EP3158030A1

EP3158030A1 - Fischer tropsch derived diesel fuel formulation

Info

Publication number: EP3158030A1
Application number: EP15731033.5A
Authority: EP
Inventors: Richard Hugh Clark; Paul Anthony Stevenson; Ratchatapong BOONWATSAKUL
Original assignee: Shell Internationale Research Maatschappij BV
Current assignee: Shell Internationale Research Maatschappij BV
Priority date: 2014-06-18
Filing date: 2015-06-18
Publication date: 2017-04-26
Anticipated expiration: 2035-06-18
Also published as: WO2015193463A1; US20150368576A1; JP6719392B2; JP2017523269A; DK3158030T3; EP3158030B1

Abstract

Use of a species selected from: (i) detergents; (ii) mixtures containing both a lubricity improver and a conductivity improver; and (iii) combinations of (i) and (ii), in a diesel fuel formulation containing 10% v/v or more of paraffinic hydrocarbons and also an antioxidant, for the purpose of increasing the oxidative stability of the formulation and/or of reducing the concentration of an antioxidant which is present in the formulation. The formulation may comprise a Fischer-Tropsch derived diesel fuel component or mixture thereof.

Description

FISCHER TROPSCH DERIVED DIESEL FUEL FORMULATION

Field of the Invention

This invention relates to the use of certain compounds in diesel fuel formulations, and in diesel fuel additive compositions, for new purposes.

Background to the Invention

Hydrocarbon fuels are prone to degradation through oxidation, especially at high temperatures. This degradation manifests itself as changes in the colour and acidity of the fuel, and in extreme cases in the

formation of deposits, such as gums and particulates, which can cause operational problems in fuel storage and distribution systems and in engines and other systems in which the fuel is used. Stability of hydrocarbon fuels is a balance between the natural propensity of the hydrocarbon to oxidize versus the level of natural antioxidancy present. In the case of synthetic

paraffinic fuels, paraffin molecules are inherently highly stable towards oxidation, but there is a low level of natural antioxidant. Provided there are no factors to promote oxidation, such fuels have excellent stability.

Operating conditions in internal combustion engines and other fuel-consuming systems are becoming

increasingly severe, in particular the operating

temperatures and pressures to which the fuel is exposed. This means that oxidative stability will be more of an issue for fuel formulators in the future.

It is known to include antioxidant additives in fuel formulations to mitigate the above described problems. Many such additives are known and commercially available; examples include hindered phenols and aromatic amines. It can be desirable to improve the performance of such antioxidant additives, and/or to provide alternative antioxidant additives with comparable or ideally superior performance, so as in turn to improve the oxidative stability of vulnerable fuel formulations.

It may also be desirable to reduce the

concentrations of antioxidant additives in fuel

formulations. This may be driven by consumer preferences and/or by technical or economic considerations.

Reductions in additive concentrations can be achieved through improvements in additive performance, and/or through the provision of better-performing alternatives. Statements of the Invention

According to a first aspect of the present invention there is provided the use of a species selected from:

(i) detergents;

(ii) mixtures containing both a lubricity improver and a conductivity improver; and

(iii) combinations of (i) and (ii) ,

in a diesel fuel formulation containing synthetically- derived paraffinic hydrocarbons and also an antioxidant, for the purpose of increasing the oxidative stability of the formulation. The increase in stability may be measured relative to that achieved using the antioxidant alone (ie in the absence of species (i), (ii) or (iii)), at the same concentration.

It has surprisingly been found that when species

(i) , (ii) or (iii) is combined with an antioxidant, in a relatively high paraffin content diesel fuel formulation, the oxidative stability of the formulation is increased compared to that achieved using the antioxidant alone. This synergy appears possible even where the species (i) ,

(ii) or (iii) is not itself active as an antioxidant. Indeed, species (i), (ii) and (iii) would not be expected to contribute significant antioxidant activity to a fuel formulation .

The combination of species (i), (ii) or (iii) with an antioxidant, in a relatively high paraffin content diesel fuel formulation, also appears to lead to an overall antioxidant effect which is greater than might be predicted from the sums of the antioxidant effects of the relevant individual additive components. Thus, in accordance with the invention, species (i) , (ii) or (iii) may be used in the diesel fuel formulation for the purpose of increasing the oxidative stability of the formulation by an amount which is greater than the sum of the increases in oxidative stability caused by species (i) , (ii) or (iii) and the antioxidant individually.

In effect, therefore, species (i) , (ii) or (iii) may be used to increase the effectiveness of the antioxidant, and its presence may allow the use of a lower

concentration of the antioxidant than would otherwise have been necessary or desirable. Instead or in

addition, its presence may allow the use of an

alternative antioxidant, for example one which gives a smaller antioxidant effect than would otherwise have been necessary or desirable.

These effects can offer greater flexibility for the fuel formulator, in terms of types and concentrations of additives which can be used to achieve a desired level of oxidative stability in a diesel fuel formulation.

In the present context, an antioxidant is a

substance which is capable of reducing the rate of oxidation of a fuel formulation to which it is added, or of a component of such a formulation. It is therefore capable of increasing the oxidative stability of such a fuel formulation or component. Typically, antioxidants inhibit the oxidation of other molecules by removing free radical intermediates, a process which involves their own oxidation: they are therefore usually reducing agents.

According to the invention, an exemplary antioxidant may be selected from phenolic antioxidants, in particular hindered phenols such as butylated hydroxytoluene ;

quinones; hydroquinones ; amines, in particular aromatic amines; and mixtures thereof. It may be selected from phenolic antioxidants, in particular hindered phenols; amines, in particular aromatic amines; and mixtures thereof .

In an embodiment, the antioxidant is a phenolic antioxidant, in particular a hindered phenol. It may for example be selected from 2, 6-di-t-butyl-4-methylphenol

(also known as 2, 6-di-t-butyl-p-cresol, 3, 5-di-t-butyl-4- hydroxytoluene or butylated hydroxytoluene (BHT) ) ; 2,4- dimethyl-6-t-butylphenol ; 2 , 6-di-t-butylphenol ; and mixtures of t-butylphenols . The antioxidant may in particular be BHT.

Such phenolic antioxidants may in particular be used (a) when the diesel fuel formulation comprises a Fischer- Tropsch derived diesel fuel component (as described below) , a hydrogenated vegetable oil (HVO) , or a mixture thereof, and a detergent (i) is used to increase the oxidative stability of the formulation; (b) when the diesel fuel formulation comprises a Fischer-Tropsch derived diesel fuel component, or a combination of a HVO and a Fischer-Tropsch derived diesel fuel component, and a mixture (ii) is used to increase oxidative stability; or (c) when the diesel fuel formulation comprises a Fischer-Tropsch derived diesel fuel component, or a combination of a HVO and a Fischer-Tropsch derived diesel fuel component, and a combination (iii) is used to increase oxidative stability.

In an embodiment, the antioxidant is an amine. It may be an aromatic amine, in particular a phenylene diamine containing one or more alkyl and/or aryl groups.

It may for example be selected from N, ' -di-2-butyl-l , 4- phenylenediamine ; N-isopropyl- ' -phenyl-p-phenylene diamine; N- (1, 3-dimethyl butyl ) - ' -phenyl-p-phenylene diamine ; N- ( 1-methylheptyl ) - ' -phenyl-p-phenylene diamine; N-cyclohexyl- ' -phenyl-p-phenylene diamine;

N, ' -di-see-butyl-p-phenylene diamine; N, ' -diisopropyl- p-phenylene diamine; N, ' -diphenyl-p-phenylene diamine; N, ' -ditolyl-p-phenylene diamine; N-tolyl- ' -xylenyl-p- phenylene diamine; and mixtures thereof. In an

embodiment, it is N, ' -di-t-butyl-1, 4-phenylenediamine .

Such amine antioxidants may be used when a mixture (ii) or a combination (iii), more particularly a mixture (ii), is used to increase the oxidative stability of the fuel formulation. They may in particular be used when the fuel formulation comprises a Fischer-Tropsch derived diesel fuel component and/or a HVO, more particularly a Fischer-Tropsch derived diesel fuel component.

Such amine antioxidants may be used (a) when the diesel fuel formulation comprises a Fischer-Tropsch derived diesel fuel component or a combination of a

Fischer-Tropsch derived diesel fuel component and a HVO, and a detergent (i) is used to increase the oxidative stability of the formulation; (b) when the diesel fuel formulation comprises a Fischer-Tropsch derived diesel fuel component and/or a HVO and a mixture (ii) is used to increase oxidative stability; or (c) when the diesel fuel formulation comprises a HVO, or a combination of a HVO and a Fischer-Tropsch derived diesel fuel component, and a combination (iii) is used to increase oxidative stability .

In an embodiment, the antioxidant is selected from BHT; N, ' -di-t-butyl-1 , 4-phenylenediamine ; and mixtures thereof.

According to the invention, the diesel fuel

formulation may contain a mixture of two or more

antioxidants .

The antioxidant may for example be used in the diesel fuel formulation at an (active matter)

concentration of up to 1,000 ppmw or up to 750 or 500 ppmw. It may for example be used at a concentration of 10 ppmw or greater, or 50 or 100 or 200 or 250 ppmw or greater, for example from 10 to 1,000 ppmw or from 50 to 500 ppmw. It may be used at a concentration below its normal treat rate, due to the additional stabilising effect of the species (i) , (ii) or (iii) .

The diesel fuel formulation in which species (i) , (ii) or (iii) is used contains an antioxidant and also 10% v/v or more of paraffinic hydrocarbons. In other respects it may be any type of diesel fuel formulation, typically in liquid form, suitable and/or adapted for use as a combustible fuel in a compression ignition fuel- consuming system. It may be hydrocarbon-based, ie comprising a major proportion (for example 80% v/v or more, or 85 or 90 or 95% v/v or more) of hydrocarbon fuel components such as alkanes, cycloalkanes, alkenes and aromatic hydrocarbons. The hydrocarbon fuel components may be mineral-derived, or derived from a biological source, or synthetic. Such a formulation may contain one or more fuel components in addition to its hydrocarbon fuel components, for example selected from oxygenates and fuel additives. A diesel fuel formulation may be suitable and/or adapted for use in a diesel fuel-consuming system such as an engine (in particular an internal combustion engine) or a heating appliance. It may be selected from

automotive diesel fuel formulations, marine diesel fuel formulations, industrial gas oil formulations, and heating oil formulations. In an embodiment, it is an automotive diesel fuel formulation.

