GB2066288A - Diesel fuel compositions and process for their production - Google Patents

Diesel fuel compositions and process for their production Download PDF

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Publication number
GB2066288A
GB2066288A GB8036177A GB8036177A GB2066288A GB 2066288 A GB2066288 A GB 2066288A GB 8036177 A GB8036177 A GB 8036177A GB 8036177 A GB8036177 A GB 8036177A GB 2066288 A GB2066288 A GB 2066288A
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vol
water
diesel fuel
volume
emulsifying
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GB2066288B (en
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Labofina SA
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Labofina SA
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Priority claimed from LU81921A external-priority patent/LU81921A1/en
Priority claimed from LU82566A external-priority patent/LU82566A1/en
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Classifications

    • 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
    • C10L1/02Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C10L1/026Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for compression ignition
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G67/00Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only
    • C10G67/02Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only
    • C10G67/06Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only including a sorption process as the refining step in the absence of hydrogen
    • 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
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B3/00Engines characterised by air compression and subsequent fuel addition
    • F02B3/06Engines characterised by air compression and subsequent fuel addition with compression ignition

Abstract

A diesel fuel, of the water in oil type, comprises 97 to 90 volume % of a mixture comprising a major amount of usual diesel fuel and a minor amount of at least 5 vol. %, based on the volume of the emulsion, of an aqueous solution of methanol and/or ethanol, and to 10 vol. % of an emulsifying blend of sorbitan monooleate and water soluble, ethoxylated non-ionic surfactant.

