Claims
- 1. Storage-stable, one package quick-curing epoxide resin moulding materials consisting essentially of:
- a. pre-adducts containing aromatic constituents and free epoxide groups and formed from epoxide resins and polyamines,
- b. pre-adducts containing free amino groups and formed from polyamines containing cycloaliphatic or heterocyclic groups with polyglycidyl compounds, as curing agents, wherein the ratio of the number of reactive hydrogen atoms of the polyamine on the amine nitrogen atoms to that of the epoxide groups of the epoxide is in the range of 3:1 to 5:1, and
- c. mineral or organic pulverulent or fibrous fillers, with the epoxide resin pre-adducts and the curing agents softening between 45.degree. and 120.degree.C, and melting 5.degree. to 30.degree.C above the softening point, and the resin pre-adducts and the curing agents being present in the moulding materials predominantly as discrete particles.
- 2. Epoxide resin moulding materials according to claim 1 which also contain lubricants.
- 3. Epoxide resin moulding materials according to claim 1 wherein the epoxide resin pre-adduct is an adduct from a low-molecular, glycidylated bisphenol A having an epoxide group content of at least 2 equivalents per kg of resin and a diamine.
- 4. Epoxide resin moulding materials according to claim 1 wherein the diamine is diaminodiphenylmethane.
- 5. Epoxide resin moulding materials according to claim 1 wherein the epoxide resin pre-adduct has an epoxide group content of more than 4.5 equivalents per kg.
- 6. Epoxide resin moulding material according to claim 1 containing
- a. 242 parts by weight of a solid resin adduct with epoxide group equivalents/kg = 3.00, softening point = 58.degree.C, melting point = 72.degree.C, produced from bisphenol-A epoxide resin with less than the equivalent amount of 4,4'-diamino-diphenylmethane,
- b. 88 parts by weight of a curing agent adduct with amino group equivalents/kg = 4.18, softening point = 63.degree.C, melting point = 78.degree.C, produced from 340.6 parts by weight of 3-aminomethyl-3,3,5-trimethylcyclohexylamine and 377.5 parts by weight of bisphenol-A-epoxide resin with 5.3 epoxide group equivalents/kg.
- c. 663 parts by weight of calcined kaolin,
- d. 20 parts by weight of a partially esterified polymethylene wax and
- e. 50 parts by weight of gas black.
- 7. Epoxide resin moulding material according to claim 1 containing
- a. 196 parts by weight of a solid resin adduct with epoxide group equivalents/kg = 3.00, softening point = 58.degree.C, melting point = 72.degree.C, produced from bisphenol-A-epoxide resin with less than the equivalent amount of 4,4'-diamino-diphenylmethane,
- b. 64 parts by weight of a curing agent adduct with amino group equivalents/kg = 3.52, softening point = 59.degree.C, melting point = 70.degree.C, produced from 4,4'-diamino-3,3'-dimethyl-dicyclohexylmethane and a low molecular bisphenol-A-epoxide with 5.34 epoxide group equivalents/kg, in the molar ratio of 2:1,
- c. 500 parts by weight of wollastonite,
- d. 230 parts by weight of aluminium oxide trihydrate,
- e. 3 parts by weight of a partially esterified polymethylene wax and
- f. 3 parts by weight of a pigment from burnt sienna and umber 1:1.
- 8. Process for the production of storage-stable, quick-curing moulding materials, in which process a polyamine containing cycloaliphatic or heterocyclic groups and a polyglycidyl compound are reacted together in such amounts that the ratio of the number of the reactive hydrogen atoms on the amine nitrogen atoms so that of the epoxide groups is in the range of 3:1 to 5:1, the formed curing agent pre-adduct, which has a softening point within the range of 45.degree. to 120.degree.C and a melting point higher than the softening point by 5.degree. to 30.degree.C, is then mixed together with a pre-adduct, containing free epoxide groups, of an epoxide resin with a polyamine, the epoxide resin pre-adduct containing aromatic constituents, softening between 45.degree. and 120.degree.C, and possessing a melting point 5.degree. to 30.degree.C above the said softening point, and also with a filler; and the mixture subsequently ground, whereby there may occur to a slight degree at the very most a fusing together of the particles of the resin pre-adduct and those of the curing agent.
- 9. Process according to claim 8 wherein lubricants are also added.
- 10. Process according to claim 8, wherein the ratio of the number of reactive hydrogen atoms on the amino nitrogen atoms to that of the epoxide groups in the polyamine and in the polyglycidyl compound is, in the production of the curing agent pre-adduct, between 3,5 : 1 and 4.5 : 1.
- 11. Process according to claim 1, wherein the formation of the curing agent pre-adduct is effected in the absence of solvents, and at a temperature of between 50.degree. and 200.degree.C.
- 12. Process according to claim 8, wherein the formation of the curing agent pre-adduct is effected in the absence of solvents, and at a temperature of between 120.degree. and 170.degree.C.
- 13. Process according to claim 8, wherein the epoxide resin pre-adduct added for the production of the moulding materials is an adduct from a low-molecular, glycidylated bisphenol A having an epoxide group content of more than 3, particularly more than 4.5, equivalents/kg of resin, and a diamine.
- 14. Process according to claim 8, wherein the curing agent pre-adduct employed is an adduct from a cycloaliphatic or heterocyclic diamine with a low-molecular polyglycidyl compound.
Priority Claims (1)
Number |
Date |
Country |
Kind |
8703/70 |
Jun 1971 |
CH |
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Parent Case Info
This is a continuation of application Ser. No. 257,749 filed on May 30, 1972, now abandoned.
US Referenced Citations (2)
Number |
Name |
Date |
Kind |
3288747 |
Sussman |
Nov 1966 |
|
3409591 |
Landua et al. |
Nov 1968 |
|
Foreign Referenced Citations (1)
Number |
Date |
Country |
1,204,224 |
Sep 1970 |
UK |
Non-Patent Literature Citations (1)
Entry |
The Condensed Chemical Dictionary; Reinhold Publishing Corp.; 1966; pp. 37, 38, 1020. |
Continuations (1)
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Number |
Date |
Country |
Parent |
257749 |
May 1972 |
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