EP2304006B1 - Zylinderschmiermittel für einen zweitakt-schiffsmotor - Google Patents
Zylinderschmiermittel für einen zweitakt-schiffsmotor Download PDFInfo
- Publication number
- EP2304006B1 EP2304006B1 EP09766015.3A EP09766015A EP2304006B1 EP 2304006 B1 EP2304006 B1 EP 2304006B1 EP 09766015 A EP09766015 A EP 09766015A EP 2304006 B1 EP2304006 B1 EP 2304006B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lubricant
- cylinder
- milligrams
- per gram
- detergents
- 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.)
- Active
Links
- 239000000314 lubricant Substances 0.000 title claims description 247
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 140
- 150000001412 amines Chemical class 0.000 claims description 127
- 239000003599 detergent Substances 0.000 claims description 104
- 229910052751 metal Inorganic materials 0.000 claims description 63
- 239000002184 metal Substances 0.000 claims description 63
- 229940072033 potash Drugs 0.000 claims description 56
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 56
- 235000015320 potassium carbonate Nutrition 0.000 claims description 56
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 53
- 239000003921 oil Substances 0.000 claims description 43
- 239000000295 fuel oil Substances 0.000 claims description 39
- 150000003839 salts Chemical class 0.000 claims description 38
- 150000001875 compounds Chemical class 0.000 claims description 29
- 239000002199 base oil Substances 0.000 claims description 27
- 230000007935 neutral effect Effects 0.000 claims description 23
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 18
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 16
- -1 alkaline-earth metal carbonates Chemical class 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 230000001050 lubricating effect Effects 0.000 claims description 12
- 239000000344 soap Substances 0.000 claims description 12
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 10
- 239000011575 calcium Substances 0.000 claims description 10
- 229910052791 calcium Inorganic materials 0.000 claims description 10
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 10
- 239000000194 fatty acid Substances 0.000 claims description 10
- 229930195729 fatty acid Natural products 0.000 claims description 10
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 9
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 9
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 9
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 9
- 150000004665 fatty acids Chemical class 0.000 claims description 9
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 8
- 239000005642 Oleic acid Substances 0.000 claims description 8
- 150000004985 diamines Chemical class 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 8
- 229910052749 magnesium Inorganic materials 0.000 claims description 8
- 239000003513 alkali Substances 0.000 claims description 7
- 150000005323 carbonate salts Chemical class 0.000 claims description 7
- 229920000768 polyamine Polymers 0.000 claims description 7
- 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 claims description 6
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 6
- 229910052788 barium Inorganic materials 0.000 claims description 6
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 238000002485 combustion reaction Methods 0.000 claims description 6
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 6
- 150000003873 salicylate salts Chemical class 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- 239000011734 sodium Substances 0.000 claims description 6
- 230000008719 thickening Effects 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 125000005609 naphthenate group Chemical group 0.000 claims description 5
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 5
- 239000003760 tallow Substances 0.000 claims description 5
- 150000007942 carboxylates Chemical class 0.000 claims description 4
- 238000005260 corrosion Methods 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 4
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 4
- 229920000742 Cotton Polymers 0.000 claims description 3
- 235000010469 Glycine max Nutrition 0.000 claims description 3
- 244000020551 Helianthus annuus Species 0.000 claims description 3
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 3
- 235000015278 beef Nutrition 0.000 claims description 3
- 230000007797 corrosion Effects 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- 150000002889 oleic acids Chemical class 0.000 claims description 3
- 235000003441 saturated fatty acids Nutrition 0.000 claims description 3
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 3
- 241001133760 Acoelorraphe Species 0.000 claims description 2
- 235000017060 Arachis glabrata Nutrition 0.000 claims description 2
- 244000105624 Arachis hypogaea Species 0.000 claims description 2
- 235000010777 Arachis hypogaea Nutrition 0.000 claims description 2
- 235000018262 Arachis monticola Nutrition 0.000 claims description 2
- 244000068988 Glycine max Species 0.000 claims description 2
- 244000299507 Gossypium hirsutum Species 0.000 claims description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 2
- 240000007817 Olea europaea Species 0.000 claims description 2
- 235000020778 linoleic acid Nutrition 0.000 claims description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims description 2
- 235000020232 peanut Nutrition 0.000 claims description 2
- 239000005864 Sulphur Substances 0.000 claims 5
- 240000002791 Brassica napus Species 0.000 claims 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 claims 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 claims 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 description 54
- 239000011593 sulfur Substances 0.000 description 54
- 235000019198 oils Nutrition 0.000 description 44
- 239000000203 mixture Substances 0.000 description 38
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 36
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 35
- 239000012141 concentrate Substances 0.000 description 31
- 238000006386 neutralization reaction Methods 0.000 description 28
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 27
- 239000000654 additive Substances 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 18
- 229910000019 calcium carbonate Inorganic materials 0.000 description 17
- 235000010216 calcium carbonate Nutrition 0.000 description 16
- 239000002253 acid Substances 0.000 description 12
- 239000002585 base Substances 0.000 description 12
- 238000009472 formulation Methods 0.000 description 12
- 239000007866 anti-wear additive Substances 0.000 description 11
- 239000010727 cylinder oil Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 239000002270 dispersing agent Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 239000000446 fuel Substances 0.000 description 9
- 239000000693 micelle Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 8
- 235000021313 oleic acid Nutrition 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 7
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 6
- 239000013538 functional additive Substances 0.000 description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 description 6
- 238000005461 lubrication Methods 0.000 description 6
- 239000011707 mineral Substances 0.000 description 6
- 235000010755 mineral Nutrition 0.000 description 6
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 6
- 229960001860 salicylate Drugs 0.000 description 6
- 241000209504 Poaceae Species 0.000 description 5
- 229920002367 Polyisobutene Polymers 0.000 description 5
- 229910002092 carbon dioxide Inorganic materials 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 230000035484 reaction time Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 5
- 239000011701 zinc Substances 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
- 238000010348 incorporation Methods 0.000 description 4
- 239000003879 lubricant additive Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical group O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 235000019484 Rapeseed oil Nutrition 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 238000004364 calculation method Methods 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 235000019197 fats Nutrition 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 150000003335 secondary amines Chemical class 0.000 description 3
- 150000003871 sulfonates Chemical class 0.000 description 3
- 229910052815 sulfur oxide Inorganic materials 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 239000005069 Extreme pressure additive Substances 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 230000001687 destabilization Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229940082150 encore Drugs 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000004530 micro-emulsion Substances 0.000 description 2
- 238000005457 optimization Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920013639 polyalphaolefin Polymers 0.000 description 2
- 229920001083 polybutene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 2
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 2
- KWTWDQCKEHXFFR-SMDDNHRTSA-N tapentadol Chemical compound CN(C)C[C@H](C)[C@@H](CC)C1=CC=CC(O)=C1 KWTWDQCKEHXFFR-SMDDNHRTSA-N 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 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
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 241000273930 Brevoortia tyrannus Species 0.000 description 1
- 101100037762 Caenorhabditis elegans rnh-2 gene Proteins 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- SYNHCENRCUAUNM-UHFFFAOYSA-N Nitrogen mustard N-oxide hydrochloride Chemical class Cl.ClCC[N+]([O-])(C)CCCl SYNHCENRCUAUNM-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- BTHAQRDGBHUQMR-UHFFFAOYSA-N [S]P(=O)=O Chemical compound [S]P(=O)=O BTHAQRDGBHUQMR-UHFFFAOYSA-N 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 125000004429 atom Chemical group 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
- 229910052796 boron Inorganic materials 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- ZMRQTIAUOLVKOX-UHFFFAOYSA-L calcium;diphenoxide Chemical compound [Ca+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 ZMRQTIAUOLVKOX-UHFFFAOYSA-L 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 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
- 150000002148 esters Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 239000010763 heavy fuel oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000013528 metallic particle 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
- 238000012544 monitoring process Methods 0.000 description 1
- TUFJPPAQOXUHRI-KTKRTIGZSA-N n'-[(z)-octadec-9-enyl]propane-1,3-diamine Chemical compound CCCCCCCC\C=C/CCCCCCCCNCCCN TUFJPPAQOXUHRI-KTKRTIGZSA-N 0.000 description 1
- NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- MWMPEAHGUXCSMY-UHFFFAOYSA-N pentacosanoic acid Chemical class CCCCCCCCCCCCCCCCCCCCCCCCC(O)=O MWMPEAHGUXCSMY-UHFFFAOYSA-N 0.000 description 1
- 125000002958 pentadecyl 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])[H] 0.000 description 1
- 150000002989 phenols Chemical group 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 229920006112 polar polymer Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000010729 system oil Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 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
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Images
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
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2207/027—Neutral salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/28—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/046—Overbasedsulfonic acid salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/52—Base number [TBN]
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
- C10N2040/26—Two-strokes or two-cycle engines
Definitions
- the present invention relates to a two-cycle marine engine cylinder lubricant for use with both high sulfur and low sulfur fuel oils. It relates more particularly to a lubricant having sufficient neutralization capacity vis-à-vis the sulfuric acid formed during the combustion of high-sulfur fuel oil, while limiting the formation of deposits during the use of fuel oils. low sulfur content.
- the document FR2094182 discloses lubricants containing an anti-rust and anti-corrosion additive based on polyalkoxylated compounds, including a C18 amine.
- the amount of amine used is very small. It is further indicated that carbonate is the compound used to provide the basicity of the lubricant.
- the marine oils used in slow-moving 2-stroke engines are of two types.
- the cylinder oils on the one hand, ensuring the lubrication of the cylinder piston assembly, and the system oils on the other hand, ensuring the lubrication of all moving parts out of the cylinder piston assembly.
