ZA200408311B - Diesel fuel compositions - Google Patents
Diesel fuel compositions Download PDFInfo
- Publication number
- ZA200408311B ZA200408311B ZA200408311A ZA200408311A ZA200408311B ZA 200408311 B ZA200408311 B ZA 200408311B ZA 200408311 A ZA200408311 A ZA 200408311A ZA 200408311 A ZA200408311 A ZA 200408311A ZA 200408311 B ZA200408311 B ZA 200408311B
- Authority
- ZA
- South Africa
- Prior art keywords
- engine
- fuel composition
- fischer
- diesel
- deposits
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 91
- 239000002283 diesel fuel Substances 0.000 title claims description 39
- 239000000446 fuel Substances 0.000 claims description 95
- 239000003921 oil Substances 0.000 claims description 53
- 238000002485 combustion reaction Methods 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 32
- 239000003599 detergent Substances 0.000 claims description 29
- 230000006835 compression Effects 0.000 claims description 2
- 238000007906 compression Methods 0.000 claims description 2
- 239000007789 gas Substances 0.000 description 51
- 238000002347 injection Methods 0.000 description 14
- 239000007924 injection Substances 0.000 description 14
- 238000003786 synthesis reaction Methods 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 13
- 239000000654 additive Substances 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 239000005864 Sulphur Substances 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 5
- -1 amine succinamides Chemical class 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 229920002367 Polyisobutene Polymers 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 238000004517 catalytic hydrocracking Methods 0.000 description 3
- 239000006280 diesel fuel additive Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003623 enhancer Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000006317 isomerization reaction Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- NKRVGWFEFKCZAP-UHFFFAOYSA-N 2-ethylhexyl nitrate Chemical compound CCCCC(CC)CO[N+]([O-])=O NKRVGWFEFKCZAP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000010771 distillate fuel oil Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003443 succinic acid derivatives Chemical class 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- GGQRKYMKYMRZTF-UHFFFAOYSA-N 2,2,3,3-tetrakis(prop-1-enyl)butanedioic acid Chemical class CC=CC(C=CC)(C(O)=O)C(C=CC)(C=CC)C(O)=O GGQRKYMKYMRZTF-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004146 Propane-1,2-diol Substances 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007866 anti-wear additive Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000013556 antirust agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical class NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HLYOOCIMLHNMOG-UHFFFAOYSA-N cyclohexyl nitrate Chemical compound [O-][N+](=O)OC1CCCCC1 HLYOOCIMLHNMOG-UHFFFAOYSA-N 0.000 description 1
- 238000006114 decarboxylation reaction Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000002816 fuel additive Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000001755 magnesium gluconate Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical class O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
- C10L1/08—Liquid carbonaceous fuels essentially based on blends of hydrocarbons for compression ignition
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/06—Use of additives to fuels or fires for particular purposes for facilitating soot removal
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Combined Controls Of Internal Combustion Engines (AREA)
- Testing Of Engines (AREA)
Description
. .
Diesel fuel compositions : This invention relates to diesel fuel compositions, their preparation and their use in diesel engines, and to the use of certain types of fuel in diesel fuel compositions.
Typical diesel fuels comprise liquid hydrocarbon middle distillate fuel oils having boiling points from about 150 to 400°C. Examples of such fuels include the reaction products of Fischer-Tropsch methane condensation processes, for example the process known as Shell Middle
Distillate Synthesis (van der Burgt et al, “The Shell
Middle Distillate Synthesis Process”, paper delivered at the 5% Synfuels Worldwide Symposium, Washington DC,
November 1985; see also the November 1989 publication of the same title from Shell International Petroleum Company
Ltd, London, UK). These Fischer-Tropsch derived gas oils are low in undesirable fuel components such as sulphur, nitrogen and aromatics and tend to lead to lower vehicle emissions. They are typically blended with other diesel base fuels, for instance petroleum derived gas oils, at concentrations of for instance from 10 to 30% w/w, to modify the base fuel properties. ~ Compression-ignition (diesel) engines running on conventional diesel fuels can suffer from the build up of combustion related deposits in their fuel injection systems, in particular in the injector nozzles. This . injector fouling can impair engine performance. To reduce fouling, a detergent-containing additive may be included in
N WO 03/091364 PCT/EP03/04339 ~ . , the fuel, or the proportion of heavier components in the . | fuel may be adjusted so as to lower its endpoint.
