CA2171924C - Extended life rust and oxidation oils - Google Patents
Extended life rust and oxidation oils Download PDFInfo
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- CA2171924C CA2171924C CA002171924A CA2171924A CA2171924C CA 2171924 C CA2171924 C CA 2171924C CA 002171924 A CA002171924 A CA 002171924A CA 2171924 A CA2171924 A CA 2171924A CA 2171924 C CA2171924 C CA 2171924C
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/10—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
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- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
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- C10M135/12—Thio-acids; Thiocyanates; Derivatives thereof
- C10M135/14—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
- C10M135/18—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond thiocarbamic type, e.g. containing the groups
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- C10M141/08—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic sulfur-, selenium- or tellurium-containing compound
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M2215/065—Phenyl-Naphthyl amines
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- C10M2215/068—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings having amino groups bound to polycyclic aromatic ring systems, i.e. systems with three or more condensed rings
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Abstract
In a rust and oxidation (R&O) inhibited lubricant composition comprising a base oil and rust and oxidation inhibitors, the invention is directed to the improvement wherein the lubricant composition includes (a) a dithiocarbamate compound represented by the formula
Description
EXTENDED LIFE RUST AND OXIDATION OILS
BACKGROUND OF THE INVENTION
1. Field of the Invention. This invention relates to the field of improved thermal and oxidative stability of lubricating fluids.
BACKGROUND OF THE INVENTION
1. Field of the Invention. This invention relates to the field of improved thermal and oxidative stability of lubricating fluids.
2. Description of the Prior Art.
Lubricating oils such as circulating oils, turbine oils, hydraulic fluids and transformer oils as well as others require good oxidation stability and good rust inhibition properties. Extended life for such fluids where desired rust and oxidation (R&O) inhibition properties are maintained for extended periods of use is demanded by industrial users and provides important economic benefit. R&O oils are widely used in turbine and compressor circulating systems. Their thermal and oxidative stability are of particular importance. In addition, R&O oils provide rust protection, corrosion protection and metal passivation. Antiwear protection is sometimes needed.
U. S. Patent 4,125,479 to Chesluk et al. discloses an oxidation inhibited lubricating oil with a combination of additives comprising methylenebis(di-n-butyldithiocarbamate)and 4-methyl-2,6-ditertiary butyl phenol, said to provide enhanced oxidation inhibition. U. S. Patent 4,880,551 to Doe discloses an antioxidant composition consisting of a 1-(di(4-octylphenyl) aminomethyl)tolutriazole and at least one antioxidant selected from the group consisting essentially of methylenebis(di-n-butyldithiocarbamate); 2,6-di-t-butyl-4-sec-butylphenol; 2,6-di-t-butyl-4-methylphenol and butylated phenol mixture. International PCT Publication Number WO 92/19703, published 12 November 1992, to Lubrizol Corporation discloses thermally stable lubricant and functional fluid compositions containing hydrocarbyl phosphate in combination with at least one basic alkali or alkaline earth metal salt of an acidic organic compound and a metal deactivator, the composition may additionally contain a dithiocarbamate compound for an antiwear agent. These references do not teach or suggest the combination of components claimed herein.
There is an increasing demand for inhibited oils with extended lifetimes. R&O lubricant concentrate packages typically contain phenolic, amino and other antioxidants, rust inhibitor(s), a metal deactivator, and a demulsifying agent. They may include additional components such as an antiwear agent depending on the final performance properties desired. The principle function of the antioxidants is the inhibition of oxidative degradation of R&O oils that are obtained by blending the R&O lubricant concentrate package in a particular basestock oil of choice. Basestock oils have varying degrees of thermal and oxidative stability.
This invention will serve to improve the thermal and oxidative properties of even those basestock oils that are known to have less than satisfactory stability. The current invention relates to the use of certain components that contribute directly to prolonging the life of R&O oils.
SUMMARY OF THE INVENTION
In a rust and oxidation (R&O) inhibited lubricant ccmposition comprising a base oil and rust and oxidation inhibitors, the invention is directed to the improvement wherein said lubricant composition comprises (a) a dithiocarbamate compound represented by the formula RS S S RS
N - S - S - -- -Ra Ra 2171924 __ wherein R4 is a hydrocarbylene group having 1 to 10 carbon atoms, each Rsis a hydrogen or a hydrocarbyl group having1 to 18 carbon atoms, and each R3 a hydrocarbyl group having 1 to 18 carbon is atoms; and (b) an alkylphenyl-a-naphthylamine. The lubricant composition further optionally comprises (c) a hydrocarbyl phosphate represented by the formula (R60)3P
where each R6 is independently C1 to C18 alkyl, Cz to C18 alkenyl, or C6 to Cle aryl. Each component (a) and (b) , or (a) , (b) and (c) is present in an amount sufficient to provide improved inhibition of oxidation to the R&O lubricant composition.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The additive combinations of this invention may be used in any lubricating oil where oxidation inhibition is required. This may include circulating oils used in compressor and turbine circulating systems, transformer oils, engine oils and other oils which are subjected to conditions where oxidation is a problem. It has been found that a dithiocarbamate compound in combination with an alkylphenyl-a-naphthylamine, in effective amounts, and that combination in further combination with an effective amount of hydrocarbyl phosphate, provide important and unexpected enhancement of thermal and oxidation stability, with resulting improvement in the life of the R&O oil.
