CN106967474A - 具有延长防抖动耐久性的无级变速器流体 - Google Patents
具有延长防抖动耐久性的无级变速器流体 Download PDFInfo
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- CN106967474A CN106967474A CN201710216758.2A CN201710216758A CN106967474A CN 106967474 A CN106967474 A CN 106967474A CN 201710216758 A CN201710216758 A CN 201710216758A CN 106967474 A CN106967474 A CN 106967474A
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- amine
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- 230000006641 stabilisation Effects 0.000 title description 12
- 238000011105 stabilization Methods 0.000 title description 12
- 239000002270 dispersing agent Substances 0.000 claims abstract description 100
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 63
- 239000000203 mixture Substances 0.000 claims abstract description 59
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 53
- 239000000314 lubricant Substances 0.000 claims abstract description 45
- 239000000463 material Substances 0.000 claims abstract description 40
- 239000002253 acid Substances 0.000 claims abstract description 20
- 150000001408 amides Chemical class 0.000 claims abstract description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 16
- 150000003512 tertiary amines Chemical class 0.000 claims abstract description 10
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 8
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- 150000001412 amines Chemical class 0.000 claims description 55
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 51
- 239000003921 oil Substances 0.000 claims description 49
- -1 hydroxyl alkane Chemical class 0.000 claims description 43
- 239000003795 chemical substances by application Substances 0.000 claims description 41
- 229910052751 metal Inorganic materials 0.000 claims description 31
- 239000002184 metal Substances 0.000 claims description 31
- 239000004327 boric acid Substances 0.000 claims description 27
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 15
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 15
- 150000003018 phosphorus compounds Chemical class 0.000 claims description 13
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 10
- 150000003335 secondary amines Chemical class 0.000 claims description 9
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- 238000012545 processing Methods 0.000 claims description 8
- 229910052796 boron Inorganic materials 0.000 claims description 7
- 239000007859 condensation product Substances 0.000 claims description 7
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- 238000000034 method Methods 0.000 claims description 6
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical class S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 claims description 5
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- 238000010306 acid treatment Methods 0.000 claims description 4
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- OSPSWZSRKYCQPF-UHFFFAOYSA-N dibutoxy(oxo)phosphanium Chemical compound CCCCO[P+](=O)OCCCC OSPSWZSRKYCQPF-UHFFFAOYSA-N 0.000 claims 1
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
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- 229910000147 aluminium phosphate Inorganic materials 0.000 description 10
- 239000003153 chemical reaction reagent Substances 0.000 description 10
- 125000001424 substituent group Chemical group 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 125000003277 amino group Chemical group 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
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- 239000001257 hydrogen Substances 0.000 description 5
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- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
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- 229910003953 H3PO2 Inorganic materials 0.000 description 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 4
- 150000008065 acid anhydrides Chemical class 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
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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 1
- 125000001421 myristyl 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])[H] 0.000 description 1
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- 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
- 239000002245 particle Substances 0.000 description 1
- 238000009304 pastoral farming Methods 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 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
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- 229920001228 polyisocyanate Polymers 0.000 description 1
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- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 239000012925 reference material Substances 0.000 description 1
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- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
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- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 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
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
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- 238000003786 synthesis reaction Methods 0.000 description 1
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- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
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- JKIYPJDZQQTBNJ-UHFFFAOYSA-N thiophene-2,3-dithiol Chemical compound SC=1C=CSC=1S JKIYPJDZQQTBNJ-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 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
- 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
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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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
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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
- 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
