EP0092946A2 - Glycerol esters with oil-soluble copper compounds as fuel economy additives - Google Patents
Glycerol esters with oil-soluble copper compounds as fuel economy additives Download PDFInfo
- Publication number
- EP0092946A2 EP0092946A2 EP83302155A EP83302155A EP0092946A2 EP 0092946 A2 EP0092946 A2 EP 0092946A2 EP 83302155 A EP83302155 A EP 83302155A EP 83302155 A EP83302155 A EP 83302155A EP 0092946 A2 EP0092946 A2 EP 0092946A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- oil
- fuel economy
- copper
- glycerol
- composition
- 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.)
- Granted
Links
- 239000000446 fuel Substances 0.000 title claims abstract description 66
- 239000005749 Copper compound Substances 0.000 title claims abstract description 23
- 150000001880 copper compounds Chemical class 0.000 title claims abstract description 23
- 239000000654 additive Substances 0.000 title claims description 42
- 150000002314 glycerols Chemical class 0.000 title description 4
- 239000000203 mixture Substances 0.000 claims abstract description 53
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 47
- 239000010687 lubricating oil Substances 0.000 claims abstract description 32
- 239000010949 copper Substances 0.000 claims abstract description 23
- 229910052802 copper Inorganic materials 0.000 claims abstract description 22
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 20
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 18
- 229930195729 fatty acid Natural products 0.000 claims abstract description 18
- 239000000194 fatty acid Substances 0.000 claims abstract description 18
- 150000002148 esters Chemical class 0.000 claims abstract description 15
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 13
- 238000002485 combustion reaction Methods 0.000 claims abstract description 6
- 230000002301 combined effect Effects 0.000 claims abstract description 4
- 230000001747 exhibiting effect Effects 0.000 claims abstract 4
- 239000003921 oil Substances 0.000 claims description 46
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 claims description 21
- 230000000996 additive effect Effects 0.000 claims description 21
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 claims description 18
- 239000002270 dispersing agent Substances 0.000 claims description 11
- 239000007866 anti-wear additive Substances 0.000 claims description 9
- 239000003599 detergent Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- SVOAENZIOKPANY-CVBJKYQLSA-L copper;(z)-octadec-9-enoate Chemical compound [Cu+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O SVOAENZIOKPANY-CVBJKYQLSA-L 0.000 claims description 4
- 230000001050 lubricating effect Effects 0.000 claims description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 3
- AFSHUZFNMVJNKX-UHFFFAOYSA-N 1,2-di-(9Z-octadecenoyl)glycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCC=CCCCCCCCC AFSHUZFNMVJNKX-UHFFFAOYSA-N 0.000 claims description 3
- AFSHUZFNMVJNKX-LLWMBOQKSA-N 1,2-dioleoyl-sn-glycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](CO)OC(=O)CCCCCCC\C=C/CCCCCCCC AFSHUZFNMVJNKX-LLWMBOQKSA-N 0.000 claims description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 3
- 239000011701 zinc Substances 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 239000005642 Oleic acid Substances 0.000 claims description 2
- -1 glycerol fatty acid ester Chemical class 0.000 description 28
- 238000012360 testing method Methods 0.000 description 13
- 239000003963 antioxidant agent Substances 0.000 description 12
- 235000006708 antioxidants Nutrition 0.000 description 12
- 230000003078 antioxidant effect Effects 0.000 description 11
- 238000009472 formulation Methods 0.000 description 7
- 239000003607 modifier Substances 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 239000002480 mineral oil Substances 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 5
- 235000010446 mineral oil Nutrition 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 229910052728 basic metal Inorganic materials 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000003502 gasoline Substances 0.000 description 4
- 235000020778 linoleic acid Nutrition 0.000 description 4
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 4
- 229920000768 polyamine Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 150000003818 basic metals Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 150000001879 copper Chemical class 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 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
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical class CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000001186 cumulative effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- FABAOYOFJNAVHB-KVVVOXFISA-N (z)-octadec-9-enoic acid;propane-1,2,3-triol Chemical class OCC(O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O FABAOYOFJNAVHB-KVVVOXFISA-N 0.000 description 1
- 150000005206 1,2-dihydroxybenzenes Chemical class 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
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- JXSRRBVHLUJJFC-UHFFFAOYSA-N 7-amino-2-methylsulfanyl-[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile Chemical compound N1=CC(C#N)=C(N)N2N=C(SC)N=C21 JXSRRBVHLUJJFC-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical class [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 229920000089 Cyclic olefin copolymer Chemical class 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical class C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- 125000005595 acetylacetonate group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006388 chemical passivation reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000010835 comparative analysis Methods 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- KGGZTXSNARMULX-UHFFFAOYSA-L copper;dicarbamodithioate Chemical class [Cu+2].NC([S-])=S.NC([S-])=S KGGZTXSNARMULX-UHFFFAOYSA-L 0.000 description 1
- VNZQQAVATKSIBR-UHFFFAOYSA-L copper;octanoate Chemical compound [Cu+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O VNZQQAVATKSIBR-UHFFFAOYSA-L 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 239000003879 lubricant additive Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 239000010707 multi-grade lubricating oil Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 125000005608 naphthenic acid group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/04—Hydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/28—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/38—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
- C10M129/40—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms monocarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/56—Acids of unknown or incompletely defined constitution
- C10M129/58—Naphthenic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/68—Esters
- C10M129/76—Esters containing free hydroxy or carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
-
- 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
- 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
- C10M2205/026—Butene
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/06—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing conjugated dienes
-
- 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
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Definitions
- British Application 2097813A published November 10, 1982, discloses the use of 0.05 to 0.2 wt% glycerol partial esters of C 16 -C 18 fatty acids as fuel economy additives.
- the present invention is an improvement over said British application.
- West German Application P-2949940 and P-2949910 of Chevron Research Company both published July 3, 1980, disclose the use of glycerol fatty esters as fuel economy additives. These references state that the addition of 0.25 to 2 weight percent, preferably 0.40 to 1.25 weight percent, of a fatty acid ester will offer a fuel economy credit of 2-3 percent in both gasoline and diesel engines. Glycerol oleic acid esters are preferred.
