EP1159604A1 - Tensioactifs - Google Patents
TensioactifsInfo
- Publication number
- EP1159604A1 EP1159604A1 EP00909529A EP00909529A EP1159604A1 EP 1159604 A1 EP1159604 A1 EP 1159604A1 EP 00909529 A EP00909529 A EP 00909529A EP 00909529 A EP00909529 A EP 00909529A EP 1159604 A1 EP1159604 A1 EP 1159604A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fuel
- conductivity
- composition according
- fuel composition
- 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.)
- Withdrawn
Links
- 239000004094 surface-active agent Substances 0.000 title claims description 13
- 239000000446 fuel Substances 0.000 claims abstract description 95
- 239000000203 mixture Substances 0.000 claims abstract description 70
- 238000000034 method Methods 0.000 claims abstract description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 31
- 239000003502 gasoline Substances 0.000 claims description 14
- 239000004215 Carbon black (E152) Substances 0.000 claims description 11
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 9
- 229930195729 fatty acid Natural products 0.000 claims description 9
- 239000000194 fatty acid Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000003607 modifier Substances 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 4
- -1 fatty acid ester Chemical class 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims 2
- 229960000541 cetyl alcohol Drugs 0.000 claims 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical group CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 claims 1
- 229910001868 water Inorganic materials 0.000 description 12
- 101100001093 Arabidopsis thaliana AAE7 gene Proteins 0.000 description 10
- 150000001298 alcohols Chemical class 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000005259 measurement Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- ZZNDQCACFUJAKJ-UHFFFAOYSA-N 1-phenyltridecan-1-one Chemical compound CCCCCCCCCCCCC(=O)C1=CC=CC=C1 ZZNDQCACFUJAKJ-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical group COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001983 dialkylethers Chemical class 0.000 description 2
- 239000002283 diesel fuel Substances 0.000 description 2
- 238000007046 ethoxylation reaction Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000002816 fuel additive Substances 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- LPMBTLLQQJBUOO-KTKRTIGZSA-N (z)-n,n-bis(2-hydroxyethyl)octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CCO)CCO LPMBTLLQQJBUOO-KTKRTIGZSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
- C10L1/023—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark ignition
-
- 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
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
-
- 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
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/02—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
- G01N27/04—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
- G01N27/06—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a liquid
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/26—Oils; Viscous liquids; Paints; Inks
- G01N33/28—Oils, i.e. hydrocarbon liquids
- G01N33/2829—Mixtures of fuels
-
- 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
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1852—Ethers; Acetals; Ketals; Orthoesters
-
- 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
- C10L1/1985—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
-
- C—CHEMISTRY; METALLURGY
- 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
- C10L1/224—Amides; Imides carboxylic acid amides, imides
-
- 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
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
- C10L1/2431—Organic compounds containing sulfur, selenium and/or tellurium sulfur bond to oxygen, e.g. sulfones, sulfoxides
- C10L1/2437—Sulfonic acids; Derivatives thereof, e.g. sulfonamides, sulfosuccinic acid esters
Definitions
- This invention relates to novel method of determining the homogeneity of a fuel composition which comprises measuring the conductivity of the composition.
- British Patent No 2217229 describes a solubilising compound as a fuel additive.
- a composition comprising;
- a polyglycol ether such as ethoxylated oleic acid.
- compositions are useful as fuel additives and enable the solubilisation of water in fuels thus reducing its potential corrosive effect.
- the compositions are disadvantageous in that, inter alia, they require a high additive to fuel ratio.
- they do not address the problems of emissions of gases such as CO, CO 2 and NOX.
- WO '745 especially describes fuel compositions comprising, ter alia, an additive made up of a fatty acid diethanolamide, an alcohol ethoxylate and an ethoxylate of a fatty acid, the degree of ethoxylation being selected so that a long term stable fuel composition is formed and, in particular, wherein, by carefully selecting the degree of ethoxylation, a balanced molecule can be produced, such that the molecular weight ratios of each of the three components are substantially equivalent.
- LAMBDA is the theoretical stoichiometric amount of a fuel divided by the actual performing stoichiometry, therefore normally LAMBDA is 1 if the engine performance is at its optimum.
- the cloud point as referred to herein is defined as the temperature at which a substance begins to separate from solution, e.g. when a petroleum oil is chilled under definite prescribed conditions.
