JP2003137966A5 - - Google Patents

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Publication number
JP2003137966A5
JP2003137966A5 JP2001334468A JP2001334468A JP2003137966A5 JP 2003137966 A5 JP2003137966 A5 JP 2003137966A5 JP 2001334468 A JP2001334468 A JP 2001334468A JP 2001334468 A JP2001334468 A JP 2001334468A JP 2003137966 A5 JP2003137966 A5 JP 2003137966A5
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JP
Japan
Prior art keywords
nitrogen atoms
polyisocyanate
atoms constituting
curing agent
group
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Pending
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JP2001334468A
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Japanese (ja)
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JP2003137966A (en
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Priority to JP2001334468A priority Critical patent/JP2003137966A/en
Priority claimed from JP2001334468A external-priority patent/JP2003137966A/en
Publication of JP2003137966A publication Critical patent/JP2003137966A/en
Publication of JP2003137966A5 publication Critical patent/JP2003137966A5/ja
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Claims (5)

脂肪族炭化水素の炭素に結合したイソシアネート基を2個以上有するポリイソシアネート(A)と、炭素原子数6〜20のモノアルコール(B)とを反応せしめた後、未反応成分を除去して得られる数平均分子量400〜1000のポリイソシアネート混合物からなる硬化剤であって、該ポリイソシアネート混合物中に含有される全窒素原子に対する、アロファネート基を構成する窒素原子の割合が40%以上、イソシアネート基を構成する窒素原子の割合が40%以上、ウレタン結合を構成する窒素原子の割合が10%以下、イソシアヌレート基を構成する窒素原子の割合が5%以下、ウレトジオン基を構成する窒素原子の割合が5%以下であることを特徴とする、ポリイソシアネート硬化剤。And polyisocyanates having Lee isocyanate group attached to a carbon of the aliphatic hydrocarbon at least two (A), after reacted with monoalcohol having 6 to 20 carbon atoms (B), to remove unreacted components A curing agent comprising a polyisocyanate mixture having a number average molecular weight of 400 to 1000 obtained in this manner, wherein the ratio of nitrogen atoms constituting allophanate groups to the total nitrogen atoms contained in the polyisocyanate mixture is 40% or more, isocyanate The proportion of nitrogen atoms constituting the group is 40% or more, the proportion of nitrogen atoms constituting the urethane bond is 10% or less, the proportion of nitrogen atoms constituting the isocyanurate group is 5% or less, and the nitrogen atoms constituting the uretdione group A polyisocyanate curing agent having a ratio of 5% or less. ポリイソシアネート(A)が、イソシアネート基結合した脂肪族炭化水素の炭素原子数が4〜15のジイソシアネートである、請求項1記載のポリイソシアネート硬化剤。The polyisocyanate curing agent according to claim 1, wherein the polyisocyanate (A) is a diisocyanate having 4 to 15 carbon atoms of an aliphatic hydrocarbon to which an isocyanate group is bonded. ポリイソシアネート混合物中に含有される全窒素原子に対する、アロファネート基を構成する窒素原子の割合が42%以上、イソシアネート基を構成する窒素原子の割合が42%以上、ウレタン結合を構成する窒素原子の割合が10%以下、イソシアヌレート基を構成する窒素原子の割合が1%以下、ウレトジオン基を構成する窒素原子の割合が5%以下である、請求項2記載のポリイソシアネート硬化剤。  The ratio of nitrogen atoms constituting the allophanate group to 42% or more, the ratio of nitrogen atoms constituting the isocyanate group to 42% or more, and the ratio of nitrogen atoms constituting the urethane bond to the total nitrogen atoms contained in the polyisocyanate mixture The polyisocyanate curing agent according to claim 2, wherein the proportion of nitrogen atoms constituting the isocyanurate group is 1% or less and the proportion of nitrogen atoms constituting the uretdione group is 5% or less. ポリイソシアネート混合物が、カルボン酸金属塩とクロロカルボン酸とを反応させてなるアロファネート化触媒、又は、2−ヒドロキシルアルキル・トリアルキルアンモニウム・カルボン酸塩とクロロカルボン酸とを反応させてなるアロファネート化触媒の存在下で、ポリイソシアネート(A)とモノアルコール(B)とを反応せしめた後、未反応成分を除去して得られたものである、請求項2記載のポリイソシアネート硬化剤。  Allophanate catalyst in which polyisocyanate mixture reacts carboxylic acid metal salt and chlorocarboxylic acid, or allophanate catalyst in which 2-hydroxylalkyl / trialkylammonium carboxylate and chlorocarboxylic acid react The polyisocyanate curing agent according to claim 2, wherein the polyisocyanate curing agent is obtained by reacting the polyisocyanate (A) with the monoalcohol (B) in the presence of and then removing unreacted components. ポリイソシアネート混合物が、カルボン酸金属塩とクロロカルボン酸とを反応させてなるアロファネート化触媒、又は、2−ヒドロキシルアルキル・トリアルキルアンモニウム・カルボン酸塩とクロロカルボン酸とを反応させてなるアロファネート化触媒の存在下で、ポリイソシアネート(A)とモノアルコール(B)とを反応せしめた後、蒸留により未反応成分を除去して得られたものである、請求項3記載のポリイソシアネート硬化剤。  Allophanate catalyst in which polyisocyanate mixture reacts carboxylic acid metal salt and chlorocarboxylic acid, or allophanate catalyst in which 2-hydroxylalkyl / trialkylammonium carboxylate and chlorocarboxylic acid react The polyisocyanate curing agent according to claim 3, which is obtained by reacting the polyisocyanate (A) with the monoalcohol (B) in the presence of and then removing unreacted components by distillation.
JP2001334468A 2001-10-31 2001-10-31 Polyisocyanate curing agent Pending JP2003137966A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001334468A JP2003137966A (en) 2001-10-31 2001-10-31 Polyisocyanate curing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001334468A JP2003137966A (en) 2001-10-31 2001-10-31 Polyisocyanate curing agent

Publications (2)

Publication Number Publication Date
JP2003137966A JP2003137966A (en) 2003-05-14
JP2003137966A5 true JP2003137966A5 (en) 2005-06-30

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ID=19149590

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001334468A Pending JP2003137966A (en) 2001-10-31 2001-10-31 Polyisocyanate curing agent

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JP (1) JP2003137966A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0617366B1 (en) * 2005-10-21 2018-01-23 Asahi Kasei Chemicals Corporation POLYOSOCYANATE COMPOSITION AND COATING COMPOSITION
JP5334361B2 (en) * 2006-07-21 2013-11-06 旭化成ケミカルズ株式会社 Polyisocyanate composition and coating composition
JP5445451B2 (en) * 2008-04-24 2014-03-19 日本ポリウレタン工業株式会社 Polyisocyanate composition and two-component coating composition using the same
JP5499474B2 (en) * 2008-12-26 2014-05-21 日本ポリウレタン工業株式会社 Curing agent composition for two-component curable paint
CN109942791A (en) * 2019-02-22 2019-06-28 上海稻畑精细化工有限公司 A kind of preparation process of polyurethane curing agent
CN111072917B (en) * 2020-01-02 2021-06-29 万华化学集团股份有限公司 Polyisocyanate composition with stable storage and preparation method thereof

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