US20160017251A1 - Lubricating composition for a marine engine - Google Patents
Lubricating composition for a marine engine Download PDFInfo
- Publication number
- US20160017251A1 US20160017251A1 US14/772,997 US201414772997A US2016017251A1 US 20160017251 A1 US20160017251 A1 US 20160017251A1 US 201414772997 A US201414772997 A US 201414772997A US 2016017251 A1 US2016017251 A1 US 2016017251A1
- Authority
- US
- United States
- Prior art keywords
- lubricant composition
- composition according
- carbon atoms
- group
- lubricant
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 202
- 230000001050 lubricating effect Effects 0.000 title description 7
- 239000000314 lubricant Substances 0.000 claims abstract description 179
- 150000001412 amines Chemical class 0.000 claims abstract description 77
- 239000003599 detergent Substances 0.000 claims abstract description 73
- 229920001577 copolymer Polymers 0.000 claims abstract description 58
- 239000002199 base oil Substances 0.000 claims abstract description 31
- 239000000446 fuel Substances 0.000 claims description 52
- 125000004432 carbon atom Chemical group C* 0.000 claims description 48
- 239000002270 dispersing agent Substances 0.000 claims description 28
- 150000001875 compounds Chemical class 0.000 claims description 26
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 22
- 230000003749 cleanliness Effects 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 239000000654 additive Substances 0.000 claims description 15
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 15
- 239000003513 alkali Substances 0.000 claims description 11
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 11
- 239000000194 fatty acid Substances 0.000 claims description 11
- 229930195729 fatty acid Natural products 0.000 claims description 11
- 150000004665 fatty acids Chemical class 0.000 claims description 11
- -1 alkaline-earth metal salicylates Chemical class 0.000 claims description 10
- 239000007866 anti-wear additive Substances 0.000 claims description 9
- 230000000996 additive effect Effects 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 229920006395 saturated elastomer Polymers 0.000 claims description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- VBIGULIJWJPALH-UHFFFAOYSA-L calcium;2-carboxyphenolate Chemical class [Ca+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O VBIGULIJWJPALH-UHFFFAOYSA-L 0.000 claims description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical group CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 239000002562 thickening agent Substances 0.000 claims description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 36
- 239000003921 oil Substances 0.000 description 24
- 235000019198 oils Nutrition 0.000 description 24
- 238000012360 testing method Methods 0.000 description 22
- 239000012141 concentrate Substances 0.000 description 16
- PWSBCLRIHVDWRH-SSDVNMTOSA-N methyl 2-[4-(4-chlorophenyl)-2-[(e)-(4-chlorophenyl)methylideneamino]-1,3-thiazol-5-yl]acetate Chemical compound N=1C(C=2C=CC(Cl)=CC=2)=C(CC(=O)OC)SC=1\N=C\C1=CC=C(Cl)C=C1 PWSBCLRIHVDWRH-SSDVNMTOSA-N 0.000 description 11
- 125000002947 alkylene group Chemical group 0.000 description 10
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 229920002367 Polyisobutene Polymers 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 239000005864 Sulphur Substances 0.000 description 6
- 239000010705 motor oil Substances 0.000 description 6
- 0 C.C.C.C.C.C.C.C.C.[4*]N([5*]N(C[H])C[H])C[H] Chemical compound C.C.C.C.C.C.C.C.C.[4*]N([5*]N(C[H])C[H])C[H] 0.000 description 5
- 150000001342 alkaline earth metals Chemical class 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 238000005461 lubrication Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 150000004985 diamines Chemical class 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229920000768 polyamine Polymers 0.000 description 4
- 229960001860 salicylate Drugs 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical class CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical group O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000019486 Sunflower oil Nutrition 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 230000003254 anti-foaming effect Effects 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 239000010727 cylinder oil Substances 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 239000000693 micelle Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 229920013639 polyalphaolefin Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 3
- 239000002600 sunflower oil Substances 0.000 description 3
- 239000010729 system oil Substances 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- GQWWGRUJOCIUKI-UHFFFAOYSA-N 2-[3-(2-methyl-1-oxopyrrolo[1,2-a]pyrazin-3-yl)propyl]guanidine Chemical compound O=C1N(C)C(CCCN=C(N)N)=CN2C=CC=C21 GQWWGRUJOCIUKI-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 125000005609 naphthenate group Chemical class 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 150000003443 succinic acid derivatives Chemical class 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 125000006681 (C2-C10) alkylene group Chemical group 0.000 description 1
- NKJOXAZJBOMXID-UHFFFAOYSA-N 1,1'-Oxybisoctane Chemical compound CCCCCCCCOCCCCCCCC NKJOXAZJBOMXID-UHFFFAOYSA-N 0.000 description 1
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 1
- 241001133760 Acoelorraphe Species 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 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
- 241000219146 Gossypium Species 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
- 241001465754 Metazoa Species 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- PFRUBEOIWWEFOL-UHFFFAOYSA-N [N].[S] Chemical compound [N].[S] PFRUBEOIWWEFOL-UHFFFAOYSA-N 0.000 description 1
- QCJQWJKKTGJDCM-UHFFFAOYSA-N [P].[S] Chemical compound [P].[S] QCJQWJKKTGJDCM-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 description 1
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000006185 dispersion Substances 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
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 239000003879 lubricant additive Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000001457 metallic cations Chemical class 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical compound C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl 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])C([H])([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
- 239000002245 particle Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 150000002989 phenols Chemical group 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229920006112 polar polymer Polymers 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 239000005076 polymer ester Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- JDVPQXZIJDEHAN-UHFFFAOYSA-N succinamic acid Chemical class NC(=O)CCC(O)=O JDVPQXZIJDEHAN-UHFFFAOYSA-N 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 1
- 239000010728 trunk piston oil Substances 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/04—Hydroxy compounds
- C10M129/10—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
- C10M129/14—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring containing at least 2 hydroxy groups
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/48—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring
- C10M129/54—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups
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- C10M167/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound, a non-macromolecular compound and a compound of unknown or incompletely defined constitution, each of these compounds being essential
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- 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
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- 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
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/06—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing conjugated dienes
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/028—Overbased salts thereof
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/26—Overbased carboxylic acid salts
- C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
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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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- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
- C10M2227/062—Cyclic esters
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/02—Unspecified siloxanes; Silicones
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
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- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/04—Detergent property or dispersant property
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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- 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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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
Definitions
- the present invention relates to the field of lubricants, and more particularly to the field of lubricants for a marine engine, in particular for a four-stroke or two-stroke marine engine, preferentially for a four-stroke marine engine. More particularly, the present invention relates to a lubricant composition comprising at least one base oil, at least one alkoxylated fatty amine, at least one hydrogenated styrene-isoprene copolymer and at least one detergent.
- the lubricant composition according to the invention simultaneously has good fuel economy properties and good engine cleanliness properties, in particular crankcase cleanliness.
- the present invention also relates to a method for reducing the fuel consumption of a vessel utilizing this lubricant composition.
- the present invention also relates to a composition of the additives-concentrate type comprising at least one alkoxylated fatty amine, at least one hydrogenated styrene-isoprene copolymer and at least one detergent.
- European Driving Cycle according to European Directive 70/220/EEC are 5% at low temperature (urban cycle) and 1.5% at high temperature (extra-urban cycle) with average gains of 2.5%.
- the formulation of a “fuel-eco” lubricant must not be detrimental to the lubricant's other performances.
- wear-resistance, demulsification, neutralizing ability, and engine cleanliness (piston and/or crankcase) should not be impaired.
- Document FR 2 974 111 describes a cylinder lubricant for a two-stroke marine engine comprising at least one overbased detergent, at least one neutral detergent and at least one alkoxylated fatty amine having a BN (Base Number) determined according to the ASTM D-2896 standard ranging from 100 to 600 milligrams of potassium hydroxide per gram of amine.
- BN Base Number
- An objective of the present invention is to provide a lubricant composition that overcomes all or part of the aforementioned drawbacks.
- Another objective of the invention is to provide a lubricant composition the formulation of which is easy to implement.
- Another objective of the present invention is to provide a lubrication method allowing fuel economies.
- a subject of the invention is thus a lubricant composition for a 4-stroke or 2-stroke marine engine comprising:
- lubricant compositions for marine engines making it possible to reduce the consumption of fuel, while maintaining or even improving engine cleanliness, in particular crankcase cleanliness, with respect to standard lubricant compositions for marine engines.
- a lubricant composition comprising at least one base oil, at least one alkoxylated fatty amine, at least one hydrogenated styrene-isoprene copolymer and at least one detergent.
- the present invention makes it possible to formulate lubricant compositions for a 4-stroke or 2-stroke marine engine, making it possible to combine both engine cleanliness and gains in fuel economies.
- the lubricant compositions according to the invention have an improved heat resistance under severe conditions, and more particularly in the presence of fuel.
- the lubricant compositions according to the invention have an improved stability on storage, as well as a viscosity that varies very little or not at all over time.
- the invention relates to a lubricant composition for a 4-stroke or 2-stroke marine engine comprising:
- the lubricant composition essentially consists of:
- the lubricant composition essentially consists of:
- the invention also relates to a trunk piston engine oil (TPEO) comprising a lubricant composition as defined above.
- TPEO trunk piston engine oil
- TPEO oil is meant any oily composition intended for lubricating 4-stroke marine engines, in particular the crankcase and cylinders.
- the invention also relates to an cylinder oil comprising a lubricant composition as defined above.
- cylinder oil is meant any oily composition intended for lubricating the cylinders of 2-stroke marine engines.
- the invention also relates to an system oil comprising a lubricant composition as defined above.
- system oil is meant any oily composition intended for lubricating the bottom part of 2-stroke marine engines, in particular the crankcase and crankshafts.
- the invention also relates to the use of a lubricant composition as defined above for lubricating a 4-stroke or 2-stroke marine engine.
- the invention also relates to the use of a lubricant composition as defined above for reducing the fuel consumption of a 4-stroke or 2-stroke marine engine.
- the invention also relates to the use of at least one alkoxylated fatty amine in a lubricant composition for 2-stroke or 4-stroke marine engines comprising at least one base oil, at least one hydrogenated styrene-isoprene copolymer and at least one detergent, for improving the engine cleanliness of 4-stroke or 2-stroke marine engines, preferably the cleanliness of the crankcase of 4-stroke or 2-stroke marine engines.
- the invention also relates to a composition of the additives-concentrate type comprising:
- the invention also relates to a method for lubricating a 4-stroke or 2-stroke marine engine comprising at least one step of bringing the engine into contact with a lubricant composition as defined above or obtained from the composition of the additives-concentrate type as described previously.
- the invention also relates to a method for reducing the fuel consumption of 4-stroke or 2-stroke marine engines comprising at least one step of bringing a mechanical part of the engine into contact with a lubricant composition as defined above or obtained from the composition of the additives-concentrate type as defined above.
- the lubricant composition comprises at least one alkoxylated fatty amine.
- alkoxylated fatty amine is meant, within the meaning of the present invention, a molecule comprising at least one amine function substituted with at least one alkyl group and at least one alkylene oxide group.
- the alkyl group can be chosen from the C 8 -0 30 alkyl groups, preferably C 10 -C 24 , more preferentially C 12 -C 22 and even more preferentially C 16 -C 20 .
- the alkylene oxide group can be chosen from the (C 2 -C 10 )-alkylene oxide groups, preferably (C 2 -C 4 )-alkylene and more preferentially (C 2 -C 3 )-alkylene.
- the alkoxylated fatty amine is chosen from the alkoxylated fatty monoamines or the alkoxylated fatty polyamines.
- the alkoxylated fatty amine can be chosen from the alkoxylated fatty monoamines or the alkoxylated fatty diamines comprising one or more fatty aliphatic chains, preferably comprising a C 8 -C 30 alkyl group, more preferentially a C 10 -C 24 alkyl group, even more preferentially a C 12 -C 22 alkyl group and advantageously a C 16 -C 20 alkyl group.
- the intrinsic BN of the alkoxylated fatty amines used in the lubricant composition according to invention can range from 100 to 600 milligrams of potassium hydroxide per gram of alkoxylated fatty amine, preferentially from 100 to 500 milligrams of potassium hydroxide per gram of alkoxylated fatty amine, more preferentially from 100 to 300 milligrams of potassium hydroxide per gram of alkoxylated fatty amine.
- Alkoxylated fatty amine can be considered as a cationic-type surfactant the polar head of which is constituted by at least one nitrogen atom and by at least one oxygen atom provided by the alkoxylation and the lipophilic part of which is constituted by the fatty aliphatic chain(s).
