GB659103A - Complex esters - Google Patents
Complex estersInfo
- Publication number
- GB659103A GB659103A GB31036/48A GB3103648A GB659103A GB 659103 A GB659103 A GB 659103A GB 31036/48 A GB31036/48 A GB 31036/48A GB 3103648 A GB3103648 A GB 3103648A GB 659103 A GB659103 A GB 659103A
- Authority
- GB
- United Kingdom
- Prior art keywords
- atoms
- atom
- radicals
- ether oxygen
- aliphatic hydrocarbon
- 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
- 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
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/30—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
- C10M2207/302—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids derived from the combination of monocarboxylic acids, dicarboxylic acids and dihydroxy compounds only and having no free hydroxy or carboxyl groups
-
- 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
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/11—Complex polyesters
- C10M2209/111—Complex polyesters having dicarboxylic acid centres
-
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/085—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing carboxyl groups; Derivatives thereof
-
- 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
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/04—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2221/043—Polyoxyalkylene ethers with a thioether group
-
- 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
- C10N2050/10—Semi-solids; greasy
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
A complex ester is prepared by esterifying a saturated aliphatic mono-carboxylic acid with an equimolar proportion of a glycol to form a half ester, and esterifying two molar proportions thereof with one of an aliphatic or aromatic dicarboxylic acid. Esters for use as lubricants may have the formula <FORM:0659103/IV (a)/1> where R1 and R11 are saturated C2-C20 aliphatic hydrocarbon radicals or a series of such C2 or higher radicals linked by one or more ether oxygen and/or thioether sulphur atoms, the total number of C, O, and S atoms being 5-80 and the number of S atoms not more than 2, R2 and R12 are C1-C22 saturated aliphatic hydrocarbon radicals or similar radicals wherein up to 5 of the C atoms are replaced by ether oxygen atoms, there being at least 1 C atom between the carboxyl group and the first O atom, and at least 2 C atoms between each pair of O atoms, or wherein 1 C atom has been replaced by a thioether sulphur atom; R3 is an aliphatic hydrocarbon radical containing up to 30 C atoms or a series of C2 or higher, such radicals linked by 1 or more ether oxygen and/or thioether sulphur atoms, the total number of C, O, and S atoms being 3-80 and the number of S atoms not more than 2, and there being at least 1 C atom between each carboxyl group and the nearest O or S or R3 is an aromatic nucleus containing not more than 2 and preferably 1 aromatic ring with or without aliphatic substituents up to a total of 16 C atoms; and the starting materials are so chosen that the molecular weight of the product is at least 300 and its viscosity at 210 DEG F. not more than 150 Saybolt seconds. Preferred glycols are polyethylene glycols HO(CH2CH2O)nCH2CH2OH, where n is 1-26. Preferred monocarboxylic acids are fatty acids of 2-10 C atoms; preferred dicarboxylic acids are straight-chain paraffinic acids of 6-10 C atoms. Numerous examples of these are given. The preparation and properties of esters from valeric, caproic, caprylic, acetic, propionic or butyric acid; ethylene glycol or tri-, tetra- or higher polyglycols or thiodiglycol; and adipic and/or sebacic, thiodipropionic or terephthalic acid are described. They may be blended with mineral oils, and antioxidants, and other additives incorporated.ALSO:A complex ester is prepared by esterifying a saturated aliphatic monocarboxylic acid with an equimolar proportion of a glycol to form a half ester, and esterifying two molar proportions thereof with one of an aliphatic or aromatic dicarboxylic acid. Esters for use as lubricants may have the formula R2.COO-R1-OOC-R3-COO.R11 -OOC.R12 where R1 and R11 are saturated C2-C20 aliphatic hydrocarbon radicals or a series of such C2 or higher radicals linked by one or more ether oxygen and/or thioether sulphur atoms, the total number of p C, O, and S atoms being 5-80 and the number of S atoms not more than 2; R2 and R12 are C1-C22 saturated aliphatic hydrocarbon radicals or similar radicals wherein up to 5 of the C atoms are replaced by ether oxygen atoms, there being at least 1 C atom between the carboxyl group and the first O atom, and at least 2 C atoms between each pair of O atoms, or wherein 1 C atom has been replaced by a thioether sulphur atom; R3 is an aliphatic hydrocarbon radical containing up to 30 C atoms or a series of C2 or higher such radicals linked by 1 or more ether oxygen and/or thioether sulphur atoms, the total number of C, O, and S atoms being 3-80 and the number of S atoms not more than 2, and there being at least 1 C atom between each carboxyl group and the nearest O or S, or R3 is an aromatic nucleus containing not more than 2 and preferably 1 aromatic ring with or without aliphatic substituents up to a total of 16 C atoms; and the starting materials are so chosen that the molecular weight of the product is at least 300 and its viscosity at 210 DEG F. not more than 150 Saybolt seconds. Preferred glycols are polyethylene glycols HO(CH2CH2 O)nCH2CH2OH where n is 1-26. Preferred monocarboxylic acids are fatty acids of 2-10 C atoms; preferred dicarboxylic acids are straight chain paraffinic acids of 6-10 C atoms. Numerous examples of these are given. The preparation and properties of esters from valeric, caproic, caprylic, acetic, propionic or butyric acid; ethylene glycol or tri-, tetra- or higher