GB889720A - Improvements in or relating to the manufacture of polymeric materials - Google Patents

Improvements in or relating to the manufacture of polymeric materials

Info

Publication number
GB889720A
GB889720A GB30174/58A GB3017458A GB889720A GB 889720 A GB889720 A GB 889720A GB 30174/58 A GB30174/58 A GB 30174/58A GB 3017458 A GB3017458 A GB 3017458A GB 889720 A GB889720 A GB 889720A
Authority
GB
United Kingdom
Prior art keywords
atoms
oxide
halogen
phthalic anhydride
polyesters
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
GB30174/58A
Inventor
John Frederick Chapman
Brian Francis Jones
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
Priority to GB30174/58A priority Critical patent/GB889720A/en
Publication of GB889720A publication Critical patent/GB889720A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08K5/0066Flame-proofing or flame-retarding additives
    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/01Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/016Flame-proofing or flame-retarding additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

A process for the manufacture of polymeric materials by interacting an organic polyisocyanate with a hydroxyl group-containing material such as a polyether, polyester or polyesteramide is characterized in that there are incorporated in the reaction mixture an oxide or sulphide of antimony, bismuth or arsenic and an organic halogen compound which, in addition to carbon, hydrogen and halogen atoms, may optionally contain oxygen, nitrogen or sulphur atoms in the molecule but no other atoms. Specified halogen compounds are ethyl iodide, ethyl bromide, benzotrichloride, bromoform, benzyl bromide, 2:3-dibromopropanol, chloral hydrate and 4-chloro-2-amino-toluene hydrochloride. Fluorine compounds are also mentioned. Usually 5 to 30% of the specified oxides (based on the weight of hydroxy-containing polymer), and an equal proportion of the halogen compound are used. There are listed polyethers (with which glycidol, glycerol, trimethylolpropanes and 3-hydroxymethyl oxacyclobutanes may be copolymerized), polyisocyanates and reactants from which the polyesters and polyesteramides can be prepared. In Example (1) a mixture of a hydroxy-polyester from pentaerythritol, 1:3-butylene glycol, adipic acid and phthalic anhydride, with water, an octylcresolethylene oxide condensation product, 2:3-dibromopropanol and antimony oxide is reacted with diphenyl methane diisocyanate (containing some triisocyanate) to give a foamed product. Other examples employ polyesters from castor oil and citric acid and hexanetriol, adipic acid and phthalic anhydride; N:N-dimethyl benzylamine lactate as catalyst. Specification 733,624 is referred to.ALSO:A process for the manufacture of foamed polymeric materials by interacting an organic polyisocyanate with a hydroxyl group containing material such as a polyether, polyester or polyesteramide is characterised in that there are incorporated in the reaction mixture an oxide or sulphide of antimony, bismuth or arsenic and an organic halogen compound which in addition to carbon, hydrogen and halogen atoms, may optionally contain oxygen, nitrogen or sulphur atoms in the molecule but no other atoms. Specified halogen compounds are ethyl iodide, ethyl bromide, benzotrichloride, bromoform, benzyl bromide, 2 : 3-dibromoproponol, chloral hydrate and 4-chloro-2-amino-toluene hydrochloride. Fluorine compounds are also mentioned. Usually 5 to 30% of the specified oxides (based on the weight of hydroxy-containing polymer) and an equal proportion of the halogen compound are used. Listed are polyethers (with which glycidol, glycerol, trimethylolpropanes and 3-hydroxymethyl oxacyclobutanes may be copolymerised), polyisocyanates, and reactants from which the polyesters and polyesteramides can be prepared. In Example 11 a mixture of a hydroxypolyester from pentaerythritol, 1 : 3-butylene glycol, adipic acid and phthalic anhydride, with water, an octyl cresol-ethylene oxide condensation product, 2 : 3-dibromopropanol and antimony oxide is reacted with diphenyl methane diisocyanate (containing some triisocyanate) to give a foamed product. Other examples employ polyesters from castor oil and citric acid and hexanetriol, adipic acid and phthalic anhydride; and N : N-dimethyl benzylamine lactate as catalyst. Specification 733,624 is referred to.
GB30174/58A 1958-09-22 1958-09-22 Improvements in or relating to the manufacture of polymeric materials Expired GB889720A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB30174/58A GB889720A (en) 1958-09-22 1958-09-22 Improvements in or relating to the manufacture of polymeric materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB30174/58A GB889720A (en) 1958-09-22 1958-09-22 Improvements in or relating to the manufacture of polymeric materials

Publications (1)

Publication Number Publication Date
GB889720A true GB889720A (en) 1962-02-21

Family

ID=10303450

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30174/58A Expired GB889720A (en) 1958-09-22 1958-09-22 Improvements in or relating to the manufacture of polymeric materials

Country Status (1)

Country Link
GB (1) GB889720A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3997449A (en) * 1975-09-29 1976-12-14 Michigan Chemical Corporation Low viscosity flame retardant
US4232085A (en) * 1979-08-14 1980-11-04 Freeman Chemical Corporation Flexible polyurethane foam having a low flame spread index
FR2458571A1 (en) * 1979-06-07 1981-01-02 Naphtachimie Sa POLYURETHANE MATERIAL, APPLICABLE TO THE PRODUCTION OF FIREWALL WALLS
GB2191208A (en) * 1986-06-05 1987-12-09 Basf Corp High resiliency molded polyurethane foams
DE4301992A1 (en) * 1993-01-26 1993-06-24 Tech In Gmbh Technologien Fuer Flameproofing plastics with synergistic fire retardants - by microencapsulating fire retardants, e.g. antimony tri:oxide and organic bromo cpd., in material which is compatible with the host plastic

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3997449A (en) * 1975-09-29 1976-12-14 Michigan Chemical Corporation Low viscosity flame retardant
FR2458571A1 (en) * 1979-06-07 1981-01-02 Naphtachimie Sa POLYURETHANE MATERIAL, APPLICABLE TO THE PRODUCTION OF FIREWALL WALLS
US4232085A (en) * 1979-08-14 1980-11-04 Freeman Chemical Corporation Flexible polyurethane foam having a low flame spread index
GB2191208A (en) * 1986-06-05 1987-12-09 Basf Corp High resiliency molded polyurethane foams
DE4301992A1 (en) * 1993-01-26 1993-06-24 Tech In Gmbh Technologien Fuer Flameproofing plastics with synergistic fire retardants - by microencapsulating fire retardants, e.g. antimony tri:oxide and organic bromo cpd., in material which is compatible with the host plastic

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