EP1252268B1 - Verfahren zur verringerung des dampfdruckes von ethanolhaltigen motortreibstoffen für funkengezündete verbrennungsmotoren - Google Patents
Verfahren zur verringerung des dampfdruckes von ethanolhaltigen motortreibstoffen für funkengezündete verbrennungsmotoren Download PDFInfo
- Publication number
- EP1252268B1 EP1252268B1 EP01942659A EP01942659A EP1252268B1 EP 1252268 B1 EP1252268 B1 EP 1252268B1 EP 01942659 A EP01942659 A EP 01942659A EP 01942659 A EP01942659 A EP 01942659A EP 1252268 B1 EP1252268 B1 EP 1252268B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- ethanol
- volume
- dvpe
- gasoline
- kpa
- 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.)
- Expired - Lifetime
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 679
- 239000000446 fuel Substances 0.000 title claims abstract description 249
- 238000000034 method Methods 0.000 title claims abstract description 32
- 238000002485 combustion reaction Methods 0.000 title claims abstract description 22
- 239000000203 mixture Substances 0.000 claims abstract description 248
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 119
- 239000001301 oxygen Substances 0.000 claims abstract description 81
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 81
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 80
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 75
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- -1 C12 hydrocarbon Chemical class 0.000 claims abstract description 15
- 150000002576 ketones Chemical class 0.000 claims abstract description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims abstract description 6
- AOWPVIWVMWUSBD-RNFRBKRXSA-N [(3r)-3-hydroxybutyl] (3r)-3-hydroxybutanoate Chemical compound C[C@@H](O)CCOC(=O)C[C@@H](C)O AOWPVIWVMWUSBD-RNFRBKRXSA-N 0.000 claims abstract description 3
- 239000003502 gasoline Substances 0.000 claims description 224
- 150000002430 hydrocarbons Chemical class 0.000 claims description 82
- 238000009835 boiling Methods 0.000 claims description 81
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 79
- 239000007789 gas Substances 0.000 claims description 31
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 21
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 claims description 17
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 claims description 16
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 12
- 238000001704 evaporation Methods 0.000 claims description 12
- 230000008020 evaporation Effects 0.000 claims description 12
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 10
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims description 10
- SGVYKUFIHHTIFL-UHFFFAOYSA-N 2-methylnonane Chemical compound CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 claims description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 239000008096 xylene Substances 0.000 claims description 7
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000005864 Sulphur Substances 0.000 claims description 6
- ZUBZATZOEPUUQF-UHFFFAOYSA-N isononane Chemical compound CCCCCCC(C)C ZUBZATZOEPUUQF-UHFFFAOYSA-N 0.000 claims description 6
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 claims description 6
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-methyltetrahydrofuran Chemical compound CC1CCCO1 JWUJQDFVADABEY-UHFFFAOYSA-N 0.000 claims description 5
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 235000001510 limonene Nutrition 0.000 claims description 5
- 229940087305 limonene Drugs 0.000 claims description 5
- 238000012545 processing Methods 0.000 claims description 5
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 claims description 5
- GQVMHMFBVWSSPF-SOYUKNQTSA-N (4E,6E)-2,6-dimethylocta-2,4,6-triene Chemical compound C\C=C(/C)\C=C\C=C(C)C GQVMHMFBVWSSPF-SOYUKNQTSA-N 0.000 claims description 4
- AXHVNJGQOJFMHT-UHFFFAOYSA-N 1-tert-butyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C(C)(C)C AXHVNJGQOJFMHT-UHFFFAOYSA-N 0.000 claims description 4
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 238000004821 distillation Methods 0.000 claims description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 4
- 238000003786 synthesis reaction Methods 0.000 claims description 4
- RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 claims description 3
- GDEQPEBFOWYWSA-UHFFFAOYSA-N 1,2-dimethyl-3-propan-2-ylbenzene Chemical group CC(C)C1=CC=CC(C)=C1C GDEQPEBFOWYWSA-UHFFFAOYSA-N 0.000 claims description 3
- QRBAXYYNPFDZAX-UHFFFAOYSA-N 1-tert-butyl-2,3-dimethylbenzene Chemical group CC1=CC=CC(C(C)(C)C)=C1C QRBAXYYNPFDZAX-UHFFFAOYSA-N 0.000 claims description 3
- DFVOXRAAHOJJBN-UHFFFAOYSA-N 6-methylhept-1-ene Chemical compound CC(C)CCCC=C DFVOXRAAHOJJBN-UHFFFAOYSA-N 0.000 claims description 3
- UAEPNZWRGJTJPN-UHFFFAOYSA-N Methylcyclohexane Natural products CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims description 3
- 239000011347 resin Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- XTVMZZBLCLWBPM-UHFFFAOYSA-N tert-butylcyclohexane Chemical compound CC(C)(C)C1CCCCC1 XTVMZZBLCLWBPM-UHFFFAOYSA-N 0.000 claims description 3
- CDLDJGNSVFBIAG-UHFFFAOYSA-N 2,2,3,3-tetramethyloxolane Chemical compound CC1(C)CCOC1(C)C CDLDJGNSVFBIAG-UHFFFAOYSA-N 0.000 claims description 2
- YBDQLHBVNXARAU-UHFFFAOYSA-N 2-methyloxane Chemical compound CC1CCCCO1 YBDQLHBVNXARAU-UHFFFAOYSA-N 0.000 claims description 2
- AAQDYYFAFXGBFZ-UHFFFAOYSA-N Tetrahydrofurfuryl acetate Chemical compound CC(=O)OCC1CCCO1 AAQDYYFAFXGBFZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 claims description 2
- 239000002802 bituminous coal Substances 0.000 claims description 2
- 238000003763 carbonization Methods 0.000 claims description 2
- 150000001983 dialkylethers Chemical class 0.000 claims description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 claims description 2
- 239000003345 natural gas Substances 0.000 claims description 2
- 238000005504 petroleum refining Methods 0.000 claims description 2
- 238000011084 recovery Methods 0.000 claims description 2
- 239000000654 additive Substances 0.000 abstract description 80
- 230000000996 additive effect Effects 0.000 abstract description 57
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 8
- 150000002148 esters Chemical class 0.000 abstract description 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 124
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 103
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 39
- 238000009472 formulation Methods 0.000 description 33
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 29
- 239000003208 petroleum Substances 0.000 description 24
- 229940035429 isobutyl alcohol Drugs 0.000 description 22
- 229910002092 carbon dioxide Inorganic materials 0.000 description 21
- 238000012360 testing method Methods 0.000 description 21
- XCYJPXQACVEIOS-UHFFFAOYSA-N 1-isopropyl-3-methylbenzene Chemical compound CC(C)C1=CC=CC(C)=C1 XCYJPXQACVEIOS-UHFFFAOYSA-N 0.000 description 20
- 230000033228 biological regulation Effects 0.000 description 13
- 238000002156 mixing Methods 0.000 description 13
- 229920006395 saturated elastomer Polymers 0.000 description 12
- 125000001931 aliphatic group Chemical group 0.000 description 11
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 10
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 10
- 230000007423 decrease Effects 0.000 description 9
- 125000002723 alicyclic group Chemical group 0.000 description 8
- 150000002170 ethers Chemical class 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 6
- 239000002816 fuel additive Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- 239000011593 sulfur Substances 0.000 description 6
- 231100000331 toxic Toxicity 0.000 description 6
- 230000002588 toxic effect Effects 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 5
- 150000004996 alkyl benzenes Chemical class 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000001569 carbon dioxide Substances 0.000 description 5
- 239000006184 cosolvent Substances 0.000 description 5
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 5
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 5
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000010779 crude oil Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 description 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 4
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 4
- 238000007655 standard test method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 4
- NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- 239000002028 Biomass Substances 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 description 3
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 3
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 2
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 2
- RQUBQBFVDOLUKC-UHFFFAOYSA-N 1-ethoxy-2-methylpropane Chemical compound CCOCC(C)C RQUBQBFVDOLUKC-UHFFFAOYSA-N 0.000 description 2
- GFAZHVHNLUBROE-UHFFFAOYSA-N 1-hydroxybutan-2-one Chemical compound CCC(=O)CO GFAZHVHNLUBROE-UHFFFAOYSA-N 0.000 description 2
- ZQAYBCWERYRAMF-UHFFFAOYSA-N 1-methoxy-3-methylbutane Chemical compound COCCC(C)C ZQAYBCWERYRAMF-UHFFFAOYSA-N 0.000 description 2
- OXMIDRBAFOEOQT-UHFFFAOYSA-N 2,5-dimethyloxolane Chemical compound CC1CCC(C)O1 OXMIDRBAFOEOQT-UHFFFAOYSA-N 0.000 description 2
- RXGUIWHIADMCFC-UHFFFAOYSA-N 2-Methylpropyl 2-methylpropionate Chemical compound CC(C)COC(=O)C(C)C RXGUIWHIADMCFC-UHFFFAOYSA-N 0.000 description 2
- FZXRXKLUIMKDEL-UHFFFAOYSA-N 2-Methylpropyl propanoate Chemical compound CCC(=O)OCC(C)C FZXRXKLUIMKDEL-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 description 2
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 2
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 2
- POSWICCRDBKBMH-UHFFFAOYSA-N 3,3,5-trimethylcyclohexan-1-one Chemical compound CC1CC(=O)CC(C)(C)C1 POSWICCRDBKBMH-UHFFFAOYSA-N 0.000 description 2
- MQWCXKGKQLNYQG-UHFFFAOYSA-N 4-methylcyclohexan-1-ol Chemical compound CC1CCC(O)CC1 MQWCXKGKQLNYQG-UHFFFAOYSA-N 0.000 description 2
- ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 2
- KDUIUFJBNGTBMD-VXMYFEMYSA-N cyclooctatetraene Chemical compound C1=C\C=C/C=C\C=C1 KDUIUFJBNGTBMD-VXMYFEMYSA-N 0.000 description 2
- AQEFLFZSWDEAIP-UHFFFAOYSA-N di-tert-butyl ether Chemical class CC(C)(C)OC(C)(C)C AQEFLFZSWDEAIP-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- MLFHJEHSLIIPHL-UHFFFAOYSA-N isoamyl acetate Chemical compound CC(C)CCOC(C)=O MLFHJEHSLIIPHL-UHFFFAOYSA-N 0.000 description 2
- XAOGXQMKWQFZEM-UHFFFAOYSA-N isoamyl propanoate Chemical compound CCC(=O)OCCC(C)C XAOGXQMKWQFZEM-UHFFFAOYSA-N 0.000 description 2
- 229930007744 linalool Natural products 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 description 2
- PGMYKACGEOXYJE-UHFFFAOYSA-N pentyl acetate Chemical compound CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 2
- 150000003377 silicon compounds Chemical class 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- ZPDIRKNRUWXYLJ-UHFFFAOYSA-N 2,2-dimethyloxolane Chemical compound CC1(C)CCCO1 ZPDIRKNRUWXYLJ-UHFFFAOYSA-N 0.000 description 1
- ZNRVRWHPZZOTIE-UHFFFAOYSA-N 2,4,4-trimethylpentan-1-ol Chemical compound OCC(C)CC(C)(C)C ZNRVRWHPZZOTIE-UHFFFAOYSA-N 0.000 description 1
- BAYAKMPRFGNNFW-UHFFFAOYSA-N 2,4-dimethylpentan-3-ol Chemical compound CC(C)C(O)C(C)C BAYAKMPRFGNNFW-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- KBMDBLCFKPRPOC-UHFFFAOYSA-N 2-bromo-3,3,3-trifluoro-2-(trifluoromethyl)propanenitrile Chemical compound FC(F)(F)C(Br)(C#N)C(F)(F)F KBMDBLCFKPRPOC-UHFFFAOYSA-N 0.000 description 1
- DTFKRVXLBCAIOZ-UHFFFAOYSA-N 2-methylanisole Chemical compound COC1=CC=CC=C1C DTFKRVXLBCAIOZ-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- NPHCXUPGMINOPP-UHFFFAOYSA-N 3,6-dimethyloctan-3-ol Chemical compound CCC(C)CCC(C)(O)CC NPHCXUPGMINOPP-UHFFFAOYSA-N 0.000 description 1
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
- DCUYGCJQVJXUHU-UHFFFAOYSA-N 4-methyloxan-4-ol Chemical compound CC1(O)CCOCC1 DCUYGCJQVJXUHU-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- YYLLIJHXUHJATK-UHFFFAOYSA-N Cyclohexyl acetate Chemical compound CC(=O)OC1CCCCC1 YYLLIJHXUHJATK-UHFFFAOYSA-N 0.000 description 1
- AQZGPSLYZOOYQP-UHFFFAOYSA-N Diisoamyl ether Chemical compound CC(C)CCOCCC(C)C AQZGPSLYZOOYQP-UHFFFAOYSA-N 0.000 description 1
- HXQPUEQDBSPXTE-UHFFFAOYSA-N Diisobutylcarbinol Chemical compound CC(C)CC(O)CC(C)C HXQPUEQDBSPXTE-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- WRQNANDWMGAFTP-UHFFFAOYSA-N Methylacetoacetic acid Chemical compound COC(=O)CC(C)=O WRQNANDWMGAFTP-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 229960004217 benzyl alcohol Drugs 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000003034 coal gas Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 229940075894 denatured ethanol Drugs 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 229940117955 isoamyl acetate Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 229940095102 methyl benzoate Drugs 0.000 description 1
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003498 natural gas condensate Substances 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- 150000004880 oxines Chemical class 0.000 description 1
- DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229940049953 phenylacetate Drugs 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 102220082318 rs755636317 Human genes 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- HVZJRWJGKQPSFL-UHFFFAOYSA-N tert-Amyl methyl ether Chemical compound CCC(C)(C)OC HVZJRWJGKQPSFL-UHFFFAOYSA-N 0.000 description 1
- JKUYRAMKJLMYLO-UHFFFAOYSA-N tert-butyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OC(C)(C)C JKUYRAMKJLMYLO-UHFFFAOYSA-N 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
Images
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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
-
- 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
-
- 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
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/10—Use of additives to fuels or fires for particular purposes for improving the octane number
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1608—Well defined compounds, e.g. hexane, benzene
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1616—Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1824—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1852—Ethers; Acetals; Ketals; Orthoesters
- C10L1/1855—Cyclic ethers, e.g. epoxides, lactides, lactones
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1857—Aldehydes; Ketones
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
Definitions
- This invention relates to motor fuel for spark ignition internal combustion engines. More particularly the invention relates to a method for lowering the dry vapour pressure equivalent (DVPE) of a fuel composition including a hydrocarbon liquid and ethanol by using an oxygen-containing additive.
