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US20070144061A1 - Alkoxylated unsaturated carboxylic acid additives for low-sulfur fuels - Google Patents

Alkoxylated unsaturated carboxylic acid additives for low-sulfur fuels Download PDF

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Publication number
US20070144061A1
US20070144061A1 US11/567,610 US56761006A US2007144061A1 US 20070144061 A1 US20070144061 A1 US 20070144061A1 US 56761006 A US56761006 A US 56761006A US 2007144061 A1 US2007144061 A1 US 2007144061A1
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composition according
weight
composition
additive
diesel
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US11/567,610
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Frank Bongardt
Juergen Roeder
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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
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/08—Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
    • C10L1/191—Esters ester radical containing compounds; ester ethers; carbonic acid esters of di- or polyhydroxyalcohols

Definitions

  • Fuels based on petroleum or petroleum derivatives generally contain small amounts of sulfur. Crude oils normally contain between 2 and 0.5% by weight of sulfur. In the combustion of these sulfur-containing fuels, sulfur dioxide is formed as a combustion product and is oxidized in air to sulfuric acid which can cause serious environmental damage in the form of acid rain. Accordingly, there has long been a demand to reduce the sulfur content in petroleum products, more particularly in fuels. However, not only does sulfur have adverse effects, it also serves in the small quantities in which it is normally present as a lubricant improver which is entirely desirable in many technical applications, for example as a fuel for combustion engines. Accordingly, the use of low-sulfur fuels often leads to problems to do with the friction of the correspondingly fuelled machine parts.
  • the present invention relates, in general, to low-sulfur fuel compositions which contain certain alkoxylated esters as additives.
  • formula (I) R—COO—(C n H 2n —O) k —H
  • the fuel compositions according to the invention are further distinguished by the fact that the sulfur content is at most 0.2% by weight, based on the fuel composition.
  • Fuels in the context of the present invention are understood to be any energy-yielding working materials of which the free combustion energy is converted into mechanical work. Such materials include all types of motor and aircraft fuels which are liquid at room temperature and normal pressure. Motor fuels, for example for automobile and truck engines, generally contain hydrocarbons, for example gasoline or higher-boiling petroleum fractions.
  • Diesel fuels are low-inflammability mixtures of liquid hydrocarbons which are used as fuels for constant-pressure or compression-ignition engines (diesel engines) and which consist predominantly of paraffins with impurities in the form of olefins, naphthenes and aromatic hydrocarbons. Their composition is variable and depends in particular upon the production method. Diesel is obtained, for example, from gas oil by cracking or from tars obtained in the low-temperature carbonization of brown coal or hard coal. Typical products have densities of 0.83 to 0.88 g/cm 3 , boiling points in the range from 170 to 360° C. and flash points of 70 to 100° C. Diesel oils for stationary plant and for marine engines are similar in composition to heavy fuel oil while those for automobiles, buses and trucks correspond to fuel oil.
  • Ignition response is the capacity of a motor fuel to ignite relatively easily or with relative difficulty in an engine operating on the diesel principle. With every fuel, this requires not only atomization, pressure and temperature, but also a conditioning interval (ignition delay) before discernible combustion.
  • Good ignition response of a fuel means favorable starting behavior and quiet running of the diesel engine by virtue of a short conditioning interval or small ignition delay. With a large ignition delay, the known phenomenon of “knocking” comes audibly into play.
  • the requirements for diesel fuels are a cetane number of 20 to 40 for slow-running engines and a cetane number of >45 for small and fast-running engines. Other desirable properties include a low pour point, a low content of incombustible or soot-forming substances and a low sulfur content.
  • the fuel compositions according to the invention contain diesel, gasoline, kerosene or other hydrocarbons liquid at room temperature, for example hexane or pentane. Fuel compositions containing diesel as fuel are particularly preferred. In principle, the fuel compositions according to the invention may also contain mixtures of, for example, gasoline and kerosene in any ratio.
  • the additives of formula (I) are alkoxylated carboxylic acid esters known per se. It is one of the key aspects of the present invention that the carboxylic acids must be unsaturated carboxylic acids containing 11 to 17 carbon atoms in the alkyl chain. Compounds of formula (I), in which R is an unsaturated group containing 17 carbon atoms, are particularly preferred. Oleic acid is particularly preferred for the purposes of the invention.
  • the alkoxylation i.e. the reaction of the acid with ethylene oxide and/or propylene oxide, is carried out in known manner, cf. for example U.S. Pat. No. 5,326,891 or U.S. Pat. No.
  • the fuel compositions according to the invention contain the additives of formula (I) in quantities of preferably 0.001 to 0.01% by weight and more preferably 0.001 to 0.005% by weight. Oleic acid esters containing 1 part ethylene oxide are particularly preferred.
  • the additives of formula (I) according to the invention are used in fuel compositions with an extremely low sulfur content, i.e. a sulfur content of 0.005 to at most 0.05% by weight. In a most particularly preferred embodiment, they are used in fuel compositions with a sulfur content below 0.005% by weight.
  • the aromatics content of the claimed fuel compositions should be below 25% by volume and is preferably below 20% by volume. Fuel compositions containing less than 5% by volume of aromatics are particularly preferred, fuel compositions free from aromatics being most particularly preferred.
  • diesel If diesel is selected as the actual fuel, it should have a cetane number below 50 and preferably below 45. The cetane number of the diesel should be below 50.
  • the HFRR value at 60° C. being 600 ⁇ m, preferably at most 500 ⁇ m and more particularly 400 ⁇ m or less.
  • the HFFR (high-frequency reciprocating rig) value is used to measure the friction of fuels in use. A detailed description of this method can be found in ISO/TC22/SC7/WG6/N188.
  • the fuels according to the invention may contain other typical additives, for example cetane number improvers (saltpeter or nitrous ester), corrosion inhibitors, flow enhancers, surfactants (which keep the fuel injectors clean), defoamers and smoke reducers.
  • cetane number improvers saltpeter or nitrous ester
  • corrosion inhibitors corrosion inhibitors
  • flow enhancers surfactants (which keep the fuel injectors clean)
  • defoamers and smoke reducers for example cetane number improvers (saltpeter or nitrous ester), corrosion inhibitors, flow enhancers, surfactants (which keep the fuel injectors clean), defoamers and smoke reducers.
  • the HFRR value of the additive-free diesel was 591 ⁇ m. A value of 529 ⁇ m was measured for the GMO-containing diesel whereas the additive according to the invention achieved an HFRR value of 500 ⁇ m.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Abstract

Compositions comprising: (i) a fuel component selected from the group consisting of diesel, gasoline, kerosene, other hydrocarbons which are liquid at room temperature and mixtures thereof; and (ii) and an additive of the general formula (I) are described:
R—COO—(CnH2n—O)k—H  (I) wherein R represents a mono- or poly-unsaturated alkylene group having from 10 to 17 carbon atoms, n is 2 or 3, and k represents a number of from 0.5 to 3; wherein the fuel component is present in an amount of more than 50% by weight, wherein the additive is present in an amount of from 0.001 to 0.1% by weight; and wherein the composition has a sulfur content of 0.2% by weight or less, all weight percents based on the composition.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation of application Ser. No. 10/495,802, filed May 17, 2004, which is a national stage entry of International Application No. PCT/EP02112371, filed on Nov. 6, 2002 which designated the United States of America and which claims priority of German Patent Application number DE 10156024.9, filed Nov. 15, 2001, the entire contents of each of which are hereby incorporated by reference.
    • BACKGROUND OF THE INVENTION
  • Fuels based on petroleum or petroleum derivatives generally contain small amounts of sulfur. Crude oils normally contain between 2 and 0.5% by weight of sulfur. In the combustion of these sulfur-containing fuels, sulfur dioxide is formed as a combustion product and is oxidized in air to sulfuric acid which can cause serious environmental damage in the form of acid rain. Accordingly, there has long been a demand to reduce the sulfur content in petroleum products, more particularly in fuels. However, not only does sulfur have adverse effects, it also serves in the small quantities in which it is normally present as a lubricant improver which is entirely desirable in many technical applications, for example as a fuel for combustion engines. Accordingly, the use of low-sulfur fuels often leads to problems to do with the friction of the correspondingly fuelled machine parts. In order to meet environmental and emission control requirements on the one hand and friction coefficient requirements on the other hand, additives are normally incorporated in the fuels. It is known from WO 94/17160 that esters of carboxylic acids and alcohols containing more than 1 carbon atom are added to low-sulfur fuels, preferably diesel fuels, to adjust the corresponding friction coefficients. Esters of C2-50 carboxylic acids and polyols are preferably used. However, the problem arises that, with small additions of expensive additives, the lubricating effect of the fuels thus obtained is not always satisfactory. Accordingly, the problem addressed by the present invention was to provide an additive for low-sulfur fuels which, even in small amounts, would enable the lubricating effect of fuels to be adequately improved.
    • BRIEF SUMMARY OF THE INVENTION
  • The present invention relates, in general, to low-sulfur fuel compositions which contain certain alkoxylated esters as additives.
  • Accordingly, the present invention relates to fuel compositions containing more than 50% by weight of diesel, gasoline, kerosene or other hydrocarbons liquid at room temperature, these fuel compositions containing an additive corresponding to formula (I):
    R—COO—(CnH2n—O)k—H  (I)
    where R is a mono- or polyunsaturated alkylene group containing 10 to 17 carbon atoms and n=2 or 3 and k is a number of 0.5 to 3, in quantities of 0.001 to 0.1% by weight, with the proviso that the fuel composition has a sulfur content of at most 0.2% by weight.
  • The fuel compositions according to the invention are further distinguished by the fact that the sulfur content is at most 0.2% by weight, based on the fuel composition.
    • DETAILED DESCRIPTION OF THE INVENTION
  • Fuels in the context of the present invention are understood to be any energy-yielding working materials of which the free combustion energy is converted into mechanical work. Such materials include all types of motor and aircraft fuels which are liquid at room temperature and normal pressure. Motor fuels, for example for automobile and truck engines, generally contain hydrocarbons, for example gasoline or higher-boiling petroleum fractions.
  • Diesel fuels are low-inflammability mixtures of liquid hydrocarbons which are used as fuels for constant-pressure or compression-ignition engines (diesel engines) and which consist predominantly of paraffins with impurities in the form of olefins, naphthenes and aromatic hydrocarbons. Their composition is variable and depends in particular upon the production method. Diesel is obtained, for example, from gas oil by cracking or from tars obtained in the low-temperature carbonization of brown coal or hard coal. Typical products have densities of 0.83 to 0.88 g/cm3, boiling points in the range from 170 to 360° C. and flash points of 70 to 100° C. Diesel oils for stationary plant and for marine engines are similar in composition to heavy fuel oil while those for automobiles, buses and trucks correspond to fuel oil.
  • During combustion in a diesel engine, air is taken into the cylinder, heated to 550-900° C. by high compression (compression ratio 14:1 to 25:1), so that a jet of diesel injected in ignites spontaneously and reaches a combustion pressure of 50-80 bar at a combustion temperature of 1500-2200° C. so that the piston is moved and work is done. 13 m3 air are used in the combustion of 1 liter of diesel in the diesel engine. The combustion energy released amounts to ca. 42,000 kJ/kg.
  • A key factor for the usability of diesel fuels is their ignition response which is quantitatively expressed by the cetane number. Ignition response is the capacity of a motor fuel to ignite relatively easily or with relative difficulty in an engine operating on the diesel principle. With every fuel, this requires not only atomization, pressure and temperature, but also a conditioning interval (ignition delay) before discernible combustion. Good ignition response of a fuel means favorable starting behavior and quiet running of the diesel engine by virtue of a short conditioning interval or small ignition delay. With a large ignition delay, the known phenomenon of “knocking” comes audibly into play. The requirements for diesel fuels are a cetane number of 20 to 40 for slow-running engines and a cetane number of >45 for small and fast-running engines. Other desirable properties include a low pour point, a low content of incombustible or soot-forming substances and a low sulfur content.
  • The fuel compositions according to the invention contain diesel, gasoline, kerosene or other hydrocarbons liquid at room temperature, for example hexane or pentane. Fuel compositions containing diesel as fuel are particularly preferred. In principle, the fuel compositions according to the invention may also contain mixtures of, for example, gasoline and kerosene in any ratio.
  • The additives of formula (I) are alkoxylated carboxylic acid esters known per se. It is one of the key aspects of the present invention that the carboxylic acids must be unsaturated carboxylic acids containing 11 to 17 carbon atoms in the alkyl chain. Compounds of formula (I), in which R is an unsaturated group containing 17 carbon atoms, are particularly preferred. Oleic acid is particularly preferred for the purposes of the invention. The alkoxylation, i.e. the reaction of the acid with ethylene oxide and/or propylene oxide, is carried out in known manner, cf. for example U.S. Pat. No. 5,326,891 or U.S. Pat. No. 5,292,910 which describe the synthesis of such compounds where the acids are reacted with the alkoxides in the presence of selected hydrotalcite catalysts to form the required alkoxylated compounds. Also of relevance in this regard is the disclosure of WO 98/25878 which describes a process for the synthesis of these “short-ethoxylated” fatty acids by reaction of the fatty acids in the presence of alkanolamines.
  • One feature of the present additives of formula (I) is that the number of alkoxide units per molecule is strictly limited and is preferably 1, i.e. 1 part acid and 1 part alkoxide have reacted. Since, in addition, the use of modern catalysts does not provide for uniform products, mixtures of different alkoxylated compounds are usually present which is expressed in the partly broken number k in formula (I). Compounds of formula (I) where n=2, i.e. ethoxylated fatty acids, are particularly preferred. The index k should preferably have a value of 0.5 to 1.5, compounds of formula (I) where k=1 being most particularly preferred. Compounds of formula (I) where k=1 and n=2 are also preferred. The fuel compositions according to the invention contain the additives of formula (I) in quantities of preferably 0.001 to 0.01% by weight and more preferably 0.001 to 0.005% by weight. Oleic acid esters containing 1 part ethylene oxide are particularly preferred.
  • In a particularly preferred embodiment, the additives of formula (I) according to the invention are used in fuel compositions with an extremely low sulfur content, i.e. a sulfur content of 0.005 to at most 0.05% by weight. In a most particularly preferred embodiment, they are used in fuel compositions with a sulfur content below 0.005% by weight. The aromatics content of the claimed fuel compositions should be below 25% by volume and is preferably below 20% by volume. Fuel compositions containing less than 5% by volume of aromatics are particularly preferred, fuel compositions free from aromatics being most particularly preferred.
  • If diesel is selected as the actual fuel, it should have a cetane number below 50 and preferably below 45. The cetane number of the diesel should be below 50.
  • The addition of the compounds of formula (I) leads to a good broad effect of the corresponding fuels, the HFRR value at 60° C. being 600 μm, preferably at most 500 μm and more particularly 400 μm or less. The HFFR (high-frequency reciprocating rig) value is used to measure the friction of fuels in use. A detailed description of this method can be found in ISO/TC22/SC7/WG6/N188.
  • The fuels according to the invention may contain other typical additives, for example cetane number improvers (saltpeter or nitrous ester), corrosion inhibitors, flow enhancers, surfactants (which keep the fuel injectors clean), defoamers and smoke reducers.
  • In choosing the additives for the fuel compositions according to the invention, it is important to bear in mind that the use of, for example, fatty alcohols and/or alkoxylated fatty alcohols and/or alkanolamides and/or derivatives thereof is preferably ruled out. Fuel compositions which contain only the additives of formula (I) for reducing friction are most particularly preferred.
  • The use of the above-defined compounds of formula (I) in fuels, more particularly in diesel fuels, leads on the one hand to satisfactory lubrication behavior of the fuels without any of the adverse ecological consequences typical of low-sulfur fuels. In addition, the fuels containing the additives according to the invention show excellent low-temperature behavior with no flocculation, even at low temperatures.
    • EXAMPLES
  • An oleic acid ester containing 1 mol ethylene oxide per mol fatty acid was tested for its effectiveness in reducing the friction coefficient of diesel (HFRR) by comparison with a commercially available glycerol mono-oleic acid ester (GMO). The additive was used in a quantity of 50 ppm. Additive-free diesel was used as the reference fuel.
  • The HFRR value of the additive-free diesel was 591 μm. A value of 529 μm was measured for the GMO-containing diesel whereas the additive according to the invention achieved an HFRR value of 500 μm.

Claims (20)

1-16. (canceled)
17. A composition comprising: (i) a fuel component selected from the group consisting of diesel, gasoline, kerosene, other hydrocarbons which are liquid at room temperature and mixtures thereof; and (ii) and an additive of the general formula (I):

R—COO—(CnH2n—O)k—H  (I)
wherein R represents a mono- or poly-unsaturated alkylene group having from 10 to 17 carbon atoms, n is 2 or 3, and k represents a number of from 0.5 to 3; wherein the fuel component is present in an amount of more than 50% by weight, wherein the additive is present in an amount of from 0.001 to 0.1% by weight; and wherein the composition has a sulfur content of 0.2% by weight or less, all weight percents based on the composition.
18. The composition according to claim 17, wherein n is 2.
19. The composition according to claim 17, wherein k represents a number of from 0.5 to 1.5.
20. The composition according to claim 17, wherein k is 1.
21. The composition according to claim 18, wherein k represents a number of from 0.5 to 1.5.
22. The composition according to claim 18, wherein k is 1.
23. The composition according to claim 17, wherein R represents a mono- or poly-unsaturated alkylene group having 17 carbon atoms.
24. The composition according to claim 17, wherein R represents a mono-unsaturated alkylene group having 17 carbon atoms.
25. The composition according to claim 21, wherein R represents a mono- or poly-unsaturated alkylene group having 17 carbon atoms.
26. The composition according to claim 21, wherein R represents a mono-unsaturated alkylene group having 17 carbon atoms.
27. The composition according to claim 17, wherein the additive is present in an amount of from 0.001 to 0.01% by weight.
28. The composition according to claim 23, wherein the additive is present in an amount of from 0.001 to 0.01% by weight.
29. The composition according to claim 25, wherein the additive is present in an amount of from 0.001 to 0.01% by weight.
30. The composition according to claim 17, wherein the composition has a sulfur content of from 0.005 to 0.05% by weight.
31. The composition according to claim 17, wherein the composition has a sulfur content of 0.005% by weight or less.
32. The composition according to claim 17, wherein the composition has an aromatic content of less than 25% by volume.
33. The composition according to claim 17, wherein the fuel component comprises a diesel having a cetane number below 50.
34. The composition according to claim 17, wherein the composition has an HFRR friction coefficient at 60° C. of at most 500 μm.
35. The composition according to claim 17, wherein the composition is free of fatty alcohols, alkoxylated fatty alcohols and alkanolamides.
US11/567,610 2001-11-15 2006-12-06 Alkoxylated unsaturated carboxylic acid additives for low-sulfur fuels Abandoned US20070144061A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/567,610 US20070144061A1 (en) 2001-11-15 2006-12-06 Alkoxylated unsaturated carboxylic acid additives for low-sulfur fuels

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
DE10156024A DE10156024A1 (en) 2001-11-15 2001-11-15 Additives for low sulfur fuels
DEDE10156024.9 2001-11-15
PCT/EP2002/012371 WO2003042335A2 (en) 2001-11-15 2002-11-06 Additives for low-sulfur fuels
US10/495,802 US20040255510A1 (en) 2001-11-15 2002-11-06 Additives for low-sulfur fuels
US11/567,610 US20070144061A1 (en) 2001-11-15 2006-12-06 Alkoxylated unsaturated carboxylic acid additives for low-sulfur fuels

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
PCT/EP2002/012371 Continuation WO2003042335A2 (en) 2001-11-15 2002-11-06 Additives for low-sulfur fuels
US10/495,802 Continuation US20040255510A1 (en) 2001-11-15 2002-11-06 Additives for low-sulfur fuels

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US20070144061A1 true US20070144061A1 (en) 2007-06-28

