Patent Grant
9139795
This application is a 371 of PCT/JP2010/058189, filed May 14, 2010. The present invention relates to a lubricating oil composition. More specifically, the present invention relates to a biodegradable lubricating oil composition usable for a step-up gear used, in particular, for wind power generation.
In recent years, due to exhaustion of fossil fuels and environmental issues, wind power generation, which uses natural energy, has been receiving considerable attention. Since wind power generation requires an increased power generation efficiency due to a low rotation speed of a rotor, a step-up gear is provided in a power generator. A so-called gear oil is used to lubricate a gear mechanism used in the step-up gear, and is required to provide a considerably high lubricity.
Typically, a lubricating oil whose base oil is PAO (polyalphaolefin) has been used as a step-up gear oil. Since a wind power generator is frequently used on the ocean or under the natural environment, the step-up gear oil should be highly biodegradable. The typical PAO lubricating oil, however, has little biodegradability, so that an alternative thereto has been sought for.
As a lubricating oil intended to be used for a step-up gear in a wind power generator, a lubricating oil whose base oil is ester can be applicable because such a lubricating oil needs to be biodegradable (see, for instance, Patent Literatures 1 and 2). Each of Patent Literatures 1 and 2 has suggested a biodegradable lubricating oil whose base oil is a complex ester obtained from a polyhydric alcohol and a polycarboxylic acid.
The biodegradable lubricating oils disclosed in Patent Literature 1 and 2 do not have a sufficient oxidation stability, so that when being used for a step-up gear in a wind power generator, the biodegradable lubricating oils are unlikely to continuously exhibit properties as a lubricating oil for a long time.
Accordingly, an object of the invention is to provide a biodegradable lubricating oil composition that is excellent in lubricity, oxidation stability and biodegradability and is suitable for a step-up gear used in a wind power generator.
In order to solve the above problem, the following biodegradable lubricating oil composition is provided according to an aspect of the invention.
(1) A biodegradable lubricating oil composition including (A) an ester represented by a formula (1) below; (B) an ester being obtained by reacting a straight-chain saturated aliphatic carboxylic acid with a polyhydric alcohol, the ester having an acid value of 0.5 mgKOH/g or less; and (C) a phosphate amine salt being obtained by reacting an acidic phosphate with an alkylamine.
In the formula, Ra is a hydrocarbyl group having 4 to 20 carbon atoms, Rb is a hydrocarbyl group having 4 to 18 carbon atoms, Rc is an acyl group having 1 to 10 carbon atoms, and n is an integer of 3 to 15.
(2) In the component (A) of the biodegradable lubricating oil composition, Ra is an alkyl group having 4 to 20 carbon atoms, and Rb is an alkyl group having 4 to 18 carbon atoms.
(3) In the biodegradable lubricating oil composition, the straight-chain saturated aliphatic carboxylic acid used to provide the ester of the component (B) has 6 to 12 carbon atoms.
(4) In the biodegradable lubricating oil composition, the polyhydric alcohol used to provide the ester of the component (B) is at least one of pentaerythritol and trimethylolpropane.
(5) In the biodegradable lubricating oil composition, a blend ratio of the component (B) is 10 mass % or more of a total amount of the lubricating oil composition.
(6) In the biodegradable lubricating oil composition, the acidic phosphate used to provide the component (C) has 8 to 13 carbon atoms.
(7) In the biodegradable lubricating oil composition, a blend ratio of the phosphate amine salt in the component (C) is in a range from 0.2 mass % to 1 mass %.
(8) In the biodegradable lubricating oil composition, the biodegradable lubricating oil composition is a gear oil.
The biodegradable lubricating oil composition according to the aspect of the invention is excellent in lubricity, oxidation stability and biodegradability, and thus is suitable for a step-up gear used in a wind power generator.
A biodegradable lubricating oil composition according to an exemplary embodiment of the invention (hereinafter also referred to simply as “the composition”) is provided by blending (A) a predetermined 2-hydroxy(hydrocarbyl) carboxylic acid, (B) an ester being obtained by reacting a straight-chain saturated aliphatic carboxylic acid with a polyhydric alcohol, and (C) a phosphate amine salt being obtained by reacting an acidic phosphate with an alkylamine. A detailed description of this exemplary embodiment will be made below.
Component (A)
The component (A) of the exemplary embodiment is an ester formed from monoalcohol and 2-hydroxy(hydrocarbyl) carboxylic acid as shown by the following formula (1).
In the formula, Ra is a hydrocarbyl group having 4 to 20 carbon atoms, preferably an alkyl group. When Ra has 3 carbon atoms or less, dehydrocondensation cannot smoothly proceed because the boiling point of an alcohol used for condensation of an ester is low, which makes condensation of the ester difficult. Particularly preferred examples of Ra include butyl group, hexyl group, octyl group, decanyl group, dodecanyl group, tetradecanyl group, hexadecanyl group and octadecanyl group. Each of the above groups may have a straight-chain or branched structure. In contrast, Ra having 21 carbon atoms or more unfavorably results in a lowered low-temperature fluidity.