Description

SPECIFICATION Diesel fuel compositions and process for their production This invention relates to new Diesel fuel compositions and to a process for their production.
More particularly, the invention relates to water-in-oil emulsions containing a Diesel fuel, an alcohol, water and an emulsifier.
The use of substitute fuels in order to reduce the consumption of crude oil has become of substantial importance in the last years. The research work in this field has been directed more particularly to the gasoline engines or engines with ignition by spark plugs. An attractive solution consists in using mixtures of gasoline and alcohols; methanol and ethanol can be mixed with gasoline in all proportions and they have a high octane number (about 87 to 90).
However, the incorporation of alcohols into Diesel fuels gives rise to some difficulties. It is known that a trouble free running of Diesel engines (or spontaneous ignition engines) requires the use of fuels with a cetane number of at least 26. But the octane numbers of methanol and ethanol are low (respectively 3 and 8) and the cetane number of a Diesel fuel, more particularly gasoil and light fuel oil, is comprised between 34 and 55. Therefore, the range of mixtures containing a Diesel fuel and alcohol and exhibiting a suitable cetane number is relatively small.
Moreover, methanol and ethanol and practically immiscible with the diesel fuel and mixtures of these components cannot be prepared beforehand. The sole solution which has been suggested consists in using a bimodal feeding system. Such a system requires mechanical modifications, i.e. two tanks, a monitoring device for the alcohol, etc.
It is an object of this invention to provide Diesel fuel compositions which overcome these drawbacks. Another object is to provide stable, substitute fuels having a suitable cetane number.
A further object is to provide water-in-oil emulsions containing a Diesel fuel and an alcohol. It is also an object of this invention to provide a process for producing these emulsions.
The combustible water-in-oil emulsions of the present invention comprise: 97 to 90 volume % of a mixture containing a major part of a Diesel fuel selected from the group consisting of gasoil and light fuel oil, and a lower amount of an aqueous solution of methanol and/or ethanol, and 3 to 10 volume % of an emulsifying blend containing sorbitan monooleate and a watersoluble, non ionic, ethoxylated sufactant.
According to an embodiment of this invention wherein gasoil is used as Diesel fuel, the emulsion comprises from 55 to 92 vol. % of gasoil, from 5 to 35 vol. % of an aqueous solution of alcohol, the volume percentage of water in said solution being comprises between 43 + 0.20 S and 74, wherein S is the vol. percentage of ethanol based on the total volume of alcohol, and 3 to 10 vol. S6 of emulsifying blend.
According to another embodiment wherein light fuel oil is used as Diesel fuel, the emulsion comprises from 45 to 92 vol. % of light fuel oil, from 5 to 45 vol. % of an aqueous solution of alcohol, the volume percentage of water is said solution being comprises between 45.7 + 0.229 S and 74.3, wherein S is the vol. percentage of ethanol based in the total volume of alcohol, and 3 to TO vol. % of emulsifying blend.
The alcohol is preferably methanol or ethanol or their mixtures. These alcohols may contain a low amount of another aliphatic alcohol with a low molecular weight or of a denaturing agent such as methyl ethyl ketone. Consequently, denaturated alcohols containing generally up to 3% of denaturating agent may be used in the compositions of this invention.
These new compositions are stable water-in-oil emulsions, which exhibit a low viscosity and a suitable cetane number. Therefore, they can be used as substitute fuels for diesel engines and for heating purposes. Moreover, they are stable and they do not give rise to a demixing and a settling of water in bottom of the tanks; a settling of water is a serious drawback, as said water would be first injected into the engine or the burner and would cause its breakdown. The term ''stable emulsion" is understood to mean that practically no demixing occurs during a period of time of at least 72 hours; a ring of Diesel fuel may however appear, inasmuch that the amount of demixed fuel is not higher than 3 vol. % of the fuel present in the emulsion. In case of demixing, the emulsion is easily restored by stirring.
The stability of the emulsions of this invention depends upon many factors, such as type of Diesel fuel, nature and amount of emulsifying agent, HLB (hydrophilic-lipophilic balance) of the emulsifying blend, respective amounts of alcohol and water, type of alcohol, mode of preparation.
When the emulsion is used to feed Diesel engines, the upper amount of aqueous solution of alcohol in the emulsion is set by cetane number consideration. Amounts of aqueous solution as high as 45 vol. % may be used, but generally emulsions containing not more than 40 vol. % of aqueous solution of alcohol are more suitable when the Diesel fuel is light fuel-oil. When the emulsion is prepared from gasoii, the amount of aqueous solution of alcohol should not generally exceed 35 viol. 9/o. When the emulsions are used for heating purposes, the calorific value is the main limitative factor and emulsions containing up to 45 vol. % of aqueous solutions of alcohol may be employed.On the other hand, emulsions having a content in aqueous solution of alcohol lower than 5 vol. % are not very attractive, as the fuel economy is negligible.
The HLB of the emulsifying blend plays also a role with respect to the emulsion stability.
