CN105018181A - 润滑油组合物 - Google Patents
润滑油组合物 Download PDFInfo
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- CN105018181A CN105018181A CN201510299705.2A CN201510299705A CN105018181A CN 105018181 A CN105018181 A CN 105018181A CN 201510299705 A CN201510299705 A CN 201510299705A CN 105018181 A CN105018181 A CN 105018181A
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- lubricating oil
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- 239000000203 mixture Substances 0.000 title claims abstract description 148
- 239000010687 lubricating oil Substances 0.000 title claims abstract description 88
- -1 alkali metal borate Chemical class 0.000 claims abstract description 184
- 239000003921 oil Substances 0.000 claims abstract description 80
- 239000002551 biofuel Substances 0.000 claims abstract description 28
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 17
- 239000000446 fuel Substances 0.000 claims abstract description 15
- 239000003963 antioxidant agent Substances 0.000 claims description 39
- 230000003078 antioxidant effect Effects 0.000 claims description 39
- 239000003795 chemical substances by application Substances 0.000 claims description 34
- 229910052751 metal Inorganic materials 0.000 claims description 33
- 239000002184 metal Substances 0.000 claims description 31
- 239000003925 fat Substances 0.000 claims description 25
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 24
- 239000002199 base oil Substances 0.000 claims description 21
- 150000001412 amines Chemical class 0.000 claims description 20
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 19
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 17
- 239000005864 Sulphur Substances 0.000 claims description 17
- KZNICNPSHKQLFF-UHFFFAOYSA-N dihydromaleimide Natural products O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 17
- 229910052750 molybdenum Inorganic materials 0.000 claims description 17
- 239000011733 molybdenum Substances 0.000 claims description 16
- 238000000746 purification Methods 0.000 claims description 16
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 14
- 229960002317 succinimide Drugs 0.000 claims description 14
- 239000002270 dispersing agent Substances 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 11
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
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- 150000003818 basic metals Chemical class 0.000 claims description 8
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- 238000012360 testing method Methods 0.000 description 15
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 14
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- 125000003342 alkenyl group Chemical group 0.000 description 9
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 9
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- 238000000034 method Methods 0.000 description 9
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 8
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- 125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
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- 159000000007 calcium salts Chemical class 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 239000002480 mineral oil Substances 0.000 description 6
- 235000010446 mineral oil Nutrition 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
- 229910052796 boron Inorganic materials 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 239000010705 motor oil Substances 0.000 description 5
- 239000011574 phosphorus Substances 0.000 description 5
- 229910052698 phosphorus Inorganic materials 0.000 description 5
- 229920001748 polybutylene Polymers 0.000 description 5
- 229920000098 polyolefin Polymers 0.000 description 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 4
- SIFDSJCMINUPDM-UHFFFAOYSA-N 3-dodecyl-2-hydroxybenzoic acid Chemical compound CCCCCCCCCCCCC1=CC=CC(C(O)=O)=C1O SIFDSJCMINUPDM-UHFFFAOYSA-N 0.000 description 4
- RPEMQNHWDRJDHW-UHFFFAOYSA-N 3-hexadecyl-2-hydroxybenzoic acid Chemical compound CCCCCCCCCCCCCCCCC1=CC=CC(C(O)=O)=C1O RPEMQNHWDRJDHW-UHFFFAOYSA-N 0.000 description 4
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 description 4
