JP2001261798A5 - - Google Patents

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JP2001261798A5
JP2001261798A5 JP2000082942A JP2000082942A JP2001261798A5 JP 2001261798 A5 JP2001261798 A5 JP 2001261798A5 JP 2000082942 A JP2000082942 A JP 2000082942A JP 2000082942 A JP2000082942 A JP 2000082942A JP 2001261798 A5 JP2001261798 A5 JP 2001261798A5
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lactone
reaction
weight
based polyol
polyol
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JP2000082942A
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Japanese (ja)
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JP5121085B2 (en
JP2001261798A (en
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Priority claimed from JP2000082942A external-priority patent/JP5121085B2/en
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Publication of JP2001261798A5 publication Critical patent/JP2001261798A5/ja
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【特許請求の範囲】
【請求項1】 多価アルコール又は多価アミンからなる活性水素を有する開始剤に対し、有機スズ系触媒であるオクチル酸スズ又はジブチルスズオキサイド又はジブチルスズジラウレート0.0001〜0.001重量%の存在下で、ラクトンモノマーを反応温度165℃〜175℃で開環重合反応させ、ラクトンモノマーが0.5重量%以下になった時点で反応を終了させて得られるラクトン系ポリオールで、そのポリオール中の反応副生成物である環状エステル化合物が、トータル量で0.5重量%以下であることを特徴とするラクトン系ポリオールの製造方法。
【請求項2】 請求項1の製造方法で得られたラクトン系ポリオールを用いた事を特徴とするポリウレタン樹脂。
[Claims]
1. An organotin-based catalyst such as tin octylate or dibutyltin oxide or dibutyltin dilaurate in an amount of 0.0001 to 0.001% by weight based on an initiator having active hydrogen comprising a polyhydric alcohol or a polyhydric amine. A lactone-based polyol obtained by subjecting a lactone monomer to a ring-opening polymerization reaction at a reaction temperature of 165 ° C. to 175 ° C. and terminating the reaction when the lactone monomer becomes 0.5% by weight or less, the reaction in the polyol A method for producing a lactone-based polyol, wherein the total amount of the by-product cyclic ester compound is 0.5% by weight or less.
2. A polyurethane resin using the lactone-based polyol obtained by the production method according to claim 1.

即ち、本発明は、多価アルコール又は多価アミンからなる活性水素を有する開始剤に対し、有機スズ系触媒であるオクチル酸スズ又はジブチルスズオキサイド又はジブチルスズジラウレート0.0001〜0.001重量%の存在下で、ラクトンモノマーを反応温度165℃〜175℃で開環重合反応させ、ラクトンモノマーが0.5重量%以下になった時点で反応を終了させて得られるラクトン系ポリオールで、そのポリオール中の反応副生成物である環状エステル化合物が、トータル量で0.5重量%以下であることを特徴とするラクトン系ポリオールの製造方法を提供するものである。また、このポリウレタン樹脂用ラクトンポリオールを用いることにより強度物性低下、ブレード抑制や糸切れ防止を可能にした優れたウレタン樹脂を提供するものである。 That is, the present invention relates to the presence of 0.0001 to 0.001% by weight of an organotin-based catalyst, tin octylate or dibutyltin oxide or dibutyltin dilaurate, based on an initiator having active hydrogen composed of a polyhydric alcohol or a polyamine. A lactone-based polyol obtained by subjecting a lactone monomer to a ring-opening polymerization reaction at a reaction temperature of 165 ° C. to 175 ° C. and terminating the reaction when the lactone monomer becomes 0.5% by weight or less, An object of the present invention is to provide a method for producing a lactone-based polyol, wherein the total amount of the cyclic ester compound as a reaction by-product is 0.5% by weight or less. It is another object of the present invention to provide an excellent urethane resin capable of reducing strength properties, suppressing blades and preventing yarn breakage by using the lactone polyol for a polyurethane resin.

本発明の触媒としては、例えば、オクチル酸スズ、ジブチルスズオキサイド、ジブチルスズジラウレートが挙げられる。無機系スズ触媒は、有機系スズ触媒に比べ、活性が強く、開環重合のコントロールが困難である。また、ラクトン系ポリオールを溶融状態で貯蔵した場合、その活性により、重合反応の進行および環状エステル化合物の生成を引き起こし、増加させてしまうため、有機スズ系触媒の方がより好ましい。

The catalyst of the present invention, for example, tin octylate, dibutyltin oxide, and dibutyltin dilaurate. Inorganic tin catalysts have higher activity than organic tin catalysts, and it is difficult to control ring-opening polymerization. In addition, when the lactone-based polyol is stored in a molten state, the activity of the lactone-based polyol causes the polymerization reaction and the formation of a cyclic ester compound to be caused to increase, so that an organotin-based catalyst is more preferable.

JP2000082942A 2000-03-23 2000-03-23 Method for producing lactone-based polyol and polyurethane resin using the same Expired - Lifetime JP5121085B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000082942A JP5121085B2 (en) 2000-03-23 2000-03-23 Method for producing lactone-based polyol and polyurethane resin using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000082942A JP5121085B2 (en) 2000-03-23 2000-03-23 Method for producing lactone-based polyol and polyurethane resin using the same

Publications (3)

Publication Number Publication Date
JP2001261798A JP2001261798A (en) 2001-09-26
JP2001261798A5 true JP2001261798A5 (en) 2007-04-05
JP5121085B2 JP5121085B2 (en) 2013-01-16

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JP2000082942A Expired - Lifetime JP5121085B2 (en) 2000-03-23 2000-03-23 Method for producing lactone-based polyol and polyurethane resin using the same

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Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2004087783A1 (en) * 2003-03-31 2006-06-29 ダイセル化学工業株式会社 Lactone polyester polyol and method for producing the same
WO2006009157A1 (en) * 2004-07-23 2006-01-26 Daicel Chemical Industries, Ltd. Process for production of polylactone polyols, polylactone polyol compositions, and compositions for polyurethane resins
JP2021008605A (en) * 2019-06-28 2021-01-28 花王株式会社 Modified hydroxycarboxylic acid polymer

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3791566B2 (en) * 1997-05-14 2006-06-28 ダイセル化学工業株式会社   Method for producing lactone polymer

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