US20030163946A1 - Low emissions fuel emulsion - Google Patents

Low emissions fuel emulsion Download PDF

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Publication number
US20030163946A1
US20030163946A1 US10/086,775 US8677502A US2003163946A1 US 20030163946 A1 US20030163946 A1 US 20030163946A1 US 8677502 A US8677502 A US 8677502A US 2003163946 A1 US2003163946 A1 US 2003163946A1
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fuel
hydrocarbon
emulsion
water
range
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US10/086,775
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Paul Berlowitz
Robert Wittenbrink
Tapan Chakrabarty
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ExxonMobil Technology and Engineering Co
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Priority to US10/086,775 priority Critical patent/US20030163946A1/en
Assigned to EXXONMOBIL RESEARCH & ENGINEERING COMPANY reassignment EXXONMOBIL RESEARCH & ENGINEERING COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHAKRANBATY, TAPAN, WITTENBRINK, ROBERT J., BERLOWITZ, PAUL J.
Priority to BR0307567-2A priority patent/BR0307567A/en
Priority to KR10-2004-7013556A priority patent/KR20040106282A/en
Priority to CA2482339A priority patent/CA2482339C/en
Priority to CA2702107A priority patent/CA2702107A1/en
Priority to CNB038050773A priority patent/CN100526441C/en
Priority to AU2003212975A priority patent/AU2003212975B2/en
Priority to EP03709019A priority patent/EP1481042B1/en
Priority to AT03709019T priority patent/ATE541916T1/en
Priority to CA2702115A priority patent/CA2702115A1/en
Priority to PCT/US2003/003850 priority patent/WO2003074638A1/en
Priority to JP2003573092A priority patent/JP4518798B2/en
Priority to TW092103004A priority patent/TWI282816B/en
Priority to MYPI20030549A priority patent/MY142387A/en
Publication of US20030163946A1 publication Critical patent/US20030163946A1/en
Priority to ZA200406035A priority patent/ZA200406035B/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/32Liquid carbonaceous fuels consisting of coal-oil suspensions or aqueous emulsions or oil emulsions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/32Liquid carbonaceous fuels consisting of coal-oil suspensions or aqueous emulsions or oil emulsions
    • C10L1/328Oil emulsions containing water or any other hydrophilic phase

