EP2636725B1 - Schmierölzusammensetzung für die Schmierung eines Automobilmotors - Google Patents
Schmierölzusammensetzung für die Schmierung eines Automobilmotors Download PDFInfo
- Publication number
- EP2636725B1 EP2636725B1 EP13157940.1A EP13157940A EP2636725B1 EP 2636725 B1 EP2636725 B1 EP 2636725B1 EP 13157940 A EP13157940 A EP 13157940A EP 2636725 B1 EP2636725 B1 EP 2636725B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lubricating oil
- viscosity
- oil composition
- mass
- base oil
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
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- 239000000203 mixture Substances 0.000 title claims description 83
- 239000010687 lubricating oil Substances 0.000 title claims description 75
- 238000005461 lubrication Methods 0.000 title claims description 9
- 239000002199 base oil Substances 0.000 claims description 62
- -1 amine compounds Chemical class 0.000 claims description 28
- 239000003795 chemical substances by application Substances 0.000 claims description 28
- 239000003963 antioxidant agent Substances 0.000 claims description 25
- 239000002270 dispersing agent Substances 0.000 claims description 20
- 238000001704 evaporation Methods 0.000 claims description 20
- 230000008020 evaporation Effects 0.000 claims description 20
- 239000002480 mineral oil Substances 0.000 claims description 20
- 235000010446 mineral oil Nutrition 0.000 claims description 20
- 239000000654 additive Substances 0.000 claims description 17
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- 230000003078 antioxidant effect Effects 0.000 claims description 14
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 239000011574 phosphorus Substances 0.000 claims description 13
- 229910052698 phosphorus Inorganic materials 0.000 claims description 13
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 12
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 12
- 239000003502 gasoline Substances 0.000 claims description 12
- 239000003599 detergent Substances 0.000 claims description 11
- 230000001050 lubricating effect Effects 0.000 claims description 10
- 230000000996 additive effect Effects 0.000 claims description 7
- 238000005984 hydrogenation reaction Methods 0.000 claims description 7
- 238000006317 isomerization reaction Methods 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 229920000193 polymethacrylate Polymers 0.000 claims description 7
- 239000007789 gas Substances 0.000 claims description 6
- 150000002898 organic sulfur compounds Chemical class 0.000 claims description 6
- 238000004821 distillation Methods 0.000 claims description 5
- 239000005078 molybdenum compound Substances 0.000 claims description 5
- 150000002752 molybdenum compounds Chemical class 0.000 claims description 5
- 150000002989 phenols Chemical class 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- KZNICNPSHKQLFF-UHFFFAOYSA-N dihydromaleimide Natural products O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 36
- 235000006708 antioxidants Nutrition 0.000 description 24
- 239000011575 calcium Substances 0.000 description 23
- 239000011701 zinc Substances 0.000 description 19
- 239000010705 motor oil Substances 0.000 description 18
- 229960002317 succinimide Drugs 0.000 description 18
- 229910052725 zinc Inorganic materials 0.000 description 18
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 17
- 125000000217 alkyl group Chemical group 0.000 description 17
- 229910052791 calcium Inorganic materials 0.000 description 17
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 16
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000001993 wax Substances 0.000 description 10
- 239000003921 oil Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 229910017464 nitrogen compound Inorganic materials 0.000 description 8
- 150000002830 nitrogen compounds Chemical class 0.000 description 8
- 239000004129 EU approved improving agent Substances 0.000 description 7
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
- 239000002585 base Substances 0.000 description 7
- 239000000446 fuel Substances 0.000 description 7
- 229910052750 molybdenum Inorganic materials 0.000 description 7
- 239000011733 molybdenum Substances 0.000 description 7
- 238000005086 pumping Methods 0.000 description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229920001083 polybutene Polymers 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 5
- 229920000768 polyamine Polymers 0.000 description 5
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical group ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 4
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- ZMRQTIAUOLVKOX-UHFFFAOYSA-L calcium;diphenoxide Chemical compound [Ca+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 ZMRQTIAUOLVKOX-UHFFFAOYSA-L 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 229920001281 polyalkylene Polymers 0.000 description 4
- 229920013639 polyalphaolefin Polymers 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- 229940014800 succinic anhydride Drugs 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 125000005266 diarylamine group Chemical group 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 150000003138 primary alcohols Chemical class 0.000 description 3
- 150000003333 secondary alcohols Chemical class 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 239000003981 vehicle Substances 0.000 description 3
- PZBGMTRNNJMLGH-UHFFFAOYSA-L C1(=CC=CC=C1)CS(=O)(=O)[O-].[Ca+2].C1(=CC=CC=C1)CS(=O)(=O)[O-] Chemical class C1(=CC=CC=C1)CS(=O)(=O)[O-].[Ca+2].C1(=CC=CC=C1)CS(=O)(=O)[O-] PZBGMTRNNJMLGH-UHFFFAOYSA-L 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000013556 antirust agent Substances 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- VJOCYCQXNTWNGC-UHFFFAOYSA-L calcium;benzenesulfonate Chemical class [Ca+2].[O-]S(=O)(=O)C1=CC=CC=C1.[O-]S(=O)(=O)C1=CC=CC=C1 VJOCYCQXNTWNGC-UHFFFAOYSA-L 0.000 description 2
- 125000005521 carbonamide group Chemical group 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000994 depressogenic effect Effects 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000012990 dithiocarbamate Substances 0.000 description 2
- 150000004659 dithiocarbamates Chemical class 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 239000010711 gasoline engine oil Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
- YFHKLSPMRRWLKI-UHFFFAOYSA-N 2-tert-butyl-4-(3-tert-butyl-4-hydroxy-5-methylphenyl)sulfanyl-6-methylphenol Chemical compound CC(C)(C)C1=C(O)C(C)=CC(SC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 YFHKLSPMRRWLKI-UHFFFAOYSA-N 0.000 description 1
