EP3331975A1 - Utilisation d'une amine grasse pour prevenir et/ou reduire les pertes métalliques des pièces dans un moteur - Google Patents
Utilisation d'une amine grasse pour prevenir et/ou reduire les pertes métalliques des pièces dans un moteurInfo
- Publication number
- EP3331975A1 EP3331975A1 EP16745760.5A EP16745760A EP3331975A1 EP 3331975 A1 EP3331975 A1 EP 3331975A1 EP 16745760 A EP16745760 A EP 16745760A EP 3331975 A1 EP3331975 A1 EP 3331975A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- carbon atoms
- linear
- saturated
- alkyl group
- branched
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 150000001412 amines Chemical class 0.000 title claims abstract description 150
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 51
- 239000002184 metal Substances 0.000 title claims abstract description 51
- 239000000203 mixture Substances 0.000 claims abstract description 145
- 230000001050 lubricating effect Effects 0.000 claims abstract description 59
- 125000004432 carbon atom Chemical group C* 0.000 claims description 154
- 125000000217 alkyl group Chemical group 0.000 claims description 70
- 229920006395 saturated elastomer Polymers 0.000 claims description 69
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 58
- 239000000314 lubricant Substances 0.000 claims description 48
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 46
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 41
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 41
- 229910052760 oxygen Inorganic materials 0.000 claims description 41
- 239000001301 oxygen Substances 0.000 claims description 41
- 229910052717 sulfur Inorganic materials 0.000 claims description 41
- 239000011593 sulfur Substances 0.000 claims description 41
- 150000001875 compounds Chemical class 0.000 claims description 36
- 229910052757 nitrogen Inorganic materials 0.000 claims description 34
- 125000005842 heteroatom Chemical group 0.000 claims description 31
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 28
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 22
- 239000000295 fuel oil Substances 0.000 claims description 20
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 15
- 238000002485 combustion reaction Methods 0.000 claims description 14
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 8
- 239000000446 fuel Substances 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 238000000034 method Methods 0.000 abstract description 15
- 230000008569 process Effects 0.000 abstract description 11
- 239000003599 detergent Substances 0.000 description 43
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 42
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 42
- 150000002430 hydrocarbons Chemical group 0.000 description 29
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 229940072033 potash Drugs 0.000 description 15
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 15
- 235000015320 potassium carbonate Nutrition 0.000 description 15
- 150000003839 salts Chemical class 0.000 description 15
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- 229930195729 fatty acid Natural products 0.000 description 14
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- 150000004665 fatty acids Chemical class 0.000 description 14
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- 230000007935 neutral effect Effects 0.000 description 10
- -1 phenate Chemical compound 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 8
- 238000007278 cyanoethylation reaction Methods 0.000 description 8
- 150000004985 diamines Chemical class 0.000 description 7
- 238000005984 hydrogenation reaction Methods 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 239000007866 anti-wear additive Substances 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 6
- 150000007942 carboxylates Chemical class 0.000 description 6
- 150000001735 carboxylic acids Chemical class 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 6
- 239000010687 lubricating oil Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 235000013311 vegetables Nutrition 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 5
- 235000019486 Sunflower oil Nutrition 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
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- 238000006386 neutralization reaction Methods 0.000 description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 150000003873 salicylate salts Chemical class 0.000 description 5
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 5
- 239000002600 sunflower oil Substances 0.000 description 5
- 239000003760 tallow Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- 235000019484 Rapeseed oil Nutrition 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 229910052788 barium Inorganic materials 0.000 description 4
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- 229910052791 calcium Inorganic materials 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 239000003240 coconut oil Substances 0.000 description 4
- 235000019864 coconut oil Nutrition 0.000 description 4
- 239000010727 cylinder oil Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 239000000693 micelle Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 235000019482 Palm oil Nutrition 0.000 description 3
- 229920002367 Polyisobutene Polymers 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 238000005461 lubrication Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 125000005609 naphthenate group Chemical class 0.000 description 3
- 239000002540 palm oil Substances 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 3
- 229960001860 salicylate Drugs 0.000 description 3
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 description 3
- 235000012424 soybean oil Nutrition 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 3
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 3
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 3
- GWHCXVQVJPWHRF-KTKRTIGZSA-N (15Z)-tetracosenoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCCC(O)=O GWHCXVQVJPWHRF-KTKRTIGZSA-N 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 2
- 240000006240 Linum usitatissimum Species 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- XJXROGWVRIJYMO-SJDLZYGOSA-N Nervonic acid Natural products O=C(O)[C@@H](/C=C/CCCCCCCC)CCCCCCCCCCCC XJXROGWVRIJYMO-SJDLZYGOSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 235000021319 Palmitoleic acid Nutrition 0.000 description 2
- 235000019483 Peanut oil Nutrition 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
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- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
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- 150000001768 cations Chemical class 0.000 description 2
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 2
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- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
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- 239000004530 micro-emulsion Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical compound C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- ISYWECDDZWTKFF-UHFFFAOYSA-N nonadecanoic acid Chemical class CCCCCCCCCCCCCCCCCCC(O)=O ISYWECDDZWTKFF-UHFFFAOYSA-N 0.000 description 1
- 235000014593 oils and fats Nutrition 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
- 229920000058 polyacrylate 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
- 238000002360 preparation method Methods 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
- 229910052815 sulfur oxide Inorganic materials 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000010729 system oil Substances 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical group [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M149/00—Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
- C10M149/12—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M149/14—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds a condensation reaction being involved
- C10M149/22—Polyamines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/52—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
- C10M133/54—Amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/041—Mixtures of base-materials and additives the additives being macromolecular compounds only
-
- 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
- C10M2215/26—Amines
-
- 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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
-
- 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
- C10N2040/252—Diesel engines
-
- 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
-
- 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 the prevention and / or reduction of metallic losses of parts of an engine, in particular of a marine engine. More particularly, the present invention relates to the prevention and / or reduction of metallic losses of parts of a marine engine due to the contact of these parts with an acid medium.
- the present invention relates to the use of one or more fatty amines soluble in a lubricant composition for preventing and / or reducing the metal losses of the parts of an engine, in particular a marine engine.
- the present invention also relates to a method for preventing and / or reducing the metallic losses of the parts of an engine, in particular a marine engine in which said parts are put in contact with one or more fatty amines soluble in a composition lubricating.
- the combustion of fuel oils generates the formation of acid gases, in particular sulfur oxides (SO 2 , SO 3 ).
- acid gases are, among other things, combustion residues of the fuel oils; these residues are in contact with the lubricating oil, and therefore are also in contact with the engine parts.
- these acid gases hydrolyze to sulphurous acid (HS0 3 ) or sulfuric acid (H 2 SO 4 ), which are in turn in contact with each other. with the engine parts.
