EP0008193B1 - Composition lubrifiante et procédé pour la lubrification d'un moteur Diesel marin - Google Patents
Composition lubrifiante et procédé pour la lubrification d'un moteur Diesel marin Download PDFInfo
- Publication number
- EP0008193B1 EP0008193B1 EP79301536A EP79301536A EP0008193B1 EP 0008193 B1 EP0008193 B1 EP 0008193B1 EP 79301536 A EP79301536 A EP 79301536A EP 79301536 A EP79301536 A EP 79301536A EP 0008193 B1 EP0008193 B1 EP 0008193B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lubricating
- composition
- lubricating composition
- dispersant
- base oil
- 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.)
- Expired
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- 239000000203 mixture Substances 0.000 title claims description 43
- 230000001050 lubricating effect Effects 0.000 title claims description 36
- 239000002270 dispersing agent Substances 0.000 claims description 27
- -1 hydrocarbyl amine Chemical class 0.000 claims description 27
- 239000002199 base oil Substances 0.000 claims description 25
- 239000004530 micro-emulsion Substances 0.000 claims description 24
- 239000000314 lubricant Substances 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 239000003995 emulsifying agent Substances 0.000 claims description 9
- 229920000768 polyamine Polymers 0.000 claims description 9
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 8
- 229960002317 succinimide Drugs 0.000 claims description 7
- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052788 barium Inorganic materials 0.000 claims description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical group [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 229920001281 polyalkylene Polymers 0.000 claims description 3
- 150000007942 carboxylates Chemical class 0.000 claims description 2
- NESLWCLHZZISNB-UHFFFAOYSA-M sodium phenolate Chemical compound [Na+].[O-]C1=CC=CC=C1 NESLWCLHZZISNB-UHFFFAOYSA-M 0.000 claims description 2
- 239000000654 additive Substances 0.000 description 15
- 239000003921 oil Substances 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 11
- 150000001412 amines Chemical class 0.000 description 9
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 9
- 239000003599 detergent Substances 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 7
- 239000010687 lubricating oil Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 6
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- ZMRQTIAUOLVKOX-UHFFFAOYSA-L calcium;diphenoxide Chemical compound [Ca+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 ZMRQTIAUOLVKOX-UHFFFAOYSA-L 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 4
- 239000005642 Oleic acid Substances 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001414 amino alcohols Chemical class 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- 240000005020 Acaciella glauca Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241001323490 Colias gigantea Species 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- 239000004907 Macro-emulsion Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid ester group Chemical group C(CCCCCCCCCCC)(=O)O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 239000003879 lubricant additive Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002943 palmitic acids Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000003499 redwood Nutrition 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229960001124 trientine Drugs 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
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution 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
- 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
- C10M141/06—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 nitrogen-containing compound
-
- 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
- C10M2201/02—Water
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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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- 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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- 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
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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
- 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
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/18—Tall oil acids
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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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
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- C10M2215/00—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
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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
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/044—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms having cycloaliphatic groups
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- 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
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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
- C10M2215/086—Imides [having hydrocarbon substituents containing less than thirty carbon atoms]
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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
- 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
- C10M2215/26—Amines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- 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
- 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
- C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
-
- 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
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
-
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- 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
- C10N2010/02—Groups 1 or 11
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
- C10N2040/253—Small diesel engines
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B3/00—Engines characterised by air compression and subsequent fuel addition
- F02B3/06—Engines characterised by air compression and subsequent fuel addition with compression ignition
Definitions
- This invention relates to lubricating compositions suitable for use in marine diesel engines.
- a cylinder lubricant having a highly basic nature, i.e. having a high total base number.
- These lubricants usually contain an overbased metal salt such as an over-based calcium or barium phenate or sulphonate.
- metal-containing salts are ash forming, i.e. when they are burnt there is a metal containing residue. It would be desirable to reduce or eliminate the use of ash-forming additives for such applications by replacing at least a proportion of such additives with ashless additives.
- a lubricant containing an ashless basic additive viz a lubricating composition
- a lubricating composition comprising a branched chain alkyl or alkenyl polyamine in which the alkyl or alkenyl group has a number average molecular weight of 350 to 500 and which has a total base number of at least 200.
