AU2004298630A1 - Fuel for homogeneous charge compression ignition (HCCI) systems and a process for production of said fuel - Google Patents
Fuel for homogeneous charge compression ignition (HCCI) systems and a process for production of said fuel Download PDFInfo
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- AU2004298630A1 AU2004298630A1 AU2004298630A AU2004298630A AU2004298630A1 AU 2004298630 A1 AU2004298630 A1 AU 2004298630A1 AU 2004298630 A AU2004298630 A AU 2004298630A AU 2004298630 A AU2004298630 A AU 2004298630A AU 2004298630 A1 AU2004298630 A1 AU 2004298630A1
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- 239000000446 fuel Substances 0.000 title claims description 133
- 238000000034 method Methods 0.000 title claims description 23
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 230000006835 compression Effects 0.000 title description 5
- 238000007906 compression Methods 0.000 title description 5
- 239000000047 product Substances 0.000 claims description 16
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- 238000004821 distillation Methods 0.000 claims description 11
- 239000005864 Sulphur Substances 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 10
- 150000001336 alkenes Chemical class 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 229910052760 oxygen Chemical group 0.000 claims description 7
- 239000001301 oxygen Chemical group 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 238000004517 catalytic hydrocracking Methods 0.000 claims description 5
- 238000003786 synthesis reaction Methods 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 description 13
- 150000002430 hydrocarbons Chemical class 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- 238000002485 combustion reaction Methods 0.000 description 10
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 10
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 9
- 239000004215 Carbon black (E152) Substances 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 238000005194 fractionation Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 230000001934 delay Effects 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000003502 gasoline Substances 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002816 fuel additive Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000000769 gas chromatography-flame ionisation detection Methods 0.000 description 1
- 238000001165 gas chromatography-thermal conductivity detection Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000010977 unit operation Methods 0.000 description 1
- 239000010457 zeolite Substances 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
- C10L10/02—Use of additives to fuels or fires for particular purposes for reducing smoke development
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Luminescent Compositions (AREA)
- Fuel-Injection Apparatus (AREA)
Description
WO 2005/059063 PCT/ZA2004/000157 FUEL FOR HOMOGENEOUS CHARGE COMPRESSION IGNITION (HCCI) SYSTEMS AND A PROCESS FOR PRODUCTION OF SAID FUEL 5 Field of the Invention The invention relates to a fuel for Homogeneous Charge Compression Ignition (HCCI) systems and to a process for producing such a fuel. 10 Background to the Invention The HCCI engine is a relatively new concept under development by several institutions and companies. The principle of HCCI combustion is that a dilute, premixed, homogenous mixture of fuel and air reacts and burns volumetrically 15 throughout the cylinder as it is compressed by the piston. Combustion reactions start when the mixture reaches a sufficiently high temperature to autoignite. These reactions initiate at multiple locations simultaneously, proceed very quickly, and there is a complete absence of localized high-temperature regions or flame-fronts. 20 In essence, the HCCI combustion process seeks to combine the low nitrogen oxides (NOx), exhaust emissions associated with the gasoline engine, with the high thermal efficiency associated with the diesel or compression ignition (CI) engine. In theory, HCCI offers the potential for sootless combustion and very low emissions of nitrogen oxides (NOx), together with an energy efficiency that can exceed that of the Cl engine. 25 Successful implementation of HCCI combustion would therefore increase the competitiveness of the internal combustion (IC) engine against emerging technologies such as fuel cells, thereby extending its lifespan. 30 Because HCCI is effectively an evolution of the IC engine, there are no external barriers to its implementation, and the gradual adoption of this technology may see it eventually being implemented in the majority of automotive IC engines, in one form or another. A 2001 report by the US Department of Energy to the US Congress WO 2005/059063 PCT/ZA2004/000157 2 speculated that, with successful R&D, passenger car HCCI engines might be commercialised by 2010. Thus a need exists for a fuel for HCCI systems and engines. 5 Summary of the Invention 10 According to one aspect of the invention, there is provided a HCCI fuel, which fuel includes at least n-paraffins and iso-paraffins, and which fuel has an ignition delay of less than 7 ms. The HCCI fuel may also be used as a fuel component. Typically, the fuel contains hydrocarbon species having from 7 to 14 carbon atoms. 15 The fuel may be substantially cyclo-paraffins free. Thus, the fuel may have less than 5 mass%, typically less than 1 mass% cyclo-paraffins. Moreover, it contains less than 1 wt % of aromatic and negligible levels of sulphur. 20 In this specification, the ignition delay is measured using the ASTM Method D6890 in a constant volume combustion bomb, Ignition Quality Tester (IQTTM) The ignition delay of the fuel may be less than 5 ms. 25 The ignition delay of the fuel may be between 2 and 5 ms. The weight % of the n-paraffins may exceed that of any other single component in the fuel. 30 The n-paraffins may be in excess of 25% by weight of the fuel The n-paraffins may be in excess of 50% by weight of the fuel. 35 The n-paraffins may be in excess of 80% by weight of the fuel.