Preferably, the HLB of the emulsifying blend is at least 5, but generally does not exceed about 7 when the fuel to be emulsified is light fuel oil or even about 6.5 in case of gasoil. The type of emulsifying blend is also another factor and said blend preferably contains sorbitan monooleate tegether with a water-soluble, non ionic, ethoxylated surfactant. Illustrative surfactants include ethoxylated sorbitan monooleate containing from 20 to 40 moles of ethylene oxide (or E O); ethoxylated sorbitan monolaurate with 11 - 40 E 0; ethoxylated nonylphenol with 8 - 50 E O; ethoxylated fatty alcohols with 6 - 50 E 0; monooleate of polyethyleneglycol having a molecular weight comprises between about 480 and 1 200. The selection of the surfactant depends upon some factors, such a availability, price and efficacity.The emulsion stability depends also on the type of fuel to be emulsified; by way of example, emulsions prepared from gasoil are more stable than similar emulsions prepared from light fuel oil when ethoxylated fatty alcohols are used as surfactants.
The required HLB may be reached by varying the respective amounts of sorbitan monooleate and surfactant. The amounts to be used will be easily determined by the skilled in the art worker.
The emulsion stability depends also upon the proportion of water in the aqueous solution of alcohol. This proportion varies according to the type of alcohol (methanol, ethanol or their mixtures) and the type of fuel to be emulsified. For the production of light fuel oil based emulsions, the volume percent of water in the aqueous solution is generally comprised between 45.7 + 0.229 S and 74.3, wherein S is the volume percent of ethanol based on the total volume of alcohol. For gasoil based emulsions, the volume percent of water in the aqueous solution is generally comprised between 43 + 0.20 S and 74. Aqueous solutions of alcohol containing amounts of water lying outside these limits are generally less convenient for producing stable emulsions.
The process employed for producing the emulsions of this invention has been found to exercise an influence over the emulsion stability. According to a further embodiment of the present invention, the emulsions are produced by a process which comprises i) preparing a first mixture of Diesel fuel and emulsifying blend, ii) preparing the aqueous solution of alcohol, and iii) adding, while stirring, said aqueous solution to the first mixture. Other methods of production present some drawbacks. For example, the addition of the first mixture to the aqueous solution of alcohol results in less stable emulsions. The addition of separate streams of water and alcohol to the first mixture requires the use of high shearing agitator, which induces an A increase of the mixture temperature and some evaporation of the alcohol.
In order to more fully illustrate this invention, the following non-limitative examples are presented.
Example 1.
Various emulsions were prepared by adding while stirring an aqueous solution containing 1 5 cc methanol and 20 cc water to a mixture containing 61 cc light fuel oil and 4 cc of emulsifying blend.
The emulsifying blends were as follows: A : sorbitan monooleate + ethoxylated sorbitan monooleate (20 E O) B : sorbitan monooleate + ethoxylated sorbitan monolaurate (20 E O) C : sorbitan monooleate + monooleate of polyethyleneglycol (M.W.: 600) D : sorbitan monooleate + ethoxylated nonylphenol (1 5 E O) The HLB of these blends were comprises between 4.3 and 8.5. These various HLB were obtained by varying the respective amounts of the components of these blends.
The stability of the obtained emulsions were determined 96 hours after their production. The results are given in the following Table 1.
TABLE 1 Emulsifying HBL index blend 4.3 5 5.5 6 6.5 7 7.5 8 8.5 A + ++ ++ ++ ++ ++ + - B + ++ ++ ++ ++ ++ + - C + ++ ++ ++ ++ ++ + - D + ++ ++ ++ ++ ++ + - (+ + : stable; +: partial demixing; - : total demixing) By way of comparison, the following emulsifying blends were used: X : monooleate of polyehtyleneglycol (MW 200) + monooleate of polyethyleneglycol (MW 600) Y : ethoxylated fatty alcohol (2 E O) + ethoxylated fatty alcohol (5 E 0).
Various blends wherein the respective amounts of surfactants were adjusted to cover a wide range of HLB were prepared. Emulsions were produced by using these blends, but they were not stable.
Example 2.
The procedure described in Example 1 was repeated for producing emulsions with various contents in emulsifying blends and various HLB.
The total volume of each emulsion was 100 cc and the compositions were the following: methanol : 1 5 cc water : 20 cc emulsifying blend : from 1 to 10 cc (blend A of Example 1) light fuel oil : from 55 to 64 cc The results of the stability tests were as follows (Table 2).
TABLE 2 Emulsifying blend (vol %) HLB 1 2 3 4 5 6 8 10 5 - - ++ ++ ++ ++ + ++ 5.5 - - + + +f ++ ++ ++ ++ 6 - - ++ ++ ++ ++ ++ ++ 6.5 - - + + + + + + + + + + + + 7 - - ++ ++ ++ ++ ++ ++ (+ + : stable after 96 hrs; - : demixing) The same results were obtained by using the emulsifying blends B and C described in Example 1. The same results were obtained by using the emulsifying blends B and C described in Example 1.
Example 3.
To a stirred mixture of 61 cc of light fuel oil and 4 cc of emulsifying blend A(HLB = 6) was added an aqueous solution containing 15 cc of methanol and 20 cc water.
The resulting emulsion was stable after 96 hours.
Another portion of this emulsion was cooied during 96 hours at - 20"C; it remained stable.
By way of comparison, the same amounts of components were used, but other procedures were used: a) separate streams of methanol and water were added to the stirred mixture of fuel and emulsifying blend: total demixing after 72 hours b) a mixture of fuel and emulsifying blend was added to the stirred aqueous solution of methanol: total demixing after 24 hours.
Example 4.
