US20050005506A1 - Distillate fuel compositions for improved combustion and engine cleanliness - Google Patents

Distillate fuel compositions for improved combustion and engine cleanliness Download PDF

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US20050005506A1
US20050005506A1 US10/614,771 US61477103A US2005005506A1 US 20050005506 A1 US20050005506 A1 US 20050005506A1 US 61477103 A US61477103 A US 61477103A US 2005005506 A1 US2005005506 A1 US 2005005506A1
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fuel
fuel additive
calcium sulfonate
overbased calcium
alkyl
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Timothy Henly
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Afton Chemical Corp
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Afton Chemical Corp
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Assigned to ETHYL PETROLEUM ADDITIVES, INC. reassignment ETHYL PETROLEUM ADDITIVES, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HENLY, TIMOTHY J.
Priority to AU2004202402A priority patent/AU2004202402A1/en
Priority to EP04013112A priority patent/EP1496100A1/en
Priority to CA002469766A priority patent/CA2469766A1/en
Assigned to SUNTRUST BANK, AS ADMINISTRATIVE AGENT reassignment SUNTRUST BANK, AS ADMINISTRATIVE AGENT SECURITY AGREEMENT Assignors: ETHYL PETROLEUM ADDITIVES, INC.
Priority to SG200404323A priority patent/SG108978A1/en
Priority to CNB200410063711XA priority patent/CN100506955C/en
Priority to JP2004202279A priority patent/JP2005029796A/en
Assigned to AFTON CHEMICAL CORPORATION reassignment AFTON CHEMICAL CORPORATION CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: ETHYL PETROLEUM ADDITIVES, INC.
Publication of US20050005506A1 publication Critical patent/US20050005506A1/en
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    • 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
    • C10L1/143Organic 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
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/1822Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
    • C10L1/1824Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
    • 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
    • C10L1/188Carboxylic acids; metal salts thereof
    • C10L1/1881Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
    • C10L1/1883Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom polycarboxylic acid
    • 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
    • C10L1/1985Macromolecular 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 polyethers, e.g. di- polygylcols and derivatives; ethers - esters
    • 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
    • C10L1/2383Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
    • 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
    • C10L1/24Organic compounds containing sulfur, selenium and/or tellurium
    • C10L1/2431Organic compounds containing sulfur, selenium and/or tellurium sulfur bond to oxygen, e.g. sulfones, sulfoxides
    • C10L1/2437Sulfonic acids; Derivatives thereof, e.g. sulfonamides, sulfosuccinic acid esters
    • 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
    • C10L1/30Organic compounds compounds not mentioned before (complexes)
    • C10L1/305Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)

