WO2010039282A1 - Fuel additive useful for increasing horsepower - Google Patents

Fuel additive useful for increasing horsepower Download PDF

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Publication number
WO2010039282A1
WO2010039282A1 PCT/US2009/039173 US2009039173W WO2010039282A1 WO 2010039282 A1 WO2010039282 A1 WO 2010039282A1 US 2009039173 W US2009039173 W US 2009039173W WO 2010039282 A1 WO2010039282 A1 WO 2010039282A1
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WO
WIPO (PCT)
Prior art keywords
additive
fuel
resin
component
horsepower
Prior art date
Application number
PCT/US2009/039173
Other languages
French (fr)
Inventor
Joseph L. Stark
Koral B. Johnson
Original Assignee
Baker Hughes Incorporated
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US12/243,753 external-priority patent/US20090090047A1/en
Priority claimed from US12/246,057 external-priority patent/US20090090655A1/en
Application filed by Baker Hughes Incorporated filed Critical Baker Hughes Incorporated
Publication of WO2010039282A1 publication Critical patent/WO2010039282A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/04Condensation polymers of aldehydes or ketones with phenols only of aldehydes
    • C08G8/08Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
    • C08G8/12Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with monohydric phenols having only one hydrocarbon substituent ortho on para to the OH group, e.g. p-tert.-butyl phenol
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/143Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/146Macromolecular compounds according to different macromolecular groups, mixtures thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/198Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
    • C10L1/1981Condensation polymers of aldehydes or ketones
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/02Use of additives to fuels or fires for particular purposes for reducing smoke development
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/222Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/224Amides; Imides carboxylic acid amides, imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/234Macromolecular compounds
    • C10L1/238Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds

Definitions

  • the present invention relates to fuel additives.
  • the present invention particularly relates to fuel additives useful for increasing horsepower.
  • fuel oils also known as heavy fuel oils
  • fuel oils have been considered to be those compounds resulting from the refining of crude oil having a vapor pressure at ambient too low to allow for easy combustion. If it could be heated and pumped, it was considered a fuel oil and used in engines that could burn such heavy fuels.
  • Exemplary applications included marine engines, locomotive engines, turbines, and use in boilers such as those oils used for power generation.
  • fuel oil may include those coming from other sources, both synthetic and non-synthetic.
  • one synthetic source fuel oil is the so called Fischer-Tropsch fuels.
  • Fischer-Tropsch fuels also known as FT fuels, include those described as gas-to-liquid (GTL) fuels, biomass-to-liquid (BTL) fuels and coal conversion fuels.
  • GTL gas-to-liquid
  • BTL biomass-to-liquid
  • coal conversion fuels coal conversion fuels.
  • syngas (CO + H (2)) is first generated and then converted to normal paraffins by a Fischer-Tropsch process.
  • the normal paraffins may then be modified by processes such as catalytic cracking/reforming or isomerisation, hydrocracking and hydroisomerisation to yield a variety of hydrocarbons such as iso-paraffins, cyclo-paraffins and aromatic compounds.
  • the resulting FT fuel can be used as such or in combination with other fuel components and fuel types such as those mentioned elsewhere in the specification.
  • Even fuels derived from natural sources such as bio-diesels and plant oils may result in the production of at least some heavy fuel oils.
  • fuels oils today are the subject of specifications due to the requirements of both governmental regulations and less forgiving apparatus for using the fuel oils. It may be desirable in the art to produce fuel oils that meet such specifications and also have improved horsepower in comparison to conventional fuel oils.
  • the invention is an additive for increasing the horse power of fuel comprising at least a first component which is an alkylphenol resin.
  • the invention is an additive for increasing the horsepower of fuel comprising at least a first component which is an alkylphenol resin and further comprising a second component selected from the group consisting of a fatty acid amide, a mannich resin and mixtures thereof.
  • the invention is a method for increasing the horsepower of an engine burning a fuel comprising admixing a fuel with an additive comprising at least a first component which is an alkylphenol resin and using that fuel to power the engine.
  • Another aspect of the invention is an admixture of a fuel and an additive for increasing the horsepower of fuels, the additive comprising at least a first component which is an alkylphenol resin.
  • the present invention is an additive useful for increasing the horsepower of a fuel.
  • Horsepower is a measurement of the force exerted by an engine. It has been defined as a unit of power in the U.S. Customary System, equal to 745.7 watts or 33,000 foot-pounds per minute.
  • the phrase "increasing the horsepower of a fuel” is defined to mean “increasing the power output of an engine powered by a fuel of the disclosure as compared to the output of the same engine powered by a conventional, but otherwise identical fuel.”
  • the additives useful for creating this increase in horsepower are those comprising at least a first component which is an alkylphenol resin.
  • the alkyl phenol resins useful as the first component of the additives of the invention include those prepared by reacting an alkyl phenol with an aldehyde.
  • the alkyl phenol may be nonyl phenol but other alkyl phenols may be used.
  • Exemplary alkyl phenols useful for preparing the alkyl phenol resin of the invention include those having the general formula:
  • R is an alkyl group having from 4 to 18 carbons.
  • the alkyl phenol resin may be prepared by reacting the alkyl phenol with an aldehyde.
  • Aldehydes useful for preparing the alkyl phenol resins include formaldehyde, but higher aldehydes may also be used. Higher aldehydes which may be used to prepare the alkyl phenol resins include those aldehydes having from 2 to about 5 carbons.
  • the alkyl phenol resins may have a molecular weight (M w ) of from about two thousand to about twenty five thousand Daltons. In one embodiment, the alkyl phenol resin has a molecular weight of from about four to about twenty thousand Daltons.
  • the alkyl phenol resin has a molecular weight of from about five to about ten thousand Daltons. While the structure of the alkyl phenol resins useful with the invention has been described as the reaction product certain starting materials, the alkyl phenol resins may be prepared by any means known to those skilled in art to be useful for preparing such resins.
  • the additives of the invention may also include a second component selected from the group consisting of fatty acid amides, mannich resins and mixtures thereof.
  • the fatty acid amides useful with the invention include those prepared using a fatty acid having from 8 to about 26 carbons.
  • the amides may be prepared using a hydroxyl alkyl amine such as 2-(2-amino ethylamine) ethanol, diethanolamine, or aminoethyl ethanolamine or other hydroxyl alkyl amine having from about 4 to about 8 carbons. While the structure of the fatty acid amides useful with the invention has been described as the reaction product certain starting materials, the fatty acid amides may be prepared by any means known to those skilled in art to be useful for preparing such resins.
  • Mannich resins useful with the invention include those which may be prepared using an alkyl phenol, an aldehyde and a polyamine.
  • the alkyl phenols useful in preparing the Mannich resins include those already described above, namely those phenols also having an alkyl group on the aromatic ring having from about 4 to about 36 carbons.