- RKLRVTKRKFEVQG-UHFFFAOYSA-N 2-tert-butyl-4-[(3-tert-butyl-4-hydroxy-5-methylphenyl)methyl]-6-methylphenol Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 RKLRVTKRKFEVQG-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
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 1
- CFXCGWWYIDZIMU-UHFFFAOYSA-N Octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate Chemical compound CCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 CFXCGWWYIDZIMU-UHFFFAOYSA-N 0.000 description 1
- QAPVYZRWKDXNDK-UHFFFAOYSA-N P,P-Dioctyldiphenylamine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=C(CCCCCCCC)C=C1 QAPVYZRWKDXNDK-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- GLOYGJPNNKTDIG-UHFFFAOYSA-N SC=1N=NSC=1S Chemical class SC=1N=NSC=1S GLOYGJPNNKTDIG-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- WGQKYBSKWIADBV-UHFFFAOYSA-N aminomethyl benzene Natural products NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 1
- SCJNCDSAIRBRIA-DOFZRALJSA-N arachidonyl-2'-chloroethylamide Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NCCCl SCJNCDSAIRBRIA-DOFZRALJSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- 150000005676 cyclic carbonates Chemical class 0.000 description 1
- LMODBLQHQHXPEI-UHFFFAOYSA-N dibutylcarbamothioylsulfanylmethyl n,n-dibutylcarbamodithioate Chemical compound CCCCN(CCCC)C(=S)SCSC(=S)N(CCCC)CCCC LMODBLQHQHXPEI-UHFFFAOYSA-N 0.000 description 1
- 229940035422 diphenylamine Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000003949 imides Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 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
- KDOVHSDPJGQWKL-UHFFFAOYSA-N octyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CCCCCCCCOC(=O)CCC1=CC(C)=C(O)C(C(C)(C)C)=C1 KDOVHSDPJGQWKL-UHFFFAOYSA-N 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 229940113162 oleylamide Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 125000005541 phosphonamide group Chemical group 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-L phosphoramidate Chemical compound NP([O-])([O-])=O PTMHPRAIXMAOOB-UHFFFAOYSA-L 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 150000003580 thiophosphoric acid esters Chemical class 0.000 description 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 1
- MBBWTVUFIXOUBE-UHFFFAOYSA-L zinc;dicarbamodithioate Chemical compound [Zn+2].NC([S-])=S.NC([S-])=S MBBWTVUFIXOUBE-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M161/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M125/00—Lubricating compositions characterised by the additive being an inorganic material
- C10M125/24—Compounds containing phosphorus, arsenic or antimony
-
- 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
- C10M125/00—Lubricating compositions characterised by the additive being an inorganic material
- C10M125/20—Compounds containing nitrogen
-
- 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
- C10M169/06—Mixtures of thickeners 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions 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
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/022—Ethene
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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
- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
- C10M2205/163—Paraffin waxes; Petrolatum, e.g. slack wax used as base material
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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
- C10M2205/17—Fisher Tropsch reaction products
- C10M2205/173—Fisher Tropsch reaction products used as base material
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- 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
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- 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
- C10M2207/028—Overbased salts thereof
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—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
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- 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
- C10M2215/28—Amides; Imides
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/022—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of hydrocarbons, e.g. olefines
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/046—Overbasedsulfonic acid salts
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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
- C10M2223/045—Metal containing thio derivatives
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/12—Groups 6 or 16
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- 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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- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/54—Fuel economy
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- 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
- C10N2030/68—Shear stability
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- 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
- C10N2030/74—Noack Volatility
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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
- C10N2040/25—Internal-combustion engines
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
Definitions
- the present invention relates to an excellent fuel-efficient, low-viscosity lubricating oil composition for an automobile engine, and in particular, relates to a lubricating oil composition for automobile engine lubrication that, while being an excellent fuel-efficient, low-viscosity lubricating oil composition for engine lubrication, also shows high wear resistance.
- the present invention relates to a low-viscosity lubricating oil composition that is particularly suitable for lubricating a motorcycle four-cycle gasoline engine or a diesel engine having an exhaust gas after-treatment device.
- engine oil lubricating oil composition
- engine oils that have an SAE viscosity grade of 5W20 and a high-temperature high-shear viscosity (value measured at 150°C when the shear velocity or shear rate is 10 6 s -1 ) of 2.6 mPa ⁇ s are already being used for practical purposes as fuel-efficient lubricating oil compositions for gasoline engines in four-wheel drive vehicles.
- the engine oil is also used to lubricate the transmission system and there is a chance that wear of the energy-transmission devices, such as the transmission gears, will increase (wear resistance will decrease) as a result of a reduction in viscosity of the engine oil.
- JASO T903-2006 stipulates that the engine oils for motorcycle four-cycle gasoline engines have a high-temperature, high-shear (10 6 s -1 ) viscosity of 2.9 mPa ⁇ s or greater.
