EP2346970A1 - Compositions lubrifiantes pour transmissions - Google Patents
Compositions lubrifiantes pour transmissionsInfo
- Publication number
- EP2346970A1 EP2346970A1 EP09740194A EP09740194A EP2346970A1 EP 2346970 A1 EP2346970 A1 EP 2346970A1 EP 09740194 A EP09740194 A EP 09740194A EP 09740194 A EP09740194 A EP 09740194A EP 2346970 A1 EP2346970 A1 EP 2346970A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- fatty acid
- lubricating composition
- methyl ester
- carbon atoms
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 124
- 230000001050 lubricating effect Effects 0.000 title claims abstract description 67
- 230000005540 biological transmission Effects 0.000 title abstract description 17
- 239000000446 fuel Substances 0.000 claims abstract description 35
- 239000003921 oil Substances 0.000 claims description 85
- 235000019387 fatty acid methyl ester Nutrition 0.000 claims description 62
- 239000000314 lubricant Substances 0.000 claims description 47
- 238000012360 testing method Methods 0.000 claims description 39
- 125000004432 carbon atom Chemical group C* 0.000 claims description 36
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 36
- 229930195729 fatty acid Natural products 0.000 claims description 36
- 239000000194 fatty acid Substances 0.000 claims description 36
- -1 s Chemical class 0.000 claims description 35
- 150000004702 methyl esters Chemical class 0.000 claims description 33
- 229920000193 polymethacrylate Polymers 0.000 claims description 33
- 150000002148 esters Chemical class 0.000 claims description 28
- 229920013639 polyalphaolefin Polymers 0.000 claims description 25
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 23
- 150000004665 fatty acids Chemical class 0.000 claims description 23
- 229910052717 sulfur Inorganic materials 0.000 claims description 23
- 239000011593 sulfur Substances 0.000 claims description 23
- 125000004429 atom Chemical group 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 21
- 229910052698 phosphorus Inorganic materials 0.000 claims description 16
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 14
- 239000011574 phosphorus Substances 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 11
- 239000005069 Extreme pressure additive Substances 0.000 claims description 9
- 239000007866 anti-wear additive Substances 0.000 claims description 9
- BTHAQRDGBHUQMR-UHFFFAOYSA-N [S]P(=O)=O Chemical compound [S]P(=O)=O BTHAQRDGBHUQMR-UHFFFAOYSA-N 0.000 claims description 8
- 239000004165 Methyl ester of fatty acids Substances 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 206010021118 Hypotonia Diseases 0.000 claims 1
- 235000019198 oils Nutrition 0.000 description 84
- 239000002585 base Substances 0.000 description 54
- 239000000654 additive Substances 0.000 description 27
- 239000003981 vehicle Substances 0.000 description 27
- 239000002562 thickening agent Substances 0.000 description 13
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 10
- 201000008752 progressive muscular atrophy Diseases 0.000 description 10
- 150000001336 alkenes Chemical class 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 9
- 238000007254 oxidation reaction Methods 0.000 description 9
- 239000002199 base oil Substances 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- 230000008719 thickening Effects 0.000 description 8
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 7
- 230000005587 bubbling Effects 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000003344 environmental pollutant 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
- 231100000719 pollutant Toxicity 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 4
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 235000006708 antioxidants Nutrition 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000006184 cosolvent Substances 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000003878 thermal aging Methods 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- 229920002943 EPDM rubber Polymers 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 235000015278 beef Nutrition 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000005809 transesterification reaction Methods 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1 -dodecene Natural products CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 240000002791 Brassica napus Species 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical class CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 235000019483 Peanut oil Nutrition 0.000 description 2
- 235000019484 Rapeseed oil Nutrition 0.000 description 2
- 235000019486 Sunflower oil Nutrition 0.000 description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 239000000809 air pollutant Substances 0.000 description 2
- 231100001243 air pollutant Toxicity 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000002596 correlated effect Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 229940069096 dodecene Drugs 0.000 description 2
- 229920001038 ethylene copolymer Polymers 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 235000021281 monounsaturated fatty acids Nutrition 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- TYQTYRXEMJXFJG-UHFFFAOYSA-N phosphorothious acid Chemical compound OP(O)S TYQTYRXEMJXFJG-UHFFFAOYSA-N 0.000 description 2
- 229920002959 polymer blend Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000002600 sunflower oil Substances 0.000 description 2
- 229940095068 tetradecene Drugs 0.000 description 2
- 150000005691 triesters Chemical class 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- GXJLQJFVFMCVHG-QXMHVHEDSA-N 2-methylpropyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(C)C GXJLQJFVFMCVHG-QXMHVHEDSA-N 0.000 description 1
- 241001133760 Acoelorraphe Species 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 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
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- QCJQWJKKTGJDCM-UHFFFAOYSA-N [P].[S] Chemical class [P].[S] QCJQWJKKTGJDCM-UHFFFAOYSA-N 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000005600 alkyl phosphonate group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000003078 antioxidant effect Effects 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
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- NLAMRLZPVVKXTK-UHFFFAOYSA-N but-1-enyl acetate Chemical class CCC=COC(C)=O NLAMRLZPVVKXTK-UHFFFAOYSA-N 0.000 description 1
- LMZSPXZNYGLPAV-UHFFFAOYSA-N butoxy-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCOP(O)(O)=S LMZSPXZNYGLPAV-UHFFFAOYSA-N 0.000 description 1
- MNVKBJFKKJDBGR-UHFFFAOYSA-N butylsulfanylphosphonous acid Chemical compound CCCCSP(O)O MNVKBJFKKJDBGR-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 238000011033 desalting Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- CAVXVJGHUYVTRI-UHFFFAOYSA-N dihydroxy-octoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCCCCCOP(O)(O)=S CAVXVJGHUYVTRI-UHFFFAOYSA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- ORDPXYVBSFJMAW-UHFFFAOYSA-N diphenoxy(phenylsulfanyl)phosphane Chemical compound C=1C=CC=CC=1OP(SC=1C=CC=CC=1)OC1=CC=CC=C1 ORDPXYVBSFJMAW-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- ISWBBUXCFWZBKC-UHFFFAOYSA-N dodecoxy-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCCCCCCCCCOP(O)(O)=S ISWBBUXCFWZBKC-UHFFFAOYSA-N 0.000 description 1
- FQERTQNSHXPBQS-UHFFFAOYSA-N dodecylsulfanylphosphonous acid Chemical compound CCCCCCCCCCCCSP(O)O FQERTQNSHXPBQS-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical class C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 description 1
- 150000002460 imidazoles Chemical class 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 150000002751 molybdenum Chemical class 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- DSKNRIRUAYEWCO-UHFFFAOYSA-N octylsulfanylphosphonous acid Chemical compound CCCCCCCCSP(O)O DSKNRIRUAYEWCO-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- PZQSQRCNMZGWFT-QXMHVHEDSA-N propan-2-yl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC(C)C PZQSQRCNMZGWFT-QXMHVHEDSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 235000011044 succinic acid Nutrition 0.000 description 1
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 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 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 150000003580 thiophosphoric acid esters Chemical class 0.000 description 1
- PPEZWDDRWXDXOQ-UHFFFAOYSA-N tributoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound CCCCOP(=S)(OCCCC)OCCCC PPEZWDDRWXDXOQ-UHFFFAOYSA-N 0.000 description 1
- IKXFIBBKEARMLL-UHFFFAOYSA-N triphenoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 IKXFIBBKEARMLL-UHFFFAOYSA-N 0.000 description 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$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 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 150000003712 vitamin E derivatives Chemical class 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
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M169/041—Mixtures of base-materials and additives the additives being macromolecular compounds only
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M169/044—Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/0206—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
- C10M2205/0285—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2207/2815—Esters of (cyclo)aliphatic monocarboxylic acids used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
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- 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
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/02—Viscosity; Viscosity index
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/04—Molecular weight; Molecular weight distribution
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/065—Saturated Compounds
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/067—Unsaturated Compounds
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/02—Pour-point; Viscosity index
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/36—Seal compatibility, e.g. with rubber
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/54—Fuel economy
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/042—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/044—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
Definitions
- the present invention relates to lubricating compositions for transmissions, in particular for gearboxes, and to their use for limiting the fuel consumption of motor vehicles.
