EP0082688A2 - Brennstoffzusammensetzung - Google Patents
Brennstoffzusammensetzung Download PDFInfo
- Publication number
- EP0082688A2 EP0082688A2 EP82306743A EP82306743A EP0082688A2 EP 0082688 A2 EP0082688 A2 EP 0082688A2 EP 82306743 A EP82306743 A EP 82306743A EP 82306743 A EP82306743 A EP 82306743A EP 0082688 A2 EP0082688 A2 EP 0082688A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- volume
- carbonate
- gasoline
- fuel composition
- fuel
- 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- Withdrawn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
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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- 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
Definitions
- This invention relates to a fuel composition suitable for use in spark ignition internal combustion engines.
- Certain oxygenated organic compounds have been known to be potentially suitable as fuels for internal combustion engines for many years. Interest in such components as fuels declined when crude oil became cheap and plentiful, but has revived in recent years.
- the most commonly proposed compounds are alcohols e.g. methanol, ethanol or tertiary butyl alcohol and ethers e.g. methyl tertiary butyl ether.
- Oxygenated organic compounds can be used as fuels per se, but normally they are proposed for use in admixture with conventional hydrocarbon fuels, thereby avoiding the need for any major modification of engines using the fuels.
- the oxygenated organic compounds should have a number of particular physical and chemical characteristics such as total miscibility, suitable volatility, and, preferably, low water solubility.
- One of the most important characteristics for spark ignition engine fuels is the blending octane value, both in respect of the Research Octane Number (RON) and the Motor Octane Number (MON). It is desirable that the oxygenated compounds used should have blending octane values that enhance rather than depress the Octane Numbers of the neat hydrocarbon fuel.
- a fuel composition suitable for use in internal combustion engines comprises a gasoline and a dialkyl carbonate having a boiling point of not more than 150°C.
- the alkyl groups may be the same or different and, to keep the boiling point at not more than 150°C, the alkyl groups may be methyl, ethyl or isopropyl.
- the dialkyl carbonate boils below 130°C.
- Preferred compounds are dimethyl carbonate which boils at 91°C and diethyl carbonate which boils at 126°C.
- the proportion of dialkyl carbonate may be from 0.1 to 50% by volume, preferably from 5 to 25X by volume of the fuel composition.
- Dialkyl carbonates may be produced by any of the known methods, such as for example by reacting an alkanol with carbon monoxide in the presence of a catalyst, e.g. palladium or platinum salts or a copper complex catalyst. It may thus be produced from relatively cheap and abundant reactants.
- a catalyst e.g. palladium or platinum salts or a copper complex catalyst. It may thus be produced from relatively cheap and abundant reactants.
- the gasoline has, before the addition of the dialkyl carbonate, a RON of from 85 to 105, more preferably from 90 to 98 and a MON of from 75 to 95, more preferably from 80 to 88.
- the gasoline may contain the following proportions of olefins, aromatics and saturates;
- the fuel may contain a lead alkyl anti-knock agent in an amount up to 0.45g Pb/1, more preferably up to 0.15g Pb/1.
- a lead alkyl anti-knock agent in an amount up to 0.45g Pb/1, more preferably up to 0.15g Pb/1.
- Other known fuel components may be included in the compositions e.g. a scavenger, other oxygenated compounds and anti-icing or other known additives.
- dialkyl carbonates have been tested in a range of gasolines, both aromatic and olefinic and both leaded and unleaded. Blending octane values for the dialkyl carbonates have been found to range from 106 to 112 RON and 96 to 106 MON, when added to gasoline at a concentration of 10% by volume.
- Dimethyl carbonate was admixed with two gasolines, one an aromatic basestock and the other an olefinic basestock.
- the aromatic basestock comprised 47.3% by volume aromatics and 52.7% by volume saturates.
- the olefinic basestock comprised 31.0% by volume aromatics, 53.8% by volume saturates and 15.2% by volume olefins.
- the Research and Motor Octane Numbers of the gasolines and the blends containing dimethyl carbonate were determined in a CFR engine.
