DE69119823T2 - Automatische Kraftübertragungsflüssigkeiten und Additive dafür - Google Patents
Automatische Kraftübertragungsflüssigkeiten und Additive dafürInfo
- Publication number
- DE69119823T2 DE69119823T2 DE69119823T DE69119823T DE69119823T2 DE 69119823 T2 DE69119823 T2 DE 69119823T2 DE 69119823 T DE69119823 T DE 69119823T DE 69119823 T DE69119823 T DE 69119823T DE 69119823 T2 DE69119823 T2 DE 69119823T2
- Authority
- DE
- Germany
- Prior art keywords
- viscosity
- weight
- composition
- cst
- index improver
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Revoked
Links
- 239000012530 fluid Substances 0.000 title claims description 7
- 230000005540 biological transmission Effects 0.000 title claims description 6
- 239000000654 additive Substances 0.000 title claims description 4
- 239000000203 mixture Substances 0.000 claims description 27
- KZNICNPSHKQLFF-UHFFFAOYSA-N dihydromaleimide Natural products O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 12
- 239000002480 mineral oil Substances 0.000 claims description 12
- 235000010446 mineral oil Nutrition 0.000 claims description 11
- -1 alkenyl succinimide Chemical compound 0.000 claims description 10
- 229960002317 succinimide Drugs 0.000 claims description 9
- 239000002270 dispersing agent Substances 0.000 claims description 8
- 230000007935 neutral effect Effects 0.000 claims description 7
- 229920013639 polyalphaolefin Polymers 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- 239000003963 antioxidant agent Substances 0.000 claims description 6
- 239000012141 concentrate Substances 0.000 claims description 6
- 239000010687 lubricating oil Substances 0.000 claims description 6
- 230000003078 antioxidant effect Effects 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 229920000768 polyamine Polymers 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000010688 mineral lubricating oil Substances 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 230000001050 lubricating effect Effects 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 2
- 229920001281 polyalkylene Polymers 0.000 claims 2
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims 2
- 239000004698 Polyethylene Substances 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 239000002199 base oil Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 3
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- OFMNOWYDHUOSEI-UHFFFAOYSA-N 2,6-ditert-butyl-6-methylcyclohexa-2,4-dien-1-ol Chemical compound CC(C)(C)C1=CC=CC(C)(C(C)(C)C)C1O OFMNOWYDHUOSEI-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
Classifications
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- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/044—Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
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- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
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- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/02—Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
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- 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
- C10M129/04—Hydroxy compounds
- C10M129/10—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
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- 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
- C10M129/04—Hydroxy compounds
- C10M129/10—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
- C10M129/14—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring containing at least 2 hydroxy groups
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- 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
- C10M133/12—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to a carbon atom of a six-membered aromatic ring
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- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/52—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
- C10M133/56—Amides; Imides
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- C10M145/14—Acrylate; Methacrylate
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- C10M145/16—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 polycarboxylic
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/104—Aromatic fractions
- C10M2203/1045—Aromatic fractions used as base material
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/106—Naphthenic fractions
- C10M2203/1065—Naphthenic fractions used as base material
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
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- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/027—Neutral salts thereof
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- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
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- C10M2209/086—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 polycarboxylic, e.g. maleic acid
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Description
- Mindestens ein Hersteller von originalteilen hat den Wunsch, die Anforderung an die Brookfield-Viskosität bei -40ºC (Flüssigkeit für automatische Getriebe = automatic transmission fluid = ATF) vom derzeitigen Maximum von 50.000 cP auf 20.000 cP zu senken. Dieses Ziel läßt sich zwar durch Zusatz von leichten Mineralbasisölen zu den bei der Formulierung von ATF verwendeten Basisölen erreichen, es müssen jedoch erhebliche zusätzliche Mengen an einem Mittel zur Verbesserung des Viskositätsindex zugegeben werden, um die Viskosität bei hoher Temperatur zu erhöhen und die daraus resultierende schlechtere Scherstabilität der Flüssigkeit wettzumachen. Die Zugabe von zusätzlichem Mittel zur Verbesserung des Viskositätsindex ist wegen möglicher Probleme in bezug auf Verschleiß, Oxidation und Scherkraft bedenklich. Darüber hinaus stehen nicht allen ATF-Herstellern die leichten Mineralbasisöle zur Verfügung, die man braucht, um diese Eigenschaften bei niedrigen Temperaturen zu erzielen.
