EP2683798B1 - Utilisation de camphène en carburants de type essence - Google Patents

Utilisation de camphène en carburants de type essence Download PDF

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Publication number
EP2683798B1
EP2683798B1 EP12707804.6A EP12707804A EP2683798B1 EP 2683798 B1 EP2683798 B1 EP 2683798B1 EP 12707804 A EP12707804 A EP 12707804A EP 2683798 B1 EP2683798 B1 EP 2683798B1
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Prior art keywords
fuel
formulation
component
base
camphene
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German (de)
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EP2683798A1 (fr
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Richard John Price
Martin Tom CROFT
Renate UITZ
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Shell Internationale Research Maatschappij BV
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Shell Internationale Research Maatschappij BV
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G29/00Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
    • C10G29/20Organic compounds not containing metal atoms
    • C10G29/22Organic compounds not containing metal atoms containing oxygen as the only hetero atom
    • 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
    • C10L1/02Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C10L1/023Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark ignition
    • 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
    • C10L1/04Liquid carbonaceous fuels essentially based on blends of hydrocarbons
    • C10L1/06Liquid carbonaceous fuels essentially based on blends of hydrocarbons for spark ignition
    • 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
    • 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
    • C10L1/16Hydrocarbons
    • C10L1/1608Well defined compounds, e.g. hexane, benzene
    • 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
    • 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
    • C10L10/04Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
    • 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
    • C10L10/08Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
    • 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
    • C10L10/10Use of additives to fuels or fires for particular purposes for improving the octane number
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/20Characteristics of the feedstock or the products
    • C10G2300/30Physical properties of feedstocks or products
    • C10G2300/305Octane number, e.g. motor octane number [MON], research octane number [RON]
    • 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

Definitions

  • This invention relates to the use of certain materials in fuel formulations for new purposes.
  • bio-derived components biofuels
  • Bio-derived fuel components are derived from biological sources, which result in a reduction in "well-to-wheels" (i.e. from source to combustion) greenhouse gas emissions.
  • gasoline fuels for use in spark ignition (petrol) engines the most common bio-derived components are oxygenates such as alcohols, in particular ethanol. These are typically blended with more traditional gasoline fuel components.
  • oxygenates such as alcohols, in particular ethanol.
  • Ethanol also impacts the distillation properties of gasoline fuels, increasing their E70 and E100 values.
  • a gasoline base fuel typically has to be specially reformulated if it is to be blended with ethanol, to ensure that the resultant blend meets gasoline specifications around the world. This reformulation naturally increases the cost and complexity of the fuel manufacturing process, and can limit the concentration at which ethanol can practically be included in gasoline fuels.
  • camphene a monoterpene component
  • Monoterpenes are a large and varied class of organic compounds, produced primarily by a wide variety of plants, particularly conifers, and also by some insects.
  • Monoterpenes may be synthetic or naturally occurring, and may be bio-derived, particularly from gum turpentine and crude sulphate turpentine (produced by the wood pulping industry). Structurally, monoterpenes comprise isomers of C 10 H 16 and may consist of two isoprene units.
  • Monoterpenes may be linear (acyclic) or may contain rings. Acyclic monoterpenes include myrcene and ocimene, and the various stereoisomers thereof.
  • Monocyclic monoterpenes include limonene, ⁇ -terpinene, ⁇ - and ⁇ -phellandrene, ⁇ - and ⁇ -terpinolene, and the various stereoisomers thereof.
  • Bicyclic monoterpenes include 3-carene, ⁇ - and ⁇ -pinene, ⁇ -fenchene, and camphene, and the various stereoisomers thereof.
  • WO 01/53437A1 proposes further reduction of vapour pressure of a fuel formulation comprising a C 3 to C 12 hydrocarbon component, ethanol, and a second oxygenate, by the incorporation of from 0 to 99% by volume of an individual hydrocarbon selected from C 6 to C 12 aliphatic or alicyclic, saturated or unsaturated hydrocarbons; suitable examples include limonene and myrcene. Limonene is also proposed for use in fuel blends in US-A-4 818 250 in an amount up to 20% by volume. Terpenes comprising at least 60%wt pinenes are proposed for use with a gasoline base fuel in EP-A1-2 290 037 , in particular as a corrosion inhibitor, in an amount from 0.1 to 40% by volume.
  • US-A-3 274 224 proposes the use of a small amount (from 0.33 to about 6% by weight) of terpenes comprising at least 60%wt ⁇ -pinene, to provide thermal stability for tetraethyl lead antiknock blends; camphene is mentioned as a minor impurity (4 to 8%) in one of three sources of terpenes. More recently, terpenes have been proposed in WO 2010/017099 for use as an optional component of a modified fuel comprising a base fuel, a lower alcohol and a triglyceride derived from a fatty acid, in an amount of less than 1% by volume; the modified fuel as a whole is said to provide increased horsepower and/or increased octane.
  • RU-2105041 C1 appears to disclose a fuel composition
  • a fuel composition comprising a base fuel, a fatty acid-based soluble iron compound and 0.006 to 0.03%wt of a camphene to increase both octane number in gasolines and cetane number in diesel fuels.
  • a base fuel a fatty acid-based soluble iron compound
  • 0.006 to 0.03%wt of a camphene to increase both octane number in gasolines and cetane number in diesel fuels.
  • DE 3031158 A1 proposes the use of from 0.1 to 1% of bicyclic monoterpene hydrocarbons, amongst other options, in a mixture also containing 70 to 85% vol of water and ethanol; the mixture is used with gasoline, naphtha, gas oil or fuel oil to increase acceleration and octane number with reduced NOx in exhaust gases.