- the compositions according to the invention are suitable for all types of vehicles, especially light vehicles, and are particularly suitable for vehicles with hybrid engines.
- the lubricants used in these bodies must be able to reduce frictional and bubbling losses to the lowest possible level. It is known to those skilled in the art that lowering the viscosity of the lubricating oil is a means of improving the fuel economy achieved in the transmissions.
- the viscosity behavior of the oils strongly depends on the bases used in their formulation to at least 50% by weight in general.
- the formulation of transmission oils with a strong effect on fuel savings, or strong fuel-saving properties or so-called "fuel eco" properties will preferentially use lubricating bases having a viscosity index or VI very high.
- the viscosity index or VI of a base measured according to the ASTM D2270 standard, quantifies its ability to limit its variations in viscosities as a function of temperature, from the measurement of its kinematic viscosity at 40 ° C. (KV40) and 100 ° C. 0 C (KV100) measured according to ASTM D445.
- the VI of known conventional mineral bases is at most of the order of 200.
- Some synthetic oils make it possible to reach very high VI's, of the order of 400, but this high VI is accompanied by either a high viscosity, or solubility constraints additives, which do not provide the lubricant gear protection properties, friction control, ..., expected by the manufacturer. It is therefore difficult to formulate a transmission oil with fuel eco properties mainly from these bases. Their cost and availability are also problematic for the large-scale industrialization of lubricants incorporating them in a majority way.
- esters inherently have a very high VI, of the order of 250 or even 300 and above, combined with low viscosity.
- those skilled in the art are not encouraged to use these esters for automotive lubricants, in particular engine and transmissions, since the esters of this type which are liquid at ambient temperature have at least one double bond on their acid chain, which gives them a very low resistance to oxidation, resulting in a risk of degradation in service.
- esters used as bases, do not particularly satisfy the high temperature oxidation tests, catalysed or not, which are part of the specifications of the car manufacturers for these applications.
- transmissions oils of very high VI greater than 250 or even 280, preferably greater than 300, or even of the order of 320 and beyond, from natural origin bases of fatty acid methyl ester types, and having a service life comparable to that of existing commercial products.
- Gearbox oils in particular must be designed for "full-life" conditions, that is, they are never drained throughout the life of the vehicle.
- the present invention relates to lubricating compositions for gearboxes, of kinematic viscosity at 100 ° C., measured according to the ASTM D445 standard of between 5.5 and 7 mmVs, comprising
- kinematic viscosity at 100 ° C. measured according to the ASTM D445 standard of between 1.5 and 6 mnrVs, with a kinematic viscosity at 40 ° C., measured according to the ASTM D445 standard, included between 4 and 32 mnrVs, and a weight-average molecular weight of less than 500 daltons, in combination with one or more polymethacrylate-type compounds of molecular weight less than 30,000 daltons.
- the lubricating composition comprises at least 20% by weight of at least one fatty acid methyl ester of formula R1COOCH3, where R1 is a mono, di or tri unsaturated olefinic group containing from 11 to 23, preferably from 15 to 19 atoms, preferably 17 carbon atoms.
- the lubricating composition comprises at least 20% by weight of at least one fatty acid methyl ester of formula R 2 COOCH 3, where R 2 is a monounsaturated olefinic group containing from 11 to 23, preferably from 15 to 19 atoms, preferably 17 carbon atoms.
- the unsaturations of the olefinic groups R 1 and / or R 2 are in the cis configuration
- the weight percentage of polyalphaolefin (s) heavy is at least 10% and the mass percentage of fatty acid methyl ester (s) is at least 60%
- the lubricating composition comprises at least 50% by weight, preferably at least 55% by weight, of at least one ester.
- the lubricating composition comprises at least 45% by weight, preferably at least 50% by weight, of at least one fatty acid methyl ester of formula R 2 COOCH 3, where R 2 is a monounsaturated olefinic group containing from 11 to 23, preferably from 15 to 19 atoms, preferably 17 carbon atoms.
- the weight percentage of light polyalphaolefin (s) is at least 10% and the weight percentage of the mixture of polymethacrylate (s) and methyl ester (s) of acid (s) fat is at least 60%
- the ratio between the weight percentage of polymethacrylate (s) and the mass percentage of ester (s) of fatty acid (s) is between 0.8 and 1.2.
