KR920703766A - Automobile fuel additive composition and preparation method thereof - Google Patents

Automobile fuel additive composition and preparation method thereof

Info

Publication number
KR920703766A
KR920703766A KR1019920702149A KR920702149A KR920703766A KR 920703766 A KR920703766 A KR 920703766A KR 1019920702149 A KR1019920702149 A KR 1019920702149A KR 920702149 A KR920702149 A KR 920702149A KR 920703766 A KR920703766 A KR 920703766A
Authority
KR
South Korea
Prior art keywords
range
weight
radical
additive
carbon atoms
Prior art date
Application number
KR1019920702149A
Other languages
Korean (ko)
Other versions
KR0151409B1 (en
Inventor
리챠드 넬슨 알프레드
넬슨 마크 엘
엘. 넬슨 쥬니어 오티스
Original Assignee
원본 미기재
폴라 몰리큘라 코오포레이션
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by 원본 미기재, 폴라 몰리큘라 코오포레이션 filed Critical 원본 미기재
Publication of KR920703766A publication Critical patent/KR920703766A/en
Application granted granted Critical
Publication of KR0151409B1 publication Critical patent/KR0151409B1/en

Links

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
    • C10L1/10—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
    • 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
    • C10L1/16—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
    • C10L1/16—Hydrocarbons
    • C10L1/1625—Hydrocarbons macromolecular compounds
    • C10L1/1633—Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds
    • C10L1/1641—Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds from compounds containing aliphatic monomers
    • 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
    • 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
    • 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
    • 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
    • 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
    • C10L1/1985—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 polyethers, e.g. di- polygylcols and derivatives; ethers - esters
    • 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
    • C10L1/22—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)
    • C10L1/2387—Polyoxyalkyleneamines (poly)oxyalkylene amines and 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
    • C10L1/30—Organic compounds compounds not mentioned before (complexes)
    • C10L1/305—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)
    • C10L1/306—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond) organo Pb compounds

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)
  • Combustion & Propulsion (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Abstract

A motor fuel additive composition comprises a mixture of:(a) from 5-50 weight percent, based upon the total weight of the additive, of a detergent component selected from the group consisting of (i) at least one nonionic compound having a molecular weight in the range of 200-1500, (ii) a reaction product of a substituted hydrocarbon and an amino compound, and (iii) a polybutylamine or polyisobutylamine; and (b) a fuel conditioner component comprising (i) from 2-50 weight percent, based upon the total weight of the additive, of a polar oxygenated hydrocarbon compound and (ii) from 2-50 weight percent, based upon the total weight of the additive, of an oxygenated compatibilizing agent. The fuel conditioner component may additionally comprise a hydrophilic separant, an aromatic hydrocarbon, or mixtures thereof. The additive may also additionally comprise a carrier oil or fluidizer. The additive is prepared by mixing together the detergent and fuel conditioner components, and is advantageous in that the detergent and fuel conditioner components synergistically interact to reduce both fuel intake system deposit formation and combustion chamber deposit formation, thereby inhibiting engine ORI.

Description

자동차 연료 첨가제 조성물 및 이의 제조방법Automobile fuel additive composition and preparation method thereof

[도면의 간단한 설명][Brief Description of Drawings]

제1도는 본 발명의 첨가제를 함유하는 자동차 연료 조성물을 포함하는, 각종 자동차 연료 조성물에 대한 엔진 테스트 스탠드[engine test stand] 실험의 결과를 도시한 도면이다,FIG. 1 shows the results of engine test stand experiments on various automotive fuel compositions, including automotive fuel compositions containing the additives of the present invention.

제2도는 본 발명의 첨가제를 함유하는 자동차 연료 조성물을 포함하는, 각종 자동차 연료 조성물에 대한, 제1도에 나타낸 엔진 테스트스탠드 실험의 결과를 연소실 등급 대 흡입 밸브 침전물(mg)로 도시한 도면이다.FIG. 2 shows the results of the engine test stand experiment shown in FIG. 1 in terms of combustion chamber grade vs. intake valve deposits (mg) for various automotive fuel compositions, including automotive fuel compositions containing the additives of the present invention. .

