EP2385977A1 - Additifs pour carburants permettant de réduire l'arrachement de métal - Google Patents

Additifs pour carburants permettant de réduire l'arrachement de métal

Info

Publication number
EP2385977A1
EP2385977A1 EP09737254A EP09737254A EP2385977A1 EP 2385977 A1 EP2385977 A1 EP 2385977A1 EP 09737254 A EP09737254 A EP 09737254A EP 09737254 A EP09737254 A EP 09737254A EP 2385977 A1 EP2385977 A1 EP 2385977A1
Authority
EP
European Patent Office
Prior art keywords
fuel
additive
substituted
hydrocarbon
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP09737254A
Other languages
German (de)
English (en)
Other versions
EP2385977B1 (fr
EP2385977B2 (fr
Inventor
Robert H. Barbour
Paul R. Stevenson
Emma Fahey
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lubrizol Corp
Original Assignee
Lubrizol Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41565924&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2385977(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to EP16185196.9A priority Critical patent/EP3127992B1/fr
Priority to DK16185196.9T priority patent/DK3127992T3/en
Priority to PL16185196T priority patent/PL3127992T3/pl
Priority to EP18211764.8A priority patent/EP3486300A1/fr
Priority to PL09737254T priority patent/PL2385977T5/pl
Application filed by Lubrizol Corp filed Critical Lubrizol Corp
Publication of EP2385977A1 publication Critical patent/EP2385977A1/fr
Publication of EP2385977B1 publication Critical patent/EP2385977B1/fr
Publication of EP2385977B2 publication Critical patent/EP2385977B2/fr
Application granted granted Critical
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • C10L1/188—Carboxylic acids; metal salts 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
    • C10L1/198—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
    • 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
    • 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
    • C10L1/18—Organic compounds containing oxygen
    • C10L1/188—Carboxylic acids; metal salts thereof
    • C10L1/1881—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
    • C10L1/1883—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom polycarboxylic acid
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/234—Macromolecular compounds
    • C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)

Definitions

  • the present invention relates to fuel additives, fuel additive compositions and fuel compositions as well as a method for fueling an internal combustion engine, providing reduced oxidative metal pick-up in fuels.
  • Trace metals like these can enter the fuel distribution system through contamination, or through the pick-up (dissolution) of metal, by the fuel, from metals parts that make up part of the fuel distribution system with which the fuel comes into contact.
  • diesel fuel may pick up zinc from galvanized steel surfaces in fuel tanks, resulting in elevated zinc levels in fuels, which may lead to the accelerated injector fouling, discussed above.
  • Zinc, and other metals may also be picked up by the fuel by contacting such metal-containing surfaces in the vehicle fuel injection system.
  • Fuel additives, fuel additive compositions and fuel compositions have been discovered which reduce the amount of metal pick-up seen in fuel compositions.
  • the present invention provides for such compositions as well as a method of reducing contaminant metal pick-up, such as zinc pick-up, in fuel compositions.
  • an additive comprising a hydrocarbon substituted with at least two carboxy functionalities in the form of acids or at least one carboxy functionality in the form an anhydride
  • adding an additive comprising a hydrocarbon substituted with at least two carboxy functionalities in the form of acids or at least one carboxy functionality in the form an anhydride
  • the substituted hydrocarbon additive is a hydrocarbyl substituted acylating agent with at least two carboxy functionalities in the form of acids or anhydrides.
  • the substituted hydrocarbon additive and/or hydrocarbyl substituted acylating agent has di-acid functionality.
  • the additive is a succinic acylating agent.
  • the hydrocarbyl group of the additive is derived from polyiso- butylene.
  • the metal, for which pick-up is being reduced include group IV transition metals.
  • the metal is V, Cr, Mn, Fe, Co, Ni, Cu, Zn, or combinations thereof.
  • the metal may be selected from the group consisting of copper, zinc, iron, or combinations thereof.
  • the oxidative metal is zinc.
  • the oxidative metal, for which the tendency of fuel composition to pick up is being reduced may be any of the metals, or groups of metals, described above except iron.
  • the substituted hydrocarbon additive may be: (a) a hydrocarbyl substituted succinic anhydride; (b) a hydrolyzed hydrocarbyl substituted succinic anhydride; or (c) combinations thereof.
  • the fuel being treated in the method is susceptible to pick up of oxidative metals to a level greater than 0.5 ppm when left in contact for an extended period of time with solid materials containing said metal.
  • the method of the present invention may also result in the reduction of injector deposits in an engine in which the fuel composition of the method is applied.
  • the present invention also provides a fuel composition comprising: (a) a fuel; (b) an additive comprising the substituted hydrocarbon additive describe herein; and (c) optional additional performance additives.
  • a fuel additive composition comprising: (a) an optional solvent; (b) the substituted hydrocarbon additive described herein; and (c) optional additional performance additives.
  • the present invention involves a fuel additive, a fuel additive composition, a fuel composition and a method for fueling an internal combustion engine.
  • the invention provides a method of reducing metal-pick, and in some embodiments zinc pick-up, in a fuel composition, in some embodiment during the operation of an internal combustion engine.
  • composition of the present invention may be used in fuel compositions to reduce their tendency to pick-up metals from surfaces with which they come into contact.
  • the additive compositions of the present invention may also provide comparable and/or improved detergency, specifically improved engine deposit control when they are used in fuel compositions. These characteristics allow for improved engine performance, including but not limited to reductions in injector fouling, reduced deposit-caused engine power losses, reduced deposit-caused fuel economy losses and reduced deposit-caused engine emissions.
  • the substituted hydrocarbon additive of the present invention comprises a hydrocarbon substituted with at least two carboxy functionalities in the form of acids or at least one carboxy functionality in the form an anhydride.
