EP0049921B1 - Clear liquid fuel mixture for combustion engines - Google Patents
Clear liquid fuel mixture for combustion engines Download PDFInfo
- Publication number
- EP0049921B1 EP0049921B1 EP81201092A EP81201092A EP0049921B1 EP 0049921 B1 EP0049921 B1 EP 0049921B1 EP 81201092 A EP81201092 A EP 81201092A EP 81201092 A EP81201092 A EP 81201092A EP 0049921 B1 EP0049921 B1 EP 0049921B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- water
- weight
- mixture
- methanol
- alcohols
- 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.)
- Expired
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- 239000000203 mixture Substances 0.000 title claims abstract description 81
- 239000000446 fuel Substances 0.000 title claims abstract description 33
- 239000007788 liquid Substances 0.000 title claims abstract description 30
- 238000002485 combustion reaction Methods 0.000 title claims abstract description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 105
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 68
- 150000001298 alcohols Chemical class 0.000 claims abstract description 43
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000013543 active substance Substances 0.000 claims abstract description 17
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 10
- 238000007036 catalytic synthesis reaction Methods 0.000 claims description 3
- 238000000629 steam reforming Methods 0.000 claims description 2
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 claims 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical group CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 10
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000004530 micro-emulsion Substances 0.000 description 3
- 238000005191 phase separation Methods 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical group CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- -1 alkyl phenols Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000001193 catalytic steam reforming Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material 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
- C10L1/32—Liquid carbonaceous fuels consisting of coal-oil suspensions or aqueous emulsions or oil emulsions
- C10L1/328—Oil emulsions containing water or any other hydrophilic phase
-
- 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
-
- 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
- C10L1/12—Inorganic compounds
- C10L1/1233—Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof
- C10L1/125—Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof water
-
- 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
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1824—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
Definitions
- the invention relates to a clear liquid mixture for application as fuel in combustion engines, comprising:
- the fuel mixture described in this patent specification consists of:
- a special combination of surface-active agents is required for the dispersion of alcohol and water in petrol or oil in order to obtain a stable water-containing fuel mixture with a water-soluble alcohol, such as methanol.
- a water-soluble alcohol such as methanol.
- alcohol fully soluble in water, methanol, ethanol, propanol or a mixture of these alcohols is applied.
- the Dutch patent application 7416290 relates to the operation of Otto and rotary piston engine, using petrol as fuel simultaneously with water-containing crude methanol. It is true that the alcohol used is cheap, but this is amply offset by the disadvantage that for each motor vehicle separate tanks and separate injection systems for the petrol and for the water-containing crude methanol are required. When combined in advance, such a mixture will show phase separation, which makes application impossible. In order to be able to use this fuel each motor vehicle, will require the necessary investments.
- the European patent application 12345 relates to engine and turbine fuels containing water and alcohol and using a special and expensive nonionogenic emulsifier to obtain good stability, even in coldness. Relatively much stirring energy is required in order to prepare a milky emulsion of the various components. Another disadvantage is that, if this fuel mixture has been left to stand for some time, or if unfortunately water has found its way into it, further stirring energy will be required again in order to obtain an emulsion. This is rather problematical if this fuel mixture is contained in the tank of a motor vehicle. Furthermore, it is difficult to determine if phase separation has already taken place. The stability in coldness, too, is not quite satisfactory.
- the purpose of the invention is to remove the said disadvantages and to provide a clear liquid fuel mixture for combustion engines, as stated in the preamble, which fuel mixture is cheap, does not separate out even after it has been left to stand for a long time, which is stable at -20°C and which allows the various components to be mixed with each other virtually without use of stirring energy to form a clear liquid mixture.
- a further purpose of the invention is to provide a fuel mixture containing relatively few petroleum- recovered hydrocarbons and relatively many liquid raw materials which can be prepared from natural gas and/or coal. Furthermore, the fuel mixture must be applicable in the existing engines.