- the Blending Octane Values (B.O.V.) were also calculated from the measured RONs and MONs of the gasolines and the dimethyl carbonate/gasoline blends, using the formula; where,
- the dimethyl carbonate was a commercial material supplied by the Aldrich Chemical Company. It had a boiling point of 91°C.
- the method measures the amount of water which can be added to a motor fuel, which may consist of a blend of hydrocarbons with a watersoluble constituent such as alcohol, without causing separation into two phases, at a specified temperature.
- the method comprises cooling a sample of the blend to about 4°C and adding water until separation into two layers occurs. The sample is, then warmed until miscibility occurs and then cooled slowly. The temperature at which the first signs of cloudiness occurs is recorded. The test is repeated with different volumes of water and the water tolerance at specified temperatures obtained from a graph of volume of water against temperature of immiscibility.
- Table 2 shows that the inclusion of 10% vol of dimethyl carbonate gives a significant increase in both the RON and the MON. This is because of intrinsically high RON and MON of the dimethyl carbonate itself.
- diethyl carbonate 10% by volume diethyl carbonate was admixed with a gasoline from an aromatic base-stock comprising 40.2% by volume aromatics and 59.8% by volume saturates.
- the diethyl carbonate was a commercial product supplied by Aldrich Chemical Company.
- the boiling point of the diethyl carbonate was 125°C.
- a test was carried out to simulate adverse tank storage conditions. 5 cm 3 of mains tap water were added to 100 cm 3 of the gasoline/diethyl carbonate blend and the mixture was agitated for about 30 seconds. The mixture was allowed to stand for one week and a sample of the bottom layer, i.e. the water phase, was subjected to IR analysis to determine the amount of diethyl carbonate in this layer. The water phase contained less than 1% by volume of diethyl carbonate.
- Blending Octane Values for the diethyl carbonate were calculated from the Research and Motor Octane Numbers determined in a CFR engine.
- the CFR engine results are given in Table 4.
- dimethyl carbonate 10X by volume of dimethyl carbonate was admixed with a gasoline containing 0.15g Pb/l as Tetra ethyl lead.
- the dimethyl carbonate was the same as used in Example 1.
- the RON and MON of the gasoline and the blend were determined in a CFR engine and the Blending Octane Values calculated from the measured RONs and MONs.
- the results given in Table 5 show that the dialkyl carbonate is also useful in leaded gasoline.
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)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8138607 | 1981-12-22 | ||
| GB8138607 | 1981-12-22 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0082688A2 true EP0082688A2 (de) | 1983-06-29 |
| EP0082688A3 EP0082688A3 (de) | 1984-09-26 |
Family
ID=10526772
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP82306743A Withdrawn EP0082688A3 (de) | 1981-12-22 | 1982-12-17 | Brennstoffzusammensetzung |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0082688A3 (de) |
| AU (1) | AU9142782A (de) |
| DK (1) | DK562982A (de) |
| NO (1) | NO824258L (de) |
| ZA (1) | ZA829195B (de) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0098691A3 (de) * | 1982-06-21 | 1984-12-12 | Imperial Chemical Industries Plc | Brennstoffzusammensetzungen |
| US4600408A (en) * | 1985-04-29 | 1986-07-15 | Union Oil Company Of California | Gasoline compositions containing carbonates |
| US4647292A (en) * | 1985-04-29 | 1987-03-03 | Union Oil Company Of Company | Gasoline composition containing acid anhydrides |
| US4781728A (en) * | 1985-04-29 | 1988-11-01 | Union Oil Company Of California | Octane enhancers for fuel compositions |
