EP2612897A2 - Aviation Gasoline Composition, It's Preparation And Use - Google Patents
Aviation Gasoline Composition, It's Preparation And Use Download PDFInfo
- Publication number
- EP2612897A2 EP2612897A2 EP13160668.3A EP13160668A EP2612897A2 EP 2612897 A2 EP2612897 A2 EP 2612897A2 EP 13160668 A EP13160668 A EP 13160668A EP 2612897 A2 EP2612897 A2 EP 2612897A2
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- EP
- European Patent Office
- Prior art keywords
- composition
- vol
- amount
- tri
- present
- 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.)
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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
- C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
- C10L1/06—Liquid carbonaceous fuels essentially based on blends of hydrocarbons for spark ignition
Abstract
Description
- The present invention relates in general to a fuel composition and in particular to an aviation gasoline (Avgas).
- International Patent Publication
WO 02/40620 - There is a need for an aviation fuel which can be used in moderately powered engines (such as presently use leaded aviation gasoline with a MON of at least 91) as well as in high performance engines (such as presently use leaded aviation gasoline with a MON of at least 99.5 MON) which have been modified to use lower octane number fuels.
- Thus, according to the present invention there is provided an aviation gasoline composition comprising at least one tri-methyl pentane hydrocarbon and at least one C4 or C5 alkane wherein the amount of the at least one tri-methyl pentane in said composition is 10 to 90 vol %, the composition is substantially free of any lead compounds and the composition has a motor octane number of at least 92 and less than 98.
- The composition of the present invention solves the technical problem defined above by the presence of at least one tri-methyl pentane compound in an amount of 10 - 90 vol. % in the composition which, in the substantial absence of lead compounds, provides a fuel with a motor octane number of at least 92 and less than 98.
- The composition of the present invention can provide the same performance in full size spark ignition aviation engines as known leaded 91/96 or 91/98 aviation gasoline, the higher MON value compensating for the absence of lead compounds such as tetraethyl lead.
- The motor octane number is defined according to ASTM D2700 standard, which is known in the art.
- The composition of the present invention preferably has a MON of at least 93 and more preferably of at least 94.
- By substantially free of lead compounds is meant that the amount of lead compounds in the composition according to the present invention is not greater than 0.003g of lead per litre. Lead compounds in particular which should be absent include tetraethyl lead.
- The at least one tri-methyl pentane preferably comprises 2,2,4-trimethylpentane (herein referred to as iso-octane). Iso-octane may be prepared as described in
WO 02/40620 - The at least one tri-methyl pentane may be provided as a substantially pure component and/or as a component in one or more alkylate process streams.
- The composition of the present invention comprises at least one tri-methyl pentane (from whatever source) in an amount of 10 - 90 vol %, preferably 40 - 90 vol %, more preferably 60 - 90 vol %.
- The composition of the present invention may comprise at least 0.01 vol % C4 alkane. The composition of the present invention may comprise less than 5 vol %, preferably less than 2 vol % C4 alkane. The composition of the present invention may comprise at least 10 vol % C5 alkane. The composition of the present invention may comprise less than 40 vol %, preferably less than 20 vol % C5 alkane. 2-methyl butane is preferred over n-pentane.
- The composition of the present invention may optionally comprise alkylate in an amount of up to 90 vol %, for example up to 70 vol %. Preferably, the alkylate if present in the composition of the present invention, has been distilled such that it has a boiling point not greater than 170 °C. The alkylate component may comprise at least one tri-methyl pentane.
- The composition of the present invention may comprise isomerate and/or isopentane (2-methyl butane) in a combined total amount of up to 40 vol %, preferably in an amount of less than 20 vol %. Isopentane used in the composition of the present invention may be provided as a substantially pure component and/or as a component in a C5 refinery stream, for example from an isomerisation unit.
- The composition of the present invention may optionally comprise hydrocrackate. If present in the composition of the present invention, the amount of hydrocrackate is preferably up to 40 vol %, more preferably up to 20 vol %.
- Aromatics may optionally be present in the composition of the present invention in an amount of up to 30 vol %, preferably up to 25 vol %. Toluene is optionally present in the composition of the present invention in an amount of up to 30 vol %. Preferably, the amount of toluene, if present in the composition of the present invention, is less than 20 vol %, more preferably not greater than 10 vol %. Other aromatic compounds, for example ethylbenzene and xylene, may be present in the composition of the present invention in place of or in addition to toluene. Such aromatic compounds may be obtained by distillation of a process stream from a catalytic reformer.