- lubricating oils are classified into two categories: cylinder oils, on the one hand, ensuring the lubrication of the cylinder piston assembly, and system oils on the other hand, ensuring the lubrication of all moving parts other than those of the cylinder piston assembly. More specifically, it is within the piston cylinder assembly that the combustion residues containing acid gases are in contact with the lubricating oil.
- the neutralization of these acids is carried out 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 the standard ASTM D-2896 and is expressed in equivalent weight of potash per gram of oil or mg of KOH / g of oil.
- 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. fuel, and likely to be converted into sulfuric acid by combustion and hydrolysis.
- marine oils available on the market have a BN ranging from 5 to 130 mg KOH / g oil.
- This basicity is in particular provided by detergents which are overbased by insoluble metal salts, in particular metal carbonates.
- 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 comprised between 150 and 700 mg of potash per gram of detergent.
- Part of the BN can also be provided by non-overbased or "neutral" detergents of BN typically less than 150 mg of potash per gram of detergent.
- the Applicant has found that during the combustion of fuel oil, the neutral and / or overbased detergents present in the lubricant composition chemically deteriorated and therefore formed ash, also called residues or deposits that favored engine fouling , especially the marine engine.
- the applicant has replaced part of the detergents supplying the entire BN of the lubricating composition with compounds providing BN and forming no or little ash during the combustion of fuel oil.
- the Applicant has therefore developed lubricating compositions in which a portion of the detergents providing the BN of the lubricating composition is replaced by amino compounds.
- WO 2009/153453 discloses a cylinder lubricating composition having a BN greater than or equal to 40 milligrams of potash per gram of lubricant and comprising a base oil, an alkali metal or alkaline earth based detergent, overbased by carbonate metal salts , a neutral detergent and a fatty amine and / or oil-soluble fatty amine derivative having a BN of between 150 and 600 milligrams of potash per gram of lubricant.
- WO 2014/180843 discloses a lubricating composition for a cylinder having a BN greater than or equal to 50 milligrams of potash per gram of lubricant comprising a base oil, a detergent based on alkali or alkaline metals earthy, overbased by carbonate metal salts, a neutral detergent and a fatty amine mixture having four amine units.
- EP 2 486 13 discloses a marine engine lubricating oil comprising a monoamine comprising a base oil, a detergent and a disubstituted monoamine by a hydrogen atom or a hydrocarbon group having 1 to 50 carbon atoms.
- the Applicant has surprisingly discovered that the amine compounds, usually used to replace part of the BN of the lubricating composition while decreasing the ash content formed during the combustion of fuel oil, also make it possible to prevent and / or to reduce the metallic losses of the parts of an engine, in particular of a marine engine, when these are in contact with acids resulting from the combustion of fuel oil.
- the fatty amine being chosen from:
- R 1 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising at least 12 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 , R 4 or R 5 independently represents a hydrogen atom or a saturated or unsaturated hydrocarbon group, linear or branched, and optionally comprising at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 3 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising one or more carbon atom (s), and optionally comprising at least one heteroatom selected from nitrogen, sulfur or oxygen, preferably oxygen,
- M is an integer greater than or equal to 1, preferably between 1 and 10, more preferably between 1 and 6, even more preferably is chosen from 1, 2 or 3, or
- R identical or different, represents a linear or branched alkyl group comprising from 8 to 22 carbon atoms
- N and z independently of each other, represent 0, 1, 2 or 3
- said mixture comprising at least 3% by weight of branched compounds such that at least one of n or z is greater than or equal to 1, or of their derivatives, or
- fatty amines of formula (I) included in a lubricant composition are known per se in the applications WO 2009/153453 and WO 2014/180843 filed by the Applicant. The applicant has now discovered a new use of these fatty amines.
- a first subject of the invention relates to the use of one or more fatty amines soluble in a lubricating composition for preventing and / or reducing the metallic losses of parts of an engine, preferably of a marine engine, the fatty amine being chosen from:
- Ri represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising at least 12 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 , R 4 or R 5 independently represents a hydrogen atom or a saturated or unsaturated hydrocarbon group, linear or branched, and optionally comprising at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 3 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising one or more carbon atom (s), and optionally comprising at least one heteroatom selected from nitrogen, sulfur or oxygen, preferably oxygen,
- M is an integer greater than or equal to 1, preferably between 1 and 10, more preferably between 1 and 6, even more preferably is chosen from 1, 2 or 3; or
- R identical or different, represents a linear or branched alkyl group comprising from 8 to 22 carbon atoms
- N and z represent, independently of one another, 0, 1, 2 or 3, and
- o and p represent, independently of one another, 0, 1, 2 or 3,
- said mixture comprising at least 3% by weight of branched compounds such that at least one of n or z is greater than or equal to 1, or of their derivatives; or
- the Applicant has surprisingly observed that the fatty amines according to the invention not only allow to bring organic BN to the lubricating composition while providing little or no ash during the combustion of fuel oil but also prevent and / or reduce the metal losses of parts of an engine, especially in a marine engine, when they are brought into contact with the acids from the combustion of fuel oil. More specifically, the Applicant has unexpectedly discovered that these fatty amines soluble in a lubricant composition in the presence of a large excess of sulfuric acid make it possible to reduce and / or reduce the metallic losses of the parts directly in contact with said lubricating composition. and the large excess of sulfuric acid. This limitation and / or reduction of the metallic losses of the parts is probably due to the passivation of all or part of the surface of the metal parts by said fatty amines.
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 12 to 22 carbon atoms, preferably from 14 to 22 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen, and / or
- R 2 , R 4 or R 5 independently represents a hydrogen atom; a saturated or unsaturated, linear or branched alkyl group comprising between 1 and 22 carbon atoms, preferably between 14 and 22 carbon atoms, more preferably between 16 and 22 carbon atoms; or a group (R 6 -O) q -H in which R 6 is a saturated alkyl group, linear or branched, comprising at least 2 carbon atoms, preferably between 2 and 6 carbon atoms, more preferably between 2 and 4 carbon atoms and q represents an integer greater than or equal to 1, preferably between 1 and 6, more preferably between 1 and 4, and / or ⁇ R 3 represents a saturated or unsaturated, linear or branched alkyl group comprising between 2 and 6 carbon atoms, preferably between 2 and 4 carbon atoms.
- ⁇ M is 1, 2 or 3
- R 1 represents a saturated or unsaturated, linear or branched alkyl group comprising from 12 to 20 carbon atoms, preferably from 14 to 20 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 independently represents a hydrogen atom or a saturated, linear or branched alkyl group comprising from 1 to 20 carbon atoms, preferably from 16 to 20 carbon atoms, more preferably from 16 to 18 carbon atoms,
- R 3 represents a saturated and linear alkyl group comprising between 2 and 6 carbon atoms, preferably between 2 and 4 carbon atoms,
- R 4 and R 5 represent a hydrogen atom or a methyl group, preferably a hydrogen atom.