  • the additive is a hydrocarbon substituted with at least two carboxy functionalities in the form of acids or anhydrides.
  • the additive is a hydrocarbyl-substituted succinic acylating agent.
  • the substituted hydrocarbon additive is a dimer acid compound.
  • the substituted hydrocarbon additive of the present invention includes a combination of two or more of the additives described in this section.
  • the substituted hydrocarbon additives of the present invention when used in the compositions and method described herein, reduce the tendency of fuel compositions in which they are used to pick up metals.
  • the substituted hydrocarbon additives include dimer acids. Dimer acids are a type of di-acid polymer derived from fatty acids and/or polyolefins, including the ployalkenes described herein, which contain acid functionality. IN some embodiments, the dimer acid used in the present invention is derived from ClO to C20 polyolefins, C 12 to Cl 8 polyolefins, and/or C 16 to C18 polyolfines.
  • the substituted hydrocarbon additives include succinic acids, halides, anhydrides and combination thereof.
  • the agents are acids or anhydrides, and in other embodiments the agents are anhydrides, and in still other embodiments the agents are hydro lyzed anhydrides.
  • the hydrocarbon of the substituted hydrocarbon additive and/or the primary hydrocarbyl group of the hydrocarbyl-substituted succinic acylating agent generally contains an average of at least about 8, or about 30, or about 35 up to about 350, or to about 200, or to about 100 carbon atoms.
  • the hydrocarbyl group is derived from a polyalkene.
  • the polyalkene may be characterized by a Mn (number average molecular weight) of at least about 300.
  • Mn number average molecular weight
  • the polyalkene is characterized by an Mn of about 500, or about 700, or about 800, or even about 900 up to about 5000, or to about 2500, or to about 2000, or even to about 1500.
  • n varies between about 300, or about 500, or about 700 up to about 1200 or to about 1300.
  • the polyalkenes include homopolymers and interpolymers of poly- merizable olefin monomers of 2 to about 16 or to about 6, or to about 4 carbon atoms.
  • the olefins may be monoolefins such as ethylene, propylene, 1-butene, isobutene, and 1-octene; or a polyolefinic monomer, such as diolefinic monomer, such 1,3-butadiene and isoprene.
  • the interpolymer is a homopolymer.
  • An example of a polymer is a polybutene. In one instance about 50% of the polybutene is derived from isobutylene.
  • the polyalkenes are prepared by conventional procedures.
  • the hydrocarbyl groups are derived from polyalkenes having an n of at least about 1300, or about 1500, or about 1600 up to about 5000, or to about 3000, or to about 2500, or to about 2000, or to about 1800, and the Mw/Mn is from about 1.5 or about 1.8, or about 2, or to about 2.5 to about 3.6, or to about 3.2.
  • the polyalkene is polyisobu- tylene with a molecular weight of 800 to 1200.
  • the substituted hydrocarbon and/or succinic acylating agents are prepared by reacting the above described polyalkene with an excess of maleic anhydride to provide substituted succinic acylating agents wherein the number of succinic groups for each equivalent weight of substituent group is at least 1.3, or to about 1.5, or to about 1.7, or to about 1.8. The maximum number generally will not exceed 4.5, or to about 2.5, or to about 2.1, or to about 2.0.
  • the polyalkene here may be any of those described above.
  • the hydrocarbon and/or hydrocarbyl group contains an average from about 8, or about 10, or about 12 up to about 40, or to about 30, or to about 24, or to about 20 carbon atoms. In one embodiment, the hydrocarbyl group contains an average from about 16 to about 18 carbon atoms. In another embodiment, the hydrocarbyl group is tetrapropenyl group. In one embodiment, the hydrocarbyl group is an alkenyl group.
  • the hydrocarbon and/or hydrocarbyl group may be derived from one or more olefins having from about 2 to about 40 carbon atoms or oligomers thereof. These olefins are preferably alpha-olefins (sometimes referred to as mono- 1 -olefins) or isomerized alpha-olefins.
  • alpha-olefins examples include ethylene, propylene, butylene, 1-octene, 1-nonene, 1-decene, 1- dodecene, 1-tridecene, 1-tetradecene, 1-pentadecene, 1-hexadecene, 1- heptadecene, 1-octadecene, 1-nonadecene, 1-eicosene, 1-henicosene, 1- docosene, 1-tetracosene, etc.
  • alpha-olefin fractions that may be used include the Cis_i8 alpha-olefins, C 12-16 alpha-olefins, Ci4_i6 alpha- olefins, Ci4_i8 alpha-olefins, C 16-18 alpha-olefins, C16-20 alpha-olefins, C22-28 alpha-olefins, etc.
  • the olefins are Ci 6 and C 16-18 alpha- olefins.
  • C 30 + alpha-olefin fractions such as those available from Gulf Oil Company under the name Gulftene can be used.
  • the olefin monomers include ethylene, propylene and 1-butene.
  • Isomerized alpha-olefins are alpha-olefins that have been converted to internal olefins.
  • the isomerized alpha-olefins suitable for use herein are usually in the form of mixtures of internal olefins with some alpha-olefins present.
  • the procedures for isomerizing alpha-olefins are well known to those in the art. Briefly these procedures involve contacting alpha-olefin with a cation exchange resin at a temperature in a range of about 80° to about 130 0 C until the desired degree of isomerization is achieved.
  • the mono-olefins may be derived from the cracking of paraffin wax.
  • the wax cracking process yields both even and odd number C6-20 liquid olefins of which 85% to 90% are straight chain 1-olefins.
  • the balance of the cracked wax olefins is made up of internal olefins, branched olefins, diolefins, aromatics and impurities.
  • mono-olefins can be derived from the ethylene chain growth process. This process yields even numbered straight-chain 1-olefins from a controlled Ziegler polymerization.