Various emulsions were prepared with different amounts of methanol and water, but the total volume of methanol + water was the same in each emulsion.
The emulsifying blend (blend A of Example 1) had a HLB of 6.
The compositions (in vol. %) of the emulsions and the results of the stability tests are summarized in Table 3.
TABLE 3 Light fuel oil 61 61 61 61 61 61 61 61 57 Emulsifying blend 4 4 4 4 4 4 4 4 8 Methanol 7 8 9 16 17 18 19 20 20 Water 28 27 26 19 18 17 16 15 15 Stability - - + + + + + + + + + + - Example 5.
Various emulsions were prepared with different amounts of light fuel oil. For each emulsion, the amount of water in the aqueous solution of methanol was 57.1 vol. %.
The emulsifying blend (blend A of Example 1) had a HLB of 6.
The compositions (in vol. %) of the emulsions and the results of the stability tests are given in Table 4.
TABLE 4 Light fuel oil 91 81 71 51 Emulsifying blend 4 4 4 4 Methanol + water 5 15 25 45 Stability + + + + + + + + Example 6.
Various mixtures were prepared from 61 cc of light fuel oil and 4 cc of each of the emulsifying blends A to D described in Example 1. The HLB of these blends was comprised within the range from 4.3 to 8.5.
An aqueous solution of ethanol was prepared from 25 vol. % of water and 10 vol. % of ethanol.
The procedure described in Example 1 was used to prepare the emulsions; the total volume of each emulsion was 100 cc.
The results of the stability tests (after 96 hrs) are given in Table 5.
TABLE 5 Emulsifying HLB blend 4.3 5 5.5 6 6.5 7 7.5 8 8.5 A - ++ ++ ++ ++ ++ - - B - ++ ++ ++ ++ ++ - - C - ++ ++ ++ ++ ++ - - D - ++ ++ ++ ++ ++ - - Example 7.
Various emulsions were prepared from light fuel oil, emulsifying blend of Example 1 (HLB: from 5 to 7), water and ethanol. The total volume of each emulsion wass 100 cc. The emulsions contained 25 cc of water, 10 cc of ethanol, from 1 to 10 cc of emulsifying blend and respectively from 54 to 64 cc of fuel.
The results with respect to stability are given in Table 6.
TABLE 6 Emulsifying blend (vol. %) HLB 1 2 3 4 5 6 8 10 5 - - ++ ++ ++ ++ ++ ++ 5.5 - - + + + + + + + + + + + + 6 - - ++ ++ ++ ++ ++ ++ 7 - - ++ ++ ++ ++ ++ ++ Example 8.
Various emulsions were prepared from light fuel oil, emulsifying blend A of Example 1 (HLB = 7) and an aqueous solution of ethanol (vol. %) of water: 73.4).
The compositions (vol. %) and results of stability tests are given in Table 7.
TABLE 7 Light fuel oil 91 8hi 71 51 Emulsifying blend 4 4 4 4 Aqueous solution of 5 15 25 45 ethanol Stability ++ ++ ++ ++ Example 9.
Various emulsions were prepared by using aqueous solutions containing methanol and ethanol.
The respective volumes of the components and the results of the stability tests are given in Table 8.
TABLE 8 Experiment 1 2 3 4 5 5 6 7 8 Light fuel oil 61 61 61 61 61 61 61 61 Emulsifying blend A 4 4 4 4 4 4 4 4 (HLB = 7) Methanol 16.8 14.0 14.0 10.6 7 1.75 1.76 3.5 Ethanol 0.9 1.75 3.5 1.75 3.5 7 8.75 10.5 Water 17.5 19.25 17.5 22.75 24.5 26.25 24.5 21 Stability ++ ++ - ++ ++ ++ ++ Experiments 3 and 8 are comparative experiments. The amount of water is Bower than the required minimum amount. In experiment 3, the amount of water in the aqueous solution of alcohols is 50% and the minimum should be 45.7 + (0.229 X 20) or 50.28%. In experiment 8, the amount of water in the aqueous solution of alcohols is 60% and the minimum should be 45.7 + (0.229 X 75) or 62.87%.
Example 10.
Various emulsions were prepared. For each emulsion, a mixture of 35 cc of methanol and 16 cc of water was added, while stirring, to a mixture containing 64 cc of gasoil and 4 cc of emulsifying blend.
The he used emulsifying blends A to D of Example 1 and blend E containing sorbitan monooleate and ethoxylated fatty alcohol (9EO). The HLB of these blends (from 5 to 120) were obtained by varying the respective amounts of components.
The results are given in Table 9.
TABLE 9 Emulsifying HLB blend 5 5.5 6 6.5 7 5 10 12 A + + + + + + -" - - - B ++ ++ ++ ++ + - - C ++ ++ ++ ++ + - - D ++ ++ ++ ++ + - - E ++ ++ ++ ++ + - - (++ : stable after 96 hours; + partial dernixing; - : total demixing) By way of comparison, the following emulsifying blends were used to prepare similar emulsions.
F : sorbitan monooleate + monooleate of polyethyleneglycol (MW : 300)(not soluble in water) G . sorbitan monooleate 9 ethoxylated nonylphenol (4 E G) (insoluble) H sorbitan inonooleate + ethoxylated fatty alcohol (3 E O) (insoluble) I : sorbitan monolaurate + ethoxylated sorbitan monoleurate (2û E O) (soluble) J . monooleate of polyethyleneglycol (MW : 200) + monooleate of polyethyleneglycol (MW : 600) (soluble) K : ethoxylated nonylphenol (4 E O) + ethoxylated nonylphenol (15 E O) L : ethoxylated fatty alcohol (3 E O) + ethoxylated fatty alcohol (9 E 0).
The emulsions prepared by using these emulsifying blends were not stable.
Example ii.
An emulsifying was prepared from gasoil (64 vol. %), emulsifying blend A of Example 1(4 vol. %), methanol (16 vol. %) and water (16 vol. %).
The cetane number of the emulsion was 26.
The emulsion was used to feed a Diesel engine.
A road test (80 km) was carried out and the emulsion consumption was 48.3 liters or a gasoil consumption of 30.9 liters. The same test was conducted but by feeding the Diesel engine with gasoil : the consumption was 39.3 liters.
Example 12.
Emulsions containing different amounts of emulsifying blend (blend A; HLB varying from 5.5.
to 6.5) were prepared.
Each emulsion had a total volume of 100 cc. It contained 22.5 cc of water and 12.5 cc of ethanol. The amount of emulsifying was varying between 1 and 10 cc and the amount of gasoil was varying between 55 and 64 cc.
The results of the stability tests are given in Table 10.
TABLE 10 Emulsifying blend (vol. %) HLB 1 2 3 4 5 6 8 10 5.5 - - + + + + + + + + + + + + 6 - - ++ ++ ++ ++ ++ ++ 6.5 - - + + + + + + + + + + + +