- the ethanol and DVPE adjusting components used to obtain the fuel composition are preferably derived from renewable raw materials.
- motor fuels containing up to 20 % by volume of ethanol meeting standard requirements for spark ignition internal combustion engines operating with gasoline are obtainable.
- Gasoline is the major fuel for spark ignition internal combustion engines.
- the extensive use of gasoline results in the pollution of the environment.
- the combustion of gasoline derived from crude oil or mineral gas disturbs the carbon dioxide balance in the atmosphere, and causes the greenhouse effect. Crude oil reserves are decreasing steadily with some countries already facing crude oil shortages.
- U.S. Patent No. 2,365,009, issued in 1944 describes the combination of C 1-5 , alcohols and C 3-5 hydrocarbons for use as a fuel.
- U.S. Patent No. 4,818,250 issued in 1989 it is proposed to use limonene obtained from citrus and other plants as a motor fuel, or as a component in blends with gasoline.
- U.S. Patent No. 5,607,486 issued in 1997 there are disclosed novel engine fuel additives comprising terpenes, aliphatic hydrocarbons and lower alcohols.
- Zudkevitch D. et al. in "Thermodynamics of reformulated automotive fuels" Hydrocarbon processing, vol 74, No. 6, 1995 disclose in table 5 thereof two fuel compositions comprising base gasoline, ethanol (5% and 3.2%, respectively) and 12% of ETBE. Using the vapour pressure data given in table 5 it can be calculated that the two fuel compositions exhibit a remaining ethanol induced vapour pressure increase of 32.1 and 30.3%, respectively.
- tert-butyl ethers are widely used as components of gasolines.
- Motor fuels comprising tert-butyl ethers are described in U.S. Patent No. 4,468,233 issued in 1984.
- the major portion of these ethers is obtained from petroleum refining, but can equally be produced from renewable resources.
- Ethanol is a most promising product for use as a motor fuel component in mixtures with gasoline.
- Ethanol is obtained from the processing of renewable raw material, known generically as biomass, which, in turn, is derived from carbon dioxide under the influence of solar energy.
- Figure 1 shows the behaviour of the dry vapour pressure equivalent (DVPE) as a function of the ethanol content of mixtures of ethanol and gasoline A92 summer, and gasoline A95 summer and winter at 37.8°C.
- the gasolines known as A92 and A95 are standard gasolines purchased at gas stations in the United States and Sweden.
- Gasoline A92 originated in the United States and gasoline A95, in Sweden.
- the ethanol employed was fuel grade ethanol produced by Williams, USA.
- the DVPE of the mixtures was determined according to the standard ASTM D5191 method at the SGS laboratory in Sweden.
- Fig. 1 For the range of concentrations by volume of ethanol between 5 and 10% which is of particular interest for use as a motor fuel for standard spark ignition engines, the data in Fig. 1 show that the DVPE of mixtures of gasoline and ethanol can exceed the DVPE of source gasoline by more than 10%. Since the commercial petroleum companies normally supply the market with gasoline already at the maximum allowed DVPE, which is strictly limited by current regulations, the addition of ethanol to such presently commercially available gasolines is not possible.
- U.S. Patent No. 5,688,295 granted on November 18, 1997 provides a chemical compound as an additive to gasoline or as a fuel for standard gasoline engines.
- an alcohol-based fuel additive is proposed.
- the fuel additive comprises from 20 - 70% alcohol, from 2.5 - 20% ketone and ether, from 0.03 - 20% aliphatic and silicon compounds, from 5 - 20% toluene and from 4 - 45% mineral spirits.
- the alcohol is methanol or ethanol. It is noted in the patent that the additive improves gasoline quality and specifically decreases DVPE.
- the disadvantages of this method of motor fuel DVPE adjustment are that there is a need for large quantities of the additive, namely, not less than 15 % by volume of the mixture; and the use of silicon compounds, which form silicon oxide upon combustion, results in increased engine wear.
- a spark ignition motor fuel composition including a hydrocarbon component of C 5 - C 8 straight-chained or branched alkanes, essentially free of olefins, aromatics, benzene and sulphur, in which the hydrocarbon component has a minimum anti-knock index of 65, according to ASTM D2699 and D2700 and a maximum DVPE of 15 psi, according to ASTM D5191; a fuel grade alcohol; and a co-solvent for the hydrocarbon component and alcohol in which the components of the fuel composition are present in amounts selected to provide a motor fuel with a minimum anti-knock index of 87 and a maximum DVPE of 15 psi.
- the co-solvent used is biomass-derived 2-methyltetrahydrofuran (MTHF) and other heterocyclical ether
- the present inventors have found that specific types of compounds exhibiting an oxygen-containing group surprisingly lower the vapour pressure of a gasoline-ethanol mixture.
- up to about 20 % by volume of fuel grade ethanol (b) can be used in the whole fuel compositions.
- the oxygen-containing additives (c) used can be obtained from renewable raw materials, and the hydrocarbon component (a) used can for example be any standard gasoline (which does not have to be reformulated) and can optionally contain aromatic fractions and sulphur, and also hydrocarbons obtained from renewable raw materials.
- fuels for standard spark ignition internal combustion engines can be prepared, which fuels allow such engines to have the same maximum performance as when operated on standard gasoline currently on the market.
- a decrease in the level of toxic emissions in the exhaust and a decrease in the fuel consumption can also be obtained by using the method of the invention.
- the anti-knock index in addition to the dry vapour pressure equivalent (DVPE), the anti-knock index (octane number) can also be desirably controlled.
- the mixture of (b), (c), and (d) can also be used per se as a fuel for modified engines, i.e., not standard-type gasoline engines.
- the additive mixture can also be used for adjusting the octane number and/or for lowering the vapour pressure of a high vapour pressure hydrocarbon component.
- the present method enables the use of C 3 - C 12 hydrocarbon fractions as hydrocarbon component (a), including narrower ranges within this broader range, without restriction on the presence of saturated and unsaturated hydrocarbons, aromatics and sulphur.
- the hydrocarbon component can be a standard gasoline currently on the market, as well as other mixtures of hydrocarbons obtained in the refining of petroleum, off-gas of chemical-recovery coal carbonisation, natural gas and synthesis gas. Hydrocarbons obtained from renewable raw materials can also be included.
- the C 3 - C 12 fractions are usually prepared by fractional distillation or by blending various hydrocarbons.
- the component (a) can contain aromatics and sulphur, which are either co-produced or naturally found in the hydrocarbon component.
- the DVPE can be reduced for fuel mixtures containing up to 20% volume of ethanol, calculated as pure ethanol.
- the vapour pressure of the hydrocarbon based ethanol-containing fuel mixture is reduced by 80% of the ethanol-induced vapour pressure increase, and more preferably the vapour pressure of the hydrocarbon based ethanol-containing fuel mixture is reduced to a vapour pressure corresponding to that of the hydrocarbon component alone.
- the DVPE can be reduced if desired to a level even lower than that of the hydrocarbon component used.
- the other properties of the fuel such as for example the octane number, are kept within the required standard limits.
- the oxygen-containing organic compound enables adjustment of (i) the dry vapour pressure equivalent, (ii) the anti-knock index and other performance parameters of the motor fuel composition as well as (iii) the reduction of the fuel consumption and the reduction of toxic substances in the engine exhaust emissions.
- the oxygen-containing compound (c) has oxygen bound in at least any one of the following functional groups:
- Such functional groups are present, for example, in the following classes of organic compounds and which can be used in the present invention: alcohols, ketones, ethers, esters, hydroxy-ketones, ketone esters, and heterocyclics with oxygen-containing rings.
- the fuel additive can be derived from fossil-based sources or preferably from renewable sources such as biomass.
- the oxygen-containing fuel additive (c) can typically be an alcohol, other than ethanol.
- aliphatic or alicyclic alcohols both saturated and unsaturated, preferably alkanols, are employed. More preferably, alkanols of the general formula: R-OH where R is alkyl with 3 to 10 carbon atoms, most preferably 3 to 8 carbon atoms, such as propanol, isopropanol, n-butanol, isobutanol, tert-butanol, n-pentanol, isopentanol, tert-pentanol, 4-methyl-2-pentanol, diethylcarbinol, diisopropylcarbinol, 2-ethylhexanol, 2,4,4-trimethylpentanol, 2,6-dimethyl-4-heptanol, linalool, 3,6-dimethyl-3-octanol, phenol, phenyl
- the component (c) can also be an aliphatic or alicyclic ketone, both saturated and unsaturated, of the general formula where R and R' are the same or different and are each C 1 -C 6 hydrocarbons, which also can be cyclic, and are preferably C 1 -C 4 hydrocarbons.
