EP3990592A1 - 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 - Google Patents
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 vehicleInfo
- Publication number
- EP3990592A1 EP3990592A1 EP20736271.6A EP20736271A EP3990592A1 EP 3990592 A1 EP3990592 A1 EP 3990592A1 EP 20736271 A EP20736271 A EP 20736271A EP 3990592 A1 EP3990592 A1 EP 3990592A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- additives
- sulfur
- additive
- amine
- electric
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 163
- 239000000654 additive Substances 0.000 title claims abstract description 86
- 238000005260 corrosion Methods 0.000 title claims abstract description 44
- 230000000996 additive effect Effects 0.000 title claims abstract description 32
- -1 triazole compound Chemical class 0.000 title claims abstract description 20
- 239000000314 lubricant Substances 0.000 title abstract description 21
- 230000001050 lubricating effect Effects 0.000 claims abstract description 87
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 78
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 60
- 239000011593 sulfur Substances 0.000 claims abstract description 57
- 239000007866 anti-wear additive Substances 0.000 claims abstract description 55
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 18
- 150000003852 triazoles Chemical class 0.000 claims description 57
- 150000001875 compounds Chemical class 0.000 claims description 55
- 150000001412 amines Chemical class 0.000 claims description 38
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical class S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 claims description 21
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical class CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 241000534944 Thia Species 0.000 claims description 13
- 150000001565 benzotriazoles Chemical class 0.000 claims description 13
- 230000005540 biological transmission Effects 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- QWENRTYMTSOGBR-UHFFFAOYSA-N 1H-1,2,3-Triazole Chemical compound C=1C=NNN=1 QWENRTYMTSOGBR-UHFFFAOYSA-N 0.000 claims description 8
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 229920001021 polysulfide Polymers 0.000 claims description 6
- 230000009467 reduction Effects 0.000 claims description 6
- DHTAIMJOUCYGOL-UHFFFAOYSA-N 2-ethyl-n-(2-ethylhexyl)-n-[(4-methylbenzotriazol-1-yl)methyl]hexan-1-amine Chemical compound C1=CC=C2N(CN(CC(CC)CCCC)CC(CC)CCCC)N=NC2=C1C DHTAIMJOUCYGOL-UHFFFAOYSA-N 0.000 claims description 5
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- BTHAQRDGBHUQMR-UHFFFAOYSA-N [S]P(=O)=O Chemical compound [S]P(=O)=O BTHAQRDGBHUQMR-UHFFFAOYSA-N 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
- 235000021317 phosphate Nutrition 0.000 claims description 3
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 1
- 239000002199 base oil Substances 0.000 description 30
- 239000003963 antioxidant agent Substances 0.000 description 22
- 230000007797 corrosion Effects 0.000 description 12
- 239000003599 detergent Substances 0.000 description 12
- 229920013639 polyalphaolefin Polymers 0.000 description 12
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- 125000003118 aryl group Chemical group 0.000 description 9
- 150000003851 azoles Chemical class 0.000 description 9
- 239000002270 dispersing agent Substances 0.000 description 9
- 239000002184 metal Substances 0.000 description 8
- 229920001515 polyalkylene glycol Polymers 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- GLOYGJPNNKTDIG-UHFFFAOYSA-N SC=1N=NSC=1S Chemical class SC=1N=NSC=1S GLOYGJPNNKTDIG-UHFFFAOYSA-N 0.000 description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
- 239000012964 benzotriazole Substances 0.000 description 6
- 150000001735 carboxylic acids Chemical class 0.000 description 6
- 239000003638 chemical reducing agent Substances 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 150000004867 thiadiazoles Chemical class 0.000 description 6
- KWBXQDNGHQLAMB-UHFFFAOYSA-N 4-sulfanyl-3h-1,3-thiazole-2-thione Chemical class SC1=CSC(=S)N1 KWBXQDNGHQLAMB-UHFFFAOYSA-N 0.000 description 5
- 239000002518 antifoaming agent Substances 0.000 description 5
- 150000004982 aromatic amines Chemical class 0.000 description 5
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 5
- 230000000994 depressogenic effect Effects 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 description 5
- 238000007654 immersion Methods 0.000 description 5
- 239000003607 modifier Substances 0.000 description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 description 5
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 230000009972 noncorrosive effect Effects 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000005077 polysulfide Substances 0.000 description 3
- 150000008117 polysulfides Polymers 0.000 description 3
- 125000004434 sulfur atom Chemical group 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- OTNSJAUBOYWVEB-UHFFFAOYSA-N 1,2,4-thiadiazolidine-3,5-dithione Chemical compound S=C1NSC(=S)N1 OTNSJAUBOYWVEB-UHFFFAOYSA-N 0.000 description 2
- QQADCAPKFRAHQW-UHFFFAOYSA-N 1,2,5-thiadiazole;1,3,4-thiadiazole Chemical compound C=1C=NSN=1.C1=NN=CS1 QQADCAPKFRAHQW-UHFFFAOYSA-N 0.000 description 2
- AJBLKZFBURBYPT-UHFFFAOYSA-N 1,2,5-thiadiazolidine-3,4-dithione Chemical compound SC1=NSN=C1S AJBLKZFBURBYPT-UHFFFAOYSA-N 0.000 description 2
- XEGAKAFEBOXGPV-UHFFFAOYSA-N 2,3,3a,4-tetrahydro-1h-benzotriazole Chemical class C1C=CC=C2NNNC12 XEGAKAFEBOXGPV-UHFFFAOYSA-N 0.000 description 2
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 2
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 230000002596 correlated effect Effects 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical group C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010292 electrical insulation Methods 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000002462 imidazolines Chemical class 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 229960002317 succinimide Drugs 0.000 description 2
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- UGUHFDPGDQDVGX-UHFFFAOYSA-N 1,2,3-thiadiazole Chemical compound C1=CSN=N1 UGUHFDPGDQDVGX-UHFFFAOYSA-N 0.000 description 1
- 150000000177 1,2,3-triazoles Chemical group 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical class ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 101000582320 Homo sapiens Neurogenic differentiation factor 6 Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N N-methylaminoacetic acid Natural products C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- 102100030589 Neurogenic differentiation factor 6 Human genes 0.000 description 1
- DIOYAVUHUXAUPX-KHPPLWFESA-N Oleoyl sarcosine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CC(O)=O DIOYAVUHUXAUPX-KHPPLWFESA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- IWBMUDDLRPGWNJ-UHFFFAOYSA-N SC1=NSC(=N1)S.SC=1N=NSC1S Chemical compound SC1=NSC(=N1)S.SC=1N=NSC1S IWBMUDDLRPGWNJ-UHFFFAOYSA-N 0.000 description 1
- 108010077895 Sarcosine Proteins 0.000 description 1
- 125000005595 acetylacetonate group Chemical group 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012809 cooling fluid Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- KGGZTXSNARMULX-UHFFFAOYSA-L copper;dicarbamodithioate Chemical class [Cu+2].NC([S-])=S.NC([S-])=S KGGZTXSNARMULX-UHFFFAOYSA-L 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000001457 metallic cations Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical class 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000010363 phase shift Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 229940043230 sarcosine Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- NGOGGDKKCYGLOD-UHFFFAOYSA-N thiadiazole;1,2,4-thiadiazole Chemical compound C1=CSN=N1.C=1N=CSN=1 NGOGGDKKCYGLOD-UHFFFAOYSA-N 0.000 description 1
- 150000007979 thiazole derivatives Chemical class 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil 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
- 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
- C10M141/08—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 sulfur-, selenium- or tellurium-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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
-
- 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
- C10M141/06—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 nitrogen-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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/68—Esters
- C10M129/70—Esters of monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
- C10M133/46—Imidazoles
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/52—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
- C10M133/56—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
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/32—Heterocyclic sulfur, selenium or tellurium compounds
- C10M135/36—Heterocyclic sulfur, selenium or tellurium compounds the ring containing sulfur and carbon with nitrogen or oxygen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/003—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions 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
- 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
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/223—Five-membered rings containing nitrogen and carbon only
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/30—Heterocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/022—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of hydrocarbons, e.g. olefines
-
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/106—Thiadiazoles
-
- 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
- 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
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
-
- 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
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
Definitions
- the present invention relates to the field of lubricating compositions for a propulsion system of an electric or hybrid vehicle. It relates more particularly to the use of compounds of triazole type, as additives for improving the anti-corrosion properties of a lubricating composition incorporating one or more anti-wear additive (s) amine (s) and / or sulfur (s). .