- R 1 represents a saturated or unsaturated, linear or branched alkyl group comprising from 12 to 20 carbon atoms, preferably from 14 to 20 carbon atoms, more preferably from 16 to 20 carbon atoms, and optionally at least one chosen heteroatom; among nitrogen, sulfur or oxygen,
- R 2 independently represents a hydrogen atom or a saturated alkyl group, linear or branched, comprising from 16 to 18 carbon atoms,
- R 3 represents an ethyl or propyl group
- R 4 and R 5 represent a hydrogen atom.
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 14 to 20 carbon atoms, preferably from 16 to 20 carbon atoms,
- R 2 , R 4 and R 5 independently represent a hydrogen atom or a group (R 6 -O) q -H in which R 6 is a linear saturated alkyl group comprising between 2 and 6 carbon atoms, more preferably between 2 and 4 carbon atoms and q representing an integer between 1 and 6, more preferably between 1 and 4,
- R 3 represents a saturated and linear alkyl group comprising between 2 and 6 carbon atoms, preferably between 2 and 4 carbon atoms.
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 14 to 20 carbon atoms, preferably from 16 to 20 carbon atoms,
- R 2 , R 4 and R 5 independently represent a hydrogen atom or a group (R 6 -O) q -H in which R 6 is a linear saturated alkyl group comprising between 2 and 4 carbon atoms and q representing an integer between 1 and 4,
- R 3 represents an ethyl or propyl group.
- fatty amine of formulas (I), (III) and / or (IV) makes it possible to prevent and / or reduce the metallic losses of the parts in the hot parts, in particular the segment-piston-jacket zone.
- SPC segment-piston-jacket zone.
- the fuel oil has a sulfur content of less than 3.5% by weight relative to the total weight of the fuel oil. Detailed description of the invention.
- An object of the invention relates to the use of one or more fatty amines soluble in a lubricant composition for preventing and / or reducing the metallic losses of parts of an engine, preferably a marine engine,
- the fatty amine is chosen from:
- Ri represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising at least 12 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 , R 4 or R 5 independently represents a hydrogen atom or a saturated or unsaturated hydrocarbon group, linear or branched, and optionally comprising at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 3 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising one or more carbon atom (s), and optionally comprising at least one heteroatom selected from nitrogen, sulfur or oxygen, preferably oxygen,
- M is an integer greater than or equal to 1, preferably between 1 and 10, more preferably between 1 and 6, even more preferably is chosen from 1, 2 or 3; or
- R identical or different, represents a linear or branched alkyl group comprising from 8 to 22 carbon atoms
- N and z represent, independently of one another, 0, 1, 2 or 3, and
- o and p represent, independently of one another, 0, 1, 2 or 3,
- said mixture comprising at least 3% by weight of branched compounds such that at least one of n or z is greater than or equal to 1, or of their derivatives; or
- another subject of the invention relates to the use of one or more fatty amines soluble in a lubricant composition to prevent and / or to reduce the metallic losses of the parts of an engine, preferably of a marine engine, the fatty amine is of formula (I):
- Ri represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising at least 12 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 , R 4 or R 5 independently represents a hydrogen atom or a saturated or unsaturated hydrocarbon group, linear or branched, and optionally comprising at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 3 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising one or more carbon atom (s), and optionally comprising at least one heteroatom selected from nitrogen, sulfur or oxygen, preferably oxygen, m is an integer greater than or equal to 1, preferably between 1 and 10, more preferably between 1 and 6, still more preferably is selected from 1, 2 or 3.
- another subject of the invention relates to the use of one or more fatty amines soluble in a lubricating composition for preventing and / or reducing the metallic losses of the parts of an engine, preferably of a marine engine, the fatty amine being a mixture of fatty polyalkylamines comprising one or more polyalkylamines of formulas (III) and / or (IV):
- R identical or different, represents a linear or branched alkyl group comprising from 8 to 22 carbon atoms
- N and z represent, independently of one another, 0, 1, 2 or 3, and
- o and p represent, independently of one another, 0, 1, 2 or 3,
- said mixture comprising at least 3% by weight of branched compounds such that at least one of n or z is greater than or equal to 1, or of their derivatives.
- fatty amine according to the invention is understood to mean an amine of formula (I),
- (III) or (IV) comprising one or more hydrocarbon groups, saturated or unsaturated, linear or branched, and optionally comprising at least one heteroatom chosen from nitrogen, sulfur or oxygen, preferably oxygen.
- severe fatty amines according to the invention is meant a mixture of fatty amines of which at least one fatty amine is of formulas (I), (III) and / or
- the fatty amine is of formula (I):
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 12 to 22 carbon atoms, preferably from 14 to 22 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen, and / or
- R 2 , R 4 or R 5 independently represents a hydrogen atom; a saturated or unsaturated, linear or branched alkyl group comprising between 1 and 22 carbon atoms, preferably between 14 and 22 carbon atoms, more preferably between 16 and 22 carbon atoms; or a group (R 6 -O) q -H in which R 6 is a saturated alkyl group, linear or branched, comprising at least 2 carbon atoms, preferably between 2 and 6 carbon atoms, more preferably between 2 and 4 carbon atoms and q represents an integer greater than or equal to 1, preferably between 1 and 6, more preferably between 1 and 4, and / or • R 3 represents a linear or branched, saturated or unsaturated alkyl group comprising between 2 and 6 carbon atoms. carbon, preferably between 2 and 4 carbon atoms.
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 14 to 20 carbon atoms, preferably from 16 to 20 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 independently represents a hydrogen atom or a saturated, linear or branched alkyl group comprising from 1 to 20 carbon atoms, more preferably from 16 to 20 carbon atoms, more preferably from 16 to 18 carbon atoms,
- R 3 represents a saturated and linear alkyl group comprising between 2 and 6 carbon atoms, preferably between 2 and 4 carbon atoms,
- R 4 and R 5 represent a hydrogen atom or a methyl group, preferably a hydrogen atom.
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 14 to 20 carbon atoms, preferably from 16 to 20 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 independently represents a hydrogen atom or a saturated alkyl group, linear or branched, comprising from 16 to 18 carbon atoms,
- R 3 represents an ethyl or propyl group
- R 4 and R 5 represent a hydrogen atom.