The diesel fuel formulation suitably comprises a diesel base fuel. A diesel base fuel may be any fuel component, or mixture thereof, which is suitable and/or adapted for combustion within a compression ignition fuel-consuming system. It may be a liquid hydrocarbon middle distillate fuel, for example, a gas oil. It may be petroleum-derived (ie mineral) . It may be or contain a kerosene fuel component . It may be or contain a synthetic fuel component, for instance a product of a Fischer-Tropsch condensation process as described below. It may be or contain a fuel component derived from a biological source. It may be or contain an oxygenate such as a fatty acid alkyl ester, in particular a fatty acid methyl ester (FAME) such as rapeseed methyl ester (RME) or palm oil methyl ester (POME) .

A diesel base fuel will typically boil in the range from 150 or 180 to 370°C (ASTM D86 or EN ISO 3405) . It will suitably have a measured cetane number (ASTM D613) of from 40 to 70 or from 40 to 65 or from 51 to 65 or 70.

A diesel fuel formulation prepared or used according to the invention may comprise a diesel base fuel at a concentration of 50% v/v or greater, or 60 or 70 or 80% v/v or greater, or 85 or 90 or 95 or 98% v/v or greater. The base fuel concentration may be up to 99.99% v/v, or up to 99.95% v/v, or up to 99.9 or 99.8 or 99.5% v/v. 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% v/v.

Where the diesel fuel formulation comprises an oxygenate and/or a biologically derived component such as a FAME, its concentration may be 1% v/v or greater, or 2 or 5% v/v or greater, based on the overall formulation, or in cases 7 or 10% v/v or greater. The FAME

concentration may be up to 30% v/v, or up to 25 or 20% v/v. Oxidative stability can be more of an issue in fuel formulations containing oxygenates, and the present invention may therefore be of particular use in such cases. The FAME concentration may be between 1 and 5% v/v, or between 5 and 10% v/v, or between 10 and 20% v/v.

A diesel fuel formulation prepared or used according to the invention will suitably comply with applicable current standard diesel fuel specification ( s ) such as for example EN 590 (for Europe) or ASTM D975 (for the USA) . By way of example, the overall formulation may have a density from 820 to 845 kg/m³ at 15°C (ASTM D4052 or EN ISO 3675); a T95 boiling point (ASTM D86 or EN ISO 3405) of 360°C or less; a measured cetane number (ASTM D613) of 40 or greater, ideally of 51 or greater; a kinematic viscosity at 40°C (VK40) (ASTM D445 or EN ISO 3104) from 2 to 4.5 centistokes (mm²/s); a flash point (ASTM D93 or EN ISO 2719) of 55°C or greater; a sulphur content (ASTM

D2622 or EN ISO 20846) of 50 mg/kg or less, preferably 10 mg/kg or less; a cloud point (IP 219) of less than -10°C; and/or a polycyclic aromatic hydrocarbons (PAH) content (EN 12916) of less than 8% w/w. Relevant specifications may however differ from country to country, from season to season and from year to year, and may depend on the intended use of the formulation. Moreover a formulation prepared or used according to the invention may contain individual fuel components with properties outside of these ranges .

A diesel fuel formulation prepared or used according to the invention may comprise, in addition to the antioxidant and species (i) , (ii) or (iii) , one or more fuel or refinery additives. Many such additives are known and commercially available and may be present in a base fuel, or may be added to the formulation at any point during its preparation. Non-limiting examples of additives which can be included in a diesel base fuel or diesel fuel formulation include cetane improvers, antistatic additives, lubricity additives, cold flow additives, detergents, and combinations thereof, as well as solvents, diluents and carriers therefor. Such additives may be included in the fuel formulation at a concentration of up to 4,000 ppmw (parts per million by weight), or up to 3,000 or 2,000 or 1,000 or 500 or 300 ppmw, for example from 50 to 4,000 ppmw or from 50 to 1,500 ppmw or from 50 to 1,000 ppmw or from 50 to 500 ppmw or from 50 to 300 ppmw.

In an embodiment of the invention, the diesel fuel formulation contains a Fischer-Tropsch derived diesel fuel component or mixture thereof. It may for instance contain 15% v/v or greater, or 25% v/v or greater, or 50% v/v or greater of a Fischer-Tropsch derived diesel fuel component or mixture thereof. It may contain up to 50% v/v of such a component or mixture, or up to 75% v/v, or up to 100% v/v. It may contain, for example, from 15 to 25% v/v, or from 25% to 50% v/v, or from 40 to 60% v/v, or from 50% to 75% v/v, or from 75% to 100% v/v of a

Fischer-Tropsch derived diesel fuel component or mixture thereof. In an embodiment, the diesel fuel formulation consists essentially of one or more Fischer-Tropsch derived diesel fuel components, ie in addition to the antioxidant, the species (i) , (ii) or (iii) and any optional diesel fuel additives, it contains only Fischer- Tropsch derived diesel fuel components.

By "Fischer-Tropsch derived diesel fuel component" is meant a hydrocarbon mixture that is, or derives from, a synthesis product of a Fischer- Tropsch condensation process. The Fischer-Tropsch reaction converts carbon monoxide and hydrogen into longer chain, usually

paraffinic, hydrocarbons:

n (CO + 2H₂) = (-CH₂-)_n + nH₂0 + heat, in the presence of an appropriate catalyst and typically at elevated temperatures (e.g., 125 to 300°C, preferably 175 to 250°C) and/or pressures (e.g., 5 to 100 bar, preferably 12 to 50 bar) . Ratios of hydrogen to carbon monoxide other than 2:1 may be employed if desired.

The carbon monoxide and hydrogen may themselves be derived from organic or inorganic, natural or synthetic sources, typically either from natural gas or from organically derived methane.

A middle distillate fuel product may be obtained directly from the Fischer-Tropsch reaction, or indirectly for instance by fractionation of a Fischer-Tropsch synthesis product or from a hydrotreated Fischer-Tropsch synthesis product. Hydrotreatment can involve

hydrocracking to adjust the boiling range of the product (see, e. g. GB2077289 and EP0147873) and/or

hydroisomerisation which can improve cold flow properties by increasing the proportion of branched paraffins.

EP0583836 describes a two-step hydrotreatment process in which a Fischer-Tropsch synthesis product is firstly subjected to hydroconversion under conditions such that it undergoes substantially no isomerisation or hydrocracking (this hydrogenates the olefinic and oxygen- containing components), and then at least part of the resultant product is hydroconverted under conditions such that hydrocracking and isomerisation occur to yield a substantially paraffinic hydrocarbon fuel. The desired middle distillate fuel fraction (s) may subsequently be isolated for instance by distillation.

Typical catalysts for the Fischer-Tropsch synthesis of paraffinic hydrocarbons comprise, as the catalytically active component, a Group VIII metal, in particular ruthenium, iron, cobalt or nickel. Suitable catalysts are described for instance in EP0583836.

An example of a Fischer-Tropsch based process is the SMDS (Shell Middle Distillate Synthesis) described in "The Shell Middle Distillate Synthesis Process", van der

Burgt et al (vide supra) . This process produces middle distillate range products by conversion of a natural gas (primarily methane) derived synthesis gas into a heavy long-chain hydrocarbon (paraffin) wax which can then be hydroconverted and fractionated to produce liquid transport fuels such as the gas oils useable in diesel fuel compositions. Versions of the SMDS process, utilising fixed-bed reactors for the catalytic conversion step, are currently in use in Bintulu, Malaysia, and in Pearl GTL, Ras Laffan, Qatar. Middle distillate fuels prepared by the SMDS process are commercially available for instance from the Royal Dutch/Shell Group of

Companies. Such Fischer-Tropsch middle distillate fuels are described in Technical Specification CEN TS 15940.

A Fischer-Tropsch derived diesel fuel component may suitably have a cetane number (ISO 5165) of 70 or greater; a density at 15°C (ISO 3675) of from 770 to 800 kg/m³; a sulphur content (ISO 14596) of 3.0 mg/kg or less; a total aromatics content (EN 12916) of 0.5% w/w or less; a polycyclic aromatics content (EN 12916) of 0.1% w/w or less; a total olefin content (ASTM D1159) of 0.1% w/w or less; a paraffin content of 97% w/w or more; a kinematic viscosity at 40°C (ISO 3104) of from 2.0 to 4.5 mm²/s; a flash point (EN 2719) of 68°C or greater; and/or a cold filter plugging point (EN 116) of -9°C or lower or (in particular for use in or as a winter grade fuel) of - 20°C or lower. Such a component may suitably have a distillation curve (ISO 3405) such that the recovery at

250°C is 65% v/v or less; the recovery at 350°C is 85% v/v or greater; and/or 95% v/v recovery is achieved at 360°C or less.

A diesel fuel formulation prepared or used according to the invention may comprise a mixture of (a) one or more Fischer-Tropsch derived diesel fuel components and (b) one or more other diesel fuel components, for example petroleum-derived, optionally with one or more diesel fuel additives. In such a mixture, the volume ratio of the Fischer-Tropsch derived diesel fuel component (s) to the other diesel fuel component (s) may for example be from 1:10 to 10:1; or from 1:5 to 5:1; or from 1:4 to 4:1; or from 1:3 to 3:1; or from 1:2 or 2:1. In an embodiment, the diesel fuel formulation comprises a 1:1 v/v mixture of (a) one or more Fischer-Tropsch derived diesel fuel components and (b) one or more other diesel fuel components, for example petroleum-derived diesel fuel components.

