Classifications

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  • 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
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  • C10L1/00—Liquid carbonaceous fuels
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  • C10L10/00—Use of additives to fuels or fires for particular purposes
  • C10L10/14—Use of additives to fuels or fires for particular purposes for improving low temperature properties
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  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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  • C10L10/00—Use of additives to fuels or fires for particular purposes
  • C10L10/14—Use of additives to fuels or fires for particular purposes for improving low temperature properties
  • C10L10/16—Pour-point depressants
• • C—CHEMISTRY; METALLURGY
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  • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/10—Liquid carbonaceous fuels containing additives
  • C10L1/14—Organic compounds
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  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/10—Liquid carbonaceous fuels containing additives
  • C10L1/14—Organic compounds
  • C10L1/16—Hydrocarbons
  • C10L1/1616—Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
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  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/10—Liquid carbonaceous fuels containing additives
  • C10L1/14—Organic compounds
  • C10L1/16—Hydrocarbons
  • C10L1/1625—Hydrocarbons macromolecular compounds
  • C10L1/1633—Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds
  • C10L1/1641—Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds from compounds containing aliphatic monomers
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  • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/10—Liquid carbonaceous fuels containing additives
  • C10L1/14—Organic compounds
  • C10L1/18—Organic compounds containing oxygen
  • C10L1/192—Macromolecular compounds
  • C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
  • C10L1/1981—Condensation polymers of aldehydes or ketones
• • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/10—Liquid carbonaceous fuels containing additives
  • C10L1/14—Organic compounds
  • C10L1/18—Organic compounds containing oxygen
  • C10L1/192—Macromolecular compounds
  • C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
  • C10L1/1983—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyesters
• • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/10—Liquid carbonaceous fuels containing additives
  • C10L1/14—Organic compounds
  • C10L1/18—Organic compounds containing oxygen
  • C10L1/192—Macromolecular compounds
  • C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
  • C10L1/1985—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
• • C—CHEMISTRY; METALLURGY
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  • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • 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 cold additives for middle distillates which have improved manageability at low temperatures, and to the use thereof for improvement of cold properties and lubricity of middle distillates, and to the corresponding middle distillates.
• paraffin-richer fuel oils In view of decreasing global oil reserves, ever heavier and hence paraffin-richer crude oils are being extracted and processed, which consequently also lead to paraffin-richer fuel oils.
• Even 0.1 to 0.3% by weight of crystallized paraffins in the oil are sufficient to block the fuel filter.
• paraffin problem is additionally aggravated by the hydrogenating desulfurization of fuel oils, which has to be undertaken for environmental protection reasons for the purpose of lowering the sulfur content, and leads to an increased proportion of cold-critical paraffins and to a reduced proportion of mono- and polycyclic aromatics, which improve the solubility of paraffins, in the fuel oil.
• the cold flow properties of middle distillates are often improved by adding chemical additives known as cold flow improvers or flow improvers, which modify the crystal structure and agglomeration tendency of the paraffins which precipitate out such that the oils thus additized can still be pumped and used at temperatures which are often more than 20° C. lower than in the case of unadditized oils.
• the cold flow improvers used are typically oil-soluble copolymers of ethylene and unsaturated esters.
• oil-soluble copolymers of ethylene and vinyl acetate having a molecular weight between about 1000 and 3000 are added to mineral oil distillate fuels having a boiling range between about 120 and 400° C.
• U.S. Pat. No. 3,447,916 discloses condensation polymers formed from alkenylsuccinic anhydrides, polyols and fatty acids for lowering of the pour point of hydrocarbon oils. In these polymers, the hydroxyl groups of the polyol have been very substantially esterified. The document does not give any indications of combined use with further additives.
• DE-A-19 20 849 discloses condensation polymers of alkenylsuccinic anhydrides, polyols having at least 4 OH groups and fatty acids for lowering of the pour point of hydrocarbon oils.
• the stoichiometry of the reactants used for the condensation is preferably selected such that the number of moles of OH groups and carboxyl groups is the same, i.e. there is essentially complete esterification.
• these polymers according to the information in the disclosure, have an efficacy superior to the additives of U.S. Pat. No. 3,447,916. This document does not give any indications of combined use with further additives either.
• DE-A-24 51 047 discloses light, low-viscosity distillate fuel oils which do not comprise any residues and have been additized with ethylene copolymers and comb polymers having C 18 -C 44 side chains.
• the comb polymers used include polyesters of alk(en)ylsuccinic anhydride with a C 16 -C 44 -alk(en)yl radical, a polyol having 2-6 OH groups and a C 20 -C 44 -monocarboxylic acid.
• the three components of the polyester are preferably condensed in equimolar amounts, so as to result in essentially complete esterification of OH and also COOH groups.
• polymer G is a polycondensate of equimolar amounts of C 22-28 -alkenylsuccinic anhydride, trimethylolpropane and C 20-22 fatty acids.
• US-A-2008/0295397 discloses additives for lowering the pour point of diesel oils, which comprise polyglyceryl esters and optionally further pour point depressants, for example ethylene/vinyl ester copolymers.
• the hydroxyl groups of the polyglycerol may be fully or partially esterified.
• Such polyol partial esters have pronounced emulsification properties and are therefore undesirable in fuels.
• Additive combinations of copolymers of ethylene and unsaturated esters and comb polymers are typically used as concentrates in organic solvents in order to improve the manageability thereof.
• the active ingredient concentration in the concentrates should be at a maximum in order to minimize the volume of the additive concentrates to be transported and stored.
• the prior art comb polymers prepared by polycondensation exhibit, as concentrates in organic solvents, and also in a blend with copolymers of ethylene and unsaturated esters in organic solvents, often comparatively high intrinsic pour points of more than 20° C. in some cases.
• heated storage of the additive concentrates is often impossible. Dilution of the additives is undesirable for logistical reasons since the volumes to be transported and stored then increase significantly.
• additive combinations which comprise solutions of copolymers of ethylene and unsaturated esters, and specific polycondensates of dicarboxylic acids or dicarboxylic anhydrides bearing linear C 16 -C 40 -alkyl radicals or C 16 -C 40 -alkenyl radicals, and polyols having two primary and at least one secondary OH group, in organic solvents are free-flowing in concentrated form and have good solubility in middle distillates even at low temperatures of below 10° C., often below 0° C., in some cases below ⁇ 10° C., for example below ⁇ 20° C. In addition, they have excellent properties as cold flow improvers without impairing the filterability of the oils additized therewith.
