EP0353116B1 - Rezepte von stickstoffhaltigen Zusätzen für Motorkraftstoffe und diese enthaltende Motorkraftstoffe - Google Patents
Rezepte von stickstoffhaltigen Zusätzen für Motorkraftstoffe und diese enthaltende Motorkraftstoffe Download PDFInfo
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- EP0353116B1 EP0353116B1 EP89401846A EP89401846A EP0353116B1 EP 0353116 B1 EP0353116 B1 EP 0353116B1 EP 89401846 A EP89401846 A EP 89401846A EP 89401846 A EP89401846 A EP 89401846A EP 0353116 B1 EP0353116 B1 EP 0353116B1
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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
- C10L1/143—Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular compounds
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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
- C10L1/22—Organic compounds containing nitrogen
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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
- C10L1/146—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
- C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
- C10L1/1985—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
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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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/224—Amides; Imides carboxylic acid amides, imides
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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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/232—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
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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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
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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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
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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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
- C10L1/2387—Polyoxyalkyleneamines (poly)oxyalkylene amines and derivatives thereof (substituted by a macromolecular group containing 30C)
Definitions
- the present invention relates to additive formulations which, when added, for example, to engine fuels, significantly reduce their tendency to deposit and corrode various parts of the engine.
- the use of conventional fuels very often leads to fouling of the different parts of the engine as a result of the incomplete vaporization and combustion of the fuel in the intake system and / or in the combustion chamber and as a result of the presence traces of lubricants.
- the accumulation of these deposits can be done at the injectors, the carburetor and the intake valves.
- Such an accumulation has harmful consequences both in terms of driving pleasure, with the appearance of unstable idling and misfires in spark-ignition engines, and in terms of optimal engine operation by changing the richness as a result. fuel adsorption-desorption phenomena on the deposits formed.
- the accumulation of deposits in the engines and in particular on the intake valves can also be reduced by the use of fuels containing certain additives, for example detergent-type additives possibly combined for example with anticorrosion additives or anti-deposit for room combustion.
- fuels containing certain additives for example detergent-type additives possibly combined for example with anticorrosion additives or anti-deposit for room combustion.
- Additives well known in the trade, for example those of the polyisobutene-amine type, are usually associated with a mineral or synthetic oil and are capable of causing increased fouling of the combustion chambers and therefore an increase in the octane requirement of the motor with greater sensitivity to the rattling phenomenon.
- the invention provides formulations of additives, in particular for engine fuels, which make it possible to substantially reduce the abovementioned drawbacks.
- the additive formulations of the present invention can be used in particular as multifunctional fuel additives; in particular for fuels used in spark ignition engines.
- the additive formulations of the invention have excellent detergent properties at the intake valves and the carburetor and have very good anti-corrosion properties.
- the additive formulations of the invention used in particular in fuels for positive-ignition engines make it possible to greatly reduce the formation of deposits on the intake valves, and the fouling of carburetors or injectors.
- these additive formulations reduce the corrosion of the various mechanical parts with which the fuel comes into contact.
- These additive formulations can be used without the addition of mineral oil, which makes it possible to overcome the drawbacks mentioned above and related to the use of a mineral oil.
- these additive formulations include: a component (A) and a component (B) said component (A) consisting of at least one nitrogenous compound resulting from the reaction of at least one succinic derivative chosen from the group formed by alkenylsuccinic acids and anhydrides and acids and polyalkenylsuccinic anhydrides on at least one polyamine corresponding to the general formula in which R1 represents a hydrogen atom or a hydrocarbon group having from 1 to 60 carbon atoms, Z is chosen from the groups -O- and -NR3- in which R3 represents a hydrogen atom or a hydrocarbon group having 1 to 60 carbon atoms, R1 and R3 can form together with the nitrogen atom to which they are linked a heterocycle, each R2 independently represents a hydrogen atom or a hydrocarbon group having from 1 to 4 carbon atoms, n is an integer from 2 to 6, m is an integer from 1 to 10 when Z is -NR3- and an integer from 2 to 10 when Z is
- the additive formulations according to the present invention further comprise at least one component (C) consisting of at least one polyglycol, soluble in said fuel, of molecular weight number 480 to 2100 and of general formula (III): (III) HO - R - (- O - R--) x -O - R - OH wherein each of the R groups independently represents a hydrocarbon group having 2 to 6 carbon atoms and x represents the average degree of polymerization.
