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GB597326A - Treatment of polymeric materials - Google Patents

Treatment of polymeric materials

Info

Publication number
GB597326A
GB597326A GB15297/41A GB1529741A GB597326A GB 597326 A GB597326 A GB 597326A GB 15297/41 A GB15297/41 A GB 15297/41A GB 1529741 A GB1529741 A GB 1529741A GB 597326 A GB597326 A GB 597326A
Authority
GB
United Kingdom
Prior art keywords
acid
heated
interpolyamide
paraformaldehyde
minutes
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
GB15297/41A
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of GB597326A publication Critical patent/GB597326A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/48Polymers modified by chemical after-treatment
    • C08G69/50Polymers modified by chemical after-treatment with aldehydes

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The properties of synthetic linear polyamides are modified by mixing the polyamide with a formaldehyde-liberating substance, not in preponderating amount, and then heating said mixture whilst or after forming it into shaped articles. It is preferred to include in the mixture an acid, an acid anhydride or an acid-reacting salt, or there may be included a material which is neutral and remains so during mixing, but which develops acidity on heating. Specified formaldehyde-liberating substances are paraformaldehyde, trioxane, dimethylolurea, trimethylolmelamine, hexamethylolmelamine, diphenylolpropane tetraalcohol, methylolchloracetamide, methylol stearamide, N-methylol-p-toluenesulphonamide, dimethylolurea dimethyl ether, dimethylolurea dibutyl ether, N : N1-dimethyloluron dimethyl ether, 1 : 2-glycol methylene ether, di-(b -hydroxy-ethyl) formal and hexamethylenetetramine-zinc chloride complexes. Specified acid substances which may be added, are formic, glycollic, oxalic, succinic, maleic, stearic, adipic, tartaric, salicylic, anthranilic, phthalic, citric, tannic, boric and phosphoric acids, phthalic and maleic anhydrides, phthalimide, and ammonium, potassium and sodium dihydrogen phosphate. Specified neutral materials developing acidity on heating are butadiene sulphone, 2 : 3-dimethylbutadiene sulphone, butadiene tetrabromide, styrene dibromide, acetylene tetrabromide, tribromohydroquinone, 1-bromo-2-naphthol, 1 : 6-dibromo-2-naphthol, 1 : 4 : 6-tribromo-2-naphthol, 2 : 4-dibromo-1-naphthol, methyl a : b -dibromopropionate, b -chloroethyl a : b -dibromoisobutyrate, ethyl a -bromopropionate, phenyl trichloroacetate, a : a : b -trichloropropionitrile trichloroacetamide, trichloroacetyldiethylamide, N - trichloroacetylanilide, N : N1-di-(trichloroacetyl)methylene-diamine, N : N1 - di - (trichloroacetyl)ethylenediamine, interpolymers of asymmetrical dichloroethylene and vinyl chloride, and chloranil. Plasticizers, anti-oxidants, pigments and fillers may be added to the mix. According to examples: (1) an interpolyamide from o -aminocaproic acid and hexamethylenediammonium sebacate is milled with paraformaldehyde and phthalic anhydride at 60-70 DEG C., and the compounded material is heated in a mould, under pressure, at 141 DEG C. for 25 minutes; (2) the paraformaldehyde in (1) is replaced by dimethylolurea dimethylol ether; (3) a film is cast from a solution of an interpolyamide from hexamethylenediammonium adipate and caprolactam, dimethylolurea dimethyl ether and phthalic anhydride in aqueous ethanol, and the film is then heated at 110 DEG C. for 25 minutes; (4) an interpolyamide from hexamethylenediammonium adipate, hexamethylenediammonium sebacate and caprolactam is plasticized with butylphthalyl butyl glycollate and diphenylol octadecane, and then milled with dimethylolurea dimethyl ether and phthalic anhydride at 50-60 DEG C. The compounded material is heated in a mould, under pressure, at 141 DEG C. for 15 minutes; (5) the interpolyamide of (4) is dissolved, with dimethylolurea dimethyl ether, in aqueous ethanol, and a film, cast from the solution, is heated at 150 DEG C. for 25 minutes; (6) an interpolyamide from 12-amino-stearic acid and o -aminocaproic acid is milled with phthalic anhydride and paraformaldehyde at 70-80 DEG C., and the compounded material is heated in a mould, under pressure, at 141 DEG C. for 30 minutes; (7) a polyamide from 12-amino-stearic acid is milled with paraformaldehyde and phthalic acid, and the compounded material is heated in a mould, under pressure, at 141 DEG C. for 30 minutes; (8) an interpolyamide from hexamethylenediammonium sebacate and 12-amino stearic acid is treated as in (7); (9) a polyester-amide from hexamethylene diammonium adipate, ethylene glycol and adipic acid is compounded with carbon black, paraformaldehyde and phthalic anhydride at 60-80 DEG C., and the compounded material is heated in a mould, under pressure, at 141 DEG C.; (10) an interpolyamide from hexamethylenediammonium sebacate and N : N1-dimethyl-hexamethylene diammonium sebacate is milled, at 70-90 DEG C., with paraformaldehyde and 1-bromo-2-naphthol. The compounded material is heated in a mould, under pressure, at 125 DEG C. for 45 minutes. Specifications 461,237, 534,698, 540,135, 540,576, 557,544 and 580,524 are referred to.
GB15297/41A 1941-11-27 1941-11-27 Treatment of polymeric materials Expired GB597326A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB916439X 1941-11-27

Publications (1)

Publication Number Publication Date
GB597326A true GB597326A (en) 1948-01-23

Family

ID=10707497

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15297/41A Expired GB597326A (en) 1941-11-27 1941-11-27 Treatment of polymeric materials

Country Status (3)

Country Link
BE (1) BE462554A (en)
FR (1) FR916439A (en)
GB (1) GB597326A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3325144A1 (en) * 1982-07-13 1984-01-19 L'Oreal, 75008 Paris CROSSLINKED POLY- (BETA) ALANINE AND THE USE THEREOF
EP0285692A1 (en) * 1987-04-09 1988-10-12 General Electric Company Thermoplastic blends with end-group controlled polyamide resin
US5280088A (en) * 1986-02-28 1994-01-18 General Electric Company Thermoplastic blends of a polyamide having low amine end-group concentration and a polymer containing carbonate linkages
US5725941A (en) * 1994-08-31 1998-03-10 Mercedes-Benz Ag Powdered lacquer for coating substrates such as automobile bodies
CN115073728A (en) * 2022-07-14 2022-09-20 江苏富琪森新材料有限公司 Glass-like thermosetting resin and preparation method thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3325144A1 (en) * 1982-07-13 1984-01-19 L'Oreal, 75008 Paris CROSSLINKED POLY- (BETA) ALANINE AND THE USE THEREOF
US5280088A (en) * 1986-02-28 1994-01-18 General Electric Company Thermoplastic blends of a polyamide having low amine end-group concentration and a polymer containing carbonate linkages
EP0285692A1 (en) * 1987-04-09 1988-10-12 General Electric Company Thermoplastic blends with end-group controlled polyamide resin
US5725941A (en) * 1994-08-31 1998-03-10 Mercedes-Benz Ag Powdered lacquer for coating substrates such as automobile bodies
CN115073728A (en) * 2022-07-14 2022-09-20 江苏富琪森新材料有限公司 Glass-like thermosetting resin and preparation method thereof
CN115073728B (en) * 2022-07-14 2023-12-05 江苏富琪森新材料有限公司 Glass-like thermosetting resin and preparation method thereof

Also Published As

Publication number Publication date
FR916439A (en) 1946-12-05
BE462554A (en)

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