GB807737A - Mineral oil compositions - Google Patents

Mineral oil compositions

Info

Publication number
GB807737A
GB807737A GB2327756A GB2327756A GB807737A GB 807737 A GB807737 A GB 807737A GB 2327756 A GB2327756 A GB 2327756A GB 2327756 A GB2327756 A GB 2327756A GB 807737 A GB807737 A GB 807737A
Authority
GB
United Kingdom
Prior art keywords
parts
alcohol
oil
weight
maleic anhydride
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
GB2327756A
Inventor
Peter Joseph Vermont Jam Agius
Joan Daphne Bryan
Thomas Arnold Garbett
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 GB2327756A priority Critical patent/GB807737A/en
Publication of GB807737A publication Critical patent/GB807737A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F22/00Homopolymers and 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 a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
    • C08F22/04Anhydrides, e.g. cyclic anhydrides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/195Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/196Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
    • C10L1/1966Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof poly-carboxylic
    • 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

Landscapes

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

Abstract

Lubricating and fuel oil compositions comprise a mineral oil and an oil-soluble copolymer derived from 1 to 10 parts (by weight) of maleic anhydride, 10 to 30 parts of an ester of a vinyl alcohol and a C2-12 monocarboxylic acid, and 50 to 90 parts by weight of an ester of fumaric or maleic acid and a C8-18 alcohol. The C8-18 alcohol is preferably a natural alcohol, e.g. palm kernel alcohol or lauryl alcohol. The compositions may be oil concentrates of the polymers, which when present as about 5 per cent wt. of the final oil impart good pour point, viscosity index and detergency characteristics to the oil. Optional additives mentioned are oil-soluble sulphonates, metal salts of alkyl phenol sulphides and E.P., anti-wear and anti-oxidant additives. Examples comprise a mineral oil having viscosities of 180 cs./100 DEG F. and 12 cs./210 DEG F. (V.I. = 104) and copolymers prepared from the following ingredients at 60 DEG C. under reflux for 24 hours using 2 per cent benzoyl peroxide as catalyst: (i) 75 parts (weight) lauryl fumarate, 19 parts vinyl acetate, 4 parts maleic anhydride, and 2 parts lauryl alcohol; and (ii) 79, 16, 3 and 2 parts respectively of the same monomers. The Provisional Specification refers to the similar use of copolymers of maleic anhydride with one or more copolymerizable organic compounds. Examples of such compounds are vinyl esters of C3-20 acids e.g. of tiglic, acrylic, methacrylic, oleic or lauric acids; unsaturated hydrocarbons e.g. simple C3-10 mono olefines, polymerized olefines e.g. ethylene or alkylated styrene, and diolefines e.g. isoprene, ethers and acrylonitrile. The use of the copolymers in animal or vegetable oils or synthetic lubricating oils such as complex esters and diesters is also mentioned.ALSO:Lubricating and fuel oil compositions comprise a mineral oil and an oil-soluble copolymer derived from 1 to 10 parts (by weight) of maleic anhydride; 10 to 30 parts of an ester of a vinyl alcohol and a C2-12 monocarboxylic acid; and 50 to 90 parts by weight of an ester of fumaric or maleic acid and a C8-18 alcohol. The C8-18 alcohol is preferably a natural alcohol, e.g. palm kernel alcohol or lauryl alcohol. Examples comprise a mineral oil having viscosities of 180 cs./100 DEG F. and 12 cs./210 DEG F. (V.I.=104) and copolymers prepared from the following ingredients at 60 DEG C. under reflux for 24 hours using 2 per cent benzoyl peroxide as catalyst: (i) 75 parts (weight) lauryl fumarate, 19 parts vinyl acetate, 4 parts maleic anhydride, and 2 parts lauryl alcohol; and (ii) 79, 16, 3, and 2 parts respectively of the same monomers.
GB2327756A 1956-07-27 1956-07-27 Mineral oil compositions Expired GB807737A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2327756A GB807737A (en) 1956-07-27 1956-07-27 Mineral oil compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2327756A GB807737A (en) 1956-07-27 1956-07-27 Mineral oil compositions

Publications (1)

Publication Number Publication Date
GB807737A true GB807737A (en) 1959-01-21

Family

ID=10193062

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2327756A Expired GB807737A (en) 1956-07-27 1956-07-27 Mineral oil compositions

Country Status (1)

Country Link
GB (1) GB807737A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3184413A (en) * 1962-06-21 1965-05-18 Exxon Research Engineering Co Polymeric lubricating oil additives containing iodine and uses thereof
US3227532A (en) * 1961-08-14 1966-01-04 Exxon Research Engineering Co Polymer-containing motor fuel composition
US3257318A (en) * 1960-09-15 1966-06-21 Exxon Research Engineering Co Lubricating compositions containing a synergistic mixture of additives
US3388977A (en) * 1965-01-06 1968-06-18 Exxon Research Engineering Co Pour point depressant for middle distillates
US3462249A (en) * 1967-03-31 1969-08-19 Exxon Research Engineering Co Fuel oil compositions containing grafted polymers

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3257318A (en) * 1960-09-15 1966-06-21 Exxon Research Engineering Co Lubricating compositions containing a synergistic mixture of additives
US3227532A (en) * 1961-08-14 1966-01-04 Exxon Research Engineering Co Polymer-containing motor fuel composition
US3184413A (en) * 1962-06-21 1965-05-18 Exxon Research Engineering Co Polymeric lubricating oil additives containing iodine and uses thereof
US3388977A (en) * 1965-01-06 1968-06-18 Exxon Research Engineering Co Pour point depressant for middle distillates
US3462249A (en) * 1967-03-31 1969-08-19 Exxon Research Engineering Co Fuel oil compositions containing grafted polymers

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