Rb is a hydrocarbyl group having 4 to 18 carbon atoms, preferably an alkyl group. When Rb has 3 carbon atoms or less, the resulting ester is not always in a liquid phase at room temperature (25 degrees C.), and thus is not appropriate as a lubricating oil. Rb having 19 carbon atoms or more unpractically results in a raised pour point due to crystallization of the ester. Rb is preferably an alkyl group having 6 to 12 carbon atoms, particularly preferably a hexyl group, octyl group, decyl group or dodecanyl group. Each of the above groups may have a straight-chain or branched structure.
Rc is hydrogen or an acyl group having 1 to 10 carbon atoms. If Rc is not hydrogen, preferred examples of a group at the terminal position of the acyl group include hydrogen (formyl group), methyl group (acetyl group), propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group and nonyl group. Each of the above groups may have a straight-chain or branched structure. Preferably, Rc is an acyl group having 2 to 4 carbon atoms so that an unreacted material can be removed by distillation.
n represents the number of chains per 2-hydroxy carboxylic acid, and is an integer of 3 to 15, preferably an integer of 7 to 10. When n is an integer of 2 or smaller, the viscosity of the composition is too low to be used as a lubricating oil. When n is an integer of 16 or larger, the biodegradability of the composition is lowered.
When Rc in the ester of the component (A) is hydrogen, the ester can be composited as follows: an alcohol containing Ra of the formula (1) is mixed with a 2-hydroxy carboxylic acid represented by the following formula (2); the mixture is heated in the presence of an acid such as sulfuric acid; and a theoretical amount of water produced by reaction is removed by distillation. Incidentally, when the alcohol and the 2-hydroxy carboxylic acid are reacted together, the theoretical amount of the water produced by reaction is twice as large as the number of moles of the added 2-hydroxy carboxylic acid. The acid value of the resulting ester is preferably 0.5 mgKOH/g or less in terms of oxidation stability.
When Rc in the ester as the component (A) is an acyl group, the ester may be prepared by performing esterification reaction on, for instance, the above ester (Rc is hydrogen) using a predetermined carboxylic acid.
In the formula, Rb is a hydrocarbyl group having 4 to 18 carbon atoms, preferably an alkyl group. Examples of Rb are the same as those in the formula (1).
By adjusting the number of chains per 2-hydroxy carboxylic acid, which is represented by n, in the above (1) representing the ester of the component (A), the biodegradability of the ester compound is controllable. The number of chains per 2-hydroxy(hydrocarbyl) carboxylic acid is controllable based on the respective feed ratios of starting materials, i.e., the alcohol and 2-hydroxy carboxylic acid or 2-hydrocarbyl carboxylic acid. For instance, in reacting the alcohol and 2-hydroxy carboxylic acid, when the feed amount of the alcohol is represented as AL(mol) and the feed amount of the 2-hydroxy carboxylic acid is represented as H(mol), the number of chains n is calculated as follows.
n=H/AL
The actual number of chains per 2-hydroxy carboxylic acid in the ester compound is measured by proton NMR. The actual number of chains is approximately equal to the above calculated number.
The viscosity of the ester of the formula (1) is controllable based on the chain length of each of Ra and Rb in addition to the number of chains n. A kinematic viscosity at 40 degrees C. is preferably in a range from 300 mm2/s to 1000 mm2/s. When the kinematic viscosity at 40 degrees C. is less than 300 mm2/s, the resulting lubricating oil composition is unlikely to have a viscosity required for maintaining lubricity. When the kinematic viscosity at 40 degrees C. is more than 1000 mm2/s, the biodegradability of the resulting lubricating oil composition is likely to be lowered.
As the alcohol and the 2-hydroxy carboxylic acid, i.e., materials for the ester of the formula (1), any commercial ones is usable without any particular limitation. The 2-hydroxy carboxylic acid in the formula (2) can be composited by, for instance, Hell-Volhard-Zelinskii reaction (Org. Synth., Coll. Vol. 4,848 (1965)) of a carboxylic acid and the subsequent hydrolysis.
As for a method of producing the ester of the formula (1), a reaction time may be approximately in a range from 6 hours to 20 hours and a reaction temperature may be approximately in 100 degrees C. to 130 degrees C. A usable solvent is preferably heptane, octane, toluene, xylene or the like.
Component (B)
The component (B) of the exemplary embodiment is an ester obtained by reacting a straight-chain saturated aliphatic carboxylic acid with a polyhydric alcohol.
For providing both biodegradability and low-temperature fluidity, a carboxylic acid having 6 to 12 carbon atoms is preferably used as the straight-chain saturated aliphatic carboxylic acid. Examples of such a carboxylic acid include monocarboxylic acids such as caproic acid, enanthic acid, caprylic acid, pelargonic acid, capric acid, undecane acid and lauric acid.
As the polyhydric alcohol, a so-called hindered polyol is suitably used. Examples of the hindered polyol include neopentyl glycol, 2-ethyl-2-methyl-1,3-propanediol, 2,2-diethyl-1,3-propanediol, trimethylol ethane, trimethylol propane, trimethylol butane, trimethylol pentane, trimethylol hexane, trimethylol heptane, pentaerythritol, 2,2,6,6-tetramethyl-4-oxa-1,7-heptanediol, 2,2,6,6,10,10-hexamethyl-4,8-dioxa-1,11-undecanediol, 2,2,6,6,10,10,14,14-octamethyl-4,8,12-trioxa-1,15-pentadecanediol, 2,6-dihydroxymethyl-2,6-dimethyl-4-oxa-1,7-heptanediol, 2,6,10-trihydroxymethyl-2,6,10-trimethyl-4,8-dioxa-1,11-undecanediol, 2,6,10,14-tetrahydroxymethyl-2,6,10,14-tetramethyl-4,8,12-trioxa-1,15-pentadecanediol, di(pentaerythritol), tri(pentaerythritol), tetra(pentaerythritol), and penta(pentaerythritol). Particularly preferred examples of the hindered polyol include pentaerythritol and trimethylolpropane.
