FI60885C - SMOERJMEDELKOMPOSITION - Google Patents
SMOERJMEDELKOMPOSITION Download PDFInfo
- Publication number
- FI60885C FI60885C FI762327A FI762327A FI60885C FI 60885 C FI60885 C FI 60885C FI 762327 A FI762327 A FI 762327A FI 762327 A FI762327 A FI 762327A FI 60885 C FI60885 C FI 60885C
- Authority
- FI
- Finland
- Prior art keywords
- nickel
- lubricant
- oil
- oils
- lubricating
- Prior art date
Links
- 239000000314 lubricant Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 19
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 17
- 239000003921 oil Substances 0.000 claims description 14
- 239000006185 dispersion Substances 0.000 claims description 8
- 239000010687 lubricating oil Substances 0.000 claims description 7
- 230000001050 lubricating effect Effects 0.000 claims description 6
- 239000002480 mineral oil Substances 0.000 claims description 6
- 150000002816 nickel compounds Chemical class 0.000 claims description 6
- 239000010720 hydraulic oil Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 235000010446 mineral oil Nutrition 0.000 claims description 2
- OXKHCBPOFYEKCZ-UHFFFAOYSA-N nickel;7-thiabicyclo[4.1.0]hepta-2,4-dien-6-ol Chemical compound [Ni].C1=CC=CC2(O)C1S2 OXKHCBPOFYEKCZ-UHFFFAOYSA-N 0.000 claims description 2
- 230000000087 stabilizing effect Effects 0.000 claims description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- 239000004519 grease Substances 0.000 claims 1
- 239000002199 base oil Substances 0.000 description 11
- 150000002815 nickel Chemical class 0.000 description 11
- 229910052759 nickel Inorganic materials 0.000 description 7
- 239000000654 additive Substances 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 5
- 125000001741 organic sulfur group Chemical group 0.000 description 5
- -1 2-ethyl Chemical group 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 101100175010 Caenorhabditis elegans gbf-1 gene Proteins 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000005189 flocculation Methods 0.000 description 3
- 230000016615 flocculation Effects 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- FSOIDCQVEPKDOS-UHFFFAOYSA-L [Ni+2].OC1=CC=CC=C1.[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 Chemical class [Ni+2].OC1=CC=CC=C1.[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 FSOIDCQVEPKDOS-UHFFFAOYSA-L 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 239000012208 gear oil Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000000326 ultraviolet stabilizing agent Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
- ZCILGMFPJBRCNO-UHFFFAOYSA-N 4-phenyl-2H-benzotriazol-5-ol Chemical class OC1=CC=C2NN=NC2=C1C1=CC=CC=C1 ZCILGMFPJBRCNO-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- FUSRPUUSAXOXGU-UHFFFAOYSA-J C1(=C(C(=CC=C1)[S-])[S-])C=CC1=CC=CC=C1.C1(=C(C(=CC=C1)[S-])[S-])C=CC1=CC=CC=C1.[Ni+4] Chemical compound C1(=C(C(=CC=C1)[S-])[S-])C=CC1=CC=CC=C1.C1(=C(C(=CC=C1)[S-])[S-])C=CC1=CC=CC=C1.[Ni+4] FUSRPUUSAXOXGU-UHFFFAOYSA-J 0.000 description 1
- XBTFJZOTEFKFJM-UHFFFAOYSA-N C12(C(C=CC=C1)S2)[O-].C2(=CC=CC=C2)O.[Ni+2].C21(C(C=CC=C2)S1)[O-] Chemical compound C12(C(C=CC=C1)S2)[O-].C2(=CC=CC=C2)O.[Ni+2].C21(C(C=CC=C2)S1)[O-] XBTFJZOTEFKFJM-UHFFFAOYSA-N 0.000 description 1
- 241000689227 Cora <basidiomycete fungus> Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- VRORVIHOPFVJKO-UHFFFAOYSA-N S1SC(C=C1)C(=O)O.C1(=CC=CC=C1)C=CC1=CC=CC=C1 Chemical compound S1SC(C=C1)C(=O)O.C1(=CC=CC=C1)C=CC1=CC=CC=C1 VRORVIHOPFVJKO-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical class [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 230000007760 free radical scavenging Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- TXIYCNRKHPXJMW-UHFFFAOYSA-N nickel;1-octyl-2-(2-octylphenyl)sulfanylbenzene Chemical compound [Ni].CCCCCCCCC1=CC=CC=C1SC1=CC=CC=C1CCCCCCCC TXIYCNRKHPXJMW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003672 ureas Chemical class 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
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/18—Complexes with metals
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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
- 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
