EP2692841A1 - Lubricating oil composition - Google Patents
Lubricating oil composition Download PDFInfo
- Publication number
- EP2692841A1 EP2692841A1 EP11862708.2A EP11862708A EP2692841A1 EP 2692841 A1 EP2692841 A1 EP 2692841A1 EP 11862708 A EP11862708 A EP 11862708A EP 2692841 A1 EP2692841 A1 EP 2692841A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mass
- composition
- lubricating oil
- group
- lubricating
- 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.)
- Ceased
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 86
- 239000010687 lubricating oil Substances 0.000 title claims abstract description 50
- -1 phosphorus compound Chemical class 0.000 claims abstract description 56
- 239000002199 base oil Substances 0.000 claims abstract description 53
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 35
- 239000011574 phosphorus Substances 0.000 claims abstract description 35
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 26
- 230000005540 biological transmission Effects 0.000 claims abstract description 26
- 239000002270 dispersing agent Substances 0.000 claims abstract description 25
- 230000001050 lubricating effect Effects 0.000 claims abstract description 25
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 13
- 150000003018 phosphorus compounds Chemical class 0.000 claims abstract description 13
- 239000006185 dispersion Substances 0.000 claims abstract description 8
- 125000000524 functional group Chemical group 0.000 claims abstract description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 7
- 125000003396 thiol group Chemical group [H]S* 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 25
- 239000000446 fuel Substances 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 238000009413 insulation Methods 0.000 abstract description 11
- 230000000573 anti-seizure effect Effects 0.000 abstract description 8
- 239000003921 oil Substances 0.000 description 33
- 150000001875 compounds Chemical class 0.000 description 32
- 150000002430 hydrocarbons Chemical group 0.000 description 19
- 238000007670 refining Methods 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- 229910052500 inorganic mineral Inorganic materials 0.000 description 11
- 239000011707 mineral Substances 0.000 description 11
- 239000000654 additive Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 9
- 238000007254 oxidation reaction Methods 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 239000002518 antifoaming agent Substances 0.000 description 7
- 239000003112 inhibitor Substances 0.000 description 7
- 239000003963 antioxidant agent Substances 0.000 description 6
- 235000006708 antioxidants Nutrition 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 6
- 230000008961 swelling Effects 0.000 description 6
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 230000003078 antioxidant effect Effects 0.000 description 5
- 238000004517 catalytic hydrocracking Methods 0.000 description 5
- 239000003599 detergent Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000002480 mineral oil Substances 0.000 description 5
- 125000005702 oxyalkylene group Chemical group 0.000 description 5
- 229920013639 polyalphaolefin Polymers 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 150000004996 alkyl benzenes Chemical class 0.000 description 4
- 150000001412 amines Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 239000010779 crude oil Substances 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000006078 metal deactivator Substances 0.000 description 4
- 239000003607 modifier Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 239000013256 coordination polymer Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 150000005690 diesters Chemical class 0.000 description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 150000003014 phosphoric acid esters Chemical class 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical class O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
- 229960002317 succinimide Drugs 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- QTKIQLNGOKOPOE-UHFFFAOYSA-N 1,1'-biphenyl;propane Chemical group CCC.C1=CC=CC=C1C1=CC=CC=C1 QTKIQLNGOKOPOE-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 230000000994 depressogenic effect Effects 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- VDTIMXCBOXBHER-UHFFFAOYSA-N hydroxy-bis(sulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound OP(S)(S)=S VDTIMXCBOXBHER-UHFFFAOYSA-N 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000012184 mineral wax Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- ZXRDVSMSMOZCPT-UHFFFAOYSA-N phosphorodithious acid Chemical compound OP(S)S ZXRDVSMSMOZCPT-UHFFFAOYSA-N 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 2
- ITRFOBBKTCNNFN-UHFFFAOYSA-N tris(sulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound SP(S)(S)=S ITRFOBBKTCNNFN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- UGUHFDPGDQDVGX-UHFFFAOYSA-N 1,2,3-thiadiazole Chemical compound C1=CSN=N1 UGUHFDPGDQDVGX-UHFFFAOYSA-N 0.000 description 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-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
- VRMHHVOBVLFRFB-UHFFFAOYSA-N 2-(2-cyanoethylsulfanylmethyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1CSCCC#N VRMHHVOBVLFRFB-UHFFFAOYSA-N 0.000 description 1
- LLEFDCACDRGBKD-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;nonanoic acid Chemical compound CCC(CO)(CO)CO.CCCCCCCCC(O)=O LLEFDCACDRGBKD-UHFFFAOYSA-N 0.000 description 1
- CWTQBXKJKDAOSQ-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;octanoic acid Chemical compound CCC(CO)(CO)CO.CCCCCCCC(O)=O CWTQBXKJKDAOSQ-UHFFFAOYSA-N 0.000 description 1
- ALKCLFLTXBBMMP-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl hexanoate Chemical compound CCCCCC(=O)OC(C)(C=C)CCC=C(C)C ALKCLFLTXBBMMP-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
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229930185605 Bisphenol Natural products 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
- DJBVDAUKGXUPLO-QEMDMZNVSA-N C(C)C(C(=O)O)CCCC.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O Chemical compound C(C)C(C(=O)O)CCCC.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O DJBVDAUKGXUPLO-QEMDMZNVSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical class CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical class COC(=O)C(C)=C VVQNEPGJFQJSBK-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
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- URGQBRTWLCYCMR-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] nonanoate Chemical compound CCCCCCCCC(=O)OCC(CO)(CO)CO URGQBRTWLCYCMR-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- ZDWGXBPVPXVXMQ-UHFFFAOYSA-N bis(2-ethylhexyl) nonanedioate Chemical compound CCCCC(CC)COC(=O)CCCCCCCC(=O)OCC(CC)CCCC ZDWGXBPVPXVXMQ-UHFFFAOYSA-N 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- VFFDVELHRCMPLY-UHFFFAOYSA-N dimethyldodecyl amine Natural products CC(C)CCCCCCCCCCCN VFFDVELHRCMPLY-UHFFFAOYSA-N 0.000 description 1
- WDNQRCVBPNOTNV-UHFFFAOYSA-N dinonylnaphthylsulfonic acid Chemical class C1=CC=C2C(S(O)(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1 WDNQRCVBPNOTNV-UHFFFAOYSA-N 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- LZJUZSYHFSVIGJ-UHFFFAOYSA-N ditridecyl hexanedioate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCC LZJUZSYHFSVIGJ-UHFFFAOYSA-N 0.000 description 1
- FVBSDVQDRFRKRF-UHFFFAOYSA-N ditridecyl pentanedioate Chemical compound CCCCCCCCCCCCCOC(=O)CCCC(=O)OCCCCCCCCCCCCC FVBSDVQDRFRKRF-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- KAJZYANLDWUIES-UHFFFAOYSA-N heptadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCN KAJZYANLDWUIES-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
- 150000005002 naphthylamines Chemical class 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000010689 synthetic lubricating oil Substances 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
-
- 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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/10—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
- C10M2207/2825—Esters of (cyclo)aliphatic oolycarboxylic acids 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
- 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
-
- 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
- C10M2215/08—Amides
-
- 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
- C10M2215/28—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
-
- 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
- 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
-
- 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
- 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
- C10M2223/043—Ammonium or amine salts thereof
-
- 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
- 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
- C10M2223/047—Thioderivatives not containing metallic elements
-
- 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
- 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
- C10M2223/049—Phosphite
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- 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
-
- 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
-
- 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
- C10N2030/40—Low content or no content compositions
-
- 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
- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
Definitions
- the present invention relates to lubricating oil compositions with excellent insulation properties and lubricity.
- a variety of electronic control devices have been used in the mechanisms of an automobile. Some of them may be used in lubricating oil and thus the insulation properties thereof have become important.
- lubricating oils for the transmission, both the transmission and electric motor, or the device in which a lubricating system is shared by the transmission and electric motor, mounted in a fuel cell electric vehicle, an electric vehicle or a hybrid vehicle have been required to have higher insulation properties because these devices operate using a high electric voltage.
- the transmission has been required to be improved in power transmission efficiency and down-sized as well as weight-reduced so as to improve fuel efficiency and thus has been applied with a higher load.
- the lubricating oil has, therefore, been demanded to have insulation properties as well as more improved anti-wear properties and anti-seizure properties.
- the lubricating oil for transmissions are required to have friction characteristics conforming with the characteristics of a clutch, viscosity characteristics ranging from low temperatures to high temperatures so that an appropriate hydraulic pressure control can be achieved, i.e., viscosity retention which is not affected on temperature as much as possible, and oxidation stability and detergent dispersibility to keep the device clean so that the control device thereof can operate appropriately. Furthermore, these characteristics are generally needed to be retained during the working life of the device. For this purpose, a variety of additives are used in a transmission lubricating oil.
- an automobile transmission oil composition comprising a base oil selected from mineral oils, synthetic oils and mixtures thereof and a phosphorus compound selected from hydrocarbon group-containing zinc dithiophosphate, triaryl phosphate, triaryl thiophosphate and a mixture thereof in an amount of 0.1 to 15.0 percent by mass on the total mass composition basis and having a 80°C volume resistivity of 1 ⁇ 10 7 ⁇ m or greater
- Patent Literature 1 a transmission oil composition
- a transmission oil composition comprising a base oil selected from mineral oils, poly- ⁇ -olefins and hydrogenated compounds thereof, alkylbenzenes, ester-based compounds and mixtures thereof and having a 80°C kinematic viscosity of 1.5 to 4.0 mm 2 /s, a phosphorus compound selected from hydrocarbon group-containing zinc dithiophosphate, triaryl thiophosphates and mixtures thereof in an amount of 0.1 to 4.0 percent by mass on the total composition mass basis,
- the present invention aims at providing a lubricating oil composition maintaining properties necessary for a transmission and having more excellent insulation properties and anti-wear properties and more improved anti-seizure properties than the prior art.
