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GB923190A - Antioxidant compositions - Google Patents

Antioxidant compositions

Info

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
Application number
GB12983/61A
Inventor
Harold David Orloff
Gordon Grayson Knapp
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.)
Ethyl Corp
Original Assignee
Ethyl Corp
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
Priority to US21099A priority Critical patent/US3115465A/en
Application filed by Ethyl Corp filed Critical Ethyl Corp
Priority to FR858326A priority patent/FR1299534A/en
Priority to GB12983/61A priority patent/GB923190A/en
Publication of GB923190A publication Critical patent/GB923190A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, 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
    • C11B5/00Preserving by using additives, e.g. anti-oxidants
    • C11B5/0092Mixtures
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/52Phosphorus bound to oxygen only
    • C08K5/524Esters of phosphorous acids, e.g. of H3PO3
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/52Phosphorus bound to oxygen only
    • C08K5/524Esters of phosphorous acids, e.g. of H3PO3
    • C08K5/526Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K15/00Anti-oxidant compositions; Compositions inhibiting chemical change
    • C09K15/04Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
    • C09K15/32Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing two or more of boron, silicon, phosphorus, selenium, tellurium or a metal
    • C09K15/322Anti-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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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/103Liquid carbonaceous fuels containing additives stabilisation of anti-knock agents
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    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
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    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/183Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom
    • C10L1/1835Organic 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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    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/26Organic compounds containing phosphorus
    • C10L1/2633Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
    • C10L1/2641Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) oxygen bonds only
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102Aliphatic fractions
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    • C10M2203/104Aromatic fractions
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    • C10M2203/106Naphthenic fractions
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    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/026Butene
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/22Alkylation reaction products with aromatic type compounds, e.g. Friedel-crafts
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2207/028Overbased salts thereof
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    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/046Hydroxy ethers
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    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2070/00Specific manufacturing methods for lubricant compositions
    • C10N2070/02Concentrating of additives
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B3/00Engines characterised by air compression and subsequent fuel addition
    • F02B3/06Engines 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).
GB12983/61A 1960-04-11 1961-04-11 Antioxidant compositions Expired GB923190A (en)

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

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GB923190A true GB923190A (en) 1963-04-10

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Cited By (5)

* Cited by examiner, † Cited by third party
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

Cited By (10)

* Cited by examiner, † Cited by third party
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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