  • dodecyl phenol may be used to prepare the Mannich resins useful with the invention.
  • the Mannich resins useful with the invention include those made made with formaldehyde but may also include those prepared with higher aldehydes.
  • Higher aldehydes which may be used to prepare the Mannich resins include those aldehydes having from 2 to about 5 carbons.
  • the polyamines useful for preparing the mannich resins include ethylene diamine, but other amines may also be used. Any amine having at least two amino groups and from 2 to 22 carbons may be used to prepare the Mannich resins.
  • the Mannich resins may have a molecular weight (M w ) of from about two thousand to about twenty five thousand Daltons. In one embodiment, the Mannich resin has a molecular weight of from about four to about twenty thousand Daltons. In still another embodiment, the Mannich resin has a molecular weight of from about five to about ten thousand Daltons. While the structure of the Mannich resins useful with the invention has been described as the reaction product certain starting materials, the Mannich resins may be prepared by any means known to those skilled in art to be useful for preparing such resins.
  • the additives of the disclosure may be admixed with fuel oils using any method known by those of ordinary skill in the art to be useful.
  • the additives are admixed with fuel oils when the fuel oils are being prepared by admixing oils of varying viscosity to achieve a target viscosity.
  • the additives are admixed when the fuel oils being subjected to treatment are being metered into a truck, ship or other vessel.
  • the actual means of admixing a fuel oil with an additive of the invention may include any apparatus useful for same.
  • Exemplary apparatus include static mixers, blade mixers, stirred vessels, vessels having recycles lines incorporating static or blade mixers and the like. Any apparatus for mixing known to be useful to those of ordinary skill in the art may be used with the method of the invention.
  • the concentration of the additives needed to increase the horsepower of a given fuel will vary depending upon the properties of the subject fuel. Still, in at least one embodiment, the method of the invention may be practiced by admixing sufficient additive to achieve a concentration of from 10 to about 3000 ppm (by weight) of additive in the fuel being treated. In other embodiments, the concentration is from about 10 to 2000 ppm. In still other embodiments, the concentration is from about 50 to about 1000 ppm.
  • the additives of the invention may be used with any fuel.
  • the fuels which are most likely to need the additives of the invention are those characterized as having a boiling point greater than about 104T (40°C).
  • These include heavy fuel oils which are often used as fuel in marine engines and locomotives. Such heavy oils are often also used for firing boilers for electricity generation or steam generation.
  • Any fuel capable of being used in a compression engine may be improved using the additives of the disclosure to increase the horsepower of an engine employing the fuel.
  • an improvement in horsepower of an engine is accompanied by a degradation of emissions parameters.
  • the additives of the disclosure may be employed to increase horsepower with negligible degradation of emission parameters.
  • the emissions of an engine may be improved along with horse power. Exemplary of such parameters are CO emissions, CO 2 emissions, and NO x emissions. Improvements may also be seen in engine efficiency when additives are used in the fuel.
  • a fuel was prepared by admixing a first oil having the properties listed in the table below with an Ultra Low Sulfur Diesel in a ratio of 86.5:13.5 to prepare a fuel having a viscosity of 183 cSt at 50 0 C.
  • the first oil had an asphaltenes concentration of 8.5%, a sulfur content of 2.65%, an API gravity value of 12.8 and a specific gravity of 0.9806.
  • the Ultra Low Sulfur Diesel had an API gravity value of 33.4 and specific gravity of 0.8581.
  • the additive is prepared using the components shown in the Table.
  • the alkyl phenol resin is an alkyl phenol resin prepared using nonyl phenol and formaldehyde and has a molecular weight (M w ) of 2000 to 5000 g/mole done using a GPC and polystyrene standard.
  • the Mannich resin is prepared using dodecyl phenol, formaldehyde and ethylene diamine. It has a molecular weight similar to that of the alkyl phenol resin.
  • the fatty acid amide is prepared using a Ci 8 fatty acid and aminoethyl ethanol amine.
  • Additive 1 -4 was tested for its ability to improve the horsepower of a fuel oil.
  • the testing was conducted using a Detroit Diesel (8V-921 A) 560 BHP engine, with Marine Diesel Oil (MDO) having 500 ppm of the additive, the engine being used to pump pressurized water.
  • MDO Marine Diesel Oil
  • the experiments were conducted at 2000 RPM and water conducted at 2000 RPM and water pressure -4000 PSI. Horsepower for the engine was calculated based on the measured flow rate of the pressurized water.
  • the emissions were monitored using a Mobile Emissions Tester, which monitored the following real time parameters: CO concentration, NO concentration, NO 2 concentration, O 2 concentration, exhaust temperature, and exhaust flow rate. Combustion efficiency and CO 2 concentration were calculated based on various thermodynamic formulas. All horsepower and emission measurements were conducted with the following protocol:
  • Step 1 5 minutes warm up on idle
  • Step 2 4 minutes of running at 2000 RPM
  • Step 3 Turn on the Load
  • Step 4 1 minutes of running with Load switched on
  • Step 5 Turn on the Mobile Emissions Tester
  • Step 6 20 minutes of continuous monitoring of BHP and emissions
  • Step 7 Turn off the BPC mobile emissions tester
  • Step 8 Turn off the load
  • Step 9 Turn off the engine for 20 minutes for cooling for period.
  • Step 10 Repeat step 1 -9 to check for reproducibility.