- the present invention relates to a lubricating oil composition
- a lubricating oil composition comprising: (A) a lubricating oil base oil; (B) at least one type of phosphorus compound selected from the group consisting of phosphorus compounds having at least one hydroxyl group and/or at least one thiol group; and (C) an ashless dispersant having a functional group containing as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the total composition mass basis or no such an ashless dispersant at all, the composition having a 80°C volume resistivity of 5 ⁇ 10 8 ⁇ m or greater.
- the present invention also relates to the above-described lubricating oil composition wherein (B) the phosphorus compound having a hydrocarbon group having 16 or fewer carbon atoms.
- the present invention also relates to the above-described lubricating oil composition used for the transmission, both transmission and electric motor, or the device in which a lubricating system is shared by the transmission and electric motor, mounted in a fuel cell electric vehicle, an electric vehicle or a hybrid vehicle.
- the lubricating oil composition of the present invention maintains properties necessary to lubricate a transmission and other devices and has more excellent insulation properties and anti-wear properties than the prior art and can be improved in anti-seizure properties.
- the lubricating base oil referred to as Component (A) used in the present invention may be a mineral base oil and/or a synthetic base oil or alternatively a mixture of two or more types of mineral oils or synthetic base oils, or a mixture of a mineral base oil and a synthetic base oil.
- the mix ratio in these mixtures may be selected arbitrarily.
- These base oils may be used alone or in combination at an arbitrary ratio.
- Examples of preferred mineral lubricating base oils include the following base oils:
- any refining process having been conventionally used upon production of a lubricating base oil examples include (a) hydro-refining processes such as hydrocracking and hydrofinishing, (b) solvent refining such as furfural extraction, (c) dewaxing such as solvent dewaxing and catalytic dewaxing, (d) clay refining with acidic clay or active clay and (e) chemical (acid or alkali) refining such as sulfuric acid treatment and sodium hydroxide treatment.
- any one or more of these refining processes may be used in any combination and order.
- the mineral lubricating base oil used in the present invention is particularly preferably a base oil produced by further subjecting a base oil selected from (1) to (8) described above to the following treatments.
- a hydrocracked mineral oil and/or wax-isomerized isoparaffinic base oil produced by hydrocracking or wax-isomerizing a base oil selected from (1) to (8) described above as it is or a lubricating fraction recovered therefrom and subjecting the resulting product as it is or a lubricating fraction recovered therefrom to dewaxing such as solvent dewaxing or catalytic dewaxing, followed by solvent refining or followed by solvent refining and then dewaxing such as solvent dewaxing or catalytic dewaxing.
- dewaxing such as solvent dewaxing or catalytic dewaxing
- the hydrocracked mineral oil and/or wax-isomerized isoparaffinic base oil are used in an amount of preferably 30 percent by mass or more, more preferably 50 percent by mass or more, and particularly preferably 70 percent by mass or more, on the total base oil mass basis.
- the lubricating base oil referred to as Component (A) used in the transmission lubricating oil composition of the present invention is a lubricating base oil adjusted so that the 100°C kinematic viscosity is from 1.5 to 4.5 mm 2 /s.
- Component (A) is preferably one or more types selected from the following (A-a) to (A-c):
- Mineral base oils (A-a) to (A-b) have a %C A of preferably 2 or less, more preferably 1 or less, more preferably 0.5 or less, particularly preferably substantially 0.
- Lubricating oil (A-c) has a %C A of substantially 0. The use of lubricating base oil (A) having a %C A of 2 or less renders it possible to produce a lubricating oil composition with an excellent oxidation stability.
- %C A used herein denotes the percentage of the aromatic carbon number in the total carbon number, determined in accordance with ASTM D 3238-85.
- viscosity index of lubricating base oils (A-a) to (A-c) which is, however, preferably 80 or greater, more preferably 100 or greater, particularly preferably 120 or greater and usually 200 or less, preferably 160 or less.
- the use of a lubricating base oil having a viscosity index of greater than 80 renders it possible to produce a composition exhibiting excellent viscosity characteristics from low temperatures to high temperatures.
- the use of a lubricating base oil having a too high viscosity index results in a too much normal paraffins in the resulting composition and also deteriorates the low temperature fluidity thereof.
- any one or more of the above-described base oils (A-a) to (A-c) may be used.
- (A-a) and (A-b)and/or(A-c) are used in combination.
- the content of Component (A-c) is preferably 1 to 50 percent by mass, more preferably 3 to 20 percent by mass, more preferably 3 to 10 percent by mass on the total base oil mass basis.
- blending of Component (A-c) in an amount of on the order of 3 to 10 percent by mass renders it possible to produce a composition exhibiting excellent effects in fatigue life, low temperature characteristics, and oxidation stability at a low cost.
- Lubricating base oil (A) used in the present invention has a 100°C kinematic viscosity of preferably 1.5 to 4.5 mm 2 /s, more preferably 2.8 to 4.0 mm 2 /s, particularly preferably 3.6 to 3.9 mm 2 /s.
- the use of a lubricating base oil with a 100°C kinematic viscosity of 4.5 mm 2 /s or lower renders it possible to produce a lubricating oil composition having a smaller frictional resistance at lubricating sites because of its small fluid resistance and thus having excellent low temperature viscosity (for example, the -40°C Brookfield viscosity is 20,000 Pa ⁇ s or less).
- a lubricating base oil with a 100°C kinematic viscosity of 1.5 mm 2 /s or higher renders it possible to produce a lubricating oil composition which is sufficient in oil film formation and thus more excellent in lubricity and less in evaporation loss of the base oil under elevated temperature conditions.
- the synthetic oil referred to as (A-c) may be a synthetic lubricating oil such as poly- ⁇ -olefins (1-octene oligomer, 1-decene oligomer, ethylene-propylene cooligomer) and hydrogenated compounds thereof; isobutene oligomers and hydrogenated compounds thereof; isoparaffins; alkylbenzenes; alkylnaphthalenes; alkyldiphenyl ethanes; monoisopropyl biphenyl; dimethyl silicone; diesters (ditridecyl glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate and di-2-ethylhexyl sebacate); polyol esters (trimethylolpropane caprylate, trimethylolpropane pelargonate, pentaerythritol 2-ethylhexan
- oils preferably used are poly- ⁇ -olefins and hydrogenated compounds thereof; isobutene oligomers and hydrogenated compounds thereof; isoparaffins; alkylbenzenes; alkylnaphthalenes; alkyldiphenylethane; monoisopropyl biphenyl; and dimethyl silicone because they have a 80°C volume resistivity of 1 ⁇ 10 13 ⁇ m or greater and thus can enhance the insulation properties of the resulting lubricating oil composition.
- ester-based compounds have a 80°C volume resistivity of on the order of 1 ⁇ 10 9 to 1 ⁇ 10 13 ⁇ m and are preferably those from which the remaining moisture and impurities have been sufficiently removed.
- the synthetic oil used in the present invention is preferably selected from poly- ⁇ -olefins and hydrogenated compounds thereof, alkylbenzenes, ester-based compounds and mixtures thereof.
- the resulting composition can maintain low temperature fluidity and low volatility in well-balance under the conditions where it is used.
- poly- ⁇ -olefins include oligomers or cooligomers of ⁇ -olefins having 2 to 32, preferably 6 to 16 carbon atoms, such as 1-octene oligomer, 1-decene oligomer, ethylene-propylene cooligomer, and hydrogenated compounds thereof.
- synthetic oils may be used alone. No particular limitation is imposed on the viscosity thereof. However, synthetic oils with different viscosities may be used in combination so that the 100°C kinematic viscosity is adjusted to preferably from 1.5 to 4.5 mm 2 /s. This is because the combination of a synthetic oil having a high viscosity with that of a low viscosity results in a base oil having a higher viscosity index.
- the lubricating oil base oil referred to as Component (A) in the present invention is as described above but is preferably mixed with a solvent refined base oil having a kinematic viscosity of 20 mm 2 /s to 50 mm 2 /s if the resulting composition has a problem in fatigue life. Furthermore, it is preferably mixed with such a solvent refined oil in such an extent that the mixture is adjusted to have a %C A of 2 or less and a 100°C kinematic viscosity of 1.5 to 4.5 mm 2 /s.
- the lubricating oil composition of the present invention contains (B) at least one type of phosphorus compound selected from phosphorus compounds having at least one hydroxyl group and/or at least one thiol group.
- the phosphorus compound referred to as Component (B) in the present invention is at least one type of compound selected from phosphorus compounds represented by formula (1), phosphorus compounds represented by formula (2), amine salts thereof, and derivatives thereof.
- X 1 , X 2 and X 3 are each independently oxygen or sulfur and at least one of them is preferably oxygen, at least one of R 1 , R 2 and R 3 is hydrogen and the others are hydrocarbon groups having 1 to 30 carbon atoms.
- X 4 , X 5 , X 6 and X 7 are each independently oxygen or sulfur (one or two of X 4 , X 5 and X 6 may be a single bond or (poly) oxyalkylene group) and at least one of them is preferably oxygen, at least one of R 4 , R 5 and R 6 is hydrogen and the others are hydrocarbon groups having 1 to 30 carbon atoms.
- hydrocarbon groups having 1 to 30 carbon atoms for R 1 to R 6 include alkyl, cycloalkyl, alkenyl, alkyl-substituted cycloalkyl, aryl, alkyl-substituted aryl, and arylalkyl groups.
- the hydrocarbon groups are preferably alkyl groups having 1 to 30 carbon atoms and aryl groups having 6 to 24 carbon atoms, more preferably alkyl groups having 3 to 18 carbon atoms, more preferably alkyl groups having 4 to 12 carbon atoms.