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- 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
- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M2207/40—Fatty vegetable or animal oils
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
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- 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
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
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- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/10—Amides of carbonic or haloformic acids
- C10M2215/102—Ureas; Semicarbazides; Allophanates
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/066—Thiocarbamic type compounds
- C10M2219/068—Thiocarbamate metal salts
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/088—Neutral salts
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/089—Overbased salts
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/02—Esters of silicic acids
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- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/04—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having a silicon-to-carbon bond, e.g. organo-silanes
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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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/08—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
- C10M2227/081—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds with a metal carbon bond belonging to a ring, e.g. ferocene
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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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/02—Unspecified siloxanes; Silicones
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- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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- C10N2010/14—Group 7
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
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- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
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Description
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C (45) Patentti ny'Snn; tty 13 04 190C Patent me Idolit ^ ^ (51) Kv.lk.3/lnt.CI.3 C 10 M 1/38 SUOMI — FINLAND (21) P«*nulh»k«mu* — Pattmintökninf 762327 (22) Htkemlipllvl — Aiu0knlngtdi| 13.00.76 ^ ' (23) Alkuptlvt—Glltljh*t*d»j 13.08.76 (41) Tulkit Julkiseksi — Bllvlt offcntllg 16.02.77C (45) Patent ny'Snn; tty 13 04 190C Patent me Idolit ^ ^ (51) Kv.lk.3 / lnt.CI.3 C 10 M 1/38 FINLAND - FINLAND (21) P «* nulh» k «mu * - Pattmintökninf 762327 (22) Htkemlipllvl - Aiu0knlngtdi | 13.00.76 ^ '(23) Alkuptlvt — Glltljh * t * d »j 13.08.76 (41) Interpreters for Public - Bllvlt offcntllg 16.02.77
Patentti- ja rekisterihallitus .... ........, . . , . ^ . .. . , (44) Nlhtlvlktlpsnon jt kuul.Julktliun pvm. —Patent and Registration Office .... ........, . . ,. ^. ... , (44) Nlhtlvlktlpsnon et al. -
Patent- och registerstyreisen ' ' Ansekan utlagd och utl.skriften publkarad 31.12.8l (32)(33)(31) Pyydetty etuoikeus —Beglid prloritet 15*08.75 USA (US) 601+977 (71) Mobil Oil Corporation, 150 East l+2nd Street, New York, N.Y., USA(US) (72) Eldon Lester Armstrong, Mullica Hill, N.J., Samuel Joseph Leonardi,Patent and Registration Office '' Ansekan utlagd och utl.skriften publkarad 31.12.8l (32) (33) (31) Claim requested privilege —Beglid prloritet 15 * 08.75 USA (US) 601 + 977 (71) Mobil Oil Corporation, 150 East l + 2nd Street, New York, NY, USA (72) Eldon Lester Armstrong, Mullica Hill, NJ, Samuel Joseph Leonardi,
Pitman, N.J., USA(US) (7I+) Berggren Oy Ah (5U) Voiteluaineseos - Smörjmedelkomposition Tämä keksintö koskee voiteluaineseoksia ja tarkemmin sanoen Voitelu-aineseoksia, jotka normaalisti joutuvat alttiiksi ultraviolettivalon aiheuttamalle hajaantumiselle, jota valoa on läsnä esimerkiksi sellaisissa valokemiallisen säteilyn lähteissä kuten auringon valossa.This invention relates to lubricant compositions, and more particularly to lubricant compositions which are normally exposed to scattering by ultraviolet light, such as light present in photochemical radiation such as photochemical radiation. in the light of.
