GB774457A - Synthetic ester lubricant blends - Google Patents

Synthetic ester lubricant blends

Info

Publication number
GB774457A
GB774457A GB15987/55A GB1598755A GB774457A GB 774457 A GB774457 A GB 774457A GB 15987/55 A GB15987/55 A GB 15987/55A GB 1598755 A GB1598755 A GB 1598755A GB 774457 A GB774457 A GB 774457A
Authority
GB
United Kingdom
Prior art keywords
phenothiazine
diester
acid
per cent
complex ester
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
GB15987/55A
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
Publication of GB774457A publication Critical patent/GB774457A/en
Expired legal-status Critical Current

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    • 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
    • C10M3/00Liquid 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
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    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/025Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with condensed rings
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/287Partial esters
    • C10M2207/289Partial esters containing free hydroxy groups
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/30Complex 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/30Complex 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
    • C10M2207/302Complex 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/30Complex 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
    • C10M2207/304Complex 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 monohydroxy compounds, dihydroxy compounds and dicarboxylic acids only and having no free hydroxy or carboxyl groups
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/11Complex polyesters
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/11Complex polyesters
    • C10M2209/111Complex polyesters having dicarboxylic acid centres
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/11Complex polyesters
    • C10M2209/112Complex polyesters having dihydric acid centres
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/14Containing carbon-to-nitrogen double bounds, e.g. guanidines, hydrazones, semicarbazones
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/085Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing carboxyl groups; Derivatives thereof
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/108Phenothiazine
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    • C10M2221/00Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2221/04Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2221/043Polyoxyalkylene ethers with a thioether group
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/041Triaryl phosphates
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/10Phosphatides, e.g. lecithin, cephalin
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    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/02Unspecified siloxanes; Silicones
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    • C10M2229/04Siloxanes with specific structure
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/08Resistance to extreme temperature
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/12Gas-turbines
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/12Gas-turbines
    • C10N2040/13Aircraft turbines

