GB969221A - Improvements in or relating to hardenable condensation products - Google Patents

Improvements in or relating to hardenable condensation products

Info

Publication number
GB969221A
GB969221A GB295061A GB295061A GB969221A GB 969221 A GB969221 A GB 969221A GB 295061 A GB295061 A GB 295061A GB 295061 A GB295061 A GB 295061A GB 969221 A GB969221 A GB 969221A
Authority
GB
United Kingdom
Prior art keywords
cresol
epoxy compound
novolak
mols
phenol
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
GB295061A
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.)
Dynamit Nobel AG
Original Assignee
Dynamit Nobel 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 Dynamit Nobel AG filed Critical Dynamit Nobel AG
Publication of GB969221A publication Critical patent/GB969221A/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
    • C08G59/02Polycondensates containing more than one epoxy group per molecule
    • C08G59/04Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
    • C08G59/06Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
    • C08G59/08Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols from phenol-aldehyde condensates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Epoxy Resins (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Hardenable condensation products are prepared by reacting, in an alkaline medium and in the absence of free phenolic compounds of phenyl glycidyl ether, a chlorine-containing epoxy compound and a substantially anhydrous novolak formed from more than 3 mols of o-cresol with 2 mols formaldehyde and containing fewer than 3 o-cresol nuclei per molecule. Suitable epoxy compounds are epichlorhydrin and glycerol dichlorhydrin. The o-cresol starting material may contain small amounts of phenol, m or p-cresol, or xylenol. The alkali is preferably added to the mixture of novolak and epoxy compound and may be added in stages. Reaction may be in a solvent, which may be an excess of the epoxy compound.ALSO:Hardenable condensation products are prepared by reacting, in an alkaline medium and in the absence of free phenolic compounds of phenyl glycidyl ether, a chlorine-containing epoxy compound and a substantially anhydrous novolak formed from acid condensation of more than 3 mols of o-cresol with 2 mols of formaldehyde, said novolak containing fewer than three o-cresol nuclei per molecule. Suitable epoxy compound are epichlorohydrin and glycerol dichlorohydrin. The o-cresol used for making the novolak may contain small amounts of phenol, m-cresol, p-cresol, or xylenol. The alkali is preferably added to the mixture of novolak and epoxy compound. Reaction may be performed in a solvent, which may be provided as an excess of epoxy compound-afterwards removed by distillation. The products may be hardened with bases, acids, acid anhydrides or Friedel-Crafts catalysts. They may be processed together with phenol-, melamine-, or urea-aldehyde resins or with other epoxy resins and may be used for lacquers, adhesives, casting or moulding.
GB295061A 1960-01-27 1961-01-25 Improvements in or relating to hardenable condensation products Expired GB969221A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DED0032442 1960-01-27

Publications (1)

Publication Number Publication Date
GB969221A true GB969221A (en) 1964-09-09

Family

ID=7041314

Family Applications (1)

Application Number Title Priority Date Filing Date
GB295061A Expired GB969221A (en) 1960-01-27 1961-01-25 Improvements in or relating to hardenable condensation products

Country Status (4)

Country Link
BE (1) BE599388A (en)
CH (1) CH436730A (en)
GB (1) GB969221A (en)
NL (1) NL260464A (en)

Also Published As

Publication number Publication date
NL260464A (en)
CH436730A (en) 1967-05-31
BE599388A (en)

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