AU2012204549B2 - Continuously variable transmission fluid with extended anti-shudder durability - Google Patents
Continuously variable transmission fluid with extended anti-shudder durability Download PDFInfo
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- AU2012204549B2 AU2012204549B2 AU2012204549A AU2012204549A AU2012204549B2 AU 2012204549 B2 AU2012204549 B2 AU 2012204549B2 AU 2012204549 A AU2012204549 A AU 2012204549A AU 2012204549 A AU2012204549 A AU 2012204549A AU 2012204549 B2 AU2012204549 B2 AU 2012204549B2
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- carbon atoms
- Prior art date
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- 230000005540 biological transmission Effects 0.000 title claims description 23
- 239000012530 fluid Substances 0.000 title description 21
- 239000000203 mixture Substances 0.000 claims abstract description 65
- 239000000463 material Substances 0.000 claims abstract description 36
- 239000000314 lubricant Substances 0.000 claims abstract description 29
- 150000001408 amides Chemical class 0.000 claims abstract description 21
- 230000001050 lubricating effect Effects 0.000 claims abstract description 20
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000002270 dispersing agent Substances 0.000 claims description 109
- -1 phosphorus compound Chemical class 0.000 claims description 62
- 125000004432 carbon atom Chemical group C* 0.000 claims description 57
- 239000003921 oil Substances 0.000 claims description 54
- 239000003795 chemical substances by application Substances 0.000 claims description 48
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- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 37
- 229910052751 metal Inorganic materials 0.000 claims description 35
- 239000002184 metal Substances 0.000 claims description 34
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 32
- 229910052698 phosphorus Inorganic materials 0.000 claims description 30
- 239000011574 phosphorus Substances 0.000 claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 29
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical compound S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 claims description 15
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- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 15
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 15
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- 125000003118 aryl group Chemical group 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
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- 229910052796 boron Inorganic materials 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 5
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- 238000005260 corrosion Methods 0.000 claims description 5
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- 125000006539 C12 alkyl 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 claims description 2
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- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 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 1
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- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
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- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
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- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical class C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 1
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- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- VGTPKLINSHNZRD-UHFFFAOYSA-N oxoborinic acid Chemical compound OB=O VGTPKLINSHNZRD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
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- 239000011541 reaction mixture Substances 0.000 description 1
