US20200339898A1 - A method for reducing particulate emissions - Google Patents
A method for reducing particulate emissions Download PDFInfo
- Publication number
- US20200339898A1 US20200339898A1 US16/960,846 US201916960846A US2020339898A1 US 20200339898 A1 US20200339898 A1 US 20200339898A1 US 201916960846 A US201916960846 A US 201916960846A US 2020339898 A1 US2020339898 A1 US 2020339898A1
- Authority
- US
- United States
- Prior art keywords
- base fuel
- aromatics
- particulate emissions
- gasoline composition
- fuel
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 24
- 239000000446 fuel Substances 0.000 claims abstract description 71
- 239000000203 mixture Substances 0.000 claims abstract description 43
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 23
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 23
- 238000002347 injection Methods 0.000 claims abstract description 20
- 239000007924 injection Substances 0.000 claims abstract description 20
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 19
- 238000009835 boiling Methods 0.000 claims abstract description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
- 150000001336 alkenes Chemical class 0.000 claims description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 6
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims description 3
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 235000006708 antioxidants Nutrition 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- -1 ethyl tert.butyl ether Chemical compound 0.000 description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000013618 particulate matter Substances 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ZISSAWUMDACLOM-UHFFFAOYSA-N triptane Chemical compound CC(C)C(C)(C)C ZISSAWUMDACLOM-UHFFFAOYSA-N 0.000 description 2
- LAAVYEUJEMRIGF-UHFFFAOYSA-N 2,4,4-trimethylpent-2-ene Chemical compound CC(C)=CC(C)(C)C LAAVYEUJEMRIGF-UHFFFAOYSA-N 0.000 description 1
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical class CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 1
- DFVOXRAAHOJJBN-UHFFFAOYSA-N 6-methylhept-1-ene Chemical class CC(C)CCCC=C DFVOXRAAHOJJBN-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- FDPIMTJIUBPUKL-UHFFFAOYSA-N dimethylacetone Natural products CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012847 fine chemical Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical class [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000013638 trimer 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
- C10L1/06—Liquid carbonaceous fuels essentially based on blends of hydrocarbons for spark 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
- C10L1/023—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark 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
-
- 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
- C10L2200/00—Components of fuel compositions
- C10L2200/04—Organic compounds
- C10L2200/0407—Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
- C10L2200/0415—Light distillates, e.g. LPG, naphtha
- C10L2200/0423—Gasoline
-
- 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
- C10L2270/00—Specifically adapted fuels
- C10L2270/02—Specifically adapted fuels for internal combustion engines
- C10L2270/023—Specifically adapted fuels for internal combustion engines for gasoline engines
Definitions
- This invention relates to a method for reducing particulate emissions from a direct injection spark-ignition engine.
- WO2004/113476 discloses gasoline compositions meeting certain parameters whose use as a fuel in a spark ignition engine results in improved stability of engine crank case lubricant. However, there is no mention in this document of the use of such a fuel for providing reduced particulate emissions in a direct-injection spark ignition engine.
- a method for reducing particulate emissions from a direct injection spark-ignition engine comprising fuelling the engine with a gasoline composition, wherein the gasoline composition comprises a hydrocarbon base fuel comprising not greater than 5% v aromatics of at least 9 carbon atoms, based on the base fuel, a T90 of up to 150° C. and a final boiling point not greater than 190° C.
- gasoline composition for reducing particulate emissions from a direct injection spark-ignition engine
- gasoline composition comprises a hydrocarbon base fuel comprising not greater than 5% v aromatics of at least 9 carbon atoms, based on the base fuel, a T90 of less than 150° C. and a final boiling point not greater than 190° C.
- Low C9+ aromatics content together with a T90 of less than 150° C. and a final boiling point of not greater than 190° C. are believed to be key parameters in achieving reduced particulate emissions from a direct-injection spark ignition internal combustion engines fuelled by gasoline compositions of the present invention.
- the hydrocarbon base fuel contains amounts of aromatics having 9 carbon atoms or more, respectively in the range 0 to 5% v, based on the base fuel.
- the uses and methods of the present invention may be used to achieve any degree of reduction in particulate emissions from a direct-injection spark ignition engine, including reduction to zero (i.e. eliminating particulate emissions). It may be used for the purpose of achieving a desired target level of particulate emissions.
