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Aromatic polyester-polycarbonate

Assignee: Mitsubishi Chemical Corp
•
Filing: 1979-08-20
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Granted: 1981-04-07
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Expires: 1999-08-20
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Abstract

Abstract An aromatic polyester-polycarbonate resin which comprises a polymer material composed of repeating units of structures I-III: <IMAGE> I <IMAGE> II <IMAGE> III wherein X is a divalent organic radical and the divalent aromatic entities in structures I, II and III may be substituted by hydrocarbon residues.

Inventors

  • 👤 Hajime Mori
  • 👤 Katsuhisa Kohyama
  • 👤 Katsuhiko Nakamura
  • 👤 Katsuyuki Sakata

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-28 20:49
CPC Classifications
C; C08; C08G; C08G63/00; C08G63/64; C08G63/66

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 174 words
An aromatic polyester-polycarbonate resin having a glass transition point ranging from 160° C. to 190° C. and having a terminal carboxyl group content of not more than 10μ equivalents/g of resin, comprising: a polymer material composed of repeating units of structures I-III: ##STR4## wherein X is a divalent organic radical and the divalent aromatic entities in structures in I, II and III may be substituted by hydrocarbon substituents and wherein the molar proportion of dihydroxy-diaryl units to benzene dicarboxylic acid units to carbonate units ranges from 1:0.33-0.75:0.67-0.25 with the molar ratio of the terephthalic acid units to isophthalic acid units of said benzene dicarboxylic acid units ranging from 9:1 to 2:8, said terephthalic acid units and said isophthalic acid units being formed in said polymer material by the presence of a terephthaloyl chloride compound selected from the group consisting of terephthaloyl chloride, methyl terephthaloyl chloride and 2,5-dimethyl terephthaloyl chloride and an isophthaloyl chloride compound selected from the goup consisting of isophthaloyl chloride and 2-methylisophthaloyl chloride in the reacting monomers which form said polymer material.
Claim 2
Dependent Claim 174 words
An aromatic polyester-polycarbonate resin having a glass transition point ranging from 160° C. to 190° C. and having a terminal carboxyl group content of not more than 10μ equivalents/g of resin, comprising: a polymer material composed of repeating units of structures I-III: ##STR4## wherein X is a divalent organic radical and the divalent aromatic entities in structures in I, II and III may be substituted by hydrocarbon substituents and wherein the molar proportion of dihydroxy-diaryl units to benzene dicarboxylic acid units to carbonate units ranges from 1:0.33-0.75:0.67-0.25 with the molar ratio of the terephthalic acid units to isophthalic acid units of said benzene dicarboxylic acid units ranging from 9:1 to 2:8, said terephthalic acid units and said isophthalic acid units being formed in said polymer material by the presence of a terephthaloyl chloride compound selected from the group consisting of terephthaloyl chloride, methyl terephthaloyl chloride and 2,5-dimethyl terephthaloyl chloride and an isophthaloyl chloride compound selected from the goup consisting of isophthaloyl chloride and 2-methylisophthaloyl chloride in the reacting monomers which form said polymer material.
Claim 3
Dependent Claim 20 words
The resin of claim 1, wherein said resin has an intrinsic viscosity ranging from 0.4 to 1.5 at 20° C.
Claim 4
Dependent Claim 35 words
The resin of claim 1, wherein the dihydroxydiaryl monomer which forms said dihydroxy-diaryl units in said polymer material is selected from the group consisting of bis-(hydroxyaryl)-alkanes, bis-(hydroxyaryl)-cycloalkanes, dihydroxy-diarylethers, dihydroxy-diaryl sulfides, dihydroxydiaryl sulfoxides and dihydroxy-diaryl sulfones.
Claim 5
Dependent Claim 14 words
The resin of claim 1, wherein said molar ratio ranges from 8:2 to 3:7.
Claim 6
Dependent Claim 12 words
The resin of claim 1, wherein said molar proportion ranges from 1:0.33-0.49:0.67-0.51.
Claim 7
Independent Claim 92 words
A method of preparting an aromatic polyester-polycarbonate resin, comprising: polycondensing a dihydroxy-diaryl compound in an aqueous alkaline solution with a combination of a terephthaloyl chloride compound and an isophthaloyl chloride compound in an organic solvent thereby forming a low molecular weight polyester oligomer having terminal OH groups; reacting said oligomer with phosgene thereby converting said terminal OH groups into terminal OCOCl groups; condensing the product of reaction between said oligomer and said phosgene with a dihydroxy-diaryl compound in an aqueous alkaline solution; and separating the product polyester-polycarbonate resin from said reaction medium.
Claim 8
Independent Claim 92 words
A method of preparting an aromatic polyester-polycarbonate resin, comprising: polycondensing a dihydroxy-diaryl compound in an aqueous alkaline solution with a combination of a terephthaloyl chloride compound and an isophthaloyl chloride compound in an organic solvent thereby forming a low molecular weight polyester oligomer having terminal OH groups; reacting said oligomer with phosgene thereby converting said terminal OH groups into terminal OCOCl groups; condensing the product of reaction between said oligomer and said phosgene with a dihydroxy-diaryl compound in an aqueous alkaline solution; and separating the product polyester-polycarbonate resin from said reaction medium.
Claim 9
Dependent Claim 50 words
The method of claim 6, wherein said dihydroxy-diaryl compound has the formula: ##STR5## wherein X is a divalent radical selected from the group consisting of >CRR, >C═R', --O--, --S--, --SO-- and --SO 2 -- and R is hydrogen or a monovalent hydrocarbon radical and R' is a divalent hydrocarbon radical.
Claim 10
Dependent Claim 43 words
The method of claim 7, wherein said terephthaloyl chloride compound is selected from the group consisting of terephthaloyl chloride, methyl terephthaloyl chloride and 2,5-dimethyl terephthaloyl chloride, and said isophthaloyl chloride compound is selected from the group consisting of isophthaloyl chloride and 2-methylisophthaloyl chloride.

References Cited (Backward Citations)

US3169121A Cited
US3133898A Cited
US3395119A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-04-06 1984-10-06 1985-04-07 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-04-06 1988-10-06 1989-04-07 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-04-06 1992-10-06 1993-04-07 $7700.00 Window Closed / Lapsed

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