- Die britische Patentschrift GB-A-2 057 494 beschreibt flüssige Zusammensetzungen für Zentralsysteme, die ein Kohlenwasserstoffbasisöl mit einem Dec-1-enoligomer und einer Erdölschmierfraktion sowie einen speziellen Typ eines Mittels zur Verbesserung des Viskositätsindex aus Polymethacrylat enthalten.
- Diese Erfindung besteht aus der Entdeckung, daß es möglich ist, die vorstehenden Probleme zu vermeiden, indem man zusammen mit den bei der Formulierung von ATF-Zusammensetzungen verwendeten Mineralschmierölen eine bestimmte, nachstehend beschriebene Komponentenkombination zum Einsatz bringt.
- Insbesondere hat sich herausgestellt, daß es möglich ist, ATF-Zusammensetzungen mit Brookfield-Viskositäten von 20.000 cP oder weniger herzustellen, ohne daß übermäßige Mengen an Mitteln zur Verbesserung des Viskositätsindex verwendet werden müssen, um die Viskosität bei hoher Temperatur zu erhöhen.
- Erfindungsgemäß zur Verfügung gestellt wird in einer Ausführungsform eine Schmiermittelzusammensetzung, die besonders für die Verwendung als Flüssigkeit für automatische Getriebe geeignet ist und
- a> 50 bis 85 Gew.-% eines Mineralöls mit einer Viskosität bei 100ºC im Bereich von 3 bis 5 cSt,
- b> 5 bis 35 Gew.-% eines Poly-α-olefin-Schmieröls mit einer Viskosität bei 100ºC im Bereich von 1 bis 8 cSt und
- c) 8 bis 15 Gew.-% einer Kombination aus einem Alkenylsuccinimid-Dispergiermittel, einem Mittel zur Verbesserung des Viskositätsindex und einem Antioxidans enthält,
- wobei die Zusammensetzung außerdem dadurch gekennzeichnet ist, daß sie weniger als 7,0 Gew.-% des Mittels zur Verbesserung des Viskositätsindex enthält und eine Brookfield-Viskosität bei -40ºC von nicht mehr als 20.000 cP aufweist. Bevorzugt entspricht das Mineralschmieröl solcher Formulierungen einem Solvent 100 neutralen Mineralöl oder ist so gemischt, daß es Solvent 100 neutralem Mineralöl entspricht. Es können jedoch auch Mineralöle mit Viskositätseigenschaften verwendet werden, die denen von Solvent 100 neutralem Mineralöl vergleichbar sind oder sich in diesem Bereich bewegen.
- Eine weitere Ausführungsform der Erfindung besteht aus der Bereitstellung eines Additivkonzentrats, das in Mischung mit Solvent 100 neutralem Mineralöl besonders für die Verwendung bei der Herstellung einer Flüssigkeit für automatische Getriebe geeignet ist und a) ein Poly-α-olefin-Schmieröl mit einer Viskosität bei 100ºC im Bereich von 1 bis 5 cSt und b) eine Kombination aus einem Alkenylsuccinimid-Dispergiermittel, einem Mittel zur Verbesserung des Viskositätsindex und einem Antioxidans enthält, wobei das Konzentrat außerdem dadurch gekennzeichnet ist, daß es weniger als 7,0 Gew.-% des Mittels zur Verbesserung des Viskositätsindex enthält und in Mischung mit 100 Solvent neutralem Mineralöl bei einer Konzentration von 20 bis 30 Gew.-% eine Zusammensetzung mit einer Brookfield-Viskosität bei -40ºC von nicht mehr als 20.000 cP bildet.
- Bevorzugt weist das in den erfindungsgemäßen Zusammensetzungen verwendete Poly-α-olefin-Schmieröl eine Viskosität bei 100ºC von 2 bis 4 cSt auf.
