some embodiments, the polyepoxide compound may be represented by the general formula (VIII):
In general formula (VIII), R6, R7, R8, R9 and R10 are each independently a hydrogen atom or a hydrocarbyl group. R11 is a divalent hydrocarbon group. The hydrocarbyl groups designated by R6, R7, R8, R9, and R10 in general formula (VIII) may have the same meaning as described above with respect to R1 in general formula (III). The divalent hydrocarbon group designated by R11 in general formula (VIII) may have the same meaning as described above with respect to R2 in general formula (IV). In certain embodiments, R6 and R7, together with the two carbons of the oxirane ring, form a cyclic structure. In other embodiments, R8 and R9, together with the two carbons of the oxirane ring, form a cyclic structure. As such, the polyepoxide compound of general formula (VIII) may include one, two, or more than two, cyclic rings. Furthermore, in certain embodiments, at least one, or at least two, of the oxirane oxygens in general formula (VIII) is directly bonded to two cyclic carbons, i.e., carbons which form part of a cyclic ring.
Alternatively, the polyepoxide compound may be represented by general formula (IX) shown below:
In general formula (IX), each Z may have the same meaning as described above with respect to general formula (IX). In general formula (IX), R12 is a divalent hydrocarbon group. R12 may have the same meaning as described above with respect to R2 in general formula (IV). It should be appreciated that the divalent hydrocarbon group designated by R12 may be bonded to various atoms in the divalent hydrocarbon group designated by Z. For example, the divalent hydrocarbon group designated by R12 may be bonded directly to one or more oxirane ring carbons in certain embodiments. Alternatively, the divalent hydrocarbon group designated by R12 may be bonded to non-oxirane ring carbon atoms in the hydrocarbon group designated by Z.
The polyepoxide compound of general formula (IX) may be exemplified by:
In one embodiment, the polyepoxide compound may be a polyepoxide ester compound including at least two oxirane rings. In certain embodiments, the polyepoxide ester compound may be exemplified by the general formula (X):
In general formula (X), each Z may have the same meaning as described above with respect to general formula (VII). In general formula (X), R13 is a divalent hydrocarbon group. R13 may have the same meaning as described above with respect to R2 in general formula (IV). It should be appreciated that the divalent hydrocarbon group designated by R13 may be bonded to various atoms in the divalent hydrocarbon group designated by Z. For example, the divalent hydrocarbon group designated by R13 may be bonded directly to one or more oxirane ring carbons in certain embodiments. Alternatively, the divalent hydrocarbon group designated by R13 may be bonded to non-oxirane ring carbon atoms in the ring designated by Z. In one embodiment, the epoxide compound of general formula (X) is a 3,4-epoxycycloalkyl, 3,4-epoxycycloalkyl carboxylate, such as 3,4-epoxycyclohexylmethyl, 3,4-epoxy-cyclohexane carboxylate. The polyepoxide ester compound of general formula (X) may be exemplified by:
Alternatively still, the epoxide compound may be exemplified by general formula (XI):
[A]w[B]x (XI)
In general formula (XI), each A is independently a hydrocarbyl group or a divalent hydrocarbon group and each B is an epoxy group. The group designated by A may have the same meaning as described above with respect to R1 in general formula (III) or R2 in general formula (IV). “w” is an integer having a value of from 0 to 50, and “x” is an integer having a value of from 0 to 10, where w+x≧1, and with the proviso that if x=0, at least one moiety designated by A is a hydrocarbyl group including an epoxy substituent group. “w” may be an integer having a value of from 1 to 40, 1 to 30, 1 to 20, 1 to 10, 1 to 8, 1 to 5, or 1 to 3, and “x” may be an integer having a value of 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1. It should be appreciated that groups A and B in general formula (XI) may be bonded to one another in any order, with varying number of iterations.
The epoxide compound may be exemplified by the following compounds:
It should be appreciated that all of these exemplary compounds fall within the scope of one or more of the general formulas (III), (IV), (V), (VI), (VII), (VIII), (IX), (X), and (XI) and/or within the scope of the written description of the epoxide compound herein.
In certain embodiments, the epoxide compound may be free from nitrogen, sulfur, phosphorous, chlorine, bromine, and/or iodine atoms. As described above, the epoxide compound may be aliphatic, cyclic, acyclic, and/or aromatic.
The epoxide compound may have a weight average molecular weight of from 44 to 1000, 50 to 750, 100 to 500, 100 to 400, or 100 to 200. Alternatively still, the epoxide compound may have a weight average molecular weight of at least 30, at least 50, at least 70, at least 90, at least 110, or at least 130. Alternatively, the epoxide compound may have a weight average molecular weight of less than 1500, less than 1300, less than 1100, less than 900, less than 700, less than 500, less than 400, or less than 300.
The epoxide compound may have an epoxide equivalent weight of from 75 to 300, 75 to 250, 75 to 200, 85 to 190, 85 to 175, 95 to 160, or 100 to 145, g per mole of oxirane ring of the epoxide compound. Alternatively, the epoxide compound may have an epoxide equivalent weight of at least 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, or 150, g per mole of oxirane ring of the epoxide compound. As referred to throughout this disclosure, the term “epoxide equivalent weight” is the numerical value which is obtained by dividing the weight average molecular weight of the epoxide compound by the number of oxirane rings in the molecule.
The basicity effect of the epoxide compound can be determined by acid titration. The resulting neutralization number is expressed as the total base number (TBN), and can be measured using various methods. ASTM D4739 is a potentiometric hydrochloric acid titration. The ASTM D4739 method is favored in engine tests and with used oils to measure TBN depletion/retention. When testing used engine lubricants, it should be recognized that certain weak bases are the result of the service rather than having been built into the oil. This test method can be used to indicate relative changes that occur in lubricant composition during use under oxidizing or other service conditions regardless of the color or other properties of the resulting lubricant composition.
In some embodiments, the epoxide compound does not negatively affect the total base number of the lubricant composition. Alternatively, the epoxide compound may improve the TBN of the lubricant composition by, at least 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 10, or 15, mg KOH/g of epoxide compound. The TBN value of the lubricant composition can be determined according to ASTM D2896 and/or ASTM D4739 as will be described below.
In certain embodiments, the epoxide compound is monomeric. The term “monomeric” is intended to indicate that the subject compound does not include more than three, more than two, or more than one, repeating monomer units bonded to one another. Alternatively, the term monomeric may refer to compounds that do not include any repeating monomer units. In other words, the term “monomeric” is intended to exclude compounds which are either oligomeric or polymeric. In certain embodiments, the monomeric epoxide compound excludes oils or alkyl fatty acid esters which have been epoxidized to include one or more oxirane rings, such as epoxidized vegetable oils. Alternatively, the lubricant composition or additive package may include less than 5, 4, 3, 2, 1, 0.5, 0.1, or 0.01, wt. %, of an epoxidized fatty acid ester or epoxidized oil based on a total weight of the lubricant composition. As used herein, the term “epoxidized oil” refers to a natural oil which was epoxidized to include at least 1, at least 2, at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, or at least 9, epoxide groups per molecule and/or has an epoxide equivalent weight of greater than 200, 250, 300, or 350. As used herein, the term “epoxidized fatty acid ester” refers to a natural fatty acid ester or acid that includes at least 1, at least 2, at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, or at least 9, epoxide groups per molecule and/or has a epoxide equivalent weight of greater than 200, 250, 300, or 350. As used herein, the term “natural” refers to compounds which are naturally-occurring.
The epoxide compound may have a boiling point of at least 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, or 150, ° C., at 1 atmosphere of pressure. Alternatively, the epoxide compound has a boiling point of from 50 to 450, 55 to 450, 65 to 450, 75 to 450, 85 to 450, 100 to 450, 115 to 450, 125 to 450, 135 to 450, 150 to 450, or from 200 to 400, ° C., at 1 atmosphere of pressure. Furthermore, in certain embodiments, the epoxide compound is a liquid at a steady state temperature of 50° C. and a steady state pressure of 1 atmosphere of pressure.
The epoxide compound may have a flash point of from 25 to 250, 50 to 250, 65 to 250, 75 to 250, 100 to 250, or from 115 to 250, ° C. at 1 atmosphere of pressure. Alternatively, the epoxide compound may have a flash point of at least 25, 35, 45, 55, 65, 75, 85, 95, 105, 115, 125, or 135, ° C. at 1 atmosphere of pressure.
The epoxide compound may be prepared using various methods as will be appreciated by one of ordinary skill in the art. For example, the epoxide compound may be prepared by the epoxidation of an allyl ether, α,β-unsaturated amide to the corresponding glycidyl ether, glycidic ester, or glycidic amide. Alternatively, an olefin may be epoxidized with hydrogen peroxide and an organic peracid to produce the epoxide compound. Alternatively, the olefin can be epoxidized in the presence of a transition metal catalyst and a co-oxidant to form the epoxide compound. Suitable co-oxidants include hydrogen peroxide, tert-butyl hydroperoxide, iodosylbenzene, sodium hypocholorite, and the like. Alternatively, glycidic esters may be prepared by Darzens condensation of an α-halo ester and an aldehyde or ketone, in the presence of a base.
In some embodiments, the lubricant composition and/or additive package is free of, or contains less than 5, 3, 1, 0.5, 0.1, or 0.05, wt. %, of an epoxide reaction catalyst, based on the total weight of the lubricant composition. The epoxide reaction catalyst may be a metal salt, such as a metallic salt of fatty acids, naphthenates, phenolates, alcoholates, carboxylates, and the corresponding thio analogues, sulfonates, and sulphinates. The epoxide reaction catalyst may also refer to calcium cetyl alcoholate, barium isoamyl thiiphenolate, calcium naphthnate, and metal salts of alkyl substituted benzene sulphonic acid. In some embodiments, the epoxide reaction catalyst is defined as a component that catalyzes the reaction of the epoxide compound with an additional component in the lubricant composition at a temperature less than 100, 80, or, 60, ° C. The additional component may include, but is not limited to, any compound described in this specification other than the epoxide reaction catalyst and the epoxide compound. For example, the additional component referred to above may be a dispersant, an anti-wear additive, an antioxidant, or a component that affects the total base number of the lubricant composition.
Conventional uses of epoxide compounds in lubricant compositions involve forming a reaction product between a conventional dispersant and a conventional epoxide compound. In these applications, the conventional epoxide compound is consumed by chemical reactions such that the ultimately formed lubricant composition does not contain appreciable amounts of the conventional epoxide compound in an unreacted state. The conventional epoxide compound may react via an addition reaction such that the addition of one or more small molecules to the lubricant composition may cause the epoxide group of the conventional epoxide compound to ring-open without eliminating or cleaving any part of the conventional epoxide compound.