-
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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
- 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
-
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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
- 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
- C10M2215/082—Amides 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
- C10M2215/28—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
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- 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
参比1参比2实施例1 | |
粘度特征 | |
运动粘度,100℃(mm2/s) | 7.22 7.26 5.36 |
运动粘度,40℃ | 33.7 31.7 24.3 |
粘度指数 | 186 205 163 |
布氏粘度,-40℃ | 9460 9640 6270 |
VT20耐久性试验 | |
摩擦系数–顶端比 | 0.0976 0.0996 0.1027 |
–超速传动比 | 0.09610.09760.0962 |
–低比 | 0.08100.08100.0899 |
防抖动耐久性,JASO LVFA M349 | |
抖动以前的小时数(负斜率) | 96 144 552 |
Claims (14)
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US201161429535P | 2011-01-04 | 2011-01-04 | |
US61/429,535 | 2011-01-04 | ||
CN2012800114478A CN103403136A (zh) | 2011-01-04 | 2012-01-03 | 具有延长防抖动耐久性的无级变速器流体 |
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CN2012800114478A Pending CN103403136A (zh) | 2011-01-04 | 2012-01-03 | 具有延长防抖动耐久性的无级变速器流体 |
CN201710216758.2A Pending CN106967474A (zh) | 2011-01-04 | 2012-01-03 | 具有延长防抖动耐久性的无级变速器流体 |
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CN2012800114478A Pending CN103403136A (zh) | 2011-01-04 | 2012-01-03 | 具有延长防抖动耐久性的无级变速器流体 |
Country Status (8)
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US (1) | US9567547B2 (zh) |
EP (1) | EP2661482B1 (zh) |
JP (1) | JP5992439B2 (zh) |
KR (1) | KR101882041B1 (zh) |
CN (2) | CN103403136A (zh) |
AU (1) | AU2012204549B2 (zh) |
CA (1) | CA2823623A1 (zh) |
WO (1) | WO2012094275A1 (zh) |
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---|---|---|---|---|
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CN110770330B (zh) * | 2018-02-28 | 2022-07-19 | 出光兴产株式会社 | 润滑油组合物 |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101360811A (zh) * | 2005-12-15 | 2009-02-04 | 卢布里佐尔公司 | 用于最终传动轴的润滑剂组合物 |
CN101421380A (zh) * | 2006-04-12 | 2009-04-29 | 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 |
US20100144565A1 (en) * | 2006-12-18 | 2010-06-10 | Masahiko Ikeda | Functional Fluid |
Family Cites Families (31)
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 |
WO1999025677A1 (en) | 1997-11-13 | 1999-05-27 | 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 |
KR101022920B1 (ko) * | 2002-07-12 | 2011-03-16 | 더루우브리졸코오포레이션 | 변속기용 윤활유에 항진동 성능 향상과 높은 정지 마찰을제공하기 위한 마찰 개질제 |
US20050041395A1 (en) * | 2003-08-21 | 2005-02-24 | The Lubrizol Corporation | Multifunctional dispersants |
US7439213B2 (en) * | 2004-10-19 | 2008-10-21 | The Lubrizol Corporation | Secondary and tertiary amines as friction modifiers for automatic transmission fluids |
EP1851292B1 (en) * | 2005-02-18 | 2017-08-30 | The Lubrizol Corporation | Lubricant additive formulation containing multifunctional dispersant |
KR101325824B1 (ko) | 2005-10-11 | 2013-11-06 | 더루우브리졸코오포레이션 | 마찰조정제로서 아민과 하이드록시산의 생성물을 포함하는 윤활 조성물을 이용한 변속기의 윤활방법 |
AU2006327315A1 (en) | 2005-12-23 | 2007-06-28 | Astrazeneca Ab | Imidazole derivatives for the treatment of gastrointestinal disorders |
US20080182770A1 (en) * | 2007-01-26 | 2008-07-31 | The Lubrizol Corporation | Antiwear Agent and Lubricating Compositions Thereof |
EP2152838B1 (en) | 2007-05-24 | 2012-10-17 | The Lubrizol Corporation | Lubricating composition containing ashfree antiwear agent based on tartaric acid derivative and a molybdenum compound |
-
2012
- 2012-01-03 AU AU2012204549A patent/AU2012204549B2/en not_active Ceased
- 2012-01-03 CA CA2823623A patent/CA2823623A1/en not_active Abandoned
- 2012-01-03 US US13/976,670 patent/US9567547B2/en 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 EP EP12700738.3A patent/EP2661482B1/en active Active
- 2012-01-03 CN CN201710216758.2A patent/CN106967474A/zh active Pending
- 2012-01-03 KR KR1020137020379A patent/KR101882041B1/ko active IP Right Grant
- 2012-01-03 WO PCT/US2012/020014 patent/WO2012094275A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101360811A (zh) * | 2005-12-15 | 2009-02-04 | 卢布里佐尔公司 | 用于最终传动轴的润滑剂组合物 |
CN101421380A (zh) * | 2006-04-12 | 2009-04-29 | 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 |
US20100144565A1 (en) * | 2006-12-18 | 2010-06-10 | Masahiko Ikeda | Functional Fluid |
Non-Patent Citations (1)
Title |
---|
王汝霖: "《润滑剂摩擦化学》", 31 October 1994, 中国石化出版社 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116042287A (zh) * | 2023-02-06 | 2023-05-02 | 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 |
Also Published As
Publication number | Publication date |
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KR20130139334A (ko) | 2013-12-20 |
CA2823623A1 (en) | 2012-07-12 |
KR101882041B1 (ko) | 2018-07-26 |
JP2014501326A (ja) | 2014-01-20 |
JP5992439B2 (ja) | 2016-09-14 |
CN103403136A (zh) | 2013-11-20 |
AU2012204549B2 (en) | 2017-04-27 |
EP2661482A1 (en) | 2013-11-13 |
US9567547B2 (en) | 2017-02-14 |
AU2012204549A1 (en) | 2013-07-18 |
US20140031268A1 (en) | 2014-01-30 |
WO2012094275A1 (en) | 2012-07-12 |
EP2661482B1 (en) | 2016-12-28 |
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Application publication date: 20170721 Assignee: Lubrizol additive (Zhuhai) Co.,Ltd. Assignor: THE LUBRIZOL Corp. Contract record no.: 2018990000081 Denomination of invention: Continuously variable transmission fluid with extended anti-shudder durability License type: Common License Record date: 20180410 |
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Application publication date: 20170721 Assignee: Lubrizol additive (Zhuhai) Co.,Ltd. Assignor: THE LUBRIZOL Corp. Contract record no.: 2019990000109 Denomination of invention: Continuously variable transmission fluid with extended anti-shudder durability License type: Common License Record date: 20190403 |
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