For esterification, one of the above examples of the hindered polyol may be used alone or, alternatively, two or more thereof may be used in combination.
The component (B) preferably has a kinematic viscosity in a range from 20 mm2/s to 40 mm2/s at 40 degrees C. When the kinematic viscosity is less than 20 mm2/s, the lubricity of the resulting lubricating oil composition is unfavorably lowered. When the kinematic viscosity is more than 40 mm2/s, the low temperature fluidity of the resulting lubricating oil composition is likely to be deteriorated.
The component (B) is required to have an acid value of 0.5 mgKOH/g or less. When the acid value is more than 0.5 mgKOH/g, the oxidation stability of the resulting lubricating oil composition is likely to be deteriorated.
Incidentally, an ester as the component (B) is typically obtained by reacting the above predetermined carboxylic acid and polyhydric alcohol together. However, the ester may be obtained in a different way as long as the resulting ester structure includes the above carboxylic acid residue and polyhydric alcohol residue. It is not necessary that starting materials (reactants) are the above carboxylic acid and polyhydric alcohol, and, furthermore, the component (B) does not necessarily have to be composited based on dehydration reaction thereof. The component (B) may be composited from other materials in a different way. For instance, the component (B) may be produced by transesterification.
The blend ratio of the component (B) of the exemplary embodiment is preferably 10 mass % or more of the total amount of the composition in terms of biodegradability.
Component (C)
The component (C) of the exemplary embodiment is a phosphate amine salt obtained by reacting an acidic phosphate with an alkylamine.
The acidic phosphate used to provide the component (C) is exemplified by one having the structure represented by, for instance, the following formula (3).
In the formula, X1 is a hydrogen atom or an alkyl group having 6 to 20 carbon atoms, and X2 is an alkyl group having 6 to 20 carbon atoms. The above alkyl group having 6 to 20 carbon atoms may have a straight-chaine, branched, or cyclic structure. Examples of the alkyl group include various hexyl groups, octyl groups, decyl groups, dodecyl groups, tetradecyl groups, hexadecyl groups, octadecyl groups and icosyl groups. Among the above, an alkyl group having 8 to 18 carbon atoms is preferable and an alkyl group having 8 to 13 carbon atoms is more preferable.
Examples of acidic alkyl phosphates represented by the formula (3) include acidic monophosphates such as monooctyl acid phosphate, monodecyl acid phosphate, monoisodecyl acid phosphate, monolauryl acid phosphate, mono(tridecyl) acid phosphate, monomyristyl acid phosphate, monopalmityl acid phosphate and monostearyl acid phosphate; and acidic diphosphates such as dioctyl acid phosphate, didecyl acid phosphate, diisodecyl acid phosphate, dilauryl acid phosphate, di(tridecyl) acid phosphate, dipalmityl acid phosphate and distearyl acid phosphate.
The component (C) may be provided using one of the above examples of the acidic phosphate alone or a combination of two or more thereof. Incidentally, the content of phosphorus (P) is preferably in a range from 150 mass ppm to 500 mass ppm of the total amount of the resulting composition. If the content of P is less than 150 mass ppm, the composition is unlikely to exhibit a sufficient seizure resistance when used as a gear oil. On the other hand, if the content of P is more than 500 mass ppm, the fatigue resistance (FZG micropitting resistance) of the composition is likely to be lowered. The content of P is preferably in a range from 250 mass ppm to 450 mass ppm, more preferably in a range from 350 mass ppm to 400 mass ppm.
The alkylamine used to provide the component (C) may be any one of primary amine, secondary amine and tertiary amine, but is preferably dialkylamine or trialkylamine in terms of improvement of seizure resistance. An alkyl group having 6 to 20 carbon atoms is preferable so that the phosphate amine salt is in a liquid phase.
Examples of dialkylamines include dihexylamine, dicyclohexylamine, dioctylamine, dilaurylamine and distearylamine. Examples of trialkylamines include trihexylamine, tricyclohexylamine, trioctylamine, trilaurylamine and tristearylamine.
One of the above examples of the alkylamine may be used alone or, alternatively, two or more thereof may be used in combination. In terms of seizure resistance, the alkylamine is favorably selected from the trialkyamines.
The blend ratio of the component (C) is preferably in a range from 0.2 mass % to 1 mass % of the total amount of the composition. The blend ratio less than 0.2 mass % results in a less effectiveness in reducing friction. When the blend ratio is more than 1 mass %, the fatigue resistance (FZG micropitting resistance) is likely to be lowered.
The component (C) may be blended with the other components to prepare the composition after being provided as the acidic phosphate amine salt. Alternatively, the acidic phosphate and the alkylamine may be independently blended to prepare the composition.