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 14 to 20 carbon atoms, preferably from 16 to 20 carbon atoms,
- R 2 , R 4 and R 5 independently represent a hydrogen atom or a group (R 6 -O) q -H in which R 6 is a linear saturated alkyl group comprising between 2 and 6 carbon atoms, more preferably between 2 and 4 carbon atoms and q representing an integer between 1 and 6, more preferably between 1 and 4,
- R 3 represents a saturated and linear alkyl group comprising between 2 and 6 carbon atoms, preferably between 2 and 4 carbon atoms.
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 14 to 20 carbon atoms, preferably from 16 to 20 carbon atoms,
- R 2 , R 4 and R 5 independently represent a hydrogen atom or a group (R 6 -O) q -H in which R 6 is a linear saturated alkyl group comprising between 2 and 4 carbon atoms and q representing an integer between 1 and 4,
- R 3 represents an ethyl or propyl group.
- the fatty amines of formula (I) according to the invention are mainly obtained from carboxylic acids. These acids are dehydrated in the presence of ammonia to give nitriles, and then undergo catalytic hydrogenation to lead in particular to fatty amines.
- the fatty amine of formula (I) is obtained from at least one carboxylic acid, preferably at least one fatty acid.
- the alkyl group of the fatty amine of formula (I) has a number of carbon atoms corresponding to the number of carbon atoms of the carbon chain of the carboxylic acid, preferably corresponding to the number of carbon atoms in the carbon chain of the fatty acid
- a same fatty amine of formula (I) may be substituted with several alkyl groups obtained from several identical or different carboxylic acids, preferably obtained from several identical or different fatty acids.
- the alkyl group is obtained from fatty acid chosen from caprylic, pelargonic, capric, undecylenic, lauric, tridecylenic, myristic, pentadecylic, palmitic, margaric, stearic and nonadecylic acids.
- arachic henicosanoic, behenic, tricosanoic, lignoceric, pentacosanoic, cerotic, heptacosanoic, montanic, nonacosanoic, melissic, hentriacontanoic, laceroic, and their derivatives or unsaturated fatty acids such as palmitoleic acid, oleic acid, erucic acid, nervonic acid, linoleic acid, -linolenic, c-linolenic, di-homo-c-linolenic, arachidonic, eicosapentaenoic, docosahexanoic, and their derivatives.
- unsaturated fatty acids such as palmitoleic acid, oleic acid, erucic acid, nervonic acid, linoleic acid, -linolenic, c-linolenic,
- the 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, soya oil, of cotton, flax, beef tallow.
- vegetable and animal oils such as coconut oil, palm oil, olive oil, peanut oil, rapeseed oil, sunflower oil, soya oil, of cotton, 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 oil.
- the fatty amine of formula (I) according to the invention is preferably obtained from natural, vegetable or animal resources. Treatments for producing fatty amines from natural oils can lead to mixtures of primary, secondary and tertiary polyamines.
- fatty amines of formula (I) when several fatty amines of formula (I) are used to prevent and / or reduce the metallic losses of the parts of an engine, said fatty amines form a mixture of fatty amines comprising in particular variable proportions, all or part of the compounds corresponding to the following formulas (Ia), (Ib) and (Ie):
- Ri represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising at least 12 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 , R 4 or R 5 independently represents a hydrogen atom or a saturated or unsaturated hydrocarbon group, linear or branched, and optionally comprising at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 3 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising one or more carbon atom (s), and optionally comprising at least one heteroatom selected from nitrogen, sulfur or oxygen, preferably oxygen,
- the mixture of fatty amines of formula (I) is in a purified form, that is to say comprising mainly a single type of amine of formula (Ia), (Ib) or (Ie), for example predominantly diamines of formula (Ia), triamines of formula (Ib) or predominantly tetramines of formula (Ic).
- the mixture of fatty amines comprises predominantly tetramines of formula (Ic).
- the mixture of fatty amines of formula (I) mainly comprises:
- the mixture of fatty amines of formula (I) mainly comprises diamines of formula (Ia) in which:
- R 1 represents a linear or branched, saturated or unsaturated alkyl group comprising from 12 to 20 carbon atoms, preferably from 14 to 20 carbon atoms, more preferably from 16 to 20 carbon atoms,
- R 2 represents a saturated, linear or branched alkyl group comprising from 1 to 5 carbon atoms, preferably from 1 to 3 carbon atoms, more preferably a methyl group,
- R 3 represents an ethyl or propyl group
- R 4 and R 5 independently represent a linear or branched, saturated alkyl group comprising from 1 to 5 carbon atoms, preferably from 1 to 3 carbon atoms, more preferably a methyl group.
- the mixture of fatty amines of formula (I) mainly comprises diamines of formula R 1 - [(NR 2 ) -R 3 ] -NI-12 (Ma), triamines of formula R 1 - [(NR 2 ) -R3] 2-NH 2 (Mb), or tetramines of formula R 1 - [(NR 2 ) -R 3 ] 3 -NH 2 (IIc), in which:
- R 1 or R 2 represents at least one alkyl group, saturated or unsaturated, obtained from a fatty acid derived from tallow fat, or soybean oil, or coconut oil, or from sunflower oil (oleic), and
- R 3 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising at least 2 carbon atoms.
- R 1 or R 2 represents a saturated alkyl group
- said saturated alkyl is obtained from a saturated fatty acid or from a hydrogenated unsaturated fatty acid, in particular from the whole of these double bonds.
- the mixture of fatty amines of formula (I) comprising predominantly tetramines of formula R [(NR 2 ) -R 3] 3 -NH 2 (Ile) is in the form:
- R 1 represents a saturated or unsaturated, linear or branched alkyl group comprising from 14 to 16 carbon atoms
- R 2 represents a hydrogen atom
- R 3 represents a linear saturated alkyl group comprising from 2 to 6 carbon atoms
- the mixture of fatty amines of formula (I) comprising predominantly tetramines of formula R 1 - [(NR 2 ) -R 3] 3 -NH 2 (Ile) is in the form:
- the sum of the weight content of said fatty amines of formula (IIc) being greater than 90% relative to the weight of said mixture of fatty amines.
- the mixture of fatty amines of formula (I) comprising predominantly tetramines of formula R 1 - [(NR 2 ) -R 3 ] 3 -NH-12 (Ile) is also in the form:
- R 1 represents a linear or branched unsaturated alkyl group comprising from 16 to 20 carbon atoms, preferably from 18 to 20 carbon atoms
- R 2 represents a hydrogen atom
- R 3 represents a linear saturated alkyl group comprising from 2 to 6 carbon atoms and
- R 1 represents a saturated linear or branched alkyl group comprising from 16 to 20 carbon atoms, preferably from 18 to 20 carbon atoms
- R 2 represents a hydrogen atom
- R 3 represents a linear saturated alkyl group comprising from 2 to 6 carbon atoms.