  • Camphene [CAS no. 79-92-5] is a monoterpene with a bicyclic structure, as shown in Table 1. It is a white crystalline solid with a boiling point of 159 °C, i.e. within the normal gasoline boiling range.
  • the monoterpene component comprises at least 90% or even at least 95% v/v of camphene, based on the total volume of the component.
  • the monoterpene component is substantially free of tricyclene and/or tricyclic monoterpenes. "Substantially free” may refer to a concentration of less than 2% v/v based on the total volume of the component.
  • the monoterpene component may exclude tricyclene.
  • the monoterpene component may be obtained by any suitable method.
  • the monoterpene component may be synthetic or naturally occurring.
  • the monoterpene component is bio-derived, by which is meant that it has been obtained - either directly or indirectly - from a biological source.
  • the monoterpene component may advantageously comprise at least about 0.1 dpm/gC of carbon-14. It is known in the art that carbon-14 (C-14), which has a half-life of about 5,700 years, is found in bio-derived materials but not in fossil fuels. Thus, the term "bio-derived” as used herein may be defined as “comprising at least about 0.1 dpm/gC of carbon-14".
  • the monoterpene is used in the fuel formulation in an amount in the range of from 5 to 10 % v/v of which at least 90% by volume, more preferably at least 95% by volume, is camphene.
  • the monoterpene component should ideally be dissolved in the fuel formulation, suitably fully dissolved. It may be present in a carrier fluid, for example a solvent selected from alkanes (for example n-heptane or other n-alkanes, or iso-octane); alcohols (for example ethanol or butanol); ethers (for example methyl t-butyl ether or ethyl t-butyl ether); alkenes such as diisobutylene; fuel components such as alkylates, isomerates, naphthas, straight run tops, light and heavy catalytically cracked gasolines or reformates; and mixtures thereof.
  • a carrier fluid for example a solvent selected from alkanes (for example n-heptane or other n-alkanes, or iso-octane); alcohols (for example ethanol or butanol); ethers (for example methyl t-butyl ether or e
  • the monoterpene component may be used, in accordance with the invention, in a gasoline fuel formulation (e.g. automotive).
  • a gasoline fuel formulation e.g. automotive
  • it may be used in a gasoline fuel formulation comprising a base fuel, preferably as defined below.
  • the monoterpene component may be used in a gasoline fuel formulation comprising a base fuel and one or more additional components, such as, for example, a bio-derived component or an oxygenate (e.g. ethanol).
  • additional components such as, for example, a bio-derived component or an oxygenate (e.g. ethanol).
  • Preferred additional components in particular bio-derived components and oxygenates, are described below.
  • an individual bio-derived component e.g. ethanol
  • the natures and concentrations of the components of such a combination can be chosen so as to achieve desired properties for the overall fuel formulation which contains it, and thus to increase the total bio-derived content of the formulation without unduly impairing its performance. This in turn can assist the fuel formulator in meeting increasingly stringent fuel specifications.
  • vapour pressure as used herein may refer to the dry vapour pressure equivalent (DVPE) and should be construed as such unless context requires otherwise.
  • the DVPE of a formulation is the vapour pressure of that formulation at 37.8 °C. DVPE values may be measured using the standard test method EN 13016-1 or ASTM D4953-06 or an analogous method.
  • Blending rules allow for calculation of the DVPE of a blend of components from the blending DVPE values of its individual components.
  • the blending DVPE of a fuel formulation component is a measure of how the DVPE of the fuel formulation may change with the addition of that component.
  • bDVPE n DVPE base + n 1.25 ⁇ DVPE base + n 1.25 1 ⁇ v n v n 0.8
  • bDVPE n the blending dry vapour pressure equivalent of a component or mixture n
  • DVPE base is the dry vapour pressure equivalent of the base fuel
  • DVPE base+n is the dry vapour pressure equivalent of the blend
  • v n the volume fraction of n in the blend.
  • the monoterpene component may be used, for example, in fuel formulations having a DVPE of 100 kPa or less.
  • the DVPE of such fuel formulations may be 90 or 95 or 80 or - in particular where it is intended for use as a summer grade fuel - 70 or 60 kPa or less.
  • the use of a monoterpene component according to the invention has been found to be particularly beneficial in fuel formulations having a DVPE of 45 kPa or more, such as, for example 50 or 55 or 60 kPa or more.
  • fuel formulations typically comprise a base fuel and may also contain additional components such as bio-derived or oxygenate components.
  • the monoterpene component may be used, according to the invention, for the purpose of reducing the vapour pressure of a fuel formulation to a level below the vapour pressure of a bio-derived or oxygenate component comprised in the fuel formulation.
  • the monoterpene component may be used for the purpose of reducing the vapour pressure of the formulation to a level below the vapour pressure of a mixture of a base fuel and a bio-derived or oxygenate component comprised in the fuel formulation.
  • the monoterpene component may even be used for the purpose of reducing the vapour pressure of the formulation to a level below the vapour pressure of a base fuel comprised in the fuel formulation.
  • the monoterpene component is used in such a fuel formulation, optionally further comprising a bio-derived component or oxygenate, to adjust or reduce the DVPE of the fuel formulation such that there is no increase in DVPE relative to the base fuel. That is to say: ⁇ DVPE ⁇ 0 kPa where ⁇ DVPE is the difference between the DVPE of the overall fuel formulation and that of the base fuel.
  • the ⁇ DVPE may also be the difference between the DVPE of the overall fuel formulation and that of the same formulation in the absence of a monoterpene component and any additional bio-derived or oxygenate component(s).
  • the monoterpene component may advantageously be used for the purpose of adjusting or reducing the vapour pressure of the fuel formulation to be neutral or close to neutral with respect to the vapour pressure of the base fuel.
