SG194415A1 - Additives to reduce metal pick-up in fuels - Google Patents
Additives to reduce metal pick-up in fuels Download PDFInfo
- Publication number
- SG194415A1 SG194415A1 SG2013075635A SG2013075635A SG194415A1 SG 194415 A1 SG194415 A1 SG 194415A1 SG 2013075635 A SG2013075635 A SG 2013075635A SG 2013075635 A SG2013075635 A SG 2013075635A SG 194415 A1 SG194415 A1 SG 194415A1
- Authority
- SG
- Singapore
- Prior art keywords
- fuel
- additive
- substituted
- hydrocarbon
- composition
- Prior art date
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- 239000000446 fuel Substances 0.000 title claims abstract description 145
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 58
- 239000002184 metal Substances 0.000 title claims abstract description 58
- 239000000654 additive Substances 0.000 title claims description 111
- 239000000203 mixture Substances 0.000 claims abstract description 147
- 238000000034 method Methods 0.000 claims abstract description 58
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 57
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- 239000002253 acid Substances 0.000 claims abstract description 23
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- 230000000996 additive effect Effects 0.000 claims description 67
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- 150000002739 metals Chemical class 0.000 claims description 20
- 230000001590 oxidative effect Effects 0.000 claims description 19
- 239000002270 dispersing agent Substances 0.000 claims description 18
- 239000011701 zinc Substances 0.000 claims description 18
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 17
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- 150000002989 phenols Chemical class 0.000 description 1
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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
- C10L1/18—Organic compounds containing oxygen
- C10L1/188—Carboxylic acids; metal salts thereof
-
- 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
- C10L1/192—Macromolecular compounds
- C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/143—Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1881—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
- C10L1/1883—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom polycarboxylic acid
-
- 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
-
- 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
- C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
-
- 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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
-
- 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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Combustion & Propulsion (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10430408P | 2008-10-10 | 2008-10-10 |
Publications (1)
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| SG194415A1 true SG194415A1 (en) | 2013-11-29 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG2013075635A SG194415A1 (en) | 2008-10-10 | 2009-10-01 | Additives to reduce metal pick-up in fuels |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20110219674A1 (fr) |
| EP (3) | EP2385977B2 (fr) |
| JP (4) | JP6046347B2 (fr) |
| KR (1) | KR101722272B1 (fr) |
| CN (2) | CN102239238A (fr) |
| AU (3) | AU2009302649A1 (fr) |
| BR (2) | BR122018075929B1 (fr) |
| CA (2) | CA3025740C (fr) |
| DK (2) | DK3127992T3 (fr) |
| PL (2) | PL2385977T5 (fr) |
| SG (1) | SG194415A1 (fr) |
| WO (1) | WO2010042378A1 (fr) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| DK2571963T3 (da) | 2010-05-18 | 2020-04-27 | Lubrizol Corp | Sammensætninger, der tilvejebringer renseegenskab |
| WO2011159742A1 (fr) * | 2010-06-15 | 2011-12-22 | The Lubrizol Corporation | Méthode d'élimination de dépôts dans les applications pétrolières et gazières |