WO 2005/059063 PCT/ZA2004/000157 3 The n-paraffins may be in the order of 95% by weight of the fuel. The n-paraffins may be Fischer-Tropsch (FT) reaction derived n-paraffins. 5 The iso-paraffins may be FT reaction derived iso-paraffins. The fuel may include olefins. 10 The HCCI fuel may include oxygenates. The HCCI fuel may be substantially sulphur free. The HCCI fuel may be substantially oxygenate free. 15 The fuel may have an ASTM D86 distillation range from 90 0 C to 270 0 C. The fuel may include a lubricity improver or other fuel additives to make meeting product specifications possible. 20 The fuel may be used as blending component with conventional fuel. The invention extends to a process for preparing a HCCI fuel or fuel component, which fuel or fuel component includes at least n-paraffins and iso-paraffins, which fuel has an ignition delay of less than 7 ms, said process including one or more steps 25 selected from: a) hydrotreating at least a Condensate fraction of a Fischer-Tropsch (FT) synthesis reaction product, or a derivative thereof; b) hydroconverting a Wax fraction of the FT synthesis product or a derivative thereof; 30 c) fractionating in a single unit or in separate units, one or more of the hydrotreated Condensate fractions of step a) and the hydroconverted fraction of step b) to obtain the desired HCCI fuel or fuel component; and d) optionally, blending two or more of said components from step c) in a desired ratio to obtain the desired HCCI fuel.
WO 2005/059063 PCT/ZA2004/000157 4 The hydroconversion may be by way of hydrocracking. The properties of the fuel made according to the process may be as disclosed above 5 and elsewhere in the specification. The blending of step d) may be the blending of FT condensate derivative and hydroconverted FT wax derivative from 1:99 to 99:1 by volume 10 The table below gives a typical composition of the two fractions. Typical FT product after separation into two fractions (vol % distilled) FT Condensate FT Wax (<270 0 C fraction) (> 270 0 C fraction) C5-1600C 44 3 160-2700C 43 4 270-3700C 13 25 370-5000C 40 > 5000C 28 The >1600C fraction, contains a considerable amount of hydrocarbon material, which 15 boils higher than the normal naphtha range. The 1600C to 2700C fraction may be regarded as a light diesel fuel. This means that all material heavier than 270C00 needs to be converted into lighter materials by means of a catalytic process often referred to as hydroprocessing, for example, hydrocracking. 20 Catalysts for this step are typically of the bifunctional type; i.e. they contain sites active for cracking and for hydrogenation. Catalytic metals active for hydrogenation include group VIII noble metals, such as platinum or palladium, or a sulphided Group VIII base metals, e.g. nickel, cobalt, which may or may not include a sulphided Group VI metal, e.g. molybdenum. The support for the metals can be any refractory 25 oxide, such as silica, alumina, titania, zirconia, vanadia and other Group III, IV, V and WO 2005/059063 PCT/ZA2004/000157 5 VI oxides, alone or in combination with other refractory oxides. Alternatively, the support can partly or totally consist of zeolite. 5 Specific Description and Examples The following table summarises the origin and carbon number ranges for the proposed fuels usable in HCCI engines of this invention: WO 2005/059063 PCT/ZA2004/000157 6 Class Typical (LTFT) Composition Carbon Number range Feedstock
C
7
-C
9
C
7
-C
14
C
10
-C