In such conventional uses, more than 50 wt. % of the conventional epoxide compound is typically reacted with the conventional dispersants or other compounds based on the total weight of the conventional epoxide compound in the lubricant composition prior to the reaction. In certain embodiments, at least 50, 60, 70, 80 or, 90, wt. % of the epoxide compound remains unreacted in the lubricant composition based on a total weight of the epoxide compound utilized to form the lubricant composition prior to any reaction in the lubricant composition. Alternatively, at least 95, 96, 97, 98, or 99, wt. %, of the epoxide compound remains unreacted in the lubricant composition based on a total weight of the epoxide compound prior to any reaction in the lubricant composition.
In certain embodiments, the lubricant composition includes less than 10, 5, 1, 0.5, 0.1, 0.01, 0.001, or 0.0001, wt. %, of compounds which would react with the epoxide compound at a temperature less than 150, less than 125, less than 100, or less than 80, ° C., based on a total weight of the lubricant composition. Exemplary types of compounds which may react with the epoxide compound at a temperature less than 100° C. include acids, amine curing agents, anyhydrides, triazoles, and/or oxides. In certain embodiments, the lubricant composition may include a collective amount of acids, amine curing agents, anhydrides, triazoles, and/or oxides which is less than 5, 3, 1, 0.5, or 0.1, wt. % based on a total weight of the lubricant composition. Alternatively, the lubricant composition may include a collective amount of acids, amine curing agents, anhydrides, triazoles, and/or oxides which is less than 0.01, 0.001, or 0.0001, wt. %, based on the total weight of the lubricant composition. Alternatively still, the lubricant composition may be free of acids, amine curing agents, anhydrides, triazoles, and/or oxides.
In other conventional uses, conventional epoxide compounds undergo tribopolymerization in lubricant compositions to form protective lubricating films. In the tribopolymerization process, polymer-formers are adsorbed on a solid surface and polymerize under rubbing conditions to form organic polymeric films directly on the rubbing surface. In such conventional uses, more than 50 wt. % of the conventional epoxide compound is typically reacted via tribopolymerization. In contrast, the inventive lubricant compositions may contain a significant amount of the epoxide compound that does not react via tribopolymerization. In certain embodiments, at least 50, 60, 70, 80, or 90, wt. %, of the epoxide compound does not react via tribopolymerization in the lubricant composition at a temperature less than 100, 80, or 60, ° C., based on the total weight of epoxide compound utilized to form the lubricant composition. Alternatively, at least 95, 96, 97, 98, or 99, wt. %, of the epoxide compound does not react via tribopolymerization in the lubricant composition at a temperature less than 100, 80, or 60, ° C., based on a total weight of the epoxide compound in the lubricant composition.
In other embodiments, the seal compatibility additive is the boroxine compound. As such, the boroxine compound may be included in a lubricant composition or an additive package for a lubricant composition to improve the seal compatibility of the lubricant composition.
The boroxine compound may be represented by general formula (XII):
In general formula (XII), each R14 is independently an alkyl group having equal to or fewer than 7 carbon atoms. For example, each R14 may independently be an alkyl group having from 1 to 7, 1 to 6, 1 to 5, 1 to 4, 1 to 3, or 1 to 2, carbon atoms. Each R14 may independently be linear or branched. In one formulation, each R14 may be a methyl group. Exemplary R14 groups may independently include methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl, and n-hexyl groups.
The boroxine compound may include, but is not limited to, trimethoxy boroxine, tripropoxy boroxine, triisopropoxy boroxine, tributoxy boroxine, tripentoxy boroxine, trihexoxy boroxine, and triheptoxy boroxine. By way of example, trimethoxy boroxine may be exemplified by the formula:
In certain embodiments, each R14 may represent distinct alkyl groups. For example, the boroxine compound may be exemplified by the formula:
where one group designated by R14 in general formula (XII) is methyl, one group designated by R14 in formula (XII) is ethyl, and one group designated by R14 in formula (XII) is propyl. Alternatively still, groups designated by R14 may be the same, and one group designated by R14 may be different in general formula (XII).
The boroxine compound may be prepared via numerous methods. As but one example, the boroxine compound can be prepared by reacting 2 mole of orthoboric acid (H3BO3) with 1 mole tri-alkyl borate. The alkyl borate may have from 1 to 7 carbon atoms, depending on the number of carbon atoms desired in the groups designated by R14 in general formula (XII). The reaction can be conducted at a temperature ranging from 50 to 150° C. in order to remove 1 mol H2O.
Conventional uses of conventional boron compounds involve forming a reaction product between a conventional amine compound and a conventional boron compound. The conventional boron compound may be exemplified by reactive borate esters and boric acids. In these applications, the conventional boron compound is consumed by chemical reactions such that the ultimately formed lubricant composition does not contain appreciable amounts of the conventional boron compound. Furthermore, in these applications, the conventional amine compound is reacted with the conventional boron compound to form a salt. The salt formation is evidenced by the electronic impact upon the reaction of the conventional boron compound and the conventional amine compound, which is visible as a chemical shift in NMR spectroscopy. There are also physical indications that a reaction takes place, such as the evolution of heat and the thickening of the solution (cross-linking).
In such applications of conventional boron compounds, more than 50 wt. % of the conventional boron compound is typically reacted with the conventional amine compounds, or is hydrolyzed, based on the total weight of the conventional boron compound before reaction. The lubricant composition may be free from a salt formed through the reaction of the boroxine compound, or may contain less than 10, less than 5, or less than 1, wt. %, of the salt formed through the reaction of the boroxine compound based on the total weight of the lubricant composition after any reaction.
In certain embodiments, at least 50, at least 60, at least 70, at least 80, or at least 90, wt. %, of the boroxine compound remains unreacted in the lubricant composition based on a total weight of boroxine compound utilized to form the lubricant composition prior to any reaction in the lubricant composition. Alternatively, at least 95, at least 96, at least 97, at least 98, or at least 99, wt. %, of the boroxine compound remains unreacted in the lubricant composition based on a total weight of the boroxine compound prior to any reaction in the lubricant composition.
In one embodiment, the percentage of the boroxine compound that remains unreacted is determined after all of the components which are present in the lubricant composition reach equilibrium with one another. The time period necessary to reach equilibrium in the lubricant composition may vary widely. For example, the amount of time necessary to reach equilibrium may range from a single minute to many days, or even weeks. In certain embodiments, the percentage of the boroxine compound that remains unreacted in the lubricant composition is determined after 1 minute, 1 hour, 5 hours, 12 hours, 1 day, 2 days, 3 days, 1 week, 1 month, 6 months, or 1 year. Generally, the percentage of the boroxine compound that remains unreacted in the lubricant composition is determined before an end use.
In certain embodiments, the lubricant composition includes less than 0.1, less than 0.01, less than 0.001, or less than 0.0001, wt. %, of compounds which would react with the boroxine compound based on the total weight of the lubricant composition.
The lubricant composition may include less than 100, less than 50, less than 10, or less than 5, ppm B(OH)3− ions, based the total weight of the lubricant composition. Conventional boroxine compounds may be hydrolyzed before they are combined with a conventional lubricant composition such that more than 100 ppm B(OH)3− ions are present in the conventional lubricant composition. In other words, at least 50, at least 60, at least 70, at least 80, at least 90, at least 95, or at least 99, wt. %, of the boroxine compound is in an unhydrolyzed state in the lubricant composition based on the total weight of the boroxine compound. The amount of the boroxine compound which is hydrolyzed is accounted for when determining the amount of the boroxine compound which remains unreacted.
Furthermore, the boroxine compound does not negatively affect the total base number (TBN) of the lubricant composition. The TBN value of the lubricant composition can be determined according to ASTM D2896 and ASTM D4739 as will be described below.
In other embodiments, the seal compatibility additive is the sulfonate ester. As such, the sulfonate ester may be included in a lubricant composition or an additive package for a lubricant composition to improve the seal compatibility of the lubricant composition.
It should be understood that, in certain aspects, the sulfonate ester may take many forms, so long as the sulfonate ester includes a sulfonate group. For example, the sulfonate ester may refer to mono-sulfonate esters, di-sulfonate esters, tri-sulfonate esters, and sulfonate esters including four or more sulfonate groups. It is also contemplated that two or more different, or two or more of the same, sulfonate groups may be present in the same sulfonate ester. For example, the sulfonate ester may include at least one mesylate group and at least one tosylate group in the same molecule.
In one aspect, the sulfonate ester has the following general formula (XIII):
wherein R15 and R16 are each independently selected hydrocarbyl groups. Each hydrocarbyl group designated by R15 and R16 may independently be substituted or unsubstituted, straight or branched, alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, alkylaryl, arylalkyl group, or combinations thereof. Each hydrocarbyl group designated by R15 and R16 may independently include from 1 to 100, 1 to 50, 1 to 40, 1 to 30, 1 to 20, 1 to 17, 1 to 15, 1 to 10, 1 to 6, or 1 to 4, carbon atoms. Alternatively, each hydrocarbyl group designated by R15 and R16 may independently include less than 20, less than 15, less than 12, or less than 10, carbon atoms. Exemplary alkyl groups include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, 2-ethylhexyl, octyl, cetyl, 3,5,5-trimethylhexyl, 2,5,9-trimethyldecyl, and dodecyl groups. Exemplary cycloalkyl groups cyclopropyl, cyclopentyl and cyclohexyl groups. Exemplary aryl groups include phenyl and naphthalenyl groups. Exemplary arylalkyl groups include benzyl, phenylethyl, and (2-naphthyl)-methyl.
In some embodiments, the sulfonate ester is free from, or includes a limited number of certain substituent groups. For example, the sulfonate ester may include fewer than three, fewer than two, one, or be completely free from, carbonyl groups. In other aspects, the sulfonate ester is free from an estolide groups (and is not an estolide). In still other aspects, the sulfonate ester is free from metal ions and/or other ions.
In certain aspects, each hydrocarbyl group designated by R15 and R16 may be independently substituted, and include at least one heteroatom, such as oxygen, nitrogen, sulfur, chlorine, fluorine, bromine, or iodine, and/or at least one heterogroup, such as pyridyl, furyl, thienyl, and imidazolyl. Alternatively, or in addition to including heteroatoms and heterogroups, each hydrocarbyl group designated by R15 and R16 may independently include at least one substituent group selected from alkoxy, amide, amine, carboxyl, epoxy, ester, ether, hydroxyl, keto, sulfonate, sulfuryl, and thiol groups. For example, each hydrocarbyl group designated by R15 and R16 may include a hydrocarbyl group that includes a sulfonate group. Alternatively still at least one hydrocarbyl group designated by R15 and R16 may include a hydrocarbyl group that includes at least two sulfonate groups.