It has now been found that Fischer-Tropsch derived : fuels can themselves contribute to a reduction in, and/or reversal of, injector fouling. A fuel composition containing such components can therefore be used to help maintain and/or improve engine cleanliness.
According to a first aspect of the present invention there is provided the use of a Fischer-Tropsch derived gas 0il in a diesel fuel composition, for the purpose of reducing subsequent combustion related deposits in a diesel engine into which the fuel composition is introduced.
The Fischer-Tropsch derived gas oil may instead or in addition be used for the purpose of removing previously incurred combustion related deposits (ie, to “clean up” the engine). .
In the context of the present invention, “reducing” includes complete prevention and “removing” embraces both complete and partial removal. “Use” of the Fischer-Tropsch derived gas oil in a fuel composition means incorporating the fuel into the composition, typically as a blend (ie, a physical mixture) with one or more other fuels, conveniently before the composition is introduced into the engine.
The Fischer-Tropsch derived gas oil should be suitable for use as a diesel fuel. Its components (or the majority, : for instance 95% w/w or greater, thereof) should therefore . have boiling points within the typical diesel fuel (“gas 0il”) range, ie, from about 150 to 400°C or from 170 to
~ , 370°C. It will suitably have a 90% w/w distillation ’ temperature of from 300 to 370°C.
By “Fischer-Tropsch derived” is meant that the fuel : 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 + 2Hp) = (-CHp-)p + nH20 + heat, in the presence of an appropriate catalyst and typically at elevated temperatures (eg, 125 to 300°C, preferably 175 to 250°C) and/or pressures (eg, 5 to 100 bar, preferably 12 to 50 bar). Hydrogen:carbon monoxide ratios other than 2:1 may be employed if desired.
A gas oil product may be obtained directly from this 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 (see, eg,
GB-B-2077289 and EP-A-0147873) and/or hydroisomerisation . 20 which can improve cold flow properties by increasing the proportion of branched paraffins. EP-A-0583836 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 © 25 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 i - 4 - desired gas oil fraction (s) may subsequently be isolated ’ for instance by distillation.
Other post-synthesis treatments, such as ' polymerisation, alkylation, distillation, cracking- decarboxylation, isomerisation and hydroreforming, may be employed to modify the properties of Fischer-Tropsch condensation products, as described for instance in
US-A-4125566 and US-A-4478955.
Typical catalysts for the Fischer-Tropsch synthesis of paraffinic hydrocarbons comprise, as the catalytically active component, a metal from Group VIII of the periodic table, in particular ruthenium, iron, cobalt or nickel.
Suitable such catalysts are described for instance in
EP-A-0583836 (pages 3 and 4).
An example of a Fischer-Tropsch based process 1s the
SMDS (Shell Middle Distillate Synthesis) described in “The
Shell Middle Distillate Synthesis Process”, van der Burgt et al (supra). This process produces middle distillate range products by conversion of a natural gas (primarily methane) derived synthesis gas into a heavy long-chain oo 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. A version of the SMDS process, utilising a fixed-bed reactor for the catalytic conversion step, is currently in use in
Bintulu, Malaysia and its products have been used in petroleum derived gas oil blends in commercially available : automotive fuels.
Gas oils prepared by the SMDS process are commercially available for instance from the Royal Dutch/Shell Group of
. Ce
Companies. Further examples of Fischer-Tropsch derived gas . oils are described in EP-A-0583836, EP-A-1101813,
WO-A-97/14768, WO-A-97/14769, WO-A-00/20534, WO-A-00/20535, : WO-A-00/11116, WO-A-00/11117, WO-A-01/83406, WO-A-01/83641,
WO-A-01/83647, WO-A-01/83648 and US-A-6204426. i Suitably, in accordance with the present invention, the Fischer-Tropsch derived gas oil will consist of at least 70% w/w, preferably at least 80% w/w, more preferably at least 90% w/w, most preferably at least 95% w/w, of paraffinic components, preferably iso- and linear paraffins. The weight ratio of iso-paraffins to normal : paraffins will suitably be greater than 0.3 and may be up to 12; suitably it is from 2 to 6. The actual value for this ratio will be determined, in part, by the hydroconversion process used to prepare the gas oil from the Fischer-Tropsch synthesis product. Some cyclic paraffins may also be present. : . By virtue of the Fischer-Tropsch process, a Fischer-
Tropsch derived gas oil has essentially no, or undetectable levels of, sulphur and nitrogen. Compounds containing these hetercatoms tend to act as poisons for Fischer-
Tropsch catalysts and are therefore removed from the synthesis gas feed. Further, the process as usually operated produces no or virtually no aromatic components.