- the combustion residues containing acid gases are in contact with the lubricating oil.
- Acid gases are formed from the combustion of fuel oils; they are in particular sulfur oxides (SO 2 , SO 3 ), which are then hydrolysed when in contact with the moisture present in the combustion gases and / or in the oil. This hydrolysis generates sulfurous acid (HSO 3 ) or sulfuric acid (H 2 SO 4 ).
- these acids must be neutralized, which is usually done by reaction with the basic sites included in the lubricant.
- the capacity of neutralization of an oil is measured by its BN or Base Number in English, characterizing its basicity. It is measured according to ASTM D-2896 and is expressed in equivalent weight of potash per gram of oil or mg of KOH / g.
- the BN is a standard criterion for adjusting the basicity of cylinder oils to the sulfur content of the fuel used, in order to neutralize all the sulfur contained in the fuel, and likely to be converted into sulfuric acid by combustion and hydrolysis.
- BN ranging from 5 to 100 mg KOH / g.
- the detergents mainly of the anionic type, are, for example, metal salicylate, phenate, sulphonate or carboxylate soaps which form micelles in which the insoluble metal salt particles are kept in suspension.
- the usual overbased detergents intrinsically have a BN conventionally between 150 and 700 mg KOH per gram of detergent. Their mass percentage is fixed in the lubricant as a function of the level of BN that one wishes to achieve.
- a part of the BN can also be provided by non-overbased or "neutral” detergents with a NO 2 typically of less than 150.
- neutral detergents with a NO 2 typically of less than 150.
- the insoluble metal salts of the overbased detergents for example calcium carbonate, thus contribute significantly to the BN of the usual lubricants. It can be considered that at least 50%, typically 75%, of the BN of the cylinder lubricants is thus provided by these insoluble salts.
- the detergent part itself, or metal soaps, found in both neutral and overbased detergents typically provides the bulk of the BN complement.
- MARPOL Annex 6 (Regulations for the Prevention of air pollution from ships) of the IMO (International Maritime Organization) entered into force in May 2005. It sets a maximum sulfur content of 4.5% m / m of fuel oils. and the creation of Sulfur Oxide Controlled Emission Zones (SOx Emission Control Areas). Vessels entering these areas must use fuel with a maximum sulfur content of 1.5% m / m or other alternative treatment to limit SOx emissions to meet the specified values.
- the notation% m / m denotes the weight percentage of a compound relative to the total weight of fuel oil or lubricating composition in which it is included.
- the switching between these two categories of fuel oil may require adaptation of the operating conditions of the engine, in particular the use of appropriate cylinder lubricants.
- marine lubricants with a BN of about 70 are used.
- marine lubricants with a BN of about 40 are used (this value will in the future be reduced).
- each of these lubricants has limitations of use resulting from the following observations: the use of a BN 70 cylinder lubricant in the presence of a low sulfur fuel oil (1.5% w / w and less) and at fixed lubrication rate, creates a large excess of basic sites (strong BN) and a risk of destabilization of micelles of unused overbased detergents, which contain insoluble metal salts. This destabilization results in the formation of insoluble metal salt deposits and having a high hardness (for example calcium carbonate), mainly on the piston ring, and eventually can lead to a risk of excessive wear polishing shirt.
- a BN 70 cylinder lubricant in the presence of a low sulfur fuel oil (1.5% w / w and less) and at fixed lubrication rate, creates a large excess of basic sites (strong BN) and a risk of destabilization of micelles of unused overbased detergents, which contain insoluble metal salts. This destabilization results in the formation of insoluble metal salt deposits
- the optimization of the cylinder lubrication of a slow 2-stroke engine then requires the selection of the lubricant with the BN adapted to the fuel oil and to the operating conditions of the engine. This optimization reduces the operating flexibility of the engine and requires a high degree of technical skill of the crew in defining the conditions under which the changeover from one type of lubricant to the other must be achieved.
- the object of the present invention is to provide a lubricating oil that can ensure good lubrication of the marine engine cylinder and can withstand the stresses of high sulfur fuel oils and the stresses of low sulfur fuel oils.
- the present invention relates to lubricating formulations having a BN sufficiently high to effectively neutralize the sulfuric acid formed in the use of high sulfur fuel oils, a significant portion of said BN being provided by oil soluble species. do not give rise to metal deposits when they are partially consumed, when using low-sulfur fuel oil.
- the Applicant has found that it is possible to formulate cylinder lubricants where a significant part of BN is provided by oil-soluble fatty amines, while maintaining the level of performance compared to conventional equivalent BN formulations.
- insoluble metal salts also have a favorable antiwear effect provided that they are kept dispersed in the lubricant in the form of stable micelles.
- the Applicant has also found, surprisingly, that in the presence of a significant contribution of BN by said fatty amines, an excessively high intake (greater than 20 mg of potassium hydroxide / gram of lubricant), BN by insoluble metal salts. overbased detergents (typically metalcarbonates) had an adverse effect on the ability of the cylinder lubricants to neutralize.
- the BN supplied by the insoluble metal salts is typically of the order of 30 mg of potash per gram of lubricant.
- the cylinder lubricants according to the present invention are suitable both for the high fuel oils. sulfur content and for low sulfur fuels.
- the alternative BN provided by the oil-soluble fatty amines represents at least 15% preferably at least 30%, preferably at least 50% of the BN of said cylinder lubricant. Or, especially for BN formulas of the order of 55, the BN supplied by the oil-soluble fatty amines represents at least 55%, or at least 60%, or at least 70% of the BN of said lubricant cylinder .
- the present invention provides a cylinder lubricant having a BN determined according to the ASTM D-2896 standard of between 40 and 80 milligrams of potash per gram of lubricant, preferably between 65 and 75, or even more preferably equal to 70 milligrams of potash. per gram of lubricant.
- the BN of the lubricants according to the present invention is between 45 and 60 milligrams of potash per gram of lubricant, preferably between 45 and 55, or even more preferably equal to 50 milligrams of potash per gram of lubricant.
- the BN of the lubricants according to the present invention is between 54 and 60 milligrams of potash per gram of lubricant, preferably equal to 57, or even more preferably equal to 55 milligrams of potash per gram of lubricant.
- the BN of the lubricants according to the present invention is between 40 and 50 milligrams of potash per gram of lubricant, preferably equal to 45 milligrams of potash per gram of lubricant. .
- the oil-soluble fatty amine (s) is (are) obtained from palm, olive, peanut, conventional or oleic rapeseed oil, of conventional or oleic sunflower, soya, cotton, from beef tallow, or palmitic, stearic, oleic, linoleic acid.
- the fatty amines are chosen from amines obtained from fatty acids comprising between 16 and 18 carbon atoms.
- fatty amines containing between 16 and 22 carbon atoms In order to avoid the gellation phenomenon sometimes observed with a high mass content of fatty amines in the lubricant, it will be preferred to work with fatty amines containing between 16 and 22 carbon atoms.
- the fatty amines are mono or polyamines, preferentially diamines.
- they are polyamines corresponding to the general formula R- [NH (CH 2 ) 3 ] n -NH 2 , where n is an integer between 1 and 3, and R represents the fatty chain of fatty acids. saturated or unsaturated compounds containing at least 16 carbon atoms, preferably the fatty chain of oleic acid.
- Particularly preferred diamines of the general formula R-NH (CH 2 ) 3 NH 2 wherein R represents the fatty chain of saturated or unsaturated fatty acids having at least 16 carbon atoms, preferably the fatty chain of the oleic acid.
- fatty amine derivatives according to the present invention which are for example the amine derivatives described above. These derivatives are, for example, chosen from ethoxylated amines having from 1 to 5 ethylene oxide units and oxyamines.
- the overbased and / or neutral detergents are preferably chosen from carboxylates, sulphonates, salicylates, naphthenates, phenates, and mixed detergents combining at least two of these types of detergents.
- these are compounds based on metals selected from the group consisting of calcium, magnesium, sodium or barium, preferably calcium or magnesium.
- insoluble metal salts selected from the group of alkali and alkaline earth metal carbonates, preferentially calcium carbonate.
- detergents provide the complement of BN not provided by oil-soluble fatty amines in the cylinder lubricants according to the invention.
- the weight percentage of overbased detergents relative to the total weight of lubricant is chosen so that the BN supplied by the carbonate metal salts represents a contribution of at least 5 milligrams of potash per gram of lubricant, preferably at least 10 milligrams of potash per gram of lubricant to the total BN of said lubricant cylinder.
- the weight percentage of overbased detergents, and possibly neutral, relative to the total weight of lubricant is chosen so that the organic BN, provided by the detergent metal soaps, represents a contribution of at least 5. milligrams of potash per gram of lubricant, preferably at least 10 milligrams of potash per gram of lubricant, in the cylinder lubricants according to the present invention.
- the lubricant according to the invention comprises from 50 to 90% by weight of base oil, from 4 to 30% by weight of at least one detergent based on alkaline or alkaline earth metals, overbased with metal salts of carbonate, optionally in combination with one or more neutral detergents, and from 2 to 40% by weight, one or more fatty amines as described above.
- the lubricants according to the invention may contain one or more functional additives chosen from dispersant additives, anti-wear additives, anti-foam additives, anti-oxidant and / or anti-rust additives.
- they may contain from 0.01% to 6%, preferably from 0.1% to 4% by weight of one or more antiwear additives.
- They may also contain from 0.1% to 4%, preferably from 0.4% to 2% by weight of a dispersing additive.