• the invention provides cold additives for middle distillates comprising
• the invention further provides a process for improving the cold flow properties of fuel oils, by adding to a middle distillate an additive which comprises
• the invention further provides a process for improving the lubricity of fuel oils, by adding to a middle distillate having a sulfur content of less than 0.05% by weight an additive which comprises
• the invention further provides fuel oils comprising a middle distillate and a cold additive which comprises
• the comb polymer A bearing hydroxyl groups is generally obtained by the polycondensation of a dicarboxylic acid bearing a C 16 - to C 40 -alkyl radical or -alkenyl radical, also referred to collectively hereinafter as C 16 -C 40 -alk(en)yl radical, with the primary hydroxyl groups of the polyol. It is preferable that the secondary OH groups remain essentially unesterified.
• the preferred structure of the comb polymer A bearing hydroxyl groups can thus be illustrated, for example, in accordance with formula A1:
• Preferred dicarboxylic acids which bear C 16 -C 40 -alkyl- and/or alkenyl radicals and are suitable for preparation of the comb polymers A) bearing hydroxyl groups correspond to the general formula 1
• R 1 to R 4 radicals in which one of the R 1 to R 4 radicals is a linear C 16 -C 40 -alkyl or -alkenyl radical and the other R 1 to R 4 radicals are each independently hydrogen or an alkyl radical having 1 to 3 carbon atoms and R 5 is a C—C bond or an alkylene radical having 1 to 6 carbon atoms.
• one of the R 1 to R 4 radicals is a linear C 16 -C 40 -alkyl or -alkenyl radical, one is a methyl group and the rest are hydrogen.
• one of the R 1 to R 4 radicals is a linear C 16 -C 40 -alkyl or -alkenyl radical and the others are hydrogen.
• R 5 is a C—C single bond. More particularly, one of the R 1 to R 4 radicals is a linear C 16 -C 40 -alkyl or -alkenyl radical, the other R 1 to R 4 radicals are hydrogen and R 5 is a C—C single bond.
• the dicarboxylic acids or anhydrides thereof bearing alkyl and/or alkenyl radicals can be prepared by known processes. For example, they can be prepared by heating ethylenically unsaturated dicarboxylic acids with olefins (“ene reaction”) or with chloroalkanes. Preference is given to the thermal addition of olefins onto ethylenically unsaturated dicarboxylic acids, which is typically performed at temperatures between 100 and 250° C.
• the dicarboxylic acids and dicarboxylic anhydrides bearing alkenyl radicals formed can be hydrogenated to dicarboxylic acids and dicarboxylic anhydrides bearing alkyl radicals.
• Dicarboxylic acids and anhydrides thereof preferred for the reaction with olefins are maleic acid and more preferably maleic anhydride. Additionally suitable are itaconic acid, citraconic acid and the anhydrides thereof, and the esters of the aforementioned acids, especially those with lower C 1 -C 8 -alcohols, for example methanol, ethanol, propanol and butanol.
• linear olefins having 16 to 40 carbon atoms and especially having 18 to 36 carbon atoms, for example having 19 to 32 carbon atoms.
• mixtures of olefins with different chain lengths are used.
• olefins may also contain minor amounts of shorter- and/or longer-chain olefins, but preferably not more than 10% by weight and especially not more than 0.1 to 5% by weight.
• Preferred olefins have a linear or at least substantially linear alkyl chain. “Linear or substantially linear” is understood to mean that at least 50% by weight, preferably 70 to 99% by weight, especially 75 to 95% by weight, for example 80 to 90% by weight, of the olefins have a linear component having 16 to 40 carbon atoms. Suitable olefins are preferably technical alkene mixtures.
• These contain preferably at least 50% by weight, more preferably 60 to 99% by weight and especially 70 to 95% by weight, for example 75 to 90% by weight, of terminal double bonds ( ⁇ -olefins).
• they may contain up to 50% by weight, preferably 1 to 40% by weight and especially 5 to 30% by weight, for example 10 to 25% by weight, of olefins having an internal double bond, for example having vinylidene double bonds with the structural element R 17 —CH ⁇ C(CH 3 ) 2 , where R 17 is an alkyl radical having 12 to 36 carbon atoms and especially having 14 to 32 carbon atoms, for example having 15 to 28 carbon atoms.
• Preferred comb polymers A) bearing hydroxyl groups are preparable by reaction of alkyl- or alkenylsuccinic acids bearing a linear C 16 -C 40 -alkyl or -alkenyl radical and/or anhydrides thereof with polyols which bear two primary and at least one secondary hydroxyl group.
• Preferred polyols are glycerol, poly(glycerol) and mixtures thereof.
• Poly(glycerol) is understood to mean especially structures derivable from glycerol by polycondensation.
• the degree of condensation of poly(glycerols) preferred in accordance with the invention is between 2 and 50, more preferably between 3 and 25 and especially between 4 and 20, for example between 5 and 15.
• the preparation of poly(glycerol) is known in the prior art. It can be effected, for example, via addition of 2,3-epoxy-1-propanol (glycide) onto glycerol.
• the preparation of poly(glycerol) can be effected by polycondensation of glycerol, which is known per se.
• the reaction temperature in the polycondensation is generally between 150 and 300° C., preferably between 200 and 250° C.
• the polycondensation is normally performed at atmospheric pressure.
• Examples of catalyzing acids include HCl, H 2 SO 4 , organic sulfonic acids or H 3 PO 4 , and examples of catalyzing bases NaOH or KOH.
• the catalysts are added to the reaction mixture preferably in amounts of 0.01 to 10% by weight, more preferably 0.1 to 5% by weight, based on the weight of the reaction mixture.
• the polycondensation can be performed in a solvent-free manner or else in the presence of solvents.
• the proportion thereof in the reaction mixture is preferably 0.1 to 70% by weight, for example 10 to 60% by weight.
• Preferred solvents are the solvents which are also used as component C) for the additive mixture.