14 SR FT FT Condensate Paraffins, olefins X X X and oxygenates HT SR FT FT Condensate Mostly linear X X X paraffins HX FT FT Wax Mostly iso-paraffins X X X FT Condensate GTL and Wax Fully paraffinic X X X and Wax Definitions 5 * SR FT Straight Run Fischer-Tropsch * HT SR FT Hydrotreated Straight Run Fischer-Tropsch * HX FT Hydrocracked Fischer-Tropsch * GTL Hydroconverted Product as expected from a Fischer-Tropsch Gas-to-Liquid plant 10 The fuel might contain hydrocarbon species having from 7 to 14 carbon atoms and has been found to define unique characteristics with respect to vapour pressure and ignition delay. Moreover, the criteria also made consideration to the highly paraffinic nature of the fuel as well as the high linearity of the hydrocarbon species. 15 The C7 to C14 carbon number range has been found to exclude hydrocarbons like pentane or hexane that have high vapour pressures. Adequate volatility is important to establish a homogeneous gaseous charge in the combustion chamber, with enough cetane character (propensity to auto-ignite) to effect the homogeneous 20 ignition throughout the whole volume. Furthermore, the C7 to C14 carbon number range has been found to exclude hydrocarbons like n-hexadecane that conventionally has cetane number of 100. The WO 2005/059063 PCT/ZA2004/000157 7 cetane number of the HCCI fuel must not be too high and its ignition delay not too short to ensure controlled in-cylinder combustion. The inventors believe that the abovementioned twelve options cover almost all 5 practical options for FT-based synthetic HCCI fuels. The key quality requirements for these fuels are summarised in Table 1. 10 Table 1 Selected Quality Characteristics of Synthetic FT HCCI Fuels Analytical Desired Range Procedure Procedure Distillation Range 90-270oC ASTM D86 Density 0.65-0.78 kg/I ASTM D1298 Composition hydrocarbon GC-FID Ignition delay (IQT) 2-7 ms ASTM D6890-03 Cetane Number 25-75 ASTM D613-03a ASTM D5186-99 Aromatics content <1.0% wt ASTM D6591-00 ASTM D6591-00 Sulfur content < 1 ppm wt ASTM D5453 Oxygen content <5000 ppm GC-TCD The ignition delay is a good indication of the elevated pressure, high temperature 15 autoignition characteristics of the fuel and can be correlated to the distillation range and cetane number of the fuel, which in turn relate to its chemical composition. The conditions at which the ignition delay is determined in the IQTTM; at 22.4 bar air pressure and 565 0C, are comparable to the conditions that an HCCI fuel could experience in an HCCI engine, thus the ignition delay (ID) can be used as an 20 appropriate yardstick for HCCI fuel ignition quality. The implications are that fuels with a high propensity for autoignition under compression will have short ignition delays (~2-4 ms), while fuels with increased resistance against autoignition (equivalent to high octane spark ignition gasoline) will have longer ignition delays (-7-11ms). 25 Since the resistance against autoignition is no different to a resistance against oxidation at the specific pressure and temperature conditions to which the fuel is exposed in an HCCI engine's combustion chamber, it follows that those sulphur (S) WO 2005/059063 PCT/ZA2004/000157 8 and nitrogen (N) heteroatoms present in crude oil derived HCCI fuel will act as oxidation inhibitors, leading to longer ignition delays and a lower propensity towards autoignition. 5 FT fuels are virtually sulphur free, with lower levels of nitrogen-containing compounds, and the absence of these naturally occurring anti-oxidants represent a benefit when FT fuels are applied in HCCI engines. This results in FT fuels outperforming conventional fuels in terms of their propensity to autoignite under HCCI conditions. t10 Process Scheme A generic block diagram flow scheme is included as figure 1. The process options for all four classes of HCCI fuels are shown in a simple format. The following table 2 summarises the basic processing for these fuels and feeds. 