- Examples of phosphorus compounds represented by formula (1) include phosphorous acid; monothiophosphorous acid; dithiophosphorous acid; phosphorous acid monoesters, monothiophosphorous acid monoesters, dithiophosphorous acid monoesters, and trithiophosphorous acid monoesters, each having any one of the above-described hydrocarbon groups having 1 to 30 carbon atoms; and phosphorous acid diesters, monothiophosphorous acid diesters, dithiophosphorous acid diesters, and trithsophosphorous acid diesters, each having any two of the above-described hydrocarbon groups having 1 to 30 carbon atoms; and a mixture thereof.
- X 1 to X 3 in formula (1) are oxygen.
- Examples of phosphorus compounds represented by formula (2) include phosphoric acid; monothiophosphoric acid; dithiophosphoric acid; trithiophosphoric acid; tetrathiophosphoric acid; phosphoric acid monoesters, monothiophospharic acid monoesters, dithiophosphoric acid monoesters, trithiophosphoric acid monoesters, and tetrathiophosphoric acid monoesters, each having any one of the above-described hydrocarbon groups having 1 to 30 carbon atoms; phosphoric acid diesters, monothiophosphoric acid diesters, dithiophosphoric acid diesters, trithiophosphoric acid diesters, and tetrathiophosphoric acid diesters, each having any two of the above-described hydrocarbon groups having 1 to 30 carbon atoms; phosphonic acid, phosphonic acid monoesters, and phosphonic acid diesters, each having any one or two of the above-described hydrocarbon groups having 1 to 30 carbon atoms; the phosphoric acid compounds exemplified
- X 4 to X 7 in formula (2) are oxygen.
- One or two of X 4 , X 5 and X 6 may be a single bond or a (poly)oxyalkylene group.
- Examples of the salts of phosphorus compounds represented by formula (1) or (2) include salts produced by allowing a nitrogen compound such as ammonia or an amine compound having in its molecules only a hydrocarbon group having 1 to 30 carbon atoms or a hydroxyl group-containing hydrocarbon group having 1 to 30 carbon atoms to react with a phosphorus compound and neutralize the whole or part of the remaining acid hydrogen.
- a nitrogen compound such as ammonia or an amine compound having in its molecules only a hydrocarbon group having 1 to 30 carbon atoms or a hydroxyl group-containing hydrocarbon group having 1 to 30 carbon atoms
- nitrogen-containing compound examples include ammonia, monoamines, diamines, and polyamines.
- Preferred examples include aliphatic amines having an alkyl or alkenyl group having 10 to 20 carbon atoms, which may be straight-chain or branched, such as decylamine, dodecylamine, dimethyldodecylamine, tridecylamine, heptadecylamine, octadecylamine, oleylamine, and stearyl amine.
- the phosphorus compound referred to as Component (B) is preferably at least one type of compound selected from the group consisting of amine salts of phosphorus compounds of formula (1) wherein all of X 1 , X 2 and X 3 are oxygen and amine salts of phosphorus compounds of formula (2) wherein all of X 4 , x 5 , X 6 and X 7 are oxygen (one or two of X 4 , and X 6 may be a single bond or a (poly) oxyalkylene group) because they are excellent in oxidation stability.
- the phosphorus compound referred to as Component (B) is preferably a phosphorus compound of formula (2) wherein all of X 4 , X 5 , X 6 and X 7 are oxygen (one or two of X 4 , X 5 and X 6 may be a single bond or a (poly)oxyalkylene group), at least one of R 4 , R 5 and R 6 is hydrogen and the others are each independently a hydrocarbon group having 1 to 30 carbon atoms in terms of oxidation stability.
- the hydrocarbon group of the phosphorus compound referred to as Component (B) has preferably 16 or fewer carbon atoms. This is based on the fact that fewer the carbon atoms, higher the volume resistivity is as set forth in Table 1 below.
- the volume resistivity designates the value measured at an oil temperature of 80°C in accordance with JIS C 2101 24. (volume resistivity test).
- each of the phosphorus compound was added and dissolved in a mineral base oil so that it is contained in an amount of 100 mass ppm on the basis of phosphorus.
- Component (B) that is the above-described phosphorus compound of the lubricating oil composition of the present invention, which is, however, 0.01 percent by mass or more, preferably 0.02 percent by mass or more, particularly preferably 0.03 percent by mass or more and preferably 0.1 percent by mass or less, more preferably 0.08 percent by mass or less, particularly preferably 0.05 percent by mass or less on the basis of phosphorus on the composition mass basis. If the content of the phosphorus compound is less than 0.01 percent by mass on the basis of phosphorus, the resulting composition would be less effective in anti-wear properties. Whilst, if the content of the phosphorus compound is more than 0.1 percent by mass on the basis of phosphorus, the resulting composition would be poor in insulation properties, degraded in oxidation stability and enhanced in aggressivity against sealing materials.
- the lubricating oil composition of the present invention is characterized in that it contains (C) an ashless dispersant having a functional group containing nitrogen as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the composition mass basis or does not contain such an ashless dispersant at all.
- the lubricating oil composition of the present invention contains (B) at least one type of phosphorus compound selected from phosphorus compounds having at least one hydroxyl group and/or at least one thiol group.
- the inclusion of the phosphorus compound enhances significantly the anti-wear properties and anti-seizure properties of the composition.
- this type of phosphorus compound degrades drastically the volume resistance of the composition compared with a phosphorus compound having no hydroxyl group and/or thiol group if an ashless dispersant having a functional group containing nitrogen as a dispersion group is contained.
- the composition contains necessarily (C) an ashless dispersant having a functional group containing nitrogen as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the composition mass basis or does not contain such an ashless dispersant at all in order to improve the anti-wear properties and anti-seizure properties of the composition.
- Examples of the ashless dispersant having a functional group containing nitrogen as a dispersion group referred to as Component (C) include succinimide, benzylamine, and polyamines, each having a hydrocarbon group having 40 to 400 carbon atoms.
- an ashless dispersant having a functional group containing nitrogen as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the composition mass basis is a structure or amount wherein even though an ashless dispersant has an amino group remained so as to be able to constitute a salt structure with Component (B) that is the phosphorus compound, the content thereof is such a level that the volume resistance at 80°C of the resulting composition is 5 ⁇ 10 8 ⁇ m or greater.
- the ashless dispersant is contained in such an amount that nitrogen is contained in an amount of less than 0.001 percent by mass, more preferably less than 0.0008 percent by mass on the composition mass basis.
- the lubricating oil composition of the present invention has a 80°C volume resistivity of preferably 5 ⁇ 10 8 ⁇ m or greater, more preferably 6 ⁇ 10 8 ⁇ m or greater, particularly preferably 10x10 8 ⁇ m or greater.
- the composition having a 80°C volume resistivity of 5 ⁇ 10 8 ⁇ m or greater can keep the insulation properties high not only when it is fresh but also when it is degraded thereby avoiding an electric motor from having a trouble such as shorting out for a long period of time.
- the lubricating oil composition of the present invention may be blended with various additives such as viscosity index improvers, extreme pressure additives, dispersants other than the above-described dispersant compounds, metallic detergents, friction modifiers, anti-oxidants, corrosion inhibitors, rust inhibitors, demulsifiers, metal deactivators, pour point depressants, seal swelling agents, anti-foaming agents, and dyes, alone or in combination in order to further enhance the properties of the composition or impart the composition with properties required for a lubricating oil.
- additives such as viscosity index improvers, extreme pressure additives, dispersants other than the above-described dispersant compounds, metallic detergents, friction modifiers, anti-oxidants, corrosion inhibitors, rust inhibitors, demulsifiers, metal deactivators, pour point depressants, seal swelling agents, anti-foaming agents, and dyes, alone or in combination in order to further enhance the properties of the composition or impart the composition with properties required for a lubricating oil.
- viscosity index improvers examples include non-dispersant or dispersant type poly(meth)acrylate; non-dispersant or dispersant type ethylene- ⁇ -olefin copolymers and hydrogenated compounds thereof; polyisobutylene and hydrogenated compounds thereof; styrene-diene hydrogenated copolymers; styrene-maleic anhydride ester copolymers; polyalkylstyrenes; and copolymers of (meth) acrylate monomers represented by formula (1) and unsaturated monomers such as ethylene/propylene/styrene/maleic anhydride.
- the amount of the viscosity index improver in the lubricating oil composition of the present invention is such an amount that the resulting composition has a 100°C kinematic viscosity of 5 to 10 mm 2 /s, preferably 6 to 9 mm 2 /s and a viscosity index of 120 to 270, preferably 150 to 250, more preferably 170 to 220. More specifically, the amount is 15 percent by mass or less, preferably 10 percent by mass or less, more preferably 8 percent by mass or less and 2 percent by mass or more, preferably 4 percent by mass or more, more preferably 5 percent by mass or more on the composition mass basis. An amount of more than 15 percent by mass causes a too high viscosity while an amount of less than 2 percent by mass causes a too high viscosity and thus cannot secure a sufficient composition viscosity.
- the metallic detergent examples include those such as alkaline earth metal sulfonates, alkaline earth metal phenates, and alkaline earth metal salicylates.
- Any one or more compounds selected from these metallic detergents may be contained in an amount of usually 0.01 to 10 percent by mass, preferably 0.1 to 5 percent by mass on the total composition mass basis.
- the friction modifier may be any compound that has been generally used as a friction modifier for lubricating oils.
- Specific examples include amine compounds, imide compounds, fatty acid esters, fatty acid amides, and fatty acid metal salts, each having per molecule at least one alkyl or alkenyl group having 6 to 30 carbon atoms, particularly a straight-chain alkyl or alkenyl group having 6 to 30 carbon atoms.
- Any one or more compounds selected from these friction modifiers may be contained in an amount of usually 0.01 to 5.0 percent by mass, preferably 0.03 to 3.0 percent by mass on the total composition mass basis.
- the anti-oxidant may be any anti-oxidant that has been usually used in lubricating oils, such as phenol- or amine-based compounds.