In one embodiment, the sulfonate ester of general formula (XIII) is cyclic, meaning that at least one group designated by R15 and R16 is cyclic, or that R15 or R16 include a pendant cyclic group. In other aspects, the sulfonate ester of general formula (XIII) is acyclic hydrocarbyl groups, meaning that both R15 and R16 are acyclic and that R15 and R16 are free from pendant cyclic groups. Alternatively still, with respect to general formula (XIII), R15 is a methyl group and R16 is a hydrocarbyl group having from 1 to 17 carbon atoms; R15 is a methyl group and R16 may be an alkyl group having from 1 to 17 carbon atoms; R15 is a methylbenzyl group and R16 is a hydrocarbyl group having from 1 to 17 carbon atoms; or R15 is a methylbenzyl group and R16 may be an alkyl group having from 1 to 17 carbon atoms.
Alternatively, as contemplated by general formula (XIII), in other aspects, R15 is selected from a p-nitrobenzenesulfonate and a p-bromobenzenesulfonate, and R16 is a hydrocarbyl group having from 1 to 17 carbon atoms.
In some aspects, the sulfonate ester is free from ionic bonds. In other words, the bonds present between the atoms of the sulfonate ester in this aspect consist solely of covalent bonds.
As such, the sulfonate ester is not a salt.
The sulfonate ester may have a weight average molecular weight ranging from 96 to 1500, 100 to 1000, 100 to 500, 150 to 500, or 250 to 400.
In some aspects, the sulfonate ester may include 1 to 50, 1 to 40, 5 to 30, 5 to 25, or 10 to 25, mole % sulfur, based on the total number of moles in the sulfonate ester.
By way of example, the sulfonate esters encompassed by general formula (XIII) and the above description may be exemplified by one or more of the following compounds:
The sulfonate ester may be synthesized in a variety of ways. For example, the sulfonate may be formed by alcoholysis of sulfonyl chlorides by the following reaction mechanism:
R15SO2Cl+R16OH→R15SO2OR16+HCl,
where R15 and R16 are each independently hydrocarbyl groups as described above in general formula (XIII). However, it should be appreciated that other methods of synthesizing the sulfonate ester are also contemplated.
In certain embodiments, at least 50, at least 60, at least 70, at least 80 or, at least 90, wt. %, of the sulfonate ester remains unreacted in the additive package and/or lubricant composition based on the total weight of sulfonate ester utilized to form the additive package and/or the lubricant composition prior to any reaction in the additive package or the lubricant composition. Alternatively, at least 95, at least 96, at least 97, at least 98, or at least 99, wt. %, of the sulfonate ester remains unreacted in the additive package and/or the lubricant composition based on the total weight of the sulfonate ester prior to any reaction in the additive package or the lubricant composition.
As also introduced above, the additive package (or resultant lubricant composition) may further include one or more amine compounds. If utilized, the amine compound may be present in the additive package in an amount ranging from 0.1 to 99, from 0.1 to 50, or from 0.1 to 10, wt. %, based on the total weight of the additive package.
The amine compound includes at least one nitrogen atom. Furthermore, in some configurations, the amine compound does not include triazoles, triazines, or similar compounds where there are three or more nitrogen atoms in the body of a cyclic ring. The amine compound may be aliphatic.
In certain embodiments, the amine compound has a total base number (TBN) value of at least 10 mg KOH/g when tested according to ASTM D4739. Alternatively, the amine compound has a TBN value of at least 15, at least 20, at least 25, at least 90, at least 100, at least 110, at least 120, at least 130, at least 140, at least 150, or at least 160, mg KOH/g, when tested according to ASTM D4739. Alternatively still, the amine compound may have a TBN value of from 80 to 200, 90 to 190, 100 to 180, or 100 to 150, mg KOH/g, when tested according to ASTM D4739.
In some embodiments, the amine compound does not negatively affect the TBN of the lubricant composition. Alternatively, the amine compound may improve the TBN of the lubricant composition by, at least 0.5, at least 1, at least 1.5, at least 2, at least 2.5, at least 3, at least 3.5, at least 4, at least 4.5, at least 5, at least 10, or at least 15, mg KOH/g of the amine compound. The TBN value of the lubricant composition can be determined according to ASTM D2896.
In some embodiments, the amine compound consists of, or consists essentially of, hydrogen, carbon, nitrogen, and oxygen. Alternatively, the amine compound may consist of, or consist essentially of, hydrogen, carbon, and nitrogen. In the context of the amine compound, the phrase “consist essentially of” refers to compounds where at least 95 mole % of the amine compound are the recited atoms (i.e., hydrogen, carbon, nitrogen, and oxygen; or hydrogen, carbon, and nitrogen). For example, if the amine compound consists essentially of hydrogen, carbon, nitrogen, and oxygen, at least 95 mole % of the amine compound is hydrogen, carbon, nitrogen, and oxygen. In certain configurations, at least 96, at least 97, at least 98, at least 99, or at least 99.9, mole %, of the amine compound are hydrogen, carbon, nitrogen and oxygen, or, in other embodiments, are carbon, nitrogen, and hydrogen.
The amine compound may consist of covalent bonds. The phrase “consist of covalent bonds” is intended to exclude those compounds which bond to the amine compound through an ionic association with at least one ionic atom or compound. That is, in configurations where the amine compound consists of covalent bonds, the amine compound excludes salts of amine compounds, for example, phosphate amine salts and ammonium salts. As such, in certain embodiments, the lubricant composition is free of a salt of the amine compound. More specifically, the lubricant composition may be free of a phosphate amine salt, ammonium salt, and/or amine sulfate salt.
The amine compound may include a monomeric acyclic amine compound having a weight average molecular weight of less than 500. Alternatively, the monomeric acyclic amine compound may have a weight average molecular weight of less than 450, less than 400, less than 350, less than 300, less than 250, less than 200, or less than 150. Alternatively still, the amine compound may have a weight average molecular weight of at least 30, at least 50, at least 75, at least 100, at least 150, at least 200, or at least 250.
The phrase “acyclic amine compound” is intended to refer to amine compounds which are free from any cyclic structures and to exclude aromatic structures. For example, the monomeric acyclic amine compound does not include compounds having a ring having at least three atoms bonded together in a cyclic structure and those compounds including benzyl, phenyl, or triazole groups.
The monomeric acyclic amine compound may be exemplified by general formula (XIV):
where each R17 is independently a hydrogen atom or a hydrocarbyl group. Each hydrocarbyl group designated by R17 may independently be substituted or unsubstituted, straight or branched, alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, alkylaryl, arylalkyl group, or combinations thereof. Each hydrocarbyl group designated by R17 may independently include from 1 to 100, 1 to 50, 1 to 40, 1 to 30, 1 to 20, 1 to 15, 1 to 10, 1 to 6, or 1 to 4, carbon atoms. Alternatively, each hydrocarbyl group designated by R17 may independently include less than 20, less than 15, less than 12, or less than 10, carbon atoms.
Alternatively, each hydrocarbyl group designated by R17 may be independently substituted, and include at least one heteroatom, such as oxygen, nitrogen, sulfur, chlorine, fluorine, bromine, or iodine, and/or at least one heterogroup, such as pyridyl, furyl, thienyl, and imidazolyl. Alternatively, or in addition to including heteroatoms and heterogroups, each hydrocarbyl group designated by R17 may independently include at least one substituent group selected from alkoxy, amide, amine, carboxyl, epoxy, ester, ether, hydroxyl, keto, metal salt, sulfuryl, and thiol groups. Alternatively, each hydrocarbyl group designated by R17 may be independently unsubstituted.
Exemplary alkyl groups include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, 2-ethylhexyl, octyl and dodecyl groups. Exemplary cycloalkyl groups cyclopropyl, cyclopentyl and cyclohexyl groups. Exemplary aryl groups include phenyl and naphthalenyl groups. Exemplary arylalkyl groups include benzyl, phenylethyl, and (2-naphthyl)-methyl.
The monomeric acyclic amine compound includes monoamines and polyamines (including two or more amine groups). In certain embodiments, at least one group designated by R17 is unsubstituted. Alternatively, two or three groups designated by R17 are unsubstituted. Alternatively still, it is contemplated that one, two, or three groups designated by R17 are substituted.
Exemplary monomeric acyclic amine compounds include, but are not limited to, primary, secondary, and tertiary amines, such as:
The monomeric acyclic amine compound may alternatively include at least one primary amines such as ethylamine, n-propylamine, isopropylamine, n-butylamine, isobutylamine, sec-butylamine, tert-butylamine, pentylamine, and hexylamine; primary amines of the formulas: CH3—O—C2H4—NH2, C2H5—O—C2H4—NH2, CH3—O—C3H—NH2, C2H5—O—C3H6—NH2, C4H9—O—C4H8—NH2, HO—C2H4—NH2, HO—C3H6—NH2 and HO—C4H8—NH2; secondary amines, for example diethylamine, methylethylamine, di-n-propylamine, diisopropylamine, diisobutylamine, di-sec-butylamine, di-tert-butylamine, dipentylamine, dihexylamine; and also secondary amines of the formulas: (CH3—O—C2H4)2NH, (C2H5—O—C2H4)2NH, (CH3—O—C3H6)2NH, (C2H5—O—C3H6)2NH, (n-C4H9—O—C4H8)2NH, (HO—C2H4)2NH, (HO—C3H6)2NH and (HO—C4H8)2NH: and polyamines, such as n-propylenediamine, 1,4-butanediamine, 1,6-hexanediamine, diethylenetriamine, triethylenetetramine and tetraethylenepentamines, and also their alkylation products, for example 3-(dimethylamino)-n-propylamine, N,N-dimethyl ethylenediamine, N,N-diethylethylenediamine, and N,N,N′,N′-tetramethyldiethylenetriamine.
Alternatively, the amine compound may be a monomeric cyclic amine compound. The monomeric cyclic amine compound may have a weight average molecular weight of from 100 to 1200, 200 to 800, or 200 to 600. Alternatively, the monomeric cyclic amine compound may have a weight average molecular weight of less than 500, or at least 50. In some embodiments, the monomeric cyclic amine compound is free from aromatic groups, such as phenyl and benzyl rings. In other embodiments, the monomeric cyclic amine compound is aliphatic.