- the cylinder lubricants according to the invention preferentially have a kinematic viscosity at 100 ° C. of between 12.5 and 26.1 cSt (SAE 40, 50, 60 grades), preferably between 16.3 and 21.9 cSt (grade SAE 50).
- the cylinder lubricants according to the invention have a kinematic viscosity at 100 ° C. of between 18 and 21.5 cSt, preferably between 19 and 21.5 cSt.
- the cylinder lubricants according to the invention comprise from 60% to 90% relative to the total weight of lubricant a mixture of one or more base oils, belonging to Groups 1 to 5 defined according to the nomenclature of API, preferentially Groups 1 or 2 according to this same nomenclature.
- This mixture of base oils may contain from 10 to 25% by weight, based on the total weight of lubricant, of a BSS type I group base oil (distillation residue, kinematic viscosity at 100 ° C. of 30 mm 2 / s, typically between 28 and 32 mm 2 / s, and of density at 15 ° C between 895 and 915 kg / m3), and from 50 to 70% by weight, relative to the total weight lubricant, a Neutral Solvent group I base oil (distillate, density at 15 ° C between 880 and 900 kg / m3, kinematic viscosity at 100 ° C close to 11 mm 2 / s for the 500 NS, or close to 12 mm 2 / s for the 600NS).
- BSS type I group base oil distillation residue, kinematic viscosity at 100 ° C. of 30 mm 2 / s, typically between 28 and 32 mm 2 / s, and of density at 15
- the base oil or oils are partially or totally substituted with one or more thickening and / or VI-improving polymers.
- the invention relates to the use of a lubricant as described above as a single cylinder lubricant that can be used with any type of fuel oil whose sulfur content is less than 4.5%, preferably of which the Sulfur content is 0.5 to 4% w / w.
- the single-cylinder lubricant according to the invention can be used both with fuel oil with a sulfur content of less than 1.5% w / w and with fuel oil with a sulfur content greater than 3% w / w, or greater than 3.5% m / m.
- the single-cylinder lubricant according to the invention can be used both with fuel oil with a sulfur content of less than 1% w / w and with fuel oil with a sulfur content of more than 3% w / w.
- the invention relates to the use of a lubricant as described above to prevent corrosion and / or reduce the formation of deposit insoluble metal salts in two-stroke marine engines during the combustion of any type of fuel oil with a sulfur content of less than 4.5% m / m.
- the application as filed describes the use of one or more compounds chosen from oil-soluble fatty amines and their derivatives, for example the fatty amines and their derivatives described above, to provide an alternative BN that does not generate any hard metal deposits in cylinder lubricants for two-stroke marine diesel engine having a BN, measured by ASTM D-2896, greater than or equal to 15, preferably greater than 20, preferably greater than 30, advantageously greater than 40 milligrams of potash per gram of lubricant.
- the application as filed discloses a method of manufacturing a lubricant as described above wherein the fatty amine (s) and / or their derivatives are added as a separate component of the cylinder lubricant having a BN determined according to ASTM D- 2896 greater than or equal to 15, preferably greater than 20, preferably greater than 30, advantageously greater than 40 milligrams of potash per gram of lubricant and optionally comprising one or more functional additives.
- the lubricant described in the application as filed is prepared by diluting one or more marine lubricant additive concentrates in which the fatty amine (s) and / or their derivatives are incorporated.
- the application as filed discloses an additive concentrate, for the preparation of cylinder lubricant having a BN determined according to ASTM D-2896 greater than or equal to 15, preferably greater than 20, preferably greater than 30, preferably greater than 30.
- the fatty amines used in the lubricants described in the application as filed are primary, secondary or tertiary monoamines, or polyamines containing one or more aliphatic chains, or their derivatives.
- the intrinsic BN of the fatty amines and derivatives described in the application as filed, measured according to the ASTM D-2896 standard, is typically between 150 and 600 milligrams of potash per gram, preferably between 200 and 500 milligrams of potash per gram.
- surfactants of cationic type whose polar head is constituted by the nitrogen atom, (and possibly by one or more oxygen atoms for the oxyamine derivatives and ethoxylated amines) and the lipophilic part by the one or more aliphatic chains.
- Fatty amines are mainly obtained from carboxylic acids. These acids are dehydrated in the presence of ammonia to give nitriles, which then undergo catalytic hydrogenation to lead to primary, secondary or tertiary amines.
- the starting fatty acids for obtaining fatty amines are, for example, caprylic, pelargonic, capric, undecylenic, lauric, tridecylenic, myristic, pentadecyl, palmitic, margaric, stearic, nonadecylic, arachic, heneicosanoic, behenic, tricosanoic, lignoceric, pentacosanoic acids.
- the preferred fatty acids are derived from the hydrolysis of triglycerides present in vegetable and animal oils, such as coconut oil, palm oil, olive oil, peanut oil, rapeseed oil, sunflower oil, soy oil and cotton oil. , flax, beef tallow, .... natural oils may have been genetically modified to enrich their content of certain fatty acids, for example rapeseed oil or oleic sunflower.
- the fatty amines used in the lubricants according to the invention are preferably obtained from natural resources, plant or animal. Treatments that result in fatty amines from natural oils can result in mixtures of secondary and tertiary primary monoamines and polyamines.
- products containing, in variable proportions, all or part of the compounds corresponding to the following formulas may be incorporated into the lubricants according to the present invention: RNH 2, R-NH-R R-NHCH 2 -R R- [NH (CH 2 ) 3 ] 2 -NH 2 R- [NH (CH 2 ) 3 ] n -NH 2 where n is an integer greater than or equal to 1 and R is a fatty chain derived from the fatty acid or acids present in the starting oil.
- R is a fatty chain derived from the fatty acid or acids present in the starting oil.
- the same fat mono or polyamine may also contain several fatty chains from different fatty acids.
- These products can also be used in purified form, mainly containing a single type of amines, for example mainly diamines.
- amines obtained from oleic acid in particular diamines of formula R- [NH (CH 2 ) 3 ] 2 -NH 2 where R is the fatty chain of oleic acid, are advantageously used.
- the amines according to the present invention are soluble in the oil matrix to facilitate their incorporation into the lubricant and to be able to more easily reach the droplets of neutralizing acid dispersed in said oil matrix, so as to be more efficient.
- the fatty amines of the lubricants according to the present invention are not in emulsion or microemulsion form, but well dispersed in the oil matrix.
- the fatty amines according to the present invention are therefore those which comprise at least one aliphatic chain consisting of at least 16 carbon atoms, preferably at least 18 carbon atoms.
- fatty amines containing between 16 and 22 carbon atoms are particularly preferred.
- the BN of the amines according to the invention being between 150 and 600, and the number of points of minimum BN provided by these amines being 10 milligram of potash per gram of lubricant, it is necessary to use them at levels minimum of the order of 2% by weight in the lubricant, but which can typically rise to values of the order of 20% by weight, for example to bring 40 BN points with an amine of BN 200, or to of the.
- the BN alternative to overbased detergents can be provided by fatty amine derivatives.
- fatty amine derivatives are, for example, ethoxylated amines, obtained by condensation of ethylene oxide with primary or secondary amines, aminoxides, resulting from the reaction of tertiary fatty amines with hydrogen peroxide, or ammonium salts. quaternaries synthesized from tertiary amines.
- the BN of the lubricants described in the application as filed is provided by the neutral or overbased detergents based on alkali or alkaline earth metals and one or more fatty amines and / or their derivatives.
- the value of this BN measured according to ASTM D-2896 can vary from 5 to 100 mg KOH / g, or beyond.
- a lubricant of BN value fixed will be chosen according to the conditions of use of said lubricants and in particular according to the sulfur content of the fuel oil used and in combination with the cylinder lubricants.
- the lubricants according to the present invention are suitable for use as a cylinder lubricant, irrespective of the sulfur content of the fuel oil used as fuel in the engine.
- the cylinder lubricants for two-stroke marine engines according to the invention have a BN greater than or equal to 15, preferably greater than 20, preferably greater than 30, advantageously greater than 40, and preferably between 40 and 80.
- the lubricant formulation has a level of BN, measured according to the ASTM D-2896 standard, adapted for use with high-sulfur fuel oils containing of the order of 4, 5% w / w sulfur, that is to say a BN between 65 and 75, or equal to 70.
- the BN of the lubricants according to the present invention is between 45 and 60, preferably between 45 and 55, or equal to 50.
- the BN of the lubricants according to the present invention is between 55 and 60, or equal to 57, or equal to 55.
- the fatty amines and derivatives provide at least 14% of the BN.
- the fatty amines and derivatives provide at least 18% of the BN.
- fatty amines and derivatives provide at least 25% of BN.
- these fatty amines and their derivatives themselves have a BN between 100 and 600, preferably between 200 and 400, the mass percentage of these compounds in the lubricants described in the application as filed is greater than 1.7% (contribution of 10 BN points with an amine of BN 600), generally greater than 2%.
- Fatty amines do not provide all the BN in the lubricants according to the present invention.
- the applicant has found that the incorporation of high-grade fatty amines induces a significant drop in viscosity, so that beyond a maximum percentage of fatty amines, it is no longer possible to formulate lubricants. having the viscosity grade required for lubricant application cylinder, except to incorporate extremely high amounts of thickening additives, which would lead to unrealistic formulas from an economic point of view and deteriorate other properties of the lubricant.
- a BN of about 55, or 57, or 70, providing at least 10 BN points per second. overbased detergents.
- a maximum of 60 points of BN will generally be provided by the fatty amines, which corresponds to a maximum mass percentage of fatty amines of the order of 10, 15, 30 or 40%, for amines respectively of BN 600, 400, 200 or 150.