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- 230000000717 retained effect Effects 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 125000004079 stearyl 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])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- DLVYHYUFIXLWKV-UHFFFAOYSA-N tris(2-ethylhexyl) borate Chemical compound CCCCC(CC)COB(OCC(CC)CCCC)OCC(CC)CCCC DLVYHYUFIXLWKV-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
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
- 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
-
- 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
-
- 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
- C10M133/16—Amides; Imides
-
- 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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
-
- 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
- C10M2201/085—Phosphorus oxides, acids or salts
-
- 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
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/042—Epoxides
-
- 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
- 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
-
- 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
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl 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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated derivatives
-
- 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
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
-
- 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
- C10M2223/049—Phosphite
-
- 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
- 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
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
-
- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- 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
- C10N2030/02—Pour-point; Viscosity index
-
- 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
- C10N2030/76—Reduction of noise, shudder, or vibrations
-
- 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
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/045—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for continuous variable transmission [CVT]
-
- 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
- C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
- C10N2060/10—Chemical after-treatment of the constituents of the lubricating composition by sulfur or a compound containing sulfur
-
- 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
- C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
- C10N2060/14—Chemical after-treatment of the constituents of the lubricating composition by boron or a compound containing boron
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161429535P | 2011-01-04 | 2011-01-04 | |
| US61/429,535 | 2011-01-04 | ||
| PCT/US2012/020014 WO2012094275A1 (en) | 2011-01-04 | 2012-01-03 | Continuously variable transmission fluid with extended anti-shudder durability |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2012204549A1 AU2012204549A1 (en) | 2013-07-18 |
| AU2012204549B2 true AU2012204549B2 (en) | 2017-04-27 |
Family
ID=45509732
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2012204549A Ceased AU2012204549B2 (en) | 2011-01-04 | 2012-01-03 | Continuously variable transmission fluid with extended anti-shudder durability |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9567547B2 (https=) |
| EP (1) | EP2661482B1 (https=) |
| JP (1) | JP5992439B2 (https=) |
| KR (1) | KR101882041B1 (https=) |
| CN (2) | CN106967474A (https=) |
| AU (1) | AU2012204549B2 (https=) |
| CA (1) | CA2823623A1 (https=) |
| WO (1) | WO2012094275A1 (https=) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2997119B1 (en) * | 2013-05-14 | 2021-08-04 | The Lubrizol Corporation | Lubricating composition and method of lubricating a transmission |
| WO2016081111A1 (en) * | 2014-11-21 | 2016-05-26 | The Lubrizol Corporation | Lubricating oil composition |
| JP6551727B2 (ja) * | 2015-03-31 | 2019-07-31 | 出光興産株式会社 | 潤滑油組成物 |
| JP6789615B2 (ja) * | 2015-03-31 | 2020-11-25 | 出光興産株式会社 | 変速機用潤滑油組成物 |