The aromatics content of a Fischer-Tropsch gas oil, as determined by ASTM D 4629, will typically be below 1% w/w, preferably below 0.5% w/w and more preferably below 0.1% - w/w.
The Fischer-Tropsch derived gas oil used in the present invention will typically have a density from 0.76
) Z 6 - to 0.79 g/cm3 at 15°C; a cetane number (ASTM D613) greater ’ than 70, ‘suitably from 74 to 85; a kinematic viscosity from 2.0 to 4.5, preferably from 2.5 to 4.0, more preferably ’ from 2.9 to 3.7, centistokes at 40°C; and a sulphur content of 5 ppmw (parts per million by weight) or less.
Preferably it is a product prepared by a Fischer-
Tropsch methane condensation reaction using a hydrogen/carbon monoxide ratio of less than 2.5, preferably less than 1.75, more preferably from 0.4 to 1.5, and ideally using a cobalt containing catalyst. Suitably it will have been obtained from a hydrocracked Fischer-Tropsch synthesis product (for instance as described in
GB-B-2077289 and/or EP-A-0147873), or more preferably a product from a two-stage hydroconversion process such as that described in EP-A-0583836 (see above). In the latter case, preferred features of the hydroconversion process may be as disclosed at pages 4 to 6, and in the examples, of’
EP-A-0583836. :
The level of combustion related deposits in a diesel engine may be measured in its fuel injection system, with reference to the degree of fouling of the injector nozzles.
Degree of nozzle fouling may be assessed in a number of ways, for instance visually, by measuring the mass of deposits in a fouled nozzle or by measuring the fluid flow (for instance, fuel flow or more preferably air flow) ’ properties of the fouled nozzle relative to those of the clean nozzle.
An appropriate test might for example determine the degree of nozzle fouling (conveniently in the form of a percentage injector fouling index) under steady state
- 7 = conditions in a suitable diesel engine, for instance based ’ on the change in air flow rate through one or more of the nozzles as a result of using the fuel composition.
Conveniently the results are averaged over all of the injector nozzles of the engine. A suitable test protocol, using an indirect injection diesel engine, is described below in connection with the experimental examples. The : CEC standard test method F-23-T-00, which again involves injector nozzle air flow measurements, may also be used to assess engine fouling.
The invention may be applicable where the fuel composition is used or intended to be used in a direct injection diesel engine, for example of the rotary pump, in-line pump, unit pump, electronic unit injector or common rail type, or in an indirect injection diesel engine. The fuel composition may be suitable for use in heavy and/or light duty diesel engines.
The amount of the Fischer-Tropsch derived gas oil used may be from 0.5 to 100% w/w of the overall diesel fuel composition, suitably from 1 to 60% w/w, preferably from 5 to 50% w/w, more preferably from 10 to 30% w/w. It may be . desirable for the composition to contain 8% w/w or greater, more preferably 10% w/w or greater, most preferably 20% w/w or greater, of the Fischer-Tropsch gas oil.
Other fuel components of the composition may be diesel fuels of conventional type, typically comprising liquid hydrocarbon middle distillate fuel oils, for instance petroleum derived gas oils. Such fuel components will typically have boiling points within the usual diesel range of 150 to 400°C, depending on grade and use.
The diesel fuel composition may, in order to achieve a : reduction and/or removal of engine deposits, consist essentially of the Fischer-Tropsch derived gas oil - in other words it may contain a major proportion (by which is ] 5 meant preferably 99% w/w or more of the fuel composition, more preferably 99.5% w/w or more, most preferably 99.8% w/w or more, even up to 100% w/w) of the Fischer-
Tropsch derived gas oil, optionally with a minor proportion of one or more diesel fuel additives such as are known in the art but with no other diesel fuels.