Definitions

  • the present invention relates to an improved fuel which has reduced particulate matter emission characteristics. More particularly the invention is directed to fuels that are in the form of hydrocarbon-in-water emulsions.
  • Hydrocarbon-in-water emulsions have many potential uses, such as in internal combustion engines and as a fuel for heating purposes. Indeed, various studies have suggested that burning hydrocarbon-in-water emulsions has the advantage of lowering the nitrogen oxide emissions normally associated with burning hydrocarbons. Emulsions are believed to reduce nitrogen oxide (NO x ) emissions by lowering the peak flame temperature during their combustion. A lower flame temperature, however, often is associated with an increase in the emission of particulate matter (Pm). This phenomenon, known as the Pm—NO x trade off, is believed to limit the improvements one can make to diesel emissions.
  • NO x nitrogen oxide
  • Pm particulate matter
  • an object of the present invention is to develop a method of more effectively controlling particulate emissions without adversely impacting presently achievable reduced nitrogen oxide emission levels demonstrated for emulsified fuels.
  • Another object of the invention is to provide an improved diesel fuel having reduced particulate matter emission characteristics.
  • emulsion of a hydrocarbon and water in which the hydrocarbon is a Fischer-Tropsch (FT) derived hydrocarbon fuel or a mixture of a FT fuel and a conventional hydrocarbon fuel and in which emulsion a major portion of the hydrocarbon has particle sizes of 1 micron or less.
  • the emulsion is a hydrocarbon-in-water emulsion.
  • the hydrocarbon is a FT derived hydrocarbon boiling in the diesel fuel range.
  • FIG. 1 is a diagrammatic illustration of one arrangement of multiple static mixers used to prepare an emulsion according to the invention.
  • FIGS. 2 and 3 graphically compare the performance of an emulsion of the invention with two non-emulsified fuels in a diesel engine without timing adjustments.
  • FIGS. 4 and 5 graphically compare the performance of the fuels of FIGS. 2 and 3 with timing adjustment.
  • the emulsions of the present invention contain as the hydrocarbon, a Fischer-Tropsch derived hydrocarbon fuel or a mixture of a FT fuel and a conventional hydrocarbon fuel.
  • the hydrocarbon is a FT derived fuel.
  • the hydrocarbon fuels produced in the Fischer-Tropsch process may be separated from the product crude by standard distillation techniques. Additionally, however, the waxy component of the crude may be converted into fuels by known techniques such as hydrotreating, hydroisomerization and hydrocracking. An example of one such process can be found in U.S. Pat. No. 5,378,348, which is incorporated herein by reference.
  • the Fischer-Tropsch derived hydrocarbon fuel may comprise either the direct liquid product (C 5 +) from the Fischer-Tropsch process, a converted Fischer-Tropsch product, or a blend of the foregoing.
  • Fischer-Tropsch products boiling in the range of from about 25° C. to about 450° C. are suitable.
  • Such fuels include that disclosed in U.S. Pat. No. 5,807,413 which patent is incorporated herein by reference.
  • Also included are more convention Fischer-Tropsch products such as those boiling, in the range of about 140° C. to about 370° C. and preferably in the range of about 160° C. to about 350° C.
  • the water of the emulsion of the invention may be that typically used in forming fuel emulsions such as tap water, distilled or deionized water.
  • water from the Fischer-Tropsch process constitutes the continuous phase of the emulsion.
  • Fischer-Tropsch process water typically contains about ⁇ 2 wt % of oxygenates.
  • a typical composition is shown in Table 1 below: TABLE 1 Oxygenates Amount C 1 —C 12 alcohols 0.05-2 wt % C 2 —C 6 acids 0-50 wppm C 2 —C 6 ketones, aldehydes, acetates 0-50 wppm other 0—500 wppm
  • the amount of water used in forming the emulsion may be varied over a wide range.
  • the volume ratio of Fischer-Tropsch hydrocarbon fuel to water may range from about 95:5 to about 60:40.
  • the emulsions of the present invention also include a nonionic surfactant or mixture of nonionic surfactants.
  • the type of nonionic surfactants suitable include ethoxylated alcohols, ethoxylated alkyl phenols, ethoxylated carboxylic esters, glycerol esters, sorbital esters and the like.
  • the nonionic surfactant will have an HLB in the range of 5 to 30 and preferably 8 to 15.
  • suitable surfactants ethoxylated alkyl phenols having from about 5 to about 30 and preferably 10 to 15 mole of ethylene oxide groups deserve special mention.
  • the amount of surfactant or mixtures thereof in the emulsion will range from about 0.05 wt % to about 5.0 wt % based on the total weight of hydrocarbons and water with 0.05 wt % to about 2 wt % being typical.
  • the emulsion compositions of the invention may include minor but effective amounts of conventional additives such as emulsions stabilizers, antioxidants and the like.
  • conventional additives such as emulsions stabilizers, antioxidants and the like.
  • the fuel may also contain conventional quantities of diesel fuel additives such as cetane improvers, detergents, heat stabilizers and the like.