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  • Oil, Petroleum & Natural Gas (AREA)
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Abstract

Alkylphenol resins, either with or without components selected from the group consisting of fatty acid amides, mannich resins and mixtures thereof; are effective additives for increasing the horsepower of fuel oils. The additives may also simultaneously improve emission performance. It is emphasized that this abstract is provided to comply with the rules requiring an abstract which will allow a searcher or other reader to quickly ascertain the subject matter of the technical disclosure. It is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims. 37 CFR 1.72(b)

Description

FUEL ADDITIVE USEFUL FOR INCREASING HORSEPOWER
Inventors: Joseph L. Stark Koral B. Johnson
BACKGROUND OF THE INVENTION
1. Field of the Invention
[0001] The present invention relates to fuel additives. The present invention particularly relates to fuel additives useful for increasing horsepower.
2. Background of the Art
[0002] Historically, fuel oils, also known as heavy fuel oils, have been considered to be those compounds resulting from the refining of crude oil having a vapor pressure at ambient too low to allow for easy combustion. If it could be heated and pumped, it was considered a fuel oil and used in engines that could burn such heavy fuels. Exemplary applications included marine engines, locomotive engines, turbines, and use in boilers such as those oils used for power generation.
[0003] More recently, fuel oil may include those coming from other sources, both synthetic and non-synthetic. For example, one synthetic source fuel oil is the so called Fischer-Tropsch fuels. Fischer-Tropsch fuels, also known as FT fuels, include those described as gas-to-liquid (GTL) fuels, biomass-to-liquid (BTL) fuels and coal conversion fuels. To make such fuels, syngas (CO + H (2)) is first generated and then converted to normal paraffins by a Fischer-Tropsch process. The normal paraffins may then be modified by processes such as catalytic cracking/reforming or isomerisation, hydrocracking and hydroisomerisation to yield a variety of hydrocarbons such as iso-paraffins, cyclo-paraffins and aromatic compounds. The resulting FT fuel can be used as such or in combination with other fuel components and fuel types such as those mentioned elsewhere in the specification. [0004] Even fuels derived from natural sources such as bio-diesels and plant oils may result in the production of at least some heavy fuel oils. [0005] Whatever their source, fuels oils today are the subject of specifications due to the requirements of both governmental regulations and less forgiving apparatus for using the fuel oils. It may be desirable in the art to produce fuel oils that meet such specifications and also have improved horsepower in comparison to conventional fuel oils.
SUMMARY OF THE INVENTION
[0006] In one aspect, the invention is an additive for increasing the horse power of fuel comprising at least a first component which is an alkylphenol resin.
[0007] In another aspect, the invention is an additive for increasing the horsepower of fuel comprising at least a first component which is an alkylphenol resin and further comprising a second component selected from the group consisting of a fatty acid amide, a mannich resin and mixtures thereof.
[0008] In still another aspect, the invention is a method for increasing the horsepower of an engine burning a fuel comprising admixing a fuel with an additive comprising at least a first component which is an alkylphenol resin and using that fuel to power the engine.
[0009] Another aspect of the invention is an admixture of a fuel and an additive for increasing the horsepower of fuels, the additive comprising at least a first component which is an alkylphenol resin. Description of the Preferred Embodiments
[0010] In one embodiment, the present invention is an additive useful for increasing the horsepower of a fuel. Horsepower is a measurement of the force exerted by an engine. It has been defined as a unit of power in the U.S. Customary System, equal to 745.7 watts or 33,000 foot-pounds per minute. For the purposes of this application, the phrase "increasing the horsepower of a fuel" is defined to mean "increasing the power output of an engine powered by a fuel of the disclosure as compared to the output of the same engine powered by a conventional, but otherwise identical fuel."
[0011] The additives useful for creating this increase in horsepower are those comprising at least a first component which is an alkylphenol resin. The alkyl phenol resins useful as the first component of the additives of the invention include those prepared by reacting an alkyl phenol with an aldehyde. The alkyl phenol may be nonyl phenol but other alkyl phenols may be used. Exemplary alkyl phenols useful for preparing the alkyl phenol resin of the invention include those having the general formula:
Figure imgf000004_0001
wherein R is an alkyl group having from 4 to 18 carbons.
[0012] The alkyl phenol resin may be prepared by reacting the alkyl phenol with an aldehyde. Aldehydes useful for preparing the alkyl phenol resins include formaldehyde, but higher aldehydes may also be used. Higher aldehydes which may be used to prepare the alkyl phenol resins include those aldehydes having from 2 to about 5 carbons. [0013]The alkyl phenol resins may have a molecular weight (Mw) of from about two thousand to about twenty five thousand Daltons. In one embodiment, the alkyl phenol resin has a molecular weight of from about four to about twenty thousand Daltons. In still another embodiment, the alkyl phenol resin has a molecular weight of from about five to about ten thousand Daltons. While the structure of the alkyl phenol resins useful with the invention has been described as the reaction product certain starting materials, the alkyl phenol resins may be prepared by any means known to those skilled in art to be useful for preparing such resins.
[0014] In another embodiment, the additives of the invention may also include a second component selected from the group consisting of fatty acid amides, mannich resins and mixtures thereof. The fatty acid amides useful with the invention include those prepared using a fatty acid having from 8 to about 26 carbons. The amides may be prepared using a hydroxyl alkyl amine such as 2-(2-amino ethylamine) ethanol, diethanolamine, or aminoethyl ethanolamine or other hydroxyl alkyl amine having from about 4 to about 8 carbons. While the structure of the fatty acid amides useful with the invention has been described as the reaction product certain starting materials, the fatty acid amides may be prepared by any means known to those skilled in art to be useful for preparing such resins.
[0015] Mannich resins useful with the invention include those which may be prepared using an alkyl phenol, an aldehyde and a polyamine. The alkyl phenols useful in preparing the Mannich resins include those already described above, namely those phenols also having an alkyl group on the aromatic ring having from about 4 to about 36 carbons. For example dodecyl phenol may be used to prepare the Mannich resins useful with the invention.
[0016] Similarly the Mannich resins useful with the invention include those made made with formaldehyde but may also include those prepared with higher aldehydes. Higher aldehydes which may be used to prepare the Mannich resins include those aldehydes having from 2 to about 5 carbons. [0017]The polyamines useful for preparing the mannich resins include ethylene diamine, but other amines may also be used. Any amine having at least two amino groups and from 2 to 22 carbons may be used to prepare the Mannich resins.
[0018] The Mannich resins may have a molecular weight (Mw) of from about two thousand to about twenty five thousand Daltons. In one embodiment, the Mannich resin has a molecular weight of from about four to about twenty thousand Daltons. In still another embodiment, the Mannich resin has a molecular weight of from about five to about ten thousand Daltons. While the structure of the Mannich resins useful with the invention has been described as the reaction product certain starting materials, the Mannich resins may be prepared by any means known to those skilled in art to be useful for preparing such resins.
[0019]The additives of the disclosure may be admixed with fuel oils using any method known by those of ordinary skill in the art to be useful. For example, in one embodiment, the additives are admixed with fuel oils when the fuel oils are being prepared by admixing oils of varying viscosity to achieve a target viscosity. In another embodiment, the additives are admixed when the fuel oils being subjected to treatment are being metered into a truck, ship or other vessel.
[0020]The actual means of admixing a fuel oil with an additive of the invention may include any apparatus useful for same. Exemplary apparatus include static mixers, blade mixers, stirred vessels, vessels having recycles lines incorporating static or blade mixers and the like. Any apparatus for mixing known to be useful to those of ordinary skill in the art may be used with the method of the invention. Passive with the method of the invention. Passive admixing may be accomplished where the additives are introduced into a vessel or transfer line or pipeline and admixing is effected by means of turbulence.