- the stability range i.e. the range in which a clear mixture is obtained and/or kept, to be as wide as possible, particularly at -20°C. This will strongly reduce the risk of phase separation at fluctuations in the composition of the mixture. Furthermore, it will also give greater freedom in the composition of the fuel mixture.
- the fuel mixture consists of:
- the alcohols with 4-12 C atoms not or sparingly solubility in water may also be divalent alcohols, such as diols. Preference, however, is given to monovalent alcohols.
- Sparingly soluble in water is understood here to mean that only very subordinate quantities will dissolve in water, i.e. smaller than 25% by weight, preferably smaller than 10% weight.
- the mixture can be converted very simply into a clear whole. This can be done by shaking, filling of the storage tank or simply by transport.
- Another major advantage of the invention is that, without adversely effecting the clearness and stability of the fuel mixture, the quantities of water-soluble alcohols and alcohols not or sparingly soluble in water can be varied in respect of each other.
- methanol water and higher alcohol may be present in such amounts that the fuel mixture contains 1-10% by weight of water; 0,1-25% by weight of methanol; 0,01-20% by weight of alcohols with 4 to 12 C atoms not or sparingly soluble in water and 5-10% by weight of alcohols with 2-4 C atoms fully soluble in water.
- Another liquid mixture according to the invention may contain methanol, water and higher alcohols in such an amount that the fuel mixture contains 1-10 by weight of water, 0,1-25% by weight of methanol, 5-20% by weight of alcohols with 4-12 C atoms not or sparingly soluble in water and 0,01 -5% by weight of alcohols with 2-4 C atoms fully soluble in water.
- the alcohol with 2-4 C atoms fully soluble in water is preferably tertiary butanol, together with the small quantities of alcohols not or sparingly soluble in water.
- the alcohol with 4-12 C atoms not or sparingly soluble in water is n-butanol or n-pentanol.
- the quantities of water and methanol in the liquid mixture can be varied in respect of each other.
- the liquid mixture according to the invention preferably methanol, water and higher alcohols are present in such amounts that the fuel mixture contains 1-5% by weight of water and 2-15% by weight of methanol.
- micro-emulsion is formed, which is understood to mean a transparent, stable, liquid system consisting of at least two liquids which cannot or hardly be mixed, in which system one liquid is dispersed by means of one or more surface-active substances in the other.
- the drop size is substantially smaller than that of an ordinary emulsion and, in consequence, a micro-emulsion, unlike an ordinary emulsion, is transparent.
- the formation of micro-emulsions requires no special measures. They are formed spontaneously as soon as the various components are brought together. Preferably anionogenic or nonionogenic surface-active substances and specifically combinations thereof are applied.
- a mixture of surface-active acid and salts of these acids as surface-active substances have the greatest preference, because these have been found very suitable and are, moreover, cheap.
- the liquid mixture preferably contains 0.1-10% by weight of surface-active substances. The quantity can easily be determined by one skilled in the art. If a nonclear emulsion is formed, the quantity must be increased.
- a mixture of methanol, water and alcohols not or sparingly soluble in water can be obtained directly by catalytic steam reforming of methane an successive catalytic synthesis of the gas mixture obtained, without successive purification, such as removal of water and higher alcohols.
- the mixture formed is extremely suitable for dispersion in petrol by means of surface-active substances and optionally a higher alcohol, in which process a mixture is obtained which remains clear and stable within a wide temperature range (-20°C to +30°C).
- the mixture obtained contains, in respect of methanol, 10-25% by volume of water and 0.05-0.5% by volume or more of higher alcohols.
- the mixture may additionally contain an ether with 2-8 C atoms, specifically methyl-tertiary butylether.
- the alcohol not soluble in water can then be partly replaced by the said ether.
- the mixture of surface-active substances was dissolved in the alcohol mixture and as such added to the petrol.
- the mixture contains 10 ml regular petrol (RON 88; MON 82), 0.8 g ammonium oleate-oleic acid mixture in the proportion of 60:40; 1.8 g crude methanol of the composition as in example I.