| JP6533689B2 (ja) * | 2015-04-22 | 2019-06-19 | 出光興産株式会社 | 自動変速機油 |
| JP6590442B2 (ja) * | 2016-02-25 | 2019-10-16 | 出光興産株式会社 | 潤滑油組成物 |
| CN108779410B (zh) * | 2016-03-15 | 2022-03-01 | 出光兴产株式会社 | 润滑油组合物、润滑方法、和变速器 |
| JP6718349B2 (ja) * | 2016-09-27 | 2020-07-08 | Ｊｘｔｇエネルギー株式会社 | 無段変速機用潤滑油組成物 |
| JP6753608B2 (ja) * | 2016-10-19 | 2020-09-09 | 出光興産株式会社 | 潤滑油組成物、潤滑方法、及び変速機 |
| JP6962677B2 (ja) * | 2016-10-27 | 2021-11-05 | Ｅｍｇルブリカンツ合同会社 | 潤滑油組成物 |
| JP6864461B2 (ja) * | 2016-11-04 | 2021-04-28 | Ｅｍｇルブリカンツ合同会社 | 潤滑油組成物 |
| CA3045129A1 (en) * | 2016-12-16 | 2018-06-21 | The Lubrizol Corporation | Lubrication of an automatic transmission with reduced wear on a needle bearing |
| EP3571271A1 (en) * | 2017-01-17 | 2019-11-27 | The Lubrizol Corporation | Engine lubricant containing polyether compounds |
| EP3650521B1 (en) * | 2018-02-28 | 2022-06-01 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
| ES2983476T3 (es) * | 2018-06-18 | 2024-10-23 | Chemetall Us Inc | Sistemas combinados de organosilano funcionalizado con amina / organofosfato como agentes EP / inhibidores de la corrosión en composiciones para el tratamiento de superficies metálicas |
| US11319634B2 (en) | 2019-12-16 | 2022-05-03 | Saudi Arabian Oil Company | Corrosion inhibitors for a refinery |
| US11046901B1 (en) | 2020-06-15 | 2021-06-29 | Saudi Arabian Oil Company | Naphthenic acid corrosion inhibitors for a refinery |
| US11441094B2 (en) * | 2020-10-02 | 2022-09-13 | Jatco Ltd | Rejuvenation and/or extension of the lifetime of frictional performance in transmission fluids |
| US11434413B1 (en) | 2021-05-07 | 2022-09-06 | Saudi Arabian Oil Company | Flourinated aromatic compound as refinery corrosion inhibitor |
| EP4469542A1 (en) * | 2022-01-25 | 2024-12-04 | Chevron Japan Ltd. | Lubricating oil composition |
| CN116042287B (zh) * | 2023-02-06 | 2024-07-30 | 瑞孚化工（上海）有限公司 | 一种耐磨抗氧化润滑油及其制备方法和应用 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050041395A1 (en) * | 2003-08-21 | 2005-02-24 | The Lubrizol Corporation | Multifunctional dispersants |
| WO2006091371A1 (en) * | 2005-02-18 | 2006-08-31 | The Lubrizol Corporation | Lubricant additive formulation containing multifunctional dispersant |
| WO2008076825A1 (en) * | 2006-12-18 | 2008-06-26 | The Lubrizol Corporation | Functional fluid |
| US7618929B2 (en) * | 2004-10-19 | 2009-11-17 | The Lubrizol Corporation | Secondary and tertiary amines as friction modifiers for automatic transmission fluids |
| US20090312207A1 (en) * | 2005-10-11 | 2009-12-17 | Bartley Stuart L | Product of Amines with Hydroxy Acid as Friction Modifiers Suitable for Automatic Transmission Fluids |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2501731A (en) | 1946-10-14 | 1950-03-28 | Union Oil Co | Modified lubricating oil |
| US2616925A (en) | 1951-03-16 | 1952-11-04 | Lubrizol Corp | Organic alkaline earth metal complexes formed by use of thiophosphoric promoters |
| US2616911A (en) | 1951-03-16 | 1952-11-04 | Lubrizol Corp | Organic alkaline earth metal complexes formed by use of sulfonic promoters |
| US2616905A (en) | 1952-03-13 | 1952-11-04 | Lubrizol Corp | Organic alkaline earth metal complexes and methods of making same |
| US2777874A (en) | 1952-11-03 | 1957-01-15 | Lubrizol Corp | Metal complexes and methods of making same |
| DE1248643B (de) | 1959-03-30 | 1967-08-31 | The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) | Verfahren zur Herstellung von öllöslichen aeylierten Aminen |
| US3488284A (en) | 1959-12-10 | 1970-01-06 | Lubrizol Corp | Organic metal compositions and methods of preparing same |
| US3282835A (en) | 1963-02-12 | 1966-11-01 | Lubrizol Corp | Carbonated bright stock sulfonates and lubricants containing them |
| US3381022A (en) | 1963-04-23 | 1968-04-30 | Lubrizol Corp | Polymerized olefin substituted succinic acid esters |
| US3320162A (en) | 1964-05-22 | 1967-05-16 | Phillips Petroleum Co | Increasing the base number of calcium petroleum sulfonate |
| US3318809A (en) | 1965-07-13 | 1967-05-09 | Bray Oil Co | Counter current carbonation process |