The overall fuel composition preferably has a low or ultra low sulphur content, for instance at most 1000 ppmw (parts per million by weight), preferably no more than 500 ppmw, most preferably no more than 100 or 50 or even 10 ppmw. It preferably has a cetane number (ASTM D613) from 40 to 85, more preferably from 45 to 75. Its density will typically be from 0.75 to 0.9 g/cm3, preferably from 0.8 to 0.85 g/cm3, at 15°C.
The Fischer-Tropsch derived gas oil may in particular be used to enhance the performance of a fuel or fuel blend which would otherwise cause relatively high levels of combustion related deposits, for instance a fuel having a relatively high endpoint and/or containing relatively high levels of aromatic components, and/or of a fuel or blend which causes, after three hours’ engine running, a reduction in the achievable air flow rate through one or more of the engine nozzles of greater than 35 or 40 or 45% for instance measured using the test protocol described below.
- Cs
Although in general the diesel fuel composition may or may not contain additives, it is preferred that it includes a detergent, since this may enhance the cleaning effect of the Fischer-Tropsch derived gas oil. The first aspect of ] 5 the present invention may therefore involve the use of both a Fischer-Tropsch derived gas oil and a detergent, in a
E diesel fuel composition, for the purpose of reducing subsequent combustion related deposits in a diesel engine into which the fuel composition is introduced and/or for the purpose of removing previously incurred combustion related deposits.
By “detergent” is meant an agent (suitably a surfactant) which can act to remove, and/or to prevent the build up of, combustion related deposits within the engine,
Cs in particular in the fuel injection system such as in the injector nozzles. Such materials are sometimes referred to as dispersant additives.
The Fischer-Tropsch derived gas oil, or alternatively the combination of the Fischer-Tropsch derived gas oil and the detergent, is preferably included in the fuel composition at a concentration sufficient to achieve a reduction in engine fouling (measured for instance as outlined above) of at least 5%, preferably at least 8%, more preferably at least 10%, most preferably at least 20%, 25 . as compared to that which results from using (under the same or comparable conditions) the same fuel composition but without the Fischer-Tropsch gas oil. Alternatively the ’ reduction may be relative to the degree of engine fouling which results from the use (under the same or comparable conditions) of a fuel composition containing no, or less than 1% w/w, Fischer-Tropsch derived fuels and no, or less : than 50 or even 20 ppmw of, detergent. . More preferably, the Fischer-Tropsch derived gas oil, ) or alternatively the combination of the Fischer-Tropsch derived gas oil and the detergent, is included at a concentration sufficient to remove, at least partially, combustion related deposits which have built up in the engine's fuel injection system, in particular in the injector nozzles, during a previous period of running using another diesel fuel (typically a fuel containing no, or less than 1% w/w, Fischer-Tropsch derived fuels and no, or less than 50 or even 20 ppmw of, detergent), when the engine is subsequently run on the Fischer-Tropsch fuel containing composition. This concentration is preferably sufficient to remove at least 5% of the previously incurred injector deposits (measured for instance as described above), more preferably at least 10%, most preferably at least 15 or 20 or 25 or 30%. :
The removal of combustion related deposits may be achieved by running the engine on the Fischer-Tropsch fuel containing composition for instance for the same period of time as that during which the deposits accumulated, or more preferably for 75%, yet more preferably 50% or even 40% or 30%, of the period of deposit accumulation, conveniently under comparable conditions. Ideally at least partial removal of combustion related deposits is achieved by running the engine on the Fischer-Tropsch fuel containing : composition for five hours or less, preferably for three hours cor less, more preferably for two hours or less.
- Ca
Where the fuel composition includes a detergent, preferred concentrations lie in the range 20 to 500 ppmw active matter detergent based on the overall fuel ’ composition, more preferably 40 to 500 ppmw, most preferably 40 to 300 ppmw or 100 to 300 ppmw or 150 to 300 ppmw. In the case of most commercially available detergent containing diesel fuel additives, this may mean that the additive is incorporated at levels higher than the standard recommended single treat rate, for example between 1.2 and 3 times, preferably between 1.5 and 2.5 times, such as about twice the standard single treat rate. Lower detergent levels (for example, corresponding to between 0.5 and 1.2 times, preferably the same as, the standard single treat rate) may however be used to help reduce or prevent further engine fouling and/or power loss.
Examples of detergents suitable for use in accordance with the present invention include polyolefin substituted succinimides or succinamides of polyamines, for instance polyisobutylene succinimides or polyisobutylene amine succinamides, aliphatic amines, Mannich bases or amines and polyolefin (eg, polyisobutylene) maleic anhydrides.
