EP3322780B1 - Inhibiteurs de corrosion pour carburants - Google Patents
Inhibiteurs de corrosion pour carburants Download PDFInfo
- Publication number
- EP3322780B1 EP3322780B1 EP16736891.9A EP16736891A EP3322780B1 EP 3322780 B1 EP3322780 B1 EP 3322780B1 EP 16736891 A EP16736891 A EP 16736891A EP 3322780 B1 EP3322780 B1 EP 3322780B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- acid
- use according
- esters
- carbon atoms
- olefin
- 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
- 239000000446 fuel Substances 0.000 title claims description 50
- 238000005260 corrosion Methods 0.000 title claims description 38
- 230000007797 corrosion Effects 0.000 title claims description 38
- 239000003112 inhibitor Substances 0.000 title claims description 22
- 229920001577 copolymer Polymers 0.000 claims description 72
- 239000000203 mixture Substances 0.000 claims description 64
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 54
- 239000000178 monomer Substances 0.000 claims description 51
- 150000001336 alkenes Chemical class 0.000 claims description 42
- 125000004432 carbon atom Chemical group C* 0.000 claims description 37
- 238000006243 chemical reaction Methods 0.000 claims description 30
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 27
- 239000004711 α-olefin Substances 0.000 claims description 23
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 22
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 22
- 150000008064 anhydrides Chemical group 0.000 claims description 21
- 229920000642 polymer Polymers 0.000 claims description 20
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 19
- 150000002148 esters Chemical class 0.000 claims description 18
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 16
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 15
- 229910052783 alkali metal Inorganic materials 0.000 claims description 14
- 150000001340 alkali metals Chemical class 0.000 claims description 14
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical compound CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 14
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 13
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 12
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 12
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 12
- 239000011701 zinc Substances 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 11
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 11
- 229910052725 zinc Inorganic materials 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
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- 229910052791 calcium Inorganic materials 0.000 claims description 5
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- 239000010959 steel Substances 0.000 claims description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 4
- 150000004808 allyl alcohols Chemical class 0.000 claims description 4
- 150000002170 ethers Chemical class 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- 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 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 230000005764 inhibitory process Effects 0.000 claims description 3
- 239000011777 magnesium Substances 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
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- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims 2
- 150000003926 acrylamides Chemical class 0.000 claims 1
- -1 C12 dicarboxylic acids Chemical class 0.000 description 65
- 239000000654 additive Substances 0.000 description 36
- 239000002253 acid Substances 0.000 description 22
- 239000007795 chemical reaction product Substances 0.000 description 22
- 239000002199 base oil Substances 0.000 description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- 150000001412 amines Chemical class 0.000 description 17
- 238000009472 formulation Methods 0.000 description 17
- 239000004215 Carbon black (E152) Substances 0.000 description 15
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 15
- 235000014113 dietary fatty acids Nutrition 0.000 description 15
- 229930195729 fatty acid Natural products 0.000 description 15
- 239000000194 fatty acid Substances 0.000 description 15
- 229930195733 hydrocarbon Natural products 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 14
- 229920002367 Polyisobutene Polymers 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 13
- 150000004665 fatty acids Chemical class 0.000 description 13
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 12
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 12
- 239000002283 diesel fuel Substances 0.000 description 12
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 12
- 229920000768 polyamine Polymers 0.000 description 12
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 10
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 239000003599 detergent Substances 0.000 description 10
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
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- 238000003786 synthesis reaction Methods 0.000 description 10
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- 125000003368 amide group Chemical group 0.000 description 9
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 8
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- 239000003513 alkali Substances 0.000 description 8
- 150000002430 hydrocarbons Chemical class 0.000 description 8
- 229910052500 inorganic mineral Inorganic materials 0.000 description 8
- 239000011707 mineral Substances 0.000 description 8