In an embodiment, the diesel fuel formulation contains 0.5% v/v or greater, or 1 or 5% v/v or greater, of non-Fischer-Tropsch paraffinic diesel components such as hydrotreated vegetable oils or fats or a mixture thereof (hereafter referred to as HVO) . HVO is also known as "Hydrogenation-Derived Renewable Diesel" (HDRD) and, in the context of the U.S. Renewable Fuel Standard, as "Non-ester renewable diesel" (ref. 40CFR Part 80:

Subpart M in the Code of Federal Regulations) . It may contain up to 75% v/v of such a component or mixture, or up to 50% v/v, for example from 0.5 to 75% v/v or from 5 to 75% v/v or from 5 to 50% v/v. In an embodiment, the diesel fuel formulation consists essentially of one or more hydrogenated vegetable oils, ie in addition to the antioxidant, the species (i) , (ii) or (iii) and any optional diesel fuel additives, it contains only HVO diesel fuel components.

In this context, the HVO component or mixture should be suitable and/or adapted for use as a diesel fuel component. Such products are commercially available, for example the NExBTL renewable diesel products ex Neste Oil . They may be used in the form of a blend containing two or more HVOs selected for example from soybean, palm, canola and rapeseed oils; animal tallow; vegetable oil waste and brown trap grease; and mixtures thereof.

The HVO component or mixture will, in certain embodiments, have a paraffin content of at least 97% by weight, a cetane number of at least 70, a density at 15°C of between 770 and 790 kg/m3, an aromatics content of not greater than 1% by weight, a polyaromatics content of not greater than 0.1% by weight, a sulfur content of not greater than 5 ppm, and a flash point of at least 59°C.

The diesel fuel formulation may comprise a mixture of (a) one or more HVO diesel fuel components and (b) one or more other diesel fuel components, for example petroleum-derived, optionally with one or more diesel fuel additives. In such a mixture, the volume ratio of the HVO diesel fuel component (s) to the other diesel fuel component (s) may for example be from 1:200 to 3:1, or from 1:20 to 2:1, or from 1:20 to 1:1, such as about 1:1. In an embodiment, the diesel fuel formulation comprises a 1:1 v/v mixture of (a) one or more HVO diesel fuel components and (b) one or more other diesel fuel

components, for example petroleum-derived diesel fuel components .

In an embodiment, the diesel fuel formulation comprises a mixture of (a) one or more Fischer-Tropsch derived diesel fuel components and (b) one or more HVO diesel fuel components, optionally with one or more diesel fuel additives. In such a mixture, the volume ratio of the Fischer-Tropsch derived diesel fuel

component (s) to the HVO diesel fuel component (s) may for example be from 1:10,000 to 10,000:1, or from 1:990 to

990:1, or from 1:99 to 99:1, or from 1:9 to 9:1, or from 1:5 to 5:1, or from 1:3 to 3:1, or from 1:2 to 2:1, such as about 1:1. In an embodiment, the diesel fuel

formulation comprises a 1:1 v/v mixture of (a) one or more Fischer-Tropsch derived diesel fuel components and

(b) one or more HVO diesel fuel components.

Thus in an embodiment of the invention, the diesel fuel formulation is selected from (1) a formulation consisting essentially of one or more Fischer-Tropsch derived diesel fuel components; (2) a formulation consisting essentially of one or more HVO diesel fuel components; (3) a mixture of one or more Fischer-Tropsch derived diesel fuel components and one or more HVO diesel fuel components; and (4) a mixture of one or more

Fischer-Tropsch derived diesel fuel components and one or more petroleum-derived diesel fuel components. It may be selected from (1) a formulation consisting essentially of one or more Fischer-Tropsch derived diesel fuel components; (2) a formulation consisting essentially of one or more HVO diesel fuel components; and (3) a mixture of one or more Fischer-Tropsch derived diesel fuel components and one or more HVO diesel fuel components.

Even in embodiments where the diesel fuel

formulation includes a mixture of two or more diesel fuel components, the overall formulation shall contain 10% v/v or more of paraffinic hydrocarbons. A paraffinic hydrocarbon is a saturated hydrocarbon (alkane) ; it may be a straight chain (normal) paraffin or a branched chain

(iso) paraffin. The diesel fuel formulation suitably comprises a mixture of normal and isoparaffins, since such mixtures can provide a suitable balance between low freezing point (isoparaffins ) and good ignition quality (normal paraffins) . Typically the weight ratio of isoparaffins to normal paraffins in a paraffinic

hydrocarbon mixture employed in a diesel fuel formulation will be from 0.5 to 10, preferably from 1 to 9. A paraffinic hydrocarbon will typically contain from 5 to 40 carbon atoms, for example from 9 to 30 carbon atoms.

In an embodiment of the invention, the diesel fuel formulation contains 20% v/v or more of paraffinic hydrocarbons. It may contain 30 or 40 or 50 or 60% v/v or more of paraffinic hydrocarbons. It may for example contain up to 99% v/v of paraffinic hydrocarbons, or up to 90 or 80 or 75% v/v, such as from 20 to 99% v/v or from 30 or 50 or 60 to 99% v/v. In an embodiment, it consists essentially of paraffinic hydrocarbons, ie it contains at least 99% v/v, or at least 99.5 or 99.8 or 99.9 or 99.95% v/v, of paraffinic hydrocarbons, together with relatively small concentrations of the antioxidant and other optional diesel fuel additives.

In certain cases, it may be preferred for the diesel fuel formulations that include the species (i) , (ii) or (iii) that such formulations do not to contain a

petroleum-derived fuel components, or to contain less than 50% v/v of such components, or less than 40 or 30 or 20% v/v, or that such formulations contain between 10 and

20% v/v, or between 20 and 30% v/v.

According to the invention, a species (i) , (ii) or (iii) may be used in the diesel fuel formulation to enhance its oxidative stability beyond what is achieved by the already-present antioxidant. Each of species (i) ,

(ii) and (iii) should be suitable and/or adapted for use as an additive in a diesel fuel formulation, in

particular an automotive diesel fuel formulation.

The species (i) is a detergent, by which is meant an agent (suitably a surfactant) which, when added to a fuel formulation, can act to remove, and/or to prevent the accumulation of, deposits such as combustion-related deposits within a fuel-consuming system in which the formulation is used, in particular within a fuel

injection system such as in or on the fuel injector nozzles. Many such materials are known and commercially available for use as diesel fuel additives.

Detergents suitable for use in fuel formulations include those disclosed in WO-A-2009/50287, which is incorporated herein by reference.

Suitable detergents typically have at least one hydrophobic hydrocarbon radical having a number average molecular weight (Mn) of from 85 to 20,000 and at least one polar moiety selected from:

(1) mono- or polyamino groups having up to 6 nitrogen atoms, of which at least one nitrogen atom has basic properties ;

(2) polyoxy-C2- to -C4-alkylene groups which are terminated by hydroxyl groups, mono- or polyamino groups, in which at least one nitrogen atom has basic properties, or by carbamate groups;

(3) moieties derived from succinic anhydride and having hydroxyl and/or amino and/or amido and/or imido groups; and/or;

(4) moieties obtained by Mannich reaction of substituted phenols with aldehydes and mono- or polyamines.

The hydrophobic hydrocarbon radical in the above detergents, which ensures adequate solubility in the base fluid, has a number average molecular weight (Mn) of from 85 to 20,000, especially from 113 to 10,000, in

particular from 300 to 5000. Typical hydrophobic hydrocarbon radicals, especially in conjunction with the polar moieties (1), (3) and (4), include polyalkenes

(polyolefins ) , such as polypropenyl, polybutenyl or polyisobutenyl radicals each having Mn of from 300 to 5000, or from 500 to 2500, or from 700 to 2300, such as from 700 to 1000.

Detergents comprising mono- or polyamino groups (1) may be polyalkenemono- or polyalkenepolyamines based on polypropene or conventional (ie having predominantly internal double bonds) polybutene or polyisobutene having Mn of from 300 to 5000.

Other suitable detergents comprising monoamino groups (1) are the hydrogenation products of the reaction products of polyisobutenes having an average degree of polymerisation of from 5 to 100, with nitrogen oxides or mixtures of nitrogen oxides and oxygen, as described in particular in WO-A-97/03946.

Additional suitable detergents comprising monoamino groups (1) are the compounds obtainable from

polyisobutene epoxides by reaction with amines and subsequent dehydration and reduction of the amino alcohols, as described in particular in DE-A-196 20 262.

Detergents comprising polyoxy-C2-to-C4-alkylene moieties (2) may be polyethers or polyetheramines which are obtainable by reaction of C2- to C60-alkanols, C6- to

C30-alkanediols, mono- or di-C2-to-C30-alkylamines, Cl- to-C30-alkylcyclohexanols or Cl-C30-alkylphenols with from 1 to 30 mol of ethylene oxide and/or propylene oxide and/or butylene oxide per hydroxyl group or amino group and, in the case of the polyether-amines, by subsequent reductive amination with ammonia, monoamines or

polyamines . Such products are described in particular in EP-A-310 875, EP-A-356 725, EP-A-700 985 and US Pat. No. 4,877,416. In the case of polyethers, such products also have carrier oil properties. Typical examples of these are tridecanol butoxylates, isotridecanol butoxylates, isononylphenol butoxylates and polyisobutenol butoxylates and propoxylates and also the corresponding reaction products with ammonia.

Detergents comprising moieties (3) derived from succinic anhydride and having hydroxyl and/or amino and/or amido and/or imido groups may be corresponding derivatives of polyisobutenylsuccinic anhydride which are obtainable by reacting conventional or highly reactive polyisobutene having Mn of from 300 to 5000 with maleic anhydride by a thermal route or via the chlorinated polyisobutene. Of particular interest are derivatives with aliphatic polyamines such as ethylenediamine, diethylenetriamine , triethylenetetramine or

tetraethylenepentamine . Such additives are described in particular in US Pat. No. 4,849,572.