- ACEA C1-08 and C2-08 which are the European standards for engine oils appropriate for lubrication of diesel engine vehicles having diesel particulate filters, set the lower limit of high-temperature, high-shear (10 6 s -1 ) viscosity of engine oils at 2.9 mPa ⁇ s and, in order to limit evaporation loss of engine oils, the upper limit of NOACK evaporation loss at 13%.
- Patent Document JP (Kokai) 6-306384 describes a fuel-efficient lubricating oil for an internal combustion engine wherein a predetermined amount of an organic molybdenum compound is added to a mineral oil base oil having a dynamic viscosity at 100°C of 3 to 5 cSt, a viscosity index of 135 or higher, and a paraffin to total carbon ratio (%Cp) of 90% or higher.
- Patent Document JP (Kohyo) 2003-505533 describes a lubricating oil composition that, as a molybdenum additive-free, fuel-efficient, low-volatility lubricating oil composition having a NOACK volatility of 15 wt% or less, contains a predetermined amount of a calcium detergent and a predetermined amount of an oil-soluble organic wear-improving agent, as well as a base oil comprising at least 50 wt% of mineral oil; has a dynamic viscosity at 100°C of 4.0 to 5.5 mm 2 /s; contains 95 wt% or more of saturated product and 25 wt% or less of naphthenes; has a viscosity index of at least 120; and has an NOACK volatility of 15.5 wt% or less.
- Patent Document JP (Kokai) 2000-87070 describes an excellent fuel-efficient motorcycle four-cycle engine composition having an oil consumption-lowering effect that contains a hydrocarbon lubricating oil base oil having a dynamic viscosity at 100°C of 3 to 10 mm 2 /s and a viscosity index of 120 or higher, or a mixed base oil containing at least 15 mass% of this base oil, a zinc dialkyl dithiophosphate, a metal detergent, an ash-free dispersant, a wear regulator, and a viscosity index-improving agent that brings dynamic viscosity at 100°C of this composition to 9.3 to 16.5 mm 2 /s.
- it describes a motorcycle four-cycle engine composition having an SAE viscosity grade of 10W30 or 10W40.
- US2009/163393 A1 discloses lubricating oil for high performance engines comprising a Group III base oil and a combination of ester base stocks.
- a lubricating oil composition that has an SAE viscosity grade of 5W20 and yet a viscosity index within a range of 140 to 230, a high-shear (10 6 s -1 ) viscosity at 150°C of 2.9 mPa ⁇ s or higher, a NOACK evaporation loss of 13% or less, and excellent wear resistance by using a base oil such as has been recently supplied to the market and is primarily isoparaffin, has an ultrahigh viscosity index wherein the viscosity index is within a range of approximately 133 to 160, and is obtained by hydrogenation and isomerization of a slack wax or a synthetic wax produced by the Fischer-Tropsch method and distillation and dewaxing treatment, and by optimizing the combination of additive components added to the base oil and the amount of each lubricant component.
- SAE viscosity grade 5W20 are already known
- the present invention is a lubricating oil composition for automobile engine lubrication, which is a lubricating oil composition comprising a base oil and the following additive components and having an SAE viscosity grade of 5W20, wherein the viscosity index is within a range of 140 to 230, the high-shear viscosity at 150°C is 2.9 mPa ⁇ s or higher, and the NOACK evaporation loss is 13% or less, further comprising:
- lubricating oil composition having an SAE viscosity grade of 5W20 of the present invention refers to a lubricating oil composition that satisfies the viscosity property of "5W20" described in “SAE viscosity grades for engine oils” of the American Petroleum Institute (revised in 2007).
- high-shear viscosity refers to the measured value (shear viscosity) when the shear speed or shear rate is 10 6 s -1 .
- the present invention also is a method for lubricating a motorcycle four-cycle gasoline engine or a diesel engine having an exhaust gas after-treatment device.
- the lubricating oil composition for lubricating an automobile engine provided by the present invention is a lubricating oil composition having an SAE viscosity grade that is low at 5W20, while having a high-temperature, high-shear viscosity of 2.9 mPa ⁇ s or higher, and shows excellent fuel efficiency and wear resistance.
- the lubricating oil compositor of the present invention therefore is an excellent fuel-efficient, wear-resistant lubricating oil that is particularly suitable for lubricating a motorcycle four-cycle gasoline engine or a diesel engine having an exhaust gas after-treatment device.
- the base oil of the lubricating oil composition of the present invention is preferably a mineral oil. It can also be a mixture of a relatively large amount (at least 50 mass%) of a mineral oil and a relatively small amount (less than 50 mass%) of a synthetic oil.
- the base oil used in the lubricating oil composition of the present invention is a base oil that is primarily an isoparaffin and has a kinematic viscosity at 100°C of 2 to 9 mm 2 /s, a saturated component content of 95 mass% or higher (particularly 98 mass% or higher), and a viscosity index of 133 or higher (particularly 135 or higher, further 145 or higher).
- a base oil having such properties and composition can be used alone, or a combination of two or more types can be used.
- the base oil composition after mixing will still have the above-mentioned properties and composition.
- the base oil having the above-mentioned properties and composition preferably has an evaporation loss (ASTM D5800) of 16% or less (particularly 15% or less, further 13% or less).