Incidentally, in the instance where the acidic phosphate and the alkylamine are independently blended, the blend ratio of the component (C) corresponds to the total amount of the acidic phosphate and the alkylamine.
The composition may further be added with a predetermined sulfur compound as a component (D) to enhance the lubricity thereof. For instance, it is preferable to use a sulfur compound that does not contain a sulfur condensation of three (—S—S—S—) or more in a molecule (D-1) and in which sulfur atoms (S) are contained in the molecule at 15 mass % or more. Further, the component (D-1) is additionally blended with a sulfur compound (D-2), which is preferably a trihydrocarbyl thiophosphate represented by the following formula (4).
(RO—)3P═S (4)
In the formula (4), R is a hydrocarbyl group having 6 to 20 carbon atoms.
When the sulfur compound as the component (D-1) is a compound having a sulfur condensation of three (—S—S—S—) or more contained in the molecule, a lot of sludge is likely to be generated in an oxidation stability test (described below) and, furthermore, the FZG micropitting resistance is likely to be lowered. When the content of S in the molecule is less than 15 mass %, the addition effect of the sulfur compound is not sufficiently exhibited, resulting in a shortage of the seizure resistance.
Examples of the sulfur compound based on the component (D-1) having the above properties include, for instance, the following compounds.
(1) mono- or di-olefin sulfide
(2) dihydrocarbyl mono- or di-sulfide
(3) thiadiazole compound
(4) dithiocarbamate compound
(5) ester compound having a disulfide structure
(6) other sulfur compounds
Mono- or Di-olefin Sulfide
The olefin sulfide can be exemplified by a compound represented by the following formula (5).
R1—Sa-R2 (5)
In the formula (5), R1 is an alkenyl group having 2 to 15 carbon atoms, R2 is an alkyl or alkenyl group having 2 to 15 carbon atoms, and a is an integer of 1 or 2. Such a compound is obtained by reacting an olefin having 2 to 15 carbon atoms or any one of the dimer to tetramer thereof with a sulfurizing agent such as sulfur, sulfur chloride or the like. Preferred examples of the olefin include propylene, isobutene and diisobutene.
Dihydrocarbyl Mono- or Di-sulfide
The dihydrocarbyl mono- or di-sulfide can be exemplified by a compound represented by the following formula (6).
R3−Sb—R4 (6)
In the formula (6), each of R3 and R4 is an alkyl or cyclic alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an alkylaryl group having 7 to 20 carbon atoms or an arylalkyl group having 7 to 20 carbon atoms, R3 and R4 may be mutually the same or different, and b is an integer of 1 or 2. When R3 and R4 are both alkyl groups, the compound is referred to as alkyl sulfide.
Preferred examples of the dihydrocarbyl mono- or di-sulfide include dibenzil mono- or di-sulfides, various dinonyl mono- or di-sulfides, various didodecyl mono- or di-sulfides, various dibutyl mono- or di-sulfides, various dioctyl mono- or di-sulfides, diphenyl mono- or di-sulfides, and dicyclohexyl mono- or di-sulfides.
Thiadiazole Compound
Preferred examples of the thiadiazole compound include 2,5-bis(n-hexyldithio)-1,3,4-thiadiazole, 2,5-bis(n-octyldithio)-1,3,4-thiadiazole, 2,5-bis(n-nonyldithio)-1,3,4-thiadiazole, 2,5-bis(1,1,3,3-tetramethylbutyldithio)-1,3,4-thiadiazole, 3,5-bis(n-hexyldithio)-1,2,4-thiadiazole, 3,6-bis(n-octyldithio)-1,2,4-thiadiazole, 3,5-bis(n-nonyldithio)-1,2,4-thiadiazole, 3,5-bis(1,1,3,3-tetramethylbutyldithio)-1,2,4-thiadiazole, 4,5-bis(n-octyldithio)-1,2,3-thiadiazole, 4,5-bis(n-nonyldithio)-1,2,3-thiadiazole, and 4,5-bis(1,1,3,3-tetramethylbutyldithio)-1,2,3-thiadiazole.
Dithiocarbamate Compound
Examples of the dithiocarbamate compound include alkylene bisdialkyl dithiocarbamates, among which preferred is a compound containing an alkylene group having 1 to 3 carbon atoms, a straight-chaine or branched saturated or unsaturated alkyl group having 3 to 20 carbon atoms, or a cyclic alkyl group having 6 to 20 carbon atoms. Examples of the above dithiocarbamate compound include methylene bisdibutyldithiocarbamate, methylene bisdioctyldithiocarbamate and methylene bistridecyldithiocarbamate.
Ester Compound Having Disulfide Structure
Examples of the ester compound having a disulfide structure include a disulfide compound represented by the following formula (7) and a compound represented by the following formula (8).
R5OOC-A1-S—S-A2-COOR6 (7)
R11OOC—CR13R14—CR15(COOR12)—S—S—CR20(COOR17)—CR18R19—COOR16 (8)
In the formula (7), R5 and R6 each independently represent a hydrocarbyl group having 1 to 30 carbon atoms, preferably 1 to 20 carbon atoms, more preferably 2 to 18 carbon atoms, particularly preferably 3 to 18 carbon atoms. Such a hydrocarbyl group may have a straight-chaine, branched or cyclic structure and may contain an oxygen atom, sulfur atom or nitrogen atom. R5 and R6 may be mutually the same or different, but are preferably the same in terms of manufacturing reasons.