  • neutral or close to neutral is meant that the vapour pressure of the formulation is adjusted to lie within plus or minus 15%, preferably plus or minus 10% of the vapour pressure of the base fuel.
  • Vapour pressure is an indicator of volatility: the higher the vapour pressure, the more volatile the fuel.
  • certain other fuel properties such as distillation properties (e.g. as discussed below), boiling points (e.g. initial and final boiling points), and alternative measurements of vapour pressure, such as air-saturated vapour pressure (ASVP), are dependent on DVPE.
  • distillation properties e.g. as discussed below
  • boiling points e.g. initial and final boiling points
  • ASVP air-saturated vapour pressure
  • vapour pressure Reducing the vapour pressure of a fuel formulation may hence comprise influencing or adjusting any fuel property dependent on vapour pressure.
  • the distillation properties of a fuel formulation may be expressed in terms of E-values and T-values.
  • E70 value for a formulation is the volume percentage of the formulation that has been distilled at 70°C
  • E100 value is the volume percentage of the formulation that has been distilled at 100°C. Both E70 and E100 values, as well as other E-values, can be measured using the standard test method EN ISO 3405.
  • T70 value for a formulation is the temperature on its distillation curve at which 70% of its volume has evaporated at standard atmospheric pressure
  • T100 value for a formulation is the temperature on its distillation curve at which 100% of its volume has evaporated at standard atmospheric pressure. Both T70 and T100 values, as well as other T-values, can be measured using the standard test method EN ISO 3405.
  • the monoterpene component according to the first aspect may preferably be for the purpose of influencing or adjusting the E70 and E100 values of the fuel formulation.
  • the monoterpene component, or particularly the combination or use of the monoterpene component with any additional bio-derived components or oxygenates in the fuel formulation does not significantly alter the E70 and E100 values for the fuel formulation as a whole compared to the values for a base fuel of the formulation alone.
  • both the E70 value and the E100 value of the fuel formulation are maintained within 25%, or within 20%, or within 15%, of both the E70 value and the E100 value of the base fuel, and/or that the value of (E70 + E100) for the fuel formulation is maintained within 15%, or within 10%, or within 5% of the value of (E70 + E100) for the base fuel.
  • the monoterpene component is used for the purpose of achieving: ⁇ 20 % v / v ⁇ ⁇ E 70 + ⁇ E 100 ⁇ 20 % v / v , where ⁇ E70 is the difference between the E70 of the overall fuel formulation and that of the same formulation in the absence of the monoterpene component and any additional bio-derived component(s) or oxygenate(s); and ⁇ E100 is the difference between the E100 of the overall fuel formulation and that of the same formulation in the absence of any monoterpene component and the additional bio-derived component(s) or oxygenate(s).
  • ⁇ E70 may be seen as the difference between the E70 of the overall fuel formulation and that of the base fuel alone, and ⁇ E100 as the difference between the E100 of the overall fuel formulation and that of the base fuel alone.
  • ⁇ 15 % v / v ⁇ ⁇ E 70 + ⁇ E 100 ⁇ 15 % v / v , or that: ⁇ 10 % v / v ⁇ ⁇ E 70 + ⁇ E 100 ⁇ 10 % v / v , or that: ⁇ 5 % v / v ⁇ ⁇ E 70 + ⁇ E 100 ⁇ 5 % v / v , or that: ⁇ 1 % v / v ⁇ ⁇ E 70 + ⁇ E 100 ⁇ 1 % v / v , or in cases that : ⁇ E 70 + ⁇ E 100 0 % v / v .
  • ⁇ E70 to counter, at least partially, ⁇ E100.
  • a blend containing ethanol as well as a monoterpene component can be tailored to have acceptable distillation properties, as can a blend containing one or more additional bio-derived components or oxygenates with a monoterpene component, a base fuel and optionally ethanol.
  • a second aspect resides in the use of a monoterpene component which comprises camphene in a fuel formulation, for the purpose of improving or maintaining one or more properties of the fuel formulation selected from: lubricity, oxidative stability, deposit-forming tendency, elastomer compatibility and especially octane number relative to the relevant property in: (i) a bio-derived or oxygenate component comprised in the fuel formulation; and/or (ii) a mixture of a base fuel and a bio-derived or oxygenate component comprised in the fuel formulation and/or (iii) a base fuel comprised in the fuel formulation.
  • Use according to the second aspect may in particular be for the purpose of achieving a desired target property, particularly by mitigating a detrimental effect on the property of other bio-derived or oxygenate components, such as ethanol, within the formulation.
  • the lubricity of a fuel formulation can be assessed by any suitable method.
  • One such method involves measuring the wear scar produced on an oscillating ball from contact with a stationary plate whilst immersed in the formulation. This "wear scar” may be measured for example using the test described in Example 4 below.
  • An “improvement” in the lubricity of a formulation may be manifested for example by a lower degree of wear scar, or of other friction-induced damage, in two relatively-moving components which are exposed to the formulation.
  • the oxidative stability of a fuel formulation can be assessed by any suitable method.
  • One such method involves measuring the concentration of peroxides in the fuel formulation before storage and upon storage of the fuel formulation at various temperatures and time intervals. For example, peroxide concentration may be measured initially, and may then be measured again after a three-month storage of the fuel formulation at 0-2 °C. A similar experiment may be performed with the storage occurring at 40 °C.
  • Peroxide concentrations which provide a suitable metric for the oxidative stability of a fuel formulation, can be measured using the standard test method SMS 359 or an analogous method.
  • the oxidative stability of a fuel formulation can also be assessed using the induction period after a period of storage at a specified temperature (e.g. 3 months at 0-2 °C or 40 °C).
  • the induction period which provides a suitable metric for the oxidative stability of a fuel formulation, can be measured using the standard test method EN ISO 7536 or an analogous method.