- In den erfindungsgemäßen Zusammensetzungen können verschiedene Alkenylsuccinimid-Dispergiermittel verwendet werden. Dazu gehören mit acyclischem Hydrocarbyl substituierte Succinimide, die mit verschiedenen in der Patentliteratur hinreichend offenbarten Ammen oder Aminderivaten gebildet werden (siehe z.B. US-A- 4,234,435). Die Verwendung von Alkenylsuccinimiden, die mit einer anorganischen Phosphorsäure (oder einem Anhydrid davon) und einem Borierungsmittel behandelt wurden, werden für die Verwendung in den erfindungsgemäßen Zusammensetzungen bevorzugt, da sie viel besser kompatibel mit elastomeren Dichtungen aus Substanzen wie Fluorelastomeren und siliciumhaltigen Elastomeren sind (siehe US-A-4,857,214). Aus Polyisobutenylbernsteinsäureanhydrid hergestellte Polyisobutenylsuccinimide und ein Alkylenpolyamin wie Triethylentetramin oder Tetraethylenpentamin, in denen der Polyisobutenylsubstituent von Polyisobuten mit einem zahlenmittleren Molekulargewicht im Bereich von 500 bis 5.000 (bevorzugt 8000 bis 2.500) abgeleitet ist, sind besonders gut geeignet, vor allem wenn sie wie in US-A-4,857,214 beschrieben mit Phosphor- und Borverbindungen behandelt werden. Die fertige ATF-Zusammensetzung enthält üblicherweise 1,5 bis 4,0 Gew.-% an solchen Dispergiermitteln.
- Mittel zur Verbesserung des Viskositätsindex, die ebenfalls in den erfindungsgemäßen Zusammensetzungen enthalten sein können, sind unter anderem Substanzen wie Polymethacrylat-Polymere, Polyacrylat-Polymere, Styrol- Maleinsäureester-Copolymere und ähnliche polymere Substanzen einschließlich Homopolymere, Copolymere und Pfropfcopolymere. Wie vorstehend bereits ausgeführt, enthält die fertige ATF zusammensetzung normalerweise weniger als 7 Gew.-% des Mittels zur Verbesserung des Viskositätsindex.
- Oxidationshemmende Mittel oder Stabilisierungsmittel, die sich für die erfindungsgemäßen Zusammensetzungen eignen, sind unter anderem Phenyl-α-naphthylamin, Phenyl-β-naphthylamin, Diphenylamin, bis-alkylierte Diphenylamine (z.B. p,p'-Bis(alkylphenyl)amine, in denen die Alkylgruppen jeweils 8 bis 12 Kohlenstoffatome enthalten), sterisch gehinderte Phenole (z.B. 2,6-Di-tert-butylphenol oder 2-Methyl-2,6-di-tertbutylphenol) und Bisphenole (z.B. 4,4'-Methylenbis(2,6- di-tert-butylphenol)) u.ä. Typisch sind Mengen im Bereich von 0,1 bis 0,7 Gew.-% in der fertigen ATF- Zusammensetzung.
- Die erfindungsgemäßen Additivkonzentrate enthalten das Dispergiermittel, Mittel zur Verbesserung des Viskositätsindex, ein oxidationshemmendes Mittel und Poly-α- olefinöl in einem solchen Verhältnis, daß bei Zugabe des Konzentrats in einer Konzentration von 12,0 bis 45,0 zu einem geeigneten Mineralöl die resultierende Flüssigkeit jeden der Inhaltsstoffe in der erwünschten Konzentration enthält. Natürlich ist es auch möglich, wenn auch weniger wünschenswert, die Komponenten getrennt oder in Unterkombinationen mit dem Mineralöl zu mischen.
Claims (7)
1. Schmiermittelzusammensetzung, die besonders für die
Verwendung als Flüssigkeit für automatische Getriebe
geeignet ist und
a) 50 bis 85 Gew.-% eines Mineralöls mit einer
Viskosität bei 100ºC im Bereich von 3 bis 5 cSt,
b) 5 bis 35 Gew.-% eines Poly-α-olefin-Schmieröls
mit einer Viskosität bei 100ºC im Bereich von 1
bis 8 cSt und
c) 8 bis 15 Gew.-% einer Kombination aus einem
Alkenylsuccinimid-Dispergiermittel, einem Mittel zur
Verbesserung des Viskositätsindex und einem
Antioxidans enthält,
wobei die Zusammensetzung außerdem dadurch
gekennzeichnet ist, daß sie weniger als 7,0 Gew.-% des
Mittels zur Verbesserung des Viskositätsindex
enthält und eine Brookfield-Viskosität bei 40ºC von
nicht mehr als 20.000 cP aufweist.
2. Zusammensetzung nach Anspruch 1, in der das
Mineralschmieröl ein Solvent 100 neutrales Mineralöl ist.