A1 and A2 each independently represent CR7R8 or CR7R8—CR9R10, in which R7 to R10 each independently a hydrogen atom or a hydrocarbyl group having 1 to 20 carbon atoms. Such a hydrocarbyl group is preferably one having 1 to 12 carbon atoms, more preferably one having 1 to 8 carbon atoms. A1 and A2 may be mutually the same or different, but are preferably the same in terms of manufacturing reasons.
In the formula (8), R11, R12, R16 and R17 each independently represent a hydrocarbyl group having 1 to 30 carbon atoms, preferably 1 to 20 carbon atoms, more preferably 2 to 18 carbon atoms, particularly preferably 3 to 18 carbon atoms. Such a hydrocarbyl group may have a straight-chaine, branched or cyclic structure and may contain an oxygen atom, sulfur atom or nitrogen atom. R11, R12, R16 and R17 may be mutually the same or different, but are preferably the same in terms of manufacturing reasons.
R13 to R15 and R18 to R20 each independently represent a hydrogen atom or a hydrocarbyl group having 1 to 5 carbon atoms. A hydrogen atom is preferred because materials are easily available.
Examples of the disulfide compound represented by the formula (7) include bis(methoxycarbonyl-methyl)disulfide, bis(ethoxycarbonylmethyl)disulfide, bis(n-propoxycarbonylmethyl)disulfide, bis(isopropoxycarbonylmethyl)disulfide, bis(cyclopropoxycarbonylmethyl)disulfide, 1,1-bis(1-methoxycarbonylethyl)disulfide, 1,1-bis(1-methoxycarbonyl-n-propyl)disulfide, 1,1-bis(1-methoxycarbonyl-n-butyl)disulfide, 1,1-bis(1-methoxycarbonyl-n-hexyl)disulfide, 1,1-bis(1-methoxycarbonyl-n-octyl)disulfide, 2,2-bis(2-methoxycarbonyl-n-propyl)disulfide, alpha,alpha-bis(alpha-methoxycarbonylbenzyl)disulfide, 1,1-bis(2-methoxycarbonylethyl)disulfide, 1,1-bis(2-ethoxycarbonylethyl)disulfide, 1,1-bis(2-n-propoxycarbonylethyl)disulfide, 1,1-bis(2-isopropoxycarbonylethyl)disulfide, 1,1-bis(2-cyclopropoxycarbonylethyl)disulfide, 1,1-bis(2-methoxycarbonyl-n-propyl)disulfide, 1,1-bis(2-methoxycarbonyl-n-butyl)disulfide, 1,1-bis(2-methoxycarbonyl-n-hexyl)disulfide, 1,1-bis(2-methoxycarbonyl-n-propyl)disulfide, 2,2-bis(3-methoxycarbonyl-n-pentyl)disulfide, and 1,1-bis(2-methoxycarbonyl-1-phenylethyl)disulfide.
Examples of the disulfide compound represented by the formula (8) include dimercaptosuccinic acid tetramethyl, dimercaptosuccinic acid tetraethyl, dimercaptosuccinic acid tetra-1-propyl, dimercaptosuccinic acid tetra-2-propyl, dimercaptosuccinic acid tetra-1-butyl, dimercaptosuccinic acid tetra-2-butyl, dimercaptosuccinic acid tetraisobutyl, dimercaptosuccinic acid tetra-1-hexyl, dimercaptosuccinic acid tetra-1-octyl, dimercaptosuccinic acid tetra-1-(2-ethyl)hexyl, dimercaptosuccinic acid tetra-1-(3,5,5-trimethyl)hexyl, dimercaptosuccinic acid tetra-1-decyl, dimercaptosuccinic acid tetra-1-dodecyl, dimercaptosuccinic acid tetra-1-hexadecyl, dimercaptosuccinic acid tetra-1-octadecyl, dimercaptosuccinic acid tetrabenzyl, dimercaptosuccinic acid tetra-alpha-(methyl)benzyl, dimercaptosuccinic acid tetra alpha,alpha-dimethylbenzyl, dimercaptosuccinic acid tetra-1-(2-methoxy)ethyl, dimercaptosuccinic acid tetra-1-(2-ethoxy)ethyl, dimercaptosuccinic acid tetra-1-(2-butoxy)ethyl, dimercaptosuccinic acid tetra-1-(2-ethoxy)ethyl, dimercaptosuccinic acid tetra-1-(2-butoxy-butoxy)ethyl, and dimercaptosuccinic acid tetra-1-(2-phenoxy)ethyl.
Other Sulfur Compounds
Examples of other sulfur compounds include sulfurized fats and oils such as sulfurized lard, sulfurized rape seed oil, sulfurized castor oil, sulfurized soybean oil and sulfurized rice bran oil; sulfurized fatty acids such as thioglycolic acid and sulfurized oleic acid; dialkyl thiodipropionate compounds such as dilauryl thiodipropionate, distearyl thiodipropionate and dimyristyl thiodipropionate; and thioterpene compounds obtained by reacting phosphorus pentasulfide with pinene.