- the polar head of the alkoxylated fatty amine can be constituted by amine functions a short distance from one another (typically separated by 2 to 3 carbon atoms), and preferentially restricted in number (typically one or two amine functions), and preferentially alkoxylated with a limited number of alkylene oxide functions, typically between 1 and 15, preferentially between 2 and 10, more preferentially between 3 and 7, even more preferentially between 3 and 4.
- the alkylene oxide group can be chosen from the (C 2 -C 4 )-alkylene oxide groups. This makes it possible to constitute a “compact” polar head, and therefore to confer a surfactant nature on these alkoxylated fatty amines.
- the alkoxylated fatty amine can be obtained by known alkoxylation methods, for example described in the application FR 2 094 182, by bringing at least one fatty amine into contact with at least one alkylene oxide, at temperatures for example comprised between 100 and 200° C., in the presence of a basic catalyst such as NaOH, KOH or NaOCH 3 .
- the starting fatty amine is mainly obtained from carboxylic acids. These acids are dehydrated in the presence of ammonia in order to produce nitriles, which then undergo catalytic hydrogenation in order to produce primary, secondary or tertiary amines.
- the starting fatty amine is obtained from carboxylic acids, preferably from fatty acids.
- fatty acid is meant, within the meaning of the invention, a carboxylic acid with a saturated or unsaturated aliphatic chain, comprising from 8 to 30 carbon atoms, preferably from 10 to 24 carbon atoms, more preferentially from 12 to 22 carbon atoms and even more preferentially from 16 to 20 carbon atoms.
- the starting fatty acids can be chosen from caprylic, pelargonic, capric, undecylenic, lauric, tridecylenic, myristic, pentadecylic, palmitic, margaric, stearic, nonadecylic, arachic, heneicosanoic, behenic, tricosanoic, lignoceric, pentacosanoic, cerotic, heptacosanoic, montanic, nonacosanoic, melissic, hentriacontanoic, laceroic acids or unsaturated fatty acids such as palmitoleic, oleic, erucic, nervonic, linoleic, ⁇ -linolenic, ⁇ -linolenic, di-homo-y-linolenic, arachidonic, eicosapentaeno
- the alkoxylated fatty amine is obtained from fatty acids comprising from 10 to 24 carbon atoms, preferably from 12 to 22 carbon atoms, more preferentially from 16 to 20 carbon atoms and even more preferentially from 16 to 18 carbon atoms.
- the fatty acids can originate from the hydrolysis of the triglycerides present in vegetable and animal oils, such as coconut, palm, olive, peanut, rapeseed, sunflower, soya, cotton, linseed oil or beef tallow.
- vegetable and animal oils such as coconut, palm, olive, peanut, rapeseed, sunflower, soya, cotton, linseed oil or beef tallow.
- the natural oils may have been genetically modified so as to enrich their content of certain fatty acids, for example rapeseed oil or oleic sunflower oil.
- the fatty amine used for preparing the alkoxylated fatty amine present in the lubricant composition according to the invention is obtained from natural, vegetable or animal resources.
- the treatments making it possible to produce fatty amines starting from natural oils can lead to mixtures of primary, secondary and tertiary monoamines, and polyamines.
- a fatty monoamine or polyamine can contain several fatty chains originating from different fatty acids.
- a product constituted by primary monoamines of formula R 1 NH 2 will be used, wherein R 1 can represent a plurality of fatty acids originating from a natural resource, for example tallow fat, or soya oil, or coconut oil, or (oleic) sunflower oil.
- R 1 can represent a plurality of fatty acids originating from a natural resource, for example tallow fat, or soya oil, or coconut oil, or (oleic) sunflower oil.
- R 1 can represent a plurality of fatty acids originating from a natural resource, for example tallow fat, or soya oil, or coconut oil, or (oleic) sunflower oil.
- amines obtained from oleic acid are advantageously used, in particular primary monoamines of formula R 1 NH 2 or diamines of formula R 1 —[NH(CH 2 ) 3 ]—NH 2 wherein R 1 is the fatty chain of oleic acid.
- the alkoxylated fatty amine present in the lubricant composition according to the invention is soluble in the base oil matrix.
- the solubility of the alkoxylated fatty amine is initially due to its fatty chain(s). It is also all the more soluble as it comprises a limited number of alkylene oxide functions.
- the alkoxylated fatty amine is all the more soluble as it comprises no more than 15 alkylene oxide functions per amine molecule, preferably no more than 10 alkylene oxide functions, more preferentially no more than 7 alkylene oxide functions and even more preferentially no more than 4 alkylene oxide functions.
- the alkoxylated fatty amine is chosen from the monoamines comprising a ternary nitrogen.
- the alkoxylated fatty amine present in the lubricant composition according to the invention is therefore all the more effective, as it is well dispersed or even solubilized in the oil matrix.
- the alkoxylated fatty amine present in the lubricant composition according to the invention is not present in the form of an emulsion or a microemulsion, but in dispersed form, or even solubilized in the oil matrix.
- the alkoxylated fatty amine comprises at least one aliphatic chain comprising at least 8 carbon atoms, preferably at least 10 carbon atoms, preferentially at least 12 carbon atoms, preferentially at least 14 carbon atoms, more preferentially at least 16 carbon atoms, advantageously from 16 to 20 carbon atoms.
- the lubricant composition according to the invention can comprise at least one alkoxylated fatty amine of formula (I):
- the lubricant composition according to the invention can comprise at least one alkoxylated fatty amine of formula (I) in which:
- alkoxylated fatty amine is chosen from the compounds of formula (Ia):
- alkoxylated fatty amine is a compound of formula (la) in which:
- the content by weight of alkoxylated fatty amine ranges from 0.1 to 10%, preferably from 1 to 9%, advantageously from 2 to 8% with respect to the total weight of the lubricant composition.
- the lubricant composition according to the invention comprises at least one hydrogenated styrene-isoprene copolymer.
- the hydrogenated styrene-isoprene copolymer can be chosen from straight-chain hydrogenated styrene-isoprene copolymers or star-shaped hydrogenated styrene-isoprene copolymers (also called “star polymers”), preferably chosen from the star-shaped hydrogenated styrene-isoprene copolymers.
- the hydrogenated styrene-isoprene copolymer can be chosen from the hydrogenated styrene-isoprene block copolymers or the hydrogenated styrene-isoprene random copolymers.
- the hydrogenated styrene-isoprene copolymer has a content of hydrogenated isoprene units, ranging from 50% to 98%, preferably from 60% to 98%, more preferentially from 70% to 97%, even more preferentially from 75% to 96% by mass, with respect to the mass of hydrogenated styrene-isoprene copolymer.
- the hydrogenated styrene-isoprene copolymer has a content of styrene units ranging from 2% to 50%, preferably from 2% to 40%, more preferentially from 3% to 30%, even more preferentially from 4% to 25% by mass with respect to the mass of hydrogenated styrene-isoprene copolymer.
- the hydrogenated styrene-isoprene copolymer according to the invention has a weight-average molecular weight M w ranging from 100,000 to 800,000 daltons, preferably from 200,000 to 700,000 daltons, more preferentially from 300,000 to 600,000 daltons, even more preferentially from 400,000 to 500,000 daltons.
- the hydrogenated styrene-isoprene copolymer according to the invention has a number-average molecular weight M n ranging from 50,000 to 800,000 daltons, preferably from 75,000 to 600,000, more preferentially from 100,000 to 500,000, even more preferentially from 100,000 to 200,000.
- the hydrogenated styrene-isoprene copolymer according to the invention has a polydispersity index ranging from 1 to 4, preferably from 1.2 to 3.5, more preferentially from 1.5 to 3.5, even more preferentially from 2 to 3.
- the content by weight of hydrogenated styrene-isoprene copolymer in the lubricant composition according to the invention is from 0.1% to 15% by mass, with respect to the total mass of the lubricant composition, preferably from 0.1% to 10%, more preferentially from 0.2% to 5%, advantageously from 0.5 to 2%.
- this quantity is meant a quantity of active polymer material.
- the hydrogenated styrene-isoprene copolymer used in the context of the present invention can be presented in the form of a dispersion in a mineral or synthetic oil, and more particularly in an oil of Group I according to the API classification.
- the lubricant composition according to the invention comprises at least one detergent.
- the detergent used in the lubricant composition according to the invention can be chosen from the detergents commonly used in lubricant compositions.
- the detergent commonly used in the formulation of lubricant compositions is typically an anionic compound comprising a long lipophilic hydrocarbon-containing chain and a hydrophilic head.
- the associated cation is typically a metallic cation of an alkali or alkaline-earth metal.
- the detergent can be chosen from the alkali or alkaline-earth metal salts of carboxylic acids, sulphonates, salicylates, naphthenates, and phenates alone or in a mixture.
- the detergents are named according to the nature of the hydrophobic chain, carboxylate, sulphonate, salicylate, naphthenate or phenate.
- the alkali and alkaline-earth metals are chosen from calcium, magnesium, sodium or barium, preferentially calcium.
- the detergent can be chosen from the non-overbased (or neutral) detergents or overbased detergents.
- non-overbased or “neutral” detergents is used when the metallic salts contain the metal in an approximately stoichiometric quantity with respect to the anionic group(s) of the detergent.
- overbased detergents is used when the metal is in excess (in a quantity greater than the stoichiometric quantity with respect to the anionic group(s) of the detergent).
- the metal in excess providing the overbased character to the detergent is presented in the form of metallic salts that are insoluble in oil.
- the overbased detergents are presented in the form of micelles.
- These micelles can contain one or more types of insoluble metallic salts, stabilized by one or more types of detergents.
- the overbased detergents will be referred to as of mixed type if the micelles comprise several types of detergents which differ from each other in the nature of their hydrophobic chain.
- the detergent is chosen from the alkali and alkaline-earth metal salicylates, carboxylates, sulphonates and/or phenates, alone or in a mixture, preferentially from the calcium salicylates, sulphonates and/or phenates.
- the detergent present in the lubricant composition according to the invention can also be chosen from the non-metallic and non-overbased detergents.
- the detergent is chosen from the amine- and borate-containing compounds.
- the detergent can be an amine- and borate-containing compound originating from the reaction between an alkylated derivative of salicylic acid and a dialkoxylated amine, in the presence of boric acid.
- the detergent can thus be obtained by implementation of the method described in document WO 2007/081494.
- the detergent can be chosen from the amine- and borate-containing derivatives of salicylic acid.
- the detergent is a compound of formula (II)
- the R 6 and R 7 groups are identical and both represent a linear or branched alkyl group comprising from 12 to 20 carbon atoms.
- the detergent is chosen from alkali or alkaline-earth metal salicylates or phenates, alone or in a mixture.
- the detergent is chosen from calcium salicylates or calcium phenates, alone or in a mixture.
- the detergent is a mixture of an alkali or alkaline-earth metal salicylate and of a compound of formula (II).
- the detergent is a mixture of an alkali or alkaline-earth metal phenate and of a compound of formula (II).
- the detergent is a mixture of an alkali or alkaline-earth metal phenate, an alkali or alkaline-earth metal salicylate and a compound of formula (II).
- the combination of a compound of formula (II) and an alkali or alkaline-earth metal phenate and/or salicylate makes it possible to enhance the heat resistance of the lubricant composition according to the invention, in particular under severe conditions, and more particularly in the presence of fuel.
- the content by weight of detergents in the lubricant composition according to the invention ranges from 1% to 20%, preferentially from 1% to 15%, more preferentially from 2% to 10% with respect to the total weight of the lubricant composition.
- the BN of the lubricant compositions according to the present invention is provided by the alkoxylated fatty amine and by the detergent(s).
- the BN value of the lubricant compositions according to the present invention can vary from 5 to 100 mg of KOH/g of lubricant composition, preferably from 7 to 80 mg of KOH/g of lubricant composition, more preferentially from 10 to 60 mg of KOH/g of lubricant composition.
- the BN value is chosen depending on the conditions of use of the lubricant compositions and in particular according to the sulphur content of the fuel used.
- the BN value is significant and preferably comprised between 20 and 80 mg of KOH/g of lubricant composition, more preferentially between 30 and 65 mg of KOH/g of lubricant composition.
- the BN value is low and preferably comprised between 5 and 20 mg of KOH/g of lubricant composition, more preferentially between 10 and 15 mg of KOH/g of lubricant composition.
- the base oils used for the formulation of lubricant compositions according to the invention can be chosen from oils of mineral, synthetic or vegetable origin as well as mixtures thereof.