Definitions

  • the present invention relates to a synergistic interaction between an overbased calcium sulfonate detergent and an ashless succinimide dispersant that allows for the formulation of improved distillate fuel additive packages.
  • the additive compositions contain an organometallic complex of manganese. Distillate fuels treated with the additive compositions exhibit improved combustion because of the detergent and the organometallic manganese compound and good fuel system cleanliness because of the detergent/dispersant interaction.
  • distillate fuel additive compositions to provide environmental benefits when the fuel is combusted.
  • Such benefits include, for example, reduced emissions of noxious pollutants such as oxides of nitrogen and particulate matter, reduced acidity of emitted particulates, and better fuel economy (which amounts to lower emissions of carbon dioxide per amount of fuel burned).
  • noxious pollutants such as oxides of nitrogen and particulate matter
  • reduced acidity of emitted particulates reduced acidity of emitted particulates
  • better fuel economy which amounts to lower emissions of carbon dioxide per amount of fuel burned.
  • An embodiment presented herein provides a fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent of TBN above about 200.
  • the TBN of the overbased calcium sulfonate is about 300.
  • Another embodiment provides a fuel comprising a major amount of a middle distillate fuel and a minor amount of a fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent of TBN above about 200.
  • a method of for improving the cleanliness of a fuel intake systems by use in the fuel intake system of a fuel containing a fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent of TBN about 300.
  • distillate fuel additive compositions for use in distillate fuels that provide enhanced fuel combustion and, at the same time, superior cleanliness of fuel intake systems.
  • Distillate fuels are defined herein as petroleum-based hydrocarbon fuels boiling in the range of about 140-360° C. [284-680° F.] and encompass diesel and biodiesel fuels, jet fuels, marine fuels and home heating oils. Distillate fuels containing the additive compositions of the invention show enhanced combustion characteristics.
  • fuels containing the additive packages also show excellent fuel injector cleanliness as measured by the Cummins L10 diesel detergency test. This injector cleanliness is exhibited as an injector rating of at most 10.0 in the Cummins L10 diesel detergency test.
  • inventions herein provide an additive composition, a distillate fuel containing the additive composition, and a method of improving the cleanliness of fuel intake systems by use of the fuel containing the additive composition.
  • the additive composition contains at least an organometallic complex of manganese, an overbased calcium sulfonate detergent and an ashless succinimide dispersant such that when the additive composition is dissolved in a distillate fuel, the following relationship is satisfied: ⁇ 0.159 x+ 0.243 y ⁇ 0.0143 xy ⁇ 8.4 where
  • the organometallic manganese compound does not affect injector cleanliness.
  • the organometallic manganese compound may be present in the fuel at concentrations of up to about 20 PTB.
  • the amount of organometallic manganese compound was shown to have no significant adverse effect on injector ratings and is therefore not constrained by the model represented by equation 3. As an economic matter only, the amount of manganese compound is, in an embodiment, limited to 20 PTB or less.
  • the benefits derived from the inclusion of a manganese compound are not directly related to injector ratings, but are much more prevalent in the areas of particulate emission reduction, reduced NO x and SO x , reduced hydrocarbons, improved fuel economy, and combustion improvement.
  • MMT® methylcyclopentadienylmanganese tricarbonyl
  • succinimide prepared from 850 to 2100-MW PIBSA and a polyalkylene polyamine approximating tetraethylenepentamine in composition as the ashless dispersant
  • MMT® is available from Ethyl Corporation, Richmond, Va.
  • the diesel fuel used in the Cummins L10 study was a high-sulfur (0.4wgt % sulfur) fuel, but any diesel fuel (including low-sulfur and ultralow-sulfur fuels) may be used.
  • a separate L10 experiment has shown that the addition of 2-ethylhexyl nitrate cetane improver to a fuel containing the inventive additive does not degrade the detergent performance.
  • the European components D-5021 (demulsifier) and HiTEC® 536 (corrosion inhibitor) were replaced with the North American components Tolad 9310 and 50% dodecenylsuccinic acid, respectively, on an equivalent weight basis. These components were held constant at the above concentrations in every test.
  • the components expected to have significant effects on Cummins L10 ratings were HiTEC® 9645 (a succinimide-based dispersant), HiTEC® 611 (overbased calcium sulfonate) and HiTEC® 3062 (62% MMT® in aromatic solvent).
  • FIG. 1 The resulting two-level, three-factor (2 3 ) design is shown in FIG. 1 ; the numbers along the axes denote concentrations in PTB.
  • HiTEC® 3062 and the higher-order terms AC, BC and ABC were significant at less than the 85% confidence level and are therefore excluded.
  • the model coefficients are as follows:
  • HiTEC® 9645 unexpectedly decreases the CRC response (a beneficial effect, since lower CRC ratings indicate less injector depositing), while HiTEC® 611 increases the ratings.
  • HiTEC® 9645 has a significant negative interaction between HiTEC® 9645 and HiTEC® 611, meaning that the deleterious effect of HiTEC® 611 on CRC rating at low concentrations of dispersant is more than cancelled out at high dispersant concentrations.
  • HiTEC® 611 improves CRC ratings when in the presence of high amounts of HiTEC® 9645. This effect is shown graphically by the interaction diagram in FIG. 2 .
  • HiTEC® 611 Ordinarily, a p-value of 0.13 would result in HiTEC® 611 alone being excluded from the model: this value indicates that the coefficient is different from zero only at the 87% confidence level. However, if the model contains an interaction between HiTEC® 9645 and HiTEC® 611, the HiTEC® 611 term should also be included to preserve model hierarchy.
  • any combination of HiTEC® 9645 and HiTEC 611 to the right of the 10.0 contour (the dashed line) in FIG. 3 should give a passing Cummins L10 rating.
  • Three points were selected on the 9.0 contour (the solid line) in the L10 test.
  • the additive combinations corresponding to these points were:
  • a simple 2 3 experimental design has determined the quantitative effects of various components in a Greenburn® Diesel Fuel Additive package on Cummins L10 performance. It was found that the succinimide dispersant (HiTEC® 9645) had a beneficial effect on injector ratings, while the overbased calcium sulfonate detergent (HiTEC® 611) harmed those ratings. In addition, a strong interaction between these two components was observed which reduced the undesirable effect of the detergent. MMT® (as HiTEC® 3062) had no significant effect on injector cleanliness. The model derived from the experimental design was used to formulate modified Greenburn®-type packages that passed the Cummins L10 test.
  • each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims.