The additive combinations of this invention can be incorporated in a wide variety of lubricants and functional fluids in effective amounts to provide suitable active ingredient concentrations. The base oils useful herein can be hydrocarbon oils of suitable viscosities; synthetic oils such as hydrogenated polyolefin oils;
poly-a-olefin oligomers (such as hydrogenated poly-1-decene); alkyl esters of dicarboxylic acids; complex esters of dicarboxylic acid,
Lubricating oils such as circulating oils, turbine oils, hydraulic fluids and transformer oils as well as others require good oxidation stability and good rust inhibition properties. Extended life for such fluids where desired rust and oxidation (R&O) inhibition properties are maintained for extended periods of use is demanded by industrial users and provides important economic benefit. R&O oils are widely used in turbine and compressor circulating systems. Their thermal and oxidative stability are of particular importance. In addition, R&O oils provide rust protection, corrosion protection and metal passivation. Antiwear protection is sometimes needed.
U. S. Patent 4,125,479 to Chesluk et al. discloses an oxidation inhibited lubricating oil with a combination of additives comprising methylenebis(di-n-butyldithiocarbamate)and 4-methyl-2,6-ditertiary butyl phenol, said to provide enhanced oxidation inhibition. U. S. Patent 4,880,551 to Doe discloses an antioxidant composition consisting of a 1-(di(4-octylphenyl) aminomethyl)tolutriazole and at least one antioxidant selected from the group consisting essentially of methylenebis(di-n-butyldithiocarbamate); 2,6-di-t-butyl-4-sec-butylphenol; 2,6-di-t-butyl-4-methylphenol and butylated phenol mixture. International PCT Publication Number WO 92/19703, published 12 November 1992, to Lubrizol Corporation discloses thermally stable lubricant and functional fluid compositions containing hydrocarbyl phosphate in combination with at least one basic alkali or alkaline earth metal salt of an acidic organic compound and a metal deactivator, the composition may additionally contain a dithiocarbamate compound for an antiwear agent. These references do not teach or suggest the combination of components claimed herein.
There is an increasing demand for inhibited oils with extended lifetimes. R&O lubricant concentrate packages typically contain phenolic, amino and other antioxidants, rust inhibitor(s), a metal deactivator, and a demulsifying agent. They may include additional components such as an antiwear agent depending on the final performance properties desired. The principle function of the antioxidants is the inhibition of oxidative degradation of R&O oils that are obtained by blending the R&O lubricant concentrate package in a particular basestock oil of choice. Basestock oils have varying degrees of thermal and oxidative stability.
This invention will serve to improve the thermal and oxidative properties of even those basestock oils that are known to have less than satisfactory stability. The current invention relates to the use of certain components that contribute directly to prolonging the life of R&O oils.
SUMMARY OF THE INVENTION
In a rust and oxidation (R&O) inhibited lubricant ccmposition comprising a base oil and rust and oxidation inhibitors, the invention is directed to the improvement wherein said lubricant composition comprises (a) a dithiocarbamate compound represented by the formula RS S S RS
N - S - S - -- -Ra Ra 2171924 __ wherein R4 is a hydrocarbylene group having 1 to 10 carbon atoms, each Rsis a hydrogen or a hydrocarbyl group having1 to 18 carbon atoms, and each R3 a hydrocarbyl group having 1 to 18 carbon is atoms; and (b) an alkylphenyl-a-naphthylamine. The lubricant composition further optionally comprises (c) a hydrocarbyl phosphate represented by the formula (R60)3P
where each R6 is independently C1 to C18 alkyl, Cz to C18 alkenyl, or C6 to Cle aryl. Each component (a) and (b) , or (a) , (b) and (c) is present in an amount sufficient to provide improved inhibition of oxidation to the R&O lubricant composition.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The additive combinations of this invention may be used in any lubricating oil where oxidation inhibition is required. This may include circulating oils used in compressor and turbine circulating systems, transformer oils, engine oils and other oils which are subjected to conditions where oxidation is a problem. It has been found that a dithiocarbamate compound in combination with an alkylphenyl-a-naphthylamine, in effective amounts, and that combination in further combination with an effective amount of hydrocarbyl phosphate, provide important and unexpected enhancement of thermal and oxidation stability, with resulting improvement in the life of the R&O oil.
The additive combinations of this invention can be incorporated in a wide variety of lubricants and functional fluids in effective amounts to provide suitable active ingredient concentrations. The base oils useful herein can be hydrocarbon oils of suitable viscosities; synthetic oils such as hydrogenated polyolefin oils;
poly-a-olefin oligomers (such as hydrogenated poly-1-decene); alkyl esters of dicarboxylic acids; complex esters of dicarboxylic acid,
3 polyglycol and alcohol; alkyl esters of carbonic or phosphoric acids; polysilicones; fluorohydrocarbon oils; and mixtures of mineral, natural and/or synthetic oils in any proportion, etc. The term "base oil" for this disclosure includes all the foregoing and mixtures thereof.
The dithiocarbamate compound to be included in the combination of the invention is represented by the formula RS S S RS
N - - - S C --Rj R3 wherein R4 is a hydrocarbylene group having 1 to 10 carbon atoms, preferably 1 to 4 carbon atoms. Preferably, R4 is an alkylene group, most preferably a methylene or ethylene group. Each Rsis a hydrogen or a hydrocarbyl group having 1 to 18 carbon atoms, preferably 2 to 10, more preferably 2 to 6_ Each R3 is a hydrocarbyl group having 1 to 18 carbon atoms, preferably 2 to 10, more preferably 2 to 6. A commercially available dithiocarbamate compound appropriate for use in the invention is VANLUBE 7723, methylenebis(di-n-butyldithiocarbamate).