- component (C) consisting of at least one polyglycol, soluble in said fuel, of molecular weight number 480 to 2100 and of general formula (III): (III) HO - R - (- O - R--) x -O - R - OH wherein each of the R groups independently represents a hydrocarbon group having 2 to 6 carbon atoms and x represents the average degree of polymerization.
- the constituent (C) is preferably a polyglycol of general formula (III) above in which each of the groups R independently represents an alkylene group, linear or branched, having from 2 to 4 atoms carbon and most often an ethylene or propylene group.
- each of the groups R independently represents an alkylene group, linear or branched, having from 2 to 4 atoms carbon and most often an ethylene or propylene group.
- the polyglycols, of general formula (III) which are particularly preferred, mention may be made of those in which each of the groups R represents a propylene group of formula: CH3-CH-CH2-
- Component (C) is preferably a polyglycol of number average molecular weight from 600 to 1800 and most often from 650 to 1250.
- the polydispersity index of the polyglycol, used as component (C), in the formulations according to the present invention, is usually about 1 to 1.25 and most often about 1 to 1.15.
- One of the characteristics of the invention relates to the synergistic effect observed when a constituent (A) and a constituent (B) are combined in a fuel.
- This synergistic effect is manifested in particular by a notable reduction in the tendency of the fuel to form deposits on the intake valves; one could not foresee such a significant reduction by considering the separate effects of constituents (A) and (B).
- This synergy is also manifested by a noticeable improvement in the cleanliness of the carburetor after a fixed operating time, an improvement which could not have been foreseen by considering the separate effects of the constituents (A) and (B).
- the molar ratio of the constituent (A) to the constituent ( B) or from 0.2: 1 to 5: 1, preferably from 0.2: 1 to 1: 1, most preferably from 0.3: 1 to 0.9: 1 and better still from 0, 4: 1 to 0.8: 1.
- the succinic acid and / or anhydride used to form component (A) and component (B) may be the same or different. It is possible to use a single succinic derivative or a mixture of several succinic derivatives.
- the succinic acid and / or anhydride used in the context of the present invention usually has a number average molecular weight of about 200 to 3000, preferably 500 to 2000 and most often 700 to 1500.
- These derivatives succinics are widely described in the prior art; they are for example obtained by the action of at least one alpha olefin or of a chlorinated hydrocarbon on maleic acid or anhydride.
- the alpha olefin or the chlorinated hydrocarbon used in this synthesis can be linear or branched, and usually contain from 10 to 150 carbon atoms, preferably from 15 to 80 carbon atoms and most often from 20 to 75 carbon atoms in their molecule.
- This olefin can also be an oligomer, for example a dimer, a trimer or a tetramer, or a polymer of a lower olefin, for example having 2 to 10 carbon atoms, such as ethylene, propylene, n -butene-1, isobutene, n-hexene-1, n-octene-1, methyl-2-heptene-1 or methyl-2-propyl-5-hexene-1. It is possible to use mixtures of olefins or mixtures of chlorinated hydrocarbons.
- succinic anhydrides mention may be made of n-octadecenylsuccinic anhydride, dodecenylsuccinic anhydride and polyisobutenyl succinic anhydrides, often called PIBSA, having a number-average molecular mass as defined above.