Vielä tarkemmin keksintö koskee sellaisia voiteluaineseoksia, kuten voiteluviskositeetin omaavia öljyä, hydrokrakattuja voiteluöljyjä, hydraulisia öljyjä, mineraaliöljyjä tai niiden jakeita, autoöljyjä, hammaspyöräöljyjä, voimansiirtonesteitä, vahoja, rasvoja ja muita voiteluaineiden muotoja, jotka normaalisti vaativat stabilointiaineiden mukanaoloa ultraviolettivalon hajotusvaikutuksia vastaan.More particularly, the invention relates to lubricant compositions such as lubricating viscosity oils, hydrocracked lubricating oils, hydraulic oils, mineral oils or fractions thereof, automotive oils, gear oils, lubricating agents, ultra-lubricating agents, waxes, greases and other forms of lubricants.
Yleensä voiteluaineseosten, esimerkiksi hydrokrakkauksella valmistettujen voiteluöljyjen valmistus saa aikaan suhteellisen korkean viskositeetti-indeksin ja tekee mahdolliseksi tiettyjen raaka-aineiden käytön, jotka olisivat sopimattomia muihin prosesseihin. Toisaalta kuitenkin hydrokrakatut voiteluöljyt pyrkivät kohti huonoa stabiili-suutta ultraviolettivalohajaantumista vastaan muodostaen nopeasti 2 60885 suspendoitunutta ja/tai saostunutta liukenematonta materiaalia joutuessaan alttiiksi ultraviolettivalolle, kuten auringon valolle tai muille valokemiallisen säteilyn lähteille. Yhdisteillä, jotka kykenevät absorboimaan ultraviolettivaloa, esim. hydroksibensofenonei11 a ja hydroksifenyylibensotriatsoleilla on saavutettu jonkin verran parannusta hydrokrakattujen öljyjen valostabiilisuudessa. Tavanomaisilla antioksidanteilla on myös aikaansaatu jotakin hyötyä.In general, the preparation of lubricant blends, for example hydrocracked lubricating oils, provides a relatively high viscosity index and allows the use of certain raw materials that would be unsuitable for other processes. On the other hand, however, hydrocracked lubricating oils tend to have poor stability against ultraviolet light scattering, rapidly forming 2,608,85 suspended and / or precipitated insoluble materials when exposed to ultraviolet light, such as sunlight or other sources of photochemical radiation. Compounds capable of absorbing ultraviolet light, e.g., hydroxybenzophenone 11a and hydroxyphenylbenzotriazoles, have provided some improvement in the light stability of hydrocracked oils. Conventional antioxidants have also provided some benefit.