- ASTM D5800 evaporation loss
- base oil there are no particular restrictions to the type of base oil showing the above-mentioned properties and composition, but when the base oil is a mineral oil, preferably it is a high-viscosity index base oil (base oil having a viscosity index between 133 and 160) the primary component of which is isoparaffin obtained by subjecting the slack wax that is the by-product of dewaxing during the production of mineral oil lubricating base oils, or synthetic wax synthesized using natural gas as the starting material (by the Fischer-Tropsche method), to hydrogenation and isomerization and then distillation and dewaxing.
- base oil is a mineral oil
- base oil base oil having a viscosity index between 133 and 160
- base oil base oil having a viscosity index between 133 and 160
- isoparaffin obtained by subjecting the slack wax that is the by-product of dewaxing during the production of mineral oil lubricating base oils, or synthetic wax synthesized using natural gas as the
- Such a high viscosity index base oil has a relatively high dynamic viscosity at 100°C, but has good low-temperature viscosity properties and therefore, can have a reduced evaporation loss and is ideal as the base oil of the lubricating oil composition of the present invention.
- the high-viscosity-index base oil which is the above-mentioned mineral oil
- a synthetic oil can be used together with a synthetic oil.
- the synthetic oil has the above-mentioned properties and composition.
- the preferred synthetic oil can be selected from a variety of conventional synthetic oils, and examples of such synthetic oils are various esters, alkylbenzenes, and polyalphaolefins (PAO). Polyalphaolefins (PAOs) are particularly preferred.
- the lubricating oil composition of the present invention comprises a nitrogen-containing ash-free dispersant (component a) in an amount within a range of 0.01 to 0.3 mass% in terms of the nitrogen content.
- a nitrogen-containing ash-free dispersant component a
- the mass-average molecular weight of the nitrogen-containing ash-free dispersant is within a range of 4,500 to 20,000.
- the phrase "mass-average molecular weight" used in the present specification is the molecular weight determined by GPC analysis with polystyrene as the standard substance.
- Typical examples of the nitrogen-containing ash-free dispersant used in the lubricating oil composition of the present invention are alkenyl and alkyl succinimides derived from polyolefins and derivatives of these succinimides. The amount added is within a range of 0.01 to 0.3 mass% in terms of the nitrogen content based on the total mass of the lubricating oil composition.
- Typical succinimides are obtained by reacting a succinic anhydride substituted by alkenyl or alkyl groups and having a high molecular weight and a polyalkylene polyamine containing an average of four to ten (preferably five to seven) nitrogen atoms per molecule.
- the succinimide anhydride that is substituted by alkenyl or alkyl groups and has a high molecular weight is preferably a polyolefin having a number-average molecular weight of approximately 900 to 5,000, particularly polybutene.
- chlorination by chlorine is used during the step for obtaining a polybutenyl succinimide by reacting polybutene and maleic anhydride.
- reactivity is good by this method, it has the effect of a large amount of chlorine (for instance, approximately 2,000 ppm) remaining in the succinimide final product.
- thermal reaction that does not use chlorine is employed, the residual chlorine contained in the final product can be kept to a very low level (for instance, 30 ppm or less).
- the succinimide that is used is produced by obtaining a polybutenyl succinimide anhydride by thermal reaction using highly reactive polybutene and then reacting this polybutenyl succinic anhydride with a polyalkylene polyamine having an average of four to ten nitrogen atoms (per one molecule).
- This succinimide can be further reacted with boric acid or an alcohol, aldehyde, ketone, alkyl phenol, cyclic carbonate, organic acid, and the like and used as a so-called modified succinimide.
- a boric acid-containing alkenyl (or alkyl) succinimide obtained by reaction with boric acid or a boron compound can be used in order to efficiently increase thermal and oxidation stability.
- this succinimide are mono-types, bis-types, and poly-types in accordance with the number of imide structures per molecule, but the bis-type or poly-type is preferred as the succinimide used for the purpose of the present invention.
- nitrogen-containing ash-free dispersants examples include polymeric succinimide dispersants derived from ethylene- ⁇ -olefin copolymer (having a molecular weight of 1,000 to 15,000, for instance) and alkenyl benzylamine ash-free dispersants.
- Nitrogen-containing dispersion-type viscosity index improvers can also be used in place of the nitrogen-containing ash-free dispersant.
- a nitrogen-containing olefin polymer or a nitrogen-containing polymethacrylate having a mass-average molecular weight of 90,000 or greater is used as the nitrogen-containing dispersion-type viscosity index-improving agent. Taking thermal stability into consideration, the former nitrogen-containing olefin copolymer is effective.
- the lubricating oil composition of the present invention contains a nitrogen-containing ash-free dispersant and/or nitrogen-containing dispersion-type viscosity index-improving agent as an active ingredient. These can also be used in combination with another ash-free dispersant, such as an alkenyl succinic acid ester ash-free dispersant.
- the lubricating oil composition of the present invention contains, as a metal-containing detergent, an alkaline earth metal-containing detergent (component (b)) in an amount within a range of 0.08 to 0.4 mass%.
- alkaline earth metals are calcium, barium, and magnesium, but calcium is preferred.
- a sulfonate or phenate of the alkaline earth metal is used as the metal-containing detergent.
- a combination of a sulfonate of an alkaline earth metal and a phenate of an alkaline earth metal can also be used. It is also possible to use a combination of these metal-containing detergents and a metal-containing detergent such as an alkyl salicylate and/or alkyl carboxylate of an alkaline earth metal (particularly calcium).