Landscapes
- 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)
Abstract
Description
- The invention relates to a clear liquid mixture for application as fuel in combustion engines, comprising:
- a liquid hydrocarbon mixture;
- water;
- an alcohol fully soluble in water;
- surface-active substances.
- Such a clear, liquid fuel mixture is known from United States patent 4,002,435.
- The fuel mixture described in this patent specification consists of:
- a. petrol or diesel oil;
- b. 0.1-10% of water;
- c. 0.1-20% of an alcohol fully soluble in water and
- d. a combination of surface-active agents, consisting of:
- 1. a salt of saturated or unsaturated higher fatty acid;
- 2. an unsaturated organic acid; and
- 3. an ethylene oxide condensation product.
- According to this patent specification, a special combination of surface-active agents is required for the dispersion of alcohol and water in petrol or oil in order to obtain a stable water-containing fuel mixture with a water-soluble alcohol, such as methanol. As alcohol fully soluble in water, methanol, ethanol, propanol or a mixture of these alcohols is applied.
- The disadvantage of this fuel mixture is that it is relatively expensive, because special surface-active agents are necessary for dispersing the alcohols fully soluble in water in petrol to a mixture which is stable over a wide temperature range.
- The Dutch patent application 7416290 relates to the operation of Otto and rotary piston engine, using petrol as fuel simultaneously with water-containing crude methanol. It is true that the alcohol used is cheap, but this is amply offset by the disadvantage that for each motor vehicle separate tanks and separate injection systems for the petrol and for the water-containing crude methanol are required. When combined in advance, such a mixture will show phase separation, which makes application impossible. In order to be able to use this fuel each motor vehicle, will require the necessary investments.
- The European patent application 12345 relates to engine and turbine fuels containing water and alcohol and using a special and expensive nonionogenic emulsifier to obtain good stability, even in coldness. Relatively much stirring energy is required in order to prepare a milky emulsion of the various components. Another disadvantage is that, if this fuel mixture has been left to stand for some time, or if unfortunately water has found its way into it, further stirring energy will be required again in order to obtain an emulsion. This is rather problematical if this fuel mixture is contained in the tank of a motor vehicle. Furthermore, it is difficult to determine if phase separation has already taken place. The stability in coldness, too, is not quite satisfactory.
- From FR-A-2114465 a one phase system of a combustion fuel is known which discloses a complex mixture of a fuel, purified methanol and further additives.
- The purpose of the invention is to remove the said disadvantages and to provide a clear liquid fuel mixture for combustion engines, as stated in the preamble, which fuel mixture is cheap, does not separate out even after it has been left to stand for a long time, which is stable at -20°C and which allows the various components to be mixed with each other virtually without use of stirring energy to form a clear liquid mixture.
- A further purpose of the invention is to provide a fuel mixture containing relatively few petroleum- recovered hydrocarbons and relatively many liquid raw materials which can be prepared from natural gas and/or coal. Furthermore, the fuel mixture must be applicable in the existing engines.
- It has been found that higher alcohols not or sparingly soluble in water have a positive effect on the increase of the stability range of clear fuel mixtures containing hydrocarbons, methanol and water, even if these higher alcohols are present in very small quantities. Very small quantities are understood to mean quantities in the order of 0.02% by volume.
- It is very important for the stability range, i.e. the range in which a clear mixture is obtained and/or kept, to be as wide as possible, particularly at -20°C. This will strongly reduce the risk of phase separation at fluctuations in the composition of the mixture. Furthermore, it will also give greater freedom in the composition of the fuel mixture.
- According to the invention the fuel mixture consists of:
- a. a liquid hydrocarbon mixture;
- b. a mixture of methanol, water and higher alcohols, that has been obtained by steam reforming of methane and subsequent catalytic synthesis of the gas mixture obtained, in such amount that the fuel mixture contains 1-10% by weight of water; 0,1-25% by weight of methanol and 0,01-20% by weight of alcohols with 4 to 12 C atoms not or sparingly soluble in water;
- c. 0.1-15% by weight of surface-active substances; and optionally
- d. 5-20% by weight of an alcohol with 2-12 C atoms, and/or
- e. 0,01-15% by weight of an ether with 2-8 C atoms.