  • a monoterpene in a fuel formulation can improve or maintain deposit-forming tendencies of the fuel formulation.
  • 'improve or maintain deposit-forming tendencies' is meant that there is a decreased or equal tendency of the monoterpene-containing fuel formulation to form deposits, particularly gum deposits, relative to the relevant reference point.
  • the deposit-forming tendencies of a fuel formulation can be assessed by any suitable method.
  • One such method is the MIHPT (multiple inclined hot plate rig test) method. This method uses an intake valve deposit simulator test corresponding closely to that described in SAE Paper 890215, Daneshgari et al, "The Influence of Temperature upon Gasoline Deposit Build-Up on the Intake Valves", Detroit, USA, 27 February to 3 March 1989 , and is described in Example 6 below.
  • Elastomer compatibility is a measure of a fuel formulation's tendency to cause elastomer-damaging effects, ie effects that reduce the ability of an elastomeric material to function correctly in a fuel-consuming system and/or in the presence of the fuel formulation.
  • An example of an elastomer damaging effect is swelling of the elastomer when in contact with the fuel formulation. Elastomer damage also includes a change (typically a reduction) in the hardness and/or flexibility of the elastomer when in contact with the fuel formulation.
  • Elastomer swell measurements in particular provide a measure of the compatibility of elastomeric materials, such as are used in fuel pump seals and other engine components, with a fuel component or formulation.
  • this compatibility is evaluated by assessing changes in the properties of an elastomer due to its immersion in a test fluid.
  • the elastomer swelling effects of a fuel formulation may for instance be assessed by measuring the increase or percentage increase in volume or mass of an elastomeric material on immersion in the formulation for a predetermined period of time. A smaller volume or mass increase indicates a reduction in elastomer swelling effects. This assessment may for example be carried out for nitrile and/or fluorocarbon elastomers.
  • a standard test method such as DIN 51605-1 or ISO 1817:1998 may be used to measure elastomer swell effects. Changes in the hardness and/or flexibility of an elastomeric material may be assessed using standard test methods such as the Shore hardness test or TMS 556.
  • a monoterpene component especially one which comprises camphene
  • a fuel formulation can improve or maintain an octane number of the formulation.
  • Octane number may refer to research octane number (RON) and/or motor octane number (MON).
  • the research octane number (RON) may be measured by any suitable method. It can be measured using the standard test methods ASTM D2699 or EN 25164 or analogous methods such as PrEN ISO 5164.
  • the motor octane number (MON) may be measured by any suitable method. It can be measured using the standard test methods ASTM D2700 or EN 25163 or analogous methods such as PrEN ISO 5163.
  • the effectiveness of the monoterpene component in improving or maintaining octane number depends on the one hand on the octane number of the fuel formulation to which it is added and on the other hand on the structure of the monoterpene(s) present in the monoterpene component.
  • the monoterpene component may be used to maintain or improve the octane number of a fuel formulation having a RON of 100 or less or 99 or 98 or 95 or less and/or a MON of 95 or less, or 90 or 88 or less.
  • camphene is especially effective in improving or maintaining the octane number (especially RON) of fuel formulations. Accordingly, a third, preferred, aspect, resides in use of camphene in a fuel formulation for the purpose of improving, maintaining or achieving a target octane number of the fuel formulation.
  • the third aspect embraces use of camphene in a fuel formulation to achieve: ⁇ RON ⁇ 0 where ⁇ RON is the difference between the RON of the camphene-containing fuel formulation and that of the base fuel alone.
  • the ⁇ RON may also be the difference between the RON of the overall fuel formulation and that of the same formulation in the absence of camphene and any additional bio-derived or oxygenate component(s).
  • MON values can be calculated from the respective blending values in a similar manner.
  • the purposive uses may alternatively be expressed as methods of achieving one or more target properties in a fuel formulation by blending an effective amount of a monoterpene, especially camphene, component with the fuel formulation.
  • a fourth aspect resides in a method of achieving a target vapour pressure in a fuel formulation, the method comprising blending an effective amount of a monoterpene component with the fuel formulation.
  • a fifth aspect resides in a method of achieving a target lubricity, oxidative stability, deposit-forming tendency, elastomer compatibility or octane number in a fuel formulation, the method comprising blending an effective amount of a monoterpene component which comprises camphene with the fuel formulation.
  • a sixth aspect provides a method of achieving a target octane number in a fuel formulation, the method comprising blending an effective amount of camphene with the fuel formulation.
  • a seventh aspect provides the use of a bio-derived monoterpene component which comprises camphene, in a fuel formulation, particularly a fuel formulation comprising another bio-derived component or oxygenate, for the purpose of increasing the bio-derived content of the formulation without, or without unduly, increasing the vapour pressure of the formulation.
  • An eighth aspect provides the use of a bio-derived monoterpene component which comprises camphene, in a fuel formulation, particularly a fuel formulation comprising another bio-derived component or oxygenate, for the purpose of increasing the bio-derived content of the formulation without, or without unduly, reducing an octane number of the formulation.
  • a ninth aspect provides the use of a monoterpene which comprises camphene in a gasoline fuel formulation, for the purpose of replacing, at least partially, a bio-derived component and/or an oxygenate in the formulation.
  • the monoterpene component is biologically derived.
  • the monoterpene component may thus be used as a substitute for at least some of the bio-derived component or oxygenate which would otherwise have been included in the formulation, for example so as to achieve a desired target specification such as a minimum bio-derived content.
  • a quantity of biologically derived monoterpene component may be included in a fuel formulation in place of the same or a similar quantity of ethanol, allowing a target minimum bio-derived content to be achieved but without, or with fewer of, the drawbacks associated with the use of ethanol alone.