The above component (D-1) may be provided using one of the above sulfur compounds alone or using a combination of two or more thereof. The blend ratio of the component (D-1) is preferably in a range from 0.2 mass % to 0.6 mass % of the total amount of the composition in terms of the amount of sulfur. The blend ratio less than 0.2 mass % can result in an insufficient seizure resistance. On the other hand, the blend ratio more than 0.6 mass % can result in not only a deteriorated fatigue resistance such as FZG micropitting resistance but also generation of a lot of sludge in an oxidation stability test (compliant with ASTM D 2893). The blend ratio is preferably in a range from 0.3 mass % to 0.5 mass %.
In blending the above component (D-1), preferably, the trihydrocarbyl thiophosphate represented by the formula (4) is also blended as the component (D-2) as desired.
In the formula (4), R is a hydrocarbyl group having 6 to 20 carbon atoms. Such a hydrocarbyl group is a straight-chaine, branched or cyclic alkyl group or alkenyl group having 6 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, or an aralkyl group having 7 to 20 carbon atoms. In the aryl group and aralkyl group, one or more alkyl group(s) may be introduced into an aromatic ring. The three RO groups may be mutually the same or different.
Examples of the alkyl group and alkenyl group each having 6 to 20 carbon atoms include various hexyl groups, various octyl groups, various decyl groups, various dodecyl groups, various tetradecyl groups, various hexadecyl groups, various octadecyl groups, cyclohexyl group, various hexenyl groups, various octenyl groups, various decenyl groups, various dodecenyl groups, various tetradecenyl groups, various hexadecenyl groups, various octadecenyl groups and cyclohexenyl group.
Examples of the aryl group having 6 to 20 carbon atoms include phenyl group, tolyl group, xylyl group, decylphenyl group, 2,4-didecylphenyl group and naphthyl group. Examples of the aralkyl group having 7 to 20 carbon atoms include benzyl group, phenethyl group, naphthylmethyl group, methylbenzyl group, methylphenethyl group and methylnaphthylmethyl group.
Examples of the trihydrocarbyl thiophosphate represented by the above formula (4) include trihexyl thiophosphate, tri2-ethylhexyl thiophosphate, tris(decyl)thiophosphate, trilauryl thiophosphate, trimyristyl thiophosphate, tripalmityl thiophosphate, tristearyl thiophosphate, trioleyl thiophosphate, tricresyl thiophosphate, trixylyl thiophosphate, tris(decylphenyl)thiophosphate and tris[2,4-isoalkyl(C9,C10)phenyl]thiophosphate. One of the above examples of the trihydrocarbyl thiophosphate may be used alone or, alternatively, two or more thereof may be used in combination.
The trihydrocarbyl thiophosphate as the component (D-2) is intended to be blended as desired in order to enhance the effectiveness of adding the sulfur compound as the above component (D-1). The blend ratio of the trihydrocarbyl thiophosphate is preferably in a range from 0.1 mass % to 1 mass % of the total amount of the composition in terms of the amount of sulfur, more preferably in a range from 0.2 mass % to 0.5 mass %.
As long as an object of the invention is not impaired, the composition may be added with at least one selected from various additives such as ashless detergent dispersant, antioxidant, rust inhibitor, metal deactivator, viscosity index improver, pour point depressant and antifoaming agent if necessary.
Examples of the ashless detergent dispersant include succinimides, boron-containing succinimides, benzylamines, boron-containing benzylamines, succinic acid esters, and carboxylic acid amides of mono- or di-carboxylic acid, a typical example of which is a fatty acid or succinic acid. The blend ratio of the ashless detergent dispersant is set approximately in a range from 0.01 mass % to 5 mass % of the total amount of the composition in view of a balance between the resulting effect and economic efficiency and the like.
As the antioxidant, ones typically used in a lubricating oil, i.e., an aminic antioxidant, phenolic antioxidant and sulfuric antioxidant, are usable. One of the above antioxidants may be used alone or, alternatively, two or more thereof may be used in combination. Examples of the aminic antioxidant include monoalkyldiphenylamine compounds such as monooctyldiphenylamine and monononyldiphenylamine; dialkyldiphenylamine compounds such as 4,4′-dibutyldiphenylamine, 4,4′-dibenzyldiphenylamine, 4,4′-dihexyldiphenylamine, 4,4′-diheptyldiphenylamine, 4,4′-dioctyldiphenylamine and 4,4′-dinonyldiphenylamine; polyalkyldiphenylamine compounds such as tetrabutyldiphenylamine, tetrahexyldiphenylamine, tetraoctyldiphenylamine and tetranonyldiphenylamine; and naphthylamine compounds such as alpha-naphthylamine, phenyl-alpha-naphthylamine, butylphenyl-alpha-naphthylamine, benzylphenyl-alpha-naphthylamine, hexylphenyl-alpha-naphthylamine, heptylphenyl-alpha-naphthylamine, octylphenyl-alpha-naphthylamine and nonylphenyl-alpha-naphthylamine.
Examples of the phenolic antioxidant include monophenol compounds such as 2,6-di-tert-butyl-4-methylphenyl, 2,6-di-tert-butyl-4-ethylphenyl and octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate; and diphenol compounds such as 4,4′-methylenebis(2,6-di-tert-butylphenol) and 2,2′-methylenebis(4-ethyl-6-tert-butylphenol).