- lubricants combining a BN supply with amines and overbased detergents did not exhibit a satisfactory neutralization efficiency (that is to say of the order of 100 or above), only up to a maximum level of BN provided by the metal carbonate salts of the overbased detergents.
- BN carbonate or BN CaCo3
- Conventional oils of BN greater than or equal to 40 thus reformulated according to the invention by substituting fatty amines for overbased detergents, so that they provide at least 10 points of BN in the lubricant, preferably at least 30 points of BN in the lubricant, can correctly prevent corrosion problems when using high-sulfur fuel oils (of the order of 4.5% m / m).
- the lubricants according to the present invention and in particular those of BN between 65 and 75, for example BN 70, can be used with both high and low sulfur fuel oils.
- the detergents used in the lubricant compositions according to the present invention are well known to those skilled in the art.
- the detergents commonly used in the formulation of lubricating compositions are typically anionic compounds having a long lipophilic hydrocarbon chain and a hydrophilic head.
- the associated cation is typically a metal cation of an alkali or alkaline earth metal.
- the detergents are preferably chosen from alkali metal or alkaline earth metal salts of carboxylic acids, sulphonates, salicylates and naphthenates, as well as the salts of phenates.
- the alkaline and alkaline earth metals are preferably calcium, magnesium, sodium or barium.
- metal salts may contain the metal in an approximately stoichiometric amount.
- neutral detergents typically have a BN, measured according to ASTM D2896, less than 150 mg KOH / g, or less than 100, or even less than 80 mg KOH / g.
- neutral detergents can contribute in part to the BN lubricants according to the present invention.
- neutral detergents of carboxylates, sulphonates, salicylates, phenates, alkali metal and alkaline earth metal naphthenates, for example calcium, sodium, magnesium or barium will be used.
- BN is high, greater than 150 mg KOH / g, typically between 200 and 700 mg KOH / g, generally between 250 and 450 mg KOH / g.
- the excess metal providing the overbased detergent character is in the form of oil insoluble metal salts, for example carbonate, hydroxide, oxalate, acetate, glutamate, preferably carbonate.
- the metals of these insoluble salts may be the same as those of the oil-soluble detergents or may be different. They are preferably selected from calcium, magnesium, sodium or barium.
- the overbased detergents are thus in the form of micelles composed of insoluble metal salts maintained in suspension in the lubricating composition by the detergents in the form of oil-soluble metal salts.
- These micelles may contain one or more types of insoluble metal salts, stabilized by one or more detergent types.
- Overbased detergents with a single type of detergent soluble metal salt will generally be named after the nature of the hydrophobic chain of the latter detergent.
- the overbased detergents will be said to be of mixed type if the micelles comprise several types of detergents, different from each other by the nature of their hydrophobic chain.
- the oil-soluble metal salts will preferably be phenates, sulphonates salicylates, and mixed detergents phenate-sulphonate and / or salicylates calcium, magnesium, sodium or barium.
- the insoluble metal salts providing the overbased character are alkali and alkaline earth metal carbonates, preferentially calcium carbonate.
- the overbased detergents used in the lubricating compositions according to the present invention will preferably be phenates, sulphonates, salicylates and mixed detergents phenates-sulphonates-salicylates, overbased with calcium carbonate.
- part of the BN is provided by the insoluble metal salts of the overbased detergents, in particular the metal carbonates.
- the weight percentage of overbased detergents relative to the total weight of lubricant is thus chosen so that the BN supplied by the carbonate metal salts represents a contribution of at most 20 milligrams of potash per gram of lubricant to the total BN of said lubricant cylinder.
- the BN supplied by the carbonate metal salts is measured on the overbased detergent alone and / or on the final lubricant according to the method described in Example 1.
- the BN supplied by the metal salts of carbonate represents 50 to 95% of the total BN of the overbased detergent alone.
- insoluble metal salts also have a favorable anti-wear effect provided that they are kept dispersed in the lubricant in the form of stable micelles, which is not the case when they are in excess of the amount of sulfuric acid to neutralize in service.
- the insoluble metal salts of the overbased detergents provide at least 5 milligrams of potash per gram of lubricant (or 5 "points of BN") in the lubricants according to the present invention, preferably at least 10 BN points.
- the detergents themselves which are metal soaps of the essentially phenate or salicylate type, or sulfonate, also contribute to the BN of the lubricants according to the present invention.
- This BN contribution hereinafter referred to as “organic BN", comes from both neutral and overbased detergents.
- the lubricants according to the present invention have a certain portion of their BN provided by these metal soaps.
- the organic BN provided by the metal soaps represents a contribution of at least 5 milligrams of potash per gram of lubricant, preferably at least 10 milligrams of potash per gram of lubricant, in the cylinder lubricants according to the present invention.
- the base oils used for the formulation of lubricants according to the present invention can be oils of mineral, synthetic or vegetable origin as well as their mixtures.
- the mineral or synthetic oils generally used in the application belong to one of the classes defined in the API classification as summarized in the table below.
- Saturated content Sulfur content Viscosity index Group 1 Mineral oils ⁇ 90% > 0.03% 80 ⁇ VI ⁇ 120 Group 2 Hydrocracked oils ⁇ 90% ⁇ 0.03% 80 ⁇ VI ⁇ 120 Group 3 Hydroisomerized oils ⁇ 90% ⁇ 0.03% ⁇ 120 Group 4 PAO Group 5 Other bases not included in groups 1 to 4
- the Group 1 mineral oils can be obtained by distillation of selected naphthenic or paraffinic crudes and then purification of these distillates by methods such as solvent extraction, solvent or catalytic dewaxing, hydrotreatment or hydrogenation.
- the oils of Groups 2 and 3 are obtained by more severe purification methods, for example a combination among hydrotreatment, hydrocracking, hydrogenation and catalytic dewaxing.
- Group 4 and 5 synthetic bases include poly-alpha olefins, polybutenes, polyisobutenes, alkylbenzenes.
- base oils can be used alone or as a mixture.
- a mineral oil can be combined with a synthetic oil.
- Cylinder oils for 2-stroke marine diesel engines have a SAE-40 SAE-40 viscometric grade, typically SAE-50 equivalent to a kinematic viscosity at 100 ° C of between 16.3 and 21.9 mm 2 / s.
- Grade 40 oils have a kinematic viscosity at 100 ° C of between 12.5 and 16.3 cSt.
- Grade 50 oils have a kinematic viscosity at 100 ° C of 16.3 to 21.9 cSt.
- Grade 60 oils have a kinematic viscosity at 100 ° C of 21.9 to 26.1 cSt.
- cylinder oils for 2-stroke marine diesel engines having a kinematic viscosity at 100 ° C. of between 18 and 21.5, preferably between 19 and 21.5 mm 2 / s (Cst).
- This viscosity can be obtained by mixing additives and base oils, for example containing Group 1 mineral bases such as Neutral Solvent (for example 500NS or 600 NS) and Brightstock bases. Any other combination of mineral, synthetic or vegetable bases having, in admixture with the additives, a viscosity compatible with the grade SAE-50 may be used.
- Group 1 mineral bases such as Neutral Solvent (for example 500NS or 600 NS) and Brightstock bases.
- Neutral Solvent for example 500NS or 600 NS
- Brightstock bases for example 500NS or 600 NS
- Any other combination of mineral, synthetic or vegetable bases having, in admixture with the additives, a viscosity compatible with the grade SAE-50 may be used.
- a conventional cylinder lubricant formulation for slow 2-cycle marine diesel engines is SAE 40 to SAE60, preferably SAE50 (SA37 J300) and includes at least 50% by weight of original lubricating base oil.
- mineral and / or synthetic, suitable for use in a marine engine for example of API Group 1, that is to say obtained by distillation of selected crudes and purification of these distillates by processes such as solvent extraction , solvent or catalytic dewaxing, hydrotreatment or hydrogenation.
- Their Viscosity Index (VI) is between 80 and 120; their sulfur content is greater than 0.03% and their saturated content is less than 90%.
- a conventional cylinder lubricant formulation for slow 2-stroke marine diesel engines contains from 18 to 25% by weight, based on the total weight of lubricant, of a BSS type I base oil base oil (residue). distillation, kinematic viscosity at 100 ° C close to 30 mm 2 / s, typically between 28 and 32 mm 2 / s, and density at 15 ° C between 895 and 915 kg / m3), and 50 to 60% by weight, based on the total weight of lubricant, of a Group 600 NS type base oil (distillate, density at 15 ° C between 880 and 900 kg / m3, kinematic viscosity at 100 ° C close to 12 mm 2 / s).
- the applicant has demonstrated that the introduction of significant amounts of fatty amines (typically of the order of 5 to 15%, or greater than 10%, or of the order 20% by weight) has the effect of lowering the viscosity of the lubricant.
- fatty amines typically of the order of 5 to 15%, or greater than 10%, or of the order 20% by weight
- This makes it possible to formulate viscosimetric-grade cylinder lubricants adapted to their use.
- the base oil or oils are partially or totally substituted by one or more thickening additives whose role is to increase the viscosity of the composition, as hot as cold, or by viscosity index (VI) improving additives.
- thickening additives whose role is to increase the viscosity of the composition, as hot as cold, or by viscosity index (VI) improving additives.
- PIBs of the order of 2000 daltons
- polyacrylate or poly methacrylates of the order of 30000 daltons
- olefin-copolymers olefin and alpha olefin copolymers
- EPDM polybutenes
- Poly-alphaolefins high molecular weight viscosity 100 ° C> 150
- Styrene-Olefin copolymers hydrogenated or not.