Succinimide dispersant additives are described for example in GB-A-960493, EP-A-0147240, EP-A-0482253, EP-A-0613938,
EP-A-0557561 and WO-A-98/42808. Particularly preferred are polyolefin substituted succinimides such as polyisobutylene succinimides.
Detergent-containing diesel fuel additives are known and commercially available, for instance from Infineum (eg,
F7661 and F7685) and Octel (eg, OMA 4130D).
The fuel composition may contain other components in : addition to the Fischer-Tropsch derived fuel and if applicable the detergent. Typically such components will ) be incorporated in fuel additives, for instance in combination with a detergent. Examples are lubricity : enhancers such as EC 832 and PARADYNE™ (ex Infineum),
HITEC™ E580 (ex Ethyl Corporation) and VEKTRON™ 6010 (ex
Infineum) and amide-based additives such as those available from the Lubrizol Chemical Company, for instance LZ 539 C; dehazers, eg, alkoxylated phenol formaldehyde polymers such as those commercially available as NALCO™ EC5462A (formerly 7D07) (ex Nalco), and TOLAD™ 2683 (ex Petrolite); anti- foaming agents (eg, the polyether-modified polysiloxanes commercially available as TEGOPREN™ 5851 and Q 25907 (ex
Dow Corning), SAG™ TP-325 (ex 0Si) and RHODORSIL™ (ex Rhone - Poulenc)); ignition improvers (cetane improvers) (eg, 2- ethylhexyl nitrate (EHN), cyclohexyl nitrate, di-tert-butyl peroxide and those disclosed in US-4208190 at column 2, line 27 to column 3, line 21); anti-rust agents (eg, that ~~ sold commercially by Rhein Chemie, Mannheim, Germany as “RC 4801”, a propane-1, 2-diol semi-ester of tetrapropenyl succinic acid, or polyhydric alcohol esters of a succinic acid derivative, the succinic acid derivative having on at least one of its alpha-carbon atoms an unsubstituted or substituted aliphatic hydrocarbon group containing from 20 to 500 carbon atoms, eg, the pentaerythritol diester of polyisobutylene-substituted succinic acid); corrosion : inhibitors; reodorants; anti-wear additives; anti-oxidants (eg, phenolics such as 2,6-di-tert-butylphenol, or phenylenediamines such as N,N’'-di-sec-butyl-p- oo : phenylenediamine); and metal deactivators.
Unless otherwise stated, the (active matter) : concentration of each such additional component in the overall fuel composition is preferably up to 1% w/w, more preferably in the range from 5 to 1000 ppmw, advantageously from 75 to 300 ppmw, such as from 95 to 150 ppmw.
It is particularly preferred that a lubricity enhancer be included in the fuel composition, especially when it has a low (eg, 500 ppmw or less) sulphur content. The lubricity enhancer is conveniently present at a concentration from 50 to 1000 ppmw, preferably from 100 to 1000 ppmw, based on the overall fuel composition.
The (active matter) concentration of any dehazer in the fuel composition will preferably be in the range from 1 to 20 ppmw, more preferably from 1 to 15 ppmw, still more
CC preferably from 1 to 10 ppmw and advantageously from 1 to 5 ppmw. The (active matter) concentration of any ignition improver present will preferably be 600 ppmw or less, more . preferably 500 ppmw or less, conveniently from 300 to 500 ppmw. :
A second aspect of the present invention provides a method of operating a diesel engine, and/or a vehicle which is driven by a diesel engine, which method involves introducing into a combustion chamber of the engine a diesel fuel composition incorporating a Fischer-Tropsch derived gas oil, and optionally also a detergent, for the : purpose of reducing subsequent combustion related depecsits in the engine and/or removing previously incurred ’ 30 combustion related deposits in the engine.
"preferred features of the second aspect of the . invention, for instance regarding the engine type, the nature of the diesel fuel composition, the nature and : concentration of the Fischer-Tropsch derived gas oil and if present the detergent, as well as of other components of the fuel composition, and the ways in which engine fouling may be assessed, may all be as described above in connection with the first aspect.