- the method and use herein preferably achieves a 5% reduction or more in particulate emissions from a direct injection spark ignition engine, more preferably a 10% reduction or more in particulate emissions from a direct injection spark ignition engine, even more preferably a 15% reduction or more in particulate emissions from a direct injection spark ignition engine, and especially a 30% reduction or more in from a direct injection spark ignition engine, compared with the use of a gasoline fuel composition having a final boiling point of greater than 190° C., a T90 of 150° C. or more and comprising greater than 5v % of aromatics having 9 carbon atoms or more.
- Any suitable method for measuring particulate emissions from direct injection spark ignition engines can be used herein.
- An example of a suitable method for measuring particulate emissions can be found in the following SAE paper: SAE 2010-01-2115 published 25th October 2010 which measures the reduction of particulate emissions by a decrease in PM index of the gasoline composition.
- Gasoline compositions suitable for use in the present invention preferably have a PM index as measured according to the test method disclosed in SAE 2010-01-2115 of 1.0 or less, more preferably 0.95 or less, even more preferably 0.9 or less.
- Gasolines contain mixtures of hydrocarbons, the optimal boiling ranges and distillation curves thereof varying according to climate and season of the year.
- the hydrocarbons in a gasoline as defined above may conveniently be derived in known manner from straight-run gasoline, synthetically-produced aromatic hydrocarbon mixtures, thermally or catalytically cracked hydrocarbons, hydrocracked petroleum fractions or catalytically reformed hydrocarbons and mixtures of these.
- Oxygenates both fossil- or bio-sourced
- MTBE methyl tert.butyl ether
- ETBE ethyl tert.butyl ether
- preferred gasoline compositions of the present invention contain 0 to 10% by volume of at least one oxygenate selected from methanol, ethanol, isopropanol and isobutanol.
- gasoline compositions of the present invention contain up to 10% by volume of ethanol, preferably 2 to 10% v, more preferably 4 to 10% v, e.g. 5 to 10% v ethanol.
- DEC diethyl carbonate
- esters such as ethyl acetate and ketone such as methyl ethyl ketone.
- Oxygenates can help to reduce PN emissions through chemical means.
- Gasoline compositions according to the present invention are advantageously lead-free (unleaded), and this may be required by law. Where permitted, lead-free anti-knock compounds and/or valve-seat recession protectant compounds (e.g. known potassium salts, sodium salts or phosphorus compounds) may be present.
- lead-free anti-knock compounds and/or valve-seat recession protectant compounds e.g. known potassium salts, sodium salts or phosphorus compounds
- the octane level can be defined by RON, MON or the anti-knock index (Aki) ((RON+MON)/2). If RON is specified, it will generally be greater than 92. If anti-knock index is specified it will generally be above 85.
- Modern gasolines are inherently low-sulphur fuels, e.g. containing less than 200 ppmw sulphur, preferably not greater than 50 ppmw sulphur.
- Hydrocarbon base fuels as defined above may conveniently be prepared in known manner by blending suitable hydrocarbon, e.g. refinery, streams in order to meet the defined parameters, as will readily be understood by those skilled in the art.
- Olefin content may be boosted by inclusion of olefin-rich refinery streams and/or by addition of synthetic components such as diisobutylene, in any relative proportions.
- Diisobutylene also known as 2,4,4-trimethyl-1-pentene (Sigma-Aldrich Fine Chemicals)
- 2,4,4-trimethyl-1-pentene is typically a mixture of isomers (2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene) prepared by heating the sulphuric acid extract of isobutylene from a butene isomer separation process to about 90° C.
- yield is typically 90%, of a mixture of 80% dimers and 20% trimers.
- Gasoline compositions as defined above may variously include one or more additives such as anti-oxidants, corrosion inhibitors, ashless detergents, dehazers, dyes, lubricity improvers and synthetic or mineral oil carrier fluids.
- additives such as anti-oxidants, corrosion inhibitors, ashless detergents, dehazers, dyes, lubricity improvers and synthetic or mineral oil carrier fluids. Examples of suitable such additives are described generally in U.S. Pat. No. 5,855,629 and DE-A-19955651.
- Additive components can be added separately to the gasoline or can be blended with one or more diluents, forming an additive concentrate, and together added to base fuel.