- ketones have a total (R+R') of 4 to 9 carbon atoms and include methylethyl ketone, methylpropyl ketone, diethylketone, methylisobutyl ketone, 3-heptanone, 2-octanone, diisobutyl ketone, cyclohexanon, acetofenone, trimethylcycohexanone, or similar ketones, and mixtures thereof.
- the component (c) can also be an aliphatic or alicyclic ether, including both saturated and unsaturated ethers, of the general formula R-O-R', wherein R and R' are the same or different and are each a C 1 -C 10 hydrocarbon group.
- R and R' are the same or different and are each a C 1 -C 10 hydrocarbon group.
- lower (C 1 -C 6 ) dialkyl ethers are preferred.
- the total number of carbon atoms in the ether is preferably from 6 to 10.
- Typical ethers include methyltertamyl ether, methylisoamyl ether, ethylisobutyl ether, ethyltertbutyl ether, dibutyl ether, diisobutyl ether, diisoamyl ether, anisole, methylanisole, phenetole or similar ethers and mixtures thereof.
- the component (c) may further be an aliphatic or alicyclic ester, including saturated and unsaturated esters, of the general formula where R and R' are the same or different.
- R and R' are preferably hydrocarbon groups, more preferably alkyl groups and most preferably alkyl and phenyl having 1 to 6 carbon atoms. Especially preferred is an ester where R is C 1 -C 4 and R' is C 4 -C 6 .
- Typical esters are alkyl esters of alkanoic acids, including n-butylacetate, isobutylacetate, tert-butylacetate, isobutylpropionate, isobutylisobutyrate, n-amylacetate, isoamylacetate, isoamylpropionate, methylbenzoate, phenylacetate, cyclohexylacetate, or similar esters and mixtures thereof. In general, it is preferred to employ an ester having from 5 to 8 carbon atoms.
- the additive (c) can simultaneously contain two oxygen-containing groups connected in the same molecule with different carbon atoms.
- the additive (c) can be a hydroxyketone.
- a preferred hydroxyketone has the general formula: where R is hydrocarbyl, and R 1 is hydrogen or hydrocarbyl, preferably lower alkyl, i.e. (C 1 -C 4 ). In general, it is preferred to employ a ketol having 4 to 6 carbon atoms.
- Typical hydroxy-ketones include 1-hydroxy-2-butanone, 3-hydroxy-2-butanone, 4-hydroxy-4-methyl-2-pentanone, or similar ketols or mixture thereof.
- the fuel additive (c) is a ketone ester, preferably of the general formula: where R is hydrocarbyl, preferably lower alkyl, i.e. (C 1 -C 4 ).
- Typical ketone esters include methylacetoacetate, ethyl acetoacetate and tert-butyl acetoacetate. Preferably, such ketone esters have 6 to 8 carbon atoms.
- the additive (c) can also be a ring-oxygen-containing heterocyclic compound and, preferably, the oxygen-containing heterocycle has a C 4 - C 5 ring. More preferably, the heterocycle additive has a total of 5 to 8 carbon atoms.
- the additive can preferably have the formula (1) or (2) as follows: where R is hydrogen or hydrocarbyl, preferably -CH 3 , and R 1 is -CH 3 , or -OH, or -CH 2 OH, or CH 3 CO 2 CH 2 -.
- a typical heterocyclic additive (c) is tetrahydrofurfuryl alcohol, tetrahydrofurfurylacetate, dimethyltetrahydrofurane, tetramethyltetrahydrofurane, methyltetrahydropyrane, 4-methyl-4-oxytetrahydropyrane or similar heterocyclic additives, or mixtures thereof.
- Component (c) can also be a mixture of any of the compounds set out above from one or more of the above-mentioned different compound classes.
- Suitable fuel grade ethanol (b) to be used according to the present invention can readily be identified by the person skilled in the art.
- a suitable example of the ethanol component is ethanol containing 99.5% of the main substance.
- Any impurities included in the ethanol in an amount of at least 0.5 % by volume thereof and falling within the above-mentioned definition of component (c) should be taken into account when determining the amount used of component (c). That is, such impurities must be included in an amount of at least 0.5% in the ethanol in order to be taken into account as a part of component (c).
- Any water, if present in the ethanol should preferably amount to no more than about 0.25 % by volume of the total fuel mixture, in order to meet the current standard requirements on fuels for gasoline engines.
- a denatured ethanol mixture as supplied to the market containing about 92% of ethanol, hydrocarbons and by-products, can also be used as the ethanol component in the fuel composition according to the invention.
- the ethanol (b) is employed in amounts from 0.1% to 20%, typically from about 1% to 20 % by volume, preferably 3% to 15 % by volume and more preferably from about 5 to 10 % by volume.
- the oxygen-containing additive (c) is generally employed in amounts from 0.05% to about 15 % by volume, more generally from 0.1 to about 15 % by volume, preferably from about 3 - 10 % by volume and most preferably from about 5 to 10 % by volume.
- the total volume of ethanol (b) and oxygen-containing additive (c) employed is from 0.15 to 25 % by volume, normally from about 0.5 to 25 % by volume, preferably from about 1 to 20 % by volume, more preferably from 3 to 15 % by volume, and most preferably from 5 to 15 % by volume.
- the ratio of ethanol (b) to oxygen-containing additive (c) in the motor fuel composition is thus generally from 1:150 to 400:1, and is more preferably from 1:10 to 10:1.
- the total oxygen content of motor fuel composition based on the ethanol and the oxygen additive is preferably no greater than about 7 wt.%, more preferably no greater than about 5 wt.%.
- a motor fuel suitable for the operation of a standard spark ignition internal combustion engine the aforesaid hydrocarbon component, ethanol, and additional oxygen-containing component are admixed to obtain the following properties of the resulting motor fuel composition:
- the hydrocarbon component and ethanol should be added together, followed by the addition of the additional oxygen-containing compound or compounds to the mix. Afterwards, the resulting motor fuel composition should preferably be maintained at a temperature not lower than -35°C, for at least about one hour. It is a feature of this invention that the components of the motor fuel composition can be merely added to each other to form the desired composition. It is generally not required to agitate or otherwise provide any significant mixing to form the composition.
- oxygen-containing component(s) originating from renewable raw material(s).
- Component (d) is used for further lowering the vapour pressure of the fuel mixture of components (a), (b) and (c).
- An individual hydrocarbon selected from a C 6 - C 12 fraction of aliphatic or alicyclic saturated and unsaturated hydrocarbons can be used as component (d).
- the hydrocarbon component (d) is selected from a C 8 -C 11 fraction.
- Suitable examples of (d) are benzene, toluene, xylene, ethylbenzene, isopropylbenzene, isopropyltoluene, diethylbenzene, isopropylxylene, tert-butylbenzene, tert-butyltoluene, tert-butylxylene, cyclooctadiene, cyclooctotetraene, limonene, isooctane, isononane, isodecane, isooctene, myrcene, allocymene, tert-butylcyclohexane or similar hydrocarbons and mixtures hereof.
- Hydrocarbon component (d) can also be a fraction boiling at 100-200°C, obtained in the distillation of oil, bituminous coal resin, or synthesis gas processing products.
- the invention further relates to an additive mixture consisting of components (b) and (c) and, optionally also component (d), which subsequently can be added to the hydrocarbon component (a) and is also possible to use as such as a fuel for a modified spark ignition combustion engine.
- the additive mixture preferably has a ratio of ethanol (b) to additive (c) of 1: 150 to 200:1 by volume.
- said mixture comprises the oxygen-containing component (c) in an amount from 0.5 up to 99.5 % by volume, and ethanol (b) in an amount from 0.5 up to 99.5 % by volume, and component (d) comprising at least one C 6 - C 12 hydrocarbon, more preferably C 8 -C 11 hydrocarbon, in an amount from 0 up to 99 % by volume, preferably from 0% up to 90%, more preferably from 0 up to 79,5%, and most preferably from 5 up to 77% of the additive mixture.
- the additive mixture has a ratio of ethanol (b) to the sum of the other additive components (c)+(d) from 1:200 to 200:1 by volume, more preferable a ratio of ethanol (b) to the sum of the components (c) + (d) is from 1:10 to 10:1 by volume.
- the octane number of the additive mixture can be established, and the mixture be used to adjust the octane number of the component (a) to a desired level by admixing a corresponding portion of the mixture (b), (c), (d) to component (a).
- the drivability testing was performed on a 1987 VOLVO 240 DL according to the standard test method EU2000 NEDC EC 98/69.
- EU 2000 European 2000
- NEDC New European Driving Cycle
- 91/441 EEC resp. ECE-R 83/01 and 93/116 EEC
- These standardised EU tests include city driving cycles and extra urban driving cycles and require that specific emission regulations be met.
- Exhaust emission analysis is conducted with a constant volume sampling procedure and utilises a flame ionisation detector for hydrocarbon determination.
- Exhaust Emission Directive 91/441 EEC Phase I
- EU Fuel Consumption Directive 93/116 EEC (1996) implements consumption standards.
- the testing was performed on a 1987 Volvo 240 DL with a B230F, 4-cylinder, 2.32 litre engine (No. LG4F20-87) developing 83 kW at 90 revolutions/second and a torque of 185 Nm at 46 revolutions/ second.
- Example 1 demonstrates the possibility of reducing the dry vapour pressure equivalent of the ethanol-containing motor fuel for the cases when gasolines with dry vapour pressure equivalent according to ASTM D-5191 at a level of 90 kPa (about 13 psi) are used as a hydrocarbon base.
- Fig. 1 demonstrates the behaviour of the DVPE of the ethanol-containing motor fuel based on winter A95 gasoline.
- the ethanol-containing motor fuels based on winter A92 and A98 used in this example also demonstrate a similar behaviour.
- the source gasoline comprised aliphatic and alicyclic C 4 -C 12 hydrocarbons, including both saturated and unsaturated ones.
- the following different embodiments of the fuels 1-3 demonstrate the possibility of adjusting the dry vapor pressure equivalent (DVPE) of the ethanol-containing motor fuel based on winter A92 gasoline.
- DVPE dry vapor pressure equivalent
- the inventive fuel 1-3 contained A92 winter gasoline (a), ethanol (b), oxygen-containing additives (c) and hydrocarbons C 6 -C 12 (d), and had the following properties for the various compositions:
- A92 : Ethanol : Isoamyl alcohol : Alkylate 79 : 9 : 2 : 10 % by volume
- Ethanol : Isobutyl acetate : Naphtha 80 : 5 : 5 : 10 % by volume
- Ethanol: Tert-butanol: Naphtha 81 : 5 : 5 : 9 % by volume
- the boiling temperature for the naphtha is
- the motor fuel compositions below demonstrate that it is not always necessary to reduce the excess DVPE of the motor fuel induced by the presence of ethanol to the level of DVPE of the source gasoline. In some cases it is sufficient just to bring it in compliance with the requirements of the regulations in force for the corresponding gasoline.
- the DVPE level for the winter gasoline is 90 kPa.
- compositions 1-6 demonstrate the possibility of adjusting the dry vapor pressure equivalent (DVPE) of the ethanol-containing motor fuel based on winter A98 gasoline.
- the fuel 1-6 contained A98 winter gasoline (a), ethanol (b), oxygen-containing additives (c), and C 6 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- A98 : Ethanol: Isobutanol : Naphtha 80 : 5 : 5 : 10 % by volume The boiling point of the naphtha is 100-200°C.
- the motor fuel compositions below demonstrate that it is not always necessary to reduce the excess DVPE of the motor fuel caused by presence of ethanol to the level of DVPE of the source gasoline. In some cases it is sufficient just to bring it in compliance with the requirements of the regulations in force for the corresponding gasoline.