- the mineral or synthetic oils generally used in the marine engine oil application belong to one of the classes defined in the API classification as summarized in the table below.
- the mineral oils of Group I can be obtained by distillation of selected naphthenic or paraffinic crude oils, then by purification of these distillates by methods such as solvent extraction, solvent or catalytic dewaxing, hydrotreating or hydrogenation.
- the mineral bases of Group I are for example the bases called Neutral Solvent (such as for example 150NS, 330NS, 500NS or 600NS) or Brightstock.
- the oils of Groups II and III are obtained by more stringent purification methods, for example a combination of hydrotreating, hydrocracking, hydrogenation and catalytic dewaxing.
- Examples of synthetic bases of Groups IV and V include the poly-alpha olefins, polybutenes, polyisobutenes and alkylbenzenes.
- base oils can be used alone or in a mixture.
- a mineral oil can be combined with a synthetic oil.
- the lubricant base oil is chosen from the base oils of Group I or Group II, alone or in a mixture.
- the lubricant composition according to the invention can be characterized by a viscosity grade of SAE-20, SAE-30, SAE-40, SAE-50 or SAE-60 according to the SAEJ300 classification.
- Grade 20 oils have a kinematic viscosity at 100° C. comprised between 5.6 and 9.3 cSt.
- Grade 30 oils have a kinematic viscosity at 100° C. comprised between 9.3 and 12.5 cSt.
- Grade 40 oils have a kinematic viscosity at 100° C. comprised between 12.5 and 16.3 cSt.
- Grade 50 oils have a kinematic viscosity at 100° C. comprised between 16.3 and 21.9 cSt.
- Grade 60 oils have a kinematic viscosity at 100° C. comprised between 21.9 and 26.1 cSt.
- the kinematic viscosity is measured according to the ASTM D7279 standard at 100° C.
- the lubricant composition according to the invention has a kinematic viscosity measured according to the ASTM D7279 standard at 100° C. comprised between 5.6 and 26.1 cSt, preferably between 9.3 and 21.9 cSt, more preferentially between 12.5 and 16.3 cSt.
- the content by weight of base oil in the lubricant composition according to the invention is from 30% to 90%, preferably from 40% to 90%, more preferentially from 50% to 85%, advantageously from 65 to 85% with respect to the total weight of the lubricant composition.
- the lubricant composition is not presented in the form of an emulsion.
- the lubricant composition according to the invention is presented in the form of an anhydrous composition.
- the lubricant composition according to the invention can also comprise a dispersant.
- the dispersants are well-known additives used in the formulation of lubricant compositions, in particular for application in the marine field. Their first role is to keep in suspension the particles originally present or appearing in the lubricant composition during its use in the engine. They prevent their agglomeration by acting on the steric hindrance. They can also have a synergistic effect on the neutralization.
- the dispersants used as lubricant additives typically contain a polar group, associated with a relatively long hydrocarbon-containing chain, generally containing from 50 to 400 carbon atoms.
- the polar group typically contains at least one nitrogen, oxygen or phosphorus element.
- the dispersant can be chosen from the succinic acid derivatives.
- succinic acid derivatives is meant, within the meaning of the invention, the succinic acid esters or succinic acid amide esters.
- the dispersant is chosen from the compounds comprising at least one succinimide group.
- These compounds can be then treated with various compounds, in particular sulphur, oxygen, formaldehyde, carboxylic acids and compounds containing boron or zinc in order to produce, for example, borated succinimides or zinc-blocked succinimides.
- the dispersant is chosen from the borated compounds comprising at least one succinimide group.
- the dispersant can be chosen from the borated compounds comprising at least one substituted succinimide group or the borated compounds comprising at least two substituted succinimide groups, the succinimide groups being able to be linked at their vertex bearing a nitrogen atom, by a polyamine group.
- substituted succinimide group within the meaning of the present invention, is meant a succinimide group at least one of the vertices of which is substituted with a hydrocarbon group comprising from 8 to 400 carbon atoms.
- the dispersant is chosen from the borated compounds comprising at least one succinimide group substituted with a polyisobutene group.
- the dispersant is chosen from the borated compounds comprising at least two succinimide groups each substituted with a polyisobutene group.
- the dispersant is chosen from the borated compounds comprising at least two succinimide groups each substituted with a polyisobutene group and characterized by:
- the product T161B from the Tianhe company can be mentioned.
- Mannich bases obtained by polycondensation of phenols substituted with alkyl groups, formaldehyde and primary or secondary amines, can also be used as dispersants in the lubricant composition according to the invention.
- the content by weight of dispersant is at least 0.1%, preferably from 0.1% to 10%, advantageously from 1% to 6% with respect to the total weight of the lubricant composition.
- the lubricant composition according to the invention can comprise at least one additional additive, in particular chosen from those commonly used by a person skilled in the art.
- the additional additive can be chosen from anti-wear additives, antioxidants, additional polymers improving the viscosity index, pour point improvers, anti-foaming agents, thickeners and mixtures thereof.
- the anti-wear additives protect the friction surfaces by the formation of a protective film adsorbed on these surfaces.
- the phosphorus- and sulphur-containing additives such as the metallic alkylthiophosphates, in particular the zinc alkylthiophosphates, and more specifically the zinc dialkyldithiophosphates (or ZnDTP) can thus be mentioned.
- the alkyl groups of these zinc dialkyldithiophosphates preferentially comprise from 1 to 18 carbon atoms.
- the amine phosphates, the polysulphides, in particular the sulphur-containing olefins are also commonly used anti-wear additives.
- Anti-wear additives of the nitrogen- and sulphur-containing type such as for example metallic dithiocarbamates, in particular molybdenum dithiocarbamate are also encountered.
- the preferred anti-wear additive is ZnDTP.
- the content by weight of anti-wear additive in the lubricant according to the invention is from 0.1% to 5%, preferably from 0.2% to 4%, more preferentially from 0.2% to 2% with respect to the total weight of the lubricant composition.
- additional polymers improving the viscosity index is meant any polymer improving the viscosity index other than the hydrogenated styrene-isoprene copolymer according to the invention.
- polymers improving the viscosity index can be chosen from the polymer esters, olefin copolymers (OCP) or polymethacrylates (PMA).
- OCP olefin copolymers
- PMA polymethacrylates
- the anti-foaming additives can be chosen from the polar polymers such as polymethylsiloxanes or polyacrylates.
- additives are generally present in a content by weight of 0.01 to 3% with respect to the total weight of the lubricant composition.
- a subject of the invention is also a lubricant composition for a 4-stroke or 2-stroke marine engine comprising:
- the lubricant composition essentially consists of:
- a subject of the invention is also a lubricant composition for a 4-stroke or 2-stroke marine engine comprising:
- the lubricant composition essentially consists of:
- the lubricant composition according to the invention can be used in 4-stroke or 2-stroke marine engines.
- the lubricant composition is used in high-speed or medium-speed 4-stroke engines, which operate with distillates and bunker fuels or heavy fuel respectively.
- the fuel economy applies in particular to the distillates used in high-speed 4-stroke engines.
- High-speed 4-stroke engines are used for the propulsion of small vessels and as electricity generating units on board larger vessels.
- Medium-speed 4-stroke engines are used for the propulsion of numerous vessels, such as cargo ships, tankers, ferries, or even certain container ships. They can moreover be used as electricity generating units on board large vessels or in diesel electricity generating stations.
- the lubricant composition is appropriate for 4-stroke engines as trunk piston oil (TPEO).
- the lubricant composition is appropriate for 2-stroke engines as system oil or cylinder oil.
- a subject of the invention is also the use of a lubricant composition as defined above for the lubrication of 4-stroke or 2-stroke marine engines.
- the invention relates to the use of a lubricant composition as defined above for the lubrication of 4-stroke marine engines. All the characteristics and preferences presented for the lubricant composition apply to the above use.
- the invention also relates to the use of a lubricant composition as defined above for reducing the fuel consumption of 4-stroke or 2-stroke marine engines.
- the invention relates to the use of a lubricant composition as defined above for reducing the fuel consumption of 4-stroke marine engines.
- the reduction in fuel consumption is in particular evaluated by testing on a marine engine test bench or by evaluation of the coefficient of traction on a machine, in particular on a mini traction machine (MTM).
- MTM mini traction machine
- the invention also relates to the use of at least one alkoxylated fatty amine in a lubricant composition for 2-stroke or 4-stroke marine engines comprising at least one base oil, at least one hydrogenated styrene-isoprene copolymer and at least one detergent, for improving the engine cleanliness of 4-stroke or 2-stroke marine engines, preferably the cleanliness of the crankcase of 4-stroke or 2-stroke marine engines.
- the engine cleanliness is in particular evaluated by the continuous ECBT and continuous fuel ECBT methods.
- the compounds as defined above contained in the lubricant composition according to the invention can be incorporated in the lubricant composition as separate additives, in particular by the separate addition of the latter to the base oils.
- a subject of the invention is also a composition of the additives-concentrate type comprising:
- a subject of the invention is also a composition of the additives-concentrate type comprising:
- composition of the additives-concentrate type can comprise:
- composition of the additives-concentrate type can comprise:
- At least one oil base can be added to the composition of the additives-concentrate type according to the invention in order to obtain a lubricant composition according to the invention.
- Another subject of the invention relates to a method for lubricating a 4-stroke or 2-stroke marine engine, said method comprising at least one step of bringing the engine into contact with the lubricant composition as described previously or obtained from the composition of the additives-concentrate type as described previously.
- Another subject of the invention relates to a method for reducing the fuel consumption of a 4-stroke or 2-stroke marine engine comprising at least one step of bringing a mechanical part of the engine into contact with the lubricant composition as defined above or obtained from the composition of the additives-concentrate type as defined above.
- the heat resistance of lubricant compositions according to the invention is evaluated by implementation of the continuous ECBT test, thus simulating the engine cleanliness in the presence of such compositions.
- the content of 13.70% of overbased detergent in the composition L 1 corresponds to a content of 8% of overbased detergent in the presence of ethoxylated oleic monoamine, this content making it possible to obtain a stable composition and being able to be evaluated.
- compositions L 1 to L 5 are described in Table II.
- Composition L 2 comprises no hydrogenated styrene-isoprene copolymer, which explains the drop in the viscosity index and the increase in kinematic viscosity.
- compositions L 1 to L 5 were therefore evaluated by means of the continuous ECBT test, whereby the mass of deposits (in mg) generated under defined conditions is measured. The lower this mass, the better the heat resistance and therefore the better the engine cleanliness.
- This test simulates an engine piston heated to a high temperature, onto which the lubricant originating from the crankcase is sprayed.
- the test utilizes aluminium beakers which simulate the shape of pistons. These beakers were placed in a glass container maintained at a controlled temperature of the order of 60° C.
- the lubricant was placed in these containers, themselves equipped with a wire brush, partially immersed in the lubricant. This brush was rotated at a speed of 1000 rpm, which creates a spray of lubricant onto the lower surface of the beaker.
- the beaker was maintained at a temperature of 310° C. by an electrical heating resistance, regulated by a thermocouple.
- the test had a duration of 12 hours and the spraying of lubricant was continuous. This procedure makes it possible to simulate the formation of deposits in the piston-ring assembly. The result is the weight of deposits measured on the beaker.
- compositions according to the invention have good heat resistance and thus make it possible to improve engine cleanliness.
- the lubricant compositions have improved heat resistance with respect to lubricant compositions comprising a hydrogenated styrene-isoprene copolymer alone.
- the lubricant compositions according to the invention retain good heat resistance, despite the presence of the hydrogenated styrene-isoprene copolymer which is known for its very poor heat resistance.
- the heat resistance of lubricant compositions according to the invention under severe conditions in the presence of fuel is evaluated by the implementation of the continuous ECBT fuel test, thus simulating engine cleanliness in the presence of such compositions under severe conditions.
- the continuous ECBT fuel test simulates an engine piston heated to high temperature, onto which the lubricant originating from the crankcase is sprayed.
- the lubricant has been polluted with heavy fuel (2.5% m/m with respect to the quantity of lubricant) in order to simulate the pollution of an engine lubricant with residues and unburned substances from the fuel following combustion.
- the equipment is identical to that of the continuous ECBT test of Example 1.
- the lubricant mixed with the heavy fuel was placed in the glass container maintained at a temperature of approximately 60° C.
- the metal beaker was maintained at a temperature of 250° C., the test had a duration of 12 hours and the spraying of the lubricant was continued throughout these 12 hours.
- compositions according to the invention have good heat resistance, and thus make it possible to retain good engine cleanliness, even under severe conditions, in particular in the presence of heavy fuel.