  • emulsions can be formed by any number of procedures. Central to all of these is providing sufficient shearing of the components to cause emulsification.
  • the fuel is added to a mixture of water and surfactant and sheared under conditions sufficient to produce hydrocarbon particles of predominantly 1 micron in size or less. Stated differently, the particles are substantially uniform in size, i.e., greater than 50% are in the range of about 0.1 to about 1.0 microns in size.
  • extensive shearing results in the formation of a “gel” and consequently the shearing will be less than that which would produce a gel.
  • static mixtures such as those described in U.S. Pat. Nos. 5,405,439; 5,236,624; and 4,832,747.
  • more than one mixer will be used and the mixers will not be of the same size (length, diameter, number of internal elements). Rather the number, size and elements are selected to adjust mixing efficiency and emulsion particle size.
  • a combination of static mixtures is selected to provide sufficient shearing of the hydrocarbon and water to produce an emulsion having particle sizes predominantly 1 micron or less and less shearing than that which would produce a “gel”.
  • FIG. 1 A diagrammatic illustration of one arrangement of static mixers suitable for carrying out the emulsification of this invention is shown in the accompanying Figure. As shown, each of the six mixers have different dimensions. Obviously, different members and sizes of mixers may be used so long as the requisite shearing is achieved. The dimensions of the illustrated mixers are given in Table 2 below. TABLE 2 Mixer Length, inches Diameter, inches 1 12 1/2 2 6 1/2 3 4 1/4 4 4 1/4 5 6 3/16 6 4 3/16
  • a water and sulfactant solution is fed to the mixer 1 via line 7 and the Fischer-Tropsch derived hydrocarbon fuel via line 8 .
  • the product of each mixer is sequentially fed to the next mixer in the series, e.g., the product of mixer 1 is fed to mixer 2 ; the product of mixer 2 is fed to mixer 3 and so on.
  • the emulsion exiting mixer 6 via line 9 has a particle size predominantly less than 1 micron.
  • the emulsion in the instance where the Fisher-Tropsch fuel is a diesel fuel has a viscosity in the range of about 50 to 200 mm 2 /sec at 20° C.
  • a non-ionic surfactant an ethoxylated nonyl phenol having 10 mols of ethylene oxide groups
  • a Fischer-Tropsch diesel fuel (boiling range ⁇ 40° C. to 300° C.) comprising 90 + % of C 6 to C 16 linear paraffins was also fed with the water and surfactant through the four mixers.
  • the volume ratio of fuel to water was 70:30.
  • the hydrocarbon flow rate was 2650 ml/min and the water surfactant solution flow rate was 1380 ml/min.
  • the temperature was 24° C.
  • the product of mixer 4 was not a hydrocarbon-in-water emulsion.
  • Comparative Example 1 The same ingredients and amounts described in Comparative Example 1 were fed through mixers 1 to 6 shown in the Figure. The flow rate and temperature was the same as in Comparative Example 1.
  • the product of mixer 6 was hydrocarbon-in-water emulsion having a density of 0.82 gm/cc and a viscosity of 150 mm 2 /sec at 20° C.
  • the hydrocarbon particles averaged 0.7 microns with 95% below 1 micron in size. This emulsion was shelf stable for more than 6 months.
  • Example 1 The performance of the emulsified Fischer-Tropsch fuel of Example 1 was compared to the same but not emulsified Fischer-Tropsch diesel fuel and to Swedish Class 1 Diesel fuel using a Catapillar 1 Y 540 single cylinder heavy duty Research engine. Two conditions were measured, low load (1500 rpm, 60 Nn torque and 3.0 bar BMEP and medium load (1500 rpm, 110 Nm torques and 5.5 bar BMEP.
  • Swedish Class 1 Diesel fuel also called Urban Diesel ECI
  • Urban Diesel ECI is a standard low emissions reference diesel fuel that produces about 10% to 20% lower NOx and 40% to 50% lower particulate matter (Pm) than conventional diesel fuel.
  • Pm particulate matter
  • Table 3 TABLE 3 Cetane >50 Cloud Point Summer 0° C. Winter ⁇ 16° C. Density, kg/m 3 800-820 IBP, ° C. 180 T 95 , ° C. 285 maximum Viscosity at 40° C., mm 2 /second 1.2 to 4.0 Sulfur, ppm 10 maximum Aromatics, vol % 5 maximum Poly aromatics not detectable
  • the unemulsified Fischer-Tropsch fuel has been shown to have excellent emissions performance (see U.S. Pat. No. 5,807,413) with NO x reductions of 10-25% and Pm reductions of 40-60% compared with conventional diesel fuels.
  • FIGS. 2 and 3 show the relative emissions performance of the Fischer-Tropsch fuel and an emulsion of the invention (Example 1) vs. Swedish Class I Diesel fuel at low and medium load.
  • the FTF exhibits similar behavior to Swedish Class I Diesel Fuel whereas the a fuel emulsion of the invention shows NO x emissions 22% below Swedish Class 1 and Pm 53% below.
  • FIG. 3 a fuel emulsion of the invention shows even larger PM reduction (91.5%) than Swedish Class 1 fuel.
  • FIGS. 4 and 5 the Pm/NO x performance of the fuels is plotted against change in spark timing. As can be seen in the case of the FTF and Swedish claim 1 fuels one can retard the timing to lower the NO x emissions.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