- the polyamines of formula (I) are preferably those in which R1 is a hydrogen atom or a hydrocarbon group having from 1 to 30 carbon atoms, Z is preferably a group -NR3- in which R3 preferably represents an atom of hydrogen or a hydrocarbon group having from 1 to 30 carbon atoms, each of the R2 independently represents preferably a hydrogen atom or a methyl group, n is an integer from 2 to 4 and when Z is a group -NR3- m is preferably an integer from 1 to 5.
- Z is -NR3-, R1, R2 and R3 each represent a hydrogen atom, n is equal to 2 and m is an integer from 1 to 5 or those in which R1 represents a hydrocarbon group preferably having from 5 to 24 carbon atoms, Z represents a group -NR3- in which R3 is a hydrogen atom, R2 represents a hydrogen atom, n is a number integer from 2 to 4, preferably 3, and m is an integer from 1 to 5, preferably 1.
- the hydrocarbon groups R1 and R3 are usually alkyl, alkenyl, linear or branched, aryl, aryl-alkyl (aralkyl), alkyl-aryl (alkaryl) or cycloaliphatic groups.
- the R1 and R3 groups are preferably alkyl or alkenyl groups, linear or branched.
- the hydrocarbon group R2 is usually an alkyl group, preferably linear, and for example methyl, ethyl, n-propyl or n-butyl.
- N-alkyl diamino-1,3 propane for example N-dodecyldiamino-1,3 propane, N-tetradecyldiamino-1,3 propane, N-hexadecyldiamino-1,3 propane, N-octadecyldiamino-1,3 propane, N-eicosyldiamino-1,3 propane and N-docosyldiamino-1,3 propane; mention may also be made of N-alkyldipropylene triamines, for example N-hexadecyldipropylene triamine, N-octadecyldipropylene triamine, N-eicosy
- N, N diamines examples include N, N-diethyl-1,2-diamino ethane, N, N-diisopropyl diamino-1,2 ethane, N, N-dibutyl diamino-1,2 ethane, N, N-diethyl diamino-1,4 butane, N, N-dimethyl diamino-1,3 propane, N, N 1,3-diethyl diamino-1,3 propane, N, N-dioctyl diamino-1,3 propane, N, N-didecyl diamino-1,3 propane, N, N-N-didodecyl diamino-1,3 propane, N , N-dissetradécyl diamino-1,3 propane, N, N-dihexadécyl diamino-1,3 propane, N, N-dioctadécyl di
- etheramines examples include N- (octyloxy-3-propyl) diamino-1,3 propane, N- (decyloxy-3 propyl) diamino-1,3 propane, N- (trimethyl- 2,4,6 decyl) oxy-3 propyl diamino-1,3 propane.
- the polyamines of formulas (II) are preferably those in which R1 and R3 each represent a hydrogen atom A, B, C and D identical or different each represent an alkylidene group having 2 to 4 carbon atoms, for example ethylidene , propylidene, isopropylidene, butylidene and isobutylidene, a is an integer from 1 to 60 and b and c are zero; or a is an integer from 1 to 59, c is zero or an integer such that the sum a + c is from 1 to 59 and b is an integer from 1 to 50; with in each case the sum a + b + c equal to an integer from 1 to 60.
- the reaction for the formation of component (A) is usually carried out by progressive addition of the polyamine to a solution or to a dispersion of the succinic derivative in an organic solvent, at ordinary temperature, then heating to a temperature usually between 65 and 250 ° C. and preferably between 80 and 200 ° C.
- the organic solvent used in this preparation has a boiling point of between 65 and 250 ° C. and is usually chosen so as to allow the elimination of the water formed during the condensation of the polyamine on the succinic derivative, preferably in the form of a water-organic solvent azeotrope.
- An organic solvent will usually be used such as for example benzene, toluene, xylenes, ethylbenzene or a hydrocarbon cut such as for example the commercial cut SOLVESSO 150 (190-209 ° C) containing 99% by weight of aromatic compounds.
- the duration of the heating after the end of the addition of the polyamine is usually 0.5 to 7 hours, preferably 1 to 5 hours.