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
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- 230000015572 biosynthetic process Effects 0.000 description 4
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- 230000000052 comparative effect Effects 0.000 description 4
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- KWUZCAVKPCRJPO-UHFFFAOYSA-N n-ethyl-4-(6-methyl-1,3-benzothiazol-2-yl)aniline Chemical compound C1=CC(NCC)=CC=C1C1=NC2=CC=C(C)C=C2S1 KWUZCAVKPCRJPO-UHFFFAOYSA-N 0.000 description 4
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- UPHOPMSGKZNELG-UHFFFAOYSA-N 2-hydroxynaphthalene-1-carboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=C(O)C=CC2=C1 UPHOPMSGKZNELG-UHFFFAOYSA-N 0.000 description 3
- HPOHQPXRFJSLRG-UHFFFAOYSA-N 3-dodecyl-2-hydroxynaphthalene-1-carboxylic acid Chemical compound C1=CC=C2C(C(O)=O)=C(O)C(CCCCCCCCCCCC)=CC2=C1 HPOHQPXRFJSLRG-UHFFFAOYSA-N 0.000 description 3
- YAXXOCZAXKLLCV-UHFFFAOYSA-N 3-dodecyloxolane-2,5-dione Chemical class CCCCCCCCCCCCC1CC(=O)OC1=O YAXXOCZAXKLLCV-UHFFFAOYSA-N 0.000 description 3
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- ACFSYJJKCORIPD-UHFFFAOYSA-N 3-hexyl-2-hydroxynaphthalene-1-carboxylic acid Chemical compound C1=CC=C2C(C(O)=O)=C(O)C(CCCCCC)=CC2=C1 ACFSYJJKCORIPD-UHFFFAOYSA-N 0.000 description 3
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- 229910000077 silane Inorganic materials 0.000 description 2
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- 235000019865 palm kernel oil Nutrition 0.000 description 1
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- 239000000312 peanut oil Substances 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 150000003873 salicylate salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
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- 238000000638 solvent extraction Methods 0.000 description 1
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- 238000005987 sulfurization reaction Methods 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 239000010496 thistle oil Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- QFKMMXYLAPZKIB-UHFFFAOYSA-N undecan-1-amine Chemical compound CCCCCCCCCCCN QFKMMXYLAPZKIB-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- MBBWTVUFIXOUBE-UHFFFAOYSA-L zinc;dicarbamodithioate Chemical compound [Zn+2].NC([S-])=S.NC([S-])=S MBBWTVUFIXOUBE-UHFFFAOYSA-L 0.000 description 1
Classifications
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10M141/02—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 oxygen-containing compound
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- C10M125/00—Lubricating compositions characterised by the additive being an inorganic material
- C10M125/26—Compounds containing silicon or boron, e.g. silica, sand
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- 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
- C10M141/12—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 compound containing atoms of elements not provided for in groups C10M141/02 - C10M141/10
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/087—Boron oxides, acids or salts
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
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- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
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- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M2207/26—Overbased carboxylic acid salts
- C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
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- C10M2207/28—Esters
- C10M2207/284—Esters of aromatic monocarboxylic acids
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- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/289—Partial esters containing free hydroxy groups
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
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- C10M2215/064—Di- and triaryl amines
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/223—Five-membered rings containing nitrogen and carbon only
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/28—Amides; Imides
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/09—Complexes with metals