- the polymers used to partially or totally substitute one or more of the base oils are preferably the aforementioned thickeners of the PIB type (for example marketed under the name Indopol H2100).
- Anti-wear additives are:
- Lubricants according to the present invention contain, at BN equivalent, a lower amount of overbased detergents than that present in conventional cylinder lubricants.
- a BN 70 cylinder lubricant usually contains about 25% by weight of overbased detergents, whereas in the lubricants of the BN 70 invention, this content can fall around 15% or even be less than 5%. .
- these compounds can have a positive anti-wear effect.
- the cylinder lubricants according to the invention will preferably comprise antiwear additives.
- the anti-wear additives protect the friction surfaces by forming a protective film adsorbed on these surfaces.
- the most commonly used is Zinc di thiophosphate or DTPZn. This category also contains various phosphorus, sulfur, nitrogen, chlorine and boron compounds.
- anti-wear additives there is a wide variety of anti-wear additives, but the most used category is that of phospho-sulfur-containing additives such as metal alkylthiophosphates, in particular zinc alkylthiophosphates, and more specifically zinc dialkyldithiophosphates or DTPZn.
- the preferred compounds have the formula Zn ((SP (S) (OR 1) (OR 2)) 2, or R 1 and R 2 are alkyl groups, preferably containing 1 to 18 carbon atoms, and DTPZn is typically present at in the range of 0.1 to 2% by weight.
- Amine phosphates, polysulfides, especially sulfur-containing olefins, are also commonly used antiwear additives.
- Lubricating compositions containing nitrogenous and sulfur-containing anti-wear and extreme pressure additives such as, for example, metal dithiocarbamates, in particular molybdenum dithiocarbamate, are also usually encountered in lubricating compositions.
- Glycerol esters are also anti-wear additives. Mention may be made, for example, of mono, di and trioleates, monopalmitates and monomyristates.
- the anti-wear and extreme pressure additives are present in lubricant compositions at contents of between 0.01 and 6%, preferably between 0.1 and 4%.
- the cylinder lubricants according to the present invention contain at least 0.5% by weight of one or more anti-wear additives.
- the preferred anti-wear agents are of the DTPZn type.
- Dispersants are well known additives used in the formulation of lubricating composition, especially for application in the marine field. Their primary role is to maintain in suspension the particles present initially or appearing in the lubricant composition during its use in the engine. They prevent their agglomeration by playing on 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 chain, generally containing from 50 to 400 carbon atoms.
- the polar group typically contains at least one nitrogen, oxygen or phosphorus element.
- the compounds derived from succinic acid are dispersants particularly used as lubrication additives.
- succinimides obtained by condensation of succinic anhydrides and amines
- succinic esters obtained by condensation of succinic anhydrides and alcohols or polyols.
- These compounds can then be treated with various compounds including sulfur, oxygen, formaldehyde, carboxylic acids and compounds containing boron or zinc to produce, for example, borated succinimides or zinc-blocked succinimides.
- Mannich bases obtained by polycondensation of phenols substituted with alkyl groups, formaldehyde and primary or secondary amines, are also compounds used as dispersants in lubricants.
- At least 0.1% of a dispersing additive is used. It is possible to use a dispersant in the family of succinimide PIBs, for example borated or blocked with zinc.
- the lubricant formulation according to the present invention may also contain any functional additives adapted to their use, for example anti-foam additives to counteract the effect of detergents, which may for example be polar polymers such as polymethylsiloxanes, polyacrylates, antioxidant additives and / or or anti rust, for example organo metal detergents or thiadiazoles. These are known to those skilled in the art. These additives are generally present at a content by weight of 0.1 to 5%.
- compositions of the lubricants described refer to the compounds taken separately before mixing, it being understood that said compounds may or may not retain the same chemical form before and after mixing.
- the lubricants according to the present invention obtained by mixing the compounds taken separately are not in the form of emulsion or microemulsion.
- the fatty amines and derivatives contained in the lubricants described in the application as filed may in particular be incorporated in a lubricant as separate additives. However, the fatty amines and derivatives contained in the lubricants described in the application as filed may also be incorporated into a marine lubricant additive concentrate.
- Conventional marine cylinder lubricant additive concentrates generally consist of a mixture of the constituents described above, detergents, dispersants, other functional additives, pre-dilution base oil, in proportions which make it possible to obtain, after dilution, in a base oil for cylinder lubricants having a BN determined according to ASTM D-2896 greater than or equal to 15, preferably greater than 20, preferably greater than 30, advantageously greater than 40 milligrams of potash per gram of lubricant.
- This mixture generally contains, relative to the total weight of concentrate, a detergent content greater than 80%, preferably greater than 90%, a dispersant additive content of 2 to 15%, preferably 5 to 10%, a content of other functional additives from 0 to 5%, preferably from 0.1 to 1%.
- the BN of said concentrates measured according to ASTM D 2896, is generally between 250 and 300 milligrams of potash per gram of concentrate, typically of the order of 275 milligrams of potash per gram of concentrate.
- the application as filed discloses an additive concentrate, for the preparation of cylinder lubricant having a BN determined according to ASTM D-2896 greater than or equal to 15, preferably greater than 20, preferably greater than 30, preferably greater than 30.
- the mass percentage of said fatty amines and / or derivatives in the concentrate is chosen so as to bring to said concentrate a BN contribution determined according to the ASTM D-2896 standard of between 60 (25 % of 250) and 225 (75 % of 300). ) milligrams of potash per gram of concentrate.
- the mass percentage of said fatty amines and / or derivatives in the concentrate is chosen so as to provide said concentrate with a BN contribution determined according to ASTM D-2896 between 135 (55 % of 250) and 225 (75 % of 300). ) milligrams of potash per gram of concentrate.
- fatty amines of the concentrates described in the application as filed are those described above and in the examples below as a source of BN alternative detergents.
- the concentrates described in the application as filed also contain base oil in a small amount, but sufficient to facilitate the use of said additive concentrates.
- This measurement is characterized by a neutralization efficiency index measured according to the enthalpic test method described precisely in the examples and in which the progress of the exothermic neutralization reaction is followed by the rise in temperature observed when said lubricant containing the basic sites is put in the presence of sulfuric acid.
- Example 1 This example is intended to describe the method for measuring the contribution of the insoluble metal salts present in the BN-based overbased detergents of the lubricant compositions containing said overbased detergents:
- the reaction vessel may be pyrex, glass, polycarbonate, ... or any other material that promotes heat exchange with the surrounding environment, so that the internal temperature of the vessel equilibrates rapidly with that of the ambient environment.
- a small amount of 600 NS type fluid base oil is introduced into the reaction vessel containing a small magnet bar. About 2 ml of concentrated sulfuric acid is placed in the reaction vessel, being careful not to stir the medium at this stage.
- the cap and pressure gauge assembly is screwed onto the reaction vessel. The threads can be greased. We tighten to have a perfect seal. Stirring is started, and the time required for the pressure to stabilize and the temperature to equilibrate with the ambient medium is stirred. A time of 30 minutes is enough. Note the pressure increase P and the ambient temperature T ° C ( ⁇ ). The whole is cleaned with a solvent of the heptane type.
- the result obtained is the BN CaCO3 expressed in mgKOH / g.
- the BN supplied by the metallic soaps of detergents also designated by "organic BN" is obtained by difference between the total BN according to ASTM D2896 and the BN CaCO3 thus measured.
- Example 2 This example aims to describe the enthalpic test for measuring the neutralization efficiency of lubricants vis-à-vis sulfuric acid.
- the acid-base neutralization reactions are generally exothermic and it is therefore possible to measure the heat release obtained by reaction of sulfuric acid with the lubricants to be tested. This evolution is followed by the evolution of the temperature over time in an adiabatic reactor of the DEWAR type.
- BN of the lubricants to be tested is preferably in excess of the BN required to neutralize the amount of added acid.
- BN 70 lubricants the following examples thus add an amount of acid corresponding to the neutralization of 55 BN points.
- the duration S is equal to the difference t f - t i between the time at the end of reaction temperature and the time at the reaction start temperature.
- the time t i at the reaction start temperature corresponds to the first rise in temperature after stirring is started.
- the time t f at the final reaction temperature is that from which the temperature signal remains stable for a duration greater than or equal to the half-duration of reaction.
- the lubricant is all the more effective as it leads to short periods of neutralization and therefore to a high index.
- the reactor and agitator geometries as well as the operating conditions were chosen so as to be in a chemical regime, where the effect of the diffusional stresses in the oil phase is negligible.
- the fluid height must be equal to the inside diameter of the reactor, and the stirring propeller must be positioned at about 1/3 of the height of the fluid.
- the apparatus consists of a cylindrical adiabatic reactor of 300 ml, the inner diameter of which is 52 mm and the internal height 185 mm, of a stirring rod provided with a propeller with inclined blades, 22 mm in diameter; the diameter of the blades is between 0.3 and 0.5 times the diameter of the DEWAR, that is to say from 15.6 to 26 mm.
- the position of the propeller is set at a distance of about 15 mm from the bottom of the reactor.
- the stirring system is driven by a variable speed motor of 10 to 5000 rpm and a temperature acquisition system as a function of time.
- This system is suitable for measuring reaction times of the order of 5 to 20 seconds and the temperature rise measurement of a few tens of degrees from a temperature of about 20 ° C to 35 ° C preferably about 30 ° C.
- the position of the temperature acquisition system in the DEWAR is fixed.
- the stirring system will be adjusted so that the reaction proceeds in a chemical regime: in the configuration of the present experiment, the speed of rotation is set at 2000 rpm, and the position of the system is fixed.