| WO2008072039A1 (en) * | 2006-12-12 | 2008-06-19 | Rosario Rocco Tulino | Tetra-component additive for the octaning and oxygenating reformulation of ecological petrol for motor-traction |
| US8557001B2 (en) | 2009-11-24 | 2013-10-15 | Shell Oil Company | Fuel formulations |
| EP2664608A1 (de) * | 2012-05-17 | 2013-11-20 | Beijing Jinjiao Biomass Chemical Industry Co., Ltd | Umweltfreundlicher flüssiger Brennstoff und Herstellungsverfahren dafür |
| US8663346B2 (en) | 2009-11-24 | 2014-03-04 | Shell Oil Company | Fuel formulations |
| EP2868737A1 (de) * | 2013-10-31 | 2015-05-06 | Shell Internationale Research Maatschappij B.V. | Hochoktaniges bleifreies Flugbenzin |
| EP3399008A1 (de) * | 2017-05-02 | 2018-11-07 | ASG Analytik-Service Gesellschaft mbH | Potenziell co2-neutraler und umweltschonender ottokraftstoff auf basis der c1-chemie |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2331386A (en) * | 1939-11-03 | 1943-10-12 | Standard Oil Dev Co | Modified fuel |
-
1982
- 1982-12-13 AU AU91427/82A patent/AU9142782A/en not_active Abandoned
- 1982-12-14 ZA ZA829195A patent/ZA829195B/xx unknown
- 1982-12-17 EP EP82306743A patent/EP0082688A3/de not_active Withdrawn
- 1982-12-17 NO NO824258A patent/NO824258L/no unknown
- 1982-12-20 DK DK562982A patent/DK562982A/da not_active Application Discontinuation
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0098691A3 (de) * | 1982-06-21 | 1984-12-12 | Imperial Chemical Industries Plc | Brennstoffzusammensetzungen |
| US4600408A (en) * | 1985-04-29 | 1986-07-15 | Union Oil Company Of California | Gasoline compositions containing carbonates |
| US4647292A (en) * | 1985-04-29 | 1987-03-03 | Union Oil Company Of Company | Gasoline composition containing acid anhydrides |
| US4781728A (en) * | 1985-04-29 | 1988-11-01 | Union Oil Company Of California | Octane enhancers for fuel compositions |
| WO2008072039A1 (en) * | 2006-12-12 | 2008-06-19 | Rosario Rocco Tulino | Tetra-component additive for the octaning and oxygenating reformulation of ecological petrol for motor-traction |
| US8557001B2 (en) | 2009-11-24 | 2013-10-15 | Shell Oil Company | Fuel formulations |
| US8663346B2 (en) | 2009-11-24 | 2014-03-04 | Shell Oil Company | Fuel formulations |
| EP2664608A1 (de) * | 2012-05-17 | 2013-11-20 | Beijing Jinjiao Biomass Chemical Industry Co., Ltd | Umweltfreundlicher flüssiger Brennstoff und Herstellungsverfahren dafür |
| EP2868737A1 (de) * | 2013-10-31 | 2015-05-06 | Shell Internationale Research Maatschappij B.V. | Hochoktaniges bleifreies Flugbenzin |
| AU2014206204B2 (en) * | 2013-10-31 | 2015-11-12 | Shell Internationale Research Maatschappij B.V. | High octane unleaded aviation gasoline |
| US9388359B2 (en) | 2013-10-31 | 2016-07-12 | Shell Oil Company | High octane unleaded aviation gasoline |
| EP3399008A1 (de) * | 2017-05-02 | 2018-11-07 | ASG Analytik-Service Gesellschaft mbH | Potenziell co2-neutraler und umweltschonender ottokraftstoff auf basis der c1-chemie |
Also Published As
| Publication number | Publication date |
|---|---|
| ZA829195B (en) | 1984-07-25 |
| DK562982A (da) | 1983-06-23 |
| NO824258L (no) | 1983-06-23 |
| AU9142782A (en) | 1983-06-30 |
| EP0082688A3 (de) | 1984-09-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Designated state(s): AT BE DE FR GB IT NL SE |
|
| PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
| AK | Designated contracting states |
Designated state(s): AT BE DE FR GB IT NL SE |
|
| 17P | Request for examination filed |
Effective date: 19850325 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
| 18D | Application deemed to be withdrawn |
Effective date: 19860325 |
|
| RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: BRETHERICK, LESLIE |