Detergents comprising moieties (4) obtained by Mannich reaction of substituted phenols with aldehydes and mono- or polyamines may be reaction products of polyisobutene-substituted phenols with formaldehyde and mono- or polyamines such as ethylenediamine ,

diethylenetriamine , triethylenetetramine,

tetraethylenepentamine or dimethylaminopropylamine . The polyisobutenyl-substituted phenols may stem from

conventional or highly reactive polyisobutene having Mn of from 300 to 5000. Such "polyisobutene-Mannich bases" are described in particular in EP-A-831 141.

In an embodiment of the invention, a detergent (i) used in the diesel fuel formulation is a nitrogen- containing detergent, in particular an amine- or

polyamine-containing detergent. In an embodiment, such a detergent contains a hydrophobic hydrocarbon radical having a number average molecular weight in the range from 300 to 5000. The nitrogen-containing detergent may be selected from the group comprising polyalkene

monoamines, polyetheramines , polyalkene Mannich amines, polyalkene succinimides , and mixtures thereof.

Conveniently, the nitrogen-containing detergent may be a polyalkene monoamine. It may be a succinimide, in particular a polyalkene succinimide.

In an embodiment of the invention, the detergent (i) is a detergent of the type referred to as (1) above, for example a polyisobutenyl (PIB) succinimide.

According to the invention, a mixture of two or more detergents (i), for example of the types defined above, may be used in the diesel fuel formulation.

The detergent (i) may for example be used in the diesel fuel formulation at an (active matter)

concentration of up to 1,500 ppmw or up to 1,000 or 500 ppmw. It may for example be used at a concentration of 250 ppmw or greater, or 500 or 1,000 ppmw or greater, for example from 250 to 1,500 ppmw or from 250 to 1,000 ppmw.

According to the invention, a mixture (ii) of a lubricity improver and a conductivity improver may be used in the diesel fuel formulation to enhance its oxidative stability. By "lubricity improver" is meant an agent which is capable of improving the lubricity of a diesel fuel formulation to which it is added, and/or imparting anti-wear effects when such a formulation is used in an engine or other fuel-consuming system. Many such compounds are known and commercially available for use as diesel fuel additives, for example the "R" series of additives ex Infineum (trade mark) or the Hitec (trade mark) additives ex Afton.

Known lubricity improvers include acid-based, ester- based and amide-based agents. They can be available in the form of lubricity additives, which may contain one or more additional active ingredients as well as the lubricity improver, for example dehazers, anti-rust agents, conductivity improvers, and combinations thereof.

An acid-based lubricity improver comprises an acid, typically a mono-acid, more typically an organic acid, as a lubricity-enhancing active ingredient. The acid may for example be a carboxylic acid, such as a fatty acid or aromatic acid, in particular the former. Such fatty acids may be saturated or unsaturated (which includes polyunsaturated) . They may contain from 1 or 2 to 30 carbon atoms, or from 10 to 22 carbon atoms, or from 12 to 22 or from 14 to 20 carbon atoms, or from 16 to 20 or 16 to 18 carbon atoms, such as 18 carbon atoms. Examples include oleic acid, linoleic acid, linolenic acid, linolic acid, stearic acid, palmitic acid and myristic acid. Of these, oleic, linoleic and linolenic acids may be used, in particular oleic and linoleic acids. Examples of acid-based lubricity additives are known and commercially available, for example as R650 (trade mark) , ex Infineum; products in the Lz 539 (trade mark) series, ex Lubrizol; and ADX4101B™ (ex Adibis) .

An ester-based lubricity improver comprises, as a lubricity-enhancing active ingredient, an ester such as a carboxylic acid ester, in particular an ester of a fatty acid. Such fatty acids may be as described above in connection with acid-based lubricity improvers. Ester- based lubricity improvers may alternatively be based on ester-functionalised oligomers or polymers (eg olefin oligomers) . Such esters may be mono-alcohol esters such as methyl esters, or more suitably may be polyol esters such as glycerol esters. In an embodiment of the invention, an ester-based lubricity improver contains a mono-, di- or tri-glyceride of a fatty acid, or a mixture of two or more such species.

An amide-based lubricity improver may for example comprise, as a lubricity-enhancing active ingredient, a fatty acid amide. The fatty acid element of such an ingredient may be as described above in connection with acid-based lubricity improvers. The ingredient may for example be a fatty acid amide of a mono- or in particular di-alkanolamine such as diethanolamine .

Other suitable lubricity improvers are described for example in:

• the paper by Danping Wei and HA Spikes, "The

Lubricity of Diesel Fuels", Wear, III (1986) 217-235;

• WO-A-95/33805 - cold flow improvers to enhance lubricity of low sulphur fuels;

• WO-A-94/17160 - certain esters of a carboxylic acid and an alcohol wherein the acid has from 2 to 50 carbon atoms and the alcohol has 1 or more carbon atoms, particularly glycerol monooleate and di-isodecyl adipate, as fuel additives for wear reduction in a diesel engine injection system;

• US Pat. No. 5,490,864 - certain dithiophosphoric diester-dialcohols as anti-wear lubricity additives for low sulphur diesel fuels; and

• WO-A-98/01516 - certain alkyl aromatic compounds having at least one carboxyl group attached to their aromatic nuclei, to confer anti-wear lubricity effects particularly in low sulphur diesel fuels.

In an embodiment of the invention, the lubricity improver used in the mixture (ii) is an ester-based lubricity improver. In an embodiment, it is used in the form of the lubricity-enhancing additive R662 (trade mark) , ex Infineum, which is described by the supplier as a combination of ester chemistry lubricity improver and conductivity additives .

According to the invention, a mixture of two or more lubricity improvers, for example of the types defined above, may be used in the diesel fuel formulation.

The lubricity improver may for example be used in the diesel fuel formulation at a concentration of up to 1,000 ppmw or up to 750 or 500 ppmw. It may for example be used at a concentration of 50 ppmw or greater, or 100 or 150 or 250 ppmw or greater, for example from 50 to

1,000 ppmw or from 50 to 500 ppmw.

By "conductivity improver" is meant an agent which is capable of increasing the electrical conductivity of a diesel fuel formulation to which it is added. Also referred to as "static dissipaters" or "antistatic additives", they reduce the risk of electrostatic charge accumulation, which can occur for example during pumping of a fuel and can increase fire and explosion hazards during subsequent fuel handling.

Fuels with an inherently lower conductivity

generally require higher levels of conductivity

improvers. Low conductivity fuels include in particular those which are low in polar fuel components such as aromatics and sulphur- or nitrogen-containing compounds : Fischer-Tropsch derived fuels can fall into this

category. As pressure to reduce sulphur levels in fuels, in particular automotive fuels, increases, this in turn increases the need for conductivity improvers.

A conductivity improver may for example comprise an active ingredient selected from organic acids, in particular (benzene ) sulphonic acids; amines, in

particular polyamines; sulphones, in particular

polysulphones ; and other hydrocarbon-soluble (co) polymers such as vinyl (co) polymers, in particular those

containing cationic monomer units .

Examples of conductivity improvers include those having components selected from aliphatic amines- fluorinated polyolefins (US 3,652,238); chromium salts and amine phosphates (US 3,758,283); alpha-olefin- sulphone copolymer clas s—polysulphone and quaternary ammonium salt (US 3,811,848); polysulphone and quaternary ammonium salt amine/epichlorhydrin adducts;

dinonylnaphthylsulphonic acid (US 3,917,466); copolymers of alkyl vinyl monomers and cationic vinyl monomers (US 5,672,183); alpha-olefin-maleic anhydride copolymer class (US 3,677,725 and US 4,416,668); methyl vinyl ether- maleic anhydride copolymers and amines (US 3,578,421); alpha-olefin-acrylonitriles (US 4,333,741 and US

4,388,452); alpha-olefin-acrylonitrile copolymers and polymeric polyamines (US 4,259,087); copolymers of an alkylvinyl monomer, a cationic vinyl monomer and a polysulphone (US 6,391,070); ethoxylated quaternary ammonium compounds (US 5,863,466); hydrocarbyl monoamines or hydrocarbyl-substituted poly (alkyleneamine (US

6,793,695); acrylic-type ester-acrylonitrile copolymers and polymeric polyamines (US 4,537,601 and US 4,491,651); and diamine succinamides reacted with adducts of a ketone and S0₂ (β-sutlone chemistry) (US 4,252,542).

Commercially available static dissipaters, for use as fuel additives, include Stadis (trade mark) 450 and Stadis 425 (both ex Innospec) , Tolad (trade mark) 3514

(ex Baker-Petrolite) and HiTEC (trade mark) 4545 (ex Afton Chemical) . Stadis 450 for example contains dinonylnaphthyl sulphonic acid as an active ingredient; it is typically used in distillate fuels, solvents, commercial jet fuels and certain military fuels. Stadis

425 contains similar active (s) to Stadis 450 and is typically used in distillate fuels and solvents. Tolad 3514 contains a hydrocarbon-soluble copolymer of an alkylvinyl monomer and a cationic vinyl monomer.

A conductivity improver may be included in a diesel fuel additive package in combination with one or more additional active ingredients, such as a lubricity improver .

In an embodiment of the invention, the conductivity improver used in the mixture (ii) is a sulphonic acid, in particular a naphthyl sulphonic acid, more particularly an alkylnaphthyl sulphonic acid such as dinonylnaphthyl sulphonic acid. In an embodiment, it is used in the form of the combined lubricity-enhancing and conductivity- improving additive R662 (trade mark) , ex Infineum.

According to the invention, a mixture of two or more conductivity improvers, for example of the types defined above, may be used in the diesel fuel formulation. The conductivity improver may for example be used in the diesel fuel formulation at a concentration of up to 10 ppmw or up to 5 or 3 or 2 or 1 ppmw . It may for example be used at a concentration of 0.1 ppmw or greater, or 0.5 ppmw or greater, for example from 0.1 to

5 ppmw or from 0.1 to 3 ppmw.

