GB980269A - Improved motor fuel composition - Google Patents
Improved motor fuel compositionInfo
- Publication number
- GB980269A GB980269A GB33023/62A GB3302362A GB980269A GB 980269 A GB980269 A GB 980269A GB 33023/62 A GB33023/62 A GB 33023/62A GB 3302362 A GB3302362 A GB 3302362A GB 980269 A GB980269 A GB 980269A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- specifications
- phosphosulphurized
- referred
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/404—2,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
- C07D207/408—Radicals containing only hydrogen and carbon atoms attached to ring carbon atoms
- C07D207/412—Acyclic radicals containing more than six carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/86—Oxygen atoms
- C07D211/88—Oxygen atoms attached in positions 2 and 6, e.g. glutarimide
-
- 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
- C10L1/16—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
- C10L1/22—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)
-
- 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
- C10L1/26—Organic compounds containing phosphorus
- C10L1/2691—Compounds of uncertain formula; reaction of organic compounds (hydrocarbons acids, esters) with Px Sy, Px Sy Halz or sulfur and phosphorus containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Lubricants (AREA)
Abstract
In Example 7, a bright stock solvent having a viscosity of 32 cs. at 210 DEG F. is reacted with 10 wt. per cent of P2S5 and the resulting phospho-sulphurized product is at least partially neutralized with 10 wt. per cent ethylene oxide at 285 DEG F. Specifications 792,553 and 838,928 are referred to.ALSO:An inside derivative of a polyisobutenyl methyl succinic acid is prepared by reacting a polyisobutylene having a viscosity of between 200 and 10,000 S.S.U. at 210 DEG F. with itaconic acid to form an anhydride which is then reacted in exylene solution with tripropylene diamine to form the imide (see Example 2). Specifications 792,553 and 838,928 are referred to.ALSO:A motor fuel composition comprises a major amount of a liquid petroleum motor fuel boiling in the gasoline range and a minor amount of a mixture of (1) a dispersant additive having the general formula <FORM:0980269/C4-C5/1> where R is a radical derived from a polymer of a C2- 6 olefin having a M.W. of 600-3000, R1 is hydrogen or C1- 4 alkyl, R11 is a methylene or ethylene radical which may be substituted by C1- 4 alkyl radicals, R111 is a C1- 4 alkylene radical, and x is 1-6, and (2) an oil soluble detergent additive of M.W. less than 20,000, the additive components being present in a weight ratio of dispersant to detergent of from 5 : 1 to 1 : 5. The detergent additive may be an alkali or alkaline earth petroleum sulphonate, an alkyl phenol sulphide or salt thereof, or a phenate, but is preferably a phosphosulphurized hydrocarbon or a hydrolysed and/or neutralization reaction product thereof. Hydrocarbon which may be phosphosulphurized include paraffins, olefins and diolefins, acetylenes, aromatics, cyclic aliphatics, mixtures thereof such as a bright stock residuum, or polymers of C2- 6 olefins (particularly polyisobutylene). The neutralization of phosphosulphurized hydrocarbons may be achieved, using alkali or alkaline earth metal hydroxides, carbonates and oxides, ammonia, amines, polyamines, epoxides (particually C2- 6 alkylene oxides), urea, thiourea, guanidine, ammonium and amine salts of carbonic acid, urethanes, urylenes and carbamates. Optional additives which may be present include alkyl and olefinic lead anti-knock agents (e.g. triethyl vinyl lead, TEL), other organometallic additives containing Pb, Ni, Fe, Si or Mn, tert-butyl acetate, tri-b -chloroethyl phosphate, isopropanol, hexylene glycol, and ethylene dibromide and dichloride. Specifications 792,553 and 838,928 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US137037A US3223495A (en) | 1961-09-11 | 1961-09-11 | Motor fuel composition |