Beyond a certain level, the dithiocarbamate compound may start hurting or interfering with relevent bench tests other than R&O
tests. Higher levels of dithiocarbamate compound may result in deterioration of thermal stability, causing undesired sludge in thermal stability tests. Also rust problems may occur at higher dithiocarbamate compound levels, which may result in failure of specified rust tests. An effective amount of dithiocarbamate compound is up to 1.0 weight percent of the finished lubricant *Trade-mark
The dithiocarbamate compound to be included in the combination of the invention is represented by the formula RS S S RS
N - - - S C --Rj R3 wherein R4 is a hydrocarbylene group having 1 to 10 carbon atoms, preferably 1 to 4 carbon atoms. Preferably, R4 is an alkylene group, most preferably a methylene or ethylene group. Each Rsis a hydrogen or a hydrocarbyl group having 1 to 18 carbon atoms, preferably 2 to 10, more preferably 2 to 6_ Each R3 is a hydrocarbyl group having 1 to 18 carbon atoms, preferably 2 to 10, more preferably 2 to 6. A commercially available dithiocarbamate compound appropriate for use in the invention is VANLUBE 7723, methylenebis(di-n-butyldithiocarbamate).
Beyond a certain level, the dithiocarbamate compound may start hurting or interfering with relevent bench tests other than R&O
tests. Higher levels of dithiocarbamate compound may result in deterioration of thermal stability, causing undesired sludge in thermal stability tests. Also rust problems may occur at higher dithiocarbamate compound levels, which may result in failure of specified rust tests. An effective amount of dithiocarbamate compound is up to 1.0 weight percent of the finished lubricant *Trade-mark
4 21 l 1924 composition, for example 0.01 to 1.0 weight percent, 0.02 to 0.5 preferred, 0.03-0.2 most preferred.
The alkylphenyl-a-naphthylamine for use in the invention is represented by the formula Rz H
' N O
wherein Rl and RZ are independently hydrogen or Cl to Cl8 alkyl. For purposes herein, "alkylphenyl-a-naphthylamine" includes phenyl-a-naphthylamine (PANA), where both R1 and RZ are hydrogen. An effective amount of alkylphenyl-a-naphthylamine for use in the invention is up to 0.15 weight percent of the finished lubricant composition, for example 0.025 to 0.15 weight percent, 0.03 to 0.125 weight percent preferred.
The hydrocarbyl phosphate compound for use in the invention is represented by the formula:
(R60)3P
where each R6 is independently C1 to C18 alkyl, Cz to C18 alkenyl, or C6 to C18 aryl. In preferred compounds, each Rsis independently C3 to C12 alkyl or C6 to C18 aryl. In most preferred compounds, R6 is C6 to C18 aryl, including triphenylphosphite, tricresylphos-phite, trinonylphenylphosphite (C15), tridodecylphenylphosphite, and mixtures thereof. An effective amount of the hydrocarbyl phosphate compound for use in the invention is up to 0.075 weight percent of the finished lubricant composition, for example 0.005 to 0.075 a weight percent, 0.01 to 0.06 preferred.
R&O oils will typically contain a conventional quantity of one or more antioxidants in order to protect the composition from premature degradation in the presence of air, especially at elevated temperatures. Typical antioxidants include various alkylated phenols, hindered phenols and phenol derivatives such as t-butyl hydroquinone, butylated hydroxyanisole, polybutylated bisphenol A, butylated hydroxy toluene, alkylated hydroquinone, 2,5-ditertaryl hydroquinone; 2,6-ditert-butyl-para-cresol; 2,2'-methylenebis(6-tert-butyl-p-cresol); 1,5-naphthalenediol; 4,4'-thiobis(t-tert-butyl-m-cresol); p,p-biphenol; 4,4'-butylidenebis(6-tert-butyl-m-cresol); 4-methoxy-2,6-di-tert-butylphenol; and the like; also amino antioxidants such as aldehyde amines, ketone amines, ketone-diarylamines, alkylated diphenylamines, phenylenediamines, and the phenolic amines; secondary aromatic amine antioxidants, sulfurized phenolic antioxidants, oil-soluble copper compounds, phosphorus-containing antioxidants, and the like as well as mixtures of antioxidants. Phenolic antioxidants are known and may be represented by the general formula:
where R-, is hydrogen or an alkyl group with 1 to 4 carbons, Re is an alkyl group with 1 to 4 carbons or a benzylic group, and R9 is hydrogen, an alkyl group with 1 to 6 carbons, or an alkoxy group with 1 to 6 carbons. In one example of a phenolic antioxidant for use with the invention, R, is hydrogen, Re is an alkyl group with 1 to 4 carbons, and R9 is an alkyl group with 1 to 6 carbons; most preferably both Re and R9 are t-butyl. In a second example R9 is hydrogen, R., is an alkyl group with 1 to 4 carbons, and Re is an -. ;
alkyl group with 1 to 4 carbons; most preferably both R, and Re are t-butyl.
The R&O oil compositions useful herein will also typically comprise a rust inhibitor and a metal deactivator. These are commonly selected from alkenyl succinic acid esters and from triazoles and triazole derivatives, known for these purposes_ It is also useful to this invention to employ in the lubricant compositions and additive concentrates a suitable quantity of a corrosion inhibitor. This may be a single compound or a mixture of compounds having the property of inhibiting corrosion of metallic surfaces. One type of such additives are inhibitors of copper' corrosion. Such compounds include thiazoles, triazoles and thiadizoles. Examples of such compounds include benzotriazole, tolytriazole, octyltriazole, decyltriazole, dodecyltriazoie, 2-mercaptobenzothiazole, 2, 5-dimercapto-1, 3, 4-thiadiazole, 2-mercapto-5-hydrocarbylthio-1,3,4-thiadiazoles, 2-mercapto-5-hydrocarbyldithio-1, 3, 4-thiadiazoles, 2, 5-bis(hydrocarbylthio)-l, 3, 4-thiadiazoles, and 2, 5- (bis) hydrocarbyldithio) , 1, 3, 4-thiadiazoles. The preferred compounds are the 1, 3, 4-thiadiazoles, a number of which are available as articles of commerce. Such compounds are generally synthesized from hydrazine and carbon disulfide by known procedures. See for example U.S.
