Polymer compositions and substrates for high temperature transparent conductive film applications

US2017190903A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017190903-A1
Application numberUS-201615285767-A
CountryUS
Kind codeA1
Filing dateOct 5, 2016
Priority dateNov 24, 2015
Publication dateJul 6, 2017
Grant date

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Described are polymer compositions that include a blend of copolyester polymers based on monomers that include on terephthalic acid (TPA), isophthalic acid (IPA) and 1,4-cyclohexanedimethanol (CHDM), wherein the blend includes a first copolyester that is semi-crystalline and a second copolyester that is amorphous; and films made from the polymer compositions useful for transparent high temperature conductive film applications.

First claim

Opening claim text (preview).

We claim: 1 . A polymer composition comprising a blend of a first PCTA copolyester and a second PCTA copolyester, said first PCTA copolyester comprising: (a) diacid residues comprising from about 90 to about 99 mole percent of terephthalic acid (TPA) residues and from about 1 to about 10 mole percent isophthalic acid (IPA) residues; and (b) diol residues comprising at least 85 mole percent of 1,4-cyclohexanedimethanol (CHDM) residues, wherein the first PCTA copolyester comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues; said second PCTA copolyester comprising: (a) diacid residues comprising from about 60 to about 90 mole percent of TPA residues and from about 10 to about 40 mole percent IPA residues; and (b) diol residues comprising at least 85 mole percent of CHDM residues, wherein the second PCTA copolyester comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues; wherein the first PCTA copolyester is semi-crystalline; wherein the second PCTA copolyester is amorphous; and wherein the blend comprises diacid residues comprising from about 5 to about 20 net mole percent of IPA residues, wherein the blend comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues. 2 . The polymer composition according to claim 1 , wherein the first PCTA copolyester comprises diacid residues comprising from 3 to 7 mole percent IPA residues. 3 . The polymer composition according to claim 2 , wherein the second PCTA copolyester comprises diacid residues comprising from 20 to 30 mole percent IPA residues. 4 . The polymer composition according to claim 3 , wherein the first PCTA copolyester and second PCTA copolyester each comprise diol residues comprising 100 mole percent CHDM residues. 5 . The polymer composition according to claim 1 , wherein the first PCTA copolyester has a degree of crystallinity of about 40% or greater. 6 . The polymer composition according to claim 1 , wherein the second PCTA copolyester is capable of being crystallized by heating or stretching. 7 . The polymer composition according to claim 1 , wherein the blend comprises diacid residues comprising from about 7 to about 12 net mole percent of IPA residues, wherein the blend comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues. 8 . The polymer composition according to claim 1 , wherein the blend comprises the first PCTA polyester in an amount from about 70 to about 80 wt % and the second PCTA polyester in an amount from about 20 to about 30 wt %. 9 . The polymer composition according to claim 1 , wherein the blend comprises less than 2 wt % of any additional additives. 10 . The polymer composition according to claim 1 , wherein the blend has a T g of at least 85° C., and a T m of at least 255° C. 11 . A polyester film comprising a melt formed polyester blend, wherein said polyester blend comprises a first PCTA copolyester and a second PCTA copolyester, said first PCTA copolyester comprising: (a) diacid residues comprising from about 90 to about 99 mole percent of terephthalic acid (TPA) residues and from about 1 to about 10 mole percent isophthalic acid (IPA) residues; and (b) diol residues comprising at least 85 mole percent of 1,4-cyclohexanedimethanol (CHDM) residues, wherein the first PCTA copolyester comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues; said second PCTA copolyester comprising: (a) diacid residues comprising from about 60 to about 90 mole percent of TPA residues and from about 10 to about 40 mole percent IPA residues; and (b) diol residues comprising at least 85 mole percent of CHDM residues, wherein the second PCTA copolyester comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues; wherein the first PCTA copolyester is semi-crystalline; wherein the second PCTA copolyester is amorphous; wherein said blend comprises diacid residues comprising from about 5 to about 20 net mole percent of IPA residues, wherein the blend comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues; and wherein the film has a thickness in the range from about 25 to about 250 microns. 12 . The polyester film according to claim 11 , wherein the film has an IV greater than 0.7 dL/g. 13 . The polyester film according to claim 11 , wherein said polyester film is biaxially oriented and has a haze of less than 1%. 14 . The polyester film according to claim 13 , wherein the polyester film is capable of being annealed at a temperature of 150° C. for 90 minutes and maintaining a haze of less than 1%. 15 . The polyester film according to claim 11 , further comprising an ITO coating and having a sheet resistance of less than about 100 Ω/□. 16 . A method of making a biaxially oriented polyester film, said method comprising blending a first PCTA copolyester and a second PCTA copolyester; forming a melt processable polymer composition from the blend; melt forming the melt processable polymer composition to form a sheet; and biaxially stretching the sheet to form a film, wherein said polyester blend comprises a first PCTA copolyester and a second PCTA copolyester, said first PCTA copolyester comprising: (a) diacid residues comprising from about 90 to about 99 mole percent of terephthalic acid (TPA) residues and from about 1 to about 10 mole percent isophthalic acid (IPA) residues; and (b) diol residues comprising at least 85 mole percent of 1,4-cyclohexanedimethanol (CHDM) residues, wherein the first PCTA copolyester comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues; said second PCTA copolyester comprising: (a) diacid residues comprising from about 60 to about 90 mole percent of TPA residues and from about 10 to about 40 mole percent IPA residues; and (b) diol residues comprising at least 90 mole percent of CHDM residues, wherein the second PCTA copolyester comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues; wherein the first PCTA copolyester is semi-crystalline; wherein the second PCTA copolyester is amorphous; wherein said blend comprises diacid residues comprising from about 5 to about 20 net mole percent of IPA residues, wherein the blend comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues. 17 . The method according to claim 16 , wherein the blend comprises diacid residues comprising from about 7 to about 12 net mole percent of IPA residues, wherein the blend comprises a total of 100 mole percent diacid residues and a total of 100 mole percent diol residues. 18 . The method according to claim 16 , wherein the melt forming step comprises extruding the blend at a temperature at or below 580° F. (304° C.) using an extruder, and wherein the motor load on the extruder is lower for the blend compared to extruding only the first PCTA polymer under similar conditions. 19 . The method according to claim 16 , wherein the polyester film has a haze of less than 1%. 20 . The method according to claim 19 , wherein the polyester film is capable of being annealed at a temperature of 150° C. for 90 minutes and maintaining a haze of less than 1%.

Assignees

Inventors

Classifications

  • Use of polyesters {or derivatives thereof}, as moulding material · CPC title

  • characterised by the choice of material · CPC title

  • Polyesters derived from dicarboxylic acids and dihydroxy compounds (C08J2467/06 takes precedence) · CPC title

  • Combinations of extrusion moulding with other shaping operations · CPC title

  • C08L67/02Primary

    Polyesters derived from dicarboxylic acids and dihydroxy compounds (C08L67/06 takes precedence) · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US2017190903A1 cover?
Described are polymer compositions that include a blend of copolyester polymers based on monomers that include on terephthalic acid (TPA), isophthalic acid (IPA) and 1,4-cyclohexanedimethanol (CHDM), wherein the blend includes a first copolyester that is semi-crystalline and a second copolyester that is amorphous; and films made from the polymer compositions useful for transparent high temperat…
Who is the assignee on this patent?
Eastman Chem Co
What technology area does this patent fall under?
Primary CPC classification C08L67/02. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jul 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).