GB767829A - Epoxide-containing ester adhesives, and a process for gluing together materials - Google Patents

Epoxide-containing ester adhesives, and a process for gluing together materials

Info

Publication number
GB767829A
GB767829A GB30303/53A GB3030353A GB767829A GB 767829 A GB767829 A GB 767829A GB 30303/53 A GB30303/53 A GB 30303/53A GB 3030353 A GB3030353 A GB 3030353A GB 767829 A GB767829 A GB 767829A
Authority
GB
United Kingdom
Prior art keywords
acid
anhydride
glycide
esters
adhesives
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
GB30303/53A
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of GB767829A publication Critical patent/GB767829A/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
    • C08G59/12Polycondensates containing more than one epoxy group per molecule of polycarboxylic acids with epihalohydrins or precursors thereof
    • 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
    • C08G59/40Macromolecules 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 curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

Adhesive compositions contain a 1,2-epoxy-alkyl ester of an aromatic polycarboxylic acid mixed with an acidic substance. The epoxyalkyl esters may be prepared by the methods of Specifications 735,001 and 766,771. The aromatic polycarboxylic acid may be a polyester prepared from glycol or glycerine with excess of an aromatic polycarboxylic acid. The acidic substance may be an inorganic or organic acid, acid chloride, anhydride or acid salt, or a phenol. A list of suitable substances is given in the Specification. The esters may be partially condensed before use by heating alone or in presence of an epoxy resin curing agent, e.g. piperidine or phthalic anhydride. Glycidyl esters of carboxyl-containing polyesters may also be employed. Non-acid catalysts, e.g. cyanamide, dicyandiamide, melamine, acetamide or adipic acid diamide may also be included in the compositions. Plasticisers, e.g. dibutylphthalate or tricresylphosphate, and other epoxy compounds, e.g. glycidyl ethers of polyhydric phenols, phenyl glycidyl ether, glycidyl esters of fatty acids, epoxidised drying oils, butadiene epoxides or glycide may also be added. The esters may be used in solution, in volatile solvents, e.g. ethers or ketones, as powders to be melted or on sheets, e.g. of paper or fabric. One part of the composition may be applied to one surface to be stuck and the remainder to the other. Hardening is preferably effected at raised temperature. Fillers, e.g. wood meal, mica, stone dust, and other adhesives, e.g. animal glue, starch derivatives, cellulose derivatives, phenylformaldehyde resins, urea or melamine resin may be added to the adhesives. The adhesives may be used for all combinations of material, as binders for moulded articles or for laminating sheets of all kinds. In many of the examples: a resin prepared from dipotassium phthalate and epichlorhydrin is used as an adhesive together with phthalic anhydride, maleic anhydride, mixtures of maleic and adipic anhydrides, o-phenylcyclophosphoric acid, monobutylorthophosphoric acid, b ,b -(4-hydroxyphenyl)-propane, resorcinol, p-toluene-sulphonic acid or terephthalic acid dichloride. In some cases the resin is first reacted to a limited extent with maleic anhydride, phthalic anhydride, or piperidine. In other examples, there is also present in the adhesive compositions: a linseed oil-maleic acid adduct, a copolymer of 2-methylol-2-chloromethyl - oxacyclobutane and 2 - methylol, 2-ethoxymethyl oxacyclobutane, 2,6 - dioxa - 3,3 - spiroheptane, tricresylphosphate, dibutylphthalate, or acetone or dioxane as a solvent. Other examples describe the use of the adhesives to impregnate paper for use in laminating beech veneers, or the formation of a hard brittle resin which either in powder form or as an extruded piece may be used for adhesion. Still other examples describe the use of resins either from terephthalic acid dichloride and glycide in presence of triethylamine, or from dipotassium terephthalate and glycide. Reference has been directed by the Comptroller to Specifications 518,057, [Group IV], and 723,777.ALSO:Epoxyalkyl esters of aromatic polycarboxylic acids are formed from epichlorhydrin and the alkali metal salt of the acid or from glycide and the acid chloride or anhydride. In examples: (1) finely powdered dipotassium phthalate and epichlorhydrin are reacted in an autoclave at 50 atmospheres pressure of nitrogen and 140-150 DEG C. Salt is filtered off and washed with epichlorhydrin. The filtrate is distilled and the epoxy ester (average mol. weight 442) remains; (14) terephthalic acid dichloride, glycide and triethylamine are mixed in toluene with cooling. Triethylamine hydrochloride is removed by filtration and the epoxy ester (mol. weight 480) remains as residue after distillation of the filtrate; (22) glycide is reacted with a mixture of phthalic acid anhydride and adipic acid anhydride. Specifications 735,001 and 766,771 are referred to. Reference has been directed by the Comptroller to Specifications 518,057, [Group IV], and 723,777.
GB30303/53A 1952-11-17 1953-11-03 Epoxide-containing ester adhesives, and a process for gluing together materials Expired GB767829A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE334649X 1952-11-17

Publications (1)

Publication Number Publication Date
GB767829A true GB767829A (en) 1957-02-06

Family

ID=6217751

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30303/53A Expired GB767829A (en) 1952-11-17 1953-11-03 Epoxide-containing ester adhesives, and a process for gluing together materials

Country Status (4)

Country Link
BE (1) BE523739A (en)
CH (1) CH334649A (en)
FR (1) FR1090578A (en)
GB (1) GB767829A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111437430A (en) * 2020-04-29 2020-07-24 深圳兰度生物材料有限公司 Adhesive polymer and medical adhesive and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1234382B (en) * 1962-10-04 1967-02-16 Dunlop Gummi Cie Ag Deutsche Process for firmly bonding rubber to metals

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111437430A (en) * 2020-04-29 2020-07-24 深圳兰度生物材料有限公司 Adhesive polymer and medical adhesive and preparation method thereof

Also Published As

Publication number Publication date
CH334649A (en) 1958-12-15
BE523739A (en)
FR1090578A (en) 1955-03-31

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