- the DVPE level for the winter gasoline is 90 kPa.
- the motor fuel compositions below demonstrate that it might be necessary to reduce the excess DVPE of the motor fuel caused by presence of ethanol below the level of DVPE of the source gasoline. Normally, this is required when DVPE of the source gasoline is higher than the limits of the regulations in force for the corresponding spending gasoline. In this way, for example, it is possible to transform the winter grade gasoline into the summer grade gasoline.
- the DVPE level for the summer gasoline is 70 kPa.
- A98 : Ethanol : Isobutanol : Isooctane : Naphtha 60 : 9.5 : 0.5 : 15 : 15 % by volume
- the boiling point of the naphtha is 100-200°C.
- the following fuels 1-9 and 1-10 demonstrate the possibility of adjusting the dry vapor pressure equivalent (DVPE) of the ethanol-containing motor fuel based on winter A95 gasoline.
- DVPE dry vapor pressure equivalent
- the fuel 1-9 contained A95 winter gasoline (a), ethanol (b), the oxygen-containing additives (c), and C 6 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- A95 : Ethanol: Isoamyl alcohol : Alkylate 83.7 : 5 : 2 : 9.3 % by volume
- the motor fuel compositions below demonstrate that it is not always necessary to reduce the excess DVPE of the motor fuel caused by presence of ethanol to the level of DVPE of the source gasoline. In some cases it is sufficient just to bring it in compliance with the requirements of the regulations in force for the corresponding gasoline.
- the DVPE level for the winter gasoline is 90 kPa.
- the motor fuel compositions below demonstrate that it might be necessary to reduce the excess DVPE of the motor fuel caused by presence of ethanol below the level of DVPE of the source gasoline. Normally, this is required when DVPE of the source gasoline is higher than the limits of the regulations in force for the corresponding gasoline. In this way, for example, it is possible to transform the winter grade gasoline into the summer grade gasoline.
- the DVPE level for the summer gasoline is 70 kPa.
- A95 : Ethanol : Isobutanol : Isoamyl alcohol : Naphtha : Isooctane 60 : 9.2 : 0.2 : 0.6 : 15 : 15 % by volume
- the boiling temperature of the naphtha is 100-200°C.
- Ethanol: Tert-butyl acetate : Naphtha 60 : 9 : 1 : 30 % by volume
- the boiling temperature of the naphtha is 100-200°C.
- the fuel 1-10 contains 75 % by volume A95 winter gasoline, 9.6 % by volume ethanol, 0.4 % by volume isobutyl alcohol, 4.5 % by volume m-isopropyl toluene and 10.5 % by volume naphtha with boiling temperature of 100-200°C.
- This fuel formulation demonstrates the possibility of decreasing the DVPE, increasing the octane number, decreasing the level of toxic emissions in the exhaust and decreasing the fuel consumption in comparison with the reference mixture of gasoline and ethanol (RFM 1).
- the motor fuel composition has the following properties: density at 15°C, according to ASTM D 4052 749.2 kg /m3; initial boiling point, according to ASTM D 86 29°C; vaporizable portion - 70°C 47.6 % by volume; vaporizable portion - 100°C 55.6 % by volume; vaporizable portion - 150°C 84.2 % by volume; vaporizable portion - 180°C 97.5 % by volume; final boiling point 194.9°C; evaporation residue 1.3 % by volume; loss by evaporation 1.6 % by volume; oxygen content, according to ASTM D4815 acidity, according to ASTM D 1613 3.7%w/w; weight% HAc 0.004; pH, according to ASTM D1287 6.6; sulfur content, according to ASTM D 5453 18mg/kg; gum content, according to ASTM D381 1 mg/100ml; water content, according to ASTM D6304 aromatics, according to SS 155120,
- the motor fuel formulation 1-10 was tested in accordance with the standard test method EU 2000 NEDC EC 98/69 and the following results, as compared to winter A95 gasoline, were obtained: CO -21%; HC -9%; NOx + 12.8%; CO2 +2.38%; NMHC -6.4%; Fuel consumption, Fc 1/100km +3.2%
- the fuel formulations 1-1 to 1-10 showed reduced DVPE over the tested ethanol-containing motor fuels based on summer grade gasoline. Similar results are obtained when other oxygen-containing compounds of this invention are substituted for the additives of the examples 1-1 to 1-10.
- Example 2 demonstrates the possibility of reducing the dry vapour pressure equivalent of the ethanol-containing motor fuel for the cases when gasolines with a dry vapour pressure equivalent according to ASTM D-5191 at a level of 70 kPa (about 10 psi) are used as a hydrocarbon base.
- the source gasoline comprised aliphatic and alicyclic C 4 -C 12 hydrocarbons, including saturated and unsaturated ones.
- Figure 1 shows the behaviour of the DVPE of the ethanol-containing motor fuel based on summer A95 gasoline.
- the fuel 2-3 contained A92 summer gasoline (a), ethanol (b), the oxygen-containing additives (c), and C 6 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- Ethanol Me
- the motor fuel compositions below demonstrate that it is not always necessary to reduce the excess DVPE of the motor fuel caused by presence of ethanol to the level of DVPE of the source gasoline. In some cases it is sufficient just to bring it in compliance with the requirements of the regulations in force for the corresponding gasoline.
- the DVPE level for the summer gasoline is 70 kPa.
- the following fuels 2-6 demonstrate the possibility of adjusting the dry vapour pressure equivalent (DVPE) of the ethanol-containing motor fuel based on summer A98 gasoline.
- DVPE dry vapour pressure equivalent
- the fuel 2-6 contained A98 summer gasoline (a), ethanol (b), the oxygen-containing additives (c), and C 6 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- the motor fuel compositions below demonstrate that it is not always necessary to reduce the excess DVPE of the motor fuel caused by the presence of ethanol to the level of DVPE of the source gasoline. In some cases it is sufficient just to bring it in compliance with the requirements of the regulations in force for the corresponding gasoline.
- the DVPE level for the summer gasoline is 70 kPa.
- the following fuels 2-9 to 2-10 demonstrate the possibility of adjusting the dry vapour pressure equivalent (DVPE) of the ethanol-containing motor fuel based on summer A95 gasoline.
- DVPE dry vapour pressure equivalent
- the fuel 2-9 contained A95 summer gasoline (a), ethanol (b), the oxygen-containing additives (c), and C 6 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- Ethanol: Diethylketone : Xylene 80 : 9.5
- the motor fuel compositions below demonstrate that it is not always necessary to reduce the excess DVPE of the motor fuel caused by the presence of ethanol to the level of DVPE of the source gasoline. In some cases it is sufficient just to bring it in compliance with the requirements of the regulations in force for the corresponding gasoline.
- the DVPE level for the summer gasoline is 70 kPa.
- the fuel formulation 2-10 contained 81.5% by volume of A95 summer gasoline, 8.5% by volume of m-isopropyltoluene, 9.2% by volume of ethanol, and 0.8% by volume of isoamyl alcohol.
- Formulation 2-10 was tested to demonstrate how the inventive composition maintained the dry vapour pressure equivalent at a same level as the source gasoline while increasing the octane number, while decreasing the level of toxic emissions in the exhaust and decreasing the fuel consumption in comparison with the mixture RFM 2 of gasoline and ethanol.
- Formulation 2-10 had the following specific properties: density at 15°C, according to ASTM D4052 754.1kg/m3; initial boiling point, according to ASTM D 86 26.6°C; vaporisable portion - 70°C 45.2 % by volume; vaporisable portion - 100°C 56.4 % by volume; vaporisable portion - 150°C 88.8 % by volume; vaporisable portion - 180°C 97.6 % by volume; final boiling point 186.3°C; evaporation residue 1.6 % by volume; loss by evaporation 0.1 % by volume; oxygen content, according to ASTM D4815 3.56% w/w; acidity, according to ASTM D1613 weight% HAc 0.007; pH, according to ASTM D 1287 8.9; sulfur content, according to ASTM D 5453 16mg/kg; gum content, according to ASTM D381 ⁇ 1mg/100ml; water content, according to ASTM D6304 0.12% w/w; aromatic
- the motor fuel Formulation 2-10 was tested in accordance with test method EU 2000 NEDC EC 98/69 as above and gave the following results in comparison (+) or (-)% with the results for the source A95 summer gasoline: CO -0.18% HC -8.5%; NOx +5.3%; CO 2 +2.8%; NMHC -9%; Fuel consumption, Fc, 1/100km +3.1%
- the fuel formulations 2-1 to 2-10 showed reduced DVPE over the tested ethanol-containing motor fuels based on summer grade gasoline. Similar results are obtained when other oxygen-containing additives of the invention are substituted for the additives of the examples 2-1 to 2-10.
- Figure 2 shows the behaviour of the dry vapour pressure equivalent (DVPE) as a function of the ethanol content when mixing summer A95 gasoline with the additive mixture 3 comprising 35 % by volume of ethanol , 5 % by volume of isoamyl alcohol, and 60 % by volume of naphtha boiling at temperatures between 100-170°C.
- DVPE dry vapour pressure equivalent
- Figure 2 demonstrates that varying the ethanol content in gasoline within the range from 0 to 20% does not induce an increase of the vapour pressure for these compositions higher than the requirements of the standards for DVPE of the summer grade gasolines, which is 70 kPa.
- the ratio between ethanol and the oxygen-containing compound other than ethanol in the additive mixture, which is used for preparation of the ethanol-containing gasolines, is of substantial importance.
- the ratio between the components of the additive established by the present invention enables to adjust the vapour pressure of the ethanol-containing gasolines over a wide range.
- the additive mixture comprising ethanol and the oxygen-containing compound of this invention other than ethanol with the ratio of the present invention can be used as an independent motor fuel for the engines adapted for operation on ethanol.
- Example 3 demonstrates the possibility of reducing the dry vapour pressure equivalent of the ethanol-containing motor fuel for the cases when gasolines with dry vapour pressure equivalent according to ASTM D-5191 at a level of 48 kPa (about 7 pSi) are used as the hydrocarbon base.
- the source gasolines comprised aliphatic and alicyclic C 5 -C 12 hydrocarbons, including both saturated and unsaturated ones.
- Fig. 1 shows the behaviour of the DVPE of the ethanol-containing motor fuel based on US summer grade A92 gasoline.
- the fuel 3-3 contained US A92 summer gasoline (a), ethanol (b), the oxygen-containing additives (c), and C 6 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- A92 Ethanol : Isoamyl alcohol : Isobut
- the motor fuel compositions below demonstrate that it is not always necessary to reduce the excess DVPE of the motor fuel caused by the presence of ethanol to the level of DVPE of the source gasoline. In some cases it is sufficient just to bring it in compliance with the requirements of the regulations in force for the corresponding gasoline.
- the DVPE level for the US summer grade gasoline is 7 psi, which corresponds to 48.28 kPa.
- the fuel 3-6 contained US A98 summer gasoline (a), ethanol (b), the oxygen-containing additives (c), and C 6 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- A98 : Ethanol : Isoamyl alcohol : Isobutyl alcohol : Naphtha 75 : 9.2 : 0.3 : 0.1 : 15.4 % by volume
- the US summer A95 gasoline was used as a reference fuel for the testing performed according to EU2000 NEDC EC 98/69 test cycle on a 1987 Volvo 240 DL with a B230F, 4-cylinder, 2.32 litre engine (No. LG4F20-87) developing 83 kW at 90 revolutions/second and a torque of 185 Nm at 46 revolutions/second.