- West German Application P-2949940 illustrates the preferred embodiment showing the use of the glycerol ester at the same treat level in combination with zinc dihydrocarbyl dithiophosphate additives.
- U.S. Patent 4,304,678 discloses hydroxyl-containing esters including glycerol oleates as being effective friction modifiers only at levels of 1-4 wt% with no benefit observed at levels less than 1% by wt. in oil.
- the present invention is based upon the discovery that very low levels of glycerol esters; that is, up to about 0.2 percent by weight, in combination with certain amounts of oil-soluble organic copper compounds, provide enhanced performance of these fuel economy lubricating oils. No benefit is obtainable in using relatively higher amounts and in some cases substantial debits in terms of formulation stability or adverse performance may occur.
- U.S. Patent 3,933,659 shows a multi-component functional fluid, one component of which can be a polyol ester friction modifier or a fatty acid amide friction modifier.
- the primary use disclosed in that reference is for automatic transmission fluids.
- U.S. Patent 3,273,981 discloses antiwear additives comprising a mixture of dimer acids and a partial ester of a polyhydric alcohol, the additive being noted as improving lubricity as well as functioning in the anti-wear category.
- U.S. Patent 3,112,271 discloses glycerol mono-oleate as an extreme pressure additive as does U.S. 3,112,269 and U.S. 3,041,284.
- U.S. 2,493,483 discloses marine engine lubricants which contain a partial ester of glycerol or other polyol fatty acid esters in amounts of from 0.05 to 1 percent.
- oil-soluble copper compounds at levels of about 5 to 500 parts per million (ppm) of copper by weight, based on the total weight of lubricating oil composition,as a highly effective antioxidant is a relatively recent development of additive technology and is disclosed in European Published Application No. 0024146, published on February 25, 1981.
- fuel economy improving lubricating oil compositions for internal combustion engines which comprise an oil of lubricating viscosity and, as the fuel economy additive, a combination from 0.05 to 0.20 weight percent of a glycerol partial ester of a C 16 -C 18 fatty acid with from 5 to 500 ppm (parts per million) copper present in the form of an oil-soluble copper compound, preferably about 60 to 200 ppm copper being present, based upon the weight of the total composition, the copper compound also functioning as an antioxidant.
- the lubricating oil compositions of the present invention comprise both straight grade and multigrade lubricating oil formulations for both gasoline and diesel (compression ignition) engines.
- the lubricating oil compositions will contain those additive systems formulated to meet the viscosity requirements or other specifications as required for qualification as a gasoline engine or diesel lubricating oil.
- a straight grade lubricating oil formulation will normally contain conventional amounts of an ashless dispersant, a normal or basic metal detergent, an anti-wear additive and an antioxidant and a multi-grade oil will contain, in addition to the foregoing, a viscosity index improver or viscosity modifier.
- very small proportions of other special purpose additives such as pour depressants, rust inhibitors, anti-foamants and the like are conventionally blended into lubricating oil compositions.
- the ester component of the fuel economy additive of the present invention is preferably a glycerol mono- or diester of a saturated or unsaturated C 16 -C 18 fatty acid, such as oleic or linoleic acid.
- Optimum efficiency has been found to be at about the 0.1 to 0.2 weight percent level and use in the excess of this amount may even be detrimental to the overall performance of the lubricating oil composition.
- Oil-soluble copper components useful herein include both cuprous or cupric compounds which are oil-soluble under normal blending conditions in the oil additive package. Particularly preferred are the copper salts of C 10 -C 22 fatty acids, such as stearic or palmitic acid, but copper salts of unsaturated acids, such as oleic acid, linoleic acid, naphthenic acid of 200-500 molecular weight or synthetic carboxylic acids are preferred.
- the particularly preferred embodiment is copper (cupric) oleate when present in an amount to provide about 100 to 150 ppm copper in the lubricating oil composition.
- Crankcase oil formulations to which the present invention relates are those which contain a major amount of lubricating oil and effective amounts of conventional additives in addition to the aforesaid fuel economy additive, the copper compound serving the dual function of being both an antioxidant and, in combination with the glycerol oleate, a fuel economy additive.
- Percentages of additives as described herein are by weight based on the total weight of lubricating oil formulation unless otherwise indicated.
- Detergents useful in the formulations include the normal, basic or overbased metal, that is, calcium, magnesium and so forth, salts of petroleum naphthenic acids, petroleum sulfonic acids, alkyl benzene sulfonic acids, alkyl phenols, alkylene-bis-phenol, oil-soluble fatty acids and the like.
- the preferred materials are the normal or overbased calcium or magnesium phenates, sulfurized phenates and/or sulfonates, and these metal-containing detergent additives are typically used in amounts of from 1 to 3 wt % based on the total weight of lubricating oil compositions.
- Suitable pour point depressants which are usually present in amounts of about 0.01 to 1 wt.%, include wax alkylated aromatic hydrocarbons, olefin polymers and copolymers, acrylate and methacrylate polymers and copolymers.
- Anti-wear additives generally are the oil-soluble zinc dihydrocarbyl dithiophosphates having a least a total of 5 carbon atoms, the alkyl group being preferably C 2 -C S . These are typically present in amounts of from 0.01 to 5 wt. %, preferably 0.5 to 1.5 wt. %, in the lubricating oil.
- Suitable conventional viscosity index improvers, or viscosity modifiers are the olefin polymers such as polybutene, ethylene-propylene copolymers, hydrogenated polymers and copolymers and terpolymers of styrene with isoprene and/or butadiene, polymers of alkyl acrylates or alkyl methacrylates, copolymers of alkylmethacrylates with N-vinyl pyrrolidone or dimethylaminoalkyl methacrylate, post-grafted polymers of ethylene-propylene with an active monomer, such as maleic anhydride, which may be further reacted with an alcohol or an alkylene polyamine, styrene-maleic anhydride polymers post- reacted with alcohols and amines and the like. These additives are used in amounts of about 1.5% to 15% by wt., depending on the exact viscosity specifications desired.
- antioxidants include phenols, hindered phenols, bis-pheno1s, sulfurized phenols, catechol, alkylated and sulfurized alkylated catechols, diphenylamine, alkylated diphenylamines and phenyl-l-naphthylamines, alkyl and aryl borates, phosphites and phosphates, trialkyl and triaryl dithiophosphates and the like.