- the mixture of fatty amines of formula (I) comprising predominantly tetramines of formula R 1 - [(NR 2 ) -R 3] 3 -NH 2 (Ile) is in the form:
- R 1 represents a linear or branched unsaturated alkyl group comprising from 16 to 20 carbon atoms, preferably from 18 to 20 carbon atoms
- R 2 represents a hydrogen atom
- R 3 represents a saturated, linear alkyl group comprising from 2 to 6 carbon atoms
- R 1 represents a saturated linear or branched alkyl group comprising from 16 to 20 carbon atoms, preferably from 18 to 20 carbon atoms
- R 2 represents a hydrogen atom
- R 3 represents a saturated, linear alkyl group comprising from 2 to 6 carbon atoms
- the fatty amine mixture of formula (I) does not comprise fatty amines other than fatty amines corresponding to formula (IIc).
- a single fatty amine of formula (I) when used to prevent and / or reduce the metallic losses of the parts of an engine, said fatty amine corresponds to one of the formulas next : a diamine of formula (IIa), or
- Ri represents a linear or branched saturated hydrocarbon group comprising at least 14 carbon atoms
- R 2 independently represents a hydrogen atom or a saturated hydrocarbon group, linear or branched, comprising at least 14 carbon atoms,
- R 3 represents a linear saturated hydrocarbon group comprising at least 2 carbon atoms.
- the fatty amine of formula (I) is preferably a tetramine of formula (IIc) in which,
- Ri represents a linear or branched saturated alkyl group comprising between 14 and 18 carbon atoms
- R 2 independently represents a hydrogen atom or a saturated hydrocarbon group, linear or branched, comprising between 14 and 18 carbon atoms,
- R 3 represents a linear saturated hydrocarbon group comprising between 2 and 6 carbon atoms.
- the fatty amine of formula (I) is advantageously a tetramine of formula (IIc) in which,
- Ri represents a linear or branched saturated alkyl group comprising between 16 and 18 carbon atoms
- R 2 independently represents a hydrogen atom or a saturated hydrocarbon group, linear or branched, comprising between 16 and 18 carbon atoms,
- R 3 represents an ethyl or propyl group.
- the fatty amine is a mixture of polyalkylamines of formulas (III) and / or (IV)
- the polyalkylamine mixtures comprise at least 5% by weight of compounds having a pure linear structure, since these compounds have been found to have an acceptable viscosity profile.
- the polyalkylamine mixtures comprise at least 4% by weight (% m / m), preferably at least 5% w / w, preferably at least 6% w / w, preferably more than 7% w / w, preferably more than 7.5% w / w, preferably more than 10% w / w, preferably more than 20% w / w of branched compounds of which at least one of n or z is greater than or equal to 1.
- n For the products of formula (III), this means that for the branched products, n must be greater than or equal to 1.
- the fatty amine is a mixture of polyalkylamines of formulas (III) and / or (IV)
- n, o, p or z is equal to 0
- the hydrogen atom present at the end of the chain is covalently bound to the corresponding secondary nitrogen atom.
- the fatty amine is a mixture of polyalkylamines of formulas (III) and / or (IV)
- the mixture comprises compounds of formulas (III) and / or (IV) in which n, o, p and z when they are different from 0, are equal to 1 or 2, preferably when n, o, p and z are different from 0 they are equal to 1.
- the mixture essentially comprises compounds of formulas (III) and / or (IV) for which n, o, p or z are independently 0, 1 or 2, preferably n, o, p or z are independently 0 or 1.
- the fatty amine when the fatty amine is a mixture of polyalkylamines of formulas (III) and / or (IV), the mixture essentially comprises compounds of formulas (III) and / or (IV) and their derivatives for wherein n, o, p and z are independently 0, 1 or 2, preferably n, o, p and z are independently 0 or 1.
- each R group is, independently of one another, a linear or branched alkyl group comprising from 14 to 22 carbon atoms, preferably from 14 to 20 carbon atoms, preferably from 16 to 20 carbon atoms.
- the fatty amines of formula (III) and (IV) according to the invention are mainly obtained from carboxylic acids. These acids are dehydrated in the presence of ammonia to give nitriles, and then undergo catalytic hydrogenation to lead in particular to fatty amines.
- the fatty amines of formula (III) and (IV) are obtained from at least one carboxylic acid, preferably at least one fatty acid.
- (III) and (IV) have a number of carbon atoms corresponding to the number of carbon atoms of the carbon chain of the carboxylic acid, preferably corresponding to the number of carbon atoms of the carbon chain of the fatty acid
- a same fatty amine of formula (I) may be substituted with several alkyl groups obtained from several identical or different carboxylic acids, preferably obtained from several identical or different fatty acids.
- a same fatty amine of formula (I) may be substituted with several alkyl groups obtained from several identical or different carboxylic acids, preferably obtained from several identical or different fatty acids.
- the two R groups may be different, they are, according to a preferred embodiment, identical, such compounds being produced more economically. Regardless of whether they are identical or not, one or both R groups, independently, are derived from chemical or natural raw material such as natural oils and fats.
- each group R can have a particular distribution in the length of the carbon chain.
- R is derived from oil or fat of animal or vegetable origin such as tallow, coconut oil and palm oil. Since the preparation of the di-alkyl fatty polyalkylamines according to the invention comprises a hydrogenation step, it may be advantageous during the process for preparing the products of the invention to use hydrogenated R groups.
- the group R is a hydrogenated tallow group.
- the group R of the raw material is unsaturated and is (partially) hydrogenated during the process for preparing the fatty polyalkylamine.
- the alkyl group R is obtained from fatty acid chosen from caprylic acids. , pelargonic, capric, undecylenic, lauric, tridecylenic, myristic, pentadecylic, palmitic, margaric, stearic, nonadecylic, arachic, henicosanoic, behenic, tricosanoic, lignoceric, pentacosanoic, cerotic, heptacosanoic, montanic, nonacosanoic, melissic, hentriacontanoic, laceroic, and their derivatives or unsaturated fatty acids such as palmitoleic acid, oleic acid, erucic acid, nervonic acid, linoleic acid, ⁇ -l
- the 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, soya oil, of cotton, flax, beef tallow.
- vegetable and animal oils such as coconut oil, palm oil, olive oil, peanut oil, rapeseed oil, sunflower oil, soya oil, of cotton, 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 oil.
- the di-alkyl fatty polyalkylamine derivative compositions of formulas (III) and / or (IV) according to the invention comprise compounds for which one or more NH fragments of the fatty polyalkylamine of the invention are methylated, alkoxylated, or two. Such compounds have been found to have advantageous solubility, particularly in lubricating oils.