- the anti-oxidant include alkylphenols such as 2-6-di-tert-butyl-4-methylphenol; bisphenols such as methylene-4,4-bisphenol(2,6-di-tert-butyl-4-methylphenol); naphthylamines such as phenyl- ⁇ -naphthylamine; dialkyldiphenylamines; zinc dialkyldithiophosphoric acids such as di-2-ethylhexyldithiophosphoric acid; and esters of (3,5-di-tert-butyl-4-hydroxyphenyl)fatty acid (propionic acid) or (3-methyl-5-tert-butyl-4-hydroxyphenyl)fatty acid (propionic acid) with a monohydric or polyhydric alcohol such as methanol, octanol, octadecanol, 1,6-hexanediol, neopentyl glycol, thiodiethylene glycol,
- Any one or more of compounds selected from these compounds may be contained in any amount, which is, however, usually from 0.01 to 5 percent by mass, preferably from 0.1 to 3 percent by mass on the total composition mass basis.
- corrosion inhibitor examples include benzotriazole-, tolyltriazole-, thiadiazole-, and imidazole-types compounds.
- rust inhibitor examples include petroleum sulfonates, alkylbenzene sulfonates, dinonylnaphthalene sulfonates, alkenyl succinic acid esters, and polyhydric alcohol esters.
- demulsifier examples include polyalkylene glycol-based non-ionic surfactants such as polyoxyethylenealkyl ethers, polyoxyethylenealkylphenyl ethers, and polyoxyethylenealkylnaphthyl ethers.
- metal deactivator examples include imidazolines, pyrimidine derivatives, alkylthiadiazoles, mercaptobenzothiazoles, benzotriazoles and derivatives thereof, 1,3,4-thiadiazolepolysulfide, 1,3,4-thiadiazolyl-2,5-bisdialkyldithiocarbamate, 2-(alkyldithio)benzoimidazole, and ⁇ -(o-carboxybenzylthio)propionitrile.
- the pour point depressant may be any of the known pour point depressants selected depending on the type of lubricating base oil but are preferably poly(meth)acrylates having a weight average molecular weight of preferably 20, 000 to 500,000, more preferably 50,000 to 300,000, particularly preferably 80,000 to 200,000.
- the anti-foaming agent may be any compound that has been usually used as an anti-foaming agent for lubricating oils.
- examples of such an anti-foaming agent include silicones such as dimethylsilicone and fluorosilicone. Any one or more of compounds selected from these compounds may be contained in any amount.
- the seal swelling agent may be any compound that has been usually used as a seal swelling agent for lubricating oils.
- seal swelling agents include ester-, sulfur- and aromatic-based seal swelling agents.
- the dye may be any compound that has been usually used and may be blended in any amount.
- the amount is usually from 0.001 to 1.0 percent by mass on the total composition mass basis.
- the corrosion inhibitor, rust inhibitor, and anti-foaming agent are each contained in an amount of 0.005 to 5 percent by mass
- the pour point depressant and metal deactivator are each contained in an amount of 0.005 to 2 percent by mass
- the seal swelling agent is contained in an amount of 0.01 to 5 percent by mass
- the anti-foaming agent is contained in an amount of 0.0005 to 1 percent by mass, all on the total composition mass basis.
- Lubricating oil compositions according to the present invention (Examples 1 to 6) and those for comparison (Comparative Examples 1 to 5) were prepared in accordance with the formulations set forth in Table 2. The performances of each composition were evaluated with the following tests. The results are set forth in Table 2.
- kinematic viscosity (100°C) 4.3mm 2 /s, viscosity index 125, %C P 78.5, %C N 21.5, %C A 0 2) kinematic viscosity (40°C) 22.7mm 2 /s, kinematic viscosity (100°C) 4.3mm 2 /s, viscosity index 102, %C P 66.4, %C N 29.0, %C A 4.6 3) di-2-ethylhexyl azelate kinematic viscosity (40°C) 10.1mm 2 /s.
- kinematic viscosity (100°C) 3.0mm 2 /s, viscosity index 144 4) amine salt of acidic phosphoric acid ester (P content: 10%, phosphoric acid ester: 2-ethylhexyl, amine: mixed amine of C11 to 14) 5) hydrogen phosphine, isoC4 P content 16% 6) acidic phosphoric acid ester, 2-ethylhexyl P: 9.4% 7) trioleylphosphite P: 3.7% 8) boronated succinimide, PIS M w 2000, bis type, TEPA crosslinking 9) succinimide, PIB M w 1000, bis type.
- the lubricating oil composition of the present invention is a composition improved in anti-wear properties and anti-seizure properties and can be used as a lubricating oil for an electric motor-equipped vehicle such as an electric vehicle or a hybrid vehicle, an electric motor oil, an oil both for a transmission and an electric motor, and an oil for a device wherein a transmission and an electric motor are packaged in one and a lubricating system is shared by the transmission and an electric motor.
- the present invention can provide the above-described transmission, electric motor and device including the lubricating oil composition of the present invention and a method for lubricating, insulating and cooling the above-described transmission, electric motor and device using the lubricating oil composition of the present invention.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Description
- The present invention relates to lubricating oil compositions with excellent insulation properties and lubricity.
- A variety of electronic control devices have been used in the mechanisms of an automobile. Some of them may be used in lubricating oil and thus the insulation properties thereof have become important. In particular, lubricating oils for the transmission, both the transmission and electric motor, or the device in which a lubricating system is shared by the transmission and electric motor, mounted in a fuel cell electric vehicle, an electric vehicle or a hybrid vehicle have been required to have higher insulation properties because these devices operate using a high electric voltage. Furthermore, in recent years, the transmission has been required to be improved in power transmission efficiency and down-sized as well as weight-reduced so as to improve fuel efficiency and thus has been applied with a higher load. The lubricating oil has, therefore, been demanded to have insulation properties as well as more improved anti-wear properties and anti-seizure properties.
- In addition to the above-described properties, the lubricating oil for transmissions are required to have friction characteristics conforming with the characteristics of a clutch, viscosity characteristics ranging from low temperatures to high temperatures so that an appropriate hydraulic pressure control can be achieved, i.e., viscosity retention which is not affected on temperature as much as possible, and oxidation stability and detergent dispersibility to keep the device clean so that the control device thereof can operate appropriately. Furthermore, these characteristics are generally needed to be retained during the working life of the device. For this purpose, a variety of additives are used in a transmission lubricating oil.
- So far, as such transmission lubricating oils, some oils have been proposed such as an automobile transmission oil composition comprising a base oil selected from mineral oils, synthetic oils and mixtures thereof and a phosphorus compound selected from hydrocarbon group-containing zinc dithiophosphate, triaryl phosphate, triaryl thiophosphate and a mixture thereof in an amount of 0.1 to 15.0 percent by mass on the total mass composition basis and having a 80°C volume resistivity of 1×107 Ω·m or greater (Patent Literature 1) and a transmission oil composition comprising a base oil selected from mineral oils, poly-α-olefins and hydrogenated compounds thereof, alkylbenzenes, ester-based compounds and mixtures thereof and having a 80°C kinematic viscosity of 1.5 to 4.0 mm2/s, a phosphorus compound selected from hydrocarbon group-containing zinc dithiophosphate, triaryl thiophosphates and mixtures thereof in an amount of 0.1 to 4.0 percent by mass on the total composition mass basis, and an ashless dispersant and having a 80°C volume resistivity of 1×108 Ω·m or greater (Patent Literature 2).
-
- Patent Literature 1:
WO2002/097017 - Patent Literature 2: Japanese Patent Application Publication
2008-285682 - As described above, a variety of additives are used in a transmission oil but would alone or in combination degrade the insulation properties, anti-wear properties or anti-seizure properties. The present invention aims at providing a lubricating oil composition maintaining properties necessary for a transmission and having more excellent insulation properties and anti-wear properties and more improved anti-seizure properties than the prior art.
- That is, the present invention relates to a lubricating oil composition comprising: (A) a lubricating oil base oil; (B) at least one type of phosphorus compound selected from the group consisting of phosphorus compounds having at least one hydroxyl group and/or at least one thiol group; and (C) an ashless dispersant having a functional group containing as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the total composition mass basis or no such an ashless dispersant at all, the composition having a 80°C volume resistivity of 5×108 Ω·m or greater.
- The present invention also relates to the above-described lubricating oil composition wherein (B) the phosphorus compound having a hydrocarbon group having 16 or fewer carbon atoms.
- The present invention also relates to the above-described lubricating oil composition used for the transmission, both transmission and electric motor, or the device in which a lubricating system is shared by the transmission and electric motor, mounted in a fuel cell electric vehicle, an electric vehicle or a hybrid vehicle.
- The lubricating oil composition of the present invention maintains properties necessary to lubricate a transmission and other devices and has more excellent insulation properties and anti-wear properties than the prior art and can be improved in anti-seizure properties.
- The present invention will be described in more detail below.
- The lubricating base oil referred to as Component (A) used in the present invention may be a mineral base oil and/or a synthetic base oil or alternatively a mixture of two or more types of mineral oils or synthetic base oils, or a mixture of a mineral base oil and a synthetic base oil. The mix ratio in these mixtures may be selected arbitrarily.
- Examples of the mineral lubricating base oil which may be used in the present invention include paraffinic or naphthenic mineral base oils which can be produced by subjecting a lubricating oil fraction produced by atmospheric- or vacuum-distillation of a crude oil, to any one of or any suitable combination of refining processes selected from solvent deasphalting, solvent extraction, hydrocracking, solvent dewaxing, catalytic dewaxing, hydrorefining, sulfuric acid treatment, and clay treatment; n-paraffins; and iso-paraffins. These base oils may be used alone or in combination at an arbitrary ratio.
