KR890010089A - Curable Resin Composition - Google Patents

Curable Resin Composition Download PDF

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KR890010089A
KR890010089A KR1019880016354A KR880016354A KR890010089A KR 890010089 A KR890010089 A KR 890010089A KR 1019880016354 A KR1019880016354 A KR 1019880016354A KR 880016354 A KR880016354 A KR 880016354A KR 890010089 A KR890010089 A KR 890010089A
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group
resin
composition
polymerizable unsaturated
atom
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KR1019880016354A
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Korean (ko)
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KR910008608B1 (en
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오사무 이소자끼
나오즈미 이와사와
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야마다 모또조오
간사이뻬인또 가부시끼가이샤
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Priority claimed from JP31165287A external-priority patent/JP2612457B2/en
Priority claimed from JP62311653A external-priority patent/JP2609881B2/en
Application filed by 야마다 모또조오, 간사이뻬인또 가부시끼가이샤 filed Critical 야마다 모또조오
Publication of KR890010089A publication Critical patent/KR890010089A/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L57/00Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/24Crosslinking, e.g. vulcanising, of macromolecules
    • C08J3/246Intercrosslinking of at least two polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F290/00Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
    • C08F290/08Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
    • C08F290/14Polymers provided for in subclass C08G
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F299/00Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
    • C08F299/02Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L87/00Compositions of unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

내용 없음No content

Description

경화성 수지 조성물Curable Resin Composition

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (16)