- the fuel 3-9 contained US A95 summer gasoline (a), ethanol (b), the oxygen-containing additives (c), and C 6 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- A95 : Ethanol : Isoamyl alcohol : Isobutyl alcohol : Naphtha 75 : 9.2 : 0.3 : 0.1 : 15.4 % by volume
- the motor fuel compositions below demonstrate that it is not always necessary to reduce the excess DVPE of the motor fuel caused by the presence of ethanol to the level of DVPE of the source gasoline. In some cases it is sufficient just to bring it in compliance with the requirements of the regulations in force for the corresponding gasoline.
- the DVPE level for the US summer grade gasoline is 7 pSi, which corresponds to 48.28 kPa.
- the boiling temperature for the naphtha is 100-200°C.
- the fuel formulation 3-10 contained 76 % by volume of US A95 summer gasoline, 9.2 % by volume of ethanol, 0.25 % by volume of isoamyl alcohol, 0.05 % by volume of isobutyl alcohol, 11.5 % by volume of naphtha with boiling temperature of 100-200°C, and 3 % by volume of isopropyltoluene.
- Formulation 3-10 was tested to demonstrate how the invention enables the production of ethanol-containing gasoline entirely meeting the requirements of the standards in force, firstly for the level of the DVPE and also for the other parameters. At the same time this gasoline secures a decrease of toxic emissions in the exhaust and lower fuel consumption in comparison to the mixture RFM 3 of source US A95 summer gasoline with 10% of ethanol.
- Formulation 3-10 had the following specific properties: density at 15°C, according to ASTM D4052 774.9kg /m3; initial boiling point, according to ASTM D 86 36.1°C; vaporisable portion - 70°C 33.6 % by volume; vaporisable portion - 100°C 50.8 % by volume; vaporisable portion - 150°C 86.1 % by volume; vaporisable portion - 190°C 97.0 % by volume; final boiling point 204.8°C; evaporation residue 1.5 % by volume; loss by evaporation 1.5 % by volume; oxygen content, according to ASTM D4815 3.37% w/w; acidity, according to ASTM D1613 weight% HAc 0.007; pH, according to ASTM D1287 7.58; sulfur content, according to ASTM D 5453 47mg/kg; gum content, according to ASTM D381 2.8mg/ 100ml; water content, according to ASTM D6304 0.02% w/w; aromatics, according
- the motor fuel Formulation 3-10 was tested on a 1987 Volvo 240 DL with a B230F, 4-cylinder, 2.32 litre engine (No. LG4F20-87) in accordance with test method EU 2000 NEDC EC 98/69 as above and gave the following results in comparison (+) or (-)% with the results for the source US A95 summer gasoline: CO -15.1% HC -5.6%; NOx +0.5%; CO2 unchanged; NMHC -4.5%; Fuel consumption, Fc, 1/100km unchanged.
- Figure 2 shows the behaviour of the dry vapour pressure equivalent (DVPE) as a function of the ethanol content in the mixtures of US summer A92 gasoline and the additive mixture 4 comprising 35 % by volume of ethanol, 1 % by volume of isoamyl alcohol, 0.2 % by volume of isobutanol, 43.8 % by volume of naphtha boiling at temperatures between 100-170°C, and 20% of isopropyl toluene.
- Figure 2 demonstrates that employment of this additive mixture in formulation of ethanol-containing gasoline enables the reduction of more than 100% of the excess vapour pressure induced by the presence of ethanol.
- the additive mixture comprising ethanol, the oxygen-containing compound other than ethanol, and C 6 -C 12 hydrocarbons in the proportion and composition of the present invention, can be used as an independent motor fuel for the engines adopted for operation on ethanol.
- Example 4 demonstrates the possibility of reducing the dry vapour pressure equivalent of the ethanol-containing motor fuel for the cases when the hydrocarbon base of the fuel is a non-standard gasoline with a dry vapour pressure equivalent according to ASTM D-5191 at a level of 110 kPa (about 16 psi).
- the hydrocarbon component (HCC) for the motor fuel compositions was prepared by mixing about 85 % by volume of winter A92, A95 or A98 gasoline with about 15 % by volume of gas condensate hydrocarbon liquid (GC).
- hydrocarbon component (HCC) for the fuel formulations 4-1 to 4-10 of this motor fuel composition, about 85 % by volume of winter A92, A95 or A98 gasoline was first mixed with the gas condensate hydrocarbon liquid (GC). The obtained hydrocarbon component (HCC) was then allowed to stand for 24 hours. The resulting gasoline contained aliphatic and alicyclic C 3 -C 12 hydrocarbons, including saturated and unsaturated ones.
- Fig. 1 demonstrates the behaviour of the DVPE of the ethanol-containing motor fuel based on winter A98 gasoline and gas condensate.
- the fuel 4-3 contained winter A92 gasoline, gas condensate (GC), ethanol, the oxygen-containing additive and C 6 -C 12 hydrocarbons and had the following properties for the various compositions:
- A92 : GC : Ethanol : Tert-butylethyl ether : Naphtha 68 : 12 : 9.5 : 0.5 : 10 % by volume
- the boiling temperature for the naphtha is 100-200°C.
- the fuel compositions below demonstrate that the invention enables the reduction of the excess DVPE of the non-standard gasoline to the level of the corresponding standrd gasoline.
- the DVPE for the standard A92 winter gasoline is 90 kPa.
- A92 : GC : Ethanol : Isoamyl alcohol : Naphtha : Alkylate 55 : 10 : 9.5 : 0.5 : 12.5 : 12.5 % by volume
- the boiling temperature for the naphtha is 100-200°C.
- the boiling temperature for the alkylate is 100-130°C.
- compositions demonstrate the possibility of adjusting the dry vapour pressure equivalent (DVPE) of the ethanol-containing fuel mixtures based on about 85 % by volume of winter A98 gasoline and about 15 % by volume of gas condensate.
- DVPE dry vapour pressure equivalent
- the motor fuel compositions below demonstrate that the invention enables the reduction of the excess DVPE of non-standard gasoline to the level of DVPE of the corresponding standard gasoline.
- the DVPE for the standard winter A98 gasoline is 90.0 kPa.
- A92 : GC : Ethanol: Isoamyl alcohol: Naphtha : Alkylate 55 : 10 : 9.5 : 0.5 : 12.5 : 12.5 % by volume
- the boiling temperature for the naphtha is 100-200°C.
- the boiling temperature for the alkylate is 100-130°C.
- A92 : GC : Ethanol : Isobutanol : Naphtha : Isopropyltoluene 55 : 10 : 5 : 5 : 20 : 5 % by volume
- the boiling temperature for the naphtha is 100-200°C.
- compositions demonstrate the possibility of adjusting the dry vapour pressure equivalent (DVPE) of the ethanol-containing fuel mixtures based on about 85 % by volume of winter A95 gasoline and about 15 % by volume of gas condensate.
- DVPE dry vapour pressure equivalent
- HCC hydrocarbon component
- GC gas condensate
- the reference fuel mixture (RFM4) comprising 80.75% of winter A95 gasoline, 14.25% of gas condensate (GC) and 5% of ethanol was tested as described above and gave the following results in comparison (+) or (-)% with the results for the gasoline comprising 85 % by volume of winter gasoline A95 and 15 % by volume of gas condensate (GC): CO -6.98% HC -7.3%; NOx +12.1%; CO2 + 1.1%; NMHC -5.3%; Fuel consumption, Fc, 1/100km +2.62%.
- the motor fuel compositions below demonstrate that the invention enables the reduction of the excess vapour pressure equivalent (DVPE) of the non-standard gasoline to the level of the corresponding standard gasoline.
- the DVPE of the standard winter gasoline A95 is 90.0 kPa.
- A95 : GC : Ethanol: Isoamyl alcohol : Isobutanol : Naphtha : Alkylate 55 : 10 : 9.2 : 0.6 : 0.2 : 12.5 : 12.5 % by volume
- the boiling temperature for the naphtha is 100-200°C.
- the boiling temperature for the alkylate is 100-130°C.
- the motor fuel 4-10 contained 55% by volume of A95 winter gasoline, 10% by volume of gas condensate (GC), 5% by volume of ethanol, 5% by volume of tert-butanol, 20% by volume of naphtha with boiling temperature of 100-200°C and 5% by volume of isopropyltoluene.
- Formulation 4-10 was tested to demonstrate how the invention enables the formulation of ethanol-containing gasoline entirely meeting requirements of the standards in force, firstly in respect of the dry vapour pressure equivalent limit, and also for the other parameters of the fuel, even when the source hydrocarbon component (HCC) has a DVPE considerably higher than the requirements of the standards.
- HCC source hydrocarbon component
- the formulation 4-10 had the following specific properties: density at 15°C, according to ASTM D4052 698.6 kg/m3; initial boiling point, according to ASTM D 86 20.5°C; vaporisable portion - 70°C 47.0 % by volume; vaporisable portion - 100°C 65.2 % by volume; vaporisable portion - 150°C 92.4 % by volume; vaporisable portion - 180°C 97.3 % by volume; final boiling point 189.9°C; evaporation residue 0.5 % by volume; loss by evaporation 1.1 % by volume; oxygen content, according to ASTM D4815 3.2% w/w; acidity, according to ASTM D1613 weight% HAc 0.001; pH, according to ASTM D 1287 7.0; sulfur content, according to ASTM D 5453 18 mg/kg; gum content,
- the motor fuel Formulation 4-10 was tested as above and gave the following results in comparison (+) or (-)% with the results for the motor fuel comprising 85 % by volume of winter A95 gasoline and 15 % by volume of gas condensate: CO -14.0% HC -8.6%; NOx unchanged; CO 2 + 1.0%; NMHC -6.7%; Fuel consumption, Fc, 1/100km +2.0%.
- HCC hydrocarbon component
- GC gas condensate
- inventive fuel formulations demonstrated the possibility of adjusting the vapour pressure of the ethanol-ccontaining motor fuels for the standard internal combustion spark ignition engines based on non-standard gasolines having a high vapour pressure.
- Example 5 demonstrates the possibility of reducing the dry vapour pressure equivalent of the ethanol-containing motor fuel for the cases when the hydrocarbon base base of the fuel is a reformulated gasoline with dry vapour pressure equivalent according to ASTM D-5191 at a level of 27.5 kPa (about 4 psi).
- the hydrocarbon component (HCC) for the motor fuel compositions was prepared by mixing about 85 % by volume of winter A92, A95 or A98 gasoline with about 15 % by volume of gas condensate hydrocarbon liquid (GC).
- the source gasolines comprised aliphatic and alicyclic C 6 -C 12 hydrocarbons, including saturated and unsaturated.
- Fig. 1 demonstrates the behaviour of the DVPE of the ethanol-containing motor fuel based on reformulated gasoline A92 and Petroleum benzine. Similar behaviour was observed for the ethanol-containing motor fuel based on reformulated A95 and A98 gasoline, and Petroleum benzine.
- the fuel 5-3 contained reformulated A92 gasoline, Petroleum benzine (PB), ethanol, the oxygen-containing additives and also C 8 -C 12 hydrocarbons and had the following properties for the various compositions:
- the boiling temperature for the naphtha is 140-200°C.
- the fuel 5-6 contained A98 reformulated gasoline, Petroleum benzine (PB), ethanol, the oxygen-containing additives, and C 8 -C 12 hydrocarbons (d) and had the following properties for the various compositions:
- the boiling temperature for the naphtha is 140-200°C.
- HCC hydrocarbon component
- PB Petroleum benzine
- the reference fuel mixture (RFM5) comprising 72 % by volume of reformulated A95 gasoline, 18 % by volume of Petroleum benzine (PB) and 10 % by volume of ethanol was tested on a 1987 Volvo 240 DL with a B230F, 4-cylinder, 2.32 litre engine (No.
