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US3905942A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for making polyetherimides and products produced thereby

Assignee: General Electric Co
•
Filing: 1974-09-13
•
Granted: 1975-09-16
•
Expires: 1994-09-13
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Abstract

Abstract A method is provided for making polyetherimides involving the reaction of aromatic bis(etherdicarboxylic) acids and organic diamines in the presence of a non-polar organic solvent, or phenolic solvent, at temperatures of at least 130*C. The polyetherimides are useful as injection molding compounds.

Inventors

  • 👤 Tohru Takekoshi
  • 👤 John E Kochanowski

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 22:09
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/1046; C08G73/1053; C08G73/1003; C08G73/1007; C08G73/1028; C08G73/1032; C08G73/1057; C08G73/1064; C08G73/1067; C08G73/1071

Claims Analysis

Total Claims: 20
Claim 1
Independent Claim 14 words
IN THE METHOD FOR MAKING POLYETHERIMIDE IN A STEPWIDE MANNER INVOLVING THE STEPS OF
Claim 2
Dependent Claim 14 words
IN THE METHOD FOR MAKING POLYETHERIMIDE IN A STEPWIDE MANNER INVOLVING THE STEPS OF
Claim 3
Dependent Claim 19 words
EFFECTING REACTION AT AMBIENT TEMPERATURES IN THE PRESENCE OF AN ORGANIC POLAR SOLVENT BETWEEN A TETRA-ACID OF THE FORMULA
Claim 4
Dependent Claim 19 words
EFFECTING REACTION AT AMBIENT TEMPERATURES IN THE PRESENCE OF AN ORGANIC POLAR SOLVENT BETWEEN A TETRA-ACID OF THE FORMULA
Claim 5
Dependent Claim 83 words
heating the polyamide acid of (1) to a temperature of at least 200*C to produce a polyetherimide, which comprises the improvement of reacting the tetra acid and the organic diamine of (1) in the presence of a non-polar or phenolic solvent at a temperature of at least 130*C, whereby the requirement of forming the polyamide acid in a polar organic solvent at ambient temperatures is avoided, where R is a member selected from the class consisting of (a) the following divalent organic radicals:
Claim 6
Dependent Claim 83 words
heating the polyamide acid of (1) to a temperature of at least 200*C to produce a polyetherimide, which comprises the improvement of reacting the tetra acid and the organic diamine of (1) in the presence of a non-polar or phenolic solvent at a temperature of at least 130*C, whereby the requirement of forming the polyamide acid in a polar organic solvent at ambient temperatures is avoided, where R is a member selected from the class consisting of (a) the following divalent organic radicals:
Claim 7
Dependent Claim 83 words
HEATING THE POLYAMIDE ACID OF (1) TO A TEMPERATURE OF AT LEAST 200*C TO PRODUCE A POLYETHERIMIDE, WHICH COMPRISES THE IMPROVEMENT OF REACTING THE TETRA ACID AND THE ORGANIC DIAMINE OF (1) IN THE PRESENCE OF A NON-POLAR OR PHENOLIC SOLVENT AT A TEMPERATURE OF AT LEAST 130*C, WHEREBY THE REQUIREMENT OF FORMING THE POLYAMIDE ACID IN A POLAR ORGANIC SOLVENT AT AMBIENT TEMPERATURES IS AVOIDED, WHERE R IS A MEMBER SELECTED FROM THE CLASS CONSISTING OF (A) THE FOLLOWING DIVALENT ORGANIC RADICALS:
Claim 8
Dependent Claim 83 words
HEATING THE POLYAMIDE ACID OF (1) TO A TEMPERATURE OF AT LEAST 200*C TO PRODUCE A POLYETHERIMIDE, WHICH COMPRISES THE IMPROVEMENT OF REACTING THE TETRA ACID AND THE ORGANIC DIAMINE OF (1) IN THE PRESENCE OF A NON-POLAR OR PHENOLIC SOLVENT AT A TEMPERATURE OF AT LEAST 130*C, WHEREBY THE REQUIREMENT OF FORMING THE POLYAMIDE ACID IN A POLAR ORGANIC SOLVENT AT AMBIENT TEMPERATURES IS AVOIDED, WHERE R IS A MEMBER SELECTED FROM THE CLASS CONSISTING OF (A) THE FOLLOWING DIVALENT ORGANIC RADICALS:
Claim 9
Dependent Claim 20 words
A method in accordance with claim 1, using a mixture of a phenolic solvent and a low boiling azeotropic solvent.
Claim 10
Dependent Claim 20 words
A method in accordance with claim 1, using a mixture of a non-polar solvent and a low boiling azeotropic solvent.
Claim 11
Dependent Claim 12 words
A method in accordance with claim 1, where the tetra-acid is 2,2-bis(4-(3,4-dicarboxyphenoxy)phenyl)propane.
Claim 12
Dependent Claim 12 words
A method in accordance with claim 1, where the tetra-acid is 2,2-bis(4-(2,3-diccarboxyphenoxy)phenyl)propane.
Claim 13
Dependent Claim 13 words
A method in accordance with claim 1, where the tetra-acid is 4,4''bis(3,4-dicarboxyphenoxy)diphenyl sulfide.
Claim 14
Dependent Claim 12 words
A method in accordance with claim 1, where the tetra-acid is 1,4-bis(3,4-dicarboxyphenoxy)benzene.
Claim 15
Dependent Claim 13 words
A method in accordance with claim 1, where the tetra-acid is 4,4''-bis(2,3-dicarboxyphenoxy)diphenyl ether.
Claim 16
Dependent Claim 14 words
A method in accordance with claim 1, where the organic diamine is bis(4-aminobutyl)tetramethyl disiloxane.
Claim 17
Dependent Claim 13 words
A method in accordance with claim 1, where the organic diamine is 4,4''-diaminodiphenylether.
Claim 18
Dependent Claim 14 words
A method in accordance with claim 1, where the organic diamine is 4,4''-diaminodiphenyl methane.
Claim 19
Dependent Claim 14 words
A method in accordance with claim 1, where the organic diamine is hexamethylene diamine.
Claim 20
Dependent Claim 14 words
A method in accordance with claim 1, where the organic diamine is m-phenylene diamine.

References Cited (Backward Citations)

US3699075A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1978-09-15 1979-03-17 1979-09-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1982-09-15 1983-03-17 1983-09-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1986-09-15 1987-03-17 1987-09-16 $7700.00 Window Closed / Lapsed

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