Kirjallisuudessa Heskins ja Guillet artikkelissa "Mechanism of Ultraviolet Stabilization of Polymers", Macromolecules 1, 97 (1968) ehdottivat ensimmäisinä ultraviolettisuoj auksen energiansi irtomekanismi n . Kaupallisesti saatavat ultraviolettistabilisaattorit on myös lueteltu luokan ja toiminnan mukaan ja identifioitu rakenteen suhteen Kirk-Othmer-kokoomateoksessa "Encyclopedia of Chemical Technology"; toinen painos, Voi. 21, sivut 115-122. Uri mainitsee artikkelissa "Thermal and Photochemical Oxidation of Polymers and Its Prevention", Chemistry and Industry, 1. maaliskuuta 1975, sivut 199-203 bis(stilbeeni-ditiolaatto)nikkelin tavanomaisista hapetuksenestovaikutuksista (hydroperoksidihajaantumisen ja vapaaradikaalisieppaus) ja sen ulta-violettivaloa hillitsevistä ominaisuuksista. Brittiläisessä patentissa 1 263 910 (1972) esitetään bis(stilbeeniditiolaatto)nikkeli muovimateriaalien antioksidanttina. Patentissa mainitaan myös tämän lisäaineen erinomainen hydroperoksidin hajotuskyky. US-patentissa 3 832 304 esitetään aromaattisten atsoyhdisteiden käyttö hydrokrakat-tujen öljyjen stabile ntiin. Misään edellä olevista paljastuksista ei esitetä voiteluaineseoksia, jotka sisältävät tässä kuvattuja orgaanisia rikkiä sisältäviä nikkelikomplekseja.In the literature, Heskins and Guillet, in the article "Mechanism of Ultraviolet Stabilization of Polymers", Macromolecules 1, 97 (1968) were the first to propose the loose mechanism of ultraviolet shielding energy. Commercially available ultraviolet stabilizers are also listed by class and function and identified in structure in the Kirk-Othmer compilation "Encyclopedia of Chemical Technology"; second edition, Oh. 21, pages 115-122. Uri mentions in the article "Thermal and Photochemical Oxidation of Polymers and Its Prevention", Chemistry and Industry, March 1, 1975, pages 199-203 bis (stilbene dithiolate) on the conventional antioxidant effects of nickel (hydroperoxide decomposition and free radical scavenging) and its Ulta-violet light. British Patent 1,263,910 (1972) discloses bis (stilbene dithiolate) nickel as an antioxidant in plastic materials. The patent also mentions the excellent hydroperoxide degradability of this additive. U.S. Patent 3,832,304 discloses the use of aromatic azo compounds to stabilize hydrocracked oils. None of the above disclosures discloses lubricant compositions comprising the organic sulfur-containing nickel complexes described herein.
Tämän keksinnön mukaisesti olemme havainneet, että suojaaminen ultraviolettivalon aiheuttamaa hajaantumista vastaan, jota valoa on läsnä auringonvalossa tai muissa valokemiallisen säteilyn lähteissä, voidaan tehokkaasti saada aikaan voiteluaineseoksille liittämällä niihin orgaanisia rikkiä sisältäviä nikkelikomplekseja. Nämä nikkelikomp-leksit ovat erityisen tehokkaita ultraviolettihajaantumista vastaan sellaisissa voiteluväliaineissa, kuten voiteluviskositeetin omaavissa öljyissä, hydrokrakatuissa voiteluöljyissä, hydraulisissa öljyissä, mineraaliöljyissä tai niiden jakeissa, autoöljyissä, hammaspyöräöl-jyissä, voimansiirtonesteissä, vahoissa, rasvoissa ja muissa voitelu-a.i neseouten muodoissa, jotka normaalisti vaativat stabilointiaineiden Jäsnäoioa ultraviolettivalon hajottavaa vaikutusta vastaan.In accordance with the present invention, we have found that protection against scattering by ultraviolet light, which is present in sunlight or other sources of photochemical radiation, can be effectively provided to lubricant mixtures by incorporating nickel complexes containing organic sulfur. These nickel complexes are particularly effective against ultraviolet dispersion in lubricating media such as oils with lubricating viscosity, hydrocracked lubricating oils, hydraulic oils, mineral oils or their fractions, lubricating oils, lubricating oils, gear oils, transmission oils, the presence of stabilizers against the diffusing effect of ultraviolet light.
6088560885
Keksintö tarkoittaa näin ollen voiteluaineseosta, joka sisältää ultraviolettihajaantumista vastaan stabiloivan määrän orgaanista nikkeliyhdistettä, ja keksintö on tunnettu siitä, että nikkeli- yhdiste on nikkelifenolisulfidi, jolla on kaava ^ ^ Ni -The invention thus relates to a lubricant mixture containing a stabilizing amount of an organic nickel compound against ultraviolet dispersion, and the invention is characterized in that the nickel compound is a nickel phenol sulphide of the formula
R RR R
tai nikkelifenoli-fenolaattisulfidi, jolla on kaava ö— ?—0or nickel phenol phenolate sulfide of the formula?