- the polyamine component of the additive e.g. a polyalkylene polyamine
- the branched chain alkyl or alkenyl group e.g. a polyisobutenyl group
- solubilising branched chain alkyl or alkenyl group in the additive is relatively bulky, and there would be advantages in being able to use a simple polyamine without the added solubilising group.
- microemulsions in which the continuous phase is a liquid hydrocarbon medium are known from US Patent No. 3346494.
- the microemulsified phase may be a volatile medium such as water (which is preferred), methanol, or aqueous or methanolic solutions of inorganic salts and bases (oxides and hydroxides) or it may be a non-volatile medium such as ethylene glycol or glycerol.
- organic bases such as amines can also form the microemulsified phase in lubricating oils in the absence of water or methanol or other solvent. Since the amine is present to react with acidic products of combustion, e.g. sulphur oxides, it has also been found that the lubricating composition should contain a dispersant.
- a lubricating composition comprising a lubricating base oil as a continuous phase and a hydrocarbon insoluble compound as a microemulsified phase is characterised in that the microemulsified phase is a hydrocarbyl amine and the lubricating composition also contains a dispersant for hydrocarbyl amine salts which may be formed during use of the lubricating composition.
- the hydrocarbyl amine may be an aryl, cycloalkyl or alkylamine.
- Alkylene polyamines are preferred, particularly polyalkylene polyamines and more particularly polyethylene polyamines. Since it is not necessary to have a large hydrocarbyl group to solubilise the amine, the hydrocarbyl amine may have a total of from 1 to 20 carbon atoms. Such a low content of hydrocarbyl groups means that the amine has a high total base number, e.g. a TBN of the order of 1000mgKOH/g.
- suitable amines are ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine and pentaethylene hexamine.
- the lubricating base oil may be any known lubricating oil and may be synthetic or natural.
- synthetic oils may be the diesters or complex esters known as synthetic lubricants, or liquid polymers formed from low molecular weight olefins.
- the oils are mineral oils derived from petroleum, e.g. petroleum fractions boiling above 300°C. These fractions may be distillate fractions boiling in the range 300 to 600°C or de- ashphalted residual fractions.
- the choice of base oil will be determined by the proposed use and, for the preferred lubricating compositions for use as cylinder lubricants for diesel engines, the oils may have a viscosity of from 8 to 23 x 10- e m z /s at 100°C.
- Microemulsions of a hydrocarbon insoluble component in a liquid hydrocarbon medium, particularly a mineral oil, can be formed by simple mixing provided the type and quantity of emulsifiers are correctly chosen.
- the disperse phase droplets are small, e.g. in the range 60-1000A, and the microemulsions are stable at ambient temperature almost indefinitely.
- the emulsifiers noramlly required for forming microemulsions are a fatty acid and an alkyl phenol with an amino alcohol as co-surfactant.
- the ratio in parts by weight of the three components may be:-
- the amino alcohol co-surfactant can be an optional component in the present invention where the microemulsified phase is a hydrocarbyl amine.
- the fatty acid may have from 12 to 25 carbon atoms and may be saturated or unsaturated.
- suitable acids are stearic, oleic, linoleic, lauric and palmitic acids. Mixtures of acids, e.g. tall oil fatty acids may also be used.
- the alkyl phenol may be mono or polyhydroxy and the alkyl group is preferably a straight chain alkyl group and has preferably, from 6 to 15 carbon atoms. There may be additional C l -C l5 alkyl groups on the aromatic ring, although this is not necessary.
- Preferred alkyl phenols are octyl and nonyl phenols and octyl and nonyl cresols.
- the amino alcohol if present, is preferably an alkanolarnine, which may be a primary, secondary or tertiary amine and the alkyl group or groups of which may have from 2 to 6 carbon atoms.
- alkanolarnine which may be a primary, secondary or tertiary amine and the alkyl group or groups of which may have from 2 to 6 carbon atoms.
- suitable alkanolamines are mono-, di- and tri-isopropanolamines.
- microemuisions As compared with macroemulsions, microemuisions have a relatively high proportion of emulsifiers in relation to the microemulsified phase and the continuous phase.
- the microemulsified phase is a hydrocarbyl amine the total quantity of emulsifiers is preferably from 2 to 25% wt. by weight of the total composition.