  • a tenth aspect resides in a fuel formulation obtainable by or resulting from the use or method of any of the first to ninth aspects of the invention.
  • the base fuel component of a fuel formulation in the context of the invention is typically a liquid hydrocarbon distillate gasoline fuel component, or mixture of such components, containing hydrocarbons that boil in the range from 0 to 250°C (ASTM D86 or EN ISO 3405) or from 20 or 25 to 200 or 230°C.
  • the optimal boiling ranges and distillation curves for such base fuels will typically vary according to the conditions of their intended use, for example the climate, the season and any applicable local regulatory standards or consumer preferences.
  • the hydrocarbon fuel component(s) in the base fuel may be obtained from any suitable source. They may for example be derived from petroleum, coal tar, natural gas or wood, in particular petroleum.
  • they may be synthetic products such as from a Fischer-Tropsch synthesis. Conveniently they may be derived in any known manner from straight-run gasoline, synthetically-produced aromatic hydrocarbon mixtures, thermally or catalytically cracked hydrocarbons, hydrocracked petroleum fractions, catalytically reformed hydrocarbons or mixtures of these.
  • base fuels comprise components selected from one or more of the following groups: saturated hydrocarbons, olefinic hydrocarbons, and aromatic hydrocarbons.
  • the olefinic hydrocarbon content of a base fuel is in the range from 0 to 40% v/v; it may for instance be in the range from 0 to 30% v/v.
  • the aromatic hydrocarbon content of a base fuel is from 0 to 70% v/v; it may for instance be from 10 to 60% v/v.
  • the benzene content of a base fuel is typically at most 10% v/v, or at most 5% v/v, or at most 1% v/v.
  • the saturated hydrocarbon content of a base fuel is at least 40% v/v; it may for instance be from 40 to 80% v/v.
  • the base fuel suitably has a low or ultra low sulphur content, for instance at most 1000 ppmw (parts per million by weight) of sulphur, or no more than 500 ppmw, or no more than 100 ppmw, or no more than 50 or even 10 ppmw. It also suitably has a low total lead content, such as at most 0.005 g/l; in an embodiment it is lead free (“unleaded”), ie having no lead compounds in it.
  • a base fuel will typically have a research octane number (RON) (ASTM D2699 or EN 25164) of 80 or greater, or of 85 or 90 or 93 or 94 or 95 or 98 or greater, for example from 80 to 110 or from 85 to 115 or from 90 to 105 or from 93 to 102 or from 94 to 100.
  • RON research octane number
  • a monoterpene component may advantageously be used in a fuel formulation comprising a base fuel having a RON of 115 or less, or of 105 or 102 or 100 or 99 or even 98 or less.
  • a base fuel will typically have a motor octane number (MON) (ASTM D2700 or EN 25163) of 70 or greater, or of 75 or 80 or 84 or 85 or greater, for example from 70 to 110 or from 75 to 105 or from 84 to 95.
  • MON motor octane number
  • a monoterpene component may advantageously be used in a fuel formulation comprising a base fuel having a MON of 110 or less, or of 105 or 100 or 95 or 90 or even 88 or less.
  • a base fuel will typically have an E70 value of 10% v/v or greater, or of 14 or 15 or 20 or 22% v/v or greater. Its E70 value might typically be up to 55% v/v, or up to 51 or 50 or 48% v/v. Its E70 value might for example be from 10 to 55% v/v, or from 14 to 51% v/v, or from 14 to 50% v/v, or from 20 to 50% v/v. In an embodiment, it has an E70 value of from 20 to 48% v/v. In an alternative embodiment, it has an E70 value of from 22 to 50% v/v.
  • the base fuel will typically have an E100 value of 35% v/v or greater, or of 40 or 45 or 46% v/v or greater. Its E100 value might typically be up to 75% v/v, or up to 72 or 71% v/v. Its E100 value might for example be from 35 to 75% v/v, or from 40 to 72% v/v, or from 40 to 71% v/v, or from 46 to 71% v/v.
  • the base fuel may be a reformulated base fuel, for example one which has been reformulated so as to accommodate the addition of an oxygenate such as ethanol.
  • a base fuel might typically have a density from 0.720 to 0.775 kg/m 3 at 15°C (ASTM D4052, EN ISO 3675, or EN ISO 12185.
  • a base fuel might typically have a vapour pressure at 37.8°C (DVPE) of from 45 to 70 kPa or from 45 to 60 kPa (EN ISO 3405, EN 13016-1 or ASTM D4953-06).
  • DVPE vapour pressure at 37.8°C
  • DVPE vapour pressure at 37.8°C
  • Suitable base fuels include those having an olefinic hydrocarbon content of from 0 to 20% v/v (ASTM D1319), and/or an aromatic hydrocarbon content of from 0 to 50% v/v (ASTM D1319), and/or a benzene content of at most 1% v/v.
  • the base fuel complies with the current European gasoline fuel standard EN 228. In an embodiment, it complies with the current US gasoline fuel standard ASTM D4814-08b.
  • the concentration of the base fuel may be up to 99.99% v/v, or up to 99.95% v/v, or up to 99.9 or 99.5% v/v based on the total volume of the fuel formulation. It may be up to 99% v/v, for example up to 98 or 95 or 90% v/v, or in cases up to 85 or 80 or 75 or 70 or 65 or 60% v/v based on the total volume of the fuel formulation.
  • the base fuel will typically represent the major proportion, i.e. more than 50% v/v, of a fuel formulation
  • a fuel formulation may also contain one or more additional fuel components.
  • the fuel formulation may comprise at least one additional fuel component which causes an increase in vapour pressure relative to the vapour pressure of the base fuel.