- the lubricant compositions have improved heat resistance under severe conditions, with respect to lubricant compositions comprising a hydrogenated styrene-isoprene copolymer alone.
- the lubricant compositions according to the invention retain good heat resistance under severe conditions, despite the presence of the hydrogenated styrene-isoprene copolymer which is known for its very poor heat resistance under such conditions.
- the fuel consumption economy properties achieved by the use of lubricant compositions according to the invention were determined by simulation, by evaluating the coefficient of traction on a mini traction machine (MTM) according to the method described below. The tests were carried out on a PCS MTM machine in contact with an ultra-polished 10006 ball (AISI 52100 standard steel) with a diameter equal to 19.05 mm against a flat disc having the same material and surface state characteristics as the balls.
- MTM mini traction machine
- the measured coefficient of traction allows effective prediction of the gain in fuel consumption with a lubricant composition; the lower the coefficient of traction, the better the gain in fuel consumption.
- compositions L 1 to L 4 were evaluated according to the above method; the results representing the coefficient of traction of each composition are summarized in Table V.
- the reference lubricant and composition L 4 were evaluated.
- Example 3 The results confirm the results of Example 3, in that the lubricant composition L 4 according to the invention makes it possible to reduce the fuel consumption of a marine engine.
- the above examples show that the lubricant compositions according to the invention have both good heat resistance, and therefore make it possible to increase the engine cleanliness, while significantly reducing the fuel consumption.
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Abstract
The present invention relates to a lubricant composition for a marine engine, in particular for a four-stroke or two-stroke marine engine, comprising at least one base oil, at least one alkoxylated fatty amine, at least one hydrogenated styrene-isoprene copolymer and at least one detergent.
Description
- The present invention relates to the field of lubricants, and more particularly to the field of lubricants for a marine engine, in particular for a four-stroke or two-stroke marine engine, preferentially for a four-stroke marine engine. More particularly, the present invention relates to a lubricant composition comprising at least one base oil, at least one alkoxylated fatty amine, at least one hydrogenated styrene-isoprene copolymer and at least one detergent. The lubricant composition according to the invention simultaneously has good fuel economy properties and good engine cleanliness properties, in particular crankcase cleanliness. The present invention also relates to a method for reducing the fuel consumption of a vessel utilizing this lubricant composition.
- The present invention also relates to a composition of the additives-concentrate type comprising at least one alkoxylated fatty amine, at least one hydrogenated styrene-isoprene copolymer and at least one detergent.
- In the automotive field, due to environmental concerns, it is increasingly sought to reduce pollutant emissions and achieve fuel economies. The nature of engine lubricants for automobiles has an influence on these two phenomena. This is why so-called “fuel-eco” engine lubricants for automobiles have been developed. It is mainly the quality of the lubricant bases, alone or in combination with polymers improving the viscosity index and/or friction-modifying additives, which give the lubricant its “fuel-eco” properties. The fuel economies generated by means of “fuel-eco” engine lubricants are essentially achieved during cold starts, when the engine has not yet reached stabilized mode, and not at high temperature in stabilized mode. In general, gains in fuel efficiency in the NEDC (New
- European Driving Cycle) according to European Directive 70/220/EEC are 5% at low temperature (urban cycle) and 1.5% at high temperature (extra-urban cycle) with average gains of 2.5%.
- Now, in the field of marine lubricants, marine engines operate at a steady speed, and there are very few cold starts. Thus, the “fuel-eco” solutions suited to automobile engines are not suited to marine engines. In particular the fuel efficiency obtained in the automotive field cannot be obtained in the marine field.
- Moreover, the formulation of a “fuel-eco” lubricant must not be detrimental to the lubricant's other performances. In particular, wear-resistance, demulsification, neutralizing ability, and engine cleanliness (piston and/or crankcase) should not be impaired.
- Document FR 2 974 111 describes a cylinder lubricant for a two-stroke marine engine comprising at least one overbased detergent, at least one neutral detergent and at least one alkoxylated fatty amine having a BN (Base Number) determined according to the ASTM D-2896 standard ranging from 100 to 600 milligrams of potassium hydroxide per gram of amine. However, this document neither describes nor suggests the presence of a hydrogenated styrene-isoprene copolymer. Furthermore, this document gives no indication of fuel economy properties or heat-resistance properties under severe conditions, in particular in the presence of fuel.
- It would therefore be desirable to have available a lubricant for a marine engine which allows satisfactory reductions in fuel consumption, while maintaining the lubricant's other performances, in particular engine cleanliness, more specifically the cleanliness of the crankcase.
- It would also be desirable to have available a lubricant for a marine engine exhibiting good heat resistance under severe conditions of use, and more particularly in the presence of fuel. In fact, during the combustion of the fuel within the engine, combustion residues and unburned substances can pollute the lubricant and thus impair its heat resistance and detergent properties.
- An objective of the present invention is to provide a lubricant composition that overcomes all or part of the aforementioned drawbacks.
- Another objective of the invention is to provide a lubricant composition the formulation of which is easy to implement. Another objective of the present invention is to provide a lubrication method allowing fuel economies.
- A subject of the invention is thus a lubricant composition for a 4-stroke or 2-stroke marine engine comprising:
-
- a) at least one base oil,
- b) at least one alkoxylated fatty amine,
- c) at least one hydrogenated styrene-isoprene copolymer,
- d) at least one detergent.
- Surprisingly, the applicant found that it was possible to formulate lubricant compositions for marine engines making it possible to reduce the consumption of fuel, while maintaining or even improving engine cleanliness, in particular crankcase cleanliness, with respect to standard lubricant compositions for marine engines. This is made possible by means of a lubricant composition comprising at least one base oil, at least one alkoxylated fatty amine, at least one hydrogenated styrene-isoprene copolymer and at least one detergent.
- Thus, the present invention makes it possible to formulate lubricant compositions for a 4-stroke or 2-stroke marine engine, making it possible to combine both engine cleanliness and gains in fuel economies.
- Advantageously, the lubricant compositions according to the invention have an improved heat resistance under severe conditions, and more particularly in the presence of fuel.
- Advantageously, the lubricant compositions according to the invention have an improved stability on storage, as well as a viscosity that varies very little or not at all over time.
- In an embodiment, the invention relates to a lubricant composition for a 4-stroke or 2-stroke marine engine comprising:
-
- a) at least one base oil,
- b) at least one alkoxylated fatty amine,
- c) at least one hydrogenated styrene-isoprene copolymer,
- d) at least one detergent,
- e) at least one dispersant.
- In an embodiment, the lubricant composition essentially consists of:
-
- a) at least one base oil,
- b) at least one alkoxylated fatty amine,
- c) at least one hydrogenated styrene-isoprene copolymer,
- d) at least one detergent.
- In an embodiment, the lubricant composition essentially consists of:
-
- a) at least one base oil,
- b) at least one alkoxylated fatty amine,
- c) at least one hydrogenated styrene-isoprene copolymer,
- d) at least one detergent,
- e) at least one dispersant.
- The invention also relates to a trunk piston engine oil (TPEO) comprising a lubricant composition as defined above.
- By TPEO oil according to the invention, is meant any oily composition intended for lubricating 4-stroke marine engines, in particular the crankcase and cylinders.
- The invention also relates to an cylinder oil comprising a lubricant composition as defined above.
- By cylinder oil according to the invention, is meant any oily composition intended for lubricating the cylinders of 2-stroke marine engines.
- The invention also relates to an system oil comprising a lubricant composition as defined above.
- By system oil according to the invention, is meant any oily composition intended for lubricating the bottom part of 2-stroke marine engines, in particular the crankcase and crankshafts.
- The invention also relates to the use of a lubricant composition as defined above for lubricating a 4-stroke or 2-stroke marine engine.
- The invention also relates to the use of a lubricant composition as defined above for reducing the fuel consumption of a 4-stroke or 2-stroke marine engine.
- The invention also relates to the use of at least one alkoxylated fatty amine in a lubricant composition for 2-stroke or 4-stroke marine engines comprising at least one base oil, at least one hydrogenated styrene-isoprene copolymer and at least one detergent, for improving the engine cleanliness of 4-stroke or 2-stroke marine engines, preferably the cleanliness of the crankcase of 4-stroke or 2-stroke marine engines.
- The invention also relates to a composition of the additives-concentrate type comprising:
-
- at least one alkoxylated fatty amine,
- at least one hydrogenated styrene-isoprene copolymer,
- at least one detergent.
- The invention also relates to a method for lubricating a 4-stroke or 2-stroke marine engine comprising at least one step of bringing the engine into contact with a lubricant composition as defined above or obtained from the composition of the additives-concentrate type as described previously.
- The invention also relates to a method for reducing the fuel consumption of 4-stroke or 2-stroke marine engines comprising at least one step of bringing a mechanical part of the engine into contact with a lubricant composition as defined above or obtained from the composition of the additives-concentrate type as defined above.
- The percentages indicated below correspond to percentages of active material.
- Alkoxylated Fatty Amine
- The lubricant composition comprises at least one alkoxylated fatty amine. By alkoxylated fatty amine is meant, within the meaning of the present invention, a molecule comprising at least one amine function substituted with at least one alkyl group and at least one alkylene oxide group.
- In an embodiment, the alkyl group can be chosen from the C8-030 alkyl groups, preferably C10-C24, more preferentially C12-C22 and even more preferentially C16-C20.
- In an embodiment, the alkylene oxide group can be chosen from the (C2-C10)-alkylene oxide groups, preferably (C2-C4)-alkylene and more preferentially (C2-C3)-alkylene.
- According to the invention, the alkoxylated fatty amine is chosen from the alkoxylated fatty monoamines or the alkoxylated fatty polyamines.
- In an embodiment, the alkoxylated fatty amine can be chosen from the alkoxylated fatty monoamines or the alkoxylated fatty diamines comprising one or more fatty aliphatic chains, preferably comprising a C8-C30 alkyl group, more preferentially a C10-C24 alkyl group, even more preferentially a C12-C22 alkyl group and advantageously a C16-C20 alkyl group.
- These compounds, which have an intrinsic basicity and therefore an intrinsic BN, thus contribute to the BN of the lubricant compositions according to the invention. In an embodiment, the intrinsic BN of the alkoxylated fatty amines used in the lubricant composition according to invention, measured according to the ASTM D-2896 standard, can range from 100 to 600 milligrams of potassium hydroxide per gram of alkoxylated fatty amine, preferentially from 100 to 500 milligrams of potassium hydroxide per gram of alkoxylated fatty amine, more preferentially from 100 to 300 milligrams of potassium hydroxide per gram of alkoxylated fatty amine.
- Alkoxylated fatty amine can be considered as a cationic-type surfactant the polar head of which is constituted by at least one nitrogen atom and by at least one oxygen atom provided by the alkoxylation and the lipophilic part of which is constituted by the fatty aliphatic chain(s).
- Thus, in an embodiment, the polar head of the alkoxylated fatty amine can be constituted by amine functions a short distance from one another (typically separated by 2 to 3 carbon atoms), and preferentially restricted in number (typically one or two amine functions), and preferentially alkoxylated with a limited number of alkylene oxide functions, typically between 1 and 15, preferentially between 2 and 10, more preferentially between 3 and 7, even more preferentially between 3 and 4. Advantageously, the alkylene oxide group can be chosen from the (C2-C4)-alkylene oxide groups. This makes it possible to constitute a “compact” polar head, and therefore to confer a surfactant nature on these alkoxylated fatty amines.
- The alkoxylated fatty amine can be obtained by known alkoxylation methods, for example described in the application FR 2 094 182, by bringing at least one fatty amine into contact with at least one alkylene oxide, at temperatures for example comprised between 100 and 200° C., in the presence of a basic catalyst such as NaOH, KOH or NaOCH3. The starting fatty amine is mainly obtained from carboxylic acids. These acids are dehydrated in the presence of ammonia in order to produce nitriles, which then undergo catalytic hydrogenation in order to produce primary, secondary or tertiary amines.
- The starting fatty amine is obtained from carboxylic acids, preferably from fatty acids. By fatty acid is meant, within the meaning of the invention, a carboxylic acid with a saturated or unsaturated aliphatic chain, comprising from 8 to 30 carbon atoms, preferably from 10 to 24 carbon atoms, more preferentially from 12 to 22 carbon atoms and even more preferentially from 16 to 20 carbon atoms.
