ES2263627T3 - GASOLINE COMPOSITION. - Google Patents
GASOLINE COMPOSITION.Info
- Publication number
- ES2263627T3 ES2263627T3 ES01942375T ES01942375T ES2263627T3 ES 2263627 T3 ES2263627 T3 ES 2263627T3 ES 01942375 T ES01942375 T ES 01942375T ES 01942375 T ES01942375 T ES 01942375T ES 2263627 T3 ES2263627 T3 ES 2263627T3
- Authority
- ES
- Spain
- Prior art keywords
- gasoline
- composition according
- reducing additive
- ppm
- friction reducing
- 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 - Lifetime
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, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/08—Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
-
- 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
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1881—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
-
- 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
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1881—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
- C10L1/1883—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom polycarboxylic acid
-
- 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
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1888—Carboxylic acids; metal salts thereof tall oil
-
- 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
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid 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
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Combustion & Propulsion (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Composición de gasolina.Gasoline composition
Esta invención se refiere a composiciones de gasolina con bajo contenido de azufre, que tienen una respuesta mejorada a aditivos que reducen la fricción.This invention relates to compositions of low sulfur gasoline, which have an answer Enhanced to additives that reduce friction.
Los combustibles tales como gasolinas y diesel se usan bastante ampliamente en el transporte de automoción y para proporcionar energía a equipo de gran rendimiento, especialmente motores diesel debido a su elevada economía de combustible. Sin embargo, uno de los problemas cuando se queman tales combustibles en motores de combustión interna es su baja lubricidad. Esta reducción de la lubricidad surge debido a que, puesto que el contenido de azufre en el combustible se ve reducido, por ejemplo mediante hidrodesulfuración, este proceso también elimina, dicho sea de paso, la lubricidad que proporcionan las moléculas polares o reductoras de fricción, tales como, por ejemplo, los compuestos nitrogenados presentes en tales combustibles. Un documento SAE nº 962010 publicado anteriormente por Wei Dan Ping et al., titulado "Comparison of the Lubricity of Gasoline and Diesel Fuels" (1996), describe los efectos de diversos aditivos sobre tales combustibles, incluyendo los combustibles con bajo contenido de azufre. Aunque hasta ahora se han realizado esfuerzos para la adición de tales compuestos nitrogenados que reducen la fricción en los combustibles tras la hidrodesulfuración, para restaurar la lubricidad del combustible, se ha prestado poca atención a la naturaleza del propio combustible, a fin de mejorar la eficacia de tales combustibles.Fuels such as gasoline and diesel are used quite widely in automotive transportation and to provide power to high performance equipment, especially diesel engines due to their high fuel economy. However, one of the problems when burning such fuels in internal combustion engines is their low lubricity. This reduction in lubricity arises because, since the sulfur content in the fuel is reduced, for example by hydrodesulfurization, this process also eliminates, incidentally, the lubricity provided by polar or friction reducing molecules, such as, for example, the nitrogen compounds present in such fuels. An SAE document No. 962010 previously published by Wei Dan Ping et al ., Entitled "Comparison of the Lubricity of Gasoline and Diesel Fuels" (1996), describes the effects of various additives on such fuels, including low sulfur fuels. Although efforts have been made so far for the addition of such nitrogen compounds that reduce friction in fuels after hydrodesulfurization, to restore the lubricity of the fuel, little attention has been paid to the nature of the fuel itself, in order to improve the efficiency of such fuels.
Los documentos GB-A-2306246 y GB-A-2307247 publicados previamente se refieren al uso de derivados de ácido carboxílico como un aditivo para mejorar la lubricidad de los combustibles con bajo contenido de azufre, que son principalmente combustibles destilados medios tales como, por ejemplo, diesel, combustibles para motores a reacción y combustibles de biodiesel. Sin embargo, en estos documentos, no se mencionan las gasolinas o combustibles que tienen un contenido de azufre menor que 30 ppm.Documents GB-A-2306246 and GB-A-2307247 previously published refer to the use of carboxylic acid derivatives as an additive to improve the lubricity of fuels with a low content of sulfur, which are mainly middle distillate fuels such such as diesel fuel for jet engines and biodiesel fuels However, in these documents, I don't know they mention gasoline or fuels that have a content of sulfur less than 30 ppm.