- the term “electric vehicle” is intended to denote a vehicle comprising an electric motor as the sole means of propulsion, unlike a hybrid vehicle which comprises a combustion engine and an electric motor as combined propulsion means. .
- propulsion system within the meaning of the present invention, is meant a system comprising the mechanical parts necessary for the propulsion of an electric vehicle.
- the propulsion system thus more particularly includes an electric motor, comprising the rotor-stator assembly of the power electronics (dedicated to speed regulation), a transmission and a battery.
- lubricating compositions also called “lubricants”, for the main purposes of reducing the frictional forces between the various parts of the system. propulsion of the vehicle, especially between moving metal parts in engines.
- lubricating compositions are also effective in preventing premature wear or even damage to these parts, and in particular to their surface.
- a lubricating composition is conventionally composed of one or more base oil (s), which are generally associated with several additives dedicated to stimulating the lubricating performance of the base oil, such as, for example, friction modifying additives, but also to provide additional performance.
- base oil s
- additives dedicated to stimulating the lubricating performance of the base oil, such as, for example, friction modifying additives, but also to provide additional performance.
- antioxidants are considered in order to reduce the wear of parts of the propulsion system, in particular of the mechanical parts of the engine, and thus to prevent degradation of the durability of the engine.
- anti-wear additives for example, dimercaptothiadiazoles, polysulfides, in particular sulfur-containing olefins, amine phosphates, or else phospho-sulfur additives, such as metal alkylthiophosphates, in in particular zinc alkylthiophosphates, and more specifically zinc dialkyldithiophosphates or ZnDTP.
- antiwear additives preference is given in particular to amine and / or sulfur antiwear agents, such as dimercaptothiadiazoles, zinc dithiophosphate or polysulphides.
- the lubricant is insulating in order to avoid any failure in the electrical components.
- a conductive lubricant can lead to a risk of electric current leakage from the stator and rotor windings, thus reducing the efficiency of the propulsion systems, and creating a possible overheating at the level of the electrical components, even up to 'damage the system. It is therefore crucial, in within the framework of the implementation of lubricants for power systems of electric or hybrid vehicles, that the lubricants have good “electrical” properties in addition to non-corrosive properties.
- the present invention aims precisely to overcome this drawback.
- the present invention relates to the use of at least one compound of triazole type, as an additive for improving the anti-corrosion properties of a lubricating composition, intended for a propulsion system of an electric or hybrid vehicle. and comprising one or more anti-wear additive (s) amine (s) and / or sulfur (s).
- a compound of triazole type as an additive for improving the anti-corrosion properties of a lubricating composition, intended for a propulsion system of an electric or hybrid vehicle. and comprising one or more anti-wear additive (s) amine (s) and / or sulfur (s).
- triazoles for example triazoles, in particular 1,2,3-triazole and their derivatives or else benzotriazole and its derivatives, are already known for their corrosion inhibiting properties, as described for example in the document
- the specific combination of at least one compound of triazole type and of at least one amino and / or sulfur anti-wear additive makes it possible to reduce, or even avoid, the phenomenon of corrosion induced in particular by the presence in of the lubricating composition of said additive (s) anti-wear amine (s) and / or sulfur (s).
- anti-corrosion additive is intended to denote an additive making it possible to prevent or reduce the corrosion of metal parts. An anti- corrosion thus makes it possible to confer good “anti-corrosion properties” on a composition containing it.
- the corrosive (or corroding) power of a compound can be evaluated according to a test implementing the study of the variation in the value of the electrical resistance of a copper wire of a predetermined diameter, as a function of the duration immersing this yarn in a composition comprising, in a non-corrosive medium, for example in one or more base oils, said compound to be tested.
- the variation in the value of this electrical resistance is correlated directly with the variation in the diameter of the wire tested.
- a compound is qualified as “non-corrosive” when the loss in diameter of the copper wire studied is less than or equal to 0.5 mm after immersion for 80 hours, in particular less than or equal to. at 0.2 mm after immersion for 20 hours in the composition comprising said compound.
- the dielectric properties of a lubricant are represented in particular by the electrical resistivity and the dielectric loss (tan d), and they can be measured according to standard IEC 60247.
- Electrical resistivity represents the material's ability to oppose the flow of electric current. It is expressed in ohm-meter (W.ih). The resistivity should not be low to avoid electrical conduction.
- the electrical dissipation factor or the tangent of the loss angle is the complementary angle of the phase shift between the applied voltage and the alternating current. This factor reflects the energy losses by the Joule effect. The temperature rises are therefore directly linked to the value of d.
- Transmission oil typically has a tan value of on the order of one at room temperature. A good insulating lubricant should maintain a low level of tan d.
- the compound of triazole type used according to the invention is chosen from triazoles, in particular 1,2,3-triazole, optionally substituted; the benzotriazoles and their derivatives, in particular tolyltriazole (also called tolutriazole) and its derivatives, and tetrahydrobenzotriazoles and their derivatives; and their mixtures.
- the triazole type compound is a benzotriazole or one of its derivatives, preferably a benzotriazole derivative, more preferably a tolyltriazole derivative.
- a lubricating composition intended for a propulsion system of an electric or hybrid vehicle of one or more compound (s) of triazole type according to the invention thus advantageously allows the implementation, in the composition, additive (s) anti-wear amine (s) and / or sulfur (s), such as dimercaptothiadiazoles, without causing an undesirable corrosive effect.
- Amino and / or sulfur anti-wear additives used in a lubricating composition according to the invention are more particularly detailed in the remainder of the text. They are preferably chosen from amino and sulfur antiwear additives. They may preferably be compounds of the thia (di) azoles type, in particular dimercaptothiadiazole derivatives. Also, a composition suitable for the invention has the advantage of being easy to formulate. In addition to good anti-wear and anti-corrosion performance, it has good stability, in particular to oxidation, as well as good properties in terms of electrical insulation.