15 Table 2 Generic Requirement for FT Feedstock Processing Process Step Process Description Reference Distillation Atmospheric Distillation (1) * H 2 saturation of olefinic double bonds. n* H 2 saturation of oxygen-containing Hydrotreatment hydrocarbons with formation of water US 6,475,375 * Other hydroconversion reactions * Cracking of heavy molecules (mostly paraffinic) Hydrocracking H 2 saturation of olefinic double bonds. EP 1129155 * H 2 saturation of oxygen-containing hydrocarbons with formation of water * Other hydroconversion reactions 20 (1) There are many references for this unit operation. For example, refer to PA Schweitzer, Handbook of Separation Techniques for Chemical Engineers (McGraw Hill, 1979) or RH Perry and CH Chilton, Chemical Engineers' Handbook (McGraw-Hill, 5 th Edition, 1973) 25 The production of the synthetic HCCI fuel components can be achieved following at least four process configurations. The selection of one for a specific plant is an WO 2005/059063 PCT/ZA2004/000157 9 exercise in process synthesis that demands additional site and market specific information. A first group of HCCI fuels - named SR FT in this description - can be produced by 5 fractionation of a light synthetic FT hydrocarbon stream 10 in Distillation unit 1. The operation of this fractionation unit to the required product specification results in the group of products 11. A second group of HCCI fuels - named SR HT FT in this description - can be obtained 10 from a light synthetic FT hydrocarbon stream 10 which is first hydrogenated in hydrogenation unit 2 to saturate the olefinic double bonds and remove the oxygen from the oxygenate species. Then the hydrogenated products can be fractionated in fractionation unit 3 to the required specification, obtaining the group of products 13. 15 .A third group of HCCI fuels - named HX FT in this description - can be obtained from a heavy synthetic FT hydrocarbon stream 14 which is hydrocracked in hydrocracking unit 4 to result in lighter saturated hydrocarbon species. Then the hydrocracked products can be fractionated in fractionation unit 5 to the required specification, obtaining the group of products 16. 20 An alternative to produce a fourth group of HCCI fuels - named GTL (GTL = gas to liquid) in this description - can be produced by direct blending of the hydrotreated and hydrocracked products described above. This can be done in an optimised way by using a common fractionator unit 6 to the required specification, obtaining the group of 25 products 18. It is also possible to blend the products 11 and 16, either by sharing a common fractionator or after fractionation to also obtain synthetic HCCI fuels. 30 In all of these process options there is co-production of non-HCCI hydrocarbon stream, both lighter and heavier than the designed HCCI synthetic products. The former can be described as a light naphtha and the latter as a heavy diesel stream. These can be used in fuel and non-fuel applications.
WO 2005/059063 PCT/ZA2004/000157 10 All fuels in any of these four groups can be used as blends components for final HCCI fuels. Emissions Performance of the Synthetic FT HCCI Fuels 5 There is wide acceptance to the fact that the synthetic FT fuels produce less noxious emissions than conventional fuel. This point has been brought into the public domain several times - for example refer to "Processing of Fischer-Tropsch Syncrude and Benefits of Integrating its Products with Conventional Fueld' presented at the National 10 Petrochemical & Refiners Association Annual Meeting held in March 2000 in San Antonio, Texas - paper AM-00-51. This document makes reference to both FT naphthas and FT diesels. Typical Quality of Synthetic FT HCCI Fuels 15 Table 3 contains the typical quality of synthetic FT HCCI fuels produced as described and conforming to the selected requirements. Table 4 shows a comparison between HT SR FT fuel and crude derived fuel. 20 Table 3 Typical Quality of Synthetic FT HCCI Fuels SR FT HT SR FT Desired Range C7-C9 C-C14 C10-C14 C7-C9 C7-C4 CI Distillation Range 90-270 103- 103- 164- 90- 90- 165 Distillation Range 90-270 00 13 21 21C6 5 5 183 251 251 160 254 254 