- the chemical regime of the reaction is also dependent on the oil height introduced into the DEWAR, which must be equal to the diameter of the latter, and which corresponds in this experiment to a mass of about 86. g of the lubricant tested.
- the amount of acid corresponding to the neutralization of 55 BN points is introduced into the reactor.
- This oil is obtained from a mineral base obtained by mixing a distillate of density at 15 ° C of between 880 and 900 Kg / m 3 with a distillation residue having a density of between 895 and 915 Kg / m. 3 (Brightstock) in a distillate / residue ratio of 3.
- a concentrate in which there is a BN overbased calcium sulfonate equal to 400 mg KOH / g, a dispersant, a BN-based calcium phenate equal to 250 mg KOH / g.
- This oil is formulated specifically to have sufficient neutralization capacity to be used with high sulfur fuels, namely S contents above 3% or even 3.5%.
- the reference lubricant contains 25.50% by weight of this concentrate. Its BN of 70 is exclusively provided by the overbased detergents (phenates and overbased sulfonates) contained in said concentrate.
- This reference lubricant has a viscosity at 100 ° C of between 18 and 21.5 mm 2 / s.
- the neutralization reaction time of this oil (hereinafter referred to as Href) is 10.59 seconds and its neutralization efficiency index is set to 100.
- EXAMPLE 3 This example describes, by way of comparison, the influence of the contribution of the BN provided by the carbonate metal salts on the performance of the cylinder oils, namely their neutralization efficiency.
- BN 70 cylinder oils A, B, C are used, where part of the BN is supplied, as in the reference oil, with a concentrate of overbased detergents, and another part is provided by a mixture of of fatty polyamines obtained from tallow, mainly containing palmitic, stearic and oleic acids.
- This amine mixture has a BN of 460 mg KOH / g. It consists of compounds of formula R [NH- (CH 2 ) 3 ] n NH 2 , where R represents the fatty chain of palmitic, stearic or oleic acids, and n is an integer between 0 and 3.
- the reference is the two-stroke marine engine cylinder oil of BN 70 referenced Href in the previous example.
- Table 1 below lists the characteristics of the reference and the samples tested, as well as the values of their efficiency indices.
- Table 1 H ref AT B VS Composition% mass Concentrated phenates + overbased sulfonates 25.50 21,30 17,10 12,90 (Poly) fatty amines, BN 460 mg KOH / g, ASTM D2896 0.00 2.50 5.00 7.50 Gr I base oils 74.50 76.20 77.90 79,60 properties KV 100 (Cst), ASTMD445 20.5 19.21 18.36 16.51 KV 40 (Cst), ASTMD445 243.7 221.1 208.3 178 Total BN (mg KOH / g, ASTM D-2896.) 70.1 71 69.4 73.4 Of which BN supplied with fatty amines (mg KOH / g, ASTM D-2896) 0 (0% of the BN) 11.50 (16%) 23 (33%) 34.50 (47%) Of which BN CaCO3 (m
- lubricant neutralization efficiency index is significantly less than 100 when the contribution of BN provided by the metal carbonate salts is greater than 20 milligrams of potassium hydroxide per gram of lubricant.
- Example 4 This example according to the invention describes the influence of the contribution of the BN provided by the metal salts of carbonate on the performance of the cylinder oils, namely the neutralization efficiency.
- the reference is the two-stroke marine engine cylinder oil of BN 70 referenced Href in Example 1.
- the oils G to J comprise, as a source of BN alternative to overbased detergents, a compound comprising predominantly a fatty diamine obtained from oleic acid, of formula RNH (CH 2 ) 3 NH 2 , where R represents the fatty chain of oleic acid.
- the BN of this compound is 320 mg KOH / g (Dinoram O).
- the oils K and L comprise, as source of BN alternative to overbased detergents, a compound comprising predominantly a C16 fatty amine of nature dimethyl hexadecyl amine.
- the BN of this compound is 200 mg KOH / g (Genamine 16R).
- Fatty amines bring, in this example, about 40 BN points out of a total of 70, or about 57%.
- the remainder of the BN is provided by neutral phenate, overbased phenate and overbased sulfonate detergents.
- the lubricant neutralization efficiency index is greater than 100 when the contribution of BN provided by the metal carbonate salts is less than 20 milligrams of potassium hydroxide per gram of lubricant.
- PIB has been introduced into the formulas.
- oil G exhibited poor anti-wear performance (as measured, for example, in the ASTM D2670 test carried out in the FALEX pin & vee block machine), compared with the Href reference.
- overbased detergents which, in the form of stable micelles, has a positive anti-wear effect (conversely, when the micelles are destabilized, for example when the overbased detergents are in excess over the amount of acid generated in operation, there is formation of hard metal deposits that generate wear).
- the characteristics and the performances of the oils thus formulated are summarized in Table 2.
- the oils H, I, J, K are preferred oils according to the invention, with an efficiency index comparable to or even greater than that of the reference, and a viscosity grade for use as a cylinder lubricant.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Claims (17)
- Zylinderschmiermittel mit einer nach der Norm ASTM D-2896 bestimmten Basenzahl, die größer oder gleich 15 ist, vorzugsweise größer als 20, bevorzugter als 30, noch bevorzugter größer als 40 Milligramm Kaliumchlorid pro Gramm Schmiermittel ist, umfassend:a) eines oder mehrere Basisschmieröle für einen Schiffsmotor,b) mindestens ein Detergens auf Basis von Alkali- oder Erdalkalimetallen, das mit Metallcarbonatsalzen, überbasiert ist, gegebenenfalls in Verbindung mit einem oder mehreren neutralen Detergenzien,c) eine oder mehrere öllösliche Fettamine mit einer, nach der Norm ASTM D-2896 bestimmten Basenzahl, die im Bereich von 150 bis 600 Milligramm Kaliumchlorid pro Gramm, vorzugsweise von 200 bis 500 Milligramm Kaliumchlorid pro Gramm liegt,wobei der Massenprozentsatz der Fettamine, bezogen auf das Gesamtgewicht des Schmiermittels so ausgewählt ist, dass die, von den Verbindungen bereitgestellte Basenzahl einen Beitrag an die Gesamtbasenzahl des Zylinderschmiermittels von mindestens 10 Milligramm Kaliumchlorid pro Gramm Schmiermittel, vorzugsweise von mindestens 20 Milligramm Kaliumchlorid pro Gramm Schmiermittel, bevorzugter von mindestens 30 Milligramm Kaliumchlorid pro Gramm, noch bevorzugter mindestens von 40 Milligramm Kaliumchlorid pro Gramm darstellt, wobei der Massenprozentsatz der überbasierten Detergenzien, bezogen auf das Gesamtgewicht des Schmiermittels so ausgewählt ist, dass die, von den Metallcarbonatsalzen bereitgestellte Basenzahl einen Beitrag an die Gesamtbasenzahl des Zylinderschmiermittels von höchstens 20 Milligramm Kaliumchlorid pro Gramm Schmiermittel darstellt, und wobei das Fettamin mindestens eine, aus mindestens 16 Kohlenstoffatomen bestehende, aliphatische Kette aufweist.
- Zylinderschmiermittel nach Anspruch 1, wobei der Massenprozentsatz der Fettamine, bezogen auf das Gesamtgewicht des Schmiermittels so ausgewählt ist, dass die, von den Verbindungen bereitgestellte Basenzahl mindestens 15%, vorzugsweise mindestens 30%, noch bevorzugter mindestens 50% der Basenzahl des Zylinderschmiermittels darstellt.
- Zylinderschmiermittel nach Ansprüchen 1 oder 2, das eine, im Bereich von 40 und 80 Milligramm Kaliumchlorid pro Gramm Schmiermittel liegende, gemäß der Norm ASTM D-2896 festgelegte Basenzahl aufweist.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 3, wobei das oder die öllöslichen Fettamine aus Palmöl, Olivenöl, Erdnussöl, klassischem Rapsöl oder Rapsoleinöl, klassischem Sonnenblumenöl oder Sonnenblumenoleinöl, Sojaöl, Baumwollsamenöl, Rinderschmalz, oder aus Palmitinsäure, Stearinsäure, Ölsäure, Linolsäure erhalten werden.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 4, wobei die öllöslichen Fettamine aus, zwischen 16 und 18 Kohlenstoffatome aufweisende Fettsäuren erhalten werden.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 5, wobei die Fettamine Polyamine der allgemeinen Formel R-[NH(CH2)3]2-NH2 sind, wobei n eine ganze, zwischen 1 und 3 liegende Zahl ist und R die Fettkette von gesättigten oder ungesättigten Fettsäuren mit mindesten 16 Kohlenstoffatomen, vorzugsweise die Fettkette aus Ölsäure darstellt.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 6, wobei die Fettamine Diamine der allgemeinen Formel R-NH-(CH2)3-NH2 sind, wobei R die Fettkette von gesättigten oder ungesättigten Fettsäuren mit mindesten 16 Kohlenstoffatomen, vorzugsweise die Fettkette aus Ölsäure darstellt.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 7, wobei die überbasierten und/oder neutralen Detergenzien aus den Carboxylaten, Sulfonaten, Salicylaten, Naphthenaten, Phenolaten ausgewählt sind, und wobei die gemischten Detergenzien mindestens zwei von diesen Detergenzarten miteinander verbinden.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 8, wobei die überbasierten und/oder neutralen Detergenzien Metallverbindungen sind, die ausgewählt sind aus der Gruppe bestehend aus Calcium, Magnesium, Natrium oder Barium, vorzugsweise Calcium oder Magnesium.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 9, wobei die überbasierten Detergenzien durch unlösliche Metallsalze, ausgewählt aus der Gruppe der Carbonaten der Alkali- oder Erdalkalimetalle überbasiert sind.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 10, wobei der Massenprozentsatz von überbasierten Detergenzien, bezogen auf das Gesamtgewicht des Schmiermittels so ausgewählt ist, dass die, von den Metallcarbonatsalzen bereitgestellte Basenzahl einen Beitrag an die Gesamtbasenzahl des Zylinderschmiermittels von mindestens 5 Milligramm Kaliumchlorid pro Gramm Schmiermittel vorzugsweise von mindestens 10 Milligramm Kaliumchlorid pro Gramm Schmiermittel darstellt.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 11, wobei der Massenprozentsatz von überbasierten und eventuell neutralen Detergenzien, bezogen auf das Gesamtgewicht des Schmiermittels so ausgewählt ist, dass die, von detergierenden Metallseifen bereitgestellte organische Basenzahl einen Beitrag von mindestens 5 Milligramm Kaliumchlorid pro Gramm Schmiermittel, vorzugsweise von mindestens 10 Milligramm Kaliumchlorid pro Gramm Schmiermittel in den erfindungsgemäßen Zylinderschmiermitteln darstellt.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 12, dessen, gemäß der Norm ASTM D445 errechnete kinematische Viskosität bei 100°C zwischen 12,5 und 26,1 cSt, vorzugsweise zwischen 16,3 und 21,9 cSt liegt.