Where a mixture (ii) of a lubricity improver and a conductivity improver is used in the present invention, the two components may be added to the diesel fuel formulation together (for example as part of a multi^¬ functional additive package) or separately. In an embodiment, they are added together. They may be added in the form of an additive composition which contains one or more other fuel additives in addition to the lubricity improver and the conductivity improver.

In an embodiment, the mixture (ii) is a mixture of an ester-based lubricity improver and a sulphonic acid (in particular a naphthyl sulphonic acid) conductivity improver. In particular, it may be the commercially available combined lubricity-enhancing and conductivity- improving additive R662.

Other products which contain mixtures of lubricity improvers and conductivity improvers, and which can therefore be used as the component (ii) in accordance with the present invention, include the PC 32xx (trade mark) range available from Total Group; the OLI-9101.X (trade mark) range from Innospec; and HiTec 4898AS (trade mark) from Afton Chemical.

In the mixture (ii) , the weight ratio of the lubricity improver to the conductivity improver may for example be up to 2,500, or up to 1,000, or up to 500 or 250. The ratio may for example be 20 or greater, or 50 or 75 or 100 or greater, such as from 100 to 250. In accordance with the invention, a combination (iii) of a detergent (i) and a lubricity improver/conductivity improver mixture (ii) may be used to enhance the

oxidative stability of the diesel fuel formulation. In the combination (iii) , the natures of the species (i) and

(ii) may be as described above. Moreover, the species (i) and (ii) may be used in the diesel fuel formulation at concentrations as described above. However, due to their combined effect on antioxidant activity, it may be possible to use a lower concentration of either or both of the individual species (i) and (ii) .

Where species (iii) is used in the present

invention, the two component species (i) and (ii) may be added to the diesel fuel formulation together (such as part of a multi-functional additive package) or

separately. In an embodiment, they are added together.

In a combination (iii) , the weight ratio of the detergent (i) to the mixture (ii) may for example be from 0.5:1 to 10:1, or from 0.5:1 to 2:1, or from 2:1 to 4:1, or from 4:1 to 6:1, or from 6:1 to 8:1, or from 8:1 to

10:1. The ratio may for example be 0.5:1 or greater, or 1:1 or greater, or 2:1 or greater. The ratio may for example be 10:1 or less, 5:1 or less, 2:1 or less.

In an embodiment of the invention, a detergent (i) is used to increase the oxidative stability of the diesel fuel formulation. In an embodiment, a mixture (ii) of a lubricity improver and a conductivity improver is used to increase the oxidative stability of the diesel fuel formulation. In an embodiment, a combination (iii) of a detergent (i) and a mixture (ii) of a lubricity improver and a conductivity improver is used to increase the oxidative stability of the diesel fuel formulation.

In embodiments of the invention, the weight ratio, in the diesel fuel formulation, of the antioxidant to the species (i) , (ii) or (iii) may for example be up to 0.02, or up to 0.1, or up to 0.4, or up to 0.6, or up to 0.8 or up to 1. The ratio may for example be less than 1, or less than 0.8, or less than 0.6, or less than 0.4, or less than 0.2, or less than 0.1, or less than 0.05. In certain embodiments, the ratio may be between 0.02 and 1, alternatively between 0.02 and 0.1, or between 0.1 and 0.2, or between 0.2 and 0.4, or between 0.4 and 0.6, or between 0.6 and 0.8, or between 0.8 and 1.

According to the present invention, the species (i) , (ii) or (iii) may be used to achieve any degree of improvement in the oxidative stability of the diesel fuel formulation, and/or to achieve or exceed a desired target level of oxidative stability.

Oxidative stability may be determined using any suitable method, for instance ASTM D7545-09 "Standard test method for oxidation stability of middle distillate fuels: Rapid small-scale oxidation test (RSSOT)", as in the examples below. Another suitable test method is EN

16091:2011 "Liquid petroleum products - Middle

distillates and fatty acid methyl ester (FAME) fuels and blends - Determination of oxidation stability by rapid small scale oxidation method", available from the

European Committee for Standardisation (CEN) , which involves subjecting a test fuel to accelerated oxidation conditions, and measuring the induction period to breakpoint in a pressure bomb apparatus, to provide a measure of the oxidation stability of the fuel. As for ASTM D7545-09, a longer measured induction period indicates that a more oxidation resistant test fuel.

Another potentially suitable test method is the standard test method ASTM D2274-03, which measures residues of oxidation products generated in a test fuel under specified conditions, a lower residue indicating a higher oxidative stability. D2274-03 is equivalent to IP 388 (Energy Institute, London) and EN ISO 12205:1996 (CEN) .

In general terms, the oxidative stability of a fuel formulation may be assessed with reference to the generation of an oxidation product, such as a carboxylic acid or peroxide, in the formulation. For a fuel formulation containing a biodiesel component such as a FAME, for example, CEN Test Method EN 15751:2009 "Fatty acid methyl ester (FAME) fuel and blends with diesel fuel - Determination of oxidation stability by accelerated oxidation method" (also known as a "Modified Rancimat" test method) may be used to assess oxidative stability.

The invention may additionally or alternatively be used to adjust any property of the diesel fuel

formulation which is equivalent to or associated with oxidative stability. For example, improved oxidative stability may be associated with reduced deposit

formation, with improved combustion and energy efficiency for a system running on the fuel formulation, with improved storage stability and/or with overall better retention of fuel properties .

In accordance with the invention, species (i), (ii) or (iii) may be added to the diesel fuel formulation at any suitable time and location. It may be premixed with the antioxidant and the resultant premix then added to the fuel formulation, or alternatively species (i) , (ii) or (iii) may be added separately, to a diesel fuel formulation which already contains, and/or is

subsequently to be mixed with, an antioxidant. A premixed additive composition comprising species (i), (ii) or (iii) and an antioxidant may constitute an essential element for the carrying out of the present invention. Such an additive composition may comprise one or more appropriate solvents or carriers, as described below in connection with the second aspect of the invention. It may contain one or more additional diesel fuel additives.

According to a second aspect, the present invention provides the use of a species selected from (i) , (ii) and (iii) as defined above, in a diesel fuel additive composition containing an antioxidant, for the purpose of increasing the antioxidant activity of the composition.

A diesel fuel additive composition is a composition which contains a diesel fuel additive and which is suitable and/or adapted and/or intended, in particular suitable and/or adapted, for use in a diesel fuel formulation, for instance a diesel fuel formulation of the type described above in connection with the first aspect of the invention. In particular, a diesel fuel additive composition prepared or used according to the second aspect of the invention may be suitable and/or adapted and/or intended, in particular suitable and/or adapted, for use in a diesel fuel formulation containing 10% v/v or more of paraffinic hydrocarbons.

An increase in the antioxidant activity of the additive composition means that the composition causes a greater increase in the oxidative stability of a diesel fuel formulation to which it is added. The increase may be measured relative to that achieved using the

antioxidant alone (ie in the absence of species (i) , (ii) or (iii)), at the same concentration.

An additive composition prepared or used according to the second aspect of the invention may comprise a solvent or other carrier, or mixture thereof, for the additives present in it. Suitable such solvents are well known and commercially available. They may in particular be liquid carriers . They may conveniently be of low polarity, and/or hydrophobic, and/or non-aqueous, to render them suitable for use in diesel fuel formulations.

Commonly used additive solvents include hydrocarbon solvents such as alkanes, alkenes and aromatic

hydrocarbons; mixtures of hydrocarbons such as in distillate fractions; and more polar solvents such as alcohols and ethers. The nature of the carrier or carrier mixture used in the additive composition (in particular its polarity) may be chosen to suit the natures and polarities of the additives present, as well as of a diesel fuel formulation in which the additive composition is to be used, so as to optimise the

stability and efficacy of the composition during use.

A detergent (i) may be used in the additive

composition at a concentration sufficient to provide a level of detergent in the finished fuel of 100 ppmw or greater, or 250 ppmw or greater, or 500 ppmw or greater, or 1000 ppmw or greater. It may be used at a

concentration of up to 250 ppmw, or up to 500 ppmw, or up to 1000 ppmw, or up to 2000 ppmw, for example from 100 to 2000 ppmw, or between 100 and 250 ppmw, or between 250 and 500 ppmw, or between 500 and 1000 ppmw, or between

1000 and 2000 ppmw.

A mixture (ii) of a lubricity improver and a conductivity improver may be used in the additive composition at a concentration sufficient to provide a level of (ii) in the finished fuel of 25 ppmw or greater, or of 50 ppmw or greater, or 100 ppmw or greater, or 200 ppmw or greater, or 300 ppmw or greater. It may be used at a concentration of up to 50 ppmw, or up to 100 ppmw, or up to 200 ppmw, or up to 300 ppmw, or up to 500 ppmw, for example from 25 to 500 ppmw, or from 25-100 ppmw, or from 100 to 200 ppmw, or from 200 to 300 ppmw, or from 300 to 500 ppmw.

Where a combination (iii) is used in the additive composition, the concentrations of its component species

(i) and (ii) may be as just described. However, due to their combined effect on antioxidant activity, it may be possible to use a lower concentration of either or both of the individual species (i) and (ii) .

The antioxidant may be used in the additive

composition at a concentration sufficient to provide a level in the finished fuel of 20 ppmw or greater, or 50 ppmw or greater, or 100 ppmw or greater, or 250 ppmw or greater. It may be used at a concentration of up to 50 ppmw, or up to 100 ppmw, or up to 250 ppmw, or up to 500 ppmw, for example from 10 to 500 ppmw, or from 20 to 250 ppmw, or from 20 to 100 ppmw.