• the polycondensation generally takes 3 to 10 hours.
• the reaction of the dicarboxylic acids bearing alkyl radicals, the anhydrides thereof or esters thereof with the polyol is effected preferably in a molar ratio of 1:2 to 2:1, more preferably in a molar ratio of 1:1.5 to 1.5:1, and especially in a molar ratio of 1:1.2 to 1.2:1, for example an equimolar ratio.
• Particular preference is given to effecting the reaction with an excess of polyol.
• Particularly useful molar excesses have been found to be from 1 to 10 mol % and especially 1.5 to 5 mol %, based on the amount of dicarboxylic acid used.
• the condensation is effected preferably by heating C 16 -C 40 -alkyl or -alkenyl-substituted dicarboxylic acid or the anhydride or ester thereof with the polyol to temperatures above 100° C. and preferably to temperatures between 120 and 320° C., for example to temperatures between 150 and 290° C.
• To accelerate the polycondensation it has often been found to be useful to add catalysts to the reaction mixture. Suitable catalysts are known acidic, basic and organometallic compounds.
• the dicarboxylic acids bearing alk(en)yl radicals, anhydrides thereof or esters thereof is replaced by one or more monocarboxylic acids.
• the comb polymers A) bearing hydroxyl groups are prepared in the absence of monocarboxylic acids.
• minor amounts of the polyol in the reaction mixture are replaced by C 1 - to C 30 -monoalcohols, preferably C 2 - to C 24 -monoalcohols and especially C 3 - to C 18 -monoalcohols, for example C 4 - to C 12 -monoalcohols.
• C 1 - to C 30 -monoalcohols preferably C 2 - to C 24 -monoalcohols and especially C 3 - to C 18 -monoalcohols, for example C 4 - to C 12 -monoalcohols.
• Preferably at most 20 mol % and more preferably 0.1 to 10 mol %, for example 0.5 to 5 mol %, of the polyol is replaced by one or more monoalcohols.
• the comb polymers A) bearing hydroxyl groups are prepared in the absence of monoalcohols.
• the polyol bearing two primary hydroxyl groups and at least one secondary hydroxyl group may also be replaced in minor amounts of up to 10 mol %, for example 0.01 to 5 mol %, by one or more diols.
• diols such as ethylene glycol, propylene glycol and/or neopentyl glycol, for example.
• the comb polymers A) bearing hydroxyl groups are prepared in the absence of diols.
• the mean degree of condensation of the inventive comb polymers A) bearing hydroxyl groups is preferably between 4 and 200, more preferably between 5 and 150 and especially between 7 and 100, for example between 10 and 50 repeat units of dicarboxylic acid and polyol.
• the weight-average molecular weight Mw of the comb polymers A) bearing hydroxyl groups determined in THF by means of GPC against poly(ethylene glycol) standards, is preferably between 1500 and 100 000 g/mol and especially between 2500 and 50 000 g/mol, for example between 4000 and 20 000 g/mol.
• the acid number of the comb polymers A) bearing hydroxyl groups is preferably less than 40 mg KOH/g and more preferably less than 30 mg KOH/g, for example less than 20 mg KOH/g.
• the acid number can be determined, for example, by titration of the polymer with alcoholic tetra-n-butylammonium hydroxide solution in xylene/isopropanol.
• the hydroxyl number of the comb polymers A) is between 45 and 500 mg KOH/g, more preferably between 50 and 300 mg KOH/g and especially between 60 and 250 mg KOH/g.
• the hydroxyl number can be determined, after reaction of the free OH groups with isocyanate, by means of 1 H NMR spectroscopy by quantitative determination of the urethane formed.
• Preferred copolymers of ethylene and olefinically unsaturated esters B) are especially those which, as well as ethylene, contain 8 to 21 mol % and especially 10 to 19 mol % of olefinically unsaturated esters as comonomers.
• the olefinically unsaturated esters are preferably vinyl esters, acrylic esters and/or methacrylic esters. It is possible for one or more esters to be present as comonomers in the polymer.
• the vinyl esters are preferably those of the formula 2
• R 12 is C 1 - to C 30 -alkyl, preferably C 1 - to C 16 -alkyl, especially C 1 - to C 12 -alkyl.
• the alkyl groups mentioned may be substituted by one or more hydroxyl groups.
• Particularly preferred vinyl esters derive from secondary and especially tertiary carboxylic acids whose branch is in the alpha-position to the carbonyl group.
• R 12 in these vinyl esters is C 4 - to C 16 -alkyl and especially C 6 - to C 12 -alkyl.
• R 12 is a branched alkyl radical or a neoalkyl radical having 7 to 11 carbon atoms, especially having 8, 9 or 10 carbon atoms.
• Suitable vinyl esters include vinyl acetate, vinyl propionate, vinyl butyrate, vinyl isobutyrate, vinyl hexanoate, vinyl heptanoate, vinyl octanoate, vinyl pivalate, vinyl 2-ethylhexanoate, vinyl laurate, vinyl stearate and Versatic esters such as vinyl neononanoate, vinyl neodecanoate, vinyl neoundecanoate.
• these ethylene copolymers contain vinyl acetate and at least one further vinyl ester of the formula 2 in which R 12 is C 4 - to C 30 -alkyl, preferably C 4 - to C 16 -alkyl, especially C 6 - to C 12 -alkyl. More preferably, the further vinyl esters are alpha-branched.
• the acrylic and methacrylic esters are preferably those of the formula 3
• R 13 is hydrogen or methyl and R 14 is C 1 - to C 30 -alkyl, preferably C 4 - to C 16 -alkyl, especially C 6 - to C 12 -alkyl.
• Suitable acrylic esters include, for example, 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 these comonomers.
• the alkyl groups mentioned may be substituted by one or more hydroxyl groups.
• An example of such an acrylic ester is hydroxyethyl methacrylate.
• the copolymers B) may, as well as olefinically unsaturated esters, also contain further olefinically unsaturated compounds as comonomers.
• Preferred comonomers of this kind are alkyl vinyl ethers and alkenes.
• alkyl vinyl ethers are preferably compounds of the formula 4
• R 15 is C 1 - to C 30 -alkyl, preferably C 4 - to C 16 -alkyl, especially C 6 - to C 12 -alkyl.
• examples include methyl vinyl ether, ethyl vinyl ether, isobutyl vinyl ether.
• the alkyl groups mentioned may be substituted by one or more hydroxyl groups.
• the alkenes are preferably monounsaturated hydrocarbons having 3 to 30 carbon atoms, especially 4 to 16 carbon atoms and especially 5 to 12 carbon atoms.
• Suitable alkenes include propene, butene, isobutylene, pentene, hexene, 4-methylpentene, octene, diisobutylene and norbornene and derivatives thereof such as methylnorbornene and vinylnorbornene.
• the alkyl groups mentioned may be substituted by one or more hydroxyl groups.
• particularly preferred terpolymers contain 3.5 to 20 mol %, especially 8 to 15 mol %, of vinyl acetate, and 0.1 to 12 mol %, especially 0.2 to 5 mol %, of at least one relatively long-chain and preferably branched vinyl ester, for example vinyl 2-ethylhexanoate, vinyl neononanoate or vinyl neodecanoate, the total comonomer content of the terpolymers being preferably between 8.1 and 21 mol %, especially between 8.2 and 19 mol %, for example between 12 and 18 mol %.
• copolymers contain, in addition to ethylene and 8 to 18 mol % of vinyl esters of C 2 - to C 12 -carboxylic acids, also 0.5 to 10 mol % of olefins such as propene, butene, isobutylene, hexene, 4-methylpentene, octene, diisobutylene and/or norbornene, the total comonomer content being preferably between 8.5 and 21 mol % and especially between 9.0 and 19 mol %.
• olefins such as propene, butene, isobutylene, hexene, 4-methylpentene, octene, diisobutylene and/or norbornene
• These ethylene co- and terpolymers preferably have melt viscosities at 140° C. of at most 5000 mPas, more preferably of 20 to 2500 mPas, particularly of 30 to 1000 mPas, especially of 50 to 500 mPas.
• the degrees of branching determined by means of 1 H NMR spectroscopy are preferably between 1 and 9 CH 3 /100 CH 2 groups, especially between 2 and 6 CH 3 /100 CH 2 groups, which do not originate from the comonomers.
• the polymers on which the mixtures are based differ in at least one characteristic.
• they may contain different comonomers, or have different comonomer contents, molecular weights and/or degrees of branching.
• mixtures of ethylene copolymers having different comonomer contents have been found to be particularly useful, the comonomer contents thereof differing by at least 2 mol % and especially more than 3 mol %.
• the inventive cold additives contain preferably 25 to 95% by weight and preferably 28 to 80% by weight, for example 35 to 70% by weight, of at least one organic solvent C).
• Preferred solvents are relatively high-boiling, low-viscosity organic solvents. These solvents preferably contain only minor amounts of heteroatoms, and they especially consist only of hydrocarbons. Additionally preferably, the kinematic viscosity thereof, measured at 20° C., is below 10 mm 2 /s and especially below 6 mm 2 /s.
• Particularly preferred solvents are aliphatic and aromatic hydrocarbons and mixtures thereof.
• Aliphatic hydrocarbons preferred as solvents have 9 to 20 carbon atoms and especially 10 to 16 carbon atoms. They may be linear, branched and/or cyclic. They may also be saturated or unsaturated; they are preferably saturated or at least very substantially saturated.
• Aromatic hydrocarbons preferred as solvents have 7 to 20 carbon atoms and especially 8 to 16, for example 9 to 13, carbon atoms.
• Preferred aromatic hydrocarbons are mono-, di-, tri- and polycyclic aromatics. In a preferred embodiment, these bear one or more, for example two, three, four, five or more, substituents. In the case of a plurality of substituents, these may be the same or different.
• Preferred substituents are alkyl radicals having 1 to 20 and especially having 1 to 5 carbon atoms, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, tert-pentyl and neopentyl radical.
• suitable aromatics are alkylbenzenes and alkylnaphthalenes.
• Particularly suitable examples are aliphatic and/or aromatic hydrocarbons or hydrocarbon mixtures, for example gasoline fractions, kerosene, decane, pentadecane, toluene, xylene, ethylbenzene, or commercial solvent mixtures such as Solvent Naphtha, Shellsoll® AB, Solvesso® 150, Solvesso® 200, Exxsol®, ISOPAR® and Shellsol® D products.
• the solvent mixtures specified contain different amounts of aliphatic and/or aromatic hydrocarbons.
• the solvent C) may optionally also contain polar solubilizers, for example alcohols, organic acids, ethers and/or esters of organic acids.
• Preferred solubilizers have 4 to 24 carbon atoms, more preferably 6 to 18 and especially 8 to 16 carbon atoms.
• suitable solubilizers are butanol, 2-ethylhexanol, decanol, isodecanol, isotridecanol, nonylphenol, benzoic acid, oleic acid, dihexyl ether, dioctyl ether, 2-ethylhexyl acid butyrate, ethyl octanoate, ethyl hexanoate, butyl 2-ethylhexanoate and 2-ethylhexyl butyrate, and higher ethers and/or higher esters, for example di(2-ethylhexyl) ether, 2-ethylhexyl 2-ethylhexanoate and 2-ethylhexyl stearate.
• the proportion of polar solubilizers in the solvent C) is preferably 5 to 80% by weight and especially 10 to 65% by weight.
• suitable solvents C) are those based on renewable raw materials, for example biodiesel based on vegetable oils and the methyl esters derived therefrom, especially rapeseed oil methyl ester, and synthetic hydrocarbons obtainable, for example, from the Fischer-Tropsch process. Mixtures of the solvents mentioned are also suitable.
• the inventive cold additives contain preferably 1.5 to 73.5%, particularly 15 to 70% and especially 25 to 60% by weight of constituent B).
• the inventive cold additives contain preferably 0.1 to 50%, particularly 0.5 to 30% and especially 1 to 20% by weight of constituent A).
• the inventive cold additives are added to middle distillates preferably in amounts of 0.001 to 1.0% by weight, more preferably 0.002 to 0.5% by weight, for example 0.005 to 0.2% by weight.
• inventive cold additives can be used together with one or more further cold flow improvers. They are preferably used together with one or more of cold flow improvers III) to VII):
• Further suitable cold flow improvers are oil-soluble polar nitrogen compounds (constituent III). These are preferably reaction products of fatty amines with compounds which contain an acyl group.
• the preferred amines are compounds of the formula NR 6 R 7 R 8 in which R 6 , R 7 and R 8 may be the same or different, and at least one of these groups is C 8 -C 36 -alkyl, C 6 -C 36 -cycloalkyl or C 5 -C 36 -alkenyl, especially C 12 -C 24 -alkyl, C 12 -C 24 -alkenyl or cyclohexyl, and the remaining groups are hydrogen, C 1 -C 36 -alkyl, C 2 -C 36 -alkenyl, cyclohexyl or a group of the formulae -(A-O) x -E or —(CH 2 ) k —NYZ in which A is an ethyl or propyl group, x
• the alkyl and alkenyl radicals may each be linear or branched and contain up to two double bonds. They are preferably linear and substantially saturated, i.e. they have iodine numbers of less than 75 g of I 2 /g, preferably less than 60 g of I 2 /g and especially between 1 and 10 g of I 2 /g.
• Suitable fatty amines are, for example, octylamine, decylamine, dodecylamine, tetradecylamine, hexadecylamine, octadecylamine, eicosylamine, behenylamine, didecylamine, didodecylamine, ditetradecylamine, dihexadecylamine, dioctadecylamine, dieicosylamine, dibehenylamine and mixtures thereof.
• the amines especially contain chain cuts based on natural raw materials, for example coconut fatty amine, tallow fatty amine, hydrogenated tallow fatty amine, dicoconut fatty amine, ditallow fatty amine and di(hydrogenated tallow fatty amine).
• Particularly preferred amine derivatives are amine salts, imides and/or amides, for example amide-ammonium salts of secondary fatty amines, especially of dicoconut fatty amine, ditallow fatty amine and distearylamine.
• Acyl group is understood here to mean a functional group of the following formula:
• Carbonyl compounds suitable for the reaction with amines are either monomeric or polymeric compounds having one or more carboxyl groups. Preference is given to those monomeric carbonyl compounds having 2, 3 or 4 carbonyl groups. They may also contain heteroatoms such as oxygen, sulfur and nitrogen.
• Suitable carboxylic acids are, for example, maleic acid, fumaric acid, crotonic acid, itaconic acid, succinic acid, C 1 -C 40 -alk(en)ylsuccinic acid, adipic acid, glutaric acid, sebacic acid and malonic acid, and also benzoic acid, phthalic acid, trimellitic acid and pyromellitic acid, nitrilotriacetic acid, ethylenediaminetetraacetic acid and their reactive derivatives, for example esters, anhydrides and acid halides.
• Useful polymeric carbonyl compounds have been found to be especially copolymers of ethylenically unsaturated acids, for example acrylic acid, methacrylic acid, maleic acid, fumaric acid and itaconic acid; particular preference is given to copolymers of maleic anhydride.
• Suitable comonomers are those which impart oil solubility to the copolymer. Oil-soluble means here that the copolymer, after reaction with the fatty amine, dissolves without residue in the middle distillate to be additized in practically relevant dosages.
• Suitable comonomers are, for example, olefins, alkyl esters of acrylic acid and methacrylic acid, alkyl vinyl esters and alkyl vinyl ethers each having 2 to 75, preferably 4 to 40 and especially 8 to 20 carbon atoms in the alkyl radical.
• the carbon number is based on the alkyl radical attached to the double bond.
• the molecular weights of the polymeric carbonyl compounds are preferably between 400 and 20 000, more preferably between 500 and 10 000, for example between 1000 and 5000.
• oil-soluble polar nitrogen compounds are those which are 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 (cf. U.S. Pat. No. 4,211,534).
• oil-soluble polar nitrogen compounds are amides and ammonium salts of aminoalkylenepolycarboxylic acids such as nitrilotriacetic acid or ethylenediamine-tetraacetic acid with secondary amines (cf. EP-A-0 398 101).
• oil-soluble polar nitrogen compounds are copolymers of maleic anhydride and ⁇ , ⁇ -unsaturated compounds which may optionally be reacted with primary monoalkylamines and/or aliphatic alcohols (cf. EP-A-0 154 177, EP-A-0 777 712), the reaction products of alkenyl-spiro-bislactones with amines (cf. EP-A-0 413 279 B1) and, according to 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 between the inventive cold additives A) and oil-soluble polar nitrogen compounds as constituent III may vary depending upon the application.
• Such additive mixtures preferably contain, based on the active ingredients, 0.1 to 10 parts by weight, preferably 0.2 to 5 parts by weight, of at least one oil-soluble polar nitrogen compound (constituent III) per part by weight of the inventive additive combination of A) and B).
• resins of phenol derivatives bearing alkyl radicals and aldehydes as constituent IV are resins of phenol derivatives bearing alkyl radicals and aldehydes as constituent IV.
• they are phenol-formaldehyde resins which contain oligo- or polymers with a repeat structural unit of the formula
• R 11 is C 1 -C 200 -alkyl or -alkenyl, O—R 10 or O—C(O)—R 10
• R 10 is C 1 -C 200 -alkyl or -alkenyl and h is a number from 2 to 100.
• R 10 is preferably C 1 -C 20 -alkyl or -alkenyl and especially C 4 -C 16 -alkyl or -alkenyl, for example C 6 -C 12 -alkyl or -alkenyl.
• R 11 is more preferably C 1 -C 20 -alkyl or -alkenyl and especially C 4 -C 16 -alkyl or -alkenyl, for example C 6 -C 12 -alkyl or -alkenyl.
• h is preferably a number from 2 to 50 and especially a number from 3 to 25, for example a number from 5 to 15.
• constituent IV comprises those resins which derive from alkylphenols having one or two alkyl radicals in ortho and/or para positions to the OH group.
• Particularly preferred starting materials are alkylphenols which bear, on the aromatic, at least two hydrogen atoms capable of condensation with aldehydes, and especially monoalkylated phenols.
• the alkyl radical is more preferably in the para position to the phenolic OH group.
• alkyl radicals may be the same or different in the alkylphenol-aldehyde resins usable in the process according to the invention, they may be saturated or unsaturated and have 1-200, preferably 1-20, especially 4-16, for example 6-12, carbon atoms; they are preferably n-, iso- and tert-butyl, n- and isopentyl, n- and isohexyl, n- and isooctyl, n- and isononyl, n- and isodecyl, n- and isododecyl, tetradecyl, hexadecyl, octadecyl, tripropenyl, tetrapropenyl, poly(propenyl) and poly(isobutenyl) radicals.
• the alkylphenol resins are prepared by using mixtures of alkylphenols with different alkyl radicals.
• resins based firstly on butylphenol and secondly on octyl-, nonyl- and/or dodecylphenol in a molar ratio of 1:10 to 10:1 have been found to be particularly useful.
• Resins suitable as constituent IV may also contain or consist of structural units of further phenol analogs such as salicylic acid, hydroxybenzoic acid, aminophenol and derivatives thereof, such as esters, amides and salts.
• Suitable aldehydes for the preparation of the resins are those having 1 to 12 carbon atoms and preferably having 1 to 4 carbon atoms, for example formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, 2-ethylhexanal, benzaldehyde, glyoxalic acid and their reactive equivalents such as paraformaldehyde and trioxane. Particular preference is given to formaldehyde in the form of paraformaldehyde and especially formalin.
• the molecular weight of suitable resins measured by means of gel permeation chromatography against poly(styrene) standards in THF, is preferably 500-25 000 g/mol, more preferably 800-10 000 g/mol and especially 1000-5000 g/mol, for example 1500-3000 g/mol.
• a prerequisite here is that the resins are oil-soluble at least in concentrations relevant to use of 0.001 to 1% by weight.
• Suitable comb polymers are, for example, copolymers of ethylenically unsaturated dicarboxylic acids such as maleic acid or fumaric acid with other ethylenically unsaturated monomers such as olefins or vinyl esters, for example vinyl acetate.
• Particularly suitable olefins are ⁇ -olefins having 10 to 36 carbon atoms and especially having 12 to 24 carbon atoms, for example 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene and mixtures thereof.
• comonomers are longer-chain olefins based on oligomerized C 2 -C 6 -olefins, for example poly(isobutylene) with a high proportion of terminal double bonds. These copolymers are typically esterified to an extent of at least 50% with alcohols having 10 to 22 carbon atoms. Suitable alcohols include n-decan-1-ol, n-dodecan-1-ol, n-tetradecan-1-ol, n-hexadecan-1-ol, n-octadecan-1-ol, n-eicosan-1-ol and mixtures thereof.
• comb polymers are poly(alkyl acrylates), poly(alkyl methacrylates) and poly(alkyl vinyl ethers) which derive from alcohols having 12 to 20 carbon atoms, and poly(vinyl esters) which derive from fatty acids having 12 to 20 carbon atoms.
• homo- and copolymers of olefins having 2 to 30 carbon atoms are suitable as further cold flow improvers.
• these may derive directly from monoethylenically unsaturated monomers or be prepared indirectly by hydrogenation of polymers which derive from polyunsaturated monomers such as isoprene or butadiene.
• Preferred copolymers contain, as well as ethylene, structural units which derive from ⁇ -olefins having 3 to 24 carbon atoms and have molecular weights of up to 120 000 g/mol.
• Preferred ⁇ -olefins are propylene, butene, isobutene, n-hexene, isohexene, n-octene, isooctene, n-decene, isodecene.
• the comonomer content of olefins is preferably between 15 and 50 mol %, more preferably between 20 and 35 mol % and especially between 30 and 45 mol %.
• These copolymers may also contain small amounts, for example up to 10 mol %, of further comonomers, for example nonterminal olefins or nonconjugated olefins. Particular preference is given to ethylene-propylene copolymers.
• copolymers of different olefins having 5 to 30 carbon atoms for example poly(hexene-co-decene).
• the olefin homo- and copolymers can be prepared by known methods, for example by means of Ziegler or metallocene catalysts.
• olefin copolymers are block copolymers which contain blocks of olefinically unsaturated, aromatic monomers A and blocks of hydrogenated polyolefins B.
• Particularly suitable block copolymers are those of the (AB) c A and (AB) d structure where c is a number between 1 and 10 and d is a number between 2 and 10.
• oil-soluble polyoxyalkylene compounds for example esters, ethers and ether/esters of polyols, which bear at least one alkyl radical having 12 to 30 carbon atoms.
• the oil-soluble polyoxyalkylene compounds possess at least 2, for example 3, 4 or 5, aliphatic hydrocarbon radicals. These radicals preferably independently possess 16 to 26 carbon atoms, for example 17 to 24 carbon atoms.
• These radicals of the oil-soluble polyoxyalkylene compounds are preferably linear. Additionally preferably, they are very substantially saturated, and are especially alkyl radicals. Esters are particularly preferred.
• Polyols which are particularly suitable in accordance with the invention are polyethylene glycols, polypropylene glycols, polybutylene glycols and copolymers thereof with a molecular weight of approx. 100 to approx. 5000 g/mol, preferably 200 to 2000 g/mol.
• the oil-soluble polyoxyalkylene compounds derive from polyols having 3 or more OH groups, preferably from polyols having 3 to about 50 OH groups, for example 4 to 10 OH groups, especially from neopentyl glycol, glycerol, trimethylolethane, trimethylolpropane, sorbitan, pentaerythritol, and the oligomers which are obtainable therefrom by condensation and have 2 to 10 monomer units, for example polyglycerol.
• polystyrene resin for example sorbitol, sucrose, glucose, fructose and oligomers thereof, for example cyclodextrin, provided that the esterified or etherified alkoxylates thereof are oil-soluble at least in application-relevant amounts.
• Preferred polyoxyalkylene compounds thus have a branched polyoxyalkylene core to which a plurality of alkyl radicals which impart oil solubility are bonded.
• the polyols are generally reacted with 3 to 70 mol of alkylene oxide, preferably 4 to 50 mol and especially 5 to 20 mol of alkylene oxide per hydroxyl group of the polyol.
• Preferred alkylene oxides are ethylene oxide, propylene oxide and/or butylene oxide.
• the alkoxylation is effected by known processes.
• the fatty acids suitable for the esterification of the alkoxylated polyols have preferably 12 to 30 and especially 16 to 26 carbon atoms.
• Suitable fatty acids are, for example, lauric acid, tridecanoic acid, myristic acid, pentadecanoic acid, palmitic acid, margaric acid, stearic acid, isostearic acid, arachic acid and behenic acid, oleic acid and erucic acid, palmitoleic acid, myristoleic acid, ricinoleic acid, and fatty acid mixtures obtained from natural fats and oils.
• Preferred fatty acid mixtures contain more than 50 mol % of fatty acids having at least 20 carbon atoms.
• the fatty acids used for esterification contain double bonds, particularly less than 10 mol %; they are especially very substantially saturated.
• the esterification may also proceed from reactive derivatives of the fatty acids, such as esters with lower alcohols (e.g. methyl or ethyl esters) or anhydrides.
• very substantially saturated is understood to mean an iodine number of the fatty acid used or of the fatty alcohol used of up to 5 g of l per 100 g of fatty acid or fatty alcohol.
• Polyol and fatty acid are used for the esterification, based on the content of hydroxyl groups on the one hand and carboxyl groups on the other hand, in a ratio of 1.5:1 to 1:1.5, preferably in a ratio of 1.1:1 to 1:1.1 and especially in equimolar amounts.
• the acid number of the esters formed is generally less than 15 mg KOH/g, preferably less than 10 mg KOH/g, especially less than 5 mg KOH/g.
• the OH number of the esters is preferably less than 20 mg KOH/g and especially less than 10 mg KOH/g.
• the terminal hydroxyl groups are converted to terminal carboxyl groups, for example by oxidation or by reaction with dicarboxylic acids.
• Reaction with fatty alcohols having 8 to 50, particularly 12 to 30 and especially 16 to 26 carbon atoms likewise affords inventive polyoxyalkylene esters.
• Preferred fatty alcohols or fatty alcohol mixtures contain more than 50 mol % of fatty alcohols having at least 20 carbon atoms.
• Preferably less than 50 mol % of the fatty alcohols used for esterification contain double bonds, particularly less than 10 mol %; they are especially very substantially saturated.
• Esters of alkoxylated fatty alcohols with fatty acids which contain abovementioned proportions of poly(alkylene oxides) and whose fatty alcohol and fatty acid possess abovementioned alkyl chain lengths and degrees of saturation, are also suitable in accordance with the invention.
• alkoxylated polyols can be converted to polyoxyalkylene compounds suitable in accordance with the invention by etherification with fatty alcohols having 8 to 50, particularly 12 to 30 and especially 16 to 26 carbon atoms.
• the fatty alcohols preferred for this purpose are linear and very substantially saturated.
• the etherification is preferably effected completely or at least very substantially completely. The etherification is performed by known processes.
• Particularly preferred polyoxyalkylene compounds derive from polyols having 3, 4 and 5 OH groups, which bear about 5 to 10 mol of structural units derived from ethylene oxide per hydroxyl group of the polyol and are very substantially completely esterified with very substantially saturated C 17 -C 24 fatty acids.
• Further particularly preferred polyoxyalkylene compounds are polyethylene glycols which have been esterified with very substantially saturated C 17 -C 24 fatty acids and have molecular weights of about 350 to 1000 g/mol.
• polyoxyalkylene compounds are polyethylene glycols which have been esterified with stearic acid and especially behenic acid and have molecular weights between 350 and 800 g/mol; neopentyl glycol 14-ethylene oxide distearate (neopentyl glycol which has been alkoxylated with 14 mol of ethylene oxide and then esterified with 2 mol of stearic acid) and especially neopentyl glycol 14-ethylene oxide dibehenate; glycerol 20-ethylene oxide tristearate, glycerol 20-ethylene oxide dibehenate and especially glycerol 20-ethylene oxide tribehenate; trimethylolpropane 22-ethylene oxide tribehenate; sorbitan 25-ethylene oxide tristearate, sorbitan 25-ethylene oxide tetrastearate, sorbitan 25-ethylene oxide tribehenate and especially sorbitan 25-ethylene oxide tetrabehenate; pentaerythritol 30-ethylene oxide tribehen
• the mixing ratio between the inventive cold additives and the further cold flow improvers IV, V, VI and VII is generally in each case between 50:1 and 1:1, preferably between 10:1 and 2:1 by weight, based on the weights of (A+B):(IV, V, VI and VII).
• the inventive cold additives improve especially the cold properties of those middle distillates which are obtained by distillation of crude oil and boil in the range from about 150 to 410° C. and especially in the range from about 170 to 380° C., or consist predominantly thereof, for example kerosene, jet fuel, diesel and heating oil.
• Middle distillates typically contain about 5 to 50% by weight, for example about 10 to 35% by weight, of n-paraffins, among which the longer-chain paraffins can crystallize out in the course of cooling and impair the flowability of the middle distillate.
• the inventive cold additives are particularly advantageous in middle distillates having a high content of cold-critical constituents with an n-alkyl chain having a carbon chain length of 16 or more carbon atoms.
• n-paraffins of fossil origin but also n-paraffins which have been obtained by hydrogenation or cohydrogenation of animal and/or vegetable fats, and esters of saturated fatty acids with lower alcohols such as methanol or ethanol.
• middle distillates having a content of more than 4% by weight and especially with 6 to 20% by weight, for example with 7 to 15% by weight, of these cold-critical constituents, the inventive cold additives have been found to be particularly useful.
• the inventive cold additives are additionally particularly advantageous in those oils which contain only a very low proportion of very long-chain n-paraffins having 28 or more carbon atoms, which function as natural nucleators for paraffin crystallization.
• inventive cold additives have been found to be especially useful in oils which contain less than 1% by weight and especially less than 0.5% by weight, for example less than 0.3% by weight, of long-chain n-paraffins having 28 or more carbon atoms. Specific advantages are exhibited by the inventive cold additives especially in those oils which contain a high content of cold-critical constituents with an n-alkyl chain having 16 or more carbon atoms, and at the same time a very low proportion of very long-chain n-paraffins having 28 or more carbon atoms.
• the content of n-paraffins and any further cold-critical components, for example fatty acid methyl esters, is typically determined by means of gas chromatography.