- the present invention also relates to G use, for lubricating a propulsion system of an electric or hybrid vehicle, in particular for lubricating the electric motor and the power electronics of an electric or hybrid vehicle, of a lubricating composition comprising :
- the present invention also relates to a method of lubricating a propulsion system of an electric or hybrid vehicle, comprising at least one step of bringing at least one mechanical part of said system into contact with a lubricating composition comprising at least an additive of triazole type as defined in the invention and at least one amine and / or sulfur anti-wear additive as defined in the invention.
- a lubricating composition according to the invention is used to lubricate the electric motor itself, in particular the bearings located between the rotor and the stator of an electric motor, and / or the transmission, in particular the reduction gear, in an electric or hybrid vehicle.
- the compounds of triazole type according to the invention will emerge more clearly on reading the description and the examples which follow, given by way of illustration and not by way of limitation of the invention.
- FIG 1 schematically represents an electric or hybrid vehicle propulsion system.
- the additive used as an anti-corrosion agent according to the invention, together with one or more anti-wear amine and / or sulfur additives, in a lubricating composition for a vehicle engine system electric or hybrid is a triazole type compound.
- Triazole compounds are mono or polycyclic compounds comprising at least one 5-membered ring incorporating three nitrogen atoms.
- the compounds of triazole type are more particularly chosen from triazoles and their derivatives.
- the triazoles of general formula C2H3N3, can exist in the following forms, respectively 1H-1,2,3-triazole, 2H-1,2, 3 -triazole, 1H-1,2,4-triazole and 4H-1, 2,4-triazole: [Chem 1]
- Benzotriazole-type compounds are specific triazole derivatives comprising a triazole ring coupled to a benzene ring, as shown below:
- the triazole compound used according to the invention is preferably chosen from triazoles, in particular 1,2,3-triazole, optionally substituted; benzotriazoles and their derivatives, in particular tolyltriazole and its derivatives and tetrahydrobenzotriazoles and their derivatives; and their mixtures.
- the compound of triazole type can be chosen from triazoles, in particular 1,2,3-triazole, optionally substituted; benzotriazoles and their derivatives; and mixtures thereof, preferably is a benzotriazole derivative, more preferably a tolyltriazole derivative.
- 1,2,3-triazoles substituted with one or more groups chosen from alkyl, aryl amine and acyl groups there may be mentioned in particular 1,2,3-triazoles substituted with one or more groups chosen from alkyl, aryl amine and acyl groups.
- the additive of triazole type used according to the invention can be chosen from 1,2,3-triazole and its derivatives, corresponding to the following formula (I): [Chem 3]
- R, R 'and R ” are chosen, independently of each other, from hydrogen, an alkyl group, preferably C 1 to C 24 , an amine group such as a group -NR 1 R 2 , a acyl group such as a -COR 3 group, or an aryl group such as a phenyl or tolyl group; with R 1 , R 2 and R 3 being chosen, independently of one another, from a hydrogen atom or a C 1 to C 24 , preferably C 2 to C 18 alkyl group
- benzotriazole derivatives there may be mentioned in particular the benzotriazoles substituted with one or more groups chosen for example from alkyl groups, such as for example tolutriazole (also called tolyltriazole), 1 ethyl lbenzotriazole, I 'hexy lbenzotriazole, 1 'octyl benzotriazole, etc., alkyl groups substituted by one or more amine functions, aryl groups, such as for example a phenolbenzotriazole, alkylaryl or arylalkyl groups, or other substituents such as hydroxy, alkoxy, halogen groups, etc.
- alkyl groups such as for example tolutriazole (also called tolyltriazole), 1 ethyl lbenzotriazole, I 'hexy lbenzotriazole, 1 'octyl benzotriazole, etc.
- alkyl groups substituted by one or more amine functions
- the additive of triazole type used according to the invention can be chosen from benzotriazole and its derivatives, in particular corresponding to the following formula (II):
- R and R ' are chosen, independently of one another from a hydrogen atom, a C 1 to C 24 alkyl group, optionally substituted by one or more groups -NR 4 R 5 ; an -NR 1 R 2 group ; an acyl group of -COR 3 type and a aryl group such as a phenyl or tolyl group;
- R 1 , R 2 and R 3 being chosen, independently of each other, from a hydrogen atom or a C 1 to C 24 , preferably C 2 to C 18 alkyl group;
- R 4 and R 5 representing, independently of one another, a hydrogen atom, a linear or branched, preferably branched, C3 to C14, preferably alkyl group.
- the triazole compound is tolyltriazole or a derivative thereof.
- the compound of triazole type is a tolyltriazole derivative of the following formula (IIa):
- R 4 and R 5 are, independently of one another, as defined above for formula (II);
- -A- represents an alkylene group, linear or branched, preferably linear, C 1 to C 6 , preferably C 1 to C 3 and more preferably a methylene group (-CH 2 -), in particular, said derivative of tolyltriazole being 2-ethyl-N- (2-ethylhexyl) -N - [(4-methylbenzotriazol-1-yl) methyl] hexan-1-amine.
- the compound of triazole type is of formula (Ha), in which R 4 and R 5 represent branched C 1 to C 12 alkyl groups and -A- represents a C 1 to C 3 alkylene group , preferably a methylene group.
- a halogen represents an atom selected from fluorine, chlorine, bromine or iodine.
- An alkyl group represents a linear or branched hydrocarbon chain.
- a C x -C z alkyl group represents a linear or branched hydrocarbon chain comprising from x to z carbon atoms.
- alkylene group a divalent, linear or branched alkyl group.
- a group C x -C z alkylene represents a divalent hydrocarbon chain of x to z carbon atoms, linear or branched.
- An aikoxy group represents an —O-alkyl radical, in which the alkyl group is as defined above.
- An aryl group represents an aromatic mono- or polycyclic group, in particular comprising between 6 and 10 carbon atoms.
- an aryl group mention may be made of phenyl or naphthyl groups.
- the triazole type compound is a benzotriazole or one of its derivatives, preferably a benzotriazole derivative, more preferably a tolyltriazole derivative.
- the triazole-type compounds required according to the invention can be commercially available, or else prepared according to synthetic methods known to those skilled in the art.
- the invention is not limited to the triazole-type compounds specifically described above.
- Other compounds of the triazole type in particular derivatives of triazole or of benzotriazole, in particular derivatives of tolyltriazole, can be used as anti-corrosion additives according to the invention.
- a compound of triazole type can be in the form of a mixture of at least two compounds of triazole type, in particular as defined above.
- the compound (s) of triazole type in particular as defined above, can be used in a lubricating composition according to the invention, in an amount of 0.01 to 5% by weight, in particular from 0.1 to 3% by mass, and more particularly from 0.5 to 2% by mass, relative to the total mass of the lubricating composition.
- a lubricating composition considered according to the invention comprises one or more anti-wear amine and / or sulfur additives.
- amine and / or sulfur anti-wear additive is intended to denote an additive chosen from amine anti-wear additives, sulfur anti-wear additives and amine and sulfur anti-wear additives.
- anti-wear additive is intended to denote a compound which, used in a lubricating composition, in particular a lubricating composition for a propulsion system of an electric or hybrid vehicle, makes it possible to improve the anti-wear properties of the composition.