[0021] The concentration of the additives needed to increase the horsepower of a given fuel will vary depending upon the properties of the subject fuel. Still, in at least one embodiment, the method of the invention may be practiced by admixing sufficient additive to achieve a concentration of from 10 to about 3000 ppm (by weight) of additive in the fuel being treated. In other embodiments, the concentration is from about 10 to 2000 ppm. In still other embodiments, the concentration is from about 50 to about 1000 ppm.
[0022]The additives of the invention may be used with any fuel. The fuels which are most likely to need the additives of the invention are those characterized as having a boiling point greater than about 104T (40°C). These include heavy fuel oils which are often used as fuel in marine engines and locomotives. Such heavy oils are often also used for firing boilers for electricity generation or steam generation. Any fuel capable of being used in a compression engine may be improved using the additives of the disclosure to increase the horsepower of an engine employing the fuel.
[0023] Generally, an improvement in horsepower of an engine is accompanied by a degradation of emissions parameters. In some embodiments, the additives of the disclosure may be employed to increase horsepower with negligible degradation of emission parameters. In some embodiments, the emissions of an engine may be improved along with horse power. Exemplary of such parameters are CO emissions, CO2 emissions, and NOx emissions. Improvements may also be seen in engine efficiency when additives are used in the fuel. EXAMPLES
[0024] The following examples are provided to illustrate the invention. The examples are not intended to limit the scope of the invention and they should not be so interpreted. Amounts are in weight parts or weight percentages unless otherwise indicated.
Example 1
[0025] A fuel was prepared by admixing a first oil having the properties listed in the table below with an Ultra Low Sulfur Diesel in a ratio of 86.5:13.5 to prepare a fuel having a viscosity of 183 cSt at 500C. The first oil had an asphaltenes concentration of 8.5%, a sulfur content of 2.65%, an API gravity value of 12.8 and a specific gravity of 0.9806. The Ultra Low Sulfur Diesel had an API gravity value of 33.4 and specific gravity of 0.8581.
[0026] The additive is prepared using the components shown in the Table. The alkyl phenol resin is an alkyl phenol resin prepared using nonyl phenol and formaldehyde and has a molecular weight (Mw) of 2000 to 5000 g/mole done using a GPC and polystyrene standard. The Mannich resin is prepared using dodecyl phenol, formaldehyde and ethylene diamine. It has a molecular weight similar to that of the alkyl phenol resin. The fatty acid amide is prepared using a Ci8 fatty acid and aminoethyl ethanol amine.
Example 2
[0027] Additive 1 -4 was tested for its ability to improve the horsepower of a fuel oil. The testing was conducted using a Detroit Diesel (8V-921 A) 560 BHP engine, with Marine Diesel Oil (MDO) having 500 ppm of the additive, the engine being used to pump pressurized water. The experiments were conducted at 2000 RPM and water conducted at 2000 RPM and water pressure -4000 PSI. Horsepower for the engine was calculated based on the measured flow rate of the pressurized water.
[0028]The emissions were monitored using a Mobile Emissions Tester, which monitored the following real time parameters: CO concentration, NO concentration, NO2 concentration, O2 concentration, exhaust temperature, and exhaust flow rate. Combustion efficiency and CO2 concentration were calculated based on various thermodynamic formulas. All horsepower and emission measurements were conducted with the following protocol:
Step 1 : 5 minutes warm up on idle;
Step 2: 4 minutes of running at 2000 RPM;
Step 3: Turn on the Load;
Step 4: 1 minutes of running with Load switched on;
Step 5: Turn on the Mobile Emissions Tester;
Step 6: 20 minutes of continuous monitoring of BHP and emissions;
Step 7: Turn off the BPC mobile emissions tester;
Step 8: Turn off the load;
Step 9: Turn off the engine for 20 minutes for cooling for period; and
Step 10: Repeat step 1 -9 to check for reproducibility.
[0029] The fuel and additive is compared to a blank with the following results:
Average % Horsepower increase: 2.7
Maximum % Horsepower Increase: 4.6
Average % Increase in Engine Efficiency: 2.4
Maximum % Increase in Engine Efficiency: 4.4
Increase in Engine Temperature: 0
Change (%) in Exhaust Temperature: -0.6
Change in CO Emissions (%): -6.9
Change in CO2 Emissions (%): -0.9
Change in NOx Emissions (%): +0.1 Table
Figure imgf000010_0001
Brief Discussion of the Examples
[0030] The Examples illustrate that the additive of the disclosure was useful in increasing generally the horsepower of an engine as compared to running the engine with an untreated fuel. Surprisingly, the horsepower improvements were noted with a general improvement in the emissions characteristics of the engine.

