JP6067027B2 - トランスミッション用潤滑剤組成物 - Google Patents
トランスミッション用潤滑剤組成物 Download PDFInfo
- Publication number
- JP6067027B2 JP6067027B2 JP2014546551A JP2014546551A JP6067027B2 JP 6067027 B2 JP6067027 B2 JP 6067027B2 JP 2014546551 A JP2014546551 A JP 2014546551A JP 2014546551 A JP2014546551 A JP 2014546551A JP 6067027 B2 JP6067027 B2 JP 6067027B2
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- JP
- Japan
- Prior art keywords
- lubricant composition
- composition according
- amine
- formula
- alkyl group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- 239000000203 mixture Substances 0.000 title claims description 113
- 239000000314 lubricant Substances 0.000 title claims description 111
- 230000005540 biological transmission Effects 0.000 title claims description 15
- 239000004711 α-olefin Substances 0.000 claims description 36
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 31
- 239000005977 Ethylene Substances 0.000 claims description 31
- 125000004432 carbon atom Chemical group C* 0.000 claims description 30
- 229920001577 copolymer Polymers 0.000 claims description 29
- -1 amine thiophosphate Chemical class 0.000 claims description 28
- 229910052717 sulfur Inorganic materials 0.000 claims description 28
- 239000002199 base oil Substances 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 229920000193 polymethacrylate Polymers 0.000 claims description 18
- 125000004434 sulfur atom Chemical group 0.000 claims description 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 230000001050 lubricating effect Effects 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 8
- 229920002367 Polyisobutene Polymers 0.000 claims description 7
- GLOYGJPNNKTDIG-UHFFFAOYSA-N SC=1N=NSC=1S Chemical class SC=1N=NSC=1S GLOYGJPNNKTDIG-UHFFFAOYSA-N 0.000 claims description 7
- 239000003963 antioxidant agent Substances 0.000 claims description 7
- 239000000446 fuel Substances 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 5
- 239000002270 dispersing agent Substances 0.000 claims description 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
- 150000003141 primary amines Chemical class 0.000 claims description 5
- 150000003335 secondary amines Chemical class 0.000 claims description 4
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- 230000003078 antioxidant effect Effects 0.000 claims description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical class S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 description 25
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 17
- 239000011593 sulfur Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 12
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 9
- 150000001336 alkenes Chemical class 0.000 description 8
- JRZJOMJEPLMPRA-UHFFFAOYSA-N 1-nonene Chemical compound CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 6
- 230000007246 mechanism Effects 0.000 description 6
- 229910052698 phosphorus Inorganic materials 0.000 description 6
- 239000011574 phosphorus Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 235000010755 mineral Nutrition 0.000 description 5
- 239000003607 modifier Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 229920013639 polyalphaolefin Polymers 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 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
- AJBLKZFBURBYPT-UHFFFAOYSA-N 1,2,5-thiadiazolidine-3,4-dithione Chemical class SC1=NSN=C1S AJBLKZFBURBYPT-UHFFFAOYSA-N 0.000 description 2
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- 229920005652 polyisobutylene succinic anhydride Polymers 0.000 description 2