| WO2011159764A1 (fr) * | 2010-06-15 | 2011-12-22 | Champion Technologies, Inc. | Inhibition de la fissuration par corrosion sous contrainte d'un métal exposé à des concentrations modérées à élevées d'éthanol |
| US8668749B2 (en) | 2010-11-03 | 2014-03-11 | Afton Chemical Corporation | Diesel fuel additive |
| CN109081797A (zh) | 2012-10-23 | 2018-12-25 | 路博润公司 | 不具有低分子量损失的柴油清净剂 |
| MX2015011122A (es) * | 2013-03-07 | 2015-11-13 | Lubrizol Corp | Inhibidores de la corrosion tolerante a iones y combinaciones de inhibidores para combustibles. |
| MX2016000389A (es) * | 2013-07-12 | 2016-12-14 | Basf Se | Uso de un acido dicarboxilico sustituido con hidrocarbilo para mejorar o aumentar la separacion del agua de aceites de combustible y combustibles de gasolina. |
| RU2695543C2 (ru) | 2014-01-29 | 2019-07-24 | Басф Се | Основанные на поликарбоновой кислоте присадки к топливам и смазочным материалам |
| BR112016028067A2 (pt) | 2014-05-30 | 2017-08-22 | Lubrizol Corp | Amida/éster de alto peso molecular contendo sais de amônio quaternário |
| SG11201609885XA (en) | 2014-05-30 | 2016-12-29 | Lubrizol Corp | Branched amine containing quaternary ammonium salts |
| CN106661473A (zh) | 2014-05-30 | 2017-05-10 | 路博润公司 | 环氧化物季铵化的季铵盐 |
| CN106536687B (zh) | 2014-05-30 | 2021-09-21 | 路博润公司 | 低分子量含酰亚胺季铵盐 |
| BR112016028032A2 (pt) | 2014-05-30 | 2017-08-22 | Lubrizol Corp | Sais de amônio quaternário acoplados |
| ES2746533T3 (es) * | 2014-05-30 | 2020-03-06 | Lubrizol Corp | Paquetes de aditivos de combustible multifuncionales concentrados |
| EP3517593A1 (fr) | 2014-05-30 | 2019-07-31 | The Lubrizol Corporation | Amide/ester à faible poids moléculaire contenant des sels d'ammonium quaternaires |
| EP3524663A1 (fr) | 2014-05-30 | 2019-08-14 | The Lubrizol Corporation | Imidazole contenant des sels d'ammonium quaternaire |
| CN106536686A (zh) | 2014-05-30 | 2017-03-22 | 路博润公司 | 高分子量含酰亚胺季铵盐 |
| WO2016083090A1 (fr) | 2014-11-25 | 2016-06-02 | Basf Se | Inhibiteurs de corrosion pour carburants et lubrifiants |
| CN107849471B (zh) | 2015-07-16 | 2021-07-16 | 巴斯夫欧洲公司 | 作为用于燃料和润滑剂的添加剂的共聚物 |
| DE212016000150U1 (de) | 2015-07-24 | 2018-03-16 | Basf Se | Korrosionsinhibitoren für Kraft- und Schmierstoffe |
| SG10202005167TA (en) | 2015-12-02 | 2020-07-29 | Lubrizol Corp | Ultra-low molecular weight amide/ester containing quaternary ammonium salts having short hydrocarbon tails |
| EP3383979A1 (fr) | 2015-12-02 | 2018-10-10 | The Lubrizol Corporation | Imide de masse moléculaire ultra-faible contenant des sels d'ammonium quaternaire ayant des queues hydrocarbures courtes |
| US11078418B2 (en) | 2016-07-05 | 2021-08-03 | Basf Se | Corrosion inhibitors for fuels and lubricants |
| EP3481922B1 (fr) | 2016-07-05 | 2020-12-30 | Basf Se | Inhibiteurs de corrosion pour carburants et lubrifiants |
| CN109963929A (zh) | 2016-09-21 | 2019-07-02 | 路博润公司 | 用于柴油燃料的聚丙烯酸酯消泡组分 |
| GB201705088D0 (en) | 2017-03-30 | 2017-05-17 | Innospec Ltd | Composition, method and use |
| US20200270537A1 (en) | 2017-09-21 | 2020-08-27 | The Lubrizol Corporation | Polyacrylate antifoam components for use in fuels |
| WO2019183050A1 (fr) | 2018-03-21 | 2019-09-26 | The Lubrizol Corporation | Composants anti-mousse de polyacrylamide destinés à être utilisés dans des carburants diesel |
| US20230002699A1 (en) | 2019-06-24 | 2023-01-05 | The Lubrizol Corporation | Continuous acoustic mixing for performance additives and compositions including the same |
| CA3162057A1 (fr) | 2019-12-18 | 2021-06-24 | James D. Burrington | Compose tensioactif polymere |
| WO2021126342A1 (fr) | 2019-12-19 | 2021-06-24 | The Lubrizol Corporation | Composition d'additif de suspension de cire pour utilisation dans des carburants diesel |
| WO2024030591A1 (fr) | 2022-08-05 | 2024-02-08 | The Lubrizol Corporation | Procédés de production de produits de réaction comprenant des sels d'ammonium quaternaire |
| WO2024163826A1 (fr) | 2023-02-03 | 2024-08-08 | The Lubrizol Corporation | Procédés de production de produits de réaction comprenant des sels d'ammonium quaternaire |