- the heating is usually continued, at the chosen temperature, most often at reflux, until the end of the evolution of the water formed during the reaction.
- the product obtained is then optionally isolated by removing, for example by vacuum distillation, the solvent used in the preparation.
- the amount of water removed during the reaction is usually about 0.8 to 1.2 moles and most often about 1 mole of water per mole of succinic derivative.
- the polyamine is preferably diluted in an organic solvent, for example one of those mentioned above and preferably the same as that used to form the solution or dispersion of the succinic derivative; this dilution facilitates the gradual addition of the polyamine.
- the amount of polyamine employed is usually at least 0.5 mole per mole of succinic derivative, for example from 0.5: 1 to 2: 1 and preferably from 0.8: 1 to 1.2: 1. most often uses an amount of about 1 mole of polyamine per mole of succinic derivative.
- the constituent (A) used can be a commercial compound, for example the compound sold by the company OCTEL under the reference OMA 41OG, which is based on a condensation product of tetraethylene pentamine on a PIBSA.
- the 1- (2-hydroxyethyl -) - imidazolines substituted in position 2 by an alkyl or alkenyl radical having from 1 to 25 carbon atoms used for the preparation of component (B) can be commercial compounds or can be synthesized for example by reaction of at least one organic acid with N- (2-hydroxyethyl) -ethylenediamine. The reaction proceeds by a first amidation step followed by cyclization.
- the organic acids used usually have from 2 to 26 carbon atoms; they are preferably aliphatic monocarboxylic acids.
- Examples include acetic acid, propanoic acid, butanoic acid, acid caproic, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, cerotic acid and the following unsaturated fatty acids:
- component (B) 1- (2-hydroxyethyl) -2 heptadecenylimidazoline is marketed by the company CIBA-GEIGY under the name "Amine-O" and by the company PROTEX under the name "Imidazoline-O".
- the preparation of component (B) is usually carried out by progressive addition of imidazoline, for example diluted in an organic solvent to a solution or to a dispersion of the succinic derivative in an organic solvent.
- the solvents used are preferably identical and they are, for example, chosen from those mentioned above in the description of the preparation of component (A).
- the addition of imidazoline to the succinic derivative is usually carried out at room temperature; after the end of the addition, the mixture is heated to a temperature usually around 65 to 250 ° C, preferably around 80 to 200 ° C.
- the duration of the heating, after the end of the addition of imidazoline is usually 0.5 to 7 hours, preferably 1 to 5 hours. Heating is usually continued, at the chosen temperature, most often at reflux, until the end of the evolution of the water formed during the reaction.
- the product obtained is then optionally isolated by removing, for example by vacuum distillation, the solvent used in the preparation.
- the amount of water removed during the reaction is usually about 0.2 to 0.8 moles and most often about 0.3 to 0.6 moles of water per mole of succinic derivative.
- the amount of imidazoline used in the reaction is usually at least 0.5 mole per mole of succinic derivative, for example from 0.5: 1 to 1.5: 1 and preferably from 0.9: 1 a 1.1: 1. Most of the time, approximately 1 mole of imidazoline is used per mole of succinic derivative.
- the formulations of the present invention can be used in the form of a solution in the reaction medium having served for the preparation of each of the constituents.
- the formulations can also be added directly to the fuel or be previously diluted in a solvent chosen, for example, from those mentioned above for the preparation of each of the constituents.
- the formulations of the present invention are mainly used as multifunctional additives for a fuel for engines, for example a fuel based on hydrocarbons or based on a mixture of hydrocarbons and at least one oxygenated compound chosen from the group formed. by alcohols and ethers, or a non-hydrocarbon fuel such as for example an alcohol or a mixture of alcohols.
- the formulations of the present invention are particularly well suited for use as additives for fuels used in spark ignition engines. Examples of fuels that may be mentioned include gasolines such as, for example, those defined by standard ASTM D-439, gas oils or diesel fuels, such as, for example, those defined by standard ASTM D-975.