- 229960002317 succinimide Drugs 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 150000003580 thiophosphoric acid esters Chemical class 0.000 description 2
- 150000005691 triesters Chemical class 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- UGUHFDPGDQDVGX-UHFFFAOYSA-N 1,2,3-thiadiazole Chemical compound C1=CSN=N1 UGUHFDPGDQDVGX-UHFFFAOYSA-N 0.000 description 1
- UDGKZGLPXCRRAM-UHFFFAOYSA-N 1,2,5-thiadiazole Chemical compound C=1C=NSN=1 UDGKZGLPXCRRAM-UHFFFAOYSA-N 0.000 description 1
- MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical compound C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 description 1
- SPSPIUSUWPLVKD-UHFFFAOYSA-N 2,3-dibutyl-6-methylphenol Chemical compound CCCCC1=CC=C(C)C(O)=C1CCCC SPSPIUSUWPLVKD-UHFFFAOYSA-N 0.000 description 1
- DRHABPMHZRIRAH-UHFFFAOYSA-N 2,4,4,6,6-pentamethylhept-2-ene Chemical group CC(C)=CC(C)(C)CC(C)(C)C DRHABPMHZRIRAH-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 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
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical class C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- LJBWYKSPKREPMZ-UHFFFAOYSA-N P(=S)(OSCCCCCCCCCCCC)(OCCCC)OCCCC Chemical class P(=S)(OSCCCCCCCCCCCC)(OCCCC)OCCCC LJBWYKSPKREPMZ-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005600 alkyl phosphonate group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- GXVWJQNUQYSLNR-UHFFFAOYSA-N butoxy(butylsulfanyl)phosphinous acid Chemical class P(SCCCC)(OCCCC)O GXVWJQNUQYSLNR-UHFFFAOYSA-N 0.000 description 1
- LMZSPXZNYGLPAV-UHFFFAOYSA-N butoxy-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical class CCCCOP(O)(O)=S LMZSPXZNYGLPAV-UHFFFAOYSA-N 0.000 description 1
- MNVKBJFKKJDBGR-UHFFFAOYSA-N butylsulfanylphosphonous acid Chemical class CCCCSP(O)O MNVKBJFKKJDBGR-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 150000001923 cyclic compounds Chemical group 0.000 description 1
- RNIDAJHSDZPOSN-UHFFFAOYSA-N dibutoxy(butylsulfanyl)phosphane Chemical class CCCCOP(OCCCC)SCCCC RNIDAJHSDZPOSN-UHFFFAOYSA-N 0.000 description 1
- BVXOPEOQUQWRHQ-UHFFFAOYSA-N dibutyl phosphite Chemical compound CCCCOP([O-])OCCCC BVXOPEOQUQWRHQ-UHFFFAOYSA-N 0.000 description 1
- BEAIULUXYSRQHO-UHFFFAOYSA-N didodecoxy-hydroxy-sulfanylidene-$l^{5}-phosphane Chemical class CCCCCCCCCCCCOP(O)(=S)OCCCCCCCCCCCC BEAIULUXYSRQHO-UHFFFAOYSA-N 0.000 description 1
- CAVXVJGHUYVTRI-UHFFFAOYSA-N dihydroxy-octoxy-sulfanylidene-$l^{5}-phosphane Chemical class CCCCCCCCOP(O)(O)=S CAVXVJGHUYVTRI-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- UMAHARXOTKOOHK-UHFFFAOYSA-N dioctoxy(octylsulfanyl)phosphane Chemical class CCCCCCCCOP(OCCCCCCCC)SCCCCCCCC UMAHARXOTKOOHK-UHFFFAOYSA-N 0.000 description 1
- ORDPXYVBSFJMAW-UHFFFAOYSA-N diphenoxy(phenylsulfanyl)phosphane Chemical class C=1C=CC=CC=1OP(SC=1C=CC=CC=1)OC1=CC=CC=C1 ORDPXYVBSFJMAW-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- VOBCOZODXKKZJQ-UHFFFAOYSA-N dodecoxy(dodecylsulfanyl)phosphinous acid Chemical class CCCCCCCCCCCCOP(O)SCCCCCCCCCCCC VOBCOZODXKKZJQ-UHFFFAOYSA-N 0.000 description 1
