JP2006124529A5 - - Google Patents
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- JP2006124529A5 JP2006124529A5 JP2004315358A JP2004315358A JP2006124529A5 JP 2006124529 A5 JP2006124529 A5 JP 2006124529A5 JP 2004315358 A JP2004315358 A JP 2004315358A JP 2004315358 A JP2004315358 A JP 2004315358A JP 2006124529 A5 JP2006124529 A5 JP 2006124529A5
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- polyethylene terephthalate
- ethylene glycol
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Description
本発明のポリエチレンテレフタレートは、エチレングリコールを500ppm以上含むポリエチレンテレフタレートを150℃以上の温度で30分以上加熱することにより好適に得ることが出来る。含有させるエチレングリコールはジエチレングリコールなどの縮合物を一部含んでいてもかまわない。 The polyethylene terephthalate of the present invention can be suitably obtained by heating polyethylene terephthalate containing 500 ppm or more of ethylene glycol at a temperature of 150 ° C. or more for 30 minutes or more. The ethylene glycol to be contained may contain a part of a condensate such as diethylene glycol.
(使用原料)
本発明に係るポリエチレンテレフタレートは、テレフタル酸と、エチレングリコールとを原料として製造される。テレフタル酸はモノアルコールとのエステルまたは酸無水物等、そのエステル形成性誘導体であっても良く、エチレングリコールは1塩基酸とのエステルや脱水縮合物等、そのエステル形成性誘導体であっても良い。なお、エチレングリコールを以下EGと略記することがある。
(Raw materials used)
Polyethylene terephthalate according to the present invention is produced and terephthalic acid and ethylene glycol as raw materials. Terephthalic acid may be an ester-forming derivative such as an ester or acid anhydride with monoalcohol, and ethylene glycol may be an ester-forming derivative such as an ester with monobasic acid or a dehydration condensate. . Hereinafter, ethylene glycol may be abbreviated as EG.
また、エチレングリコールとともに、トリメチレングリコール、プロピレングリコール、テトラメチレングリコール、ネオペンチルグリコール、ヘキサメチレングリコール、ドデカメチレングリコールなどの脂肪族ジオール;シクロヘキサンジメタノールなどの脂環族グリコール;ビスフェノール、ハイドロキノン、2,2−ビス(4−β-ヒドロキシエトキシフェニル)プロパン類などの芳香族ジオールなどを原料として使用することができる。
さらに本発明では、トリメシン酸、トリメチロールエタン、トリメチロールプロパン、トリメチロールメタン、ペンタエリスリトールなどの多官能性化合物を原料として使用することができる。
Further, the ethylene glycol, Application Benefits glycol, propylene glycol, tetramethylene glycol, neopentyl glycol, hexamethylene glycol, aliphatic diols, such as dodecamethylene glycol; alicyclic glycols such as cyclohexanedimethanol; bisphenol, hydroquinone, 2 , Aromatic diols such as 2-bis (4-β-hydroxyethoxyphenyl) propanes can be used as raw materials.
Furthermore, in this invention, polyfunctional compounds, such as a trimesic acid, a trimethylol ethane, a trimethylol propane, a trimethylol methane, a pentaerythritol, can be used as a raw material.
このようなスラリーにはテレフタル酸またはそのエステル形成性誘導体1モルに対して、通常1.005〜1.4モル、好ましくは1.01〜1.3モルのエチレングリコールまたはそのエステル形成性誘導体が含まれる。
エステル化反応は連続式、バッチ式で行われ、一段としても多段としてもよい。エステル化反応は好ましくは2個以上のエステル化反応器を直列に連結した装置を用いてエチレングリコールが還流する条件下で、反応によって生成した水を精留塔で系外に除去しながら行う。
In such a slurry, 1.005 to 1.4 mol, preferably 1.01 to 1.3 mol of ethylene glycol or an ester-forming derivative thereof is usually used with respect to 1 mol of terephthalic acid or an ester-forming derivative thereof. included.
The esterification reaction is carried out continuously or batchwise, and may be one stage or multistage. The esterification reaction is preferably carried out using an apparatus in which two or more esterification reactors are connected in series under conditions where ethylene glycol is refluxed while removing water generated by the reaction from the system using a rectification column.
重縮合反応は、1段階で行ってもよく、複数段階に分けて行ってもよい。例えば、重縮合反応が複数段階で行われる場合には、第1段目の重縮合反応は、反応温度が250〜290℃、好ましくは260〜280℃、圧力が0.07〜0.003MPa(500〜20Torr)、好ましくは0.03〜0.004MPa(200〜30Torr)の条件下で行われ、最終段の重縮合反応は、反応温度が265〜300℃、好ましくは270〜295℃、圧力が1〜0.01kPa(10〜0.1Torr)、好ましくは0.7〜0.07kPa(5〜0.5Torr)の条件下で行われる。 The polycondensation reaction may be performed in one stage or may be performed in a plurality of stages. For example, when the polycondensation reaction is performed in a plurality of stages, the first stage polycondensation reaction has a reaction temperature of 250 to 290 ° C., preferably 260 to 280 ° C., and a pressure of 0.07 to 0.003 MPa ( 500 to 20 Torr), preferably 0.03 to 0.004 MPa (200 to 30 Torr). The final stage polycondensation reaction is performed at a reaction temperature of 265 to 300 ° C, preferably 270 to 295 ° C, pressure Is carried out under conditions of 1 to 0.01 kPa (10 to 0.1 Torr), preferably 0.7 to 0.07 kPa (5 to 0.5 Torr).
Claims (4)
エチレングリコールの含有量が40ppm以上であり、エチレングリコールとテレフタル酸の線状三量体(I)含有量が80ppm以上であり、線状二量体(II)含有量が80ppm以上であり、ビス(2−ヒドロキシエチル)テレフタレート(III)含有量が60ppm以上であり、環状三量体量(IV)含有量が0.40wt%以下であるポリエチレンテレフタレート。
The ethylene glycol content is 40 ppm or more, the ethylene trimer and terephthalic acid linear trimer (I) content is 80 ppm or more, the linear dimer (II) content is 80 ppm or more, bis Polyethylene terephthalate having a (2-hydroxyethyl) terephthalate (III) content of 60 ppm or more and a cyclic trimer content (IV) content of 0.40 wt% or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004315358A JP2006124529A (en) | 2004-10-29 | 2004-10-29 | Polyethylene terephthalate and hollow molded product formed out of the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004315358A JP2006124529A (en) | 2004-10-29 | 2004-10-29 | Polyethylene terephthalate and hollow molded product formed out of the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2006124529A JP2006124529A (en) | 2006-05-18 |
JP2006124529A5 true JP2006124529A5 (en) | 2007-12-13 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004315358A Pending JP2006124529A (en) | 2004-10-29 | 2004-10-29 | Polyethylene terephthalate and hollow molded product formed out of the same |
Country Status (1)
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JP (1) | JP2006124529A (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3470304B2 (en) * | 1994-10-20 | 2003-11-25 | 東洋紡績株式会社 | Polyester production method |
JP3465764B2 (en) * | 1995-01-25 | 2003-11-10 | 東洋紡績株式会社 | Polyester and method for producing the same |
JP4167159B2 (en) * | 2002-10-02 | 2008-10-15 | 三菱化学株式会社 | Production method of polyester resin |
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2004
- 2004-10-29 JP JP2004315358A patent/JP2006124529A/en active Pending
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