- These fuels may also contain other additives as the formulations of the present invention for example anti-knock additives such as lead compounds (for example tetraethyl lead), methyltertiobutylether, methyl-tertioamylether or a mixture of methanol and tert-butyl alcohol, anti-freeze additives and octane reducers.
- anti-knock additives such as lead compounds (for example tetraethyl lead), methyltertiobutylether, methyl-tertioamylether or a mixture of methanol and tert-butyl alcohol, anti-freeze additives and octane reducers.
- the formulations of the present invention are used in an amount sufficient to obtain a significant reduction in deposits on the various components of the engine, in particular at the level of the intake valves and of the carburetor.
- amounts are used representing from 10 to 3000 ppm by weight of active material relative to the weight of the fuel, preferably from 10 to 1000 ppm and most often from 50 to 700 ppm.
- the amount of the constituent (C) is usually from 10 to 2000 ppm, most often from 10 to 900 ppm so preferred from 30 to 800 ppm.
- Examples 1 to 5 describe the preparation of constituents (A) and (B) used for the preparation of the formulations according to the invention.
- the progress of the reaction can also be followed by infrared spectrometry at the level of the absorption band of the imine function at 1660 cm ⁇ 1 which gradually disappears during the reaction, while two bands appear (1710 cm ⁇ 1 and 1770 cm ⁇ 1) characteristics of the succinimide function.
- the infrared spectrum shows an imine band at 1660 cm ⁇ 1 and in nuclear magnetic resonance spectrometry, the presence of the two methylene groups of the imidazoline ring and the presence of the methyl group in position 2 on the imidazoline ring are detected. Elemental analysis provides a percentage of nitrogen of 22.1% by weight for a calculated percentage of 21.8%.
- the procedure described in Example 1 is repeated, replacing 1- (2-hydroxyethyl) -2-heptadecenylimidazoline with 1- (2-hydroxyethyl) -2-methylimidazoline prepared above.
- Example 1 The procedure described in Example 1 is repeated, replacing the imidazoline with a tallow diamine such as that sold under the brand Dinoram S by the company CECA and corresponding to cut E, the characteristics of which have been mentioned in table I below. -before. 306 g (0.3 mole) of PIBSA diluted in 306 g of xylene and 108 g (0.3 mole) of Dinoram S diluted in 108 g of xylene were used. The reflux is maintained for 5 hours. The reaction water is eliminated as it is formed; this elimination mainly occurs during the first 4 hours of reaction. A solution is thus obtained, adjusted to 50% by weight of active material, in xylene, of component A2.
- Example 3 The procedure of Example 3 is repeated, replacing Dinoram S with 0.3 mole of tetraetriylenepentamine (56 g) diluted in 56 g of xylene. The reflux is maintained for 5 hours. The reaction water is eliminated as it is formed; this elimination mainly occurs during the first 4 hours of reaction. A solution is thus obtained, at 50% by weight of active material, in xylene, of the constituent A3.
- Example 2 The procedure described in Example 1 is repeated, replacing the imidazoline with the polyoxyalkyleneamine sold by the company TEXACO under the name Jeffamine D-400 with a number average molecular mass of 400.
- the Jeffamine D-400 is added in the form of a solution in xylene containing 164 g (0.41 mole) of Jeffamine D-400.
- the reflux is maintained throughout the elimination of the reaction water by azeotropic distillation, then for an additional hour.
- a solution is thus obtained, adjusted to 50% by weight of active material, in the xylene of the constituent A4.
- the engine test procedure is carried out following European standard R5-CEC-FO3-T-81. The results are expressed in terms of merit from zero to ten. A merit 10 corresponds to a clean carburetor and a merit 0 to a very dirty carburetor. The tests are carried out using the fuels C1 to C10 described in Example 6. The results obtained are presented in Table III below.
