CN103597062A - 含有羧酸的盐的润滑组合物 - Google Patents
含有羧酸的盐的润滑组合物 Download PDFInfo
- Publication number
- CN103597062A CN103597062A CN201280029312.4A CN201280029312A CN103597062A CN 103597062 A CN103597062 A CN 103597062A CN 201280029312 A CN201280029312 A CN 201280029312A CN 103597062 A CN103597062 A CN 103597062A
- Authority
- CN
- China
- Prior art keywords
- lubricating composition
- amine
- weight
- carboxylic acid
- alkyl
- Prior art date
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- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 147
- 230000001050 lubricating effect Effects 0.000 title claims abstract description 82
- 150000001732 carboxylic acid derivatives Chemical class 0.000 title claims abstract description 43
- 150000003839 salts Chemical class 0.000 title claims abstract description 14
- -1 carboxylic acid compound Chemical class 0.000 claims abstract description 69
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 48
- 150000001412 amines Chemical class 0.000 claims abstract description 43
- 125000003118 aryl group Chemical group 0.000 claims abstract description 31
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical class N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 19
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 11
- 239000003921 oil Substances 0.000 claims description 57
- 125000000217 alkyl group Chemical group 0.000 claims description 42
- 239000000314 lubricant Substances 0.000 claims description 40
- 229910052799 carbon Inorganic materials 0.000 claims description 29
- 150000001721 carbon Chemical group 0.000 claims description 28
- 150000001875 compounds Chemical class 0.000 claims description 25
- 239000002270 dispersing agent Substances 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 239000003599 detergent Substances 0.000 claims description 18
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 18
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 claims description 15
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 15
- 239000004215 Carbon black (E152) Substances 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 14
- 125000003545 alkoxy group Chemical group 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 claims description 14
- 235000004515 gallic acid Nutrition 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 10
- 229940074391 gallic acid Drugs 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims description 9
- 239000011574 phosphorus Substances 0.000 claims description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 8
- 239000005864 Sulphur Substances 0.000 claims description 6
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 claims description 6
- 229960001860 salicylate Drugs 0.000 claims description 6
- 150000003512 tertiary amines Chemical class 0.000 claims description 6
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 5
- 150000003335 secondary amines Chemical class 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- VILAVOFMIJHSJA-UHFFFAOYSA-N dicarbon monoxide Chemical compound [C]=C=O VILAVOFMIJHSJA-UHFFFAOYSA-N 0.000 claims description 4
- 150000003141 primary amines Chemical class 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 150000004668 long chain fatty acids Chemical class 0.000 claims description 3
- 229940095064 tartrate Drugs 0.000 claims description 3
- 150000002118 epoxides Chemical class 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 abstract description 6
- 239000000654 additive Substances 0.000 description 25
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 22
- 230000000996 additive effect Effects 0.000 description 20
- 239000006185 dispersion Substances 0.000 description 18
- 229910052757 nitrogen Inorganic materials 0.000 description 17
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- 238000005260 corrosion Methods 0.000 description 10
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- 239000000463 material Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