Abstract

The invention provides a distillate fuel additive composition, and also a fuel composition containing a distillate fuel, an overbased calcium sulfonate detergent, a succinimide dispersant, and an organomanganese compound. Also provided is a method for improving the cleanliness of diesel fuel intake systems by the combustion in said systems of a distillate fuel containing the fuel additive composition.

Description

    FIELD
  • The present invention relates to a synergistic interaction between an overbased calcium sulfonate detergent and an ashless succinimide dispersant that allows for the formulation of improved distillate fuel additive packages. In addition to the metallic detergent and the ashless dispersant, the additive compositions contain an organometallic complex of manganese. Distillate fuels treated with the additive compositions exhibit improved combustion because of the detergent and the organometallic manganese compound and good fuel system cleanliness because of the detergent/dispersant interaction.
  • BACKGROUND
  • A great deal of prior art has been devoted to formulating distillate fuel additive compositions to provide environmental benefits when the fuel is combusted. Such benefits include, for example, reduced emissions of noxious pollutants such as oxides of nitrogen and particulate matter, reduced acidity of emitted particulates, and better fuel economy (which amounts to lower emissions of carbon dioxide per amount of fuel burned). The effects of these fuels on the cleanliness of fuel systems, e.g., on the buildup of carbon and lacquer on the fuel injectors found in diesel engines, has received less study.
  • A need exists for a distillate fuel additive composition that provides for the simultaneous achievement of improved combustion, fuel and combustion system cleanliness, improved fuel economy, and reduction in pollutant generation.
  • SUMMARY OF THE EMBODIMENTS
  • An embodiment presented herein provides a fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent of TBN above about 200. In another embodiment the TBN of the overbased calcium sulfonate is about 300.
  • Another embodiment provides a fuel comprising a major amount of a middle distillate fuel and a minor amount of a fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent of TBN above about 200.
  • Accordingly, in one example herein is provided a method of for improving the cleanliness of a fuel intake systems by use in the fuel intake system of a fuel containing a fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent of TBN about 300.
  • It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are intended to provide further explanation of the present invention, as claimed.
  • DETAILED DESCRIPTION OF EMBODIMENTS
  • In one embodiment is provided herein distillate fuel additive compositions for use in distillate fuels that provide enhanced fuel combustion and, at the same time, superior cleanliness of fuel intake systems. Distillate fuels are defined herein as petroleum-based hydrocarbon fuels boiling in the range of about 140-360° C. [284-680° F.] and encompass diesel and biodiesel fuels, jet fuels, marine fuels and home heating oils. Distillate fuels containing the additive compositions of the invention show enhanced combustion characteristics.
  • If certain components of the additive packages described herein are present in specific proportions, fuels containing the additive packages also show excellent fuel injector cleanliness as measured by the Cummins L10 diesel detergency test. This injector cleanliness is exhibited as an injector rating of at most 10.0 in the Cummins L10 diesel detergency test.
  • Other embodiments herein provide an additive composition, a distillate fuel containing the additive composition, and a method of improving the cleanliness of fuel intake systems by use of the fuel containing the additive composition.
  • In an embodiment, the additive composition contains at least an organometallic complex of manganese, an overbased calcium sulfonate detergent and an ashless succinimide dispersant such that when the additive composition is dissolved in a distillate fuel, the following relationship is satisfied:
    −0.159x+0.243y−0.0143xy≦−8.4
    where
      • x=concentration of succinimide (in pounds per thousand barrels)
      • y=concentration of overbased calcium sulfonate (in PTB)