- the amine and / or sulfur antiwear additive can for example be chosen from additives of the thia (di) azole type, in particular derivatives of dimercaptothiadiazole; polysulphide additives, in particular sulfur olefins; amine phosphates; phospho-sulfur additives such as alkylthiophosphates; and their mixtures.
- a lubricating composition considered according to the invention comprises at least one anti-wear additive of the thia (di) azoles type.
- Thia (di) azole compounds are compounds that contain both a sulfur atom and at least one nitrogen atom in a five-atom ring.
- Benzothiazoles are a special type of thia (di) azoles.
- This term thia (di) azole includes, besides cyclic compounds containing one sulfur atom and one nitrogen atom per five atom ring, also thiadiazoles which contain sulfur and two nitrogen atoms in such a ring.
- thia (di) azole type compounds can be chosen from benzothiazole derivatives, thiazole derivatives and thiadiazole derivatives.
- the antiwear additive can be a thiadiazole derivative.
- Thiadiazoles are heterocyclic compounds comprising two nitrogen atoms, one sulfur atom, two carbon atoms and two double bonds, of general formula C2N2SH2, which may exist in the following forms, respectively: 1,2,3-thiadiazole; 1,2,4-thiadiazole; 1,2,5-thiadiazole; 1,3,4-thiadiazole:
- the thiadiazole derivative is a derivative of dimercaptothiadiazole.
- a lubricating composition according to the invention comprises at least one anti-wear additive chosen from derivatives of dimercaptothiazole.
- dimercaptothiadiazole derivative means chemical compounds derived from the following four dimercaptothiadiazole molecules, below: 4,5-dimercapto 1,2,3-thiadiazole, 3,5-dimercapto-1,2,4 -thiadiazole, 3,4-dimercapto-l, 2,5-thiadiazole, 2,5-dimercapto-l, 3,4-thiadiazole, taken alone or as a mixture:
- R 1 is chosen from a hydrogen atom, a linear or branched, saturated or unsaturated alkyl group comprising from 1 to 24 carbon atoms, preferably from 2 to 18, more preferably from 4 to 16, even more preferably from 8 to 12 or an aromatic substituent.
- 2,5-dimercapto-1,3,4-thiadiazole is molecules of the following formulas taken alone or as a mixture:
- group or groups R 1 represent, independently of one another, hydrogen atoms, linear or branched alkyl or alkenyl groups, comprising from 1 to 24 carbon atoms, preferably from 2 to 18, more preferably from 4 to 16, again more preferably from 8 to 12 or aromatic substituents, n being, independently of one another, integers equal to 1, 2, 3 or 4, preferably n being equal to 1.
- R 1 represent, independently of one another, linear alkyl groups, C 1 to C 24 , preferably C 2 to C 18 , in particular C 4 to C 16, more particularly C 8 to C 12 and preferably C 12 .
- dimercaptothiadiazole derivatives used in the present invention may be commercially available, for example from the suppliers Vanderbilt, Rhein Chemie or Afton.
- the amine and / or sulfur antiwear additive or additives used in a lubricating composition according to the invention can still be chosen from among sulfurized antiwear additives of the poly sulfide type, in particular sulfur olefins.
- the sulfur-containing olefins used in a lubricating composition according to the invention can in particular be dialkyl sulfides represented by the general formula R a -S x -R b , where R a and R b are alkyl groups comprising from 3 to 15 carbon atoms. , preferably from 1 to 5 carbon atoms, preferentially 3 carbon atoms, and x is an integer between 2 and 6.
- the poly sulfide additive is chosen from dialkyl trisulfides.
- the anti-wear additive present in a composition used according to the invention is chosen from amino and sulfur anti-wear additives, and advantageously from thia (di) azole compounds as described above and more preferably among the derivatives of dimercaptothiadiazole.
- a lubricating composition considered according to the invention can comprise from 0.01% to 5% by mass, in particular from 0.1% to 3% by mass and more particularly from 0.5% to 2% by mass of additive (s ) anti-wear amines and / or sulfur, preferably of thia (di) azole type and more preferably chosen from derivatives of dimercaptothiadiazole, relative to the total mass of the lubricating composition.
- additive s
- anti-wear amines and / or sulfur preferably of thia (di) azole type and more preferably chosen from derivatives of dimercaptothiadiazole
- anti-wear additives known in particular for lubricants for propulsion systems, distinct from amine and / or sulfur additives, can be envisaged, provided that they do not affect the properties conferred by the combination. of said compound of triazole type and of said amino and / or sulfur antiwear additive (s) according to the invention.
- a lubricant composition required according to the invention is free of antiwear additive other than said amine and / or sulfur antiwear additive (s) used according to the invention.
- a lubricating composition considered according to the invention combines:
- additives of triazole type chosen from benzotriazole derivatives, preferably tolyltriazole derivatives, and in particular those of formula (Ha) indicated above;
- amino and sulfur antiwear additives preferably chosen from derivatives of dimercaptothiazole, in particular as defined above.
- a lubricating composition considered according to the invention combines, as an amine and / or sulfur antiwear additive, a derivative of 2,5-dimercapto-l, 3,4-thiadiazole and, as a compound of triazole type, a tolyltriazole derivative, in particular 2-ethyl-N- (2-ethylhexyl) -N - [(4-methylbenzotriazol-1-yl) methyl] hexan-1-amine.
- a composition used according to the invention may comprise, in addition to one or more additives of triazole type and one or more anti-wear additives amine (s) and / or sulfur (s), in particular as defined above, one or more base oils, as well as other additives, conventionally considered in lubricating compositions.
- a lubricating composition considered according to the invention can thus comprise one or more base oils.
- base oils can be chosen from the base oils conventionally used in the field of lubricating oils, such as mineral, synthetic or natural, animal or vegetable oils or their mixtures.
- base oils can be a mixture of several base oils, for example a mixture of two, three, or four base oils.
- the name “fluid base” will denote the oil or the mixture of base oils of the lubricating composition considered according to the invention.
- the base oils of the lubricating compositions considered according to the invention can in particular be oils of mineral or synthetic origins belonging to groups I to V according to the classes defined in the API classification (or their equivalents according to the ATIEL classification) and presented in Table 1 below or their mixtures.
- Mineral base oils include all types of base oils obtained by atmospheric and vacuum distillation of crude oil, followed by refining operations such as solvent extraction, dealphating, solvent dewaxing, hydrotreatment, hydrocracking, hydroisomerization and hydrofinishing. .
- Mixtures of synthetic and mineral oils, which can be biobased, can also be used.
- the base oils of the compositions used according to the invention can also be chosen from synthetic oils, such as certain esters of carboxylic acids and alcohols, polyalphaolefins (PAO), and polyalkylene glycols (PAG) obtained by polymerization or copolymerization of alkylene oxides comprising from 2 to 8 carbon atoms, in particular from 2 to 4 carbon atoms.
- synthetic oils such as certain esters of carboxylic acids and alcohols, polyalphaolefins (PAO), and polyalkylene glycols (PAG) obtained by polymerization or copolymerization of alkylene oxides comprising from 2 to 8 carbon atoms, in particular from 2 to 4 carbon atoms.
- the PAOs used as base oils are for example obtained from monomers comprising from 4 to 32 carbon atoms, for example from octene or decene.