According to a third aspect of the invention, there is . 10 provided a diesel fuel composition which includes a major proportion of a fuel or fuel blend for an internal combustion engine of the compression ignition type, wherein the fuel or fuel blend comprises at least 30% w/w of a
Fischer-Tropsch derived gas oil, preferably at least 40%
W/W, more preferably at least 50% w/w, most preferably at least 60% w/w. The fuel or. fuel blend may comprise up to 100% w/w of the Fischer-Tropsch derived gas oil, preferably up to 95% w/w, more preferably up to 90% w/w, most preferably up to 80% w/w or 70% w/w. :
This fuel composition preferably also contains a minor proportion of a detergent-containing additive. By “minor proportion” is meant preferably less than 1% w/w of the fuel composition, more preferably less than 0.5% w/w (5000 ppmw) and most preferably less than 0.2% w/w (2000 ppmw); references to “major proportion” may be construed accordingly.
As described above, in accordance with the present : invention a fuel or fuel blend may be additivated (additive-containing) or unadditivated (additive-free). If : 30 additivated, it will contain a minor proportion of one or id WO 03/091364 PCT/EP03/04359 more additives, in particular a detergent containing : additive. Such additives may be added at various stages during the production of the fuel composition; those added : at the refinery for example might be selected from anti- static agents, pipeline drag reducers, flow improvers (eg, ethylene/vinyl acetate copolymers or acrylate/maleic anhydride copolymers} and wax anti-settling agents (eg, those commercially available under the Trade Marks “PARAFLOW” (eg, PARAFLOW™ 450, ex Infineum), “OCTEL” (eg,
OCTEL™ W 5000, ex Octel) and “DODIFLOW” (eg, DODIFLOW™ wv 3958, ex Hoechst).
In accordance with a fourth aspect of the invention, there is provided a method of operating a diesel engine, and/or a vehicle which is driven by a diesel engine, which method involves introducing into a combustion chamber of the engine a diesel fuel composition according to the third aspect.
A fifth aspect of the invention provides a process for the preparation of a diesel fuel composition, such as a composition according to the third aspect, which process involves blending a Fischer-Tropsch derived gas oil with a non Fischer-Tropsch derived diesel fuel, optionally together with a detergent. Again the blending is ideally carried out with the aim of reducing subsequent combustion related deposits in a diesel engine into which the fuel composition is introduced and/or for the purpose of removing previously incurred combustion related deposits in : the engine.
The discovery that Fischer-Tropsch gas oils can at ) 30 least partly remove existing engine deposits may be put to use in the “clean-up” of a fouled engine. Thus, according : to a sixth aspect of the present invention, there is provided the use of a Fischer-Tropsch derived gas oil, ’ and/or of a fuel composition containing a Fischer-Tropsch derived gas o0il, to clean (ie, to remove combustion related deposits from) the fuel injection system of a diesel engine. “Use” in this way means running the engine, or a part thereof such as its fuel injection system, on the gas 0il or fuel composition for a period of time sufficient to effect at least partial removal of the combustion related " deposits. It need not necessarily involve driving the vehicle.
A Fischer-Tropsch derived gas oil, or a fuel composition containing such a gas oil, may therefore in accordance with the invention be packaged together with instructions for its use to clean a diesel engine in the manner described above.
The sixth aspect of the invention also encompasses a method of cleaning the fuel injection system of a diesel engine, by introducing into a combustion chamber of the engine a Fischer-Tropsch derived gas oil and/or a fuel composition containing a Fischer-Tropsch derived gas oil.
Preferred features of the third to the sixth aspects of the invention, for instance regarding the nature and concentrations of the Fischer-Tropsch derived gas oil, any detergent present and any other fuel components and additives present, may be as described above in connection : with the first and second aspects of the invention.
i -17 -
According to a seventh aspect, the present invention . provides a method for assessing the performance of a candidate diesel fuel composition, comprising the steps of: : 1) measuring the level of combustion related deposits in a diesel engine running on a “standard” diesel fuel composition, which “standard” fuel composition contains no, or less than 1% w/w of, Fischer-Tropsch derived gas oils; 2) subjecting the engine to a first test cycle running on the standard fuel composition; . 3) measuring the level of combustion related deposits in the engine after the first test cycle; 4) calculating the increase in deposits during the first test cycle; 5) subjecting the engine to a second test cycle running on the candidate diesel fuel composition; 6) measuring the level of combustion related deposits in the engine after the second test cycle; 7) calculating the increase in deposits (if any) during the second test cycle; and ©0020 8) if applicable, calculating the extent of removal of deposits during the second test cycle.