- Suitable hydrocarbon base stocks are those mineral oils of lubricating viscosity as measured by ASTM D-455 of from about 2 to 40, preferably 5 to 20 centistokes at 99 0 C.
- the reference oil used in this example was a formulated straight grade 20W30 crankcase mineral lubricating oil (corresponding to ASTM "HR" oil) to which was added 0.2 weight percent of a glycerol monooleate (GMO) fuel economy additive or 0.2 weight percent of a fuel economy additive being a mixture (GMO/GDO) of glycerol monooleate and glycerol dioleate in a weight ratio of 3 parts of GMO to 2 parts of GDO in said mixture.
- the reference oil contained 2.10 wt % dispersant, 1.10 wt. % antioxidant, 1.00 wt. % basic metal detergent, 1. 95 wt.
- results are expressed as a percentage fuel economy credit with respect to the referenced oil, as are all fuel economy credit results reported in the Examples.
- Results at the 0.2 wt. % treat level for both GMO and the GMO/GDO mixture are set forth in Table I.
- Example 1 The Laboratory Fuel Economy Test of Example 1 was repeated utilizing a 10W40 multigrade mineral oil containing 0.09 wt. % of the GMO/GDO mixture as the fuel economy additive.
- the oil contained about 14% by wt. of a multifunctional dispersant viscosity index improver (acryloid 1155), 0.5% dispersant, 1.85% of basic metal detergent, 0.75 wt.% of anti-wear additive and 0.75% antioxidant.
- Table III shows the fuel economy credits over the oil used as the reference in Example 1. Laboratory Fuel economy results were confirmed in the Proposed ASTM 5 Car Interim Fuel Economy Procedure which utilized the EPA car certification cycle in 5 automobiles having engine sizes of 2.3 liter, 2.8 liter, 3.7 liter, 3.8 liter and 5.0 liter. Five Car average fuel economy credit of 1.64% was obtained in one series of fuel economy tests.
- Example 6 This will be demonstrated in Example 6.
- Example 1-4 and 6 are presented here to illustrate these principles.
- the LEFET test was carried out using an Oil * equivalent to the HR straight grade oil of Example 1 except that 0.3 wt. % of a 40 wt% solution of copper oleate in mineral oil, which is equivalent to 120 ppm copper was used in place of the anti- oxidant reported in Example 1.
- the LEFET results for this test are below in Table IV:
- oils containing both the oil-soluble organic copper compound and glycerol ester friction modifier would exhibit any complementary effect
- different oils were formulated and tested in Ford 2.3 liter 4-cylinder engine.
- the purpose of these tests was to evaluate the increase in fuel economy credits when the copper compound and the glycerol ester were combined over the credits obtained with these additives separately in the same engine.
- Fuel economy credit values will vary among engines of differing sizes. This is due to the inherent differences in engine design and operating conditions. It is known therefore that the values for a 2.3 liter 4-cylinder engine will be lower than fuel economy credit values for a 5 liter 8-cylinder used in these examples.
- balance is basestock mineral oil.
- Oil D represents the advantage of this invention. Oils B, C, E show the maximum values one can expect to obtain based on the credits due only to the copper compound. Oil D, however, achieves a value of 0.9%. This result is not expected because it is known, as a general principle, that merely increasing the treatment level of a given fuel economy additive does not increase the credit obtained.
- Oil G was a formulated lubricating oil having 4 wt% dispersant, 1 wt% overbased metal sulfonate, 1.5 wt% antioxidant and 2 wt% anti-wear additive.
- Oil H was the same as Oil G , except for the inclusion of 0.1 wt% dimerized linoleic acid ester of diethylene glycol as disclosed in U.S. Patent 4, 105, 571.
- Oil I was the same as Oil G except 0.2 wt% of the GMO/GDO ester was added.
- Oil J was the same as Oil G except both 0.1 wt% of the dimerized linoleic acid ester and 0.2 wt% of the GMO/GDO were added. Fuel economy results for these four oils are shown below in Table V I .
- Oil K contained 5.5 wt% dispersant, 1 wt% overbased metal sulfonate, 1.4 wt% anti-wear additive and 1 wt% anti-oxidant.
- Oil L was the same as Oil K with .0.3 wt% of a 40 wt% solution of copper oleate (120 ppm copper) included and Oil M was the same as Oil L except 0.1 wt% of the GMO/GDO glycerol oleate was included.
- Fuel economy credits are in Table VII below.
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Abstract
Description
- This invention relates to lubricating oil compositions which exhibit marked improvements in fuel economy. More particularly, this invention relates to lubricating oil compositions which contain very minor proportions of a glycerol fatty acid ester fuel economy additive in combination with an oil-soluble organic copper compound.
- It is a current objective of the industry to provide lubricating oil compositions which exhibit improvements in fuel savings in gasoline and diesel engine vehicles. To meet that current goal, a new category of additives commonly referred to as fuel economy additives are being developed which function primarily to increase the miles or kilometers obtained per unit volume of fuel. Since modern day lubricating oil compositions are complex formulations, such additives must be compatible with the other components of such compositions and should not adversely affect the numerous other functions of conventional lubricant additives such as dispersancy, viscosity stability, corrosion and oxidation inhibition, and the like.
- Illustrative of recent patents reflecting developments in this field are U.S. Patents 4,201,684 and 4,208,293. These patents show the use of fatty acid amides and sulfurized amides as additives which have fuel economy benefits as demonstrated by friction reducing data.
- The present invention concerns the use of glycerol fatty acid esters as such fuel economy additives, specifically glycerol esters of C16-C18 fatty acids in combination with oil-soluble copper organic compounds. There is prior art disclosing the use of each of these materials in lubricating oil compositions which is discussed hereinbelow.
- British Application 2097813A, published November 10, 1982, discloses the use of 0.05 to 0.2 wt% glycerol partial esters of C16-C18 fatty acids as fuel economy additives. The present invention is an improvement over said British application.