The monomeric cyclic amine compound may include two or fewer nitrogen atoms per molecule. Alternatively, the monomeric cyclic amine compound may include only one nitrogen per molecule. The phrase “nitrogen per molecule” refers to the total number of nitrogen atoms in the entire molecule, including the body of the molecule and any substituent groups. In certain embodiments, the monomeric cyclic amine compound includes one or two nitrogen atoms in the cyclic ring of the monomeric cyclic amine compound.
The monomeric cyclic amine compound may be exemplified by the general formula (XV):
general formula (XVI):
In general formulas (XV) and (XVI), Y represents the type and number of atoms necessary to complete the cyclic ring of general formulas (XV) or (XVI). The ring designated by Y may include from 2 to 20, 3 to 15, 5 to 15, or 5 to 10, carbon atoms. The ring designated by Y may be a substituted or unsubstituted, branched or unbranched, divalent hydrocarbon group that includes at least one hetero atom, such as oxygen, or sulfur, and may include at least one heterogroup. In addition to including heteroatoms and/or heterogroups, the ring designated by Y may include at least one hydrocarbyl substituent group, as described above with respect to R1 in general formula (III). In certain embodiments, the ring designated by Y is free from nitrogen heteroatoms, or free from any heteroatoms. The heteroatoms, heterogroups, and/or substituent groups may be bonded to different atoms in the divalent hydrocarbon group designated by Y. The substituent nitrogen atom in general formula (XVI) may be bonded to at least one hydrogen atom, or may be bonded to one or two hydrocarbyl groups.
In formula (XV), R18 is a hydrogen atom or a hydrocarbyl group. The hydrocarbyl group designated by R18 may have the same meaning as R1 described above with respect to formula (III). For example, R18 may be an alcohol group, an amino group, an alkyl group, an amide group, an ether group, or an ester group. R18 may have 1 to 50, 1 to 25, 1 to 17, 1 to 15, 1 to 12, 1 to 8, 1 to 6, or 1 to 4, carbon atoms. R18 may be straight or branched. For example, each R18 may be an alcohol group, amino group, alkyl group, amide group, ether group, or ester group having 1 to 50 carbon atoms, with the designated functional group (alcohol, etc.), heteroatom, or heterogroup bonded at various positions on the carbon atoms in the backbone. The substituent nitrogen atom in general formula (XVI) may be bonded to at least one hydrogen atom, or may be bonded to one or two hydrocarbyl groups, such as those described above with respect to R18.
In one embodiment, the monomeric cyclic amine compound may be exemplified by general formula (XVII):
In general formula (XVII), each R19 is independently a hydrogen atom or a hydrocarbyl group having from 1 to 17 carbon atoms. The hydrocarbyl group designated by R19 may have the same meaning as R1 in general formula (III). For example, each R19 may independently be substituted with an alcohol group, an amino group, an amide group, an ether group, or an ester group. Each R19 may independently have from 1 to 17, 1 to 15, 1 to 12, 1 to 8, 1 to 6, or 1 to 4, carbon atoms. In certain embodiments, at least one group designated by R19 is unsubstituted. Alternatively, at least two, three, four, five, or six groups designated by R19 are unsubstituted. Alternatively still, it is contemplated that one, two, three, four, five, or six groups designated by R19 are substituted. For example, each R19 may be an alcohol group, amino group, alkyl group, amide group, ether group, or ester group having 1 to 17 carbon atoms, with the designated functional group (alcohol, etc) bonded at various positions on the carbon chain.
Exemplary monomeric cyclic amine compounds include:
In some embodiments, the amine compound, such as the monomeric acyclic amine compound or the monomeric cyclic amine compound may be a sterically hindered amine compound. The sterically hindered amine compound may have a weight average molecular weight of from 100 to 1200. Alternatively, the sterically hindered amine compound may have a weight average molecular weight of from 200 to 800, or 200 to 600. Alternatively still, the sterically hindered amine compound may have a weight average molecular weight of less than 500.
As used herein, the term “sterically hindered amine compound” means an organic molecule having fewer than two hydrogen atoms bonded to at least one alpha-carbon with reference to a secondary or tertiary nitrogen atom. In other embodiments, the term “sterically hindered amine compound” means an organic molecule having no hydrogen atoms bonded to at least one alpha-carbon with reference to a secondary or tertiary nitrogen atom. In still other embodiments, the term “sterically hindered amine compound” means an organic molecule having no hydrogen atoms bonded to each of at least two alpha-carbons with reference to a secondary or tertiary nitrogen atom.
The sterically hindered amine compound may have general formula (XVIII) or (XIX):
In general formula (XVIII), each R20 is independently a hydrogen atom or a hydrocarbyl group having from 1 to 17 carbon atoms, wherein at least two of R20 are an alkyl group in one molecule; and R21 is independently a hydrogen atom or a hydrocarbyl group having from 1 to 17 carbon atoms. In general formula (XIX), each R22 is independently a hydrogen atom or a hydrocarbyl group having from 1 to 17 carbon atoms, wherein at least two of R22 are an alkyl group, and each R22 is independently a hydrogen atom or a hydrocarbyl group having from 1 to 17 carbon atoms. The groups designated by R20, R21, R22, and R23 may have the same meaning as R1 described above with respect to general formula (III). For example, each R20, R21, R22, and R23 may independently substituted with an alcohol group, an amide group, an ether group, or an ester group, and each R20, R21, R22, and R23 may independently have from 1 to 17, 1 to 15, 1 to 12, 1 to 8, 1 to 6, or 1 to 4, carbon atoms.
In certain embodiments, at least one group designated by R20, R21, R22, and R23 is unsubstituted. Alternatively, at least two, three, four, five, or six groups designated by R20, R21, R22, and R23 are unsubstituted. In other embodiments, every group designated by R20, R21, R22, and R23 is unsubstituted. Alternatively still, it is contemplated that one, two, three, four, five, or six groups designated by R20, R21, R22, and R23 are substituted.
Exemplary R20, R21, R22, and R23 groups may be independently selected from methyl, ethyl, n-propyl, n-butyl, sec-butyl, tert-butyl, n-hexyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-hexadecyl, or n-octadecyl.
In general formula (XVIII), at least two, at least three, or all four groups, designated by R22 are each independently an alkyl group. Similarly, in general formula (XIX), at least two groups designated by R22 are an alkyl group. Alternatively, at least three, or all four groups, designated by R22 are an alkyl group.
The sterically hindered amine compound of general formula (XVIII) may be exemplified by the following compounds:
The sterically hindered amine compound of general formula (XIX) is acyclic. The term “acyclic” is intended to mean that the sterically hindered amine compound of general formula (XIX) is free from any cyclic structures and aromatic structures. The sterically hindered amine compound of general formula (XIX) can be exemplified by:
The sterically hindered amine compound may alternatively be exemplified by the general formula (XX):
In general formula (XX), each R20 and R21 are as described above, wherein at least three of R20 are each independently an alkyl group. The sterically hindered amine compound of general formula (XX) may be exemplified by the following compounds:
The sterically hindered amine compound may include a single ester group. However, the sterically hindered amine compound may alternatively be free from ester groups. In certain embodiments, the sterically hindered amine compound may include at least one, or only one, piperidine ring.
The additive package may include the total weight of the seal compatibility additive and the amine compound in a weight ratio ranging from 1:100 to 10:1, from 1:80 to 2:1; from 1:50 to 10:1, or from 1:10 to 10:1. Alternatively, the additive package may include the total weight of the seal compatibility additive and the amine compound in a weight ratio ranging from 1:3 to 1:6.
As also introduced above, the additive package (or resultant lubricant composition) may further include one or more polyol esters. If utilized, the polyol ester may be present in the additive package in an amount ranging from 0.1 to 99, from 0.1 to 50, or from 0.1 to 10, wt. %, based on the total weight of the additive package. Suitable examples of polyol esters are commercially available from BASF of Florham Park, N.J. under the tradename Synative®, such as Synative® ES 2925.
As also introduced above, the additive package (or resultant lubricant composition) may further include one or more dispersants. The dispersant may be a polyalkene amine or other amine dispersant. As such, depending on the composition of the dispersant, the dispersant may be encompassed by at least one of the descriptions of the amine compound provided above. If utilized, the dispersant may be present in the additive package in an amount ranging from 1 to 99, from 25 to 75, or from 45 to 55, wt. %, based on the total weight of the additive package. The amounts may be in addition to the amounts of the amine compound utilized in the additive package.
The TBN value of the amine dispersant may be least 15, at least 25, or at least 30, mg KOH/g of the amine dispersant. Alternatively, the TBN value of the amine dispersant may range from 15 to 100, from 15 to 80, or from 15 to 75, mg KOH/g of the amine dispersant.
The polyalkene amine includes a polyalkene moiety. The polyalkene moiety is the polymerization product of identical or different, straight-chain or branched C2-6 olefin monomers. Examples of suitable olefin monomers are ethylene, propylene, 1-butene, isobutene, 1-pentene, 2-methyl butene, 1-hexene, 2-methylpentene, 3-methylpentene, and 4-methylpentene. The polyalkene moiety has a weight average molecular weight of from 200 to 10000, 500 to 10000, or 800 to 5000.
In one embodiment, the polyalkene amine is derived from polyisobutenes. Particularly suitable polysiobutenes are known as “highly reactive” polyisobutenes which feature a high content of terminal double bonds. Terminal double bonds are alpha-olefinic double bonds of the type shown in general formula (XXI):
The bonds shown in general formula (XXI) are known as vinylidene double bones. Suitable highly reactive polypolyisobutenes are, for example, polyisobutenes which have a fraction of vinylidene double bonds of greater than 70, 80, or 85, mole %. Preference is given in particular to polyisobutenes which have uniform polymer frameworks. Uniform polymer frameworks have in particular those polyisobutenes which are composed of at least 85, 90, or 95, wt. %, of isobutene units. Such highly reactive polyisobutenes may have a number-average molecular weight in the abovementioned range. In addition, the highly reactive polyisobutenes may have a polydispersity of from 1.05 to 7, or 1.1 to 2.5. The highly reactive polyisobutenes may have a polydispersity less than 1.9, or less than 1.5. Polydispersity refers to the quotients of weight-average molecular weight Mw divided by the number-average molecular weight Mn.
The dispersant may include moieties derived from succinic anhydride and having hydroxyl and/or amino and/or amido and/or imido groups. For example, the dispersant may be derived from polyisobutenylsuccinic anhydride which is obtainable by reacting conventional or highly reactive polyisobutene having a weight average molecular weight of from 500 to 5000 with maleic anhydride by a thermal route or via the chlorinated polyisobutene. For examples, derivatives with aliphatic polyamines such as ethylenediamine, diethylenetriamine, triethylenetetramine or tetraethylenepentamine may be used.