Pat. Nos. 2,765,289; 2,749, 311; 2,760,933; 2,850,453; 2,910,439;
3,663,561; 3,862,798; and 3,840,549. Other types of corrosion inhibitors are known and suitable for use in the compositions of this invention. Suitable corrosion inhibitors include ether amines; acid phosphates; amines; polyethoxylated compounds such as ethoxylated amines, ethoxylated and/or propoxylated phenols, and ethoxylated alcohols; imidazolines; and the like. Materials of these types are well known to those skilled in the art and a number of such materials are available as articles of commerce.
The lubricating composition of the present invention may further contain other additives such as extreme pressure agents and/or antiwear agents.
The additives of the present invention can be incorporated into a lubricating oil in any convenient way. The compounds, or mixtures thereof, can be added directly to the oil at the desired level or by adding concentrates of the additive to the oil.
Accordingly, the additive compounds can be blended with a suitable oil soluble solvent such as mineral spirits and/or base oil to form a concentrate and then the concentrate may be blended with lubricating oil to obtain a final formulation. A complete R&O
lubricant concentrate package can be prepared containing antioxidants, rust inhibitor, metal, deactivator, demulsifier, additional desired components as well as the components of the invention, i.e. the dithiocarbamate compound and the alkylphenyl-a-naphthylamine compound; or the dithiocarbamate compound, the alkylphenyl-a-naphthylamine compound, and the hydrocarbyl phosphate. The components are present in the lubricant concentrate package at a level sufficient to provide an effective level in the finished composition to provide the enhanced oxidation inhibition properties.
EXAMPLES
The following tests were performed to demonstrate the advantages of the invention:
(a) The American Society for Testing and Materials {ASTM) provides a Standard Test Method for Oxidation Characteristics of Inhibited Mineral Oils {ASTM D943-81{Reapproved 1991)). The D943 test method was developed for, and is used to evaluate the oxidation stability of inhibited steam turbine oils and other oils containing R&O inhibitors in the presence of oxygen, water, and copper and iron metals at an elevated temperature and is considered of value in the industry in estimating the oxidation stability of lubricants, especially those that are prone to water contamination_ (b) ASTM D-2272-85(Reapproved 1991), Standard Test Method for Oxidation Stability of Steam Turbine Oils by Rotating Bomb, (RBOT) utilizes an oxygen-pressured bomb to evaluate the oxidation stability of new and in service turbine oils having the same composition (base stock and additives) in the presence of water and a copper catalyst coil at 150°C.
(c) The Cincinnati Milacron Thermal Stability Test procedure "A" (CM "A") is intended to check the thermal stability of a designated oil sample by immersing copper and iron rods into an oil sample, heating in an oil bath or oven (135-138° C) for one week (168 hours), and determining the weight of resulting residue or "sludge".
HiTec 575 Ashless Rust & Oxidation Inhibitor is a lubricant additive concentrate package commercially available from Ethyl Corporation. This is fully formulated for high-performance, turbine-quality hydraulic fluids. It provides extended oxidation life, excellent rust control, demulsibility and filterability, and is compatible with other additives commonly used in hydraulic fluids. HiTec 575 lubricant additive represents a typical R&O
package and has been used in the studies reported herein to demonstrate the improved oxidation properties obtained with the present invention. Texaco''ISO 46 basestock oil was used in preparing the formulation of the examples below. In Example 1, HiTec 575 lubricant additive was blended with the basestock oil at its recommended dosage, 0.80 weight percent. HiTec 575 lubricant additive contains PANA in an amount that provides 0.10 weight percent to the blended lubricant composition at this recommended dosage. For Examples 2 through 6 below, the PANA was removed from the HiTec 575 lubricant additive. The HiTec 575 lubricant additive without PANA was blended with the Texaco ISO 46 basestock oil at *trade-mark 9 ~_, 0.80 weight percent dosage, and the dithiocarbamate compound and triphenylphosphite were added in the amounts indicated. Far Examples 7 through 14, commercially available HiTec 575 lubricant additive was blended with the basestock at 0.80 weight percent dosage, and the dithiocarbamate compound and triphenylphosphite were added in the amounts indicated. A commercially available dithiocarbamate compound, VANLUBE° 7723, methylenebis(di-n-butyldithiocarbamate), was used in the Examples in the amounts indicated. Table I below provides the composition of Examples 1-11 and the results of D943 and RBOT testing and CM "A" Sludge testing.
The composition and the results of RBOT testing for Examples 12-14 are also provided in Table I.
2171924.-.
TABLE I
Example PANA DITHIO- TPP RBOT CM "A" D943 ~AM~ SLUDGE
wt % wt % wt o minutes mg/100m1 hours 1 0.10 - - 745 14.00 2644 2 - - - 708 14.03 2634 3 - 0.025 - 765 9.92 2756 4 - 0.025 0.025 775 19.5 2523 - 0.050 - 805 12.25 2922 6 - 0.050 0.025 826 20.08 2526 7 0.10 0.025 0.025 945 23.05 2724 8 0.10 0.050 0.025 1048 22.10 3852 9 0.10 0.050 0.050 986 25.40 3684 0.10 0.100 0.025 1130 19.75 )3700*
11 0.10 0.100 0.050 1195 29.03 3850 12 0.10 0.05 - 942 13 0.10 0.10 - 1080 14 0.10 0.20 - 1335 * Test still running at time of filing
The alkylphenyl-a-naphthylamine for use in the invention is represented by the formula Rz H
' N O
wherein Rl and RZ are independently hydrogen or Cl to Cl8 alkyl. For purposes herein, "alkylphenyl-a-naphthylamine" includes phenyl-a-naphthylamine (PANA), where both R1 and RZ are hydrogen. An effective amount of alkylphenyl-a-naphthylamine for use in the invention is up to 0.15 weight percent of the finished lubricant composition, for example 0.025 to 0.15 weight percent, 0.03 to 0.125 weight percent preferred.
