EP1594943B1 - Lubricating oil compositions - Google Patents
Lubricating oil compositions Download PDFInfo
- Publication number
- EP1594943B1 EP1594943B1 EP04712057.1A EP04712057A EP1594943B1 EP 1594943 B1 EP1594943 B1 EP 1594943B1 EP 04712057 A EP04712057 A EP 04712057A EP 1594943 B1 EP1594943 B1 EP 1594943B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lubricating oil
- oil
- composition
- base oil
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000010687 lubricating oil Substances 0.000 title claims description 99
- 239000000203 mixture Substances 0.000 title claims description 72
- 239000002199 base oil Substances 0.000 claims description 103
- 239000003921 oil Substances 0.000 claims description 31
- 239000000654 additive Substances 0.000 claims description 24
- 239000012530 fluid Substances 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- 239000010720 hydraulic oil Substances 0.000 claims description 14
- 150000003141 primary amines Chemical class 0.000 claims description 14
- 239000003963 antioxidant agent Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 11
- 239000004129 EU approved improving agent Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 239000013556 antirust agent Substances 0.000 claims description 8
- 239000002270 dispersing agent Substances 0.000 claims description 7
- 238000005259 measurement Methods 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 238000004945 emulsification Methods 0.000 claims description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 239000005864 Sulphur Substances 0.000 claims description 4
- 239000002518 antifoaming agent Substances 0.000 claims description 4
- 238000004140 cleaning Methods 0.000 claims description 4
- 239000010725 compressor oil Substances 0.000 claims description 4
- 239000012208 gear oil Substances 0.000 claims description 4
- 239000012188 paraffin wax Substances 0.000 claims description 4
- 239000010723 turbine oil Substances 0.000 claims description 4
- 239000005069 Extreme pressure additive Substances 0.000 claims description 3
- 238000010998 test method Methods 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000006078 metal deactivator Substances 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- -1 amine compound Chemical class 0.000 description 52
- 150000003956 methylamines Chemical group 0.000 description 33
- BAVYZALUXZFZLV-UHFFFAOYSA-N mono-methylamine Natural products NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 33
- 235000019198 oils Nutrition 0.000 description 29
- 150000001412 amines Chemical class 0.000 description 24
- 238000012360 testing method Methods 0.000 description 15
- 239000002904 solvent Substances 0.000 description 13
- 230000000996 additive effect Effects 0.000 description 12
- 235000006708 antioxidants Nutrition 0.000 description 10
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 10
- 238000003860 storage Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 238000004134 energy conservation Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 230000003078 antioxidant effect Effects 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 229920013639 polyalphaolefin Polymers 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 150000003973 alkyl amines Chemical class 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000013016 damping Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 229940042472 mineral oil Drugs 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 2
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 2
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 2
- DIOYAVUHUXAUPX-ZHACJKMWSA-N 2-[methyl-[(e)-octadec-9-enoyl]amino]acetic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(=O)N(C)CC(O)=O DIOYAVUHUXAUPX-ZHACJKMWSA-N 0.000 description 2
- FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 description 2
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 2
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 2
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 2
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- CGRTZESQZZGAAU-UHFFFAOYSA-N [2-[3-[1-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]-2-methylpropan-2-yl]-2,4,8,10-tetraoxaspiro[5.5]undecan-9-yl]-2-methylpropyl] 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCC(C)(C)C2OCC3(CO2)COC(OC3)C(C)(C)COC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 CGRTZESQZZGAAU-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 150000001556 benzimidazoles Chemical class 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- 150000001565 benzotriazoles Chemical class 0.000 description 2
- LUFPJJNWMYZRQE-UHFFFAOYSA-N benzylsulfanylmethylbenzene Chemical compound C=1C=CC=CC=1CSCC1=CC=CC=C1 LUFPJJNWMYZRQE-UHFFFAOYSA-N 0.000 description 2
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000004523 catalytic cracking Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229950000688 phenothiazine Drugs 0.000 description 2
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical compound OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 150000000183 1,3-benzoxazoles Chemical class 0.000 description 1
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 1
- PWNBRRGFUVBTQG-UHFFFAOYSA-N 1-n,4-n-di(propan-2-yl)benzene-1,4-diamine Chemical compound CC(C)NC1=CC=C(NC(C)C)C=C1 PWNBRRGFUVBTQG-UHFFFAOYSA-N 0.000 description 1