- the lubricating composition comprises at least 85% by weight, preferably at least 90% by weight, even more preferably at least 95% by weight, of one or more fatty acid methyl esters of formula RCOOCH 3, where R is a paraffinic or olefinic group containing from 11 to 23, preferably from 13 to 19 carbon atoms, relative to the total weight of fatty acid esters present in said lubricating composition
- the lubricating composition comprises at least 75% by weight, preferably at least 80% by weight of at least one fatty acid methyl ester of formula R1COOCH3, where R1 is a mono, di or tri unsaturated olefinic group. containing from 11 to 23, preferably from 15 to 19 atoms, preferably 17 carbon atoms, relative to the total weight of fatty acid esters present in said lubricating composition
- the lubricating composition comprises at least 65% by weight, preferably at least 70% by weight, of at least one fatty acid methyl ester of formula R 2 COOCH 3, where R 2 is a monounsaturated olefinic group containing from 11 to 23 preferably from 15 to 19 atoms, preferably 17 carbon atoms, relative to the total weight of fatty acid esters present in said lubricating composition.
- the unsaturations of the olefinic groups R 1 and / or R 2 are in the cis configuration.
- the lubricating composition comprises at most 15% by weight, preferably at most 10% by weight, of saturated fatty acid esters, relative to the total weight of fatty acid esters present in said lubricating composition.
- the S / P ratio between the sulfur element mass content measured according to the ASTM D2622 standard and the phosphorus element content measured according to the ASTM D5185 standard in said lubricating compositions is between 3 and 60, preferably less than 30, preferably less than 20, even more preferably less than 10, or even between 5 and 10.
- the lubricating composition has a VI, measured according to the ASTM D2270 standard, greater than 250, preferably greater than 280, and even more preferably greater than 300.
- Another aspect of the invention relates to the use of lubricant compositions for gearboxes described above, to generate fuel savings greater than 1%, preferably greater than 2.5%, measured under the standard conditions of the test.
- NEDC according to Directive EEC 90 / C81 / 01 on national emission ceilings for certain atmospheric pollutants ("test emission cycles for the certification of light duty vehicles in Europe", Brussels, 2001), on motor vehicles, equipped with boxes manual or automatic gears, or automated manual gearboxes.
- the fuel savings are generated on light-duty vehicle engines, preferably hybrid vehicles.
- a preferred use is for vehicles equipped with manual gearboxes or automated manual gearboxes.
- the present invention relates to the use of fatty acid methyl ester bases containing at least 85% by weight, preferably at least 90%, even more preferably at least 90% of fatty acid methyl esters, of formula RCOOCH3 where R is a paraffinic or olefinic group containing from 11 to 23, preferably from 13 to 19 carbon atoms, VI greater than 250, and kinematic viscosity at 100 ° C of less than 7 mm 2 / s, as a lubricating base for formulating gearbox oils generating fuel savings greater than 1%, preferably greater than 2.5%, measured under the standard conditions of the NEDC test according to EEC Directive 90 / C81 / 01 01 setting emission ceilings for certain atmospheric pollutants ("test emission cycles for the certification of light duty vehicles in Europe", Brussels, 2001).
- compositions which comprise at least 75% by weight, preferably at least 80% by weight of at least one methyl ester, are preferably used.
- compositions which comprise at least 65% by weight, preferably at least 70% by weight, of at least one fatty acid methyl ester of formula R 2 COOCH 3, where R 2 is a monounsaturated olefinic group containing from II to 23, preferably from 15 to 19 atoms, preferably 17 carbon atoms.
- compositions are used in which the unsaturations of the olefinic groups R 1 and / or R 2 are in the cis configuration.
- the lubricant compositions according to the invention are compositions for transmissions, more particularly for gearboxes, making it possible to significantly save fuel on vehicles, in particular light vehicles, especially hybrid vehicles.
- the oils according to the invention have a kinematic viscosity at 100 ° C. imposed by the manufacturers of between 5.5 and 7 mm 2 / s, preferably between 6 and 7 mnrVs, even more preferentially between 6 and 6.7 mmVs, measured according to ASTM D445.
- oils according to the invention must, to ensure their role of protecting the mechanical parts while generating fuel savings, have VI (ASTM 2270) high, greater than 250, preferably greater than 280, even more preferably greater than 300, or of the order of 320 and beyond.
- oils according to the invention are formulated from lubricating bases of the fatty acid methyl ester type, high VI (greater than 250), and kinematic viscosity at 100 ° C. of less than 7 mm 2 / s. , such as those described below, combined with heavy PAOs, or light PAOs in combination with PMAs, and / or possibly certain other compounds known to those skilled in the art as thickening additives.
- the oils according to the invention contain at least 30% by weight of at least one fatty acid methyl ester of formula RCOOCH3, where R is a paraffinic or olefinic group containing from 11 to 23, preferably from 13 to 19 carbon atoms. This minimum content achieves high VI and low viscosity in service generating the fuel economy effect.
- the oils according to the invention may contain at least 35, at least 50, or at least 60, 70, or 80% of such fatty acid methyl esters. It should be noted that very high levels of such esters, above 70% by weight, or above 80% by weight, may have an adverse effect on the level of insolubles formed during the aging of the oils. .
- the predominant fatty acid methyl esters are of formula R 1 COOCH 3, where R 1 is a mono, di or tri unsaturated olefinic group containing from 11 to 23, preferably from 15 to 19 atoms, preferably 17 carbon atoms.
- the lubricant compositions for gearboxes according to the invention preferentially contain at least 20% by weight, preferably at least 25% by weight of such esters.
- the methyl esters of predominant fatty acids are of formula R 2 COOCH 3, where R 2 is a monounsaturated olefinic group containing from 11 to 23, preferably from 15 to 19 atoms, preferably 17 carbon atoms.
- the lubricant compositions for gearboxes according to the invention preferably contain at least 20% by weight of such esters.
- esters are preferably derived from fatty acid methyl ester bases as described below.
- the basic system of the lubricants according to the present invention can also be completed by other bases, insofar as the VI of said lubricating compositions is greater than 250, preferably greater than 280, still more preferably greater than 300 or of the order 320 and beyond, and the kinematic viscosity at 100 ° C of said lubricant compositions is between 5.5 and 7 mmVs, preferably between 6 and 6.5 mm 2 / s.
- bases of mineral origin can be bases of mineral origin, synthetic or natural.
- fatty acid ester bases used in the formulation of lubricants according to the invention are in fact mixtures of fatty acid esters, comprising at least 85% by weight, preferably at least 90% or at least 92%, preferably at least 95%, still more preferably at least 98% or at least 99% by weight of fatty acid methyl esters of formula RCOOCH 3, where R is a paraffinic or olefinic group containing from 11 to 23, preferably from 13 to 19 carbon atoms.
- the fatty acid methyl ester bases used in the lubricants according to the invention are also preferably substantially free of impurities of the ethyl ester type or, more generally, esters of alcohols containing 2 or more carbon atoms.