- Zylinderschmiermittel nach einem der Ansprüche 1 bis 13, wobei eines oder mehrere Basisöle teilweise oder vollkommen durch einen oder mehrere verdickende Polymere und/oder einen Verbesserer des Viskositätsindex VI substituiert sind.
- Verwendung eines Zylinderschmiermittels nach einem der Ansprüche 1 bis 14, als einziges Zylinderschmiermittel, das gleichzeitig mit Heizölen verwendet werden kann, deren Schwefelgehalt niedriger als 1,5% m/m ist, und mit Heizölen, deren Schwefelgehalt höher als 3,5% m/m ist.
- Verwendung eines Zylinderschmiermittels nach einem der Ansprüche 1 bis 14, als einziges Zylinderschmiermittel, das gleichzeitig mit Heizölen verwendet werden kann, deren Schwefelgehalt niedriger als 1% m/m ist, und mit Heizölen, deren Schwefelgehalt höher als 3% m/m ist.
- Verwendung eines Schmiermittels nach einem der Ansprüche 1 bis 14, zur Vermeidung von Korrosion und/oder zur Reduzierung von Ablagerungen von unlöslichen Metallsalzen in den Zweitaktschiffsmotoren während der Verbrennung jeder Art von Heizölen, deren Schwefelgehalt niedriger als 4,5% m/m ist.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0803396A FR2932813B1 (fr) | 2008-06-18 | 2008-06-18 | Lubrifiant cylindre pour moteur marin deux temps |
PCT/FR2009/000721 WO2009153453A2 (fr) | 2008-06-18 | 2009-06-17 | Lubrifiant cylindre pour moteur marin deux temps |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2304006A2 EP2304006A2 (de) | 2011-04-06 |
EP2304006B1 true EP2304006B1 (de) | 2018-08-01 |
Family
ID=40352276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP09766015.3A Active EP2304006B1 (de) | 2008-06-18 | 2009-06-17 | Zylinderschmiermittel für einen zweitakt-schiffsmotor |
Country Status (12)
Country | Link |
---|---|
US (1) | US8334245B2 (de) |
EP (1) | EP2304006B1 (de) |
JP (1) | JP5517311B2 (de) |
KR (1) | KR101575692B1 (de) |
CN (1) | CN102066535B (de) |
BR (1) | BRPI0915185B1 (de) |
ES (1) | ES2693130T3 (de) |
FR (1) | FR2932813B1 (de) |
PT (1) | PT2304006T (de) |
RU (1) | RU2507245C2 (de) |
TR (1) | TR201816003T4 (de) |
WO (1) | WO2009153453A2 (de) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101722380B1 (ko) * | 2009-10-09 | 2017-04-05 | 쉘 인터내셔날 리써취 마트샤피지 비.브이. | 윤활 조성물 |
JP5483329B2 (ja) * | 2009-12-24 | 2014-05-07 | Jx日鉱日石エネルギー株式会社 | クロスヘッド型ディーゼル機関用シリンダー潤滑油組成物 |
EP2531585B1 (de) * | 2010-02-01 | 2018-06-20 | ExxonMobil Research and Engineering Company | Verwendung von motorölzusammensetzungen zur verbesserung der kraftstoffeffizienz für grosse gasmotoren mit niedriger und mittlerer geschwindigkeit mittels reduzierung des traktionskoeffizienten |
CN103459572A (zh) | 2011-04-05 | 2013-12-18 | 雪佛龙奥伦耐有限责任公司 | 低粘度船用气缸润滑油组合物 |
FR2974111B1 (fr) * | 2011-04-14 | 2013-05-10 | Total Raffinage Marketing | Lubrifiant cylindre pour moteur marin deux temps |
FR2980799B1 (fr) | 2011-09-29 | 2013-10-04 | Total Raffinage Marketing | Composition lubrifiante pour moteur marin |
FR2987052B1 (fr) | 2012-02-17 | 2014-09-12 | Total Raffinage Marketing | Additifs ameliorant la resistance a l'usure et au lacquering de carburants de type gazole ou biogazole |
CN103289795B (zh) * | 2012-02-22 | 2015-06-10 | 中国石油化工股份有限公司 | 船用发动机油组合物及其用途 |
FR2990213B1 (fr) | 2012-05-04 | 2015-04-24 | Total Raffinage Marketing | Composition lubrifiante pour moteur |
FR2992655B1 (fr) | 2012-06-29 | 2015-07-31 | Total Raffinage Marketing | Composition lubrifiante |
FR2998303B1 (fr) | 2012-11-16 | 2015-04-10 | Total Raffinage Marketing | Composition lubrifiante |
FR3000103B1 (fr) | 2012-12-21 | 2015-04-03 | Total Raffinage Marketing | Composition lubrifiante a base d'ether de polyglycerol |
FR3005474B1 (fr) * | 2013-05-07 | 2016-09-09 | Total Raffinage Marketing | Lubrifiant pour moteur marin |
US20160289588A1 (en) | 2013-11-04 | 2016-10-06 | Basf Se | Lubricant Composition |
FR3017876B1 (fr) | 2014-02-24 | 2016-03-11 | Total Marketing Services | Composition d'additifs et carburant de performance comprenant une telle composition |
FR3017875B1 (fr) | 2014-02-24 | 2016-03-11 | Total Marketing Services | Composition d'additifs et carburant de performance comprenant une telle composition |
FR3018079B1 (fr) | 2014-02-28 | 2017-06-23 | Total Marketing Services | Composition lubrifiante a base de nanoparticules metalliques |
FR3027607B1 (fr) * | 2014-10-27 | 2018-01-05 | Total Marketing Services | Lubrifiant pour moteur marin |
US10577556B2 (en) | 2015-06-12 | 2020-03-03 | The Lubrizol Corporation | Michael adduct amino esters as total base number boosters for marine diesel engine lubricating compositions |
FR3039835B1 (fr) * | 2015-08-03 | 2019-07-05 | Total Marketing Services | Utilisation d'une amine grasse pour prevenir et/ou reduire les pertes metalliques des pieces dans un moteur |
EP3211062B1 (de) | 2016-02-29 | 2022-07-27 | TotalEnergies OneTech | Schmiermittel für einen zweitaktschiffsmotor |
EP3257919B1 (de) | 2016-06-17 | 2020-08-19 | Total Marketing Services | Schmiermittelpolymere |
EP3257920A1 (de) * | 2016-06-17 | 2017-12-20 | Total Marketing Services | Schmiermittelpolymere |
FR3053049A1 (fr) | 2016-06-28 | 2017-12-29 | Total Marketing Services | Reduction des oxydes d'azote |
KR102517043B1 (ko) * | 2016-08-29 | 2023-04-04 | 셰브런 오로나이트 테크놀로지 비.브이. | 선박용 디젤 실린더 윤활유 조성물 |
US11427780B2 (en) | 2016-09-12 | 2022-08-30 | The Lubrizol Corporation | Total base number boosters for marine diesel engine lubricating compositions |
FR3065964B1 (fr) | 2017-05-04 | 2020-03-13 | Total Marketing Services | Utilisation d'une amine grasse pour reduire et/ou controler la combustion anormale du gaz dans un moteur marin |
FR3071252B1 (fr) | 2017-09-19 | 2020-04-03 | Total Marketing Services | Utilisation d'ester dans une composition lubrifiante pour ameliorer la proprete moteur |
CN110646564A (zh) * | 2018-06-26 | 2020-01-03 | 中国石油天然气股份有限公司 | 一种评价清净剂的碱值保持性的方法 |
KR20220093338A (ko) * | 2019-11-07 | 2022-07-05 | 토탈에너지스 원테크 | 선박 엔진용 윤활제 |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5128644B1 (de) * | 1970-06-11 | 1976-08-20 | ||
US3711406A (en) * | 1970-06-11 | 1973-01-16 | Chevron Res | Lubricating oil containing an hydroxylated amine and an overbased sulfonate or phenate |
JPS54160402A (en) * | 1978-05-25 | 1979-12-19 | Nippon Oil Co Ltd | General lubricating oil composition |
CA1118750A (en) * | 1978-08-01 | 1982-02-23 | Ernst L. Neustadter | Lubricating composition |
US6242394B1 (en) * | 1991-05-30 | 2001-06-05 | The Lubrizol Corporation | Two-stroke cycle lubricant and method of using same |
RU1829401C (ru) * | 1991-06-28 | 1996-02-20 | Всероссийский научно-исследовательский институт по переработке нефти | Смазочная композиция |
GB9225337D0 (en) * | 1992-12-03 | 1993-01-27 | Exxon Chemical Patents Inc | Lubricating oil additives |
US6004910A (en) * | 1994-04-28 | 1999-12-21 | Exxon Chemical Patents Inc. | Crankcase lubricant for modern heavy duty diesel and gasoline fueled engines |
US5441653A (en) * | 1994-08-09 | 1995-08-15 | The Lubrizol Corporation | Two-stroke cycle engine lubricant and method of using same |
JP3827039B2 (ja) * | 1997-08-20 | 2006-09-27 | 株式会社コスモ総合研究所 | 舶用エンジン油組成物 |
DE69828628T2 (de) * | 1997-10-03 | 2006-04-06 | Infineum Usa L.P. | Schmierölzusammensetzungen |
FR2774387B1 (fr) * | 1998-02-02 | 2000-12-01 | Elf Antar France | Lubrifiant marin pour moteur deux temps |
US5906969A (en) * | 1998-05-01 | 1999-05-25 | Exxon Research And Engineering Company | High fuel economy passenger car engine oil |
JP4047136B2 (ja) | 2002-11-07 | 2008-02-13 | 三菱化工機株式会社 | 遠心分離機による固液分離方法 |
JP2005054609A (ja) | 2003-08-07 | 2005-03-03 | Nissan Motor Co Ltd | 高圧燃料ポンプ |
ES2604192T3 (es) * | 2003-10-09 | 2017-03-03 | Infineum International Limited | Composición lubricante |
JP4511154B2 (ja) * | 2003-11-11 | 2010-07-28 | 新日本石油株式会社 | エンジン油用潤滑油組成物 |
BRPI0405935A (pt) | 2003-12-19 | 2005-10-04 | Shell Int Research | Métodos de produzir um produto de petróleo bruto e combustìvel de transporte, combustìvel de aquecimento, lubrificantes ou substâncias quìmicas e produto de petróleo bruto |