- ZBRNSXOKGALPHF-UHFFFAOYSA-N 10-[(3,5-ditert-butyl-4-hydroxyphenyl)methylsulfanyl]decanoic acid Chemical compound CC(C)(C)C1=CC(CSCCCCCCCCCC(O)=O)=CC(C(C)(C)C)=C1O ZBRNSXOKGALPHF-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 description 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 description 1
- ZBADMMCYTSORHN-UHFFFAOYSA-N 2,5-bis(dodecyldisulfanyl)-1,3,4-thiadiazole Chemical compound CCCCCCCCCCCCSSC1=NN=C(SSCCCCCCCCCCCC)S1 ZBADMMCYTSORHN-UHFFFAOYSA-N 0.000 description 1
- ZGWOXISFZXPTGJ-UHFFFAOYSA-N 2,5-bis(heptyldisulfanyl)-1,3,4-thiadiazole Chemical compound CCCCCCCSSC1=NN=C(SSCCCCCCC)S1 ZGWOXISFZXPTGJ-UHFFFAOYSA-N 0.000 description 1
- MGEQSWVPSCZGEK-UHFFFAOYSA-N 2,5-bis(nonyldisulfanyl)-1,3,4-thiadiazole Chemical compound CCCCCCCCCSSC1=NN=C(SSCCCCCCCCC)S1 MGEQSWVPSCZGEK-UHFFFAOYSA-N 0.000 description 1
- JZODKRWQWUWGCD-UHFFFAOYSA-N 2,5-di-tert-butylbenzene-1,4-diol Chemical compound CC(C)(C)C1=CC(O)=C(C(C)(C)C)C=C1O JZODKRWQWUWGCD-UHFFFAOYSA-N 0.000 description 1
- LKALLEFLBKHPTQ-UHFFFAOYSA-N 2,6-bis[(3-tert-butyl-2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound OC=1C(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=CC(C)=CC=1CC1=CC(C)=CC(C(C)(C)C)=C1O LKALLEFLBKHPTQ-UHFFFAOYSA-N 0.000 description 1
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 description 1
- SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 description 1
- QHPKIUDQDCWRKO-UHFFFAOYSA-N 2,6-ditert-butyl-4-[2-(3,5-ditert-butyl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 QHPKIUDQDCWRKO-UHFFFAOYSA-N 0.000 description 1
- YQQQXXUABFURLN-UHFFFAOYSA-N 2,6-ditert-butyl-4-ethoxyphenol Chemical compound CCOC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 YQQQXXUABFURLN-UHFFFAOYSA-N 0.000 description 1
- HYXVEQIONZKDIA-UHFFFAOYSA-N 2-(decyldisulfanyl)-1,3-benzoxazole Chemical compound C1=CC=C2OC(SSCCCCCCCCCC)=NC2=C1 HYXVEQIONZKDIA-UHFFFAOYSA-N 0.000 description 1
- XTYDQWTYBIZARF-UHFFFAOYSA-N 2-(decyldisulfanyl)-1h-benzimidazole Chemical compound C1=CC=C2NC(SSCCCCCCCCCC)=NC2=C1 XTYDQWTYBIZARF-UHFFFAOYSA-N 0.000 description 1
- ITJODUNSZXNTOI-UHFFFAOYSA-N 2-(dodecyldisulfanyl)-1h-benzimidazole Chemical compound C1=CC=C2NC(SSCCCCCCCCCCCC)=NC2=C1 ITJODUNSZXNTOI-UHFFFAOYSA-N 0.000 description 1
- HVHWMYUBPWXAIK-UHFFFAOYSA-N 2-(hexyldisulfanyl)-1,3-benzothiazole Chemical compound C1=CC=C2SC(SSCCCCCC)=NC2=C1 HVHWMYUBPWXAIK-UHFFFAOYSA-N 0.000 description 1
- CYXWNSBYVBWROX-UHFFFAOYSA-N 2-(octyldisulfanyl)-1,3-benzothiazole Chemical compound C1=CC=C2SC(SSCCCCCCCC)=NC2=C1 CYXWNSBYVBWROX-UHFFFAOYSA-N 0.000 description 1
- LFAMMXHEBNTRPL-UHFFFAOYSA-N 2-(octyldisulfanyl)-1,3-benzoxazole Chemical compound C1=CC=C2OC(SSCCCCCCCC)=NC2=C1 LFAMMXHEBNTRPL-UHFFFAOYSA-N 0.000 description 1
- ZYLBDGBVCLZOII-UHFFFAOYSA-N 2-(octyldisulfanyl)-1h-benzimidazole Chemical compound C1=CC=C2NC(SSCCCCCCCC)=NC2=C1 ZYLBDGBVCLZOII-UHFFFAOYSA-N 0.000 description 1
- ROHFBIREHKPELA-UHFFFAOYSA-N 2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]prop-2-enoic acid;methane Chemical compound C.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O ROHFBIREHKPELA-UHFFFAOYSA-N 0.000 description 1
- XXQHMEUBVSZQON-UHFFFAOYSA-N 2-[(3-dodecoxy-3-oxopropyl)sulfanylmethyl]icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCC(CSCCC(=O)OCCCCCCCCCCCC)C(=O)O XXQHMEUBVSZQON-UHFFFAOYSA-N 0.000 description 1
- QSRJVOOOWGXUDY-UHFFFAOYSA-N 2-[2-[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCCOCCOCCOC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 QSRJVOOOWGXUDY-UHFFFAOYSA-N 0.000 description 1
- XVEYHYHXRYVWJW-UHFFFAOYSA-N 2-ethyl-n-(2-ethyl-4-nonylphenyl)-4-nonylaniline Chemical compound CCC1=CC(CCCCCCCCC)=CC=C1NC1=CC=C(CCCCCCCCC)C=C1CC XVEYHYHXRYVWJW-UHFFFAOYSA-N 0.000 description 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 0.000 description 1
- IMOYOUMVYICGCA-UHFFFAOYSA-N 2-tert-butyl-4-hydroxyanisole Chemical compound COC1=CC=C(O)C=C1C(C)(C)C IMOYOUMVYICGCA-UHFFFAOYSA-N 0.000 description 1
- GPNYZBKIGXGYNU-UHFFFAOYSA-N 2-tert-butyl-6-[(3-tert-butyl-5-ethyl-2-hydroxyphenyl)methyl]-4-ethylphenol Chemical compound CC(C)(C)C1=CC(CC)=CC(CC=2C(=C(C=C(CC)C=2)C(C)(C)C)O)=C1O GPNYZBKIGXGYNU-UHFFFAOYSA-N 0.000 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical class OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 description 1
- STGFANHLXUILNY-UHFFFAOYSA-N 3,7-dioctyl-10h-phenothiazine Chemical compound C1=C(CCCCCCCC)C=C2SC3=CC(CCCCCCCC)=CC=C3NC2=C1 STGFANHLXUILNY-UHFFFAOYSA-N 0.000 description 1
- MRBKEAMVRSLQPH-UHFFFAOYSA-N 3-tert-butyl-4-hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1 MRBKEAMVRSLQPH-UHFFFAOYSA-N 0.000 description 1
- MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- JHCCIUPVUCVKIJ-UHFFFAOYSA-N 4,6-ditert-butyl-2-(3,5-ditert-butyl-2,6-dihydroxyphenyl)sulfanylbenzene-1,3-diol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=C(O)C(SC=2C(=C(C=C(C=2O)C(C)(C)C)C(C)(C)C)O)=C1O JHCCIUPVUCVKIJ-UHFFFAOYSA-N 0.000 description 1
- PRWJPWSKLXYEPD-UHFFFAOYSA-N 4-[4,4-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butan-2-yl]-2-tert-butyl-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C)CC(C=1C(=CC(O)=C(C=1)C(C)(C)C)C)C1=CC(C(C)(C)C)=C(O)C=C1C PRWJPWSKLXYEPD-UHFFFAOYSA-N 0.000 description 1
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 description 1