- Such impurities can indeed have an impact on the viscosity level and the VI of the ester bases, leading in particular to values of VI lower than desired (VI less than 250).
- the total contents of such impurities will be less than 15% by weight, preferably less than 10%, or 8% or 5% by weight in the ester bases used to formulate the lubricants according to the invention. more preferably less than 2% or less than 1% by weight.
- fatty acid methyl ester bases preferably contain at least 70% by weight, preferably at least 75%, even more preferably at least 80% by weight of at least one fatty acid methyl ester of formula R 1 COOCH 3, where R 1 is a mono, di or tri unsaturated olefinic group containing from 11 to 23, preferentially from 15 to 19 atoms, preferably 17 carbon atoms,
- these fatty acid methyl ester bases contain at least 65% by weight, preferably at least 70% by weight of at least one fatty acid methyl ester of formula R 2 COOCH 3, where R 2 is a mono-unsaturated olefinic group containing 11 to 23, preferably from 15 to 19 atoms, preferably 17 carbon atoms
- the average chain length of the fatty acids composing the esters of said base is between 17 and 19.
- fatty acid methyl esters, the unsaturations of the groups R 1 and / or R 2 are preferably in cis form.
- the cis or trans configuration of said monounsaturated fatty acid methyl esters affects their technical characteristics.
- a cis double bond creates a bend in the carbon chain while the trans double bond has an extended structure.
- Unsaturated fatty acids are predominantly present in their "cis” form in their natural state.
- the "trans” form is present in the natural state at about 2 to 8% by weight in the milk fats, at about 4.5% by weight in the fats of beef and beef. sheep. However, it is mainly obtained during industrial processes for the hydrogenation of polyunsaturated fatty chains present in certain oils.
- these fatty acid methyl ester bases contain less than 5% by weight of unsaturated fatty acid methyl esters having at least one unsaturation of their olefinic chain in trans form (hereinafter "unsaturated fatty acid methyl esters”). trans ").
- the fatty acid esters may be obtained from fatty acids themselves derived from natural resources or from synthetic fatty acids, obtained for example from petroleum fractions.
- fatty acids denotes linear hydrocarbon-based monoacids containing from 8 to 24 carbon atoms. They can be saturated, monounsaturated, or polyunsaturated. The fatty acids from natural resources have an even number of carbon atoms.
- the methyl ester of oleic acid is particularly preferred (18-1).
- methyl esters of the above fatty acids the predominant compound is those of palmitoleic (16-1), oleic (18-1) and linoleic (18-2) acids.
- the methyl ester of oleic acid is particularly preferred.
- oils are present, for example, in vegetable oils in the form of triglycerides, or triesters of glycerol.
- the hydrolysis of triglycerides leads to the corresponding fatty acids and glycerol.
- Methyl esters are obtained by esterification of fatty acids or directly by transesterification of the oils with methanol.
- a natural oil mention may be made of conventional or genetically modified copra, palm, olive, peanut, rapeseed and sunflower oils so as to enrich their oleic acid content (rapeseed and oleic sunflower), soybean, cotton, beef tallow, etc.
- the fatty acid methyl ester bases used in the invention are of natural origin, particularly of vegetable origin, obtained for example from palm oil, olive oil, peanut oil, rapeseed oil or sunflower oil. classic or oleic.
- the fatty acid methyl ester bases used in the invention typically have a kinematic viscosity at 100 ° C, measured by ASTM D445, of between 1.5 and 10 m ⁇ vVs, preferably between 1.5 and 7 mnrVs, and an IV (ASTM 2270) of the order of 250 to 400.
- the VI of these bases is typically greater than 250, preferably greater than 280, or greater than 300, or of the order of 320 and beyond.
- compositions according to the present invention are used as a lubricating base in the compositions according to the present invention, and represent at least 30% by weight of the finished lubricant, preferably at least 35% by weight. They may be present up to levels of the order of at least 50%, or 60%, or 70%, or even at least 80% by weight relative to the total weight of lubricant.
- the lubricants according to the invention formulated with the high-VI fatty acid methyl ester bases described above, show excellent results in fuel economy when they are used for example as gearbox oil.
- the minimum amount of 30% of fatty acid methyl esters present in the compositions according to the invention, and the minimum quantity of 85% of fatty acid methyl esters present in the Fatty acid methyl ester type bases described above do not take into account any esters in the form of sulfur, phosphorus or phosphorus-sulfur compounds which are known as anti-wear and extreme pressure agents.
- Heavy Polvalphaolefines The polyalphaolefins employed in the lubricating compositions according to the present invention are called heavy polyalphaolefins or viscosity. They allow, in mixture with the esters, and optionally PMA, described above, to achieve in the lubricant compositions according to the invention the target of desired viscosity (between 5.5 and 7 mmVs, preferably between 6 and 7 mmVs, still more preferably between 6 and 6.7 mmVs at 100 0 C), without degrading VI, which remains greater than 250.
- desired viscosity between 5.5 and 7 mmVs, preferably between 6 and 7 mmVs, still more preferably between 6 and 6.7 mmVs at 100 0 C
- PAO polyalphaolefin
- viscosity viscosity
- Mw Their molecular weight in weight Mw is greater than 2500 daltons, typically of the order of 4000 to 50000 approximately.
- Mn has a number-average molecular weight, typically between 3000 and 20000, preferably between 3000 and 10000, preferably between 3000 and 7000.
- polyalphaolefins are for example obtained from monomers such as octene, decene, dodecene, tetradecene, hexadecene, etc., alone or mixed with other olefins.
- compositions according to the invention can be used alone or as a mixture in the compositions according to the invention, and represent at least 10% by weight of said compositions.
- Their mass percentage is preferably less than 30% by weight in said compositions, so as to avoid additive solubility constraints or excessively high viscosity.
- the mass percentage of heavy polyalphaolefins will be sufficiently high to give the compositions the required viscosity, but will have to remain within certain limits to avoid leading to too viscous compositions or to generate problems of solubility of the additives.
- It is typically between 10 and 25%, or 10 and 20% by weight, or between 15 and 25% by weight, or between 10 and 18% by weight, preferably between 15 and 18% by weight of lubricants for gearbox according to the invention.
- the percentage of fatty acid methyl esters of formula RCOOCH 3, where R is a paraffinic or olefinic group containing 11 to 23, preferably 13 to 19 carbon atoms, in said compositions is greater than 60%.