  • Other methods for preparing the mono- olefins include chlorination-dehydrochlorination of paraffin and catalytic dehydrogenation of paraffins.
  • Succinic acylating agents are prepared by reacting the above- described olefins, isomerized olefins or oligomers thereof with unsaturated carboxylic acylating agents, such as itaconic, citraconic, or maleic acylating agents at a temperature of about 160°, or about 185°C up to about 240 0 C, or to about 210 0 C.
  • unsaturated carboxylic acylating agents such as itaconic, citraconic, or maleic acylating agents at a temperature of about 160°, or about 185°C up to about 240 0 C, or to about 210 0 C.
  • Maleic acylating agents are the preferred unsaturated acylating agent.
  • the procedures for preparing the acylating agents are well known to those skilled in the art and have been described for example in U.S.
  • the alkenyl group is derived from oligomers of lower olefins, i.e., olefins containing from 2 to about 6, or about 4 carbon atoms. Examples of these olefins include ethylene, propylene and butylene.
  • the olefin, olefin oligomer, or polyalkene may be reacted with the carboxylic reagent such that there is at least one mole of carboxylic reagent for each mole of olefin, olefin oligomer, or polyalkene that reacts.
  • an excess of carboxylic reagent is used. In one embodiment, this excess is between about 5% to about 25%. In another embodiment, the excess is greater than 40%, or greater than 50%, and even greater than 70%.
  • the substituted hydrocarbon additives and/or hydrocarbyl substituted succinic acylating agents suitable for use in the present invention contain di-acid functionality.
  • the hydrocarbyl group of the hydrocarbyl substituted succinic acylating agent is derived from polyisobutylene and the di-acid functionality of the agent is derived from carboxylic acid groups, such as hydrocarbyl substituted succinic acid.
  • the hydrocarbyl substituted acylating agent comprises one or more hydrocarbyl substituted succinic anhydride groups.
  • the hydrocarbyl substituted acylating agent comprises one or more hydrolyzed hydrocarbyl substituted succinic anhydride groups.
  • the hydrocarbyl substituents of the acylating agents described above are derived from homopolymers and/or copolymers containing 2 to 10 carbon atoms. In some embodiments the hydrocarbyl substituents of any of the acylating agents described above are derived from polyisobutylene.
  • the fuel additives of the present invention can be solids, semi-solids, or liquids (oils) depending on the particular alcohol(s) and/or amine(s) used in preparing them.
  • the fuel additives are advantageously soluble and/or stably dispersible in such oleaginous compositions.
  • compositions intended for use in fuels are typically fuel-soluble and/or stably dispersible in a fuel in which they are to be used.
  • fuel-soluble as used in this specification and appended claims does not necessarily mean that all the compositions in question are miscible or soluble in all proportions in all fuels.
  • composition is soluble in a fuel (hydrocarbon, non-hydrocarbon, mixtures, etc) in which it is intended to function to an extent which permits the solution to exhibit one or more of the desired properties.
  • a fuel hydrocarbon, non-hydrocarbon, mixtures, etc
  • solutions it is not necessary that such "solutions" be true solutions in the strict physical or chemical sense. They may instead be micro-emulsions or colloidal dispersions which, for the purpose of this invention, exhibit proper- ties sufficiently close to those of true solutions to be, for practical purposes, interchangeable with them within the context of this invention.
  • the anti-metal pick-up additives of this invention are useful as additives for fuels, in which they may also function as detergents.
  • the fuel additives of the present invention can be present in fuel compositions at 1 to 10,000 ppm (where ppm is calculated on a weightweight basis).
  • the fuel additive is present in fuel compositions in ranges with lower limits of 1, 3, 5, 10, 50, 100, 150 and 200 ppm and upper limits of 10,000, 7,500, 5,000, and 2,500 where any upper limit may be combined with any lower limit to provide a range for the fuel additive present in the fuel compositions.
  • the additives of the present invention may form salts or other complexes and/or derivatives, when interacting with other components of the compositions in which they are used. Such forms of these additives are also part of the present invention and are include in the embodiment described herein.
  • Some of the succinic acylating agents of the present invention and the processes for making them are disclosed in U.S. Pat. Nos. 5,739,356; 5,777,142; 5,786,490; 5,856,524; 6,020,500; and 6,114,547 which are hereby incorporated by reference.
  • Other methods of making the hydrocarbyl substituted acylating agent can be found in U.S. Pat. Nos.
  • succinic acylating agents of the present invention are prepared by the thermal process and/or chlorine free process only, as described in EP0355895 hereby incorporated by reference.
  • the fuel additive composition of the present invention comprises the fuel additive described above and further comprises a solvent and/or one or more additional performance additives. These additive compositions, also known as additive concentrates and/or concentrates, may be used to prepare fuel compositions by adding the additive composition to an non-additized fuel.
  • the solvents suitable for use in the present invention include hydrocarbon solvents that provide for the additive composition's compatibility and/or homogeneity and to facilitate their handling and transfer and may include a fuel as described below.
  • the solvent can be an aliphatic hydrocarbon, an aromatic hydrocarbon, an oxygen-containing composition, or a mixture thereof. In some embodiments the flash point of the solvent is generally about 25°C or higher.
  • the hydrocarbon solvent is an aromatic naphtha having a flash point above 62°C or an aromatic naphtha having a flash point of 40 0 C or a kerosene with a 16% aromatic content having a flash point above 62°C.
  • Aliphatic hydrocarbons include various naphtha and kerosene boiling point fractions that have a majority of aliphatic components.
  • Aromatic hydrocarbons include benzene, toluene, xylenes and various naphtha and kerosene boiling point fractions that have a majority of aromatic components.
  • Alcohols are usually aliphatic alcohols having about 2 to 10 carbon atoms and include ethanol, 1-propanol, isopropyl alcohol, 1-butanol, isobutyl alcohol, amyl alcohol, and 2-methyl- 1-butanol.
  • the oxygen containing composition can include an alcohol, a ketone, an ester of a carboxylic acid, a glycol and/or a polyglycol, or a mixture thereof.
  • the solvent in an embodiment of the invention will be substantially free of to free of sulphur having a sulphur content in several instances that is below 50 ppm, 25 ppm, below 18 ppm, below 10 ppm, below 8 ppm, below 4 ppm, or below 2 ppm.
  • the solvent can be present in the additive concentrate composition at 0 to 99 percent by weight, and in other instances at 3 to 80 percent by weight, or 10 to 70 percent by weight.
  • the friction modifier of the present invention and the additional performance additives taken separately or in combination can be present in the additive concentrate composition at 0.01 to 100 percent by weight, and in other instances can be present at 0.01 to 95 percent by weight, at 0.01 to 90 percent by weight, or at 0.1 to 80 percent by weight.
  • the additive concentrate may comprise the fuel additive of the present invention and be substantially free of any additional solvent.
  • the additive concentrate containing the fuel additive of the present invention is neat, in that it does not contain any additional solvent added to improve the material handling characteristics of the concentrate, such as its viscosity.
  • the fuel composition, fuel additive concentrate, and/or the fuel additive itself are substantially free of or free of at least one member selected from the group consisting of sulphur, phosphorus, sulfated ash, and combinations thereof, and in other embodiments the fuel composition contains less than 50 ppm, 20 ppm, less than 15 ppm, less than 10 ppm, or less than 1 ppm of any one or all of these members.
  • the additive concentrate composition, or a fuel composition containing the fuel additive of the present invention may be prepared by admixing or mixing the components of the composition at ambient to elevated temperatures usually up to 6O 0 C until the composition is homogeneous.
  • the fuel composition of the present invention comprises the fuel additive described above and a liquid fuel, and is useful in fueling an internal combustion engine.
  • a fuel may also be a component of the additive compositions described above.
  • the fuels suitable for use in the present invention include any commercially available fuels, and in some embodiments any commercially available diesel fuels and/or biofuels. In other embodiments, the fuels suitable for use in the present invention include any commercially available fuels which are susceptible to metal pick up, and in some embodi- ments any commercially available diesel fuels and/or biofuels susceptible to metal pick up.
  • the fuels suitable for use in the present invention are any fuels, or any diesel fuels and/or biofuels, which are susceptible to pick up of oxidative metals to a level greater than 0.5 ppm when left in contact for an extended period of time with solid materials containing said metal.
  • the exposure time involved is greater than 72 hours, greater than 48 hours, or greater than 24 hours.
  • the present invention includes fuel compositions and fuel additive concentrate compositions which may contain fuel.
  • the fuel used in these compositions may or may not exhibit a propensity to pick up oxidative metal, and may in fact be any of the fuels described in this application or combinations thereof.
  • the fuel used in these compositions need not be the same fuel to which the additive of the present invention may be added in the methods described herein. That is, the additive of the present invention may be present in a composition that also comprises a fuel. This fuel may or may not exhibit a propensity to pick up oxidative metal.
  • the additive-containing composition may then be added to a fuel and/or fuel additive composition.
  • the identity of the fuel present in this composition is independent of the identity of the optional fuel component in the additive containing composition.
  • the oxidative metal pick-up propensity of the fuel and/or fuel additive composition may be a result of the properties of the fuel and/or the properties of one or more of the additives present in the fuel and /or additive composition.
  • the addition of the additive- containing compositions, as described in the method and compositions of the present invention result in a reduction of the oxidative metal pick-up propensity of the fuel and/or fuel additive compositions.
  • Fuels suitable for use in the present invention are not overly limited. Generally, suitable fuels are normally liquid at ambient conditions e.g., room temperature (20 to 30 0 C). The liquid fuel can be a hydrocarbon fuel, a non- hydrocarbon fuel, or a mixture thereof.
  • the hydrocarbon fuel can be a petroleum distillate, including a gasoline as defined by ASTM specification D4814, or a diesel fuel, as defined by ASTM specification D975.
  • the liquid fuel is a gasoline, and in another embodiment the liquid fuel is a non-leaded gasoline.
  • the liquid fuel is a diesel fuel.
  • the hydrocarbon fuel can be a hydrocarbon prepared by a gas to liquid process to include for example hydrocarbons prepared by a process such as the Fischer-Tropsch process.
  • the fuel used in the present invention is a diesel fuel, a biodiesel fuel, or combinations thereof.
  • the non-hydrocarbon fuel can be an oxygen containing composition, often referred to as an oxygenate, which includes an alcohol, an ether, a ketone, an ester of a carboxylic acid, a nitroalkane, or a mixture thereof.
  • the non- hydrocarbon fuel can include for example methanol, ethanol, methyl t-butyl ether, methyl ethyl ketone, transesterified oils and/or fats from plants and animals such as rapeseed methyl ester and soybean methyl ester, and nitro- methane.
  • Mixtures of hydrocarbon and non-hydrocarbon fuels can include, for example, gasoline and methanol and/or ethanol, diesel fuel and ethanol, and diesel fuel and a transesterified plant oil such as rapeseed methyl ester and other bio-derived fuels.
  • the liquid fuel is an emulsion of water in a hydrocarbon fuel, a non-hydrocarbon fuel, or a mixture thereof.
  • the liquid fuel can have a sulphur content on a weight basis that is 5000 ppm or less, 1000 ppm or less, 300 ppm or less, 200 ppm or less, 30 ppm or less, or 10 ppm or less.
  • the liquid fuel of the invention is present in a fuel composition in a major amount that is generally greater than 95% by weight, and in other embodiments is present at greater than 97% by weight, greater than 99.5% by weight, or greater than 99.9% by weight. Additional Performance Additives
  • the additive compositions and fuel compositions of the present invention can further comprise one or more additional performance additives.
  • Additional performance additives can be added to a fuel composition depending on several factors to include the type of internal combustion engine and the type of fuel being used in that engine, the quality of the fuel, and the service conditions under which the engine is being operated.
  • the additional performance additives described herein may increase the tendency of a fuel composition to pick-up metals such as zinc.
  • the use of the present invention in such situations can reduce and/or eliminate this impact of the additional additives.
  • the additional performance additives can include: an antioxidant such as a hindered phenol or derivative thereof and/or a diarylamine or derivative thereof; a corrosion inhibitor; and/or a detergent/dispersant additive, other than the fuel additive of the present invention, such as a polyetheramine or nitrogen containing detergent, including but not limited to PIB amine dispers- ants, quaternary salt dispersants, and succinimide dispersants including deri- vates of succinimide dispersants such as quaternary ammonium salts thereof.
  • an antioxidant such as a hindered phenol or derivative thereof and/or a diarylamine or derivative thereof
  • a corrosion inhibitor such as a corrosion inhibitor
  • a detergent/dispersant additive other than the fuel additive of the present invention, such as a polyetheramine or nitrogen containing detergent, including but not limited to PIB amine dispers- ants, quaternary salt dispersants, and succinimide dispersants including deri- vates of succinimide dispersants such
  • the additional performance additives may also include: a cold flow improver such as an esterified copolymer of maleic anhydride and styrene and/or a copolymer of ethylene and vinyl acetate; a foam inhibitor and/or antifoam agent such as a silicone fluid; a demulsifier such as a polyalkoxylated alcohol; a lubricity agent such as a fatty carboxylic acid; a metal deactivator such as an aromatic triazole or derivative thereof, including but not limited to benzotriazole; and/or a valve seat recession additive such as an alkali metal sulfosuccinate salt.
  • a cold flow improver such as an esterified copolymer of maleic anhydride and styrene and/or a copolymer of ethylene and vinyl acetate
  • a foam inhibitor and/or antifoam agent such as a silicone fluid
  • a demulsifier such as a polyalkoxylated alcohol
  • Suitable antifoams also include organic silicones such as polydi- methyl siloxane, polyethylsiloxane, polydiethylsiloxane, polyacrylates and polymethacrylates, trimethyl-triflouro-propylmethyl siloxane and the like.
  • the additional additives may also include a biocide; an antistatic agent, a deicer, a fluidizer such as a mineral oil and/or a poly(alpha-olefin) and/or a polyether, and a combustion improver such as an octane or cetane improver.
  • the additional performance additives which may be present in the fuel additive compositions and fuel compositions of the present invention, also include di-ester, di-amide, ester-amide, and ester-imide friction modifiers prepared by reacting a dicarboxylic acid (such as tartaric acid) and/or a tricarboxylic acid (such as citric acid), with an amine and/or alcohol, optionally in the presence of a known esterification catalyst.
  • These friction modifiers often derived from tartaric acid, citric acid, or derivatives thereof, may be derived from amines and/or alcohols that are branched so that the friction modifier itself has significant amounts of branched hydrocarbyl groups present within it structure. Examples of a suitable branched alcohols used to prepare these friction modifiers include 2-ethylhexanol, isotridecanol, Guerbet alcohols, or mixtures thereof.
  • the additional performance additives may comprise a high TBN nitrogen containing dispersant, such as a succinimide dispersant, that is the condensation product of a hydrocarbyl-substituted succinic anhydride with a poly (alky leneamine).
  • a succinimide dispersant that is the condensation product of a hydrocarbyl-substituted succinic anhydride with a poly (alky leneamine).
  • Succnimide dispersants are very well known in the art of lubricant formulation. Such molecules are commonly derived from reaction of an alkenyl acylating agent with a polyamine, and a wide variety of linkages between the two moieties is possible including a simple imide structure as well as a variety of amides and quaternary ammonium salts. Succinimide dispersants are more fully described in U.S. Patents 4,234,435 and 3,172,892. Such materials may also contain ester linkages or ester functionality.
  • Mannich bases are materials which are formed by the condensation of a higher molecular weight, alkyl substituted phenol, an alkylene polyamine, and an aldehyde such as formaldehyde. Such materials are described in more detail in U.S. Patent 3,634,515.
  • nitrogen-containing dispersants include polymeric dispersant additives, which are generally hydrocarbon-based polymers which contain nintrogen-containing polar functionality to impart dispersancy characteristics to the polymer.
  • An amine is typically employed in preparing the high TBN nitrogen- containing dispersant.
  • One or more poly(alkyleneamine)s may be used, and these may comprise one or more poly(ethyleneamine)s having 3 to 5 ethylene units and 4 to 6 nitrogens.
  • Such materials include triethylenetetramine (TETA), tetraethylenepentamine (TEPA), and pentaethylenehexamine (PEHA).
  • TETA triethylenetetramine
  • TEPA tetraethylenepentamine
  • PEHA pentaethylenehexamine
  • Such materials are typically commercially available as mixtures of various isomers containing a range number of ethylene units and nitrogen atoms, as well as a variety of isomeric structures, including various cyclic structures.
  • the poly (alky leneamine) may likewise comprise relatively higher molecular weight amines known in the industry as ethylene amine still bottoms.
  • the additional performance additives may comprise a quaternary salt comprising the reaction product of: (i) at least one compound selected from the group consisting of: (a) the condensation product of a hydrocarbyl-substituted acylating agent and a compound having an oxygen or nitrogen atom capable of condensing with said acylating agent and said condensation product further having a tertiary amino group; (b) a polyalkene-substituted amine having at least one tertiary amino group; and (c) a Mannich reaction product having a tertiary amino group, said Mannich reaction product being prepared from the reaction of a hydrocarbyl-subsituted phenol, an aldehyde, and an amine; and (ii) a quaternizing agent suitable for converting the tertiary amino group of compound (i) to a quaternary nitrogen, wherein the quaternizing agent is selected from the group consisting of dialkyl sulfates,
  • the quaternary salt comprises the reaction product of (i) at least one compound selected from the group consisting of: a polyalkene-substituted amine having at least one tertiary amino group and/or a Mannich reaction product having a tertiary amino group; and (ii) a quaternizing agent.
  • the quaternary salt comprises the reaction product of (i) the reaction product of a succinic anhydride and an amine; and (ii) a quaternizing agent.
  • the succinic anhydride may be derived from polyisobutylene and an anhydride, where the polyisobutylene has a number average molecular weight of about 800 to about 1600. In some embodiments the succinic anhydride is chlorine free.
  • the hydrocarbyl substituted acylating agent of component (i)(a) described above is the reaction product of a long chain hydrocarbon, generally a polyolefin substituted with a monounsaturated carboxylic acid reactant such as (1) monounsaturated C 4 to C 10 dicarboxylic acid such as fumaric acid, itaconic acid, maleic acid.; (2) derivatives of (1) such as anhydrides or Ci to C 5 alcohol derived mono- or di-esters of (1); (3) monounsaturated C3 to Cio mono carboxylic acid such as acrylic acid and methacrylic acid.; or (iv4 derivatives of (3) such as Ci to C5 alcohol derived esters of (3) with any compound containing an olefinic bond represented by the general formula:
  • Olefin polymers for reaction with the monounsaturated carboxylic acids can include polymers comprising a major molar amount of C 2 to C20, e.g. C 2 to C5 monoolefin.
  • Such olefins include ethylene, propylene, butylene, isobutylene, pentene, octene-1, or styrene.
  • the polymers can be homopolymers such as polyisobutylene, as well as copolymers of two or more of such olefins such as copolymers of; ethylene and propylene; butylene and isobutylene; propylene and isobutylene.
  • Other copolymers include those in which a minor molar amount of the copolymer monomers e.g., 1 to 10 mole % is a C 4 to C 18 diolefin, e.g., a copolymer of isobutylene and butadiene; or a copolymer of ethylene, propylene and 1,4-hexadiene.
  • At least one R of formula (I) is derived from polybutene, that is, polymers of C 4 olefins, including 1-butene, 2-butene and isobutylene.
  • C 4 polymers can include polyisobutylene.
  • at least one R of formula (I) is derived from ethylene-alpha olefin polymers, including ethylene-propylene-diene polymers.
  • Ethylene-alpha olefin copoly- mers and ethylene-lower olefin-diene terpolymers are described in numerous patent documents, including European patent publication EP0279863 and the following United States patents: 3,598,738; 4,026,809; 4,032,700; 4,137,185; 4,156,061; 4,320,019; 4,357,250; 4,658,078; 4,668,834; 4,937,299; 5,324,800 each of which are incorporated herein by reference for relevant disclosures of these ethylene based polymers.
  • the olefinic bonds of formula (I) are predominantly vinylidene groups, represented by the following formulas:
  • R 2 is a hydrocarbyl group, and in some embodiments both R 2 groups are methyl groups
  • the vinylidene content of formula (I) can comprise at least about 30 mole % vinylidene groups, at least about 50 mole % vinylidene groups, or at least about 70 mole % vinylidene groups.
  • Such material and methods for preparing them are described in U.S. Pat. Nos. 5,071,919; 5,137,978; 5,137,980; 5,286,823, 5,408,018, 6,562,913, 6,683,138, 7,037,999 and U.S. Publication Nos.
  • the hydrocarbyl substituted acylating agent can be made from the reaction of at least one carboxylic reactant represented by the following formulas: (R 4 C(O)(R 5 ) n C(O))R 4 (IV) and
  • each R 4 is independently H or a hydrocarbyl group
  • each R 5 is a divalent hydrocarbylene group and n is 0 or 1 with any compound containing an olefin bond as represented by formula (I).
  • Compounds and the processes for making these compounds are disclosed in U.S. Pat. Nos. 5,739,356; 5,777,142; 5,786,490; 5,856,524; 6,020,500; and 6,114,547 which are hereby incorporated by reference.
  • Other methods of making the hydrocarbyl substituted acylating agent can be found in the following reference, U.S. Pat. Nos. 5,912,213; 5,851,966; and 5,885,944 which are hereby incorporated by reference.
  • the compound having an oxygen or nitrogen atom capable of condensing with the acylating agent and further having a tertiary amino group can be represented by the following formulas:
  • N—X—N wherein X is a alkylene group containing about 1 to about 4 carbon atoms; and wherein each R 6 is independently a hydrocarbyl group, and R 6 can be hydrogen or a hydrocarbyl group.
  • Examples of the nitrogen or oxygen contain compounds capable of condensing with the acylating agent and further having a tertiary amino group can include but are not limited to: ethylenedi amine, 1 ,2-propylenediamine, 1,3- propylene diamine, the isomeric butylenediamines, pentanediamines, hex- anediamines, heptanediamines, diethylenetri amine, dipropylenetriamine, dibuty- lenetriamine, triethylenetetraamine, tetraethylenepentaamine, pentaethylene- hexaamine, hexamethylenetetramine, and bis(hexamethylene) triamine, the diaminobenzenes, the diaminopyridines or mixtures thereof.
  • nitrogen or oxygen contain compounds which may be alkylated to contain a tertiary amino group may also used.
  • examples of the nitrogen or oxygen contain compounds capable of condensing with the acylating agent after being alkylated to having a tertiary amino group can include but are not limited to: dimethyl- aminopropylamine, N,N-dimethyl-aminopropylamine, N,N-diethyl- aminopropylamine, N,N-dimethyl-aminoethylamine or mixtures thereof.
  • the nitrogen or oxygen containing compounds capable of condensing with the acylating agent and further having a tertiary amino group can further include aminoalkyl substituted heterocyclic compounds such as l-(3-aminopropyl)imidazole and 4-(3-aminopropyl)morpholine, l-(2-aminoethyl)piperidine, 3,3-diamino-N-methyldipropylamine,
  • Another type of nitrogen or oxygen containing compounds capable of condensing with the acylating agent and having a tertiary amino group include alkanolamines including but not limited to triethanolamine, N,N-dimethylaminopropanol, N,N-diethylaminopropanol, N,N-diethylaminobutanol, N,N,N-tris(hydroxyethyl)amine, or mixtures thereof.
  • the additional performance additives can each be added directly to the additive and/or the fuel compositions of the present invention, but they are generally mixed with the fuel additive to form an additive composition, or concentrate, which is then mixed with fuel to result in a fuel composition.
  • the additive concentrate compositions are described in more detail above.
  • these additional performance additives described above may be the cause and/or a contributing factor to the propensity of a fuel to pick up oxidative metal in the fuel compositions in which they are used.
  • the additives described above may have no impact on the metal pick-up properties of the fuel composition in which they are used.
  • the additive compositions and methods of the present invention can counter the potential effect of these additives and reduce the tendency of fuel compositions to pick-up metals, whether that tendency is caused, exacerbated by, or not significantly changes by, the additional performance additives described above.
  • the invention is useful for a liquid fuel and/or for the operation of an internal combustion engine, including either compression ignition engines or spark ignited engines.
  • the internal combustion engine includes 2-stroke or 4-stroke engines fuelled with gasoline, diesel, a natural gas, a mixed gasoline/alcohol or any of the fuels described in the sections above.
  • the compression ignition engines include both light duty and heavy duty diesel engines.
  • the spark ignited engines include port and direct injection gasoline engines.
  • the invention is useful in additive compositions in that the fuel additive and methods described above reduce metal pick-up in fuel compositions, thus preventing elevated levels of metals, such as zinc, in the fuel.
  • the additive compositions of the present invention may be used in a lubricating composition such that the additives are present in the lubricating system of the engine.
  • the additives may also enter the combustion chamber of the engine during operation of the engine by the transfer of small amounts of the additive containing lubricating composition to the combustion chamber due to a phenomenon referred to as "blow by" where the lubricating composition, and in this case the additive composition, pass around the piston heads inside the cylinder, moving from the lubricating system of the engine into the combustion chamber.
  • the methods and/or compositions of the present invention provide a reduction in metal pick-up of at least 5%, at least 20% or even at least 50%. In some of these embodiments the reduction is in regards to the 7 day and/or 14 day result of the test procedure used in the examples below. In other embodiments the methods and/or compositions of the present invention ensure the metal level of a fuel composition does not rise above 10 ppm, 5 ppm, 1 ppm. 0.5 ppm, 0.3 ppm or even 0.1 ppm of metal content. In some of these embodiments the reduction is in regards to the 7 day and/or 14 day result of the test procedure used in the examples below.
  • the methods and/or compositions of the present invention when evaluated at 7 days by the test described in the examples below, provide a reduction in metal levels of at least 30%, or at least 80% and/or ensure metal levels to not rise above 1 ppm. In some embodiments, the methods and/or compositions of the present invention, when evaluated at 14 days by the test described in the examples below, provide a reduction in metal levels of at least 40%, or at least 80% and/or ensure metal levels to not rise above 8 ppm, or even 1 ppm.
  • the present invention includes the use of the substituted hydrocarbon and/or hydrocarbyl substituted acylating agents described herein as additives in fuel compositions, as well as the additive itself and the fuel and fuel additive compositions containing said additive.
  • the additives of the present invention may be delivered to the fuel compositions and/or fuel additive compositions in any of the means known in the art and the timing of the additive is not limited.
  • the additive of the present invention may be added to a fuel composition before, during, or after the production and/or blending of the fuel and/or additive composition.
  • the additive of the invention may be added to fuel and/or additive composition before, during, or after the addition of other performance additives which may be used in the compositions.
  • the additive of the invention may be added as a top treat to fuel and/or additive compositions or be incorporated into the production and/or distribution of the fuel and/or additive compositions in which it is used.
  • hydrocarbyl substituent or “hydrocarbyl group” is used in its ordinary sense, which is well-known to those skilled in the art. Specifically, it refers to a group having a carbon atom directly attached to the remainder of the molecule and having predominantly hydrocarbon character.
  • hydrocarbyl groups include: hydrocarbon substituents, that is, aliphatic (e.g., alkyl or alkenyl), alicyclic (e.g., cycloalkyl, cycloalkenyl) substituents, and aromatic-, aliphatic-, and alicyclic-substituted aromatic substituents, as well as cyclic substituents wherein the ring is completed through another portion of the molecule (e.g., two substituents together form a ring); substituted hydrocarbon substituents, that is, substituents containing non- hydrocarbon groups which, in the context of this invention, do not alter the predominantly hydrocarbon nature of the substituent (e.g., halo (especially chloro and fluoro), hydroxy, alkoxy, mercapto, alkylmercapto, nitro, nitroso, and sulfoxy); hetero substituents, that is, substituents which, while having a predominantly hydrocarbon character, in the context of this invention,
  • Heteroatoms include sulfur, oxygen, nitrogen, and encompass substituents as pyridyl, furyl, thienyl and imidazolyl.