- the proportion of hydrocarbyl amine to lubricating base oil will depend on the total base number of the amine and that required in the finished oil.
- the TBN of the finished oil may be from 5 to 500 mgKOH/g preferably 20 to 100, and the proportion of hydrocarbyl amine may be from 1 to 20% by weight of total composition.
- the microemulsions may be prepared by simple mixing at room temperature.
- the emulsifiers are added to the base oil and then the hydrocarbyl amine.
- the primary function of the hydrocarbyl amine is to react with acidic products of combustion of the engine being lubricated. With high sulphur content fuels these combustion products will be sulphur oxides or acids giving amine sulphates as the reaction products. Amine sulphates tend to be crystalline solids with a tendency to settle out on cooler parts of the engine. It is necessary, therefore, for the lubricating composition to have a dispersant capable of holding the amine salts in suspension so that they are removed from the cylinder with the lubricant and other exhaust products.
- Dispersant additives capable of holding particulate solids, e.g. carbon, in suspension are well known in the lubricating oil art and suitable dispersants for use in the present invention may be selected from the known dispersant additives by suitable experiments and/or engine tests.
- Preferred dispersants are the polyisobutenyl succinimides. They may be of the mono- or bis- type, preferably the latter.
- the polyisobutenyl group may have from 8 to 200 carbon atoms and the amine used to form the compound may be a hydrocarbyl amine of the same type as that in the microemulsified phase, preferably an alkylene polyamine having a total of from 1 to 20 carbon atoms.
- the dispersant may be a known detergent additive, e.g. a barium, calcium or sodium phenate, sulphonate or carboxylate.
- a known detergent additive e.g. a barium, calcium or sodium phenate, sulphonate or carboxylate.
- Such additives are known ash-forming detergent additives, so in this embodiment the lubricant will be a low-ash rather than a wholly ashless composition.
- the amount of ash-forming material can be significantly reduced and may be from 0.1 to 5% wt. of the total composition.
- the hydrocarbyl amine is likely to have a relatively high TBN per unit of weight (particularly the preferred hydrocarbyl amines with from 1 to 20 C atoms) and could make a significant contribution to the TBN of the composition even if present in relatively small amounts by weight.
- Preferred compositions may contain from 1 to 10% wt. of hydrocarbyl amine and from 1 to 15% wt. of ash-forming detergent
- the contribution of the ash-forming detergent additive to the overall dispersancy may, however, not be sufficient in itself and may be supplemented by another dispersant additive, e.g. a polyisobutenyl succinimide as described above or one or more of the dispersants described below.
- another dispersant additive e.g. a polyisobutenyl succinimide as described above or one or more of the dispersants described below.
- Other dispersants for the hydrocarbyl amine sulphate reaction products may be alcohols and phenols having surfactant properties. These can be, for example, the type of organic compounds used to form the salts and overbased salts referred to above.
- Preferred compounds are alkyl and alkeny! alcohols or pheno!s having from 6 to 100 carbon atoms in the alkyl or alkenyl group. The group preferably has from 9 to 20 carbon atoms and is preferably a straight chain group.
- Exampes of suitable compounds are nonyl phenol, dodecanol, lauryl alcohol and stearyl alcohol.
- VI improvers are not normally required in marine diesel lubricants
- another type of dispersant may be a dispersant polymer used as a VI improver, e.g. a polyalkylmethacrylate.
- compositions of the present invention may contain other known additives suitable for use in diesel cylinder lubricants, e.g. corrosion inhibitors such as metal sulphonates.
- the total amount of dispersant may be from 1 to 30% wt., preferably from 5 to 20% wt. by weight of the total composition.
- some of the compounds contributing to the dispersancy may be present partly for other reasons and for other functions.
- a conventional ash-forming detergent may be present as indicated above and may contribute to the dispersancy.
- some of the dispersants listed above may be the same as the emulsifiers used to form the microemulsion (e.g. alkyl phenols). In such circumstances the quantity quoted above is the total quantity of dispersant in the composition irrespective of whether the dispersant has additional functions or not, it being impractical to apportion the total amount in respect of differing functions.
- a microemulsion of tetraethylene pentamine in a lubricating base oil was prepared using the following amounts of components by weight:-
- the polyisobutenyl mono-succinimide was an ashless dispersant sold by Orobis Limited under the Trade Name Oloa 1200.