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (22)

하기 (a) 및 (b)의 혼합물을 포함하는 자동차 연료 첨가제 조성물: (a) 하기의 (ⅰ), (ⅱ) 및 (ⅲ)으로 구성된 군에서 선택한, 첨가제 총중량의 5-50중량%의 세정제: (ⅰ) 분자량의 범위가 200-1500인 비이온성 화합물 1종 이상, (ⅱ) 하기 (A) 및 (B)화합물의 반응 생성물; (A) 하기 일반식(Ⅰ)의 치환 탄화수소Automotive fuel additive composition comprising a mixture of the following (a) and (b): (a) 5-50% by weight of the total weight of the additive selected from the group consisting of (i), (ii) and (iii) (Iii) at least one nonionic compound having a molecular weight in the range of 200-1500, (ii) a reaction product of the following (A) and (B) compounds; (A) Substituted hydrocarbon of the general formula (I) R1-X (Ⅰ)R 1 -X (Ⅰ) (식중, R1은 분자량의 범위가 150-10,000인 히드로카르빌 라디칼이며, X는 할로겐, 숙신산 무수물 및 숙신이염기산으로 구성된 군에서 선택된다), 및 (B) 하기 일반식(Ⅱ)의 아미노 화합물(Wherein R 1 is a hydrocarbyl radical having a molecular weight in the range of 150-10,000, X is selected from the group consisting of halogen, succinic anhydride and succinic dibasic acid), and (B) amino of general formula (II) compound H-(NH-(A)m)n-Y-R2(Ⅱ)H- (NH- (A) m ) n -YR 2 (II) (식중, Y는 O또는 NR5(R5는 H 또는 탄소 원자수 1-30의 히드로카르빌 라디칼이다)이고; A는 탄소원자수 1-30의 직쇄 또는 측쇄의 알킬렌 라디칼이며; m은 1-15범위의 값이고; n은 0-6범위의 값이며; R2는 H, 분자량의 범위가 15-10,000인 히드로카르빌 라디칼 및 하기 일반식(Ⅲ)의 동종 중합성 또는 헤테로 중합성 폴리옥시알킬렌라디칼로 구성된 군에서 선택된다.Wherein Y is O or NR 5 (R 5 is H or a hydrocarbyl radical of 1-30 carbon atoms); A is a straight or branched alkylene radical of 1-30 carbon atoms; m is 1 A value in the range -15; n is a value in the range 0-6; R 2 is H, a hydrocarbyl radical having a molecular weight in the range of 15-10,000 and a homopolymerizable or heteropolymerizable poly of formula (III) It is selected from the group consisting of oxyalkylene radicals. R3-((Q)a(T)b(Z)c)d- (Ⅲ)R 3 -((Q) a (T) b (Z) c ) d- (III) (식중, R3은 H 또는 탄소원자수 1-30의 히드로카르빌 라디칼이고, Q, T 및 Z는 탄소원자수 1-6의 폴리옥시알킬렌부분이며, a, b 및 c는 각각 0-30범위의 값이고, d는 1-50범위의 값이다), 및 (ⅲ) 하기 일반식(Ⅳ)의 폴리부틸아민 또는 폴리이소부틸아민;Wherein R 3 is H or a hydrocarbyl radical of 1-30 carbon atoms, Q, T and Z are polyoxyalkylene moieties of 1-6 carbon atoms, and a, b and c are each in the range 0-30 D is a value in the range 1-50), and (iii) polybutylamine or polyisobutylamine of the following general formula (IV); (식중, R11은 이소부텐 및 20중량%이하의 n-부텐으로부터 유도된 폴리부틸 또는 폴리이소부틸 라디칼이고, R12및 R13은 동일 또는 상이하고, 각각 수소, 지방족 또는 방향족 탄화수소, 1차 또는 2차, 방향족 또는 지방족 아미노알킬렌 라디칼 또는 폴리아미노알킬렌 라디칼, 폴리옥시알킬렌 라디칼 또는 헤트아릴 또는 헤테로고리라디칼이거나, R12및 R13이 결합되어 있는 질소원자와 함께 헤테로 원자가 추가로 존재할 수 있는 고리를 형성한다); 및 (b) 하기의 (ⅰ) 및 (ⅱ)를 포함하는 연료 조절제 성분: (ⅰ) 평균 분자량의 범위가 250-500이고, 산가(acid number)의 범위가 25-175이며, 비누화값의 범위가 약 30-250인, 첨가제 총중량의 2-50중량%의 극성 산화 탄화수소, 및 (ⅱ) 용해도 지수의 범위가 약 8.8-11.5이고, 적당한 강한 수소 결합 능력을 지니는, 첨가제 총 중량의 2-50중량%의 산화 상용화제.Wherein R 11 is a polybutyl or polyisobutyl radical derived from isobutene and up to 20% by weight of n-butene, R 12 and R 13 are the same or different and each is hydrogen, aliphatic or aromatic hydrocarbon, primary Or is a secondary, aromatic or aliphatic aminoalkylene radical or polyaminoalkylene radical, polyoxyalkylene radical