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2229/02—Unspecified siloxanes; Silicones
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- C10N2010/02—Groups 1 or 11
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- C10N2010/04—Groups 2 or 12
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- C10N2010/00—Metal present as such or in compounds
- C10N2010/12—Groups 6 or 16
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- C10N2030/02—Pour-point; Viscosity index
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- C10N2030/04—Detergent property or dispersant property
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- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/08—Resistance to extreme temperature
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/40—Low content or no content compositions
- C10N2030/42—Phosphor free or low phosphor content compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/40—Low content or no content compositions
- C10N2030/43—Sulfur free or low sulfur content compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/40—Low content or no content compositions
- C10N2030/45—Ash-less or low ash content
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/74—Noack Volatility
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/78—Fuel contamination
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
- C10N2040/253—Small diesel engines
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Lubricants (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007-269380 | 2007-10-16 | ||
JP2007269380 | 2007-10-16 | ||
CN200880112470A CN101821368A (zh) | 2007-10-16 | 2008-09-22 | 润滑油组合物 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN200880112470A Division CN101821368A (zh) | 2007-10-16 | 2008-09-22 | 润滑油组合物 |
Publications (1)
Publication Number | Publication Date |
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CN105018181A true CN105018181A (zh) | 2015-11-04 |
Family
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Application Number | Title | Priority Date | Filing Date |
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CN201510299705.2A Pending CN105018181A (zh) | 2007-10-16 | 2008-09-22 | 润滑油组合物 |
CN200880112470A Pending CN101821368A (zh) | 2007-10-16 | 2008-09-22 | 润滑油组合物 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
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CN200880112470A Pending CN101821368A (zh) | 2007-10-16 | 2008-09-22 | 润滑油组合物 |
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Country | Link |
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US (2) | US20100249000A1 (ja) |
EP (1) | EP2204438A4 (ja) |
JP (1) | JP5431947B2 (ja) |
KR (1) | KR20100061839A (ja) |
CN (2) | CN105018181A (ja) |
WO (1) | WO2009050984A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106947576A (zh) * | 2017-04-01 | 2017-07-14 | 江苏奥克化学有限公司 | 一种液压油组合物、液压油及其制备方法 |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7960322B2 (en) * | 2007-10-26 | 2011-06-14 | Chevron Oronite Company Llc | Lubricating oil compositions comprising a biodiesel fuel and an antioxidant |
US7838474B2 (en) * | 2007-10-31 | 2010-11-23 | Chevron Oronite Company Llc | Lubricating oil compositions comprising a biodiesel fuel and a detergent |
DE102008024382B4 (de) * | 2008-05-20 | 2014-03-27 | Jürgen Krahl | Verfahren zur Verminderung der Motorölverdünnung bei Verbrennungskraftmaschinen und/oder deren Auswirkung |
ATE550411T1 (de) * | 2009-08-24 | 2012-04-15 | Infineum Int Ltd | Schmierölzusammensetzung |
JP2011252073A (ja) * | 2010-06-01 | 2011-12-15 | Idemitsu Kosan Co Ltd | 低摩擦摺動材料用潤滑油組成物、及びこれを用いた摺動機構 |
RU2013124369A (ru) * | 2010-10-29 | 2014-12-10 | Эвоник Ойл Эддитивс ГмбХ | Дизельный двигатель, обладающий улучшенными свойствами |
CA2836598A1 (en) * | 2011-06-15 | 2012-12-20 | The Lubrizol Corporation | Lubricating composition containing a salt of a carboxylic acid |
WO2012174075A1 (en) * | 2011-06-15 | 2012-12-20 | The Lubrizol Corporation | Lubricating composition containing an ester of an aromatic carboxylic acid |
CN105229128B (zh) | 2013-05-20 | 2018-07-06 | 出光兴产株式会社 | 润滑油组合物 |
US9567554B2 (en) * | 2014-01-10 | 2017-02-14 | General Electric Company | Apparatus, method, and solvent for cleaning turbine components |