- West German Application P-2949940 and P-2949910 of Chevron Research Company, both published July 3, 1980, disclose the use of glycerol fatty esters as fuel economy additives. These references state that the addition of 0.25 to 2 weight percent, preferably 0.40 to 1.25 weight percent, of a fatty acid ester will offer a fuel economy credit of 2-3 percent in both gasoline and diesel engines. Glycerol oleic acid esters are preferred. West German Application P-2949940 illustrates the preferred embodiment showing the use of the glycerol ester at the same treat level in combination with zinc dihydrocarbyl dithiophosphate additives. Similarly U.S. Patent 4,304,678 discloses hydroxyl-containing esters including glycerol oleates as being effective friction modifiers only at levels of 1-4 wt% with no benefit observed at levels less than 1% by wt. in oil.
- In contrast to the teachings of these references, the present invention is based upon the discovery that very low levels of glycerol esters; that is, up to about 0.2 percent by weight, in combination with certain amounts of oil-soluble organic copper compounds, provide enhanced performance of these fuel economy lubricating oils. No benefit is obtainable in using relatively higher amounts and in some cases substantial debits in terms of formulation stability or adverse performance may occur.
- Another reference disclosing the use of polyol- carboxylic acid esters in lubricating oil compositions is U.S. Patent 3,933,659, which shows a multi-component functional fluid, one component of which can be a polyol ester friction modifier or a fatty acid amide friction modifier. The primary use disclosed in that reference is for automatic transmission fluids. U.S. Patent 3,273,981 discloses antiwear additives comprising a mixture of dimer acids and a partial ester of a polyhydric alcohol, the additive being noted as improving lubricity as well as functioning in the anti-wear category. U.S. Patent 3,112,271 discloses glycerol mono-oleate as an extreme pressure additive as does U.S. 3,112,269 and U.S. 3,041,284. U.S. 2,493,483 discloses marine engine lubricants which contain a partial ester of glycerol or other polyol fatty acid esters in amounts of from 0.05 to 1 percent.
- Other references disclosing polyol esters of fatty acids are represented.by U.S. 2,788,326, which discloses these compounds as being useful in extreme pressure lubricants and U.S. Patent 2,527,889, which shows the same polyol esters, such as glycerol monooleate, being useful as anti-corrosion agents in turbine oils and diesel fuels.
- The use of oil-soluble copper compounds at levels of about 5 to 500 parts per million (ppm) of copper by weight, based on the total weight of lubricating oil composition,as a highly effective antioxidant is a relatively recent development of additive technology and is disclosed in European Published Application No. 0024146, published on February 25, 1981.
- The present invention is based on the discovery that these copper compounds, when used in an oil in combination with glycerol esters, e.g. oleates, act cooperatively with the glycerol ester in substantially increasing the fuel economy of the formulated oil. The cumulative effect observed would not be expected by adding the fuel economy credit obtained in oils which contain one or the other of the glycerol ester or copper compound. Data obtained therefore provide the basis for an unexpected additive effect upon fuel economy due to more effective lubrication of an internal combustion engine operated using the oils of the present invention.
- The prior art also recognizes that copper components per se can be favorable friction reducing agents in certain circumstances. German Democratic Republic Patents 145,469 and 145,470 disclose the reduction of wear and friction in iron/iron and iron/bronze friction interfaces using polyol or mineral oil lubricants containing copper compounds such as copper naphthenate, copper octoate, copper stearate and reaction products of lubricants themselves with copper, copper oxide and copper salts of inorganic acids. These references indicate that the friction reduction is achieved by deposition on the substrate being lubricated of a film reaction layer of copper with adequate adhesion properties. It is recommended in these references that the concentration of the copper compound in the lubricant provide a copper content of 0.001 to 5 volume % relative to the lubricant. These references however did not evaluate lubricating oil compositions for internal combustion engines.
- In accordance with the present invention, there are provided fuel economy improving lubricating oil compositions for internal combustion engines which comprise an oil of lubricating viscosity and, as the fuel economy additive, a combination from 0.05 to 0.20 weight percent of a glycerol partial ester of a C16-C18 fatty acid with from 5 to 500 ppm (parts per million) copper present in the form of an oil-soluble copper compound, preferably about 60 to 200 ppm copper being present, based upon the weight of the total composition, the copper compound also functioning as an antioxidant.
- The lubricating oil compositions of the present invention comprise both straight grade and multigrade lubricating oil formulations for both gasoline and diesel (compression ignition) engines. Thus, in the practice of the present invention the lubricating oil compositions will contain those additive systems formulated to meet the viscosity requirements or other specifications as required for qualification as a gasoline engine or diesel lubricating oil. A straight grade lubricating oil formulation will normally contain conventional amounts of an ashless dispersant, a normal or basic metal detergent, an anti-wear additive and an antioxidant and a multi-grade oil will contain, in addition to the foregoing, a viscosity index improver or viscosity modifier. In addition to these principal additives, very small proportions of other special purpose additives, such as pour depressants, rust inhibitors, anti-foamants and the like are conventionally blended into lubricating oil compositions.
- The ester component of the fuel economy additive of the present invention is preferably a glycerol mono- or diester of a saturated or unsaturated C16-C18 fatty acid, such as oleic or linoleic acid. Optimum efficiency has been found to be at about the 0.1 to 0.2 weight percent level and use in the excess of this amount may even be detrimental to the overall performance of the lubricating oil composition.
- Oil-soluble copper components useful herein include both cuprous or cupric compounds which are oil-soluble under normal blending conditions in the oil additive package. Particularly preferred are the copper salts of C10-C22 fatty acids, such as stearic or palmitic acid, but copper salts of unsaturated acids, such as oleic acid, linoleic acid, naphthenic acid of 200-500 molecular weight or synthetic carboxylic acids are preferred. The particularly preferred embodiment is copper (cupric) oleate when present in an amount to provide about 100 to 150 ppm copper in the lubricating oil composition.
- Other suitable copper compounds include the same as those disclosed in said European Published Application 0024146 and these include copper dithiocarbamates of the formula (RR'NCSS)nCu where n is 1 or 2 and R and R' are the same or different Cl-Cl8 hydrocarbyl radicals, preferably C2-C8 alkyl, copper sulphonates, copper phenates and acetyl acetonates as well as copper dihydrocarbyl dithiophosphate, the hydrocarbyl being C1-C18 and preferably C2-C8 alkyl, such as a hexyl or isooctyl.