De forma similar, los documentos EP-A-0860494, EP-A-0739970 y EP-A-0635558 se refieren a gasóleos diesel con bajo contenido de azufre y gasóleos (combustibles para motores diesel), respectivamente, que contienen ésteres derivados mediante transesterificación de aceites vegetales, ésteres de glicerina con ácidos grasos y ésteres de alquilos inferiores de una mezcla de ácidos grasos saturados e insaturados derivados de semillas oleaginosas, respectivamente, como agente mejorador de la lubricidad. En cada caso, no se mencionan gasolinas con bajo contenido de azufre, especialmente gasolinas que tienen un contenido de azufre < 30 ppm.Similarly, the documents EP-A-0860494, EP-A-0739970 and EP-A-0635558 refers to diesel low sulfur diesel and diesel (fuels for diesel engines), respectively, containing derived esters by transesterification of vegetable oils, esters of glycerin with fatty acids and lower alkyl esters of a mixture of saturated and unsaturated fatty acids derived from oilseeds, respectively, as an agent that improves lubricity. In each case, no gasoline is mentioned with low sulfur content, especially gasoline that have a content of sulfur <30 ppm.
El documento EP-A-0829527 describe aditivos para gasolinas que contienen modificadores de la fricción sin cenizas, entre otros constituyentes.The document EP-A-0829527 describes additives for gasoline containing ashless friction modifiers, among other constituents.
El documento WO 99/00467 describe una composición combustible de lubricidad mejorada que comprende un combustible de ignición por chispa y una alcanolamida de un ácido graso o de un ácido graso modificado, que tienen un contenido máximo de azufre de 0,05% basado en la masa. Sin embargo, no se mencionan las gasolinas, y todos los ejemplos se refieren a diesel, especialmente el combustible diesel con bajo contenido de azufre Clase Sueca I (Swedish Class I). No hay tampoco ninguna referencia al índice de bromo o a la absorbancia de UV de los combustibles ensayados o reivindicados.WO 99/00467 describes a improved lubricity fuel composition comprising a spark ignition fuel and an acid alkanolamide fatty or a modified fatty acid, which have a maximum content 0.05% sulfur based on mass. However, they are not mentioned gasoline, and all examples refer to diesel, especially diesel fuel with low sulfur content Swedish Class I (Swedish Class I). There is also no reference at bromine index or UV absorbance of fuels tested or claimed.
Ahora se ha encontrado que la eficacia de los aditivos reductores de fricción se pueden mejorar significativamente mezclando los mismos con combustibles de características predeterminadas específicas.It has now been found that the effectiveness of friction reducing additives can be significantly improved mixing them with characteristic fuels specific default.
En consecuencia, la presente invención, como se describe en los términos de la reivindicación 1 independiente, es una composición que comprende (i) una gasolina con bajo contenido de azufre, que tiene un contenido de azufre menor que 30 ppm, un índice de bromo menor que 10 y una absorbancia de ultravioleta a 319 nm por debajo de 0,15, y (ii) menos de 1000 mg por kg de la gasolina con bajo contenido de azufre de un aditivo reductor de la fricción sin cenizas, que es un ácido graso que tiene 10-30 átomos de carbono, derivado de grasas y aceites de origen natural, o un derivado de los mismos seleccionado de las sales de alquilamina, alquilamidas y ésteres alquílicos de tales ácidos y sus oligómeros.Accordingly, the present invention, as described in the terms of independent claim 1, is a composition comprising (i) a gasoline with a low content of sulfur, which has a sulfur content less than 30 ppm, an index of bromine less than 10 and an ultraviolet absorbance at 319 nm per below 0.15, and (ii) less than 1000 mg per kg of gasoline with low sulfur content of a friction reducing additive without ashes, which is a fatty acid that is 10-30 carbon atoms, derived from fats and oils of natural origin, or a derivative thereof selected from the alkylamine salts, alkylamides and alkyl esters of such acids and their oligomers
La gasolina tiene un índice de bromo (que se refiere a la cantidad de olefinas en el combustible) por debajo de 10, adecuadamente por debajo de 5, y preferiblemente por debajo de 4,5. Además, la gasolina tiene un contenido de azufre por debajo de 30 ppm, adecuadamente por debajo de 20 ppm y preferiblemente por debajo de 10 ppm. Nuevamente, la absorbancia de UV del combustible a 319 nm puede ser preferiblemente por debajo de 0,1, de forma adecuada por debajo de 0,07, y más preferiblemente por debajo de 0,05.Gasoline has a bromine index (which is refers to the amount of olefins in the fuel) below 10, suitably below 5, and preferably below 4,5. In addition, gasoline has a sulfur content below 30 ppm, suitably below 20 ppm and preferably by below 10 ppm. Again, the UV absorbance of the fuel at 319 nm may preferably be below 0.1, so suitable below 0.07, and more preferably below 0.05
El aditivo reductor de la fricción sin cenizas en la composición es adecuadamente un líquido a temperatura y presión ambiente, y se selecciona de ácidos grasos de C10-C30, preferiblemente un ácido graso C10-C24 derivado de grasas y aceites de origen natural, y los derivados seleccionados de las sales de alquilamina, alquilamidas y ésteres alquílicos de tales ácidos y sus oligómeros. Un ejemplo de una sal de carboxilato de alquilamina es oleato de n-butilamina, y un ejemplo de otro ácido graso de origen natural es una sustancia que comprende un ácido graso, un ácido graso de taloil.The ash-free friction reducing additive in the composition it is suitably a liquid at temperature and ambient pressure, and is selected from fatty acids of C10-C30, preferably a fatty acid C10-C24 derived from fats and oils of origin natural, and the derivatives selected from the alkylamine salts, alkylamides and alkyl esters of such acids and their oligomers. An example of an alkylamine carboxylate salt is n-butylamine, and an example of another fatty acid of Natural origin is a substance that comprises a fatty acid, a taloyl fatty acid.
