GB1124437A - Copolymers - Google Patents
CopolymersInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F218/00—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 or of a haloformic acid
- C08F218/02—Esters of monocarboxylic acids
- C08F218/04—Vinyl esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—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
- C08F222/10—Esters
- C08F222/12—Esters of phenols or saturated alcohols
- C08F222/14—Esters having no free carboxylic acid groups, e.g. dialkyl maleates or fumarates
- C08F222/145—Esters having no free carboxylic acid groups, e.g. dialkyl maleates or fumarates the ester chains containing seven or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular 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
- C10M2209/086—Macromolecular 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B3/00—Engines characterised by air compression and subsequent fuel addition
- F02B3/06—Engines characterised by air compression and subsequent fuel addition with compression ignition
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B47/00—Methods 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.
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)
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 |
-
1967
- 1967-07-28 GB GB34856/67A patent/GB1124437A/en not_active Expired
Cited By (5)
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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