  • the fuel formulation may include one or more gasoline fuel additives, of the type well known in the art.
  • the fuel formulation may contain one or more additional bio-derived components.
  • additional fuel components may have boiling points within the normal gasoline boiling range, and in the case of bio-derived components will have been derived - whether directly or indirectly - from biological sources.
  • The, or each, additional bio-derived fuel component may comprise at least about 0.1 dpm/gC of carbon-14.
  • the formulation may contain one or more oxygenates, which may for example be selected from alcohols, ethers (including cyclic ethers), esters, carboxylic acids and their derivatives, aldehydes, ketones, and mixtures thereof.
  • the formulation contains one or more oxygenates selected from alcohols, ethers, esters and mixtures thereof.
  • it contains one or more oxygenates selected from alcohols, ethers and mixtures thereof.
  • oxygenates are suitably bio-derived components.
  • Alcohols suitable for inclusion in a fuel formulation in the context of the invention include C1 to C5 saturated or unsaturated alcohols, in particular C1 to C4 aliphatic alcohols such as ethanol and butanol.
  • a formulation may include ethanol. It may include ethanol and one or more - for example one - additional bio-derived components. It may include ethanol and one or more - for example one - additional oxygenates.
  • Ethers suitable for inclusion in a fuel formulation include dialkyl ethers, in particular alkyl t-butyl ethers, more particularly (C1 to C3 alkyl) t-butyl ethers such as methyl t-butyl ether and ethyl t-butyl ether.
  • Other suitable ethers include furans; C5 and C5+ ethers having boiling points below 210°C; and C7 ethers - in particular ethyl ethers - such as 2-ethoxy-2-methylbutane and 1-ethoxy-3-methylbutane.
  • a formulation may include ethanol together with one or more ethers selected from (C1 to C3 alkyl) t-butyl ethers and mixtures thereof.
  • a fuel formulation contains a bio-derived or oxygenate component, especially ethanol
  • the bio-derived/oxygenate or ethanol concentration may for example be 1 or 2 or 5% v/v or greater, or 8 or 10 or 15 or 20 or 25 or 30% v/v or greater, based on the total volume of the formulation.
  • the ethanol or bio-derived/oxygenate concentration may be up to 50% v/v, or up to 45 or 40 or 35% v/v. In cases it may be up to 30 or 25 or 20 or 15 or 10% v/v.
  • the amount of oxygenate is usefully such as to provide a fuel formulation having an oxygen content of from 0 to 5% w/w (EN 1601).
  • the volume ratio of the monoterpene component to the ethanol or bio-derived/oxygenate component may be for example 1:100 or greater, or 1:50 or 1:10 or greater, for example 1:5 or 1:2 or greater, or 1:1 or 1.5:1 or greater. It may be up to 5:1, or up to 4:1 or 3:1 or 2:1 or 1:1.
  • the volume ratio of the monoterpene component to ethanol may be 1:1 or greater, or 1.2:1 or greater, or 1.5:1 or greater, or 1.8:1 or greater; in this case the ratio may for example be up to 5:1, or up to 4:1 or 3:1 or 2.5:1, for example from 1.5:1 to 3:1.
  • the concentration of the combination in the formulation may be 3 or 4 or 5% v/v or greater.
  • the concentration of the combination may be up to 50% v/v, or up to 40 or 30% v/v, or up to 25 or 20 or 15 or 10% v/v. These concentrations are for the combination as a whole in the overall fuel formulation, even if one or more components of the combination are in practice added individually when preparing the formulation.
  • the formulation resulting from uses according to the invention should be suitable for use in a spark ignition (petrol) internal combustion engine. It may in particular be suitable for use as an automotive fuel.
  • the RON of a formulation resulting from the uses of the invention is suitably 80 or greater. It may be 85 or 90 or 93 or 94 or 95 or 98 or 98.4 or greater. The RON may for example be from 80 to 110 or from 85 to 115 or from 90 to 105 or from 93 to 102 or from 94 to 100.
  • the MON of a fuel formulation resulting from the uses of the invention is suitably 70 or greater, or 75 or 80 or greater. It may be 84 or 85 or greater. The MON may for example be from 70 to 110 or from 75 to 105 or from 84 to 95.
  • achieving a desired target property also embraces - and in an embodiment involves - improving on the relevant target.
  • a monoterpene component may be used to produce a fuel formulation that has an octane number above a desired target value, or a vapour pressure below a desired target value.
  • a monoterpene component in a fuel formulation means incorporating a monoterpene component into the formulation, typically as a blend (i.e. a physical mixture) with one or more other fuel components such as a base fuel and optionally one or more additional bio-derived components or oxygenates.
  • the monoterpene may conveniently be incorporated before the formulation is introduced into an engine or other system that is to be run on the formulation.
  • “Use” of a monoterpene component in the ways described above may also embrace supplying the monoterpene component together with instructions for its use in a fuel formulation to achieve the purpose(s) of any of the aspects of the invention.
  • the monoterpene component may itself be supplied as part of a composition which is suitable for and/or intended for use as a fuel additive, in which case the monoterpene component may be included in such a composition for the purpose of influencing its relevant effects on a fuel formulation.
  • GBF2 The properties of GBF2 are summarised in Table 2 below.