Claims (6)

1. Diesel fuel emulsions of the water-in-oil type comprising: 97 to 90 vol. % of a mixture comprising a major amount of usual diesel fuel and a minor amount of at least 5 vol. % based on the volume of the emulsion, of an aqueous solution of methanol and/or ethanol, and to 10 vol. % of an emulsifying blend of sorbitan monooleate and water soluble, ethoxylated non-ionic surfactant.
2. Diesel fuel emulsions according to Claim 1, comprising from 55 to 92 vol. % of gasoil, from 5 to 35 vol. % of aqueous solution of methanol and/or ethanol, the volume percentage of water in said solution being comprised between 43 + 0.20 S and 74, wherein S is the volume percentage of ethanol based on the total volume of alcohol, and from 3 to 10% volume of emulsifying blend having a HLB comprised between 5 and 6.5.
3. Diesel fuel emulsion according to Claim 2 wherein the surfactant is an ethoxylated sorbitan monooleate containing 20-40 moles of ethylene oxide, an ethoxylated sorbitan monolaurate containing 11-40 moles of ethylene oxide, an ethoxylated nonylphenol containing 8-50 moles of ethylene oxide, and ethoxylated fatty alcohol containing 6-50 moles of ethylene oxide and/or monooleate of polyethyleneglycol having a molecular weight comprising between 480 and 1200.
4. Diesel fuel emulsions according to Claim 1, comprising from 45 to 92 volume % of light fuel oil, from 5 to 45 vol. % of an aqueous solution of methanol and/or ethanol, the volume percentage of water in said solution being comprised between 45.7 + 0.229 S and 74.3, wherein S is the volume percentage of ethanol based on the total volume of alcohol and from 3 to 10% volume of emulsifying blend having a HLB QfiLB comprised between 5 and 7.
5. Diesel fuel emulsions according to claim 4, wherein the surfactant is an ethoxylated sorbitan monooleate containing 20-40 moles of ethylene oxide, and ethoxylated sorbitan monolaurate containing 11-40 moles of ethylene oxide, and ethoxylated nonylphenol containing 8-50 moles of ethylene oxide and/or a monooleate of polyethyleneglycol having a molecular weight comprised between 480 and 1200.
6. A process for producing the emulsions according to any of claims 1 to 4, which comprises adding while stirring the aqueous solution of alcohol to a mixture of fuel and emulsifying blend.
GB8036177A 1979-11-22 1980-11-11 Diesel fuel compositions and process for their production Expired GB2066288B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
LU81921A LU81921A1 (en) 1979-11-22 1979-11-22 FUEL COMPOSITIONS FOR A DIESEL ENGINE AND PROCESS FOR PREPARING THE SAME
US10627479A 1979-12-21 1979-12-21
LU82566A LU82566A1 (en) 1980-06-27 1980-06-27 FUEL COMPOSITIONS AND PROCESS FOR PREPARING THE SAME