| US3365396A (en) | 1965-12-28 | 1968-01-23 | Texaco Inc | Overbased calcium sulfonate |
| US3384585A (en) | 1966-08-29 | 1968-05-21 | Phillips Petroleum Co | Overbasing lube oil additives |
| US3629109A (en) | 1968-12-19 | 1971-12-21 | Lubrizol Corp | Basic magnesium salts processes and lubricants and fuels containing the same |
| 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 |
| US5697988A (en) | 1991-11-18 | 1997-12-16 | Ethyl Corporation | Fuel compositions |
| US5750477A (en) | 1995-07-10 | 1998-05-12 | The Lubrizol Corporation | Lubricant compositions to reduce noise in a push belt continuous variable transmission |
| CA2277469C (en) | 1997-11-13 | 2005-07-05 | Lubrizol Adibis Holdings (Uk) Limited | Salicyclic calixarenes and their use as lubricant additives |
| US6103673A (en) | 1998-09-14 | 2000-08-15 | The Lubrizol Corporation | Compositions containing friction modifiers for continuously variable transmissions |
| US6451745B1 (en) | 1999-05-19 | 2002-09-17 | The Lubrizol Corporation | High boron formulations for fluids continuously variable transmissions |
| EP1254100A1 (en) | 2000-02-07 | 2002-11-06 | Bp Oil International Limited | Calixarenes and their use as lubricant additives |
| US6458172B1 (en) | 2000-03-03 | 2002-10-01 | The Lubrizol Corporation | Fuel additive compositions and fuel compositions containing detergents and fluidizers |
| JP4741088B2 (ja) * | 2001-02-02 | 2011-08-03 | Ｊｘ日鉱日石エネルギー株式会社 | 潤滑油組成物 |
| JP4526386B2 (ja) * | 2002-07-12 | 2010-08-18 | ザ ルブリゾル コーポレイション | トランスミッション流体中の改善された抗震え性能および高い静止摩擦のための摩擦調節剤 |
| CN101360811B (zh) * | 2005-12-15 | 2011-12-28 | 卢布里佐尔公司 | 用于最终传动轴的润滑剂组合物 |
| KR20080091452A (ko) | 2005-12-23 | 2008-10-13 | 아스트라제네카 아베 | 위장 장애의 치료를 위한 이미다졸 유도체 |
| CN101421380B (zh) * | 2006-04-12 | 2012-05-02 | 卢布里佐尔公司 | 作为自动传动液的摩擦改进剂的含羟基叔胺 |
| US20080182770A1 (en) * | 2007-01-26 | 2008-07-31 | The Lubrizol Corporation | Antiwear Agent and Lubricating Compositions Thereof |
| CN101679900A (zh) | 2007-05-24 | 2010-03-24 | 卢布里佐尔公司 | 包含基于羟基多羧酸衍生物和钼化合物的无灰抗磨剂的润滑组合物 |
-
2012
- 2012-01-03 EP EP12700738.3A patent/EP2661482B1/en active Active
- 2012-01-03 US US13/976,670 patent/US9567547B2/en active Active
- 2012-01-03 CA CA2823623A patent/CA2823623A1/en not_active Abandoned
- 2012-01-03 WO PCT/US2012/020014 patent/WO2012094275A1/en not_active Ceased
- 2012-01-03 CN CN201710216758.2A patent/CN106967474A/zh active Pending
- 2012-01-03 KR KR1020137020379A patent/KR101882041B1/ko active Active
- 2012-01-03 JP JP2013547716A patent/JP5992439B2/ja active Active
- 2012-01-03 CN CN2012800114478A patent/CN103403136A/zh active Pending
- 2012-01-03 AU AU2012204549A patent/AU2012204549B2/en not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050041395A1 (en) * | 2003-08-21 | 2005-02-24 | The Lubrizol Corporation | Multifunctional dispersants |
| US7618929B2 (en) * | 2004-10-19 | 2009-11-17 | The Lubrizol Corporation | Secondary and tertiary amines as friction modifiers for automatic transmission fluids |
| WO2006091371A1 (en) * | 2005-02-18 | 2006-08-31 | The Lubrizol Corporation | Lubricant additive formulation containing multifunctional dispersant |
| US20090312207A1 (en) * | 2005-10-11 | 2009-12-17 | Bartley Stuart L | Product of Amines with Hydroxy Acid as Friction Modifiers Suitable for Automatic Transmission Fluids |
| WO2008076825A1 (en) * | 2006-12-18 | 2008-06-26 | The Lubrizol Corporation | Functional fluid |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2823623A1 (en) | 2012-07-12 |
| US20140031268A1 (en) | 2014-01-30 |
| KR101882041B1 (ko) | 2018-07-26 |
| CN106967474A (zh) | 2017-07-21 |
| JP2014501326A (ja) | 2014-01-20 |
| US9567547B2 (en) | 2017-02-14 |
| CN103403136A (zh) | 2013-11-20 |
| WO2012094275A1 (en) | 2012-07-12 |
| EP2661482A1 (en) | 2013-11-13 |
| AU2012204549A1 (en) | 2013-07-18 |
| EP2661482B1 (en) | 2016-12-28 |
| KR20130139334A (ko) | 2013-12-20 |
| JP5992439B2 (ja) | 2016-09-14 |
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