- a measure of when a fuel composition is at or near its cloud point is the conductivity of the fuel.
- water has a conductivity of 100 mS cm “1 and an alcohol, e.g. ethanol, a conductivity of 20 to 30 mS cm “1 .
- Fuels, such as gasoline or diesel, being non-ionic, generally have a conductivity of substantially zero.
- a non-homogenous mixture of a fuel, such as gasoline or diesel will have a relatively high conductivity reading, and as homogeneity is approached, the conductivity will reduce and will reach a minimum when the composition is a clear homogenous solution.
- a method of determining the homogeneity of a fuel composition which comprises measuring the conductivity of the composition.
- the conductivity may be measured at varying temperatures. However, we have found that measuring at substantially ambient temperature is preferred and particularly at 27.1 °C. Conductivity values given hereinafter generally relate to such values when measured at 27.1°C. Furthermore, since it is known that conductivity may vary with temperature, any conductivity values taken at differing temperatures should be calibrated as if measured at 27.1°C.
- a method of determining the homogeneity of a fuel composition which comprises a fuel and an oxygenator.
- a method of determining the conductivity in a composition as herein before described which is not less than 1 mS cm "1 for a light fraction hydrocarbon and not more than 1 mS cm "1 for a heavier fraction hydrocarbon.
- a fuel composition comprising an oxygenator and a hydrocarbon fuel which together form a continuous homogenous phase.
- the conductivity may vary depending on the hydrocarbon fuel.
- Hydrocarbon fuels which may be used in the course of the invention may be alkanes from C5 to C50. Particularly preferred fuels are gasoline, diesel, aviation fuel, etc.
- the conductivity should be not less than lmS cm " for a light fraction hydrocarbon and not more than lmS cm "1 for a heavier fraction hydrocarbon.
- a heavy fraction fuel eg a diesel fuel, composition as herein before described which has a conductivity of not greater than 1 mS cm “1 i.e. from 0 to lmScm "1 .
- a light fraction fuel eg a gasoline fuel, composition as herein before described which has a conductivity of not less than 1 mS cm “1 , for example, from 1 to 2 mS cm “1 .
- compositions with conductivity levels as described may be achieved by inclusion of a modifier, although this is not deemed essential.
- the homogenous fuel mixture may preferentially comprise a mixture of a fuel, an oxygenator and surfactant additive.
- Preferred surfactant additives are those which have the relative molecular weights substantially balanced.
- Particularly preferred surfactant additives are those described in International Patent Application No WO98/17745 which is incorporated herein by reference.
- Oxygenators which may be used include water, ethers, furans and the like and especially alcohols. Suitable alcohols are alkyl Cl to 10 alcohols, preferably alkyl Cl to 5 alcohols. Particular alcohols which may be mentioned are methanol, ethanol and propanol, but a preferred alcohol is ethanol.
- the oxygenator comprises an ether
- dialkyl ethers are preferred. Any conventionally known dialkyl ethers used as fuel oxygenators may be included in the formulation. However, a preferred ether is methyl t-butyl ether (MTBE).
- the amount of oxygenator present may vary depending upon, mter alia, the fuel and the oxygenator.
- the oxygenator is present as from 10 to 20% w/w of the composition, preferably from 12 to 18% w/w and especially 15% w/w.
- the storage characteristics of the fuel may be improved by the addition of a higher alcohol.
- higher alcohol we generally mean an alkyl alcohol with more than 10 carbon atoms, e.g. alkyl CIO to 50 alcohols.
- One object of the present invention is to provide a permanent, clear fuel with a consistent conductivity reading which will, ter alia, increase the performance of the vehicle enormous.
- AAE 7 is a surfactant composition comprising 50% w/w of an ethoxylated alcohol, said alcohol having a ratio of 3:1 of ethoxylate groups to Cl l alcohol; 25% w/w of a fatty acid diethanolamine and an ethoxylated fatty acid.
- AAE 7 comprises:
- a 30 litre tank was filled with water and maintained at a temperature of 27.1°C. The samples were placed in the tank and a temperature equilibrium was formed.
