GB1024810A - Process for preparing copolymers of formaldehyde - Google Patents

Process for preparing copolymers of formaldehyde

Info

Publication number
GB1024810A
GB1024810A GB4361064A GB4361064A GB1024810A GB 1024810 A GB1024810 A GB 1024810A GB 4361064 A GB4361064 A GB 4361064A GB 4361064 A GB4361064 A GB 4361064A GB 1024810 A GB1024810 A GB 1024810A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
specified
formal
dioxolane
halides
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
GB4361064A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst 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 Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB1024810A publication Critical patent/GB1024810A/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
    • C08G2/00Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
    • C08G2/18Copolymerisation of aldehydes or ketones
    • C08G2/24Copolymerisation of aldehydes or ketones with acetals
    • 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
    • C08G2/00Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
    • C08G2/06Catalysts
    • 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
    • C08G4/00Condensation polymers of aldehydes or ketones with polyalcohols; Addition polymers of heterocyclic oxygen compounds containing in the ring at least once the grouping —O—C—O—

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)

Abstract

Formaldehyde is polymerized in an inert solvent with 1 to 50% based on the monomer mixture of a cyclic formal in the presence of 0.01 to 1.0% of a cationic catalyst at +20 to +100 DEG C. Specified cyclic formals are 1,3-dioxolane, 4 - phenyl - 1,3 - dioxolane, 1,3-dioxane, 5 - dimethyl - 1,3 - dioxane, 1,3-dioxoacyclopeptane, 1,3,6 - trioxyacyclooctane, 1,4 - butane diol formal and diethylene glycol formal. Specified catalysts are the halides of boron, aluminium, titanium, zinc, iron and especially antimony or tin and their complex compounds with, e.g. ethers or organic acids and the oxonium compounds of these halides, e.g. triethyl oxonium fluoroborate or their diazonium complex compounds, e.g. p-nitrophenyl diazonium fluoroborate-preferred catalysts are SbCl5 and SnCl4 and [(C6H5)3O] SbCl6 and [(C2H5)3O]SnCl6. The polymerization may take place in a mixture of solvents. Specified are aliphatic or aromatic hydrocarbons, halogenated hydrocarbons and ethers. The formaldehyde may be added and the polymerization batch then stirred for 10 minutes to 5 hours at 20 DEG to 100 DEG C., the polymer sucked off, and treated with a base before or after washing with a solvent.
GB4361064A 1963-10-26 1964-10-26 Process for preparing copolymers of formaldehyde Expired GB1024810A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF0041106 1963-10-26

Publications (1)

Publication Number Publication Date
GB1024810A true GB1024810A (en) 1966-04-06

Family

ID=7098519

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4361064A Expired GB1024810A (en) 1963-10-26 1964-10-26 Process for preparing copolymers of formaldehyde

Country Status (4)

Country Link
BE (1) BE654836A (en)
DE (1) DE1495754B2 (en)
GB (1) GB1024810A (en)
NL (1) NL6412355A (en)

Also Published As

Publication number Publication date
NL6412355A (en) 1965-04-27
DE1495754A1 (en) 1969-07-17
DE1495754B2 (en) 1972-02-10
BE654836A (en) 1965-04-26

Similar Documents

Publication Publication Date Title
US2989509A (en) Trioxane polymer stabilization
US3453240A (en) Polyester resin treatment with ethylene glycol
GB943684A (en) Process for the manufacture of polyoxymethylenes
GB1024810A (en) Process for preparing copolymers of formaldehyde
US3144418A (en) Polymerization of epoxides
GB1527154A (en) Unsaturated epoxides as coupling agents for carbon fibres and unsaturated matrix resins
GB1039936A (en) Process for the manufacture of copolymers of acetals
Dickson et al. Radiation curing of epoxies
GB1390976A (en) Process for preparing homo- and copolymers of cyclic acetals
US3030316A (en) Polymerization of epoxides
US3275598A (en) Polymerization of oxirane monoepoxides in the presence of an organometallic compoundand an alcohol
Bal et al. Photopolymerization of 1, 2-epoxypropane and 1, 2-epoxybutane by arenediazonium salts: evidence for anion dependence of the extent of polymerization
GB875558A (en) Process for the production of eupolyoxymethylenes
US3417033A (en) 1,4-endoxacyclohexane polyethers and process for preparing them
IL28509A (en) Producing oxymethylene polymers by cationic polymerization
US3417035A (en) Trihydropolyfluoroalkylene glycidyl ethers, methods for making said ethers, and polymers and copolymer of said ethers
US3030315A (en) Polymerization of epoxides
US3399149A (en) Polymerization of oxirane monoepoxides using an organometallic compound with water as cocatalysts
US3424725A (en) Copolymers of trioxane,cyclic ethers,and bifunctional epoxides and a process for their manufacture
US3287330A (en) Polyether polymers having unsaturated side chains
US3274129A (en) Polymerization of epoxides
US3268482A (en) Preparation of polyesters
GB1061659A (en) Polymers and copolymers of cyclic acetals and process for preparing them
Hein Ring‐opening polymerizations of cyclic olefins
GB1045784A (en) Process for preparing trioxane homo- and copolymers