      • with the following limitations:
      • x=20-35, preferably 25-30, and y=10-120, preferably 30-50.
  • The organometallic manganese compound does not affect injector cleanliness. In an embodiment, the organometallic manganese compound may be present in the fuel at concentrations of up to about 20 PTB.
  • It has been discovered that the combustion-improving conventional additive packages previously known do not necessarily pass the Cummins L10 diesel detergency test (where a pass is defined as an average injector rating of 10.0 or less). To identify the components in the additive composition that affect injector ratings, an experimental design was carried out. A synergy (i.e. a nonlinear interaction) was observed between the overbased calcium sulfonate detergent and the succinimide dispersant. This was a surprising result which is not anticipated by any prior art.
  • The results of the experimental design were used to generate a model for average injector rating, as follows:
    Rating=−0.159x+0.243y−0.0143xy+18.4   (1)
    where
      • x=concentration of succinimide (in pounds per thousand barrels, or PTB)
      • y=concentration of overbased calcium sulfonate (in PTB)
        Since the average injector rating must be 10.0 or lower for a pass in the Cummins L10 test, the equation becomes:
        10.0≧−0.159x+0.243y−0.0143xy+18.4   (2)
        or
        −0.159x+0.243y−0.0143xy≦≦8.4   (3)
        The detergent/dispersant synergy is represented by the xy term.
  • The model was validated by the testing of three new formulations that satisfy the above equation:
      • 1. x=28 PTB, y=32 PTB
      • 2. x=26 PTB, y=40 PTB
      • 3. x=25 PTB, y=48 PTB
  • All three formulations gave an average injector rating of below 10.0, in accordance with the model. Of course, there are an infinite number of solutions for x and y in equation 3. Examples of currently practical solutions are the following ranges:
      • x=20-35, preferably 25-30
      • y=10-120, preferably 30-50
  • The amount of organometallic manganese compound was shown to have no significant adverse effect on injector ratings and is therefore not constrained by the model represented by equation 3. As an economic matter only, the amount of manganese compound is, in an embodiment, limited to 20 PTB or less. The benefits derived from the inclusion of a manganese compound are not directly related to injector ratings, but are much more prevalent in the areas of particulate emission reduction, reduced NOx and SOx, reduced hydrocarbons, improved fuel economy, and combustion improvement.
  • Especially useful herein is methylcyclopentadienylmanganese tricarbonyl (MMT®) as the organometallic manganese compound, a succinimide prepared from 850 to 2100-MW PIBSA and a polyalkylene polyamine approximating tetraethylenepentamine in composition as the ashless dispersant, and an overbased calcium sulfonate of TBN up to about 300 as the detergent. MMT® is available from Ethyl Corporation, Richmond, Va. The diesel fuel used in the Cummins L10 study was a high-sulfur (0.4wgt % sulfur) fuel, but any diesel fuel (including low-sulfur and ultralow-sulfur fuels) may be used. A separate L10 experiment has shown that the addition of 2-ethylhexyl nitrate cetane improver to a fuel containing the inventive additive does not degrade the detergent performance.
  • The following examples further illustrate aspects of the present invention but do not limit the present invention.
  • EXAMPLES
  • Since the Cummins L10 test was designed to evaluate additives and fuels for on-road use in North America, HiTEC®-4080 Fuel Additive was used in this example. This additive is Ethyl Corporation's antifoam-free Greenburn® road diesel fuel additive package, used with a recommended treat rate of 500 ppm (w/w). The formulation is shown in Table 1.
    TABLE 1
    Composition of HiTEC ® 4080
    ppm component PTB component
    Component % weight at 500 ppm total at 500 ppm total
    HiTEC ®
    9645 15.34 76.7 22.8
    2-ethylhexanol 46.22 231.1 68.8
    HiTEC ® 611 32.16 160.8 47.9
    HiTEC ® 536 0.93 4.7 1.4
    D-5021 0.97 4.9 1.5
    HiTEC ® 3062 4.38 21.9 6.6