H Ni" HH Ni "H
R RR R
taior
I Ni - OHI Ni - OH
: ^ " i -^: ^ "i - ^
HO " I "OHHO "I" OH
R RR R
joissa kaavoissa R tarkoittaa vetyatomia tai enintään 30 hiiliatomia sisältävää alkyyliryhmää.in which R represents a hydrogen atom or an alkyl group having up to 30 carbon atoms.
4 608854 60885
Orgaanisia rikkiä sisältäviä nikkelikomplekseja voidaan tehokkaasti käyttää mikä tahansa määrä, joka riittää antamaan voiteluaineelle halutun suojausasteen ultraviolettihajaantumista vastaan. Monissa tapauksissa nikkelikompleksia käytetään tehokkaasti n. 0,01-b paino-%:n määrä ja mieluummin n. 0,1-2 paino-$:n määrä voitelu-aineseoksen kokonaismäärästä. Sanonnan "nikkelikompleksi" tarkoitetaan tässä käytettynä sisältävän nikkeliyhdisteet, joilla on kelaattirengasmuodostus. Kuten edellä mainittiin orgaaniset rikkiä sisältävät nikkelikompleksit voidaan liittää mihin tahansa voiteluväliaineeseen, joka voi sisältää voiteluviskositeetin omaa-via öljyjä, ja myös rasvoihin, joissa jotakin yllä mainituista öljyistä käytetään apuaineina. Yleensä synteettisiä öljyjä voidaan myös tehokkaasti suojata ultraviolettihajaantumista vastaan tai voidaan myös käyttää mineraaliöljyjen yhteydessä tai rasvan apuaineina. Tyypillisiä synteettisiä apuaineita ovat polyiso-butyleeni, polybuteenit, hydratut polydeseenit, polypropyleenigly-koli, polyetyleeniglykoli, trimetylolipropaaniesterit, neopentyyli-ja pentaerytritoliesterit,di(2-etyyliheksyyli) sebasaatti, di(2-etyyliheksyyli) adipaatti, dibutyyliftalaatti, fluorihiilivedyt, silikaattiesterit, silaanit, fosforia sisältävien happojen esterit, nestemäiset ureat, ferroseenijohdannaiset, hydratut mineraaliöljyt, ketjutyyppiset polyfenolit, siloksaanit ja silikonit (polysiloksaa-nit), alkyylisubstituoidut difenyylieetterit, joista tyypillisiä esimerkkejä ovat butyylisubstituoitu bis-(p-fenoksifenyyli)eetteri, fenoksifenyylieetteri jne.Organic sulfur-containing nickel complexes can be effectively used in any amount sufficient to give the lubricant the desired degree of protection against ultraviolet dispersion. In many cases, the nickel complex is effectively used in an amount of about 0.01 to b% by weight, and preferably in an amount of about 0.1 to 2% by weight of the total amount of the lubricant mixture. The term "nickel complex" as used herein is intended to include nickel compounds having chelate ring formation. As mentioned above, organic sulfur-containing nickel complexes can be incorporated into any lubricating medium which may contain oils having a lubricating viscosity, and also to fats in which one of the above oils is used as an excipient. In general, synthetic oils can also be effectively protected against ultraviolet dispersion or can also be used in conjunction with mineral oils or as fat excipients. Typical synthetic excipients include polyisobutylene, polybutenes, hydrogenated polydenes, polypropylene glycol, polyethylene glycol, trimethylolpropane esters, neopentyl and pentaerythritol esters, di (2-ethylhexyl) sebacate, di (2-ethylhexyl) sebacate, di (2-ethyl) esters of phosphorus-containing acids, liquid ureas, ferrocene derivatives, hydrogenated mineral oils, chain-type polyphenols, siloxanes and silicones (polysiloxanes), alkyl-substituted diphenyl ethers, etc., of which are butyl-substituted bis (p-phenoxy) phenis,
Rikkiä sisältävät nikkelifenoli-fenolaatit ovat hyödyllisiä aineita. Niitä kuvataan esimerkiksi US-patenteissa n:ot 2 971 9^0 ja 2 971 9^1. Ne koostuvat bis-fenolisulfidien nikkelisuoloista, joissa vain osa koko fenyylivedystä on korvattu nikkelillä.Sulfur-containing nickel phenol phenolates are useful substances. They are described, for example, in U.S. Patent Nos. 2,971,9 ^ 2 and 2,971,9 ^ 1. They consist of nickel salts of bis-phenol sulphides in which only part of the total phenylhydrogen has been replaced by nickel.
