GB923190A - Antioxidant compositions - Google Patents
Antioxidant compositionsInfo
- Publication number
- GB923190A GB923190A GB12983/61A GB1298361A GB923190A GB 923190 A GB923190 A GB 923190A GB 12983/61 A GB12983/61 A GB 12983/61A GB 1298361 A GB1298361 A GB 1298361A GB 923190 A GB923190 A GB 923190A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- formula
- oils
- alkyl group
- hydrogen
- 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
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B5/00—Preserving by using additives, e.g. anti-oxidants
- C11B5/0092—Mixtures
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
- C08K5/526—Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/32—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing two or more of boron, silicon, phosphorus, selenium, tellurium or a metal
- C09K15/322—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing two or more of boron, silicon, phosphorus, selenium, tellurium or a metal containing only phosphorus
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/103—Liquid carbonaceous fuels containing additives stabilisation of anti-knock agents
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- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
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- 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
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- C10L—FUELS 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
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- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/183—Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom
- C10L1/1835—Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom having at least two hydroxy substituted non condensed benzene rings
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- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/26—Organic compounds containing phosphorus
- C10L1/2633—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
- C10L1/2641—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) oxygen bonds only
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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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
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- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Lubricants (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Fats and fatty oils, e.g. lard, beef tallow, fish oils, and vegetable oils and shortenings; waxes; liquid hydrocarbon fuels such as gasoline, which may contain antiknock agents such as tetraethyl lead and halogen- and phosphorus-containing scavengers, kerosene, diesel oils, fuel oils and turbine oils; hydrocarbon lubricating oils which may contain barium sulphonate detergents, and insulating oils; synthetic diester lubricating oils, such as the adipates and sebacates; polyalkylene glycol lubricants; hydraulic fluids; and greases obtained by adding metallic soaps (including resin soaps) to lubricating oils together with such further additives as fats, fatty acids, alkalis, glycerol, fatty alcohols, resin, wool grease, water, and modifiers and peptizers; contain a synergistic antioxidant composition which comprises (a) a phosphite ester of formula <FORM:0923190/III/1> wherein R1, R2 and R3 are alkyl, alkoxyalkyl, haloalkyl, cycloalkyl, halocycloalkyl, aralkyl, alkaryl, haloaryl or haloalkaryl radicals, and R3 may also be hydrogen, and (b) a methylene bisphenol of formula <FORM:0923190/III/2> wherein R4 is a C3-12- alkyl group which is branched on the a -carbon atom and R5 is a C1-12- alkyl group, the weight ratio (b) to (a) being 0,005-1000. In general the material to be stabilized contains 0,025-4% of (a) and 0,01-5%, preferably 0,1-3% of (b) by weight, there preferably being present 0,5-5 moles of (a) per mole of (b). (a) is most suitably a di-C1-12-alkyl hydrogen phosphite, and (b) is preferably 4:41-methylene bis(2:6-diisopropylphenol) or 4:41-methylene bis(6-tert.butyl-o-cresol).ALSO:Addition polymers such as polystyrene, polyvinyl chloride and acetate and particularly polymers of C2-5- mono-olefins such as butylene, isobutylene, 2-methyl-4-butene, and 2-methyl-3-butene, but especially polyethylene and-propylene; condensation polymers such as epoxide, polyester and alkyd resins; elastomers such as natural rubber, oil extended and sulphur-vulcanized rubbers, and synthetic rubbers such as polybutadiene, methyl rubber, polybutadiene rubber, butyl rubber, GR-S and GR-N rubbers, piperylene rubber and dimethylbutadiene rubber; and silicone lubricants, contan a synergistic antioxidant composition which comprises (a) a phosphite ester of formula <FORM:0923190/IV(a)/1> wherein R1, R2 and R3 are alkyl, alkoxyalkyl, haloalkyl, cycloalkyl, halocycloalkyl, aralkyl, alkaryl, haloaryl or haloalkaryl radicals, and R3 may also be hydrogen, and (b) a methylene bisphenol of formula <FORM:0923190/IV(a)/2> wherein R4 is a C3-12- alkyl group which is branched on the a -carbon atom and R5 is a C1-12- alkyl group, the weight ratio (b) to (a) being 0,005-1000. In general the material to be stabilized contains 0,025-4% of (a) and 0,01-5%, preferably 0,1-3% of (b) by weight, there preferably being present 0,5-5 moles of (a) per mole of (b). (a) is most suitably a di-C1-12-alkyl hydrogen phosphite, and (b) is preferably 4:41-methylene