- the weight average molecular weight of PAO can vary quite widely. Preferably, the weight average molecular mass of the PAO is less than 600 Da.
- the weight-average molecular mass of PAO can also range from 100 to 600 Da, from 150 to 600 Da, or even from 200 to 600 Da.
- oil or the base oils of the composition used according to the invention are chosen from polyalphaolefins (PAO), polyalkylene glycol (PAG) and esters of carboxylic acids and alcohols.
- PAO polyalphaolefins
- PAG polyalkylene glycol
- esters of carboxylic acids and alcohols are chosen from polyalphaolefins (PAO), polyalkylene glycol (PAG) and esters of carboxylic acids and alcohols.
- the base oil (s) of the composition used according to the invention is (are) chosen from oils of group III, IV or V, and their mixtures, preferably is an oil of group III base.
- the oil or the base oils of the composition used according to the invention can be chosen from the base oils of group II.
- a lubricating composition considered according to the invention may comprise at least 50% by mass of base oil (s) relative to its total mass, in particular from 60% to 99% by mass of base oil (s).
- a lubricating composition suitable for the invention may also further comprise all types of additives, distinct from additives of the triazole type and anti-wear additives amine (s) and / or sulfur (s) defined in the context of the present invention. , suitable for use in a lubricant for a propulsion system of an electric or hybrid vehicle.
- additives used are chosen so as not to affect the properties in terms of anti-wear and anti-corrosion performance conferred by the combination of said compound (s) of triazole type and of said additive (s). amine (s) and / or sulfur (s) used according to the invention.
- Such additives known to those skilled in the art in the field of lubricating and / or cooling the propulsion systems of electric or hybrid vehicles, can be chosen from friction modifiers, viscosity index modifiers, detergents, extreme pressure additives, dispersants, antioxidants, pour point depressants, defoamers and mixtures thereof.
- composition suitable for the invention comprises at least one additional additive chosen from antioxidants, detergents, dispersants, pour point depressant additives, anti-foam agents, and mixtures thereof.
- additives can be introduced individually and / or in the form of a mixture like those already available for sale for commercial lubricant formulations for vehicle engines, with a performance level as defined by ACEA ( Association of European Automobile Manufacturers) and / or API (American Petroleum Institute), well known to those skilled in the art.
- ACEA Association of European Automobile Manufacturers
- API American Petroleum Institute
- a lubricating composition suitable for the invention may comprise at least one friction modifier additive.
- the friction modifier additive can be chosen from a compound providing metallic elements and an ash-free compound.
- the compounds providing metallic elements mention may be made of transition metal complexes such as Mo, Sb, Sn, Fe, Cu, Zn, the ligands of which may be hydrocarbon compounds comprising oxygen, nitrogen or carbon atoms. sulfur or phosphorus.
- the ash-free friction modifying additives are generally of organic origin and can be chosen from fatty acid and polyol monoesters, alkoxylated amines, alkoxylated fatty amines, fatty epoxides, borate fatty epoxides; fatty amines or fatty acid glycerol esters.
- the fatty compounds comprise at least one hydrocarbon group comprising from 10 to 24 carbon atoms.
- a lubricating composition suitable for the invention may comprise from 0.01 to 2% by weight or from 0.01 to 5% by weight, preferably from 0.1 to 1.5% by weight or from 0.1 to 2%. by weight of friction modifier additive, relative to the total weight of the composition.
- a lubricating composition used according to the invention can comprise at least one antioxidant additive.
- the antioxidant additive generally makes it possible to delay the degradation of the composition in service. This degradation can be reflected in particular by the formation of deposits, by the presence of sludge or by an increase in the viscosity of the composition.
- Antioxidant additives act in particular as radical inhibitors or destroyers of hydroperoxides.
- antioxidant additives currently used, there may be mentioned antioxidant additives of phenolic type, antioxidant additives of amine type, phosphosulfurized antioxidant additives. Some of these antioxidant additives, for example phosphosulfurized antioxidant additives, can generate ash.
- the phenolic antioxidant additives can be ash-free or in the form of neutral or basic metal salts.
- the antioxidant additives can in particular be chosen from sterically hindered phenols, sterically hindered phenol esters and sterically hindered phenols comprising a thioether bridge, diphenylamines, diphenylamines substituted with at least one C 1 - C 12 alkyl group, N , N'-dialkyl-aryl-diamines and mixtures thereof.
- the sterically hindered phenols are chosen from compounds comprising a phenol group of which at least one carbon vicinal of the carbon carrying the alcohol function is substituted by at least one C 1 - C 10 alkyl group, preferably one.
- C 1 -C 6 alkyl group preferably a C 4 alkyl group, preferably by the tert-butyl group.
- Amino compounds are another class of antioxidant additives that can be used, optionally in combination with phenolic antioxidant additives.
- Examples of amino compounds are aromatic amines, for example aromatic amines of formula NR 4 R 5 R 6 in which R 4 represents an aliphatic group or an aromatic group, optionally substituted, R 5 represents an aromatic group, optionally substituted, R 6 represents a hydrogen atom, an alkyl group, an aryl group or a group of formula R 7 S (0) z R 8 in which R 7 represents an alkylene group or an alkenylene group, R 8 represents an alkyl group, a alkenyl group or an aryl group and z represents 0, 1 or 2.
- Sulfurized alkyl phenols or their alkali and alkaline earth metal salts can also be used as antioxidant additives.
- antioxidant additives are copper compounds, for example copper thio- or dithio-phosphates, salts of copper and carboxylic acids, copper dithiocarbamates, sulphonates, phenates, acetylacetonates. Copper I and II salts, salts of succinic acid or anhydride can also be used.
- a lubricating composition used according to the invention can contain all types of antioxidant additives known to those skilled in the art.
- a lubricating composition used according to the invention comprises at least one antioxidant additive free of ash.
- a lubricating composition used according to the invention can comprise from 0.5 to 2% by weight of at least one antioxidant additive, relative to the total weight of the composition.
- a lubricating composition used according to the invention is free from an antioxidant additive of aromatic amine type or of sterically hindered phenol type.
- a lubricating composition suitable for the invention can also include at least one detergent additive.
- Detergent additives generally reduce the formation of deposits on the surface of metal parts by dissolving by-products of oxidation and combustion.
- the detergent additives which can be used in a lubricating composition used according to the invention are generally known to those skilled in the art.
- the detergent additives can be anionic compounds comprising a long lipophilic hydrocarbon chain and a hydrophilic head.
- the associated cation can be a metallic cation of an alkali or alkaline earth metal.
- the detergent additives are preferably chosen from alkali metal or alkaline earth metal salts of carboxylic acids, sulphonates, salicylates, naphthenates, as well as salts of phenates.
- the alkali metals and alkaline earth metals are preferably calcium, magnesium, sodium or barium.
- metal salts generally include the metal in a stoichiometric amount or else in excess, therefore in an amount greater than the stoichiometric amount.
- overbased detergent additives the excess metal providing the overbased character to the detergent additive is then generally in the form of a metal salt insoluble in oil, for example a carbonate, a hydroxide, an oxalate, an acetate, a glutamate, preferably a carbonate .