  • substituents as pyridyl, furyl, thienyl and imidazolyl.
  • no more than two, preferably no more than one, non-hydrocarbon substituent will be present for every ten carbon atoms in the hydrocarbyl group; typically, there will be no non- hydrocarbon substituents in the hydrocarbyl group.
  • Example Set 1 Fuel treated with a succinimide dispersant.
  • An EU certification diesel fuel known as RF-06, is treated with 200 ppm of a commercially available succinimide dispersant.
  • Seven 500 ML graduated cylinder are prepared for testing by placing in each a 4 cm section of a Goodfellow Zn rod ZN007902, having a length of 200 mm and a diameter of 2.0 mm. The weight of each rod section is recorded and an amount of fuel is added to each cylinder so that the combined mixture of fuel composition and zinc rod is 1 % by weight zinc.
  • Each cylinder is charged with a slightly different amount of fuel to ensure the zinc content of each sample is the same.
  • One of the seven samples (1-1) is kept as a baseline.
  • the other seven samples (1-2 to 1-7) are each independently treated at 200 ppm with an additional additive, as shown the in the table below.
  • Example Set 1 The containers are stored at ambient conditions in a dark test location for 14 days. Each sample is tested at the 7 day mark and the 14 day mark by Inductively Coupled Plasma (ICP) analysis to determine zinc content.
  • ICP Inductively Coupled Plasma
  • Example Set 2 Biodiesel.
  • Example set 1 is repeated except that the succinimide dispersant treated diesel fuel is replaced with BlOO, a commercially available biodiesel fuel.
  • each additional additive in samples 2-2 to 2-7 are present in the fuel composition at 500 ppm.
  • Samples 2-1 to 2-7 are tested in the same manner described above and the results are summarized in the table below.
  • Table 3 Results from Example Set 2.
  • each chemical component is presented exclusive of any solvent or diluent, which may be customarily present in the commercial material, unless otherwise indicated. It is to be understood that the upper and lower amount, range, and ratio limits set forth herein may be independently combined. Similarly, the ranges and amounts for each element of the invention can be used together with ranges or amounts for any of the other elements. As used herein, the expression "consisting essentially of permits the inclusion of substances that do not materially affect the basic and novel characteristics of the composition under consideration.

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Abstract

L'invention concerne des additifs pour carburant, des compositions d'additifs pour carburant et des compositions de carburant, ainsi qu'un procédé d'alimentation d'un moteur à combustion interne, procurant une réduction de l'arrachement de métal par les carburants, les compositions de la présente invention contenant un hydrocarbure substitué avec au moins deux fonctionnalités carboxy sous la forme d'acides ou au moins une fonctionnalité carboxy sous la forme d'un anhydride.
EP09737254.4A 2008-10-10 2009-10-01 Additifs pour carburants permettant de réduire l'arrachement de métal Active EP2385977B2 (fr)

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DK16185196.9T DK3127992T3 (en) 2008-10-10 2009-10-01 ADDITIVES TO REDUCE METAL COLLECTION IN FUELS
PL16185196T PL3127992T3 (pl) 2008-10-10 2009-10-01 Dodatki do obniżania odbioru metalu w paliwach
EP18211764.8A EP3486300A1 (fr) 2008-10-10 2009-10-01 Additifs pour carburants permettant de réduire l'arrachement de métal
PL09737254T PL2385977T5 (pl) 2008-10-10 2009-10-01 Dodatki do obniżania odbioru metalu w paliwach
EP16185196.9A EP3127992B1 (fr) 2008-10-10 2009-10-01 Additifs pour carburants permettant de réduire l'arrachement de métal

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PCT/US2009/059164 WO2010042378A1 (fr) 2008-10-10 2009-10-01 Additifs pour carburants permettant de réduire l'arrachement de métal

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EP18211764.8A Division EP3486300A1 (fr) 2008-10-10 2009-10-01 Additifs pour carburants permettant de réduire l'arrachement de métal
EP16185196.9A Division EP3127992B1 (fr) 2008-10-10 2009-10-01 Additifs pour carburants permettant de réduire l'arrachement de métal
EP16185196.9A Division-Into EP3127992B1 (fr) 2008-10-10 2009-10-01 Additifs pour carburants permettant de réduire l'arrachement de métal

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CN106753620A (zh) 2017-05-31
PL2385977T5 (pl) 2020-07-27
WO2010042378A1 (fr) 2010-04-15
EP2385977B1 (fr) 2016-08-24
EP3127992A1 (fr) 2017-02-08
CA2739432A1 (fr) 2010-04-15
JP6046347B2 (ja) 2016-12-14
KR20110069846A (ko) 2011-06-23
EP2385977B2 (fr) 2020-01-01
CA3025740C (fr) 2021-11-09
DK2385977T4 (da) 2020-03-09
AU2017251765B2 (en) 2019-05-09
CA3025740A1 (fr) 2010-04-15
AU2016204848A1 (en) 2016-07-28
SG194415A1 (en) 2013-11-29
AU2009302649A1 (en) 2010-04-15
CA2739432C (fr) 2018-12-04
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JP2015147942A (ja) 2015-08-20
PL2385977T3 (pl) 2017-02-28
BR122018075929B1 (pt) 2022-09-27
CN102239238A (zh) 2011-11-09
DK3127992T3 (en) 2019-03-18
PL3127992T3 (pl) 2019-06-28
JP2017101259A (ja) 2017-06-08
US20110219674A1 (en) 2011-09-15
BRPI0920665B1 (pt) 2022-09-20
EP3486300A1 (fr) 2019-05-22
JP2013234336A (ja) 2013-11-21
JP2012505291A (ja) 2012-03-01
BRPI0920665A2 (pt) 2018-06-26
EP3127992B1 (fr) 2018-12-12

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