  • Table 2 F uel property Units GBF2 RON (PrEN ISO 5164) 98.2 MON (PrEN ISO 5163) 87.5 DVPE (EN ISO 3405) kPa 63.3 Density @ 15°C (EN 12185) g/kg 746.7 Initial boiling point (EN ISO 3405) °C 33.0 T5 °C 47.5 T10 °C 54.6 T20 °C 66.4 T30 °C 78.7 T40 °C 92.0 T50 °C 103.3 T60 °C 111.7 T70 °C 120.2 T80 °C 132.6 T85 °C 142.7 T90 °C 154.8 T95 °C 168.7 Final boiling point °C 194.4 Total recovery % v/v 97.8 Percent residue % v/v 1.1 Corrected loss % v/v 1.1 E50 % v/v 6.7 E70 %
  • myrcene (95% purity), S(-) limonene (96% purity), and camphene (95% purity) were sourced from Sigma-Aldrich; ocimene (90% purity), ⁇ -pinene (98% purity) and ⁇ -pinene (99% purity) from Aldrich; and R(+) limonene (97% purity) from Sigma.
  • Myrcene and ocimene are acyclic monoterpenes.
  • Limonene is a monocyclic monoterpene.
  • Pinene and camphene are bicyclic monoterpenes.
  • DVPE values were measured in accordance with EN ISO 3405 for various monoterpenes when blended at 10% v/v with the base fuel GBF2. These values are shown in Table 3 below. Table 3 Added component Concentration of added component (% v / v) DVPE (kPa) E70 (% v / v) E100 (% v / v) E150 (% v / v) None (GBF2 alone) - 63.3 23.0 46.9 88.0 Ethanol 10 69.4 40.3 52.5 89.0 Myrcene 10 58.8 19.9 40.6 81.3 Ocimene 10 58.3 20.2 41.3 80.1 S(-)Limonene 10 58.3 19.6 40.7 79.9 R(+)Limonene 10 58.8 19.9 41.0 80.4 ⁇ -Pinene 10 58.6 19.1 40.3 84.9 ⁇ -Pinene 10 58.3 19.4 40.4 82.1 Camphene
  • Table 3 illustrates that all monoterpenes tested reduce the DVPE in the 10% v/v blend, relative to base fuel alone and relative to the ethanol 10 % v/v blend, reflecting the relatively high boiling point of these molecules.
  • the high reduction of 6 kPa (from 63.3 kPa for the base fuel to 56.2 kPa for the base fuel + 10% v/v camphene) for the camphene blend in particular was unexpected.
  • monoterpenes in the fuel formulation can compensate the impact of ethanol on the vapour pressure and distillation properties of the fuel formulation. This means that through combining monoterpenes, and especially camphene, with ethanol containing base-fuel no further adjustment for DVPE and E70 and E100 is needed (e.g. to the base fuel).
  • Blending DVPE values obtained for each of the monoterpene components when blended with GBF2 were calculated according to Equation 1 above and are shown in Table 4 below.
  • Table 4 Added component Concentration of added component (% v / v) bDVPE (kPa) None (GBF2 alone) - 63.3 Ethanol 10 119.7 Myrcene 10 11.6 Ocimene 10 3.0 S(-)Limonene 10 3.0 R(+)Limonene 10 11.6 ⁇ -Pinene 10 8.4 ⁇ -Pinene 10 3.0 Camphene 10 0* *bDVPE data on 10% v/v blends indicates a physically impossible negative vapour pressure for the camphene - containing blend. The blending DVPE of these components has consequently been assigned as zero.
  • a number of monoterpene components were blended with GBF2.
  • the monoterpene components and base fuel were the same as those detailed in Example 1 above.
  • RON and MON values were measured (using the standard test methods PrEN ISO 5164 and PrEN ISO 5163 respectively) for each of the resultant blends of 5 and 10% v/v monoterpene component. RON and MON values were also recorded for the base fuel alone, and for blends of 5 and 10% v/v ethanol in the base fuel.
  • Tables 5 and 6 illustrate the superior octane properties of camphene compared to the other monoterpenes tested. Its blending RON is significantly higher than those of the other monoterpenes. Since its blending RON is >98.2 at 10% v/v there is no RON penalty when camphene is blended with a base fuel such as GBF2. By contrast, there is a small RON penalty and larger MON penalty when adding the other monoterpenes to the base fuel. Thus, camphene can be seen to be superior to the other monoterpenes in terms of its fit with typical gasoline fuel octane number specifications, making it particularly suitable for use as a gasoline fuel component.
  • the elastomer swell caused by the eight formulations prepared in Example 2 was assessed using the standard test method DIN 51605-1 (measurements taken in triplicate and averaged).
  • the elastomer tested was the nitrile elastomer SRE-NBR 34. The results are shown in Table 7 below.
  • each of the monoterpenes and especially camphene causes significantly less elastomer swell than ethanol, and indeed that each has an elastomer compatibility similar to that of the base fuel alone.
  • each of the monoterpenes and especially camphene could be substituted for at least a proportion of the ethanol in an ethanol/base fuel blend, in order to mitigate the elastomer damaging effects caused by the ethanol.
  • Gasoline fuel formulations were prepared by blending the base fuel GBF2 with 10% v/v of each of the monoterpene components and ethanol, as in Example 3.
  • a sample of the fuel or blend under test was placed in a test reservoir which was maintained at a specified test temperature.
  • a fixed steel ball was held in a vertically mounted chuck and forced against a horizontally mounted stationary steel plate with an applied load.
  • the test ball was oscillated at a fixed frequency and stroke length while the interface with the plate was fully immersed in the fluid reservoir.
  • the metallurgies of the ball and plate, and the temperature, load, frequency, and stroke length were as specified in ISO 12156.
  • the ambient conditions during the test were then used to correct the size of the wear scar generated on the test ball to a standard set of ambient conditions, again as per ISO 12156.
  • the corrected wear scar diameter provides a measure of the test fluid lubricity: the lower the wear scar diameter, the higher the lubricity improvement.