- compositions according to the invention can be formulated with high levels of unsaturated fatty acid methyl base (50% by weight of base, or even 60, 70% and beyond, which respectively corresponds to methyl ester percentages.
- compositions have the disadvantage of not being compatible with all the qualities of elastomeric seals, in particular those of the acrylate and fluoroelastomeric type.
- a portion of the amount of ester base used is substituted for one or more polymethacrylate (PMA) compounds, which are compounds that are well known to the person skilled in the art. profession, intervening in particular as thickening polymers in the lubricating formulation.
- PMA polymethacrylate
- the PMAs of the present invention have a kinematic viscosity at 100 ° C., measured according to the ASTM D445 standard, preferably less than 500 mnrVs, or even lower than 250 mmVs, or of the order of 200 m ⁇ rVs.
- the weight percentage of PMA will be chosen so that the mixture of fatty acid methyl ester and PMA represents at least 60% by weight in the lubricants according to the invention.
- the mass percentage of PMA will be substantially equivalent to that of the fatty acid methyl esters, that is to say that the ratio between the mass percentage of polymethacrylate (s) and the mass percentage of ester (s) of fatty acid (s) is between 0.8 and 1.2.
- the commercial polymethacrylates are in the form of polymer compounds in a predilution base oil.
- Said polymethacrylate compounds thus consist of 30 to 60% by weight, typically 50% by weight, of polymer (active ingredient), in the predilution oil.
- the mass percentages of PMA mentioned in the present description refer to the percentage of compound consisting of the polymer mixture (active ingredient) plus predilution oil.
- the PMAs employed in the compositions according to the invention have a relatively low molecular weight by weight of less than 30,000 daltons. Their incorporation however requires the incorporation of a co-solvent, which will also make it possible to respect the kinematic viscosity target at 100 ° C. of between 5.5 and 7 mmVs and to improve the compatibility with the elastomers for the lubricants according to US Pat. 'invention.
- This co-solvent must not degrade the VI of the compositions.
- the PMAs as described above are thickening additives well known to those skilled in the art, whose role is to increase the viscosity when hot or cold.
- one alternative to these PMAs is one or more other thickening additives also known to those skilled in the art, in combination with the light polyalphaolefins described hereinafter as co-solvent.
- These other thickening additives can be used alone or as a mixture, and optionally in admixture with the LDCs, exactly under the same conditions as the LDCs.
- thickeners will be selected for their high VI (greater than 200, preferably 250, or 280, or 300, preferably of the order of 320 or above), and for their shear strength adapted to use in lubricants for gearboxes.
- polyalphaolefms (PAO) / ethylene copolymers such as, for example, LUCANTG marketed by Mitsui, or ethylene-propylene dimers (EPDM), such as for example TRILENE CP 80 marketed by LYON Copolymers, or Styrene-Acrylate copolymers or derivatives or copolymers of PMA.
- PEO polyalphaolefms
- EPDM ethylene-propylene dimers
- PIBs polyisubutenes
- Some of these compounds, such as EPDMs are in the form of liquid compounds almost exclusively made of polymeric active material (ie for example that Trilene consists almost exclusively of EPDM)
- Others are in the form of compounds consisting of polymer (active material) in a predilution base oil. This is the case, for example, of PAO / ethylene copolymers, which consist of 30 to 60% by weight, typically 50% by weight, of polymer (active material), in the predilution oil.
- the mass percentages of thickeners mentioned in the present description refer to the percentage of compound consisting of the polymer mixture (active ingredient) plus predilution oil.
- the mass percentage of these thickeners will be chosen so that the mixture of fatty acid methyl ester, thickener (s), and optionally PMA, represents at least 60% by weight in the lubricants according to the invention.
- the weight percentage of the thickener or thickener mixture and PMA will be substantially equivalent to that of the fatty acid methyl esters.
- the ratio between the mass percentage of the thickener (s), or thickener mixture and PMA, and the mass percentage of ester (s) of fatty acid (s) is between 0.8 and 1.2.
- the light polyalphaolefins are for example obtained from monomers such as octene, decene, dodecene, tetradecene, hexadecene, etc., alone or mixed with other olefins. They can also be used alone or as a mixture in the compositions according to the invention.
- the so-called light PAOs have a kinematic viscosity at 100 ° C., measured according to the ASTM D445 standard of between 1.5 and 6 mmVs, preferably less than 3 nmV, of the order of 2 mnrVs, a kinematic viscosity at 40 ° C. measured according to the standard.
- ASTM D445 between 4 and 32 mnfVs, preferably less than 6 mmVs, of the order of 5 mmVs, and a molecular weight in weight (obtained by gas chromato graphie), less than 500, preferably less than 300, typically of order of 290 or 285 daltons.
- lubricants for gearboxes according to the invention.
- Their weight percentage is preferably less than 30% by weight in said lubricants, so as to avoid solubility of the additives.
- the weight percentage of light polyalphaolefins will be sufficiently high to solubilize the amount of PMA (and / or other thickeners as described above) necessary to give the compositions the required viscosity, but must remain within certain limits to avoid solubility problems of additives.
- their weight percentage is between 10 and 25%, preferably between 15 and 25% by weight, or between compositions according to the invention.
- the weight percentage of light PAO is at least 10% and the mass percentage of PMA (s) (and / or other thickeners described above) will be chosen so that the mixture of fatty acid methyl ester with the PMA (s) and / or with the other thickeners as described above, represents at least 60% by weight in the lubricating compositions for gearboxes according to the invention.
- the weight percentage of PMA (s) and / or other thickener (s) as described above will be substantially equivalent to that of the fatty acid methyl esters, that is to say that the ratio between the weight percentage of polymethacrylate (s) and the mass percentage of ester (s) of fatty acid (s) is between 0.8 and 1.2.
- compositions according to the invention thus formulated with fatty acid methyl ester bases, PMA and light PAO, have less aggressiveness than the variants containing only the methyl ester and the heavy PAO, during dynamic tests carried out on joints of various qualities. In particular, there is less variation in volume and deterioration of mechanical properties on fluoroelastomer seals.
- the lubricating compositions according to the invention may contain, as lubricating bases, in addition to the fatty acid methyl esters described above, in combination with heavy PAOs, or light PAOs and PMAs, all types of lubricating bases known to those skilled in the art, insofar as the VI of said lubricating compositions is greater than 250, preferably greater than 280, still more preferably greater than 300 or of the order of 320 and beyond, and the kinematic viscosity at 100 ° C said lubricating compositions is between 5.5 and 7 mmVs.
- These base oils can be of mineral, synthetic or natural origin.