Emulsions of a hydrocarbon and water in which the hydrocarbon preferably is a Fischer-Tropsch derived hydrocarbon fuel and in which emulsion a major portion of the hydrocarbon has particle sizes of 1 micron or less produce reduced particulate matter emissions upon combustion.

Description

    FIELD OF INVENTION
  • The present invention relates to an improved fuel which has reduced particulate matter emission characteristics. More particularly the invention is directed to fuels that are in the form of hydrocarbon-in-water emulsions. [0001]
  • BACKGROUND OF The INVENTION
  • Hydrocarbon-in-water emulsions have many potential uses, such as in internal combustion engines and as a fuel for heating purposes. Indeed, various studies have suggested that burning hydrocarbon-in-water emulsions has the advantage of lowering the nitrogen oxide emissions normally associated with burning hydrocarbons. Emulsions are believed to reduce nitrogen oxide (NO[0002] x) emissions by lowering the peak flame temperature during their combustion. A lower flame temperature, however, often is associated with an increase in the emission of particulate matter (Pm). This phenomenon, known as the Pm—NOx trade off, is believed to limit the improvements one can make to diesel emissions.
  • In recent years there has been a tendency for more stringent emission regulations, including particulate emissions. Therefore, an object of the present invention is to develop a method of more effectively controlling particulate emissions without adversely impacting presently achievable reduced nitrogen oxide emission levels demonstrated for emulsified fuels. [0003]
  • In the instance of diesel fueled engines, the reduction of particulate emissions is particularly important. Consequently, another object of the invention is to provide an improved diesel fuel having reduced particulate matter emission characteristics. [0004]
  • SUMMARY OF INVENTION
  • In accordance with the invention reduced particulate matter emissions are achieved with an emulsion of a hydrocarbon and water in which the hydrocarbon is a Fischer-Tropsch (FT) derived hydrocarbon fuel or a mixture of a FT fuel and a conventional hydrocarbon fuel and in which emulsion a major portion of the hydrocarbon has particle sizes of 1 micron or less. Preferably, the emulsion is a hydrocarbon-in-water emulsion. [0005]
  • In a particularly preferred embodiment of the invention the hydrocarbon is a FT derived hydrocarbon boiling in the diesel fuel range. [0006]
  • These and other embodiments will become apparent upon a reading of the detailed description of the invention which follows.[0007]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a diagrammatic illustration of one arrangement of multiple static mixers used to prepare an emulsion according to the invention. [0008]
  • FIGS. 2 and 3 graphically compare the performance of an emulsion of the invention with two non-emulsified fuels in a diesel engine without timing adjustments. [0009]
  • FIGS. 4 and 5 graphically compare the performance of the fuels of FIGS. 2 and 3 with timing adjustment. [0010]
  • DETAILED DESCRIPTION OF THE INVENTION
  • The emulsions of the present invention contain as the hydrocarbon, a Fischer-Tropsch derived hydrocarbon fuel or a mixture of a FT fuel and a conventional hydrocarbon fuel. Preferably, the hydrocarbon is a FT derived fuel. [0011]
  • As is well known in the art the Fischer-Tropsch process involves the reaction of a hydrogen and carbon monoxide containing feed in the presence of a suitable catalyst to produce a largely normal paraffin synthetic crude. The process is described, for example, in U.S. Pat. Nos. 5,348,982 and 5,545,674, and suitable catalysts in U.S. Pat. No. 4,568,663, each of which is incorporated herein by reference. [0012]
  • The hydrocarbon fuels produced in the Fischer-Tropsch process may be separated from the product crude by standard distillation techniques. Additionally, however, the waxy component of the crude may be converted into fuels by known techniques such as hydrotreating, hydroisomerization and hydrocracking. An example of one such process can be found in U.S. Pat. No. 5,378,348, which is incorporated herein by reference. [0013]