The “standard” fuel composition suitably contains no, or less than 50 or even 20 ppmw, active matter detergent.
It is suitably a low or ultra low sulphur diesel fuel, as described above, and is preferably unadditivated.
The level of combustion related deposits may be measured by assessing the degree of fouling of the injector . nozzles in the fuel injection system of the engine, as described above.
i WO 03/091364 PCT/EP03/04359
The test cycles involve running the engine on the ‘ relevant fuel composition for a given period of time and/or for a given number of miles. The tests may be conducted on the engine alone or driving a vehicle - in the latter case they may be conducted under simulated driving conditions (such as using a chassis dynamometer) or involve regular road driving (preferably under urban as opposed to motorway conditions). The engine running and/or driving conditions should be the same or comparable for both the first and the second test cycles. : By way of example, the duration of the first test cycle should be sufficient to cause a significant, and at least detectable, build up of combustion related deposits “compared to that measured in step 1 of the test. A typical first test cycle might last from 1 to 5 hours, preferably 2 hours or more, more preferably 3 hours or more.
An appropriate duration for the second test cycle is typically from 10 to 100%, preferably from 50 to 100%, most suitably 100%, of that of the first -test cycle. It may in cases be 80% or 75% or even 50% or less of the duration of the first test cycle. For assessing reductions in (as opposed to removal of) combustion related deposits, it may be up to 120% or 150% or even 200% of the duration of the first test cycle.
The engine used for the test may for instance be an indirect injection diesel engine, such as a Volkswagen™
Passat™ engine, for instance the Passat™ AAZ 1.9 TD engine. ’ The test may be conducted on only a part of the engine (eg, the fuel injection system) or on a simulated engine or engine part.
The assessment method of the invention is particularly applicable to a candidate diesel fuel composition which incorporates a Fischer-Tropsch derived gas oil, more : particularly to one which also incorporates a detergent.
The method may therefore be used to identify and/or evaluate fuel compositions according to the third aspect of the invention.
The method may also be used to assess the performance of a diesel engine, and/or to assess the performance of a fuel injection system for use in a diesel engine, and/or to assess the performance of a vehicle driven by a diesel : engine.
An eighth aspect of the present invention provides a diesel fuel composition which, when used as the candidate fuel composition in the assessment method of the seventh aspect, leads to removal of at least 5%, preferably at least 10% or 15% or 20% or 25% or 30%, of the combustion related deposits accumulated in the engine prior to step 5 of the test, when the duration of the second test cycle is the same as or less than, more preferably 80% or 75% ox even 50% or less of, the duration of the first test cycle, and the duration of the first test cycle is preferably at least 2 hours, more preferably 3 hours or more.
Such a fuel composition ideally contains, in accordance with the present invention, a Fischer-Tropsch derived gas oil, preferably together with a detergent.
The present invention will be further understood from ’ the following examples, which illustrate the effects of using Fischer-Tropsch derived gas oils in diesel fuel compositions, on the degree of fuel injector fouling.
Claims (13)
1. Use of a Fischer-Tropsch derived gas oil in a diesel fuel composition, for the purpose of reducing subsequent combustion related deposits in a diesel engine into which the fuel composition is introduced and/or of removing previously incurred combustion related deposits from the engine.
2. Use according to claim 1, wherein the amount of the Fischer-Tropsch derived gas oil used in the fuel composition is 10% w/w or greater.
3. Use according to claim 1 or claim 2, wherein the fuel composition includes a detergent.
4. A method of operating a diesel engine, and/or a vehicle which is driven by a diesel engine, which method involves introducing into a combustion chamber of the engine a diesel fuel composition incorporating a Fischer- Tropsch derived gas oil, and optionally also a detergent, for the purpose of reducing subsequent combustion related deposits in the engine and/or removing previously incurred combustion related deposits in the engine.
5. Use of a Fischer-Tropsch derived gas oil, and/or of a fuel composition containing a Fischer-Tropsch derived gas oil, to remove combustion related deposits from a diesel engine.
6. Use according to claim 5, wherein the Fischer-Tropsch derived gas oil and/or the fuel composition is used together with a detergent.
