JP2000192059A5 - - Google Patents
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- Publication number
- JP2000192059A5 JP2000192059A5 JP1999363794A JP36379499A JP2000192059A5 JP 2000192059 A5 JP2000192059 A5 JP 2000192059A5 JP 1999363794 A JP1999363794 A JP 1999363794A JP 36379499 A JP36379499 A JP 36379499A JP 2000192059 A5 JP2000192059 A5 JP 2000192059A5
- Authority
- JP
- Japan
- Prior art keywords
- additive composition
- fuel
- composition according
- group
- fuel additive
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 description 33
- 239000002816 fuel additive Substances 0.000 description 25
- 229910052739 hydrogen Inorganic materials 0.000 description 14
- 239000001257 hydrogen Substances 0.000 description 14
- 239000000446 fuel Substances 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 5
- -1 aromatic ester compound Chemical class 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 150000002430 hydrocarbons Chemical group 0.000 description 5
- 229920000768 polyamine Polymers 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229920002367 Polyisobutene Polymers 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920001281 polyalkylene Polymers 0.000 description 3
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 125000003916 ethylene diamine group Chemical group 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/218782 | 1998-12-22 | ||
| US09/218,782 US6071319A (en) | 1998-12-22 | 1998-12-22 | Fuel additive compositions containing aromatic esters of polyalkylphenoxyalkanols and aliphatic amines |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2000192059A JP2000192059A (ja) | 2000-07-11 |
| JP2000192059A5 true JP2000192059A5 (enExample) | 2007-02-08 |
| JP4790887B2 JP4790887B2 (ja) | 2011-10-12 |
Family
ID=22816493
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP36379499A Expired - Lifetime JP4790887B2 (ja) | 1998-12-22 | 1999-12-22 | ポリアルキルフェノキシアルカノールの芳香族エステルと脂肪族アミンとを含む燃料添加剤組成物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US6071319A (enExample) |
| EP (1) | EP1013745B1 (enExample) |
| JP (1) | JP4790887B2 (enExample) |
| CA (1) | CA2287766C (enExample) |
| DE (1) | DE69930597T2 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60025035D1 (de) * | 1999-11-30 | 2006-01-26 | Ici Plc | Verfahren zur Behandlung von Rohöl oder Öl in einem Raffinerieverfahren |
| ES2489815B1 (es) * | 2013-02-21 | 2015-08-10 | Centro De Investigación Príncipe Felipe | Nuevos p-terfenilos hexakis-sustituidos con grupos bilaterales para el tratamiento de la infección por el virus de la inmunodeficiencia humana tipo 1 (VIH-1) y otras enfermedades |
| KR102759010B1 (ko) * | 2018-03-23 | 2025-01-24 | 셰브런 오로나이트 컴퍼니 엘엘씨 | 스파크-점화된 내연기관용 엔진에서 저속 조기-점화를 방지 또는 감소시키기 위한 조성물 및 방법 |
| WO2022009105A1 (en) | 2020-07-07 | 2022-01-13 | Chevron Oronite Company Llc | Fuel additives for mitigating injector nozzle fouling and reducing particulate emissions |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3149933A (en) * | 1960-08-25 | 1964-09-22 | Bayer Ag | Process for stabilizing liquid fuels |
| NL284832A (enExample) * | 1961-10-30 | |||
| US3285855A (en) * | 1965-03-11 | 1966-11-15 | Geigy Chem Corp | Stabilization of organic material with esters containing an alkylhydroxy-phenyl group |
| US3574576A (en) * | 1965-08-23 | 1971-04-13 | Chevron Res | Distillate fuel compositions having a hydrocarbon substituted alkylene polyamine |
| US3434814A (en) * | 1966-06-29 | 1969-03-25 | Ethyl Corp | Emission control additive |
| US3849085A (en) * | 1972-05-08 | 1974-11-19 | Texaco Inc | Motor fuel composition |
| US3960515A (en) * | 1973-10-11 | 1976-06-01 | Chevron Research Company | Hydrocarbyl amine additives for distillate fuels |