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- 150000001639 boron compounds Chemical class 0.000 description 1
- DFMYXZSEXKBYDI-UHFFFAOYSA-N butyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 DFMYXZSEXKBYDI-UHFFFAOYSA-N 0.000 description 1
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- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- 238000012544 monitoring process Methods 0.000 description 1
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- MHJCZOMOUCUAOI-UHFFFAOYSA-N n-tert-butyl-n-phenylaniline Chemical compound C=1C=CC=CC=1N(C(C)(C)C)C1=CC=CC=C1 MHJCZOMOUCUAOI-UHFFFAOYSA-N 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JKBYAWVSVVSRIX-UHFFFAOYSA-N octadecyl 2-(1-octadecoxy-1-oxopropan-2-yl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)SC(C)C(=O)OCCCCCCCCCCCCCCCCCC JKBYAWVSVVSRIX-UHFFFAOYSA-N 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
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- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 150000002990 phenothiazines Chemical class 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
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- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
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- PDEDQSAFHNADLV-UHFFFAOYSA-M potassium;disodium;dinitrate;nitrite Chemical compound [Na+].[Na+].[K+].[O-]N=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PDEDQSAFHNADLV-UHFFFAOYSA-M 0.000 description 1
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- 230000002265 prevention Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical class [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- JDVPQXZIJDEHAN-UHFFFAOYSA-N succinamic acid Chemical compound NC(=O)CCC(O)=O JDVPQXZIJDEHAN-UHFFFAOYSA-N 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LVEOKSIILWWVEO-UHFFFAOYSA-N tetradecyl 3-(3-oxo-3-tetradecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCC LVEOKSIILWWVEO-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- JZNDMMGBXUYFNQ-UHFFFAOYSA-N tris(dodecylsulfanyl)phosphane Chemical compound CCCCCCCCCCCCSP(SCCCCCCCCCCCC)SCCCCCCCCCCCC JZNDMMGBXUYFNQ-UHFFFAOYSA-N 0.000 description 1
- QQBLOZGVRHAYGT-UHFFFAOYSA-N tris-decyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OCCCCCCCCCC QQBLOZGVRHAYGT-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- 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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
-
- 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
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/02—Specified values of viscosity or viscosity index
-
- 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
- C10M2205/0206—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers used as base material
-
- 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
- C10M2205/10—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing cycloaliphatic monomers
- C10M2205/103—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing cycloaliphatic monomers used as base material
-
- 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
- C10M2205/17—Fisher Tropsch reaction products
- C10M2205/173—Fisher Tropsch reaction products used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/017—Specific gravity or density
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/02—Viscosity; Viscosity index
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/30—Refrigerators lubricants or compressors lubricants
Definitions
- the present invention relates to lubricating oil compositions which suppress the formation of sludge and which have excellent storage stability, low friction properties, small pressure transmission loss, low supply pressure loss in pipe-work, and low flammability.
- Hydraulic systems are distinguished in that the "oil" which is the motive power transmitting medium has low compressibility and so it is possible to use higher pressures and to increase the output with respect to the weight of a machine, and for many reasons such as the fact that the division, concentration and speed control of the motive power can be achieved easily, such oils are widely used in industrial applications.
- the Hydraulic Fluid Handbook page 31, published in 1985 by the Lubrication News Agency Co. Ltd. , describes that the feed pressure loss in hydraulic pipe-work based on the Bernoulli's theorem is proportional to the density of the oil both in a vacuum pipe and in a vented pipe, elbow, branch pipe or linked pipe. That is to say, the supply pressure loss can be reduced by reducing the density if the kinematic viscosity and the pipe-work are the same, and it is also shown that at the same time an improvement in flow-rate efficiency can be devised by reducing the density. Moreover, since the supply pressure loss in hydraulic pipe-work is converted to heat and sound etc., it is suggested that the generation of heat and noise are also suppressed by reducing the density. Since reduced friction also contributes to improving energy conservation, low friction properties to an extent where stick-slip does not arise in steel-steel situations is required.
- the present invention now surprisingly enables energy conservation to be achieved by improving the performance of monograde hydraulic oils as the hydraulic media for increasing the efficiency of hydraulic energy transmission.