중합성 불포화기 및 하기 일반식(I)의 비양자성 오늄-함유기를 함유하는 경화성 수지로 구성된 경화성 수지 조성물.Curable resin composition comprised from curable resin containing a polymerizable unsaturated group and an aprotic onium-containing group of the following general formula (I). [식중 R1은 수소원자, 또는 히드록실기, 알콕시기 또는 에스테르기 또는 할로겐 원자에 의해 임의로 치환될 수 있는 1내지 8탄소원자의 탄화수소기를 의미하고;[Wherein R 1 means a hydrogen atom or a hydrocarbon group of 1 to 8 carbon atoms which may be optionally substituted by a hydroxyl group, an alkoxy group or an ester group or a halogen atom; (여기서, Z는 질소원자 또는 인 원자를 의미하고; Y는 황원자를 의미하고; R2, R3및 R4는 동일하거나 다르며 각각 1 내지 14탄소원자의 유기기를 의미하고, R2및 R3또는 R2, R3및 R4가 함께 인접한 질소, 인 또는 황원자와 함께 헤테로 시클기를 형성 할 수 있다)를 의미한다.](Wherein Z means a nitrogen atom or a phosphorus atom; Y means a sulfur atom; R 2 , R 3 and R 4 are the same or different and each represents an organic group of 1 to 14 carbon atoms, R 2 and R 3 or R 2 , R 3 and R 4 together may form a heterocycl group with adjacent nitrogen, phosphorus or sulfur atoms.] 제1항에 있어서, 상기 수지가 겔 투과 크로마토그래피에 의해 측정된 피이크 분자량이 약 250 내지 100,000인 조성물.The composition of claim 1, wherein the resin has a peak molecular weight of about 250 to 100,000 as measured by gel permeation chromatography. 제1항에 있어서, 상기 수지가 분자당 적어도 하나의 중합성 불포화기를 갖는 조성물.The composition of claim 1 wherein said resin has at least one polymerizable unsaturated group per molecule. 제1항에 있어서, 상기 수지의 수지 고체 kg당 중합성불포화기 함량이 약 0.1 내지 10몰이고, 오늄-함유기 함량이 약 0.01 내지 5몰인 조성물.The composition of claim 1 wherein the polymerizable unsaturated group content per kg solid resin of the resin is from about 0.1 to 10 moles and the onium-containing group content is from about 0.01 to 5 moles. 제1항에 있어서, 중합성 불포화기가 적어도 아크릴로일기, 메타크릴로일기, 이타코노일기, 말레오일기, 푸마로일기, 크로토노일기, 아크릴아미도기, 메타크릴아미도기, 신나모일기, 비닐기 및 알릴기로 구성 되는 군에서 선택된 것인 조성물.The polymerizable unsaturated group is at least acryloyl group, methacryloyl group, itaconoyl group, maleoyl group, fumaroyl group, crotonoyl group, acrylamido group, methacrylamido group, cinnamoyl group, vinyl Composition selected from the group consisting of a group and an allyl group. 제1항에 있어서, 상기 수지가 아크릴, 폴리에스테르, 우레탄, 알키드, 에폭시 또는 페놀형인 조성물.The composition of claim 1 wherein the resin is acrylic, polyester, urethane, alkyd, epoxy or phenolic. (a) 중합성 불포화기 -함유 수지 및 (b) 하기 일반식(I)의 비양자성 오늄-함유기를 함유하는 경화성 수지로 구성된 경화성 수지 조성물.Curable resin composition comprised from (a) polymeric unsaturated group containing resin, and (b) curable resin containing the aprotic onium-containing group of following General formula (I). [식중 R1은 수소원자, 또는 히드록실기, 알콕시기 또는 에스테르기 또는 할로겐 원자에 의해 임의로 치완될 수 있는 1 내지 8탄소원자의 탄화수소기를 의미하고;[Wherein R 1 means a hydrogen atom or a hydrocarbon group of 1 to 8 carbon atoms which may be optionally substituted by a hydroxyl group, an alkoxy group or an ester group or a halogen atom; (여기서, Z는 질소원자 또는 인 원자를 의미하고; Y는 황원자를 의미하고; R2, R3및 R4는 동일하거나 다르며 각각 1내지 14탄소원자의 유기기를 의미하고, R2및 R3또는 R2, R3및 R4가 함께 인접한 질소, 인 또는 황원자와 함께 헤테로 시클기를 형성 할 수 있다)를 의미한다.]Wherein Z is a nitrogen atom or a phosphorus atom; Y is a sulfur atom; R 2 , R 3 and R 4 are the same or different and each represents an organic group of 1 to 14 carbon atoms, R 2 and R 3 or R 2 , R 3 and R 4 together may form a heterocycl group with adjacent nitrogen, phosphorus or sulfur atoms.] 제7항에 있어서, 수지(a)가 히드록실기를 함유하는 수지인 조성물.8. The composition of claim 7, wherein the resin (a) is a resin containing a hydroxyl group. 제7항에 있어서, 수지(a)의 피이크 분자량이 겔 투과크로마토그래피 측정으로 약 250 내지 100,000인 조성물.8. The composition of claim 7, wherein the peak molecular weight of resin (a) is about 250 to 100,000 by gel permeation chromatography measurements. 제7항에 있어서, 상기 수지가 분자당 적어도 하나의 중합성 불포화기를 갖는 조성물.8. The composition of claim 7, wherein said resin has at least one polymerizable unsaturated group per molecule. 제7항에 있어서, 수지(a)의 중합성 불포화기 함량이 수지 고체 kg당 약 0.1 내지 10몰인 조성물.8. The composition of claim 7, wherein the polymerizable unsaturated group content of resin (a) is from about 0.1 to 10 moles per kg of solid resin. 제7항에 있어서, 중합성 불포화기가 적어도 아크릴로일기, 메타크릴로일기, 이타코노일기, 말레오일기, 푸마토일기, 크로토노일기, 아크릴아미도기, 메타크릴 아미도기, 신나모일기. 비닐기 및 알릴기로 구성된 군에서 선택된 것인 조성물.8. The polymerizable unsaturated group is at least an acryloyl group, methacryloyl group, itaconoyl group, maleoyl group, fumatoyl group, crotonoyl group, acrylamido group, methacryl amido group, cinnamoyl group. Composition selected from the group consisting of vinyl and allyl groups. 제7항에 있어서, 수지(a)가 아크릴, 폴리에스테르, 우레탄, 알키드. 에폭시 또는 페놀형인 조성물.8. The resin of claim 7, wherein the resin (a) is acrylic, polyester, urethane, alkyd. Compositions that are epoxy or phenolic. 제7항에 있어서, 수지(b)가 피이크분자량이 겔 투과 크로마토그래피 측정으로 약 150 내지 100,000인 조성물.8. The composition of claim 7, wherein the resin (b) has a peak molecular weight of about 150 to 100,000 by gel permeation chromatography measurements. 제7항에 있어서, 수지(b)의 오늄-함유기 함량이 수지 고체 kg당 약 0.01 내지 5몰인 조성물.8. The composition of claim 7, wherein the onium-containing content of resin (b) is about 0.01 to 5 moles per kg solid resin. 제17항에 있어서, 수지(b)가 아크릴, 폴리에스테르 우레탄, 알키드, 에폭시 또는 페놀형인 조성물.18. The composition of claim 17, wherein the resin (b) is acrylic, polyester urethane, alkyd, epoxy or phenolic. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019880016354A 1987-12-08 1988-12-08 Hardening resin composition KR910008608B1 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP311652/87 1987-12-08
JP311653/87 1987-12-08
JP31165287A JP2612457B2 (en) 1987-12-08 1987-12-08 Curable resin and its curing method
JP62-311652 1987-12-08
JP62311653A JP2609881B2 (en) 1987-12-08 1987-12-08 Curable resin composition and curing method thereof
JP62-311653 1987-12-08

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KR890010089A true KR890010089A (en) 1989-08-05
KR910008608B1 KR910008608B1 (en) 1991-10-19

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KR1019880016354A KR910008608B1 (en) 1987-12-08 1988-12-08 Hardening resin composition

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CA (1) CA1338575C (en)
DE (1) DE3841413A1 (en)
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3914407A1 (en) * 1989-04-29 1990-10-31 Basf Ag RADIATION-SENSITIVE POLYMERS AND POSITIVE WORKING RECORDING MATERIAL
JPH07114183A (en) * 1993-10-15 1995-05-02 Sony Corp Photopolymerizable composition and formation of cured coating film pattern using the same

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4338232A (en) * 1977-12-27 1982-07-06 The Dow Chemical Company Radiation-curable resins
US4857566A (en) * 1987-04-21 1989-08-15 The Dow Chemical Company Curable latex composition, films and foams formed therefrom and method for curing the composition

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DE3841413C2 (en) 1992-04-30
KR910008608B1 (en) 1991-10-19
GB2213488B (en) 1991-11-27
GB8828256D0 (en) 1989-01-05
CA1338575C (en) 1996-09-03
GB2213488A (en) 1989-08-16
DE3841413A1 (en) 1989-06-22

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