- 229920000570 polyether Polymers 0.000 description 8
- 150000003335 secondary amines Chemical class 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
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- 238000005227 gel permeation chromatography Methods 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 7
- 238000006460 hydrolysis reaction Methods 0.000 description 7
- 150000002989 phenols Chemical class 0.000 description 7
- 239000011593 sulfur Substances 0.000 description 7
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- 238000012360 testing method Methods 0.000 description 7
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 7
- OAOABCKPVCUNKO-UHFFFAOYSA-N 8-methyl Nonanoic acid Chemical compound CC(C)CCCCCCC(O)=O OAOABCKPVCUNKO-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
- 125000003342 alkenyl group Chemical group 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
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- 238000002360 preparation method Methods 0.000 description 6
- 235000011044 succinic acid Nutrition 0.000 description 6
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 5
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M145/00—Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
- C10M145/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/10—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
- C10M145/16—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate polycarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/146—Macromolecular compounds according to different macromolecular groups, mixtures thereof
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/196—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
- C10L1/1963—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof mono-carboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/196—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
- C10L1/1966—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof poly-carboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/236—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derivatives thereof
- C10L1/2366—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derivatives thereof homo- or copolymers derived from unsaturated compounds containing amine groups
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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Claims (15)
- Utilisation de copolymères, pouvant être obtenus par :- lors d'une première étape de réaction (I), la copolymérisation de :(A) au moins un acide mono- ou dicarboxylique éthyléniquement insaturé ou ses dérivés, choisis dans le groupe constitué par :- les anhydrides sous forme monomère ou polymère,- les esters mono- ou dialkyliques, et- les esters mixtes,(B) au moins une α-oléfine contenant au moins 12 à 30, inclus, atomes de carbone,(C) éventuellement au moins une oléfine aliphatique ou cycloaliphatique supplémentaire, comprenant au moins 4 atomes de carbone, qui est différente de (B), et(D) éventuellement un ou plusieurs monomères copolymérisables supplémentaires, qui sont différents des monomères (A), (B) et (C), choisis dans le groupe constitué par :(Da) les esters de vinyle,(Db) les éthers de vinyle,(Dc) les esters de l'acide (méth)acrylique d'alcools, qui comprennent au moins 5 atomes de carbone,(Dd) les alcools allyliques ou leurs éthers,(De) les composés de N-vinyle, choisis dans le groupe constitué par les composés de vinyle d'hétérocycles contenant au moins un atome d'azote, les N-vinylamides ou les N-vinyllactames,(Df) les composés aromatiques éthyléniquement insaturés,(Dg) les nitriles α,β-éthyléniquement insaturés,(Dh) les amides de l'acide (méth)acrylique et(Di) les allylamines,
suivie par- lors d'une deuxième étape de réaction optionnelle (II), l'hydrolyse partielle des fonctionnalités anhydride contenues dans le copolymère obtenu en (I) et/ou la saponification partielle des fonctionnalités ester d'acide carboxylique contenues dans le copolymère obtenu en (I), à condition que plus de 90 % des fonctionnalités anhydride et ester d'acide carboxylique restent intactes après l'étape de réaction (II),en tant qu'inhibiteurs de corrosion dans des carburants qui présentent une teneur en métaux alcalins et/ou alcalino-terreux et/ou en zinc d'au moins 0,1 ppm en poids. - Utilisation selon la revendication 1, caractérisée en ce que les métaux alcalins et/ou alcalino-terreux et/ou le zinc sont choisis dans le groupe constitué par le sodium, le zinc, le magnésium et le calcium.
- Utilisation selon l'une quelconque des revendications précédentes, caractérisée en ce que le monomère (A) est choisi dans le groupe constitué par l'acide acrylique, l'acide méthacrylique, l'ester méthylique de l'acide acrylique, l'ester éthylique de l'acide acrylique, l'ester n-butylique de l'acide acrylique, l'ester méthylique de l'acide méthacrylique et l'anhydride de l'acide maléique, de préférence l'anhydride de l'acide maléique.
- Utilisation selon l'une quelconque des revendications précédentes, caractérisée en ce que le monomère (B) consiste en une α-oléfine contenant au moins 14 à 26, inclus, atomes de carbone.
- Utilisation selon l'une quelconque des revendications précédentes, caractérisée en ce que l'oléfine (C) consiste en un polymère de propène, de 1-butène, de 2-butène ou d'iso-butène comprenant plus de 30 atomes de carbone ou en des mélanges d'oléfines contenant un tel polymère, de préférence d'iso-butène ou des mélanges d'oléfines contenant un tel polymère, ayant un poids moléculaire moyen Mw dans la plage allant de 500 à 5 000 g/mol.