  • In the context of the embodiments of the present invention the Fischer-Tropsch derived hydrocarbon fuel may comprise either the direct liquid product (C[0014] 5+) from the Fischer-Tropsch process, a converted Fischer-Tropsch product, or a blend of the foregoing. Thus, Fischer-Tropsch products boiling in the range of from about 25° C. to about 450° C. are suitable. Such fuels include that disclosed in U.S. Pat. No. 5,807,413 which patent is incorporated herein by reference. Also included are more convention Fischer-Tropsch products such as those boiling, in the range of about 140° C. to about 370° C. and preferably in the range of about 160° C. to about 350° C.
  • The water of the emulsion of the invention may be that typically used in forming fuel emulsions such as tap water, distilled or deionized water. In one embodiment, water from the Fischer-Tropsch process constitutes the continuous phase of the emulsion. Fischer-Tropsch process water typically contains about ≦2 wt % of oxygenates. A typical composition is shown in Table 1 below: [0015]
    TABLE 1
    Oxygenates Amount
    C1—C12 alcohols 0.05-2 wt %
    C2—C6 acids 0-50 wppm
    C2—C6 ketones, aldehydes, acetates 0-50 wppm
    other 0—500 wppm
  • The amount of water used in forming the emulsion may be varied over a wide range. For example, the volume ratio of Fischer-Tropsch hydrocarbon fuel to water may range from about 95:5 to about 60:40. [0016]
  • The emulsions of the present invention also include a nonionic surfactant or mixture of nonionic surfactants. The type of nonionic surfactants suitable include ethoxylated alcohols, ethoxylated alkyl phenols, ethoxylated carboxylic esters, glycerol esters, sorbital esters and the like. In general, the nonionic surfactant will have an HLB in the range of 5 to 30 and preferably 8 to 15. Among suitable surfactants ethoxylated alkyl phenols having from about 5 to about 30 and preferably 10 to 15 mole of ethylene oxide groups deserve special mention. [0017]
  • The amount of surfactant or mixtures thereof in the emulsion will range from about 0.05 wt % to about 5.0 wt % based on the total weight of hydrocarbons and water with 0.05 wt % to about 2 wt % being typical. [0018]
  • The emulsion compositions of the invention may include minor but effective amounts of conventional additives such as emulsions stabilizers, antioxidants and the like. In the case where the fuel is diesel fuel the fuel may also contain conventional quantities of diesel fuel additives such as cetane improvers, detergents, heat stabilizers and the like. [0019]
  • As is known in the art emulsions can be formed by any number of procedures. Central to all of these is providing sufficient shearing of the components to cause emulsification. In the practice of the present invention the fuel is added to a mixture of water and surfactant and sheared under conditions sufficient to produce hydrocarbon particles of predominantly 1 micron in size or less. Stated differently, the particles are substantially uniform in size, i.e., greater than 50% are in the range of about 0.1 to about 1.0 microns in size. Experience has shown that extensive shearing results in the formation of a “gel” and consequently the shearing will be less than that which would produce a gel. [0020]
  • To achieve the requisite shearing it is particularly preferred to employ one or more static mixtures such as those described in U.S. Pat. Nos. 5,405,439; 5,236,624; and 4,832,747. In general more than one mixer will be used and the mixers will not be of the same size (length, diameter, number of internal elements). Rather the number, size and elements are selected to adjust mixing efficiency and emulsion particle size. In the practice of the present invention a combination of static mixtures is selected to provide sufficient shearing of the hydrocarbon and water to produce an emulsion having particle sizes predominantly 1 micron or less and less shearing than that which would produce a “gel”. [0021]