- The alcohols with 4-12 C atoms not or sparingly solubility in water may also be divalent alcohols, such as diols. Preference, however, is given to monovalent alcohols.
- According to the invention it is possible to incorporate the mixture of methanol, water and higher alcohols in hydrocarbons just by means of surface-active substances, although it is an advantage to add optionally an extra quantity of alcohol with 2 to 12 C atoms, or with 2-8 C atoms, because the quantity of surface-active substances required may then be smaller. Optionally 5-20% by weight respectively 0,01-15% by weight of these alcohols may be added.
- Sparingly soluble in water is understood here to mean that only very subordinate quantities will dissolve in water, i.e. smaller than 25% by weight, preferably smaller than 10% weight.
- The mixture can be converted very simply into a clear whole. This can be done by shaking, filling of the storage tank or simply by transport.
- The fuel mixture according to the invention has the following advantages:
- a. it is clear;
- b. requires little or no stirring energy during its preparation;
- c. is stable to at least -20°C;
- d. gives lower emission of harmful components in the exhaust gases than petrol;
- e. gives good knock resistance so that the addition of tetra-alkyl lead to raise the octane number is not necessary.
- It has specifically been found that, in addition to small quantities of these higher alcohols not or sparingly soluble in water, a larger quantity of alcohols with 2-4 C atoms fully soluble in water has the effect that a substantially smaller quantity of surface-active agents is required.
- By the addition or use of larger quantities of alcohols with 4-12 C atoms not or sparingly soluble in water, the quantity of surface-active substances can be reduced, while a simultaneous widening of the stability range will be found.
- Another major advantage of the invention is that, without adversely effecting the clearness and stability of the fuel mixture, the quantities of water-soluble alcohols and alcohols not or sparingly soluble in water can be varied in respect of each other.
- Thus in the liquid mixture according to the invention methanol, water and higher alcohol may be present in such amounts that the fuel mixture contains 1-10% by weight of water; 0,1-25% by weight of methanol; 0,01-20% by weight of alcohols with 4 to 12 C atoms not or sparingly soluble in water and 5-10% by weight of alcohols with 2-4 C atoms fully soluble in water.
- Another liquid mixture according to the invention may contain methanol, water and higher alcohols in such an amount that the fuel mixture contains 1-10 by weight of water, 0,1-25% by weight of methanol, 5-20% by weight of alcohols with 4-12 C atoms not or sparingly soluble in water and 0,01 -5% by weight of alcohols with 2-4 C atoms fully soluble in water.
- The alcohol with 2-4 C atoms fully soluble in water is preferably tertiary butanol, together with the small quantities of alcohols not or sparingly soluble in water.
- Preferably the alcohol with 4-12 C atoms not or sparingly soluble in water is n-butanol or n-pentanol.
- As stated earlier, the quantities of water and methanol in the liquid mixture can be varied in respect of each other. In the liquid mixture according to the invention preferably methanol, water and higher alcohols are present in such amounts that the fuel mixture contains 1-5% by weight of water and 2-15% by weight of methanol.
- For dispersing the water and the alcohols in the petrol, surface-active substances are required.
- It is supposed that a so-called micro-emulsion is formed, which is understood to mean a transparent, stable, liquid system consisting of at least two liquids which cannot or hardly be mixed, in which system one liquid is dispersed by means of one or more surface-active substances in the other. The drop size is substantially smaller than that of an ordinary emulsion and, in consequence, a micro-emulsion, unlike an ordinary emulsion, is transparent. Apart from the limited amount of energy required for mixing the components, the formation of micro-emulsions requires no special measures. They are formed spontaneously as soon as the various components are brought together. Preferably anionogenic or nonionogenic surface-active substances and specifically combinations thereof are applied. A mixture of surface-active acid and salts of these acids as surface-active substances have the greatest preference, because these have been found very suitable and are, moreover, cheap. The liquid mixture preferably contains 0.1-10% by weight of surface-active substances. The quantity can easily be determined by one skilled in the art. If a nonclear emulsion is formed, the quantity must be increased.