Niiden edellä esitettyjen kaavojen mukaisten nikkelifenoli-feno-laattiyhdisteiden seos (jota nimitetään tässä "seokseksi A"), joissa R on oktyyliryhmä, on hyvä ultraviolettistabilisaattori.A mixture of nickel phenol-phenolate compounds of the above formulas (referred to herein as "mixture A") in which R is an octyl group is a good ultraviolet stabilizer.
Tämän keksinnön orgaanisten rikkiä sisältävien nikkelikompleksien tehokkuuden arvioimiseksi ultraviolettihajaantumista vastaan voi-teluaineväliaineissa käytettiin seuraavaa koetta: Tässä kokeessa käytettiin perusöljyä, nimittäin vedyllä jälkikäsiteltyä, hydrokrakattua 100 ":n öljyä, joka oli saatu poistamalla vaha 385°C:n pohjajakeesta, joka oli peräisin polttoainehydro- 5 60885 krakkaustornin ensimmäisen vaiheen tuotteesta. Lisäaineiden ja edellä mainitun hydrokrakatun perusöljyn seoksia testattiin saattamalla 20 g suljetussa n. 118 ml:n pitkänomaisessa pullossa olevaa koeöljyä päivänvalon alaiseksi ikkunalaudalla, joka oli kohti kaakkoa. Koeöljyä tarkasteltiin joka päivä suspendoituneiden, liukenemattomien tuotteiden suhteen, jotka tavallisesti etenevät samenemasta suspendoituneeseen höytälöitymään ja saostumiin, joita yleensä edeltävät samentumat tai höytälöitymät ja jotka usein koostuvat laskeutuneista samentumista tai höytälöitymistä. Seuraavassa taulukossa I on esitetty tulokset, jotka on saatu käyttämällä 0,J paino-$ lisäaineita yllämainitussa hydrokrakatussa perusöljyssä. Taulukosta huomataan, että tämän keksinnön nikkelikompleksit ovat paljon merkittävämmin tehokkaita ultraviolettihajaantumista vastaan (esimerkit 2-3) kuin parhaat kaupallisesti saatavat tavanomaiset antioksidantit ja ultraviolettivaloa absorboivat aineet (esimerkit 4-8).To evaluate the effectiveness of the organic sulfur-containing nickel complexes of this invention against ultraviolet dispersion in lubricant media, the following experiment was used: This experiment used a base oil, namely a hydrotreated 100 "hydrocracked oil obtained by removing wax from a base at 385 ° C. 5 60885. The mixtures of the additives and the above-mentioned hydrocracked base oil were tested by exposing 20 g of the test oil in a sealed elongated bottle of about 118 ml to a window facing south-east on a window facing south-east of the suspended, insoluble products. progress from turbidity to suspended flocculation and precipitation, which is usually preceded by turbidity or flocculation and often consists of settled turbidity or flocculation.The results are shown in Table I below, obtained by using 0.1% by weight of additives in the above hydrocracked base oil. It can be seen from the table that the nickel complexes of this invention are much more effective against ultraviolet scattering (Examples 2-3) than the best commercially available conventional antioxidants and ultraviolet light absorbing agents (Examples 4-8).