- Utilisation selon l'une quelconque des revendications précédentes, caractérisée en ce que le mélange de matières des oléfines (B) et (C) comprend au moins 12 atomes de carbone, moyenné sur leurs quantités de matières.
- Utilisation selon l'une quelconque des revendications précédentes, caractérisée en ce que le monomère (D) est choisi dans le groupe constitué par (Da), (Db), (Dc), (De) et (Df).
- Utilisation selon l'une quelconque des revendications précédentes, caractérisée en ce que le rapport molaire de (A)/((B) et (C)) (au total) est de 10:1 à 1:10.
- Utilisation selon la revendication 8, caractérisée en ce que le rapport molaire entre le monomère (B) et le monomère (C) est de 1:0,05 à 10.
- Utilisation selon la revendication 8 ou 9, caractérisée en ce que la proportion d'un ou de plusieurs des monomères (D), par rapport à la quantité des monomères (A), (B) et éventuellement (C) (au total) est de 5 à 200 % en moles.
- Utilisation selon l'une quelconque des revendications précédentes, caractérisée en ce que l'anhydride de l'acide maléique est utilisé en tant que composant (A) et l'étape de réaction optionnelle (II) n'est pas réalisée.
- Utilisation selon l'une quelconque des revendications 1 à 10, caractérisée en ce que l'anhydride de l'acide maléique est utilisé en tant que composant (A) et, à l'étape de réaction (II), plus de 90 % et jusqu'à 99,9 % des fonctionnalités anhydride restent intactes.
- Utilisation selon l'une quelconque des revendications précédentes, pour l'inhibition de la corrosion de surfaces en fer, en acier et/ou en métal non ferreux.
- Utilisation selon l'une quelconque des revendications 1 à 12 pour l'inhibition de la corrosion de cuivre et d'alliages contenant du cuivre.
- Utilisation selon l'une quelconque des revendications précédentes, caractérisée en ce que le carburant est un carburant diesel ou automobile.
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Application Number | Priority Date | Filing Date | Title |
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EP15177085 | 2015-07-16 | ||
PCT/EP2016/066466 WO2017009306A1 (fr) | 2015-07-16 | 2016-07-12 | Inhibiteurs de corrosion pour carburants et lubrifiants |
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EP3322780A1 EP3322780A1 (fr) | 2018-05-23 |
EP3322780B1 true EP3322780B1 (fr) | 2019-09-18 |
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US (1) | US20180201863A1 (fr) |
EP (1) | EP3322780B1 (fr) |
CN (1) | CN107849478A (fr) |
BR (1) | BR112018000797A2 (fr) |
ES (1) | ES2762999T3 (fr) |
RU (1) | RU2018105762A (fr) |
SG (1) | SG11201800399TA (fr) |
WO (1) | WO2017009306A1 (fr) |
ZA (1) | ZA201800858B (fr) |
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PL3099720T3 (pl) | 2014-01-29 | 2018-12-31 | Basf Se | Zastosowanie dodatków opartych na kwasach polikarboksylowych do paliw silnikowych |
WO2017009305A1 (fr) | 2015-07-16 | 2017-01-19 | Basf Se | Copolymères utilisés en tant qu'additifs pour carburants et lubrifiants |
PT3481920T (pt) | 2016-07-05 | 2021-11-10 | Basf Se | Utilização de inibidores de corrosão para combustíveis e lubrificantes |
CN110088253B (zh) | 2016-12-15 | 2022-03-18 | 巴斯夫欧洲公司 | 作为燃料添加剂的聚合物 |
RU2019122807A (ru) | 2016-12-20 | 2021-01-22 | Басф Се | Применение смеси комплексного сложного эфира с монокарбоновой кислотой для уменьшения трения |