An additive composition prepared or used according to the second aspect of the invention may for example be included in a diesel fuel formulation at a concentration of 100 ppmw or greater, or 250 ppmw or greater, or 500 ppmw or greater, or 750 ppmw or greater, or 1000 ppmw or greater. Its concentration may for example be up to 250 ppmw, or up to 500 ppmw, or up to 750 ppmw, or up to 1000 ppmw, or up to 2000 ppmw, such as from 100 to 2000 ppmw, or from 500 to 1000 ppmw, or from 750 to 1250 ppmw, or from 1000 to 2000 ppmw.

Other preferred features of the second aspect of the invention, for example the natures of the species (i) ,

(ii) and (iii) and the antioxidant; the purpose (s) for which, and the concentrations at which, these additives are used; and the nature of the diesel fuel formulation in which they are suitable to be used, may be as

described above in connection with the first aspect of the invention.

According to a third aspect, the invention provides a method for preparing a diesel fuel formulation, the method comprising (a) providing a diesel fuel component (for example a diesel base fuel) or mixture thereof, which contains 10% v/v or greater of paraffinic

hydrocarbons and also an antioxidant; (b) optionally assessing the oxidative stability of the component or mixture; (c) adding to the component or mixture species

(i) , (ii) or (iii) as defined above, and (d) assessing the oxidative stability of the resultant formulation. Step (d) may be carried out in order to assess the effect of species (i), (ii) or (iii) on the oxidative stability of the diesel fuel formulation and/or on the activity of the antioxidant.

In an embodiment of the third aspect of the

invention, species (i) , (ii) or (iii) is added to the diesel fuel component, or mixture thereof, in the form of an additive composition prepared according to the second aspect. One or more additional diesel fuel additives may also be added to the fuel component or mixture, either with or separately to species (i) , (ii) or (iii) .

Preferred features of the antioxidant, of species (i) ,

(ii) or (iii) and of the diesel fuel component (s) and additive (s) with which they are mixed, may be as

described above in connection with the first and second aspects of the invention, as may the ways in which oxidative stability is assessed.

Because species (i) , (ii) or (iii) can act to improve the activity of an antioxidant present in a diesel fuel formulation containing 10% v/v or greater of paraffinic hydrocarbons, it can make possible the use of lower concentrations of the, or other, antioxidant additives in the formulation or in an additive

composition for use in the formulation, without or without undue reduction in the oxidative stability of the formulation. This can in turn reduce the cost and complexity of preparing the formulation or composition, and/or can provide greater versatility in diesel fuel or additive formulation practices.

Thus, according to a fourth aspect, the invention provides the use of species (i) , (ii) or (iii) as defined above, in a diesel fuel additive composition or in a diesel fuel formulation containing 10% v/v of paraffinic hydrocarbons, in combination with an antioxidant, for the purpose of reducing the concentration of the or an antioxidant present in the composition or formulation.

In the context of the fourth aspect of the

invention, the term "reducing" embraces any degree of reduction, including reduction to zero. The reduction may for instance be 10% or more of the original

concentration of the antioxidant, or 25 or 50 or 75 or 90% or more. The reduction may for instance be 2 ppmw or more, or 5 or 10 ppmw or more, or in cases 25 or 50 or 75 ppmw or more. The reduction may be as compared to the concentration of the antioxidant which would otherwise have been incorporated into the composition or

formulation in order to achieve the properties and performance required and/or desired of it in the context of its intended use. This may be the concentration of the antioxidant which was present in the composition or formulation prior to the realisation that species (i) , (ii) or (iii) could be used in the way provided by the present invention, and/or which was present in an otherwise analogous additive composition or diesel fuel formulation which was intended (eg marketed) for use in an analogous context, prior to adding species (i), (ii) or (iii) to it in accordance with the invention.

The reduction in concentration of the antioxidant may be as compared to the concentration of the

antioxidant which would be predicted to be necessary to achieve a desired property or performance (for instance a desired level of oxidative stability) for the composition or formulation in the absence of species (i), (ii) or

(iii) . It may be as compared to the "standard treat rate" of the antioxidant in the relevant type of diesel fuel formulation.

In accordance with a fifth aspect of the invention, there is provided a method of operating a diesel fuel- consuming system, and/or apparatus (for example a vehicle, or a heating appliance) which is driven by such a system, the method comprising introducing into the system a diesel fuel formulation prepared according to the first, third or fourth aspect of the invention, or an additive composition prepared according to the second or the fourth aspect. This method may comprise introducing the formulation or the additive composition into a combustion chamber of a fuel-consuming system. The system may for example be an internal combustion engine.

A method according to the fifth aspect of the invention may be carried out with the intention of increasing the oxidative stability of the diesel fuel formulation, or of a diesel fuel formulation containing the additive composition, following its introduction into the diesel fuel-consuming system.

In the context of the present invention, "use" of species (i) , (ii) or (iii) as defined above in a diesel fuel formulation means incorporating the relevant species into the formulation, typically as a blend (ie a physical mixture) with one or more diesel fuel components, for example diesel base fuels, and optionally in combination with one or more additional diesel fuel additives.

Species (i) , (ii) or (iii) will conveniently, although not necessarily, be incorporated before the formulation is introduced into a fuel-consuming system. Instead or in addition, the use of species (i) , (ii) or (iii) may involve running a diesel fuel-consuming system on a diesel fuel formulation containing the relevant species, typically by introducing the formulation into a combustion region of the system. It may involve running a vehicle or other apparatus which is driven by a diesel fuel-consuming system, on a diesel fuel formulation containing the relevant species.

"Use" of species (i), (ii) or (iii) in the ways described above may also embrace supplying the relevant species together with instructions for its use in a diesel fuel formulation for one or more of the purposes described above in connection with the first to the fifth aspects of the invention. The species (i) , (ii) or (iii) may itself be supplied as part of a composition which is suitable and/or adapted for use as a diesel fuel

additive, in particular an additive composition prepared according to the second aspect of the invention. In this case, species (i) , (ii) or (iii) may be included in such a composition for any one or more of the purposes described above in connection with the first to the fifth aspects of the invention.

Thus species (i) , (ii) or (iii) may be used, in a diesel fuel formulation, in the form of an additive composition which has been prepared according to the second aspect of the invention, ie in which species (i) ,

(ii) or (iii) is used to enhance the activity of an antioxidant additive. "Use" of species (i) , (ii) or

(iii) may therefore comprise use of such an additive composition.

"Use" of species (i), (ii) or (iii) in an additive composition means incorporating the relevant species into the composition, typically as a blend (ie a physical mixture) with one or more solvent carriers and optionally in combination with one or more additional diesel fuel additives. Species (i) , (ii) or (iii) will conveniently, although not necessarily, be incorporated before the composition is introduced into a diesel fuel formulation or into a diesel fuel-consuming system. Instead or in addition, the use of species (i) , (ii) or (iii) may involve running a diesel fuel-consuming system on a diesel fuel formulation containing the relevant species in the additive composition, typically by introducing the formulation into a combustion region of the system. It may involve running a vehicle or other apparatus which is driven by a diesel fuel-consuming system, on a diesel fuel formulation containing species (i), (ii) or (iii) in the additive composition.

"Use" of species (i), (ii) or (iii) in the ways described above may also embrace supplying the relevant species together with instructions for its use in an additive composition for one or more of the purposes described above in connection with the first to the fifth aspects of the invention.

In general, references to "adding" a component to, or "incorporating" a component in, an additive

composition or a diesel fuel formulation may be taken to embrace addition or incorporation at any point during the production of the composition or formulation or at any time prior to its use.

In certain embodiments, the present invention may be used to produce at least 1,000 litres of an additive composition or diesel fuel formulation containing a species (i) , (ii) or (iii) , or at least 5,000 or 10,000 or 20,000 or 50,000 litres.

A diesel fuel formulation which is prepared or used according to the invention may be marketed with an indication that it benefits from an improvement due to the inclusion of species (i) , (ii) or (iii), for example increased oxidative stability and/or a lower

concentration of an antioxidant in the formulation. The marketing of such a formulation may comprise an activity selected from: (a) providing the formulation in a container that comprises the relevant indication; (b) supplying the formulation with product literature that comprises the indication; (c) providing the indication in a publication or sign (for example at the point of sale) that describes the formulation; and (d) providing the indication in a commercial which is aired for instance on the radio, television or internet. The improvement may be attributed, in such an indication, at least partly to the presence of species (i) , (ii) or (iii) . The

invention may involve assessing the relevant property of the formulation during or after its preparation. It may involve assessing the relevant property both before and after incorporation of species (i), (ii) or (iii), for example so as to confirm that the species contributes to the relevant improvement in the formulation.

A diesel fuel additive composition prepared or used according to the invention may be marketed with an indication that it benefits from an improvement due to the inclusion of species (i) , (ii) or (iii) , for example increased oxidative stability in a diesel fuel

formulation in which the composition is used, and/or a lower concentration of an antioxidant in the composition. The marketing of such a composition may comprise an activity selected from: (a) providing the composition in a container that comprises the relevant indication; (b) supplying the composition with product literature that comprises the indication; (c) providing the indication in a publication or sign (for example at the point of sale) that describes the composition; and (d) providing the indication in a commercial which is aired for instance on the radio, television or internet. The improvement may be attributed, in such an indication, at least partly to the presence of species (i) , (ii) or (iii) . The

invention may involve assessing the relevant property of the composition during or after its preparation. It may involve assessing the relevant property both before and after incorporation of the species (i) , (ii) or (iii), for example so as to confirm that the species contributes to the relevant improvement in the composition.

According to a sixth aspect, the present invention can provide the use of a species selected from:

(i) detergents;

(iii) combinations of (i) and (ii) ,

in a diesel fuel formulation containing an antioxidant, for the purpose of increasing the oxidative stability of the formulation. In other words, in certain cases the invention can have use in diesel fuel formulations having paraffinic hydrocarbon contents of less than 10% v/v.

Throughout the description and claims of this specification, the words "comprise", "include" and

"contain" and variations of these words, for example "comprising" and "comprises", mean "including but not limited to", and do not exclude other moieties,

additives, components, integers or steps. Moreover the singular encompasses the plural unless the context otherwise requires : in particular, where the indefinite article is used, the specification is to be understood as contemplating plurality as well as singularity, unless the context requires otherwise.