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- 125000001931 aliphatic group Chemical group 0.000 description 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 7
- 239000010949 copper Substances 0.000 description 7
- 229910052802 copper Inorganic materials 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
- 238000005885 boration reaction Methods 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- XXUJMEYKYHETBZ-UHFFFAOYSA-N ethyl 4-nitrophenyl ethylphosphonate Chemical compound CCOP(=O)(CC)OC1=CC=C([N+]([O-])=O)C=C1 XXUJMEYKYHETBZ-UHFFFAOYSA-N 0.000 description 6
- 239000000446 fuel Substances 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 229910052725 zinc Inorganic materials 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 description 5
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 230000029936 alkylation Effects 0.000 description 4
- 238000005804 alkylation reaction Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 3
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 150000008431 aliphatic amides Chemical class 0.000 description 3
- 239000004411 aluminium Substances 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000002199 base oil Substances 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical group OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 125000005266 diarylamine group Chemical group 0.000 description 3
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical class CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 3
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000009931 harmful effect Effects 0.000 description 3
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
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- 238000004519 manufacturing process Methods 0.000 description 3
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- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical compound C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 3
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- XSFKFBNQLMQTAL-UHFFFAOYSA-N 1,5-dimethoxycyclohexa-2,4-diene-1-carboxylic acid Chemical compound COC1=CC=CC(C(O)=O)(OC)C1 XSFKFBNQLMQTAL-UHFFFAOYSA-N 0.000 description 2
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 2
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/48—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring
- C10M129/54—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/28—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/38—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
- C10M129/44—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- 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
- 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
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M149/00—Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
- C10M149/12—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M149/14—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds a condensation reaction being involved
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M161/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
- C10M2207/128—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/144—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/221—Six-membered rings containing nitrogen and carbon only
-
- C—CHEMISTRY; METALLURGY
- 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
- 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
- C10M2215/224—Imidazoles
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
- C10M2215/226—Morpholines
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- 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
- 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
-
- 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
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Description
Claims (18)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610898881.2A CN106978231B (zh) | 2011-06-15 | 2012-06-14 | 含有羧酸的盐的润滑组合物 |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201161497146P | 2011-06-15 | 2011-06-15 | |