- LG4F20-87 in accordance with test method EU 2000 NEDC EC 98/69 as above and gave the following results in comparison (+) or (-)% with the results for the gasoline comprising 80 % by volume of reformulated gasoline A95 and 20 % by volume of Petroleum benzine (GC): CO -4.8% HC -1.3%; NOx +26.3%; CO2 +4.4%; NMHC -0.6%; Fuel consumption, Fc, 1/100km +5.7%.
- GC Petroleum benzine
- the motor fuel 5-10 contained 60% by volume of A95 reformulated gasoline, 15% by volume of Petroleum benzine (PB), 10% by volume of ethanol, 5% by volume of 2,5-Dimethyltetrahydrofuran and 10% by volume of isopropyltoluene.
- Formulation 5-10 was tested to demonstrate how the invention enables the formulation of ethanol-containing gasoline with a low vapour pressure, wherein the presence in the motor fuel composition of ethanol does not induce an increase of dry vapour pressure equivalent in comparison to the source hydrocarbon component (HCC).
- HCC source hydrocarbon component
- this gasoline secures a decrease of toxic emissions in the exhaust and a decrease of the fuel consumption in comparison with the above mixture RFM 5.
- the formulation 5-10 had the following specific properties: density at 15°C, according to ASTM D4052 764.6 kg/m3; initial boiling point, according to ASTM D 86 48.9°C; vaporisable portion - 70°C 25.3 % by volume; vaporisable portion - 100°C 50.8 % by volume; vaporisable portion - 150°C 76.5 % by volume; vaporisable portion - 190°C 95.6 % by volume; final boiling point 204.5°C; evaporation residue 1.4 % by volume; loss by evaporation 0.5 % by volume; oxygen content, according to ASTM D4815 4.6% w/w; acidity, according to ASTM D 1613 weight% HAc 0.08; pH, according to ASTM D1287 7.5; sulfur content, according to ASTM D 5453 39 mg/kg; gum content, according to ASTM D381 1.5 mg/100ml; water content, according to ASTM D6304 0.1% w/w; aromatics, according to SS
- the motor fuel Formulation 5-10 was tested as described previously and gave the following results in comparison (+) or (-)% with the results for the motor fuel comprising 80 % by volume of reformulated A95 gasoline and 20 % by volume of Petroleum benzine: CO -12.3% HC -6.2%; NOx unchanged; CO 2 +2.6%; NMHC -6.4%; Fuel consumption, Fc, 1/ 100km +3.7%
- the invention demonstrated the possibility of adjusting the vapour pressure of the ethanol-containing motor fuels for the standard internal combustion spark ignition engines based on non-standard gasolines having a low vapour pressure.
- Figure 2 shows the behaviour of the dry vapour pressure equivalent (DVPE) when mixing the hydrocarbon component (HCC), comprising 80 % by volume of reformulated A92 gasoline and 20 % by volume of Petroleum benzine, with the oxygen-containing additive mixture 5, comprising 40 % by volume of ethanol, 20 % by volume of 3,3,5-trimethylcyclohexanone, and 20 % by volume of naphtha with boiling temperature 130-170°C and 20 % by volume of tert-butyltoluene.
- HCC hydrocarbon component
- HCC hydrocarbon component
- gasolines have a vapour pressure equivalent (DVPE) not higher than the DVPE of the source hydrocarbon component (HCC).
- DVPE vapour pressure equivalent
- HCC source hydrocarbon component
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Combustion & Propulsion (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Air-Conditioning For Vehicles (AREA)
- Ignition Installations For Internal Combustion Engines (AREA)
- Output Control And Ontrol Of Special Type Engine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fuel-Injection Apparatus (AREA)
- Combustion Methods Of Internal-Combustion Engines (AREA)
Claims (9)
- Verfahren zum Vermindern des Dampfdrucks eines C3-C12 Motorentreibstoffgemisches auf Kohlenwasserstoffbasis für herkömmliche funkengezündete Verbrennungsmotoren, enthaltend 0,1 bis 20 Vol.-% Ethanol, nicht mehr als 0,25 Gew.-% Wasser gemäß ASTM D 6304 und nicht mehr als 7 Gew.-% Sauerstoff gemäß ASTM D 4815, um mindestens 80 % des durch das Ethanol verursachten Dampfdruckanstiegs, und stärker bevorzugt des Dampfdrucks des C3-C12 Kohlenwasserstoffbestandteils (a) allein, wobei zusätzlich zu dem C3-C12 Kohlenwasserstoffbestandteil (a) und einem Ethanolbestandteil (b) ein Sauerstoff enthaltender Anteil (c) in dem Treibstoffgemisch in einer Menge von 0,05 bis 15 Vol.-% des Gesamtvolumens des Treibstoffgemisches vorhanden ist; wobei Bestandteil (c) aus wenigstens einer der folgenden Arten von Verbindungen ausgewählt ist:Alkanol mit 3 bis 10 Kohlenstoffatomen;Dialkylether mit 6 bis 10 Kohlenstoffatomen;Keton mit 4 bis 9 Kohlenstoffatomen;Alkylester von Alkansäure mit 5 bis 8 Kohlenstoffatomen;Hydroxyketon mit 4 bis 6 Kohlenstoffatomen;Ketonester von Alkansäure mit 5 bis 8 Kohlenstoffatomen;Sauerstoff enthaltende heterocyclische Verbindungen, ausgewählt aus den folgenden: Tetrahydrofurfurylalkohol, Tetrahydrofurfurylacetat, Dimethyltetrahydrofuran, Tetramethyltetrahydrofuran, Methyltetrahydropyran, 4-Methyl-4-oxytetrahydropyran und Gemischen davon; und
- Verfahren gemäß Anspruch 1, dadurch gekennzeichnet, dass der Sauerstoff enthaltende Bestandteil (c) und der Bestandteil (d) dem Ethanolbestandteil (b) zugegeben werden, wobei das Gemisch aus (c), (b) und (d) nachfolgend dem Kohlenwasserstoffbestandteil (a) zugegeben wird.
- Verfahren gemäß Anspruch 1, dadurch gekennzeichnet, dass der Ethanolbestandteil (b) dem Kohlenwasserstoffbestandteil (a) zugegeben wird, dem Gemisch aus (b) und (a) der Sauerstoff enthaltende Bestandteil (c) zugegeben wird, wobei ein Gemisch aus (a), (b) und (c) erhalten wird, und diesem Gemisch Bestandteil (d) zugegeben wird.
- Verfahren nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass der C3-C12 Kohlenwasserstoffbestandteil (a) aus nicht reformuliertem Standardbenzin, einer Kohlenwasserstoffflüssigkeit aus der Erdölraffinerie, einer Kohlenwasserstoffflüssigkeit aus Erdgas, einer Kohlenwasserstoffflüssigkeit aus einem Abgas einer chemischen Rückgewinnung bei der Verkohlung, einer Kohlenwasserstoffflüssigkeit aus einer Synthesegasverarbeitung oder Gemischen davon ausgewählt ist, wobei nicht reformuliertes Standardbenzin bevorzugt ist.
- Verfahren gemäß einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass die erhaltene Treibstoffzusammensetzung die folgenden Merkmale aufweist:(i) eine Dichte bei 15°C gemäß ASTM D 4052 von mindestens 690 kg/m3;(ii) ein trockenes Dampfdruckequivalent gemäß ASTM D 5191 von 20 kPa bis 120 kPa;(iii) einen Säuregehalt gemäß ASTM D 1613 von nicht mehr als 0, 1 Gew.-% HAc;(iv) einen pH-Wert gemäß ASTM D 1287 von 5 bis 9;(v) einen Aromatengehalt gemäß SS 155120 von nicht mehr als 40 Vol.-%, wobei Benzol gemäß EN 238 in Mengen von nicht mehr als 1 Vol.-% vorhanden ist;(vi) einen Schwefelgehalt gemäß ASTM D 5453 von nicht mehr als 50 mg/kg;(vii) einen Gummigehalt gemäß ASTM D 381 von nicht mehr als 2 mg/100 ml;(viii) Destillationseigenschaften gemäß ASTM D 86, wobei der Anfangssiedepunkt mindestens 20°C beträgt, der verdampfbare Anteil bei 70°C mindestens 25 Vol.-% beträgt, der verdampfbare Anteil bei 100°C mindestens 50 Vol.-% beträgt; der verdampfbare Anteil bei 150°C mindestens 75 Vol.-% beträgt; der verdampfbare Anteil bei 190°C mindestens 95 Vol.-% beträgt; der Endsiedepunkt nicht größer als 205°C ist; und der Verdampfungsrückstand nicht mehr als 2 Vol.-% beträgt; und(ix) eine Klopffestigkeit von 0,5 (RON+MON) gemäß ASTM D 2699-86 und ASTM D 2700-86 von mindestens 80.
- Verfahren gemäß einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass der Kohlenwasserstoffbestandteil (d) aus Benzol, Toluol, Xylol, Ethylbenzol, Isopropylbenzol, Isopropyltoluol, Diethylbenzol, Isopropylxylol, tert-Butylbenzol, tert-Butyltoluol, tert-Butylxylol, Cyclooctadien, Cyclooctatetraen, Limonen, Isooctan, Isononan, Isodecan, Isoocten, Myrcen, Allocymen, tert-Butylcyclohexan und Gemischen davon ausgewählt ist.
- Verfahren gemäß einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass der Kohlenwasserstoffbestandteil (d) aus einer C8-C11 Fraktion ausgewählt ist.
- Verfahren gemäß einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass der Kohlenwasserstoffbestandteil (d) aus einer bei 100 bis 200°C siedenden Fraktion ausgewählt ist, welche beim Destillieren von Öl, Kokskohlenharz oder Synthesegasverarbeitungsprodukten erhalten wird.