- Mineral base oils may include any type of base obtained by atmospheric and vacuum distillation of crude oil, followed by refining operations such as solvent extraction, desalting, solvent dewaxing, hydrotreating, hydrocracking and hydroisomerization, hydrofinishing, and the like. ..
- Synthetic base oils may include oils belonging to groups IV, V and VI of the API classification, including polyalphaolefins, polyinternal olefins, alkyl aromatics, alkyl benzene, alkylnaphthalenes, esters, diesters, polyol esters such as as pentaerythritol esters, oligomers of aplhaolefins and esters, polyalkylene glycols.
- Viscosity and VI of the oils according to the invention are Viscosity and VI of the oils according to the invention.
- oils according to the invention are characterized by a very high VI.
- Their VI measured according to the ASTM 2270 standard, is greater than 250, preferably greater than 280 or even greater than 300, or of the order of 320 and beyond.
- the viscosity behavior of the lubricants is determined by the bases and the thickeners and VI modifiers used in their formulation.
- the VI of these unsaturated fatty acid methyl esters is strongly affected by the presence of impurities, in particular by the presence of unsaturated fatty acid esters and alcohols other than methanol, for example ethanol.
- the methyl esters of commercial fatty acids thus have VIs which can vary in a very broad range, as shown by the VI values of commercial oleates below, extracted from the Unichema catalog.
- Antiwear and / or extreme pressure additives are provided.
- the lubricating compositions according to the present invention contain at least one anti-wear agent and / or extreme phospho-sulfur, sulfur or phosphorus-containing agent, preferably present at contents of between 0.01% and 12%, preferably between 0.01% and 5%, by weight. relative to the total weight of lubricant.
- compositions according to the invention preferentially contain both the sulfur element and the phosphorus element.
- it contains either at least one phosphorus additive and at least one sulfur additive, or at least one phospho-sulfur additive.
- the sulfur element mass contents are typically of the order of 1 to 3% by weight (depending on the formulations and the objectives) and the phosphorus contents of the order of 500 to 3000 ppm (according to the formulations and the objectives).
- the anti-wear and extreme phospho-sulfur pressure additives used in the present invention are, for example and without limitation, thiophosphoric acid, thiophosphorous acid, esters of these acids, their salts, and dithiophosphates, particularly zinc dithiophosphates.
- Examples which may be mentioned as examples of phospho-sulfur-containing anti-wear and extreme pressure additives are those containing from 1 to 3 sulfur atoms, such as monobutylthiophosphate, monooctylthiophosphate, monolaurylthiophosphate, dibutylthiophosphate, dilaurylthiophosphate, tributylthiophosphate, trioctylthiophosphate, triphenylthiophosphate, trilaurylthiophosphate, monobutylthiophosphite, monooctylthiophosphite, monolaurylthiophosphite, dibutylthiophosphite, dilaurylthiophosphite, tributylthiophosphite, trioctylthiophosphite, triphenylthiophosphite, trilaurylthiophosphite and their salts.
- salts of thiophosphoric acid esters and thiophosphorous acid are those obtained by reaction with a nitrogen compound such as ammonia or an amine or zinc oxide or zinc chloride.
- Antiwear additives and extreme pressure phosphors are those obtained by reaction with a nitrogen compound such as ammonia or an amine or zinc oxide or zinc chloride.
- the lubricant compositions according to the present invention may also contain phosphorus anti-wear and extreme-pressure additives, such as, for example, alkyl phosphates or alkyl phosphonates, phosphoric acid, phopsphorous acid, mono, di and triesters of phosphorous acid and phosphoric acid, and their salts.
- phosphorus anti-wear and extreme-pressure additives such as, for example, alkyl phosphates or alkyl phosphonates, phosphoric acid, phopsphorous acid, mono, di and triesters of phosphorous acid and phosphoric acid, and their salts.
- sulfur anti-wear and extreme pressure additives examples include dithiocarbamates, thiadiazoles and benzothiazoles, sulfur-containing olefins.
- the most common sulfur-containing olefins are also called SIBs for "sulfurized isobutylenes". These sulfur-containing olefins are generally obtained by a reaction of sulfurization of olefins with sulfur, hydrogen sulphide or alkali metal sulphides hydrate, example sodium sulphide.
- Certain particular sulfurized olefins can be obtained by catalytic processes, for example by reacting hydrogen sulfide with isobutylene in the presence of catalyst. These processes lead to purer products, of better defined structure, having a higher sulfur level (ASTM D2622) and an active sulfur content (ASTM D-1662) generally lower than the commonly used SIBs.
- the sulfur content of the base oil or of the base oil mixture, as well as the respective quantities of phospho sulfur, phosphorus and sulfur-containing extreme pressure additives, in particular sulfur-containing olefins, are generally chosen so that said compositions have a ratio between their sulfur element content, measured by the ASTM D2622 standard and their phosphorus element content, measured by the ASTM D5185 standard, namely S / P, of between 3 and 60.
- Transmission lubricants having a S / P ratio greater than 30 are generally "economical" type products with a very low rate of additive treatment and reduced phosphorus contents.
- the mixed gearbox and bridge products generally have an S / P value of between 20 and 30, preferably close to 20, which corresponds to minimizing the amount of sulfur to improve compatibility with the synchros;
- Products with a ratio of less than 20 are intended for gearboxes rather than bridges.
- the lubricant compositions according to the present invention have a S / P ratio as defined above of between 3 and 60, or between 5 and 60, more preferably less than 30, preferentially less than 20, even more preferably less than 15 or 10.
- the lubricant compositions according to the invention may also contain any type of additive adapted to their use known to those skilled in the art for use in transmission oil formulations, for example one or more additives chosen from friction, antioxidant additives (eg antioxidants amines), corrosion inhibitors present at the usual levels required for the application.
- additives chosen from friction, antioxidant additives (eg antioxidants amines), corrosion inhibitors present at the usual levels required for the application.
- the friction modifying additives make it possible to limit friction in the limit or mixed lubrication regime by forming monolayers adsorbed on the surfaces of the metals;
- the methyl esters of fatty acids used as base in the lubricants according to the invention possess this property.
- their mass percentage is less than 10%, generally between 0.01 and 5% by weight relative to the total weight of lubricating composition.
- Said lubricants according to the invention may further contain, as friction modifiers, molecules such as fatty alcohols, ethoxylated fatty amines or not, fatty acids, amides obtained from fatty acids and amines, or succinimides formed by reaction of aliphatic succinic acids and primary amines, imidazoles, tertiary amines, aliphatic phosphonates, phosphates, thiophosphonates, aliphatic thiophosphates, organic Molybdenum derivatives.