- the tests consist in determining the extent of the corrosion produced on samples of polished ordinary steel, in the presence of synthetic seawater, by following the modified ASTM D 665 standard (temperature 32.2 ° C, duration 20 hours) .
- the tests are carried out using some of the fuels described in Example 6.
- the results obtained are presented in Table IV below; they are expressed as percentages (%) of the surface of the corroded test piece after hours.
- Formula F1 contains the component (A3) described in Example 4, component (B1) described in Example 1 and polypropylene glycol (component (C)) described above; the molar ratio of the number of moles of the constituent (A3) to the number of moles of the constituent (B1) is 0.7: 1; the quantity of polypropylene glycol contained in this formulation is such that the molar ratio of the sum of the number of moles of constituent (A3) and of constituent (B1) which it contains to the number of moles of polypropylene glycol which it contains ((A3) + (B1)) / (C) is 0.7: 1.
- the formulation F2 contains the constituent (A3) described in Example 4, the constituent (B1) described in Example 1 and the poylpropylene glycol (constituent ( C)) described above; the molar ratio of the number of moles of the constituent (A3) to the number of moles of the constituent (B1) is 2: 1; the quantity of polypropylene glycol contained in this formulation is such that the molar ratio of the sum of the number of moles of constituent (A3) and of constituent (B1) which it contains to the number of moles of polypropylene glycol which it contains ((A3) + (B1)) / (C) is 0.73: 1.
- Formulation F3 includes polypropylene glycol and contains neither component (A3) nor component (B1).
- the formulation F4 comprises each of the constituents (A3) and (B1) in a molar ratio of 2: 1 and does not contain polypropylene glycol.
- the formulations are added to the fuel so as to obtain a concentration, by weight of active material in the additive fuel, specified for each example in Table V below giving the results obtained.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Exhaust Gas After Treatment (AREA)
- Control Of Vehicle Engines Or Engines For Specific Uses (AREA)
Claims (15)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT89401846T ATE74950T1 (de) | 1988-06-29 | 1989-06-28 | Rezepte von stickstoffhaltigen zusaetzen fuer motorkraftstoffe und diese enthaltende motorkraftstoffe. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8808900A FR2633638B1 (fr) | 1988-06-29 | 1988-06-29 | Formulations d'additifs azotes pour carburants moteurs et les carburants moteurs les contenant |
FR8808900 | 1988-06-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0353116A1 EP0353116A1 (de) | 1990-01-31 |
EP0353116B1 true EP0353116B1 (de) | 1992-04-15 |
Family
ID=9367960
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89401846A Expired - Lifetime EP0353116B1 (de) | 1988-06-29 | 1989-06-28 | Rezepte von stickstoffhaltigen Zusätzen für Motorkraftstoffe und diese enthaltende Motorkraftstoffe |
Country Status (13)
Country | Link |
---|---|
US (1) | US4976746A (de) |
EP (1) | EP0353116B1 (de) |
JP (1) | JP2645893B2 (de) |
AT (1) | ATE74950T1 (de) |
BR (1) | BR8903221A (de) |
CA (1) | CA1340495C (de) |
DE (1) | DE68901226D1 (de) |
DK (1) | DK174037B1 (de) |
ES (1) | ES2032666T3 (de) |
FR (1) | FR2633638B1 (de) |
MY (1) | MY106959A (de) |
NO (1) | NO173554C (de) |