US61/497,146 | 2011-06-15 | ||
PCT/US2012/042361 WO2012174184A1 (en) | 2011-06-15 | 2012-06-14 | Lubricating composition containing a salt of a carboxylic acid |
Related Child Applications (1)
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CN201610898881.2A Division CN106978231B (zh) | 2011-06-15 | 2012-06-14 | 含有羧酸的盐的润滑组合物 |
Publications (2)
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CN103597062A true CN103597062A (zh) | 2014-02-19 |
CN103597062B CN103597062B (zh) | 2016-11-09 |
Family
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CN201280029312.4A Expired - Fee Related CN103597062B (zh) | 2011-06-15 | 2012-06-14 | 含有羧酸的盐的润滑组合物 |
CN201610898881.2A Expired - Fee Related CN106978231B (zh) | 2011-06-15 | 2012-06-14 | 含有羧酸的盐的润滑组合物 |
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CN201610898881.2A Expired - Fee Related CN106978231B (zh) | 2011-06-15 | 2012-06-14 | 含有羧酸的盐的润滑组合物 |
Country Status (5)
Country | Link |
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US (2) | US9243202B2 (zh) |
EP (1) | EP2721127A1 (zh) |
CN (2) | CN103597062B (zh) |
CA (1) | CA2836598A1 (zh) |
WO (1) | WO2012174184A1 (zh) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106635255A (zh) * | 2016-12-13 | 2017-05-10 | 中国科学院宁波材料技术与工程研究所 | 生物基油品分散剂、其制备方法及应用 |
CN110691838A (zh) * | 2017-05-31 | 2020-01-14 | 道达尔销售服务公司 | 包含多胺、酸和硼官能团的化合物及其作为润滑剂添加剂的用途 |
CN112313203A (zh) * | 2018-06-22 | 2021-02-02 | 松下电器产业株式会社 | 有机盐和具备该有机盐的羟基自由基传感器及检测介质 |
CN112585249A (zh) * | 2018-08-30 | 2021-03-30 | 巴斯夫欧洲公司 | 润滑剂组合物 |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2836598A1 (en) * | 2011-06-15 | 2012-12-20 | The Lubrizol Corporation | Lubricating composition containing a salt of a carboxylic acid |
CN104962351A (zh) * | 2015-06-10 | 2015-10-07 | 柳州科尔特锻造机械有限公司 | 一种轮毂锻压用油的制备方法 |
WO2018136541A1 (en) * | 2017-01-17 | 2018-07-26 | The Lubrizol Corporation | Engine lubricant containing polyether compounds |
WO2022140496A1 (en) | 2020-12-23 | 2022-06-30 | The Lubrizol Corporation | Benzazepine compounds as antioxidants for lubricant compositions |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3840462A (en) * | 1972-04-07 | 1974-10-08 | Mobil Oil Corp | Lubricant compositions |
US5667539A (en) * | 1992-10-05 | 1997-09-16 | Exxon Chemical Patents Inc. | Oleaginous compositions |
CN1361762A (zh) * | 1999-07-19 | 2002-07-31 | 新日本理化株式会社 | 二羧酸二酯、其制备方法及含该酯的冷冻机润滑油 |
US20030220209A1 (en) * | 2002-05-23 | 2003-11-27 | The Lubrizol Corporation | Use of an amide to reduce lubricant temperature |
CN101821368A (zh) * | 2007-10-16 | 2010-09-01 | 出光兴产株式会社 | 润滑油组合物 |
Family Cites Families (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE425425A (zh) | ||||
US2079643A (en) * | 1934-01-19 | 1937-05-11 | Celanese Corp | Yarn and filament and method of preparing same |
US2795548A (en) | 1954-06-29 | 1957-06-11 | California Research Corp | Lubricant compositions |
DE1248643B (de) | 1959-03-30 | 1967-08-31 | The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) | Verfahren zur Herstellung von öllöslichen aeylierten Aminen |
US3444170A (en) | 1959-03-30 | 1969-05-13 | Lubrizol Corp | Process which comprises reacting a carboxylic intermediate with an amine |
US3381022A (en) | 1963-04-23 | 1968-04-30 | Lubrizol Corp | Polymerized olefin substituted succinic acid esters |
DE1271877B (de) | 1963-04-23 | 1968-07-04 | Lubrizol Corp | Schmieroel |
USRE26433E (en) | 1963-12-11 | 1968-08-06 | Amide and imide derivatives of metal salts of substituted succinic acids | |
GB1052380A (zh) | 1964-09-08 | |||
US3336349A (en) | 1964-09-17 | 1967-08-15 | Koppers Co Inc | Alkanoyl esters of the trihydroxy benzenes |
US3316177A (en) | 1964-12-07 | 1967-04-25 | Lubrizol Corp | Functional fluid containing a sludge inhibiting detergent comprising the polyamine salt of the reaction product of maleic anhydride and an oxidized interpolymer of propylene and ethylene |