The hydrocarbyl phosphate compound for use in the invention is represented by the formula:
(R60)3P
where each R6 is independently C1 to C18 alkyl, Cz to C18 alkenyl, or C6 to C18 aryl. In preferred compounds, each Rsis independently C3 to C12 alkyl or C6 to C18 aryl. In most preferred compounds, R6 is C6 to C18 aryl, including triphenylphosphite, tricresylphos-phite, trinonylphenylphosphite (C15), tridodecylphenylphosphite, and mixtures thereof. An effective amount of the hydrocarbyl phosphate compound for use in the invention is up to 0.075 weight percent of the finished lubricant composition, for example 0.005 to 0.075 a weight percent, 0.01 to 0.06 preferred.
R&O oils will typically contain a conventional quantity of one or more antioxidants in order to protect the composition from premature degradation in the presence of air, especially at elevated temperatures. Typical antioxidants include various alkylated phenols, hindered phenols and phenol derivatives such as t-butyl hydroquinone, butylated hydroxyanisole, polybutylated bisphenol A, butylated hydroxy toluene, alkylated hydroquinone, 2,5-ditertaryl hydroquinone; 2,6-ditert-butyl-para-cresol; 2,2'-methylenebis(6-tert-butyl-p-cresol); 1,5-naphthalenediol; 4,4'-thiobis(t-tert-butyl-m-cresol); p,p-biphenol; 4,4'-butylidenebis(6-tert-butyl-m-cresol); 4-methoxy-2,6-di-tert-butylphenol; and the like; also amino antioxidants such as aldehyde amines, ketone amines, ketone-diarylamines, alkylated diphenylamines, phenylenediamines, and the phenolic amines; secondary aromatic amine antioxidants, sulfurized phenolic antioxidants, oil-soluble copper compounds, phosphorus-containing antioxidants, and the like as well as mixtures of antioxidants. Phenolic antioxidants are known and may be represented by the general formula:
where R-, is hydrogen or an alkyl group with 1 to 4 carbons, Re is an alkyl group with 1 to 4 carbons or a benzylic group, and R9 is hydrogen, an alkyl group with 1 to 6 carbons, or an alkoxy group with 1 to 6 carbons. In one example of a phenolic antioxidant for use with the invention, R, is hydrogen, Re is an alkyl group with 1 to 4 carbons, and R9 is an alkyl group with 1 to 6 carbons; most preferably both Re and R9 are t-butyl. In a second example R9 is hydrogen, R., is an alkyl group with 1 to 4 carbons, and Re is an -. ;
alkyl group with 1 to 4 carbons; most preferably both R, and Re are t-butyl.
The R&O oil compositions useful herein will also typically comprise a rust inhibitor and a metal deactivator. These are commonly selected from alkenyl succinic acid esters and from triazoles and triazole derivatives, known for these purposes_ It is also useful to this invention to employ in the lubricant compositions and additive concentrates a suitable quantity of a corrosion inhibitor. This may be a single compound or a mixture of compounds having the property of inhibiting corrosion of metallic surfaces. One type of such additives are inhibitors of copper' corrosion. Such compounds include thiazoles, triazoles and thiadizoles. Examples of such compounds include benzotriazole, tolytriazole, octyltriazole, decyltriazole, dodecyltriazoie, 2-mercaptobenzothiazole, 2, 5-dimercapto-1, 3, 4-thiadiazole, 2-mercapto-5-hydrocarbylthio-1,3,4-thiadiazoles, 2-mercapto-5-hydrocarbyldithio-1, 3, 4-thiadiazoles, 2, 5-bis(hydrocarbylthio)-l, 3, 4-thiadiazoles, and 2, 5- (bis) hydrocarbyldithio) , 1, 3, 4-thiadiazoles. The preferred compounds are the 1, 3, 4-thiadiazoles, a number of which are available as articles of commerce. Such compounds are generally synthesized from hydrazine and carbon disulfide by known procedures. See for example U.S.
Pat. Nos. 2,765,289; 2,749, 311; 2,760,933; 2,850,453; 2,910,439;
3,663,561; 3,862,798; and 3,840,549. Other types of corrosion inhibitors are known and suitable for use in the compositions of this invention. Suitable corrosion inhibitors include ether amines; acid phosphates; amines; polyethoxylated compounds such as ethoxylated amines, ethoxylated and/or propoxylated phenols, and ethoxylated alcohols; imidazolines; and the like. Materials of these types are well known to those skilled in the art and a number of such materials are available as articles of commerce.
The lubricating composition of the present invention may further contain other additives such as extreme pressure agents and/or antiwear agents.
The additives of the present invention can be incorporated into a lubricating oil in any convenient way. The compounds, or mixtures thereof, can be added directly to the oil at the desired level or by adding concentrates of the additive to the oil.
Accordingly, the additive compounds can be blended with a suitable oil soluble solvent such as mineral spirits and/or base oil to form a concentrate and then the concentrate may be blended with lubricating oil to obtain a final formulation. A complete R&O
lubricant concentrate package can be prepared containing antioxidants, rust inhibitor, metal, deactivator, demulsifier, additional desired components as well as the components of the invention, i.e. the dithiocarbamate compound and the alkylphenyl-a-naphthylamine compound; or the dithiocarbamate compound, the alkylphenyl-a-naphthylamine compound, and the hydrocarbyl phosphate. The components are present in the lubricant concentrate package at a level sufficient to provide an effective level in the finished composition to provide the enhanced oxidation inhibition properties.