Preferred features of each aspect of the invention may be as described in connection with any of the other aspects. Other features of the invention will become apparent from the following examples. Generally, the invention extends to any novel one, or any novel

combination, of the features disclosed in this

specification (including any accompanying claims and drawings). Thus features, integers, characteristics, compounds, chemical moieties or groups described in conjunction with a particular aspect, embodiment or example of the invention are to be understood to be applicable to any other aspect, embodiment or example described herein unless incompatible therewith. For example, for the avoidance of doubt, optional and preferred features (including concentrations) of the antioxidant, the species (i) to (iii) , any additional additive (s) and the diesel fuel formulation can apply to all aspects of the invention in which the antioxidant, the species (i) , (ii) or (iii) , the additional

additive (s) or the fuel formulation are mentioned.

Unless stated otherwise, any feature disclosed herein may be replaced by an alternative feature serving the same or a similar purpose. Where upper and lower limits are quoted for a property, for example, concentration of an additive or fuel component, then a range of values defined by a combination of any of the upper limits with any of the lower limits may also be implied.

In this specification, references to physical properties such as antioxidant, detergent, lubricity improver, conductivity improver, additive, fuel and fuel component properties are, unless stated otherwise, to properties measured under ambient conditions, ie at atmospheric pressure and at a temperature from 16 to 22 or 25°C, or from 18 to 22 or 25°C, for example about 20°C.

The present invention will now be further described with reference to the following non-limiting examples.

General

Fuel formulations were prepared, in accordance with the invention, by incorporating antioxidants into diesel base fuels, together with (i) a detergent, (ii) a mixture of a lubricity improver and a conductivity improver, and

(iii) a combination of (i) and (ii) . For comparison purposes, further formulations were prepared by

incorporating antioxidants into the base fuels in the absence of the components (i) to (iii) .

The oxidative stability of each fuel formulation was assessed using the standard test method ASTM D7545-09 and a Petrospec (trade mark) "PetroOxy" test apparatus. A 5 ml sample of the test formulation was introduced into a pressure chamber which was then charged with oxygen at 700 kPa and ambient temperature. The test was initiated by switching on a heater and heating the chamber to 140°C. The pressure inside the chamber was recorded continuously until a breakpoint was reached, this being the point at which the pressure had fallen by 10% from the maximum pressure attained in the chamber. The

"induction period" was defined as the time between the start of the test and the breakpoint. This provided an indication of the resistance of the test formulation to oxidation .

In the event that no breakpoint was reached within a specified time period T, the result was recorded as "greater than T" .

Induction periods recorded in these examples are averages of two measurements .

Two antioxidants were used in the tests, designated AOl and A02. AOl was butylated hydroxytoluene (BHT) , obtained as Baynox (trade mark), a 20 g/1 solution in biodiesel, ex Lanxess. BHT is employed in fuel

formulations to reduce autoxidation rates by reacting with peroxy radicals, converting them to more stable hydroperoxides and non-radical products, thereby

terminating the chain reactions that might otherwise occur. It is typically used in distillate fuels at treat rates from 10 to 200 ppmw; in these tests it was included at a concentration of 100 ppmw.

A02 was N, ' -di-2-butyl-l , 4 -phenylenediamine, available from Octel Starreon (trade mark) as AO-22. It was included in the formulations at a concentration of 20 ppmw .

Other additives used in the tests were as follows. Neither was expected to cause a large, if any, increase in oxidative stability of a fuel to which it was added.

Dl - a multi-functional diesel performance additive package suitable for use in automotive diesel fuels, ex Innospec (trade mark) . This contained as its main

(detergent) active ingredient a polyisobutenyl (PIB) succinimide of a polyamme . It also contained minor amounts of other fuel additives, including a silicone antifoaming agent and a dehazer. It was used in the test formulations at a treat rate of 500 ppmw.

LCI - a commercially available performance additive package suitable for use in automotive distillate fuels, ex Infineum (trade mark) . This contained both a fatty ester-based lubricity improver and a conductivity improver. It was used at a treat rate of 250 ppmw.

Example 1 - Base Fuel 1

This example used a Fischer-Tropsch derived diesel base fuel BFl. This was a paraffinic gas oil made from natural gas via a Fischer-Tropsch synthesis, sourced from Qatar Shell GTL . It was free of additives, such as detergents, lubricity improvers and conductivity

improvers. Its properties are summarised in Table 1 below .

Table 1

The results of the oxidative stability tests for BFl and for test formulations containing BFl blended with one or more of the additives AOl, A02, Dl and LCI are shown in Table 2 below. The third column shows the increase in induction period relative to that of BFl alone.

For formulations containing two or more different additives, the fourth column shows the predicted increase in induction period relative to that of BFl alone. These predictions assumed that the effects of a combination of additives on oxidative stability would be additive, eg that a combination of additives A and B would give an overall increase in stability equal to the sum of the increases which the two additives caused when used alone at the same concentrations. Thus, numerically, the predicted induction period (IP_mixtUre) for a fuel

formulation containing a mixture of additives A, B and C is defined by the formula:

Predicted IP_mixtUre = IPnone * [l+(% increase due to A + % increase due to B + % increase due to C) ]

where IP_n0ne is the induction period for the same formulation but without any of the three additives.

The fifth column in Table 2 shows the percentage benefit provided by the invention, ie the difference between the measured increase in induction period and the predicted increase, as a percentage of the predicted increase for the formulations containing two or more additives. A deficit (when the measured increase was smaller than predicted) is shown as a negative number. Synergistic combinations (positive benefit compared to predicted results) are indicated by positive numbers. Table 2

Test Measured Induction Predicted o.

o formulation induction period increase benefit/ period increase (hours ) deficit

(hours ) (hours )

BFl 1.419 0.00

BFl + Dl 1.933 0.51

BFl + AOl 2.224 0.80

BFl + A02 3.908 2.49

BFl + LCI 1.468 0.05 Test Measured Induction Predicted o.

o formulation induction period increase benefit/ period increase (hours ) deficit (hours ) (hours )

BFl + Dl + 2.976 1.56 1.319 18 AOl

BFl + Dl + 4.847 3.43 3.002 14 AO2

BFl + Dl + 1.858 0.44 0.563 -22 LCI

BFl + AOl + 2.434 1.01 0.853 19 LCI

BFl + A02 + 4.774 3.35 2.537 32 LCI

BFl + Dl + 2.909 1.49 1.367 9 AOl + LCI

BFl + Dl + 3.974 2.55 3.051 -16 A02 + LCI

It can be seen from Table 2 that antioxidants AOl and A02 both increased the oxidative stability (and hence the induction period) of the Fischer-Tropsch derived base fuel alone, as did the detergent Dl to a much smaller extent. The lubricity improver/conductivity improver mixture LCI did not cause any significant increase in oxidative stability, and the combination of Dl and LCI caused a significant reduction in stability.

Surprisingly, when detergent Dl was used together with the antioxidants, the combined effect on oxidative stability was greater than would have been predicted from their individual effects, indicating some form of synergistic interaction between them. The detergent appeared to enhance the activity of the antioxidants. Similar synergies were observed when LCI was used with the antioxidants. The combination of Dl and LCI also appeared to enhance the antioxidant activity of the phenolic antioxidant AOl.

In the case of this Fischer-Tropsch derived base fuel, unexpectedly good results were observed for binary additive combinations containing an antioxidant with either a detergent or a lubricity improver/conductivity improver mixture, especially the combination of the amine antioxidant A02 and the lubricity improver/conductivity improver mixture .

Example 2 - Base Fuel 2

Example 1 was repeated using a hydrogenated

vegetable oil (HVO) blend BF2 as a base fuel. BF2, ex Neste Oil, was a biodiesel fuel produced by hydrotreating vegetable oils and other biologically derived lipids. Its chemical composition was similar to that of Fischer- Tropsch derived base fuels, being paraffinic with essentially no aromatic components or sulphur, although with a relatively narrow carbon chain length

distribution. Its properties are summarised in Table 3 below .

Table 3

As indicated in Table 3, analysis revealed that BF2 comprised 99.5% w/w paraffins. More than 90% of the paraffins content of BF2 was represented by carbon chain lengths of C12 to C18. The results of the oxidative stability tests are shown in Table 4 below, for BF2 and for test formulations containing BF2 blended with one or more of the additives AOl, A02, Dl and LCI. The third, fourth and fifth columns correspond to those in Table 2. Table 4

Test Measured Induction Predicted o.

(hours ) (hours )

BF2 1 284 0 00

BF2 + Dl 1 737 0 45

BF2 + AOl 3 022 1 74

BF2 + AO2 4 097 2 81

BF2 + LCI 1 316 0 03

BF2 + Dl + 3 642 2 36 2 191 8

AOl

BF2 + Dl + 4 209 2 93 3 266 -10

AO2

BF2 + Dl + 1 686 0 40 0 485 -17

LCI

BF2 + AOl + 2 367 1 08 1 771 -39

LCI

BF2 + A02 + 5 174 3 89 2 845 37

LCI

BF2 + Dl + 3 395 2 11 2 223 -5

AOl + LCI

BF2 + Dl + 5 057 3 77 3 298 14

A02 + LCI

Table 4 shows that both antioxidants increased the oxidative stability of the HVO base fuel alone, as did detergent Dl to a much smaller extent. The lubricity improver/conductivity improver mixture LCI did not cause any significant increase in oxidative stability, and the combination of Dl and LCI caused a significant reduction.

Surprisingly, when detergent Dl was used with the phenolic antioxidant AOl, the combined effect on

oxidative stability was unexpectedly greater than would have been predicted from their individual effects, indicating some form of synergistic interaction as the detergent appeared to enhance the activity of the antioxidant. An even more marked synergy was observed when LCI was used with the amine antioxidant A02, and when a combination of Dl and LCI was used in combination with the amine antioxidant.