or hetaryl or heterocyclic radical, or further hetero atoms are present together with the nitrogen atom to which R 12 and R 13 are attached. To form a ring); And (b) a fuel regulator component comprising the following (i) and (ii): (iii) the range of average molecular weight is 250-500, the range of acid number is 25-175, and the range of saponification value Is 2-30% by weight of the total weight of the additive, about 30-250, and (ii) 2-50% of the total weight of the additive, having a solubility index in the range of about 8.8-11.5, and having moderately strong hydrogen bonding capacity. Wt% oxidation compatibilizer. 제1항에 있어서, 비이온성 화합물이 분자량의 범위가 200-1500알킬아릴 에테르 알코올 또는 알킬아릴 폴리에테르 알코올인 조성물.The composition of claim 1 wherein the nonionic compound has a molecular weight in the range 200-1500 alkylaryl ether alcohol or alkylaryl polyether alcohol. 제2항에 있어서, 비이온성 화합물이 1-10개의 에틸렌 옥시드부분을 함유하는 옥틸페닐 또는 노닐페닐 폴리에테르 알코올일 조성물.3. The composition of claim 2, wherein the nonionic compound is octylphenyl or nonylphenyl polyether alcohol containing 1-10 ethylene oxide moieties. 제1항에 있어서, 치환 탄화수소 R1-X의 아미노 화합물에 대한 몰비가 0.2:1 내지 20:1의 범위인 조성물.The composition of claim 1, wherein the molar ratio of substituted hydrocarbon R 1 -X to amino compound is in the range of 0.2: 1 to 20: 1. 제1항에 있어서, R1-X가 클로로폴리이소부틸렌 또는 폴리이소부테닐 숙신산 무수물인 조성물.The composition of claim 1 wherein R 1 -X is chloropolyisobutylene or polyisobutenyl succinic anhydride. 제1항에 있어서, H, 분자량의 범위가 15-2000인 히드로카르빌 라디칼 및 하기 일반식(Ⅲ)의 폴리옥시알킬렌 라디칼로 구성된 군에서, R2를 선택하고;The compound of claim 1, wherein R 2 is selected from the group consisting of H, a hydrocarbyl radical having a molecular weight in the range of 15-2000 and a polyoxyalkylene radical of the general formula (III) below; R3-((Q)a(T)b(Z)c)d- (Ⅲ)R 3 -((Q) a (T) b (Z) c ) d- (III) (상기 일반식(Ⅲ)에서 R3이 R3은 H 또는 탄소원자수 1-22의 히드로카르빌 라디칼이고, Q, T 및 Z는 탄소원자수 1-6의 폴리옥시알킬렌부분이며, a, b 및 c는 각각 1-25범위의 값이며; Y가 0 또는 NR5이고, 여기에서 R5는 H 또는 탄소원자수 1-22의 히드로카르빌 라디칼이며, A가 탄소원자수 1-15의 직쇄 또는 측쇄 알킬렌 라디칼이고; m이 1-12범위의 값이며; n이 0-5범위의 값임을 특징으로 하는 조성물.(The above general formula (Ⅲ) R 3 is R 3 is a hydrocarbyl radical of from 1-22 carbon atoms or H, and the polyoxyalkylene portion of Q, T and Z are carbon atoms 1-6, a, b And c are each a value ranging from 1-25; Y is 0 or NR 5 , wherein R 5 is H or a hydrocarbyl radical of 1-22 carbon atoms, and A is a straight or branched chain of 1-15 carbon atoms An alkylene radical, m is a value in the range 1-12, n is a value in the range 0-5. 제1항에 있어서, 폴리에틸렌 폴리아민, 폴리프로필렌 폴리아민 및 이의 혼합물로 구성된 군에서 일반식(Ⅱ)의 아미노 화합물을 선택함을 특징으로 하는 조성물.2. A composition according to claim 1, wherein the amino compound of formula (II) is selected from the group consisting of polyethylene polyamines, polypropylene polyamines and mixtures thereof. 제1항에 있어서, 상용화제가 탄소원자수 3이상의 알코올인 조성물.The composition of claim 1 wherein the compatibilizer is an alcohol having at least 3 carbon atoms. 제1항에 있어서, 연료 조절제 성분이 친수성 분리제(separant)를 첨가제 총 중량의 0-40중량%로 추가로 함유함을 특징으로 하는 조성물.The composition of claim 1, wherein the fuel regulator component further contains a hydrophilic separator at 0-40% by weight of the total weight of the additive. 