ZA (1) | ZA894901B (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10035757B2 (en) * | 2010-06-03 | 2018-07-31 | Instituto Mexicano Del Petroleo | Amino and imino propionic acids, process of preparation and use |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5147414A (en) * | 1989-08-03 | 1992-09-15 | Texaco Inc. | Process for producing ori control additives |
FR2680796B1 (fr) * | 1991-08-30 | 1994-10-21 | Inst Francais Du Petrole | Formulation d'additifs pour carburants comprenant des produits a fonction ester et un detergent - dispersant. |
US6860908B2 (en) | 1992-12-17 | 2005-03-01 | Institut Francais du Pétrole | Petroleum middle distillate composition containing a substance for limiting the paraffin sedimentation rate |
FR2699550B1 (fr) * | 1992-12-17 | 1995-01-27 | Inst Francais Du Petrole | Composition de distillat moyen de pétrole contenant des additifs azotés utilisables comme agents limitant la vitesse de sédimentation des paraffines. |
US5348674A (en) * | 1993-04-12 | 1994-09-20 | Mobil Oil Corporation | Amide/ester heterocyclic derivatives of hydrocarbylsuccinic anhydrides as rust/corrosion inhibiting additives for lubricants |
FR2710652B1 (fr) * | 1993-09-30 | 1995-12-01 | Elf Antar France | Composition d'additifs d'opérabilité à froid des distillats moyens. |
US5601624A (en) * | 1995-04-10 | 1997-02-11 | Mobil Oil Corporation | Fuel composition with reaction product of oxygenated amine, dicarbonyl linking agent, and hydrocarbyl(ene) amine |
FR2749756B1 (fr) * | 1996-06-14 | 1998-09-11 | Bioland | Procede de preparation d'un materiau composite implantable, materiau obtenu, implant comprenant ce materiau et kit de mise en oeuvre |
FR2792646B1 (fr) * | 1999-04-26 | 2001-07-27 | Elf Antar France | Composition d'additifs multifonctionnels d'operabilite a froid des distillats moyens |
US20030056431A1 (en) * | 2001-09-14 | 2003-03-27 | Schwab Scott D. | Deposit control additives for direct injection gasoline engines |
FR2839315B1 (fr) * | 2002-05-03 | 2006-04-28 | Totalfinaelf France | Additif pour ameliorer la stabilite thermique de compositions d'hydrocarbures |
BRPI0514160A (pt) * | 2004-08-06 | 2008-06-03 | Basf Ag | usos de um composto e de um produto de reação, composições de combustìvel e lubrificante, concentrado de aditivos, e, processo para preparar uma composição |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2568876A (en) * | 1949-11-14 | 1951-09-25 | Socony Vacuum Oil Co Inc | Reaction products of n-acylated polyalkylene-polyamines with alkenyl succinic acid anhydrides |
GB708193A (en) * | 1951-05-08 | 1954-04-28 | Thompson Prod Inc | Improvements in or relating to fuel charges for internal combustion engines |
DE1248643B (de) * | 1959-03-30 | 1967-08-31 | The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) | Verfahren zur Herstellung von öllöslichen aeylierten Aminen |
US3138610A (en) * | 1961-03-10 | 1964-06-23 | Gen Aniline & Film Corp | Substituted imidazolines |
US3458530A (en) * | 1962-11-21 | 1969-07-29 | Exxon Research Engineering Co | Multi-purpose polyalkenyl succinic acid derivative |
US3312619A (en) * | 1963-10-14 | 1967-04-04 | Monsanto Co | 2-substituted imidazolidines and their lubricant compositions |
GB1346765A (en) * | 1970-06-16 | 1974-02-13 | Shell Int Research | Fuel compositions |
FR2133072A5 (en) * | 1971-04-07 | 1972-11-24 | Lubrizol Corp | Hydrocarbon fuel additive compsn - for cleaning fuel systems in engines, furnaces etc |