- Naphtha may be present in the composition of the present invention. If present in the composition of the present invention, the amount of naphtha is preferably not greater than 30 vol %, and more preferably is less than 10 vol %.
- Olefins are preferably not present in the composition of the present invention, but their presence is not excluded.
- The composition of the present invention may comprise a dye, or may be undyed. The composition of the present invention may comprise one or more anti-oxidants such as hindered phenols.
- The composition of the present invention may comprise one or more lubricity improvers such as acids, esters and/or amides. Biofuel may also be present in the composition of the present invention. The composition of the present invention may comprise one or more additives to reduce valve seat recession, such as phosphorus, potassium or sodium based valve seat recession additives.
- The composition of the present invention may independently have one or more of the features listed in Table 1 below and preferably all of the features.
TABLE 1 Feature Range/value Vapour pressure 38 to 49 kPa Distillation properties : 10 % evaporation by 75 °C max 40 % evaporation by 75 °C min 50 % evaporation by 105 °C max 90 % evaporation by 135 °C max Final boiling point < 170 °C Supercharge Not specified, or > 96 or > 98 ON Calorific value > 43.5 Mj/kg Freezing point Less than or equal to - 58 °C - Preferably, the composition of the present invention meets the Def Stan 91-90 standard and/or ASTM D910 standards with the provisos (i) that the MON value is at least 92 and less than 98 (ii) the supercharge is unspecified or at least 96 and (iii) the composition is substantially free of any lead compounds.
- The composition of the present invention may be made by blending together one or more process streams selected from the group consisting of iso-octane, alkylate, isopentane, isomerate, hydrocrackate, aromatics and naphtha streams. Preferably, the composition of the present invention is made by adding to one or more of these process streams or a blend thereof, one or more aviation gasoline additives selected from the group consisting of dye, anti-oxidants, lubricity improvers and additives to reduce valve seat recession.
- The composition of the present invention may further comprise at least one fuel system icing inhibitor. Such icing inhibitors are preferably added at the point of use of the composition. Suitable fuel system icing inhibitors comprise alcohols or ethers for example diethylene glycol monomethyl ether and isopropanol. The icing inhibitor may be used in an amount of up to 5 % by volume in the fuel composition.
- The composition of the present invention may be used in spark ignition aviation engines. The aviation engines may be capable of operating at 30 metres or more above sea level. The aviation engines may be used to propel heavier than air craft such as light aircraft. The aviation engines may be used to propel lighter than air craft such as airships. Thus, according to a further embodiment of the present invention there is provided a method of operating a spark ignition aviation engine which comprises providing said engine with an aviation gasoline composition comprising at least one tri-methyl pentane hydrocarbon and at least one C4 or C5 alkane wherein the amount of the at least one tri-methyl pentane in said composition is 10 to 90 vol %, the composition is substantially free of any lead compounds and the composition has a motor octane number of at least 92 and less than 98.
- The present invention will now be illustrated by reference only to the following examples. Compositions were prepared by blending amounts of components as listed in Table 2 below.
TABLE 2 Component Example 1 (W02/421) Example 2 (W02/579) Amount Amount Alkylate, initial boiling point to 170 °C fraction * 24 vol % 24 vol % Naphtha 2.4 vol % - Toluene 8 vol % 8 vol % Isopentane 16 vol % 16 vol % Iso-octane 49.6 vol % 52 vol % * the alkylate fraction comprised approximately 30 vol % iso-octane such that the total amount of iso-octane in the composition was about 60 vol %. - The properties of the compositions were determined and these are listed in Table 3 below.
TABLE 3 Property Units W02/421 W02/579 MON 93.2 95.0 Supercharge 99 99 Lead gPb/litre 0.00 0.00 D 1319 FIA Aromatics % v/v 6.5 7.4 D 1319 FIA Olefins % v/v 0.6 0 D1319 FIA Saturates % v/v 92.9 92.6 D3338 Specific Energy MJ/kg 44.086 44.071 D381 Existent Gum (Air) Mg/100ml 1 <1 IP365 Composite Density kg/m3 700.9 698.8 D86 Initial Boiling Point °C 39.7 32.5 D86 Final Boiling Point °C 123.4 119.5 D86 Loss % v/v 0.6 0.5 D86 Recovery % v/v 98.3 99.0 D86 Residue % v/v 1.1 0.5 D86 10% Evaporated °C 67.1 69.5 D86 40% Evaporated °C 96.2 96.0 D86 50% Evaporated °C 99.3 98.5 D86 90% Evaporated °C 104.0 101.0 D86 Sum of 10% and 50% Evaporated temps °C 166.4 168.0 D873 16Hr Accelerated Gum Mg/100ml 3 1 D873 Lead Precipitate Mg/100ml 0 0 IP 16 Freeze point °C <-80 <-60 IP154 Copper Corrosion 2Hrs @ 100 °C - 1a 1 IP289 Water Reaction Interface Rating - 1 1b IP289 Water Reaction Volume change - 0 0 Vapour Pressure KPa 45.1 41.1 Sulphur (D2622mod) % w/w 0.0011 0.0010 Anti-oxidant mg/L 12 12 - The properties of the compositions show that these are suitable for use as aviation gasolines, in particular, the compositions of the present invention meet the Def Stan 91-90 standard and/or ASTM D910 standards with the provisos (i) that the MON value is at least 92 and less than 98 (ii) the supercharge is unspecified or at least 96 and (iii) the composition is substantially free of any lead compounds.