- Verfahren gemäß einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass das Volumenverhältnis von (b):((c)+(d)) 1:10 bis 10:1 beträgt.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05104353A EP1589091A1 (de) | 2000-01-24 | 2001-01-24 | Verfahren zur Verringerung des Dampfdruckes von ethanolhaltigen Motortreibstoffen für funkengezündete Verbrennungsmotoren |
SI200130387T SI1252268T1 (en) | 2000-01-24 | 2001-01-24 | Method of reducing the vapour pressure of ethanol-containing motor fuels for spark ignition combustion engines |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/SE2000/000139 WO2001053436A1 (en) | 2000-01-24 | 2000-01-24 | Motor fuel for spark ignition internal combustion engines |
WOPCT/SE00/00139 | 2000-01-24 | ||
PCT/SE2001/000040 WO2001053437A1 (en) | 2000-01-24 | 2001-01-24 | Method of reducing the vapour pressure of ethanol-containing motor fuels for spark ignition combustion engines |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05104353A Division EP1589091A1 (de) | 2000-01-24 | 2001-01-24 | Verfahren zur Verringerung des Dampfdruckes von ethanolhaltigen Motortreibstoffen für funkengezündete Verbrennungsmotoren |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1252268A1 EP1252268A1 (de) | 2002-10-30 |
EP1252268B1 true EP1252268B1 (de) | 2005-05-25 |
Family
ID=20278139
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05104353A Ceased EP1589091A1 (de) | 2000-01-24 | 2001-01-24 | Verfahren zur Verringerung des Dampfdruckes von ethanolhaltigen Motortreibstoffen für funkengezündete Verbrennungsmotoren |
EP01942659A Expired - Lifetime EP1252268B1 (de) | 2000-01-24 | 2001-01-24 | Verfahren zur verringerung des dampfdruckes von ethanolhaltigen motortreibstoffen für funkengezündete verbrennungsmotoren |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05104353A Ceased EP1589091A1 (de) | 2000-01-24 | 2001-01-24 | Verfahren zur Verringerung des Dampfdruckes von ethanolhaltigen Motortreibstoffen für funkengezündete Verbrennungsmotoren |
Country Status (30)
Country | Link |
---|---|
EP (2) | EP1589091A1 (de) |
JP (1) | JP4871475B2 (de) |
KR (1) | KR100545054B1 (de) |
CN (1) | CN1177914C (de) |
AT (1) | ATE296342T1 (de) |
AU (2) | AU3684800A (de) |
BG (1) | BG66039B1 (de) |
BR (1) | BR0107817B1 (de) |
CA (1) | CA2397579C (de) |
CU (1) | CU23146A3 (de) |
CZ (1) | CZ305710B6 (de) |
DE (1) | DE60111018T2 (de) |
DK (1) | DK1252268T3 (de) |
EA (1) | EA006855B1 (de) |
EE (1) | EE05647B1 (de) |
ES (1) | ES2243510T3 (de) |
HK (1) | HK1052023A1 (de) |
HR (1) | HRP20020670B1 (de) |
HU (1) | HU230551B1 (de) |
IL (1) | IL150624A (de) |
MX (1) | MXPA02007148A (de) |
NO (1) | NO336184B1 (de) |
PL (1) | PL194561B1 (de) |
PT (1) | PT1252268E (de) |
RS (1) | RS52075B (de) |
SI (1) | SI1252268T1 (de) |
SK (1) | SK287660B6 (de) |
UA (1) | UA76945C2 (de) |
WO (2) | WO2001053436A1 (de) |
ZA (1) | ZA200205833B (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3187570A1 (de) | 2015-12-29 | 2017-07-05 | Neste Oyj | Erneuerbares dvpe-einstellungsmaterial, brennstoffmischung damit und verfahren zur herstellung einer brennstoffmischung |
Families Citing this family (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6761745B2 (en) | 2000-01-24 | 2004-07-13 | Angelica Hull | Method of reducing the vapor pressure of ethanol-containing motor fuels for spark ignition combustion engines |
US7981170B1 (en) * | 2000-04-21 | 2011-07-19 | Shell Oil Company | Gasoline-oxygenate blend and method of producing the same |
US6565617B2 (en) * | 2000-08-24 | 2003-05-20 | Shell Oil Company | Gasoline composition |
WO2003062354A1 (en) * | 2002-01-21 | 2003-07-31 | Ramar Ponniah | Hydrocarbon fuel |
JP2005187706A (ja) * | 2003-12-26 | 2005-07-14 | Japan Energy Corp | エタノール含有ガソリンおよびその製造方法 |
US20090199464A1 (en) * | 2008-02-12 | 2009-08-13 | Bp Corporation North America Inc. | Reduced RVP Oxygenated Gasoline Composition And Method |
WO2006081089A1 (en) * | 2005-01-25 | 2006-08-03 | Bp Corporation North America Inc. | Reduced rvp oxygenated gasoline composition and method |
AU2011226816B2 (en) * | 2005-01-25 | 2012-08-30 | Bp Corporation North America Inc. | Reduced RVP oxygenated gasoline composition and method |
JP4624142B2 (ja) * | 2005-03-11 | 2011-02-02 | コスモ石油株式会社 | エタノール配合ガソリン |
JP4624143B2 (ja) * | 2005-03-11 | 2011-02-02 | コスモ石油株式会社 | エタノール配合ガソリン |
US7389751B2 (en) * | 2006-03-17 | 2008-06-24 | Ford Global Technology, Llc | Control for knock suppression fluid separator in a motor vehicle |
MY146612A (en) | 2006-05-26 | 2012-09-14 | Amyris Inc | Production of isoprenoids |
AU2007267914C1 (en) * | 2006-05-26 | 2012-06-07 | Amyris, Inc. | Fuel components, fuel compositions and methods of making and using same |
KR100812423B1 (ko) * | 2006-12-13 | 2008-03-10 | 현대자동차주식회사 | 연료 중의 에탄올 농도 계산 방법 및 그 장치 |
US8968426B2 (en) | 2007-01-15 | 2015-03-03 | Technische Universiteit Eindhoven | Liquid fuel composition and the use thereof |
NL1033228C2 (nl) * | 2007-01-15 | 2008-07-16 | Univ Eindhoven Tech | Vloeibare brandstofsamenstelling alsmede de toepassing daarvan. |
DE102008008818A1 (de) * | 2008-02-12 | 2009-08-20 | Deutsche Bp Ag | Kraftstoffe für Otto-Motoren |
US20110016774A1 (en) * | 2008-03-12 | 2011-01-27 | Ponnupillai Ramar | Velar Bio Hydrocarbon Fuel |
US9476004B2 (en) | 2009-09-08 | 2016-10-25 | Technische Universiteit Eindhoven | Liquid fuel composition and the use thereof |
JP5214688B2 (ja) * | 2010-09-10 | 2013-06-19 | コスモ石油株式会社 | エタノール配合ガソリンの製造方法 |
JP5144729B2 (ja) * | 2010-09-10 | 2013-02-13 | コスモ石油株式会社 | エタノール配合ガソリンの製造方法 |
CN103415600B (zh) | 2011-03-10 | 2015-11-25 | 国际壳牌研究有限公司 | 关于汽油燃料制剂改进 |
KR101700490B1 (ko) * | 2011-08-17 | 2017-01-26 | 후난 종추앙 케미칼 컴퍼니 리미티드 | 가솔린 조성물 및 이의 제조방법 |
NL2007304C2 (en) * | 2011-08-26 | 2013-02-27 | Progression Industry B V | Use of perfume composition as fuel for internal combustion engines. |
US8968429B2 (en) * | 2011-09-23 | 2015-03-03 | Butamax Advanced Biofuels Llc | Butanol compositions for fuel blending and methods for the production thereof |
CN102746909B (zh) * | 2012-07-20 | 2014-04-16 | 杨如平 | 一种甲醇燃料改性剂及汽油发动机用高比例甲醇燃料 |
CN102876404B (zh) * | 2012-10-11 | 2014-10-22 | 陕西延长石油(集团)有限责任公司研究院 | 一种降低甲醇汽油饱和蒸汽压的添加剂 |
ITMI20122006A1 (it) * | 2012-11-26 | 2014-05-27 | Eni Spa | Composizioni utili come carburanti comprendenti composti ossigenati idrofobici |
CN104004554B (zh) * | 2014-06-05 | 2016-01-20 | 上海化工研究院 | 车用醇醚替代燃料尾气改善剂及其制备方法和应用 |
BR112017005960B1 (pt) * | 2014-10-06 | 2021-08-24 | Shell Internationale Research Maatschappij B.V. | Uso de uma composição de hidrocarboneto líquida |
US11913166B2 (en) | 2015-09-21 | 2024-02-27 | Modern Meadow, Inc. | Fiber reinforced tissue composites |
RU2605954C1 (ru) * | 2015-12-25 | 2017-01-10 | Акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (АО "ВНИИ НП") | Альтернативное автомобильное топливо и способ его получения |
RU2605952C1 (ru) * | 2015-12-25 | 2017-01-10 | Акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (АО "ВНИИ НП") | Альтернативное автомобильное топливо и способ его получения |
EP3205701A1 (de) | 2016-02-11 | 2017-08-16 | Bp Oil International Limited | Kraftstoffzusammensetzungen |
EP3205702A1 (de) * | 2016-02-11 | 2017-08-16 | Bp Oil International Limited | Kraftstoffzusammensetzungen mit additiven |
EP3205703A1 (de) | 2016-02-11 | 2017-08-16 | Bp Oil International Limited | Kraftstoffadditive |
ES2806990T3 (es) | 2016-02-15 | 2021-02-19 | Modern Meadow Inc | Procedimiento para fabricar un material biofabricado que contiene fibrillas de colágeno |
RU2616606C1 (ru) * | 2016-04-14 | 2017-04-18 | Акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (АО "ВНИИ НП") | Высокооктановый автомобильный бензин и антидетонационная добавка для его получения |
EP3301144B1 (de) * | 2016-09-29 | 2021-03-17 | Neste Oyj | Dieselkraftstoff umfassend 5-nonanon |
EP3399008B1 (de) | 2017-05-02 | 2020-03-18 | ASG Analytik-Service Gesellschaft mbH | Potenziell co2-neutraler und umweltschonender ottokraftstoff auf basis der c1-chemie |
AU2018253595A1 (en) | 2017-11-13 | 2019-05-30 | Modern Meadow, Inc. | Biofabricated leather articles having zonal properties |
AU2020209847B2 (en) | 2019-01-17 | 2024-10-17 | Modern Meadow, Inc. | Layered collagen materials and methods of making the same |
RU2740554C1 (ru) * | 2020-08-13 | 2021-01-15 | федеральное государственное автономное образовательное учреждение высшего образования "Российский государственный университет нефти и газа (национальный исследовательский университет) имени И.М. Губкина" | Высокооктановый бензин |
FI129568B (en) | 2021-04-15 | 2022-04-29 | Neste Oyj | 2-BUTANONE AND ETHANOL AS FUEL COMPONENTS |
EP4433556A1 (de) * | 2021-11-16 | 2024-09-25 | Hediger, Richard | Verfahren zur herstellung eines kraftstoffzusatzes |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2104021A (en) * | 1935-04-24 | 1938-01-04 | Callis Conral Cleo | Fuel |
US2365009A (en) * | 1940-12-19 | 1944-12-12 | Standard Oil Dev Co | Motor fuels |
RO75851A2 (ro) * | 1978-02-22 | 1981-02-28 | Institutul National De Motoare Termice,Ro | Amestec combustibil |
US4207076A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with ethyl-t-butyl ether |
DK148747C (da) * | 1980-06-09 | 1986-02-24 | Inst Francais Du Petrole | Motorbraendstof |
US4328004A (en) * | 1980-08-13 | 1982-05-04 | United International Research, Inc. | Stabilization of ethanol-gasoline mixtures |
FR2493863A1 (fr) * | 1980-11-07 | 1982-05-14 | Inst Francais Du Petrole | Nouveaux carburants a base d'essence renfermant de l'ethanol hydrate et un additif |
DE3150989A1 (de) * | 1980-12-30 | 1982-08-05 | Institut Français du Pétrole, 92502 Rueil-Malmaison, Hauts-de-Seine | Brennbare kompositionen, die ein gasoel, mindestens einen fettsaeureester sowie einen alkoholischen bestandteil auf basis von n-butanol enthalten und als dieseltreibstoffe brauchbar sind |
FR2500844A1 (fr) * | 1981-03-02 | 1982-09-03 | Realisations Sarl Et | Additifs permettant l'incorporation d'alcools aux carburants et compositions carburantes renfermant lesdits additifs |
DE3116734C2 (de) * | 1981-04-28 | 1985-07-25 | Veba Oel AG, 4650 Gelsenkirchen | Vergaserkraftstoff |
US4451266A (en) * | 1982-01-22 | 1984-05-29 | John D. Barclay | Additive for improving performance of liquid hydrocarbon fuels |
US4541836A (en) * | 1982-12-09 | 1985-09-17 | Union Carbide Corporation | Fuel compositions |
EP0121089B1 (de) * | 1983-03-03 | 1989-05-31 | DEA Mineraloel Aktiengesellschaft | Motor-Kraftstoff |
DE3330165C2 (de) * | 1983-08-20 | 1985-10-03 | Union Rheinische Braunkohlen Kraftstoff AG, 5000 Köln | Motor-Kraftstoff |
US4891050A (en) * | 1985-11-08 | 1990-01-02 | Fuel Tech, Inc. | Gasoline additives and gasoline containing soluble platinum group metal compounds and use in internal combustion engines |
US4806129A (en) * | 1987-09-21 | 1989-02-21 | Prepolene Industries, Inc. | Fuel extender |
US4818250A (en) * | 1987-10-21 | 1989-04-04 | Lemco Energy, Inc. | Process for producing fuel from plant sources and fuel blends containing same |
ES2012729A6 (es) * | 1989-06-07 | 1990-04-01 | Vicente Rodriguez Heliodoro | Procedimiento para la obtencion de un componente organico oxigenado adicionable a carburantes. |