- the lubricating base oil was a petroleum lubricating oil having a viscosity of 10.09 1 x 10-emz/s at 100°C and a viscosity index of 73.
- the microemulsion was prepared as follows.
- the oleic acid and nonyl phenol were added to half the weight of the base oil and stirred at room temperature.
- the tetraethylenepentamine was then added and stirred until homogeneous and clear.
- the polyisobutylene mono-succinimide was next added followed by the isopropanolamine and the rest of the base oil.
- microemulsion was found to be stable for a period of at least 2 years. It had a total base number of 59.
- composition was tested for suitability as a cylinder lubricant for a marine diesel engine using a 24 hour test in a Ruston engine.
- the Ruston engine test is carried out in a Ruston 7XHR diesel engine.
- the engine has a single piped oil supply which is the sole source of lubricant for the piston and rings.
- the piston and its rings Prior to the test, the piston and its rings are cleaned and the rings are weighed.
- the cylinder bore is measured in two diametrical positions at 30 stations along its length, covering the extent of ring travel.
- the engine is run for the test period with the lubricant under test being supplied to the cylinder and using a fuel having a nominal viscosity of 1500 seconds Redwood No 1 (3.7x10 -4 m 2 /S) at 38°C (100°F) and a sulphur content of approximately 2.75% by weight.
- the condition of the engine is rated on a demerit system, low numbers indicating good condition.
- the piston rings are re-weighed and the cylinder bore is remeasured in order to determine the wear rates on a 1000 hour basis.
- the wear rate obtained for the microemulsion composition was comparable to that of a conventional non-ashless diesel cylinder lubricant.
- a microemulsion of tetraethylene pentamine in a lubricating base oil was prepared using the following components:-
- the base oil was a petroleum lubricating oil having a viscosity of 17.6x 10-emz/s at 100°C.
- microemulsion was prepared as follows:-
- the oleic acid and nonyl phenol were added to half the weight of the base oil and stirred.
- the tetraethylenepentamine was then added together with the rest of the base oil and stirred. The whole operation was carried out at room temperature and the finished microemulsion had a TBN of 71.
- the overbased calcium phenate was an ash-forming alkaline marine cylinder lubricant additive sold by Orobis Limited under the Trade Name Oloa 219.
- the lubricating base oil was the same as that used for the microemulsion.
- the finished oil had a TBN of 70.
- the neutralisations were carried out by adding sulphuric acid dropwise to the stirred oils which were then stirred at 90°C for 10 minutes.
- Equal weights of the two neutralised oils were mixed with stirring giving, as the final product, a 90% neutralised half-ash microemulsion.
- a half-ash microemulsion of tetraethylenepentamine in a lubricating base oil was prepared using the following components:-
- overbased calcium phenate was the same as in Example 2.
- the polyisobutenyl succinimides were also supplied by Orobis Limited under the Trade Names indicated above.
- the lubricating base oil was a blend of distillate and bright stock oil chosen so that the finished composition was of SAE 50 grade viscosity (16.7 to 17.2x 1 0 -6 m 2 /S at 100°C).
- the microemulsion was prepared as follows.
- the oleic acid and nonyl phenol were added to half the weight of the base oil and stirred.
- the tetraethylene pentamine was then added and stirred until homogeneous and clear.
- the overbased calcium phenate, the polyisobutenyl succinimides and the rest of the base oil were then added and stirred at 50°C for 15 minutes.
- the finished microemulsion had a TBN of 69.5.
- a low-ash microemulsion of tetraethylenepentamine in a lubricating base oil was prepared using the following components:-
- the polyisobutenyl mono-succinimide was the same as in Example 3.
- the dispersant/detergent package was also supplied by Orobis Limited under the Trade Name indicated above.
- the package was a blend of overbased calcium phenate, polyisobutenyl bis- succinimide and metal sulphonate.
- the lubricating base oil was a blend of distillate and bright stock oil chosen so that the finished composition was of SAE 50 grade viscosity (16.7 to 17.2 x 10- B m 2 /s at 100° C).
- the microemulsion was prepared as follows.
- the oleic acid and nonyl phenol were added to half the weight of the base oil and stirred.
- the tetraethylenepentamine was then added and stirred until homogeneous and clear.