bis(2:6-diisopropylphenol) or 4:41-methylene bis(6-tert.butyl-o-cresol).ALSO:A synergistic antioxidant composition for addition to material subject to oxidative deterioration comprises (a) a phosphite ester of formula <FORM:0923190/IV(a)/1> wherein R1, R2 and R3 are alkyl, alkoxyalkyl, haloalkyl, cycloalkyl, halocycloalkyl, aralkyl, alkaryl, haloaryl or haloalkaryl radicals, and R3 may also be hydrogen, and (b) a methylene bisphenol of formula <FORM:0923190/IV(a)/2> wherein R4 is a C3-12-alkyl group which is branched on the a -carbon atom and R5 is a C1-12-alkyl group, the weight ratio (b) to (a) being 0.005-1000. In general the material to be stabilized contains 0.025-4% of (a) and 0.01-5%, preferably 0.1-3% of (b) by weight, there preferably being present 0.0-5 moles of (a) per mole of (b). (a) is most suitably a di-C1-12-alkyl hydrogen phosphite, and (b) is preferably 4:41- methylene bis(2:6- diisopropylphenol) or 4:41-methylene bis(6-tert-.butylo-cresol). The compositions may be used to p stabilize vitamins A, D and E and certain of the B complex vitamins; halogen-containing compounds such as fluorocarbons; and phosphate esters of formula <FORM:0923190/IV(a)/3> where R, R1 and R11 are hydrogen or an organic radical at least one of the groups R, R1 and R11 being an organic radical, e.g. tricresyl phosphate.ALSO:Foodstuffs such as butter, margarine, potato chips, fried fish, doughnuts, crackers, cakes, biscuits, peanut butter, peanuts and other whole nuts, and salad dressings, fat-fortified animal feedstuffs and fish meal contain a synergistic antioxidant composition which comprises (a) a phosphite ester of formula <FORM:0923190/VI/1> wherein R1, R2 and R3 are alkyl, alkoxyalkyl, haloalkyl, cycloalkyl, halocycloalkyl, aralkyl, alkaryl, haloaryl or haloalkaryl radicals, and R3 may also be hydrogen, and (b) a methylene bisphenol of formula <FORM:0923190/VI/2> wherein R4 is a C3-12-alkyl group which is branched on the a -carbon atom and R5 is a C1-12-alkyl group, the weight ratio (b) to (a) being 0.005-1000. In general the material to be stabilized contains 0.025-4% of (a) and 0.01-5%, preferably 0.1-3% of (b) by weight, there preferably being present 0.5-5 mols. of (a) per mol. of (b). (a) is most suitably a di-C1-12-alkyl hydrogen phosphite, and (b) is preferably 4 : 41-methylene bis (2 : 6 - diisopropylphenol) or 4 : 41 - methylene bis (6-tert. butyl - o - cresol).
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21099A US3115465A (en) | 1960-04-11 | 1960-04-11 | Stabilized compositions of matter |
FR858326A FR1299534A (en) | 1961-04-11 | 1961-04-11 | New additives with antioxidant action for organic compositions such as fuels, lubricants and hydrocarbon polymers |
GB12983/61A GB923190A (en) | 1961-04-11 | 1961-04-11 | Antioxidant compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB12983/61A GB923190A (en) | 1961-04-11 | 1961-04-11 | Antioxidant compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB923190A true GB923190A (en) | 1963-04-10 |
Family
ID=10014682
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12983/61A Expired GB923190A (en) | 1960-04-11 | 1961-04-11 | Antioxidant compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB923190A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0030310A1 (en) * | 1979-11-30 | 1981-06-17 | CASSELLA Aktiengesellschaft | Internal release agent for heat-curable aminoplast resins, process for its production and its use |
WO2004013260A1 (en) * | 2002-08-06 | 2004-02-12 | The Associated Octel Company Limited | Jet fuel composition comprising a phenol derivative |
WO2005089085A2 (en) | 2003-07-14 | 2005-09-29 | Rhodia Inc | Improved color stability of isocyanates |
WO2006039006A1 (en) * | 2004-09-29 | 2006-04-13 | Chemtura Corporation | Stabilized lubricant compositions |
CN114672350A (en) * | 2021-08-20 | 2022-06-28 | 安徽速收宝网络科技有限公司 | Innovative and economical tail gas cleaning agent and preparation method thereof |
-
1961
- 1961-04-11 GB GB12983/61A patent/GB923190A/en not_active Expired
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0030310A1 (en) * | 1979-11-30 | 1981-06-17 | CASSELLA Aktiengesellschaft | Internal release agent for heat-curable aminoplast resins, process for its production and its use |
EP0030310B1 (en) * | 1979-11-30 | 1984-03-28 | CASSELLA Aktiengesellschaft | Internal release agent for heat-curable aminoplast resins, process for its production and its use |
WO2004013260A1 (en) * | 2002-08-06 | 2004-02-12 | The Associated Octel Company Limited | Jet fuel composition comprising a phenol derivative |
WO2005089085A2 (en) | 2003-07-14 | 2005-09-29 | Rhodia Inc | Improved color stability of isocyanates |
EP1732965A2 (en) * | 2003-07-14 | 2006-12-20 | Rhodia, Inc. | Improved color stability of isocyanates |
EP1732965A4 (en) * | 2003-07-14 | 2008-08-20 | Rhodia | Improved color stability of isocyanates |
WO2006039006A1 (en) * | 2004-09-29 | 2006-04-13 | Chemtura Corporation | Stabilized lubricant compositions |
US7799101B2 (en) | 2004-09-29 | 2010-09-21 | Chemtura Corporation | Stabilized lubricant compositions |
CN101065468B (en) * | 2004-09-29 | 2014-05-28 | 科聚亚公司 | Stabilized lubricant compositions |
CN114672350A (en) * | 2021-08-20 | 2022-06-28 | 安徽速收宝网络科技有限公司 | Innovative and economical tail gas cleaning agent and preparation method thereof |
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