To prepare the polyalkene amine, the polyalkene component may be aminated in a known manner. An exemplary process proceeds via the preparation of an oxo intermediate by hydroformylation and subsequent reductive amination in the presence of a suitable nitrogen compound.
The dispersant may be a poly(oxyalkyl) radical or a polyalkylene polyamine radical of the general formula (XXII):
R24—NH—(C1-C6-alkylene-NH)m—C1-C6-alkylene (XXII)
where m is an integer of from 1 to 5, R24 is a hydrogen atom or a hydrocarbyl group having from 1 to 6 carbon atoms with C1-C6 alkylene representing the corresponding bridged analogs of the alkyl radicals. The dispersant may also be a polyalkylene imine radical composed of from 1 to 10 C1-C4 alkylene imine groups; or, together with the nitrogen atom to which they are bonded, are an optionally substituted 5- to 7-membered heterocyclic ring which is optionally substituted by one to three C1-C4 alkyl radicals and optionally bears one further ring heteroatom such as oxygen or nitrogen.
Examples of suitable alkenyl radicals include mono- or polyunsaturated, mono- or diunsaturated analogs of alkyl radicals has from 2 to 18 carbon atoms, in which the double bonds may be in any position in the hydrocarbon chain. Examples of C4-C18 cycloalkyl radical include cyclobutyl, cyclopentyl and cyclohexyl, and also the analogs thereof substituted by 1 to 3 C1-C4 alkyl radicals. The C1-C4 alkyl radicals are, for example, selected from methyl, ethyl, iso- or n-propyl, n-, iso-, sec- or tert-butyl. Examples of the arylalkyl radical include a C1-C18 alkyl group and an aryl group which are derived from a monocyclic or bicyclic fused or nonfused 4- to 7-membered, in particular 6 membered, aromatic or heteroaromatic group, such as phenyl, pyridyl, naphthyl and biphenyl.
If additional dispersants other than the dispersant described above are employed, these dispersants can be of various types. Suitable examples of dispersants include polybutenylsuccinic amides or -imides, polybutenylphosphonic acid derivatives and basic magnesium, calcium and barium sulfonates and phenolates, succinate esters and alkylphenol amines (Mannich bases), and combinations thereof. Additional suitable examples of dispersants are commercially available from Infineum International Limited of Linden, N.J. under the tradename Infineum®, such as Infineum® C9268.
As also introduced above, the additive package (or resultant lubricant composition) may further include one or more detergents. Suitable examples of detergents include overbased or neutral metal sulfonates, phenates, or combinations thereof. If utilized, the detergent may be present in the additive package in an amount ranging from 1 to 99, from 1 to 50, or from 12 to 22, wt. %, based on the total weight of the additive package.
In one embodiment, the detergent is an overbased sulfonate. Sulfonates (or sulfonate esters) may be prepared from sulfonic acids which are typically obtained by the sulfonation of alkyl substituted aromatic hydrocarbons such as those obtained from the fractionation of petroleum or by the alkylation of aromatic hydrocarbons. Examples included those obtained by alkylating benzene, toluene, xylene, naphthalene, biphenyl or their halogen derivatives such as chlorobenzene, chlorotoluene and chloronaphthalene. The alkylation may be carried out in the presence of a catalyst with alkylating agents having from about 3 to more than carbon atoms. The alkaryl sulfonates usually contain from about 9 to about 80 or more carbon atoms, from about 16 to about 60 carbon atoms per alkyl substituted aromatic moiety. The oil soluble sulfonates or alkaryl sulfonic acids may be neutralized with oxides, hydroxides, alkoxides, carbonates, carboxylate, sulfides, hydrosulfides, nitrates, borates and ethers of the metal. The amount of metal compound is chosen having regard to the desired TBN of the final product but typically ranges from about 100 to 220 wt. % of that stoichiometrically required.
Metal salts of phenols and sulfurized phenols are prepared by reaction with an appropriate metal compound such as an oxide or hydroxide and neutral or overbased products may be obtained by methods well known in the art. Sulfurized phenols may be prepared by reacting a phenol with sulfur or a sulfur containing compound such as hydrogen sulfide, sulfur monohalide or sulfur dihalide, to form products which are generally mixtures of compounds in which 2 or more phenols are bridged by sulfur containing bridges.
Carboxylate detergents, e.g., salicylates, can be prepared by reacting aromatic carboxylic acid with an appropriate metal compound such as an oxide or hydroxide and neutral or overbased products may be obtained by methods well known in the art. The aromatic moiety of the aromatic carboxylic acid can contain heteroatoms, such as nitrogen and oxygen. The aromatic carboxylic acid may contain one or more aromatic moieties, such as one or more benzene rings, either fused or connected via alkylene bridges. The carboxylic moiety may be attached directly or indirectly to the aromatic moiety. The carboxylic acid group may be attached directly to a carbon atom on the aromatic moiety, such as a carbon atom on the benzene ring. The aromatic moiety also contains a second functional group, such as a hydroxy group or a sulfonate group, which can be attached directly or indirectly to a carbon atom on the aromatic moiety.
In another embodiment, the detergent is an overbased phenate. Overbased phenates, including sulfurized phenates, are typically formed in the presence of ethylene glycol which must be removed from the product. The presence of glycol in overbased phenates can cause engine varnish or lacquer. Phenates are generally the reaction product of phenol or substituted phenol with a metal or ammonium base. Often the metal base is a Group II metal compound. Substituted phenols are generally mono-, di- or tri-hydrocarbyl substituted, such as alkyl, alkenyl, aryl, aralkyl, or alkaryl. The hydrocarbyl can include low molecular weight groups such as methyl, ethyl, the isomers of propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl and the like up to high molecular weight materials having a number average molecular weight of 10,000 or more. These hydrocarbyl substituents can be intermediate molecular weight polymer olefins such as C8-C100 ethylene or propylene or butene polymers. The hydrocarbyl can be substituted with groups such as chlorine, bromine, hydroxy, nitro or sulfonic acid groups. The Group II metal compound can include a metal oxide, hydroxide, alcoholate, acetate and the like. Metals typically utilized include calcium, barium, strontium and magnesium. The metal compound may be calcium oxide or hydroxide. Phenates can contain sulfur which can be introduced by reaction of elemental sulfur or SCl2 with phenol or substituted phenol, or by reaction of elemental sulfur or SCl2 with metal phenate.
Other examples of suitable detergents include “hybrid” detergents formed with mixed surfactant systems including phenate and/or sulfonate components, e.g., phenate/salicylates, sulfonate/phenates, sulfonate/salicylates, or sulfonates/phenates/salicylates.
Additional examples of suitable detergents include synthetic calcium alkyl benzene sulfonates having a low base value, linear synthetic calcium alkyl benzene sulfonates having a high base value, long-chain linear alkyl benzene synthetic calcium sulfonates having a high base value, synthetic calcium dialkyl benzene sulfonates having a high base value, long-chain linear alkyl benzene synthetic magnesium sulfonates having a high base value, sulfurized calcium alkyl phenolates having a high base value, polyisobutenyl succinimides, polyisobutenyl succinimide borides, polyisobutenyl succinimides having a high molecular weight, polyisobutenyl succinimide borides having a high molecular weight, calcium alkyl salicylates, magnesium alkyl salicylates.
Further examples of suitable detergents include overbased salts of linear alkaryl acids. The term “overbased” means that the compound has a stoichiometric excess of base beyond the amount required to neutralize the acid component in the detergent. The detergent is a salt complex which when a carbonate can have a structure as shown in general formula XXIII.
(M+v(OH)v)m(M3-v+v)n(M+vYv−) (XXIII)
In general formula (XXIII), M+v is a metal, typically an alkali or alkaline earth metal, cation having a valence, given by v, of 1 or 2. Typical M cations include among others, one or mixtures of the following: lithium, sodium, potassium, magnesium, barium, strontium, and calcium. Y− is a, typically oil-soluble, linear alkaryl anion. The alkyl portion can have either a saturated or unsaturated hydrocarbon chain. Typical Y include, among others, one or mixtures of the following: linear alkaryl sulfonates, such as sulfonated, linear mono- or dialkyl-substituted, aromatic hydrocarbons; linear alkaryl carboxylates; linear alkyl phenates; linear alkyl salicylates; and the like. The linear alkaryl group is an aromatic hydrocarbon having alkyl substitution. The aromatic portion may have other substituents, such as hydroxyl. The alkyl group has a linear, as opposed to branched, chain of carbon atoms, and when saturated, generally contains a chain of methylene, i.e. —CH2—, groups. One or more alkyl substituent may be present, providing mono-, di- or higher alkyl substitution on the aromatic ring. Typical monoalkyl groups have at least 15, from 16 to 40, or from 18 to 24, carbon atoms. Typical dialkyl substitution has at least 18, from 20 to 50, or from 20 to 30, carbon atoms. Typical aromatic groups include benzene, phenol, naphthalene, and toluene.
The detergent is typically overbased when the sum of m+n in general formula (XXIII) is more than 0.5 per detergent molecule. The amount of overbasing may vary depending upon which cation and anion are used. For example, the amount of overbasing for alkaryl sulfonates generally ranges from above 0.5 up to 30, from 5 to 20, or from 8 to 12. The detergent can have a Total Base Number (TBN), defined as the milligram equivalents of potassium hydroxide per gram of product, which may range from 25 to 500.
The detergent can be overbased by any, including known, manner. For example, overbased carbonate detergent can be made by carbonating the linear alkaryl salt, generally in the presence of diluent solvent and promotor. One or mixtures of carbonating compounds, like Ca(OH)2 and CaO, are added until the desired level of carbonation and TBN is achieved.
Mixtures of alkyl substituents include combinations of mono- and dialkyl substituents. The proportion of mono- to dialkyl substitution may range from 90:10 to 30:70, from 80:20 to 40:60, or be 70:30, mole percent.
Additional suitable examples of detergents are commercially available from Infineum International Limited of Linden, N.J. under the tradename Infineum®, such as Infineum® C9330.