Claims

WHAT IS CLAIMED IS:
1. An additive for increasing horsepower in fuel comprising at least a first component which is an alkylphenol resin.
2. The additive of Claim 1 wherein the alkyl phenol resin is prepared using an alkyl phenol having a general formula:
Figure imgf000011_0001
wherein R is an alkyl group having from 4 to 18 carbons.
3. The additive of Claim 2 wherein the alkylphenol is reacted with formaldehyde to form the alkylphenol resin.
4. The additive of Claim 1 wherein the alkylphenol resin has a molecular weight (Mw) of from about 3,000 to about 20,000 Daltons.
5. The additive of claim 1 further comprising a second component selected from the group consisting of a fatty acid amide, a mannich resin and mixtures thereof.
6. The additive of Claim 5 wherein the second component is a fatty acid amide having from about 8 to about 26 carbons.
7. The additive of Claim 6 wherein the fatty acid amide is prepared using a compound selected from the group consisting of 2-(2-amino ethylamine)ethanol, diethanolamine, aminoethyl ethanolamine and mixtures thereof.
8. The additive of Claim 5 wherein the second component is a mannich resin prepared from a formulation including an alkyl phenol, an aldehyde and a polyamine.
9. The additive of Claim 8 wherein the alkyl phenol has a general formula:
Figure imgf000012_0001
wherein R is an alkyl group having from 4 to 18 carbons.
10. The additive of Claim 9 wherein the alkyl phenol is dodecyl phenol.
11. The additive of Claim 8 wherein the aldehyde is formaldehyde.
12. The additive of Claim 8 wherein the polyamine has from 2 to 22 carbons.
13. The additive of Claim 12 wherein the polyamine is ethylene diamine.
14. The additive of Claim 5 wherein the second component is a mannich resin having a molecular weight (Mw) of from about from about 4,000 to about 20,000 Daltons.
15. A method for increasing horsepower of a fuel comprising admixing a fuel oil with an additive comprising at least a first component which is an alkylphenol resin.
16. The method of Claim 15 wherein the additive additionally comprises a second component selected from the group consisting of a fatty acid amide, a mannich resin and mixtures thereof.
17. The method of Claim 15 wherein the additive is admixed with the fuel at a concentration of from about 10 to about 3,000 ppm.
18. The method of Claim 17 wherein the additive is admixed with the fuel at a concentration of from about 50 to about 1 ,000 ppm.
19. A composition comprising an admixture of a fuel and an additive of Claim 1.
20. The composition of Claim 19 wherein the fuel has a boiling point greater then 104T (40QC)
21. The composition of Claim 20 wherein the fuel is a heavy fuel oil.
22. The composition of Claim 21 wherein the heavy fuel oil is Bunker C oil.
23. The composition of Claim 19 wherein the additive is present at a concentration of from about 10 to about 2,000 ppm.
PCT/US2009/039173 2008-10-01 2009-04-01 Fuel additive useful for increasing horsepower WO2010039282A1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US12/243,753 2008-10-01
US12/243,753 US20090090047A1 (en) 2007-10-04 2008-10-01 Additive Useful for Stabilizing Fuel Oils
US12/246,057 US20090090655A1 (en) 2007-10-04 2008-10-06 Additive Useful for Stabilizing Crude Oil
US12/246,057 2008-10-06

Publications (1)

Publication Number Publication Date
WO2010039282A1 true WO2010039282A1 (en) 2010-04-08

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4553979A (en) * 1984-10-15 1985-11-19 Ethyl Petroleum Additives, Inc. Diesel fuel compositions
US20030226312A1 (en) * 2002-06-07 2003-12-11 Roos Joseph W. Aqueous additives in hydrocarbonaceous fuel combustion systems
US20050166447A1 (en) * 2002-03-14 2005-08-04 Corkwell Keith C. Ethanol-diesel fuel composition and methods thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4553979A (en) * 1984-10-15 1985-11-19 Ethyl Petroleum Additives, Inc. Diesel fuel compositions
US20050166447A1 (en) * 2002-03-14 2005-08-04 Corkwell Keith C. Ethanol-diesel fuel composition and methods thereof
US20030226312A1 (en) * 2002-06-07 2003-12-11 Roos Joseph W. Aqueous additives in hydrocarbonaceous fuel combustion systems

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