• the inventive compositions are additionally particularly advantageous in middle distillates with a low final boiling point, i.e. in those middle distillates which have 90% distillation points below 360° C., especially 350° C. and in special cases below 340° C., and additionally in those middle distillates which have boiling ranges between 20 and 90% distillation volume of less than 120° C. and especially of less than 110° C.
• the middle distillates may also contain minor amounts, for example up to 40% by volume, preferably 1 to 20% by volume, especially 2 to 15%, for example 3 to 10% by volume, of the oils of animal and/or vegetable origin described in detail below, for example fatty acid methyl esters.
• the middle distillates preferably do not contain any residues from the distillation of mineral oils, for example residues from atmospheric distillation and/or vacuum distillation.
• the inventive cold additives are likewise suitable for improving the cold properties of fuels based on renewable raw materials (biofuels).
• Biofuels are understood to mean oils which are obtained from animal material and preferably from vegetable material or both, and derivatives thereof, which can be used as a fuel and especially as a diesel or heating oil. They are especially triglycerides of fatty acids having 10 to 24 carbon atoms, and also the fatty acid esters of lower alcohols, such as methanol or ethanol, obtainable from them by transesterification.
• biofuels examples include rapeseed oil, coriander oil, soybean oil, cottonseed oil, sunflower oil, castor oil, olive oil, groundnut oil, corn oil, almond oil, palm kernel oil, coconut oil, mustard seed oil, bovine tallow, bone oil, fish oils and used cooking oils.
• the fatty acid alkyl esters also known as biodiesel can be derived from these oils by processes known in the prior art.
• Rapeseed oil which is a mixture of fatty acids esterified with glycerol, is preferred, since it is obtainable in large amounts and is obtainable in a simple manner by extractive pressing of rapeseed. Preference is further given to the likewise widespread oils of sunflowers, palms and soya, and mixtures thereof with rapeseed oil.
• Particularly suitable biofuels are lower alkyl esters of fatty acids.
• Useful examples here are commercial mixtures of the ethyl esters, propyl esters, butyl esters and especially methyl esters of fatty acids having 14 to 22 carbon atoms, for example of lauric acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, oleic acid, elaidic acid, petroselic acid, ricinoleic acid, eleostearic acid, linoleic acid, linolenic acid, eicosanoic acid, gadoleic acid, docosanoic acid or erucic acid.
• Preferred esters have an iodine number of 50 to 150 and especially of 90 to 125.
• Mixtures with particularly advantageous properties are those which contain mainly, i.e. to an extent of at least 50% by weight, 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 acid, linoleic acid, linolenic acid and erucic acid.
• inventive cold additives can be used alone or else together with other coadditives, for example with other pour point depressants or dewaxing assistants, with detergents, antioxidants, cetane number improvers, dehazers, demulsifiers, dispersants, antifoams, dyes, corrosion inhibitors, lubricity additives, sludge inhibitors, odorants and/or additives for lowering the cloud point.
• other pour point depressants or dewaxing assistants with detergents, antioxidants, cetane number improvers, dehazers, demulsifiers, dispersants, antifoams, dyes, corrosion inhibitors, lubricity additives, sludge inhibitors, odorants and/or additives for lowering the cloud point.
• inventive cold additives lie in a distinct improvement in intrinsic flowability under cold conditions compared to corresponding prior art additive combinations, with a simultaneous improvement in efficacy.
• these cold additives given the same active ingredient content, can also be used at lower temperatures than the prior art additives, without needing to be heated.
• more highly concentrated additives can be used, and so the expenditure for transport and storage is reduced.
• inventive cold additives surprisingly exhibit improved efficacy in the improvement of the cold flow properties of middle distillates.
• the ⁇ -olefins used were commercially available mixtures of 1-alkenes with the specified compositions.
• the acid numbers were determined by titration of an aliquot of the reaction mixture with alcoholic tetra-n-butylammonium hydroxide solution in xylene/isopropanol.
• the hydroxyl numbers were determined, after reaction of the free OH groups of the polymers with isocyanate, by means of 1 H NMR spectroscopy by quantitative determination of the urethane formed. The values reported are based on the solvent-free polymers.
• the molecular weights were determined by means of lipophilic gel permeation chromatography in THF against poly(ethylene glycol) standards and detection by means of an RI detector.
• the melt viscosity of the ethylene copolymers B) was determined by means of a rotary viscometer at a temperature of 140° C. Before the measurement, all volatile components were removed from the ethylene copolymer B) at 150° C./100 mbar.
• the pour points thereof were determined to DIN ISO 3016. A low pour point indicates good flowability and hence good manageability under cold conditions.
• the percentages reported for the additives relate to the proportions by weight of the additive constituents used.
• the proportions by weight specified for the polymers relate to solvent-free active ingredients. Any solvent components present in the polymers as a result of the synthesis are shown as solvent C).
• the efficacy of the additives was studied by means of the lowering of the CFPP value to DIN EN 116 in low-sulfur middle distillates having the characteristics shown in Table 2.
• the components with n-alkyl radical ⁇ C 16 and the n-paraffins ⁇ C 28 were determined by means of gas chromatography.
• Test oil 1 Test oil 2
• Test oil 3 Initial boiling point [° C.] 171 179 173 Final boiling point [° C.] 355 348 331
• Boiling range (20-90)% [° C.] 93 94 89 Density [g/cm 3 ] 0.8555 0.8437 0.8409 Cloud point [° C.] ⁇ 11.7 ⁇ 15.6 ⁇ 22.0 CFPP [° C.] ⁇ 12 ⁇ 15 ⁇ 22
• Sulfur content [ppm] ⁇ 10 ⁇ 10 ⁇ 10
• Components with n-alkyl [% by wt.] 11.1 9.8 8.3 radical ⁇ C 16 n-Paraffins ⁇ C 28 [% by wt.] 0.04 0.11 0.01
• test oil 3 (Table 2) were admixed with 1000 ppm of an additive according to Table 1 at the temperature specified in Table 6 in a 250 ml measuring cylinder.
• the additives were added by means of a direct displacement pipette in order to be able to manage the high viscosity of the comparative additives in particular. After rotating the measuring cylinder by 180° ten times, a visual examination was made for undissolved additive constituents.

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