CA3162057A1 (fr) * | 2019-12-18 | 2021-06-24 | James D. Burrington | Compose tensioactif polymere |
PL3940043T3 (pl) * | 2020-07-14 | 2024-02-19 | Basf Se | Inhibitory korozji do paliw silnikowych i smarów |
EP4247921A1 (fr) * | 2020-11-20 | 2023-09-27 | Basf Se | Mélanges pour améliorer ou renforcer la séparation de l'eau de carburants |
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US3382056A (en) * | 1966-06-03 | 1968-05-07 | Chevron Res | Maleic anhydride copolymers as rust inhibitors |
US3909215A (en) * | 1973-03-27 | 1975-09-30 | Chevron Res | Rust inhibitors for hydrocarbon fuels |
JPS5922791B2 (ja) * | 1978-12-25 | 1984-05-29 | 三菱化学株式会社 | 防錆剤 |
JPS59100196A (ja) * | 1982-11-30 | 1984-06-09 | Mitsubishi Chem Ind Ltd | 水性潤滑剤 |
DE3411531A1 (de) * | 1984-03-29 | 1985-10-10 | Basf Ag, 6700 Ludwigshafen | Verfahren zur umsetzung von olefinen mit maleinsaeureanhydrid und verwendung der erhaltenen bernsteinsaeureanhydride zur herstellung von korrosionsschutzmitteln und mineraloelhilfsmitteln |
JPH0668111B2 (ja) * | 1986-11-17 | 1994-08-31 | 出光興産株式会社 | 含水潤滑剤 |
DE3733172A1 (de) * | 1987-10-01 | 1989-04-20 | Basf Ag | Kraftstoffe fuer ottomotoren |
DE3730885A1 (de) * | 1987-09-15 | 1989-03-23 | Basf Ag | Kraftstoffe fuer ottomotoren |
US5422023A (en) * | 1993-10-12 | 1995-06-06 | Exxon Research And Engineering Company | Corrosion inhibitor for aviation turbine oils (PNE-628) |
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CN103384718A (zh) * | 2010-12-21 | 2013-11-06 | 路博润公司 | 官能化共聚物及其润滑组合物 |
US10131859B2 (en) * | 2011-12-30 | 2018-11-20 | Butamax Advanced Biofuels Llc | Corrosion inhibitor compositions for oxygenated gasolines |
EP2898051B1 (fr) * | 2012-09-24 | 2017-08-16 | The Lubrizol Corporation | Lubrifiante contenant un mélange d'un copolmère d'un oléfine-ester avec un copolymère d'un éthyléne-alpha-oléfine |
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US10377958B2 (en) * | 2014-01-29 | 2019-08-13 | Basf Se | Corrosion inhibitors for fuels and lubricants |
-
2016
- 2016-07-12 ES ES16736891T patent/ES2762999T3/es active Active
- 2016-07-12 US US15/743,897 patent/US20180201863A1/en not_active Abandoned
- 2016-07-12 CN CN201680041522.3A patent/CN107849478A/zh active Pending
- 2016-07-12 EP EP16736891.9A patent/EP3322780B1/fr active Active
- 2016-07-12 SG SG11201800399TA patent/SG11201800399TA/en unknown
- 2016-07-12 RU RU2018105762A patent/RU2018105762A/ru not_active Application Discontinuation
- 2016-07-12 WO PCT/EP2016/066466 patent/WO2017009306A1/fr active Application Filing
- 2016-07-12 BR BR112018000797-8A patent/BR112018000797A2/pt not_active Application Discontinuation
-
2018
- 2018-02-09 ZA ZA2018/00858A patent/ZA201800858B/en unknown
Non-Patent Citations (1)
Title |
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None * |
Also Published As
Publication number | Publication date |
---|---|
SG11201800399TA (en) | 2018-02-27 |
EP3322780A1 (fr) | 2018-05-23 |
RU2018105762A3 (fr) | 2019-10-16 |
CN107849478A (zh) | 2018-03-27 |
RU2018105762A (ru) | 2019-08-16 |
WO2017009306A1 (fr) | 2017-01-19 |
ZA201800858B (en) | 2019-06-26 |
ES2762999T3 (es) | 2020-05-26 |
US20180201863A1 (en) | 2018-07-19 |
BR112018000797A2 (pt) | 2018-09-04 |
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