- friction modifiers molecules such as fatty alcohols, ethoxylated fatty amines or not, fatty acids, amides obtained from fatty acids and amines, or succinimides formed by reaction of aliphatic succinic acids and primary amines, imidazoles, tertiary amines, aliphatic phosphonates, phosphates, thiophosphonates, aliphatic thiophosphates, organic Molybden
- the aliphatic chains of these compounds generally have a minimum of 8 carbon atoms.
- friction modifying additives may contain combinations of N-substituted dihydroxyalkylamines substituted by an aliphatic group having about 14 to 20 carbon atoms, optionally in combination with trimethyl diamines having at least one N-aliphatic substituent, or with substituted N-imidazoles. by hydroxyalkyl aliphatic groups.
- These compounds may be present, preferably, at contents of between 0.01% and 10% by weight in the lubricants according to the present invention.
- compositions according to the invention may contain one or more additives of a pour point depressant additive. It may be, for example, poly- Acrylates, Ethyl-Vinyl Acetates, ethylenic copolymers, condensation derivatives of naphthalene.
- additives may typically be present in an amount of from 0.1 to 2% by weight.
- oils according to the invention may also contain all types of additives suitable for their use, and in particular:
- Detergents such as, for example, sulphonates, phenates, calcium salycilates, sodium, magnesium and barium, present at contents of between 0 and 5% by weight
- Dispersants such as polyisobutyl butylene succinic anhydride derivatives, between 0 and 5%
- Antioxidants which may be for example Amino antioxidants (Ocatadiphenylamines, Phenyl-Alpha-Naphtyl Amines, ...), Phenolics (BHT and derivatives), Sulfurized (Phenates Sulfurized).
- Amino antioxidants Olediphenylamines, Phenyl-Alpha-Naphtyl Amines, ...), Phenolics (BHT and derivatives), Sulfurized (Phenates Sulfurized).
- the present invention also relates to the use of the lubricant compositions for gearboxes described above to generate fuel savings greater than 1%, preferably greater than 2.5%, measured under the standard conditions of the NEDC test according to EEC Directive 90 / C81 / 01 establishing national emission ceilings for certain air pollutants ("test emission cycles for the certification of light duty vehicles in Europe", Brussels, 2001), on motor vehicles.
- compositions according to the invention are particularly suitable for generating fuel savings on gasoline or diesel light vehicles, or equipped with a hybrid electric motor.
- Another aspect of the invention also relates to the use of bases of the fatty acid methyl ester type as described above as a lubricating base for formulating gearbox oils which generate fuel savings of greater than 1%, preferably greater than 1%. at 2.5%, measured under the conditions standard of the NEDC test according to EEC Directive 90 / C81 / 01 on national emission ceilings for certain atmospheric pollutants ("emission test for the certification of light duty vehicles in Europe", Brussels, 2001).
- These bases are preferably used at levels of at least 30% by weight of the finished lubricant, preferably at least 35% by weight. They may be present up to levels of the order of at least 50%, or 60%, or 70%, or even at least 80% by weight relative to the total weight of lubricant.
- Lubricating compositions according to the invention comprising at least 35% by weight of a lubricating base consisting predominantly of unsaturated fatty acid methyl esters are prepared, the characteristics of which are given in table 1. Percentages are percentages by weight relative to the total weight of lubricant
- Heavy PAO employed in the oil A is available under the commercial reference ExxonMobil Chemicals, Spectracyn 1000, having a kinematic viscosity at 100 0 C 1,000 mmVs.
- the light PAO used in oil B is marketed by Exxon Mobil Chemicals under the reference SHF-23, having a kinematic viscosity at 100 ° C. of 1.8 mm Vs.
- the polymethacrylate used in oils A and B is PAS 501 supplied by Sanyo Chemical
- compositions according to the invention thus prepared is a conventional additivation of lubricants for gearboxes.
- These compositions comprise 9.5% by weight of the gear package marketed by Lubrizol under the reference OS 215497, and containing:
- Table 2 groups together the characteristics of oils A and B according to the invention. The% indicated are% by weight relative to the total weight of lubricant.
- In-service and fuel consumption warm-up measurements are made by subjecting a test bench or actual vehicle engine to the NEDC model cycle (also referred to as ECE EUDC) according to EEC Directive 90 / C81 / 01 01 fixing national emission ceilings for certain atmospheric pollutants ("test emission cycle for the certification of light duty vehicles in Europe", Brussels, 2001).
- EEC Directive 90 / C81 / 01 01 fixing national emission ceilings for certain atmospheric pollutants (“test emission cycle for the certification of light duty vehicles in Europe", Brussels, 2001).
- the characteristics of this engine cycle are grouped together in FIG. 1, which describes the speed (in km / hour) imposed as a function of time (in seconds), respectively in the ECE 15 and EUDC cycles.
- Table 3 summarizes the overall characteristics of this cycle, representative of the average daily commute in Europe. .
- This NEDC cycle is carried out on an engine bench, which uses a 88 kW power gasoline engine, a manual gearbox and a Clemessy gearshift robot.
- the reference oil is a commercial oil for manual gearbox used in passenger light vehicles, grade 75W80, kinematic viscosity 8 mmVs at 100 0 C and VI of the order of 150, formulated with Conventional paraffinic bases of Group I (essentially Solvent Neutral 150).
- the initial temperature of the oils is 22 ° C.
- the final temperature of the gearbox oils tested at the end of the test are reported in Table 4 below.
- oils according to the invention A and B formulated with at least 35% by weight of base of the fatty acid methyl ester type, lead to heating up much lower than the commercial reference. It can also be seen that during tests simulating driving on fairly short paths, representative of the average of the daily journeys, the operating temperature of the gearbox oils is between 40 and 50 ° C.
- Fuel consumption is calculated according to EEC Directive 90 / C81 / 01 on national emission ceilings for certain air pollutants (Brussels, 2001). We measure the amount of gas emitted to the exhaust, and we go back to the mass fuel consumption.
- oils A and B there are significant fuel savings with oils A and B according to the invention.
- the heating is also limited (5 to 6 degrees less than the reference).
- the hybrid vehicle used included an automated mechanical gearbox to apply a specific shift strategy to the optimization of a hybrid operation.
- Example 5 Correlation Between Fuel Economy and Kinematic Viscosity at 40 ° C.