- As anionogenic surface-active substances the following are eligible:
- - salts of surface-active carboxylic acids, specifically fatty acids with 10 to 20 C atoms;
- - sulphuric acid esters, specifically alkyl esters with an alkyl group of 10 to 20 C atoms;
- - alkyl and alkylaryl sulphonates, in which the alkyl group has 10 to 20 C atoms and the alkylaryl group 10 to 26 C atoms;
- - paraffin sulphonates, lignin sulphonates;
- - phosphoric acid esters, specifically alkyl esters with an alkyl group of 10 to 20 C atoms;
- - salts of surface-active phosphorous and phosphoric acids.
- As nonionogenic surface-active substances the following are eligible:
- - ethylene oxide condensation products with, for instance, alcohols with 6 to 18 C atoms, alkyl phenols, polyols or propylene oxide;
- - polyhydroxy compounds, such as esters of polyols and fatty acids;
- - fatty acids, both saturated and unsaturated, with 10 to 20 C atoms.
- It is a great advantage of the present invention that a mixture can directly be applied as obtained in the preparation of methanol, starting form methane, without water and higher alcohols having to be removed.
- A mixture of methanol, water and alcohols not or sparingly soluble in water can be obtained directly by catalytic steam reforming of methane an successive catalytic synthesis of the gas mixture obtained, without successive purification, such as removal of water and higher alcohols. The mixture formed is extremely suitable for dispersion in petrol by means of surface-active substances and optionally a higher alcohol, in which process a mixture is obtained which remains clear and stable within a wide temperature range (-20°C to +30°C). The mixture obtained contains, in respect of methanol, 10-25% by volume of water and 0.05-0.5% by volume or more of higher alcohols.
- In order even further to improve the stability of the clear liquid mixture obtained even further, the mixture may additionally contain an ether with 2-8 C atoms, specifically methyl-tertiary butylether. The alcohol not soluble in water can then be partly replaced by the said ether. Preferably 0.01 to 15% by weight, specifically 0.05-10% by weight, of ether is added.
- Clear liquid mixtures were formed by bringing together in a test tube:
- Premium petrol (RON=99; MON=88; boiling range 35 to 200°C); methanol in the form of crude methanol with 21.5% by volume of water and 0.02% by volume of alcohols not or sparingly soluble in water, such as butanol, pentanol and higher alcohols, and 0.08% by volume of alcohols completely soluble in water, such as ethanol and propanol; or pure methanol with 21.5% by volume of water; a mixture of Na-oleate and oleic acid in the ratio of 80:20 and n-butanol.
- The mixture of surface-active substances was dissolved in the alcohol mixture and as such added to the petrol.
-
- With 1.00 g methanol (pure and crude) the same results are obtained.
- It is, furthermore, found that, if 0.75 to 1.75 g crude methanol is added, a clear mixture is obtained at both surfactant butanol ratios. It has, furthermore, been found that the stability range is twice as large as that when pure methanol with 21.5% by volume of water is used.
- In order to show the effects of different types of alcohol on the stability of the clear liquid mixture according to the invention, the quantities in grammes of each type of alcohol at +20°C respectively ―20°C to be added in order to obtain a clear stable liquid mixture were determined.
-
- These results show that the non-soluble alcohols, particularly n-butanol and n-pentanol, clearly produce the greatest effects.
- In this example the effect of the addition of methyl-tertiary-butylether (MTBE) on the stability of the liquid mixtures according to the invention is shown.
