JP2010031099A5 - - Google Patents

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JP2010031099A5
JP2010031099A5 JP2008192991A JP2008192991A JP2010031099A5 JP 2010031099 A5 JP2010031099 A5 JP 2010031099A5 JP 2008192991 A JP2008192991 A JP 2008192991A JP 2008192991 A JP2008192991 A JP 2008192991A JP 2010031099 A5 JP2010031099 A5 JP 2010031099A5
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hour
acid
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JP2008192991A
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JP2010031099A (en
JP5469828B2 (en
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《参考例1:ポリエステルアミド樹脂(I)の合成例》
機械式撹拌装置、温度計、脱水トラップ、コンデンサー及び乾燥窒素ガス導入口を備えたガラス製反応器に、炭素数36のダイマー酸〔水添二量体化脂肪酸、ダイマー酸含有率98%、クローダ(株)製プライポール1009〕2部、アゼライン酸188部、ピペラジン158部を入れ、3時間かけて230℃まで昇温した。このとき約150℃付近から縮合水が流出してきた。230℃で150mmHgまで減圧し、1時間保持した後にサンプリングしたところ酸価は30であった。この反応混合物に更にアゼライン酸429部、シクロヘキサン−1,4−ジメタノール341部を添加したところ、内温が150℃まで低下した。再度250℃まで昇温し、5mmHgで1時間、2mmHgで1時間、1〜2mmHgで3時間反応させ、安定剤であるN,N−ヘキサメチレンビス(3,5−ジ−t−ブチル−4−ヒドロキシシンナマイド(チバスペシャリティケミカルズ製、イルガノックス1098)1部を添加した。反応混合物をサンプリングして粘度を測定したところ、230℃において60Pa・sであったため、反応を終了し、反応混合物をテフロン(登録商標)バット上に取り出して、目的とするポリエステルアミド樹脂(I)を得た。
<< Reference Example 1: Synthesis Example of Polyesteramide Resin (I) >>
In a glass reactor equipped with a mechanical stirrer, thermometer, dehydration trap, condenser and dry nitrogen gas inlet, a dimer acid having 36 carbon atoms (hydrogenated dimerized fatty acid, dimer acid content 98%, clada (Plypole 1009, manufactured by Co., Ltd.) 2 parts, 188 parts azelaic acid, and 158 parts piperazine were added and heated to 230 ° C. over 3 hours. At this time, the condensed water flowed out from about 150 ° C. When the pressure was reduced to 150 mmHg at 230 ° C. and held for 1 hour, the acid value was 30 when sampled. When 429 parts of azelaic acid and 341 parts of cyclohexane-1,4-dimethanol were further added to this reaction mixture, the internal temperature decreased to 150 ° C. The temperature was raised again to 250 ° C., and the mixture was reacted at 5 mmHg for 1 hour, 2 mmHg for 1 hour, and 1-2 mmHg for 3 hours, and the stabilizer N, N-hexamethylenebis (3,5-di-t-butyl-4 -1 part of hydroxycinnamide (manufactured by Ciba Specialty Chemicals, Irganox 1098) was added, and the viscosity was measured by sampling the reaction mixture. The product was taken out on a Teflon (registered trademark) vat to obtain a target polyesteramide resin (I).

JP2008192991A 2008-07-28 2008-07-28 Polyesteramide resin composition Expired - Fee Related JP5469828B2 (en)

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Application Number Priority Date Filing Date Title
JP2008192991A JP5469828B2 (en) 2008-07-28 2008-07-28 Polyesteramide resin composition

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Application Number Priority Date Filing Date Title
JP2008192991A JP5469828B2 (en) 2008-07-28 2008-07-28 Polyesteramide resin composition

Publications (3)

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JP2010031099A JP2010031099A (en) 2010-02-12
JP2010031099A5 true JP2010031099A5 (en) 2011-07-07
JP5469828B2 JP5469828B2 (en) 2014-04-16

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JP2008192991A Expired - Fee Related JP5469828B2 (en) 2008-07-28 2008-07-28 Polyesteramide resin composition

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Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7271146B2 (en) * 2017-12-28 2023-05-11 日鉄ケミカル&マテリアル株式会社 Dimer diamine composition, method for producing the same, and resin film
WO2019147457A2 (en) * 2018-01-23 2019-08-01 Eastman Chemical Company Novel polyestermides, processes for the preparation thereof, and polyesteramide compositions
CN109742343A (en) * 2018-12-20 2019-05-10 中南民族大学 High-valued electrode active material of nylon engineering plastic and preparation method thereof
CN113767133A (en) * 2019-04-30 2021-12-07 巴斯夫欧洲公司 Flame-retardant polyamide

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10134816A (en) * 1996-03-29 1998-05-22 Sekisui Chem Co Ltd Nonaqueous electrolyte secondary battery
JP2000048805A (en) * 1998-07-29 2000-02-18 Sekisui Chem Co Ltd Manufacture of positive electrode or negative electrode for nonaqueous electrolyte secondary battery
JP2002003601A (en) * 2000-06-23 2002-01-09 T & K Toka Co Ltd Polyesteramide copolymer and adhesive composition for laminate using it

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