Claims (16)
- An aviation gasoline composition comprising at least one tri-methyl pentane hydrocarbon and at least one C4 or C5 alkane wherein the amount of the at least one tri-methyl pentane in said composition is 10 to 90 vol. % and the composition has a motor octane number of at least 92 and less than 98 in which: the amount of lead compounds in the composition is not greater than 0.003g of lead per litre; the composition comprises at least 10 vol.% and less than 40 vol.% C5 alkane; and the composition comprises aromatics in an amount of up to 30 vol.%.
- A composition as claimed in claim 1 in which the composition has a MON of at least 93.
- A composition as claimed in any one of the preceding claims in which the tri-methyl pentane is provided as a component in one or more alkylate process streams
- A composition as claimed in any one of the preceding claims in which the amount of the at least one tri-methyl pentane in said composition is 40 - 90 vol. %.
- A composition as claimed in any one of the preceding claims in which the amount of the at least one tri-methyl pentane in said composition is 60 - 90 vol. %.
- A composition as claimed in any one of the preceding claims in which the composition comprises alkylate in an amount of up to 90 vol. %.
- A composition as claimed in claim 6 in which the alkylate has been distilled such that it has a boiling point not greater than 170 °C.
- A composition as claimed in any one of the preceding claims in which the composition comprises isomerate and/or isopentane (2-methyl butane) in a combined total amount of up to 40 vol. %.
- A composition as claimed in any one of the preceding claims in which the composition comprises hydrocrackate in an amount of up to 40 vol. %.
- A composition as claimed in any one of the preceding claims in which the composition comprises aromatics in an amount of up to 25 vol. %.
- A composition as claimed in any one of the preceding claims in which the composition comprises toluene in an amount of up to 30 vol. %.
- A composition as claimed in any one of the preceding claims in which the composition meets the Def Stan 91-90 standard with the provisos (i) that the MON value is at least 92 and less than 98 (ii) the supercharge is unspecified or at least 96 and (iii) the composition is substantially free of any lead compounds.
- A composition as claimed in any one of the preceding claims in which the composition meets the ASTM D910 standard with the provisos (i) that the MON value is at least 92 and less than 98 (ii) the supercharge is unspecified or at least 96 and (iii) the composition is substantially free of any lead compounds.
- A method of making an aviation gasoline composition which comprises blending together one or more process streams selected from the group consisting of iso-octane, alkylate, isopentane, isomerate, hydrocrackate, aromatics and naphtha streams to make a composition as claimed in any one of claims 1 to 13.
- A method as claimed in claim 14 which further comprises adding to one or more of said process streams or a blend thereof, one or more aviation gasoline additives selected from the group consisting of dye, anti-oxidants, lubricity improvers and additives to reduce valve seat recession.