- the present invention provides a lubricating oil composition
- a lubricating oil composition comprising lubricating oil base oil and a primary amine which has a C 8 to C 20 tertiary alkyl group which can be represented by general formula (1) below wherein x is an integer of value from 1 to 17, y is an integer of value from 1 to 17, z is an integer of value from 1 to 17, and x + y + z is an integer of value from 7 to 19, wherein said composition has a kinematic viscosity at 40°C of from 18 to 60 mm 2 /s, a viscosity index of from 130 to 150 and a density at 15°C of from 0.80 to 0.84 g.cm -3 .
- a lubricating oil composition in which not only has the density been reduced by about 10% when compared with the commercial industrial lubricating oil products of the same viscosity and which surprisingly has an energy conserving effect, but which also has a flash point of at least 250°C as measured by JIS K 2265 by using a narrow-cut base oil.
- the narrow-cut base oils having a high flash point for industrial lubricating oil products are very different in terms of their molecular weight distribution from the usual base oils used by those in the industry and the proportion of high molecular weight hydrocarbon components is very small. Consequently, the solubilities of lubricating oil additives which control various aspects of performance are very low and there is a disadvantage in that turbidity and precipitates are produced, and these materials cannot be used as industrial lubricating oils.
- the high molecular weight ashless dispersants used in the automobile lubricating oils cannot be used in hydraulic applications even at treat rates of less than 1 %wt., e.g. 0.1 %wt., due to emulsification in the presence of water, which is an undesirable property therefor.
- the solubility, the low friction properties and anti-rust properties when using a specified narrow-cut base oil in industrial lubricating oils with a view to increasing energy conservation and having a high flash point may be surprisingly improved by the use of a specific amine compound.
- Japanese Unexamined Patent Application Laid Open 2002-338 983 there is disclosed a lubricating oil composition where an alkylamine has been added to a lubricating oil base oil, but the amount of anti-rust agent is greatly reduced by combining the alkylamines with the anti-rust agent and, as a result, the extreme pressure performance by the anti-rust agent is suppressed to the lowest level.
- the primary amine having a tertiary alkyl group in the present invention as the primary amine.
- the lubricating oil base oil used is preferably a base oil of which the minimum value of the kinematic viscosity at 40°C is preferably 8 mm 2 /s and more desirably 10 mm 2 /s, and the maximum value of the kinematic viscosity at 40°C is preferably 60 mm 2 /s and more desirably 40 mm 2 /s. It is also disclosed that from the viewpoint of minimising as far as possible the change in the damping force the viscosity index is preferably at least 80 and more desirably at least 95, but there is no disclosure of the lubricating oil base oil of the present invention.
- the lubricating oil base oil used is preferably a base oil of which the minimum value of the kinematic viscosity at 40°C is preferably 8 mm 2 /s and more desirably 10 mm 2 /s, and the maximum value of the kinematic viscosity at 40°C is preferably 60 mm 2 /s and more desirably 40 mm 2 /s. It is further disclosed that from the viewpoint of minimising as far as possible the change in the damping force the viscosity index is preferably at least 80 and more desirably at least 95, but there is no disclosure of the lubricating oil base oil of the present invention.
- the use of an oil of which the minimum value of the kinematic viscosity at 40°C is preferably 8 mm 2 /s and more desirably 10 mm 2 /s, and the maximum value of the kinematic viscosity at 40°C is preferably 60 mm 2 /s and more desirably 40 mm 2 /s is desirable.
- the viscosity index is preferably at least 80 and more desirably at least 95, but there is no disclosure of the fact that the viscosity index is at least 130 and the density is not more than 0.84 g.cm -3 as in the case of the lubricating oil base oil of the present invention.
- the present invention surprisingly provides a lubricating oil composition with which the formation of sludge is suppressed even when the usual lubricating oil additives are compounded, which has excellent storage stability, which has low friction properties, with which the pressure transmission loss is small, with which the supply pressure loss in pipe-work is small, and which has low flammability.
- the present invention provides a lubricating oil composition
- a lubricating oil composition comprising lubricating oil base oil, wherein said composition has a kinematic viscosity at 40°C of from 18 to 60 mm 2 /s, a viscosity index of from 130 to 150, a density at 15°C of from 0.80 to 0.84 g.cm -3 and a flash point of at least 250°C as measured by JIS K 2265.
- the lubricating oil base oil is narrow cut base oil or mixtures of narrow cut base oils, wherein the composition of the narrow-cut base oils is such that with the method of measurement laid down in ASTM D 3238, the aromatic content (%CA) is not more than 0.1 wt% and the paraffin content (%Cp) is at least 85 wt%, the iso-paraffin content is at least 80 wt%, the elemental sulphur content is not more than 50 ppm, the elemental nitrogen content is not more than 5 ppm, the total polar material is not more than 1% and the properties are: refractive index at least 1.45, aniline point at least 120°C and they are colourless and transparent, being classified as L0.5 using the colour test method laid down in ASTM D 1500.
- the lubricating oil composition further comprises a primary amine which has a C 8 to C 20 tertiary alkyl group which can be represented by general formula (1) below wherein x is an integer of value from 1 to 17, y is an integer of value from 1 to 17, z is an integer of value from 1 to 17, and x + y + z is an integer of value from 7 to 19.
- a primary amine which has a C 8 to C 20 tertiary alkyl group which can be represented by general formula (1) below wherein x is an integer of value from 1 to 17, y is an integer of value from 1 to 17, z is an integer of value from 1 to 17, and x + y + z is an integer of value from 7 to 19.
- the lubricating oil composition of the present invention contains from 0.001 to 5.0 parts by weight of the primary amine represented by general formula (1) is compounded per 100 parts by weight of the lubricating oil composition.