- In an embodiment, in order to obtain fatty amines, the starting fatty acids can be chosen from caprylic, pelargonic, capric, undecylenic, lauric, tridecylenic, myristic, pentadecylic, palmitic, margaric, stearic, nonadecylic, arachic, heneicosanoic, behenic, tricosanoic, lignoceric, pentacosanoic, cerotic, heptacosanoic, montanic, nonacosanoic, melissic, hentriacontanoic, laceroic acids or unsaturated fatty acids such as palmitoleic, oleic, erucic, nervonic, linoleic, α-linolenic, γ-linolenic, di-homo-y-linolenic, arachidonic, eicosapentaenoic or docosahexanoic acid.
- In a preferred embodiment, the alkoxylated fatty amine is obtained from fatty acids comprising from 10 to 24 carbon atoms, preferably from 12 to 22 carbon atoms, more preferentially from 16 to 20 carbon atoms and even more preferentially from 16 to 18 carbon atoms.
- In an embodiment, the fatty acids can originate from the hydrolysis of the triglycerides present in vegetable and animal oils, such as coconut, palm, olive, peanut, rapeseed, sunflower, soya, cotton, linseed oil or beef tallow. The natural oils may have been genetically modified so as to enrich their content of certain fatty acids, for example rapeseed oil or oleic sunflower oil.
- Advantageously, the fatty amine used for preparing the alkoxylated fatty amine present in the lubricant composition according to the invention is obtained from natural, vegetable or animal resources. The treatments making it possible to produce fatty amines starting from natural oils can lead to mixtures of primary, secondary and tertiary monoamines, and polyamines. It is for example possible to use, for preparing the alkoxylated fatty amine present in the lubricant composition according to the invention, products containing, in variable proportions, all or some of the fatty amines corresponding to the following formulae:
-
R1NH2, -
R1—NH—R2, -
R1—NHCH2—R2, -
R1—[NH(CH2)3]2—NH2, -
R1—[NH(CH2)r]s—NH2, - in which:
-
- s represents an integer greater than or equal to 1, preferentially ranging from 1 to 12, more preferentially from 1 to 5, advantageously from 1 to 2;
- r represents an integer ranging from 2 to 3;
- R1 and R2, identical or different, independently represent a fatty chain originating from the fatty acid(s), originating from the oil used as starting reagent.
- A fatty monoamine or polyamine can contain several fatty chains originating from different fatty acids.
- It is also possible to use these products in the purified form, predominantly containing a single type of amine, for example predominantly monoamines or predominantly diamines.
- In an embodiment, a product constituted by primary monoamines of formula R1NH2 will be used, wherein R1 can represent a plurality of fatty acids originating from a natural resource, for example tallow fat, or soya oil, or coconut oil, or (oleic) sunflower oil.
- A product constituted by diamines of formula R1—[NH(CH2)3]—NH2, will thus be advantageously used, wherein R1 can represent a plurality of fatty acids originating from a natural resource, for example tallow fat, or soya oil, or coconut oil, or (oleic) sunflower oil.
- It is also possible to use purified products. For example, amines obtained from oleic acid are advantageously used, in particular primary monoamines of formula R1NH2 or diamines of formula R1—[NH(CH2)3]—NH2wherein R1 is the fatty chain of oleic acid.
- In an embodiment, the alkoxylated fatty amine present in the lubricant composition according to the invention is soluble in the base oil matrix.
- The solubility of the alkoxylated fatty amine is initially due to its fatty chain(s). It is also all the more soluble as it comprises a limited number of alkylene oxide functions.
- In an embodiment of the invention, the alkoxylated fatty amine is all the more soluble as it comprises no more than 15 alkylene oxide functions per amine molecule, preferably no more than 10 alkylene oxide functions, more preferentially no more than 7 alkylene oxide functions and even more preferentially no more than 4 alkylene oxide functions.
- Moreover, the applicant found that an alkoxylated fatty amine where the nitrogen atoms are ternary (where there is no longer any N-H bond) is easier to solubilize.
- In an embodiment of the invention, the alkoxylated fatty amine is chosen from the monoamines comprising a ternary nitrogen.
- The alkoxylated fatty amine present in the lubricant composition according to the invention is therefore all the more effective, as it is well dispersed or even solubilized in the oil matrix.
- Thus, in an embodiment, the alkoxylated fatty amine present in the lubricant composition according to the invention is not present in the form of an emulsion or a microemulsion, but in dispersed form, or even solubilized in the oil matrix.
- Advantageously, the alkoxylated fatty amine comprises at least one aliphatic chain comprising at least 8 carbon atoms, preferably at least 10 carbon atoms, preferentially at least 12 carbon atoms, preferentially at least 14 carbon atoms, more preferentially at least 16 carbon atoms, advantageously from 16 to 20 carbon atoms.
- In an embodiment of the invention, the lubricant composition according to the invention can comprise at least one alkoxylated fatty amine of formula (I):
- in which:
-
- R3 represents an alkane-di-yl group comprising from 2 to 10 carbon atoms;
- R4 represents a linear or branched, saturated or unsaturated, alkyl group comprising from 12 to 22 carbon atoms;
- R5 represents an alkane-di-yl group comprising from 1 to 10 carbon atoms;
- m represents an integer ranging from 0 to 12;
- n represents an integer ranging from 0 to 12;
- p represents an integer ranging from 0 to 12;
- q represents 0 or 1;
- the sum m+n+p is strictly greater than 0, preferably 1<m+n+p<15, preferentially 2<m+n+p<10, more preferentially 3<m+n+p<7, advantageously 3<m+n+p<4.
- In a preferred embodiment of the invention, the lubricant composition according to the invention can comprise at least one alkoxylated fatty amine of formula (I) in which:
-
- R3 represents an alkane-di-yl group comprising from 2 to 4 carbon atoms, preferably from 2 to 3 carbon atoms;
- R4 represents a linear or branched, saturated or unsaturated, alkyl group comprising from 16 to 20 carbon atoms;
- R5 represents an alkane-di-yl group comprising from 2 to 4 carbon atoms;
- m represents 0, 1, 2, 3, 4 or 5;
- n represents 0, 1, 2, 3, 4 or 5;
- p represents 0, 1, 2, 3, 4 or 5;
- q represents 0 or 1;
- the sum m+n+p represents an integer ranging from 1 to 15, preferentially from 2 to 10, more preferentially from 3 to 7, advantageously from 3 to 4.
- Advantageously, the alkoxylated fatty amine is chosen from the compounds of formula (Ia):
- in which:
-
- R3 represents an alkane-di-yl group comprising from 2 to 4 carbon atoms, preferably from 2 to 3 carbon atoms;
- R4 represents a linear or branched, saturated or unsaturated, alkyl group comprising from 16 to 20 carbon atoms;
- m represents 0, 1 or 2;
- n represents 0, 1 or 2;
- the sum m+n represents an integer ranging from 1 to 4, preferably from 2 to 4.
- Even more advantageously, the alkoxylated fatty amine is a compound of formula (la) in which:
-
- R3 represents a —(CH2CH2)— group,
- R4 represents a linear or branched mono-unsaturated alkyl group comprising from 16 to 18 carbon atoms,
- m represents 0, 1 or 2;
- n represents 0, 1 or 2;
- the sum m+n represents 2.
- As an example of an alkoxylated fatty amine according to the invention, the product Ethomeen 0/12 marketed by the Akzo Nobel company can be mentioned.
- In an embodiment of the invention, the content by weight of alkoxylated fatty amine ranges from 0.1 to 10%, preferably from 1 to 9%, advantageously from 2 to 8% with respect to the total weight of the lubricant composition.
- Hydrogenated Styrene-Isoprene Copolymer
- The lubricant composition according to the invention comprises at least one hydrogenated styrene-isoprene copolymer.
- In an embodiment of the invention, the hydrogenated styrene-isoprene copolymer can be chosen from straight-chain hydrogenated styrene-isoprene copolymers or star-shaped hydrogenated styrene-isoprene copolymers (also called “star polymers”), preferably chosen from the star-shaped hydrogenated styrene-isoprene copolymers.
- In an embodiment of the invention, the hydrogenated styrene-isoprene copolymer can be chosen from the hydrogenated styrene-isoprene block copolymers or the hydrogenated styrene-isoprene random copolymers.
- Advantageously, the hydrogenated styrene-isoprene copolymer has a content of hydrogenated isoprene units, ranging from 50% to 98%, preferably from 60% to 98%, more preferentially from 70% to 97%, even more preferentially from 75% to 96% by mass, with respect to the mass of hydrogenated styrene-isoprene copolymer.
- Advantageously, the hydrogenated styrene-isoprene copolymer has a content of styrene units ranging from 2% to 50%, preferably from 2% to 40%, more preferentially from 3% to 30%, even more preferentially from 4% to 25% by mass with respect to the mass of hydrogenated styrene-isoprene copolymer.
- In an embodiment of the invention, the hydrogenated styrene-isoprene copolymer according to the invention has a weight-average molecular weight Mw ranging from 100,000 to 800,000 daltons, preferably from 200,000 to 700,000 daltons, more preferentially from 300,000 to 600,000 daltons, even more preferentially from 400,000 to 500,000 daltons.
- In an embodiment of the invention, the hydrogenated styrene-isoprene copolymer according to the invention has a number-average molecular weight Mn ranging from 50,000 to 800,000 daltons, preferably from 75,000 to 600,000, more preferentially from 100,000 to 500,000, even more preferentially from 100,000 to 200,000.
- In an embodiment of the invention, the hydrogenated styrene-isoprene copolymer according to the invention has a polydispersity index ranging from 1 to 4, preferably from 1.2 to 3.5, more preferentially from 1.5 to 3.5, even more preferentially from 2 to 3.
- As examples of hydrogenated styrene-isoprene copolymers according to the invention, the products Shellvis 300 or Shellvis 301 marketed by the Infineum company can be mentioned.
- In an embodiment of the invention, the content by weight of hydrogenated styrene-isoprene copolymer in the lubricant composition according to the invention is from 0.1% to 15% by mass, with respect to the total mass of the lubricant composition, preferably from 0.1% to 10%, more preferentially from 0.2% to 5%, advantageously from 0.5 to 2%. By this quantity is meant a quantity of active polymer material. In fact, the hydrogenated styrene-isoprene copolymer used in the context of the present invention can be presented in the form of a dispersion in a mineral or synthetic oil, and more particularly in an oil of Group I according to the API classification.
- Detergent
- The lubricant composition according to the invention comprises at least one detergent.
- In an embodiment, the detergent used in the lubricant composition according to the invention can be chosen from the detergents commonly used in lubricant compositions.
- The detergent commonly used in the formulation of lubricant compositions is typically an anionic compound comprising a long lipophilic hydrocarbon-containing chain and a hydrophilic head. The associated cation is typically a metallic cation of an alkali or alkaline-earth metal.
- In an embodiment of the invention, the detergent can be chosen from the alkali or alkaline-earth metal salts of carboxylic acids, sulphonates, salicylates, naphthenates, and phenates alone or in a mixture. The detergents are named according to the nature of the hydrophobic chain, carboxylate, sulphonate, salicylate, naphthenate or phenate.
- In an embodiment of the invention, the alkali and alkaline-earth metals are chosen from calcium, magnesium, sodium or barium, preferentially calcium.
- In an embodiment of the invention, the detergent can be chosen from the non-overbased (or neutral) detergents or overbased detergents.
- The term non-overbased or “neutral” detergents is used when the metallic salts contain the metal in an approximately stoichiometric quantity with respect to the anionic group(s) of the detergent.
- The term overbased detergents is used when the metal is in excess (in a quantity greater than the stoichiometric quantity with respect to the anionic group(s) of the detergent). The metal in excess providing the overbased character to the detergent is presented in the form of metallic salts that are insoluble in oil. The overbased detergents are presented in the form of micelles. These detergents constituted by metallic salts that are soluble in oil thus stabilize the insoluble metallic salts, by maintaining them in suspension in the lubricant composition.
- These micelles can contain one or more types of insoluble metallic salts, stabilized by one or more types of detergents. The overbased detergents will be referred to as of mixed type if the micelles comprise several types of detergents which differ from each other in the nature of their hydrophobic chain.
- Advantageously, the detergent is chosen from the alkali and alkaline-earth metal salicylates, carboxylates, sulphonates and/or phenates, alone or in a mixture, preferentially from the calcium salicylates, sulphonates and/or phenates.
- The detergent present in the lubricant composition according to the invention can also be chosen from the non-metallic and non-overbased detergents.
- In an embodiment, the detergent is chosen from the amine- and borate-containing compounds. In an embodiment, the detergent can be an amine- and borate-containing compound originating from the reaction between an alkylated derivative of salicylic acid and a dialkoxylated amine, in the presence of boric acid.
