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US5272248A Expired / Lapsed US ⏱️ 0.0 years remaining

Polyimide processing additives

Assignee: University of Southern California
•
Filing: 1992-05-22
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Granted: 1993-12-21
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Expires: 2012-05-22
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Abstract

Abstract A process for preparing polyamides having enhanced melt flow properties is described. The process consists of heating a mixture of a high molecular weight poly(amic acid) or polyimide with a low molecular weight amic acid or imide additive in the range of 0.05 to 15% by weight of additive. The polyimide powders so obtained show improved processability, as evidenced by lower melt viscosity by capillary rheometry. Likewise, films prepared from mixtures of polymers with additives show improved processability with earlier onset of stretching by TMA.

Inventors

  • 👤 J. Richard Pratt
  • 👤 Terry L. St. Clair
  • 👤 Diane M. Stoakley
  • 👤 Harold D. Burks

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 00:19
CPC Classifications
C; C08; C08K; C08K5/00; C08K5/16; C08K5/21; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/1067; C08K5/34; C08K5/3412; C08K5/3415

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 92 words
A low molecular weight amic acid or imide additive improving the melt processability of high molecular weight poly(amic acids) and polyimides, the additive selected from the group consisting of: ##STR5## wherein R, R', R'', and R''' are selected from the group consisting of hydrogen, alkyl, alkylaryl, alkyloxy, aryloxy, aryl, halogen, and haloalkyl; and x is a bond or is selected from the group consisting of oxo, thio, methylene, carbonyl, 2,2-hexafluoropropyl, sulfone, and 4,4'-thiodiphenoxy; and wherein arrows drawn from a group to an aromatic ring represent any amic acid isomer or isomer mixture.
Claim 2
Dependent Claim 92 words
A low molecular weight amic acid or imide additive improving the melt processability of high molecular weight poly(amic acids) and polyimides, the additive selected from the group consisting of: ##STR5## wherein R, R', R'', and R''' are selected from the group consisting of hydrogen, alkyl, alkylaryl, alkyloxy, aryloxy, aryl, halogen, and haloalkyl; and x is a bond or is selected from the group consisting of oxo, thio, methylene, carbonyl, 2,2-hexafluoropropyl, sulfone, and 4,4'-thiodiphenoxy; and wherein arrows drawn from a group to an aromatic ring represent any amic acid isomer or isomer mixture.

References Cited (Backward Citations)

US3933749A Cited
US3983093A Cited
US4107125A Cited
US4142870A Cited
US4281100A Cited
US4444979A Cited
US4603061A Cited
US4552931A Cited
US5116939A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1996-12-20 1997-06-21 1997-12-21 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2000-12-20 2001-06-21 2001-12-21 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2004-12-20 2005-06-21 2005-12-21 $7700.00 Window Closed / Lapsed

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