- Examples of preferred mineral lubricating base oils include the following base oils:
- (1) a distillate oil produced by atmospheric distillation of a paraffin base crude all and/or a mixed base crude oil;
- (2) a whole vacuum gas oil (WVGO) produced by vacuum distillation of the topped crude of a paraffin base crude oil and/or a mixed base crude oil;
- (3) a wax produced by a lubricating oil dewaxing process and/or a Fischer-Tropsch wax produced by a GTL process;
- (4) an oil produced by mild-hydrocracking (MHC) one or more oils selected from oils of (1) to (3) above;
- (5) a mixed oil of two or more oils selected from (1) to (4) above;
- (6) a deasphalted oil (DAO) produced by deasphalting an oil of (1), (2) (3), (4) or (5);
- (7) an oil produced by mild-hydrocracking (MHC) an oil of (6); and
- (8) a lubricating oil produced by subjecting a mixed oil of two or more oils selected from (1) to (7) used as a feed stock and/or a lubricating oil fraction recovered therefrom to a normal refining process and further recovering a lubricating oil fraction from the refined product.
- No particular limitation is imposed on the normal refining process used herein. Therefore, there may be used any refining process having been conventionally used upon production of a lubricating base oil. Examples of the normal refining process include (a) hydro-refining processes such as hydrocracking and hydrofinishing, (b) solvent refining such as furfural extraction, (c) dewaxing such as solvent dewaxing and catalytic dewaxing, (d) clay refining with acidic clay or active clay and (e) chemical (acid or alkali) refining such as sulfuric acid treatment and sodium hydroxide treatment. In the present invention, any one or more of these refining processes may be used in any combination and order.
- The mineral lubricating base oil used in the present invention is particularly preferably a base oil produced by further subjecting a base oil selected from (1) to (8) described above to the following treatments.
- That is, preferred are a hydrocracked mineral oil and/or wax-isomerized isoparaffinic base oil produced by hydrocracking or wax-isomerizing a base oil selected from (1) to (8) described above as it is or a lubricating fraction recovered therefrom and subjecting the resulting product as it is or a lubricating fraction recovered therefrom to dewaxing such as solvent dewaxing or catalytic dewaxing, followed by solvent refining or followed by solvent refining and then dewaxing such as solvent dewaxing or catalytic dewaxing. The hydrocracked mineral oil and/or wax-isomerized isoparaffinic base oil are used in an amount of preferably 30 percent by mass or more, more preferably 50 percent by mass or more, and particularly preferably 70 percent by mass or more, on the total base oil mass basis.
- The lubricating base oil referred to as Component (A) used in the transmission lubricating oil composition of the present invention is a lubricating base oil adjusted so that the 100°C kinematic viscosity is from 1.5 to 4.5 mm2/s.
- Component (A) is preferably one or more types selected from the following (A-a) to (A-c):
- (A-a) a mineral base oil having a 100°C kinematic viscosity of between 1.5 and lower than 3.5
mm2/s, preferably 1.9 to 3.2 mm2/s; - (A-b) a mineral base oil having a 100°C kinematic viscosity of between 3.5 and lower than 7 mm2/s, preferably 3.6 to 4.5 mm2/s; and
- (A-c) a synthetic base oil having a 100°C kinematic viscosity of between 1.5 and lower than 7 mm2/s, preferably 3.8 to 4.5 mm2/s.
- Mineral base oils (A-a) to (A-b) have a %CA of preferably 2 or less, more preferably 1 or less, more preferably 0.5 or less, particularly preferably substantially 0. Lubricating oil (A-c) has a %CA of substantially 0. The use of lubricating base oil (A) having a %CA of 2 or less renders it possible to produce a lubricating oil composition with an excellent oxidation stability.
- The %CA used herein denotes the percentage of the aromatic carbon number in the total carbon number, determined in accordance with ASTM D 3238-85.
- No particular limitation is imposed on the viscosity index of lubricating base oils (A-a) to (A-c), which is, however, preferably 80 or greater, more preferably 100 or greater, particularly preferably 120 or greater and usually 200 or less, preferably 160 or less. The use of a lubricating base oil having a viscosity index of greater than 80 renders it possible to produce a composition exhibiting excellent viscosity characteristics from low temperatures to high temperatures. The use of a lubricating base oil having a too high viscosity index results in a too much normal paraffins in the resulting composition and also deteriorates the low temperature fluidity thereof.
- No particular limitation is imposed on the sulfur content of mineral base oils (A-a) to (A-b) used in the present invention, which is, however, preferably 0.05 percent by mass or less, more preferably 0.02 percent by mass or less, particularly preferably 0.005 percent by mass or less. The sulfur content of lubricating base oil (A-c) is substantially 0%. Reduction of the sulfur content of Component (A) renders it possible to produce a composition having a more excellent oxidation stability.
- In the present invention, any one or more of the above-described base oils (A-a) to (A-c) may be used. Above all, preferably (A-a) and (A-b)and/or(A-c) are used in combination. When Component (A-a) and/or Component (A-b) and Component (A-c) are used in combination, the content of Component (A-c) is preferably 1 to 50 percent by mass, more preferably 3 to 20 percent by mass, more preferably 3 to 10 percent by mass on the total base oil mass basis. In particular, blending of Component (A-c) in an amount of on the order of 3 to 10 percent by mass renders it possible to produce a composition exhibiting excellent effects in fatigue life, low temperature characteristics, and oxidation stability at a low cost.
- Lubricating base oil (A) used in the present invention has a 100°C kinematic viscosity of preferably 1.5 to 4.5 mm2/s, more preferably 2.8 to 4.0 mm2/s, particularly preferably 3.6 to 3.9 mm2/s. The use of a lubricating base oil with a 100°C kinematic viscosity of 4.5 mm2/s or lower renders it possible to produce a lubricating oil composition having a smaller frictional resistance at lubricating sites because of its small fluid resistance and thus having excellent low temperature viscosity (for example, the -40°C Brookfield viscosity is 20,000 Pa·s or less). The use of a lubricating base oil with a 100°C kinematic viscosity of 1.5 mm2/s or higher renders it possible to produce a lubricating oil composition which is sufficient in oil film formation and thus more excellent in lubricity and less in evaporation loss of the base oil under elevated temperature conditions.
- The synthetic oil referred to as (A-c) may be a synthetic lubricating oil such as poly-α-olefins (1-octene oligomer, 1-decene oligomer, ethylene-propylene cooligomer) and hydrogenated compounds thereof; isobutene oligomers and hydrogenated compounds thereof; isoparaffins; alkylbenzenes; alkylnaphthalenes; alkyldiphenyl ethanes; monoisopropyl biphenyl; dimethyl silicone; diesters (ditridecyl glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate and di-2-ethylhexyl sebacate); polyol esters (trimethylolpropane caprylate, trimethylolpropane pelargonate, pentaerythritol 2-ethylhexanoate and pentaerythritol pelargonate); polyoxyalkylene glycols; dialkyldiphenyl ethers; polyphenyl ethers; or a mixture thereof. Among these oils, preferably used are poly-α-olefins and hydrogenated compounds thereof; isobutene oligomers and hydrogenated compounds thereof; isoparaffins; alkylbenzenes; alkylnaphthalenes; alkyldiphenylethane; monoisopropyl biphenyl; and dimethyl silicone because they have a 80°C volume resistivity of 1×1013 Ω·m or greater and thus can enhance the insulation properties of the resulting lubricating oil composition. In general, ester-based compounds have a 80°C volume resistivity of on the order of 1×109 to 1×1013 Ω·m and are preferably those from which the remaining moisture and impurities have been sufficiently removed.
- The term "80°C volume resistivity" used herein is measured in accordance with JIS C 2101 24.(volume resistivity test).
- The synthetic oil used in the present invention is preferably selected from poly-α-olefins and hydrogenated compounds thereof, alkylbenzenes, ester-based compounds and mixtures thereof. In this case, the resulting composition can maintain low temperature fluidity and low volatility in well-balance under the conditions where it is used.
- Typical examples of poly-α-olefins include oligomers or cooligomers of α-olefins having 2 to 32, preferably 6 to 16 carbon atoms, such as 1-octene oligomer, 1-decene oligomer, ethylene-propylene cooligomer, and hydrogenated compounds thereof.
- These synthetic oils may be used alone. No particular limitation is imposed on the viscosity thereof. However, synthetic oils with different viscosities may be used in combination so that the 100°C kinematic viscosity is adjusted to preferably from 1.5 to 4.5 mm2/s. This is because the combination of a synthetic oil having a high viscosity with that of a low viscosity results in a base oil having a higher viscosity index.
- The lubricating oil base oil referred to as Component (A) in the present invention is as described above but is preferably mixed with a solvent refined base oil having a kinematic viscosity of 20 mm2/s to 50 mm2/s if the resulting composition has a problem in fatigue life. Furthermore, it is preferably mixed with such a solvent refined oil in such an extent that the mixture is adjusted to have a %CA of 2 or less and a 100°C kinematic viscosity of 1.5 to 4.5 mm2/s.
- The lubricating oil composition of the present invention contains (B) at least one type of phosphorus compound selected from phosphorus compounds having at least one hydroxyl group and/or at least one thiol group.
-
-
- In formula (2), X4, X5, X6 and X7 are each independently oxygen or sulfur (one or two of X4, X5 and X6 may be a single bond or (poly) oxyalkylene group) and at least one of them is preferably oxygen, at least one of R4, R5 and R6 is hydrogen and the others are hydrocarbon groups having 1 to 30 carbon atoms.
- Examples of the hydrocarbon groups having 1 to 30 carbon atoms for R1 to R6 include alkyl, cycloalkyl, alkenyl, alkyl-substituted cycloalkyl, aryl, alkyl-substituted aryl, and arylalkyl groups. The hydrocarbon groups are preferably alkyl groups having 1 to 30 carbon atoms and aryl groups having 6 to 24 carbon atoms, more preferably alkyl groups having 3 to 18 carbon atoms, more preferably alkyl groups having 4 to 12 carbon atoms.
