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US3989670A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for making polyetherimides

Assignee: General Electric Co
•
Filing: 1974-02-06
•
Granted: 1976-11-02
•
Expires: 1994-02-06
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Abstract

Abstract A process for making polyetherimides is provided by melt polymerizing a mixture of certain aromatic bis(etheranhydride)s and organic diamines. The polyetherimides can be reinforced with various fillers to produce high performance composites.

Inventors

  • 👤 Tohru Takekoshi
  • 👤 John E. Kochanowski

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 19:54
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/1057; C08G73/106; C08G73/1003; C08G73/1007; C08G73/1028; C08G73/1042; C08G73/1046; C08G73/1053

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 88 words
A method for making polyetherimide which comprises effecting the removal of water of reaction at temperatures of from about 250° C to a temperature below about 400° C by using either stirring, an inert gas purge, or reduced pressure, from the melt of a mixture containing as essential ingredients m-phenylene diamine and aromatic bis(etheranhydride) selected from the class consisting of 2,2-bis[4-(3,4-dicarboxyphenoxy)phenyl]propane dianhydride, 2,2-bis[4-(2,3-dicarboxyphenoxy)phenyl]propane dianhydride, and 2-[4-(2,3-dicarboxyphenoxy)phenyl]-2-[ 4-(3,4-dicarboxyphenoxy)phenyl]propane dianhydride and mixtures thereof, where there is utilized from 0.5 to 2.0 moles of m-phenylene diamine per mole of aromatic bis(etheranhydride).
Claim 2
Independent Claim 88 words
A method for making polyetherimide which comprises effecting the removal of water of reaction at temperatures of from about 250° C to a temperature below about 400° C by using either stirring, an inert gas purge, or reduced pressure, from the melt of a mixture containing as essential ingredients m-phenylene diamine and aromatic bis(etheranhydride) selected from the class consisting of 2,2-bis[4-(3,4-dicarboxyphenoxy)phenyl]propane dianhydride, 2,2-bis[4-(2,3-dicarboxyphenoxy)phenyl]propane dianhydride, and 2-[4-(2,3-dicarboxyphenoxy)phenyl]-2-[ 4-(3,4-dicarboxyphenoxy)phenyl]propane dianhydride and mixtures thereof, where there is utilized from 0.5 to 2.0 moles of m-phenylene diamine per mole of aromatic bis(etheranhydride).
Claim 3
Dependent Claim 21 words
A method in accordance with claim 1, where the aromatic bis(etheranhydride) and m-phenylene diamine are present in substantially equal molar amounts.
Claim 4
Dependent Claim 10 words
A method in accordance with claim 1, utilizing 2,2-bis[4-(3,4-dicarboxyphenoxy)phenyl]propane dianhydride.
Claim 5
Dependent Claim 10 words
A method in accordance with claim 1 employing 2,2-bis[4-(2,3-dicarboxyphenoxy)phenyl]propane dianhydride.

References Cited (Backward Citations)

US3179634A Cited
US3624050A Cited
US3838101A Cited
US3649601A Cited
US3699075A Cited
US3803085A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-11-02 1980-05-03 1980-11-02 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-11-02 1984-05-03 1984-11-02 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-11-02 1988-05-03 1988-11-02 $7700.00 Window Closed / Lapsed

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