DE1595234A1 (de) | 1965-04-27 | 1970-03-05 | Roehm & Haas Gmbh | Verfahren zur Herstellung oligomerer bzw. polymerer Amine |
US3340281A (en) | 1965-06-14 | 1967-09-05 | Standard Oil Co | Method for producing lubricating oil additives |
GB1162818A (en) | 1965-12-17 | 1969-08-27 | British Petroleum Co | Synthetic Lubricants |
FR1537892A (fr) | 1966-07-21 | 1968-08-30 | British Petroleum Co | Composition de lubrifiant synthétique |
GB1180386A (en) | 1966-07-21 | 1970-02-04 | British Petroleum Co | Synthetic Lubricants for Aero Gas Turbines |
GB1180389A (en) | 1966-07-21 | 1970-02-04 | British Petroleum Co | Lubricants having improved Anti-Wear and Anti-Corrosion Properties |
US3433744A (en) | 1966-11-03 | 1969-03-18 | Lubrizol Corp | Reaction product of phosphosulfurized hydrocarbon and alkylene polycarboxylic acid or acid derivatives and lubricating oil containing the same |
US3501405A (en) | 1967-08-11 | 1970-03-17 | Rohm & Haas | Lubricating and fuel compositions comprising copolymers of n-substituted formamide-containing unsaturated esters |
US3625859A (en) * | 1968-08-06 | 1971-12-07 | San Abbott Ltd | Corrosion inhibiting composition |
US3576743A (en) | 1969-04-11 | 1971-04-27 | Lubrizol Corp | Lubricant and fuel additives and process for making the additives |
FR2063994A1 (en) | 1969-10-22 | 1971-07-16 | Schmierstoffkomb Zeitz | Stabilised lubricating oils of the ether - alcohol or ester type |
US3632511A (en) | 1969-11-10 | 1972-01-04 | Lubrizol Corp | Acylated nitrogen-containing compositions processes for their preparationand lubricants and fuels containing the same |
GB1358046A (en) | 1971-01-18 | 1974-06-26 | British Petroleum Co | Synthetic lubricating composition |
US3790478A (en) | 1971-04-30 | 1974-02-05 | British Petroleum Co | Synthetic lubricant for aero gas turbines |
US3778371A (en) | 1972-05-19 | 1973-12-11 | Ethyl Corp | Lubricant and fuel compositions |
GB1445993A (en) | 1973-06-27 | 1976-08-11 | Exxon Research Engineering Co | Lubricating oil compositions |
US4171959A (en) | 1977-12-14 | 1979-10-23 | Texaco Inc. | Fuel composition containing quaternary ammonium salts of succinimides |
US4234435A (en) | 1979-02-23 | 1980-11-18 | The Lubrizol Corporation | Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation |
US4253980A (en) | 1979-06-28 | 1981-03-03 | Texaco Inc. | Quaternary ammonium salt of ester-lactone and hydrocarbon oil containing same |
US4326973A (en) | 1981-01-13 | 1982-04-27 | Texaco Inc. | Quaternary ammonium succinimide salt composition and lubricating oil containing same |
US4338206A (en) | 1981-03-23 | 1982-07-06 | Texaco Inc. | Quaternary ammonium succinimide salt composition and lubricating oil containing same |
US4863623A (en) | 1988-03-24 | 1989-09-05 | Texaco Inc. | Novel VI improver, dispersant, and anti-oxidant additive and lubricating oil composition containing same |
GB8818711D0 (en) | 1988-08-05 | 1988-09-07 | Shell Int Research | Lubricating oil dispersants |
US5038319A (en) | 1989-04-24 | 1991-08-06 | Xerox Corporation | System for recording and remotely accessing operating data in a reproduction machine |
US5102569A (en) | 1990-10-23 | 1992-04-07 | Chevron Research And Technology Company | Method of preparing borated alkyl aromatic polyols |
US5254138A (en) | 1991-05-03 | 1993-10-19 | Uop | Fuel composition containing a quaternary ammonium salt |
US6117825A (en) | 1992-05-07 | 2000-09-12 | Ethyl Corporation | Polyisobutylene succinimide and ethylene-propylene succinimide synergistic additives for lubricating oils compositions |
US5399277A (en) | 1993-10-08 | 1995-03-21 | Exxon Chemical Patents Inc. | Fuel and lubricant additives derived from dihydroxyaromatic compounds |
GB9611318D0 (en) | 1996-05-31 | 1996-08-07 | Exxon Chemical Patents Inc | Overbased metal-containing detergents |
GB9611316D0 (en) | 1996-05-31 | 1996-08-07 | Exxon Chemical Patents Inc | Overbased metal-containing detergents |
GB9611428D0 (en) | 1996-05-31 | 1996-08-07 | Exxon Chemical Patents Inc | Overbased metal-containing detergents |