- Examples of calcium sulfonates are perbasic calcium sulfonate having a total base value of 150 to 500 mgKOH/g and low-basic calcium sulfonate having a total base value of 5 to 60 mgKOH/g.
- the perbasic calcium sulfonate is perbasic alkylated calcium benzene sulfonate or alkylated calcium toluene sulfonate having alkyl groups with 10 or more carbon atoms (usually the degree of perbasic conversion is within a range of 5 to 25).
- the low-basic calcium sulfonate is alkylated calcium benzene sulfonate or alkylated calcium toluene sulfonate having alkyl groups with ten or more carbon atoms and is usually one that is nearly a neutral salt subjected to virtually no perbasic conversion (preferably the degree of perbasic conversion is within a range of 0.1 to 1.5).
- a combination of a perbasic calcium sulfonate and a low-basic calcium sulfonate is used.
- the sulfonate can be a synthetic sulfonate as described above, or it can be a petroleum sulfonate obtained by sulfonating a lubricating oil fraction of a mineral oil to a calcium salt. Consequently, a petroleum low-basic calcium sulfonate/perbasic calcium sulfonate such as described above is preferred for the purpose of the present invention.
- Perbasic sulfurized calcium phenate having a total base value of 120 to 350 mgKOH/g is known as a calcium phenate.
- a perbasic sulfurized alkyl phenol calcium having alkyl groups with ten or more carbon atoms is preferred.
- the lubricating oil composition of the present invention contains a phosphorus-containing anti-wear agent (component c) in an amount within a range of 0.05 to 0.12 mass% in terms of the amount of phosphorus.
- Preferred phosphorus-containing anti-wear agents are zinc dihydrocarbyl dithiophosphate, zinc dihydrocarbyl monothiophate, and zinc dihydrocarbyl phosphate, which are known as lubricating oil additives that are multiperformance in that they have antioxidant performance and anti-wear performance.
- a primary or secondary alkyl group-type zinc dialkyl dithiophosphate is usually used as the zinc dihydrocarbyl dithiophosphate.
- a zinc dialkyl dithiophosphate having secondary alkyl groups derived from a C 3-18 secondary alcohol is effective in terms of anti-wear performance.
- a zinc dialkyl dithiophosphate having primary alkyl groups derived from a C 3-18 primary alcohol has a tendency toward being superior in terms of heat resistance and wear-reducing activity.
- a combination of a secondary alkyl group-type zinc dialkyl dithiophosphate and a primary alkyl group-type zinc dialkyl dithiophosphate can be used.
- a zinc dialkylaryl dithiophosphate (such as a zinc dialkylaryl dithiophosphate derived from dodecyl phenol) can also be used as the phosphorus-containing anti-wear agent.
- phosphoric acid ester phosphorus acid ester, or thiophosphoric acid ester
- phosphorus-containing anti-wear agent it is also possible to use a phosphoric acid ester, phosphorus acid ester, or thiophosphoric acid ester as the phosphorus-containing anti-wear agent.
- the lubricating oil composition of the present invention further contains, in an amount that is within a range of 0.1 to 7 mass%, at least one antioxidant (component d) selected from the group consisting of phenol compounds (phenol antioxidants), amine compounds (amine antioxidants), and molybdenum compounds (molybdenum antioxidants).
- at least one antioxidant selected from the group consisting of phenol compounds (phenol antioxidants), amine compounds (amine antioxidants), and molybdenum compounds (molybdenum antioxidants).
- a hindered phenol compound is generally used as the phenol antioxidant, and a diaryl amine compound is generally used as the amine antioxidant.
- Hindered phenol antioxidants and diaryl amine antioxidants are both also effective in improving high-temperature detergency.
- Diaryl amine antioxidants in particular have a base value derived from nitrogen and are effective in improving high-temperature detergency.
- hindered phenol antioxidants are effective in preventing oxidative degradation by NO x .
- hindered phenol antioxidants are 2,6-di-t-butyl-p-cresol, 4,4'-methylenebis(2,6-di-t-butylphenol), 4,4'-methylenebis(6-t-butyl-o-cresol), 4,4'-isoropylidenebis(2,6) ⁇ -di-t-butylphenol), 4,4'-bis(2,6-di-t-butylphenol), 2,2'-methylenebis(4-methyl-6-t-butylphenol), 4,4'-thiobis(2-methyl-6-t-butylphenol), 2,2-thiodiethylenebis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate], octyl 3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate, octadecyl 3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate, and oc
- amine antioxidants are C 4-9 mixed alkyl diphenyl amines, p,p'-dioctyldiphenylamine, phenyl- ⁇ -naphthylamine, phenyl- ⁇ -naphthylamine, alkylated- ⁇ -naphthylamine, and alkylated-phenyl- ⁇ -naphthylamine.
- molybdenum antioxidants are oxymolybdenum complexes of basic nitrogen compounds.
- preferred oxymolybdenum complexes of basic nitrogen compounds are oxymolybdenum complexes of succinimide and oxymolybdenum complexes of carbonamide.
- Oxymolybdenum complexes of basic nitrogen compounds can be produced using the following method, for instance.
- a molybdenum complex is produced by reacting an acidic molybdenum compound or salt thereof with a basic nitrogen compound, such as a succinimide, carbonamide, hydrocarbon monoamine, hydrocarbon polyamine, Mannich hydrochloric acid, phosphonamide, thiophosphonamide, phosphoric amide, dispersion-type viscosity index-improving agent (or a mixture thereof), while maintaining the reaction temperature at 120°C or lower.
