GB792702A - Curing of liquid polyepoxide resins - Google Patents

Curing of liquid polyepoxide resins

Info

Publication number
GB792702A
GB792702A GB1256354A GB1256354A GB792702A GB 792702 A GB792702 A GB 792702A GB 1256354 A GB1256354 A GB 1256354A GB 1256354 A GB1256354 A GB 1256354A GB 792702 A GB792702 A GB 792702A
Authority
GB
United Kingdom
Prior art keywords
catalyst
per cent
epichlorhydrin
butanol
hardened
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
GB1256354A
Inventor
Henry Brunner
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 GB1256354A priority Critical patent/GB792702A/en
Publication of GB792702A publication Critical patent/GB792702A/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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/68Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
    • C08G59/72Complexes of boron halides
    • 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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/14Polycondensates modified by chemical after-treatment
    • C08G59/1433Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
    • C08G59/1438Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
    • C08G59/145Compounds containing one epoxy group

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Emergency Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Reinforced Plastic Materials (AREA)
  • Laminated Bodies (AREA)

Abstract

Liquid polyepoxide resins prepared from dihydric phenols and more epichlorhydrin and having at least two epoxide groups per molecule and more epoxide groups than hydroxyl groups and free from functional groups other than hydroxyl are cured by addition of FriedelCrafts catalysts preferably in the presence of diluents neutral to the catalyst and polyepoxide, e.g. dibutyl phthalate, chlorinated polyphenols. There also may be present as diluents compounds which are polymerized by the catalyst, e.g. phenyl glycidylether, allyl glycidylether, epichlorhydrin, turpentine, styrene oxide. Suitable catalysts are boron trifluoride complexes with ether, water, acetic acid and butanol; stannic chloride, antimony pentachloride. The catalyst and resin may be applied from jets of a spray gun on to the surfaces to be united, e.g. glass cloth or laminates. In examples: (1) "Technical TPG" was hardened by addition of antimony pentachloride in butyl acetate; (3) the resin as in (1) mixed with a 10 per cent solution of boron fluoride etherate in methyl ethyl ketone and aluminium powder was poured into a mould and hardened in 3 minutes without shrinking; (5) "Technical DPG" containing 25 per cent epichlorhydrin was sprayed from one jet of a twin jet gun and a 10 per cent solution of boron fluoride/butanol in butanol was sprayed from the secondary jet to give a 4 per cent concentration of catalyst. The sprayed panels were coated with thick films of high gloss which hardened in 8 minutes.
GB1256354A 1954-04-30 1954-04-30 Curing of liquid polyepoxide resins Expired GB792702A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1256354A GB792702A (en) 1954-04-30 1954-04-30 Curing of liquid polyepoxide resins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1256354A GB792702A (en) 1954-04-30 1954-04-30 Curing of liquid polyepoxide resins

Publications (1)

Publication Number Publication Date
GB792702A true GB792702A (en) 1958-04-02

Family

ID=10006966

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1256354A Expired GB792702A (en) 1954-04-30 1954-04-30 Curing of liquid polyepoxide resins

Country Status (1)

Country Link
GB (1) GB792702A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3080341A (en) * 1959-12-16 1963-03-05 Martin Marietta Corp Processes for curing epoxy resins
US3109827A (en) * 1958-05-08 1963-11-05 Boake Roberts & Company Ltd A New reaction products of epoxidized oils and an antimony halide
US3287318A (en) * 1961-08-10 1966-11-22 Pittsburgh Plate Glass Co Substantially neutral electrophilic salts as curing catalyst for amidealdehyde resins

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3109827A (en) * 1958-05-08 1963-11-05 Boake Roberts & Company Ltd A New reaction products of epoxidized oils and an antimony halide
US3080341A (en) * 1959-12-16 1963-03-05 Martin Marietta Corp Processes for curing epoxy resins
US3287318A (en) * 1961-08-10 1966-11-22 Pittsburgh Plate Glass Co Substantially neutral electrophilic salts as curing catalyst for amidealdehyde resins

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