GB1124437A - Copolymers - Google Patents

Copolymers

Info

Publication number
GB1124437A
GB1124437A GB34856/67A GB3485667A GB1124437A GB 1124437 A GB1124437 A GB 1124437A GB 34856/67 A GB34856/67 A GB 34856/67A GB 3485667 A GB3485667 A GB 3485667A GB 1124437 A GB1124437 A GB 1124437A
Authority
GB
United Kingdom
Prior art keywords
hydrocarbyl group
alcohol
acid
prepared
substituted
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
Application number
GB34856/67A
Inventor
Roger Charles Price
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering Co
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 Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Priority to GB34856/67A priority Critical patent/GB1124437A/en
Publication of GB1124437A publication Critical patent/GB1124437A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F218/00Copolymers 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 or of a haloformic acid
    • C08F218/02Esters of monocarboxylic acids
    • C08F218/04Vinyl esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F222/00Copolymers 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 a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
    • C08F222/10Esters
    • C08F222/12Esters of phenols or saturated alcohols
    • C08F222/14Esters having no free carboxylic acid groups, e.g. dialkyl maleates or fumarates
    • C08F222/145Esters having no free carboxylic acid groups, e.g. dialkyl maleates or fumarates the ester chains containing seven or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/086Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type polycarboxylic, e.g. maleic acid
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/015Dispersions of solid lubricants
    • C10N2050/02Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B3/00Engines characterised by air compression and subsequent fuel addition
    • F02B3/06Engines characterised by air compression and subsequent fuel addition with compression ignition
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B47/00Methods of operating engines involving adding non-fuel substances or anti-knock agents to combustion air, fuel, or fuel-air mixtures of engines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

An oil-soluble copolymer is prepared by copolymerizing (A) a vinyl ester or a hydrocarbyl substituted vinyl ester of a carboxylic acid and (B) a dialkyl ester of fumaric acid, maleic acid or itaconic acid and a monohydric alcohol or a mixture of monohydric alcohols in the presence of a minor proportion by weight, based on the total weight of (A) and (B), of an allyl compound of the formula CH2=CH.CH2OR where R is hydrogen, a hydrocarbyl group, a substituted hydrocarbyl group or -OCR1, where R1 is a hydrocarbyl group, or a substituted hydrocarbyl group, said hydrocarbyl groups being saturated aliphatic groups or aryl groups in which any substituent in any benzene ring is saturated. In the examples are used: vinyl acetate, allyl alcohol, mineral oil, a dialkyl fumarate prepared from hydrogenated fatty acid alcohol, a dialkyl fumarate prepared from mixed ceto-stearyl alcohol and azo-bis-isobutyronitrile. The coconut fatty acid alcohol and mixed ceto-stearyl alcohol comprise mixtures of C8, C10, C12, C14, C16 and C18 straight chain alcohols and C14, C16 and C18 straight chain alcohols respectively. The reaction is terminated by the addition of high sulphur mineral oil. Benzoyl peroxide is used in some examples. The copolymers may be used as lubricating oil additives.ALSO:A lubricating composition comprises a mineral lubricating oil and 0.01% to 10.0% by weight based on the oil of a copolymer prepared by copolymerizing (A) a vinyl ester or a hydrocarbyl substituted vinyl ester of a carboxylic acid, and (B) a dialkyl ester of fumaric acid, maleic acid or itaconic acid and a monohydric alcohol or a mixture of monohydric alcohols in the presence of a minor proportion by weight, based on the total weight of (A) and (B), of an allyl compound of the formula CH2=CHCH2OR where R is hydrogen, a hydrocarbyl group, a substituted hydrocarbyl group or -OCR1 where R1 is hydrocarbyl group or a substituted hydrocarbyl group, said hydrocarbyl groups being saturated aliphatic groups or aryl groups in which any substituent in any benzene ring is saturated. Fuel compositions comprising diesel fuel base stocks, domestic heating oils, or refined kerosene and the copolymers may also be prepared.
GB34856/67A 1967-07-28 1967-07-28 Copolymers Expired GB1124437A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB34856/67A GB1124437A (en) 1967-07-28 1967-07-28 Copolymers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB34856/67A GB1124437A (en) 1967-07-28 1967-07-28 Copolymers

Publications (1)

Publication Number Publication Date
GB1124437A true GB1124437A (en) 1968-08-21

Family

ID=10370751

Family Applications (1)

Application Number Title Priority Date Filing Date
GB34856/67A Expired GB1124437A (en) 1967-07-28 1967-07-28 Copolymers

Country Status (1)

Country Link
GB (1) GB1124437A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4906702A (en) * 1985-04-15 1990-03-06 Henkel Kommanditgesellschaft Auf Aktien Esters of unsaturated carboxylic acids, preparation of their oil-soluble homo- and copolymers and use thereof as pour point depressants
GB2234750A (en) * 1989-08-10 1991-02-13 Basf Corp Polyvinyl acetate/allyl alcohol copolymers
GB2234751A (en) * 1989-08-10 1991-02-13 Basf Corp Rigid polyurethane foams prepared from polyvinyl acetate/allyl alcohol polyols,and process for making same
US5478368A (en) * 1990-04-19 1995-12-26 Exxon Chemical Patents Inc. Additives for distillate fuels and distillate fuels containing them
US5593466A (en) * 1985-09-06 1997-01-14 Exxon Chemical Patents Inc Oil and fuel oil compositions

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4906702A (en) * 1985-04-15 1990-03-06 Henkel Kommanditgesellschaft Auf Aktien Esters of unsaturated carboxylic acids, preparation of their oil-soluble homo- and copolymers and use thereof as pour point depressants
US5593466A (en) * 1985-09-06 1997-01-14 Exxon Chemical Patents Inc Oil and fuel oil compositions
GB2234750A (en) * 1989-08-10 1991-02-13 Basf Corp Polyvinyl acetate/allyl alcohol copolymers
GB2234751A (en) * 1989-08-10 1991-02-13 Basf Corp Rigid polyurethane foams prepared from polyvinyl acetate/allyl alcohol polyols,and process for making same
US5478368A (en) * 1990-04-19 1995-12-26 Exxon Chemical Patents Inc. Additives for distillate fuels and distillate fuels containing them

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