GB842271A - Age-resisters for plastics containing urethane groups - Google Patents
Age-resisters for plastics containing urethane groupsInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0033—Use of organic additives containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0028—Use of organic additives containing nitrogen
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
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.
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)
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 |
-
1957
- 1957-08-08 GB GB25061/57A patent/GB842271A/en not_active Expired
- 1957-08-08 FR FR1180937D patent/FR1180937A/en not_active Expired
Cited By (7)
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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