- Crankcase oil formulations to which the present invention relates are those which contain a major amount of lubricating oil and effective amounts of conventional additives in addition to the aforesaid fuel economy additive, the copper compound serving the dual function of being both an antioxidant and, in combination with the glycerol oleate, a fuel economy additive. Percentages of additives as described herein are by weight based on the total weight of lubricating oil formulation unless otherwise indicated.
- These conventional additives comprise ashless dispersants typically nitrogen-containing dispersant additives which are oil-soluble salts, amides, imides and esters made from high molecular weight mono- or di-carboxylic acids and various amines having an amino or heterocyclic nitrogen with at least one amido or hydroxy group capable of salt, amide or ester formation. Preferred are the reaction products of polyolefin (C2-C5 olefin), such as polyisobutenyl, succinic anhydride with an alkylene polyamine such as tetraethylenepentamine. The polyisobutenyl portion has between 50 and 250 carbon atoms. The alkylene polyamines are those represented by the formula:
NH2(CH2)n(NH(CH2)n)m-NH2
where n is 2 to 3 and m is a number from 0 to 10. Mixtures of alkylene polyamines which approximate tetraethylenepentamine are commercially available materials. Dispersants are used generally in amounts of from about 0.1 to 10 wt.%, preferably in the range of about 0.5 to 5 wt %, based on the weight of the lubricating oil composition. - Detergents useful in the formulations include the normal, basic or overbased metal, that is, calcium, magnesium and so forth, salts of petroleum naphthenic acids, petroleum sulfonic acids, alkyl benzene sulfonic acids, alkyl phenols, alkylene-bis-phenol, oil-soluble fatty acids and the like. The preferred materials are the normal or overbased calcium or magnesium phenates, sulfurized phenates and/or sulfonates, and these metal-containing detergent additives are typically used in amounts of from 1 to 3 wt % based on the total weight of lubricating oil compositions.
- Suitable pour point depressants, which are usually present in amounts of about 0.01 to 1 wt.%, include wax alkylated aromatic hydrocarbons, olefin polymers and copolymers, acrylate and methacrylate polymers and copolymers.
- Anti-wear additives generally are the oil-soluble zinc dihydrocarbyl dithiophosphates having a least a total of 5 carbon atoms, the alkyl group being preferably C2-CS. These are typically present in amounts of from 0.01 to 5 wt. %, preferably 0.5 to 1.5 wt. %, in the lubricating oil.
- Suitable conventional viscosity index improvers, or viscosity modifiers, are the olefin polymers such as polybutene, ethylene-propylene copolymers, hydrogenated polymers and copolymers and terpolymers of styrene with isoprene and/or butadiene, polymers of alkyl acrylates or alkyl methacrylates, copolymers of alkylmethacrylates with N-vinyl pyrrolidone or dimethylaminoalkyl methacrylate, post-grafted polymers of ethylene-propylene with an active monomer, such as maleic anhydride, which may be further reacted with an alcohol or an alkylene polyamine, styrene-maleic anhydride polymers post- reacted with alcohols and amines and the like. These additives are used in amounts of about 1.5% to 15% by wt., depending on the exact viscosity specifications desired.
- Conventionally used antioxidants include phenols, hindered phenols, bis-pheno1s, sulfurized phenols, catechol, alkylated and sulfurized alkylated catechols, diphenylamine, alkylated diphenylamines and phenyl-l-naphthylamines, alkyl and aryl borates, phosphites and phosphates, trialkyl and triaryl dithiophosphates and the like.
- Suitable hydrocarbon base stocks are those mineral oils of lubricating viscosity as measured by ASTM D-455 of from about 2 to 40, preferably 5 to 20 centistokes at 990C.
- These conventional additives are used in amounts normally necessary to provide their attendant functions in a formulated crankcase lubricating oil composition. Very small proportions of additional special purpose additives, such as anti-foam agents or rust inhibitors, may also be present in a fully formulated lubricating oil composition.
- The invention is further illustrated by the following Examples.
- The reference oil used in this example was a formulated straight grade 20W30 crankcase mineral lubricating oil (corresponding to ASTM "HR" oil) to which was added 0.2 weight percent of a glycerol monooleate (GMO) fuel economy additive or 0.2 weight percent of a fuel economy additive being a mixture (GMO/GDO) of glycerol monooleate and glycerol dioleate in a weight ratio of 3 parts of GMO to 2 parts of GDO in said mixture. The reference oil contained 2.10 wt % dispersant, 1.10 wt. % antioxidant, 1.00 wt. % basic metal detergent, 1. 95 wt. % anti- wear additive, 0.21 wt % pour depressant and 0.001 wt. % anti-foam agent. This type of reference oil, which is generally accepted by the industry for establishing fuel economy data, provides a reproducible baseline against which fuel economy credits may be measured and is considered to provide test results which accurately reflect the effect of a given fuel economy additive.
- Fuel economy was evaluated using the Laboratory Engine Fuel Economy Test (LEFET) summarized below:
- The fuel economy test used is a fired engine procedure. The engine is a 5.0 liter, V-8 Chevrolet engine coupled to a water cooled electric dynamometer. The engine is run with a dry sump by the use of external oil pumps. One pump supplies oil to the oil gallery from an external sump and a second pump scavenges the sump and returns the oil to the external sump. The conditions that the engine runs at are as follows:
-
-
- (a) Comparative evaluations utilizing increased amounts of the GMO/GDO mixture, that is, at the 0.3 weight percent and 0.5 weight percent levels showed no increase in fuel economy credit for treatment at these levels and in some cases, an adverse effect on fuel economy credits or other lubricating oil performance criteria, such as increased piston deposit formation tendencies or poor results in bearing corrosion tests.
- (b) Coefficient of friction (CF) testing using a Roxana Four-ball wear tester in acordance with the procedure described in ASTM D2266-67 at 110°C, 2.5 RPM at both 15 kg and 3 kg was carried out with a formulated mineral oil (Base oil) containing conventional amounts of dispersant (2.12 %), basic metal sulfonate (1.02%), antioxidant (0.72%), anti-wear additive (1.96%) and viscosity index improver (only present at 8.7 wt. % in test oils 5 and 6 to evaluate compatibility) to which was added varying amounts of the GDO/GMO mixture. The results in Table II below show essentially no additional friction reducing benefit at levels in excess of 0.2 wt. % and, at 0.9 wt. % in the test, potential instability or incompatibility was observed since the samples appeared hazy.
- (a) The Laboratory Fuel Economy Test of Example 1 was repeated utilizing a 10W40 multigrade mineral oil containing 0.09 wt. % of the GMO/GDO mixture as the fuel economy additive. The oil contained about 14% by wt. of a multifunctional dispersant viscosity index improver (acryloid 1155), 0.5% dispersant, 1.85% of basic metal detergent, 0.75 wt.% of anti-wear additive and 0.75% antioxidant.
- Table III shows the fuel economy credits over the oil used as the reference in Example 1.
- Based upon these results one would expect that the fuel economy credits attributed to a glycerol mono-oleate to be non-cumulative when the treatment level is increased above the range of about 0.1 wt. % to 0.2 wt. % and the inventors hereof have found this principle is generally true in fuel economy additives technology, i.e., increasing the amount of friction modifier additive does not result in a concomitant straight line proportional increase in the observed fuel economy. For example, combining the glycerol oleate mixed esters described above with a known fuel economy additive such as a dimerized linoleic acid ester as described in U.S. Patent 4,105,571 has been found to offer no better fuel economy than when either compound is used alone. This will be demonstrated in Example 6. Thus, as a general rule increasing the treat level of the friction modifier itself or increasing the treat level by adding another friction modifier known to have fuel economy benefits has not heretofore been found to offer a fuel economy improvement. Examples 1-4 and 6 are presented here to illustrate these principles.
- Evaluation of Copper Compounds for Fuel Economy
- The LEFET test was carried out using an Oil* equivalent to the HR straight grade oil of Example 1 except that 0.3 wt. % of a 40 wt% solution of copper oleate in mineral oil, which is equivalent to 120 ppm copper was used in place of the anti- oxidant reported in Example 1. The LEFET results for this test are below in Table IV:
- This example establishes that copper does provide a significant fuel economy credit in addition to its antioxidant effectiveness.
- The foregoing examples, carried out in fired engine tests using a 5.0 liter 8-cylinder engine demonstrate that the oil-soluble organic copper compounds offer a beneficial fuel economy credit and that the glycerol ester offers a fuel economy credit which does not increase to any significant degree above the 0.2 wt. % treat level.
- To determine if oils containing both the oil-soluble organic copper compound and glycerol ester friction modifier would exhibit any complementary effect, different oils were formulated and tested in Ford 2.3 liter 4-cylinder engine. The purpose of these tests was to evaluate the increase in fuel economy credits when the copper compound and the glycerol ester were combined over the credits obtained with these additives separately in the same engine. Fuel economy credit values will vary among engines of differing sizes. This is due to the inherent differences in engine design and operating conditions. It is known therefore that the values for a 2.3 liter 4-cylinder engine will be lower than fuel economy credit values for a 5 liter 8-cylinder used in these examples.
-
-
- Oil D represents the advantage of this invention. Oils B, C, E show the maximum values one can expect to obtain based on the credits due only to the copper compound. Oil D, however, achieves a value of 0.9%. This result is not expected because it is known, as a general principle, that merely increasing the treatment level of a given fuel economy additive does not increase the credit obtained.
- To demonstrate the principle that fuel economy additives, when combined together, cannot be expected to have a combined effect. The following oils G, H, I and J were evaluated for fuel economy in the 5.0 L engine using the same LEFET procedure of Example I. Oil G was a formulated lubricating oil having 4 wt% dispersant, 1 wt% overbased metal sulfonate, 1.5 wt% antioxidant and 2 wt% anti-wear additive. Oil H was the same as Oil G, except for the inclusion of 0.1 wt% dimerized linoleic acid ester of diethylene glycol as disclosed in U.S. Patent 4, 105, 571. Oil I was the same as Oil G except 0.2 wt% of the GMO/GDO ester was added. Oil J was the same as Oil G except both 0.1 wt% of the dimerized linoleic acid ester and 0.2 wt% of the GMO/GDO were added. Fuel economy results for these four oils are shown below in Table VI.
- The positive effect on fuel economy attributable to use of the two component fuel economy additive of this invention is further demonstrated by LEFET results in the 5.0 L engine and these data confirm the results shown above in Example 5. Here Oil K contained 5.5 wt% dispersant, 1 wt% overbased metal sulfonate, 1.4 wt% anti-wear additive and 1 wt% anti-oxidant. Oil L was the same as Oil K with .0.3 wt% of a 40 wt% solution of copper oleate (120 ppm copper) included and Oil M was the same as Oil L except 0.1 wt% of the GMO/GDO glycerol oleate was included. Fuel economy credits are in Table VII below.
Claims (11)
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US37100882A | 1982-04-22 | 1982-04-22 | |
US371008 | 1982-04-22 |
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EP0092946B1 EP0092946B1 (en) | 1988-03-16 |
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Cited By (28)
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FR2505355A1 (en) * | 1981-05-06 | 1982-11-12 | Exxon Research Engineering Co | LUBRICATING OIL COMPOSITION CONTAINING A PARTIAL GLYCEROL ESTER |
EP0260863A2 (en) * | 1986-09-15 | 1988-03-23 | Exxon Research And Engineering Company | Lubricating oil |
EP0280579A2 (en) * | 1987-02-27 | 1988-08-31 | Exxon Chemical Patents Inc. | Low phosphorus/low zinc lubricants |
EP0294045A2 (en) * | 1987-05-11 | 1988-12-07 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
FR2634780A1 (en) * | 1988-08-01 | 1990-02-02 | Lubrizol Corp | LUBRICATING OIL AND CONCENTRATE COMPOSITION FOR PREPARATION CONTAINING CARBOXYLIC DERIVATIVE COMPOSITION, ESTER AND DIHYDROCARBYLDITHIOPHOSPHORIC ACID METAL SALT |
US4938881A (en) * | 1988-08-01 | 1990-07-03 | The Lubrizol Corporation | Lubricating oil compositions and concentrates |
US4952328A (en) * | 1988-05-27 | 1990-08-28 | The Lubrizol Corporation | Lubricating oil compositions |
US4956108A (en) * | 1987-07-29 | 1990-09-11 | Mobil Oil Corporation | Copper salts of thiodipropionic acid derivatives as antioxidant additives process of making the same and fuel composition thereof |
US4957651A (en) * | 1988-01-15 | 1990-09-18 | The Lubrizol Corporation | Mixtures of partial fatty acid esters of polyhydric alcohols and sulfurized compositions, and use as lubricant additives |
US4981602A (en) * | 1988-06-13 | 1991-01-01 | The Lubrizol Corporation | Lubricating oil compositions and concentrates |
US5013467A (en) * | 1987-09-16 | 1991-05-07 | Exxon Chemical Patents Inc. | Novel oleaginous composition additives for improved rust inhibition |
US5021173A (en) * | 1988-02-26 | 1991-06-04 | Exxon Chemical Patents, Inc. | Friction modified oleaginous concentrates of improved stability |
US5049290A (en) * | 1987-05-11 | 1991-09-17 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
US5102566A (en) * | 1987-10-02 | 1992-04-07 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines (pt-727) |
US5141657A (en) * | 1987-10-02 | 1992-08-25 | Exxon Chemical Patents Inc. | Lubricant compositions for internal combustion engines |
US5244591A (en) * | 1992-03-23 | 1993-09-14 | Chevron Research And Technology Company | Lubricating oil compositions for internal combustion engines having silver bearing parts |
US5320765A (en) * | 1987-10-02 | 1994-06-14 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines |
EP0652279A1 (en) * | 1993-06-07 | 1995-05-10 | Ethyl Corporation | Fuel economy and oxidation inhibition in lubricant compositions for internal combustion engines |
US6254849B1 (en) * | 1999-07-28 | 2001-07-03 | Chevron U.S.A. Inc. | Zeolite SSZ-52 |
WO2001059037A2 (en) * | 2000-02-14 | 2001-08-16 | Exxonmobil Research And Engineering Company | Lubricating oils having improved fuel economy retention properties |
EP1925655A1 (en) | 2006-11-22 | 2008-05-28 | Infineum International Limited | Lubricating oil compositions |
EP2161326A1 (en) | 2008-09-05 | 2010-03-10 | Infineum International Limited | Lubricating oil compositions |
EP2390306A1 (en) | 2009-12-01 | 2011-11-30 | Infineum International Limited | A lubricating oil composition |
WO2011161406A1 (en) | 2010-06-25 | 2011-12-29 | Castrol Limited | Uses and compositions |
US9127232B2 (en) | 2010-10-26 | 2015-09-08 | Castrol Limited | Non-aqueous lubricant and fuel compositions comprising fatty acid esters of hydroxy-carboxylic acids, and uses thereof |
EP3115443A1 (en) | 2015-07-07 | 2017-01-11 | Ab Nanol Technologies Oy | Organometallic salt composition, a method for its preparation and a lubricant additive composition |
EP3252130A1 (en) | 2016-06-03 | 2017-12-06 | Infineum International Limited | Additive package and lubricating oil composition |
WO2020089212A1 (en) | 2018-10-29 | 2020-05-07 | Castrol Limited | Lubricant compositions |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JP4822473B2 (en) | 2001-04-02 | 2011-11-24 | 東燃ゼネラル石油株式会社 | Lubricating oil composition for internal combustion engines |
US6892531B2 (en) * | 2003-04-02 | 2005-05-17 | Julius J. Rim | System for and methods of operating diesel engines to reduce harmful exhaust emissions and to improve engine lubrication |
JP6027578B2 (en) * | 2013-08-30 | 2016-11-16 | 良光 長井 | Lubrication promoting liquid |
CN107964441A (en) * | 2017-10-19 | 2018-04-27 | 山东源根石油化工有限公司 | A kind of organic copper antioxidant and the diesel engine oil containing the organic copper antioxidant |
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EP0024146A1 (en) * | 1979-08-13 | 1981-02-25 | Exxon Research And Engineering Company | Improved lubricating compositions |
GB2097813A (en) * | 1981-05-06 | 1982-11-10 | Exxon Research Engineering Co | Glycerol esters in lubricating oils as fuel economy additives |
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CA1137463A (en) * | 1978-12-18 | 1982-12-14 | Thomas V. Liston | Mileage-improving lubricating oil |
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1983
- 1983-04-15 EP EP83302155A patent/EP0092946B1/en not_active Expired
- 1983-04-15 DE DE8383302155T patent/DE3376016D1/en not_active Expired
- 1983-04-21 CA CA000426360A patent/CA1205451A/en not_active Expired
- 1983-04-22 JP JP58070198A patent/JPS58191795A/en active Granted
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US2911367A (en) * | 1957-07-01 | 1959-11-03 | Gulf Oil Corp | Mineral lubricating oil composition |
EP0024146A1 (en) * | 1979-08-13 | 1981-02-25 | Exxon Research And Engineering Company | Improved lubricating compositions |
GB2097813A (en) * | 1981-05-06 | 1982-11-10 | Exxon Research Engineering Co | Glycerol esters in lubricating oils as fuel economy additives |
Cited By (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2505355A1 (en) * | 1981-05-06 | 1982-11-12 | Exxon Research Engineering Co | LUBRICATING OIL COMPOSITION CONTAINING A PARTIAL GLYCEROL ESTER |
EP0260863A2 (en) * | 1986-09-15 | 1988-03-23 | Exxon Research And Engineering Company | Lubricating oil |
EP0260863A3 (en) * | 1986-09-15 | 1989-02-15 | Exxon Research And Engineering Company | Lubricating oil |
EP0280579A3 (en) * | 1987-02-27 | 1989-03-15 | Exxon Chemical Patents Inc. | Low phosphorus/low zinc lubricants |
EP0280579A2 (en) * | 1987-02-27 | 1988-08-31 | Exxon Chemical Patents Inc. | Low phosphorus/low zinc lubricants |
US4915857A (en) * | 1987-05-11 | 1990-04-10 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
US5049290A (en) * | 1987-05-11 | 1991-09-17 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
EP0294045A3 (en) * | 1987-05-11 | 1989-03-22 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
EP0294045A2 (en) * | 1987-05-11 | 1988-12-07 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
US4956108A (en) * | 1987-07-29 | 1990-09-11 | Mobil Oil Corporation | Copper salts of thiodipropionic acid derivatives as antioxidant additives process of making the same and fuel composition thereof |
US5013467A (en) * | 1987-09-16 | 1991-05-07 | Exxon Chemical Patents Inc. | Novel oleaginous composition additives for improved rust inhibition |
US5102566A (en) * | 1987-10-02 | 1992-04-07 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines (pt-727) |
US5141657A (en) * | 1987-10-02 | 1992-08-25 | Exxon Chemical Patents Inc. | Lubricant compositions for internal combustion engines |
US5320765A (en) * | 1987-10-02 | 1994-06-14 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines |
US4957651A (en) * | 1988-01-15 | 1990-09-18 | The Lubrizol Corporation | Mixtures of partial fatty acid esters of polyhydric alcohols and sulfurized compositions, and use as lubricant additives |
US5282991A (en) * | 1988-02-26 | 1994-02-01 | Exxon Chemical Patents Inc. | Friction modified oleaginous concentrates of improved stability |
US5021173A (en) * | 1988-02-26 | 1991-06-04 | Exxon Chemical Patents, Inc. | Friction modified oleaginous concentrates of improved stability |
US4952328A (en) * | 1988-05-27 | 1990-08-28 | The Lubrizol Corporation | Lubricating oil compositions |
US4981602A (en) * | 1988-06-13 | 1991-01-01 | The Lubrizol Corporation | Lubricating oil compositions and concentrates |
US4938881A (en) * | 1988-08-01 | 1990-07-03 | The Lubrizol Corporation | Lubricating oil compositions and concentrates |
EP0389573A1 (en) * | 1988-08-01 | 1990-10-03 | Lubrizol Corp | Lubricating oil compositions and concentrates. |
US4957649A (en) * | 1988-08-01 | 1990-09-18 | The Lubrizol Corporation | Lubricating oil compositions and concentrates |
BE1001977A3 (en) * | 1988-08-01 | 1990-05-02 | Lubrizol Corp | LUBRICATING OIL COMPOSITIONS. |
FR2634780A1 (en) * | 1988-08-01 | 1990-02-02 | Lubrizol Corp | LUBRICATING OIL AND CONCENTRATE COMPOSITION FOR PREPARATION CONTAINING CARBOXYLIC DERIVATIVE COMPOSITION, ESTER AND DIHYDROCARBYLDITHIOPHOSPHORIC ACID METAL SALT |
EP0389573B1 (en) * | 1988-08-01 | 1995-01-11 | The Lubrizol Corporation | Lubricating oil compositions and concentrates |
US5244591A (en) * | 1992-03-23 | 1993-09-14 | Chevron Research And Technology Company | Lubricating oil compositions for internal combustion engines having silver bearing parts |
EP0652279A1 (en) * | 1993-06-07 | 1995-05-10 | Ethyl Corporation | Fuel economy and oxidation inhibition in lubricant compositions for internal combustion engines |
US6379531B2 (en) * | 1999-07-28 | 2002-04-30 | Chevron U.S.A. Inc. | Zeolite SSZ-52 |
US6254849B1 (en) * | 1999-07-28 | 2001-07-03 | Chevron U.S.A. Inc. | Zeolite SSZ-52 |
WO2001059037A2 (en) * | 2000-02-14 | 2001-08-16 | Exxonmobil Research And Engineering Company | Lubricating oils having improved fuel economy retention properties |
WO2001059037A3 (en) * | 2000-02-14 | 2002-01-24 | Exxonmobil Res & Eng Co | Lubricating oils having improved fuel economy retention properties |
EP1925655A1 (en) | 2006-11-22 | 2008-05-28 | Infineum International Limited | Lubricating oil compositions |
EP2161326A1 (en) | 2008-09-05 | 2010-03-10 | Infineum International Limited | Lubricating oil compositions |
EP2390306A1 (en) | 2009-12-01 | 2011-11-30 | Infineum International Limited | A lubricating oil composition |
WO2011161406A1 (en) | 2010-06-25 | 2011-12-29 | Castrol Limited | Uses and compositions |
US9080120B2 (en) | 2010-06-25 | 2015-07-14 | Castrol Limited | Uses and compositions |
US9127232B2 (en) | 2010-10-26 | 2015-09-08 | Castrol Limited | Non-aqueous lubricant and fuel compositions comprising fatty acid esters of hydroxy-carboxylic acids, and uses thereof |
US9828564B2 (en) | 2010-10-26 | 2017-11-28 | Castrol Limited | Non-aqueous lubricant and fuel compositions comprising fatty acid esters of hydroxy-carboxylic acids, and uses thereof |
EP3115443A1 (en) | 2015-07-07 | 2017-01-11 | Ab Nanol Technologies Oy | Organometallic salt composition, a method for its preparation and a lubricant additive composition |
WO2017005967A1 (en) | 2015-07-07 | 2017-01-12 | Ab Nanol Technologies Oy | Organometallic salt composition, a method for its preparation and a lubricant additive composition |
US10618865B2 (en) | 2015-07-07 | 2020-04-14 | Ab Nanol Technologies Oy | Organometallic salt composition, a method for its preparation and a lubricant additive composition |
EP3252130A1 (en) | 2016-06-03 | 2017-12-06 | Infineum International Limited | Additive package and lubricating oil composition |
WO2020089212A1 (en) | 2018-10-29 | 2020-05-07 | Castrol Limited | Lubricant compositions |
Also Published As
Publication number | Publication date |
---|---|
CA1205451A (en) | 1986-06-03 |
JPS58191795A (en) | 1983-11-09 |
EP0092946B1 (en) | 1988-03-16 |
JPH0377837B2 (en) | 1991-12-11 |
EP0092946A3 (en) | 1985-08-14 |
DE3376016D1 (en) | 1988-04-21 |
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