- the dispersant/detergent package (Oloa 853), polyisobutenyl mono-succinimide (Oloa 1200) and the rest of the base oil were added and stirred at 50°C for 15 minutes.
- the finished microemulsion had a TBN of 70.
- This composition (which had an ash content of 1.85%wt.) was tested for suitability as a cylinder lubricant for marine diesel engines using a 125 hour test in a Ruston engine.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Claims (8)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7831884 | 1978-08-01 | ||
| GB3188478 | 1978-08-01 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0008193A1 EP0008193A1 (fr) | 1980-02-20 |
| EP0008193B1 true EP0008193B1 (fr) | 1982-06-30 |
Family
ID=10498803
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP79301536A Expired EP0008193B1 (fr) | 1978-08-01 | 1979-08-01 | Composition lubrifiante et procédé pour la lubrification d'un moteur Diesel marin |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0008193B1 (fr) |
| JP (1) | JPS5521490A (fr) |
| CA (1) | CA1118750A (fr) |
| DE (1) | DE2963239D1 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0839840B2 (fr) † | 1996-10-29 | 2016-01-20 | Idemitsu Kosan Company Limited | Additif pour huile lubrifiante contenant un composé de succinimide et son utilisation dans les moteurs diesel |
| RU2598848C2 (ru) * | 2011-04-14 | 2016-09-27 | Тоталь Маркетин Сервис | Смазка цилиндра двухтактного судового двигателя |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1265506A (fr) * | 1984-11-21 | 1990-02-06 | Kirk Emerson Davis | Compositions a base d'alcoylphenol et de composes amines ainsi que huiles et carburants pour moteurs deux temps les renfermant |
| US4808325A (en) * | 1987-03-30 | 1989-02-28 | Amoco Corporation | Mannich dispersant VI-improver blended with phenolic compound for improved storage stability |
| GB8804171D0 (en) * | 1988-02-23 | 1988-03-23 | Exxon Chemical Patents Inc | Dispersant for marine diesel cylinder lubricant |
| WO1990002786A1 (fr) * | 1988-09-16 | 1990-03-22 | Idemitsu Kosan Co., Ltd. | Huile lubrifiante |
| SG55446A1 (en) | 1996-10-29 | 1998-12-21 | Idemitsu Kosan Co | Lube oil compositions for diesel engines |
| ES2447428T3 (es) * | 2006-10-11 | 2014-03-12 | Total Marketing Services | Lubricante marino para fuel con bajo y alto contenido de azufre |
| FR2932813B1 (fr) * | 2008-06-18 | 2010-09-03 | Total France | Lubrifiant cylindre pour moteur marin deux temps |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1068547A (en) * | 1963-12-26 | 1967-05-10 | Exxon Research Engineering Co | Metal carbonate overbased lubricant detergent-dispersants |
| US3346494A (en) * | 1964-04-29 | 1967-10-10 | Exxon Research Engineering Co | Microemulsions in liquid hydrocarbons |
| GB1386620A (en) * | 1972-06-01 | 1975-03-12 | British Petroleum Co | Lubricating composition |
| DE2622066A1 (de) * | 1975-05-23 | 1976-11-25 | Cooper Ltd Ethyl | Korrosionsinhibitoren fuer schmieroele |
-
1979
- 1979-07-27 CA CA000332715A patent/CA1118750A/fr not_active Expired
- 1979-07-30 JP JP9620579A patent/JPS5521490A/ja active Pending
- 1979-08-01 EP EP79301536A patent/EP0008193B1/fr not_active Expired
- 1979-08-01 DE DE7979301536T patent/DE2963239D1/de not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0839840B2 (fr) † | 1996-10-29 | 2016-01-20 | Idemitsu Kosan Company Limited | Additif pour huile lubrifiante contenant un composé de succinimide et son utilisation dans les moteurs diesel |
| RU2598848C2 (ru) * | 2011-04-14 | 2016-09-27 | Тоталь Маркетин Сервис | Смазка цилиндра двухтактного судового двигателя |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2963239D1 (en) | 1982-08-19 |
| CA1118750A (fr) | 1982-02-23 |
| JPS5521490A (en) | 1980-02-15 |
| EP0008193A1 (fr) | 1980-02-20 |
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