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GB842271A - Age-resisters for plastics containing urethane groups - Google Patents

Age-resisters for plastics containing urethane groups

Info

Publication number
GB842271A
GB842271A GB25061/57A GB2506157A GB842271A GB 842271 A GB842271 A GB 842271A GB 25061/57 A GB25061/57 A GB 25061/57A GB 2506157 A GB2506157 A GB 2506157A GB 842271 A GB842271 A GB 842271A
Authority
GB
United Kingdom
Prior art keywords
dihydroxy
methane
glycol
pyrocatechol
diphenyl
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
GB25061/57A
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.)
FARBENFABRIKEN AG
Original Assignee
FARBENFABRIKEN AG
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 FARBENFABRIKEN AG filed Critical FARBENFABRIKEN AG
Publication of GB842271A publication Critical patent/GB842271A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0014Use of organic additives
    • C08J9/0033Use of organic additives containing sulfur
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0014Use of organic additives
    • C08J9/0028Use of organic additives containing nitrogen
    • 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
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005Stabilisers against oxidation, heat, light, ozone
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention comprises a polyurethane foam containing from 0,5% to 10% by weight of an antioxidant which is a polyhydric phenol which may be acylated or etherified and which may contain one or more aromatic ring systems or condensed aromatic ring systems and the hydroxyl groups of which may be partially etherified, 2-mercapto-benzimidazole, zinc dimethyl dithiocarbamate, nickel dibutyl dithiocarbamate or polymerized trimethyl dihydroquinoline (which may be used individually or in admixture) or a mixture consisting of zinc dimethyl dithiocarbamate, nickel dibutyl dithiocarbamate or polymerized trimethyl dihydroquinoline with any of the compounds of the formula: <FORM:0842271/IV(a)/1> Suitable polyhydric phenols are tertiary butyl pyrocatechol, 4, 41-dihydroxy-diphenyl, cyclohexyl pyrocatechol, 2, 4-dihydroxydiphenyl, 2, 4-dihydroxy-benzophenone, 4-hydroxy-5-methoxybenzal acetoacetic ester, pyrocatechol, resorcin, hydroquinone, pyrogallol, 4, 41-dihydroxy-diphenyl-dimethyl methane, 4, 41-dihydroxy-diphenyl methyl ethyl methane. 2, 5-ditertiary butyl hydroquinone, bis (1-oxy-2-tert. butyl-4-ethyl phenyl)-methane, and bis-(1-oxy-2-cyclobexyl-4-methyl-phenyl)-methane. The antioxidant can be added to the reaction mixture as such or in solution in, for example, trichloroethyl phosphate. Examples illustrate the invention as applied to foams prepared from diisocyanates, activator mixtures and respectively a polythioether (from thiodiglycol and butane-dihydroxyethyl glycol), polyesters (linear or branched, and in one case with the addition of butylene-1, 4-glycol), polypropylene glycol, and a branched polythioether (from thiodiglycol, triethylene glycol and trimethylolpropane. Specifications 769,680, 769,682 and 797,576 are referred to.ALSO:The invention comprises a polyurethane foam containing from 0,5% to 10% by weight of an antioxidant which is a polyhydric phenol which may be acylated or etherified and which may contain one or more aromatic ring systems or condensed aromatic ring systems and the hydroxyl groups of which may be partially etherified, 2-mercaptobenzimidazole, zinc di-methyl dithiocarbamate, nickel dibutyl dithiocarbamate or polymerised trimethyl dihydro quinoline (which may be used individually or in admixture) or a mixture consisting of zinc dimethyl dithiocarbamate, nickel dibutyl dithiocarbamate or polymerised trimethyl dihydroquinoline with any of the compounds of the formula: <FORM:0842271/V/1> Suitable polyhydrio phenols are tertiary butyl pyrocatechol, 4,41-dihydroxy-diphenyl cyclohexyl pyrocatechol, 2, 4-dihydroxydiphenyl, 2, 4-dihydroxy-benzophenone, 4-hydroxy-5-methoxybenzol acetoacetic ester, pyrocatechol, resorcin, hydroquinone, pyrogallol, 4, 41-dihydroxy-diphenyl-dimethyl methane, 4, 41-dihydroxy-diphenyl methyl ethyl methane, 2, 5-ditertiary butyl hydroquinone, bis (1-oxy-2-tert butyl-4-ethyl phenyl)-methane, and bis-(1-oxy-2-cyclohexyl-4-methyl-phenyl)-methane. The antioxidant can be added to the reaction mixture as such or in solution in, for example, trichloroethyl phosphate. Examples illustrate the invention as applied to foams prepared from diisocyanates, activator mixtures and respectively a polythioether (from thiodiglycol and butane-dihydroxyethyl glycol), polyesters (linear or branched, and in one case with the addition of butylene-1, 4-glycol), polypropylene glycol and a branched polythioether (from thiodiglycol, triethylene glycol and trimethylol-propane. Specifications 769,680, 769,682 and 797,576 are referred to.
GB25061/57A 1956-08-09 1957-08-08 Age-resisters for plastics containing urethane groups Expired GB842271A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE842271X 1956-08-09

Publications (1)

Publication Number Publication Date
GB842271A true GB842271A (en) 1960-07-27

Family

ID=6769347

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25061/57A Expired GB842271A (en) 1956-08-09 1957-08-08 Age-resisters for plastics containing urethane groups

Country Status (2)

Country Link
FR (1) FR1180937A (en)
GB (1) GB842271A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3245923A (en) * 1962-05-11 1966-04-12 Union Carbide Corp Cellular polyurethane stabilized with a lead dialkyldithiocarbamate and process for preparing same
US3331792A (en) * 1963-08-01 1967-07-18 Uniroyal Inc Use of certain bis(hydroxy-alkylbenzylthio) compounds as antioxidants
US3429837A (en) * 1964-10-20 1969-02-25 Ici Ltd Polyurethane foams containing tertiary esters of phosphorous acid
EP2898038A4 (en) * 2012-09-24 2016-04-27 Arkema Inc Improved stability of polyurethane polyol blends containing halogenated olefin blowing agent
WO2018064521A1 (en) 2016-09-30 2018-04-05 Vanderbilt Chemicals, Llc Low emissions scorch inhibitor for polyurethane foam
WO2018175702A1 (en) 2017-03-24 2018-09-27 Invista North America S.A.R.L. Polyol compositions for foam insulation

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3245923A (en) * 1962-05-11 1966-04-12 Union Carbide Corp Cellular polyurethane stabilized with a lead dialkyldithiocarbamate and process for preparing same
US3331792A (en) * 1963-08-01 1967-07-18 Uniroyal Inc Use of certain bis(hydroxy-alkylbenzylthio) compounds as antioxidants
US3429837A (en) * 1964-10-20 1969-02-25 Ici Ltd Polyurethane foams containing tertiary esters of phosphorous acid
EP2898038A4 (en) * 2012-09-24 2016-04-27 Arkema Inc Improved stability of polyurethane polyol blends containing halogenated olefin blowing agent
WO2018064521A1 (en) 2016-09-30 2018-04-05 Vanderbilt Chemicals, Llc Low emissions scorch inhibitor for polyurethane foam
EP3519489A4 (en) * 2016-09-30 2019-10-16 Vanderbilt Chemicals, LLC Low emissions scorch inhibitor for polyurethane foam
WO2018175702A1 (en) 2017-03-24 2018-09-27 Invista North America S.A.R.L. Polyol compositions for foam insulation

Also Published As

Publication number Publication date
FR1180937A (en) 1959-06-10

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