- Table 6 correlation between fuel economy and kinematic viscosity at 40 ° C.
- oils A and B are the oils according to the invention whose characteristics are set out in Table 2, and REF the reference for the fuel consumption described above.
- the oil C is a gearbox oil having the same additivation as the oils A and B, but formulated from mineral bases of group I and III with VI G 160
- Oil H is similar to oil C, with a VI of 200
- Example 6 Insoluble levels of the oils according to the invention.
- Oils A and B are those whose characteristics are set out in Table 2. The results are summarized in Table 7 below.
- Table 7 oxidation tests at 140 ° C., GFCT-021-A-90.
- oils according to the invention are poorly resistant to high temperature oxidizing conditions, with a significant increase in their kinematic viscosity. However, their level of insoluble is low.
- oils B formulated with fatty acid methyl esters combined with light PMA and PAO, have an exceptionally low level of insolubles.
- Example 7 Thermal stability of the oils according to the invention.
- a thermal aging test was carried out on oils A and B according to the invention. This test is carried out under the conditions of the standardized test GFCT-021-A-90, at 160 ° C., but the bubbling of air is replaced by a bubbling of nitrogen so as to be placed under non-oxidizing conditions. This absence of oxygen in the air is representative of the confinement in which a gear box oil is placed in service.
- the evolution of the kinematic viscosity at 100 ° C. of the oils A and B according to the invention during the test is reported in Table 8 below:
- Table 8 Evolution of the kinematic viscosity at 100 ° C. as a function of time, thermal aging test at 160 ° C.
- oil A is very stable in temperature.
- oil B there is a significant initial increase in viscosity, and the product remains very stable over time.
- the level of insolubles measured for the two oils is very low, respectively 0.01 and 0.065 after 200 hours of testing.
- the B oil therefore has the advantage of an exceptionally low insoluble level after oxidation test, with one initial thickening found during the thermal aging tests.
- Oil A when it is very thermally stable, with insoluble levels very high during oxidation tests.
- the acid number increases from 3.5 to 6.5 for the oil A, which shows a very low degradation of the fatty acid methyl ester base;
- the acid number goes from 3.7 to 2.1 for the oil B, which is not surprising if we consider that the initial thickening phenomenon is due to a transesterification reaction of the methyl esters of fatty acids with the heavy alcohols of the PMA.
- Example 8 Measurement of service life of the oils according to the invention.
- the viscosity of the oil representative of its aging, the contents of certain metallic elements, representative of the wear of the mechanical parts, as well as the content of certain elements (in particular Ca, Zn, P, Mg, Mo, Bo, Na), the presence of which makes it possible to check if the additives of the oil are not degraded.
- the element content present in the main gearbox additives (P, Ca, Zn,) measured by ICP also remains constant at measurement errors.
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Abstract
Description
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FR0805471A FR2936812B1 (fr) | 2008-10-03 | 2008-10-03 | Compositions lubrifiantes pour transmissions. |
PCT/IB2009/007026 WO2010038147A1 (fr) | 2008-10-03 | 2009-10-02 | Compositions lubrifiantes pour transmissions |
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US (1) | US8664169B2 (fr) |
EP (1) | EP2346970B1 (fr) |
JP (1) | JP5758297B2 (fr) |
KR (1) | KR101649308B1 (fr) |
CN (1) | CN102171320A (fr) |
ES (1) | ES2561477T3 (fr) |
FR (1) | FR2936812B1 (fr) |
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CN115060825A (zh) * | 2022-06-21 | 2022-09-16 | 奇瑞汽车股份有限公司 | 车辆产品中邻苯二甲酸酯的检测方法 |
FR3137918A1 (fr) | 2022-07-13 | 2024-01-19 | Totalenergies Onetech | Composition lubrifiante à base de diester |
US11912955B1 (en) | 2022-10-28 | 2024-02-27 | Afton Chemical Corporation | Lubricating compositions for reduced low temperature valve train wear |
US11939551B1 (en) | 2023-06-27 | 2024-03-26 | Afton Chemical Corporation | Lubricating fluid for an electric motor system |
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CN1831097A (zh) | 2006-02-08 | 2006-09-13 | 新疆福克油品有限公司 | 抗磨节能润滑油 |
HRP20060287A2 (en) | 2006-08-30 | 2008-03-31 | Kuftinec Josip | Process for production of fatty acid esthers and fuels comprising fatty acid esthers |
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WO2009125075A1 (fr) | 2008-04-11 | 2009-10-15 | Total Raffinage Marketing | Fluide lubrifiant multifonctionnel |
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2008
- 2008-10-03 FR FR0805471A patent/FR2936812B1/fr not_active Expired - Fee Related
-
2009
- 2009-10-02 EP EP09740194.7A patent/EP2346970B1/fr active Active
- 2009-10-02 WO PCT/IB2009/007026 patent/WO2010038147A1/fr active Application Filing
- 2009-10-02 ES ES09740194.7T patent/ES2561477T3/es active Active
- 2009-10-02 JP JP2011529648A patent/JP5758297B2/ja not_active Expired - Fee Related
- 2009-10-02 US US13/121,428 patent/US8664169B2/en not_active Expired - Fee Related
- 2009-10-02 RU RU2011110797/04A patent/RU2509145C2/ru not_active IP Right Cessation
- 2009-10-02 CN CN200980139171XA patent/CN102171320A/zh active Pending
- 2009-10-02 KR KR1020117007605A patent/KR101649308B1/ko active IP Right Grant
- 2009-10-02 HU HUE09740194A patent/HUE026653T2/en unknown
Non-Patent Citations (1)
Title |
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See references of WO2010038147A1 * |
Also Published As
Publication number | Publication date |
---|---|
RU2011110797A (ru) | 2012-11-10 |
FR2936812A1 (fr) | 2010-04-09 |
CN102171320A (zh) | 2011-08-31 |
JP5758297B2 (ja) | 2015-08-05 |
FR2936812B1 (fr) | 2010-10-15 |
KR101649308B1 (ko) | 2016-08-18 |
RU2509145C2 (ru) | 2014-03-10 |
EP2346970B1 (fr) | 2015-12-16 |
WO2010038147A1 (fr) | 2010-04-08 |
US8664169B2 (en) | 2014-03-04 |
US20110177989A1 (en) | 2011-07-21 |
KR20110090890A (ko) | 2011-08-10 |
JP2012504677A (ja) | 2012-02-23 |
ES2561477T3 (es) | 2016-02-26 |
HUE026653T2 (en) | 2016-07-28 |
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