GB783764A - - Google Patents

Info

Publication number
GB783764A
GB783764A GB783764DA GB783764A GB 783764 A GB783764 A GB 783764A GB 783764D A GB783764D A GB 783764DA GB 783764 A GB783764 A GB 783764A
Authority
GB
United Kingdom
Prior art keywords
dibutyl tin
tin
epoxide
reacting
produced
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.)
Active
Application number
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.)
Publication of GB783764A publication Critical patent/GB783764A/en
Active 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
    • C08G59/681Metal alcoholates, phenolates or carboxylates
    • 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
    • C08G59/681Metal alcoholates, phenolates or carboxylates
    • C08G59/685Carboxylates

Landscapes

  • 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)
  • Paints Or Removers (AREA)
  • Epoxy Resins (AREA)

Abstract

783,764. Curing epoxide resins. CHEMISCHE WERKE ALBERT. April 30, 1956 [April 28, 1955], No. 13266/56. Class 2 (5). [Also in Group IV (b)] Epoxide resins having on the average more than one epoxide group per molecule are hardened by addition thereto of an organo-tin compound having the general formula where n is an integer, R 1 and R 2 , which may be the same or different, are monoacyl groups where n=1 or alternatively where n is greater than 1 are alkyl, aryl or alkaryl groups or residues of maleic acid and R 3 and R 4 are alkyl, aryl or aralkyl. R 1 and R 2 are preferably acyl groups containing 2-22 atoms. Examples of hardening agents are dibutyl tin diacetate and dibutyl tin dilaurate. The hardening agent may contain the recurring unit e.g. compounds such as dibutyl tin maleate obtained by reacting a dialkyl tin dichloride and maleic acid dibutyl tin di-ethylhexoxide polymer may also be used. The polymeric compounds may be produced by reacting a dialkyl, diaryl or diaralkyl tin halide in an anhydrous solvent with alkalimetal alkoxides or with alcohols in the presence of ammonia or tertiary amines. The hardening agent and the epoxide resin may be mixed by melting together or by solution in a mutual solvent, e.g. dichlorethylene, carbon tetrachloride, dichlorethylene ethers, monochlorbenzene. In examples: (1) 100 parts epoxide resin produced from bisphenol and epichlorhydrin are dissolved in ethylene glycol containing 1 part of dibutyl tin laurate. Films of high gloss and good chemical resistance are produced by stoving the solution on metal panels at 200‹ C.; (2) dibutyl tin maleate is used to cure the resin of (1); (3) the hardener was obtained by reacting a dispersion of metallic sodium with 2-ethylhexyl alcohol in toluene with dibutyl tin dichloride. Specification 729,258 is referred to.
GB783764D 1955-04-28 Active GB783764A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEC11148A DE1008909B (en) 1955-04-28 1955-04-28 Hardening agent for epoxy resins

Publications (1)

Publication Number Publication Date
GB783764A true GB783764A (en)

Family

ID=7014913

Family Applications (1)

Application Number Title Priority Date Filing Date
GB783764D Active GB783764A (en) 1955-04-28

Country Status (3)

Country Link
DE (1) DE1008909B (en)
FR (1) FR69456E (en)
GB (1) GB783764A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL282843A (en) * 1961-10-03
US3364159A (en) * 1965-09-27 1968-01-16 Argus Chem Curing vicinal epoxy compounds and curing compositions therefor

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL84498C (en) * 1936-10-28
NL73196C (en) * 1948-02-28
US2643243A (en) * 1951-02-26 1953-06-23 Shell Dev Curing glycidyl polyethers of dihydric phenols with sulfonic acids

Also Published As

Publication number Publication date
FR69456E (en) 1958-11-07
DE1008909B (en) 1957-05-23

Similar Documents

Publication Publication Date Title
US2864775A (en) Process for curing polyepoxides by amine adducts and resulting products
US7750107B2 (en) Substituted urea accelerator with dicyandiamide for epoxy resin systems
US3678131A (en) Adhesive compositions containing epoxy resin, carboxyl containing copolymer and 2,2,-bis-(4-hydroxyphenyl) sulfone
EP0495269B1 (en) Thermosetting reactive resin mixture, moulded article and coating made therefrom
EP0659793A1 (en) One component epoxy resin compositions containing modified epoxy-amine adducts as curing agents
KR20150072351A (en) Processing-friendly dianhydride hardener for epoxy resin systems based on 5,5'-oxybis(isobenzofuran-1,3-dione)
US3660354A (en) Quaternary ammonium and phosphonium thiocyanates and their use as accelerators for epoxy resins
GB1070581A (en) Oxazolidinone compounds and their preparation
CN110156958B (en) Bio-based phosphaphenanthrene curing agent flame-retardant epoxy resin material and preparation method thereof
US3395121A (en) Curing epoxy resins with boron trichloride-tertiary amine complexes
GB783764A (en)
JP3355658B2 (en) Epoxy resin composition
JP3476994B2 (en) Epoxy resin composition
US4379908A (en) Rapid curing epoxy-unsaturated monomer compositions
US3134754A (en) Polyepoxide compositions
EP0456603A1 (en) Tetra-N-glycedyl compound and its hardenable mixtures
DE1154624B (en) Hardeners for epoxy resins
US3945971A (en) Phenyl urea epoxy resin accelerator
JP3468597B2 (en) Epoxy resin composition
ES364920A1 (en) Curable mixtures of epoxide resins and cyclic urea derivatives
GB971525A (en) Hardened poly epoxide resins and process for their manufacture
JPH08283320A (en) Cationically polymerizable organic material composition and method for stabilizing same
JPS60231723A (en) Additive for epoxy resin
JPH1059907A (en) Polyamine, its production and lacquer containing the same, coating agent, adhesive agent, resin for impregnation, resin for immersion, and resin for casting
US5039756A (en) Vulcanizable epoxy group-containing elastomer composition