3. Additivkonzentrat, das in Mischung mit Solvent 100
neutralem Mineralöl besonders für die Verwendung bei
der Herstellung einer Flüssigkeit für automatische
Getriebe geeignet ist und a) ein Poly-α-olefin-
Schmieröl mit einer Viskosität bei 100ºC im Bereich
von 1 bis 8 cSt und b) eine Kombination aus einem
Alkenylsuccinimid-Dispergiermittel, einem Mittel zur
Verbesserung des Viskositätsindex und einem
Antioxidans enthält, wobei das Konzentrat außerdem
dadurch gekennzeichnet ist, daß es weniger als 7,
Gew.-% des Mittels zur Verbesserung des
Viskositätsindex enthält und in Mischung mit 100 Solvent
neutralem Mineralöl bei einer Konzentration von 20
bis 30 Gew.-% eine Zusammensetzung mit einer
Brookfield-Viskosität bei -40ºC von nicht mehr als 20.000
cP bildet.
4. Zusammensetzung nach einem der vorstehenden
Ansprüche, in der das Poly-α-Olefin-Schmieröl eine
Viskosität bei 100ºC von 2 bis 4 cSt aufweist.
5. Zusammensetzung nach einem der vorstehenden
Ansprüche, in der das Alkenylsuccinimid-Dispergiermittel
ein Alkenylsuccinimid ist, das mit einer
anorganischen Phosphorsäure oder einem Phosphorsäureanhydrid
und einem Borierungsmittel behandelt wurde.
6. Zusammensetzung nach Anspruch 5, in der das
Alkenylsuccinimid ein Polyisobutenylsuccinimid von
Polyalkylenpolyamin ist.
7. Zusammensetzung nach Anspruch 6, in der das
Polyalkylenpolyamin eine überwiegend aus
Polyethylenpolyaminen bestehende Mischung ist, die in ihrer
durchschnittlichen Zusammensetzung im allgemeinen
Tetraethylenpentamin entsprechen.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51240690A | 1990-04-23 | 1990-04-23 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69119823D1 DE69119823D1 (de) | 1996-07-04 |
| DE69119823T2 true DE69119823T2 (de) | 1996-10-02 |
Family
ID=24038959
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69119823T Revoked DE69119823T2 (de) | 1990-04-23 | 1991-04-22 | Automatische Kraftübertragungsflüssigkeiten und Additive dafür |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US5387346A (de) |
| EP (1) | EP0454395B1 (de) |
| DE (1) | DE69119823T2 (de) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69119823T2 (de) * | 1990-04-23 | 1996-10-02 | Ethyl Petroleum Additives Inc | Automatische Kraftübertragungsflüssigkeiten und Additive dafür |
| CA2095972A1 (en) * | 1992-05-22 | 1993-11-23 | Rolfe J. Hartley | Lubricants with enhanced low temperature properties |
| JP2859077B2 (ja) * | 1993-04-09 | 1999-02-17 | 出光興産株式会社 | 潤滑油組成物 |
| US5344579A (en) * | 1993-08-20 | 1994-09-06 | Ethyl Petroleum Additives, Inc. | Friction modifier compositions and their use |
| US5578236A (en) * | 1994-11-22 | 1996-11-26 | Ethyl Corporation | Power transmission fluids having enhanced performance capabilities |
| US5750477A (en) * | 1995-07-10 | 1998-05-12 | The Lubrizol Corporation | Lubricant compositions to reduce noise in a push belt continuous variable transmission |
| US5641732A (en) * | 1995-07-17 | 1997-06-24 | Exxon Chemical Patents Inc. | Automatic transmission fluids of improved viscometric properties |
| US5646099A (en) * | 1995-07-17 | 1997-07-08 | Exxon Chemical Patents Inc. | Automatic transmission fluids of improved viscometric properties |
| US5641733A (en) * | 1995-07-17 | 1997-06-24 | Exxon Chemical Patents Inc. | Automatic transmission fluids of improved viscometric properties |
| US6077455A (en) * | 1995-07-17 | 2000-06-20 | Exxon Chemical Patents Inc | Automatic transmission fluid of improved viscometric properties |
| AU711941B2 (en) * | 1995-07-17 | 1999-10-28 | Exxon Chemical Patents Inc. | Partial synthetic transmission fluids with improved low temperature properties |
| US5866519A (en) * | 1995-07-17 | 1999-02-02 | Exxon Chemical Patents Inc. | Automatic transmission fluids of improved viscometric properties |
| US5759965A (en) * | 1995-10-18 | 1998-06-02 | The Lubrizol Corporation | Antiwear enhancing composition for lubricants and functional fluids |