- the alkoxylated derivatives are butoxylated, propoxylated and / or ethoxylated. If two or more alkoxylating agents are used, they may be used in any order, for example EO-PO-EO, and the different aikoxy units may be Polyhedral nature and / or present in a random manner.
- a primary -NH 2 group is alkoxylated with one or more alkylene oxides in a conventional manner to form a -NH-AO-H group, where AO represents one or more alkylene-oxy units.
- the -NH-AO-H group obtained can be further alkoxylated to form -N (AO-H) 2 units .
- alkylene oxide ie, more than 8 moles of alkylene oxides per mole of polyalkylamine
- the secondary amines if present, are alkoxylated.
- all the primary and secondary amine functions of the di-alkyl polyamine of formulas (III) and / or (IV) are alkoxylated.
- the di-alkyl fatty polyalkylamines are derived by methylation of one or more NH functions in a manner known to those skilled in the art, for example by reaction with formic acid and formaldehyde.
- one or more OH functions of the alkoxylated fatty di-alkyl polyalkylamines are conventionally methylated.
- polyalkylamine mixtures of formula (IV) are preferred. If appropriate, polyalkylamine mixtures of formulas (III) and / or (IV) are used.
- the branched polyalkylamines of the invention may be produced by any synthetic route known to those skilled in the art.
- a conventional method of production can be from a diamine and involves two or more cycles, preferably two for economic reasons, each cycle having a cyanoethylation step and a hydrogenation step. This process is subsequently named a two-step process.
- one equivalent of di-alkyl diamine can react in one step with two or more equivalents of acrylonitrile, followed by hydrogenation.
- optional additional cycles involving cyanoethylation and hydrogenation steps may be considered.
- Such a one-step process may be advantageous since it requires fewer intermediate steps.
- an acid catalyst is used such as HCl or acetic acid.
- the increase of the reaction temperature during cyanoethylation also makes it possible to increase the branching in this process.
- the temperature of a subsequent cyanoethylation step is greater than the temperature of a preceding cyanoethylation step, making it possible to obtain a compound with the desired branching.
- more than one mole of acrylonitrile per mole of initial polyamine is used, which also makes it possible to increase the branching of the expected product to the desired level.
- a solvent is used.
- Preferred solvents include C 1-4 alcohols and C 2-4 diols.
- ethanol is used because it allows a particular ease of handling.
- the C 1-4 alcohols and diols C 2 -4 are not of single solvents but also have a co-catalytic activity in the cyanoethylation step.
- the amount of solvent employed may vary over a wide range. For economic reasons, the amount employed is preferably minimal.
- the amount of solvent, particularly in the cyanoethylation step is preferably less than 50, 40, 30 or 25% by weight based on the liquid reaction mixture.
- the amount of solvent, in particular in the cyanoethylation step is preferably greater than 0.1, 0.5, 1, 5 or 10% by weight relative to the liquid reaction mixture.
- the mixture of di-alkyl fatty polyalkylamines of formulas (III) and / or (IV) according to the invention is characterized by a BN measured according to the ASTM D-2896 standard of between 150 and 350 mg KOH / g of amine, preferably between 170 and 340 and even more preferably between 180 and 320.
- the percentage by weight of the dialkyl polyalkylamine mixture relative to the total weight of the lubricating composition is chosen so that the BN provided by these compounds represents a contribution between 5 and 60 mgKOH / g of lubricant, preferably between 10 and 30 mgKOH / g of lubricant, total BN of said cylinder lubricant, measured according to ASTM D-2896.
- Lubricating composition The fatty amine of formula (I), or the mixture of fatty amines of formulas (III) and / or (IV) or the mixture of fatty amines of formulas (I), (III) and / or (IV) according to the invention for preventing and / or reducing the metallic losses of the parts of an engine, preferably a marine engine, is present in a lubricating composition.
- Said lubricant composition comprises:
- At least one base oil preferably a lubricating base oil for a marine engine
- At least one detergent based on alkaline or alkaline earth metals, overbased with carbonate metal salts at least one detergent based on alkaline or alkaline earth metals, overbased with carbonate metal salts.
- the lubricating composition has a BN determined according to ASTM D-2896 greater than or equal to 15 milligrams of potash per gram of lubricant, more preferably greater than or equal to 40 milligrams.
- the lubricating composition has a BN determined according to the ASTM D-2896 standard of between 40 and 120 milligrams of potash per gram of lubricant, preferably between 50 and 100 milligrams of potash per gram of lubricant.
- the lubricating composition also has a BN determined according to the ASTM D-2896 standard of between 15 and 40 milligrams of potash per gram of lubricant, preferably between 20 and 40 milligrams of potash per gram of lubricant.
- the mass percentage of fatty amine relative to the total weight of the cylinder lubricant is chosen so that the BN supplied by this fatty amine represents a contribution of at least 2 milligrams of potassium hydroxide. per gram of total BN lubricant of said cylinder lubricant, preferably at least 5 milligrams of potash per gram of lubricant to the total BN of said cylinder lubricant.
- the part of BN provided by a fatty amine in the lubricant cylinder according to the invention is calculated from its intrinsic BN measured according to the ASTM D standard. -2896 and its mass percentage in the finished lubricant:
- Amino BN lub x. BN amine / 100
- BN amine lub contribution of amine to the BN of the finished lubricant
- Amino BN intrinsic BN of the amine alone (ASTM D-2896).
- the mass percentage of fatty amine of formulas (I), (III) and / or (IV) relative to the total weight of the cylinder lubricant is chosen so that the BN brought by this fatty amine represents a contribution of 2 to 30 milligrams of potash per gram of lubricant, more preferably 5 to 25 milligrams of potash per gram of lubricant to the total BN of said lubricant cylinder.
- the fatty amine of formula (I) or the mixture of fatty amines of formulas (III) and / or (IV) or the mixture of fatty amines of formulas (I) (III) and / or (IV) is added in an amount of from 0.1 to 15%, preferably from 0.5 to 10%, preferably from 0.5 to 8% or from 3 to 10% by weight. weight relative to the total weight of the lubricating composition.
- the fatty amine of formula (I) represents from 0.5 to 10%, preferably from 0.5 to 8% by weight relative to the total weight of the lubricating composition.
- the weight percentage of the polyalkylamine di-alkyl mixture of formulas (III) and / or (IV) relative to the total weight of lubricant is between 0.1 and 15%, preferably between 0.5 and 10%, advantageously between 3 and 10%.
- the lubricating composition further comprises at least one neutral detergent.
- the detergents commonly used in the formulation of lubricating compositions are typically anionic compounds comprising 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 carboxylates, phenates, sulphonates, salicylates, and mixed detergents phenate-sulphonate and / or salicylates of 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 are preferably carboxylates, phenates, sulphonates, salicylates and mixed detergents phenates-sulphonates-salicylates, overbased with calcium carbonate.