- Examples of phosphorus compounds represented by formula (1) include phosphorous acid; monothiophosphorous acid; dithiophosphorous acid; phosphorous acid monoesters, monothiophosphorous acid monoesters, dithiophosphorous acid monoesters, and trithiophosphorous acid monoesters, each having any one of the above-described hydrocarbon groups having 1 to 30 carbon atoms; and phosphorous acid diesters, monothiophosphorous acid diesters, dithiophosphorous acid diesters, and trithsophosphorous acid diesters, each having any two of the above-described hydrocarbon groups having 1 to 30 carbon atoms; and a mixture thereof.
- In order to further enhance the properties such as high temperature detergency and oxidation stability in the present invention, preferably two or more, particularly preferably all of X1 to X3 in formula (1) are oxygen.
- Examples of phosphorus compounds represented by formula (2) include phosphoric acid; monothiophosphoric acid; dithiophosphoric acid; trithiophosphoric acid; tetrathiophosphoric acid; phosphoric acid monoesters, monothiophospharic acid monoesters, dithiophosphoric acid monoesters, trithiophosphoric acid monoesters, and tetrathiophosphoric acid monoesters, each having any one of the above-described hydrocarbon groups having 1 to 30 carbon atoms; phosphoric acid diesters, monothiophosphoric acid diesters, dithiophosphoric acid diesters, trithiophosphoric acid diesters, and tetrathiophosphoric acid diesters, each having any two of the above-described hydrocarbon groups having 1 to 30 carbon atoms; phosphonic acid, phosphonic acid monoesters, and phosphonic acid diesters, each having any one or two of the above-described hydrocarbon groups having 1 to 30 carbon atoms; the phosphoric acid compounds exemplified above but having a (poly)oxyalkylene group having 1 to 4 carbon atoms; derivatives of the phosphorus compounds exemplified above, such as β-dithiophosphorylated propionic acid and reaction products of dithiophosphates and olefin cyclopentadiene or (methyl)methacrylates; and mixtures thereof.
- In order to further enhance the properties such as high temperature detergency and oxidation stability in the present invention, preferably two or more, more preferably three or more, particularly preferably all of X4 to X7 in formula (2) are oxygen. One or two of X4, X5 and X6 may be a single bond or a (poly)oxyalkylene group.
- Examples of the salts of phosphorus compounds represented by formula (1) or (2) include salts produced by allowing a nitrogen compound such as ammonia or an amine compound having in its molecules only a hydrocarbon group having 1 to 30 carbon atoms or a hydroxyl group-containing hydrocarbon group having 1 to 30 carbon atoms to react with a phosphorus compound and neutralize the whole or part of the remaining acid hydrogen.
- Specific examples of the nitrogen-containing compound include ammonia, monoamines, diamines, and polyamines. Preferred examples include aliphatic amines having an alkyl or alkenyl group having 10 to 20 carbon atoms, which may be straight-chain or branched, such as decylamine, dodecylamine, dimethyldodecylamine, tridecylamine, heptadecylamine, octadecylamine, oleylamine, and stearyl amine.
- The phosphorus compound referred to as Component (B) is preferably at least one type of compound selected from the group consisting of amine salts of phosphorus compounds of formula (1) wherein all of X1, X2 and X3 are oxygen and amine salts of phosphorus compounds of formula (2) wherein all of X4, x5, X6 and X7 are oxygen (one or two of X4, and X6 may be a single bond or a (poly) oxyalkylene group) because they are excellent in oxidation stability.
- Alternatively, the phosphorus compound referred to as Component (B) is preferably a phosphorus compound of formula (2) wherein all of X4, X5, X6 and X7 are oxygen (one or two of X4, X5 and X6 may be a single bond or a (poly)oxyalkylene group), at least one of R4, R5 and R6 is hydrogen and the others are each independently a hydrocarbon group having 1 to 30 carbon atoms in terms of oxidation stability.
- The hydrocarbon group of the phosphorus compound referred to as Component (B) has preferably 16 or fewer carbon atoms. This is based on the fact that fewer the carbon atoms, higher the volume resistivity is as set forth in Table 1 below.
-
[Table 1] Structure of phosphorus compound Trialkyl phosphite Dialkylhydrogen phosphine Diphenylhydrogen phosphine Dialkyl acid phosphate Structure of hydrocarbon group iC8 nC12 nC18 iC4 iC8 nC18 phenyl nC10 nC18 Carnbon number of hydrocarbon group 8 12 18 4 8 18 6 10 18 Volume resistivity 1010 Ω·m 358 315 27.9 1200 104 12.8 800 1.44 1.4 *Phosphoric compounds were each dissolved in a base oil with the following physical properties to compare the volume resistivity.
They were each added in an amount of 100 mass ppm by phosphorus.
Kinematic viscosity (40°C) 19.7mm2/s, Kinematic viscosity (100°C) 4.3mm2/s, Viscosity index 125, %CP 78.5, %CN21.5, %CA0 - In Table 1, the volume resistivity designates the value measured at an oil temperature of 80°C in accordance with JIS C 2101 24. (volume resistivity test). In the above examples, each of the phosphorus compound was added and dissolved in a mineral base oil so that it is contained in an amount of 100 mass ppm on the basis of phosphorus.
- No particular limitation is imposed on the content of Component (B) that is the above-described phosphorus compound of the lubricating oil composition of the present invention, which is, however, 0.01 percent by mass or more, preferably 0.02 percent by mass or more, particularly preferably 0.03 percent by mass or more and preferably 0.1 percent by mass or less, more preferably 0.08 percent by mass or less, particularly preferably 0.05 percent by mass or less on the basis of phosphorus on the composition mass basis. If the content of the phosphorus compound is less than 0.01 percent by mass on the basis of phosphorus, the resulting composition would be less effective in anti-wear properties. Whilst, if the content of the phosphorus compound is more than 0.1 percent by mass on the basis of phosphorus, the resulting composition would be poor in insulation properties, degraded in oxidation stability and enhanced in aggressivity against sealing materials.
- The lubricating oil composition of the present invention is characterized in that it contains (C) an ashless dispersant having a functional group containing nitrogen as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the composition mass basis or does not contain such an ashless dispersant at all.
- As described above, the lubricating oil composition of the present invention contains (B) at least one type of phosphorus compound selected from phosphorus compounds having at least one hydroxyl group and/or at least one thiol group. The inclusion of the phosphorus compound enhances significantly the anti-wear properties and anti-seizure properties of the composition. However, this type of phosphorus compound degrades drastically the volume resistance of the composition compared with a phosphorus compound having no hydroxyl group and/or thiol group if an ashless dispersant having a functional group containing nitrogen as a dispersion group is contained. Therefore, the composition contains necessarily (C) an ashless dispersant having a functional group containing nitrogen as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the composition mass basis or does not contain such an ashless dispersant at all in order to improve the anti-wear properties and anti-seizure properties of the composition.
- Examples of the ashless dispersant having a functional group containing nitrogen as a dispersion group referred to as Component (C) include succinimide, benzylamine, and polyamines, each having a hydrocarbon group having 40 to 400 carbon atoms.
- However, among these compounds, those having been modified to have a structure wherein nitrogen cannot constitute a salt structure together with Component (B) that is the phosphorus compound are excluded from the examples. Fox example, compounds wherein the amino group is acylated or modified with a boron compound or a sulfuric compound and incapable of constituting a salt structure with Component (B) that is the phosphorus compound are excluded.
- What is meant by "containing an ashless dispersant having a functional group containing nitrogen as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the composition mass basis" is a structure or amount wherein even though an ashless dispersant has an amino group remained so as to be able to constitute a salt structure with Component (B) that is the phosphorus compound, the content thereof is such a level that the volume resistance at 80°C of the resulting composition is 5×108 Ω·m or greater. Specifically, the ashless dispersant is contained in such an amount that nitrogen is contained in an amount of less than 0.001 percent by mass, more preferably less than 0.0008 percent by mass on the composition mass basis.
- No particular limitation is imposed on the use of compounds with a structure of thiadiazole or triazole that is an amine-based anti-oxidant or a corrosion inhibitor because it can be ignored if the content thereof is 1 percent by mass or less.
- The lubricating oil composition of the present invention has a 80°C volume resistivity of preferably 5×108 Ω·m or greater, more preferably 6×108 Ω·m or greater, particularly preferably 10x108 Ω·m or greater. The composition having a 80°C volume resistivity of 5×108 Ω·m or greater can keep the insulation properties high not only when it is fresh but also when it is degraded thereby avoiding an electric motor from having a trouble such as shorting out for a long period of time.
- If necessary, the lubricating oil composition of the present invention may be blended with various additives such as viscosity index improvers, extreme pressure additives, dispersants other than the above-described dispersant compounds, metallic detergents, friction modifiers, anti-oxidants, corrosion inhibitors, rust inhibitors, demulsifiers, metal deactivators, pour point depressants, seal swelling agents, anti-foaming agents, and dyes, alone or in combination in order to further enhance the properties of the composition or impart the composition with properties required for a lubricating oil.
- Examples of the viscosity index improvers include non-dispersant or dispersant type poly(meth)acrylate; non-dispersant or dispersant type ethylene-α-olefin copolymers and hydrogenated compounds thereof; polyisobutylene and hydrogenated compounds thereof; styrene-diene hydrogenated copolymers; styrene-maleic anhydride ester copolymers; polyalkylstyrenes; and copolymers of (meth) acrylate monomers represented by formula (1) and unsaturated monomers such as ethylene/propylene/styrene/maleic anhydride.