poly-glycols or thiodiglycol; and adipic and/or sebacic, thiodipropionic or terephthalic acid are described. Esterification is effected in toluene with p-toluene sulphonic acid monohydrate as catalyst. They may be blended with mineral oils, and antioxidants, and other additives incorporated.ALSO:A complex ester is prepared by esterifying a saturated aliphatic monocarboxylic acid with an equimolar proportion of a glycol to form a half ester, and esterifying two molar proportions thereof with one of an aliphatic or aromatic dicarboxylic acid. Esters for use as lubricants may have the formula R2COO-R1-OOC-R3 -COO.R11-OOC.R12 where R1 and R11 are saturated C2-C20 aliphatic hydrocarbon radicals or a series of such C2 or higher radicals linked by one or more ether oxygen and/or thioether sulphur atoms, the total number of C, O, and S atoms being 5-80 and the number of S atoms not more than 2; R2 and R12 are C1-C22 saturated aliphatic hydrocarbon radicals or similar radicals wherein up to 5 of the C atoms are replaced by ether oxygen atoms, there being at least 1 C atom between the carboxyl group and the first O atom, and at least 2 C atoms between each pair of O atoms, or wherein 1 C atom has been replaced by a thioether sulphur atom; R3 is an aliphatic hydrocarbon radical containing up to 30 C atoms or a series of C2 or higher such radicals linked by 1 or more ether oxygen and/or thioether sulphur atoms, the total number of C, O, and S atoms being 3-80 and the number of S atoms not more than 2, and there being at least 1 C atom between each carboxyl group and the nearest O or S, or R3 is an aromatic nucleus containing not more than 2 and preferably 1 aromatic ring with or without aliphatic substituents up to a total of 16 C atoms; and the starting materials are so chosen that the molecular weight of the product is at least 300 and its viscosity at 210 DEG F. not more than 150 Saybolt seconds. Preferred glycols are polyethylene glycols HO(CH2CH2O)nCH2CH2 OH where n is 1-26. Preferred monocarboxylic acids are fatty acids of 2-10 C atoms; preferred dicarboxylic acids are stright chain paraffinic acids of 6-10 C atoms. Numerous examples of these are given. The preparation and properties of esters from valeric, caproic, caprylic, acetic, propionic or butyric acid; ethylene glycol or tri-, tetra- or higher polyglycols or thiodiglycol; and adipic and/or sebacic, thiodipropionic or terephthalic acid are described. They may be blended with mineral oils, and antioxidants, and other additives incorporated.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB31036/48A GB659103A (en) | 1948-11-30 | 1948-11-30 | Complex esters |
FR991513D FR991513A (en) | 1948-11-30 | 1949-07-30 | Advanced lubricant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB31036/48A GB659103A (en) | 1948-11-30 | 1948-11-30 | Complex esters |
Publications (1)
Publication Number | Publication Date |
---|---|
GB659103A true GB659103A (en) | 1951-10-17 |
Family
ID=10316975
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31036/48A Expired GB659103A (en) | 1948-11-30 | 1948-11-30 | Complex esters |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR991513A (en) |
GB (1) | GB659103A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1135445B (en) * | 1953-07-02 | 1962-08-30 | Exxon Research Engineering Co | Process for the preparation of complex esters which can be used as lubricating oils or lubricating oil components |
DE1225628B (en) * | 1955-07-11 | 1966-09-29 | Exxon Research Engineering Co | Process for the production of mixed esters serving as lubricating oils |
EP3255128A1 (en) * | 2016-06-08 | 2017-12-13 | Peter Greven GmbH & Co. KG | Complex esters and their use |
-
1948
- 1948-11-30 GB GB31036/48A patent/GB659103A/en not_active Expired
-
1949
- 1949-07-30 FR FR991513D patent/FR991513A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1135445B (en) * | 1953-07-02 | 1962-08-30 | Exxon Research Engineering Co | Process for the preparation of complex esters which can be used as lubricating oils or lubricating oil components |
DE1225628B (en) * | 1955-07-11 | 1966-09-29 | Exxon Research Engineering Co | Process for the production of mixed esters serving as lubricating oils |
EP3255128A1 (en) * | 2016-06-08 | 2017-12-13 | Peter Greven GmbH & Co. KG | Complex esters and their use |
Also Published As
Publication number | Publication date |
---|---|
FR991513A (en) | 1951-10-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3090753A (en) | Ester oil compositions containing acid anhydride | |
US2628974A (en) | Polyester synthetic lubricants | |
US4061581A (en) | Trimethylolpropane esters useful as base lubricants for motor oils | |
US2559510A (en) | Synthetic lubricants | |
GB1037985A (en) | Alkylbutyrolactone-ª-acetic acids | |
GB659103A (en) | Complex esters | |
US2561232A (en) | Dialkylalkenylsuccinates | |
US2911368A (en) | Low temperature stability of synthetic lubricants | |
GB642410A (en) | Lubricating grease composition | |
US3804762A (en) | Antioxidants | |
GB711211A (en) | Improved lubricant blend | |
JPH04314797A (en) | Ester composition | |
US2956954A (en) | Synthetic ester lubricants | |
EP0041851B1 (en) | Lubricant composition with stabilized metal detergent additive and friction reducing ester component | |
KR940019670A (en) | Ester Compounds, Processes for Use and Uses thereof | |
GB701160A (en) | Improved motor fuel | |
US3329611A (en) | Lubricating oil composition | |
GB1441918A (en) | Ester mixtures | |
GB666697A (en) | ||
US2585862A (en) | Synthetic lubricants | |
US3290248A (en) | Siloxane ester lubricants | |
US3649570A (en) | Lubricant compositions | |
GB668663A (en) | Improvements in or relating to synthetic ester lubricants | |
US2311534A (en) | Polyester compounds and method of making same | |
JPS63125598A (en) | Flame-retardant hydraulic oil |