- The detergent can thus be obtained by implementation of the method described in document WO 2007/081494.
- In an embodiment, the detergent can be chosen from the amine- and borate-containing derivatives of salicylic acid.
- In a preferred embodiment, the detergent is a compound of formula (II)
- in which:
-
- R5 represents a linear or branched alkyl group comprising from 2 to 30 carbon atoms, preferably from 5 to 20 carbon atoms, advantageously from 15 to 20 carbon atoms;
- R6 represents a linear or branched alkyl group comprising from 2 to 30 carbon atoms, preferably from 5 to 20 carbon atoms, advantageously from 12 to 20 carbon atoms;
- R7 represents a linear or branched alkyl group comprising from 2 to 30 carbon atoms, preferably from 5 to 20 carbon atoms, advantageously from 12 to 20 carbon atoms;
- r is an integer ranging from 1 to 100.
- Advantageously, the R6 and R7 groups are identical and both represent a linear or branched alkyl group comprising from 12 to 20 carbon atoms.
- In a preferred embodiment of the invention, the detergent is chosen from alkali or alkaline-earth metal salicylates or phenates, alone or in a mixture.
- Advantageously, the detergent is chosen from calcium salicylates or calcium phenates, alone or in a mixture.
- In another preferred embodiment, the detergent is a mixture of an alkali or alkaline-earth metal salicylate and of a compound of formula (II).
- In another preferred embodiment, the detergent is a mixture of an alkali or alkaline-earth metal phenate and of a compound of formula (II).
- In another preferred embodiment, the detergent is a mixture of an alkali or alkaline-earth metal phenate, an alkali or alkaline-earth metal salicylate and a compound of formula (II).
- Advantageously, the combination of a compound of formula (II) and an alkali or alkaline-earth metal phenate and/or salicylate makes it possible to enhance the heat resistance of the lubricant composition according to the invention, in particular under severe conditions, and more particularly in the presence of fuel.
- In an embodiment of the invention, the content by weight of detergents in the lubricant composition according to the invention ranges from 1% to 20%, preferentially from 1% to 15%, more preferentially from 2% to 10% with respect to the total weight of the lubricant composition.
- The BN of the lubricant compositions according to the present invention is provided by the alkoxylated fatty amine and by the detergent(s).
- The BN value of the lubricant compositions according to the present invention, measured according to the ASTM D-2896 standard, can vary from 5 to 100 mg of KOH/g of lubricant composition, preferably from 7 to 80 mg of KOH/g of lubricant composition, more preferentially from 10 to 60 mg of KOH/g of lubricant composition. The BN value is chosen depending on the conditions of use of the lubricant compositions and in particular according to the sulphur content of the fuel used.
- Thus for fuels with a high sulphur content (in the range of 0.2% to 4.5% by weight), the BN value is significant and preferably comprised between 20 and 80 mg of KOH/g of lubricant composition, more preferentially between 30 and 65 mg of KOH/g of lubricant composition. For fuels with a low sulphur content (in the range of 0.05% to 0.2% by weight), the BN value is low and preferably comprised between 5 and 20 mg of KOH/g of lubricant composition, more preferentially between 10 and 15 mg of KOH/g of lubricant composition.
- Base Oils
- In general, the base oils used for the formulation of lubricant compositions according to the invention can be chosen from oils of mineral, synthetic or vegetable origin as well as mixtures thereof.
- The mineral or synthetic oils generally used in the marine engine oil application belong to one of the classes defined in the API classification as summarized in the table below.
-
Saturates Sulphur Viscosity index content content (VI) Group I Mineral oils <90% >0.03% 80 ≦ VI < 120 Group II ≧90% ≦0.03% 80 ≦ VI < 120 Hydrocracked oils Group III ≧90% ≦0.03% ≧120 Hydro-isomerized oils Group IV Poly-alpha-Olefins (PAO) Group V Other bases not included in bases of Groups I to IV - The mineral oils of Group I can be obtained by distillation of selected naphthenic or paraffinic crude oils, then by purification of these distillates by methods such as solvent extraction, solvent or catalytic dewaxing, hydrotreating or hydrogenation. The mineral bases of Group I are for example the bases called Neutral Solvent (such as for example 150NS, 330NS, 500NS or 600NS) or Brightstock.
- The oils of Groups II and III are obtained by more stringent purification methods, for example a combination of hydrotreating, hydrocracking, hydrogenation and catalytic dewaxing. Examples of synthetic bases of Groups IV and V include the poly-alpha olefins, polybutenes, polyisobutenes and alkylbenzenes.
- These base oils can be used alone or in a mixture. A mineral oil can be combined with a synthetic oil.
- In a preferred embodiment of the invention, the lubricant base oil is chosen from the base oils of Group I or Group II, alone or in a mixture.
- In an embodiment of the invention, the lubricant composition according to the invention can be characterized by a viscosity grade of SAE-20, SAE-30, SAE-40, SAE-50 or SAE-60 according to the SAEJ300 classification.
- Grade 20 oils have a kinematic viscosity at 100° C. comprised between 5.6 and 9.3 cSt.
- Grade 30 oils have a kinematic viscosity at 100° C. comprised between 9.3 and 12.5 cSt.
- Grade 40 oils have a kinematic viscosity at 100° C. comprised between 12.5 and 16.3 cSt.
- Grade 50 oils have a kinematic viscosity at 100° C. comprised between 16.3 and 21.9 cSt.
- Grade 60 oils have a kinematic viscosity at 100° C. comprised between 21.9 and 26.1 cSt.
- The kinematic viscosity is measured according to the ASTM D7279 standard at 100° C.
- In a preferred embodiment, the lubricant composition according to the invention has a kinematic viscosity measured according to the ASTM D7279 standard at 100° C. comprised between 5.6 and 26.1 cSt, preferably between 9.3 and 21.9 cSt, more preferentially between 12.5 and 16.3 cSt.
- In an embodiment of the invention, the content by weight of base oil in the lubricant composition according to the invention is from 30% to 90%, preferably from 40% to 90%, more preferentially from 50% to 85%, advantageously from 65 to 85% with respect to the total weight of the lubricant composition.
- In an embodiment, the lubricant composition is not presented in the form of an emulsion.
- In an embodiment, the lubricant composition according to the invention is presented in the form of an anhydrous composition.
- Other Additives
- In an embodiment, the lubricant composition according to the invention can also comprise a dispersant.
- The dispersants are well-known additives used in the formulation of lubricant compositions, in particular for application in the marine field. Their first role is to keep in suspension the particles originally present or appearing in the lubricant composition during its use in the engine. They prevent their agglomeration by acting on the steric hindrance. They can also have a synergistic effect on the neutralization.
- The dispersants used as lubricant additives typically contain a polar group, associated with a relatively long hydrocarbon-containing chain, generally containing from 50 to 400 carbon atoms. The polar group typically contains at least one nitrogen, oxygen or phosphorus element.
- In an embodiment of the invention, the dispersant can be chosen from the succinic acid derivatives. By succinic acid derivatives is meant, within the meaning of the invention, the succinic acid esters or succinic acid amide esters.
- Preferably, the dispersant is chosen from the compounds comprising at least one succinimide group.
- These compounds can be then treated with various compounds, in particular sulphur, oxygen, formaldehyde, carboxylic acids and compounds containing boron or zinc in order to produce, for example, borated succinimides or zinc-blocked succinimides.
- In a preferred embodiment of the invention, the dispersant is chosen from the borated compounds comprising at least one succinimide group.
- In a preferred embodiment of the invention, the dispersant can be chosen from the borated compounds comprising at least one substituted succinimide group or the borated compounds comprising at least two substituted succinimide groups, the succinimide groups being able to be linked at their vertex bearing a nitrogen atom, by a polyamine group.
- By substituted succinimide group within the meaning of the present invention, is meant a succinimide group at least one of the vertices of which is substituted with a hydrocarbon group comprising from 8 to 400 carbon atoms.
- Advantageously, the dispersant is chosen from the borated compounds comprising at least one succinimide group substituted with a polyisobutene group.
- Advantageously, the dispersant is chosen from the borated compounds comprising at least two succinimide groups each substituted with a polyisobutene group.
- More advantageously, the dispersant is chosen from the borated compounds comprising at least two succinimide groups each substituted with a polyisobutene group and characterized by:
-
- A number molecular weight of the polyisobutene greater than 2000 Daltons, preferably ranging from 2000 to 5000 Daltons, advantageously from 2000 to 3000 Daltons,
- A content by mass of the element boron greater than or equal to 0.35% with respect to the total mass of the dispersant.
- As an example of a dispersant additive according to the invention, the product T161B from the Tianhe company can be mentioned.
- Mannich bases, obtained by polycondensation of phenols substituted with alkyl groups, formaldehyde and primary or secondary amines, can also be used as dispersants in the lubricant composition according to the invention.
- In an embodiment of the invention, the content by weight of dispersant is at least 0.1%, preferably from 0.1% to 10%, advantageously from 1% to 6% with respect to the total weight of the lubricant composition.
- In addition to the compounds as described above, the lubricant composition according to the invention can comprise at least one additional additive, in particular chosen from those commonly used by a person skilled in the art.
- In an embodiment, the additional additive can be chosen from anti-wear additives, antioxidants, additional polymers improving the viscosity index, pour point improvers, anti-foaming agents, thickeners and mixtures thereof.
- The anti-wear additives protect the friction surfaces by the formation of a protective film adsorbed on these surfaces. A great variety of anti-wear additives exists. The phosphorus- and sulphur-containing additives, such as the metallic alkylthiophosphates, in particular the zinc alkylthiophosphates, and more specifically the zinc dialkyldithiophosphates (or ZnDTP) can thus be mentioned. The alkyl groups of these zinc dialkyldithiophosphates, preferentially comprise from 1 to 18 carbon atoms. The amine phosphates, the polysulphides, in particular the sulphur-containing olefins, are also commonly used anti-wear additives. Anti-wear additives of the nitrogen- and sulphur-containing type, such as for example metallic dithiocarbamates, in particular molybdenum dithiocarbamate are also encountered. The preferred anti-wear additive is ZnDTP.
- The content by weight of anti-wear additive in the lubricant according to the invention is from 0.1% to 5%, preferably from 0.2% to 4%, more preferentially from 0.2% to 2% with respect to the total weight of the lubricant composition.
- By additional polymers improving the viscosity index according to the invention, is meant any polymer improving the viscosity index other than the hydrogenated styrene-isoprene copolymer according to the invention.
- These additional polymers improving the viscosity index can be chosen from the polymer esters, olefin copolymers (OCP) or polymethacrylates (PMA).
- The anti-foaming additives can be chosen from the polar polymers such as polymethylsiloxanes or polyacrylates.
- These additives are generally present in a content by weight of 0.01 to 3% with respect to the total weight of the lubricant composition.
- A subject of the invention is also a lubricant composition for a 4-stroke or 2-stroke marine engine comprising:
-
- from 30 to 90% of at least one base oil,
- from 0.1 to 10% of at least one alkoxylated fatty amine,
- from 0.1 to 15% of at least one hydrogenated styrene-isoprene copolymer,
- from 1 to 20% of at least one detergent.
- In an embodiment, the lubricant composition essentially consists of:
-
- from 30 to 90% of at least one base oil,
- from 0.1 to 10% of at least one alkoxylated fatty amine,
- from 0.1 to 15% of at least one hydrogenated styrene-isoprene copolymer,
- from 1 to 20% of at least one detergent.
- All the characteristics and preferences presented for the base oil, the alkoxylated fatty amine, the hydrogenated styrene-isoprene copolymer and the detergent also apply to the above lubricant compositions.
- A subject of the invention is also a lubricant composition for a 4-stroke or 2-stroke marine engine comprising:
-
- from 30 to 90% of at least one base oil,
- from 0.1 to 10% of at least one alkoxylated fatty amine,
- from 0.1 to 15% of at least one hydrogenated styrene-isoprene copolymer,
- from 1 to 20% of at least one detergent,
- from 0.1 to 10% of at least one dispersant.
- In an embodiment, the lubricant composition essentially consists of:
-
- from 30 to 90% of at least one base oil,
- from 0.1 to 10% of at least one alkoxylated fatty amine,
- from 0.1 to 15% of at least one hydrogenated styrene-isoprene copolymer,
- from 1 to 20% of at least one detergent,
- from 0.1 to 10% of at least one dispersant.
- All the characteristics and preferences presented for the base oil, the alkoxylated fatty amine, the hydrogenated styrene-isoprene copolymer, the detergent and the dispersant also apply to the above lubricant compositions.