US3806456A (en) * | 1971-05-17 | 1974-04-23 | Lubrizol Corp | Acylated nitrogen compositions |
FR2414542A1 (fr) * | 1978-01-11 | 1979-08-10 | Orogil | Nouvelles compositions a base d'alcenylsuccinimides, derives de la tris(amino-5 thia-3 pentyl)amine, leur procede de preparation et leur application comme additifs pour lubrifiants |
US4247300A (en) * | 1978-04-27 | 1981-01-27 | Phillips Petroleum Company | Imidazoline fuel detergents |
FR2476119B1 (fr) * | 1980-02-15 | 1985-07-26 | Inst Francais Du Petrole | Ethers de succinimides n-substitues leur preparation et leur utilisation comme additifs pour carburants |
FR2510598A1 (fr) * | 1981-07-30 | 1983-02-04 | Inst Francais Du Petrole | Utilisation d'additifs azotes comme agents d'abaissement du point de trouble des distillats moyens d'hydrocarbures et compositions de distillats moyens d'hydrocarbures renfermant lesdits additifs |
EP0074724A3 (de) * | 1981-09-03 | 1984-08-01 | The Lubrizol Corporation | Acylierte Imidazoline und diese enthaltende Brennstoff- und Schmiermittelzusammensetzungen |
USRE32174E (en) * | 1981-12-14 | 1986-06-10 | The Lubrizol Corporation | Combination of hydroxy amines and carboxylic dispersants as fuel additives |
DE3343816C2 (de) * | 1983-12-03 | 1986-12-04 | UK Mineralölwerke Wenzel & Weidmann GmbH, 5180 Eschweiler | Schmiermittel |
US4531948A (en) * | 1984-06-13 | 1985-07-30 | Ethyl Corporation | Alcohol and gasohol fuels having corrosion inhibiting properties |
US4659336A (en) * | 1986-03-28 | 1987-04-21 | Texaco Inc. | Motor fuel composition |
-
1988
- 1988-06-29 FR FR8808900A patent/FR2633638B1/fr not_active Expired - Lifetime
-
1989
- 1989-06-27 NO NO892658A patent/NO173554C/no not_active IP Right Cessation
- 1989-06-27 DK DK198903194A patent/DK174037B1/da not_active IP Right Cessation
- 1989-06-27 MY MYPI89000870A patent/MY106959A/en unknown
- 1989-06-28 DE DE8989401846T patent/DE68901226D1/de not_active Expired - Fee Related
- 1989-06-28 ZA ZA894901A patent/ZA894901B/xx unknown
- 1989-06-28 ES ES198989401846T patent/ES2032666T3/es not_active Expired - Lifetime
- 1989-06-28 AT AT89401846T patent/ATE74950T1/de not_active IP Right Cessation
- 1989-06-28 EP EP89401846A patent/EP0353116B1/de not_active Expired - Lifetime
- 1989-06-28 US US07/372,598 patent/US4976746A/en not_active Expired - Lifetime
- 1989-06-29 CA CA000604407A patent/CA1340495C/fr not_active Expired - Fee Related
- 1989-06-29 JP JP1168292A patent/JP2645893B2/ja not_active Expired - Fee Related
- 1989-06-29 BR BR898903221A patent/BR8903221A/pt not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10035757B2 (en) * | 2010-06-03 | 2018-07-31 | Instituto Mexicano Del Petroleo | Amino and imino propionic acids, process of preparation and use |
Also Published As
Publication number | Publication date |
---|---|
ATE74950T1 (de) | 1992-05-15 |
DK319489A (da) | 1990-02-14 |
ES2032666T3 (es) | 1993-02-16 |
ZA894901B (en) | 1990-03-28 |
FR2633638B1 (fr) | 1991-04-19 |
CA1340495C (fr) | 1999-04-13 |
JPH02196889A (ja) | 1990-08-03 |
BR8903221A (pt) | 1990-02-13 |
EP0353116A1 (de) | 1990-01-31 |
DK174037B1 (da) | 2002-05-06 |
NO173554B (no) | 1993-09-20 |
FR2633638A1 (fr) | 1990-01-05 |
NO892658L (no) | 1990-01-02 |
DK319489D0 (da) | 1989-06-27 |
US4976746A (en) | 1990-12-11 |
DE68901226D1 (de) | 1992-05-21 |
NO173554C (no) | 1993-12-29 |
NO892658D0 (no) | 1989-06-27 |
JP2645893B2 (ja) | 1997-08-25 |
MY106959A (en) | 1995-08-30 |
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