- the present invention further provides a hydraulic oil, a machine tool oil, a gear oil, a compressor oil, a turbine oil, a bearing oil and a heat transfer fluid
- a high viscosity index signifies that the temperature dependence of the lubricating oil viscosity is small and, for example, the temperature of the hydraulic oil when hydraulic equipment is first started is low and, while a hydraulic oil which has a low viscosity index will have a high viscosity, a hydraulic oil which has a high viscosity index will have a low viscosity at low temperature and it is possible to reduce the power consumption on start-up.
- the viscosity index as defined in JIS K 2283 is from 130 to 150, preferably from 132 to 150 and most desirably from 135 to 150.
- the kinematic viscosity at 10°C is 283.06 mm 2 /s, while if the viscosity index is 130 the kinematic viscosity at 10°C is 250.1 mm 2 /s and if the viscosity index is 135 then it is 242.98 mm 2 /s and the room temperature viscosity changes markedly according to the viscosity index, and since the electrical power consumption also increases in accordance with the kinematic viscosity, a high viscosity index is also desirable for reducing the power consumption on start-up.
- the density at 15°C of the lubricating oil base oil measured by the method for measuring the density of lubricating oil defined in JIS K 2249 is from 0.80 to 0.84 g.cm -3 , preferably from 0.81 to 0.84 g.cm -3 , more desirably from 0.815 to 0.835 g.cm -3 and most desirably from 0.820 to 0.830 g.cm -3 .
- hydraulic equipment generally operates at an oil temperature of from 40 to 60°C, but in the case of a density at 15°C of 0.84 g.cm -3 , the density, when calculated using the density calculation method indicated in JIS K 2249, at 40°C is 0.8233 g.cm -3 , at 50°C is 0.8167 g.cm -3 and at 60°C is 0.8100 g.cm -3 , and so the density at 40°C is preferably not more than 0.8167 g.cm -3 , the density at 50°C is preferably not more than 0.8167 g.cm -3 and the density at 60°C is preferably not more than 0.8100 g.cm -3 .
- a lubricating oil composition which has low friction properties contributes to energy conservation, it is preferred that there are low friction properties such that stick-slip does not occur in steel-steel situations.
- the flash point of the lubricating oil base oil as measured using the Cleveland formula defined in JIS K 2265 is at least 250°C, preferably at least 252°C, more preferably at least 256°C.
- Storage stability of a lubricating oil composition is essential for providing useful performance as an industrial lubricating oil.
- troubles may arise in precision hydraulic systems, for example, in the case of lubricating oil compositions where turbidity or precipitation occurs.
- the narrow-cut base oils wherein the molecular weight distribution of the hydrocarbons in the base oil is very narrow can be cited as base oils which do satisfy these conditions.
- the Fischer-Tropsch derived base oil may any Fischer-Tropsch derived base oil as disclosed in for example EP-A-776959 , EP-A-668342 , WO-A-9721788 , WO-0015736 , WO-0014188 , WO-0014187 , WO-0014183 , WO-0014179 , WO-0008115 , WO-9941332 , EP-1029029 , WO-0118156 and WO-0157166 .
- these three types of narrow-cut base oil are used individually or in the form of mixtures so as to provide the prescribed viscosity.
- Such narrow-cut oils also exhibit especially good volatilisation resistance.
- an ISO VG 32 grade in the viscosity classification for industrial lubricating oils is prepared by combining these base oils, the result in a volatile loss test (NOACK) as defined in ASTM D 5800 is suppressed to 8% or less.
- the volatile loss test (NOACK) result in the case of an ISO VG 46 grade oil prepared in the same way is less than 5%.
- these narrow-cut base oils can also be said to be suitable for lubricating oils where involatility is required as in the case of a compressor lubricating oils for example.
- the amount of the primary amine compound represented by general formula (1) compounded in the lubricating oil composition of the present invention is preferably from 0.001 to 1.0 part by weight, preferably from 0.001 to 0.5 part by weight, and most desirably from 0.001 to 0.05 part by weight, per 100 parts by weight of the lubricating oil composition.
- Examples of the aliphatic hydrocarbyl groups represented by C x H 2x + 1 , C y H 2y +1 and C z H 2z + 1 in the above-mentioned general formula (1) include the methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, the linear chain and branched pentyl groups, the linear chain and branched hexyl groups, the linear chain and branched heptyl groups, the linear chain and branched octyl groups, the linear chain and branched nonyl groups, the linear chain and branched decyl groups, the linear chain and branched undecyl groups, the linear chain and branched dodecyl groups, the linear chain and branched tridecyl groups, the linear chain and branched tetradecyl groups, the linear chain and
- lubricating oil additives such as antioxidants, metal deactivators, extreme pressure additives, oil-improving agents, antifoaming agents, viscosity index improving agents, pour point depressants, cleaning dispersants, anti-rust agents and anti-emulsification agents can be added.
- amine-based antioxidants include dialkyldiphenylamines such as p,p'-dioctyl-diphenylamine (such as that produced under the trade designation "Sonoflex OD-3" by the Seiko Kagaku Co.), p,p'-di- ⁇ -methylbenzyl-diphenylamine and N-p-butylphenyl-N-p'-octylphenylamine, monoalkyldiphenylamines such as mono-t-butyldiphenylamine and mono-octyldiphenylamine, bis(dialkylphenyl)amines such as di-(2,4-diethylphenyl)amine and di(2-ethyl-4-nonylphenyl)amine, alkylphenyl-1-naphthylamines such as octylphenyl-1-naphthylamine and n-t-dodecylphenyl-1
- sulphur-based anti-oxidants examples include dialkylsulphites such as didodecylsulphite and dioctylsulphite, thiodipropionic acid esters such as didodecylthiodipropionate, dioctadecylthiodipropionate, dimyristylthiodipropionate and dodecyloctadecylthiodipropionate, and 2-mercaptobenzimidazole.