- a basic nitrogen compound such as a succinimide, carbonamide, hydrocarbon monoamine, hydrocarbon polyamine, Mannich hydrochloric acid, phosphonamide, thiophosphonamide, phosphoric amide, dispersion-type viscosity index-improving agent (or a mixture thereof).
- molybdenum-containing compound other than an oxymolybdenum complex of a basic nitrogen compound in place of the oxymolybdenum complex of the basic nitrogen compound, or in combination with the oxymolybdenum complex of a basic nitrogen compound.
- molybdenum-containing compounds that can be used are sulfurized oxymolybdenum dithiocarbamates and sulfurized oxymolybdenum dithiophosphates.
- the phenol antioxidant particularly hindered phenol antioxidant
- amine antioxidant particularly diaryl amine antioxidant
- molybdenum antioxidant particularly oxymolybdenum complex of basic nitrogen compound
- the lubricating oil composition of the present invention further comprises a viscosity index-improving agent (component e) in an amount within a range of 0.5 to 20 mass%.
- a viscosity index-improving agent is polymethacrylate viscosity index-improving agents such as polyalkylmethacrylate, and viscosity index-improving agents based on olefin copolymers, such as ethylene-propylene copolymer, styrene-butadiene copolymer, and polyisoprene.
- olefin copolymer viscosity index-improving agents have high thermal stability and are effective in terms of the object of the present invention.
- One having a shear stability index (SSI) of 30 or less (particularly 25 or less) is particularly preferable for the object of the present invention.
- SSI shear stability index
- a dispersion-type viscosity index-improving agent or multifunctional viscosity index-improving agent that imparts dispersion performance to these polymer compounds is preferably used.
- These viscosity index-improving agents can be used alone, or a combination of any two or more viscosity index-improving agents can be used.
- the lubricating oil composition of the present invention further comprises an organic sulfur compound that is effective in terms of wear resistance and oxidation resistance.
- organic sulfur compounds having such a property are sulfurized olefins, sulfurized esters, sulfurized oils and fats, polysulfide compound, dimercaptothiadiazoles, dithiophosphoric acid esters, and dithiocarbamates.
- alkali metal borate hydrate to the lubricating oil composition of the present invention is effective in terms of high-temperature detergency and imparting a base value.
- the amount of alkali metal borate hydrate is 5 mass% or less, particularly 0.01 to 5 mass%.
- Alkali metal borate hydrates often have an ash component, sulfur component, and the like, but taking into consideration the properties of the lubricating oil composition of the present invention, an alkali metal borate hydrate can be effectively used by adjusting the amount added.
- the lubricating oil composition of the present invention can also contain a small amount of various auxiliary additives.
- auxiliary additives are zinc dithiocarbamate and methylene bis(dibutyl dithiocarbamate), oil-soluble copper compounds, and organic amide compounds (such as oleyl amide) that function as antioxidants or anti-wear agents.
- compounds such as benzotriazole compounds and thiadiazole compounds that function as metal deactivators.
- polyoxyalkylene nonionic surfactants such as polyoxyethylene alkylphenyl ethers and copolymers of ethylene oxide and propylene oxide that function as anti-rust agents and demulsifiers.
- auxiliary additives are each used in an amount that is 3 mass% or less (particularly a range of 0.001 to 3 mass%) in terms of the lubricating oil composition.
- the lubricating oil composition of the present invention (SAE viscosity grade: 5W20, high-temperature, high-shear viscosity: 2.9 mPa ⁇ s or higher) was produced (Examples 1 and 2) using the following base oil and additives (in the following amounts). Moreover, a lubricating oil composition having an SAE viscosity grade of 5W20 (high-temperature, high-shear viscosity of approximately 2.6 mPa ⁇ s) was produced as a comparative example and a lubricating oil composition having an SAE viscosity grade of 10W30 (high-temperature, high-shear viscosity of 2.9 mPa ⁇ s or higher) was produced as a reference example.
- Base oil1 Mixture (having viscosity index of 142, a kinematic viscosity at 100°C of 4.9 mm 2 /s, and NOACK evaporation loss of 10.1%) of mineral oil base oil a (having a viscosity index of 137, a kinematic viscosity at 100°C of 4.1 mm 2 /s, and a NOACK evaporation loss of 13.6%) obtained by hydrogenation and isomerization, fractionation, and then dewaxing using slack wax as the starting material and mineral oil base oil b (having a viscosity index of 148, a kinematic viscosity at 100°C of 6.6 mm 2 /s, and NOACK evaporation loss of 5.0%) obtained by hydrogenation and isomerization, fractionation, and then dewaxing using slack wax as the starting material, at a weight ratio of 60:40 (base oil a:base oil b).
- Base oil 2 Hydrocracked mineral oil (having a viscosity index of 128, a kinematic viscosity at 100°C of 4.2 mm 2 /s, and NOACK evaporation loss of 14.2%)
- Base oil 3 Mixture (having viscosity index of 115, kinematic viscosity at 100°C of 6.7 mm 2 /s, and NOACK evaporation loss of 10.8%) of hydrocracked mineral oil a (having a viscosity index of 122, a kinematic viscosity at 100°C of 5.6 mm 2 /s, and NOACK evaporation loss of 12.4%) and hydrocracked mineral oil b (having a viscosity index of 99, a kinematic viscosity at 100°C of 10.7 mm 2 /s, and NOACK evaporation loss of 6.0%), at a weight ratio of 73:27 (mineral oil a:mineral oil b)
- Table 1 shows the properties of each of the lubricating oil compositions and the results of the Shell four spheres test of examples 1 and 2, the comparative example, and the reference example.