  • For the purposes of this example, the European components D-5021 (demulsifier) and HiTEC® 536 (corrosion inhibitor) were replaced with the North American components Tolad 9310 and 50% dodecenylsuccinic acid, respectively, on an equivalent weight basis. These components were held constant at the above concentrations in every test. The components expected to have significant effects on Cummins L10 ratings were HiTEC® 9645 (a succinimide-based dispersant), HiTEC® 611 (overbased calcium sulfonate) and HiTEC® 3062 (62% MMT® in aromatic solvent).
  • The resulting two-level, three-factor (23) design is shown in FIG. 1; the numbers along the axes denote concentrations in PTB.
  • All tests were carried out in the same Cummins L10 engine and in the same batch of high-sulfur Cat 1K fuel. The test order was randomized. The results are shown in Table 2.
    TABLE 2
    Cummins L10 results for H-4080 experimental design
    PTB H- PTB H- Avg. flow Avg. CRC
    Test no. PTB H-9645 611 3062 loss (%) rating
    D102-97-1 0 0 6.6 3.2 19.1
    D102-98-1 23 0 0 4.2 14.7
    D102-99-1 23 0 6.6 2.9 15.3
    D102-100-1 23 48 0 2.3 9.9
    D102-101-1 0 48 6.6 8.9 34.7
    D102-102-1 11.5 24 3.3 4.1 16.8
    D102-103-1 0 48 0 4.0 25.9
    D102-104-1 23 48 6.6 3.1 11.9
    D102-105-1 0 0 0 1.9 18.2
  • An analysis of variance (ANOVA) on the data in Table 2 showed that average flow loss was independent of all three factors. The ANOVA for CRC rating is shown below. Analysis of Variance for CRC
    Source Sum of Squares Df Mean Square F-Ratio P-Value
    A (H-9645) 265.651 1 265.651 29.81 0.0028
    B (H-611) 28.5012 1 28.5012 3.20 0.1337
    AB 124.031 1 124.031 13.92 0.0136
    Total error 44.5563 5 8.91125
    Total (corr.) 462.74 8
      • R-squared=90.3712 percent
      • R-squared (adjusted for d.f.)=84.5939 percent
      • Standard Error of Est.=2.98517
      • Mean absolute error=1.55556
      • Durbin-Watson statistic=2.10796
  • HiTEC® 3062 and the higher-order terms AC, BC and ABC were significant at less than the 85% confidence level and are therefore excluded. The model coefficients are as follows:
  • Regression coeffs. for CRC
    constant = 18.4375
    A (H-9645) = −0.158696
    B (H-611) = 0.242708
    AB = −0.0142663
  • The regression coefficients show that HiTEC® 9645 unexpectedly decreases the CRC response (a beneficial effect, since lower CRC ratings indicate less injector depositing), while HiTEC® 611 increases the ratings. There is a significant negative interaction between HiTEC® 9645 and HiTEC® 611, meaning that the deleterious effect of HiTEC® 611 on CRC rating at low concentrations of dispersant is more than cancelled out at high dispersant concentrations. In other words, HiTEC® 611 improves CRC ratings when in the presence of high amounts of HiTEC® 9645. This effect is shown graphically by the interaction diagram in FIG. 2. Ordinarily, a p-value of 0.13 would result in HiTEC® 611 alone being excluded from the model: this value indicates that the coefficient is different from zero only at the 87% confidence level. However, if the model contains an interaction between HiTEC® 9645 and HiTEC® 611, the HiTEC® 611 term should also be included to preserve model hierarchy.
  • Formulations of Modified Dispersant Packages to Pass the Cummins L10 Test
  • From the model developed above, it is therefore possible to adjust the components in, for example, HiTEC®D 4080 in order to hit a desired CRC target. As mentioned previously, the maximum CRC rating for a Cummins L10 pass is 10.0. Constant response curves for CRC as a function of HiTEC® 9645 and HiTEC® 611 concentrations (in PTB) are shown in FIG. 3.
  • Based on the above model for CRC, any combination of HiTEC® 9645 and HiTEC 611 to the right of the 10.0 contour (the dashed line) in FIG. 3 should give a passing Cummins L10 rating. Three points were selected on the 9.0 contour (the solid line) in the L10 test. The additive combinations corresponding to these points were:
      • 1. 28 PTB HiTEC® 9645+32 PTB HiTEC® 611
      • 2. 26 PTB HiTEC® 9645+40 PTB HiTEC® 611
      • 3. 25 PTB HiTEC® 9645+48 PTB HiTEC® 611
  • All three packages also contained 6.6 PTB of Ethyl's MMT® as HiTEC® 3062 plus solvent, demulsifier and corrosion inhibitor as described above. The resulting Cummins L10 data are shown in Table 3.
    TABLE 3
    Cummins L10 results for modified versions of HiTEC ® 4080
    Modified package Test no. Avg. flow loss (%) Avg. CRC rating
    1 D102-107-2 2.0 8.6
    2 D102-107-1 3.1 8.5
    3 D102-109-1 3.3 9.9