- the base oil included in the lubricating composition is selected from oils of mineral, synthetic or vegetable origin and mixtures thereof.
- 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.
- the Group 1 mineral oils can be obtained by distillation of selected naphthenic or paraffinic crudes and then purification of these distillates by processes such as solvent extraction, solvent or catalytic dewaxing, hydrotreating 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 viscometric grade of SAE-60, generally 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 mm 2 / s.
- Grade 50 oils have a kinematic viscosity at 100 ° C of between 16.3 and 21.9 mm 2 / s.
- Grade 60 oils have a kinematic viscosity at 100 ° C between
- cylinder oils for marine 2-stroke diesel engines having a kinematic viscosity at 100 ° C of between 18 and 21.5, preferably between 19 and 21.5 mm 2 / s.
- 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%.
- the lubricating composition may further comprise one or more thickening additives whose role is to increase the viscosity of the composition, hot or cold, or by improving additives viscosity index (VI).
- thickening additives whose role is to increase the viscosity of the composition, hot or cold, or by improving additives viscosity index (VI).
- these additives are most often polymers of low molecular weight, of the order of 2000 to 50 000 dalton (Mn).
- the base oil (s) included in the lubricating composition according to the invention may be partially or totally substituted by these additives.
- 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).
- the lubricating composition may further comprise at least one antiwear additive.
- the anti-wear additive 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.
- phospho-sulfur-containing additives such as metal alkylthiophosphates, in particular zinc alkylthiophosphates, and more specifically zinc dialkyldithiophosphates or DTPZn.
- 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 lubricating composition may further comprise at least one dispersant.
- Dispersants are well known additives used in the formulation of lubricating composition, especially for application in the marine field. Their primary role is to keep particles present initially or in suspension 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.
- the lubricating composition may furthermore comprise all types of functional additives adapted to their use, for example anti-foam additives to counteract the effect of detergents, which may be, for example, polar polymers such as polymethylsiloxanes, polyacrylates, anti-oxidant and / or anti-rust additives, for example metal organo-detergents or thiadiazoles. These are known to those skilled in the art.
- 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 use of one or more fatty amines formulas (I), (III) and / or (IV) makes it possible to prevent and / or reduce the metallic losses of the parts in an engine. marine, two-stroke or four-stroke when burning any type of fuel oil.
- the use of one or more fatty amines of formulas (I), (III) and / or (IV) according to the invention makes it possible to prevent and / or reduce metal losses. parts in hot parts, especially the SPC zone, of a marine engine, two or four times, during the combustion of any type of fuel oil.
- the fuel oil has a sulfur content of less than 3.5% by weight relative to the total weight of the fuel oil.
- Another subject of the invention covers a method for preventing and / or reducing the metallic losses of the parts of an engine, preferably of a marine engine in which said parts are put in contact with one or more fatty amines soluble in a lubricating composition,
- the fatty amine being chosen from:
- R 1 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising at least 12 carbon atoms, and optionally at least one heteroatom chosen from nitrogen, sulfur or oxygen,
- R 2 , R 4 or R 5 independently represents a hydrogen atom or a linear or branched, saturated or unsaturated hydrocarbon group, and optionally comprising at least one heteroatom selected from nitrogen, sulfur or oxygen,
- R 3 represents a saturated or unsaturated hydrocarbon group, linear or branched, comprising one or more carbon atom (s), and optionally comprising at least one heteroatom selected from nitrogen, sulfur or oxygen, preferably oxygen,
- M is an integer greater than or equal to 1, preferably between 1 and 10, more preferably between 1 and 6, even more preferably is chosen from 1, 2 or 3,
- R identical or different, represents a linear or branched alkyl group comprising from 8 to 22 carbon atoms
- N and z independently of each other, represent 0, 1, 2 or 3
- said mixture comprising at least 3% by weight of branched compounds such that at least one of n or z is greater than or equal to 1, or of their derivatives, and
- 200 g of the lubricating composition comprising one or more fatty amines according to the invention are introduced into a 700 ml test tube and this test piece is heated at 60 ° C. with vigorous stirring for a period of approximately 30 minutes.
- a cast iron plate, previously sanded, cleaned and weighed, is immersed in the test piece thus heated and stirred, then a quantity of sulfuric acid diluted to 50% is gradually added during 1 h 30 in order to neutralize all or part of the BN. total of said lubricating composition.
- the amount of 50% diluted sulfuric acid added to the lubricating composition is calculated as a function of the number of BN points to be neutralized.
- the rate of addition of sulfuric acid diluted to 50% is calculated as a function of the total amount of sulfuric acid to be added over a period of 1 hour 30 minutes.
- the lubricating composition thus acidified and comprising the plate is subsequently stirred for an additional 30 minutes to ensure that the BN neutralization reaction is complete.
- a lubricating base oil comprising a mixture of mineral oils of group I and / or II, in particular Brightstock type oils,
- a fatty amine 2 comprising predominantly tetramines of formula (I),
- a fatty amine 3 comprising predominantly diamines of formula (I),
- a fatty amine 4 comprising predominantly triamines of formula (I),
- a fatty amine comprising predominantly tetramines of formula (I).
- the L 7 compositions according to the invention are described in Table I as well as a control lubricant composition L 8 comprising only a base oil and a detergent package; the percentages given correspond to mass percentages.
- the metal part loses little material, that is to say it loses 7 mg when in contact with fatty amines according to the invention contained in a lubricating composition, unlike a metal part contacted with a lubricating composition not comprising fatty amines according to the invention for which the metal losses rise above 1 15 mg.