- a lubricating composition suitable for the invention may, for example, comprise from 2 to 4% by weight of detergent additive, relative to the total weight of the composition.
- a lubricating composition used according to the invention can comprise at least one dispersing agent.
- the dispersing agent can be chosen from Mannich bases, succinimides and their derivatives.
- a lubricating composition used according to the invention may for example comprise from 0.2 to 10% by weight of dispersing agent, relative to the total weight of the composition.
- a lubricating composition used according to the invention is free from dispersing agent of succinimide type.
- a lubricating composition suitable for the invention may further comprise at least one antifoam agent.
- the antifoam agent can be chosen from silicones.
- a lubricating composition suitable for the invention may comprise from 0.01 to 2% by mass or from 0.01 to 5% by mass, preferably from 0.1 to 1.5% by mass or from 0.1 to 2% by mass of antifoaming agent, relative to the total weight of the composition.
- a lubricating composition suitable for the invention may also include at least one pour point depressant additive (also called “PPD” agents for "For Point Depressant” in English).
- PPD pour point depressant additive
- pour point depressant additives By slowing the formation of paraffin crystals, pour point depressant additives generally improve the cold behavior of the composition.
- pour point lowering additives there may be mentioned polymethacrylates, polyacrylates, polyarylamides, polyalkylphenols, polyalkylnaphthalenes, alkylated polystyrenes.
- a lubricating composition used according to the invention may be free from dispersing agent of succinimide type and of antioxidant additive of aromatic amine type or of sterically hindered phenol type.
- said compound (s) of triazole type can be added to an oil or mixture of base oils, then the other additional additives, including the anti-wear additive (s). amino (s) and / or sulfur (s), added.
- said compound (s) of triazole type can be added to a pre-existing conventional lubricating formulation, comprising in particular one or more base oils, one or more anti-wear additives amine (s) and / or sulfur (s), and optionally additional additives.
- a lubricating composition used according to the invention has a kinematic viscosity, measured at 100 ° C. according to the ASTM D445 standard, ranging from 1 to 15 mm 2 / s.
- a lubricating composition used according to the invention has a kinematic viscosity, measured at 40 ° C. according to the ASTM D445 standard, ranging from 3 to 80 mm 2 / s.
- the values of electrical resistivity measured at 90 ° C. of the lubricating compositions used according to the invention are between 5 and 10,000 Mohm.m, more preferably between 6 and 5,000 Mohm. mr.
- the dielectric loss values measured at 90 ° C. of the lubricating compositions used according to the invention are between 0.01 and 30, more preferably between 0.02 and 25, more preferably between 0.02 and 10.
- a lubricating composition used according to the invention can be of a grade according to the SAEJ300 classification defined by formula (X) W (Y), in which X represents 0 or 5; and Y represents an integer ranging from 4 to 20, in particular ranging from 4 to 16 or from 4 to 12.
- a lubricating composition used according to the invention comprises, or even consists of:
- base oil or mixture of base oils preferably chosen from polyalphaolefins (PAO), polyalkylene glycol (PAG) and esters of carboxylic acids and alcohols;
- one or more anti-corrosion additives of the triazole type preferably chosen from benzotriazole derivatives, in particular tolyltriazole derivatives, and more preferably those of formula (Ha) indicated above;
- amino and / or sulfur antiwear additives preferably one or more amino and sulfur antiwear additives, and more preferably chosen from compounds of thia (di) azoles type, in particular dimercaptothiazole derivatives such as defined above;
- antioxidants optionally one or more additional additives chosen from antioxidants, detergents, dispersants, pour point depressant additives, defoamers, and mixtures thereof.
- a lubricating composition used according to the invention comprises, or even consists of:
- anti-corrosion additives of the triazole type of preferably chosen from benzotriazole derivatives, in particular tolyltriazole derivatives, and more preferably those of formula (Ha) indicated above;
- anti-wear additives amine and / or sulfur preferably one or more amino and sulfur anti-wear additives, and more preferably chosen from compounds of thia (di) azoles type, in particular dimercaptothiazole derivatives as defined above;
- base oil preferably chosen from polyalphaolefins (PAO), polyalkylene glycols (PAG), esters of carboxylic acids and alcohols and their mixtures;
- additives chosen from antioxidants, detergents, dispersants, pour point lowering additives, anti-foam agents, and mixtures thereof;
- a lubricating composition suitable for the invention is used as a lubricant for a propulsion system of an electric or hybrid vehicle, and more particularly of the engine and of the power electronics.
- the present invention relates to the use of a lubricating composition as defined above, combining one or more anti-corrosion additives of triazole type, in particular as defined above, preferably derived from tolyltriazole, and one or more anti-wear additives.
- the propulsion system of an electric or hybrid vehicle comprises in particular the electric motor part (1), an electric battery (2) and a transmission, and in particular a speed reducer (3).
- the electric motor typically comprises power electronics (11) connected to a stator (13) and a rotor (14).
- the stator comprises coils, in particular copper coils, which are supplied alternately by an electric current. This makes it possible to generate a rotating magnetic field.
- the rotor itself consists of coils, permanent magnets or other magnetic materials, and is rotated by the rotating magnetic field.
- a bearing (12) is generally integrated between the stator (13) and the rotor (14).
- a transmission, and in particular a speed reducer (3), makes it possible to reduce the speed of rotation at the output of the electric motor and to adapt the speed transmitted to the wheels, allowing at the same time to control the speed of the vehicle.
- the bearing (12) is particularly subjected to high mechanical stresses and poses fatigue wear problems. It is therefore necessary to lubricate the bearing in order to increase its life. Also, the reducer is subjected to high friction stresses and therefore needs to be lubricated appropriately in order to prevent it from being damaged too quickly.
- the invention relates in particular to the use of a composition as described above for lubricating an electric motor of an electric or hybrid vehicle, in particular for lubricating the bearings located between the rotor and the stator of an electric motor. .
- compositions as described above to lubricate the transmission, in particular the reduction gear, in an electric or hybrid vehicle.
- a composition according to the invention can thus be used to lubricate the various parts of a propulsion system of an electric or hybrid vehicle, in particular of the bearings located between the rotor and the stator of an electric motor and / or the transmission, in particular the reduction gear, in an electric or hybrid vehicle.
- a lubricating composition according to the invention exhibits excellent anti-wear and anti-corrosion performance.
- the invention also relates, according to another of its aspects, to a method of lubricating at least one part of a propulsion system of an electric or hybrid vehicle, in particular of the bearings located between the rotor and the stator of. an electric motor; and / or of the transmission, in particular of the reducer, comprising at least one step of bringing at least said part into contact with a composition as described above.
- the present invention thus proposes a method for simultaneously reducing the wear and corrosion of at least one part of a propulsion system of an electric or hybrid vehicle, in particular of the bearings located between the rotor and the stator of an electric vehicle. electric motor; and / or of the transmission, in particular of the reducer, said method comprising at least one step of bringing at least said part into contact with a composition as described above.
- a composition according to the invention may exhibit, in addition to lubricating properties, good electrical insulation properties.