- dialkylsulphites such as didodecylsulphite and dioctylsulphite
- thiodipropionic acid esters such as didodecylthiodipropionate, dioctadecylthiodipropionate, dimyristylthiodipropionate and dodecyloctadecylthiodipropionate
- 2-mercaptobenzimidazole examples include dialky
- phenol-based antioxidants examples include 2-t-butylphenol, 2-t-butyl-4-methylphenol, 2-t-butyl-5-methylphenol, 2,4-di-t-butylphenol, 2,4-dimethyl-6-t-butylphenol, 2-t-butyl-4-methoxyphenol, 3-t-butyl-4-methoxyphenol, 2,5-di-t-butylhydroquinone (such as that produced under the trade designation "Anteeji DBH" by the Kawaguchi Kagaku Co.,), 2,6-di-t-butyl-4-alkylphenols such as 2,6-di-t-butylphenol, 2,6-di-t-butyl-4-methylphenol and 2,6-di-t-butyl-4-ethylphenol, 2,6-di-t-butyl-4-alkoxyphenols such as 2,6-di-t-butyl-4-methoxyphenol and 2,6-di-t
- phosphorus-based antioxidants include triaryl phosphites such as triphenyl phosphite and tricresyl phosphite, trialkyl phosphites such as trioctadecyl phosphite and tridecyl phosphite, and tridodecyl trithiophosphite.
- antioxidants can be conveniently used individually or in the form of a combination of number of types in an amount within the range of from 0.01 to 2.0 parts by weight, per 100 parts by weight of lubricating oil composition.
- metal de-activating agents can be conveniently used individually or in the form of a combination of a number of types in an amount within the range of from 0.01 to 0.5 parts by weight, per 100 parts by weight of lubricating oil composition.
- antifoaming agents examples include organosilicates such as dimethylpolysiloxane, diethylsilicate and fluorosilicone, and non-silicone antifoaming agents such as polyalkylacrylates. These can be conveniently used individually or in the form of a combination of a number of types in amounts within the range of from 0.0001 to 0.1 part by weight, per 100 parts by weight of lubricating composition.
- viscosity index improving agents examples include non-dispersing type viscosity improving agents such as polymethacrylates and olefin copolymers such as ethylene-propylene copolymers and styrene-diene copolymers, and dispersing type viscosity improving agents where nitrogen-containing monomers have been copolymerized in these materials.
- the amount added can be conveniently within the range of from 0 to 20 parts by weight, per 100 parts by weight of lubricating oil composition.
- the amount of viscosity index improving agent compounded is preferably from 0 to 5 parts by weight and more desirably from 0 to 2 parts by weight, while most desirably no viscosity index improving agent is compounded at all.
- pour point depressants examples include polymethacrylate-based polymers. These can be conveniently used in amounts within the range of from 0.01 to 5 parts by weight, per 100 parts of lubricating oil composition.
- cleaning dispersing agents examples include metal-based detergents such as neutral or basic alkaline earth metal sulphonates, alkaline earth metal phenates and alkaline earth metal salicylates, and ash-less dispersants such as alkenylsuccinimides, alkenyl succinic acid esters, and modified products derived therefrom with boron compounds and sulphur compounds for example.
- metal-based detergents such as neutral or basic alkaline earth metal sulphonates, alkaline earth metal phenates and alkaline earth metal salicylates
- ash-less dispersants such as alkenylsuccinimides, alkenyl succinic acid esters, and modified products derived therefrom with boron compounds and sulphur compounds for example.
- ash-less dispersants such as alkenylsuccinimides, alkenyl succinic acid esters, and modified products derived therefrom with boron compounds and sulphur compounds for example.
- extreme pressure agents and oil-improving agents examples include the sulphur-based extreme pressure additives such as dialkysulphides, dibenzylsulphide, dialkylpolysulphides, dibenzylpolysulphide, alkylmercaptans, benzothiophene and 2,2'-dithiobis(benzothiazole), and aliphatic oil-improving agents such as fatty acid amides and fatty acid esters.
- sulphur-based extreme pressure additives such as dialkysulphides, dibenzylsulphide, dialkylpolysulphides, dibenzylpolysulphide, alkylmercaptans, benzothiophene and 2,2'-dithiobis(benzothiazole)
- aliphatic oil-improving agents such as fatty acid amides and fatty acid esters.
- These anti-rust agents can be conveniently used individually or in the form of a combination of a number of types in amounts within the range of from 0.01 to 2 parts by weight per 100 parts by weight, of lubricating oil composition
- anti-emulsification agents used generally as lubricating oil additives can be conveniently used as anti-emulsification agents in the lubricating oil compositions of the present invention. They can be conveniently used in amounts within the range of from 0.0005 to 0.5 part by weight, per 100 parts by weight of lubricating oil composition.
- the lubricating oil compositions of the present invention can be used as industrial lubricating oils and, in particular, as hydraulic oils. Moreover, they are also useful as heat transfer fluids, machine tool oils, gear oils, compressor oils, turbine oils, bearing oils and greases in view of their surprising ability to eliminate the pressure loss in hydraulic pipe-work.
- the sample oil was coated between steel test pieces moved at a slip rate of 12.7 mm/minute with a loading of 22.4 kgf using a stick-slip tester produced by the Cincinnati Milacron Co. (formerly ASTM D 2877) and whether or not sticking occurred was assessed in order to evaluate the low-friction - energy conserving properties of the sample oil.