\newpage\ newpage
El oleato de n-butilamina tiene la fórmula:The n-butylamine oleate has the formula:
CH_{3}-(CH_{2})_{7}-CH:CH-(CH_{2})_{7}-C(O)O \ ^{-+}NH_{3}C_{4}H_{9}CH 3 - (CH 2) 7 -CH: CH- (CH 2) 7 -C (O) O \ <+> - NH 3 C 4 H 9
uno de tales oleatos de n-butilamina se vende comercialmente como un modificador de la fricción como RS124 por Bitrez Ltd.one such oleate of n-butylamine is sold commercially as a friction modifier like RS124 by Bitrez Ltd.
La sustancia que comprende ácidos grasos puede
tener un 100% de ácidos grasos, o sustancialmente un 100% de ácidos
grasos, o puede ser una mezcla de ácidos grasos y/o ácidos de taloil
o sus derivados. Tal mezcla contiene adecuadamente al menos 30% p/p,
preferiblemente al menos 50% p/p de ácidos grasos. Un ejemplo de una
sustancia comercialmente disponible adecuada que contiene ácidos
grasos es TOLAD® 9103 (de Baker-Petrolite
Ltd.).The substance comprising fatty acids may have 100% fatty acids, or substantially 100% fatty acids, or it may be a mixture of fatty acids and / or taloyl acids or their derivatives. Such a mixture suitably contains at least 30% w / w, preferably at least 50% w / w fatty acids. An example of a suitable commercially available substance containing fatty acids is TOLAD® 9103 (from Baker-Petrolite
Ltd.).
El aditivo reductor de la fricción se usa en una
cantidad suficiente para proporcionar una lubricidad efectiva a la
composición. El aditivo reductor de la fricción se usa en una
cantidad menor que 1000 mg por kilogramo de combustible base en la
composición, preferiblemente de 1 a 500 mg, y más preferiblemente
de alrededor de 5 a 100 mg por kg de combustible base en la
composición. Se ha encontrado que una gasolina con estas
características es mucho más sensible, a la cantidad del agente
reductor de fricción sin cenizas especificado anteriormente añadido,
que los combustibles convencionales que no poseen estas
características. Un ejemplo típico de tal gasolina es la denominada
"gasolina de Rotterdam" que tiene adecuadamente un punto de
ebullición final por debajo de 200ºC, preferiblemente alrededor de
185ºC. El aditivo reductor de fricción sin cenizas puede ser parte
de un concentrado de aditivo que comprende un número de aditivos. En
el concentrado de aditivo, la cantidad del aditivo reductor de la
fricción es adecuadamente de 0,2-25% p/p,
preferiblemente de 0,5-20% p/p, y más
preferiblemente de 3 a 15% p/p. En base al concentrado total, el
nivel de tratamiento del aditivo reductor de la fricción en la
gasolina es adecuadamente de 4-200 ppm,
preferiblemente de 10-100 ppm y más preferiblemente
de 25-75
ppm.The friction reducing additive is used in an amount sufficient to provide effective lubricity to the composition. The friction reducing additive is used in an amount less than 1000 mg per kilogram of base fuel in the composition, preferably from 1 to 500 mg, and more preferably from about 5 to 100 mg per kg of base fuel in the composition. It has been found that a gasoline with these characteristics is much more sensitive, to the amount of friction reducing agent without ash specified above, than conventional fuels that do not possess these characteristics. A typical example of such gasoline is the so-called "Rotterdam gasoline" which suitably has a final boiling point below 200 ° C, preferably around 185 ° C. The ashless friction reducing additive may be part of an additive concentrate comprising a number of additives. In the additive concentrate, the amount of the friction reducing additive is suitably 0.2-25% w / w, preferably 0.5-20% w / w, and more preferably 3 to 15% w / w . Based on the total concentrate, the level of treatment of the friction reducing additive in gasoline is suitably from 4-200 ppm, preferably from 10-100 ppm and more preferably from 25-75
ppm.