- Table 1 Example 1 Example 2 Comparative Example Reference Example Viscosity grade 5W20 5W20 5W20 10W30 Base oil Base oil 1 Base oil 1 Base oil 2 Base oil 3 High-temperature, high-shear viscosity 2.93 2.91 2.62 3.15 Kinematic viscosity (100°C) 9.15 9.05 8.02 10.1 Kinematic viscosity (40°C) 44.1 43.7 36.3 65.7 Viscosity index 196 195 203 139 Cranking viscosity - - - 5815 -25°C -30°C 3630 3590 2800 - Pumping viscosity at -35°C Passed Passed Passed Passed ⁇ NOACK evaporation loss (%) 9.7 9.8 14.0 11.5 Shell four spheres test 0.47 0.47 0.54 0.48 Average abrasion
- the kinematic viscosity units are mm 2 /s and the cranking viscosity units are mPa ⁇ s.
- a pumping viscosity that "passed” means that the pumping viscosity satisfied the regulation for pumping viscosity (at a determination temperature of -35°C) for SAE viscosity grade 5W20.
- the determination temperature was -30°C for pumping viscosity required by 10W30 and the "passed ⁇ " indicates that the determination passed the regulation for pumping viscosity at -30°C.
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- Inorganic Chemistry (AREA)
- Lubricants (AREA)
Claims (8)
- Schmierölzusammensetzung für Kraftwagenmotorschmierung, die eine Schmierölzusammensetzung ist, umfassend ein Grundöl mit einem SAE-Viskositätsgrad von 5W20, wobei der Viskositätsindex der Schmierölzusammensetzung innerhalb des Bereichs von 140 bis 230 ist, die Hochscher-Viskosität der Schmierölzusammensetzung bei 150°C 2,9 mPa·s oder höher ist, und der NOACK-Verdampfungsverlust der Schmierölzusammensetzung 13% oder weniger ist, zudem umfassenda) ein stickstoffhaltiges, aschefreies Dispergiermittel mit 0,01 bis 0,3 Masse-% nach Stickstoffgehalt,b) ein alkalierdmetallhaltiges Dispergiermittel mit 0,08 bis 0,4 Masse-% nach Alkalierdmetallgehalt,c) ein phosphorhaltiges Antiabriebmittel mit 0,05 bis 0,12 Gew.-% nach Phosphorgehalt,d) ein Antioxidans, ausgewählt aus der Gruppe Aminverbindungen, Phenolverbindungen und Molybdänverbindungen mit 0,1 bis 7 Masse-%,e) ein Viskositätsindex-Verbesserungsmittel mit 0,5 bis 20 Masse-%, und zudem wobeidie Menge jedes Zusatzmittelbestandteils die Masse-% nach der Gesamtmenge Schmierölzusammensetzung ist;
wobei der NOACK-Verdampfungsverlust nach ASTM D5800 bestimmt wird; und
wobei der Begriff "Hochscher-Viskosität" sich auf den gemessenen Wert (Scherviskosität) bezieht, wenn die Schergeschwindigkeit oder Scherrate 106 s-1 ist, und
wobei das Grundöl istein Grundöl, umfassend als Grundölbestandteil mindestens 80 Masse-% eines Mineralöl-Grundöls mit einer kinematischen Viskosität bei 100°C, die innerhalb eines Bereichs von 2 bis 9 mm2/s ist, und einem Viskositätsindex von 133 bis 160; oderein Grundöl mit einem Viskositätsindex von 133 bis 160, das erhalten wird durch Hydrogenisierung und Isomerierung, entweder eines Gatsches oder eines synthetischen Wachses, hergestellt durch das Fischer-Tropsch-Verfahren und dann Destillierung und Entwachsungsbehandlung. - Schmierölzusammensetzung gemäß Anspruch 1, wobei das Grundöl ein Mineralöl ist mit einer kinematischen Viskosität bei 100°C, die innerhalb eines Bereichs von 2 bis 9 mm2/s ist, und einem Viskositätsindex von 133 bis 160.
- Schmierölzusammensetzung gemäß Anspruch 1, wobei das Viskositätsindex-Verbesserungsmittel ein Polymethacrylatpolymer ist mit einem Scherstabilitätsindex von 30 oder geringer.
- Schmierölzusammensetzung gemäß Anspruch 1, die zudem eine organische Schwefelverbindung als Zusatzmittelbestandteil umfasst.
- Verwendung der Schmierölzusammensetzung aus Anspruch 1 zur Schmierung eines Motorrad-Viertakt-Benzinmotors.
- Verwendung der Schmierölzusammensetzung aus Anspruch 1 zur Schmierung des Motors eines Dieselmotorfahrzeugs mit einer Abgas-Nachbehandlungsvorrichtung.
- Verfahren zum Schmieren eines Motorrad-Viertakt-Benzinmotors, das die Schmierölzusammensetzung aus Anspruch 1 verwendet.
- Verfahren zum Schmieren eines Motors eines Dieselmotorfahrzeugs mit einer Abgas-Nachbehandlungsvorrichtung, das die Schmierölzusammensetzung aus Anspruch 1 verwendet.