Density 0.65-0.78 kg/I 0.67 0.71 0.76 0.71 0.74 0.76 Composition * n-paraffins wt% 52.5 63.1 68.4 94.6 94.9 95.1 * i-paraffins wt% 0.4 1.6 2.2 5.4 5.1 4.9 * Olefins wt % 38.5 26.5 20.5 0 0 0 SOxygenates wt% 8.6 8.8 8.9 0 0 0 Ignition delay Ignition delay 2-7 ms 3.34 2.79 2.60 3.44 2.74 2.54 Cetane Number 30-70 60 75 83 58 77 86 Aromatics content <1.0 % wt % <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 Sulphur content < 1 ppm wt <1 <1 <1 <1 <1 <1 Oxygen content <5000 ppm 700 2000 2150 <80 <80 <80 (wt) WO 2005/059063 PCT/ZA2004/000157 11 __HX GTL Desired Range C-C9 C7-Cr14 C10- 7 9 14 C 0..14 7 14 Distillation Range 90-270 oC 80-163 80-250 135- 90-163 90-250 155 250 250 Density 0.65-0.78 kg/ 0.68 0.72 0.74 0.69 0.72 0.75 Composition ,._ * n-paraffins wt % 46.0 30.7 26.6 57.5 41.0 38.0 * i-paraffins wt % 54.0 69.3 73.4 42.5 59.0 62.0 * Olefins wt% 0 0 0 0 0 0 * Oxygenates wt% 0 0 0 0 0 0 Ignition delay 2-7 ms 4.92 4.06 3.50 4.55 3.34 3.08 (QT7rm) Cetane Number 30-70 41 49 57 44 60 66 Aromatics content <1.0% wt % <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 Sulphur content <1 ppm wt <1 <1 <1 <1 <1 <1 Oxygen content <5000 ppm <80 <80 <80 <80 <80 <80 (wt) WO 2005/059063 PCT/ZA2004/000157 12 Table 4 Comparison between equivalent synthetic FT Fuel for HCCI Fuels and Crude Derived Fuels HT SR FT Crude Derived Fuels Desired Range C7-C9 C7- 0C- C7-C9 07-014 C10-C14 0414 04 Distillation Range 90-270 0C 90- 90- 165- 80-159 80-257 151-257 160 254 245 Density 0.65-0.78 kg/I 0.71 0.74 0.76 0.7329 0.7715 0.7961 Composition ,,, * n-paraffins wt% 94.6 94.9 95.1 28.2 23.8 24.7 Si-paraffins wt% 5.4 5.1 4.9 32.8 53.0 55.3 * Olefins wt % 0 0 0 0.4 0.4 0.5 * Oxygenates wt% 0 0 0 0 0 0 * Aromatics wt% 0 0 0 10.3 14.2 18 W Naphthenes wt% 0 0 0 28.3 8.6 1.5 Ignition delay 2-7 ms 3.44 2.74 2.54 6.17 5.22 4.79 (IQ-i-M) 27m Cetane Number 30-70, 58 77 86 34.1 39.0 42.0 Sulphur content < 1 ppm wt <1 <1 <1 50 50 50 5 Table 5 below presents an example of the quality characteristics of blends of the C7 C9 GTL HCCI fuel with an equivalent Petroleum fraction. The benefits of including synthetic FT fuel in conventional blends are quite evident. 10 Table 5 Quality of blends of the C7-C9 GTL HCCI fuel with an equivalent Petroleum fraction GTL Fuel Content 0% 25% 50% 75% 100% Density kg/ 0.733 0.722 0.711 0.700 0.690 Composition n-paraffins wt % 28.2 35.4 42.8 50.1 57.5 i-paraffins wt % 32.8 35.1 37.6 40.0 42.5 Olefins wt % 0.4 0.3 0.2 0.1 0.0 Oxygenates wt % 0.0 0.0 0.0 0.0 0.0 Aromatics wt % 10.3 7.8 5.2 2.6 0.0 Naphthenes wt % 28.3 21.3 14.2 7.1 0.0 Total wt % 100.0 99.9 100.0 99.9 100.0 Ignition delay (IQT T M ) ms 6.17 5.75 5.22 4.75 4.55 Cetane Number 34.1 36.0 39.1 41.9 44.0 Sulphur content ppm 50 38 25 13 <1 15
Claims (22)
1. A HCCI fuel or fuel component, which fuel includes at least n-paraffins and iso paraffins having from 7 to 14 carbon atoms, and which fuel has an ignition delay of 5 less than 7 ms, according to ASTM D6890.
2. A fuel as claimed in claim 1, which fuel contains less than 1% wt of aromatic and negligible levels of sulphur. 10
3. A fuel as claimed in any one of the preceding claims, which fuel has an ignition delay of less than 5 ms.
4. A fuel as claimed in any one of the preceding claims, which fuel has an ignition delay of between 2 and 5 ms. 15
5. A fuel as claimed in any one of the preceding claims, wherein the mass %/o of the n-paraffins exceeds that of any other single component in the fuel.
6. A fuel as claimed in any one of the preceding claims, wherein the mass % of 20 the n-paraffins is in excess of 25% by mass of the fuel
7. A fuel as claimed in any one of the preceding claims, wherein the mass % of the n-paraffins is in excess of 50% by mass of the fuel. 25
8. A fuel as claimed in any one of the preceding claims, wherein the mass % of the n-paraffins is in excess of 80% by mass of the fuel.
