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Process for producing melting-anisotropic, copolymerized polyester

Assignee: Mitsubishi Chemical Corp
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Filing: 1985-02-28
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Granted: 1986-11-04
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Expires: 2005-02-28
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Abstract

Abstract PCT No. PCT/JP85/00094 Sec. 371 Date Oct. 31, 1985 Sec. 102(e) Date Oct. 31, 1985 PCT Filed Feb. 28, 1985 PCT Pub. No. WO85/03941 PCT Pub. Date Sep. 12, 1985.A process for producing a melting-anisotropic copolymerized polyester containing an alkylene terephthalate component, which comprises reacting a starting polyester composed of a dicarboxylic acid and a diol with an oxyaromatic carboxylic acid to form a copolymerized oligomer, then conducting acylating reaction by the addition of an acylating agent and further conducting polycondensating reduction thereby producing a melting-anisotropic, copolymerized polyester having a logarithmic viscosity of at least 0.2 dl/g. According to this process, a polyester of excellent physical property can be obtained at a good production efficiency.

Inventors

  • 👤 Tamotsu Yoshimura
  • 👤 Masahiko Nakamura
  • 👤 Ken Honma

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 22:05
CPC Classifications
C; C08; C08G; C08G63/00; C08G63/02; C08G63/60

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 163 words
A process for producing a melting-anisotropic, copolymerized polyester containing an alkylene terephthalate component, which comprises reacting 95 to 5 mol % of a starting polyester composed of a dicarboxylic acid and a diol having of recurring units represented by the general formula: ##STR6## where R 1 represents a divalent aromatic radical of 6 to 20 carbon atoms or a divalent cycloaliphatic radical of 4 to 20 carbon atoms, and R 2 represents a divalent aliphatic radical of 2 to 20 carbon atoms, with from 5 to 95 mol % of an oxyaromatic carboxylic acid represented by the general formula: ##STR7## where R 3 represents a hydrogen atom, a halogen atom, an alkyl or alkoxy group of 1 to 4 carbon atoms to form a copolymerized oligomer, then conducting acylating reaction by the addition of an acylating agent and, further conducting polycondensating reaction in order to increase the logarithmic viscosity thereby producing a copolymerized polyester having a logarithmic viscosity of at least 0.2 dl/g.
Claim 2
Dependent Claim 163 words
A process for producing a melting-anisotropic, copolymerized polyester containing an alkylene terephthalate component, which comprises reacting 95 to 5 mol % of a starting polyester composed of a dicarboxylic acid and a diol having of recurring units represented by the general formula: ##STR6## where R 1 represents a divalent aromatic radical of 6 to 20 carbon atoms or a divalent cycloaliphatic radical of 4 to 20 carbon atoms, and R 2 represents a divalent aliphatic radical of 2 to 20 carbon atoms, with from 5 to 95 mol % of an oxyaromatic carboxylic acid represented by the general formula: ##STR7## where R 3 represents a hydrogen atom, a halogen atom, an alkyl or alkoxy group of 1 to 4 carbon atoms to form a copolymerized oligomer, then conducting acylating reaction by the addition of an acylating agent and, further conducting polycondensating reaction in order to increase the logarithmic viscosity thereby producing a copolymerized polyester having a logarithmic viscosity of at least 0.2 dl/g.
Claim 3
Dependent Claim 27 words
The process for producing the melting-anisotropic, copolymerized polyester as defined in claim 1, wherein a polyalkylene terephthalate or the oligomer thereof is used as the starting polyester.
Claim 4
Dependent Claim 30 words
The process for producing the melting-anisotropic, copolymerized polyester as defined in claim 1, wherein para-oxybenzoic acid, 2-oxy-6-naphthoic acid, 1-oxy-5-naphthoic acid or 1-oxy-4-naphthoic acid is used as the oxyaromatic carboxylic acid.
Claim 5
Dependent Claim 22 words
The process for producing the melting-anisotropic, copolymerized polyester as defined in claim 1, wherein acetic anhydride is used as the acylating agent.

References Cited (Backward Citations)

US3778410A Cited
US3804805A Cited
US4035356A Cited
US4393191A Cited
US4542203A Cited
US4560740A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-11-03 1990-05-05 1990-11-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-11-03 1994-05-05 1994-11-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-11-03 1998-05-05 1998-11-04 $7700.00 Window Closed / Lapsed

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