-
Claims (4)
characterized in that the fuel mixture consists of:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT81201092T ATE11676T1 (en) | 1980-10-09 | 1981-10-02 | CLEAR, LIQUID FUEL MIXTURE FOR INTERNAL COMBUSTION ENGINES. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL8005581A NL8005581A (en) | 1980-10-09 | 1980-10-09 | CLEAR LIQUID FUEL MIXTURE FOR COMBUSTION ENGINES. |
NL8005581 | 1980-10-09 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0049921A1 EP0049921A1 (en) | 1982-04-21 |
EP0049921B1 true EP0049921B1 (en) | 1985-02-06 |
Family
ID=19836001
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP81201092A Expired EP0049921B1 (en) | 1980-10-09 | 1981-10-02 | Clear liquid fuel mixture for combustion engines |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0049921B1 (en) |
AT (1) | ATE11676T1 (en) |
DE (1) | DE3168809D1 (en) |
NL (1) | NL8005581A (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1224628A (en) * | 1982-12-09 | 1987-07-28 | Union Carbide Corporation | Diesel fuels |
DE3307091A1 (en) * | 1983-03-01 | 1984-09-06 | Union Rheinische Braunkohlen Kraftstoff AG, 5000 Köln | FUEL AND USE THEREOF |
DE3330165C2 (en) * | 1983-08-20 | 1985-10-03 | Union Rheinische Braunkohlen Kraftstoff AG, 5000 Köln | Engine fuel |
DE3345516A1 (en) * | 1983-12-16 | 1985-07-04 | Uni-Commerz Handelsgesellschaft mbH, 2800 Bremen | SOLUTION AGENT FOR CARBURETOR FUELS |
IT1197464B (en) * | 1985-12-19 | 1988-11-30 | Snam Progetti | COMPOSITION FOR HIGH OCTANCY OXYGEN FUEL AND METHOD FOR ITS PREPARATION |
US4744796A (en) * | 1986-02-04 | 1988-05-17 | Arco Chemical Company | Microemulsion fuel system |
US4795478A (en) * | 1986-06-17 | 1989-01-03 | Intevep, S.A. | Viscous hydrocarbon-in-water emulsions |
US4713087A (en) * | 1986-10-14 | 1987-12-15 | Texaco Inc. | Carrier composition for introducing additives to a motor fuel |
NO864988D0 (en) * | 1986-12-10 | 1986-12-10 | Dyno Industrier As | UPGRADING OF HEAVY GROWN OIL FRACTIONS FOR USE AS LIGHTING FUEL OILS OR DIESEL OILS AND UPGRADED OILS. |
GB2231061B (en) * | 1987-09-11 | 1992-05-20 | Intevep Sa | Viscous hydrocarbon-in-water emulsions |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3822119A (en) * | 1970-11-19 | 1974-07-02 | Goodyear Tire & Rubber | Anti-pollution anti-knock gasoline |
US4002435A (en) * | 1971-11-17 | 1977-01-11 | Wenzel Edward C | Clear and stable liquid fuel compositions for internal combustion engines |
US4154580A (en) * | 1974-03-22 | 1979-05-15 | Mobil Oil Corporation | Method for producing a stabilized gasoline-alcohol fuel |
US4098339A (en) * | 1976-06-21 | 1978-07-04 | Mobil Oil Corporation | Utilization of low BTU natural gas |
DE2854540A1 (en) * | 1978-12-16 | 1980-06-26 | Bayer Ag | FUELS |
-
1980
- 1980-10-09 NL NL8005581A patent/NL8005581A/en not_active Application Discontinuation
-
1981
- 1981-10-02 EP EP81201092A patent/EP0049921B1/en not_active Expired
- 1981-10-02 DE DE8181201092T patent/DE3168809D1/en not_active Expired
- 1981-10-02 AT AT81201092T patent/ATE11676T1/en active
Also Published As
Publication number | Publication date |
---|---|
NL8005581A (en) | 1982-05-03 |
DE3168809D1 (en) | 1985-03-21 |
ATE11676T1 (en) | 1985-02-15 |
EP0049921A1 (en) | 1982-04-21 |
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