- Lubricating oils where stick-slip occurred had a high coefficient of friction and were unsatisfactory in terms of energy conservation and therefore assessed a failure.
- the sample oil was introduced into a clear gloss bottle and left to stand in the dark in the open air in winter with a view to evaluating solubility, and those where there was no turbidity or precipitate formation were adjudged to have passed the test. Moreover, the open air temperature varied gradually between 5 and -5°C.
- the lubricating oil compositions of the present invention have excellent thermal oxidation stability, lubricating properties and filtration characteristics from the viewpoint of both the safety aspects and the actual performance of the compositions.
- Example 11 Comp. Ex. 16 Comp. Ex. 17 Comp. Ex. 18 Formulation Type Formulation according to the present invention containing 98.97 %wt. of Base Oil 4, 0.03 %wt. of Amine 2.
- the balance was made up of standard additive components.
- Anti-wear hydraulic oil according to WO-A-00/63325 .
- Synthetic biodegradable lubricant Synthetic biodegradable lubricant.
- Viscosity Modifier improved multigrade hydraulic conventional anti-wear hydraulic fluid.
- Mineral-oil based (HVI). A commercially available ISO VG 46 environmentally acceptable hydraulic fluid consisting of synthetic esters (HEES) and ashless additives. ISO VG 46. Mineral-oil based (HVI). Ester-based.
- the first test assessed the effects (predicted as no effect) that the relationship between altering swash plate angle or drive speed have on pump efficiency.
- the swash plate was set at different angles and then given running conditions achieved, set flow rate, speed, temperature and pressure so that the displacement of the pump was the only variable. Efficiency calculations were then performed on the data gathered and any effect was found to be below the scope of the measuring equipment, hence the relationship is assumed to be negligible.
- Denison hydraulic piston pump rig used to assess hydraulic fluids and pump efficiency, including electrical fault-finding and calibration of the torque transducer.
- a contact box with an over-current switch controls the rig, and a dial linked to an electronic control box allows the drive shaft speed to be adjusted.
- Fluid temperature is varied between room temperature and 80°C.
- Pressure is varied between 0 Bar and 130 Bar under normal test conditions, using a manual screw-in valve.
- Periodically maintenance and cleaning may be required, such as fluid changes and adjustments to the swash plate.
- Example 11 has not only a higher VI than the conventional anti-wear hydraulic oil of Comparative Example 16, but also has a significantly lower density.
- Example 11 surprisingly has the highest relative efficiency as the pump requires less energy per unit of fluid pumped. It would be expected in real systems where a much higher proportion of pipework exists that the benefit would be of the order of 5% or more, which could be determined by monitoring electricity consumption.
- the present invention makes it possible to make use of narrow-cut base oils in industrial lubricating oils to increase energy conservation and raise the flash point where necessary and to provide lubricating oil compositions which, when compared with commercial industrial lubricating oils of the same viscosity, have a density reduced by some 10% and which surprisingly have an energy conserving effect.
- lubricating oil compositions of the present invention may be used in a wide range of industrial lubricating oils, such as hydraulic oils, machine tool oils, gear oils, compressor oils, turbine oils, bearing oils, heat transfer fluids and greases.
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JP2003040127A JP5057630B2 (ja) | 2003-02-18 | 2003-02-18 | 工業用潤滑油組成物 |
PCT/EP2004/050150 WO2004074412A2 (en) | 2003-02-18 | 2004-02-18 | Lubricating oil compositions |
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US (1) | US20040224860A1 (es) |
EP (1) | EP1594943B1 (es) |
JP (1) | JP5057630B2 (es) |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006030490A1 (ja) * | 2004-09-14 | 2006-03-23 | Idemitsu Kosan Co., Ltd. | 冷凍機油組成物 |
US20060063685A1 (en) * | 2004-09-22 | 2006-03-23 | Pieter Purmer | Lubricant for manual or automated manual transmissions |
CN101321852B (zh) * | 2005-02-11 | 2012-02-22 | R.T.范德比尔特公司 | 含有二硫代氨基甲酸锑的润滑脂 |
CN101198682B (zh) * | 2005-06-23 | 2012-02-22 | 国际壳牌研究有限公司 | 电气绝缘用油配制物 |
US20100144571A1 (en) * | 2005-06-29 | 2010-06-10 | Shinichi Shirahama | Base oil for hydraulic oil and composition using the same |
CN101278036B (zh) * | 2005-09-29 | 2011-04-20 | 出光兴产株式会社 | 润滑组合物 |
JP5301078B2 (ja) | 2005-11-15 | 2013-09-25 | 出光興産株式会社 | 圧力媒体油 |
US20070197410A1 (en) * | 2006-02-21 | 2007-08-23 | Rohmax Additives Gmbh | Energy efficiency in hydraulic systems |
JP5255243B2 (ja) * | 2006-09-11 | 2013-08-07 | 昭和シェル石油株式会社 | 潤滑油組成物 |