In the case of this HVO base fuel, particularly good results were thus seen for the formulations containing an amine antioxidant and a lubricity improver/conductivity improver mixture, both with and without the detergent additive Dl .

Comparative Example 3 - Base Fuel 3

Example 1 was repeated using a petroleum-derived diesel base fuel BF3. This was a commercially available, EN 590-compliant ultra low sulphur diesel base fuel, ex Shell, formulated without fatty acid methyl esters

(FAMEs) . Its properties are summarised in Table 5 below. Table 5

The results of the oxidative stability tests for BF3-containing formulations are shown in Table 6 below. The third, fourth and fifth columns correspond to those in Table 2. Table 6

Test Measured Induction Predicted o.

(hours ) (hours )

BF3 0 733 0 00

BF3 + Dl 1 540 0 81

BF3 + AOl 1 365 0 63

BF3 + AO2 3 096 2 36

BF3 + LCI 0 940 0 21

BF3 + Dl + 1 842 1 11 1 440 -23

AOl

BF3 + Dl + 4 377 3 64 3 171 15

AO2

BF3 + Dl + 1 495 0 76 1 016 -25

LCI

BF3 + AOl + 1 440 0 71 0 840 -16

LCI

BF3 + A02 + 1 935 1 20 2 571 -53

LCI

BF3 + Dl + 1 930 1 20 1 648 -27

AOl + LCI

BF3 + Dl + 4 248 3 52 3 378 4

A02 + LCI

Table 6 shows that the surprising effects of the present invention were not generally observed in the case of the petroleum-derived base fuel BF3, which had a relatively low paraffin content. Although antioxidants AOl and A02 increased the oxidative stability of the base fuel, the detergent additive Dl only enhanced that stability for the amine antioxidant A02. The lubricity improver/conductivity improver combination LCI was detrimental to the antioxidant activities of AOl and A02, and when combined with Dl reduced the antioxidant activity of the phenolic antioxidant AOl.

Thus, with petroleum-derived diesel base fuels, improvements in oxidative stability were achieved only with the amine antioxidant A02, and only in the presence of the detergent additive. Example 4 - Base Fuel 4

Example 1 was repeated using a base fuel BF4, which was a 1:1 v/v blend of BFl and BF2 having an overall paraffinic hydrocarbon content of greater than 99% v/v.

The results of the oxidative stability tests are shown in Table 7 below. The third, fourth and fifth columns correspond to those in Table 2.

Table 7

Test Measured Induction Predicted o.

(hours ) (hours )

BF4 1 359 0 00

BF4 + Dl 1 711 0 35

BF4 + AOl 2 418 1 06

BF4 + AO2 4 210 2 85

BF4 + LCI 1 361 0 00

BF4 + Dl + 2 899 1 54 1 411 9

AOl

BF4 + Dl + 4 848 3 49 3 203 9

AO2

BF4 + Dl + 1 647 0 29 0 354 -19

LCI

BF4 + AOl + 2 493 1 13 1 061 7

LCI

BF4 + A02 + 4 670 3 31 2 853 16

LCI

BF4 + Dl + 2 821 1 46 1 413 3

AOl + LCI

BF4 + Dl + 5 534 4 18 3 205 30

A02 + LCI

Table 7 shows antioxidants AOl and A02 greatly increased oxidative stability of the Fischer-Tropsch fuel/HVO blend BF4. Detergent Dl did so to a smaller extent. The lubricity improver/conductivity improver mixture LCI did not cause any significant increase in oxidative stability, and the combination of Dl and LCI caused a significant reduction in stability.

Surprisingly, when the detergent Dl was used with the antioxidants, the combined effect on oxidative stability was greater than would have been predicted from their individual effects, indicating a synergistic interaction between them. Similar synergies were observed when LCI was used with antioxidants, and also when Dl and LCI were used to enhance antioxidant activity (despite the fact that a Dl/LCl mixture on its own caused a large reduction in the oxidative stability of BF4) .

In this case, the Fischer-Tropsch derived and HVO base fuels blend provided particularly good results for formulations containing both the amine antioxidant A02 and the lubricity improver/conductivity improver mixture LCI .

Example 5 - Base Fuel 5

Example 1 was repeated using a base fuel BF5, which was a 1:1 v/v blend of BFl and BF3, having a synthetic paraffinic hydrocarbon content of 50% v/v.

The results of the oxidative stability tests are shown in Table 8 below. The third, fourth and fifth columns correspond to those in Table 2.

Table 8

Test Measured Induction Predicted o.

(hours ) (hours )

BF5 1 444 0 00

BF5 + Dl 1 800 0 36

BF5 + AOl 1 928 0.48

BF5 + AO2 2 858 1 41

BF5 + LCI 1 551 0 11

BF5 + Dl + 1 932 0 49 0 840 -42

AOl

BF5 + Dl + 4 990 3 55 1 770 100

AO2

BF5 + Dl + 1 779 0 34 0 463 -28

LCI

BF5 + AOl + 1 755 0 31 0 591 -47

LCI

BF5 + A02 + 2 962 1 52 1 521 0

LCI Test Measured Induction Predicted o.

BF5 + Dl + 2.293 0.85 0.947 -10 AOl + LCI

BF5 + Dl + 5.565 4.12 1.877 120 A02 + LCI

Table 8 shows that antioxidants AOl and A02

increased the oxidative stability of the Fischer-Tropsch fuel/mineral fuel blend, as did detergent Dl. The lubricity improver/conductivity improver mixture LCI did not cause any sizeable increase in oxidative stability, and the combination of Dl and LCI caused a significant reduction .

Surprisingly, when detergent Dl was used together with amine antioxidant A02, the combined effect on oxidative stability was far greater than would have been predicted from their individual effects, indicating a synergistic interaction between them. A similarly high level of synergy was observed when a combination of Dl and LCI was used with the amine antioxidant .

In the case of this blend of Fischer-Tropsch derived and mineral base fuels, particularly good results were achieved using an amine antioxidant and a detergent .

This pattern reflected that observed for the mineral base fuel alone (BF3), although the addition of Fischer- Tropsch derived fuel components and the resultant increase in paraffin content appeared to enhance the synergistic interaction between the antioxidant and the detergent .

It can be seen from the above examples that species (i) , (ii) or (iii) , as defined above, can be used to enhance the antioxidant activity in a relatively high paraffin content diesel fuel formulation. It can be used to improve the oxidative stability of such formulations, which are likely to be more prone to oxidation because of the paraffinic hydrocarbons they contain. A species (i) , (ii) or (iii) can similarly be used to reduce the concentration of an antioxidant which is needed in such a diesel fuel formulation, without or without undue detriment to the oxidative stability of the formulation. The present invention thus provides more options for the diesel fuel formulator.

Moreover, these results can be achieved through the use of conventional diesel fuel additives (detergents, lubricity improvers and conductivity improvers) which can be of value in a diesel fuel formulation for other purposes as well as their effects on oxidative stability. Species (i) to (iii) are able to interact synergistically with antioxidants in higher paraffin content diesel fuel formulations. This unexpected effect can allow new uses for fuel additives which are not normally regarded as antioxidants .

Thus, in recognising that the species (i) to (iii) may be used for such novel purposes, the invention allows the formulator to achieve more than one aim through the use of a particular additive. This can allow a reduction in overall additive concentrations, with its associated processing benefits, yet without undue loss of fuel stability .

Claims

C L A I M S

1. Use of a species selected from:

(i) detergents;

(iii) combinations of (i) and (ii) ,

in a diesel fuel formulation containing 10% v/v or more of paraffinic hydrocarbons and an antioxidant, for the purpose of increasing the oxidative stability of the formulation .

2. Use according to claim 1, wherein the antioxidant is selected from phenolic antioxidants, in particular hindered phenols; amines, in particular aromatic amines; and mixtures thereof.

3. Use according to claim 2, wherein the antioxidant is selected from amines, in particular aromatic amines, and mixtures thereof.

4. Use according to any one of the preceding claims, wherein the diesel fuel formulation contains 25% v/v or greater of a Fischer-Tropsch derived diesel fuel

component or mixture thereof.

5. Use according to any one of the preceding claims, wherein the diesel fuel formulation contains 60% v/v or more of paraffinic hydrocarbons.

6. Use according to any one of the preceding claims, wherein the species (i) or (iii) comprises a nitrogen- containing detergent, in particular an amine- or

polyamine-containing detergent, for example a

polyisobutenyl (PIB) succinimide .

7. Use according to any one of the preceding claims, wherein the species (ii) or (iii) comprises an ester- based lubricity improver, in particular a fatty acid ester .

8. Use according to any one of the preceding claims, wherein the species (ii) or (iii) comprises a sulphonic acid conductivity improver, in particular a naphthyl sulphonic acid conductivity improver.

9. Use of a species selected from (i) , (ii) and (iii) as defined according to any one of the preceding claims, in a diesel fuel additive composition containing an antioxidant, for the purpose of increasing the

antioxidant activity of the composition.

10. Method for preparing a diesel fuel formulation, the method comprising (a) providing a diesel fuel component or mixture thereof, which contains 10% v/v or greater of paraffinic hydrocarbons and also an antioxidant; (b) optionally assessing the oxidative stability of the component or mixture; (c) adding to the component or mixture a species (i) , (ii) or (iii) as defined according to any one of claims 1 to 8 and (d) assessing the oxidative stability of the resultant formulation.

11. Use of a species (i), (ii) or (iii) as defined according to any one of claims 1 to 8, in a diesel fuel additive composition or in a diesel fuel formulation containing 10% v/v of paraffinic hydrocarbons, in combination with an antioxidant, for the purpose of reducing the concentration of the or an antioxidant which is present in the composition or formulation.

12. Method of operating a diesel fuel-consuming system, and/or apparatus which is driven by such a system, the method comprising introducing into the system a diesel fuel formulation prepared according to any one of claims 1 to 8, 10 or 11, or an additive composition prepared according to claim 9 or claim 11.