Examples of sulfuric antioxidant include 2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazine-2-ylamino)phenol, thioterpene compound such as a reactant of phosphorus pentasulfide and pinene, and dialkyl thiodipropionate such as dilauryl thiodipropionate and distearyl thiodipropionate.
The blend ratio of the antioxidant is set approximately in a range from 0.3 mass % to 2 mass % of the total amount of the composition in view of a balance between the resulting effect and economic efficiency and the like.
Examples of the rust inhibitor include metal sulfonate and alkenyl succinic acid ester. The blend ratio of the rust inhibitor is set approximately in a range from 0.01 mass % to 0.5 mass % in view of the blend effect thereof.
Examples of the metal deactivator (copper corrosion inhibitor) include benzotriazole compounds, tolyltriazole compounds, thiadiazole compounds, imidazole compounds and pyrimidine compounds. Among the above, benzotriazole compounds are preferable. The blend ratio of the metal deactivator is set approximately in a range from 0.01 mass % to 0.1 mass % in view of the blend effect thereof.
Examples of the viscosity index improver include polymethacrylate, dispersed polymethacrylate, olefin copolymer (e.g. ethylene-propylene copolymer), dispersed olefin copolymer and styrene copolymer (e.g. styrene-diene copolymer and styrene-isoprene copolymer). The blend ratio of the viscosity index improver is set approximately in a range from 0.5 mass % to 15 mass % in view of the blend effect thereof.
Examples of the pour point depressant include ethylene-vinyl acetate copolymer, condensate of chlorinated paraffin and naphthalene, condensate of chlorinated paraffin and phenol, polymethacrylate and polyalkylstyrene, among which polymethacrylate of, for instance, approximately 50000 to 150000 (mass average molecular weight) is preferably used. The blend ratio of the pour point depressant is set approximately in a range from 0.1 mass % to 5 mass % of the total amount of the composition.
Preferred examples of the antifoaming agent include silicone polymer antifoaming agent and polyacrylate antifoaming agent. By blending silicone polymer antifoaming agent, antifoaming capabilities can be effectively exhibited. Examples of the silicone polymer antifoaming agent include organopolysiloxanes, among which, in particular, a fluorine-containing organopolysiloxane such as trifluoropropylmethyl silicone oil is suitable. The blend ratio of the antifoaming agent is set approximately in a range from 0.005 mass % to 0.1 mass % of the total amount of the composition in view of a balance between the resulting antifoaming effect and economic efficiency and the like.
The biodegradable lubricating oil composition according to the exemplary embodiment is excellent in lubricity, oxidation stability and biodegradability, and thus can be suitably used as lubricating oils such as gear oil and bearing oil. In particular, the composition is suitable as a lubricating oil used for a power transmission device with a planet gear (e.g., step-up gear) in a wind power generator, which is intended to be continuously used outside for a long time.
Next, examples of the invention will be described below in detail. However, it should be noted that the scope of the invention is by no means limited by the examples.
Various ester base oils were blended with various additives, and the resulting lubricating oil compositions (sample oils) were evaluated in various aspects.
Details of esters used as base oils and additives are as follows. The properties of each ester used as a base oil are shown in Table 1.
(1) Ester A (Component A)
This ester was produced in the following manner.
(2-hydroxy dodecanic acid/1-dodecanol:feed mole ratio=3/1, H/AL=3)
2-hydroxy dodecanic acid (100 g), 1-dodecanole (11.42 g) and sulfuric acid (acid catalyst, 2.0 g) were mixed with heptane in a 500-ml three-necked flask. The flask was attached with a Dean-Stark apparatus and heated for reflux of the heptane. After the reflux for 6 hours, approximately 8.0 ml of water was distilled. After the solvent was distilled away, the mixture was further heated for 6 hours. The mixture was then cooled down to room temperature, and was extracted with 100 ml of 5-mass % NaCl water for three times to remove the acid catalyst. An organic layer was dried with anhydrous sodium sulfate and the heptane (solvent) was removed using a rotary evaporator to yield a water-clear or thin-yellow viscous oily material (yielded amount: 112.81 g).
n = (Ha + Ha′)/((Hal-1)/2) = 2.97
(2) Ester B (Component A)
(2-hydroxy dodecanic acid/1-butanol:feed mole ratio=6/1, H/AL=6)
The ester B was produced (yielded amount: 93.49 g) in the same manner as in Example 1 except that 1-butanol was used in place of 1-dodecanol.
n = (Ha + Ha′)/((Hal-1)/2) = 7.92
(3) Ester C
A complex ester formed from pentaerythritol, sebacic acid and isostearic acid (PRIOLUBE 1851 manufactured by Uniqema Ltd.) was used.
(4) Ester D
A complex ester formed from pentaerythritol, adipic acid and mixed monocarboxylic acid having approximately 7 to 10 carbon atoms (PAF-450 manufactured by The Nisshin OilliO Group, Ltd.) was used.
(5) Ester C
A di(pentaerythritol)oleate (TOE-500 manufactured by NOF Corporation) was used.
(6) Ester F (Component B)
An ester formed from pentaerythritol and saturated fatty acid (KAOLUBE 262 manufactured by Kao Corporation) was used.
(7) Ester G
A trimethylolpropane diisostearate was used.
(8) Phosphate Amine Salt (Component C)
Tridecyl acid phosphate and trioctylamine were used.