EP1640442B1 (de) * | 2004-09-24 | 2009-08-26 | A.P. Moller - Maersk A/S | Methode und System für die Modifizierung eines gebrauchten Kohlenwasserstoff-Fluids zur Herstellung eines Zylinderöls |
US7928043B2 (en) * | 2005-10-14 | 2011-04-19 | The Lubrizol Corporation | Lubricating compositions |
KR20070055386A (ko) * | 2005-11-25 | 2007-05-30 | 인피늄 인터내셔날 리미티드 | 선박용 또는 정치식 디젤 엔진의 작동 방법 |
EP1914295B1 (de) | 2006-10-11 | 2013-12-04 | Total Marketing Services | Schmiermittel für Schiffsmotor verwendend Treibstoff mit niedrigem oder hohem Schwefelgehalt |
US20080153723A1 (en) * | 2006-12-20 | 2008-06-26 | Chevron Oronite Company Llc | Diesel cylinder lubricant oil composition |
-
2008
- 2008-06-18 FR FR0803396A patent/FR2932813B1/fr not_active Expired - Fee Related
-
2009
- 2009-06-17 TR TR2018/16003T patent/TR201816003T4/tr unknown
- 2009-06-17 KR KR1020107028475A patent/KR101575692B1/ko active IP Right Grant
- 2009-06-17 US US13/000,051 patent/US8334245B2/en active Active
- 2009-06-17 ES ES09766015.3T patent/ES2693130T3/es active Active
- 2009-06-17 EP EP09766015.3A patent/EP2304006B1/de active Active
- 2009-06-17 RU RU2010150876/04A patent/RU2507245C2/ru active
- 2009-06-17 PT PT09766015T patent/PT2304006T/pt unknown
- 2009-06-17 JP JP2011514086A patent/JP5517311B2/ja active Active
- 2009-06-17 CN CN200980122774.9A patent/CN102066535B/zh active Active
- 2009-06-17 WO PCT/FR2009/000721 patent/WO2009153453A2/fr active Application Filing
- 2009-06-17 BR BRPI0915185-0A patent/BRPI0915185B1/pt not_active IP Right Cessation
Non-Patent Citations (1)
Title |
---|
Albemare Corporation; fiche technique de ADMA WC AMINE; - novombre 1999; CAS: 7378-99-6/1120-24-7/112-18-5/112-75-4/112-69-6/124-28-7 * |
Also Published As
Publication number | Publication date |
---|---|
KR101575692B1 (ko) | 2015-12-08 |
JP5517311B2 (ja) | 2014-06-11 |
JP2011524926A (ja) | 2011-09-08 |
PT2304006T (pt) | 2018-11-15 |
FR2932813A1 (fr) | 2009-12-25 |
KR20110033900A (ko) | 2011-04-01 |
RU2010150876A (ru) | 2012-07-27 |
BRPI0915185B1 (pt) | 2018-04-03 |
US20110092403A1 (en) | 2011-04-21 |
FR2932813B1 (fr) | 2010-09-03 |
CN102066535A (zh) | 2011-05-18 |
RU2507245C2 (ru) | 2014-02-20 |
US8334245B2 (en) | 2012-12-18 |
CN102066535B (zh) | 2015-01-21 |
TR201816003T4 (tr) | 2018-11-21 |
EP2304006A2 (de) | 2011-04-06 |
ES2693130T3 (es) | 2018-12-07 |
WO2009153453A2 (fr) | 2009-12-23 |
WO2009153453A3 (fr) | 2010-02-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2304006B1 (de) | Zylinderschmiermittel für einen zweitakt-schiffsmotor | |
EP2697344B1 (de) | Zylinderschmiermittel für einen zweitaktschiffsmotor | |
EP2994521B1 (de) | Schmiermittel für einen schiffsmotor | |
EP1914295B1 (de) | Schmiermittel für Schiffsmotor verwendend Treibstoff mit niedrigem oder hohem Schwefelgehalt | |
EP2271731B1 (de) | Schmiermittel für schiffe | |
EP2760982B1 (de) | Schmiermittelzusammensetzung für einen schiffsmotor | |
FR3039835B1 (fr) | Utilisation d'une amine grasse pour prevenir et/ou reduire les pertes metalliques des pieces dans un moteur | |
EP3212745B1 (de) | Schmiermittel für schiffsmotoren | |
WO2009101276A1 (fr) | Composition lubrifiante pour moteur quatre temps a bas taux de cendres | |
EP3523407B1 (de) | Schmierstoffzusammensetzung für einen schiffsmotor oder einen stationären motor | |
EP2964736A1 (de) | Schmierstoffzusammensetzung für einen schiffsmotor | |
WO2019057718A1 (fr) | Utilisation d'ester dans une composition lubrifiante pour améliorer la propreté moteur |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20110118 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA RS |
|
DAX | Request for extension of the european patent (deleted) | ||
17Q | First examination report despatched |
Effective date: 20121002 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: TOTAL MARKETING SERVICES |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
INTG | Intention to grant announced |
Effective date: 20180214 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK TR |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D Free format text: NOT ENGLISH |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP Ref country code: AT Ref legal event code: REF Ref document number: 1024307 Country of ref document: AT Kind code of ref document: T Effective date: 20180815 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D Free format text: LANGUAGE OF EP DOCUMENT: FRENCH |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602009053600 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: FP |
|
REG | Reference to a national code |
Ref country code: PT Ref legal event code: SC4A Ref document number: 2304006 Country of ref document: PT Date of ref document: 20181115 Kind code of ref document: T Free format text: AVAILABILITY OF NATIONAL TRANSLATION Effective date: 20181026 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2693130 Country of ref document: ES Kind code of ref document: T3 Effective date: 20181207 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 1024307 Country of ref document: AT Kind code of ref document: T Effective date: 20180801 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181101 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181102 Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181101 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181201 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602009053600 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20190503 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190617 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190630 Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190617 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190630 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: TR Payment date: 20200522 Year of fee payment: 12 Ref country code: PT Payment date: 20200520 Year of fee payment: 12 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20200701 Year of fee payment: 12 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO Effective date: 20090617 Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20211217 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180801 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20220905 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20210618 |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20230523 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R081 Ref document number: 602009053600 Country of ref document: DE Owner name: TOTALENERGIES ONETECH, FR Free format text: FORMER OWNER: TOTAL MARKETING SERVICES, PUTEAUX, FR |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: PD Owner name: TOTALENERGIES ONETECH; FR Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), OTHER; FORMER OWNER NAME: TOTALENERGIES MARKETING SERVICES Effective date: 20240423 Ref country code: BE Ref legal event code: HC Owner name: TOTALENERGIES MARKETING SERVICES; FR Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), CHANGE OF OWNER(S) NAME; FORMER OWNER NAME: TOTAL MARKETING SERVICES Effective date: 20240423 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20240620 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20240619 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20240619 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20240628 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20240619 Year of fee payment: 16 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20210617 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20240625 Year of fee payment: 16 |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: PD Owner name: TOTALENERGIES ONETECH; FR Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), ASSIGNMENT; FORMER OWNER NAME: TOTALENERGIES MARKETING SERVICES Effective date: 20240926 Ref country code: NL Ref legal event code: HC Owner name: TOTALENERGIES MARKETING SERVICES; FR Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), CHANGE OF OWNER(S) NAME; FORMER OWNER NAME: TOTAL MARKETING SERVICES Effective date: 20240926 |