EXAMPLES
The following tests were performed to demonstrate the advantages of the invention:
(a) The American Society for Testing and Materials {ASTM) provides a Standard Test Method for Oxidation Characteristics of Inhibited Mineral Oils {ASTM D943-81{Reapproved 1991)). The D943 test method was developed for, and is used to evaluate the oxidation stability of inhibited steam turbine oils and other oils containing R&O inhibitors in the presence of oxygen, water, and copper and iron metals at an elevated temperature and is considered of value in the industry in estimating the oxidation stability of lubricants, especially those that are prone to water contamination_ (b) ASTM D-2272-85(Reapproved 1991), Standard Test Method for Oxidation Stability of Steam Turbine Oils by Rotating Bomb, (RBOT) utilizes an oxygen-pressured bomb to evaluate the oxidation stability of new and in service turbine oils having the same composition (base stock and additives) in the presence of water and a copper catalyst coil at 150°C.
(c) The Cincinnati Milacron Thermal Stability Test procedure "A" (CM "A") is intended to check the thermal stability of a designated oil sample by immersing copper and iron rods into an oil sample, heating in an oil bath or oven (135-138° C) for one week (168 hours), and determining the weight of resulting residue or "sludge".
HiTec 575 Ashless Rust & Oxidation Inhibitor is a lubricant additive concentrate package commercially available from Ethyl Corporation. This is fully formulated for high-performance, turbine-quality hydraulic fluids. It provides extended oxidation life, excellent rust control, demulsibility and filterability, and is compatible with other additives commonly used in hydraulic fluids. HiTec 575 lubricant additive represents a typical R&O
package and has been used in the studies reported herein to demonstrate the improved oxidation properties obtained with the present invention. Texaco''ISO 46 basestock oil was used in preparing the formulation of the examples below. In Example 1, HiTec 575 lubricant additive was blended with the basestock oil at its recommended dosage, 0.80 weight percent. HiTec 575 lubricant additive contains PANA in an amount that provides 0.10 weight percent to the blended lubricant composition at this recommended dosage. For Examples 2 through 6 below, the PANA was removed from the HiTec 575 lubricant additive. The HiTec 575 lubricant additive without PANA was blended with the Texaco ISO 46 basestock oil at *trade-mark 9 ~_, 0.80 weight percent dosage, and the dithiocarbamate compound and triphenylphosphite were added in the amounts indicated. Far Examples 7 through 14, commercially available HiTec 575 lubricant additive was blended with the basestock at 0.80 weight percent dosage, and the dithiocarbamate compound and triphenylphosphite were added in the amounts indicated. A commercially available dithiocarbamate compound, VANLUBE° 7723, methylenebis(di-n-butyldithiocarbamate), was used in the Examples in the amounts indicated. Table I below provides the composition of Examples 1-11 and the results of D943 and RBOT testing and CM "A" Sludge testing.
The composition and the results of RBOT testing for Examples 12-14 are also provided in Table I.
2171924.-.
TABLE I
Example PANA DITHIO- TPP RBOT CM "A" D943 ~AM~ SLUDGE
wt % wt % wt o minutes mg/100m1 hours 1 0.10 - - 745 14.00 2644 2 - - - 708 14.03 2634 3 - 0.025 - 765 9.92 2756 4 - 0.025 0.025 775 19.5 2523 - 0.050 - 805 12.25 2922 6 - 0.050 0.025 826 20.08 2526 7 0.10 0.025 0.025 945 23.05 2724 8 0.10 0.050 0.025 1048 22.10 3852 9 0.10 0.050 0.050 986 25.40 3684 0.10 0.100 0.025 1130 19.75 )3700*
11 0.10 0.100 0.050 1195 29.03 3850 12 0.10 0.05 - 942 13 0.10 0.10 - 1080 14 0.10 0.20 - 1335 * Test still running at time of filing
Claims (22)
1. In a rust and oxidation inhibited lubricant composition comprising a base oil and rust and oxidation inhibitors, the improvement wherein said lubricant composition additionally comprises (a) up to 1.0 weight percent of the finished lubricant composition of a dithiocarbamate compound represented by the formula wherein R4 is a hydrocarbylene group having 1 to 10 carbon atoms, each R5 is a hydrogen or a hydrocarbyl group having 1 to 18 carbon atoms, and each R3 is a hydrocarbyl group having 1 to 18 carbon atoms; and (b) up to 0.15 weight percent of the finished lubricant composition of an alkylphenyl-.alpha.-naphthylamine compound represented by the formula wherein R1 and R2 are independently hydrogen or C1 to C18 alkyl.
2. The lubricant composition of claim 1 wherein for the dithiocarbamate compound (a) R4 is an alkylene group having 1 to 4 carbon atoms, each R5 is a hydrogen or a hydrocarbyl group having 2 to 10 carbon atoms, and each R3 has 2 to 10 carbon atoms.
3. The lubricant composition of claim 2 wherein R5 is a hydrogen and R3 has 2 to 6 carbon atoms.
4. The lubricant composition of claim 1 wherein the dithiocarbamate compound (a) is methylenebis(di-n-butyldithio-carbamate).
5. The lubricant composition of claim 1 additionally comprising (c) up to 0.075 weight percent of the finished lubricant composition of a hydrocarbyl phosphate represented by the formula (R6O)3P
where each R6 is independently C1 to C18 alkyl, C2 to C18 alkenyl, or C6 to C18 aryl.
where each R6 is independently C1 to C18 alkyl, C2 to C18 alkenyl, or C6 to C18 aryl.