CN1017061B (zh) * | 1990-02-13 | 1992-06-17 | 唐昌干 | 车船用抗暴减烟节油剂及其生产方法 |
DE4308053C2 (de) * | 1993-03-13 | 1997-05-15 | Veba Oel Ag | Flüssige unverbleite Kraftstoffe |
US5607486A (en) * | 1994-05-04 | 1997-03-04 | Wilkins, Jr.; Joe S. | Engine fuels |
US5688295A (en) * | 1996-05-08 | 1997-11-18 | H. E. W. D. Enterprises-America, Inc. | Gasoline fuel additive |
US5697987A (en) * | 1996-05-10 | 1997-12-16 | The Trustees Of Princeton University | Alternative fuel |
AU761457B2 (en) * | 1998-01-12 | 2003-06-05 | Deborah Wenzel | An additive composition also used as a fuel composition comprising water soluble alcohols |
-
2000
- 2000-01-24 AU AU36848/00A patent/AU3684800A/en not_active Abandoned
- 2000-01-24 WO PCT/SE2000/000139 patent/WO2001053436A1/en active Application Filing
-
2001
- 2001-01-11 PL PL01356843A patent/PL194561B1/pl unknown
- 2001-01-11 HU HU0204201A patent/HU230551B1/hu unknown
- 2001-01-24 DE DE60111018T patent/DE60111018T2/de not_active Expired - Lifetime
- 2001-01-24 EP EP05104353A patent/EP1589091A1/de not_active Ceased
- 2001-01-24 JP JP2001553900A patent/JP4871475B2/ja not_active Expired - Fee Related
- 2001-01-24 DK DK01942659T patent/DK1252268T3/da active
- 2001-01-24 EA EA200200796A patent/EA006855B1/ru not_active IP Right Cessation
- 2001-01-24 CN CNB018040500A patent/CN1177914C/zh not_active Expired - Fee Related
- 2001-01-24 RS YU55802A patent/RS52075B/sr unknown
- 2001-01-24 EE EEP200200407A patent/EE05647B1/xx active IP Right Revival
- 2001-01-24 CA CA2397579A patent/CA2397579C/en not_active Expired - Lifetime
- 2001-01-24 EP EP01942659A patent/EP1252268B1/de not_active Expired - Lifetime
- 2001-01-24 UA UA2002076155A patent/UA76945C2/uk unknown
- 2001-01-24 ES ES01942659T patent/ES2243510T3/es not_active Expired - Lifetime
- 2001-01-24 PT PT01942659T patent/PT1252268E/pt unknown
- 2001-01-24 WO PCT/SE2001/000040 patent/WO2001053437A1/en active IP Right Grant
- 2001-01-24 SI SI200130387T patent/SI1252268T1/xx unknown
- 2001-01-24 AU AU28949/01A patent/AU782062B2/en not_active Ceased
- 2001-01-24 KR KR1020027009521A patent/KR100545054B1/ko active IP Right Grant
- 2001-01-24 BR BRPI0107817-8A patent/BR0107817B1/pt not_active IP Right Cessation
- 2001-01-24 IL IL15062401A patent/IL150624A/xx active IP Right Grant
- 2001-01-24 AT AT01942659T patent/ATE296342T1/de active
- 2001-01-24 SK SK1222-2002A patent/SK287660B6/sk not_active IP Right Cessation
- 2001-01-24 CZ CZ2002-2869A patent/CZ305710B6/cs not_active IP Right Cessation
- 2001-01-24 MX MXPA02007148A patent/MXPA02007148A/es active IP Right Grant
-
2002
- 2002-07-17 CU CU149A patent/CU23146A3/es unknown
- 2002-07-22 ZA ZA200205833A patent/ZA200205833B/en unknown
- 2002-07-23 NO NO20023502A patent/NO336184B1/no not_active IP Right Cessation
- 2002-08-13 HR HR20020670A patent/HRP20020670B1/xx not_active IP Right Cessation
- 2002-08-15 BG BG107007A patent/BG66039B1/en unknown
-
2003
- 2003-06-11 HK HK03104130A patent/HK1052023A1/xx not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3187570A1 (de) | 2015-12-29 | 2017-07-05 | Neste Oyj | Erneuerbares dvpe-einstellungsmaterial, brennstoffmischung damit und verfahren zur herstellung einer brennstoffmischung |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1252268B1 (de) | Verfahren zur verringerung des dampfdruckes von ethanolhaltigen motortreibstoffen für funkengezündete verbrennungsmotoren | |
US6761745B2 (en) | Method of reducing the vapor pressure of ethanol-containing motor fuels for spark ignition combustion engines | |
US5697987A (en) | Alternative fuel | |
US20010034966A1 (en) | Method of reducing the vapor pressure of ethanol-containing motor fuels for spark ignition combustion engines | |
BRPI0619727A2 (pt) | combustìvel de aviação sem chumbo | |
JP2006515377A (ja) | 高アルコール代替燃料 | |
JP2000026871A (ja) | 低公害燃料組成物 | |
JP4691269B2 (ja) | ガソリンエンジン用燃料油組成物 | |
JP4920185B2 (ja) | ガソリン組成物 | |
JP4746869B2 (ja) | 高性能ガソリン | |
JPH06192667A (ja) | ガソリン組成物 | |
US20100000483A1 (en) | Gasoline compositions | |
JP2006016590A (ja) | ガソリン |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20020815 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
AX | Request for extension of the european patent |
Free format text: AL PAYMENT 20020815;LT PAYMENT 20020815;LV PAYMENT 20020815;MK PAYMENT 20020815;RO PAYMENT 20020815;SI PAYMENT 20020815 |
|
17Q | First examination report despatched |
Effective date: 20031022 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
AX | Request for extension of the european patent |
Extension state: AL LT LV MK RO SI |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REF | Corresponds to: |
Ref document number: 60111018 Country of ref document: DE Date of ref document: 20050630 Kind code of ref document: P |
|
REG | Reference to a national code |
Ref country code: SE Ref legal event code: TRGR |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: EP Ref document number: 20050402596 Country of ref document: GR |
|
REG | Reference to a national code |
Ref country code: PT Ref legal event code: SC4A Effective date: 20050729 Ref country code: CH Ref legal event code: NV Representative=s name: DR. LUSUARDI AG |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2243510 Country of ref document: ES Kind code of ref document: T3 |
|
PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
PLAX | Notice of opposition and request to file observation + time limit sent |
Free format text: ORIGINAL CODE: EPIDOSNOBS2 |
|
ET | Fr: translation filed | ||
26 | Opposition filed |
Opponent name: BP OIL INTERNATIONAL LIMITED Effective date: 20060223 |
|
NLR1 | Nl: opposition has been filed with the epo |
Opponent name: BP OIL INTERNATIONAL LIMITED |
|
PLAF | Information modified related to communication of a notice of opposition and request to file observations + time limit |
Free format text: ORIGINAL CODE: EPIDOSCOBS2 |
|
PLBB | Reply of patent proprietor to notice(s) of opposition received |
Free format text: ORIGINAL CODE: EPIDOSNOBS3 |
|
PLCK | Communication despatched that opposition was rejected |
Free format text: ORIGINAL CODE: EPIDOSNREJ1 |
|
APBM | Appeal reference recorded |
Free format text: ORIGINAL CODE: EPIDOSNREFNO |
|
APBP | Date of receipt of notice of appeal recorded |
Free format text: ORIGINAL CODE: EPIDOSNNOA2O |
|
APAH | Appeal reference modified |
Free format text: ORIGINAL CODE: EPIDOSCREFNO |
|
APBQ | Date of receipt of statement of grounds of appeal recorded |
Free format text: ORIGINAL CODE: EPIDOSNNOA3O |
|
APBU | Appeal procedure closed |
Free format text: ORIGINAL CODE: EPIDOSNNOA9O |
|
PLBN | Opposition rejected |
Free format text: ORIGINAL CODE: 0009273 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: OPPOSITION REJECTED |
|
27O | Opposition rejected |
Effective date: 20110325 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R100 Ref document number: 60111018 Country of ref document: DE Effective date: 20110325 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 60111018 Country of ref document: DE Representative=s name: WHITE & CASE LLP, DE |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 60111018 Country of ref document: DE Representative=s name: WHITE & CASE LLP, DE Effective date: 20150119 Ref country code: DE Ref legal event code: R081 Ref document number: 60111018 Country of ref document: DE Owner name: SWEDISH BIOFUELS (IP) LIMITED, GB Free format text: FORMER OWNER: HULL, ANGELICA, LIDINGOE, SE Effective date: 20150119 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: 732E Free format text: REGISTERED BETWEEN 20150205 AND 20150211 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R008 Ref document number: 60111018 Country of ref document: DE Ref country code: DE Ref legal event code: R039 Ref document number: 60111018 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: TR Payment date: 20160112 Year of fee payment: 16 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 17 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R040 Ref document number: 60111018 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 18 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: LU Payment date: 20171228 Year of fee payment: 18 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 60111018 Country of ref document: DE Representative=s name: VOSSIUS & PARTNER PATENTANWAELTE RECHTSANWAELT, DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190124 |
|
REG | Reference to a national code |
Ref country code: SI Ref legal event code: KO00 Effective date: 20190926 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20200120 Year of fee payment: 20 Ref country code: PT Payment date: 20200108 Year of fee payment: 20 Ref country code: DE Payment date: 20190920 Year of fee payment: 20 Ref country code: ES Payment date: 20200203 Year of fee payment: 20 Ref country code: AT Payment date: 20200121 Year of fee payment: 20 Ref country code: IT Payment date: 20200117 Year of fee payment: 20 Ref country code: DK Payment date: 20200122 Year of fee payment: 20 Ref country code: IE Payment date: 20200116 Year of fee payment: 20 Ref country code: SE Payment date: 20200122 Year of fee payment: 20 Ref country code: MC Payment date: 20200116 Year of fee payment: 20 Ref country code: GR Payment date: 20200121 Year of fee payment: 20 Ref country code: GB Payment date: 20200120 Year of fee payment: 20 Ref country code: FI Payment date: 20200120 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 20200120 Year of fee payment: 20 Ref country code: BE Payment date: 20200120 Year of fee payment: 20 Ref country code: CY Payment date: 20191231 Year of fee payment: 20 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R042 Ref document number: 60111018 Country of ref document: DE |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20200116 Year of fee payment: 20 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY Effective date: 20200609 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: EUP Expiry date: 20210124 |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MK Effective date: 20210123 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: PE20 Expiry date: 20210123 |
|
REG | Reference to a national code |
Ref country code: FI Ref legal event code: MAE |
|
REG | Reference to a national code |
Ref country code: SE Ref legal event code: EUG |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: MK9A |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK07 Ref document number: 296342 Country of ref document: AT Kind code of ref document: T Effective date: 20210124 |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MK Effective date: 20210124 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20210123 Ref country code: PT Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20210204 Ref country code: IE Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20210124 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20211229 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20210125 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200124 |