제1항에 있어서, 연료 조절제 성분이 방향족 탄화수소를 첨가제 총 중량의 0-50중량%로 추가로 함유함을 특징으로 하는 조성물.The composition of claim 1, wherein the fuel regulator component further contains aromatic hydrocarbons in an amount of 0-50% by weight of the total weight of the additive. 제1항에 있어서, 석유 베이스 오일, 광물유, 분자량의 범위가 500-3000인 폴리프로필렌 화합물, 분자량의 범위가 500-300인 폴리이소부틸렌 화합물, 분자량의 범위가 500-3000인 폴리옥시알킬렌 화합물 및 폴리이소부텐과 20중량% 이하의 n-부텐으로부터 유도된 폴리부틸 또는 폴리이소부틸 라디칼, 폴리부틸 또는 폴리이소부틸 알코올에 상응하는 카르복실산염 및 이의 혼합물을 함유하는 폴리부틸 및 폴리이소부틸 알코올로 구성된 군에서 선택한 캐리어 오일(carrier oil)을 첨가제 총 중량에 대해 0-80중량%로 추가로 함유함을 특징으로 하는 조성물.The petroleum base oil, mineral oil, polypropylene compound having a molecular weight in the range of 500-3000, polyisobutylene compound having a molecular weight in the range of 500-300, polyoxyalkylene having a molecular weight in the range of 500-3000 Polybutyl and polyisobutyl containing compounds and carboxylates corresponding to polybutyl or polyisobutyl radicals, polybutyl or polyisobutyl alcohols derived from polyisobutene and up to 20% by weight of n-butene and mixtures thereof And a carrier oil selected from the group consisting of alcohols in an amount of 0-80% by weight relative to the total weight of the additive. 하기 (a) 및 (b)를 혼합함을 특징으로 하는, 자동차 연료 첨가제 조성물의 제조방법. (a) 하기의 것들로 구성된 선택한, 첨가제 총중량의 5-50중량%의 세정제: (ⅰ) 분자량의 범위가 200-1500인 비이온성 화합물 1종 이상, (ⅱ) 하기 (A) 및 (B)화합물의 반응 생성물; (A) 하기 일반식(Ⅰ)의 치환 탄화수소A method for producing an automotive fuel additive composition, characterized in that the following (a) and (b) are mixed. (a) 5-50% by weight of a detergent selected from the total weight of the additive selected from the following: (iii) one or more nonionic compounds having a molecular weight in the range of 200-1500, (ii) the following (A) and (B) Reaction products of the compounds; (A) Substituted hydrocarbon of the general formula (I) R1-X (Ⅰ)R 1 -X (Ⅰ) (식중, R1은 분자량의 범위가 150-10,000인 히드로카르빌 라디칼이며, X는 할로겐, 숙신산 무수물 및 숙신이염기산으로 구성된 군에서 선택된다), 및 (B) 하기 일반식(Ⅱ)의 아미노 화합물(Wherein R 1 is a hydrocarbyl radical having a molecular weight in the range of 150-10,000, X is selected from the group consisting of halogen, succinic anhydride and succinic dibasic acid), and (B) amino of general formula (II) compound H-(NH-(A)m)n-Y-R2(Ⅱ)H- (NH- (A) m ) n -YR 2 (II) (식중, Y는 O또는 NR5(R5는 H 또는 탄소 원자수 1-30의 히드로카르빌 라디칼이다)이고; A는 탄소원자수 1-30의 직쇄 또는 측쇄의 알킬렌 라디칼이며; m은 1-15범위의 값이고; n은 0-6범위의 값이며; R2는 H, 분자량의 범위가 15-10,000인 히드로카르빌 라디칼 및 하기 일반식(Ⅲ)의 동종 중합성 또는 헤테로 중합성 폴리옥시알킬렌라디칼로 구성된 군에서 선택된다.Wherein Y is O or NR 5 (R 5 is H or a hydrocarbyl radical of 1-30 carbon atoms); A is a straight or branched alkylene radical of 1-30 carbon atoms; m is 1 A value in the range -15; n is a value in the range 0-6; R 2 is H, a hydrocarbyl radical having a molecular weight in the range of 15-10,000 and a homopolymerizable or heteropolymerizable poly of formula (III) It is selected from the group consisting of oxyalkylene radicals. R3-((Q)a(T)b(Z)c)d- (Ⅲ)R 3 -((Q) a (T) b (Z) c ) d- (III) (식중, R3은 H 또는 탄소원자수 1-30의 히드로카르빌 라디칼이고, Q, T 및 Z는 탄소원자수 1-6의 폴리옥시알킬렌부분이며, a, b 및 c는 각각 0-30범위의 값이고, d는 1-50범위의 값이다), 및 (ⅲ) 하기 일반식(Ⅳ)의 폴리부틸아민 또는 폴리이소부틸아민;Wherein R 3 is H or a hydrocarbyl radical of 1-30 carbon atoms, Q, T and Z are polyoxyalkylene moieties of 1-6 carbon atoms, and a, b and c are each in the range 0-30 D is a value in the range 1-50), and (iii) polybutylamine or polyisobutylamine of the following general formula (IV); (식중, R11은 이소부텐 및 20중량%이하의 n-부텐으로부터 유도된 폴리부틸 또는 폴리이소부틸 라디칼이고, R12및 R13은 동일 또는 상이하고, 각각 수소, 지방족 또는 방향족 탄화수소, 1차 또는 2차, 방향족 또는 지방족 아미노알킬렌 라디칼 또는 폴리아미노알킬렌 라디칼, 폴리옥시알킬렌 라디칼 또는 헤트아릴 또는 헤테로고리라디칼이거나, R12및 R13이 결합되어 있는 질소원자와 함께 헤테로 원자가 추가로 존재할 수 있는 고리를 형성한다); 및 (b) 하기의 것들을 포함하는 연료 조절제 성분: (ⅰ) 평균 분자량의 범위가 250-500이고, 산가의 범위가 25-175이며, 비누화값의 범위가 약 30-250인, 첨가제 총중량의 2-50중량%의 극성 산화 탄화수소, 및 (ⅱ) 용해도 지수의 범위가 약 8.8-11.5이고, 적당히 강한 수소 결합 능력을 지니는, 첨가제 총 중량의 2-50중량%의 산화 상용화제.Wherein R 11 is a polybutyl or polyisobutyl radical derived from isobutene and up to 20% by weight of n-butene, R 12 and R 13 are the same or different and each is hydrogen, aliphatic or aromatic hydrocarbon, primary Or is a secondary, aromatic or aliphatic aminoalkylene radical or polyaminoalkylene radical, polyoxyalkylene radical or hetaryl or heterocyclic radical, or further hetero atoms are present together with the nitrogen atom to which R 12 and R 13 are attached. To form a ring); And (b) a fuel regulator component comprising: (i) two of the total weight of the additive, wherein the average molecular weight ranges from 250-500, the acid value ranges from 25-175, and the saponification value ranges from about 30-250 2-50% by weight of an oxidizing compatibilizer with a total weight of the additive having a polar oxidation hydrocarbon of -50% by weight, and (ii) a solubility index of about 8.8-11.5, with moderately strong hydrogen bonding capacity. 제12항에 있어서, 비이온성 화합물이 분자량의 범위가 200-1500인 알킬아릴 에테르 알코올 또는 알킬아릴 폴리에테르 알코올인 방법.13. The method of claim 12, wherein the nonionic compound is an alkylaryl ether alcohol or alkylaryl polyether alcohol having a molecular weight in the range of 200-1500. 제13항에 있어서, 비이온성 화합물이 1-10개의 에틸렌 옥시드부분을 함유하는 옥틸페닐 또는 노닐페닐 폴리에테르 알코올인 방법.The method of claim 13, wherein the nonionic compound is octylphenyl or nonylphenyl polyether alcohol containing 1-10 ethylene oxide moieties. 제12항에 있어서, 치환 탄화수소 R1-X의 아미노 화합물에 대한 몰비가 0.2:1 내지 20:1의 범위인 방법.13. The process of claim 12, wherein the molar ratio of substituted hydrocarbon R 1 -X to amino compound is in the range of 0.2: 1 to 20: 1. 제12항에 있어서, R1-X가 클로로폴리이소부틸렌 또는 폴리이소부테닐 숙신산 무수물인 방법.13. The method of claim 12, wherein R 1 -X is chloropolyisobutylene or polyisobutenyl succinic anhydride. 