La presente invención se ilustra además con referencia a los siguientes Ejemplos y ensayos comparativos.The present invention is further illustrated by reference to the following Examples and comparative tests.
Se ensayaron los siguientes combustibles con
grados variables de índices de bromo, contenido de azufre y
absorbancia de UV a 319 nm para determinar su sensibilidad a un
aditivo de lubricidad. De estos, tanto las gasolinas base de
Rotterdam como la de Neste 95UL muestran contenidos de azufre
comparables, aunque el combustible de Rotterdam (que tiene un punto
de ebullición final de 186,2ºC) es más sensible al aditivo de
lubricidad. Esta sensibilidad, según se mide por el porcentaje de
reducción en la fricción con relación al combustible base (Tabla 2),
está relacionada con un índice de bromo y una absorción de UV a 319
nm sustancialmente menor de los combustibles (Tabla 1). (Nota: la
medida de la absorbancia de UV y del índice de bromo son cantidades
ambas adimen-
sionales).The following fuels with varying degrees of bromine indices, sulfur content and UV absorbance at 319 nm were tested to determine their sensitivity to a lubricity additive. Of these, both Rotterdam and Neste 95UL base gasolines show comparable sulfur contents, although Rotterdam fuel (which has a final boiling point of 186.2 ° C) is more sensitive to the lubricity additive. This sensitivity, as measured by the percentage reduction in friction relative to the base fuel (Table 2), is related to a bromine index and a substantially lower 319 nm UV absorption of fuels (Table 1). (Note: the measure of UV absorbance and bromine index are both quantities
sionales).
\vskip1.000000\baselineskip\ vskip1.000000 \ baselineskip
\newpage\ newpage
Los combustibles anteriores se ensayaron a diversas velocidades de tratamiento para determinar el cambio del coeficiente de fricción y los valores medios de fricción, y los resultados se tabulan en las Tablas 2 y 3 a continuación:Previous fuels were tested at various treatment speeds to determine the change in coefficient of friction and average friction values, and Results are tabulated in Tables 2 and 3 below:
\vskip1.000000\baselineskip\ vskip1.000000 \ baselineskip
Claims (15)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0000915 | 2000-01-14 | ||
GB0000915A GB2358192A (en) | 2000-01-14 | 2000-01-14 | Fatty acids or derivatives thereof as lubricity enhancers in low sulphur fuels |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2263627T3 true ES2263627T3 (en) | 2006-12-16 |
Family
ID=9883747
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES01942375T Expired - Lifetime ES2263627T3 (en) | 2000-01-14 | 2001-01-12 | GASOLINE COMPOSITION. |
Country Status (11)
Country | Link |
---|---|
US (1) | US20030154650A1 (en) |
EP (1) | EP1252267B1 (en) |
JP (1) | JP2003519718A (en) |
AT (1) | ATE324425T1 (en) |
CA (1) | CA2396425A1 (en) |
DE (1) | DE60119078T2 (en) |
DK (1) | DK1252267T3 (en) |
ES (1) | ES2263627T3 (en) |
GB (1) | GB2358192A (en) |
PT (1) | PT1252267E (en) |
WO (1) | WO2001051592A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004210984A (en) * | 2003-01-06 | 2004-07-29 | Chevron Texaco Japan Ltd | Fuel oil composition and fuel additive |
WO2020161265A1 (en) * | 2019-02-07 | 2020-08-13 | Shell Internationale Research Maatschappij B.V. | Fuel composition with lubricity additives |