- a 30 litre tank was filled with water and maintained at a temperature of 28°C.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Electrochemistry (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9906214 | 1999-03-18 | ||
GBGB9906214.3A GB9906214D0 (en) | 1999-03-18 | 1999-03-18 | Surfactants |
PCT/GB2000/000957 WO2000055610A1 (fr) | 1999-03-18 | 2000-03-15 | Tensioactifs |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1159604A1 true EP1159604A1 (fr) | 2001-12-05 |
Family
ID=10849858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00909529A Withdrawn EP1159604A1 (fr) | 1999-03-18 | 2000-03-15 | Tensioactifs |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1159604A1 (fr) |
AU (1) | AU3181100A (fr) |
GB (1) | GB9906214D0 (fr) |
HK (1) | HK1044042A1 (fr) |
WO (1) | WO2000055610A1 (fr) |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3822119A (en) * | 1970-11-19 | 1974-07-02 | Goodyear Tire & Rubber | Anti-pollution anti-knock gasoline |
DE2632048A1 (de) * | 1976-07-16 | 1978-01-26 | Bold Karl Wilhelm | Verfahren zur bestimmung des dispersitaetsgrades eines mehrstoffsystems |
DE2949118A1 (de) * | 1979-12-06 | 1981-06-11 | Basf Ag, 6700 Ludwigshafen | Kraftstoffe fuer dieselmotoren |
US4410334A (en) * | 1981-10-30 | 1983-10-18 | Parkinson Harold B | Hydrocarbon fuel composition |
EP0082689A3 (fr) * | 1981-12-22 | 1984-09-26 | The British Petroleum Company p.l.c. | Composition de combustible |
US4541836A (en) * | 1982-12-09 | 1985-09-17 | Union Carbide Corporation | Fuel compositions |
CA1224628A (fr) * | 1982-12-09 | 1987-07-28 | Union Carbide Corporation | Carburants diesel |
DE3478465D1 (en) * | 1983-03-03 | 1989-07-06 | Union Rheinische Braunkohlen | Motor fuel |
US4557734A (en) * | 1984-08-08 | 1985-12-10 | The United States Of America As Represented By The Secretary Of Agriculture | Microemulsions from vegetable oil and lower alcohol with octanol surfactant as alternative fuel for diesel engines |
JPS62192633A (ja) * | 1986-02-19 | 1987-08-24 | Ngk Spark Plug Co Ltd | アルコ−ル混合燃料の混合比センサ |
GB8701368D0 (en) * | 1987-01-22 | 1987-02-25 | Ecc Int Ltd | Monitoring flocculation state of particles in suspension |
GB2217229B (en) * | 1988-04-25 | 1992-07-29 | Enersolve Chemical Company Lim | Solubilising composition |
US5103181A (en) * | 1988-10-05 | 1992-04-07 | Den Norske Oljeselskap A. S. | Composition monitor and monitoring process using impedance measurements |
JPH05133926A (ja) * | 1991-07-03 | 1993-05-28 | Nippondenso Co Ltd | 液体混合比率検出装置 |
US5425790A (en) * | 1992-12-23 | 1995-06-20 | Arco Chemical Technology, L.P. | Diesel fuel |
FR2711800B1 (fr) * | 1993-10-28 | 1996-01-12 | Agronomique Inst Nat Rech | Procédé et matériel de caractérisation de la stabilité d'une émulsion. |
GB9621753D0 (en) * | 1996-10-18 | 1996-12-11 | Williamson Ian V | 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 |
GB2336120A (en) * | 1998-04-09 | 1999-10-13 | Coval Technologies Limited | Solubilising water and fuel oil |
GB9827592D0 (en) * | 1998-12-15 | 1999-02-10 | Hamelin Holdings Limited | Fuel composition |
-
1999
- 1999-03-18 GB GBGB9906214.3A patent/GB9906214D0/en active Pending
-
2000
- 2000-03-15 WO PCT/GB2000/000957 patent/WO2000055610A1/fr not_active Application Discontinuation
- 2000-03-15 EP EP00909529A patent/EP1159604A1/fr not_active Withdrawn
- 2000-03-15 AU AU31811/00A patent/AU3181100A/en not_active Abandoned
-
2002
- 2002-06-05 HK HK02104267.6A patent/HK1044042A1/zh unknown
Non-Patent Citations (1)
Title |
---|
See references of WO0055610A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2000055610A1 (fr) | 2000-09-21 |
AU3181100A (en) | 2000-10-04 |
HK1044042A1 (zh) | 2002-10-04 |
GB9906214D0 (en) | 1999-05-12 |
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