JP5180466B2 (ja) * | 2006-12-19 | 2013-04-10 | 昭和シェル石油株式会社 | 潤滑油組成物 |
JP5426829B2 (ja) * | 2007-02-07 | 2014-02-26 | 昭和シェル石油株式会社 | 油圧シリンダーのビビリ、振動、鳴き防止用潤滑油組成物 |
US20080302422A1 (en) * | 2007-06-07 | 2008-12-11 | Rohmax Additives Gmbh | Power output in hydraulic systems |
JP5623276B2 (ja) * | 2007-08-23 | 2014-11-12 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイShell Internationale Research Maatschappij Beslotenvennootshap | 潤滑油組成物の使用法 |
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JP5800449B2 (ja) * | 2008-03-25 | 2015-10-28 | Jx日鉱日石エネルギー株式会社 | 潤滑油基油及びその製造方法並びに潤滑油組成物 |
US20110021394A1 (en) * | 2008-03-27 | 2011-01-27 | Jx Nippon Oil & Energy Corporation | Lubricant composition |
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WO2010075046A2 (en) * | 2008-12-23 | 2010-07-01 | Shrieve Chemical Products, Inc. | Refrigerant lubricant composition |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2758086A (en) * | 1952-06-28 | 1956-08-07 | California Research Corp | Lubricant composition |
US3290245A (en) * | 1959-06-05 | 1966-12-06 | Castrol Ltd | Lubricating compositions containing amine tungstates |
US4101427A (en) * | 1977-02-09 | 1978-07-18 | Exxon Research & Engineering Co. | Lubricant composition |
US4917809A (en) * | 1986-11-11 | 1990-04-17 | Ciba-Geigy Corporation | High-temperature lubricants |
US5552068A (en) * | 1993-08-27 | 1996-09-03 | Exxon Research And Engineering Company | Lubricant composition containing amine phosphate |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1595701A (en) * | 1977-06-24 | 1981-08-19 | Castrol Ltd | Fluids suitable for use as hydraulic fluids electrical oils heat transfer fluids and refrigerant oils |
US4392968A (en) * | 1980-08-13 | 1983-07-12 | Nippon Oil Company, Limited | Metal deactivator and composition containing same |
US4975177A (en) * | 1985-11-01 | 1990-12-04 | Mobil Oil Corporation | High viscosity index lubricants |
US5275749A (en) * | 1992-11-06 | 1994-01-04 | King Industries, Inc. | N-acyl-N-hydrocarbonoxyalkyl aspartic acid esters as corrosion inhibitors |
EP0684298A3 (en) * | 1994-05-23 | 1996-04-03 | Lubrizol Corp | Compositions for increasing the shelf life of seals and the lubricants and functional fluids containing them. |
US5737469A (en) * | 1996-06-03 | 1998-04-07 | Witco Corporation | Filling compound for fiber optical cables |
US6180575B1 (en) * | 1998-08-04 | 2001-01-30 | Mobil Oil Corporation | High performance lubricating oils |
US6627779B2 (en) * | 2001-10-19 | 2003-09-30 | Chevron U.S.A. Inc. | Lube base oils with improved yield |
US6646174B2 (en) * | 2002-03-04 | 2003-11-11 | Bp Corporation North America Inc. | Co-oligomerization of 1-dodecene and 1-decene |
-
2003
- 2003-02-18 JP JP2003040127A patent/JP5057630B2/ja not_active Expired - Lifetime
-
2004
- 2004-02-18 WO PCT/EP2004/050150 patent/WO2004074412A2/en active Search and Examination
- 2004-02-18 CN CN200480004455A patent/CN100587048C/zh not_active Expired - Lifetime
- 2004-02-18 MX MXPA05008671A patent/MXPA05008671A/es unknown
- 2004-02-18 CA CA002516271A patent/CA2516271A1/en not_active Abandoned
- 2004-02-18 KR KR1020057015233A patent/KR20050098951A/ko not_active Application Discontinuation
- 2004-02-18 EP EP04712057.1A patent/EP1594943B1/en not_active Expired - Lifetime
- 2004-02-18 RU RU2005129121/04A patent/RU2352621C2/ru active
- 2004-02-18 BR BRPI0407521A patent/BRPI0407521B8/pt active IP Right Grant
- 2004-02-18 US US10/781,028 patent/US20040224860A1/en not_active Abandoned
-
2005
- 2005-08-03 ZA ZA200506194A patent/ZA200506194B/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2758086A (en) * | 1952-06-28 | 1956-08-07 | California Research Corp | Lubricant composition |
US3290245A (en) * | 1959-06-05 | 1966-12-06 | Castrol Ltd | Lubricating compositions containing amine tungstates |
US4101427A (en) * | 1977-02-09 | 1978-07-18 | Exxon Research & Engineering Co. | Lubricant composition |
US4917809A (en) * | 1986-11-11 | 1990-04-17 | Ciba-Geigy Corporation | High-temperature lubricants |
US5552068A (en) * | 1993-08-27 | 1996-09-03 | Exxon Research And Engineering Company | Lubricant composition containing amine phosphate |
Also Published As
Publication number | Publication date |
---|---|
EP1594943A2 (en) | 2005-11-16 |
BRPI0407521A (pt) | 2006-02-14 |
MXPA05008671A (es) | 2005-10-18 |
CN100587048C (zh) | 2010-02-03 |
WO2004074412A2 (en) | 2004-09-02 |
ZA200506194B (en) | 2006-09-27 |
JP5057630B2 (ja) | 2012-10-24 |
CA2516271A1 (en) | 2004-09-02 |
CN1751115A (zh) | 2006-03-22 |
WO2004074412A3 (en) | 2004-10-28 |
BRPI0407521B8 (pt) | 2020-04-07 |
AU2004213598A1 (en) | 2004-09-02 |
RU2005129121A (ru) | 2006-01-27 |
KR20050098951A (ko) | 2005-10-12 |
US20040224860A1 (en) | 2004-11-11 |
RU2352621C2 (ru) | 2009-04-20 |
JP2004250504A (ja) | 2004-09-09 |
BRPI0407521B1 (pt) | 2020-03-17 |
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