9. A fuel as claimed in any one of the preceding claims, wherein the mass % of the n-paraffins is in the order of 95% by mass of the fuel. 30
10. A fuel as claimed in any one of the preceding claims, wherein the n-paraffins are Fischer-Tropsch (FT) reaction derived n-paraffins. WO 2005/059063 PCT/ZA2004/000157 14
11. A fuel as claimed in any one of the preceding claims, wherein the iso-paraffins are FT reaction derived iso-paraffins.
12. A fuel as claimed in any one of the preceding claims, which fuel includes one or 5 more of: olefins, lubricity improver, and oxygenates.
13. A fuel as claimed in any one of claims 1 to 11, which fuel is substantially free of heteroatoms such as nitrogen, sulphur and oxygen! 10
14. A fuel as claimed in any one of the preceding claims, which fuel has an ASTM D86 distillation range from 90 0 C to 270oC.
15. Use of an HCCI fuel or fuel component as claimed in any one of claims 1 to 14 as a blending component with conventional fuel. 15
16. A process for preparing a HCCI fuel or fuel component, which fuel or fuel component includes at least n-paraffins and iso-paraffins, which fuel has an ignition delay of less than 7 ms, said process including one or more steps selected from: a) hydrotreating at least a Condensate fraction of a Fischer-Tropsch (FT) 20 synthesis reaction product, or a derivative thereof; b) hydroconverting a Wax fraction of the FT synthesis product or a derivative thereof; c) fractionating in a single unit or in separate units, one or more of the hydrotreated Condensate fractions of step a) and the hydroconverted fraction 25 of step b) to obtain the desired HCCI fuel or fuel component; and d) optionally, blending two or more of said components from step c) in a desired ratio to obtain the desired HCCI fuel.
17. A process as claimed in claim 16, wherein the hydroconversion is by way of 30 hydrocracking. WO 2005/059063 PCT/ZA2004/000157 15
18. A process as claimed in claim 16 or claim 17, wherein the blending of step d) is the blending of FT condensate derivative and hydroconverted FT wax derivative in a blending ratio of from 1:99 to 99:1 by volume. 5
19. A process as claimed in any one of claims 16 to 18, wherein the fuel produced by the process is a fuel as claimed in any one of claims 1 to 14.
20. A HCCI fuel or fuel component as claimed in claim 1, substantially as herein 10 described and illustrated.
21. A process as claimed in claim 16, substantially as herein described and illustrated. 15
22. A new HCCI fuel or fuel component, or a new process substantially as herein described.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53142803P | 2003-12-19 | 2003-12-19 | |
ZA2003/9849 | 2003-12-19 | ||
US60/531,428 | 2003-12-19 | ||
ZA200309849 | 2003-12-19 | ||
PCT/ZA2004/000157 WO2005059063A1 (en) | 2003-12-19 | 2004-12-17 | Fuel for homogeneous charge compression ignition (hcci) systems and a process for production of said fuel |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2004298630A1 true AU2004298630A1 (en) | 2005-06-30 |
AU2004298630B2 AU2004298630B2 (en) | 2010-06-03 |
Family
ID=34704302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2004298630A Ceased AU2004298630B2 (en) | 2003-12-19 | 2004-12-17 | Fuel for homogeneous charge compression ignition (HCCI) systems and a process for production of said fuel |
Country Status (9)
Country | Link |
---|---|
US (1) | US20090025279A1 (en) |
JP (1) | JP2007517094A (en) |
AU (1) | AU2004298630B2 (en) |
BR (1) | BRPI0417299A (en) |
CA (1) | CA2549927A1 (en) |
DE (1) | DE112004002457T5 (en) |
GB (1) | GB2423996B (en) |
WO (1) | WO2005059063A1 (en) |