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Seuraavassa taulukossa II on esitetty tulokset, jotka on saatu käyttäen 0,5 paino-% lisäaineita yllä kuvatussa taulukon I hydrokrakatussa perusöljyssä. Myös tässä huomataan taulukosta, että kun tämän keksinnön voiteluaineseoksissa rikkiä sisältävä nikkelikompleksi alistetaan yllä kuvattuun kokeeseen, se on paljon merkittävämmin tehokas ultraviolettihajaantumista (esimerkki 2) vastaan kuin parhaat edellä mainituista kaupallisesti saatavista tavanomaisista antioksidanteista ja ultraviolettivaloa absorboivista aineista (esimerkki 3-7).The following Table II shows the results obtained using 0.5% by weight of additives in the hydrocracked base oil of Table I described above. Here again, it is noted from the table that when the sulfur-containing nickel complex in the lubricant compositions of this invention is subjected to the experiment described above, it is much more effective against ultraviolet dispersion (Example 2) than the best of the above commercially available conventional antioxidants and ultraviolet light absorbing agents (Example 3-7).
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Seuraavassa taulukossa III esitetään tämän keksinnön tyypillisen, edustavan nikkelikompleksin, nimittäin nikkeli-bis(oktyylifeno]i)-sulfidin, tehokkuus 200" hydrokrakatussa perusöljyssä (perusöljy 1) ja myös toisessa perusöljyssä (perusöljy 2) nimittäin raskaassa tyh-jökaasuöljyssä. Kuten taulukossa esitetään tämän keksinnön nikkeli. -(oktyylifenoli) sulfidi oli merkittävän tehokas pienentämään molempien perusöljyjen ultaviolettihajaantumista.The following Table III shows the performance of a typical nickel complex of this invention, namely nickel-bis (octylphenyl) sulfide, in a 200 "hydrocracked base oil (base oil 1) and also in another base oil (base oil 2), namely in a heavy vacuum gas oil as shown in the table. the nickel of the invention - (octylphenol) sulfide was significantly effective in reducing the ultaviolet dispersion of both base oils.
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Seuraavassa taulukossa IV esitetään tämän keksinnön tyypillisesti edustavien nikkelikompleksien tehokkuus antioksidantteina voitelu-aineseoksissa. Edustavat lisäaineet sekoitettiin erikseen 130":n liotinpuhdistettuun parafiiniseen mineraaliöljyyn ja alistettiin standardi kiertopommihapetuskokeeseen koementelmän ASTM D-22'(2 mukaisesti.The following Table IV shows the effectiveness of representative nickel complexes of this invention as antioxidants in lubricant compositions. Representative additives were separately mixed with 130 "solvent-purified paraffinic mineral oil and subjected to a standard rotary bomb oxidation test according to ASTM D-22 '(2).
Kuten taulukosta huomataan perusöljyn hapettumisikä kasvoi huomattavasti tämän keksinnön nikkelikompleksien aikaansaaman hapettumisen-estovaikutuksen avulla.As can be seen from the table, the oxidation life of the base oil was significantly increased by the antioxidant effect of the nickel complexes of this invention.
TAULUKKO IVTABLE IV
Nikkelikompleksien hapettumisenestovaikutuksetAntioxidant effects of nickel complexes
Esimerkki Ikä kiertopommihapetus- kokeessa, minuuttia_ 1 Ei lainkaan (perusöljy) 37 3. 1 % seosta A 80Example Age in a roundabout oxidation test, minutes_ 1 Not at all (base oil) 37 3. 1% mixture A 80
Vaikka tätä keksintöä on kuvattu viitaten sen suositeltaviin seoksiin ja komponentteihin, alaan perehtyneet ymmärtävät, että poikkeama suositeltavista toteutusmuodoista voidaan tehdä tehokkaasti ja se on patenttimäärityksen -suojapiirin sisällä.Although the present invention has been described with reference to its preferred compositions and components, those skilled in the art will appreciate that deviation from the preferred embodiments may be made effectively and is within the scope of the specification.