6. The lubricant composition of claim 5 wherein each R6 is independently C3 to C12 alkyl or C6 to C18 aryl.
7. The lubricant composition of claim 5 wherein R6 is C6 to C18 aryl.
8. The lubricant composition of claim 5 wherein said hydrocarbyl phosphate compound (c) is triphenylphosphite or tricresylphosphite.
9. The lubricant composition of claim 3 additionally comprising (c) up to 0.075 weight percent of the finished lubricant composition of a hydrocarbyl phosphate represented by the formula (R6O)3P
wherein each R6 is C6 to C18 aryl.
wherein each R6 is C6 to C18 aryl.
20. The lubricant composition of claim 8 wherein the dithiocarbamate compound (a) is methylenebis(di-n-butyldithiocarbamate).
11. The lubricant composition of claim 1 comprising from 0.01 to 1.0 weight percent of the finished lubricant composition of said dithiocarbamate compound (a) and from 0.025 to 0.15 weight percent of the finished lubricant composition of said alkylphenyl-.alpha.-naphthylamine compound (b).
12. The lubricant composition of claim 11 wherein for the dithiocarbamate compound (a) R4 is an alkylene group having 1 to 4 carbon atoms, each R5 is a hydrogen or a hydrocarbyl group having 2 to 10 carbon atoms, and each R3 has 2 to 10 carbon atoms.
13. The lubricant composition of claim 12 wherein R5 is a hydrogen and R3 has 2 to 6 carbon atoms.
14. The lubricant composition of claim 11 wherein the dithiocarbamate compound (a) is methylenebis(di-n-butyldithiocarbamate).
15. The lubricant composition of claim 5 comprising from 0.01 to 1.0 weight percent of the finished lubricant composition of said dithiocarbamate compound (a); from 0.025 to 0.15 weight percent of the finished lubricant composition of said alkylphenyl-.alpha.-naphthylamine compound (b); and from 0.005 to 0.075 weight percent of the finished lubricant composition of said hydrocarbyl phosphate compound (c).
16. The lubricant composition of claim 9 comprising from 0.01 to 1.0 weight percent of the finished lubricant composition of said dithiocarbamate compound (a); from 0.025 to 0.15 weight percent of the finished lubricant composition of said alkylphenyl-.alpha.-naphthylamine compound (b); and from 0.005 to 0.075 weight percent of the finished lubricant composition of said hydrocarbyl phosphate compound (c).
17. The lubricant composition of claim 15 wherein the dithiocarbamate compound (a) is present in an amount of 0.02 to 0.5 weight percent of the finished lubricant composition; the alkylphenyl-.alpha.-naphthylamine compound (b) is present in an amount of 0.03 to 0.125 weight percent of the finished lubricant composition; and the hydrocarbyl phosphate compound (c) is present in an amount of 0.01 to 0.06 weight percent of the finished lubricant composition.
18. The lubricant composition of claim 17 wherein the dithiocarbamate compound (a) is methylenebis(di-n-butyldithiocarbamate) and the hydrocarbyl phosphate compound (c) is triphenylphosphite or tricresylphosphite.
19. The lubricant composition of claim 16 wherein the dithiocarbamate compound (a) is present in an amount of 0.02 to 0.5 weight percent of the finished lubricant composition; the alkylphenyl-.alpha.-naphthylamine compound (b) is present in an amount of 0.03 to 0.125 weight percent of the finished lubricant composition; and the hydrocarbyl phosphate compound (c) is present in an amount of 0.01 to 0.06 weight percent of the finished lubricant composition.
20. In a rust and oxidation inhibited lubricant composition comprising a base oil and rust and oxidation inhibitors, the improvement wherein said lubricant composition additionally comprises (a) methylenebis(di-n-butyldithiocarbamate) in an amount of 0.02 to 0.5 weight percent of the finished lubricant composition;
(b) an alkylphenyl-.alpha.-naphthylamine compound in an amount of 0.03 to 0.125 weight percent of the finished lubricant composition; and (c) triphenylphosphite or tricresylphosphite in an amount of 0.01 to 0.06 weight percent of the finished lubricant composition.
(b) an alkylphenyl-.alpha.-naphthylamine compound in an amount of 0.03 to 0.125 weight percent of the finished lubricant composition; and (c) triphenylphosphite or tricresylphosphite in an amount of 0.01 to 0.06 weight percent of the finished lubricant composition.
21. A method for improving the inhibition of oxidation of a lubricant composition containing rust and oxidation inhibitors, said method comprising incorporating into the lubricant composition (a) up to 1.0 weight percent of the finished lubricant composition of a dithiocarbamate compound represented by the formula wherein R4 is a hydrocarbylene group having 1 to 10 carbon atoms, each R5 is a hydrogen or a hydrocarbyl group having 1 to 18 carbon atoms, and each R3 is a hydrocarbyl group having 1 to 18 carbon atoms;
(b) up to 0.15 weight percent of the finished lubricant composition of an alkylphenyl-.alpha.-naphthylamine compound represented by the formula wherein R1 and R2 are independently hydrogen or C1 to C18 alkyl;
and (c) optionally up to 0.075 weight percent of the finished lubricant composition of a hydrocarbyl phosphite represented by the formula (R6O)3P
where each R6 is independently C1 to C18 alkyl, C2 to C18 alkenyl, or C6 to C18 aryl.
