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US4464520A Expired / Lapsed US ⏱️ 0.0 years remaining

Delayed cure bismaleimide resins

Assignee: United States Department of Energy
•
Filing: 1982-08-12
•
Granted: 1984-08-07
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Expires: 2002-08-12
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Abstract

Abstract Polybismaleimides prepared by delayed curing of bis-imides having the formula ##STR1## wherein R 1 and R 2 each independently is H, C 1-4 -alkyl, C 1-4 -alkoxy, Cl or Br, or R 1 and R 2 together form a fused 6-membered hydrocarbon aromatic ring, with the proviso that R 1 and R 2 are not t-butyl or t-butoxy; X is O, S or Se; n is 1-3; and the --(CH 2 ) n -- group, optionally, is substituted by 1-3 methyl groups or by fluorine.

Inventors

  • 👤 Johnnie E. Adams
  • 👤 Donald R. Jamieson

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 07:22
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/12; C08G73/125; C08F; C08F22/00; C08F22/36; C08F22/40; C08G73/123; C08G73/124

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 153 words
A method for delayed curing of a bismaleimide, comprising: heating the bismaleimide to a temperature equal to or greater than its melting point but lower than the temperature at which it begins to polymerize; holding the melted bismaleimide at a temperature lower than that at which it begins to polymerize for a period of time sufficient to obtain a homogeneous melt; and then heating the bismaleimide to the temperature at which it polymerizes; said bismaleimide having the formula ##STR4## wherein R 1 and R 2 each independently is H, C 1-4 -alkyl, C 1-4 -alkoxy, Cl or Br, or R 1 and R 2 together form a fused 6-membered hydrocarbon aromatic ring, with the proviso that R 1 and R 2 are not t-butyl or t-butoxy; X is O, S or Se; n is 1-3; and the --(CH 2 ) n -- group, optionally, is substituted by 1-3 methyl groups or by fluorine.
Claim 2
Independent Claim 153 words
A method for delayed curing of a bismaleimide, comprising: heating the bismaleimide to a temperature equal to or greater than its melting point but lower than the temperature at which it begins to polymerize; holding the melted bismaleimide at a temperature lower than that at which it begins to polymerize for a period of time sufficient to obtain a homogeneous melt; and then heating the bismaleimide to the temperature at which it polymerizes; said bismaleimide having the formula ##STR4## wherein R 1 and R 2 each independently is H, C 1-4 -alkyl, C 1-4 -alkoxy, Cl or Br, or R 1 and R 2 together form a fused 6-membered hydrocarbon aromatic ring, with the proviso that R 1 and R 2 are not t-butyl or t-butoxy; X is O, S or Se; n is 1-3; and the --(CH 2 ) n -- group, optionally, is substituted by 1-3 methyl groups or by fluorine.
Claim 3
Dependent Claim 10 words
The method of claim 1 wherein the bismaleimide is 1,2-bis(2-maleimidophenylthio)ethane.
Claim 4
Dependent Claim 10 words
A polybismaleimide prepared according to the process of claim 1.
Claim 5
Dependent Claim 16 words
An oxygen and heat resistant composite in which the matrix is the polybismaleimide of claim 3.

References Cited (Backward Citations)

US2818405A Cited
US3380964A Cited
US3435003A Cited
US3533996A Cited
US3627780A Cited
US3562223A Cited
US4118377A Cited
US4100140A Cited
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US4269961A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-08-07 1988-02-06 1988-08-07 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-08-07 1992-02-06 1992-08-07 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-08-07 1996-02-06 1996-08-07 $7700.00 Window Closed / Lapsed

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