Family Cites Families (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2334158A (en) * | 1941-09-29 | 1943-11-09 | Shell Dev | Rust-preventive composition |
| US2632695A (en) | 1951-09-20 | 1953-03-24 | Socony Vacuum Oil Co Inc | Rust inhibitor for light petroleum products |
| DE1248643B (de) | 1959-03-30 | 1967-08-31 | The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) | Verfahren zur Herstellung von öllöslichen aeylierten Aminen |
| NL124842C (fr) | 1959-08-24 | |||
| US3215707A (en) | 1960-06-07 | 1965-11-02 | Lubrizol Corp | Lubricant |
| US3231587A (en) | 1960-06-07 | 1966-01-25 | Lubrizol Corp | Process for the preparation of substituted succinic acid compounds |
| US3087436A (en) | 1960-12-02 | 1963-04-30 | Ross Gear And Tool Company Inc | Hydraulic pump |
| US3282836A (en) * | 1963-03-22 | 1966-11-01 | Shell Oil Co | Corrosion resistant liquid hydrocarbons containing mixture of alkyl succinic acid and polyamine salt thereof |
| US3412111A (en) | 1965-06-02 | 1968-11-19 | Gulf Research Development Co | Process for reacting an olefin with maleic anhydride to obtain an alkenyl succinic anhydride |
| US3272746A (en) | 1965-11-22 | 1966-09-13 | Lubrizol Corp | Lubricating composition containing an acylated nitrogen compound |
| DE1644941C3 (de) | 1966-09-23 | 1978-06-22 | E.I. Du Pont De Nemours And Co., Wilmington, Del. (V.St.A.) | Legiertes Mineralschmieröl |
| US3401118A (en) | 1967-09-15 | 1968-09-10 | Chevron Res | Preparation of mixed alkenyl succinimides |
| US3447918A (en) | 1967-10-26 | 1969-06-03 | Standard Oil Co | Rust inhibitors |
| US3634515A (en) | 1968-11-08 | 1972-01-11 | Standard Oil Co | Alkylene polyamide formaldehyde |
| US3778371A (en) | 1972-05-19 | 1973-12-11 | Ethyl Corp | Lubricant and fuel compositions |
| US3912764A (en) | 1972-09-29 | 1975-10-14 | Cooper Edwin Inc | Preparation of alkenyl succinic anhydrides |
| CA1022752A (fr) * | 1973-03-15 | 1977-12-20 | Benjamin F. Ward | Composes anticorrosion et methode d'utilisation sur des metaux |
| GB1457328A (en) | 1973-06-25 | 1976-12-01 | Exxon Research Engineering Co | Aminated polymers useful as additives for fuels and lubricants |
| US3899295A (en) | 1973-11-23 | 1975-08-12 | Bio Medical Sciences Inc | Integrity indicator |
| US4156061A (en) | 1974-03-06 | 1979-05-22 | Exxon Research & Engineering Co. | Epoxidized terpolymer or derivatives thereof, and oil and fuel compositions containing same |
| US4026809A (en) | 1974-12-19 | 1977-05-31 | Texaco Inc. | Lubricating compositions containing methacrylate ester graft copolymers as useful viscosity index improvers |
| US4110349A (en) | 1976-06-11 | 1978-08-29 | The Lubrizol Corporation | Two-step method for the alkenylation of maleic anhydride and related compounds |
| US4108889A (en) | 1976-11-19 | 1978-08-22 | The Procter & Gamble Company | Preparing alkane phosphonic acids and intermediates |
| US4137185A (en) | 1977-07-28 | 1979-01-30 | Exxon Research & Engineering Co. | Stabilized imide graft of ethylene copolymeric additives for lubricants |
| US4171959A (en) | 1977-12-14 | 1979-10-23 | Texaco Inc. | Fuel composition containing quaternary ammonium salts of succinimides |
| US4357250A (en) | 1978-04-17 | 1982-11-02 | The Lubrizol Corporation | Nitrogen-containing terpolymer-based compositions useful as multi-purpose lubricant additives |
| US4320019A (en) | 1978-04-17 | 1982-03-16 | The Lubrizol Corporation | Multi-purpose additive compositions and concentrates containing same |
| US4214876A (en) | 1978-12-12 | 1980-07-29 | E. I. Du Pont De Nemours & Company | Corrosion inhibitor compositions |
| US4234435A (en) | 1979-02-23 | 1980-11-18 | The Lubrizol Corporation | Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation |
| US4253980A (en) | 1979-06-28 | 1981-03-03 | Texaco Inc. | Quaternary ammonium salt of ester-lactone and hydrocarbon oil containing same |