제12항에 있어서, H, 분자량의 범위가 15-2000인 히드로카르빌 라디칼 및 하기 일반식(Ⅲ)의 폴리옥시알킬렌 라디칼로 구성된 군에서, R2를 선택하고;The compound of claim 12, wherein R 2 is selected from the group consisting of H, a hydrocarbyl radical having a molecular weight ranging from 15-2000 and a polyoxyalkylene radical of the general formula (III): R3-((Q)a(T)b(Z)c)d- (Ⅲ)R 3 -((Q) a (T) b (Z) c ) d- (III) 상기 일반식(Ⅲ)에서 R3이 H 또는 탄소원자수 1-22의 히드로카르빌 라디칼이고, Q, T 및 Z는 탄소원자수 1-6의 폴리옥시알킬렌 부분이고, a, b, c 및 d가 1-25범위의 값이며; Y가 0 또는 NR5이고, 여기에서 R5는 H 또는 탄소원자수 1-22의 히드로카르빌 라디칼이며; A가 탄소원자수 1-15의 직쇄 또는 측쇄 알킬렌 라디칼이고; m이 1-12범위의 값이며; n이 0-5범위의 값임을 특징으로 하는 방법.R 3 in formula (III) is H or a hydrocarbyl radical of 1-22 carbon atoms, Q, T and Z are polyoxyalkylene moieties of 1-6 carbon atoms, a, b, c and d Is a value in the range 1-25; Y is 0 or NR 5 , wherein R 5 is H or a hydrocarbyl radical of 1-22 carbon atoms; A is a straight or branched chain alkylene radical of 1-15 carbon atoms; m is a value in the range 1-12; and n is a value in the range 0-5. 제12항에 있어서, 폴리에틸렌 폴리아민, 폴리프로필렌 폴리아민 및 이의 혼합물로 구성된 군에서 일반식(Ⅱ)의 아미노 화합물을 선택함을 특징으로 하는 방법.13. A process according to claim 12, wherein the amino compound of formula (II) is selected from the group consisting of polyethylene polyamines, polypropylene polyamines and mixtures thereof. 제12항에 있어서, 상용화제가 탄화수소수 3이상의 알코올인 방법.13. The process of claim 12, wherein the compatibilizer is an alcohol having at least 3 hydrocarbons. 제12항에 있어서, 연료 조절제 성분이 친수성 분리제를 첨가제 총 중량의 0-40중량%로 추가로 함유함을 특징으로 하는 방법.13. The method of claim 12, wherein the fuel modifier component further contains 0-40% by weight of the total weight of the additive of the hydrophilic separator. 제12항에 있어서, 연료 조절제 성분이 방향족 탄화수소를 첨가제 총 중량의 0-80중량%로 추가로 함유함을 특징으로 하는 방법.13. The method of claim 12, wherein the fuel regulator component further comprises 0 to 80% by weight of the total weight of the aromatic hydrocarbon additive. 제12항에 있어서, 석유 베이스 오일, 광물유, 분자량의 범위가 500-3000인 폴리프로필렌 화합물, 분자량의 범위가 500-3000인 폴리이소부틸렌 화합물, 분자량의 범위가 500-3000인 폴리옥시알킬렌 화합물 및 폴리이소부텐과 20중량% 이하의 n-부텐으로부터 유도된 폴리부틸 또는 폴리이소부틸 라디칼, 폴리부틸 또는 폴리이소부틸 알코올에 상응하는 카르복실산염 및 이의 혼합물을 함유하는 폴리부틸 및 폴리이소부틸 알코올로 구성된 군에서 선택한 캐리어 오일을 첨가제 총 중량에 대해 0-80중량%로 지니는 연료조절제 성분과 반응 생성물을 혼합함을 추가적인 특징으로 하는 방법.The petroleum base oil, mineral oil, polypropylene compound having a molecular weight in the range of 500-3000, polyisobutylene compound having a molecular weight in the range of 500-3000, polyoxyalkylene having a molecular weight in the range of 500-3000 Polybutyl and polyisobutyl containing compounds and carboxylates corresponding to polybutyl or polyisobutyl radicals, polybutyl or polyisobutyl alcohols derived from polyisobutene and up to 20% by weight of n-butene and mixtures thereof Further comprising mixing the reaction product with a fuel regulator component having a carrier oil selected from the group consisting of 0-80% by weight relative to the total weight of the additive. ※ 참고사항 : 최초출원 내용에 의하여 공개되는 것임.※ Note: This is to be disclosed by the original application.
KR1019920702149A 1990-03-05 1991-03-05 Motor fuel additive composition and method for preparation thereof KR0151409B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US48867090A 1990-03-05 1990-03-05
US488,670 1990-03-05
US488670 1990-03-05
PCT/US1991/001332 WO1991013949A1 (en) 1990-03-05 1991-03-05 Motor fuel additive composition and method for preparation thereof