- A method of operating a spark ignition aviation engine which comprises providing said engine with an aviation gasoline composition as claimed in any one of claims 1 to 13 or made by a method as claimed in claim 14 or claim 15.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29421002A | 2002-11-14 | 2002-11-14 | |
GBGB0226587.4A GB0226587D0 (en) | 2002-11-14 | 2002-11-14 | Aviation gasoline composition, its preparation and use |
US49303003P | 2003-08-05 | 2003-08-05 | |
EP03811014.4A EP1560900B1 (en) | 2002-11-14 | 2003-11-05 | Aviation gasoline composition, its preparation and use |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP03811014.4A Division-Into EP1560900B1 (en) | 2002-11-14 | 2003-11-05 | Aviation gasoline composition, its preparation and use |
EP03811014.4 Division | 2003-11-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2612897A2 true EP2612897A2 (en) | 2013-07-10 |
EP2612897A3 EP2612897A3 (en) | 2013-10-23 |
Family
ID=32314754
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP03811014.4A Expired - Lifetime EP1560900B1 (en) | 2002-11-14 | 2003-11-05 | Aviation gasoline composition, its preparation and use |
EP13160668.3A Withdrawn EP2612897A3 (en) | 2002-11-14 | 2003-11-05 | Aviation Gasoline Composition, It's Preparation And Use |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP03811014.4A Expired - Lifetime EP1560900B1 (en) | 2002-11-14 | 2003-11-05 | Aviation gasoline composition, its preparation and use |
Country Status (7)
Country | Link |
---|---|
EP (2) | EP1560900B1 (en) |
AU (1) | AU2003276465A1 (en) |
GB (1) | GB0226587D0 (en) |
NO (1) | NO337019B1 (en) |
NZ (1) | NZ539863A (en) |
WO (1) | WO2004044106A1 (en) |
ZA (1) | ZA200503171B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104611074A (en) * | 2015-01-12 | 2015-05-13 | 四川帝标新能源科技有限公司 | Novel liquid fuel and preparation method thereof |
RU2554938C1 (en) * | 2014-06-06 | 2015-07-10 | Открытое акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (ОАО "ВНИИ НП") | Fuel composition of aviation gasoline |
RU2572242C2 (en) * | 2014-04-15 | 2016-01-10 | Открытое акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (ОАО "ВНИИ НП") | Fuel aviation gasoline composition |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BRPI0510496B1 (en) * | 2004-05-26 | 2014-12-23 | Shell Int Research | Process for preparing an aliphatic gasoline component |
FR2933102B1 (en) | 2008-06-30 | 2010-08-27 | Total France | AVIATION GASOLINE FOR AIRCRAFT PISTON ENGINES, PROCESS FOR PREPARING THE SAME |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002040620A2 (en) | 2000-09-01 | 2002-05-23 | Chevron U.S.A. Inc. | Aviation gasoline containing reduced amounts of tetraethyl lead |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19744109A1 (en) * | 1997-10-06 | 1999-04-15 | Thomas Dr Wilharm | Fuel for 2- and 4-stroke engines |
EG22450A (en) * | 1998-03-26 | 2003-02-26 | Bp Oil Int | Fuel composition |
US6451075B1 (en) * | 1999-12-09 | 2002-09-17 | Texas Petrochemicals Lp | Low lead aviation gasoline blend |
-
2002
- 2002-11-14 GB GBGB0226587.4A patent/GB0226587D0/en not_active Ceased
-
2003
- 2003-11-05 NZ NZ539863A patent/NZ539863A/en not_active IP Right Cessation
- 2003-11-05 EP EP03811014.4A patent/EP1560900B1/en not_active Expired - Lifetime
- 2003-11-05 AU AU2003276465A patent/AU2003276465A1/en not_active Abandoned
- 2003-11-05 EP EP13160668.3A patent/EP2612897A3/en not_active Withdrawn
- 2003-11-05 WO PCT/GB2003/004777 patent/WO2004044106A1/en not_active Application Discontinuation
-
2005
- 2005-04-19 ZA ZA200503171A patent/ZA200503171B/en unknown
- 2005-06-13 NO NO20052868A patent/NO337019B1/en not_active IP Right Cessation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002040620A2 (en) | 2000-09-01 | 2002-05-23 | Chevron U.S.A. Inc. | Aviation gasoline containing reduced amounts of tetraethyl lead |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2572242C2 (en) * | 2014-04-15 | 2016-01-10 | Открытое акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (ОАО "ВНИИ НП") | Fuel aviation gasoline composition |
RU2554938C1 (en) * | 2014-06-06 | 2015-07-10 | Открытое акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (ОАО "ВНИИ НП") | Fuel composition of aviation gasoline |
CN104611074A (en) * | 2015-01-12 | 2015-05-13 | 四川帝标新能源科技有限公司 | Novel liquid fuel and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
EP1560900B1 (en) | 2019-08-21 |
ZA200503171B (en) | 2006-10-25 |
NZ539863A (en) | 2006-11-30 |
AU2003276465A1 (en) | 2004-06-03 |
WO2004044106A1 (en) | 2004-05-27 |
EP1560900A1 (en) | 2005-08-10 |
EP2612897A3 (en) | 2013-10-23 |
GB0226587D0 (en) | 2002-12-24 |
NO337019B1 (en) | 2015-12-28 |
NO20052868L (en) | 2005-07-12 |
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