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GB2066288A true GB2066288A (en) 1981-07-08
GB2066288B GB2066288B (en) 1984-01-18

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4482666A (en) * 1982-03-12 1984-11-13 Apace Research Limited Emulsions of liquid hydrocarbons with water and/or alcohols
EP0194365A1 (en) * 1984-12-05 1986-09-17 Hydroline Australia Pty. Ltd. Emulsions
US5573336A (en) * 1995-08-31 1996-11-12 The Torrington Company Seal for a spherical plain bearing
US5782936A (en) * 1997-04-23 1998-07-21 Suburban Propane, L.P. Additive compositions for LPG fuel
ES2152188A1 (en) * 1999-08-26 2001-01-16 Petroferm Inc Enhancement of the combustion of hydrocarbon fuel consists of dispersion of water droplets to form a fuel emulsion stabilised by a surfactant
WO2003031794A1 (en) * 2001-10-09 2003-04-17 Southwest Research Institute Oxygenated fuel plus water injection for emissions control in compression ignition devices
WO2003031540A1 (en) * 2001-10-08 2003-04-17 Imperial Chemical Industries Plc Diesel fuel emulsion
JP2006506481A (en) * 2002-11-13 2006-02-23 シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイ Diesel fuel composition
US7182797B2 (en) * 2004-11-08 2007-02-27 Kenneth Mekonen Fuel compositions
NL1034160C2 (en) * 2007-07-19 2009-01-20 Univ Eindhoven Tech Fuel mixture and method for its application.

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4482666A (en) * 1982-03-12 1984-11-13 Apace Research Limited Emulsions of liquid hydrocarbons with water and/or alcohols
EP0194365A1 (en) * 1984-12-05 1986-09-17 Hydroline Australia Pty. Ltd. Emulsions
US5573336A (en) * 1995-08-31 1996-11-12 The Torrington Company Seal for a spherical plain bearing
US5782936A (en) * 1997-04-23 1998-07-21 Suburban Propane, L.P. Additive compositions for LPG fuel
ES2152188A1 (en) * 1999-08-26 2001-01-16 Petroferm Inc Enhancement of the combustion of hydrocarbon fuel consists of dispersion of water droplets to form a fuel emulsion stabilised by a surfactant
WO2003031540A1 (en) * 2001-10-08 2003-04-17 Imperial Chemical Industries Plc Diesel fuel emulsion
JP2005504875A (en) * 2001-10-08 2005-02-17 インペリアル・ケミカル・インダストリーズ・ピーエルシー Diesel fuel emulsion
JP4870905B2 (en) * 2001-10-08 2012-02-08 クローダ インターナショナル パブリック リミティド カンパニー Diesel fuel emulsion
WO2003031794A1 (en) * 2001-10-09 2003-04-17 Southwest Research Institute Oxygenated fuel plus water injection for emissions control in compression ignition devices
US6637381B2 (en) 2001-10-09 2003-10-28 Southwest Research Institute Oxygenated fuel plus water injection for emissions control in compression ignition engines
JP2006506481A (en) * 2002-11-13 2006-02-23 シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイ Diesel fuel composition
US7182797B2 (en) * 2004-11-08 2007-02-27 Kenneth Mekonen Fuel compositions
NL1034160C2 (en) * 2007-07-19 2009-01-20 Univ Eindhoven Tech Fuel mixture and method for its application.

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