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JP2012051849A JP5902005B2 (ja) | 2012-03-08 | 2012-03-08 | 自動車エンジン潤滑用潤滑油組成物 |
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KR (1) | KR101968322B1 (de) |
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CN103728212B (zh) * | 2013-11-16 | 2015-12-30 | 平湖市永光机械配件有限公司 | 一种粘度机的玛瑙座 |
CN106255742A (zh) * | 2014-03-11 | 2016-12-21 | 路博润公司 | 润滑内燃机的方法 |
US20170175029A1 (en) * | 2014-03-31 | 2017-06-22 | Idemitsu Kosan Co., Ltd. | Lubricating-oil composition |
CN104031729B (zh) * | 2014-07-02 | 2015-12-09 | 宝捷润滑油镇江有限公司 | 一种摩托车引擎专用润滑油及其制备方法 |
EP3390594B1 (de) * | 2015-12-18 | 2022-06-29 | The Lubrizol Corporation | Stickstofffunktionalisierte olefinpolymere für motorschmiermittel |
JP6927488B2 (ja) * | 2017-03-30 | 2021-09-01 | 出光興産株式会社 | 二輪車用潤滑油組成物、該潤滑油組成物を用いた二輪車の燃費向上方法、及び該潤滑油組成物の製造方法 |
JP6936041B2 (ja) * | 2017-04-25 | 2021-09-15 | シェルルブリカンツジャパン株式会社 | 内燃機関用潤滑油組成物 |
US20180371347A1 (en) * | 2017-06-27 | 2018-12-27 | Chevron Oronite Company Llc | Lubricating oil composition |
JP6744047B2 (ja) * | 2018-03-30 | 2020-08-19 | 出光興産株式会社 | 潤滑油組成物、及び潤滑油組成物の使用方法 |
JP2019206644A (ja) * | 2018-05-29 | 2019-12-05 | 出光興産株式会社 | 潤滑油組成物及びその製造方法 |
WO2020141571A1 (ja) * | 2019-01-04 | 2020-07-09 | ヤマハ発動機株式会社 | 4ストロークエンジンユニット、及び同エンジンユニットを備えた鞍乗型車両 |
WO2023162819A1 (ja) * | 2022-02-28 | 2023-08-31 | 出光興産株式会社 | 二輪自動車用潤滑油組成物 |
US12098347B2 (en) | 2022-09-21 | 2024-09-24 | Afton Chemical Corporation | Lubricating composition for fuel efficient motorcycle applications |
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JP2693698B2 (ja) | 1993-04-22 | 1997-12-24 | 株式会社ジャパンエナジー | 省燃費型潤滑油 |
GB9624441D0 (en) * | 1996-11-25 | 1997-01-15 | Exxon Research Engineering Co | Fuel economy engine oil composition |
US5863873A (en) * | 1997-04-08 | 1999-01-26 | Exxon Chemical Patents Inc | Fuel economy additive and lubricant composition containing same |
JP4076634B2 (ja) | 1998-09-09 | 2008-04-16 | 新日本石油株式会社 | 二輪車用4サイクルエンジン油組成物 |
US6333298B1 (en) | 1999-07-16 | 2001-12-25 | Infineum International Limited | Molybdenum-free low volatility lubricating oil composition |
JP4011967B2 (ja) * | 2002-05-07 | 2007-11-21 | シェブロンジャパン株式会社 | 潤滑油組成物 |
JP5565999B2 (ja) * | 2007-01-31 | 2014-08-06 | Jx日鉱日石エネルギー株式会社 | 潤滑油組成物 |
US7871966B2 (en) * | 2007-03-19 | 2011-01-18 | Nippon Oil Corporation | Lubricating oil composition |
JP5406433B2 (ja) * | 2007-04-27 | 2014-02-05 | 東燃ゼネラル石油株式会社 | 内燃機関用潤滑油組成物 |
US8530397B2 (en) * | 2007-12-12 | 2013-09-10 | Infineum International Limited | Additive compositions |
US8703677B2 (en) * | 2007-12-21 | 2014-04-22 | Chevron Japan Ltd | Lubricating oil compositions for internal combustion engines |
EP2497819B1 (de) * | 2008-10-07 | 2017-01-04 | JX Nippon Oil & Energy Corporation | Schmiermittelzusammensetzung |
JP5727713B2 (ja) * | 2010-03-19 | 2015-06-03 | 出光興産株式会社 | 内燃機関用潤滑油組成物 |
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- 2013-03-06 CN CN2013101461015A patent/CN103305318A/zh active Pending
- 2013-03-06 US US13/786,555 patent/US20130237465A1/en not_active Abandoned
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- 2013-03-06 KR KR1020130023829A patent/KR101968322B1/ko active IP Right Grant
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JP5902005B2 (ja) | 2016-04-13 |
CN103305318A (zh) | 2013-09-18 |
PH12013000076A1 (en) | 2014-11-24 |
JP2013185087A (ja) | 2013-09-19 |
US20150175929A1 (en) | 2015-06-25 |
CA2808765A1 (en) | 2013-09-08 |
KR101968322B1 (ko) | 2019-08-13 |
SG10201507189WA (en) | 2015-10-29 |
KR20130103388A (ko) | 2013-09-23 |
PH12013000076B1 (en) | 2014-11-24 |
SG193720A1 (en) | 2013-10-30 |
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US20130237465A1 (en) | 2013-09-12 |
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