GB703445A - Improvements in and relating to lubricating compositions - Google Patents
Improvements in and relating to lubricating compositionsInfo
- Publication number
- GB703445A GB703445A GB15017/51A GB1501751A GB703445A GB 703445 A GB703445 A GB 703445A GB 15017/51 A GB15017/51 A GB 15017/51A GB 1501751 A GB1501751 A GB 1501751A GB 703445 A GB703445 A GB 703445A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sebacate
- acid
- composition
- adipate
- ethylhexyl
- 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
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- 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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/044—Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/36—Esters of polycarboxylic acids
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/20—Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
- C10M107/30—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M107/32—Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
- C10M107/34—Polyoxyalkylenes
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- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/04—Hydroxy compounds
- C10M129/10—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
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- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/28—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/30—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 7 or less carbon atoms
- C10M129/36—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 7 or less carbon atoms containing hydroxy groups
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- C10M145/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/10—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
- C10M145/12—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 monocarboxylic
- C10M145/14—Acrylate; Methacrylate
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
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- C10N2040/02—Bearings
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- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
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- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
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- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
- C10N2040/13—Aircraft turbines
-
- 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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Catching Or Destruction (AREA)
- Lubricants (AREA)
Abstract
A lubricating composition comprises (1) a liquid ester of the formula R1OOCRCOOR11, wherein R is a divalent saturated aliphatic hydrocarbon radical and R1 and R11 are alkyl, aralkyl or cycloalkyl radicals of more than two carbon atoms; (2) from 2 to 30 per cent., preferably 5 to 15 per cent., based on the combined weight of ester and polymer, of a polymer of an ester of acrylic acid or a 1-alkacrylic acid and (3) a Group II metal salt of an aromatic carboxylic acid or phenol in such amount that the metal content of the composition is from 0.01 to 1.0 per cent. Suitable polymers or copolymers are derived from methyl, ethyl, n-propyl, isopropyl, isobutyl, lauryl, phenyl or benzyl esters of acrylic, methacrylic, 1-ethyl acrylic and 1-propyl acrylic acids. The polymers preferably have a relative molecular weight between 100 and 180 centistokes and may be subjected to a shearing action prior to incorporation in the composition. Typical esters are di(2-methylheptyl) adipate, di (3.5.5-trimethylhexyl) adipate or sebacate, di (3-ethylhexyl) adipate or sebacate, dihexylpimelate, di (2-ethylhexyl) sebacate, di-sec. butyl sebacate or malonate, di (1-ethylpropyl) azelate and dibutyl ethylmalonate. The metallic salt may be normal or basic and is preferably a zinc or calcium salt of benzoic, naphthoic, 4-t-butyl benzoic, 2.4-di-t-butyl-benzoic, di-isopropylsalicylic, octylsalicylic, pentadecenylsalicylic, octadecylsalicylic, stearyl-salicylic or octyl 4-hydroxybenzoic acid or of phenol, naphthol, cresol, alkylated phenols and di or tri alkylated phenols. Nuclear substituents such as halogen, alkoxy, alkyl mercapto and alkyl amino may be present in the phenol and particularly effective salts are the condensation products of substituted phenols and formaldehyde, acetaldehyde or paraformaldehyde. The composition may also contain mineral lubricating oils, extreme pressure additives such as trioctyl and tricresyl phosphates, monobutyl trichloromethanephosphonate or its di (2-ethylhexyl) amine salt, antioxidants such as alkylated phenols and diphenols and condensation products of ethylene or propylene oxide with sebacic acid and ethers or esters of these condensates. In examples the physical properties of compositions containing polymethyl acrylate or methacrylate are given.ALSO:Lubricants for use in aircraft and gas