Publications (1)
Publication Number | Publication Date |
---|---|
GB980269A true GB980269A (en) | 1965-01-13 |
Family
ID=22475540
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB33023/62A Expired GB980269A (en) | 1961-09-11 | 1962-08-28 | Improved motor fuel composition |
Country Status (3)
Country | Link |
---|---|
US (1) | US3223495A (en) |
DE (1) | DE1245209B (en) |
GB (1) | GB980269A (en) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3443918A (en) * | 1965-09-21 | 1969-05-13 | Chevron Res | Gasoline composition |
US4098585A (en) * | 1976-06-07 | 1978-07-04 | Texaco Inc. | Amine-alkenylsuccinic acid or anhydride reaction product |
US4325708A (en) * | 1977-09-09 | 1982-04-20 | Phillips Petroleum Company | Fuel detergent compositions containing lubricating oil |
US4240803A (en) * | 1978-09-11 | 1980-12-23 | Mobil Oil Corporation | Fuel containing novel detergent |
US4863487A (en) * | 1987-04-29 | 1989-09-05 | Nalco Chemical Company | Hydrocarbon fuel detergent |
US4895578A (en) * | 1987-04-29 | 1990-01-23 | Nalco Chemical Company | Hydrocarbon fuel detergent |
WO1990012857A1 (en) * | 1989-04-25 | 1990-11-01 | Mobil Oil Corporation | Novel lubricant additives |
WO1993006194A1 (en) * | 1991-09-13 | 1993-04-01 | Chevron Research And Technology Company | Fuel additive compositions containing polyisobutenyl succinimides |
CA2180498C (en) * | 1995-07-06 | 2008-03-25 | Richard E. Cherpeck | Method and composition for reduction of combustion chamber deposits |
EP1803771B1 (en) * | 2005-12-28 | 2017-12-06 | Bridgestone Corporation | A rubber composition having good wet-traction properties and a low aromatic-oil content |
US7700673B2 (en) * | 2006-12-22 | 2010-04-20 | Bridgestone Corporation | Reduced oil rubber compositions including N-substituted polyalkylene succinimide derivates and methods for preparing such compositions |
KR101596953B1 (en) | 2007-12-31 | 2016-02-23 | 가부시키가이샤 브리지스톤 | Metal Soaps Incorporated in Rubber Compositions and Method for Incorporating Such Soaps in Rubber Compositions |
WO2009158604A2 (en) * | 2008-06-26 | 2009-12-30 | Bridgestone Corporation | Rubber compositions including metal-functionalized polyisobutylene derivatives and methods for preparing such compositions |
US8389609B2 (en) | 2009-07-01 | 2013-03-05 | Bridgestone Corporation | Multiple-acid-derived metal soaps incorporated in rubber compositions and method for incorporating such soaps in rubber compositions |
US9803060B2 (en) * | 2009-09-10 | 2017-10-31 | Bridgestone Corporation | Compositions and method for making hollow nanoparticles from metal soaps |
US8802755B2 (en) | 2011-01-18 | 2014-08-12 | Bridgestone Corporation | Rubber compositions including metal phosphate esters |
WO2014071301A1 (en) | 2012-11-02 | 2014-05-08 | Bridgestone Corporation | Rubber compositions comprising metal carboxylates and processes for making the same |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2296069A (en) * | 1940-03-21 | 1942-09-15 | Allied Chem & Dye Corp | Fuel for internal combustion engines |
US2280419A (en) * | 1940-07-16 | 1942-04-21 | Chester E Wilson | Compounded oil |
US2768999A (en) * | 1952-08-27 | 1956-10-30 | Exxon Research Engineering Co | Phosphosulfurized hydrocarbons and production thereof |
US2781319A (en) * | 1954-03-22 | 1957-02-12 | Shell Dev | Lubricating compositions |
FR1131205A (en) * | 1955-09-08 | 1957-02-19 | Exxon Standard Sa | Improved lubricating oil compositions |
NL255194A (en) * | 1959-08-24 | |||
US3080223A (en) * | 1960-06-29 | 1963-03-05 | Exxon Research Engineering Co | Stabilized distillate fuels |
-
1961
- 1961-09-11 US US137037A patent/US3223495A/en not_active Expired - Lifetime
-
1962
- 1962-08-28 GB GB33023/62A patent/GB980269A/en not_active Expired
- 1962-09-05 DE DEE23484A patent/DE1245209B/en active Pending
Also Published As
Publication number | Publication date |
---|---|
DE1245209B (en) | 1967-07-20 |
US3223495A (en) | 1965-12-14 |
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