- a preferred gasoline composition for use in the method of the present invention comprises one or more antioxidants in order to improve the oxidative stability of the gasoline composition.
- Any antioxidant additive which is suitable for use in a gasoline composition can be used herein.
- a preferred anti-oxidant for use herein is a hindered phenol, for example BHT (butylated hydroxy toluene). It is preferred that the gasoline composition comprises from 10 ppmw to 100 ppmw of antioxidant.
- Non-oxygenated high octane components that can be bio-sourced and which suitable for use herein include iso-butylenes or iso-octenes, iso-octane, triptane and iso-pentenes. These non-oxygenated high octane compounds help to reduce PN emissions through ignition and combustion optimization.
- Preferred gasoline compositions used in the method of the present invention have one or more of the following features:—
- the hydrocarbon base fuel contains at least 10% v olefins, (ii) the hydrocarbon base fuel contains at least 12% v olefins, (iii) the hydrocarbon base fuel contains at least 13% v olefins, (iv) the hydrocarbon base fuel contains up to 20% v olefins, (v) the hydrocarbon base fuel contains up to 18% v olefins, (vi) the base fuel has initial boiling point (IBP) of at least 28° C., (vii) the base fuel has IBP of at least 30° C., (viii) the base fuel has IBP up to 42° C., (ix) the base fuel has IBP up to 40° C., (x) the base fuel has T 10 of at least 42° C., (xi) the base fuel has T 10 of at least 45° C., (xii) the base fuel has T 10 of at least 46° C., (xiii) the base fuel has T 10 up to 58°
- Examples of preferred combinations of the above features include (i) and (iv); (ii) and (v); (iii) and (v); (vi), (viii), (x), (xii), (xvi), (xix), (xxii), (xxv) and (xxix); (vii), (ix), (xi), (xiv), (xvii), (xx), (xxiii), (x ⁇ v) and (x ⁇ x); and (vii), (ix), (xii), (xv), (xviii), (xxi), (xxiv), (xxvii), (xxxiii) and (xxxiv).
- Use of the gasoline composition described herein can give one of a number of benefits in addition to reducing particulate emissions in a direct injection spark-ignition engine. These benefits include reduced frequency of oil changes, reduced engine wear, e.g. engine bearing wear, engine component wear (e.g. camshaft and piston crank wear), improved acceleration performance, higher maximum power output, and/or improved fuel economy.
- engine wear e.g. engine bearing wear
- engine component wear e.g. camshaft and piston crank wear
- improved acceleration performance e.g. camshaft and piston crank wear
- higher maximum power output e.g. camshaft and piston crank wear
- particulate matter emissions tests on gasoline compositions in direct injection spark ignition engines fuelled by test fuels were effected using the following procedure.
- Example 1 contains 0% v heavy aromatics
- Example 2 contains 4% v heavy aromatics
- Example 3 contains 8% v heavy aromatics
- Example 4 contains 12% v heavy aromatics.
- the gasoline compositions having a hydrocarbon base fuel comprising not greater than 5% v aromatics of at least 9 carbon atoms, based on the base fuel, a T90 of less than 150° C. and a final boiling point not greater than 190° C. provide a greater reduction in particulate emissions (as measured by a decrease in PM index).