| JP2000501126A (ja) * | 1995-11-03 | 2000-02-02 | エクソン・ケミカル・パテンツ・インク | 改良された伝達挙動を有する自動変速機液 |
| SG64414A1 (en) | 1996-01-16 | 1999-04-27 | Lubrizol Corp | Lubricating compositions |
| ZA97222B (en) * | 1996-01-16 | 1998-02-18 | Lubrizol Corp | Lubricating compositions. |
| GB9716283D0 (en) * | 1997-08-01 | 1997-10-08 | Exxon Chemical Patents Inc | Lubricating oil compositions |
| US6059955A (en) * | 1998-02-13 | 2000-05-09 | Exxon Research And Engineering Co. | Low viscosity lube basestock |
| US6103673A (en) * | 1998-09-14 | 2000-08-15 | The Lubrizol Corporation | Compositions containing friction modifiers for continuously variable transmissions |
| US6191078B1 (en) * | 1999-09-21 | 2001-02-20 | Exxonmobil Research And Engineering Company | Part-synthetic, aviation piston engine lubricant |
| US6525004B1 (en) * | 2001-05-01 | 2003-02-25 | Infineum International Inc. | Combustion improving additive for small engine lubricating oils |
| RU2283341C1 (ru) * | 2005-07-18 | 2006-09-10 | Татьяна Иосифовна Назарова | Моторно-редукторное масло для авиационной техники |
| RU2303625C1 (ru) * | 2006-08-14 | 2007-07-27 | Татьяна Иосифовна Назарова | Смазочная композиция для осевых шарниров винтов вертолетов |
| CN114574272B (zh) * | 2022-03-18 | 2022-09-06 | 中国科学院兰州化学物理研究所 | 一种润滑油组合物及其制备方法和应用 |
Family Cites Families (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1248643B (de) * | 1959-03-30 | 1967-08-31 | The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) | Verfahren zur Herstellung von öllöslichen aeylierten Aminen |
| NL124842C (de) * | 1959-08-24 | |||
| US3131150A (en) * | 1961-04-12 | 1964-04-28 | California Research Corp | Lubricating oil compositions containing n-substituted alkenyl succinimides in combination with polyamines |
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| FR2307867A1 (fr) * | 1975-04-16 | 1976-11-12 | Inst Francais Du Petrole | Nouvelles compositions d'esters complexes et leur utilisation comme constituants de bases lubrifiantes |
| US4282392A (en) * | 1976-10-28 | 1981-08-04 | Gulf Research & Development Company | Alpha-olefin oligomer synthetic lubricant |
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| JPS619497A (ja) * | 1984-06-25 | 1986-01-17 | Nippon Oil Co Ltd | 自動変速機油組成物 |
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| WO1988006616A1 (fr) * | 1987-03-02 | 1988-09-07 | Idemitsu Kosan Company Limited | Composition a base d'huile lubrifiante |
| US4992183A (en) * | 1987-04-01 | 1991-02-12 | Ethyl Corporation | Multigrade hydrogenated decene-1 oligomer engine oils |
| JP2555284B2 (ja) * | 1987-05-14 | 1996-11-20 | 出光興産株式会社 | 温度特性改良潤滑油組成物 |
| US4827073A (en) * | 1988-01-22 | 1989-05-02 | Mobil Oil Corporation | Process for manufacturing olefinic oligomers having lubricating properties |
| US4857214A (en) * | 1988-09-16 | 1989-08-15 | Ethylk Petroleum Additives, Inc. | Oil-soluble phosphorus antiwear additives for lubricants |
| DE69119823T2 (de) * | 1990-04-23 | 1996-10-02 | Ethyl Petroleum Additives Inc | Automatische Kraftübertragungsflüssigkeiten und Additive dafür |
| TW215106B (de) * | 1990-09-25 | 1993-10-21 | Shell Internat Res Schappej B V | |
| US5089156A (en) * | 1990-10-10 | 1992-02-18 | Ethyl Petroleum Additives, Inc. | Ashless or low-ash synthetic base compositions and additives therefor |
-
1991
- 1991-04-22 DE DE69119823T patent/DE69119823T2/de not_active Revoked
- 1991-04-22 EP EP91303590A patent/EP0454395B1/de not_active Revoked
-
1993
- 1993-07-19 US US08/094,482 patent/US5387346A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0454395B1 (de) | 1996-05-29 |
| EP0454395A1 (de) | 1991-10-30 |
| DE69119823D1 (de) | 1996-07-04 |
| US5387346A (en) | 1995-02-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8363 | Opposition against the patent | ||
| 8331 | Complete revocation |