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Abstract
Description
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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FR1557492A FR3039835B1 (fr) | 2015-08-03 | 2015-08-03 | Utilisation d'une amine grasse pour prevenir et/ou reduire les pertes metalliques des pieces dans un moteur |
PCT/EP2016/068477 WO2017021426A1 (fr) | 2015-08-03 | 2016-08-03 | Utilisation d'une amine grasse pour prevenir et/ou reduire les pertes métalliques des pièces dans un moteur |
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EP3331975A1 true EP3331975A1 (fr) | 2018-06-13 |
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EP16745760.5A Pending EP3331975A1 (fr) | 2015-08-03 | 2016-08-03 | Utilisation d'une amine grasse pour prevenir et/ou reduire les pertes métalliques des pièces dans un moteur |
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US (1) | US10738261B2 (fr) |
EP (1) | EP3331975A1 (fr) |
JP (1) | JP6833813B2 (fr) |
KR (1) | KR102665281B1 (fr) |
CN (1) | CN107922876B (fr) |
BR (1) | BR112018002388A2 (fr) |
FR (1) | FR3039835B1 (fr) |
HK (1) | HK1251606A1 (fr) |
RU (1) | RU2018103966A (fr) |
SG (1) | SG11201800901UA (fr) |
WO (1) | WO2017021426A1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3211062B1 (fr) * | 2016-02-29 | 2022-07-27 | TotalEnergies OneTech | Lubrifiant pour moteur marin deux temps |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
JP6556959B2 (ja) * | 2016-02-29 | 2019-08-07 | アクゾ ノーベル ケミカルズ インターナショナル ベスローテン フエンノートシャップAkzo Nobel Chemicals International B.V. | ジアルキル−ポリアルキルアミン組成物、それらの製造方法およびそれらの使用 |
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 |
JP7106579B6 (ja) | 2017-05-31 | 2022-08-17 | トータルエナジーズ マーケティング サービシーズ | ポリアミン官能基、酸性官能基およびホウ素官能基を含む化合物、ならびにその潤滑剤添加物としての使用 |
EP3630927B1 (fr) | 2017-05-31 | 2021-09-08 | Total Marketing Services | Composé comprenant des fonctionnalités polyamine, acide et bore et son utilisation comme additif pour lubrifiant |
FR3071252B1 (fr) | 2017-09-19 | 2020-04-03 | Total Marketing Services | Utilisation d'ester dans une composition lubrifiante pour ameliorer la proprete moteur |
US20220010232A1 (en) | 2018-11-09 | 2022-01-13 | Total Marketing Services | Compound comprising polyamine, carboxylate and boron functionalities and its use as a lubricant additive |
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US4250045A (en) * | 1979-06-22 | 1981-02-10 | Exxon Research & Engineering Co. | Polymerized fatty acid amine derivatives useful as friction and wear-reducing additives |
US4512903A (en) * | 1983-06-23 | 1985-04-23 | Texaco Inc. | Lubricant compositions containing amides of hydroxy-substituted aliphatic acids and fatty amines |
EP0608962A1 (fr) * | 1985-03-14 | 1994-08-03 | The Lubrizol Corporation | Condensats à haut poids moléculaire contenant de l'azote, carburants et lubrifiants les contenant |
US4957649A (en) * | 1988-08-01 | 1990-09-18 | The Lubrizol Corporation | Lubricating oil compositions and concentrates |
US4975096A (en) * | 1988-09-09 | 1990-12-04 | Chevron Research Company | Long chain aliphatic hydrocarbyl amine additives having an oxyalkylene hydroxy connecting group |
ATE146518T1 (de) * | 1992-08-03 | 1997-01-15 | Henkel Ecolab Gmbh & Co Ohg | Schmiermittelkonzentrat und wässrige schmiermittellösung auf basis von fettaminen, verfahren zu deren herstellung und deren verwendung |
WO1996001854A1 (fr) * | 1994-07-11 | 1996-01-25 | Exxon Chemical Patents Inc. | Dispersants a base de succinimide pour huiles lubrifiantes, derives de polyamines lourdes |
GB9421282D0 (en) | 1994-10-21 | 1994-12-07 | Exxon Chemical Patents Inc | Additives and oleaginous compositions |
JP5057630B2 (ja) | 2003-02-18 | 2012-10-24 | 昭和シェル石油株式会社 | 工業用潤滑油組成物 |
CA2576014A1 (fr) * | 2004-08-06 | 2006-02-16 | Basf Aktiengesellschaft | Additifs de polyamines destines aux carburants et lubrifiants |
FR2932813B1 (fr) * | 2008-06-18 | 2010-09-03 | Total France | Lubrifiant cylindre pour moteur marin deux temps |
KR101722380B1 (ko) * | 2009-10-09 | 2017-04-05 | 쉘 인터내셔날 리써취 마트샤피지 비.브이. | 윤활 조성물 |
FR2974111B1 (fr) * | 2011-04-14 | 2013-05-10 | Total Raffinage Marketing | Lubrifiant cylindre pour moteur marin deux temps |
EP2692839B1 (fr) * | 2012-07-31 | 2015-11-18 | Infineum International Limited | Composition d'huile lubrifiante contenant un inhibiteur de corrosion |
FR3005474B1 (fr) | 2013-05-07 | 2016-09-09 | Total Raffinage Marketing | Lubrifiant pour moteur marin |
EP3060638B1 (fr) * | 2013-10-25 | 2017-08-02 | Akzo Nobel Chemicals International B.V. | Sels d'amines grasses en tant que modificateurs de friction pour lubrifiants |
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 (fr) * | 2016-02-29 | 2022-07-27 | TotalEnergies OneTech | Lubrifiant pour moteur marin deux temps |
-
2015
- 2015-08-03 FR FR1557492A patent/FR3039835B1/fr active Active
-
2016
- 2016-08-03 EP EP16745760.5A patent/EP3331975A1/fr active Pending
- 2016-08-03 RU RU2018103966A patent/RU2018103966A/ru not_active Application Discontinuation
- 2016-08-03 BR BR112018002388-4A patent/BR112018002388A2/pt active Search and Examination
- 2016-08-03 KR KR1020187003438A patent/KR102665281B1/ko active IP Right Grant
- 2016-08-03 JP JP2018506315A patent/JP6833813B2/ja active Active
- 2016-08-03 WO PCT/EP2016/068477 patent/WO2017021426A1/fr active Application Filing
- 2016-08-03 CN CN201680045002.XA patent/CN107922876B/zh active Active
- 2016-08-03 US US15/750,312 patent/US10738261B2/en active Active
- 2016-08-03 SG SG11201800901UA patent/SG11201800901UA/en unknown
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2018
- 2018-08-23 HK HK18110845.6A patent/HK1251606A1/zh unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3211062B1 (fr) * | 2016-02-29 | 2022-07-27 | TotalEnergies OneTech | Lubrifiant pour moteur marin deux temps |
Also Published As
Publication number | Publication date |
---|---|
JP2018522131A (ja) | 2018-08-09 |
KR102665281B1 (ko) | 2024-05-10 |
JP6833813B2 (ja) | 2021-02-24 |
CN107922876B (zh) | 2020-11-03 |
FR3039835B1 (fr) | 2019-07-05 |
FR3039835A1 (fr) | 2017-02-10 |
RU2018103966A3 (fr) | 2019-10-07 |
KR20180036723A (ko) | 2018-04-09 |
SG11201800901UA (en) | 2018-03-28 |
US10738261B2 (en) | 2020-08-11 |
HK1251606A1 (zh) | 2019-02-01 |
WO2017021426A1 (fr) | 2017-02-09 |
US20180223218A1 (en) | 2018-08-09 |
CN107922876A (zh) | 2018-04-17 |
BR112018002388A2 (pt) | 2018-09-18 |
RU2018103966A (ru) | 2019-08-02 |
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