Publications (2)

Publication Number Publication Date
KR920703766A true KR920703766A (en) 1992-12-18
KR0151409B1 KR0151409B1 (en) 1998-10-01

Family

ID=23940646

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019920702149A KR0151409B1 (en) 1990-03-05 1991-03-05 Motor fuel additive composition and method for preparation thereof

Country Status (12)

Country Link
EP (1) EP0518966B1 (en)
JP (1) JP2966927B2 (en)
KR (1) KR0151409B1 (en)
AT (1) ATE132180T1 (en)
AU (1) AU660608B2 (en)
BR (1) BR9106137A (en)
CA (1) CA2077666C (en)
DE (1) DE69115894T2 (en)
DK (1) DK0518966T3 (en)
ES (1) ES2081472T3 (en)
GR (1) GR3019268T3 (en)
WO (1) WO1991013949A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100325574B1 (en) * 1993-07-22 2002-07-03 만셀 케이쓰 로드니 Additives and Fuel Compositions

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5089028A (en) * 1990-08-09 1992-02-18 Mobil Oil Corporation Deposit control additives and fuel compositions containing the same
WO1993006194A1 (en) * 1991-09-13 1993-04-01 Chevron Research And Technology Company Fuel additive compositions containing polyisobutenyl succinimides
CA2077616A1 (en) * 1991-09-16 1993-03-17 Lawrence Joseph Cunningham Compositions for control of induction system deposits
GB9207383D0 (en) * 1992-04-03 1992-05-13 Ass Octel Multi-functional gasoline detergent compositions
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
DE4434603A1 (en) * 1994-09-28 1996-04-04 Basf Ag Mixture of amines, hydrocarbon polymers and carrier oils suitable as a fuel and lubricant additive
GB9610781D0 (en) * 1996-05-23 1996-07-31 Ass Octel Gasoline detergent compositions
JP3802244B2 (en) * 1998-10-02 2006-07-26 三洋化成工業株式会社 Fuel oil detergent and fuel oil composition
DE10021936A1 (en) 2000-05-05 2001-11-08 Basf Ag Fuel additive composition comprises a detergent additive, a carrier oil mixture consisting of a synthetic carrier oil and a mineral carrier oil, and optionally further fuel additive components
GB0022473D0 (en) * 2000-09-13 2000-11-01 Ass Octel Composition