As also introduced above, the additive package (or resultant lubricant composition) may further include one or more antioxidants. If utilized, the antioxidants may be present in the additive package in an amount ranging from 1 to 99, from 1 to 50, or from 10 to 20, wt. %, based on the total weight of the additive package. If employed, the antioxidant can be of various types. Suitable antioxidants include alkylated monophenols, for example 2,6-di-tert-butyl-4-methylphenol, 2-tert-butyl-4,6-dimethylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butyl-4-n-butylphenol, 2,6-di-tert-butyl-4-isobutylphenol, 2,6-dicyclopentyl-4-methylphenol, 2-(a-methylcyclohexyl)-4,6-dimethylphenol, 2,6-dioctadecyl-4-methylphenol, 2,4,6-tricyclohexylphenol, 2,6-di-tert-butyl-4-methoxymethylphenol, 2,6-di-nonyl-4-methylphenol, 2,4-dimethyl-6(1′-methylundec-1′-yl)phenol, 2,4-dimethyl-6-(1′-methylheptadec-1′-yl)phenol, 2,4-dimethyl-6-(1′-methyltridec-1′-yl)phenol, and combinations thereof.
Further examples of suitable antioxidants includes alkylthiomethylphenols, for example 2,4-dioctylthiomethyl-6-tert-butylphenol, 2,4-dioctylthiomethyl-6-methylphenol, 2,4-dioctylthiomethyl-6-ethylphenol, 2,6-didodecylthiomethyl-4-nonylphenol, and combinations thereof. Hydroquinones and alkylated hydroquinones, for example 2,6-di-tert-butyl-4-methoxyphenol, 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amylhydroquinone, 2,6-diphenyl-4-octadecyloxyphenol, 2,6-di-tert-butyl hydroquinone, 2,5-di-tert-butyl-4-hydroxyanisole, 3,5-di-tert-butyl-4-hydroxyanisole, 3,5-di-tert-butyl-4-hydroxyphenyl stearate, bis-(3,5-di-tert-butyl-4-hydroxyphenyl) adipate, and combinations thereof, may also be utilized.
Furthermore, hydroxylated thiodiphenyl ethers, for example 2,2′-thiobis(6-tert-butyl-4-methylphenol), 2,2′-thiobis(4-octylphenol), 4,4′-thiobis(6-tert-butyl-3-methylphenol), 4,4′-thiobis(6-tert-butyl-2-methylphenol), 4,4′-thiobis-(3,6-di-sec-amylphenol), 4,4′-bis-(2,6-dimethyl-4-hydroxyphenyl) disulfide, and combinations thereof, may also be used.
It is also contemplated that alkylidenebisphenols, for example 2,2′-methylenebis(6-tert-butyl-4-methylphenol), 2,2′-methylenebis(6-tert-butyl-4-ethylphenol), 2,2′-methylenebis[4-methyl-6-(a-methylcyclohexyl)phenol], 2,2′-methylenebis(4-methyl-6-cyclohexylphenol), 2,2′-methylenebis(6-nonyl-4-methylphenol), 2,2′-methylenebis(4,6-di-tert-butylphenol), 2,2′-ethylidenebis (4,6-di-tert-butylphenol), 2,2′-ethylidenebis(6-tert-butyl-4-isobutylphenol), 2,2′-methylenebis [6-(a-methylbenzyl)-4-nonylphenol], 2,2′-methylenebis[6-(a,a-dimethylbenzyl)-4-nonylphenol], 4,4′-methylenebis(2,6-di-tert-butyl phenol), 4,4′-methylenebis(6-tert-butyl-2-methylphenol), 1,1-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butane, 2,6-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-methylphenol, 1,1,3-tris(5-tert-butyl-4-hydroxy-2-methylphenyl) butane, 1,1-bis(5-tert-butyl-4-hydroxy-2-methyl-phenyl)-3-n-dodecylmercapto butane, ethylene glycol bis[3,3-bis(3′-tert-butyl-4′-hydroxyphenyl)butyrate], bis(3-tert-butyl-4-hydroxy-5-methyl-phenyl)dicyclopentadiene, bis[2-(3′-tert-butyl-2′-hydroxy-5′-methylbenzyl)-6-tert-butyl-4-methylphenyl]terephthalate, 1,1-bis-(3,5-dimethyl-2-hydroxyphenyl)butane, 2,2-bis-(3,5-di-tert-butyl-4-hydroxyphenyl)propane, 2,2-bis-(5-tert-butyl-4-hydroxy-2-methylphenyl)-4-n-dodecylmercaptobutane, 1,1,5,5-tetra-(5-tert-butyl-4-hydroxy-2-methyl phenyl)pentane, and combinations thereof may be utilized as antioxidants in the lubricant composition.
O-, N- and S-benzyl compounds, for example 3,5,3′,5′-tetra-tert-butyl-4,4′-dihydroxydibenzyl ether, octadecyl-4-hydroxy-3,5-dimethylbenzylmercaptoacetate, tris-(3,5-di-tert-butyl-4-hydroxybenzyl)amine, bis(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl)dithiol terephthalate, bis(3,5-di-tert-butyl-4-hydroxybenzyl)sulfide, isooctyl-3,5di-tert-butyl-4-hydroxy benzylmercaptoacetate, and combinations thereof, may also be utilized.
Hydroxybenzylated malonates, for example dioctadecyl-2,2-bis-(3,5-di-tert-butyl-2-hydroxybenzyl)-malonate, di-octadecyl-2-(3-tert-butyl-4-hydroxy-5-methylbenzyl)-malonate, di-dodecylmercaptoethyl-2,2-bis-(3,5-di-tert-butyl-4-hydroxybenzyl)malonate, bis [4-(1,1,3,3-tetramethylbutyl)phenyl]-2,2-bis(3,5-di-tert-butyl-4-hydroxybenzyl)malonate, and combinations thereof are also suitable for use as antioxidants.
Triazine compounds, for example 2,4-bis(octylmercapto)-6-(3,5-di-tert-butyl-4-hydroxyanilino)-1,3,5-triazine, 2-octylmercapto-4,6-bis(3,5-di-tert-butyl-4-hydroxyanilino)-1,3,5-triazine, 2-octylmercapto-4,6-bis(3,5-di-tert-butyl-4-hydroxyphenoxy)-1,3,5-triazine, 2,4,6-tris(3, 5-di-tert-butyl-4-hydroxyphenoxy)-1,2,3-triazine, 1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate, 1,3,5-tris(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl 2,4,6-tris(3,5-di-tert-butyl-4-hydroxyphenylethyl)-1,3,5-triazine, 1,3,5-tris(3,5-di-tert-butyl-4-hydroxyphenyl propionyl)-hexahydro-1,3,5-triazine, 1,3,5-tris-(3,5-dicyclohexyl-4-hydroxybenzyl)-isocyanurate, and combinations thereof, may also be used.
Additional examples of antioxidants include aromatic hydroxybenzyl compounds, for example, 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene, 1,4-bis(3,5-di-tert-butyl-4-hydroxybenzyl)-2,3, 5,6-tetramethylbenzene, 2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)phenol, and combinations thereof. Benzylphosphonates, for example dimethyl-2,5-di-tert-butyl-4-hydroxybenzylphosphonate, diethyl-3,5-di-tert-butyl-4-hydroxybenzylphosphonate, dioctadecyl3,5-di-tert-butyl-4-hydroxybenzylphosphonate, dioctadecyl-5-tert-butyl-4-hydroxy3-methylbenzylphosphonate, the calcium salt of the monoethyl ester of 3,5-di-tert-butyl-4-hydroxybenzylphosphonic acid, and combinations thereof, may also be utilized. In addition, acylaminophenols, for example 4-hydroxylauranilide, 4-hydroxystearanilide, and octyl N-(3,5-di-tert-butyl-4-hydroxyphenyl)carbamate.
Esters of [3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid with mono- or polyhydric alcohols, e.g. with methanol, ethanol, octadecanol, 1,6-hexanediol, 1,9-nonanediol, ethylene glycol, 1,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl) isocyanurate, N,N′-bis(hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hydroxymethyl-1-phospha-2,6,7-trioxabicyclo[2.2.2]octane, and combinations thereof, may also be used. It is further contemplated that esters of b-(5-tert-butyl-4-hydroxy-3-methylphenyl)-propionic acid with mono- or polyhydric alcohols, e.g. with methanol, ethanol, octadecanol, 1,6-hexanediol, 1,9-nonanediol, ethylene glycol, 1,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl) isocyanurate, N,N′-bis(hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hydroxymethyl-1-phospha-2,6,7-trioxabicyclo[2.2.2]octane, and combinations thereof, may be used.
Additional examples of suitable antioxidants include those that include nitrogen, such as amides of b-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid, e.g., N,N′-bis(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)hexamethylenediamine, N,N′-bis(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)trimethylenediamine, N,N′-bis(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)hydrazine. Other suitable examples of antioxidants include aminic antioxidants such as N,N′-diisopropyl-p-phenylenediamine, N,N′-di-sec-butyl-p-phenylenediamine, N,N′-bis (1,4-dimethylpentyl)-p-phenylenediamine, N,N′-bis(1-ethyl-3-methylpentyl)-p-phenylenediamine, N,N′-bis(1-methylheptyl)-p-phenylenediamine, N,N′-dicyclohexyl-p-phenylenediamine, N,N′-diphenyl-p-phenylenediamine, N,N′-bis(2-naphthyl)-p-phenylenediamine, N-isopropyl-N′-phenyl-p-phenylenediamine, N-(1,3-dimethyl-butyl)-N′-phenyl-p-phenylenediamine, N-(1-methylheptyl)-N′-phenyl-p-phenylenediamine, N-cyclohexyl-N′-phenyl-p-phenylenediamine, 4-(p-toluenesulfamoyl)diphenyl amine, N,N′-dimethyl-N,N′-di-sec-butyl-p-phenylenediamine, diphenylamine, N-allyldiphenylamine, 4-isopropoxydiphenylamine, N-phenyl-1-naphthylamine, N-phenyl-2-naphthylamine, octylated diphenylamine, for example p,p′-di-tert-octyldiphenylamine, 4-n-butylaminophenol, 4-butyrylaminophenol, 4-nonanoylaminophenol, 4-dodecanoylaminophenol, 4-octadecanoylaminophenol, bis(4-methoxyphenyl)amine, 2,6-di-tert-butyl-4-dimethylamino methylphenol, 2,4′-diaminodiphenylmethane, 4,4′-diaminodiphenylmethane, N,N,N′,N′-tetramethyl-4,4′-diaminodiphenylmethane, 1,2-bis[(2-methyl-phenyl)amino]ethane, 1,2-bis(phenylamino)propane, (o-tolyl)biguanide, bis[4-(1′,3′-dimethylbutyl)phenyl]amine, tert-octylated N-phenyl-1-naphthylamine, a mixture of mono- and dialkylated tert-butyl/tert-octyldiphenylamines, a mixture of mono- and dialkylated isopropyl/isohexyldiphenylamines, mixtures of mono- and dialkylated tert-butyldiphenylamines, 2,3-dihydro-3,3-dimethyl-4H-1,4-benzothiazine, phenothiazine, N-allylphenothiazine, N,N,N′,N′-tetraphenyl-1,4-diaminobut-2-ene, and combinations thereof.
