EP2589647A1 - Quaternisierte Polyetheramine und deren Verwendung als Additive in Kraft- und Schmierstoffen - Google Patents

Quaternisierte Polyetheramine und deren Verwendung als Additive in Kraft- und Schmierstoffen Download PDF

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Publication number
EP2589647A1
EP2589647A1 EP11187959.9A EP11187959A EP2589647A1 EP 2589647 A1 EP2589647 A1 EP 2589647A1 EP 11187959 A EP11187959 A EP 11187959A EP 2589647 A1 EP2589647 A1 EP 2589647A1
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EP
European Patent Office
Prior art keywords
alkyl
fuel
formula
aryl
general formula
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EP11187959.9A
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German (de)
English (en)
French (fr)
Inventor
Markus Dr. Hansch
Harald Dr. Böhnke
Ludwig Dr. Völkel
Marc Dr. Walter
Wolfgang Dr. Grabarse
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BASF SE
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BASF SE
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Priority to EP11187959.9A priority Critical patent/EP2589647A1/de
Priority to HUE12780216 priority patent/HUE044181T2/hu
Priority to ES12780216T priority patent/ES2726102T3/es
Priority to KR1020147015015A priority patent/KR102033606B1/ko
Priority to AU2012331073A priority patent/AU2012331073B2/en
Priority to EP12780216.3A priority patent/EP2773729B1/de
Priority to BR112014010671A priority patent/BR112014010671A2/pt
Priority to MX2014005325A priority patent/MX2014005325A/es
Priority to PCT/EP2012/071844 priority patent/WO2013064689A1/de
Priority to CN201280065791.5A priority patent/CN104024385B/zh
Priority to TR2019/05501T priority patent/TR201905501T4/tr
Priority to CA2854421A priority patent/CA2854421C/en
Priority to PL12780216T priority patent/PL2773729T3/pl
Publication of EP2589647A1 publication Critical patent/EP2589647A1/de
Withdrawn legal-status Critical Current

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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
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
    • 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
    • C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
    • 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
    • C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
    • C10L1/2225—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates hydroxy containing
    • 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
    • C10L1/2227—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond urea; derivatives thereof; urethane
    • 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)
    • 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
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/06—Use of additives to fuels or fires for particular purposes for facilitating soot removal
    • 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
    • C10M133/08—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01—Physico-chemical properties
    • C10N2020/04—Molecular weight; Molecular weight distribution
    • 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
    • C10N2030/04—Detergent property or dispersant property
    • 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
    • C10N2030/54—Fuel economy
    • 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
    • C10N2040/252—Diesel engines
    • C10N2040/253—Small 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
    • C10N2070/00—Specific manufacturing methods for lubricant compositions
    • 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
    • C10N2070/00—Specific manufacturing methods for lubricant compositions
    • C10N2070/02—Concentrating of additives

Definitions

  • the present invention relates to novel quaternized polyetheramines and their preparation, Furthermore, the present invention relates to the use of these compounds as a fuel and lubricant additive. More particularly, the invention relates to the use of these quaternized nitrogen compounds as a fuel additive to reduce or prevent deposits in the injection systems of direct injection diesel engines, particularly in common rail injection systems, to reduce fuel consumption of direct injection diesel engines, particularly diesel engines with common rail injection systems. and to minimize the power loss in direct injection diesel engines, especially in diesel engines with common rail injection systems.
  • the invention also relates to additive packages containing these polyetheramines; as well as with it additized fuels and lubricants. Furthermore, the invention relates to the use of these quaternized nitrogen compounds as an additive for gasoline fuels, in particular for improving the intake system cleanliness of gasoline engines.
  • direct-injection diesel engines the fuel is injected through a directly into the combustion chamber-reaching multi-hole injection nozzle of the engine and finely distributed (nebulized), instead of being introduced as in the classic (chamber) diesel engine in a vortex or vortex chamber.
  • the advantage of direct-injection diesel engines lies in their high performance for diesel engines and yet low consumption. In addition, these engines achieve a very high torque even at low speeds.
  • the diesel fuel is pumped from a pump with pressures up to 2000 bar into a high-pressure line, the common rail.
  • spur lines run to the various injectors, which inject the fuel directly into the combustion chamber.
  • the full pressure is always applied to the common rail, which allows a multiple injection or a special injection form. In the other injection systems, however, only a smaller variation of the injection is possible.
  • Injection in the common rail is essentially subdivided into three groups: (1) preinjection, which substantially achieves softer combustion, so that hard combustion noises ("nails") are reduced and engine running appears quiet; (2.) main injection, which is responsible in particular for a good torque curve; and (3.) post-injection, which provides in particular for a low NO x value.
  • preinjection which substantially achieves softer combustion, so that hard combustion noises ("nails") are reduced and engine running appears quiet
  • main injection which is responsible in particular for a good torque curve
  • post-injection which provides in particular for a low NO x value.
  • the fuel is not burned in the rule, but evaporated by residual heat in the cylinder.
  • the resulting exhaust gas / fuel mixture is transported to the exhaust system, where the fuel in the presence of suitable catalysts acts as a reducing agent for the nitrogen oxides NO x .
  • deposits can form under certain conditions, for example when using biodiesel-containing fuels or fuels with metal impurities such as zinc compounds, copper compounds, lead compounds and other metal compounds, the injection behavior of the Negatively affect the performance of the engine, ie in particular reduce the power, but in part also deteriorate the combustion.
  • the formation of deposits is further enhanced by structural developments of the injectors, in particular by the change in the geometry of the nozzles (narrower, conical openings with rounded outlet). For a permanently optimal functioning of the engine and injectors, such deposits in the nozzle orifices must be prevented or reduced by suitable fuel additives.
  • Fuel metering systems are contaminated by impurities caused by dust particles from the air, unburned hydrocarbon residues from the combustion chamber and the crankcase ventilation gases directed into the gasifier.
  • the first additive generation could only prevent the formation of deposits in the intake system, but not remove already existing deposits, whereas the modern additives of the second generation can cause both (keep-clean and clean-up effect) and especially because of their excellent thermal stability at higher temperature zones, namely at the inlet valves.
  • Such detergents which can originate from a large number of chemical substance classes, for example polyalkeneamines, polyetheramines, polybutene-Mannich bases or polybutene succinimides, are generally used in combination with carrier oils and in some cases further additive components, for example corrosion inhibitors and demulsifiers.
  • the carrier oils perform a solvent or wash function in combination with the detergents.
  • Carrier oils are usually high-boiling, viscous, thermostable liquids which coat the hot metal surface and thereby prevent the formation or deposition of impurities on the metal surface.
  • Detergent-effect fuel additives of the younger generation often have quaternized nitrogen groups.
  • Polyalkene substituted quaternized amines such as, in particular, quaternized polyisobuteneamines, and their use as detergent additives to reduce inlet valve deposits and as lubricant additives for internal combustion engines are disclosed in U.S.P. US 2008/0113890 described.
  • the US 6 331 648 B1 relates to specific quaternary etheramine compounds which incorporate a 1-ethyl-1,3-propylene unit between the alkoxylate chain and quaternary nitrogen.
  • the use of these compounds as anticorrosion or detergent additives in gasoline and diesel fuels is speculated, but without demonstrating their usefulness.
  • the EP 182 669 A1 describes halogenated or sulfur-containing alkoxylated quaternary ammonium compounds of the general structure [RO (R 1) x CH 2 CH (R 2 ) HNR 3 R 4 R 6 ] + A- wherein R 1 represents an alkylene oxide block.
  • R 1 represents an alkylene oxide block.
  • Preferred anions A- are chloride, methylsulfate and ethylsulfate.
  • the U.S. 4,564,372 . US 4,581,151 . US 4,600,409 and the WO 1985/000620 refer to alkyl halides quaternized, ie halogenated, polyoxyalkyleneamine salts in which polyoxyalkylene unit and amine unit via different linker groups, in particular amine linker of the type - C (O) -NH-.
  • Use as dispersants and corrosion inhibitors in fuels is postulated, but without actually demonstrating specific functions experimentally.
  • the additives according to the invention are superior to the known additives according to the prior art in several respects and can be used simultaneously in diesel and gasoline fuels. They are characterized by their advantageous cleansing and cleansing effect on various components of internal combustion engines, such as diesel engine injectors but also on intake valves and injectors of gasoline engines, and prevent the formation of combustion chamber deposits or eliminate ready formed combustion chamber deposits of internal combustion engines. In addition, they prevent the formation of deposits in fuel filters or eliminate already formed filter contaminants.
  • FIG. 1 shows the achievable with additives of the invention injector cleanliness after a test operation with a direct-injection gasoline engine (1b and 1 c) compared to an operation with non-additive fuel (1 a).
  • halogen-free or sulfur-free means the absence of inorganic or organic halogen-containing or sulfur-containing compounds and / or their corresponding ions, such as halide anion and sulfur-containing anions, in particular sulfates.
  • halogen-free or sulfur-free includes the absence of stoichiometric amounts of halogen-containing or sulfur-containing compounds or anions.
  • Substoichiometric amounts of halogen-containing or sulfur-containing compounds or anions are e.g. in molar ratios of less than 1: 0.1, or less than 1.
  • halogen-free 0.01 or 1: 0.001, or 1: 0.0001 of quaternised nitrogen compound to halogen-containing or sulfur-containing compound or ions thereof, other than "halogen-free" or "Sulfur-free” includes in particular the complete absence of halogen-containing or sulfur-containing compounds and / or their corresponding ions, such as halide anion and sulfur-containing anions, in particular sulfates.
  • Carboxylic acids include, in particular, organic carboxylic acids, such as, in particular, monocarboxylic acids of the RCOOH type, in which R represents a short-chain hydrocarbyl radical, such as, for example, a lower alkyl or C 1 -C 4 -alkylcarboxylic acid.
  • Quadraturear nitrogen groups or amino groups include in particular primary, secondary and tertiary amino groups.
  • Hydrocarbyl is to be interpreted broadly and includes both cyclic aromatic or non-aromatic, as well as long-chain or short-chain, straight or branched hydrocarbon radicals having 1 to 50 carbon atoms, which may contain additional heteroatoms, such as O, N, NH, S, may contain in their chain or ring.
  • Hydrocarbyl includes, for example, the alkyl, alkenyl, aryl, alkylaryl, cycloalkenyl or cycloalkyl radicals and their substituted analogs as defined below.
  • Alkyl or “lower alkyl” in particular represents saturated, straight-chain or branched hydrocarbon radicals having 1 to 4, 1 to 6, 1 to 8, 1 to 10, 1 to 14 or 1 to 20 carbon atoms, such as.
  • “Hydroxyalkyl” is in particular the mono- or polysubstituted, especially monohydricated, analogs of the above-mentioned alkyl radicals, such as, for example, the monohydroxylated analogs of the above straight-chain or branched alkyl radicals, e.g. the linear hydroxyalkyl groups, e.g. those having a primary (terminal) hydroxyl group, such as hydroxymethyl, 2-hydroxyethyl, 3-hydroxypropyl, 4-hydroxybutyl, or those having non-terminal hydroxyl groups, such as 1-hydroxyethyl, 1- or 2-hydroxypropyl, 1- or 2-hydroxybutyl or 1- , 2- or 3-hydroxybutyl.
  • Alkenyl is mono- or polysubstituted, in particular monounsaturated, straight-chain or branched hydrocarbon radicals having 2 to 4, 2 to 6, 2 to 8 2 to 10 or 2 or to 20 carbon atoms and a double bond in any position, for.
  • C 2 -C 6 alkenyl such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1 propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3 Methyl 3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-1
  • Haldroxyalkenyl is in particular the mono- or polysubstituted, in particular simply hydroxylated, analogs of the above alkenyl radicals
  • aminoalkyl and “aminoalkenyl” are in particular the mono- or polysubstituted, in particular simply aminated, analogs of the above alkyl or alkenyl radicals, or analogs of the above hydroxyalkyl, where the OH group has been replaced by an amino group.
  • Alkylene represents straight-chain or mono- or poly-branched hydrocarbon bridging groups having 1 to 10 carbon atoms, such as, for example, C 1 -C 7 -alkylene groups selected from -CH 2 -, - (CH 2 ) 2 -, - (CH 2 ) 3 -, - (CH 2 ) 4 -, - (CH 2 ) 2 -CH (CH 3 ) -, -CH 2 -CH (CH 3 ) -CH 2 -, (CH 2 ) 4 -, - (CH 2 ) 5 -, - (CH 2 ) 6 , - (CH 2 ) 7 -, -CH (CH 3 ) -CH 2 -CH 2 -CH (CH 3 ) - or - CH (CH 3 ) -CH 2 -CH 2 -CH 2 -CH (CH 3 ) - or C 1 -C 4 -alkylene groups selected from -CH 2 -, - (CH 2
  • Oxyalkylene radicals correspond to the definition of the above straight-chain or mono- or polysubstituted alkylene radicals having 2 to 10 carbon atoms, the coal chain being interrupted by an oxygen heteroatom 1 or more times, in particular 1 times.
  • Aminoalkylene correspond to the definition of the above straight-chain or mono- or polysubstituted alkylene radicals having 2 to 10 carbon atoms, the coal chain being interrupted by a nitrogen group (in particular - NH group) 1 or more times, in particular 1 times.
  • Non-limiting examples are: -CH 2 -NH-CH 2 -, - (CH 2 ) 2 -NH- (CH 2 ) 2 -, - (CH 2 ) 3 -NH- (CH 2 ) 3 -, or -CH 2 -NH- (CH 2 ) 2 -, - (CH 2 ) 2 -NH- (CH 2 ) 3 -, -CH 2 -NH- (CH 2 ) 3 .
  • Cycloalkyl denotes carbocyclic radicals having from 3 to 20 carbon atoms, such as, for example, C 3 -C 12 -cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, cycloundecyl and cyclododecyl; preferred are cyclopentyl, cyclohexyl, cycloheptyl and also cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentylethyl, cyclohexylmethyl or C 3 -C 7 -cycloalkyl, such as cyclopropyl, cyclobutyl, Cyclopentyl,
  • Cycloalkenyl or mono- or polyunsaturated cycloalkyl is especially for monocyclic, mono- or polyunsaturated hydrocarbon groups having 5 to 8, preferably up to 6 carbon ring members, such as the monounsaturated radicals Cyclopenten-1-yl, cyclopenten-3-yl, cyclohexen-1-yl, cyclohexen-3-yl and cyclohexen-4-yl;
  • Aryl represents mono- or polynuclear, preferably mono- or binuclear, optionally substituted aromatic radicals having from 6 to 20, such as e.g. From 6 to 10 ring carbon atoms, e.g. Phenyl, biphenyl, naphthyl such as 1- or 2-naphthyl, tetrahydronaphthyl, fluorenyl, indenyl and phenanthrenyl. These aryl radicals may optionally carry 1, 2, 3, 4, 5 or 6 identical or different substituents.
  • Alkylaryl stands for the in any position of the ring one or more times, in particular 1- or 2-fold, alkyl-substituted analogs of the above aryl radicals, where aryl likewise has the meanings indicated above, such as, for example, C 1 -C 4 -alkyl-phenyl- in which the C 1 -C 4 -alkyl radicals can be in any desired ring position.
  • Substituents for radicals specified herein are especially selected from keto groups, -COOH, -COO-alkyl, -OH, -SH, -CN, amino, -NO 2 , alkyl, or alkenyl groups.
  • Mn number average molecular weight
  • Suitable quaternizing agents are, in principle, all compounds suitable as such.
  • the quaternizing agent is in particular selected from alkylene oxides, if appropriate in combination with acid; aliphatic or aromatic carboxylic acid esters, in particular dialkyl carboxylates; alkanoates; cyclic non-aromatic or aromatic carboxylic acid esters; dialkyl; alkyl sulfates; alkyl halides; alkylaryl halides; and mixtures thereof.
  • the quaternization of the at least one quaternizable tertiary nitrogen atom is carried out with at least one quaternizing agent selected from epoxides, in particular hydrocarbyl epoxides.
  • the R a radicals contained therein are identical or different and represent H or a hydrocarbyl radical.
  • the hydrocarbyl radical may have at least 1 to 14 carbon atoms. These are in particular aliphatic or aromatic radicals such as linear or branched C 1 - C 14 alkyl radicals or aromatic radicals, such as phenyl or C 1 -C 4 alkylphenyl.
  • hydrocarbyl epoxides are aliphatic and aromatic alkylene oxides, in particular C 2-16 -alkylene oxides, such as ethylene oxide, propylene oxide, 1,2-butylene oxide, 2,3-butylene oxide, 2-methyl-1,2-propene oxide (isobutene oxide).
  • aromatic-substituted ethylene oxides such as optionally substituted styrene oxide, in particular styrene oxide or 4-methyl-styrene oxide.
  • epoxides as quaternizing these are in the presence or absence of free acids, especially in the presence or absence of free protic acids, such as especially with C 1-12 monocarboxylic acids, such as formic acid, acetic acid or propionic acid or C 2-12 Dicarboxylic acids such as oxalic acid or adipic acid; or in the presence or absence of sulfonic acids, such as benzenesulfonic acid or toluenesulfonic acid or aqueous mineral acids, such as sulfuric acid or hydrochloric acid.
  • the quaternization product thus produced is thus either "acidic" or "acid-free" within the meaning of the present invention.
  • alkyl esters of a cycloaromatic or cycloaliphatic mono- or polycarboxylic acid in particular a mono- or dicarboxylic acid
  • alkyl esters of a cycloaromatic or cycloaliphatic mono- or polycarboxylic acid in particular a mono- or dicarboxylic acid
  • an aliphatic polycarboxylic acid in particular dicarboxylic acid
  • Particularly suitable quaternizing agents are the lower alkyl esters of salicylic acid, such as methyl salicylate, ethyl salicylate, n- and i-propyl salicylate, and n-, i- or tert-butyl salicylate.
  • An "anion resulting from the quaternization reaction" X- is, for example, a halide such as a chloride or bromide, a sulfate radical ((SO 4 ) 2- ), or the anionic radical of a mono- or polyhydric, aliphatic or aromatic carboxylic acid, or anionic radical ROC (O) O- resulting from the quaternization reaction of a dialkyl carbonate.
  • a halide such as a chloride or bromide
  • anionic radical of a mono- or polyhydric, aliphatic or aromatic carboxylic acid or anionic radical ROC (O) O- resulting from the quaternization reaction of a dialkyl carbonate.
  • the quaternizable nitrogen compound is selected from hydroxyalkyl-substituted mono- or polyamines having at least one quaternizable, primary, secondary or tertiary amino group and at least one hydroxyl group which is linkable with a polyether radical.
  • the quaternizable nitrogen compound is selected from hydroxyalkyl-substituted primary, secondary, tertiary or quaternary monoamines and hydroxyalkyl-substituted primary, secondary, tertiary or quaternary diamines.
  • Suitable "hydroxyalkyl-substituted mono- or polyamines" are those containing at least one, e.g. 1, 2, 3, 4, 5 or 6, hydroxyalkyl substituents are equipped.
  • hydroxyalkyl-substituted monoamines may be mentioned: N-hydroxyalkyl-monoamines, N, N-dihydroxyalkyl-monoamines and N, N, N-trihydroxyalkyl-monoamines, wherein the hydroxyalkyl groups are the same or different and are also as defined above , Hydroxyalkyl stands in particular for 2-hydroxyethyl, 3-hydroxypropyl or 4-hydroxybutyl.
  • hydroxyalkyl-substituted polyamines and especially “hydroxyalkyl-substituted diamines” may be mentioned: (N-hydroxyalkyl) -alkylenediamines, N, N-dihydroxyalkylalkylenediamines wherein the hydroxyalkyl groups are the same or different and are also as defined above.
  • Hydroxyalkyl stands in particular for 2-hydroxyethyl, 3-hydroxypropyl or 4-hydroxybutyl
  • Alkylene stands in particular for ethylene, propylene or butylene.
  • the amino alcohols of the general formula II can be alkoxylated in a manner known in principle, giving alkoxylated amines of the general formula Ia-1.
  • C 2 -C 16 -alkylene oxides are used, for example ethylene oxide, propylene oxide or butylene oxide. Preference is given in each case to the 1,2-alkylene oxides.
  • the alkoxylation may be a base-catalyzed alkoxylation.
  • the amino alcohols (II) can be mixed in a pressure reactor with alkali metal hydroxides, preferably potassium hydroxide or with alkali metal such as sodium methylate.
  • alkali metal hydroxides preferably potassium hydroxide or with alkali metal such as sodium methylate.
  • pressure for example ⁇ 100 mbar
  • temperature 30 to 150 ° C
  • water still present in the mixture can be withdrawn.
  • the alcohol is then present as the corresponding alkoxide. It is then inertized with inert gas (eg nitrogen) and the (the) alkylene oxide (s) at temperatures of 60 to 180 ° C up to a pressure of max. 10 bar added gradually.
  • inert gas eg nitrogen
  • the catalyst can be replaced by the addition of acid (eg Acetic or phosphoric acid) neutralized and can be filtered off if necessary.
  • acid eg Acetic or phosphoric acid
  • the basic catalyst can also be neutralized by adding commercial Mg silicates, which are then filtered off.
  • the alkoxylation can also be carried out in the presence of a solvent. This may be, for example, toluene, xylene, dimethylformamide or ethylene carbonate.
  • the alkoxylation of the amino alcohols can also be carried out by other methods, for example by acid-catalyzed alkoxylation.
  • Doppelhydroxidtone as in DE 43 25 237 A1 or double metal cyanide (DMC) catalysts can be used.
  • DMC catalysts are for example in the DE 102 43 361 A1 , in particular sections [0029] to [0041] and the literature cited therein.
  • Zn-Co type catalysts can be used.
  • the aminoalcohol can be admixed with the catalyst, the mixture can be dehydrated as described above and reacted with the alkylene oxides as described. It is usually not more than 1000 ppm catalyst used with respect to the mixture, and the catalyst can remain in the product due to this small amount.
  • the amount of catalyst can typically be less than 1000 ppm, for example 250 ppm and less.
  • the alkoxylation can alternatively be carried out by reaction of the compounds (IV) and (V) with cyclic carbonates such as ethylene carbonate.
  • alkanols R 6 OH can also be alkoxylated in a manner known in principle to give polyethers (Ib-1).
  • the polyethers thus obtained can then by reductive amination with ammonia, primary amines or secondary amines (VII) by conventional methods in continuous or batch processes using conventional hydrogenation or amination catalysts such as those, the catalytically active ingredients based on the elements Ni , Co, Cu, Fe, Pd, Pt, Ru, Rh, Re, Al, Si, Ti, Zr, Nb, Mg, Zn, Ag, Au, Os, Ir, Cr, Mo "W or combinations of these elements with each other , in usual amounts to the corresponding polyetheramines (Ib-2).
  • the reaction can be carried out without solvent or at high polyether viscosities in the presence of a solvent, preferably in the presence of branched aliphatics such as isododecane.
  • the amine component (VII) is generally used in excess, for example in 2 to 100-fold excess, preferably 10 to 80-fold excess used.
  • the reaction is carried out at pressures of 10 to 600 bar over a period of 10 minutes to 10 hours. After cooling, the catalyst is separated by filtration, excess amine component (VII) is evaporated off and the reaction water is distilled off azeotropically or under a gentle stream of nitrogen.
  • the resulting polyetheramine (Ib-2) have primary or secondary amine functionalities (R 1 and / or R 2 is H), this can subsequently be converted into a polyether amine having a tertiary amine function (R 1 and R 2 not equal to H).
  • the alkylation can be carried out in a manner known in principle by reaction with alkylating agents.
  • alkylating agents such as, for example, alkyl halides, alkylaryl halides, dialkyl sulfates, alkylene oxides, if appropriate in combination with acid, are suitable; aliphatic or aromatic carboxylic acid esters, in particular dialkylcarboxylates; alkanoates; cyclic non-aromatic or aromatic carboxylic esters; dialkyl; and mixtures thereof.
  • the reactions to the tertiary polyetheramine can also take place by reductive amination by reaction with a carbonyl compound such as formaldehyde in the presence of a reducing agent.
  • Suitable reducing agents are formic acid or hydrogen in the presence of a suitable heterogeneous or homogeneous hydrogenation catalyst.
  • the reactions can be carried out without solvent or in the presence of solvents.
  • suitable solvents are for example H 2 O, alkanols such as methanol or ethanol, or 2-ethylhexanol, aromatic solvents such as toluene, xylene or solvent mixtures of the Solvesso series, or aliphatic solvents, in particular mixtures of branched aliphatic solvents.
  • the reactions are carried out at temperatures of 10 ° C to 300 ° C at pressures of 1 to 600 bar over a period of 10 minutes to 10 hours.
  • the reducing agent is used at least stoichiometrically, preferably in excess, in particular in a 2- to 10-fold excess.
  • reaction product thus formed (polyetheramine Ib-1 or Ib-2) can theoretically be further purified or the solvent removed. Usually, however, this is not absolutely necessary, so that the reaction product can be converted into the next synthesis step, the quaternization, without further purification.
  • the reaction product or reaction mixture from stage a) above is mixed with at least one epoxide compound of the above formula (IVa), in particular in the required stoichiometric amounts, in order to achieve the desired quaternization.
  • the acid is preferably also added in stoichiometric amounts.
  • Per equivalent of quaternizable tertiary nitrogen atom can be e.g. Use 0.1 to 2.0 equivalents, or 0.5 to 1.25 equivalents, of quaternizing agent.
  • approximately equimolar amounts of the epoxide are used to quaternize a tertiary amine group.
  • higher amounts are required to quaternize a secondary or primary amine group.
  • Suitable acids are especially carboxylic acids such as acetic acid.
  • reaction time may be in the range of a few minutes or a few hours, e.g. about 10 minutes to about 24 hours.
  • the reaction may be carried out at about 0.1 to 20 bar, e.g. 1 to 10 bar pressure.
  • the pressure is usually determined by the vapor pressure of the alkylene oxide used at the respective reaction temperature.
  • an inert gas atmosphere such as e.g. Nitrogen, appropriate.
  • the reactants may be presented in a suitable organic aliphatic or aromatic solvent or a mixture thereof for epoxidation, or there may still be a sufficient amount of solvent from reaction step a).
  • suitable organic aliphatic or aromatic solvent or a mixture thereof for epoxidation or there may still be a sufficient amount of solvent from reaction step a).
  • Typical examples include Solvesso series solvents, toluene or xylene.
  • alkanols are used as solvents or as a co-solvent in admixture with the aforementioned solvents, such as methanol, ethanol, propanol, 2-ethylhexanol or 2-propylheptanol.
  • the reaction product or reaction mixture from stage a) above is mixed with at least one alkylating agent of the formula (IV), in particular in the required stoichiometric amounts, in order to achieve the desired quaternization.
  • Per equivalent of quaternizable tertiary nitrogen atom can be e.g. 0.1 to 5.0 equivalents, or 0.5 to 2.0 equivalents, of quaternizing agent.
  • approximately equimolar proportions of the alkylating agent are used to quaternize a tertiary amine group.
  • higher amounts are required to quaternize a secondary or primary amine group.
  • Particularly suitable quaternizing agents are methyl salicylate, dimethyl oxalate, dimethyl phthalate and dimethyl carbonate.
  • the reaction can be accelerated by adding catalytic or stoichiometric amounts of an acid.
  • Suitable acids are, for example, proton donors, such as aliphatic or aromatic carboxylic acids or fatty acids.
  • Lewis acids such as boron trifluoride, ZnCl 2 , MgCl 2 , AlCl 3 or FeCl 3 , are suitable.
  • the acid can be used in amounts of from 0.01 to 50% by weight, for example in the range from 0.1 to 10% by weight.
  • reaction time may be in the range of a few minutes or a few hours, e.g. about 10 minutes to about 24 hours.
  • the reaction can be at about 0.1 to 20 bar, such as. 0.5 to 10 bar pressure, done.
  • the reaction can be carried out at atmospheric pressure.
  • an inert gas atmosphere such as e.g. Nitrogen, appropriate.
  • the reactants may be presented in a suitable organic aliphatic or aromatic solvent or a mixture thereof for quaternization, or it may still be a sufficient proportion of solvent from reaction step a).
  • suitable organic aliphatic or aromatic solvent or a mixture thereof for quaternization or it may still be a sufficient proportion of solvent from reaction step a).
  • Typical examples include Solvesso series solvents, toluene or xylene.
  • alkanols are suitable as solvents or as cosolvents in a mixture with the abovementioned solvents, such as, for example, methanol, ethanol, propanol, butanol, 2-ethylhexanol or 2-propylheptanol.
  • the final reaction product thus formed can theoretically be further purified or the solvent removed. Usually, however, this is not absolutely necessary, so that the reaction product can be used without further purification as an additive, if appropriate after mixing with further additive components (see below).
  • the acid used can be removed by filtration, neutralization or extraction from the reaction product.
  • an excess of alkylating agent may be removed by distillation or by filtration.
  • the fuel additized with the quaternized additive according to the invention is a gasoline fuel or in particular a middle distillate fuel, especially a diesel fuel.
  • the fuel may contain other conventional additives to improve the effectiveness and / or wear suppression.
  • these are primarily conventional detergent additives, carrier oils, cold flow improvers, lubricity improvers, corrosion inhibitors, demulsifiers, dehazers, defoamers, cetane improvers, combustion improvers, antioxidants or stabilizers, antistatic agents, metallocenes, metal deactivators, dyes and / or Solvent.
  • the hydrophobic hydrocarbon residue in the above detergent additives which provides the sufficient solubility in the fuel has a number average molecular weight (M n ) of from 85 to 20,000, preferably from 113 to 10,000, more preferably from 300 to 5,000, more preferably from 300 to 3,000, even more preferably from 500 to 2,500 and in particular from 700 to 2,500, especially from 800 to 1,500.
  • M n number average molecular weight
  • hydrophobic hydrocarbon radical in particular in connection with the polar groups are in particular polypropenyl, polybutenyl and polyisobutenyl radicals having a number average molecular weight M n from preferably in each case 300 to 5,000, particularly preferably 300 to 3,000, more preferably 500 to 2,500, even more preferably 700 to 2,500 and in particular 800 to 1,500 into consideration.
  • monoamino (Da) -containing additives are the compounds obtainable from polyisobutene epoxides by reaction with amines and subsequent dehydration and reduction of the amino alcohols, as described in particular in US Pat DE-A 196 20 262 are described.
  • Carboxyl groups or their alkali metal or alkaline earth metal salts (Dd) containing additives are preferably copolymers of C 2 - to C 40 olefins with maleic anhydride having a total molecular weight of 500 to 20,000, their carboxyl groups wholly or partially to the alkali metal or alkaline earth metal salts and a remaining Rest of the carboxyl groups are reacted with alcohols or amines.
  • Such additives are in particular from the EP-A 307 815 known.
  • Such additives are primarily for preventing valve seat wear and can, as in the WO-A 87/01126 described, be used with advantage in combination with conventional fuel detergents such as poly (iso) -butene amines or polyetheramines.
  • Sulfonic acid groups or their alkali metal or alkaline earth metal salts (De) containing additives are preferably alkali metal or alkaline earth metal salts of a Sulfobernsteinklakylesters, as described in particular in EP-A 639 632 is described.
  • Such additives are primarily for preventing valve seat wear and can be used to advantage in combination with conventional fuel detergents such as poly (iso) buteneamines or polyetheramines.
  • Polyoxy-C 2 -C 4 -alkylene (Df) containing additives are preferably polyether or polyetheramines, which by reaction of C 2 - to C 60 -alkanols, C 6 -C 30 alkanediols, mono- or di-C 2 - to C 30 -alkylamines, C 1 - to C 30 -alkylcyclohexanols or C 1 - to C 30 -alkylphenols with 1 to 30 mol of ethylene oxide and / or propylene oxide and / or butylene oxide per hydroxyl group or amino group and, in the case of polyetheramines, are obtainable by subsequent reductive amination with ammonia, monoamines or polyamines.
  • Such products are used in particular in the EP-A 310 875 .
  • polyethers such products also meet carrier oil properties. Typical examples of these are tridecanol or Isotridecanolbutoxylate, Isononylphenolbutoxylate and Polyisobutenolbutoxylate and propoxylates and the corresponding reaction products with ammonia.
  • Carboxylic ester groups (Dg) containing additives are preferably esters of mono-, di- or tricarboxylic acids with long-chain alkanols or polyols, especially those having a minimum viscosity of 2 mm 2 / s at 100 ° C, as in particular in DE-A 38 38 918 are described.
  • mono-, di- or tricarboxylic acids it is possible to use aliphatic or aromatic acids, especially suitable ester alcohols or polyols are long-chain representatives having, for example, 6 to 24 C atoms.
  • esters are adipates, phthalates, isophthalates, terephthalates and trimellitates of iso-octanol, iso-nonanol, iso-decanol and of isotridecanol. Such products also meet carrier oil properties.
  • the groups having hydroxyl and / or amino and / or amido and / or imido groups are, for example, carboxylic acid groups, acid amides of monoamines, acid amides of diamines or polyamines which, in addition to the amide function, still have free amine groups, succinic acid derivatives with an acid and an amide function, carboximides with monoamines, carboximides with di- or polyamines which, in addition to the imide function, still have free amine groups, or diimides which are formed by reacting di- or polyamines with two succinic acid derivatives.
  • the further detergent additive according to the present invention is used only up to a maximum of 100% of the amount by weight of compounds having betaine structure.
  • Such fuel additives are well known and described, for example, in documents (1) and (2). Preference is given to the reaction products of alkyl- or alkenyl-substituted succinic acids or derivatives thereof with amines and particularly preferably to the reaction products of polyisobutenyl-substituted succinic acids or derivatives thereof with amines.
  • reaction products with aliphatic polyamines in particular ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine and hexaethyleneheptamine, which have an imide structure.
  • Mannich reaction of substituted phenols with aldehydes and mono- or polyamines produced groupings (di) -containing additives are preferably reaction products of polyisobutene-substituted phenols with formaldehyde and mono- or polyamines such as ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine or dimethylaminopropylamine.
  • One or more of said detergent additives may be added to the fuel in such an amount that the dosage rate of these detergent additives is preferably from 25 to 2500 ppm by weight, in particular from 75 to 1500 ppm by weight, especially from 150 to 1000% by weight . ppm.
  • Co-used carrier oils may be mineral or synthetic.
  • Suitable mineral carrier oils are fractions obtained in petroleum processing, such as bright stock or base oils having viscosities such as from class SN 500 to 2000, but also aromatic hydrocarbons, paraffinic hydrocarbons and alkoxyalkanols. It is also useful as a "hydrocrack oil” known and obtained in the refining of mineral oil fraction (Vakuumdestillatites with a boiling range of about 360 to 500 ° C, available from high pressure catalytically hydrogenated and isomerized and dewaxed natural mineral oil). Also suitable are mixtures of the abovementioned mineral carrier oils.
  • suitable synthetic carrier oils are polyolefins (polyalphaolefins or polyinternalolefins), (poly) esters, poly) alkoxylates, polyethers, aliphatic polyetheramines, alkylphenol-initiated polyethers, alkylphenol-initiated polyetheramines and carboxylic acid esters of long-chain alkanols.
  • suitable polyethers or polyetheramines are preferably compounds containing polyoxy-C 2 to C 4 -alkylene groups, which are prepared by reacting C 2 - to C 60 -alkanols, C 6 - to C 30 -alkanediols, mono- or di-C 2 - to C 30 -alkylamines, C 1 - to C 30 -alkyl-cyclohexanols or C 1 - to C 30 -alkylphenols with 1 to 30 mol of ethylene oxide and / or propylene oxide and / or butylene oxide per hydroxyl group or amino group and, in the case of polyetheramines , by subsequent reductive amination with ammonia, monoamines or polyamines are available.
  • EP-A 310 875 Such products are used in particular in the EP-A 310 875 .
  • EP-A 356 725 EP-A 700 985 and the US-A 4,877,416 described.
  • poly-C 2 -C 6 -alkylene oxide amines or functional derivatives thereof can be used as polyetheramines. Typical examples of these are tridecanol or Isotridecanolbutoxylate, Isononylphenolbutoxylate and Polyisobutenolbutoxylate and propoxylates and the corresponding reaction products with ammonia.
  • carboxylic acid esters of long-chain alkanols are, in particular, esters of mono-, di- or tricarboxylic acids with long-chain alkanols or polyols, as are described in particular in US Pat DE-A 38 38 918 are described.
  • mono-, di- or tricarboxylic acids it is possible to use aliphatic or aromatic acids, especially suitable ester alcohols or polyols are long-chain representatives having, for example, 6 to 24 carbon atoms.
  • esters are adipates, phthalates, isophthalates, terephthalates and trimellitates of isooctanol, isononanol, isodecanol and of isotridecanol, eg. B. di- (n- or isotridecyl) phthalate.
  • particularly suitable synthetic carrier oils are alcohol-started polyethers having about 5 to 35, preferably about 5 to 30, particularly preferably 10 to 30 and in particular 15 to 30 C 3 - to C 6 -alkylene oxide units, for.
  • suitable starter alcohols are long-chain alkanols or long-chain alkyl-substituted phenols, where the long-chain alkyl radical is in particular a straight-chain or branched C 6 - to C 18 -alkyl radical.
  • Specific examples include tridecanol and nonylphenol.
  • Particularly preferred alcohol-started polyethers are the reaction products (polyetherification products) of monohydric aliphatic C 6 - to C 18 -alcohols with C 3 - to C 6 -alkylene oxides.
  • monohydric aliphatic C 6 -C 18 -alcohols are hexanol, heptanol, octanol, 2-ethylhexanol, nonyl alcohol, decanol, 3-propylheptanol, undecanol, dodecanol, tridecanol, tetradecanol, pentadecanol, hexadecanol, octadecanol and their constitution and position isomers.
  • the alcohols can be in the form of pure isomers as well as in Form of technical mixtures are used.
  • a particularly preferred alcohol is tridecanol.
  • C 3 - to C 6 -alkylene oxides are propylene oxide, such as 1,2-propylene oxide, butylene oxide, such as 1,2-butylene oxide, 2,3-butylene oxide, isobutylene oxide or tetrahydrofuran, pentylene oxide and hexylene oxide.
  • particularly preferred are C 3 to C 4 alkylene oxides, ie, propylene oxide such as 1,2-propylene oxide and butylene oxide such as 1,2-butylene oxide, 2,3-butylene oxide and isobutylene oxide.
  • butylene oxide is used.
  • Suitable synthetic carrier oils are alkoxylated alkylphenols, as described in the DE-A 10 102 913 are described.
  • Particular carrier oils are synthetic carrier oils, the alcohol-initiated polyethers described above being particularly preferred.
  • the carrier oil or the mixture of different carrier oils is added to the fuel in an amount of preferably from 1 to 1000 ppm by weight, more preferably from 10 to 500 ppm by weight and in particular from 20 to 100 ppm by weight.
  • Suitable cold flow improvers are in principle all organic compounds which are able to improve the flow behavior of middle distillate fuels or diesel fuels in the cold. Conveniently, they must have sufficient oil solubility.
  • middle distillates of fossil origin ie for conventional mineral diesel fuels
  • used cold flow improvers (“middle distillate flow improvers", "MDFI") come into consideration.
  • MDFI middle distillate flow improvers
  • WASA wax anti-settling additive
  • Suitable C 2 to C 40 olefin monomers for the copolymers of class (K1) are, for example, those having 2 to 20, in particular 2 to 10, carbon atoms and having 1 to 3, preferably 1 or 2, in particular having a carbon-carbon double bond.
  • the carbon-carbon double bond can be arranged both terminally ( ⁇ -olefins) and internally.
  • ⁇ -olefins particularly preferably ⁇ -olefins having 2 to 6 carbon atoms, for example propene, 1-butene, 1-pentene, 1-hexene and, above all, ethylene.
  • the at least one further ethylenically unsaturated monomer is preferably selected from carboxylic alkenyl esters, (meth) acrylic esters and further olefins.
  • olefins are polymerized in, these are preferably higher molecular weight than the abovementioned C 2 to C 40 olefin base monomers. If, for example, ethylene or propene is used as the olefin base monomer, C 10 - to C 40 - ⁇ -olefins are particularly suitable as further olefins. Other olefins are polymerized in most cases only when monomers with carboxylic acid ester functions are used.
  • Suitable (meth) acrylic esters are, for example, esters of (meth) acrylic acid with C 1 - to C 20 -alkanols, in particular C 1 - to C 10 -alkanols, especially with methanol, ethanol, propanol, isopropanol, n-butanol, sec. Butanol, isobutanol, tert-butanol, pentanol, Hexanol, heptanol, octanol, 2-ethylhexanol, nonanol and decanol, and structural isomers thereof.
  • Suitable carboxylic alkenyl esters are, for example, C 2 -C 14 -alkenyl esters, for example the vinyl and propenyl esters, of carboxylic acids having 2 to 21 carbon atoms, whose hydrocarbon radical may be linear or branched. Preferred among these are the vinyl esters.
  • carboxylic acids with a branched hydrocarbon radical preference is given to those whose branching is in the ⁇ -position to the carboxyl group, the ⁇ -carbon atom being particularly preferably tertiary, ie the carboxylic acid being a so-called neocarboxylic acid.
  • the hydrocarbon radical of the carboxylic acid is linear.
  • carboxylic alkenyl esters examples include vinyl acetate, vinyl propionate, vinyl butyrate, vinyl 2-ethylhexanoate, vinyl neopentanoate, vinyl hexanoate, vinyl neononanoate, vinyl neodecanoate and the corresponding propenyl esters, with vinyl esters being preferred.
  • a particularly preferred carboxylic acid alkenyl ester is vinyl acetate; typical resulting copolymers of group (K1) are the most commonly used ethylene-vinyl acetate copolymers ("EVA").
  • copolymers of class (K1) are those which contain two or more different carboxylic acid alkenyl esters in copolymerized form, these differing in the alkenyl function and / or in the carboxylic acid group. Also suitable are copolymers which, in addition to the carboxylic acid alkenyl ester (s), contain at least one olefin and / or at least one (meth) acrylic acid ester in copolymerized form.
  • terpolymers of a C 2 - to C 40 - ⁇ -olefin, a C 1 - to C 20 alkyl ester of an ethylenically unsaturated monocarboxylic acid having 3 to 15 carbon atoms and a C 2 - to C 14 alkenyl ester of a saturated monocarboxylic acid having 2 to 21 Carbon atoms are suitable as copolymers of class (K1).
  • Such terpolymers are in the WO 2005/054314 described.
  • a typical such terpolymer is composed of ethylene, 2-ethylhexyl acrylate and vinyl acetate.
  • the at least one or the other ethylenically unsaturated monomers are present in the copolymers of class (K1) in an amount of preferably from 1 to 50% by weight, in particular from 10 to 45% by weight and especially from 20 to 40% by weight. %, based on the total copolymer, copolymerized.
  • the majority by weight of the monomer units in the copolymers of class (K1) is thus usually derived from the C 2 to C 40 based olefins.
  • the copolymers of class (K1) preferably have a number average molecular weight M n of from 1000 to 20,000, particularly preferably from 1000 to 10,000 and in particular from 1000 to 8000.
  • Typical comb polymers of component (K2) are, for example, by the copolymerization of maleic anhydride or fumaric acid with another ethylenically unsaturated monomer, for example with an ⁇ -olefin or an unsaturated ester such as vinyl acetate, and subsequent esterification of the anhydride or acid function with an alcohol having at least 10 carbon atoms available.
  • Other suitable comb polymers are copolymers of ⁇ -olefins and esterified comonomers, for example esterified copolymers of styrene and maleic anhydride or esterified copolymers of styrene and fumaric acid.
  • Suitable comb polymers may also be polyfumarates or polymaleinates.
  • homopolymers and copolymers of vinyl ethers are suitable comb polymers.
  • suitable comb polymers are, for example, those which are described in the WO 2004/035715 and in " Comb-like polymers. Structure and Properties ", NA Platé and VP Shibaev, J. Poly. Sci. Macromolecular Revs., 8, pp. 117-253 (1974 Also mixtures of comb polymers are suitable.
  • suitable polyoxyalkylenes are, for example, polyoxyalkylene esters, polyoxyalkylene ethers, mixed polyoxyalkylene ester ethers, and mixtures thereof.
  • these polyoxyalkylene contain at least one, preferably at least two linear alkyl groups each having 10 to 30 carbon atoms and a polyoxyalkylene group having a number average molecular weight of up to 5000.
  • Such polyoxyalkylene compounds are for example in the EP-A 061 895 as well as in the U.S. 4,491,455 described.
  • Special polyoxyalkylene compounds are based on polyethylene glycols and polypropylene glycols having a number average molecular weight of 100 to 5000.
  • polyoxyalkylene mono- and diesters of fatty acids having 10 to 30 carbon atoms such as stearic acid or behenic acid are suitable.
  • Polar nitrogen compounds suitable as a component of class (K4) may be of both ionic and nonionic nature, and preferably have at least one, especially at least two, tertiary nitrogen substituent of the general formula> NR 7 wherein R 7 is C 8 - C 40 hydrocarbon radical stands.
  • the nitrogen substituents may also be quaternized, that is in cationic form. Examples of such nitrogen compounds are ammonium salts and / or amides obtainable by reacting at least one amine substituted with at least one hydrocarbyl radical with a carboxylic acid having 1 to 4 carboxyl groups or with a suitable derivative thereof.
  • the amines preferably contain at least one linear C 8 - to C 40 -alkyl radical.
  • suitable primary amines for the preparation of said polar nitrogen compounds are octylamine, nonylamine, decylamine, undecylamine, dodecylamine, tetradecylamine and the higher linear homologues
  • suitable secondary amines are, for example, dioctadecylamine and methylbehenylamine.
  • amine mixtures in particular industrially available amine mixtures such as fatty amines or hydrogenated tallamines, as described, for example, in Ullmann's Encyclopedia of Industrial Chemistry, 6th edition, in the chapter "Amines, aliphatic".
  • Suitable acids for the reaction are, for example, cyclohexane-1,2-dicarboxylic acid, cyclohexene-1,2-dicarboxylic acid, cyclopentane-1,2-dicarboxylic acid, naphthalenedicarboxylic acid, phthalic acid, isophthalic acid, terephthalic acid and succinic acids substituted by long-chain hydrocarbon radicals.
  • the component of class (K4) is an oil-soluble reaction product of at least one tertiary amino group-containing poly (C 2 - to C 20 -carboxylic acids) with primary or secondary amines.
  • the poly (C 2 - to C 20 -carboxylic acids) which have at least one tertiary amino group and are based on this reaction product preferably contain at least 3 carboxyl groups, in particular 3 to 12, especially 3 to 5 carboxyl groups.
  • the carboxylic acid units in the polycarboxylic acids preferably have 2 to 10 carbon atoms, in particular they are Acetic acid units.
  • the carboxylic acid units are suitably linked to the polycarboxylic acids, usually via one or more carbon and / or nitrogen atoms. Preferably, they are attached to tertiary nitrogen atoms, which are connected in the case of several nitrogen atoms via hydrocarbon chains.
  • the component of class (K4) is an oil-soluble reaction product based on at least one tertiary amino group-containing poly (C 2 - to C 20 -carboxylic acids) of the general formula IIa or IIb in which the variable A is a straight-chain or branched C 2 - to C 6 -alkylene group or r is the grouping of the formula III and the variable B denotes a C 1 - to C 19 -alkylene group.
  • the compounds of the general formula IIa and IIb have in particular the properties of a WASA.
  • the preferred oil-soluble reaction product of component (K4) in particular that of general formula IIa or IIb, is an amide, an amide ammonium salt or an ammonium salt in which no, one or more carboxylic acid groups are converted into amide groups.
  • Straight-chain or branched C 2 -C 6 -alkylene groups of the variable A are, for example, 1,1-ethylene, 1,2-propylene, 1,3-propylene, 1,2-butylene, 1,3-butylene, 1,4- butylene, 2-methyl-1,3-propylene, 1,5-pentylene, 2-methyl-1,4-butylene, 2,2-dimethyl-1,3-propylene, 1,6-hexylene (hexamethylene) and especially 1, 2-ethylene.
  • the variable A comprises 2 to 4, in particular 2 or 3 carbon atoms.
  • C 1 - to C 19 -alkylene groups of the variables B are, for example, 1,2-ethylene, 1,3-propylene, 1,4-butylene, hexamethylene, octamethylene, decamethylene, dodecamethylene, tetradecamethylene, hexadecamethylene, octadecamethylene, nonadecamethylene and in particular methylene ,
  • the variable B comprises 1 to 10, in particular 1 to 4, carbon atoms.
  • the primary and secondary amines as reaction partners for the polycarboxylic acids to form the component (K4) are usually monoamines, in particular aliphatic monoamines. These primary and secondary amines may be selected from a variety of amines bearing hydrocarbon radicals, optionally linked together.
  • these amines are secondary amines on which the oil-soluble reaction products of component (K4) are based and have the general formula HN (R 8 ) 2 , in which the two variables R 8 are each independently straight-chain or branched C 10 - to C 30 -alkyl radicals, in particular C 14 - to C 24 -alkyl radicals.
  • These longer-chain alkyl radicals are preferably straight-chain or only slightly branched.
  • the abovementioned secondary amines are derived with regard to their longer-chain alkyl radicals from naturally occurring fatty acid or from its derivatives.
  • the two radicals R 8 are the same.
  • the abovementioned secondary amines can be bound to the polycarboxylic acids by means of amide structures or in the form of the ammonium salts, and only one part can be present as amide structures and another part as ammonium salts. Preferably, only a few or no free acid groups are present. Preferably, the oil-soluble reaction products of component (K4) are completely in the form of the amide structures.
  • Typical examples of such components (K4) are reaction products of nitrilotriacetic acid, ethylenediaminetetraacetic acid or propylene-1,2-diaminetetraacetic acid with in each case 0.5 to 1.5 mol per carboxyl group, in particular 0.8 to 1.2 mol per carboxyl group, dioleylamine, dipalmitinamine, dicoco fatty amine, distearylamine, dibehenylamine or in particular Ditalgfettamin.
  • a particularly preferred component (K4) is the reaction product of 1 mole of ethylenediaminetetraacetic acid and 4 moles of hydrogenated ditallow fatty amine.
  • component (K4) include the N, N-dialkylammonium salts of 2-N ', N'-dialkylamidobenzoates, for example the reaction product of 1 mole of phthalic anhydride and 2 moles of ditallow fatty amine, the latter may be hydrogenated or unhydrogenated, and the reaction product of 1 mole of a Alkenylspirobislactons with 2 moles of a dialkylamine, for example Ditalgfettamin and / or tallow fatty amine, the latter two may be hydrogenated or not hydrogenated, called.
  • N, N-dialkylammonium salts of 2-N ', N'-dialkylamidobenzoates for example the reaction product of 1 mole of phthalic anhydride and 2 moles of ditallow fatty amine, the latter may be hydrogenated or unhydrogenated
  • component of class (K4) are cyclic compounds with tertiary amino groups or condensates of long-chain primary or secondary amines with carboxylic acid-containing polymers, as described in US Pat WO 93/18115 are described.
  • Sulfocarboxylic acids, sulfonic acids or their derivatives which are suitable as cold flow improvers of the component of class (K5) are, for example, the oil-soluble carboxamides and carboxylic acid esters of ortho-sulfobenzoic acid in which the sulfonic acid function is present as sulfonate with alkyl-substituted ammonium cations, as described in US Pat EP-A 261 957 to be discribed.
  • suitable poly (meth) acrylic acid esters are both homo- and copolymers of acrylic and methacrylic acid esters.
  • Preferred are copolymers of at least two mutually different (meth) acrylic acid esters, which differ with respect to the fused alcohol.
  • the copolymer contains a further, different of which olefinically unsaturated monomer copolymerized.
  • the weight-average molecular weight of the polymer is preferably 50,000 to 500,000.
  • a particularly preferred polymer is a copolymer of methacrylic acid and methacrylic acid esters of saturated C 14 and C 15 alcohols, wherein the acid groups are hydrogenated tallamine are neutralized.
  • Suitable poly (meth) acrylic esters are, for example, in WO 00/44857 described.
  • the middle distillate fuel or diesel fuel is the cold flow improver or the mixture of various cold flow improvers in a total amount of preferably 10 to 5000 ppm by weight, more preferably from 20 to 2000 ppm by weight, more preferably from 50 to 1000 ppm by weight and in particular from 100 to 700 ppm by weight, for example from 200 to 500 ppm by weight, added.
  • Suitable lubricity improvers are usually based on fatty acids or fatty acid esters. Typical examples are tall oil fatty acid, such as in the WO 98/004656 described, and glycerol monooleate. Also in the US Pat. No. 6,743,266 B2 described reaction products of natural or synthetic oils, such as triglycerides, and alkanolamines are suitable as such lubricity improvers.
  • Suitable corrosion inhibitors are e.g. Succinic esters, especially with polyols, fatty acid derivatives, e.g. Oleic acid esters, oligomerized fatty acids, substituted ethanolamines, and products sold under the trade name RC 4801 (Rhein Chemie Mannheim, Germany) or HiTEC 536 (Ethyl Corporation).
  • Suitable demulsifiers are, for example, the alkali metal or alkaline earth metal salts of alkyl-substituted phenol and naphthalene sulfonates and the alkali metal or alkaline earth metal salts of fatty acids, furthermore neutral compounds such as alcohol alkoxylates, for example alcohol ethoxylates, phenol alkoxylates, for example tert-butylphenol ethoxylate or tert-pentylphenol ethoxylate, fatty acids, alkylphenols, Condensation of ethylene oxide (EO) and propylene oxide (PO), for example in the form of EO / PO block copolymers, polyethylene imines or polysiloxanes.
  • EO ethylene oxide
  • PO propylene oxide
  • Suitable dehazers are e.g. alkoxylated phenol-formaldehyde condensates such as the NALCO 7D07 (Nalco) and TOLAD 2683 (Petrolite) products available under the tradename.
  • Suitable antifoams are e.g. Polyether-modified polysiloxanes such as the TEGOPREN 5851 (Goldschmidt), Q 25907 (Dow Corning) and RHODOSIL (Rhone Poulenc) products available under the tradename.
  • Polyether-modified polysiloxanes such as the TEGOPREN 5851 (Goldschmidt), Q 25907 (Dow Corning) and RHODOSIL (Rhone Poulenc) products available under the tradename.
  • Suitable cetane number improvers are e.g. aliphatic nitrates such as 2-ethylhexyl nitrate and cyclohexyl nitrate and peroxides such as di-tert-butyl peroxide.
  • Suitable antioxidants are e.g. substituted phenols such as 2,6-di-tert-butylphenol and 6-di-tert-butyl-3-methylphenol and phenylenediamines such as N, N'-di-sec-butyl-p-phenylenediamine.
  • Suitable metal deactivators are e.g. Salicylic acid derivatives such as N, N'-disalicylidene-1,2-propanediamine.
  • Suitable are, for example, nonpolar organic solvents such as aromatic and aliphatic hydrocarbons, for example toluene, xylenes, "white spirit" and products sold under the trade name SHELLSOL (Royal Dutch / Shell Group) and EXXSOL (ExxonMobil). and polar organic solvents, for example alcohols such as 2-ethylhexanol, decanol and isotridecanol.
  • solvents usually arrive together with the aforementioned additives and co-additives which they are intended to dissolve or dilute for better handling into the diesel fuel.
  • the additive of the invention is outstandingly suitable as a fuel additive and can be used in principle in any fuels. It has a number of beneficial effects on the operation of internal combustion engines with fuels.
  • the present invention therefore also fuels, especially middle distillate fuels, with an effective as an additive to achieve beneficial effects in the operation of internal combustion engines, such as diesel engines, especially direct injection diesel engines, especially of diesel engines with common rail injection systems, effective content on the quaternized additive according to the invention.
  • This effective content is generally from 10 to 5000 ppm by weight, preferably from 20 to 1500 ppm by weight, in particular from 25 to 1000 ppm by weight, especially from 30 to 750 ppm by weight, each based on the total amount of fuel.
  • Middle distillate fuels such as diesel fuels or fuel oils
  • mineral middle distillate mineral fuels or diesel fuels available through refining
  • those produced by coal gasification or gas liquefaction [GTL] or by biomass to liquid (BTL) fuels are also included. are available, suitable. Also suitable are mixtures the aforementioned middle distillate fuels or diesel fuels with regenerative fuels, such as biodiesel or bioethanol.
  • the quaternized additive according to the invention can also be used in mixtures of such middle distillates with biofuel oils (biodiesel).
  • biofuel oils biodiesel
  • such mixtures are also encompassed by the term "middle distillate fuel”. They are commercially available and usually contain the biofuel oils in minor amounts, typically in amounts of 1 to 30 wt .-%, in particular from 3 to 10 wt .-%, based on the total amount of middle distillate of fossil, vegetable or animal origin and biofuel.
  • Biofuel oils are generally based on fatty acid esters, preferably substantially on alkyl esters of fatty acids derived from vegetable and / or animal oils and / or fats.
  • Alkyl esters are usually lower alkyl esters, in particular C 1 - to C 4 -alkyl esters, understood by transesterification of occurring in vegetable and / or animal oils and / or fats glycerides, especially triglycerides, by means of lower alcohols, for example ethanol or especially methanol (“ FAME ”) are available.
  • Typical lower alkyl esters based on vegetable and / or animal oils and / or fats which are used as biofuel oil or components thereof include, for example, sunflower methyl ester, palm oil methyl ester (“PME”), soybean oil methyl ester (“SME”) and in particular rapeseed oil methyl ester (“RME”).
  • PME palm oil methyl ester
  • SME soybean oil methyl ester
  • RME rapeseed oil methyl ester
  • the middle distillate fuels or diesel fuels are particularly preferably those with a low sulfur content, ie with a sulfur content of less than 0.05% by weight, preferably less than 0.02% by weight, in particular less as 0.005 wt .-% and especially less than 0.001 wt .-% sulfur.
  • gasoline fuels are all commercially available gasoline fuel compositions into consideration.
  • a typical representative here is the market-standard basic fuel of Eurosuper according to EN 228.
  • petrol fuel compositions of the specification are also according to WO 00/47698 Possible fields of use for the present invention.
  • the quaternized additive according to the invention is particularly suitable as a fuel additive in fuel compositions, especially in diesel fuels, to overcome the initially described problems in direct injection diesel engines, especially in those with common rail injection systems.
  • the power loss was determined according to the official test method CEC F-098-08.
  • the power loss is a direct measure of the formation of deposits in the injectors.
  • a direct injection diesel engine with common rail system was used according to test methods CEC F-098-08.
  • fuel was a commercial diesel fuel the company Haltermann (RF-06-03) used.
  • RF-06-03 the company Haltermann (RF-06-03) used.
  • 1 wt ppm zinc in the form of a zinc didodecanoate solution to artificially stimulate the formation of deposits on the injectors.
  • the results illustrate the relative power loss measured at 4000 rpm during a 12-hour continuous operation.
  • the value "t0" indicates the power loss normalized (100%) to the value after 10 minutes; the value "t1" indicates the power loss normalized to the value after one hour.
  • the measured power loss is determined by the ratio - (P1-PO) / PO.
  • Polydispersities D were determined by gel permeation chromatography.
  • N, N-dimethylethanolamine (76.7 g) is treated with potassium tert -butylate (4.1 g) in a 21-liter autoclave. It is purged three times with N 2 , a pre-pressure of about 1.3 bar N 2 adjusted and the temperature increased to 130 ° C.
  • 1,2-propylene oxide (750 g) is metered in over a period of 10 hours so that the temperature remains between 129 ° C-131 ° C.
  • the mixture is then stirred for 6 h at 130 ° C, rinsed with N 2 , cooled to 60 ° C and the reactor emptied. Excess propylene oxide is removed on a rotary evaporator in vacuo.
  • the basic crude product is neutralized using commercially available Mg silicates, which are then filtered off. 831 g of the product are obtained in the form of an orange oil (TBN 58.1 mg KOH / g; D 1.16).
  • N, N-dimethylethanolamine (47.1 g) is treated with potassium tert-butylate (5.0 g). It is purged three times with N 2 , a pre-pressure of about 1.3 bar N 2 adjusted and the temperature increased to 140 ° C.
  • 1,2-Butylene oxide (953 g) is added over a period of 9 h so that the temperature remains between 138 ° C-141 ° C.
  • the mixture is then stirred for 6 h at 140 ° C, rinsed with N 2 , cooled to 60 ° C and the reactor emptied. Excess butylene oxide is removed on a rotary evaporator in vacuo.
  • the basic crude product is neutralized using commercially available Mg silicates, which are then filtered off. 1000 g of the product are obtained in the form of a yellow oil (TBN 28.1 mg KOH / g; D 1.12).
  • Polyetheramine (B) 400 g) from Synthesis Example 2 is dissolved in Solvent Naphtha Heavy (436 g), added with styrene oxide (24.0 g) and acetic acid (12.0 g) and then at 80 ° C for 8 h touched. After cooling to room temperature, 870 g of the product are obtained.
  • 1 H NMR analysis of the quaternized polyetheramine solution thus obtained in Solvent Naphtha Heavy shows the quaternization.
  • polyetheramine (A) (305 g) from Synthesis Example 1 is dissolved in 2-ethylhexanol (341 g) and acetic acid (18.3 g) is added. It is purged three times with N 2 , a pre-pressure of about 1.3 bar N 2 adjusted and the temperature increased to 130 ° C. 1,2-propylene oxide (17.7 g) is added. The mixture is then stirred for 5 h at 130 ° C, rinsed with N 2 , cooled to 40 ° C and the reactor emptied. Excess propylene oxide is removed on a rotary evaporator in vacuo. This gives 675 g of the product in the form of an orange oil. 1 H-NMR analysis of the resulting solution of the quaternized polyetheramine in 2-ethylhexanol shows the quaternization.
  • polyetheramine (A) (518 g) from Synthesis Example 1 is dissolved in 2-ethylhexanol (570 g) and treated with conc. Acetic acid (30 g) was added. It is purged three times with N 2 , a pre-pressure of about 1.3 bar N 2 adjusted and the temperature increased to 130 ° C. Ethylene oxide (22 g) is added. The mixture is then stirred for 5 h at 130 ° C, rinsed with N 2 , cooled to 40 ° C and the reactor emptied. You get 1116 g of the product in the form of an orange oil. 1 H-NMR analysis of the resulting solution of the quaternized polyetheramine in 2-ethylhexanol shows the quaternization.
  • the polyetheramine (D) (400 g) from Synthesis Example 9 is mixed with ice-bath cooling with formic acid (65.3 g, 85% in H 2 O). The reaction mixture is then ⁇ -heated to a temperature of 45 ° C and formaldehyde solution (44.9 g, 36.5% in H 2 O) is added dropwise at this temperature, wherein the liberated carbon dioxide is discharged from the reaction vessel. The reaction mixture is stirred for 16 h at a temperature of 80 ° C. The reaction mixture is then cooled to room temperature, admixed with hydrochloric acid (37%, 35.4 g) and stirred at room temperature for 1 h.
  • the additives are used either as a pure substance (as synthesized in the above preparation examples) or in the form of an additive package.
  • Table 2 Results of the DW10 test additive dose [Mg / kg] Time [H] P0 [KW] Pend [KW] Power loss basic value 0 12 99.3 94.3 5.0% M1, according to Preparation Example 6, Keep-Clean 80 12 97.9 97.3 0.61% basic value 0 12 94.2 91.5 2.87% M2, according to Preparation Example 3, Clean-up 75 12 91.3 93.1 -1.97%

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EP11187959.9A 2011-11-04 2011-11-04 Quaternisierte Polyetheramine und deren Verwendung als Additive in Kraft- und Schmierstoffen Withdrawn EP2589647A1 (de)

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EP11187959.9A EP2589647A1 (de) 2011-11-04 2011-11-04 Quaternisierte Polyetheramine und deren Verwendung als Additive in Kraft- und Schmierstoffen
HUE12780216 HUE044181T2 (hu) 2011-11-04 2012-11-05 Kvaternizált poliéteraminok alkalmazása adalékként üzemanyagokhoz és kenõolajokhoz
ES12780216T ES2726102T3 (es) 2011-11-04 2012-11-05 Uso de polieteraminas cuaternizadas como aditivo en combustibles y lubricantes
KR1020147015015A KR102033606B1 (ko) 2011-11-04 2012-11-05 4급화된 폴리에테르아민 및 연료 및 윤활제의 첨가제로서 이의 용도
AU2012331073A AU2012331073B2 (en) 2011-11-04 2012-11-05 Quaternized polyetheramines and use thereof as additives in fuels and lubricants
EP12780216.3A EP2773729B1 (de) 2011-11-04 2012-11-05 Verwendung von quaternisierten polyetheraminen als additive in kraft- und schmierstoffen
BR112014010671A BR112014010671A2 (pt) 2011-11-04 2012-11-05 composição de combustível ou composição de lubrificante, composto de nitrogênio quaternizado, processo para preparar compostos de nitrogênio quaternizados, uso de um composto de nitrogênio quaternizado, e, concentrado de aditivo
MX2014005325A MX2014005325A (es) 2011-11-04 2012-11-05 Polieteraminas cuaternizadas y uso de las mismas como aditivos en combustibles y lubricantes.
PCT/EP2012/071844 WO2013064689A1 (de) 2011-11-04 2012-11-05 Quaternisierte polyetheramine und deren verwendung als additive in kraft- und schmierstoffen
CN201280065791.5A CN104024385B (zh) 2011-11-04 2012-11-05 季铵化聚醚胺及其在燃料和润滑剂中作为添加剂的用途
TR2019/05501T TR201905501T4 (tr) 2011-11-04 2012-11-05 Akaryakıtlarda ve yağlama maddelerinde katkı maddesi olarak kuaternize edilmiş polieter aminlerin kullanımı.
CA2854421A CA2854421C (en) 2011-11-04 2012-11-05 Quaternized polyetheramines and use thereof as additives in fuels and lubricants
PL12780216T PL2773729T3 (pl) 2011-11-04 2012-11-05 Zastosowanie czwartorzędowanych polieteroamin jako dodatków do paliw silnikowych i smarów

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KR20160037958A (ko) * 2013-07-26 2016-04-06 이노스펙 리미티드 연료 또는 윤활제 첨가제로서의 4급 암모늄 화합물
KR20160037959A (ko) * 2013-07-26 2016-04-06 이노스펙 리미티드 연료 또는 윤활제 첨가제로서의 4급 암모늄 화합물
US10351791B2 (en) 2013-07-26 2019-07-16 Innospec Limited Quaternary ammonium compounds as fuel or lubricant additives
EP3024820B1 (en) * 2013-07-26 2019-09-04 Innospec Limited Quaternary ammonium compounds as fuel or lubricant additives
EP3575385A1 (en) * 2013-07-26 2019-12-04 Innospec Limited Method for preparing a fuel composition comprising a quaternary ammonium compound
KR20210003312A (ko) * 2013-07-26 2021-01-11 이노스펙 리미티드 연료 또는 윤활제 첨가제로서의 4급 암모늄 화합물
US11066617B2 (en) 2013-07-26 2021-07-20 Innospec Limited Quaternary ammonium compounds as fuel or lubricant additives

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EP2773729B1 (de) 2019-02-13
CN104024385B (zh) 2016-03-09
PL2773729T3 (pl) 2019-07-31
WO2013064689A1 (de) 2013-05-10
AU2012331073A1 (en) 2014-06-26
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KR102033606B1 (ko) 2019-10-17
KR20140097288A (ko) 2014-08-06
EP2773729A1 (de) 2014-09-10
MX2014005325A (es) 2014-06-05
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HUE044181T2 (hu) 2019-10-28
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