- The amount of the viscosity index improver in the lubricating oil composition of the present invention is such an amount that the resulting composition has a 100°C kinematic viscosity of 5 to 10 mm2/s, preferably 6 to 9 mm2/s and a viscosity index of 120 to 270, preferably 150 to 250, more preferably 170 to 220. More specifically, the amount is 15 percent by mass or less, preferably 10 percent by mass or less, more preferably 8 percent by mass or less and 2 percent by mass or more, preferably 4 percent by mass or more, more preferably 5 percent by mass or more on the composition mass basis. An amount of more than 15 percent by mass causes a too high viscosity while an amount of less than 2 percent by mass causes a too high viscosity and thus cannot secure a sufficient composition viscosity.
- Examples of the metallic detergent include those such as alkaline earth metal sulfonates, alkaline earth metal phenates, and alkaline earth metal salicylates.
- Any one or more compounds selected from these metallic detergents may be contained in an amount of usually 0.01 to 10 percent by mass, preferably 0.1 to 5 percent by mass on the total composition mass basis.
- The friction modifier may be any compound that has been generally used as a friction modifier for lubricating oils. Specific examples include amine compounds, imide compounds, fatty acid esters, fatty acid amides, and fatty acid metal salts, each having per molecule at least one alkyl or alkenyl group having 6 to 30 carbon atoms, particularly a straight-chain alkyl or alkenyl group having 6 to 30 carbon atoms.
- Any one or more compounds selected from these friction modifiers may be contained in an amount of usually 0.01 to 5.0 percent by mass, preferably 0.03 to 3.0 percent by mass on the total composition mass basis.
- The anti-oxidant may be any anti-oxidant that has been usually used in lubricating oils, such as phenol- or amine-based compounds.
- Specific examples of the anti-oxidant include alkylphenols such as 2-6-di-tert-butyl-4-methylphenol; bisphenols such as methylene-4,4-bisphenol(2,6-di-tert-butyl-4-methylphenol); naphthylamines such as phenyl-α-naphthylamine; dialkyldiphenylamines; zinc dialkyldithiophosphoric acids such as di-2-ethylhexyldithiophosphoric acid; and esters of (3,5-di-tert-butyl-4-hydroxyphenyl)fatty acid (propionic acid) or (3-methyl-5-tert-butyl-4-hydroxyphenyl)fatty acid (propionic acid) with a monohydric or polyhydric alcohol such as methanol, octanol, octadecanol, 1,6-hexanediol, neopentyl glycol, thiodiethylene glycol, triethylene glycol and pentaerythritol.
- Any one or more of compounds selected from these compounds may be contained in any amount, which is, however, usually from 0.01 to 5 percent by mass, preferably from 0.1 to 3 percent by mass on the total composition mass basis.
- Examples of the corrosion inhibitor include benzotriazole-, tolyltriazole-, thiadiazole-, and imidazole-types compounds.
- Examples of the rust inhibitor include petroleum sulfonates, alkylbenzene sulfonates, dinonylnaphthalene sulfonates, alkenyl succinic acid esters, and polyhydric alcohol esters.
- Examples of the demulsifier include polyalkylene glycol-based non-ionic surfactants such as polyoxyethylenealkyl ethers, polyoxyethylenealkylphenyl ethers, and polyoxyethylenealkylnaphthyl ethers.
- Examples of the metal deactivator include imidazolines, pyrimidine derivatives, alkylthiadiazoles, mercaptobenzothiazoles, benzotriazoles and derivatives thereof, 1,3,4-thiadiazolepolysulfide, 1,3,4-thiadiazolyl-2,5-bisdialkyldithiocarbamate, 2-(alkyldithio)benzoimidazole, and β-(o-carboxybenzylthio)propionitrile.
- The pour point depressant may be any of the known pour point depressants selected depending on the type of lubricating base oil but are preferably poly(meth)acrylates having a weight average molecular weight of preferably 20, 000 to 500,000, more preferably 50,000 to 300,000, particularly preferably 80,000 to 200,000.
- The anti-foaming agent may be any compound that has been usually used as an anti-foaming agent for lubricating oils. Examples of such an anti-foaming agent include silicones such as dimethylsilicone and fluorosilicone. Any one or more of compounds selected from these compounds may be contained in any amount.
- The seal swelling agent may be any compound that has been usually used as a seal swelling agent for lubricating oils. Examples of such a seal swelling agents include ester-, sulfur- and aromatic-based seal swelling agents.
- The dye may be any compound that has been usually used and may be blended in any amount. The amount is usually from 0.001 to 1.0 percent by mass on the total composition mass basis.
- When these additives are blended with the lubricating oil composition of the present invention, the corrosion inhibitor, rust inhibitor, and anti-foaming agent are each contained in an amount of 0.005 to 5 percent by mass, the pour point depressant and metal deactivator are each contained in an amount of 0.005 to 2 percent by mass, the seal swelling agent is contained in an amount of 0.01 to 5 percent by mass, and the anti-foaming agent is contained in an amount of 0.0005 to 1 percent by mass, all on the total composition mass basis.
- The present invention will be described more specifically with reference to the following Examples and Comparative Examples but not limited thereto.
- (Examples 1 to 6 and Comparative Examples 1 to 5)
- Lubricating oil compositions according to the present invention (Examples 1 to 6) and those for comparison (Comparative Examples 1 to 5) were prepared in accordance with the formulations set forth in Table 2. The performances of each composition were evaluated with the following tests. The results are set forth in Table 2.
[Table 2] Base Oil Total Base Oil Mass Basis Example Example 2 Example 3 Example 4 Example 5 Example 6 Comparative Example 1 Comparative Example 2 Comparative Example 3 Comparative Example 4 Comparative Example 5 A-1 Base Oil 1 1) inmass% 100 100 100 100 100 100 100 100 100 A-2 Base Oil 2 2) inmass% 100 A-3 Base Oil 3 3) inmass% 100 Additives Total Composition Mass Basis mass% B-1 Oil soluble phosphorus additive 1 4) mass% 0.5 0.1 0.1 0.1 0.1 0.1 B-2 Oil soluble phosphorus additive 2 5) mass% 0.1 B-3 Oil soluble phosphorus additive 3 6) mass% 0.1 B-4 Oil soluble phosphorus additive 4 7) 0.3 C-1 Ashless dispersant 1 8) mass% 4 4 C-2 Ashless dispersant 2 9) 4 D-1 Viscosity index improver 10) mass% 12 12 12 17 12 12 12 12 12 12 12 Additive package 11) mass% 2.5 2.5 2.5 2.5 2.5 2.5 2.5 2.5 25 2.5 2.5 P content of the composition masspm 500 100 100 100 100 100 0 100 0 100 100 Evalution results Four - ball test 12) WL mm2/s 1961 1961 1961 1961 1961 1961 1961 1961 1961 1961 1961 LNSL % 785 785 785 785 785 785 490 785 490 785 785 Four- ball (wear scar diameter) 13) mm2/s 0.5 0.5 0.5 0.5 0.5 0.5 0.7 0.5 0.8 0.5 0.5 Volume resistivity 14) 1010 Ω·m 0.06 0.15 0.12 0.06 0.13 0.05 0.16 0.005 0.031 0.001 0.01 1) kinematic viscosity (40°C) 19.7mm2/s. kinematic viscosity (100°C) 4.3mm2/s, viscosity index 125, %CP 78.5, %CN 21.5, %CA 0
2) kinematic viscosity (40°C) 22.7mm2/s, kinematic viscosity (100°C) 4.3mm2/s, viscosity index 102, %CP 66.4, %CN 29.0, %CA4.6
3) di-2-ethylhexyl azelate kinematic viscosity (40°C) 10.1mm2/s. kinematic viscosity (100°C) 3.0mm2/s, viscosity index 144
4) amine salt of acidic phosphoric acid ester (P content: 10%, phosphoric acid ester: 2-ethylhexyl, amine: mixed amine of C11 to 14)
5) hydrogen phosphine, isoC4 P content 16%
6) acidic phosphoric acid ester, 2-ethylhexyl P: 9.4%
7) trioleylphosphite P: 3.7%
8) boronated succinimide, PIS Mw 2000, bis type, TEPA crosslinking
9) succinimide, PIB Mw 1000, bis type. TEPA crosslinking
10) non-dispersant type PMA Mw 25,000
11) containing Ca metallic detergent (0.1 mass%), metal deactivator (0.1 mass%), anti-oxidant (2.0 mass%), anti-foaming agent (30 mass ppm)
12) 1800 rpm
13) 392 N, 1800 rpm, 80°C, 30 min
14) in accordance with JIS C2101, measured at 80°C - The lubricating oil composition of the present invention is a composition improved in anti-wear properties and anti-seizure properties and can be used as a lubricating oil for an electric motor-equipped vehicle such as an electric vehicle or a hybrid vehicle, an electric motor oil, an oil both for a transmission and an electric motor, and an oil for a device wherein a transmission and an electric motor are packaged in one and a lubricating system is shared by the transmission and an electric motor.
- The present invention can provide the above-described transmission, electric motor and device including the lubricating oil composition of the present invention and a method for lubricating, insulating and cooling the above-described transmission, electric motor and device using the lubricating oil composition of the present invention.
Claims (3)
- A lubricating oil composition comprising:(A) a lubricating oil base oil;(B) at least one type of phosphorus compound selected from the group consisting of phosphorus compounds having at least one hydroxyl group and/or at least one thiol group; and(C) an ashless dispersant having a functional group containing as a dispersion group in an amount of less than 0.001 percent by mass on the basis of nitrogen on the total composition mass basis or no such an ashless dispersant at all, the composition having a 80°C volume resistivity of 5×108 Ω·m or greater.
- The lubricating oil composition according to claim 1 wherein (B) the phosphorus compound having a hydrocarbon group having 16 or fewer carbon atoms.