GB9611424D0 (en) | 1996-05-31 | 1996-08-07 | Exxon Chemical Patents Inc | Overbased metal-containing detergents |
US6165235A (en) | 1997-08-26 | 2000-12-26 | The Lubrizol Corporation | Low chlorine content compositions for use in lubricants and fuels |
US6107258A (en) | 1997-10-15 | 2000-08-22 | Ethyl Corporation | Functionalized olefin copolymer additives |
US6107257A (en) | 1997-12-09 | 2000-08-22 | Ethyl Corporation | Highly grafted, multi-functional olefin copolymer VI modifiers |
US7423000B2 (en) | 1999-01-19 | 2008-09-09 | International Lubricants, Inc. | Non-phosphorous, non-metallic anti-wear compound and friction modifier |
US6559105B2 (en) | 2000-04-03 | 2003-05-06 | The Lubrizol Corporation | Lubricant compositions containing ester-substituted hindered phenol antioxidants |
WO2003040273A2 (en) | 2001-11-05 | 2003-05-15 | The Lubrizol Corporation | Lubricating composition with improved fuel economy |
US7238650B2 (en) | 2002-06-27 | 2007-07-03 | The Lubrizol Corporation | Low-chlorine, polyolefin-substituted, with amine reacted, alpha-beta unsaturated carboxylic compounds |
CN100523156C (zh) | 2002-08-22 | 2009-08-05 | 新日本理化株式会社 | 轴承用润滑油 |
JP4578115B2 (ja) * | 2004-02-04 | 2010-11-10 | Jx日鉱日石エネルギー株式会社 | 潤滑油組成物 |
JP5070049B2 (ja) | 2004-07-30 | 2012-11-07 | ザ ルブリゾル コーポレイション | 芳香族アミンを含有する分散剤粘度調整剤 |
JP2008518059A (ja) | 2004-10-25 | 2008-05-29 | ザ ルブリゾル コーポレイション | 腐食防止 |
US7582126B2 (en) | 2005-12-20 | 2009-09-01 | Arkema France | Fatty ester compositions with improved oxidative stability |
JP2010528156A (ja) | 2007-05-24 | 2010-08-19 | ザ ルブリゾル コーポレイション | ヒドロキシポリカルボン酸誘導体に基づく無灰の磨耗防止剤およびモリブデン化合物を含有する潤滑組成物 |
CN102333851B (zh) * | 2009-02-27 | 2016-06-15 | Ntn株式会社 | 润滑脂组合物、润滑脂封入轴承、推进器轴用万向联轴器、润滑油组合物及烧结含油轴承 |
CA2836598A1 (en) * | 2011-06-15 | 2012-12-20 | The Lubrizol Corporation | Lubricating composition containing a salt of a carboxylic acid |
-
2012
- 2012-06-14 CA CA2836598A patent/CA2836598A1/en not_active Abandoned
- 2012-06-14 CN CN201280029312.4A patent/CN103597062B/zh not_active Expired - Fee Related
- 2012-06-14 EP EP12728931.2A patent/EP2721127A1/en not_active Withdrawn
- 2012-06-14 WO PCT/US2012/042361 patent/WO2012174184A1/en active Application Filing
- 2012-06-14 CN CN201610898881.2A patent/CN106978231B/zh not_active Expired - Fee Related
- 2012-06-14 US US14/117,377 patent/US9243202B2/en active Active
-
2015
- 2015-12-15 US US14/969,335 patent/US9631159B2/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3840462A (en) * | 1972-04-07 | 1974-10-08 | Mobil Oil Corp | Lubricant compositions |
US5667539A (en) * | 1992-10-05 | 1997-09-16 | Exxon Chemical Patents Inc. | Oleaginous compositions |
CN1361762A (zh) * | 1999-07-19 | 2002-07-31 | 新日本理化株式会社 | 二羧酸二酯、其制备方法及含该酯的冷冻机润滑油 |
US20030220209A1 (en) * | 2002-05-23 | 2003-11-27 | The Lubrizol Corporation | Use of an amide to reduce lubricant temperature |
CN101821368A (zh) * | 2007-10-16 | 2010-09-01 | 出光兴产株式会社 | 润滑油组合物 |
Non-Patent Citations (1)
Title |
---|
方建华等: "《润滑剂添加剂手册》", 30 September 2010 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106635255A (zh) * | 2016-12-13 | 2017-05-10 | 中国科学院宁波材料技术与工程研究所 | 生物基油品分散剂、其制备方法及应用 |
CN110691838A (zh) * | 2017-05-31 | 2020-01-14 | 道达尔销售服务公司 | 包含多胺、酸和硼官能团的化合物及其作为润滑剂添加剂的用途 |
CN112313203A (zh) * | 2018-06-22 | 2021-02-02 | 松下电器产业株式会社 | 有机盐和具备该有机盐的羟基自由基传感器及检测介质 |
CN112313203B (zh) * | 2018-06-22 | 2023-05-02 | 松下控股株式会社 | 有机盐和具备该有机盐的羟基自由基传感器及检测介质 |
CN112585249A (zh) * | 2018-08-30 | 2021-03-30 | 巴斯夫欧洲公司 | 润滑剂组合物 |
CN112585249B (zh) * | 2018-08-30 | 2022-07-08 | 巴斯夫欧洲公司 | 润滑剂组合物 |
Also Published As
Publication number | Publication date |
---|---|
CN106978231B (zh) | 2020-01-03 |
CN106978231A (zh) | 2017-07-25 |
US20150141307A1 (en) | 2015-05-21 |
WO2012174184A1 (en) | 2012-12-20 |
US9631159B2 (en) | 2017-04-25 |
US20160097018A1 (en) | 2016-04-07 |
EP2721127A1 (en) | 2014-04-23 |
CN103597062B (zh) | 2016-11-09 |
CA2836598A1 (en) | 2012-12-20 |
US9243202B2 (en) | 2016-01-26 |
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