(b) up to 0.15 weight percent of the finished lubricant composition of an alkylphenyl-.alpha.-naphthylamine compound represented by the formula wherein R1 and R2 are independently hydrogen or C1 to C18 alkyl;
and (c) optionally up to 0.075 weight percent of the finished lubricant composition of a hydrocarbyl phosphite represented by the formula (R6O)3P
where each R6 is independently C1 to C18 alkyl, C2 to C18 alkenyl, or C6 to C18 aryl.
22. A lubricant additive concentrate for formulation with a base oil to provide a rust and oxidation inhibited lubricant composition wherein said lubricant additive concentrate comprises (a) a dithiocarbamate compound represented by the formula wherein R4 is a hydrocarbylene group having 1 to 10 carbon atoms, each R5 is a hydrogen or a hydrocarbyl group having 1 to 18 carbon atoms, and each R3 is a hydrocarbyl group having 1 to 18 carbon atoms;
(b) an alkylphenyl-.alpha.-naphthylamine compound represented by the formula wherein R1 and R2 are independently hydrogen or C1 to C18 alkyl;
and optionally (c) a hydrocarbyl phosphate represented by the formula (R6O)3P
where each R6 is independently C1 to C18 alkyl, C2 to C18 alkenyl, or C6 to C18 aryl;
wherein component (a) is present in an amount sufficient to comprise up to 1.0 weight percent of the finished lubricant composition, component (b) is present in an amount sufficient to comprise up to 0.15 weight percent of the finished lubricant composition and component (c) if present, is present in an amount sufficient to comprise up to 0.075 weight percent of the finished lubricant composition.
(b) an alkylphenyl-.alpha.-naphthylamine compound represented by the formula wherein R1 and R2 are independently hydrogen or C1 to C18 alkyl;
and optionally (c) a hydrocarbyl phosphate represented by the formula (R6O)3P
where each R6 is independently C1 to C18 alkyl, C2 to C18 alkenyl, or C6 to C18 aryl;
wherein component (a) is present in an amount sufficient to comprise up to 1.0 weight percent of the finished lubricant composition, component (b) is present in an amount sufficient to comprise up to 0.15 weight percent of the finished lubricant composition and component (c) if present, is present in an amount sufficient to comprise up to 0.075 weight percent of the finished lubricant composition.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41303895A | 1995-03-28 | 1995-03-28 | |
US413,038 | 1995-03-28 |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2171924A1 CA2171924A1 (en) | 1996-09-29 |
CA2171924C true CA2171924C (en) | 2007-03-13 |
Family
ID=23635549
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002171924A Expired - Fee Related CA2171924C (en) | 1995-03-28 | 1996-03-15 | Extended life rust and oxidation oils |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0735128B1 (en) |
CA (1) | CA2171924C (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1067714C (en) * | 1998-08-27 | 2001-06-27 | 中国石油化工集团公司 | Compound additive for turbine oil |
US6326336B1 (en) * | 1998-10-16 | 2001-12-04 | Ethyl Corporation | Turbine oils with excellent high temperature oxidative stability |
JP2001158896A (en) * | 1999-12-02 | 2001-06-12 | Chevron Oronite Ltd | Lubricant oil composition for internal combustion engine especially effective for lubricant of gas engine |
US6207623B1 (en) | 2000-01-14 | 2001-03-27 | Exxonmobil Research And Engineering Company | Industrial oils of enhanced resistance to oxidation |
CN102282244B (en) * | 2009-02-02 | 2014-10-15 | 范德比尔特化学品有限责任公司 | Ashless lubricant composition |
EP2576741B1 (en) | 2010-06-02 | 2017-08-23 | The Lubrizol Corporation | Lubrication method |
CA2834078A1 (en) * | 2011-05-16 | 2012-11-22 | The Lubrizol Corporation | Lubricating compositions for turbine and hydraulic systems with improved antioxidancy |
EP3189125B1 (en) * | 2014-09-04 | 2021-03-03 | Vanderbilt Chemicals, LLC | Lubricating compositions comprising liquid ashless antioxidant additive |
CN107573987A (en) * | 2017-09-29 | 2018-01-12 | 中国石油化工股份有限公司 | Turbine oil compositions of additives and application thereof |
CN107653025A (en) * | 2017-09-29 | 2018-02-02 | 中国石油化工股份有限公司 | Turbine oil composition and application thereof |
RU2679663C1 (en) * | 2018-04-06 | 2019-02-12 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Казанский государственный энергетический университет" (ФГБОУ ВО "КГЭУ") | Transformer oil oxidation retardation method |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE557839A (en) * | 1956-05-28 | |||
US3230168A (en) * | 1964-12-08 | 1966-01-18 | Shell Oil Co | Lubricant compositions |
US4125479A (en) * | 1975-12-22 | 1978-11-14 | Texaco Inc. | Oxidation inhibited lubricating oil |
US4119551A (en) * | 1977-06-28 | 1978-10-10 | Texaco Inc. | Synthetic aircraft turbine lubricating oil compositions |
US4226732A (en) * | 1978-06-30 | 1980-10-07 | Texaco Inc. | Synthetic aircraft turbine oil |
JP3086727B2 (en) * | 1991-08-09 | 2000-09-11 | オロナイトジャパン株式会社 | Additive composition for producing low phosphorus engine oil |
US5236610A (en) * | 1992-02-03 | 1993-08-17 | The United States Of America As Represented By The Secretary Of The Commerce | Stable high temperature liquid lubricant blends and antioxidant additives for use therewith |
-
1996
- 1996-03-15 CA CA002171924A patent/CA2171924C/en not_active Expired - Fee Related
- 1996-03-28 EP EP96302164A patent/EP0735128B1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
CA2171924A1 (en) | 1996-09-29 |
EP0735128B1 (en) | 2000-08-23 |
EP0735128A3 (en) | 1997-06-11 |
EP0735128A2 (en) | 1996-10-02 |
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