EP4105301A1 (en) | 2021-06-15 | 2022-12-21 | Basf Se | New gasoline additive packages |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL7713482A (en) * | 1977-12-06 | 1979-06-08 | Beverolfabrieken | PROCESS FOR THE PREPARATION OF A HYDROCARBON FUEL WITH LUBRICATING ACTION. |
CA2045455C (en) * | 1990-07-13 | 2002-04-02 | John Vincent Hanlon | Motor fuels of enhanced properties |
US5113803A (en) * | 1991-04-01 | 1992-05-19 | Ethyl Petroleum Additives, Inc. | Reduction of Nox emissions from gasoline engines |
GB9301119D0 (en) * | 1993-01-21 | 1993-03-10 | Exxon Chemical Patents Inc | Fuel composition |
IT1270954B (en) * | 1993-07-21 | 1997-05-26 | Euron Spa | DIESEL COMPOSITION |
AU2692795A (en) * | 1994-05-31 | 1995-12-21 | William C. Orr | Vapor phase combustion methods and compositions |
GB9514480D0 (en) * | 1995-07-14 | 1995-09-13 | Exxon Chemical Patents Inc | Additives and fuel oil compositions |
JP3379866B2 (en) * | 1995-04-24 | 2003-02-24 | 花王株式会社 | Gas oil additive and gas oil composition |
GB2307246B (en) * | 1995-11-13 | 2000-04-12 | Ethyl Petroleum Additives Ltd | Fuel additive |
GB2307247B (en) * | 1995-11-13 | 1999-12-29 | Ethyl Petroleum Additives Ltd | Fuel additive |
DE69613549T2 (en) * | 1995-12-22 | 2001-10-25 | Exxon Mobil Res And Engineerin | Fuel additive concentrate |
JPH09255973A (en) * | 1996-03-25 | 1997-09-30 | Oronaito Japan Kk | Additive for gas oil and gas oil composition |
EP0829527A1 (en) * | 1996-09-12 | 1998-03-18 | Exxon Research And Engineering Company | Additive concentrate for fuel compositions |
US5730029A (en) * | 1997-02-26 | 1998-03-24 | The Lubrizol Corporation | Esters derived from vegetable oils used as additives for fuels |
US6562086B1 (en) * | 1997-06-26 | 2003-05-13 | Baker Hughes Inc. | Fatty acid amide lubricity aids and related methods for improvement of lubricity of fuels |
EP1047757B1 (en) * | 1998-01-13 | 2002-09-04 | Baker Hughes Incorporated | Composition and method to improve lubricity in fuels |
US6132479A (en) * | 1998-05-04 | 2000-10-17 | Chevron U.S.A. Inc. | Low emission, non-oxygenated fuel composition |
US6511519B1 (en) * | 2000-09-29 | 2003-01-28 | Chevron Oronite Company Llc | Fuel additive compositions containing a mannich condensation product, a poly(oxyalkylene) monool, and a carboxylic acid |
-
2000
- 2000-01-14 GB GB0000915A patent/GB2358192A/en not_active Withdrawn
-
2001
- 2001-01-12 ES ES01942375T patent/ES2263627T3/en not_active Expired - Lifetime
- 2001-01-12 CA CA002396425A patent/CA2396425A1/en not_active Abandoned
- 2001-01-12 AT AT01942375T patent/ATE324425T1/en active
- 2001-01-12 EP EP01942375A patent/EP1252267B1/en not_active Expired - Lifetime
- 2001-01-12 WO PCT/EP2001/000331 patent/WO2001051592A1/en active IP Right Grant
- 2001-01-12 PT PT01942375T patent/PT1252267E/en unknown
- 2001-01-12 DK DK01942375T patent/DK1252267T3/en active
- 2001-01-12 DE DE60119078T patent/DE60119078T2/en not_active Expired - Lifetime
- 2001-01-12 US US10/168,995 patent/US20030154650A1/en not_active Abandoned
- 2001-01-12 JP JP2001551167A patent/JP2003519718A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
PT1252267E (en) | 2006-09-29 |
JP2003519718A (en) | 2003-06-24 |
GB2358192A (en) | 2001-07-18 |
DE60119078T2 (en) | 2006-11-30 |
ATE324425T1 (en) | 2006-05-15 |
DE60119078D1 (en) | 2006-06-01 |
EP1252267A1 (en) | 2002-10-30 |
WO2001051592A1 (en) | 2001-07-19 |
US20030154650A1 (en) | 2003-08-21 |
CA2396425A1 (en) | 2001-07-19 |
GB0000915D0 (en) | 2000-03-08 |
DK1252267T3 (en) | 2006-08-28 |
EP1252267B1 (en) | 2006-04-26 |
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