    As expected from the above model and calculations, all three packages pass the Cummins L10 test.
  • A simple 23 experimental design has determined the quantitative effects of various components in a Greenburn® Diesel Fuel Additive package on Cummins L10 performance. It was found that the succinimide dispersant (HiTEC® 9645) had a beneficial effect on injector ratings, while the overbased calcium sulfonate detergent (HiTEC® 611) harmed those ratings. In addition, a strong interaction between these two components was observed which reduced the undesirable effect of the detergent. MMT® (as HiTEC® 3062) had no significant effect on injector cleanliness. The model derived from the experimental design was used to formulate modified Greenburn®-type packages that passed the Cummins L10 test.
  • Other embodiments of the present invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. As used throughout the specification and claims, “a” and/or “an” may refer to one or more than one. Unless otherwise indicated, all numbers expressing quantities of ingredients, properties such as molecular weight, percent, ratio, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the specification and claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims.

Claims (12)

1. A distillate fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent.
2. The fuel additive of claim 1 wherein the organometallic manganese compound comprises methylcyclopentadienylmanganese tricarbonyl.
3. The fuel additive of claim 1 wherein the succinimide is prepared from polyisobutylene succinic anhydride and a polyalkylene polyamine.
4. The fuel additive of claim 1 wherein the succinimide is prepared from polyisobutylene succinic anhydride and tetraethylenepentamine.
5. The fuel additive of claim 1 wherein the polyisobutylene of the alkyl-substituted succinimide is prepared from about 850 to 2100 molecular weight polyisobutylene.
6. The fuel additive of claim 1 wherein the polyisobutylene of the alkyl-substituted succinimide is prepared from about 850 to 1300 molecular weight polyisobutylene.
7. The fuel additive of claim 1 wherein the polyisobutylene of the alkyl-substituted succinimide is prepared from about 950 molecular weight polyisobutylene.
8. The fuel additive of claim 1 wherein the composition comprises an organometallic complex of manganese, an overbased calcium sulfonate detergent, and an ashless alkyl-substituted succinimide dispersant such that when the additive composition is dissolved in a distillate fuel, the following relationship is satisfied:

−0.159x+0.243y−0.0143xy≦−8.4
where
x=concentration of succinimide (in pounds per thousand barrels)
y=concentration of overbased calcium sulfonate (in PTB)
with the following limitations:
x=20-35, and y=10-120.
9. The fuel additive of claim I wherein the overbased calcium sulfonate has a TBN of above about 200.
10. The fuel additive of claim 1 wherein the overbased calcium sulfonate has a TBN of about 300.
11. A fuel comprising a major amount of a middle distillate fuel and a minor amount of a fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent of TBN about 300.
12. A method for improving the cleanliness of a fuel intake systems by use in the fuel intake system of a fuel containing a distillate fuel additive composition comprising an organometallic manganese compound, an alkyl-substituted succinimide ashless dispersant, and an overbased calcium sulfonate detergent of TBN about 300.
US10/614,771 2003-07-08 2003-07-08 Distillate fuel compositions for improved combustion and engine cleanliness Abandoned US20050005506A1 (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100199547A1 (en) * 2006-09-05 2010-08-12 Cerion Technology, Inc. Cerium dioxide nanoparticle-containing fuel additive
CN103205288A (en) * 2013-03-06 2013-07-17 陕西明瑞资源再生有限公司 Clean synthetic diesel and synthetic process thereof
US8883865B2 (en) 2006-09-05 2014-11-11 Cerion Technology, Inc. Cerium-containing nanoparticles
US10143661B2 (en) 2013-10-17 2018-12-04 Cerion, Llc Malic acid stabilized nanoceria particles
US10435639B2 (en) 2006-09-05 2019-10-08 Cerion, Llc Fuel additive containing lattice engineered cerium dioxide nanoparticles

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1790710A1 (en) 2005-11-25 2007-05-30 Infineum International Limited A Method of Operating a Marine or Stationary Diesel Engine
KR20070055386A (en) * 2005-11-25 2007-05-30 인피늄 인터내셔날 리미티드 A method of operating a marine or stationary diesel engine
EP2507347A1 (en) * 2009-11-30 2012-10-10 The Lubrizol Corporation Methods of controlling sulfur trioxide levels in internal combustion engines
US20230257670A1 (en) * 2021-11-15 2023-08-17 Infineum International Limited Marine Fuels

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3883320A (en) * 1972-12-07 1975-05-13 Standard Oil Co Reducing deposits and smoke from jet fuels with additives incorporating an ammonium salt
US4240801A (en) * 1979-05-31 1980-12-23 Ethyl Corporation Diesel fuel composition
US4247301A (en) * 1978-06-19 1981-01-27 Chevron Research Company Deposit control and dispersant additives
US4482356A (en) * 1983-12-30 1984-11-13 Ethyl Corporation Diesel fuel containing alkenyl succinimide
US4659338A (en) * 1985-08-16 1987-04-21 The Lubrizol Corporation Fuel compositions for lessening valve seat recession
US4781730A (en) * 1987-06-05 1988-11-01 The Lubrizol Corporation Fuel additive comprising a hydrocarbon soluble alkali or alkaline earth metal compound and a demulsifier
US5454843A (en) * 1994-03-02 1995-10-03 Ethyl Corporation Reducing deposit formation in gasoline engines
US5525127A (en) * 1993-12-23 1996-06-11 Ethyl Petroleum Additives Limited Evaporative burner fuels and additives therefor
US5679116A (en) * 1992-05-06 1997-10-21 Ethyl Corporation Compositions for control of induction system deposits
US5919276A (en) * 1997-02-07 1999-07-06 Ethyl Petroleum Additives Limited Use of mixed alkaline earth-alkali metal systems as emissions reducing agents in compression ignition engines
US5928392A (en) * 1996-05-14 1999-07-27 Ethyl Corporation Enhanced combustion of hydrocarbonaceous burner fuels
US5944858A (en) * 1990-09-20 1999-08-31 Ethyl Petroleum Additives, Ltd. Hydrocarbonaceous fuel compositions and additives therefor
US6652609B1 (en) * 1997-07-15 2003-11-25 Exxon Chemical Patents Inc Fuel oil compositions