- The lubricant composition according to the invention can be used in 4-stroke or 2-stroke marine engines.
- In a preferred embodiment, the lubricant composition is used in high-speed or medium-speed 4-stroke engines, which operate with distillates and bunker fuels or heavy fuel respectively. The fuel economy applies in particular to the distillates used in high-speed 4-stroke engines. High-speed 4-stroke engines are used for the propulsion of small vessels and as electricity generating units on board larger vessels. Medium-speed 4-stroke engines are used for the propulsion of numerous vessels, such as cargo ships, tankers, ferries, or even certain container ships. They can moreover be used as electricity generating units on board large vessels or in diesel electricity generating stations.
- In particular, the lubricant composition is appropriate for 4-stroke engines as trunk piston oil (TPEO).
- In particular, the lubricant composition is appropriate for 2-stroke engines as system oil or cylinder oil.
- Thus a subject of the invention is also the use of a lubricant composition as defined above for the lubrication of 4-stroke or 2-stroke marine engines.
- In a preferred embodiment, the invention relates to the use of a lubricant composition as defined above for the lubrication of 4-stroke marine engines. All the characteristics and preferences presented for the lubricant composition apply to the above use.
- The invention also relates to the use of a lubricant composition as defined above for reducing the fuel consumption of 4-stroke or 2-stroke marine engines.
- In a preferred embodiment, the invention relates to the use of a lubricant composition as defined above for reducing the fuel consumption of 4-stroke marine engines.
- The reduction in fuel consumption is in particular evaluated by testing on a marine engine test bench or by evaluation of the coefficient of traction on a machine, in particular on a mini traction machine (MTM).
- All the characteristics and preferences presented for the lubricant composition apply to the above use.
- The invention also relates to the use of at least one alkoxylated fatty amine in a lubricant composition for 2-stroke or 4-stroke marine engines comprising at least one base oil, at least one hydrogenated styrene-isoprene copolymer and at least one detergent, for improving the engine cleanliness of 4-stroke or 2-stroke marine engines, preferably the cleanliness of the crankcase of 4-stroke or 2-stroke marine engines.
- The engine cleanliness is in particular evaluated by the continuous ECBT and continuous fuel ECBT methods.
- All the characteristics and preferences presented for the base oil, the alkoxylated fatty amine, the hydrogenated styrene-isoprene copolymer and the detergent also apply to the above use.
- The compounds as defined above contained in the lubricant composition according to the invention, and more particularly the alkoxylated fatty amine, the hydrogenated styrene-isoprene copolymer, the detergent and optionally the dispersant, can be incorporated in the lubricant composition as separate additives, in particular by the separate addition of the latter to the base oils.
- However, they can also be incorporated in an additives concentrate for a marine lubricant composition.
- Thus, a subject of the invention is also a composition of the additives-concentrate type comprising:
-
- at least one alkoxylated fatty amine,
- at least one hydrogenated styrene-isoprene copolymer,
- at least one detergent.
- All the characteristics and preferences presented for the alkoxylated fatty amine, the hydrogenated styrene-isoprene copolymer and the detergent also apply to the above composition.
- A subject of the invention is also a composition of the additives-concentrate type comprising:
-
- at least one alkoxylated fatty amine,
- at least one hydrogenated styrene-isoprene copolymer,
- at least one detergent,
- at least one dispersant.
- All the characteristics and preferences presented for the alkoxylated fatty amine, the hydrogenated styrene-isoprene copolymer, the detergent and the dispersant also apply to the composition above.
- In an embodiment, the composition of the additives-concentrate type can comprise:
-
- from 0.5 to 50% of at least one alkoxylated fatty amine,
- from 1.5 to 25% of at least one hydrogenated styrene-isoprene copolymer,
- from 2.5 to 25% of at least one detergent; % by weight with respect to the total weight of the composition of the additives-concentrate type.
- In another embodiment, the composition of the additives-concentrate type can comprise:
-
- from 0.5 to 50% of at least one alkoxylated fatty amine,
- from 1.5 to 25% of at least one hydrogenated styrene-isoprene copolymer,
- from 2.5 to 25% of at least one detergent,
- from 2 to 40% of at least one dispersant; % by weight with respect to the total weight of the composition of the additives-concentrate type.
- In an embodiment of the invention, at least one oil base can be added to the composition of the additives-concentrate type according to the invention in order to obtain a lubricant composition according to the invention.
- Another subject of the invention relates to a method for lubricating a 4-stroke or 2-stroke marine engine, said method comprising at least one step of bringing the engine into contact with the lubricant composition as described previously or obtained from the composition of the additives-concentrate type as described previously.
- All the characteristics and preferences presented for the lubricant composition or for the composition of the additives-concentrate type also apply to the lubrication method according to the invention.
- Another subject of the invention relates to a method for reducing the fuel consumption of a 4-stroke or 2-stroke marine engine comprising at least one step of bringing a mechanical part of the engine into contact with the lubricant composition as defined above or obtained from the composition of the additives-concentrate type as defined above.
- All the characteristics and preferences presented for the lubricant composition or for the composition of the additives-concentrate type also apply to the method for reducing the fuel consumption according to the invention.
- The different subjects of the present invention and implementation thereof will be better understood on reading the following examples. These examples are given by way of indication, without being limitative.
- The heat resistance of lubricant compositions according to the invention is evaluated by implementation of the continuous ECBT test, thus simulating the engine cleanliness in the presence of such compositions.
- To this end, different lubricant compositions were prepared from the following compounds:
-
- Group I base oils, in particular referred to as Neutral Solvent 150NS, 330NS or 600NS, with a viscosity at 40° C. of 30 cSt, 66 cSt and 120 cSt respectively, measured according to the ASTM D7279 standard,
- a hydrogenated styrene-isoprene (HSI) copolymer having a star-shaped conformation, diluted to 9% of active material in a Group I base oil (Shellvis 301 marketed by the Infineum company),
- an ethoxylated oleic monoamine (Ethomeen O/12 marketed by the AKZO NOBEL company),
- an overbased detergent based on calcium phenates and calcium salicylates and dispersed at 25% of active material in an oil,
- a non-metallic and non-overbased detergent of formula (II) as described previously in which:
- R5 represents a C18H37 group,
- R6 and R7 both represent a C16H33 group,
- r represents an integer ranging from 1 to 100,
- a dispersant of the borated compound type comprising at least one succinimide group substituted with a polyisobutene group (T161B marketed by the Tianhe company)
- an anti-wear additive of the zinc dithiophosphate type,
- a silicone-containing anti-foaming additive.
- The different lubricant compositions L1 to L5 are described in Table I; the percentages indicated correspond to percentages by mass.
-
TABLE I L1 L2 L3 L4 L5 (compar- (compar- (inven- (inven- (inven- Compositions ative) ative) tion) tion) tion) Base oils 78.28 83.08 77.58 75.88 76.38 Anti-wear 0.5 0.5 0.5 0.5 0.5 additive Anti-foaming 0.02 0.02 0.02 0.02 0.02 additive Overbased 13.70 8 8 8 8 detergent Hydrogenated 7.5 7.5 7.5 7.5 styrene- isoprene copolymer Ethoxylated 6.4 6.4 6.4 3.2 oleic monoamine Non-metallic 4.4 and non- overbased detergent Dispersant 2 1.7 - The content of 13.70% of overbased detergent in the composition L1 corresponds to a content of 8% of overbased detergent in the presence of ethoxylated oleic monoamine, this content making it possible to obtain a stable composition and being able to be evaluated.
- The physico-chemical characteristics of compositions L1 to L5 are described in Table II.
-
TABLE II L1 L2 L3 L4 L5 (compar- (compar- (inven- (inven- (inven- Compositions ative) ative) tion) tion) tion) Kinematic 13.68 13.61 13.98 14.36 14.11 viscosity in mm2/s (measured at 100° C. according to the ASTM D7279 standard) Kinematic 101.6 137.7 107 108.3 103 viscosity in mm2/s (measured at 40° C. according to the ASTM D7279 standard) Viscosity 135 93.6 131.6 135 139.3 index (VI) - Composition L2 comprises no hydrogenated styrene-isoprene copolymer, which explains the drop in the viscosity index and the increase in kinematic viscosity.
- The heat resistance of compositions L1 to L5 was therefore evaluated by means of the continuous ECBT test, whereby the mass of deposits (in mg) generated under defined conditions is measured. The lower this mass, the better the heat resistance and therefore the better the engine cleanliness.
- This test simulates an engine piston heated to a high temperature, onto which the lubricant originating from the crankcase is sprayed.
- The test utilizes aluminium beakers which simulate the shape of pistons. These beakers were placed in a glass container maintained at a controlled temperature of the order of 60° C.
- The lubricant was placed in these containers, themselves equipped with a wire brush, partially immersed in the lubricant. This brush was rotated at a speed of 1000 rpm, which creates a spray of lubricant onto the lower surface of the beaker. The beaker was maintained at a temperature of 310° C. by an electrical heating resistance, regulated by a thermocouple.
- In the continuous ECBT test, the test had a duration of 12 hours and the spraying of lubricant was continuous. This procedure makes it possible to simulate the formation of deposits in the piston-ring assembly. The result is the weight of deposits measured on the beaker.
- A detailed description of this test is given in the publication entitled “Research and Development of Marine Lubricants in ELF ANTAR France—The relevance of laboratory tests in simulating field performance” by Jean-Philippe ROMAN, MARINE PROPULSION CONFERENCE 2000—AMSTERDAM—29-30 MARCH 2000.
- The results are summarized in Table III below.
-
TABLE III L1 L2 L3 L4 L5 (compar- (compar- (inven- (inven- (inven- Compositions ative) ative) tion) tion) tion) Continuous 506 172 350 286 386 ECBT (mg) - The results show that the compositions according to the invention have good heat resistance and thus make it possible to improve engine cleanliness.
- It is to be noted that the lubricant compositions have improved heat resistance with respect to lubricant compositions comprising a hydrogenated styrene-isoprene copolymer alone.
- It is also to be noted that the lubricant compositions according to the invention retain good heat resistance, despite the presence of the hydrogenated styrene-isoprene copolymer which is known for its very poor heat resistance.
- The heat resistance of lubricant compositions according to the invention under severe conditions in the presence of fuel is evaluated by the implementation of the continuous ECBT fuel test, thus simulating engine cleanliness in the presence of such compositions under severe conditions.
- As for the continuous ECBT test, the continuous ECBT fuel test simulates an engine piston heated to high temperature, onto which the lubricant originating from the crankcase is sprayed.
- The lubricant has been polluted with heavy fuel (2.5% m/m with respect to the quantity of lubricant) in order to simulate the pollution of an engine lubricant with residues and unburned substances from the fuel following combustion.
- The equipment is identical to that of the continuous ECBT test of Example 1.
- The lubricant mixed with the heavy fuel was placed in the glass container maintained at a temperature of approximately 60° C. The metal beaker was maintained at a temperature of 250° C., the test had a duration of 12 hours and the spraying of the lubricant was continued throughout these 12 hours.
- The results are described in Table IV and correspond to the weight of deposit measured on the metal beaker. The lower this mass, the better the heat resistance and therefore the better the engine cleanliness under severe conditions.
-
TABLE IV L1 L2 L3 L4 L5 (compar- (compar- (inven- (inven- (inven- Compositions ative) ative) tion) tion) tion) Continuous 223 43 147 129 124 fuel ECBT (mg) - The results show that the compositions according to the invention have good heat resistance, and thus make it possible to retain good engine cleanliness, even under severe conditions, in particular in the presence of heavy fuel.
- It is to be noted that the lubricant compositions have improved heat resistance under severe conditions, with respect to lubricant compositions comprising a hydrogenated styrene-isoprene copolymer alone.
- It is also to be noted that the lubricant compositions according to the invention retain good heat resistance under severe conditions, despite the presence of the hydrogenated styrene-isoprene copolymer which is known for its very poor heat resistance under such conditions.
- The fuel consumption economy properties achieved by the use of lubricant compositions according to the invention were determined by simulation, by evaluating the coefficient of traction on a mini traction machine (MTM) according to the method described below. The tests were carried out on a PCS MTM machine in contact with an ultra-polished 10006 ball (AISI 52100 standard steel) with a diameter equal to 19.05 mm against a flat disc having the same material and surface state characteristics as the balls.