| US4326973A (en) | 1981-01-13 | 1982-04-27 | Texaco Inc. | Quaternary ammonium succinimide salt composition and lubricating oil containing same |
| US4338206A (en) | 1981-03-23 | 1982-07-06 | Texaco Inc. | Quaternary ammonium succinimide salt composition and lubricating oil containing same |
| US4440545A (en) * | 1981-11-02 | 1984-04-03 | Ethyl Corporation | Gasohol having corrosion inhibiting properties |
| US4521219A (en) | 1981-11-02 | 1985-06-04 | Ethyl Corporation | Alcohol based fuels containing corrosion inhibitors |
| US4937299A (en) | 1983-06-06 | 1990-06-26 | Exxon Research & Engineering Company | Process and catalyst for producing reactor blend polyolefins |
| US5324800A (en) | 1983-06-06 | 1994-06-28 | Exxon Chemical Patents Inc. | Process and catalyst for polyolefin density and molecular weight control |
| JPS6018584A (ja) * | 1983-07-11 | 1985-01-30 | Sanyo Chem Ind Ltd | 燃料油の防錆添加剤 |
| US4531948A (en) | 1984-06-13 | 1985-07-30 | Ethyl Corporation | Alcohol and gasohol fuels having corrosion inhibiting properties |
| US4668834B1 (en) | 1985-10-16 | 1996-05-07 | Uniroyal Chem Co Inc | Low molecular weight ethylene-alphaolefin copolymer intermediates |
| EP0299119A1 (fr) | 1986-06-23 | 1989-01-18 | Petrolite Corporation | Système de carburant oxygéné inhibés contre la corrosion |
| US4658078A (en) | 1986-08-15 | 1987-04-14 | Shell Oil Company | Vinylidene olefin process |
| ATE81512T1 (de) | 1986-08-26 | 1992-10-15 | Mitsui Petrochemical Ind | Katalysator zur polymerisierung von alpha-olefin und verfahren. |
| EP0280417A1 (fr) | 1987-02-27 | 1988-08-31 | Petrolite Corporation | Additif pour injecteur de carburant diesel contenant de l'acide polyalkényl succinique, carburant diesel contenant celui-ci, et méthode d'utilisation de cela |
| JPS6436690A (en) * | 1987-07-24 | 1989-02-07 | Petrolite Corp | Alkyl or alkenyl succinate used as corrosion inhibitor for oxidized fuel |
| GB8818711D0 (en) | 1988-08-05 | 1988-09-07 | Shell Int Research | Lubricating oil dispersants |
| US5137978A (en) | 1990-05-17 | 1992-08-11 | Ethyl Petroleum Additives, Inc. | Substituted acylating agents and their production |
| US5137980A (en) | 1990-05-17 | 1992-08-11 | Ethyl Petroleum Additives, Inc. | Ashless dispersants formed from substituted acylating agents and their production and use |
| US5071919A (en) | 1990-05-17 | 1991-12-10 | Ethyl Petroleum Additives, Inc. | Substituted acylating agents and their production |
| US5254138A (en) | 1991-05-03 | 1993-10-19 | Uop | Fuel composition containing a quaternary ammonium salt |
| BE1006694A5 (fr) | 1991-06-22 | 1994-11-22 | Basf Ag | Procede de preparation de polyisobutenes extremement reactifs. |
| AU668151B2 (en) | 1992-05-06 | 1996-04-26 | Afton Chemical Corporation | Composition for control of induction system deposits |
| US6020500A (en) | 1995-08-22 | 2000-02-01 | The Lubrizol Corporation | Hydroxy-substituted monolactones useful as intermediates for preparing lubricating oil and fuel additives |
| SG64399A1 (en) | 1995-08-22 | 1999-04-27 | Lubrizol Corp | Process for preparing compositions useful as intermediates for preparing lubricanting oil and fuel additives |
| US5777142A (en) | 1995-08-22 | 1998-07-07 | The Lubrizol Corporation | Unsaturated hydroxycarboxylic compounds useful as intermediates for preparing lubricant and fuel additives |
| US5885944A (en) | 1996-05-21 | 1999-03-23 | The Lubrizol Corporation | Low chlorine polyalkylene substituted carboxylic acylating agent compositions and compounds derived therefrom |
| US6077909A (en) | 1997-02-13 | 2000-06-20 | The Lubrizol Corporation | Low chlorine content compositions for use in lubricants and fuels |
| US5851966A (en) | 1997-06-05 | 1998-12-22 | The Lubrizol Corporation | Reaction products of substituted carboxylic acylating agents and carboxylic reactants for use in fuels and lubricants |
