KR950703044A - Lead Free Methylcyclopentadienyl Manganese Tricarbonyl Fuel Composition [UNLEADED METHYLCYCLOPENTADIENYL MANGANESE TRICARBONYL (MMT) FUEL COMPOSITION] - Google Patents
Lead Free Methylcyclopentadienyl Manganese Tricarbonyl Fuel Composition [UNLEADED METHYLCYCLOPENTADIENYL MANGANESE TRICARBONYL (MMT) FUEL COMPOSITION] Download PDFInfo
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- KR950703044A KR950703044A KR1019950700815A KR19950700815A KR950703044A KR 950703044 A KR950703044 A KR 950703044A KR 1019950700815 A KR1019950700815 A KR 1019950700815A KR 19950700815 A KR19950700815 A KR 19950700815A KR 950703044 A KR950703044 A KR 950703044A
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- South Korea
- Prior art keywords
- combustion
- manganese
- emissions
- fuel
- composition
- Prior art date
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- 239000000446 fuel Substances 0.000 title claims abstract description 26
- 239000000203 mixture Substances 0.000 title claims abstract 30
- ANHQLUBMNSSPBV-UHFFFAOYSA-N 4h-pyrido[3,2-b][1,4]oxazin-3-one Chemical group C1=CN=C2NC(=O)COC2=C1 ANHQLUBMNSSPBV-UHFFFAOYSA-N 0.000 title abstract 5
- 238000002485 combustion reaction Methods 0.000 claims abstract 31
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims abstract 14
- 229910052748 manganese Inorganic materials 0.000 claims abstract 14
- 239000011572 manganese Substances 0.000 claims abstract 14
- 150000001875 compounds Chemical class 0.000 claims abstract 8
- 230000015572 biosynthetic process Effects 0.000 claims abstract 4
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 claims abstract 4
- 229930195733 hydrocarbon Natural products 0.000 claims 21
- 150000002430 hydrocarbons Chemical class 0.000 claims 21
- 238000000034 method Methods 0.000 claims 16
- 239000004215 Carbon black (E152) Substances 0.000 claims 13
- 238000009835 boiling Methods 0.000 claims 9
- 239000000758 substrate Substances 0.000 claims 7
- DEIHRWXJCZMTHF-UHFFFAOYSA-N [Mn].[CH]1C=CC=C1 Chemical compound [Mn].[CH]1C=CC=C1 DEIHRWXJCZMTHF-UHFFFAOYSA-N 0.000 claims 6
- 239000006184 cosolvent Substances 0.000 claims 6
- 238000006213 oxygenation reaction Methods 0.000 claims 6
- -1 methyloxy radical Chemical class 0.000 claims 5
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims 4
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 claims 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 3
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 claims 3
- 230000002401 inhibitory effect Effects 0.000 claims 3
- NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 0.000 claims 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 2
- HVZJRWJGKQPSFL-UHFFFAOYSA-N tert-Amyl methyl ether Chemical compound CCC(C)(C)OC HVZJRWJGKQPSFL-UHFFFAOYSA-N 0.000 claims 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical group CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 230000003247 decreasing effect Effects 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 230000001105 regulatory effect Effects 0.000 claims 1
- 239000000779 smoke Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
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Abstract
무연 연료 조성물은 사이클로메틱 망간 트리카보닐 화합물(CMT), 바람직하게는 메틸사이클로펜타디에닐 망간 트리카보닐(MMT)과, 생성된 배기 방출물이 환경적으로 허용되도록 연소 도중에 대량의 망간산화물의 형성을 감소시키는 수단을 포함한다.The lead-free fuel composition is composed of a cyclomatic manganese tricarbonyl compound (CMT), preferably methylcyclopentadienyl manganese tricarbonyl (MMT), and a large amount of manganese oxide during combustion so that the resulting exhaust emissions are environmentally acceptable. Means for reducing formation.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.
제1도는 2부류의 연료 사이의 더욱 높은 하중, 더 큰 EGT 차이를 나타낸다.Figure 1 shows the higher load, larger EGT difference between the two classes of fuel.