- a composition according to the invention can simultaneously be used to lubricate one or more parts of a propulsion system of an electric or hybrid vehicle, in particular for lubricating the sensors and solenoid valves of the engine, bearings, but also the winding located at the rotor and stator of an electric motor, or the lubrication at the transmission level, in particular the gears, sensors, solenoid valves, or the reducer that we find in an electric or hybrid vehicle, and to electrically isolate at least one part of said propulsion system, in particular from the battery.
- a lubricating composition considered according to the invention advantageously exhibits a kinematic viscosity, measured at 100 ° C according to the ASTM D445 standard, of between 2 and 8 mm 2 / s, preferably between 3 and 7 mm 2 / s. It is understood that the uses described above can be combined, a composition as described above can be used both as a lubricant, as an electrical insulator but also as a cooling fluid for the engine, the battery and the transmission of an electric or hybrid vehicle. According to the invention, the particular, advantageous or preferred characteristics of the composition according to the invention make it possible to define uses according to the invention which are also particular, advantageous or preferred.
- composition C2 comprising said anti-wear additive of dimercaptothiadiazole type, and an anti-corrosion additive of triazole type, in accordance with the invention, of above-mentioned formula (Ha): 2-ethyl-N- (2-ethylhexyl) - N - [(4-methylbenzotriazol-1-yl) methyl] hexan-1-amine;
- a C3 composition comprising said anti-wear additive of dimercaptothiadiazole type, and an anti-corrosion additive not in accordance with the invention, of alkylated organic acid ester type;
- composition C4 comprising said anti-wear additive of dimercaptothiadiazole type, and an anti-corrosion additive not in accordance with the invention, of N-acyl sarcosine type (N-oleyl sarcosine); and
- composition C 5 comprising said anti-wear additive of dimercaptothiadiazole type, and an anti-corrosion additive not in accordance with the invention, of imidazoline derivative type.
- Compositions C 1 to C 5 comprise, in addition to the aforementioned compounds, a group III base oil.
- compositions and the amounts are indicated in Table 2 below.
- the corrosive (or corroding) power of a composition can be evaluated according to a test implementing the study of the variation in the value of the electrical resistance of a copper wire having a predetermined diameter, as a function of the duration d immersion of this thread within the composition.
- the variation in the value of this electrical resistance is correlated directly with the variation in the diameter of the wire tested.
- the diameter of the wire chosen is 70mm.
- a copper wire is immersed in a test tube containing a volume of 20 mL of a composition to be tested (composition C2 being a composition according to the invention and compositions C 1 and C3 to C5 being compositions serving as comparisons).
- composition C2 being a composition according to the invention
- compositions C 1 and C3 to C5 being compositions serving as comparisons.
- the resistance of the wire is measured using an ohmmeter.
- the measurement current is 1mA.
- the temperature of the composition to be tested is brought to 150 ° C.
- the resistance of the copper wire is calculated by this equation (1):
- R is the resistance
- p is the resistivity of copper
- L is the length of the wire
- S is the section area
- the wire diameter is calculated from the section area (equation (2)):
- D is the diameter of the wire.
- the diameter of the wire decreases, therefore causing an increase in the value of the resistance.
- the wire diameter loss is therefore calculated directly from the measured resistance. When the measured resistance is infinite, it is an open circuit. So the wire broke, which defines very severe corrosion.
- a composition is “non-corrosive” when the loss of diameter of the copper wire studied is less than or equal to 0.5 mm after immersion for 80 hours, in particular less than or equal to 0.1 mm after immersion. for 20 hours in the composition.
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
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1907140A FR3097871B1 (en) | 2019-06-28 | 2019-06-28 | Use of a compound of the triazole type as an additive to improve the anti-corrosion properties of a lubricating composition |
PCT/EP2020/067819 WO2020260457A1 (en) | 2019-06-28 | 2020-06-25 | 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 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP3990592A1 true EP3990592A1 (en) | 2022-05-04 |
Family
ID=68138473
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP20736271.6A Pending EP3990592A1 (en) | 2019-06-28 | 2020-06-25 | 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 |
Country Status (8)
Country | Link |
---|---|
US (1) | US12043814B2 (en) |
EP (1) | EP3990592A1 (en) |
JP (1) | JP2022538639A (en) |
KR (1) | KR20220032564A (en) |
CN (1) | CN114555762B (en) |
FR (1) | FR3097871B1 (en) |
MX (1) | MX2021015547A (en) |
WO (1) | WO2020260457A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3109942B1 (en) * | 2020-05-05 | 2022-08-19 | Total Marketing Services | LUBRICANT COMPOSITION FOR ELECTRIC VEHICLES |
WO2024112665A1 (en) | 2022-11-23 | 2024-05-30 | The Lubrizol Corporation | Powertrain lubricant containing polyether |
WO2024206581A1 (en) * | 2023-03-29 | 2024-10-03 | The Lubrizol Corporation | Lubricant additive composition for electric vehicle |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2366074A (en) | 1942-05-26 | 1944-12-26 | Standard Oil Dev Co | Corrosion resistant composition |
US4661273A (en) | 1985-12-30 | 1987-04-28 | Mobil Oil Company | Mercapto-thiadiazole reaction products as multifunctional lubricant additives and compositions thereof |
RO111107B1 (en) | 1992-10-22 | 1996-06-28 | Inst De Cercetari Pentru Rafin | Dispersant admixtures for engines oils and preparation process thereof |
US6001780A (en) | 1998-06-30 | 1999-12-14 | Chevron Chemical Company Llc | Ashless lubricating oil formulation for natural gas engines |
US6074992A (en) | 1999-02-02 | 2000-06-13 | Union Carbide Chemicals & Plastics Technology Corporation | Functional fluid compositions |
JP2002003877A (en) * | 2000-06-23 | 2002-01-09 | Nippon Mitsubishi Oil Corp | Lubricating oil composition |
JP4805536B2 (en) | 2001-05-28 | 2011-11-02 | 日産自動車株式会社 | Transmission oil composition for automobiles |
US20030224948A1 (en) | 2002-02-14 | 2003-12-04 | Dam Willem Van | Lubricating oil additive comprising EC-treated succinimide, borated dispersant and corrosion inhibitor |
US20040259743A1 (en) | 2003-06-18 | 2004-12-23 | The Lubrizol Corporation, A Corporation Of The State Of Ohio | Lubricating oil composition with antiwear performance |
US7763574B2 (en) | 2003-10-10 | 2010-07-27 | R.T. Vanderbilt Company, Inc. | Lubricating compositions containing synthetic ester base oil, molybdenum compounds and thiadiazole-based compounds |
US7704931B2 (en) | 2004-12-10 | 2010-04-27 | Chemtura Corporation | Lubricant compositions stabilized with multiple antioxidants |