MX2018001909A (es) * | 2015-08-14 | 2018-06-19 | Vanderbilt Chemicals Llc | Composiciones antioxidantes mejoradas y composiciones lubricantes que contienen los mismos. |
CN108473905B (zh) * | 2015-12-07 | 2021-03-09 | Jxtg能源株式会社 | 内燃机用润滑油组合物 |
WO2018156304A1 (en) | 2017-02-21 | 2018-08-30 | Exxonmobil Research And Engineering Company | Lubricating oil compositions and methods of use thereof |
US20200277541A1 (en) * | 2019-02-28 | 2020-09-03 | Afton Chemical Corporation | Lubricating compositions for diesel particulate filter performance |
CN115558541B (zh) * | 2019-04-26 | 2024-05-31 | 胜牌全球产品知识产权有限公司 | 用于电动车辆和混合动力车辆的润滑剂及其使用方法 |
US12065623B2 (en) | 2019-04-26 | 2024-08-20 | Vgp Ipco Llc | Lubricant for use in electric and hybrid vehicles and methods of using the same |
US11680223B2 (en) | 2020-12-07 | 2023-06-20 | Eneos Corporation | Lubricating oil composition |
EP4317376A1 (en) * | 2021-03-30 | 2024-02-07 | Idemitsu Kosan Co.,Ltd. | Lubricating oil composition |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000226593A (ja) * | 1999-02-05 | 2000-08-15 | Idemitsu Kosan Co Ltd | 潤滑油用添加剤及び潤滑油組成物 |
JP2005306913A (ja) * | 2004-04-16 | 2005-11-04 | Chevron Texaco Japan Ltd | エンジン潤滑油組成物 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2243198A (en) * | 1939-01-28 | 1941-05-27 | Du Pont | Fuel oil |
US3929650A (en) | 1974-03-22 | 1975-12-30 | Chevron Res | Extreme pressure agent and its preparation |
US4089790A (en) | 1975-11-28 | 1978-05-16 | Chevron Research Company | Synergistic combinations of hydrated potassium borate, antiwear agents, and organic sulfide antioxidants |
JPH0322438A (ja) | 1989-06-20 | 1991-01-30 | Oki Electric Ind Co Ltd | バイポーラ型半導体集積回路装置の製造方法 |
US6051538A (en) * | 1999-01-26 | 2000-04-18 | The Procter & Gamble Company | Pour point depression of heavy cut methyl esters via alkyl methacrylate copolymer |
CA2336513C (en) * | 2000-02-17 | 2010-08-24 | Tatsuo Tateno | Process for producing fatty acid esters and fuels comprising fatty acid ester |
JP3722472B2 (ja) * | 2000-06-02 | 2005-11-30 | シェブロンテキサコジャパン株式会社 | 潤滑油組成物 |
US6569818B2 (en) * | 2000-06-02 | 2003-05-27 | Chevron Oronite Company, Llc | Lubricating oil composition |
JP5231694B2 (ja) | 2000-08-22 | 2013-07-10 | 出光興産株式会社 | ディーゼル微粒子除去装置付きディーゼルエンジン用潤滑油組成物 |
JP2003252887A (ja) | 2002-03-04 | 2003-09-10 | Asahi Denka Kogyo Kk | モリブデンアミン化合物の製造方法 |
US20050181957A1 (en) * | 2002-05-30 | 2005-08-18 | Hiroaki Koshima | Lubricating oil additive composition for internal combustion engine |
US6962896B2 (en) | 2002-05-31 | 2005-11-08 | Chevron Oronite Company Llc | Reduced color molybdenum-containing composition and a method of making same |
JP4515797B2 (ja) * | 2004-03-19 | 2010-08-04 | 新日本石油株式会社 | ディーゼルエンジン用潤滑油組成物 |
-
2008
- 2008-09-22 WO PCT/JP2008/067099 patent/WO2009050984A1/ja active Application Filing
- 2008-09-22 JP JP2009538019A patent/JP5431947B2/ja not_active Expired - Fee Related
- 2008-09-22 EP EP08839550.4A patent/EP2204438A4/en not_active Withdrawn
- 2008-09-22 CN CN201510299705.2A patent/CN105018181A/zh active Pending
- 2008-09-22 US US12/681,864 patent/US20100249000A1/en not_active Abandoned
- 2008-09-22 CN CN200880112470A patent/CN101821368A/zh active Pending
- 2008-09-22 KR KR1020107007978A patent/KR20100061839A/ko not_active Application Discontinuation
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2013
- 2013-01-14 US US13/740,326 patent/US20130130954A1/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000226593A (ja) * | 1999-02-05 | 2000-08-15 | Idemitsu Kosan Co Ltd | 潤滑油用添加剤及び潤滑油組成物 |
JP2005306913A (ja) * | 2004-04-16 | 2005-11-04 | Chevron Texaco Japan Ltd | エンジン潤滑油組成物 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106947576A (zh) * | 2017-04-01 | 2017-07-14 | 江苏奥克化学有限公司 | 一种液压油组合物、液压油及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
EP2204438A4 (en) | 2014-09-10 |
JP5431947B2 (ja) | 2014-03-05 |
EP2204438A1 (en) | 2010-07-07 |
CN101821368A (zh) | 2010-09-01 |
US20130130954A1 (en) | 2013-05-23 |
KR20100061839A (ko) | 2010-06-09 |
US20100249000A1 (en) | 2010-09-30 |
JPWO2009050984A1 (ja) | 2011-03-03 |
WO2009050984A1 (ja) | 2009-04-23 |
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