| US5912213A (en) | 1997-06-05 | 1999-06-15 | The Lubrizol Corporation | Substituted carboxylic acylating agent compositions and derivatives thereof for use in lubricants and fuels |
| US6165235A (en) | 1997-08-26 | 2000-12-26 | The Lubrizol Corporation | Low chlorine content compositions for use in lubricants and fuels |
| US6562913B1 (en) | 1999-09-16 | 2003-05-13 | Texas Petrochemicals Lp | Process for producing high vinylidene polyisobutylene |
| US7037999B2 (en) | 2001-03-28 | 2006-05-02 | Texas Petrochemicals Lp | Mid-range vinylidene content polyisobutylene polymer product and process for producing the same |
| CA2502623C (fr) * | 2002-09-13 | 2013-10-08 | Octel Starreon Llc | Procede de production d'une composition de combustible |
| US7404888B2 (en) | 2004-07-07 | 2008-07-29 | Chevron U.S.A. Inc. | Reducing metal corrosion of hydrocarbons using acidic fischer-tropsch products |
| EP1669433A1 (fr) * | 2004-12-13 | 2006-06-14 | Basf Aktiengesellschaft | acide hydrocarbyl succinique et dérivés d'acide hydrocarbyl succinique comme modificateurs de friction. |
| ES2561424T3 (es) * | 2005-06-16 | 2016-02-26 | The Lubrizol Corporation | Detergentes de sal de amonio cuaternario para su uso en combustibles |
| WO2007062304A2 (fr) | 2005-11-23 | 2007-05-31 | Novus International, Inc. | Compositions combustibles de biodiesel presentant une meilleure tenue a l'oxydation |
| BRPI0715106A2 (pt) * | 2006-07-27 | 2013-06-04 | Shell Int Research | uso de um componente de combustÍvel derivado de fischer-tropsch, e, mÉtodos para formular uma composiÇço de combustÍvel, e para operar um sistema consumidor de combustÍvel |
| EP1884556A3 (fr) * | 2006-08-04 | 2011-09-14 | Infineum International Limited | Compositions de carburant diesel contenant des espèces metalliques et des additifs détergents |
| US20080060608A1 (en) | 2006-09-07 | 2008-03-13 | Angela Priscilla Breakspear | Method and use for the prevention of fuel injector deposits |
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2009
- 2009-10-01 CA CA3025740A patent/CA3025740C/fr active Active
- 2009-10-01 DK DK16185196.9T patent/DK3127992T3/en active
- 2009-10-01 CN CN2009801487036A patent/CN102239238A/zh active Pending
- 2009-10-01 SG SG2013075635A patent/SG194415A1/en unknown
- 2009-10-01 JP JP2011531069A patent/JP6046347B2/ja active Active
- 2009-10-01 EP EP09737254.4A patent/EP2385977B2/fr active Active
- 2009-10-01 CA CA2739432A patent/CA2739432C/fr active Active
- 2009-10-01 EP EP16185196.9A patent/EP3127992B1/fr active Active
- 2009-10-01 PL PL09737254T patent/PL2385977T5/pl unknown
- 2009-10-01 CN CN201710063619.0A patent/CN106753620A/zh active Pending
- 2009-10-01 WO PCT/US2009/059164 patent/WO2010042378A1/fr active Application Filing
- 2009-10-01 EP EP18211764.8A patent/EP3486300A1/fr not_active Withdrawn
- 2009-10-01 BR BR122018075929-1A patent/BR122018075929B1/pt active IP Right Grant
- 2009-10-01 BR BRPI0920665-5A patent/BRPI0920665B1/pt active IP Right Grant
- 2009-10-01 US US13/121,714 patent/US20110219674A1/en not_active Abandoned
- 2009-10-01 KR KR1020117010466A patent/KR101722272B1/ko active IP Right Grant
- 2009-10-01 AU AU2009302649A patent/AU2009302649A1/en not_active Abandoned
- 2009-10-01 DK DK09737254.4T patent/DK2385977T4/da active
- 2009-10-01 PL PL16185196T patent/PL3127992T3/pl unknown
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2013
- 2013-08-23 JP JP2013172919A patent/JP2013234336A/ja not_active Withdrawn
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2015
- 2015-05-27 JP JP2015107040A patent/JP2015147942A/ja not_active Withdrawn
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2016
- 2016-07-11 AU AU2016204848A patent/AU2016204848A1/en not_active Abandoned
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2017
- 2017-03-03 JP JP2017040410A patent/JP2017101259A/ja active Pending
- 2017-10-25 AU AU2017251765A patent/AU2017251765B2/en active Active
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