(9) Sulfur Compound (Component D)
Methylene bisdibutyldithiocarbamate and tris(2,4-C9-C10 isoalkylphenol)thiophosphate were used.
(10) Antioxidant
IRGANOX L107 (phenol-based) manufactured by Ciba Specialty Chemicals Inc. was used. IRGANOX L57 (amine-based) manufactured by Ciba Specialty Chemicals Inc. was used.
(11) Metal Deactivator
IRGAMET39 (a benzotriazole derivative) manufactured by Ciba Japan K.K. was used.
(12) Rust Inhibitor
A polybutenyl succinimide was used.
(13) Antifoaming Agent
A silicone antifoaming agent (KF96H12500CS manufactured by Shin-Etsu Chemical Co., Ltd.) was used.
(14) Anti-emulsifier
LUBRIZOL 5957 (PAG-based) manufactured by Lubrizol Co., Ltd. was used.
Properties-measurement methods and evaluation methods for base oils and sample oils were as follows. Table 4 shows evaluation results of sample oils (biodegradability, oxidation stability, lubricity).
(1) Kinematic Viscosity
A sulfur content was measured according to JIS K 2283.
(2) Acid Value
A sulfur content was measured according to JIS K 2501.
(3) Saponification Value
A sulfur content was measured according to JIS K 2503.
(4) Biodegradability
A biodegradation rate was measured according to the modified MITI test method (OECD301C). According to the authorized standard of ECOMARK (Environmental Labeling System) revised in July, 1998, a biodegradation rate is required to be 60% or more.
(5) Friction Coefficient (LFW-1 Test)
Using a block-on-ring tester (LFW-1) according to ASTM D2174, a coefficient of friction between metals was measured to evaluate the lubricity of each sample oil. Specific testing conditions were as follows.
Test Jigs
Ring: Falex S-10 Test Ring (SAE4620 Steel)
Bock: Falex H-60 Test Block (SAE01 Steel)
Operation Conditions
Oil Temperature: 60 degrees C.
Load: 177.9 N (40 lbs)
Rotation Speed: 500 rpm
(6) Oxidation Stability Test
According to ASTM D 2893, each sample oil was oxidized with air (121 degrees C., 312 hours) under predetermined conditions, and then an increase ratio of kinematic viscosity at 100 degrees C., an acid value increment, and a sludge amount after filtering through a millipore filter were measured.
(7) FZG Seizure Test
According to ASTM D 5182-91, the test was performed under the conditions including 90 degrees C., 1450 rpm and 15 minutes, and the result was shown in a scuffing generating load stage.
Evaluation Results
As shown in Table 4, the sample oils of Examples 1 and 2, being provided by blending the components (A), (B) and (C), are excellent in all of lubricity, oxidation stability and biodegradability. Thus, it is understandable that these sample oils exhibit excellent properties as, for instance, an oil for a step-up gear used in a wind power generator. In particular, it is notable that although the biodegradability of the component (A) itself is not so high (see Table 1), the sample oil provided by blending the component (A) with other components exhibits an excellent biodegradability.
In contrast, the sample oils of Comparatives 1 to 3 are inferior in oxidation stability. It is because that each of the esters C, D and E, which are used as the base oils of these sample oils, has a structure using an unsaturated fatty acid unlike the ester A. The sample oil of Comparative 4 is inferior not only in biodegradability but also in lubricity. This sample oil uses PAO as the base oil thereof and is provided by blending the ester G (branched aliphatic carboxylic acid polyalcohol ester) at 10 mass %.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2009-118432 | May 2009 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2010/058189 | 5/14/2010 | WO | 00 | 11/15/2011 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2010/131739 | 11/18/2010 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 5552068 | Griffith | Sep 1996 | A |
| 20070225182 | Hewette | Sep 2007 | A1 |
| 20090176670 | Kawasaki | Jul 2009 | A1 |
| Number | Date | Country |
|---|---|---|
| 101070506 | Nov 2007 | CN |
| 56 044119 | Apr 1981 | JP |
| 06 062760 | Mar 1994 | JP |
| 11 012224 | Jan 1999 | JP |
| 3011696 | Feb 2000 | JP |
| 3231094 | Nov 2001 | JP |
| 3235930 | Dec 2001 | JP |
| 2003 522204 | Jul 2003 | JP |
| 3489703 | Jan 2004 | JP |
| 3515522 | Apr 2004 | JP |
| 2005 520038 | Jul 2005 | JP |
| 2008 115301 | May 2008 | JP |
| 2009 096720 | May 2009 | JP |
| WO 9916849 | Apr 1999 | WO |
| WO 2008038701 | Apr 2008 | WO |
| 2008 120581 | Oct 2008 | WO |
| Entry |
|---|
| International Search Report Issued Jun. 15, 2010 in PCT/JP10/058189 filed May 14, 2010. |
| U.S. Appl. No. 13/319,462, filed Nov. 8, 2011, Okada, et al. |
| Combined Chinese Office Action and Search Report issued on Dec. 28, 2012, in Chinese patent Application No. 201080021991.1 with English translation and English translation of category of cited documents. |
| U.S. Appl. No. 14/342,228, filed Feb. 28, 2014, Ohno, et al. |
| Number | Date | Country | |
|---|---|---|---|
| 20120065111 A1 | Mar 2012 | US |
