GB1003306A - Alkyds and polyurethanes derived from adducts of hexahalocyclopentadienes - Google Patents

Alkyds and polyurethanes derived from adducts of hexahalocyclopentadienes

Info

Publication number
GB1003306A
GB1003306A GB19103/62A GB1910362A GB1003306A GB 1003306 A GB1003306 A GB 1003306A GB 19103/62 A GB19103/62 A GB 19103/62A GB 1910362 A GB1910362 A GB 1910362A GB 1003306 A GB1003306 A GB 1003306A
Authority
GB
United Kingdom
Prior art keywords
glycidyl
polycarboxylic
alcohol
compounds
polyhydric
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
GB19103/62A
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.)
Hooker Chemical Corp
Original Assignee
Hooker Chemical 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
Application filed by Hooker Chemical Corp filed Critical Hooker Chemical Corp
Publication of GB1003306A publication Critical patent/GB1003306A/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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/68Unsaturated polyesters
    • C08G18/683Unsaturated polyesters containing cyclic groups
    • C08G18/686Unsaturated polyesters containing cyclic groups containing cycloaliphatic groups
    • 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
    • C08G63/68Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/682Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens
    • C08G63/6824Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens derived from polycarboxylic acids and polyhydroxy compounds

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)
  • Polyesters Or Polycarbonates (AREA)
  • Epoxy Resins (AREA)

Abstract

Alkyl resins based on hexahalocyclopentadiene adducts and having acid numbers of 20-90 have their viscosities reduced by reacting them with sufficient of a mono-epoxide to produce alkyd resins with acid numbers below 20. The alkyds resins may be the reaction products of (a) an adduct of a hexahalocyclopentadiene and an unsaturated polycarboxylic compound with a polyhydric alcohol at least part of which is an alcohol with at least 3 hydroxyl groups or (b) an adduct of a hexahalocyclopentadiene and an unsaturated polyhydric alcohol with a polycarboxylic compound and a polyhydric alcohol at least part of which is an alcohol with at least three hydroxyl groups or (c) an adduct of a hexahalocyclopentadiene and an unsaturated polyhydric alcohol with a polycarboxylic compound having at least three carboxyl groups. The halogen may be fluorine, chlorine or bromine. The polyhydric alcohols and polycarboxylic compounds which are reacted with the adducts may be aliphatic, cycloaliphatic, aromatic or heterocyclic and may be saturated or unsaturated. The polyhydric alcohols may contain hetero oxygen or sulphur atoms and may be substituted by halogen atoms or ester groups. The polycarboxylic compound may also be halogen-substituted. The mono-epoxide may be ethylene oxide, propylene oxide, butylene oxides, isobutylene oxides, decylene oxides, 2 : 3 - epoxyhexane, 3 - ethyl - 2 : 3 - epoxyoctane, cyclohexene oxide, styrene oxide, epichlorohydrin, epibromohydrin, glycidol, allyl glycidyl ether, methyl glycidyl ether, phenyl glycidyl ether, butyl glycidyl sulphide, glycidyl methyl sulphone, glycidyl acrylate, glycidyl methacrylate, glycidyl benzoate, glycidyl acetate, glycidyl sorbate, glycidyl allyl phthalate, phenyl-(p-octadecyloxybenzoyl) ethylene oxide, triphenyl glycidyl silane, <FORM:1003306/C3/1> or <FORM:1003306/C3/2> Fire-retardant polyurethane resins and foams are made by reacting the above alkyds with polyisocyanates or polyisothiocyanates or reaction product therewith and (1) polycarboxylic compounds, (2) polyhydric alcohols, (3) hydroxylated polyesters, (4) hydroxylated polyethers derived from mono-epoxides and polycarboxylic compounds, polyhydric alcohols or polyhydric phenols (including phenol-formaldehyde condensates) or (5) reactions products of epoxides and certain phosphorus compounds are disclosed in Specification 984,474. The usual catalysts may be used, e.g. tertiary amines, antimony compounds or tin compounds. The alkyds may also be foamed in admixture with the substances defined under (3), (4) and (5). In making the foam, the foaming agent may be water, a fluorochlorocarbon, a tertiary alcohol (see Specification 873,975), a secondary alcohol, a glycol, a polycarboxylic acid or anhydride, dimethylol urea, polymethylol phenols, formic acid or tetrahydroxymethylphosphonium chloride. The foam-forming mixture may also include a silicone emulsifier and glycerol. Specification 873,974 also is referred to.
GB19103/62A 1961-06-01 1962-05-17 Alkyds and polyurethanes derived from adducts of hexahalocyclopentadienes Expired GB1003306A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11404161A 1961-06-01 1961-06-01

Publications (1)

Publication Number Publication Date
GB1003306A true GB1003306A (en) 1965-09-02

Family

ID=22353043

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19103/62A Expired GB1003306A (en) 1961-06-01 1962-05-17 Alkyds and polyurethanes derived from adducts of hexahalocyclopentadienes

Country Status (7)

Country Link
BE (1) BE618033A (en)
CH (1) CH469764A (en)
DE (2) DE1190656B (en)
FR (1) FR1352120A (en)
GB (1) GB1003306A (en)
NL (1) NL279174A (en)
SE (1) SE305536B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT997520B (en) * 1972-09-08 1975-12-30 British Industrial Plastics IMPROVEMENT IN THE PRODUCTION PROCESS OF MODIFIED SATURATED ALCHIDIC COMPOSITIONS
DE10359763B4 (en) * 2003-12-19 2007-11-22 Teijin Monofilament Germany Gmbh Polyester fibers, process for their preparation and their use

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE492903A (en) * 1948-12-22
NL243924A (en) * 1958-10-02

Also Published As

Publication number Publication date
BE618033A (en)
CH469764A (en) 1969-03-15
DE1520053C3 (en) 1978-06-01
SE305536B (en) 1968-10-28
DE1520053B2 (en) 1974-11-14
DE1520053A1 (en) 1970-03-26
NL279174A (en)
DE1190656B (en) 1965-04-08
FR1352120A (en) 1964-02-14

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