JP2011178936A5 - - Google Patents

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JP2011178936A5
JP2011178936A5 JP2010046026A JP2010046026A JP2011178936A5 JP 2011178936 A5 JP2011178936 A5 JP 2011178936A5 JP 2010046026 A JP2010046026 A JP 2010046026A JP 2010046026 A JP2010046026 A JP 2010046026A JP 2011178936 A5 JP2011178936 A5 JP 2011178936A5
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mol
dihydroxybiphenyl
hours
liquid crystalline
crystalline polyester
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JP2010046026A
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Japanese (ja)
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JP5504978B2 (en
JP2011178936A (en
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合成例9 液晶性ポリエステル(B−2)の合成
撹拌翼、留出管を備えた5Lの反応容器にp−ヒドロキシ安息香酸759.7g(5.5モル)、4,4’−ジヒドロキシビフェニル419.0g(2.25モル)、テレフタル酸560.7g(3.375モル(4,4’−ジヒドロキシビフェニルの1.5倍モル当量))、酢酸ナトリウム0.30g(得られる液晶性ポリエステルの0.02重量%)および無水酢酸1051.5g(系の全フェノール性ヒドロキシ基に対して1.03当量)を仕込み、窒素ガス雰囲気下で撹拌しながら145℃で2時間反応させた後、395℃まで1℃/分で昇温した。その後、395℃で0.5時間保持し、1.5時間で1.0mmHg(133Pa)に減圧し、更に60分間反応を続け、トルクが21kg・cmに到達したところで重縮合を完了させた。次に反応容器内を0.1MPaに加圧し、直径10mmの円形吐出口を1個持つ口金を経由してポリマーをストランド状物に吐出し、カッターによりペレタイズした。
Synthesis Example 9 Synthesis of Liquid Crystalline Polyester (B-2) In a 5 L reaction vessel equipped with a stirring blade and a distillation tube, 759.7 g (5.5 mol) of p-hydroxybenzoic acid and 4,4′-dihydroxybiphenyl 419 0.0 g (2.25 mol), 560.7 g of terephthalic acid (3.375 mol (1.5 times the molar equivalent of 4,4′-dihydroxybiphenyl)), 0.30 g of sodium acetate (0 of the resulting liquid crystalline polyester) 0.02 wt%) and 1051.5 g of acetic anhydride (1.03 equivalents based on the total phenolic hydroxy groups in the system) were reacted at 145 ° C. for 2 hours with stirring under a nitrogen gas atmosphere, and then 395 ° C. The temperature was raised at 1 ° C./min. Thereafter, the temperature was maintained at 395 ° C. for 0.5 hour, the pressure was reduced to 1.0 mmHg (133 Pa) in 1.5 hours, and the reaction was further continued for 60 minutes. When the torque reached 21 kg · cm, the polycondensation was completed. Next, the inside of the reaction vessel was pressurized to 0.1 MPa, the polymer was discharged to a strand through a base having one circular discharge port having a diameter of 10 mm, and pelletized by a cutter.

JP2010046026A 2010-03-03 2010-03-03 Liquid crystalline polyester and liquid crystalline polyester composition Expired - Fee Related JP5504978B2 (en)

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JP2010046026A JP5504978B2 (en) 2010-03-03 2010-03-03 Liquid crystalline polyester and liquid crystalline polyester composition

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Application Number Priority Date Filing Date Title
JP2010046026A JP5504978B2 (en) 2010-03-03 2010-03-03 Liquid crystalline polyester and liquid crystalline polyester composition

Publications (3)

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JP2011178936A JP2011178936A (en) 2011-09-15
JP2011178936A5 true JP2011178936A5 (en) 2013-01-24
JP5504978B2 JP5504978B2 (en) 2014-05-28

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JP2010046026A Expired - Fee Related JP5504978B2 (en) 2010-03-03 2010-03-03 Liquid crystalline polyester and liquid crystalline polyester composition

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Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105358657A (en) 2013-06-07 2016-02-24 提克纳有限责任公司 High strength thermotropic liquid crystalline polymer
CN105837803B (en) * 2016-02-01 2017-05-31 金发科技股份有限公司 A kind of liquid crystal polyester and the moulding compound being made from it and its application
CN113604009B (en) * 2021-09-08 2022-11-15 宁波聚嘉新材料科技有限公司 High-toughness liquid crystal polymer film and preparation method thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60106832A (en) * 1983-11-15 1985-06-12 Teijin Ltd Fully aromatic polyester and its production
JPS6395224A (en) * 1986-10-08 1988-04-26 Sumitomo Chem Co Ltd Production of crystalline aromatic polyester
JP3087430B2 (en) * 1992-04-06 2000-09-11 住友化学工業株式会社 Solid state polymerization of powdery polymer
JP4770100B2 (en) * 2001-09-28 2011-09-07 住友化学株式会社 Liquid crystalline polyester resin composition for connectors and connector
JP3848880B2 (en) * 2002-01-25 2006-11-22 新日本石油化学株式会社 Method for producing blister-resistant liquid crystal polyester composition

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