Claims (23)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US93419292A | 1992-08-24 | 1992-08-24 | |
US07/934,192 | 1992-08-24 | ||
US07/935192 | 1992-08-24 | ||
PCT/US1993/007962 WO1994004636A1 (en) | 1992-08-24 | 1993-08-24 | Unleaded mmt fuel composition |
Publications (2)
Publication Number | Publication Date |
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KR950703044A true KR950703044A (en) | 1995-08-23 |
KR100307417B1 KR100307417B1 (en) | 2001-11-30 |
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ID=25465130
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019950700815A KR100307417B1 (en) | 1992-08-24 | 1993-08-24 | How to increase the economics of fuels and fuel compositions for them |
Country Status (6)
Country | Link |
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EP (1) | EP0656045A1 (en) |
JP (2) | JP3478825B2 (en) |
KR (1) | KR100307417B1 (en) |
AU (1) | AU5089593A (en) |
CA (1) | CA2142991A1 (en) |
WO (1) | WO1994004636A1 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2184490C (en) * | 1994-03-02 | 2008-07-08 | William C. Orr | Unleaded mmt fuel compositions |
AU2692795A (en) * | 1994-05-31 | 1995-12-21 | William C. Orr | Vapor phase combustion methods and compositions |
KR19990022557A (en) * | 1995-06-07 | 1999-03-25 | 윌리엄 씨. 오어 | Steam phase combustion method and composition II |
JP3948796B2 (en) * | 1997-09-30 | 2007-07-25 | 新日本石油株式会社 | Unleaded gasoline for in-cylinder direct injection gasoline engines |
US6206940B1 (en) | 1999-02-12 | 2001-03-27 | Exxon Research And Engineering Company | Fuel formulations to extend the lean limit (law770) |
AU2008237487B2 (en) * | 2007-04-04 | 2012-04-05 | The Lubrizol Corporation | A synergistic combination of a hindered phenol and nitrogen containing detergent for biodiesel fuel to improve oxidative stability |
KR100881756B1 (en) | 2007-10-15 | 2009-02-06 | 주식회사 성우지오텍 | Exhaust gas purification method and purification device using advanced oxidation method of Fenton reaction |
US8741002B2 (en) | 2009-05-25 | 2014-06-03 | Shell Oil Company | Gasoline compositions |
WO2010136437A1 (en) | 2009-05-25 | 2010-12-02 | Shell Internationale Research Maatschappij B.V. | Gasoline compositions |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4141693A (en) * | 1974-12-18 | 1979-02-27 | Standard Oil Company (Ohio) | Manganese containing fuels |
US4005993A (en) * | 1976-03-08 | 1977-02-01 | Ethyl Corporation | Novel gasoline compositions |
WO1987001384A1 (en) * | 1985-08-28 | 1987-03-12 | Orr William C | Nonleaded fuel composition |
US4988366A (en) * | 1989-10-24 | 1991-01-29 | Mobil Oil Corporation | High conversion TAME and MTBE production process |
CA2045455C (en) * | 1990-07-13 | 2002-04-02 | John Vincent Hanlon | Motor fuels of enhanced properties |
EP0474342A1 (en) * | 1990-09-05 | 1992-03-11 | ARCO Chemical Technology, L.P. | Unsymmetrical dialkyl carbonate fuel additives |
US5113803A (en) * | 1991-04-01 | 1992-05-19 | Ethyl Petroleum Additives, Inc. | Reduction of Nox emissions from gasoline engines |
-
1993
- 1993-08-24 CA CA002142991A patent/CA2142991A1/en not_active Abandoned
- 1993-08-24 AU AU50895/93A patent/AU5089593A/en not_active Abandoned
- 1993-08-24 WO PCT/US1993/007962 patent/WO1994004636A1/en not_active Application Discontinuation
- 1993-08-24 KR KR1019950700815A patent/KR100307417B1/en not_active IP Right Cessation
- 1993-08-24 EP EP93920308A patent/EP0656045A1/en active Pending
- 1993-08-24 JP JP50659894A patent/JP3478825B2/en not_active Expired - Fee Related
-
2003
- 2003-06-25 JP JP2003181643A patent/JP4054288B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP3478825B2 (en) | 2003-12-15 |
KR100307417B1 (en) | 2001-11-30 |
CA2142991A1 (en) | 1994-03-03 |
JPH08500624A (en) | 1996-01-23 |
JP2004003500A (en) | 2004-01-08 |
WO1994004636A1 (en) | 1994-03-03 |
AU5089593A (en) | 1994-03-15 |
JP4054288B2 (en) | 2008-02-27 |
EP0656045A1 (en) | 1995-06-07 |
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