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

The ingredients of a lubricating composition (see Group III) include a C6-C16 branched-chain alcohol diester of a dicarboxylic acid, a complex ester and phenothiazine. The blend of diester and complex ester may be prepared by refluxing a mixture of 2 mols. of azelaic acid, 1 mol. of a polyethylene glycol having a molecular weight of about 200 and 2.4 mols. of a C8 oxo alcohol, in the presence of toluene and sodium bisulphate, until no further formation of water occurs. The crude product may be washed, first with caustic soda and then with water, to remove acid compounds, and then distilled at reduced pressure to remove light ends. Instead of refluxing the mixture of azelaic acid, polyethylene glycol and C8 oxo alcohol, a half ester may first be prepared by refluxing a mixture of the azelaic acid and polyethylene glycol, in the presence of toluene and sodium bisulphate, until no further formation of water occurs. The C8 oxo alcohol may then be added and the mixture again refluxed until no further formation of water occurs. The finished product contains about 30-35 volume per cent diester and 65-70 volume per cent complex ester. The phenothiazine may be prepared by heating diphenylamine and sulphur in the presence of iodine. The crude product may be purified by precipitating the phenothiazine from a solution in acetone by the addition of water.ALSO:Non-corrosive lubricating compositions, suitable for use in turbo-jet and turbo-prop aircraft engines, comprise a blend of 20-95 per cent by volume of a C6-C16 branched chain alcohol diester of a dicarboxylic acid with 80-5 per cent by volume of a complex ester as defined below, 0.1-5 per cent by weight of phenothiazine and 0.1-5 per cent by weight of a condensation product of an aromatic aldehyde with a diamine, the percentages by weight being based on the total composition. The diester may be derived from C6, C7, C8 or C9 oxo alcohols and oxalic, malonic, succinic, glutaric, adipic, pimelic, suberic, azelaic or sebacic acids. The complex ester has one of the following formulae:- (I) <FORM:0774457/III/1> wherein R1 and R5 are the alkyl radicals of monocarboxylic acids, R2 and R4 are glycol residues, R3 is the alkylene radicle of a dicarboxylic acid and x is a whole number, (II) <FORM:0774457/III/2> wherein R1 and R5 are the combining radicles of the alcohols R1 OH and R5OH, R2 and R4 are the alkylene radicles of a dicarboxylic acid, R3 is a glycol residue and x is a whole number and (III) <FORM:0774457/III/3> wherein R1 is the alkyl radicle of a monohydric alcohol, R2 is the alkylene radicle of a dicarboxylic acid, R3 is a glycol residue, R4 is the alkyl radicle of a monocarboxylic acid and x is a whole number. Monohydric alcohols suitable for use in preparing the complex esters include alkanols, oleyl alcohol and ether alcohols formed by the reaction of ethylene oxide or propylene oxide with aliphatic alcohols, while suitable glycols include those containing ether oxygen atoms and/or thioether sulphur atoms, particularly polyethylene glycols. Additional ingredients which may be present in the lubricating compositions are amines (e.g. primary, secondary and tertiary alkylamines, such as bis-2 - ethyl hexyl amine( bis (di - 2 - ethylhexylamino) methane, C6-C24 primary amine mixtures, trihexylamine and octadecylamine), tricresyl phosphate, other oxidation inhibitors (e.g. polynuclear phenols and alkylated phenols), detergents (e.g. petroleum sulphonic acids and their metal salts), rust inhibitors (e.g. polyhydroxy esters such as sorbitan mono-oleate and penta-erythritol mono-oleate), lecithin, foam suppressants (e.g. silicones) and mineral oil. In an example, a lubricating composition consists of a diester (derived from C8 oxo alcohol and azelaic acid), a complex ester (derived from azelaic acid, polyethylene glycol having a molecular weight of about 200, and C8 oxo alcohol), purified or commercial phenothiazine and an ethylene diaminesalicylaldehyde condensation product. For comparison purposes, similar compositions are described in which either the phenothiazine or the amine-aldehyde condensation product is omitted. Also for comparison purposes, compositions are described consisting of a diester (derived from 2 - ethyl hexanol and sebacic acid), a complex ester derived from sebacic acid, polyethylene glycol having a molecular weight of about 200 and 2 - ethyl hexanol), tricresyl phosphate and either (a) purified phenothiazine or (b) commercial phenothiazine together with one of di - 2 - ethylhexyl amine, bis (di - 2 - ethylhexyl amino) methane and a mixture of C12-C16 aliphatic primary amines.
GB15987/55A 1954-06-25 1955-06-03 Synthetic ester lubricant blends Expired GB774457A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US439478A US2743234A (en) 1954-06-25 1954-06-25 Stabilized synthetic lubricant

Publications (1)

Publication Number Publication Date
GB774457A true GB774457A (en) 1957-05-08

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ID=23744856

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15987/55A Expired GB774457A (en) 1954-06-25 1955-06-03 Synthetic ester lubricant blends

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US (1) US2743234A (en)
GB (1) GB774457A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3236774A (en) * 1962-08-10 1966-02-22 Eastman Kodak Co Antioxidant composition and synthetic lubricant containing it
US3278434A (en) * 1963-07-30 1966-10-11 Exxon Research Engineering Co Lubricant compositions containing thiodicarboxylic acid esters
FR2187895A1 (en) * 1972-06-12 1974-01-18 Union Carbide Corp Power transfer fluid - contg dibasic acid ester and tert amine

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2190648A (en) * 1936-06-09 1940-02-20 Gulf Oil Corp Lubrication of alloy bearings
US2476271A (en) * 1946-05-29 1949-07-19 Standard Oil Co Lubricating oil additive
US2499984A (en) * 1948-12-16 1950-03-07 Rohm & Haas Oily complex esters
US2639266A (en) * 1951-04-07 1953-05-19 Texas Co Lubricating grease comprising a complex ester base and sodium myristate

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US2743234A (en) 1956-04-24

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