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US3963666A Expired / Lapsed US ⏱️ 0.0 years remaining

Storage-stable, quick-curing epoxide resin moulding materials

Assignee: Novartis Corp
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Filing: 1975-04-24
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Granted: 1976-06-15
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Expires: 1995-04-24
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Abstract

Abstract The invention relates to storage-stable, quick-curing epoxide resin moulding materials containing:

Inventors

  • 👤 Bruno Schreiber
  • 👤 Wolfgang Seiz
  • 👤 Ewald Forster

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 19:13
CPC Classifications
C; C08; C08G; C08G59/00; C08G59/18; C08G59/182; C08G59/184; C08G59/02; C08G59/10

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 133 words
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° and 120°C, and melting 5° to 30°C above the softening point, and the resin pre-adducts and the curing agents being present in the moulding materials predominantly as discrete particles.
Claim 2
Dependent Claim 133 words
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° and 120°C, and melting 5° to 30°C above the softening point, and the resin pre-adducts and the curing agents being present in the moulding materials predominantly as discrete particles.
Claim 3
Dependent Claim 12 words
Epoxide resin moulding materials according to claim 1 which also contain lubricants.
Claim 4
Dependent Claim 39 words
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.
Claim 5
Dependent Claim 13 words
Epoxide resin moulding materials according to claim 1 wherein the diamine is diaminodiphenylmethane.
Claim 6
Dependent Claim 25 words
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.
Claim 7
Dependent Claim 119 words
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°C, melting point = 72°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°C, melting point = 78°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.
Claim 8
Dependent Claim 130 words
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°C, melting point = 72°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°C, melting point = 70°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.
Claim 9
Dependent Claim 170 words
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° to 120°C and a melting point higher than the softening point by 5° to 30°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° and 120°C, and possessing a melting point 5° to 30°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.
Claim 10
Dependent Claim 170 words
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° to 120°C and a melting point higher than the softening point by 5° to 30°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° and 120°C, and possessing a melting point 5° to 30°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.
Claim 11
Dependent Claim 10 words
Process according to claim 8 wherein lubricants are also added.
Claim 12
Dependent Claim 51 words
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.
Claim 13
Dependent Claim 29 words
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° and 200°C.
Claim 14
Dependent Claim 29 words
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° and 170°C.
Claim 15
Dependent Claim 46 words
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.
Claim 16
Dependent Claim 25 words
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.

References Cited (Backward Citations)

US3288747A Cited
US3409591A Cited
GB1204224A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-06-15 1979-12-15 1980-06-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-06-15 1983-12-15 1984-06-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-06-15 1987-12-15 1988-06-15 $7700.00 Window Closed / Lapsed

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