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)
- Liquid Carbonaceous Fuels (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16/960,846 US20200339898A1 (en) | 2018-01-10 | 2019-01-08 | A method for reducing particulate emissions |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862615459P | 2018-01-10 | 2018-01-10 | |
US16/960,846 US20200339898A1 (en) | 2018-01-10 | 2019-01-08 | A method for reducing particulate emissions |
PCT/EP2019/050308 WO2019137896A1 (en) | 2018-01-10 | 2019-01-08 | A method for reducing particulate emissions |
Publications (1)
Publication Number | Publication Date |
---|---|
US20200339898A1 true US20200339898A1 (en) | 2020-10-29 |
Family
ID=65031033
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/960,846 Abandoned US20200339898A1 (en) | 2018-01-10 | 2019-01-08 | A method for reducing particulate emissions |
Country Status (9)
Country | Link |
---|---|
US (1) | US20200339898A1 (ru) |
EP (1) | EP3737735A1 (ru) |
JP (1) | JP2021510389A (ru) |
CN (1) | CN111556890A (ru) |
MX (1) | MX2020007002A (ru) |
PH (1) | PH12020500585A1 (ru) |
RU (1) | RU2020126101A (ru) |
WO (1) | WO2019137896A1 (ru) |
ZA (1) | ZA202003666B (ru) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20220356409A1 (en) * | 2019-04-01 | 2022-11-10 | Shell Oil Company | Method for reducing low speed pre-ignition |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5288393A (en) * | 1990-12-13 | 1994-02-22 | Union Oil Company Of California | Gasoline fuel |
EP0905217A1 (en) * | 1997-09-30 | 1999-03-31 | Nippon Oil Co. Ltd. | Unleaded gasoline for direct injection gasoline engine |
WO2000077130A1 (en) * | 1999-06-11 | 2000-12-21 | Bp Oil International Limited | Fuel composition |
US20050279018A1 (en) * | 2003-06-18 | 2005-12-22 | Cracknell Roger F | Gasoline composition |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW477784B (en) | 1996-04-26 | 2002-03-01 | Shell Int Research | Alkoxy acetic acid derivatives |
GB9922553D0 (en) * | 1999-09-23 | 1999-11-24 | Bp Oil Int | Fuel compositions |
DE19955651A1 (de) | 1999-11-19 | 2001-05-23 | Basf Ag | Verwendung von Festsäuresalzen von alkoxylierten Oligoaminen als Schmierfähigkeitsverbesserer für Mineralölprodukte |
US7052597B2 (en) * | 2001-03-27 | 2006-05-30 | Exxonmobil Research And Engineering Company | Tuning fuel composition for driving cycle conditions in spark ignition engines |
US20030094397A1 (en) * | 2001-08-15 | 2003-05-22 | Fortum Oyj | Clean-burning MTBE-free gasoline fuel |
JP2005054102A (ja) * | 2003-08-06 | 2005-03-03 | Nippon Oil Corp | ガソリン |
JP4938333B2 (ja) * | 2006-03-31 | 2012-05-23 | 出光興産株式会社 | ガソリン組成物 |
JP4938334B2 (ja) * | 2006-03-31 | 2012-05-23 | 出光興産株式会社 | ガソリン組成物 |
-
2019
- 2019-01-08 US US16/960,846 patent/US20200339898A1/en not_active Abandoned
- 2019-01-08 JP JP2020537760A patent/JP2021510389A/ja active Pending
- 2019-01-08 RU RU2020126101A patent/RU2020126101A/ru unknown
- 2019-01-08 CN CN201980007521.0A patent/CN111556890A/zh active Pending
- 2019-01-08 MX MX2020007002A patent/MX2020007002A/es unknown
- 2019-01-08 EP EP19700644.8A patent/EP3737735A1/en active Pending
- 2019-01-08 WO PCT/EP2019/050308 patent/WO2019137896A1/en unknown
-
2020
- 2020-06-18 ZA ZA2020/03666A patent/ZA202003666B/en unknown
- 2020-07-08 PH PH12020500585A patent/PH12020500585A1/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5288393A (en) * | 1990-12-13 | 1994-02-22 | Union Oil Company Of California | Gasoline fuel |
EP0905217A1 (en) * | 1997-09-30 | 1999-03-31 | Nippon Oil Co. Ltd. | Unleaded gasoline for direct injection gasoline engine |
WO2000077130A1 (en) * | 1999-06-11 | 2000-12-21 | Bp Oil International Limited | Fuel composition |
US20050279018A1 (en) * | 2003-06-18 | 2005-12-22 | Cracknell Roger F | Gasoline composition |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US20220356409A1 (en) * | 2019-04-01 | 2022-11-10 | Shell Oil Company | Method for reducing low speed pre-ignition |
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PH12020500585A1 (en) | 2021-06-14 |
RU2020126101A (ru) | 2022-02-10 |
JP2021510389A (ja) | 2021-04-22 |
EP3737735A1 (en) | 2020-11-18 |
MX2020007002A (es) | 2020-09-07 |
WO2019137896A1 (en) | 2019-07-18 |
ZA202003666B (en) | 2022-06-29 |
CN111556890A (zh) | 2020-08-18 |
BR112020013412A2 (pt) | 2020-12-01 |
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