  • A diagrammatic illustration of one arrangement of static mixers suitable for carrying out the emulsification of this invention is shown in the accompanying Figure. As shown, each of the six mixers have different dimensions. Obviously, different members and sizes of mixers may be used so long as the requisite shearing is achieved. The dimensions of the illustrated mixers are given in Table 2 below. [0022]
    TABLE 2
    Mixer Length, inches Diameter, inches
    1 12 1/2 
    2  6 1/2 
    3  4 1/4 
    4  4 1/4 
    5  6 3/16
    6  4 3/16
  • In the arrangement shown in the Figure, a water and sulfactant solution is fed to the [0023] mixer 1 via line 7 and the Fischer-Tropsch derived hydrocarbon fuel via line 8. The product of each mixer is sequentially fed to the next mixer in the series, e.g., the product of mixer 1 is fed to mixer 2; the product of mixer 2 is fed to mixer 3 and so on. The emulsion exiting mixer 6 via line 9 has a particle size predominantly less than 1 micron. The emulsion in the instance where the Fisher-Tropsch fuel is a diesel fuel, has a viscosity in the range of about 50 to 200 mm2/sec at 20° C.
  • EXAMPLES Comparative Example 1
  • 300 gms of a non-ionic surfactant (an ethoxylated nonyl phenol having 10 mols of ethylene oxide groups) was added to 9700 gms of water and fed through [0024] mixers 1 to 4 shown in the Figure. A Fischer-Tropsch diesel fuel (boiling range ˜40° C. to 300° C.) comprising 90+% of C6 to C16 linear paraffins was also fed with the water and surfactant through the four mixers. The volume ratio of fuel to water was 70:30. The hydrocarbon flow rate was 2650 ml/min and the water surfactant solution flow rate was 1380 ml/min. The temperature was 24° C. The product of mixer 4 was not a hydrocarbon-in-water emulsion.
  • Example 1
  • The same ingredients and amounts described in Comparative Example 1 were fed through [0025] mixers 1 to 6 shown in the Figure. The flow rate and temperature was the same as in Comparative Example 1. In this instance the product of mixer 6 was hydrocarbon-in-water emulsion having a density of 0.82 gm/cc and a viscosity of 150 mm2/sec at 20° C. The hydrocarbon particles averaged 0.7 microns with 95% below 1 micron in size. This emulsion was shelf stable for more than 6 months.
  • Example 2
  • The performance of the emulsified Fischer-Tropsch fuel of Example 1 was compared to the same but not emulsified Fischer-Tropsch diesel fuel and to [0026] Swedish Class 1 Diesel fuel using a Catapillar 1 Y 540 single cylinder heavy duty Research engine. Two conditions were measured, low load (1500 rpm, 60 Nn torque and 3.0 bar BMEP and medium load (1500 rpm, 110 Nm torques and 5.5 bar BMEP.
  • As is known [0027] Swedish Class 1 Diesel fuel (also called Urban Diesel ECI) is a standard low emissions reference diesel fuel that produces about 10% to 20% lower NOx and 40% to 50% lower particulate matter (Pm) than conventional diesel fuel. The specification for Swedish Class 1 diesel fuel are given in Table 3.
    TABLE 3
    Cetane >50
    Cloud Point
    Summer
    0° C.
    Winter −16° C.
    Density, kg/m3 800-820
    IBP, ° C. 180
    T95, ° C. 285 maximum
    Viscosity at 40° C., mm2/second 1.2 to 4.0
    Sulfur, ppm 10 maximum
    Aromatics, vol % 5 maximum
    Poly aromatics not detectable
  • The unemulsified Fischer-Tropsch fuel (FTF) has been shown to have excellent emissions performance (see U.S. Pat. No. 5,807,413) with NO[0028] x reductions of 10-25% and Pm reductions of 40-60% compared with conventional diesel fuels. FIGS. 2 and 3 show the relative emissions performance of the Fischer-Tropsch fuel and an emulsion of the invention (Example 1) vs. Swedish Class I Diesel fuel at low and medium load.
  • As can be seen in FIG. 2, the FTF exhibits similar behavior to Swedish Class I Diesel Fuel whereas the a fuel emulsion of the invention shows NO[0029] x emissions 22% below Swedish Class 1 and Pm 53% below.
  • In FIG. 3 a fuel emulsion of the invention shows even larger PM reduction (91.5%) than [0030] Swedish Class 1 fuel.
  • In FIGS. 4 and 5 the Pm/NO[0031] x performance of the fuels is plotted against change in spark timing. As can be seen in the case of the FTF and Swedish claim 1 fuels one can retard the timing to lower the NOx emissions.