FR2879621B1 (en) | 2004-12-16 | 2007-04-06 | Total France Sa | OIL FOR 4-STROKE MARINE ENGINE |
US7673497B2 (en) | 2005-10-18 | 2010-03-09 | Idq Operating, Inc. | System, methods, and compositions for detecting and inhibiting leaks in transmission systems |
WO2007052833A1 (en) | 2005-11-02 | 2007-05-10 | Nippon Oil Corporation | Lubricating oil composition |
US20080194442A1 (en) * | 2007-02-13 | 2008-08-14 | Watts Raymond F | Methods for lubricating a transmission |
JP2010521559A (en) * | 2007-03-13 | 2010-06-24 | ザ ルブリゾル コーポレイション | Multifunctional driveline fluid |
US7871966B2 (en) | 2007-03-19 | 2011-01-18 | Nippon Oil Corporation | Lubricating oil composition |
US9206379B2 (en) * | 2010-03-17 | 2015-12-08 | Shell Oil Company | Lubricating composition |
JP5779376B2 (en) | 2011-03-29 | 2015-09-16 | Jx日鉱日石エネルギー株式会社 | Lubricating oil composition |
US9068134B2 (en) | 2011-12-02 | 2015-06-30 | Exxonmobil Research And Engineering Company | Method for improving engine wear and corrosion resistance |
US8400030B1 (en) | 2012-06-11 | 2013-03-19 | Afton Chemical Corporation | Hybrid electric transmission fluid |
EP2746024B1 (en) | 2012-12-21 | 2015-05-27 | Reifenhäuser GmbH & Co. KG Maschinenfabrik | Roller frame |
JP6404934B2 (en) | 2013-09-19 | 2018-10-17 | ザ ルブリゾル コーポレイションThe Lubrizol Corporation | Lubricant composition for direct injection engines |
JP7208790B2 (en) * | 2015-08-20 | 2023-01-19 | ザ ルブリゾル コーポレイション | Azole Derivatives as Lubricant Additives |
CN108473899A (en) | 2015-11-11 | 2018-08-31 | 路博润公司 | The lubricating composition of Sulfide-containing Hindered 5-substituted phenol compounds |
JP6661435B2 (en) | 2016-03-23 | 2020-03-11 | 出光興産株式会社 | Lubricating oil composition and lubricating method |
FR3058156B1 (en) | 2016-10-27 | 2022-09-16 | Total Marketing Services | COMPOSITION FOR ELECTRIC VEHICLE |
EP3562922B1 (en) | 2016-12-27 | 2021-02-03 | The Lubrizol Corporation | Lubricating composition with alkylated naphthylamine |
JP7204738B2 (en) | 2017-08-16 | 2023-01-16 | ザ ルブリゾル コーポレイション | Lubricating composition for hybrid electric vehicle transmission |
CN108085095B (en) * | 2017-12-20 | 2021-03-02 | 山东北方淄特特种油股份有限公司 | Pure electric vehicle motor bearing long-life antifriction energy-saving lubricating grease and preparation method thereof |
FR3083801B1 (en) | 2018-07-13 | 2021-02-12 | Total Marketing Services | COOLING AND FIRE-RESISTANT COMPOSITION FOR THE PROPULSION SYSTEM OF AN ELECTRIC OR HYBRID VEHICLE |
FR3083800B1 (en) | 2018-07-13 | 2020-12-25 | Total Marketing Services | COOLING AND FIRE-RESISTANT COMPOSITION FOR THE PROPULSION SYSTEM OF AN ELECTRIC OR HYBRID VEHICLE |
FR3083802B1 (en) | 2018-07-13 | 2021-02-12 | Total Marketing Services | COOLING AND FIRE-RESISTANT COMPOSITION FOR THE PROPULSION SYSTEM OF AN ELECTRIC OR HYBRID VEHICLE |
FR3093729A1 (en) | 2019-03-13 | 2020-09-18 | Total Marketing Services | Use of an ester in a cooling composition |
FR3097872B1 (en) | 2019-06-28 | 2022-01-14 | Total Marketing Services | Use of a phosphorus compound as a non-corrosive anti-wear and extreme-pressure additive in a lubricant for the propulsion system of an electric or hybrid vehicle. |
FR3097873B1 (en) | 2019-06-28 | 2022-01-14 | Total Marketing Services | Use of a compound of the succinimide type as an anti-corrosion additive in a lubricating composition intended for a propulsion system of an electric or hybrid vehicle. |
FR3097870B1 (en) | 2019-06-28 | 2022-01-14 | Total Marketing Services | Use of a compound of aromatic amine or sterically hindered phenol type as an anti-corrosion additive in a lubricating composition |
-
2019
- 2019-06-28 FR FR1907140A patent/FR3097871B1/en active Active
-
2020
- 2020-06-25 WO PCT/EP2020/067819 patent/WO2020260457A1/en active Application Filing
- 2020-06-25 JP JP2021577604A patent/JP2022538639A/en active Pending
- 2020-06-25 MX MX2021015547A patent/MX2021015547A/en unknown
- 2020-06-25 KR KR1020227001737A patent/KR20220032564A/en unknown
- 2020-06-25 CN CN202080049716.4A patent/CN114555762B/en active Active
- 2020-06-25 EP EP20736271.6A patent/EP3990592A1/en active Pending
- 2020-06-25 US US17/619,857 patent/US12043814B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
US20220364011A1 (en) | 2022-11-17 |
WO2020260457A1 (en) | 2020-12-30 |
US12043814B2 (en) | 2024-07-23 |
CN114555762B (en) | 2023-06-20 |
KR20220032564A (en) | 2022-03-15 |
MX2021015547A (en) | 2022-02-16 |
FR3097871B1 (en) | 2022-01-14 |
FR3097871A1 (en) | 2021-01-01 |
JP2022538639A (en) | 2022-09-05 |
CN114555762A (en) | 2022-05-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3818135B1 (en) | Use and method for cooling and lubricating a propulsion system of y hybrdid or electrical vehicle | |
WO2020260458A1 (en) | Use of a succinimide compound as an anti-corrosion additive in a lubricant composition for a propulsion system of an electric or hybrid vehicle | |
EP3697876B1 (en) | Use of a composition for cooling and lubricating a drive system of a vehicle | |
EP3938459A1 (en) | Use of an ester in a cooling composition | |
EP3990588B1 (en) | Use of a sterically hindered aromatic amine or phenol compound as an anti-corrosion additive in a lubricant composition for a propulsion system of an electric or hybrid vehicle | |
EP3990592A1 (en) | 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 | |
WO2020260462A1 (en) | 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 | |
FR3109942A1 (en) | LUBRICANT COMPOSITION FOR ELECTRIC VEHICLES | |
FR3139828A1 (en) | Use of a monoester in a lubricating composition for vehicle transmissions | |
FR3137919A1 (en) | Use of a diester in a cooling composition | |
WO2024165518A1 (en) | Use of a diester in a lubricant composition for vehicle transmissions | |
WO2024165517A1 (en) | Use of a diester in a cooling and/or lubricating composition for an electronic device | |
WO2024223793A1 (en) | Composition for cooling and/or lubricating at least one element of a moving or stationary system | |
WO2022084320A1 (en) | Use of dialkylene glycol ester to reduce friction in vehicles with hybrid engines | |
FR3148238A1 (en) | Cooling and/or lubricating composition for at least one element of a mobile or stationary system |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: UNKNOWN |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
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 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20211220 |
|
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 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: TOTALENERGIES ONETECH |
|
DAV | Request for validation of the european patent (deleted) | ||
DAX | Request for extension of the european patent (deleted) | ||
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20230102 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
INTG | Intention to grant announced |
Effective date: 20240404 |
|
GRAJ | Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20240528 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
INTC | Intention to grant announced (deleted) | ||
INTG | Intention to grant announced |
Effective date: 20240724 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |