EP1526167B2 - Agent d'amélioration de l'écoulement à froid pour huiles combustibles d'origine végétale ou animale - Google Patents

Agent d'amélioration de l'écoulement à froid pour huiles combustibles d'origine végétale ou animale Download PDF

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Publication number
EP1526167B2
EP1526167B2 EP04024234.9A EP04024234A EP1526167B2 EP 1526167 B2 EP1526167 B2 EP 1526167B2 EP 04024234 A EP04024234 A EP 04024234A EP 1526167 B2 EP1526167 B2 EP 1526167B2
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Prior art keywords
monomer
fuel oil
alkyl radicals
oil composition
mol
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EP1526167B1 (fr
EP1526167A3 (fr
EP1526167A2 (fr
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Matthias Dr. Krull
Bettina Dr. Siggelkow
Martina Hess
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Clariant Produkte Deutschland GmbH
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Clariant Produkte Deutschland GmbH
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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
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C10L1/192—Macromolecular compounds
    • C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/1955—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by an alcohol, ether, aldehyde, ketonic, ketal, acetal radical
    • 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
    • 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
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C10L1/192—Macromolecular compounds
    • C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/196—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
    • C10L1/1963—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof mono-carboxylic
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C10L1/192—Macromolecular compounds
    • C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/197—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and an acyloxy group of a saturated carboxylic or carbonic acid
    • C10L1/1973—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and an acyloxy group of a saturated carboxylic or carbonic acid mono-carboxylic
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/234—Macromolecular compounds
    • C10L1/236—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derivatives thereof
    • C10L1/2364—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derivatives thereof homo- or copolymers derived from unsaturated compounds containing amide and/or imide groups
    • 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
    • C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
    • 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
    • C10L1/221—Organic compounds containing nitrogen compounds of uncertain formula; reaction products where mixtures of compounds are obtained
    • 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

Definitions

  • the present invention relates to the use of an additive as a cold flow improver for vegetable or animal fuel oils and correspondingly fueled fuel oils.
  • renewable raw materials include, in particular, natural oils and fats of plant or animal origin. These are typically triglycerides of fatty acids with 10 to 24 C atoms, which have a calorific value comparable to conventional fuels, but at the same time are considered less harmful to the environment.
  • Biofuels ie fuels derived from animal or plant material, are obtained from renewable sources and thus produce only as much CO 2 as was previously converted into biomass. It has been reported that combustion produces less carbon dioxide than equivalent amount of petroleum distillate fuel, eg, diesel fuel, and that very little sulfur dioxide is produced. In addition, they are biodegradable.
  • Oils obtained from animal or vegetable material are mainly metabolites comprising triglycerides of monocarboxylic acids, eg acids having 10 to 25 carbon atoms, and the formula in which R is an aliphatic radical of 10 to 25 carbon atoms, which may be saturated or unsaturated.
  • oils include glycerides of a variety of acids, the number and variety of which varies with the source of the oil, and may additionally contain phosphoglycerides.
  • Such oils can be obtained by methods known in the art.
  • EP-B-0 665 873 discloses a fuel oil composition
  • a fuel oil composition comprising a biofuel, a petroleum-based fuel oil and an additive which comprises (a) an oil-soluble ethylene copolymer or (b) a comb polymer or (c) a polar nitrogen compound or (d) a compound in which at least one substantially linear alkyl group having from 10 to 30 carbon atoms is bonded to a non-polymeric organic radical to provide at least one linear chain of atoms which includes the carbon atoms of the alkyl groups and one or more non-terminal oxygen atoms, or (e) one or more of the components ( a), (b), (c) and (d).
  • EP-B-0 153 176 discloses the use of polymers based on unsaturated C 4 -C 8 dicarboxylic acid dialkyl esters having average alkyl chain lengths of 12 to 14 as cold flow improvers for certain petroleum distillate fuel oils.
  • Suitable comonomers are unsaturated esters, in particular vinyl acetate, but also ⁇ -olefins.
  • US-2003/0163951 teaches multifunctional cold additives containing copolymers of dicarboxylic acid derivatives and olefins, whereupon nitrogen-containing compounds or esters are grafted on.
  • US 5391632 teaches terpolymers based on ⁇ , ⁇ -unsaturated dicarboxylic anhydrides, ⁇ , ⁇ -unsaturated compounds and polyoxyalkylene ethers according to claim 1 of US 5391632 , and a method for producing the same according to claim 5 of US 5391632 ,
  • terpolymer according to claim 1 a mixture of at least one terpolymer according to claim 1 and at least one ethylene-vinyl ester copolymer.
  • the terpolymers of the invention, as well as their mixtures, are used as paraffin inhibitors in crude oils and petroleum products.
  • US 4985048 teaches polymer blends of a copolymer (A 1 ) of 10-60 wt .-% vinyl acetate and 40-90 wt .-% of ethylene or a Copoylmer (A 2 ) of 15-50 wt .-% vinyl acetate, 0.5-20 wt % C 6 -C 24 ⁇ -olefin and 30-70% by weight of ethylene and a copolymer (B) of 10-90% by weight of C 6 -C 24 ⁇ -olefin and 10-90% by weight.
  • a 1 a copolymer of 10-60 wt .-% vinyl acetate and 40-90 wt .-% of ethylene or a Copoylmer (A 2 ) of 15-50 wt .-% vinyl acetate, 0.5-20 wt % C 6 -C 24 ⁇ -olefin and 30-70% by weight of ethylene and a copolymer (B) of 10-9
  • WO 95/22300 discloses comb polymers in which the alkyl radicals have on average less than 12 carbon atoms. These additives are particularly suitable for oils with cloud points of less than -10 ° C, where the oils may also be native hydrocarbon oils (page 21, line 16 ff.). However, native oils have cloud points from about -2 ° C upwards.
  • Another object of the invention is the use of 0.001 to 5 wt .-% of the additive defined above to improve the cold flow properties of fuel oils of animal or vegetable origin.
  • Another object of the invention is a method for improving the cold flow properties of fuel oils of animal or vegetable origin, By adding to fuel oils of animal or vegetable origin, the above-defined additive in an amount of 0.001 to 5 wt .-%.
  • Q has values from 24 to 26.
  • side chain length of olefins is meant here the alkyl radical leaving the polymer backbone, ie the chain length of the monomeric olefin minus the two olefinically bonded C atoms.
  • side chain length of olefins is meant here the alkyl radical leaving the polymer backbone, ie the chain length of the monomeric olefin minus the two olefinically bonded C atoms.
  • Suitable ethylene copolymers A) are those which contain from 8 to 21 mol% of one or more vinyl and / or (meth) acrylic esters and from 79 to 92% by weight of ethylene. Particularly preferred are ethylene copolymers with 10 to 18 mol% and especially 12 to 16 mol% of at least one vinyl ester.
  • Suitable vinyl esters are derived from fatty acids having linear or branched alkyl groups having 1 to 18 C atoms and preferably 1 to 12 C atoms.
  • vinyl acetate vinyl propionate, vinyl butyrate, vinyl hexanoate, Vinylheptanoat, vinyl octanoate, vinyl laurate and vinyl stearate and branched fatty acid based esters of vinyl alcohol such as vinyl isobutyrate, vinyl pivalate, vinyl 2-ethylhexanoate, iso-Nonanklarevinylester, Neononanklarevinylester, vinyl neodecanoate and Neoundecanklavinylester.
  • vinyl acetate vinyl propionate, vinyl butyrate, vinyl hexanoate, Vinylheptanoat, vinyl octanoate, vinyl laurate and vinyl stearate and branched fatty acid based esters of vinyl alcohol such as vinyl isobutyrate, vinyl pivalate, vinyl 2-ethylhexanoate, iso-Nonanklarevinylester, Neononanklawrevinylester, vinyl neodecan
  • esters of acrylic and methacrylic acid having 1 to 20 C atoms in the alkyl radical such as methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n- and isobutyl (meth) acrylate, hexyl , Octyl, 2-ethylhexyl, decyl, dodecyl, tetradecyl, hexadecyl, Octadecyl (meth) acrylate and mixtures of two, three, four or more of these comonomers.
  • Particularly preferred terpolymers of 2-ethylhexanoic acid vinyl ester, vinyl neononanoate or vinyl neodecanoate contain, in addition to ethylene, preferably 3.5 to 20 mol%, in particular 8 to 15 mol% vinyl acetate and 0.1 to 12 mol%, in particular 0.2 to 5 mol% of at least one long-chain, in addition to ethylene and 8 to 18 mol% vinyl esters contain from 0.5 to 10 mol% of olefins such as propene, butene, isobutylene, hexene, 4-methylpentene, octene, diisobutylene and / or norbornene.
  • olefins such as propene, butene, isobutylene, hexene, 4-methylpentene, octene, diisobutylene and / or norbornene.
  • the copolymers A preferably have molecular weights which correspond to melt viscosities at 140 ° C. of from 20 to 10,000 mPas, in particular from 30 to 5,000 mPas and especially from 50 to 1,000 mPas.
  • the determined by 1 H NMR spectroscopy degrees of branching are preferably between 1 and 9 CH 3/100 CH 2 groups, especially between 2 and 6 CH 3/100 CH 2 groups, such as 2.5 to 5 CH 3/100 CH 2 groups not derived from the comonomers.
  • the copolymers (A) can be prepared by the usual copolymerization methods such as suspension polymerization, solvent polymerization, gas phase polymerization or high-pressure bulk polymerization.
  • the high-pressure mass polymerization is preferably carried out at pressures of from 50 to 400 MPa, preferably from 100 to 300 MPa, and at temperatures of from 100 to 300 ° C., preferably from 150 to 220 ° C.
  • the polymerization takes place in a multi-zone reactor, wherein the temperature difference between the peroxide dosages along the tubular reactor is kept as low as possible, i. ⁇ 50 ° C, preferably ⁇ 30 ° C, in particular ⁇ 15 ° C.
  • the temperature maxima in the individual reaction zones preferably differ by less than 30 ° C., more preferably by less than 20 ° C. and especially by less than 10 ° C.
  • the reaction of the monomers is initiated by free radical initiators (free radical initiators).
  • This class of substance includes e.g. Oxygen, hydroperoxides, peroxides and azo compounds such as cumene hydroperoxide, t-butyl hydroperoxide, dilauroyl peroxide, dibenzoyl peroxide, bis (2-ethylhexyl) peroxide carbonate, t-butyl perpivalate, t-butyl permalate, t-butyl perbenzoate, dicumyl peroxide, t-butyl cumyl peroxide, di (t -butyl) peroxide, 2,2'-azobis (2-methylpropanonitrile), 2,2'-azobis (2-methylbutyronitrile).
  • the initiators are used individually or as a mixture of two or more substances in amounts of 0.01 to 20 wt .-%, preferably 0.05 to 10 wt .-%, based on the
  • the high-pressure mass polymerization is carried out batchwise or continuously in known high-pressure reactors , for example autoclaves or tubular reactors, tube reactors have proven particularly useful.
  • Solvents such as aliphatic and / or aromatic hydrocarbons or hydrocarbon mixtures, benzene or toluene may be present in the reaction mixture. Preferred is the substantially solvent-free operation.
  • Preferred moderators are, for example, hydrogen, saturated and unsaturated hydrocarbons such as propane or propene, aldehydes such as propionaldehyde, n-butyraldehyde or isobutyraldehyde, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone and alcohols such as butanol.
  • the comonomers as well as the moderators can be metered into the reactor both together with ethylene and separately via side streams. In this case, the monomer streams can be composed differently ( EP-A-0 271 738 and EP-A-0 922 716 ).
  • Suitable copolymers or terpolymers include, for example: ethylene-vinyl acetate copolymers with 10 to 40% by weight of vinyl acetate and 60 to 90% by weight of ethylene; from DE-A-34 43 475 known ethylene-vinyl acetate-hexene terpolymers; in the EP-B-0 203 554 described ethylene-vinyl acetate-diisobutylene terpolymers; from EP-B-0 254 284 known mixture of an ethylene-vinyl acetate-diisobutylene terpolymer and an ethylene / vinyl acetate copolymer; in the EP-B-0 405 270 disclosed blends of an ethylene-vinyl acetate copolymer and an ethylene-vinyl acetate-N-vinylpyrrolidone terpolymer; in the EP-B-0 463 518 described ethylene / vinyl acetate / iso-butyl vinyl
  • the polymers underlying the mixtures differ in at least one characteristic.
  • they may contain different comonomers, have different comonomer contents, molecular weights and / or degrees of branching.
  • the mixing ratio of the various ethylene copolymers is preferably between 20: 1 and 1:20, preferably 10: 1 to 1:10, in particular 5: 1 to 1: 5.
  • the copolymers B are preferably derived from ethylenically unsaturated dicarboxylic acids and their derivatives, such as esters and anhydrides. Preference is given to maleic acid, fumaric acid, itaconic acid and their esters with lower alcohols having 1 to 6 C atoms and their anhydrides, such as, for example, maleic anhydride. Monoolefins having from 10 to 20, in particular from 12 to 18, carbon atoms are particularly suitable as comonomers. These are preferably linear and the double bond is dicarboxylic acids and their derivatives such as esters and anhydrides.
  • Monoolefins having from 10 to 20, in particular from 12 to 18, carbon atoms are particularly suitable as comonomers. These are preferably linear and the double bond is preferably terminal such as in dodecene, tridecene, tetradecene, pentadecene, hexadecene, heptadecene and octadecene.
  • the ratio of dicarboxylic acid or dicarboxylic acid derivative to olefin or olefins in the polymer is in the range 1: 1.5 to 1.5: 1, in particular it is equimolar.
  • copolymer B which are copolymerizable with ethylenically unsaturated dicarboxylic acids and the olefins mentioned, such as, for example, and longer-chain olefins, allyl polyglycol ethers, C 1 -C 30 -alkyl (meth) acrylates, vinylaromatics or C 1 -C 20 -alkyl vinyl ethers.
  • poly (isobutylenes) having molecular weights of up to 5,000 g / mol are used, with highly reactive variants having a high content of terminal vinylidene groups being preferred.
  • poly (isobutylenes) having molecular weights of up to 5,000 g / mol are used, with highly reactive variants having a high content of terminal vinylidene groups being preferred.
  • the preferred method of preparation is solvent-free bulk polymerization, but it is also possible to carry out the polymerization in the presence of aprotic solvents such as benzene, toluene, xylene or higher-boiling aromatic, aliphatic or isoaliphatic solvents or solvent mixtures such as kerosene or solvent naphtha.
  • aprotic solvents such as benzene, toluene, xylene or higher-boiling aromatic, aliphatic or isoaliphatic solvents or solvent mixtures such as kerosene or solvent naphtha.
  • the polymerization is particularly preferably in less moderating, aliphatic or isoaliphatic solvents.
  • the proportion of solvent in the polymerization mixture is generally between 10 and 90 wt .-%, preferably between 35 and 60 wt .-%.
  • the reaction temperature can be set particularly easily by the boiling point of the solvent or by working under reduced or elevated pressure.
  • the average molecular weight of the copolymers B according to the invention is generally between 1,200 and 200,000 g / mol, in particular between 2,000 and 100,000 g / mol, measured by gel permeation chromatography (GPC) against polystyrene standards in THF.
  • Copolymers of the invention must be oil-soluble in practice-relevant dosing quantities, ie they must dissolve in the oil to be additized at 50 ° C. without residue.
  • the reaction of the monomers is initiated by free radical initiators (free radical initiators).
  • This class of substances includes, for example, oxygen, hydroperoxides and peroxides such as cumene hydroperoxide, t-butyl hydroperoxide, dilauroyl peroxide, dibenzoyl peroxide, bis (2-ethylhexyl) peroxide carbonate, t-butyl perpivalate, t-butyl permalonate, t-butyl perbenzoate, dicumyl peroxide, t-butylcumyl peroxide, Di- (t-butyl) peroxide, and azo compounds such as 2,2'-azobis (2methylpropanonitrile) or 2,2'-azobis (2-methylbutyronitrile).
  • the initiators are used individually or as a mixture of two or more substances in amounts of 0.01 to 20 wt .-%, preferably 0.05 to 10 wt .-%, based on the
  • the copolymers can be prepared either by reaction of maleic, fumaric and / or itaconic acid or derivatives thereof with the corresponding amine and subsequent copolymerization or by copolymerization of olefin or olefins with at least one unsaturated dicarboxylic acid or its derivative such as itacon and / or Maleic anhydride and subsequent reaction with amines are produced.
  • a copolymerization with anhydrides is preferably carried out and the resulting copolymer is converted after production into an amide and / or an imide.
  • reaction with amines takes place in both cases, for example by reaction with 0.8 to 2.5 moles of amine per mole of anhydride, preferably with 1.0 to 2.0 moles of amine per mole of anhydride at 50 to 300 ° C.
  • 0.8 to 2.5 moles of amine per mole of anhydride preferably with 1.0 to 2.0 moles of amine per mole of anhydride at 50 to 300 ° C.
  • about 1 mol of amine per mol of anhydride formed at reaction temperatures of about 50 to 100 ° C preferably hemiamides, which additionally carry a carboxyl group per amide group.
  • reaction temperatures of about 100 to 250 ° C arise from primary amines with elimination of water preferably imides.
  • amine preferably 2 moles of amine per mole of anhydride formed at about 50 to 200 ° C amide ammonium salts and at higher temperatures, for example, 100 - 300 ° C, preferably 120 - 250 ° C diamides.
  • the water of reaction can be distilled off by means of an inert gas stream or discharged in the presence of an organic solvent by means of azeotropic distillation. Preference is given to 20-80, in particular 30-70, especially 35-55 wt .-% of at least one organic solvent used.
  • half-amides here are considered (50% in solvent) copolymers having acid numbers of 30 - 70 mg KOH / g, preferably from 40 - 60 mg KOH / g.
  • Corresponding copolymers with acid numbers of less than 40, especially less than 30 mg KOH / g are considered diamides or imides. Particularly preferred are hemiamides and imides.
  • Suitable amines are primary and secondary amines having one or two C 8 -C 16 alkyl radicals. They can carry one, two or three amino groups which are linked via alkylene radicals having two or three carbon atoms. Preference is given to monoamines. In particular, they carry linear alkyl radicals, but they can also minor amounts, eg. B. up to 30 wt .-%, preferably up to 20 wt .-% and especially up to 10 wt .-% (in 1- or 2-position) contain branched amines. Shorter as well as longer-chain amines can be used, but their proportion is preferably less than 20 mol% and especially less than 10 mol%, for example between 1 and 5 mol%, based on the total amount of amines used.
  • primary amines are octylamine, 2-ethylhexylamine, decylamine, undecylamine, dodecylamine, n-tridecylamine, iso-tridecylamine, tetradecylamine, pentadecylamine, hexadecylamine and mixtures thereof.
  • Preferred secondary amines are dioctylamine, dinonylamine, didecylamine, didodecylamine, ditetradecylamine, dihexadecylamine, and amines having different alkyl chain lengths such as N-octyl-N-decylamine, N-decyl-N-dodecylamine, N-decyl-N-tetradecylamine, N-decyl N-hexadecylamine, N-dodecyl-N-tetradecylamine, N-dodecyl-N-hexadecylamine, N-tetradecyl-N-hexadecylamine.
  • Secondary amines which, in addition to a C 8 -C 16 -alkyl radical, bear shorter side chains having 1 to 5 C atoms, for example methyl or ethyl groups, are suitable according to the invention.
  • the alkyl chain length n is taken into account as the mean value of the alkyl chain lengths of C 8 to C 16 for the calculation of the Q factor. Shorter and longer alkyl radicals, if present, are not included in the calculation because they do not contribute to the effectiveness of the additives.
  • Particularly preferred copolymers B are hemiamides and imides of primary monoamines.
  • the effectiveness can be further adapted to specific fatty acid ester compositions.
  • the additives may also contain polymers and copolymers based on C 10 -C 24 -alkyl acrylates or methacrylates (component C).
  • These poly (alkyl acrylates) and methacrylates have molecular weights of 800 to 1,000,000 g / mol, and are preferably derived from caprylic, capric, undecyl, lauryl, myristyl, cetyl, palmitoleyl, stearyl alcohol or the like Mixtures such as coconut, palm, tallow or behenyl from.
  • mixtures of the copolymers B according to the invention are used, with the proviso that the mean value of the Q values of the mixture components again assumes values of 23 to 27 and preferably values of 24 to 26.
  • the mixing ratio of the additives A and B is (in parts by weight) 20: 1 to 1:20, preferably 10: 1 to 1:10, especially 5: 1 to 1: 2.
  • the proportion of component C in the formulations of A, B and C may be up to 40% by weight; it is preferably less than 20% by weight, in particular between 1 and 10% by weight.
  • the additives are added to oils in amounts of 0.001 to 5 wt%, preferably 0.005 to 1 wt%, and especially 0.01 to 0.5 wt%.
  • they can be dissolved or dispersed as such or else in solvents such as, for example, aliphatic and / or aromatic hydrocarbons or hydrocarbon mixtures, such as.
  • toluene xylene, ethylbenzene, decane, pentadecane, gasoline fractions, kerosene, naphtha, diesel, fuel oil, isoparaffins or commercial solvent mixtures such as Solvent Naphtha, ®Shellsol AB, ® Solvesso 150, ® Solvesso 200, ®Exxsol, ®Isopar and ®Shellsol D types are used.
  • they are dissolved in Br nnstofföl animal or vegetable origin based on fatty acid alkyl esters.
  • the additives contain 1 - 80%, especially 10 - 70%, in particular 25 - 60% solvent.
  • the fuel oil which is often referred to as “biodiesel” or “biofuel”
  • biodiesel is fatty acid alkyl esters of fatty acids having 12 to 24 carbon atoms and alcohols having 1 to 4 carbon atoms.
  • fatty acids having 12 to 24 carbon atoms and alcohols having 1 to 4 carbon atoms.
  • a major part of the fatty acids contains one, two or three double bonds.
  • oils derived from animal or vegetable material and in which the additive according to the invention can be used are rapeseed oil, coriander oil, soybean oil, cottonseed oil, sunflower oil, castor oil, olive oil, peanut oil, corn oil, almond oil, palm kernel oil, coconut oil, mustard seed oil, Beef tallow, bone oil, fish oils and used edible oils.
  • oils derived from wheat, jute, sesame, shea nut, arachis oil and linseed oil can be derived from these oils by methods known in the art.
  • Rapeseed oil which is a mixture of glycerol partially esterified fatty acids, is preferred because it is available in large quantities and is readily available by squeezing rapeseed. Furthermore, the also widespread oils of sunflower and soybeans and their mixtures with rapeseed oil are preferred.
  • Particularly suitable as biofuels are lower alkyl esters of fatty acids.
  • lower alkyl esters of fatty acids are, for example, commercially available mixtures of ethyl, propyl, butyl and especially methyl esters of fatty acids having 14 to 22 carbon atoms, for example of lauric, myristic, palmitic, palmitolic, stearic, oleic, elaidic, petroselic, ricinoleic, elaeostearic, linoleic, linolenic , Eicosanoic acid, gadoleic acid, docosanoic acid or erucic acid, which preferably have an iodine value of 50 to 150, in particular 90 to 125.
  • Mixtures with particularly advantageous properties are those which are mainly d. H. at least 50 wt .-%, contain methyl esters of fatty acids having 16 to 22 carbon atoms and 1, 2 or 3 double bonds.
  • the preferred lower alkyl esters of fatty acids are the methyl esters of oleic, linoleic, linolenic and erucic acids.
  • a biofuel is an oil obtained from plant or animal matter or both, or a derivative thereof, which can be used as a fuel and especially as a diesel or fuel oil.
  • vegetable oil derivatives are preferred, with particularly preferred biofuels being alkyl ester derivatives of rapeseed oil, cottonseed oil, soybean oil, sunflower oil, olive oil or palm oil, with methyl rapeseed oil, methyl sunflower oil and soybean oil methyl ester being most preferred.
  • particularly preferred biofuel or as a component in the biofuel are also old fat esters such as, for example, used fat methyl ester.
  • the additive may be added to the oil to be treated according to methods known in the art. If more than one additive component or co-additive component is to be used, such components may be incorporated into the oil together or separately in any combination.
  • the CFPP value of biodiesel can be adjusted to values below -20 ° C and sometimes to values below -25 ° C, as required for marketing for use, in particular in winter.
  • the pour point of biodiesel is lowered by the addition of additives.
  • the additives are particularly advantageous in problematic oils which have a high content of saturated fatty acid esters of more than 4%, in particular more than 5% and especially 7 to 25%, for example 8 to 20%, as for example in sunflower oils and soy are included.
  • Such oils are characterized by cloud points above -5 ° C and especially above -3 ° C.
  • the additives can also be used together with one or more oil-soluble co-additives, which already improve all in the cold flow properties of crude oils, lubricating oils or fuel oils.
  • oil-soluble co-additives are polar compounds which cause paraffin dispersion (paraffin dispersants) and oil-soluble amphiphiles, provided that they differ from comb polymers B.
  • Additives can be used in admixture with paraffin dispersants.
  • paraffin reduce the size of the paraffin crystals and cause the paraffin particles to not settle but remain colloidally dispersed with significantly reduced sedimentation effort.
  • Suitable paraffin dispersants are both low molecular weight and polymeric, oil-soluble compounds having ionic or polar groups such as amine salts and / or amides have proven.
  • Particularly preferred paraffin dispersants contain reaction products of secondary fatty amines having 20 to 44 carbon atoms, in particular dicocoamine, ditallow fatty amine, distearylamine and dibehenylamine with carboxylic acids and derivatives thereof.
  • Paraffin dispersants which have been obtained by reaction of aliphatic or aromatic amines, preferably long-chain aliphatic amines, with aliphatic or aromatic mono-, di-, tri- or tetracarboxylic acids or their anhydrides have proven particularly suitable (cf. US 4 211 534 ).
  • amides and ammonium salts of aminoalkylene polycarboxylic acids such as nitrilotriacetic acid or ethylenediaminetetraacetic acid with secondary amines are suitable as paraffin dispersants (cf. EP 0 398 101 ).
  • paraffin dispersants are copolymers of maleic anhydride and ⁇ , ⁇ -unsaturated compounds, which can optionally be reacted with primary monoalkylamines and / or aliphatic alcohols (cf. EP 0 154 177 ) and the reaction products of alkenyl spiro-bis-lactones with amines (cf. EP 0 413 279 B1 ) and after EP-A-0 606 055 A2 Reaction products of terpolymers based on ⁇ , ⁇ -unsaturated dicarboxylic anhydrides, ⁇ , ⁇ -unsaturated compounds and polyoxyalkylene ethers of lower unsaturated alcohols.
  • the mixing ratio (in parts by weight) of the additives with paraffin dispersants is 1:10 to 20: 1, preferably 1: 1 to 10: 1.
  • the additives can be used alone or together with other additives, e.g. with other pour point depressants or dewaxing aids, with antioxidants, cetane improvers, dehazers, demulsifiers, detergents, dispersants, defoamers, dyes, corrosion inhibitors, conductivity improvers, sludge inhibitors, odorants and / or cloud point depressants.
  • other pour point depressants or dewaxing aids with antioxidants, cetane improvers, dehazers, demulsifiers, detergents, dispersants, defoamers, dyes, corrosion inhibitors, conductivity improvers, sludge inhibitors, odorants and / or cloud point depressants.
  • the CFPP value is determined in accordance with EN 116 and the determination of the cloud point in accordance with ISO 3015.
  • the ethylene copolymers used are commercial products having the characteristics given in Table 2. The products were used as 65% and 50% (A3) settings in kerosene, respectively.
  • Table 3 Characterization of the ethylene copolymers used example Comonomer (s) V140 CH 3/100 CH 2 A1 13.6 mole% vinyl acetate 130 mPas 3.7 A2 13.7 mole percent vinyl acetate and 1.4 mole percent vinyl neodecanoate 105 mPas 5.3 A3 9.4 mol% vinyl acetate 220 mPas 6.2 A4 Mixture of EVA copolymer with 16 mol% vinyl acetate and EVA with 95 mPas 3.2 5 mol% vinyl acetate in the ratio 13: 1 350 mPas 5.7
  • the polymerization of maleic anhydride (MSA) with ⁇ -olefins is carried out in a higher boiling aromatic hydrocarbon mixture at 160 ° C in the presence of a mixture of equal parts tert-butyl peroxybenzoate and tert-butyl peroxy-2-ethylhexanoate as a radical chain initiator.
  • Table 3 shows, by way of example, various copolymers and the molar proportions of the monomers used for their preparation, as well as the chain length (R) and molar amount (based on MSA) of the amine used for the derivatization and the factor Q calculated therefrom.
  • the amines used are, unless stated otherwise, monoalkylamines.
  • the reactions with amines are carried out in the presence of solvent naphtha (50 wt .-%) at 50 to 100 ° C to the half-amide or amide ammonium salt and at 160 to 200 ° C with azeotropic culling of water of reaction to imide or diamide.
  • solvent naphtha 50 wt .-%
  • the degree of amidation is inversely proportional to the acid number.
  • the compounds listed in the table were used as 50% settings used in higher boiling solvent.
  • the K values are determined according to Ubbelohde at 25 ° C. in 5% strength toluene solution.
  • Table 5 Characterization of the poly (acrylates) used C1 Poly (octadecyl acrylate), K value 32 C2 Poly (dodecyl acrylate), K value 35.6 C3 Poly (phenyl acrylate), K value 22.4
  • the CFPP value (according to EN 116, in ° C) of various biofuels according to the above table was determined after addition of 1200 ppm, 1500 ppm and 2000 ppm of additive mixture. Percentages refer to parts by weight in the respective mixtures.
  • Tables 5 to 7 show that comb polymers with the factor Q according to the invention achieve excellent CFPP reductions even at low dosing rates and offer additional potential at higher dosing rates.
  • Table 6 CFPP testing in test oil E1 Ex.
  • the CFPP value according to DIN EN 116 is compared before and after a standardized cold-change treatment.
  • test oil E1 500 ml of biodiesel (test oil E1) are treated with the appropriate cold additive, placed in a cylinder and stored in a programmable cold chamber for one week. During this time, a program is run through which repeatedly cools to -13 ° C and then warms up again to -3 ° C. 6 cycles are consecutively run through (Table 8).
  • Cooling program for determining the resistance to cold chill section begin The End duration description A ⁇ B + 5 ° C -3 ° C 8 h Pre-cooling to cycle start temperature B ⁇ C -3 ° C -3 ° C 2 h stationary temperature, start of cycle C ⁇ D -3 ° C -13 ° C 14 h Temperature reduction, incipient crystal formation D ⁇ E -13 ° C - 13 ° C 2 h Stationary temperature, crystal growth E ⁇ F -13 ° C -3 ° C 6 h Temperature increase, melting of the crystals F ⁇ B Another 6 cycles B ⁇ F are carried out
  • the additiviere oil sample is reheated to room temperature without shaking. From each of the upper, middle and lower sections of the cylinder a sample of 50 ml is drawn for CFPP measurements.
  • Table 10 Resistance to cold-resistance of the additized oil: additive CFPP CFPP after storage example comb polymer ethylene copolymer metering before storage below ⁇ CFPP (below) center ⁇ CFPP (middle) above ⁇ CFPP (above) 39 20% B2 80% A2 1500 ppm -24 ° C -23 ° C 1K -24 ° C 0K -25 ° C -1K 40 19% B2 5% C1 76% A2 1500 ppm -24 ° C -22 ° C 2K -23 ° C 1K -24 ° C 0K 41 20% B14 80% A4 1500 ppm -23 ° C -22 ° C 1K -21 ° C 2K -22 ° C 1K 42 25% B13 75% A4 1500 ppm

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Claims (17)

  1. Composition d'huile combustible, contenant une huile combustible d'origine animale ou végétale et 0,001 à 5 % en poids d'un additif contenant les constituants A) et B) en un rapport en poids de 10:1 à 1:10
    A) un copolymère d'éthylène et de 8 à 21 % en moles d'au moins un ester acrylique ou vinylique comprenant un radical alkyle en C1-C18 et
    B) un polymère en peigne, contenant des unités structurales de
    B1) au moins une oléfine en tant que monomère 1, qui porte au moins un radical alkyle en C8-C18 sur la double liaison oléfinique et
    B2) au moins un acide dicarboxylique éthyléniquement insaturé en tant que monomère 2, qui porte au moins un radical alkyle en C8-C16 relié par un groupe amide et/ou imide, la somme Q Q = ∑ i w 1 i ⋅ n 1 i + ∑ j w 2 j ⋅ n 2 j
    Figure imgb0010
     des moyennes molaires des distributions de longueurs de chaînes C dans les radicaux alkyle du monomère 1 d'un côté et les radicaux alkyle des groupes amide et/ou imide du monomère 2 d'un autre côté étant de 23 à 27, en un rapport molaire B1) : B2) de 1:1,5 à 1,5:1,
    w1 étant la proportion molaire des longueurs de chaînes individuelles dans les radicaux alkyle du monomère 1,
    w2 étant la proportion molaire des longueurs de chaînes individuelles dans les radicaux alkyle des groupes amide et/ou imide du monomère 2,
    n1 étant les longueurs de chaînes individuelles dans les radicaux alkyle du monomère 1,
    n2 étant les longueurs de chaînes individuelles dans les radicaux alkyle des groupes amide et/ou imide du monomère 2,
    i étant la variable de contrôle pour les longueurs de chaînes individuelles dans les radicaux alkyle du monomère 1 et
    j étant la variable de contrôle pour les longueurs de chaînes individuelles dans les radicaux alkyle des groupes amide et/ou imide du monomère 2.
  2. Composition d'huile combustible selon la revendication 1, dans laquelle Q vaut de 24 à 26.
  3. Composition d'huile combustible selon la revendication 1 et/ou 2, dans laquelle, outre l'éthylène, le constituant A contient 3,5 à 20 % en moles d'acétate de vinyle et 0,1 à 12 % en moles d'ester vinylique de l'acide 2-éthylhexanoïque, d'ester vinylique de l'acide néononanoïque et/ou d'ester vinylique de l'acide néodécanoïque, la teneur totale en comonomères étant comprise entre 8 et 21 % en moles.
  4. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 3, dans laquelle, outre l'éthylène et 8 à 18 % en moles d'esters vinyliques, le constituant A contient encore 0,5 à 10 % en moles d'oléfines, choisies parmi le propène, le butène, l'isobutylène, l'hexène, le 4-méthylpentène, l'octène, le diisobutylène ou le norbornène.
  5. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 4, dans laquelle les copolymères qui composent le constituant A présentent des viscosités à l'état fondu comprises entre 20 et 10 000 mPas.
  6. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 5, dans laquelle les copolymères qui composent le constituant A présentent des degrés de ramification compris entre 1 et 9 groupes CH3/100 groupes CH2, qui ne proviennent pas des comonomères.
  7. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 6, dans laquelle les copolymères qui composent le constituant B contiennent des comonomères qui dérivent d'amides et/ou d'imides de l'acide maléique, de l'acide fumarique et/ou de l'acide itaconique.
  8. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 7, dans laquelle les amides et/ou les imides du constituant B dérivent d'amines primaires.
  9. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 8, dans laquelle les amides et/ou les imides du constituant B dérivent d'amines à radicaux alkyle linéaires.
  10. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 9, dans laquelle les amides et/ou les imides du constituant B dérivent de monoamines.
  11. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 10, dans laquelle les copolymères qui composent le constituant B contiennent des comonomères qui dérivent d'a-oléfines.
  12. Composition d'huile combustible selon une ou plusieurs des revendications 1 à 11, dans laquelle, outre les constituants A et B, un polymère ou copolymère qui comprend des unités acrylate ou méthacrylate d'alkyle en C10-C24, d'un poids moléculaire de 800 à 1 000 000 g/mol, est contenu en tant que constituant C en une quantité de jusqu'à 40 % en poids, par rapport au poids total de A, B et C.
  13. Composition d'huile combustible selon l'une quelconque des revendications 1 à 12, contenant des dispersants paraffiniques azotés polaires.
  14. Composition d'huile combustible selon la revendication 1, caractérisée en ce que l'huile combustible d'origine animale ou végétale contient un ou plusieurs esters d'un acide monocarboxylique de 14 à 24 atomes C et d'un alcool de 1 à 4 atomes C.
  15. Composition d'huile combustible selon la revendication 14, caractérisée en ce que l'alcool est le méthanol ou l'éthanol.
  16. Composition d'huile combustible selon une ou plusieurs des revendications 1, 14 ou 15, caractérisée en ce que l'huile combustible d'origine animale ou végétale contient plus de 5 % en poids d'esters d'acides gras saturés.
  17. Utilisation d'un additif contenant les constituants A) et B) en un rapport en poids de 10:1 à 1:10
    A) un copolymère d'éthylène et de 8 à 21 % en moles d'au moins un ester acrylique ou vinylique comprenant un radical alkyle en C1-C18 et
    B) un polymère en peigne, contenant des unités structurales de
    B1) au moins une oléfine en tant que monomère 1, qui porte au moins un radical alkyle en C8-C18 sur la double liaison oléfinique et
    B2) au moins un acide dicarboxylique éthyléniquement insaturé en tant que monomère 2, qui porte au moins un radical alkyle en C8-C16 relié par un groupe amide et/ou imide, la somme Q Q = ∑ i w 1 i ⋅ n 1 i + ∑ j w 2 j ⋅ n 2 j
    Figure imgb0011
     des moyennes molaires des distributions de longueurs de chaînes C dans les radicaux alkyle du monomère 1 d'un côté et les radicaux alkyle des groupes amide et/ou imide du monomère 2 d'un autre côté étant de 23 à 27, en un rapport molaire B1) : B2) de 1:1,5 à 1,5 : 1,
    w1 étant la proportion molaire des longueurs de chaînes individuelles dans les radicaux alkyle du monomère 1,
    w2 étant la proportion molaire des longueurs de chaînes individuelles dans les radicaux alkyle des groupes amide et/ou imide du monomère 2,
    n1 étant les longueurs de chaînes individuelles dans les radicaux alkyle du monomère 1,
    n2 étant les longueurs de chaînes individuelles dans les radicaux alkyle des groupes amide et/ou imide du monomère 2,
    i étant la variable de contrôle pour les longueurs de chaînes individuelles dans les radicaux alkyle du monomère 1 et
    j étant la variable de contrôle pour les longueurs de chaînes individuelles dans les radicaux alkyle des groupes amide et/ou imide du monomère 2 en une quantité de 0,001 à 5 % en poids pour l'amélioration des propriétés d'écoulement à froid d'huiles combustibles d'origine animale ou végétale.
EP04024234.9A 2003-10-25 2004-10-12 Agent d'amélioration de l'écoulement à froid pour huiles combustibles d'origine végétale ou animale Expired - Lifetime EP1526167B2 (fr)

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Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10349850C5 (de) 2003-10-25 2011-12-08 Clariant Produkte (Deutschland) Gmbh Kaltfließverbesserer für Brennstofföle pflanzlichen oder tierischen Ursprungs
DE10357880B4 (de) * 2003-12-11 2008-05-29 Clariant Produkte (Deutschland) Gmbh Brennstofföle aus Mitteldestillaten und Ölen pflanzlichen oder tierischen Ursprungs mit verbesserten Kälteeigenschaften
DE10357878C5 (de) 2003-12-11 2013-07-25 Clariant Produkte (Deutschland) Gmbh Brennstofföle aus Mitteldestillaten und Ölen pflanzlichen oder tierischen Ursprungs mit verbesserten Kälteeigenschaften
RU2377278C2 (ru) * 2004-04-06 2009-12-27 Акцо Нобель Н.В. Депрессантные присадки для композиций масел
CA2584762C (fr) * 2004-10-21 2014-03-18 Novo Nordisk A/S Dispositif d'injection a ressort de torsion et affichage rotatif
EP1866397A2 (fr) 2005-03-29 2007-12-19 Arizona Chemical Company Compositions renfermant des acides gras et/ou leurs derives et un stabilisateur a basse temperature
DE102005020264B4 (de) * 2005-04-30 2008-07-31 Clariant Produkte (Deutschland) Gmbh Additive für schwefelarme Mineralöldestillate, umfassend Aromaten, welche eine Hydroxygruppe, eine Methoxygruppe und eine Säurefunktion tragen
KR101189385B1 (ko) * 2005-06-03 2012-10-10 라이온 가부시키가이샤 엔진 연료용 지방산 ｃ1 내지 2 알킬에스테르의 유동점조정 방법
DE102006016588A1 (de) * 2006-04-06 2007-10-18 Rohmax Additives Gmbh Kraftstoffzusammensetzungen umfassend nachwachsende Rohstoffe
US20070253379A1 (en) * 2006-04-28 2007-11-01 Motorola, Inc. Method and apparatus for uplink allocation placement in an uplink frame
DE102006022719B4 (de) * 2006-05-16 2008-10-02 Clariant International Limited Kaltfließverbesserer für pflanzliche oder tierische Brennstofföle
DE102006022718B4 (de) * 2006-05-16 2008-10-02 Clariant International Limited Zusammensetzung von Brennstoffölen
DE102006022720B4 (de) * 2006-05-16 2008-10-02 Clariant International Limited Kaltfließverbesserer für pflanzliche oder tierische Brennstofföle
DE102006022698B4 (de) * 2006-05-16 2008-10-02 Clariant International Limited Zusammensetzung von Brennstoffölen
ATE451441T1 (de) * 2006-06-22 2009-12-15 Basf Se Mischung aus polaren öllöslichen stickstoffverbindungen und säureamiden als paraffindispergator für kraftstoffe
US7655055B2 (en) * 2006-09-21 2010-02-02 Southwest Research Institute Biofuel
DE102006054909A1 (de) * 2006-11-22 2008-05-29 Clariant International Limited Stockpunkt-Verbesserer für pflanzliche oder tierische Brennstofföle
US20090293344A1 (en) * 2008-05-30 2009-12-03 Baker Hughes Incorporated Process for Removing Water and Water Soluble Contaminants From Biofuels
US9127226B2 (en) 2008-06-06 2015-09-08 Baker Hughes Incorporated Process for clarifying biofuels
ES2356112T3 (es) * 2008-12-09 2011-04-05 Infineum International Limited Método para mejorar composiciones de aceite.
US9012583B2 (en) 2010-02-10 2015-04-21 Nof Corporation Flow improver for oils and fats
MY180330A (en) * 2014-01-29 2020-11-28 Basf Se Use of polycarboxylic-acid-based additives for fuels
RU2690940C2 (ru) 2014-11-27 2019-06-07 Басф Се Сополимер и его применение для уменьшения кристаллизации кристаллов парафина в топливах
US11060044B2 (en) 2016-05-24 2021-07-13 Basf Se Copolymer and use thereof for reducing crystallization of paraffin crystals in fuels
WO2018054892A1 (fr) 2016-09-21 2018-03-29 Basf Se Terpolymères d'anhydride de l'acide maléique, d'acrylates et d'alpha-oléfines, en particulier destinés à être utilisés comme agent d'amélioration de l'écoulement de pétrole
CA3044265A1 (fr) * 2016-12-07 2018-06-14 Ecolab Usa Inc. Compositions antisalissures pour charges petrolieres a traiter
CN107082849B (zh) * 2017-05-15 2019-10-01 上海应用技术大学 一种四元聚合物柴油降凝剂及其制备方法
US10421498B2 (en) * 2017-12-01 2019-09-24 Thomas Albert Blomberg Snow and rain deflector assembly for vehicles
EP3913035A1 (fr) 2020-05-20 2021-11-24 Basf Se Nouvelles compositions de réduction de cristallisation de cristaux de paraffine dans des carburants
WO2024037904A1 (fr) 2022-08-16 2024-02-22 Basf Se Composition pour réduire la cristallisation de cristaux de paraffine dans des combustibles
WO2024115211A1 (fr) 2022-11-30 2024-06-06 Basf Se Homopolymères et copolymères d'éthers vinyliques pour réduire la cristallisation de cristaux de paraffine dans des carburants

Citations (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2615845A (en) † 1948-08-02 1952-10-28 Standard Oil Dev Co Lubricating oil additives
US3003858A (en) † 1958-01-07 1961-10-10 Socony Mobil Oil Co Inc Stabilized distillate fuel oil
US4121026A (en) † 1973-03-23 1978-10-17 Petrolite Corporation Copolymers of alpha-olefins and maleic anhydride reacted with amines in the presence of Lewis acids
US4153424A (en) † 1975-03-28 1979-05-08 Exxon Research & Engineering Co. Polymer combinations useful in distillate hydrocarbon oils to improve cold flow properties
EP0100248A1 (fr) † 1982-06-04 1984-02-08 Institut Français du Pétrole Copolymères à fonctions azotées, utilisables notamment comme additifs d'abaissement du point de trouble des distillats moyens d'hydrocarbures, et compositions de distillats moyens d'hydrocarbures renfermant lesdits copolymères
JPS59126496A (ja) † 1983-01-11 1984-07-21 Nippon Zeon Co Ltd 燃料油組成物
EP0172758A1 (fr) † 1984-07-10 1986-02-26 Institut Français du Pétrole Compositions d'additifs destinees notamment a ameliorer les propriétés de filtrabilité a froid des distillats moyens de pétrole
EP0184083A2 (fr) † 1984-11-29 1986-06-11 Hoechst Aktiengesellschaft Terpolymères de l'éthylène, leur procédé de fabrication et leur application
FR2592658A1 (fr) † 1986-01-09 1987-07-10 Inst Francais Du Petrole Compositions d'additifs destinees notamment a ameliorer les proprietes de filtrabilite a froid des distillats moyens de petrole.
WO1993018115A1 (fr) † 1992-03-03 1993-09-16 Exxon Chemical Patents Inc. Additifs pour huiles
US5254652A (en) † 1990-12-29 1993-10-19 Hoechst Aktiengesellschaft Terpolymers of ethylene, their preparation, and their use as additives for mineral oil distillates
US5767190A (en) † 1996-05-18 1998-06-16 Hoechst Aktiengesellschaft Terpolymers of ethylene, their preparation and their use as additives for mineral oil distillates
WO2000032722A1 (fr) † 1998-12-02 2000-06-08 Infineum International Limited Additifs et compositions pour fiouls
US6106584A (en) † 1997-08-05 2000-08-22 Exxon Chemical Patents Inc Additives for oil compositions
WO2001048122A1 (fr) † 1999-12-28 2001-07-05 Elf Antar France Composition d'additifs multifonctionnels d'operabilite a froid des distillats moyens
US20010034968A1 (en) † 1997-07-08 2001-11-01 Matthias Krull Fuel oils based on middle distillates and copolymers of ethylene and unsaturated carboxylic esters
US6409778B1 (en) † 1997-11-21 2002-06-25 Rohmax Additives Gmbh Additive for biodiesel and biofuel oils
WO2002090470A1 (fr) † 2001-05-08 2002-11-14 Sanyo Chemical Industries, Ltd. Agent fluidifiant et composition de mazout
US20050126072A1 (en) † 2003-12-11 2005-06-16 Clariant Gmbh Fuel oils composed of middle distillates and oils of vegetable or animal origin and having improved cold flow properties
US20070266620A1 (en) † 2006-05-16 2007-11-22 Clariant International Ltd. Cold flow improvers for vegetable or animal fuel oils

Family Cites Families (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3462249A (en) * 1967-03-31 1969-08-19 Exxon Research Engineering Co Fuel oil compositions containing grafted polymers
US4137185A (en) * 1977-07-28 1979-01-30 Exxon Research & Engineering Co. Stabilized imide graft of ethylene copolymeric additives for lubricants
US4211534A (en) * 1978-05-25 1980-07-08 Exxon Research & Engineering Co. Combination of ethylene polymer, polymer having alkyl side chains, and nitrogen containing compound to improve cold flow properties of distillate fuel oils
DE3405843A1 (de) * 1984-02-17 1985-08-29 Bayer Ag, 5090 Leverkusen Copolymere auf basis von maleinsaeureanhydrid und (alpha), (beta)-ungesaettigten verbindungen, ein verfahren zu ihrer herstellung und ihre verwendung als paraffininhibitoren
EP0153176B1 (fr) * 1984-02-21 1991-11-27 Exxon Research And Engineering Company Compositions de distillat moyen à caractéristiques d'écoulement à froid
FR2572410B1 (fr) * 1984-10-25 1987-09-04 Elf Aquitaine Copolymeres d'ethylene greffes utilisables notamment comme additifs pour l'inhibition du depot de paraffines dans les huiles brutes et compositions renfermant les huiles et lesdits additifs
DE3616056A1 (de) 1985-05-29 1986-12-04 Hoechst Ag, 65929 Frankfurt Verwendung von ethylen-terpolymerisaten als additive fuer mineraloele und mineraloeldestillate
GB8521393D0 (en) * 1985-08-28 1985-10-02 Exxon Chemical Patents Inc Middle distillate compositions
DE3613247C2 (de) * 1986-04-19 1995-04-27 Roehm Gmbh Konzentrierte Emulsionen aus Ethylen-Vinylacetat-Copolymeren, Verfahren zu deren Herstellung und deren Verwendung als Stockpunktverbesserer
DE3625174A1 (de) 1986-07-25 1988-01-28 Ruhrchemie Ag Verfahren zur verbesserung der fliessfaehigkeit von mineraloelen und mineraloeldestillaten
DE3640613A1 (de) 1986-11-27 1988-06-09 Ruhrchemie Ag Verfahren zur herstellung von ethylen-mischpolymerisaten und deren verwendung als zusatz zu mineraloel und mineraloelfraktionen
GB8722016D0 (en) 1987-09-18 1987-10-28 Exxon Chemical Patents Inc Fuel oil additives
DE3742630A1 (de) 1987-12-16 1989-06-29 Hoechst Ag Polymermischungen fuer die verbesserung der fliessfaehigkeit von mineraloeldestillaten in der kaelte
US5017299A (en) * 1988-08-01 1991-05-21 Exxon Chemical Patents, Inc. Novel ethylene alpha-olefin copolymer substituted Mannich base lubricant dispersant additives
GB8820295D0 (en) * 1988-08-26 1988-09-28 Exxon Chemical Patents Inc Chemical compositions & use as fuel additives
DE3905681A1 (de) 1989-02-24 1990-08-30 Basf Ag Konzentrierte mischungen von pfropfcopolymerisaten aus estern von ungesaettigten saeuren und ethylen-vinylester-copolymerisaten
DE3916366A1 (de) 1989-05-19 1990-11-22 Basf Ag Neue umsetzungsprodukte von aminoalkylenpolycarbonsaeuren mit sekundaeren aminen und erdoelmitteldestillatzusammensetzungen, die diese enthalten
DE3921279A1 (de) 1989-06-29 1991-01-03 Hoechst Ag Verfahren zur verbesserung der fliessfaehigkeit von mineraloelen und mineraloeldestillaten
DE3926992A1 (de) * 1989-08-16 1991-02-21 Hoechst Ag Verwendung von umsetzungsprodukten von alkenylspirobislactonen und aminen als paraffindispergatoren
US5275747A (en) * 1990-02-01 1994-01-04 Exxon Chemical Patents Inc. Derivatized ethylene alpha-olefin polymer useful as multifunctional viscosity index improver additive for oleaginous composition
DE4020640A1 (de) * 1990-06-29 1992-01-02 Hoechst Ag Terpolymerisate des ethylens, ihre herstellung und ihre verwendung als additive fuer mineraloeldestillate
DE4036225A1 (de) * 1990-11-14 1992-05-21 Basf Ag Erdoelmitteldestillate mit verbesserten fliesseigenschaften in der kaelte
DE4134347A1 (de) * 1991-10-17 1993-04-22 Hoechst Ag Pfropfmischpolymer auf basis eines ethylen-copolymers mit modifizierten und verbesserten eigenschaften
DE4138429A1 (de) 1991-11-22 1993-05-27 Roehm Gmbh Verfahren zur herstellung von kompositionen mit verbessertem tieftemperaturverhalten
GB9200694D0 (en) 1992-01-14 1992-03-11 Exxon Chemical Patents Inc Additives and fuel compositions
GB9213871D0 (en) * 1992-06-30 1992-08-12 Exxon Chemical Patents Inc Oil additives and compositions
GB9213909D0 (en) 1992-06-30 1992-08-12 Exxon Chemical Patents Inc Oil additives and compositions
GB9222458D0 (en) * 1992-10-26 1992-12-09 Exxon Chemical Patents Inc Oil additives and compositions
DE4241948A1 (de) * 1992-12-12 1994-06-16 Hoechst Ag Pfropfpolymerisate, ihre Herstellung und Verwendung als Stockpunkterniedriger und Fließverbesserer für Rohöle, Rückstandsöle und Mitteldestillate
US5413725A (en) * 1992-12-18 1995-05-09 The Lubrizol Corporation Pour point depressants for high monounsaturated vegetable oils and for high monounsaturated vegetable oils/biodegradable base and fluid mixtures
ES2110124T3 (es) 1993-01-06 1998-02-01 Clariant Gmbh Termopolimeros a base de anhidridos de acidos carboxilicos alfa,beta-insaturados, de compuestos alfa,beta-insaturados y de polioxialquileneteres de alcoholes inferiores insaturados.
GB9301752D0 (en) 1993-01-29 1993-03-17 Exxon Chemical Patents Inc Oil and fuel oil compositions
GB9410820D0 (en) * 1994-05-31 1994-07-20 Exxon Chemical Patents Inc Oil additives and compositions
GB9417670D0 (en) * 1994-09-02 1994-10-19 Exxon Chemical Patents Inc Oil additives, compositions and polymers for use therein
EP0743972B1 (fr) * 1994-12-13 2000-06-14 Infineum USA L.P. Compositions de fuel-oil
JPH08165480A (ja) * 1994-12-13 1996-06-25 Nippon Oil & Fats Co Ltd 燃料油用流動性向上剤
GB9610363D0 (en) * 1996-05-17 1996-07-24 Ethyl Petroleum Additives Ltd Fuel additives and compositions
DE19620119C1 (de) * 1996-05-18 1997-10-23 Hoechst Ag Terpolymerisate des Ethylens, ihre Herstellung und ihre Verwendung als Additive für Mineralöldestillate
JP3894997B2 (ja) 1997-02-25 2007-03-22 三洋化成工業株式会社 燃料油用流動性改良添加剤および燃料油
JPH10245574A (ja) 1997-02-28 1998-09-14 Sanyo Chem Ind Ltd 燃料油用流動性改良添加剤および燃料油
DE19729055C2 (de) * 1997-07-08 2000-07-27 Clariant Gmbh Brennstofföle auf Basis von Mitteldestillaten und Copolymeren aus Ethylen und ungesättigten Carbonsäureestern
GB9725578D0 (en) * 1997-12-03 1998-02-04 Exxon Chemical Patents Inc Oil additives and compositions
DE19754555A1 (de) * 1997-12-09 1999-06-24 Clariant Gmbh Verfahren zur Herstellung von Ethylen-Mischpolymerisaten und deren Verwendung als Zusatz zu Mineralöl und Mineralöldestillaten
JP3903559B2 (ja) 1997-12-17 2007-04-11 株式会社コスモ総合研究所 燃料油組成物
DE19757830C2 (de) * 1997-12-24 2003-06-18 Clariant Gmbh Brennstofföle mit verbesserter Schmierwirkung
GB9810994D0 (en) * 1998-05-22 1998-07-22 Exxon Chemical Patents Inc Additives and oil compositions
GB9818210D0 (en) * 1998-08-20 1998-10-14 Exxon Chemical Patents Inc Oil additives and compositions
DE19901803B4 (de) * 1999-01-19 2005-04-07 Clariant Gmbh Copolymere und ihre Verwendung als Additiv zur Verbesserung der Kaltfließeigenschaften von Mitteldestillaten
KR20020070286A (ko) * 1999-11-23 2002-09-05 더 어소시에이티드 악텔 컴퍼니 리미티드 조성물
EP1116780B1 (fr) * 2000-01-11 2005-08-31 Clariant GmbH Additif polyfonctionnel pour huiles combustibles
DE10012267B4 (de) * 2000-03-14 2005-12-15 Clariant Gmbh Copolymermischungen und ihre Verwendung als Additiv zur Verbesserung der Kaltfließeigenschaften von Mitteldestillaten
DE10012269C2 (de) * 2000-03-14 2003-05-15 Clariant Gmbh Verwendung von Copolymermischungen als Additiv zur Verbesserung der Kaltfließeigenschaften von Mitteldestillaten
DE10012946B4 (de) * 2000-03-16 2006-02-02 Clariant Gmbh Verwendung von öllöslichen Amphiphilen als Lösemittel für hydroxyfunktionelle Copolymere
DE10012947A1 (de) * 2000-03-16 2001-09-27 Clariant Gmbh Mischungen aus Carbonsäuren, deren Derivate und hydroxylgruppenhaltigen Polymeren, sowie deren Verwendung zur Verbesserung der Schmierwirkung von Ölen
DE10058357B4 (de) * 2000-11-24 2005-12-15 Clariant Gmbh Fettsäuremischungen verbesserter Kältestabilität, welche Kammpolymere enthalten, sowie deren Verwendung in Brennstoffölen
JP2002338975A (ja) * 2001-05-17 2002-11-27 Sanyo Chem Ind Ltd 流動性向上剤
EP1302526A1 (fr) * 2001-10-15 2003-04-16 Infineum International Limited Compositions d'Additifs
CA2404646A1 (fr) * 2001-10-15 2003-04-15 Infineum International Limited Compositions d'additif
EP1314771A3 (fr) * 2001-11-21 2004-10-27 Infineum International Limited Additif pour combustible
US20030136046A1 (en) * 2001-11-21 2003-07-24 Graham Jackson Fuel additive
EP1380635B1 (fr) * 2002-07-09 2013-01-23 Clariant Produkte (Deutschland) GmbH Agent d'amélioration de l'écoulement à froid pour huiles combustibles d'origine animale ou végétale.
DE10349850C5 (de) 2003-10-25 2011-12-08 Clariant Produkte (Deutschland) Gmbh Kaltfließverbesserer für Brennstofföle pflanzlichen oder tierischen Ursprungs
DE10357878C5 (de) 2003-12-11 2013-07-25 Clariant Produkte (Deutschland) Gmbh Brennstofföle aus Mitteldestillaten und Ölen pflanzlichen oder tierischen Ursprungs mit verbesserten Kälteeigenschaften
DE10357877B4 (de) 2003-12-11 2008-05-29 Clariant Produkte (Deutschland) Gmbh Brennstofföle aus Mitteldestillaten und Ölen pflanzlichen oder tierischen Ursprungs mit verbesserten Kälteeigenschaften
EP1674554A1 (fr) 2004-12-24 2006-06-28 Clariant Produkte (Deutschland) GmbH Additifs pour distillats d'huiles minérales, à faible contenu en soufre, comprenant un copolymère greffé à base de copolymères d'éthylène-acétate de vinyle.
DE102006001381A1 (de) 2006-01-11 2007-07-12 Clariant International Limited Additive für schwefelarme Mineralöldestillate, umfassend Pfropfcopolymere auf Basis von Ethylen-Vinylester-Copolymeren
DE102006001380A1 (de) 2006-01-11 2007-07-26 Clariant International Limited Additive für schwefelarme Mineralöldestillate, umfassend Pfropfcopolymere auf Basis von Ethylen-Vinylacetat-Copolymeren

Patent Citations (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2615845A (en) † 1948-08-02 1952-10-28 Standard Oil Dev Co Lubricating oil additives
US3003858A (en) † 1958-01-07 1961-10-10 Socony Mobil Oil Co Inc Stabilized distillate fuel oil
US4121026A (en) † 1973-03-23 1978-10-17 Petrolite Corporation Copolymers of alpha-olefins and maleic anhydride reacted with amines in the presence of Lewis acids
US4153424A (en) † 1975-03-28 1979-05-08 Exxon Research & Engineering Co. Polymer combinations useful in distillate hydrocarbon oils to improve cold flow properties
EP0100248A1 (fr) † 1982-06-04 1984-02-08 Institut Français du Pétrole Copolymères à fonctions azotées, utilisables notamment comme additifs d'abaissement du point de trouble des distillats moyens d'hydrocarbures, et compositions de distillats moyens d'hydrocarbures renfermant lesdits copolymères
JPS59126496A (ja) † 1983-01-11 1984-07-21 Nippon Zeon Co Ltd 燃料油組成物
EP0172758A1 (fr) † 1984-07-10 1986-02-26 Institut Français du Pétrole Compositions d'additifs destinees notamment a ameliorer les propriétés de filtrabilité a froid des distillats moyens de pétrole
EP0184083A2 (fr) † 1984-11-29 1986-06-11 Hoechst Aktiengesellschaft Terpolymères de l'éthylène, leur procédé de fabrication et leur application
FR2592658A1 (fr) † 1986-01-09 1987-07-10 Inst Francais Du Petrole Compositions d'additifs destinees notamment a ameliorer les proprietes de filtrabilite a froid des distillats moyens de petrole.
US5254652A (en) † 1990-12-29 1993-10-19 Hoechst Aktiengesellschaft Terpolymers of ethylene, their preparation, and their use as additives for mineral oil distillates
WO1993018115A1 (fr) † 1992-03-03 1993-09-16 Exxon Chemical Patents Inc. Additifs pour huiles
US5767190A (en) † 1996-05-18 1998-06-16 Hoechst Aktiengesellschaft Terpolymers of ethylene, their preparation and their use as additives for mineral oil distillates
US20010034968A1 (en) † 1997-07-08 2001-11-01 Matthias Krull Fuel oils based on middle distillates and copolymers of ethylene and unsaturated carboxylic esters
US6106584A (en) † 1997-08-05 2000-08-22 Exxon Chemical Patents Inc Additives for oil compositions
US6409778B1 (en) † 1997-11-21 2002-06-25 Rohmax Additives Gmbh Additive for biodiesel and biofuel oils
WO2000032722A1 (fr) † 1998-12-02 2000-06-08 Infineum International Limited Additifs et compositions pour fiouls
WO2001048122A1 (fr) † 1999-12-28 2001-07-05 Elf Antar France Composition d'additifs multifonctionnels d'operabilite a froid des distillats moyens
WO2002090470A1 (fr) † 2001-05-08 2002-11-14 Sanyo Chemical Industries, Ltd. Agent fluidifiant et composition de mazout
US20050126072A1 (en) † 2003-12-11 2005-06-16 Clariant Gmbh Fuel oils composed of middle distillates and oils of vegetable or animal origin and having improved cold flow properties
US20070266620A1 (en) † 2006-05-16 2007-11-22 Clariant International Ltd. Cold flow improvers for vegetable or animal fuel oils

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CARBURANTS ET MOTEURS, éDITIONS TECHNIP, 1997 †

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CA2486035C (fr) 2012-03-13
PL1526167T5 (pl) 2019-09-30
EP1526167B1 (fr) 2015-05-20
KR101139274B1 (ko) 2012-04-26
JP2005126720A (ja) 2005-05-19
PL1526167T3 (pl) 2015-10-30
EP1526167A3 (fr) 2005-05-11
JP4859361B2 (ja) 2012-01-25
EP1526167A2 (fr) 2005-04-27
HUE025057T2 (en) 2016-01-28
US20050113266A1 (en) 2005-05-26
DE10349851B4 (de) 2008-06-19
US7500996B2 (en) 2009-03-10
KR20050039682A (ko) 2005-04-29
CA2486035A1 (fr) 2005-04-25

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