Claims (12)

What is claimed is:
1. A method for reducing particulate emissions during combustion of a hydrocarbon fuel which comprises combusting an emulsion of a hydrocarbon fuel and water wherein the fuel is a Fischer-Tropsch (FT) derived hydrocarbon as a mixture of a FT fuel and a conventional fuel, and in which emulsion, a major portion of the hydrocarbon has particle sizes of 1 micron or less.
2. The method of claim 1 wherein the emulsion is a hydrocarbon-in-water emulsion.
3. The method of claim 2 wherein the fuel is a FT derived fuel.
4. The method of claim 3 wherein greater than 50% of the hydrocarbon particles are in the range of about 0.1 to about 1.0 microns in size.
5. The method of claim 4 wherein the volume ratio of hydrocarbon to water is in the range of 95:5 to 60:40.
6. The method of claim 5 wherein greater than 80% of the hydrocarbon particles are in the range of about 0.1 to about 1.0 microns in size.
7. The method of claim 6 wherein the Fischer-Tropsch derived hydrocarbon boils in the diesel fuel range.
8. The method of claim 7 wherein the emulsion has a viscosity in the range of about 50 to 200 mm2/sec.
9. A method for forming a fuel in water emulsion which when combusted has reduced particulate matter emissions compared with Swedish Class I Diesel Fuel comprising shearing a Fischer-Tropsch derived hydrocarbon boiling in the diesel fuel range and water in the volume ratio of hydrocarbon to water of 95:5 to 40:60 and about 0.05 to about 5.0 wt % based on the weight of hydrocarbon and water with a non-ionic surfactant or mixtures thereof having a HLB of about 5 to about 30 under shearing conditions sufficient to produce a liquid emulsion in which a major portion of the hydrocarbon has particle sizes of 1 micron or less.
10. A liquid fuel composition comprising an emulsion of FT derived fuel in water wherein the fuel in the emulsion has fuel particle sizes predominately of 1 micron or less and the emulsion has a viscosity of above about 50 mm2/sec at 20° C.
11. The composition of claim 10 wherein greater than 50% of the fuel particles has particle sizes in the range of about 0.1 to about 1.0 microns.
12. The composition of claim 11 wherein the Fischer-Tropsch derived fuel boils in the diesel fuel range.
US10/086,775 2002-03-01 2002-03-01 Low emissions fuel emulsion Abandoned US20030163946A1 (en)

Priority Applications (15)