7. A method for assessing the performance of a candidate . diesel fuel composition, comprising the steps of: 1) measuring the level of combustion related ’ deposits in a diesel engine running on a standard diesel fuel composition, which standard fuel composition contains no, or less than 1% w/w of, Fischer-Tropsch derived gas oils; 2) subjecting the engine to a first test cycle running on the standard fuel composition; 3) measuring the level of combustion related deposits in the engine after the first test cycle; 4) calculating the increase in deposits during the first test cycle; ) 5) subjecting the engine to a second test cycle running on the candidate diesel fuel composition; 0) measuring the level of combustion related deposits in the engine after the second test cycle; 7) calculating the increase in deposits (if any) during the second test cycle; and 8) if applicable, calculating the extent of removal of deposits during the second test cycle.
8. A diesel fuel composition which, when used as the candidate fuel composition in a method according to claim 7, leads to removal of at least 5% of the combustion related deposits accumulated in the engine prior to step 5 of the test, when the duration of the second test cycle is the same as or less than that of the first test cycle.
- 9. A diesel fuel composition which includes a major proportion of a fuel or fuel blend for an internal ’ 30 combustion engine of the compression ignition type, wherein the fuel or fuel blend comprises at least 30% w/w of a Fischer-Tropsch derived gas oil.
10. A diesel fuel composition according to claim 9, additionally comprising a detergent.
11. Use according to claim 1 or 5, substantially as herein described and exemplified and/or described with reference to the examples.
12. A method according to claim 4 or 7, substantially as herein described and exemplified and/or described with reference to the examples.
13. A diesel fuel composition according to claim 8 or 9, substantially as herein described and exemplified and/or described with reference to the examples. AMENDED SHEET
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EP02252946 | 2002-04-25 |
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JP (1) | JP5179700B2 (en) |
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EP1664247A1 (en) * | 2003-09-03 | 2006-06-07 | Shell Internationale Researchmaatschappij B.V. | Fuel compositions comprising fischer-tropsch derived fuel |
-
2003
- 2003-04-23 MY MYPI20031522A patent/MY140444A/en unknown
- 2003-04-23 AR ARP030101391A patent/AR043292A1/en unknown
- 2003-04-24 BR BR0309479-0A patent/BR0309479A/en not_active IP Right Cessation
- 2003-04-24 AU AU2003229732A patent/AU2003229732B2/en not_active Ceased
- 2003-04-24 US US10/512,140 patent/US20050241216A1/en not_active Abandoned
- 2003-04-24 CN CN038115034A patent/CN1656199B/en not_active Expired - Fee Related
- 2003-04-24 JP JP2003587903A patent/JP5179700B2/en not_active Expired - Fee Related
- 2003-04-24 EP EP03722551.3A patent/EP1497398B1/en not_active Expired - Lifetime
- 2003-04-24 WO PCT/EP2003/004359 patent/WO2003091364A2/en active Application Filing
- 2003-04-24 CA CA2483200A patent/CA2483200C/en not_active Expired - Lifetime
- 2003-04-24 PL PL03371868A patent/PL371868A1/en not_active IP Right Cessation
- 2003-04-24 DK DK03722551.3T patent/DK1497398T3/en active
-
2004
- 2004-10-14 ZA ZA200408311A patent/ZA200408311B/en unknown
- 2004-11-24 NO NO20045114A patent/NO20045114L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
MY140444A (en) | 2009-12-31 |
JP5179700B2 (en) | 2013-04-10 |
AU2003229732B2 (en) | 2009-06-25 |
WO2003091364A3 (en) | 2004-04-01 |
CA2483200A1 (en) | 2003-11-06 |
AR043292A1 (en) | 2005-07-27 |
US20050241216A1 (en) | 2005-11-03 |
DK1497398T3 (en) | 2018-08-27 |
CA2483200C (en) | 2011-07-26 |
BR0309479A (en) | 2005-02-01 |
CN1656199B (en) | 2010-11-03 |
EP1497398B1 (en) | 2018-05-23 |
EP1497398A2 (en) | 2005-01-19 |
WO2003091364A2 (en) | 2003-11-06 |
AU2003229732A1 (en) | 2003-11-10 |
PL371868A1 (en) | 2005-07-11 |
NO20045114L (en) | 2004-11-24 |
CN1656199A (en) | 2005-08-17 |
JP2005523973A (en) | 2005-08-11 |
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