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0476197B1 (en) * 1990-09-20 1994-01-12 Ethyl Petroleum Additives Limited Hydrocarbonaceous fuel compositions and additives therefor
EP0476196B1 (en) * 1990-09-20 1993-11-18 Ethyl Petroleum Additives Limited Hydrocarbonaceous fuel compositions and additives therefor
GB2289287A (en) * 1994-05-04 1995-11-15 Ethyl Petroleum Additives Ltd Fuel foam control additive
GB2322138A (en) * 1997-02-17 1998-08-19 Ethyl Petroleum Additives Ltd Foam reducing fuel additive

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3883320A (en) * 1972-12-07 1975-05-13 Standard Oil Co Reducing deposits and smoke from jet fuels with additives incorporating an ammonium salt
US4247301A (en) * 1978-06-19 1981-01-27 Chevron Research Company Deposit control and dispersant additives
US4240801A (en) * 1979-05-31 1980-12-23 Ethyl Corporation Diesel fuel composition
US4482356A (en) * 1983-12-30 1984-11-13 Ethyl Corporation Diesel fuel containing alkenyl succinimide
US4659338A (en) * 1985-08-16 1987-04-21 The Lubrizol Corporation Fuel compositions for lessening valve seat recession
US4781730A (en) * 1987-06-05 1988-11-01 The Lubrizol Corporation Fuel additive comprising a hydrocarbon soluble alkali or alkaline earth metal compound and a demulsifier
US5944858A (en) * 1990-09-20 1999-08-31 Ethyl Petroleum Additives, Ltd. Hydrocarbonaceous fuel compositions and additives therefor
US5679116A (en) * 1992-05-06 1997-10-21 Ethyl Corporation Compositions for control of induction system deposits
US5525127A (en) * 1993-12-23 1996-06-11 Ethyl Petroleum Additives Limited Evaporative burner fuels and additives therefor
US5454843A (en) * 1994-03-02 1995-10-03 Ethyl Corporation Reducing deposit formation in gasoline engines
US5928392A (en) * 1996-05-14 1999-07-27 Ethyl Corporation Enhanced combustion of hydrocarbonaceous burner fuels
US5919276A (en) * 1997-02-07 1999-07-06 Ethyl Petroleum Additives Limited Use of mixed alkaline earth-alkali metal systems as emissions reducing agents in compression ignition engines
US6652609B1 (en) * 1997-07-15 2003-11-25 Exxon Chemical Patents Inc Fuel oil compositions

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100199547A1 (en) * 2006-09-05 2010-08-12 Cerion Technology, Inc. Cerium dioxide nanoparticle-containing fuel additive
US8883865B2 (en) 2006-09-05 2014-11-11 Cerion Technology, Inc. Cerium-containing nanoparticles
US9221032B2 (en) 2006-09-05 2015-12-29 Cerion, Llc Process for making cerium dioxide nanoparticles
US9303223B2 (en) 2006-09-05 2016-04-05 Cerion, Llc Method of making cerium oxide nanoparticles
US9340738B2 (en) 2006-09-05 2016-05-17 Cerion, Llc Method of making cerium oxide nanoparticles
US9993803B2 (en) 2006-09-05 2018-06-12 Cerion, Llc Method of preparing cerium dioxide nanoparticles
US10435639B2 (en) 2006-09-05 2019-10-08 Cerion, Llc Fuel additive containing lattice engineered cerium dioxide nanoparticles
CN103205288A (en) * 2013-03-06 2013-07-17 陕西明瑞资源再生有限公司 Clean synthetic diesel and synthetic process thereof
US10143661B2 (en) 2013-10-17 2018-12-04 Cerion, Llc Malic acid stabilized nanoceria particles

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