Application Number Priority Date Filing Date Title
US10/086,775 US20030163946A1 (en) 2002-03-01 2002-03-01 Low emissions fuel emulsion
JP2003573092A JP4518798B2 (en) 2002-03-01 2003-02-07 Fischer-Tropsch derived hydrocarbon containing low emission fuel emulsion
AU2003212975A AU2003212975B2 (en) 2002-03-01 2003-02-07 Low emissions fuel emulsion comprising Fischer-Tropsch derived hydrocarbon
AT03709019T ATE541916T1 (en) 2002-03-01 2003-02-07 ENVIRONMENTALLY FRIENDLY FISCHER-TROPSCH FUEL EMULSION
CA2482339A CA2482339C (en) 2002-03-01 2003-02-07 Low emissions fuel emulsion comprising fischer-tropsch derived hydrocarbon
CA2702107A CA2702107A1 (en) 2002-03-01 2003-02-07 Low emissions fuel emulsion comprising fischer-tropsch derived hydrocarbon
CNB038050773A CN100526441C (en) 2002-03-01 2003-02-07 Low emissions fuel emulsion comprising fischer-tropsch derived hydrocarbon
BR0307567-2A BR0307567A (en) 2002-03-01 2003-02-07 Method for reducing particulate emissions during combustion of a hydrocarbon fuel, method for forming an aqueous emulsion fuel, and, liquid fuel composition
EP03709019A EP1481042B1 (en) 2002-03-01 2003-02-07 Low emissions fuel emulsion comprising fischer-tropsch derived hydrocarbon
KR10-2004-7013556A KR20040106282A (en) 2002-03-01 2003-02-07 Low emissions fuel emulsion comprising fischer-tropsch derived hydrocarbon
CA2702115A CA2702115A1 (en) 2002-03-01 2003-02-07 Low emissions fuel emulsion comprising fischer-tropsch derived hydrocarbon
PCT/US2003/003850 WO2003074638A1 (en) 2002-03-01 2003-02-07 Low emissions fuel emulsion comprising fischer-tropsch derived hydrocarbon
TW092103004A TWI282816B (en) 2002-03-01 2003-02-13 Method for reducing particulate emission during combustion of a hydrocarbon fuel, method for forming a fuel in water emulsion, and liquid fuel composition
MYPI20030549A MY142387A (en) 2002-03-01 2003-02-18 Low emissions fuel emulsion comprising fischer-tropsch derived hydrocarbon
ZA200406035A ZA200406035B (en) 2002-03-01 2004-07-28 Low emmisions fuel emulsion comprising Fischer-Tropsch derived hydrocarbon

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US20060156620A1 (en) * 2004-12-23 2006-07-20 Clayton Christopher W Fuels for compression-ignition engines
US20100037513A1 (en) * 2006-04-27 2010-02-18 New Generation Biofuels, Inc. Biofuel Composition and Method of Producing a Biofuel

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NL1033989C2 (en) * 2007-06-14 2008-12-16 Hendrik Loggers Engine fuel, comprises emulsified mixture of mineral fuels, optional plant oil and emulsifier
NL1035106C2 (en) 2008-02-29 2009-09-01 Hendrik Loggers Water applying method for replacing part of e.g. normal fuel, involves feeding water into cylinder of engine, and injecting fuel into cylinder, where water is heated due to combustion of fuel to produce water vapor
JP5095517B2 (en) * 2008-06-19 2012-12-12 独立行政法人科学技術振興機構 Aluminum-containing zinc oxide n-type thermoelectric conversion material
WO2020159350A2 (en) * 2019-02-01 2020-08-06 Treviño Quintanilla Sergio Antonio Process for the production of an improved diesel fuel

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US20050241216A1 (en) * 2002-04-25 2005-11-03 Clark Richard H Diesel fuel compositions
US20050086854A1 (en) * 2003-09-03 2005-04-28 Millington Christopher R. Fuel compositions
US20050277794A1 (en) * 2003-09-03 2005-12-15 Cracknell Roger F Fuel compositions
US7737311B2 (en) * 2003-09-03 2010-06-15 Shell Oil Company Fuel compositions
US20060156620A1 (en) * 2004-12-23 2006-07-20 Clayton Christopher W Fuels for compression-ignition engines
US20100037513A1 (en) * 2006-04-27 2010-02-18 New Generation Biofuels, Inc. Biofuel Composition and Method of Producing a Biofuel

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CA2702107A1 (en) 2003-09-12
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CA2702115A1 (en) 2003-09-12
CA2482339A1 (en) 2003-09-12
ATE541916T1 (en) 2012-02-15
AU2003212975A1 (en) 2003-09-16
WO2003074638A1 (en) 2003-09-12
TW200303917A (en) 2003-09-16
EP1481042B1 (en) 2012-01-18
CN100526441C (en) 2009-08-12
KR20040106282A (en) 2004-12-17
JP2005519165A (en) 2005-06-30

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