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US10/495,802 Abandoned US20040255510A1 (en) 2001-11-15 2002-11-06 Additives for low-sulfur fuels
US11/567,610 Abandoned US20070144061A1 (en) 2001-11-15 2006-12-06 Alkoxylated unsaturated carboxylic acid additives for low-sulfur fuels

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US10/495,802 Abandoned US20040255510A1 (en) 2001-11-15 2002-11-06 Additives for low-sulfur fuels

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US (2) US20040255510A1 (en)
EP (1) EP1444312B1 (en)
CA (1) CA2467394A1 (en)
DE (2) DE10156024A1 (en)
WO (1) WO2003042335A2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102286299B (en) * 2010-06-21 2016-01-13 周向进 A kind of gasoline products of clean and effective environmental protection

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5292910A (en) * 1990-04-02 1994-03-08 Henkel Kommanditgesellschaft Auf Aktien Use of hydrophobized hydrotalcites as catalysts for ethoxylation or propoxylation
US5326891A (en) * 1990-10-29 1994-07-05 Henkel Kommanditgesellschaft Auf Aktien Hydrophobicized double layer hydroxide compounds
US5936107A (en) * 1996-12-09 1999-08-10 Henkel Kommanditgesellschaft Auf Aktien Process for the production of fatty acid polyethylene glycol esters
US6017369A (en) * 1998-11-23 2000-01-25 Pure Energy Corporation Diesel fuel composition
US6074445A (en) * 1997-10-20 2000-06-13 Pure Energy Corporation Polymeric fuel additive and method of making the same, and fuel containing the additive
US6222082B1 (en) * 1999-09-08 2001-04-24 Leonard Bloom Diesel fuel for use in diesel engine-powered vehicles
US20010003881A1 (en) * 1998-11-23 2001-06-21 Pure Energy Corporation Diesel fuel composition
US6511520B1 (en) * 1997-12-24 2003-01-28 Elf Antar France Additive for fuel oiliness
US20040060226A1 (en) * 2000-11-08 2004-04-01 Aae Technologies International Plc Alkanolamide free fuel additives

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Publication number Priority date Publication date Assignee Title
GB2307247B (en) * 1995-11-13 1999-12-29 Ethyl Petroleum Additives Ltd Fuel additive
FR2752850A1 (en) * 1996-08-27 1998-03-06 Inst Francais Du Petrole COMPOSITIONS OF ADDITIVES IMPROVING THE LUBRICATING POWER OF FUELS AND FUELS CONTAINING THEM

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5292910A (en) * 1990-04-02 1994-03-08 Henkel Kommanditgesellschaft Auf Aktien Use of hydrophobized hydrotalcites as catalysts for ethoxylation or propoxylation
US5326891A (en) * 1990-10-29 1994-07-05 Henkel Kommanditgesellschaft Auf Aktien Hydrophobicized double layer hydroxide compounds
US5936107A (en) * 1996-12-09 1999-08-10 Henkel Kommanditgesellschaft Auf Aktien Process for the production of fatty acid polyethylene glycol esters
US6074445A (en) * 1997-10-20 2000-06-13 Pure Energy Corporation Polymeric fuel additive and method of making the same, and fuel containing the additive
US6511520B1 (en) * 1997-12-24 2003-01-28 Elf Antar France Additive for fuel oiliness
US6017369A (en) * 1998-11-23 2000-01-25 Pure Energy Corporation Diesel fuel composition
US20010003881A1 (en) * 1998-11-23 2001-06-21 Pure Energy Corporation Diesel fuel composition
US6222082B1 (en) * 1999-09-08 2001-04-24 Leonard Bloom Diesel fuel for use in diesel engine-powered vehicles
US20040060226A1 (en) * 2000-11-08 2004-04-01 Aae Technologies International Plc Alkanolamide free fuel additives

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DE10156024A1 (en) 2003-05-28
WO2003042335A3 (en) 2003-09-25
US20040255510A1 (en) 2004-12-23
DE50205670D1 (en) 2006-04-06
EP1444312B1 (en) 2006-01-18
CA2467394A1 (en) 2003-05-22
WO2003042335A2 (en) 2003-05-22
EP1444312A2 (en) 2004-08-11

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