| US4320021A (en) * | 1975-10-14 | 1982-03-16 | The Lubrizol Corporation | Amino phenols useful as additives for fuels and lubricants |
| JPS5712053Y2 (enExample) * | 1976-03-29 | 1982-03-10 | ||
| US4347148A (en) * | 1976-07-15 | 1982-08-31 | The Lubrizol Corporation | Full and lubricant compositions containing nitro phenols |
| US4328322A (en) * | 1979-12-03 | 1982-05-04 | Polaroid Corporation | Synthetic polymers by polyisocyanate polyaddition process |
| US4386939A (en) * | 1979-12-10 | 1983-06-07 | The Lubrizol Corporation | Reaction products of certain heterocycles with aminophenols |
| DE3611230A1 (de) * | 1986-04-04 | 1987-10-08 | Basf Ag | Polybutyl- und polyisobutylamine, verfahren zu deren herstellung und diese enthaltende kraft- und schmierstoffzusammensetzungen |
| DE3700363A1 (de) * | 1987-01-08 | 1988-07-21 | Basf Ag | Kraft- oder schmierstoffzusammensetzung und verwendung von polybutyl- oder polyisobutylderivaten in denselben |
| US5090914A (en) * | 1988-03-04 | 1992-02-25 | Xoma Corporation | Activated polymers and conjugates thereof |
| US5196142A (en) * | 1989-03-17 | 1993-03-23 | Ciba-Geigy Corporation | Aqueous antioxidant emulsions |
| JPH0488092A (ja) * | 1990-07-30 | 1992-03-19 | Tonen Corp | ガソリン添加用組成物 |
| US5211721A (en) * | 1991-02-25 | 1993-05-18 | Texaco Inc. | Polyoxyalkylene ester compounds and ORI-inhibited motor fuel compositions |
| US5196565A (en) * | 1992-06-26 | 1993-03-23 | Ciba-Geigy Corporation | Extractive purification of phenols |
| US5427591A (en) * | 1992-12-18 | 1995-06-27 | Chevron Chemical Company | Poly(oxyalkylene) hydroxyaromatic esters and fuel compositions containing the same |
| US5366519A (en) * | 1992-12-18 | 1994-11-22 | Chevron Research And Technology Company | Fuel additive compositions containing poly(oxyalkylene) hydroxyaromatic esters and poly(oxyalkylene) amines |
| US5755835A (en) * | 1992-12-28 | 1998-05-26 | Chevron Chemical Company | Fuel additive compositions containing aliphatic amines and polyalkyl hydroxyaromatics |
| US5462567A (en) * | 1992-12-28 | 1995-10-31 | Chevron Chemical Company | Fuel additive compositions containing poly(oxyalkylene)hydroxyaromatic esters and aliphatic amines |
| US5407452A (en) * | 1993-07-28 | 1995-04-18 | Chevron Chemical Company | Fuel compositions containing poly(oxyalkylene) aromatic esters |
| JPH08505429A (ja) * | 1993-10-28 | 1996-06-11 | シェブロン ケミカル カンパニー | ポリアルキルヒドロキシ芳香族エステル及びそれを含む燃料組成物 |
| US5380345A (en) * | 1993-12-03 | 1995-01-10 | Chevron Research And Technology Company | Polyalkyl nitro and amino aromatic esters and fuel compositions containing the same |
| US5405419A (en) * | 1994-05-02 | 1995-04-11 | Chevron Chemical Company | Fuel additive compositions containing an aliphatic amine, a polyolefin and a poly(oxyalkylene) monool |
| CA2180498C (en) * | 1995-07-06 | 2008-03-25 | Richard E. Cherpeck | Method and composition for reduction of combustion chamber deposits |
| JP3786706B2 (ja) * | 1996-05-14 | 2006-06-14 | シェブロン ケミカル カンパニー | ポリアルキルフェノキシアルカノールの芳香族エステル及びポリ（オキシアルキレン）アミンを含有する燃料添加剤組成物 |
| US5618320A (en) * | 1996-05-14 | 1997-04-08 | Chevron Chemical Company | Aromatic esters of polyalkylphenoxyalkanols and fuel compositions containing the same |
-
1998
- 1998-12-22 US US09/218,782 patent/US6071319A/en not_active Expired - Lifetime
-
1999
- 1999-10-29 CA CA002287766A patent/CA2287766C/en not_active Expired - Lifetime
- 1999-11-08 EP EP99308886A patent/EP1013745B1/en not_active Expired - Lifetime
- 1999-11-08 DE DE69930597T patent/DE69930597T2/de not_active Expired - Lifetime
- 1999-12-22 JP JP36379499A patent/JP4790887B2/ja not_active Expired - Lifetime
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