- The lubricating oil composition according to claim 1 or 2 wherein the composition is used for the transmission, both transmission and electric motor, or the device in which a lubricating system is shared by the transmission and electric motor, mounted in a fuel cell electric vehicle, an electric vehicle or a hybrid vehicle.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011072464A JP5779376B2 (en) | 2011-03-29 | 2011-03-29 | Lubricating oil composition |
PCT/JP2011/070814 WO2012132055A1 (en) | 2011-03-29 | 2011-09-13 | Lubricating oil composition |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2692841A1 true EP2692841A1 (en) | 2014-02-05 |
EP2692841A4 EP2692841A4 (en) | 2014-08-27 |
Family
ID=46929864
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP11862708.2A Ceased EP2692841A4 (en) | 2011-03-29 | 2011-09-13 | Lubricating oil composition |
Country Status (6)
Country | Link |
---|---|
US (1) | US20140018271A1 (en) |
EP (1) | EP2692841A4 (en) |
JP (1) | JP5779376B2 (en) |
CN (1) | CN103443256B (en) |
CA (1) | CA2820519A1 (en) |
WO (1) | WO2012132055A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018067905A1 (en) * | 2016-10-07 | 2018-04-12 | Exxonmobil Research And Engineering Company | Method for preventing or minimizing electrostatic discharge and dielectric breakdown in electric vehicle powertrains |
WO2020260462A1 (en) * | 2019-06-28 | 2020-12-30 | Total Marketing Services | Use of a phosphorus compound as a non-corrosive extreme-pressure and anti-wear additive in a lubricant for a propulsion system of an electric or hybrid vehicle |
EP3872151A4 (en) * | 2018-10-24 | 2022-07-13 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
US12043814B2 (en) | 2019-06-28 | 2024-07-23 | Totalenergies Onetech | Use of a triazole compound as an additive for improving the anti-corrosion properties of a lubricant composition for a propulsion system of an electric or hybrid vehicle |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104177406B (en) * | 2013-05-22 | 2016-08-24 | 中国石油化工股份有限公司 | Bis-phosphite and preparation method thereof, purposes and lubricant oil composite |
JP6073748B2 (en) * | 2013-06-10 | 2017-02-01 | 東燃ゼネラル石油株式会社 | Lubricating oil composition |
JP6693033B2 (en) * | 2015-03-31 | 2020-05-13 | 出光興産株式会社 | Lubricating oil composition for electric vehicle or hybrid vehicle |
FR3072685B1 (en) * | 2017-10-20 | 2020-11-06 | Total Marketing Services | COMPOSITION FOR COOLING AND LUBRICATING A MOTORIZATION SYSTEM OF A VEHICLE |
JP2019163407A (en) * | 2018-03-20 | 2019-09-26 | 出光興産株式会社 | Lubricant base oil and lubricant composition |
CN112930389B (en) * | 2018-11-06 | 2022-11-25 | 引能仕株式会社 | Lubricating oil composition |
US10819342B2 (en) | 2018-12-20 | 2020-10-27 | Samsung Electronics Co., Ltd. | Low-power low-setup integrated clock gating cell with complex enable selection |
US11066622B2 (en) | 2019-10-24 | 2021-07-20 | Afton Chemical Corporation | Synergistic lubricants with reduced electrical conductivity |
CN116323878A (en) * | 2020-09-14 | 2023-06-23 | 雪佛龙日本有限公司 | Lubricating oil containing alkylphosphonic acid |
JP7563935B2 (en) * | 2020-10-09 | 2024-10-08 | Eneos株式会社 | Lubricating Oil Composition |
JP7523319B2 (en) | 2020-11-04 | 2024-07-26 | Eneos株式会社 | Lubricating Oil Composition |
CN112694938A (en) * | 2020-12-28 | 2021-04-23 | 广东南油石化有限公司 | Motor oil for electric automobile and preparation method thereof |
US11753599B2 (en) | 2021-06-04 | 2023-09-12 | Afton Chemical Corporation | Lubricating compositions for a hybrid engine |
KR20240137667A (en) | 2022-03-03 | 2024-09-20 | 미쓰이 가가쿠 가부시키가이샤 | Lubricant composition |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1405897A1 (en) * | 2001-05-28 | 2004-04-07 | Nissan Motor Co., Ltd. | Transmission oil composition for automobile |
EP2520640A1 (en) * | 2009-12-29 | 2012-11-07 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09137181A (en) * | 1995-11-10 | 1997-05-27 | Kao Corp | Refrigerator working fluid composition |
JP4209975B2 (en) * | 1998-10-05 | 2009-01-14 | 新日本石油株式会社 | Lubricating oil composition |
JP4316042B2 (en) * | 1999-03-05 | 2009-08-19 | 出光興産株式会社 | Refrigerator oil composition |
CN1307293C (en) * | 2000-11-29 | 2007-03-28 | 日本精工株式会社 | Conductive grease and rolling apparatus packed with the same |
US7786059B2 (en) * | 2004-12-21 | 2010-08-31 | Chevron Oronite Company Llc | Anti-wear additive composition and lubricating oil composition containing the same |
JP5062650B2 (en) * | 2005-07-29 | 2012-10-31 | 東燃ゼネラル石油株式会社 | Gear oil composition |
US20080194442A1 (en) * | 2007-02-13 | 2008-08-14 | Watts Raymond F | Methods for lubricating a transmission |
-
2011
- 2011-03-29 JP JP2011072464A patent/JP5779376B2/en active Active
- 2011-09-13 CN CN201180069358.4A patent/CN103443256B/en not_active Expired - Fee Related
- 2011-09-13 WO PCT/JP2011/070814 patent/WO2012132055A1/en active Application Filing
- 2011-09-13 EP EP11862708.2A patent/EP2692841A4/en not_active Ceased
- 2011-09-13 CA CA2820519A patent/CA2820519A1/en not_active Abandoned
- 2011-09-13 US US14/007,120 patent/US20140018271A1/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1405897A1 (en) * | 2001-05-28 | 2004-04-07 | Nissan Motor Co., Ltd. | Transmission oil composition for automobile |
EP2520640A1 (en) * | 2009-12-29 | 2012-11-07 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
Non-Patent Citations (1)
Title |
---|
See also references of WO2012132055A1 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018067905A1 (en) * | 2016-10-07 | 2018-04-12 | Exxonmobil Research And Engineering Company | Method for preventing or minimizing electrostatic discharge and dielectric breakdown in electric vehicle powertrains |
EP3872151A4 (en) * | 2018-10-24 | 2022-07-13 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
US11535808B2 (en) | 2018-10-24 | 2022-12-27 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
WO2020260462A1 (en) * | 2019-06-28 | 2020-12-30 | Total Marketing Services | Use of a phosphorus compound as a non-corrosive extreme-pressure and anti-wear additive in a lubricant for a propulsion system of an electric or hybrid vehicle |
FR3097872A1 (en) * | 2019-06-28 | 2021-01-01 | Total Marketing Services | Use of a phosphorus compound as an anti-wear and non-corrosive extreme pressure additive in a lubricant for an electric or hybrid vehicle propulsion system. |
US12043814B2 (en) | 2019-06-28 | 2024-07-23 | Totalenergies Onetech | Use of a triazole compound as an additive for improving the anti-corrosion properties of a lubricant composition for a propulsion system of an electric or hybrid vehicle |
Also Published As
Publication number | Publication date |
---|---|
CA2820519A1 (en) | 2012-10-04 |
EP2692841A4 (en) | 2014-08-27 |
WO2012132055A1 (en) | 2012-10-04 |
US20140018271A1 (en) | 2014-01-16 |
CN103443256B (en) | 2016-05-25 |
JP5779376B2 (en) | 2015-09-16 |
JP2012207083A (en) | 2012-10-25 |
CN103443256A (en) | 2013-12-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2692841A1 (en) | Lubricating oil composition | |
CN103275800B (en) | Lubricant oil composite | |
EP2813563B1 (en) | Lubricating oil composition for internal combustion engine | |
US8580719B2 (en) | Lubricating oil composition for internal combustion engine | |
EP3878928B1 (en) | Lubricant composition | |
EP2636725B1 (en) | Lubricating oil composition for automobile engine lubrication | |
WO2002097017A1 (en) | Transmission oil composition for automobile | |
EP2878653B1 (en) | Lubricant oil composition, and method for lubricating sliding material while preventing elution of copper and lead | |
EP2439256A1 (en) | Lubricant oil composition | |
EP2474602A1 (en) | Lubricant composition | |
EP2873720A1 (en) | Lubricant oil composition for internal combustion engine | |
EP3766948A1 (en) | Lubricating oil composition | |
JP5930905B2 (en) | Lubricating oil composition | |
JP5931250B2 (en) | Lubricating oil composition | |
EP4206307A1 (en) | Lubricating oil composition | |
WO2016181863A1 (en) | Lubricating oil composition | |
JP5564204B2 (en) | Lubricating oil composition | |
EP3943582B1 (en) | Lubricating oil composition | |
US20180320103A1 (en) | Lubricating Oil Composition for Internal Combustion Engine | |
JP5241122B2 (en) | Lubricating oil composition in contact with silver-containing material | |
CN112888770A (en) | Lubricating oil composition, mechanical device provided with lubricating oil composition, and method for producing lubricating oil composition | |
JP7312717B2 (en) | lubricating oil composition | |
JP6382749B2 (en) | Lubricating oil composition for final reduction gear | |
JP2022048706A (en) | Lubricant composition | |
JP2021143309A (en) | Lubricant composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20130612 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20140729 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C10M 137/00 20060101AFI20140723BHEP Ipc: C10N 30/06 20060101ALI20140723BHEP Ipc: C10N 20/04 20060101ALI20140723BHEP Ipc: C10N 40/04 20060101ALI20140723BHEP Ipc: C10M 141/10 20060101ALI20140723BHEP Ipc: C10N 10/04 20060101ALI20140723BHEP Ipc: C10M 137/02 20060101ALI20140723BHEP Ipc: C10N 20/02 20060101ALI20140723BHEP |
|
17Q | First examination report despatched |
Effective date: 20160617 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R003 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED |
|
18R | Application refused |
Effective date: 20180625 |