Even further examples of suitable antioxidants include aliphatic or aromatic phosphites, esters of thiodipropionic acid or of thiodiacetic acid, or salts of dithiocarbamic or dithiophosphoric acid, 2,2,12,12-tetramethyl-5,9-dihydroxy-3,7,1trithiatridecane and 2,2,15,15-tetramethyl-5,12-dihydroxy-3,7,10,14-tetrathiahexadecane, and combinations thereof. Furthermore, sulfurized fatty esters, sulfurized fats and sulfurized olefins, and combinations thereof, may be used. Additional suitable examples of antioxidants are commercially available from BASF of Florham Park, N.J. under the tradename Irganox®, such as Irganox® L 67 and Irganox® L 135.
As also introduced above, the additive package (or resultant lubricant composition) may further include one or more anti-wear additives. If utilized, the anti-wear may be present in the additive package in an amount ranging from 1 to 99, from 1 to 50, or from 5 to 15, wt. %, based on the total weight of the additive package. The anti-wear additive may include sulfur- and/or phosphorus- and/or halogen-containing compounds, e.g., sulfurised olefins and vegetable oils, alkylated triphenyl phosphates, tritolyl phosphate, tricresyl phosphate, chlorinated paraffins, alkyl and aryl di- and trisulfides, amine salts of mono- and dialkyl phosphates, amine salts of methylphosphonic acid, diethanolaminomethyltolyltriazole, bis(2-ethylhexyl)aminomethyltolyltriazole, derivatives of 2,5-dimercapto-1,3,4-thiadiazole, ethyl 3-[(diisopropoxyphosphinothioyl)thio]propionate, triphenyl thiophosphate (triphenylphosphorothioate), tris(alkylphenyl) phosphorothioate and mixtures thereof, diphenyl monononylphenyl phosphorothioate, isobutylphenyl diphenyl phosphorothioate, the dodecylamine salt of 3-hydroxy-1,3-thiaphosphetane 3-oxide, trithiophosphoric acid 5,5,5-tris[isooctyl 2-acetate], derivatives of 2-mercaptobenzothiazole such as 1-[N,N-bis (2-ethylhexyl)aminomethyl]-2-mercapto-1H-1,3-benzothiazole, ethoxycarbonyl-5-octyldithio carbamate, and/or combinations thereof.
In some embodiments, the anti-wear additive may be exemplified by a dihydrocarbyl dithiophosphate salt. The dihydrocarbyl dithiophosphate salt may be represented by the following general formula (XXIV):
[R25O(R26O)PS(S)]2M (XXIV)
where R25 and R26 are each hydrocarbyl groups independently having from 1 to 30, 1 to 20, 1 to 15, 1 to 10, or 1 to 5, carbon atoms, wherein M is a metal atom or an ammonium group. For example, R25 and R26 may each independently be C1-20 alkyl groups, C2-20 alkenyl groups, C3-20 cycloalkyl groups, C1-20 aralkyl groups or C3-20 aryl groups. The groups designated by R25 and R26 may be substituted or unsubstituted. The hydrocarbyl groups designated by R25 and R26 groups may have the same meaning as described above with respect to R1 in general formula III. The metal atom may be selected from the group including aluminum, lead, tin, manganese, cobalt, nickel, or zinc. The ammonium group may be derived from ammonia or a primary, secondary, or tertiary amine. The ammonium group may be of the formula R25R26R27R28N+, wherein R27, R28, R29, and R30 each independently represents a hydrogen atom or a hydrocarbyl group having from 1 to 150 carbon atoms. In certain embodiments, R27, R28, R29, and R30 may each independently be hydrocarbyl groups having from 4 to 30 carbon atoms. The hydrocarbyl groups designated by R27, R28, R29, and R30 may have the same meaning and R1 in general formula III. In one embodiment, the dihydrocarbyl dithiophosphate salt is zinc dialkyl dithiophosphate. The lubricant composition may include mixtures of different dihydrocarbyl dithiophosphate salts.
In certain embodiments, the dihydrocarbyl dithiophosphate salt includes a mixture of primary and secondary alkyl groups for, R25 and R26, wherein the secondary alkyl groups are in a major molar proportion, such as at least 60, at least 75, or at least 85, mole %, based on the number of moles of alkyl groups in the dihydrocarbyl dithiophosphate salt.
In some embodiments, the anti-wear additive may be ashless. The anti-wear additive may be further defined as a phosphate. In another embodiment, the anti-wear additive is further defined as a phosphite. In still another embodiment, the anti-wear additive is further defined as a phosphorothionate. The anti-wear additive may alternatively be further defined as a phosphorodithioate. In one embodiment, the anti-wear additive is further defined as a dithiophosphate. The anti-wear additive may also include an amine such as a secondary or tertiary amine. In one embodiment, the anti-wear additive includes an alkyl and/or dialkyl amine. Structures of suitable non-limiting examples of anti-wear additives are set forth immediately below:
In other embodiments, the anti-wear additive may include molybdenum. For example, the anti-wear additive including molybdenum may be exemplified by any suitable oil-soluble organo-molybdenum compound. Typically, the anti-wear additive including molybdenum includes a molybdenum-sulfur core formed from one or more molybdenum atoms and one or more sulfur atoms. Non-limiting examples of suitable anti-wear additives including molybdenum include molybdenum dithiocarbamates, molybdenum dithiophosphates, molybdenum dialkyldithiophosphates, molybdenum dithiophosphinates, molybdenum xanthates, molybdenum alkyl xanthates, molybdenum alkylthioxanthates, molybdenum thioxanthates, molybdenum sulfides, and combinations thereof.
In certain embodiments, the anti-wear additive including molybdenum is dinuclear or trinuclear. In one embodiment, the anti-wear additive including molybdenum is a tri-nuclear molybdenum compound that may be represented by the following general formula (XXV):
Mo3SkLnQ (XXV).
In general formula (XXV), L is an independently selected ligand having organo groups with a sufficient number of carbon atoms to render the compounds soluble or dispersible in the oil. In general formula (XXV), n is a number from 1 to 4. Also in general formula (XXV), k is a number from 4 to 7. Further in general formula (XXV), Q is selected from the group of neutral electron donating compounds such as water, amines, alcohols, phosphines, and ethers. Also in general formula (XXV), O is a number from 0 to 5. In certain embodiments, at least 21, at least 25, at least 30, or at least 35, total carbon atoms should be present among all the ligands' organo groups of the anti-wear additive including molybdenum.
In various embodiments, the anti-wear additive of the additive package or the lubricant composition may include phosphorus and molybdenum in a single compound. It is to be appreciated that one or more of the anti-wear additives including phosphorus described above may include phosphorus and molybdenum in a single compound. It is also to be appreciated that one or more of the anti-wear additives including molybdenum described above may include phosphorus and molybdenum in a single compound.
As also introduced above, the additive package (or resultant lubricant composition) may further include one or more base oils. If utilized, the base oil may be present in the additive package in an amount ranging from 1 to 99, from 1 to 50, or from 1 to 10, wt. %, based on the total weight of the additive package. The base oil is classified in accordance with the American Petroleum Institute (API) Base Oil Interchangeability Guidelines. In other words, the base oil may be further described as one or more of five types of base oils: Group I (sulphur content >0.03 wt. %, and/or <90 wt. % saturates, viscosity index 80-119); Group II (sulphur content less than or equal to 0.03 wt. %, and greater than or equal to 90 wt. % saturates, viscosity index 80-119); Group III (sulphur content less than or equal to 0.03 wt. %, and greater than or equal to 90 wt. % saturates, viscosity index greater than or equal to 119); Group IV (all polyalphaolefins (PAO's)); and Group V (all others not included in Groups I, II, III, or IV).
In some embodiments, the base oil is selected from the group of API Group I base oils; API Group II base oils; API Group III base oils; API Group IV base oils; API Group V base oils; and combinations thereof. In one embodiment, the base oil includes API Group II base oils.
The base oil may have a viscosity of from 1 to 50, 1 to 40, 1 to 30, 1 to 25, or 1 to 20, cSt, when tested according to ASTM D445 at 100° C. Alternatively, the viscosity of the base oil may range from 3 to 17, or 5 to 14, cSt, when tested according to ASTM D445 at 100° C.
The base oil may be further defined as a crankcase lubricant oil for spark-ignited and compression-ignited internal combustion engines, including automobile and truck engines, two-cycle engines, aviation piston engines, marine engines, and railroad diesel engines. Alternatively, the base oil can be further defined as an oil to be used in gas engines, diesel engines, stationary power engines, and turbines. The base oil may be further defined as heavy or light duty engine oil.
In still other embodiments, the base oil may be further defined as synthetic oil that includes one or more alkylene oxide polymers and interpolymers, and derivatives thereof. The terminal hydroxyl groups of the alkylene oxide polymers may be modified by esterification, etherification, or similar reactions. Typically, these synthetic oils are prepared through polymerization of ethylene oxide or propylene oxide to form polyoxyalkylene polymers which can be further reacted to form the synthetic oil. For example, alkyl and aryl ethers of these polyoxyalkylene polymers may be used. For example, methylpolyisopropylene glycol ether having a weight average molecular weight of 1000; diphenyl ether of polyethylene glycol having a molecular weight of 500-1000; or diethyl ether of polypropylene glycol having a weight average molecular weight of 1,000-1500 and/or mono- and polycarboxylic esters thereof, such as acetic acid esters, mixed C3-C5 fatty acid esters, and the C13 oxo acid diester of tetraethylene glycol may also be utilized as the base oil. Alternatively, the base oil may include a substantially inert, normally liquid, organic diluent, such as mineral oil, naptha, benzene, toluene, or xylene.
The base oil may include less than 90, less than 80, less than 70, less than 60, less than 50, less than 40, less than 30, less than 20, less than 10, less than 5, less than 3, less than 1, or be free from, an estolide compound (i.e., a compound including one or more estolide groups), based on the total weight of the lubricant composition.