- FQERTQNSHXPBQS-UHFFFAOYSA-N dodecylsulfanylphosphonous acid Chemical class CCCCCCCCCCCCSP(O)O FQERTQNSHXPBQS-UHFFFAOYSA-N 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052976 metal sulfide Inorganic materials 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- OTYNBGDFCPCPOU-UHFFFAOYSA-N phosphane sulfane Chemical compound S.P[H] OTYNBGDFCPCPOU-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- TYQTYRXEMJXFJG-UHFFFAOYSA-N phosphorothious acid Chemical compound OP(O)S TYQTYRXEMJXFJG-UHFFFAOYSA-N 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- JJJPTTANZGDADF-UHFFFAOYSA-N thiadiazole-4-thiol Chemical class SC1=CSN=N1 JJJPTTANZGDADF-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- PPEZWDDRWXDXOQ-UHFFFAOYSA-N tributoxy(sulfanylidene)-$l^{5}-phosphane Chemical class CCCCOP(=S)(OCCCC)OCCCC PPEZWDDRWXDXOQ-UHFFFAOYSA-N 0.000 description 1
- YVFHKLYMBACKFA-UHFFFAOYSA-N trioctoxy(sulfanylidene)-$l^{5}-phosphane Chemical class CCCCCCCCOP(=S)(OCCCCCCCC)OCCCCCCCC YVFHKLYMBACKFA-UHFFFAOYSA-N 0.000 description 1
- IKXFIBBKEARMLL-UHFFFAOYSA-N triphenoxy(sulfanylidene)-$l^{5}-phosphane Chemical class C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 IKXFIBBKEARMLL-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M161/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/022—Ethene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/024—Propene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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- 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
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/046—Overbasedsulfonic acid salts
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- 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
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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- 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
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
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- C10M2223/049—Phosphite
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- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/044—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
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- C—CHEMISTRY; METALLURGY
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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Description
・摩擦調整剤を添加せずとも低い摩擦係数を示す;
・トランスミッションの効率を向上させる;
・オイル中のポリマーの使用量を低減できる;
・高い熱安定性を示す。
・グループ3の基油(ASTM D445規格に準拠して測定される100℃での粘度が3cStであり、ASTM D2270規格に準拠して測定される粘度指数が125である。);
・一般式(I)で表されるエチレンとαオレフィンとのコポリマー(式中:Rはメチル基であり;xは約40であり;yは約40であり;ASTM D5296規格に準拠して測定される重量平均分子量Mwが約8,880である。);
・一般式(II)および/または(III)で表される化合物の混合物であるジメルカプトチアジアゾール誘導体(式中:R1およびR2は、平均炭素数が12の飽和直鎖アルキル基であり;nは1である。);
・一般式(IVa)で表されるアミンチオホスフェート化合物(式中:X1およびX2は、いずれも硫黄原子であり;R1およびR2は、炭素数6のアルキル基であり;Mは、式:R3R4R5Nで表される、第一級アミンから構成されたアンモニウムであり、その式中、R3、R4およびR5は、水素原子と炭素数11のアルキル基であり;nは1である。);
・非分散型の直鎖状ポリメタクリレート(重量平均分子量Mw(ASTM D5296規格)が16,190であり;数平均分子量Mn(ASTM D5296規格)が9,990であり;多分散指数PI(PI=Mw/Mn)が1.6であり;ASTM D445規格に準拠して測定される100℃での動粘度が170cSt以上である。)(以降、この化合物を低分子量PMAと称する場合がある。);
・非分散型の直鎖状ポリメタクリレート(重量平均分子量Mw(ASTM D5296規格)が60,000である。)(以降、この化合物を平均分子量PMAと称する場合がある。);
・分散剤(ポリイソブチレンの誘導体、特に、ポリイソブチレンコハク酸イミドの誘導体である。);
・ジフェニルアミンタイプのアミン系酸化防止剤;
・エトキシ化フェノールタイプフェノール系防食剤;
・亜鉛ジチオホスフェート(C4アルキル鎖、C6アルキル鎖およびC8アルキル鎖を有する亜鉛アルキルジチオホスフェートである);
・スルホネート化合物(カルシウムアルキルベンゼンスルホネートまたはナトリウムアルキルベンゼンスルホネートである);
・アルキルホスファイト(ジブチルホスファイトである);
・含硫黄オレフィン(含硫黄2,4,4−トリメチルペンテンである);および
・希釈用のグループ1の基油。
Claims (12)
- 少なくとも1種の基油と、
下記の一般式(II)又は(III)で表される少なくとも1種のジメルカプトチアジアゾール誘導体と、
下記の一般式(I)で表される、エチレンとαオレフィンとの少なくとも1種のコポリマーと、
下記の一般式(IVa)で表される少なくとも1種のアミンチオホスフェートと、
を含む、潤滑剤組成物。
- 請求項1に記載の潤滑剤組成物において、前記エチレンとαオレフィンとのコポリマーの含有量が、当該潤滑剤組成物の総質量に対して、質量%で、1〜20%である、潤滑剤組成物。
- 請求項1または2に記載の潤滑剤組成物において、ジメルカプトチアジアゾール誘導体の含有量が、当該潤滑剤組成物の総質量に対して、質量%で、0.1〜10%である、潤滑剤組成物。
- 請求項1から3のいずれか一項に記載の潤滑剤組成物において、アミンチオホスフェートの含有量が、当該潤滑剤組成物の総質量に対して、質量%で、0.2〜10%である、潤滑剤組成物。