- The following conditions were determined based on their being representative of the engine operation in the PRL (Piston Ring Liner) zone, the PRL zone being the zone of the engine in which most of the friction occurs and therefore the zone in which the gain in fuel efficiency can be maximized:
-
- load on the ball of 25N,
- drive speed of 2 m/s,
- SRR (slide-roll ratio) of 100%, this ratio being equivalent to the slide speed/roll speed ratio,
- temperature of 100° C.
- Thus, under these conditions, the measured coefficient of traction allows effective prediction of the gain in fuel consumption with a lubricant composition; the lower the coefficient of traction, the better the gain in fuel consumption.
- Compositions L1 to L4 were evaluated according to the above method; the results representing the coefficient of traction of each composition are summarized in Table V.
-
TABLE V L1 L2 L3 L4 (compar- (compar- (inven- (inven- Compositions ative) ative) tion) tion) Coefficient of 0.039 0.036 0.034 0.035 traction - The results show that the coefficient of traction for the lubricant compositions according to the invention are lower than those obtained with a lubricant composition comprising only a hydrogenated styrene-isoprene copolymer alone or an alkoxylated fatty amine alone.
- Thus, these results show that the lubricant compositions according to the invention can allow a significant gain in fuel consumption.
- The fuel economy properties of the lubricant compositions according to the invention were validated by a test carried out on a test bench equipped with a MAN 5L16/24 engine. The particular characteristics of this engine have been described in the publication entitled “INNOVATOR-4C, The cutting-edge MAN B&W 5L16/24 test engine”, by D. Lancon, V. Doyen and J. Christensen, CIMAC Congress 2004, KYOTO (Paper 124).
- A dedicated steady speed procedure has been developed for measuring the “fuel eco” properties of the lubricant compositions according to the following description. This procedure makes use of equipment usually found in engine test bench centres:
-
- Rinsing the engine and lubrication circuits with the candidate lubricant,
- Running-in of the engine with the candidate lubricant,
- Measurement of the consumption of distillate-type fuel oil (Marine Diesel Oil—according to the IS08217 specification). The measurements are repeated so as to ensure accuracy,
- The fuel oil consumptions obtained with the candidate lubricant are compared with those obtained when a reference lubricant is tested under the same conditions,
- The operating conditions of the engine are:
- Speed: 1000 rpm,
- Power output: 100%, 75% and 25% of the maximum power,
- Temperature of the lubricant at the engine inlet: 68-70° C.,
- Volume of lubricant: 2×200 litres,
- The tests are organized according to a precise protocol which consists of ensuring that any test carried out with a candidate lubricant is preceded and followed by tests carried out with the reference lubricant. This makes it possible to guarantee the operating stability of the engine as well as the statistically significant character of the differences in consumption measured between lubricants,
- In the present case, the reference lubricant is a commercial oil for medium-speed engines with a viscosity grade of SAE40 and BN of 30.
- The reference lubricant and composition L4 were evaluated.
- The results, representing the gain in fuel consumption for the different engine loads tested, are summarized in Table VI.
-
TABLE VI Gain in fuel Reference L4 consumption (%) lubricant (invention) At 100% engine load 0 0.69 At 75% engine load 0 0.79 At 25% engine load 0 1.74 - The results confirm the results of Example 3, in that the lubricant composition L4 according to the invention makes it possible to reduce the fuel consumption of a marine engine.
- It is to be noted that this gain remains significant even when the engine load increases.
- Thus, the above examples show that the lubricant compositions according to the invention have both good heat resistance, and therefore make it possible to increase the engine cleanliness, while significantly reducing the fuel consumption.
Claims (21)
1.-20. (canceled)
21. Lubricant composition for a 4-stroke or 2-stroke marine engine, comprising:
a) at least one base oil,
b) at least one alkoxylated fatty amine,
c) at least one hydrogenated styrene-isoprene copolymer,
d) at least one detergent.
22. Lubricant composition according to claim 21 in which the alkoxylated fatty amine is obtained from fatty acids comprising from 10 to 24 carbon atoms.
23. Lubricant composition according to claim 21 comprising at least one alkoxylated fatty amine of formula (I)
in which:
R3 represents an alkane-di-yl group comprising from 2 to 10 carbon atoms;
R4 represents a linear or branched, saturated or unsaturated, alkyl group comprising from 12 to 22 carbon atoms;
R5 represents an alkane-di-yl group comprising from 1 to 10 carbon atoms;
m represents an integer ranging from 0 to 12;
n represents an integer ranging from 0 to 12;
p represents an integer ranging from 0 to 12;
q represents 0 or 1;
the sum m+n+p is strictly greater than 0.
24. Lubricant composition according to claim 23 in which:
R3 represents an alkane-di-yl group comprising from 2 to 4 carbon atoms;
R4 represents a linear or branched, saturated or unsaturated, alkyl group comprising from 16 to 20 carbon atoms;
R5 represents an alkane-di-yl group comprising from 2 to 4 carbon atoms;
m represents 0, 1, 2, 3, 4 or 5;
n represents 0, 1, 2, 3, 4 or 5;
p represents 0, 1, 2, 3, 4 or 5;
q represents 0 or 1;
the sum m+n+p represents an integer ranging from 1 to 15.
25. Lubricant composition according to claim 21 comprising at least one alkoxylated fatty amine of formula (Ia):
in which:
R3 represents an alkane-di-yl group comprising from 2 to 4 carbon atoms;
R4 represents a linear or branched, saturated or unsaturated, alkyl group comprising from 16 to 20 carbon atoms;
m represents 0, 1 or 2;
n represents 0, 1 or 2;
the sum m+n represents an integer ranging from 1 to 4.
26. Lubricant composition according to claim 21 in which the hydrogenated styrene-isoprene copolymer has a content of hydrogenated isoprene units ranging from 50% to 98% with respect to the mass of hydrogenated styrene-isoprene copolymer.
27. Lubricant composition according to claim 21 in which the hydrogenated styrene-isoprene copolymer has a content of styrene units ranging from 2% to 50% with respect to the mass of hydrogenated styrene-isoprene copolymer.
28. Lubricant composition according to claim 21 in which the detergent is chosen from the alkali or alkaline-earth metal salicylates or phenates, alone or in a mixture.
29. Lubricant composition according to claim 28 in which the detergent is chosen from calcium salicylates or calcium phenates, alone or in a mixture.
30. Lubricant composition according to claim 21 also comprising a dispersant.
31. Lubricant composition according to claim 30 in which the dispersant is chosen from the compounds comprising at least one succinimide group.
32. Lubricant composition according to claim 30 in which the dispersant is chosen from the borated compounds comprising at least one succinimide group.
33. Lubricant composition according to claim 21 in which the base oil is chosen from the base oils of Group I or Group II, alone or in a mixture.
34. Lubricant composition according to claim 21 , also comprising at least one additional additive chosen from anti-wear additives, antioxidants, additional polymers improving the viscosity index, pour point improvers, anti-foaming agents, thickeners and mixtures thereof.
35. Lubricant composition according to claim 21 having a BN determined according to the ASTM D-2896 standard, from 5 to 100 mg of KOH/g of lubricant composition.
36. Lubricant composition according to claim 21 having a kinematic viscosity measured according to the ASTM D7279 standard at 100° C. comprised between 5.6 and 26.1 cSt.
37. Lubricant composition according to claim 21 having a BN determined according to the ASTM D-2896 standard, from 7 to 80 mg of KOH/g of lubricant composition.
38. Lubricant composition according to claim 21 having a kinematic viscosity measured according to the ASTM D7279 standard at 100° C. comprised between 9.3 and 21.9 cSt.
39. Method for reducing the fuel consumption of 4-stroke or 2-stroke marine engines, comprising adding a lubricant composition according to claim 21 into the marine engines.
40. Method for improving the engine cleanliness of 4-stroke or 2-stroke marine engines, comprising adding at least one alkoxylated fatty amine in a lubricant composition for 2-stroke or 4-stroke marine engines comprising at least one base oil, at least one hydrogenated styrene-isoprene copolymer and at least one detergent.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1352010A FR3002947B1 (en) | 2013-03-06 | 2013-03-06 | LUBRICATING COMPOSITION FOR MARINE ENGINE |
| FR1352010 | 2013-03-06 | ||
| PCT/EP2014/054280 WO2014135596A1 (en) | 2013-03-06 | 2014-03-05 | Lubricating composition for a marine engine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20160017251A1 true US20160017251A1 (en) | 2016-01-21 |
Family
ID=48521266
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US14/772,997 Abandoned US20160017251A1 (en) | 2013-03-06 | 2014-03-05 | Lubricating composition for a marine engine |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20160017251A1 (en) |
| EP (1) | EP2964736A1 (en) |
| CN (1) | CN105339477A (en) |
| AR (1) | AR094986A1 (en) |
| FR (1) | FR3002947B1 (en) |
| WO (1) | WO2014135596A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11572526B2 (en) | 2016-10-07 | 2023-02-07 | Total Marketing Services | Lubricating composition for a marine engine or a stationary engine |
| CN116496565A (en) * | 2023-05-10 | 2023-07-28 | 焦作铁路电缆有限责任公司 | Environment-friendly flame-retardant water-blocking anti-corrosion filling paste and preparation method and application thereof |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3257919B1 (en) * | 2016-06-17 | 2020-08-19 | Total Marketing Services | Lubricant polymers |
| FR3164220A1 (en) * | 2024-07-05 | 2026-01-09 | Totalenergies Onetech | USE OF ESTERS TO IMPROVE THE CLEANLINESS OF MARINE ENGINES |
| FR3164221A1 (en) | 2024-07-05 | 2026-01-09 | Totalenergies Onetech | LUBRICANT COMPOUND FOR 4-STROKE MARINE ENGINES |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3763044A (en) * | 1969-12-12 | 1973-10-02 | W Anderson | Block copolymers as viscosity index improvers for lubricating oils |
| US20110030648A1 (en) * | 2007-12-12 | 2011-02-10 | The Lubrizol Corporation | Marine Diesel Cylinder Lubricants for Fuel Efficiency |
| WO2012140215A1 (en) * | 2011-04-14 | 2012-10-18 | Total Raffinage Marketing | Cylinder lubricant for a two-stroke marine engine |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999018175A1 (en) * | 1997-10-03 | 1999-04-15 | Infineum Usa Lp | Lubricating compositions |
| US6333298B1 (en) * | 1999-07-16 | 2001-12-25 | Infineum International Limited | Molybdenum-free low volatility lubricating oil composition |
| US6715473B2 (en) * | 2002-07-30 | 2004-04-06 | Infineum International Ltd. | EGR equipped diesel engines and lubricating oil compositions |
| CN101945981A (en) * | 2008-12-05 | 2011-01-12 | 卢布里佐尔公司 | Be used for the marine diesel cylinder lubrication agent of improved fuel efficiency |
-
2013
- 2013-03-06 FR FR1352010A patent/FR3002947B1/en not_active Expired - Fee Related
-
2014
- 2014-03-05 US US14/772,997 patent/US20160017251A1/en not_active Abandoned
- 2014-03-05 CN CN201480012445.XA patent/CN105339477A/en active Pending
- 2014-03-05 AR ARP140100702A patent/AR094986A1/en unknown
- 2014-03-05 WO PCT/EP2014/054280 patent/WO2014135596A1/en not_active Ceased
- 2014-03-05 EP EP14709909.7A patent/EP2964736A1/en not_active Withdrawn
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3763044A (en) * | 1969-12-12 | 1973-10-02 | W Anderson | Block copolymers as viscosity index improvers for lubricating oils |
| US20110030648A1 (en) * | 2007-12-12 | 2011-02-10 | The Lubrizol Corporation | Marine Diesel Cylinder Lubricants for Fuel Efficiency |
| WO2012140215A1 (en) * | 2011-04-14 | 2012-10-18 | Total Raffinage Marketing | Cylinder lubricant for a two-stroke marine engine |
| US20140041610A1 (en) * | 2011-04-14 | 2014-02-13 | Total Marketing Services | Cylinder lubricant for a two-stroke marine engine |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11572526B2 (en) | 2016-10-07 | 2023-02-07 | Total Marketing Services | Lubricating composition for a marine engine or a stationary engine |
| CN116496565A (en) * | 2023-05-10 | 2023-07-28 | 焦作铁路电缆有限责任公司 | Environment-friendly flame-retardant water-blocking anti-corrosion filling paste and preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2964736A1 (en) | 2016-01-13 |
| AR094986A1 (en) | 2015-09-09 |
| FR3002947B1 (en) | 2016-03-25 |
| FR3002947A1 (en) | 2014-09-12 |
| CN105339477A (en) | 2016-02-17 |
| WO2014135596A1 (en) | 2014-09-12 |
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