The additive package may include, but is not limited to, seal compatibility additives, amine compounds, dispersants, detergents, aminic antioxidants, phenolic antioxidants, anti-foam additives, anti-wear additives, pour point depressants, viscosity modifiers, and combinations thereof. The lubricant composition may include the additive package in amount of at least 3, at least 4, at least 5, at least 6, at least 7, or at least 8, wt. %, based on a total weight of the lubricant composition. Alternatively, the lubricant composition may include the additive package in an amount of from 3 to 20, 4 to 18, 5 to 16, or 6 to 14, wt. %, based on a total weight of the lubricant composition. In some embodiments, the additive package does not account for the weight of the base oil as an additive. Although not required, the additive package includes all compounds in the lubricant composition other than the base oil. However, it is to be appreciated that certain individual components can be independently and individually added to the lubricant composition separate from the addition of the additive package to the lubricant composition, yet still be considered part of the additive package once the additive which was individually added into the lubricant composition is present in the lubricant composition along with the other additives.
The additive package refers to the collective amount of the seal compatibility additives, amine compounds, dispersants, detergents, aminic antioxidants, phenolic antioxidants, anti-foam additives, anti-wear additives, pour point depressants, viscosity modifiers, or combinations thereof in a solution, mixture, concentrate, or blend, such as the lubricant composition. In some embodiments, the term “additive package” does not require that these additives are physically packaged together or blended together before addition to the base oil. Thus, the base oil which includes the seal compatibility additive and the dispersant, each added to the base oil separately, could be interpreted to be a lubricant composition that includes an additive package comprising the seal compatibility additive and the dispersant. In other embodiments, the additive package refers to a blend of the seal compatibility additives, amine compounds, dispersants, detergents, aminic antioxidants, phenolic antioxidants, anti-foam additives, anti-wear additives, pour point depressants, viscosity modifiers, or combinations thereof. The additive package may be blended into the base oil to make the lubricant composition.
The additive package may be formulated to provide the desired concentration in the lubricant composition when the additive package is combined with a predetermined amount of base oil. It is to be appreciated that most references to the lubricant composition throughout this disclosure also apply to the description of the additive package. For example, it is to be appreciated that the additive package may include, or exclude, the same components as the lubricant composition, albeit in different amounts.
The lubricant composition may be formulated with the addition of several auxiliary components to achieve certain performance objectives for use in certain applications. For example, the lubricant composition may be a rust and oxidation lubricant formulation, a hydraulic lubricant formulation, turbine lubricant oil, and an internal combustion engine lubricant formulation. Accordingly, it is contemplated that the base oil may be formulated to achieve these objectives as discussed below.
If employed, the metal deactivator can be of various types. Suitable metal deactivators include benzotriazoles and derivatives thereof, for example 4- or 5 alkylbenzotriazoles (e.g. tolutriazole) and derivatives thereof, 4,5,6,7-tetrahydrobenzotriazole and 5,5′-methylenebisbenzotriazole; Mannich bases of benzotriazole or tolutriazole, e.g. 1-[bis(2-ethylhexyl)aminomethyl)tolutriazole and 1-[bis(2-ethylhexyl)aminomethyl)benzotriazole; and alkoxyalkylbenzotriazoles such as 1-(nonyloxymethyl)benzotriazole, 1-(1-butoxyethyl)benzotriazole and 1-(1-cyclohexyloxybutyl) tolutriazole, and combinations thereof.
Additional examples of suitable metal deactivators include 1,2,4-triazoles and derivatives thereof, and Mannich bases of 1,2,4-triazoles, such as 1-[bis(2-ethylhexyl)aminomethyl-1,2,4-triazole; alkoxyalkyl-1,2,4-triazoles such as 1-(1-butoxyethyl)-1,2,4-triazole; and acylated 3-amino-1,2,4-triazoles, imidazole derivatives, for example 4,4′-methylenebis(2-undecyl-5-methylimidazole) and bis[(N-methyl)imidazol-2-yl]carbinol octyl ether, and combinations thereof. Further examples of suitable metal deactivators include sulfur-containing heterocyclic compounds, for example 2-mercaptobenzothiazole, 2,5-dimercapto-1,3,4-thiadiazole and derivatives thereof; and 3,5-bis[di(2-ethylhexyl)aminomethyl]-1,3,4-thiadiazolin-2-one, and combinations thereof. Even further examples of metal deactivators include amino compounds, for example salicylidenepropylenediamine, salicylaminoguanidine and salts thereof, and combinations thereof.
If employed, the metal deactivator can be used in various amounts. The metal deactivator may be present in the lubricant composition in an amount of from 0.01 to 0.1, 0.05 to 0.01, or 0.07 to 0.1, wt. %, based on the total weight of the lubricant composition. Alternatively, the metal deactivator may be present in amounts of less than 1.0, less than 0.7, or less than 0.5, wt. %, based on the total weight of the lubricant composition.
If employed, the rust inhibitor and/or friction modifier can be of various types. Suitable examples of rust inhibitors and/or friction modifiers include organic acids, their esters, metal salts, for example alkyl- and alkenylsuccinic acids and their partial esters with alcohols, diols or hydroxycarboxylic acids, partial amides of alkyl- and alkenylsuccinic acids, 4-nonylphenoxyacetic acid, alkoxy- and alkoxyethoxycarboxylic acids such as dodecyloxyacetic acid, dodecyloxy(ethoxy)acetic acid, and also N-oleoylsarcosine, sorbitan monooleate, lead naphthenate, alkenylsuccinic anhydrides, for example, dodecenylsuccinic anhydride, 2-carboxymethyl-1-dodecyl-3-methylglycerol, and combinations thereof. Further examples include heterocyclic compounds, for example: substituted imidazolines and oxazolines, and 2-heptadecenyl-1-(2-hydroxyethyl)imidazoline, phosphorus-containing compounds, for example: amine salts of phosphoric acid partial esters or phosphonic acid partial esters, molybdenum-containing compounds, such as molydbenum dithiocarbamate and other sulphur and phosphorus containing derivatives, sulfur-containing compounds, for example: barium dinonylnaphthalenesulfonates, calcium petroleum sulfonates, alkylthio-substituted aliphatic carboxylic acids, esters of aliphatic 2-sulfocarboxylic acids and salts thereof, glycerol derivatives, for example: glycerol monooleate, 1-(alkylphenoxy)-3-(2-hydroxyethyl)glycerols, 1-(alkylphenoxy)-3-(2,3-dihydroxypropyl) glycerols and 2-carboxyalkyl-1,3-dialkylglycerols, and combinations thereof.
If employed, the rust inhibitor and/or friction modifier can be used in various amounts. The rust inhibitor and/or friction modifier may be present in the lubricant composition in an amount of from 0.01 to 0.1, 0.05 to 0.01, or 0.07 to 0.1, wt. %, based on the total weight of the lubricant composition. Alternatively, the rust inhibitor and/or friction modifier may be present in amounts of less than 1, less than 0.7, or less than 0.5, wt. %, based on the total weight of the lubricant composition.
If employed, the viscosity index improver can be of various types. Suitable examples of viscosity index improvers include polyacrylates, polymethacrylates, vinylpyrrolidone/methacrylate copolymers, polyvinylpyrrolidones, polybutenes, olefin copolymers, styrene/acrylate copolymers and polyethers, and combinations thereof.
If employed, the viscosity index improver can be used in various amounts. The viscosity index improver may be present in the lubricant composition in an amount of from 0.01 to 20, 1 to 15, or 1 to 10, wt. %, based on the total weight of the lubricant composition. Alternatively, the viscosity index improver may be present in amounts of less than 10, less than 8, or less than 5, wt. %, based on the total weight of the lubricant composition.
If employed, the pour point depressant can be of various types. Suitable examples of pour point depressants include polymethacrylate and alkylated naphthalene derivatives, and combinations thereof.
If employed, the pour point depressant can be used in various amounts. The pour point depressant may be present in the lubricant composition in an amount of from 0.01 to 0.1, 0.05 to 0.01, or 0.07 to 0.1, wt. %, each based on the total weight of the lubricant composition. Alternatively, the pour point depressant may be present in amounts of less than 1.0, less than 0.7, or less than 0.5, wt. %, based on the total weight of the lubricant composition.
An exemplary additive package formulation is provided in Table 1 below. The weight percent (wt. %) for each of the components below is based on a total weight of the additive package. The formulation may be formed using the method described above.
Many modifications and variations of the present disclosure are possible in light of the above teachings, and the disclosure may be practiced otherwise than as specifically described within the scope of the appended claims. The subject matter of all combinations of independent and dependent claims, both single and multiple dependent, is herein expressly contemplated. It is to be understood that the appended claims are not limited to express and particular compounds, compositions, or methods described in the detailed description, which may vary between particular embodiments which fall within the scope of the appended claims. With respect to any Markush groups relied upon herein for describing particular features or aspects of various embodiments, it is to be appreciated that different, special, and/or unexpected results may be obtained from each member of the respective Markush group independent from all other Markush members. Each member of a Markush group may be relied upon individually and or in combination and provides adequate support for specific embodiments within the scope of the appended claims.
It is also to be understood that any ranges and subranges relied upon in describing various embodiments of the present disclosure independently and collectively fall within the scope of the appended claims, and are understood to describe and contemplate all ranges including whole and/or fractional values therein, even if such values are not expressly written herein. One of skill in the art readily recognizes that the enumerated ranges and subranges sufficiently describe and enable various embodiments of the present disclosure, and such ranges and subranges may be further delineated into relevant halves, thirds, quarters, fifths, and so on. As just one example, a range “of from 0.1 to 0.9” may be further delineated into a lower third, i.e., from 0.1 to 0.3, a middle third, i.e., from 0.4 to 0.6, and an upper third, i.e., from 0.7 to 0.9, which individually and collectively are within the scope of the appended claims, and may be relied upon individually and/or collectively and provide adequate support for specific embodiments within the scope of the appended claims. In addition, with respect to the language which defines or modifies a range, such as “at least,” “greater than,” “less than,” “no more than,” and the like, it is to be understood that such language includes subranges and/or an upper or lower limit. As another example, a range of “at least 10” inherently includes a subrange of from at least 10 to 35, a subrange of from at least 10 to 25, a subrange of from 25 to 35, and so on, and each subrange may be relied upon individually and/or collectively and provides adequate support for specific embodiments within the scope of the appended claims. Finally, an individual number within a disclosed range may be relied upon and provides adequate support for specific embodiments within the scope of the appended claims. For example, a range “of from 1 to 9” includes various individual integers, such as 3, as well as individual numbers including a decimal point (or fraction), such as 4.1, which may be relied upon and provide adequate support for specific embodiments within the scope of the appended claims.
This application claims priority to U.S. Provisional Patent Application No. 62/139,223, filed on Mar. 27, 2015, which is hereby incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 62139223 | Mar 2015 | US |