  • Table 8 Added component Concentration of added component (% v / v) Wear scar diameter ( ⁇ m) None (GBF2 alone) - 886 Ethanol 10 765 Myrcene 10 900 Ocimene 10 779 S(-)Limonene 10 815 R(+)Limonene 10 747 ⁇ -Pinene 10 864 ⁇ -Pinene 10 896 Camphene 10 800
  • a gasoline fuel formulation for use according to the invention was prepared by dissolving 10 % v/v camphene in a commercially available unleaded gasoline base fuel from Germany, GBF2 (see Example 1).
  • camphene was sourced from Sigma-Aldrich. It had a purity of 95%.
  • GBF1 had an octane (RON) rating of 95.
  • MIHPT multiple inclined hot plate rig test
  • the test rig utilised four inclined plates in parallel.
  • the plates were strips of sandblasted aluminium, each 50 cm long and 2.5 cm wide, each having a 3 mm wide, 1 mm deep central groove along its length. These plates were mounted in the rig at an angle of 3 degrees relative to the horizontal. The temperature at the top end of each plate was maintained at 400°C, whilst at the middle of each plate it was maintained at 250°C.
  • test samples each contained 100 ml of the relevant fuel or fuel formulation. They were delivered at a rate of 0.6 ml/minute from glass syringes fitted with 20 gauge steel hypodermic Luer lock needles into the groove at the top end of each plate. Once sample delivery was complete, the plates were allowed to cool to ambient temperature (20°C) and were washed with n-heptane until the run-off liquid was clear. They were then left to dry before assessment of any deposit present.
  • An image was captured of a clear portion of each plate.
  • a second image was then captured of the section of the plate containing deposit.
  • the image analyser divides, pixel by corresponding pixel, the deposit image by the clean image and automatically measures the area and optical density of deposit at the pixels contained within the overall measuring frame, and calculates an integrated optical density for the image, the numerical value of which is recorded as a test rating.
  • a fuel with a high deposit-forming tendency would typically have a MIHPT scan rating of greater than 200.
  • the GBF1 base fuel was determined to have an MIHPT rating of 142, whilst the GBF1 base fuel mixed with 10 %v/v camphene gave a rating of 87. These results reflect the lower deposit-forming tendency of the camphene-containing fuel formulation, further demonstrating the suitability of camphene as a fuel component.
  • the MIHPT rating for GBF2 alone was measured as 71.
  • Examples 1 to 6 show that monoterpenes are suitable for reducing the vapour pressure of fuel formulations and that they have a number of further beneficial effects on fuel formulation properties.
  • a blend containing an oxygenate such as ethanol as well as a monoterpene component and base fuel can be tailored to have acceptable properties. Therefore, in accordance with the present invention, a monoterpene component may be used to enhance the overall bio-derived content of fuel formulations.
  • Camphene has been found to be particularly useful in fuel formulations, being capable of lowering DVPE and acting as an octane booster. It is apparent from Examples 1 to 6 that blends of camphene with a gasoline base fuel can have octane numbers, DVPEs and distillation properties within ranges which are acceptable for use in spark ignition (petrol) engines, and indeed which conform to current gasoline standards such as EN 228. Such blends can also benefit from enhanced lubricity.
  • a blend containing ethanol as well as camphene and base fuel can be tailored to have acceptable properties, as can a blend containing one or more additional bio-derived components or oxygenates with camphene, a gasoline base fuel and optionally ethanol.
  • camphene also has no negative impact on oxidative stability, whilst the MIHPT results indicate that camphene has a low tendency to form engine inlet valve deposits.

Claims (8)

  1. Utilisation, dans la gamme de 5 % V/V à 10 % V/V, rapporté au volume total, d'un constituant monoterpène qui comprend au moins 90 % en volume de camphène, dans une formulation de carburant essence dans le but d'améliorer ou maintenir l'indice d'octane recherche (RON) de la formulation de carburant.
  2. Utilisation selon la revendication 1, dans laquelle la formulation de carburant comprend un carburant à base d'essence et un constituant d'origine biologique ou oxygénat.
  3. Utilisation selon la revendication 2, dans laquelle le constituant d'origine biologique ou oxygénat est l'éthanol.
  4. Utilisation selon l'une quelconque des revendications 1 à 3, dans laquelle le camphène est utilisé dans la formulation de carburant pour obtenir : ΔRON > 0
    Figure imgb0031
    où ΔRON est la différence entre le RON de la formulation de carburant contenant du camphène et celui du carburant de base seul.
  5. Utilisation selon une quelconque revendication précédente, dans le but simultané d'améliorer ou maintenir le pouvoir lubrifiant de la formulation de carburant essence.
  6. Utilisation selon une quelconque revendication précédente, dans le but simultané d'améliorer ou maintenir la tendance à la formation de dépôts de la formulation de carburant essence.
  7. Utilisation selon une quelconque revendication précédente, dans le but simultané d'améliorer ou maintenir la compatibilité avec les élastomères de la formulation de carburant essence.
  8. Utilisation selon une quelconque revendication précédente, dans le but simultané de réduire la pression de vapeur de la formulation de carburant essence.
EP12707804.6A 2011-03-10 2012-03-12 Utilisation de camphène en carburants de type essence Not-in-force EP2683798B1 (fr)

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EP3205702A1 (fr) * 2016-02-11 2017-08-16 Bp Oil International Limited Compositions de carburant avec des additifs
EP3205703A1 (fr) 2016-02-11 2017-08-16 Bp Oil International Limited Additifs de carburant
EP3205701A1 (fr) 2016-02-11 2017-08-16 Bp Oil International Limited Composition de carburant
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IT1179351B (it) * 1980-07-07 1987-09-16 Mario Scifoni Miscela combustibile
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RU2105041C1 (ru) * 1993-08-31 1998-02-20 Александр Петрович Ильин Топливная композиция на основе моторного топлива
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