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1248643B (en) * 1959-03-30 1967-08-31 The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) Process for the preparation of oil-soluble aylated amines
US3574576A (en) * 1965-08-23 1971-04-13 Chevron Res Distillate fuel compositions having a hydrocarbon substituted alkylene polyamine
US3443918A (en) * 1965-09-21 1969-05-13 Chevron Res Gasoline composition
US3493354A (en) * 1967-02-27 1970-02-03 Monsanto Chemicals Diesel fuel additive
US3658495A (en) * 1968-08-05 1972-04-25 Lubrizol Corp Fuel compositions comprising a combination of oxy compounds and ashless dispersants
US3658494A (en) * 1969-01-21 1972-04-25 Lubrizol Corp Fuel compositions comprising a combination of monoether and ashless dispersants
US3615295A (en) * 1969-07-18 1971-10-26 Dow Chemical Co Gasoline fuel containing polyalkoxylated alkylphenol to reduce exhaust emission
US4384872A (en) * 1979-03-05 1983-05-24 Institute Of Gas Technology Stabilized gasoline-alcohol fuel compositions
FR2510598A1 (en) * 1981-07-30 1983-02-04 Inst Francais Du Petrole USE OF NITROGEN ADDITIVES AS DISORDERS OF HYDROCARBON MEDIUM DISTILLATE DISORDER POINT AND HYDROCARBON MEDIUM DISTILLATE COMPOSITIONS COMPRISING SUCH ADDITIVES
US4486573A (en) * 1982-08-09 1984-12-04 The Lubrizol Corporation Carboxylic acylating agents substituted with olefin polymers of high molecular weight mono-olefins, derivatives thereof, and fuels and lubricants containing same
DE3626102A1 (en) * 1986-01-21 1988-02-11 Polar Molecular Corp FUEL ADDITIVE
DE3611230A1 (en) * 1986-04-04 1987-10-08 Basf Ag POLYBUTYL AND POLYISOBUTYLAMINE, METHOD FOR THE PRODUCTION THEREOF AND THE FUEL AND LUBRICANT COMPOSITIONS CONTAINING THE SAME
DE3700363A1 (en) * 1987-01-08 1988-07-21 Basf Ag FUEL OR LUBRICANT COMPOSITION AND USE OF POLYBUTYL OR POLYISOBUTYL DERIVATIVES IN THE SAME

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100325574B1 (en) * 1993-07-22 2002-07-03 만셀 케이쓰 로드니 Additives and Fuel Compositions

Also Published As

Publication number Publication date
EP0518966A1 (en) 1992-12-23
JPH05505209A (en) 1993-08-05
DK0518966T3 (en) 1996-01-29
DE69115894T2 (en) 1996-05-30
CA2077666A1 (en) 1991-09-06
AU7484691A (en) 1991-10-10
EP0518966A4 (en) 1993-03-10
ATE132180T1 (en) 1996-01-15
DE69115894D1 (en) 1996-02-08
JP2966927B2 (en) 1999-10-25
EP0518966B1 (en) 1995-12-27
WO1991013949A1 (en) 1991-09-19
BR9106137A (en) 1993-03-02
ES2081472T3 (en) 1996-03-16
KR0151409B1 (en) 1998-10-01
GR3019268T3 (en) 1996-06-30
AU660608B2 (en) 1995-07-06
CA2077666C (en) 2004-06-22

Similar Documents

Publication Publication Date Title
EP0624639B1 (en) Fuel composition
KR100663774B1 (en) Fuel composition
KR100533490B1 (en) Additives for fuel compositions to reduce formation of combustion chamber deposits
KR920703766A (en) Automobile fuel additive composition and preparation method thereof
JPS63500602A (en) fuel products
US20030131527A1 (en) Alkyl-substituted aryl polyalkoxylates and their use in fuels
EP0235868A1 (en) Fuel composition
KR20010089133A (en) Fuel compositions containing propoxilate
AU2002246715B2 (en) Stabilizer blends for alcohol in hydrocarbon fuel
CN105378040A (en) Fuel additive composition
CZ20023608A3 (en) Fuel additive composition for internal combustion engines exhibiting enhanced viscosity properties and good IVD performance
MXPA02003836A (en) Use of fatty acid salts of alkoxylated oligoamines as lubricity improvers for petroleum products.
KR20010111494A (en) Polyalkenealcohol-polyalkoxylates and their use in fuels and lubricants
JPH04213390A (en) Composition for reducing attachment on guidance system
PL203764B1 (en) Fuel additive mixtures for gasolines with synergistic ivd performance
EP0323088A1 (en) Preparation of overbased magnesium sulphonate
WO1985001956A1 (en) Deposit control additives - hydroxy polyether polyamines
GB2261441A (en) Fuel compositions
WO2005121282A2 (en) Motor fuel additive composition
KR20020010600A (en) Polyalkene alcohol polyetheramines and use thereof in fuels and lubricants
WO2006098741A2 (en) Motor fuel additive composition
WO1997025392A1 (en) Gasoline detergent compositions
WO1997044415A1 (en) Gasoline detergent compositions
CA1341005C (en) Fuel compositions and lubricating oil compositions containing very long chain alkylphenyl poly(oxyalkylene) aminocarbamate
US20090158642A1 (en) Motor fuel additive composition

Legal Events

Date Code Title Description
A201 Request for examination
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20070813

Year of fee payment: 10

LAPS Lapse due to unpaid annual fee