ZA (1) | ZA200604993B (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007514013A (en) * | 2004-05-14 | 2007-05-31 | エクソンモービル・リサーチ・アンド・エンジニアリング・カンパニー | Method for limiting exhaust concentration from a direct injection premixed compression self-ignition engine |
JP4815178B2 (en) * | 2005-09-27 | 2011-11-16 | Jx日鉱日石エネルギー株式会社 | Fuel for premixed compression self-ignition engines |
WO2007114025A1 (en) | 2006-03-31 | 2007-10-11 | Nippon Oil Corporation | Gas oil composition |
KR101437700B1 (en) * | 2006-03-31 | 2014-09-03 | 제이엑스 닛코닛세키에너지주식회사 | Gas oil composition |
EP2006365B1 (en) * | 2006-03-31 | 2018-02-21 | Nippon Oil Corporation | Use of a polyfunctional hydrocarbon oil composition |
US7487663B2 (en) | 2006-04-20 | 2009-02-10 | Exxonmobil Research & Engineering Co. | Method for selecting fuel to both optimize the operating range and minimize the exhaust emissions of HCCI engines |
EP2077312A1 (en) * | 2007-12-17 | 2009-07-08 | Nippon Oil Corporation | Fuels for homogeneous charge compression ignition combustion engine |
JP5188796B2 (en) * | 2007-12-18 | 2013-04-24 | Jx日鉱日石エネルギー株式会社 | Fuel oil composition for premixed compression ignition engine and method for producing the same |
CN105441142B (en) * | 2010-06-21 | 2017-09-15 | 周向进 | A kind of gasoline products of clean and effective environmental protection |
US9688928B2 (en) | 2013-12-11 | 2017-06-27 | Phillips 66 Company | Processes for making homogeneous charge compression ignition engine fuel blends |
US10246657B2 (en) | 2013-12-11 | 2019-04-02 | Phillips 66 Company | Fuel blends for homogeneous charge compression ignition engines |
EP3080414B1 (en) | 2013-12-11 | 2020-11-04 | Phillips 66 Company | Homogeneous charge compression ignition engine fuels and process for making these fuels |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2322755T3 (en) * | 1999-04-06 | 2009-06-26 | Sasol Technology (Proprietary) Limited | SYNTHETIC NAFTA FUEL. |
US20020020107A1 (en) * | 1999-07-02 | 2002-02-21 | Bailey Brent K. | Low molecular weight compression ignition fuel |
ATE376044T1 (en) * | 2001-09-18 | 2007-11-15 | Southwest Res Inst | FUELS FOR HOMOGENEOUSLY CHARGED COMPRESSION IGNITION MACHINES |
EP1371715A1 (en) * | 2002-06-13 | 2003-12-17 | Shell Internationale Researchmaatschappij B.V. | Fuel compositions |
FR2849052B1 (en) * | 2002-12-19 | 2009-05-01 | Inst Francais Du Petrole | METHOD FOR PRODUCING FUEL FORMULATIONS FOR OPTIMUM OPERATION OF AN ENGINE DEVELOPED FOR THE HCCI COMBUSTION MODE |
-
2004
- 2004-12-17 BR BRPI0417299-0A patent/BRPI0417299A/en not_active IP Right Cessation
- 2004-12-17 GB GB0611828A patent/GB2423996B/en not_active Expired - Fee Related
- 2004-12-17 JP JP2006545624A patent/JP2007517094A/en active Pending
- 2004-12-17 CA CA002549927A patent/CA2549927A1/en not_active Abandoned
- 2004-12-17 US US10/583,391 patent/US20090025279A1/en not_active Abandoned
- 2004-12-17 WO PCT/ZA2004/000157 patent/WO2005059063A1/en active Application Filing
- 2004-12-17 AU AU2004298630A patent/AU2004298630B2/en not_active Ceased
- 2004-12-17 DE DE112004002457T patent/DE112004002457T5/en not_active Ceased
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2006
- 2006-06-19 ZA ZA2006/04993A patent/ZA200604993B/en unknown
Also Published As
Publication number | Publication date |
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BRPI0417299A (en) | 2007-03-13 |
GB2423996A (en) | 2006-09-13 |
GB2423996B (en) | 2008-07-16 |
AU2004298630B2 (en) | 2010-06-03 |
US20090025279A1 (en) | 2009-01-29 |
GB0611828D0 (en) | 2006-07-26 |
WO2005059063A1 (en) | 2005-06-30 |
DE112004002457T5 (en) | 2006-12-21 |
JP2007517094A (en) | 2007-06-28 |
ZA200604993B (en) | 2008-01-08 |
CA2549927A1 (en) | 2005-06-30 |
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