turbines comprise a saturated ester R1OOCRCOOR11, wherein R is a divalent saturated aliphatic hydrocarbon radical and R1 and R11 are alkyl, aralkyl or cycloalkyl radicals of more than two carbon atoms, from 2 to 30 per cent., based on the combined weight of polymer and ester, of a polymer of an ester of acrylic acid or a 1-alkacrylic acid and a Group II metal salt of an aromatic carboxylic acid or phenol in such amount that the metal content of the composition is from 0.01 to 1.0 per cent. Suitable polymers or copolymers are derived from methyl, ethyl, n-propyl, isopropyl, isobutyl, lauryl, phenyl or benzyl esters of acrylic, methacrylic, 1 - ethylacrylic and 1 - propylacrylic acids. The polymers preferably have a relative molecular weight between 100 and 180 centistokes and may be subjected to a shearing action prior to incorporation in the composition. Typical esters are di (2-methylheptyl) adipate, di (3.5.5-trimethylhexyl) adipate or sebacate, di (3-ethylhexyl) adipate or sebacate, dihexylpimelate, di (2-ethylhexyl) sebacate, di-sec. butyl sebacate or malonate, di (1-ethylpropyl) azelate and dibutyl ethylmalonate. The metallic salt may be normal or basic and is preferably a zinc or calcium salt of benzoic, naphthoic, 4 - t - butylbenzoic, 2.4 - di - t - butylbenzoic, di-isopropylsalicylic, octylsalicylic, pentadecenylsalicylic, octadecylsalicylic, stearylsalicylic or octyl-4-hydroxy-benzoic acid or of phenol, naphthol, cresol, alkylated phenols and di or tri alkylated phenols. Nuclear substitutes such as halogen, alkoxy, alkyl mercapto and alkyl amino may be present in the phenol and particularly effective salts are the condensation products of substituted phenols and formaldehyde, acetaldehyde or paraformaldehyde. The composition may also contain mineral lubricating oils, extreme pressure additives such as trioctyl and tricresyl phosphates, monobutyl trichloromethane-phosphonate or its di (2-ethylhexyl) amine salt, antioxidants such as alkylated phenols and diphenols and condensation products of ethylene or propylene oxide with sebacic acid and ethers or esters of these condensates. In examples the physical properties of compositions containing polymethyl acrylate or methacrylate are given.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB311808X | 1951-06-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB703445A true GB703445A (en) | 1954-02-03 |
Family
ID=10319207
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15017/51A Expired GB703445A (en) | 1951-06-25 | 1951-06-25 | Improvements in and relating to lubricating compositions |
Country Status (6)
Country | Link |
---|---|
AT (1) | AT27938B (en) |
BE (3) | BE512332A (en) |
CH (3) | CH311808A (en) |
FR (2) | FR1063912A (en) |
GB (1) | GB703445A (en) |
NL (3) | NL93187C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE972655C (en) * | 1954-06-09 | 1959-08-27 | Exxon Research Engineering Co | Synthetic lubricating oil for aircraft gas turbines |
WO2005014762A1 (en) * | 2003-07-25 | 2005-02-17 | Rohmax Additives Gmbh | A functional fluid and the use thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB786950A (en) * | 1951-06-25 | 1957-11-27 | Shell Res Ltd | Improvements in and relating to lubricating compositions containing polyoxy alkyleneliquids |
GB768905A (en) * | 1951-06-25 | 1957-02-20 | Shell Res Ltd | Improvements in and relating to lubricating compositions |
-
0
- NL NL93232D patent/NL93232C/xx active
- NL NL80589D patent/NL80589C/xx active
- BE BE546947D patent/BE546947A/xx unknown
- BE BE557647D patent/BE557647A/xx unknown
- NL NL93187D patent/NL93187C/xx active
- BE BE512332D patent/BE512332A/xx unknown
-
1906
- 1906-06-16 AT AT27938D patent/AT27938B/en active
-
1951
- 1951-06-25 GB GB15017/51A patent/GB703445A/en not_active Expired
-
1952
- 1952-06-23 CH CH311808D patent/CH311808A/en unknown
- 1952-06-24 FR FR1063912D patent/FR1063912A/en not_active Expired
-
1956
- 1956-04-12 CH CH343992D patent/CH343992A/en unknown
- 1956-04-12 FR FR69796D patent/FR69796E/en not_active Expired
-
1957
- 1957-05-20 CH CH357822D patent/CH357822A/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE972655C (en) * | 1954-06-09 | 1959-08-27 | Exxon Research Engineering Co | Synthetic lubricating oil for aircraft gas turbines |
WO2005014762A1 (en) * | 2003-07-25 | 2005-02-17 | Rohmax Additives Gmbh | A functional fluid and the use thereof |
CN100424157C (en) * | 2003-07-25 | 2008-10-08 | 罗麦斯添加剂有限公司 | A functional fluid and the use thereof |
Also Published As
Publication number | Publication date |
---|---|
NL93232C (en) | |
BE557647A (en) | |
NL80589C (en) | |
FR69796E (en) | 1958-12-30 |
CH311808A (en) | 1955-12-15 |
AT27938B (en) | 1907-03-26 |
NL93187C (en) | |
CH357822A (en) | 1961-10-31 |
BE546947A (en) | |
FR1063912A (en) | 1954-05-10 |
CH343992A (en) | 1960-01-15 |
BE512332A (en) |
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