- 請求項1から4のいずれか一項に記載の潤滑剤組成物において、当該潤滑剤組成物が、さらに、ポリメタクリレートを含む、潤滑剤組成物。
- 請求項1から5のいずれか一項に記載の潤滑剤組成物において、当該潤滑剤組成物が、さらに、ポリイソブテンから誘導された分散剤を含む、潤滑剤組成物。
- 請求項1から6のいずれか一項に記載の潤滑剤組成物において、当該潤滑剤組成物が、さらに、アミン系酸化防止剤を含む、潤滑剤組成物。
- 請求項1から7のいずれか一項に記載の潤滑剤組成物において、当該潤滑剤組成物が、さらに、フェノール系防食剤を含む、潤滑剤組成物。
- 請求項1から8のいずれか一項に記載の潤滑剤組成物において、当該潤滑剤組成物は、ASTM D445規格に準拠して測定される100℃での動粘度が、4〜40cStである、潤滑剤組成物。
- 請求項1から9のいずれか一項に記載の潤滑剤組成物の使用であって、トランスミッションを潤滑するための使用。
- 請求項1から9のいずれか一項に記載の潤滑剤組成物の使用であって、車両の燃料消費を減少させるための使用。
- 潤滑剤組成物の摩擦係数を低下させるための、
下記の一般式(I)で表される、エチレンとαオレフィンとの少なくとも1種のコポリマーと、
下記の一般式(II)又は(III)で表される少なくとも1種のジメルカプトチアジアゾール誘導体と、
および
下記の一般式(IVa)で表される少なくとも1種のアミンチオホスフェートの使用。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1161856A FR2984348B1 (fr) | 2011-12-16 | 2011-12-16 | Compositions lubrifiantes pour transmissions |
FR1161856 | 2011-12-16 | ||
PCT/EP2012/075645 WO2013087889A1 (fr) | 2011-12-16 | 2012-12-14 | Compositions lubrifiantes pour transmissions |
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JP2015500385A JP2015500385A (ja) | 2015-01-05 |
JP2015500385A5 JP2015500385A5 (ja) | 2015-12-17 |
JP6067027B2 true JP6067027B2 (ja) | 2017-01-25 |
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US (1) | US9334462B2 (ja) |
EP (1) | EP2791294B1 (ja) |
JP (1) | JP6067027B2 (ja) |
KR (1) | KR101984065B1 (ja) |
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BR (1) | BR112014014490A2 (ja) |
CA (1) | CA2858927A1 (ja) |
FR (1) | FR2984348B1 (ja) |
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FR2961823B1 (fr) | 2010-06-25 | 2013-06-14 | Total Raffinage Marketing | Compositions lubrifiantes pour transmissions automobiles |
CN102344849B (zh) | 2010-07-29 | 2013-07-31 | 中国石油化工股份有限公司 | 一种汽轮机油添加剂组合物 |
FR2968669B1 (fr) | 2010-12-13 | 2014-02-28 | Total Raffinage Marketing | Composition de graisse |
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2011
- 2011-12-16 FR FR1161856A patent/FR2984348B1/fr active Active
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- 2012-12-14 JP JP2014546551A patent/JP6067027B2/ja not_active Expired - Fee Related
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- 2012-12-14 BR BR112014014490-7A patent/BR112014014490A2/pt not_active Application Discontinuation
- 2012-12-14 WO PCT/EP2012/075645 patent/WO2013087889A1/fr active Application Filing
- 2012-12-14 MX MX2014007278A patent/MX343664B/es active IP Right Grant
- 2012-12-14 RU RU2014124015A patent/RU2612803C2/ru not_active IP Right Cessation
- 2012-12-14 KR KR1020147016039A patent/KR101984065B1/ko active IP Right Grant
- 2012-12-14 CA CA2858927A patent/CA2858927A1/fr not_active Abandoned
- 2012-12-14 CN CN201280061291.4A patent/CN104066827B/zh not_active Expired - Fee Related
- 2012-12-14 EP EP12809233.5A patent/EP2791294B1/fr active Active
Also Published As
Publication number | Publication date |
---|---|
EP2791294A1 (fr) | 2014-10-22 |
FR2984348A1 (fr) | 2013-06-21 |
CN104066827A (zh) | 2014-09-24 |
RU2014124015A (ru) | 2016-02-10 |
EP2791294B1 (fr) | 2020-09-02 |
KR101984065B1 (ko) | 2019-05-30 |
MX2014007278A (es) | 2014-08-01 |
AR089276A1 (es) | 2014-08-13 |
WO2013087889A1 (fr) | 2013-06-20 |
JP2015500385A (ja) | 2015-01-05 |
US20150218481A1 (en) | 2015-08-06 |
RU2612803C2 (ru) | 2017-03-13 |
US9334462B2 (en) | 2016-05-10 |
CN104066827B (zh) | 2016-11-16 |
FR2984348B1 (fr) | 2015-02-27 |
MX343664B (es) | 2016-11-16 |
KR20140110861A (ko) | 2014-09-17 |
CA2858927A1 (fr) | 2013-06-20 |
BR112014014490A2 (pt) | 2019-10-01 |
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