Claims (4)
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US60497775A | 1975-08-15 | 1975-08-15 | |
US60497775 | 1975-08-15 |
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CA (1) | CA1088506A (en) |
CH (1) | CH602909A5 (en) |
DE (1) | DE2636583A1 (en) |
DK (1) | DK367076A (en) |
FI (1) | FI60885C (en) |
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IT (1) | IT1066053B (en) |
MX (1) | MX145462A (en) |
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BE572057A (en) * | ||||
US2362293A (en) * | 1939-12-27 | 1944-11-07 | Standard Oil Dev Co | Lubricant |
GB800964A (en) * | 1955-12-20 | 1958-09-03 | Exxon Research Engineering Co | Improvements in or relating to lubricating oil additive compositions and to lubricating oil compositions containing them |
US2971941A (en) * | 1959-05-15 | 1961-02-14 | Ferro Corp | Nickel bis-(p-octylphenol) monosulphide stabilized polyethylene |
US2971940A (en) * | 1959-03-20 | 1961-02-14 | Ferro Corp | Nickel phenolate stabilized polypropylene |
US3215717A (en) * | 1961-12-11 | 1965-11-02 | American Cyanamid Co | Phenol sulfide nickel amine derivatives |
US3398170A (en) * | 1964-05-21 | 1968-08-20 | Universal Oil Prod Co | Mixed chelates of a schiff base, an amine, and a transition series metal |
US3450636A (en) * | 1967-08-22 | 1969-06-17 | Sinclair Research Inc | Automatic transmission fluid of reduced susceptibility oxidative degradation |
GB1204798A (en) * | 1967-12-06 | 1970-09-09 | Snam Progetti | Metal derivatives of dithiophosphoric acids and lubricating compositions containing them |
FR2077906A1 (en) * | 1970-02-23 | 1971-11-05 | Inst Francais Du Petrole |
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1976
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- 1976-08-16 AT AT608976A patent/AT362487B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FR2320981A1 (en) | 1977-03-11 |
ATA608976A (en) | 1980-10-15 |
NO143707C (en) | 1981-04-01 |
ZA764881B (en) | 1978-03-29 |
MX145462A (en) | 1982-02-19 |
FI762327A (en) | 1977-02-16 |
FI60885B (en) | 1981-12-31 |
BR7605333A (en) | 1977-08-09 |
CH602909A5 (en) | 1978-08-15 |
PT65462A (en) | 1976-09-01 |
JPS6014793B2 (en) | 1985-04-16 |
FR2320981B1 (en) | 1981-08-07 |
NO143707B (en) | 1980-12-22 |
NL7608842A (en) | 1977-02-17 |
BE845054A (en) | 1977-02-10 |
TR19122A (en) | 1978-07-01 |
NZ181648A (en) | 1978-07-28 |
IT1066053B (en) | 1985-03-04 |
AT362487B (en) | 1981-05-25 |
DK367076A (en) | 1977-02-16 |
SE421429B (en) | 1981-12-21 |
SE7608973L (en) | 1977-02-16 |
AU501498B2 (en) | 1979-06-21 |
PT65462B (en) | 1978-02-10 |
GR61121B (en) | 1978-09-14 |
AU1678676A (en) | 1978-02-16 |
NO762814L (en) | 1977-02-16 |
CA1088506A (en) | 1980-10-28 |
JPS5224203A (en) | 1977-02-23 |
DE2636583A1 (en) | 1977-02-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM | Patent lapsed |
Owner name: MOBIL OIL CORP |