KR830005273A - 페놀 발포체를 안정화시키기 위한 폴리옥시알킬렌 계면 활성제의 금속 촉매접속 제조법 - Google Patents
페놀 발포체를 안정화시키기 위한 폴리옥시알킬렌 계면 활성제의 금속 촉매접속 제조법 Download PDFInfo
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- KR830005273A KR830005273A KR1019810000178A KR810000178A KR830005273A KR 830005273 A KR830005273 A KR 830005273A KR 1019810000178 A KR1019810000178 A KR 1019810000178A KR 810000178 A KR810000178 A KR 810000178A KR 830005273 A KR830005273 A KR 830005273A
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- Prior art keywords
- acid
- maleate
- peroxide
- iii
- ferrocene
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- 229910052751 metal Inorganic materials 0.000 title claims 6
- 239000002184 metal Substances 0.000 title claims 6
- 239000006260 foam Substances 0.000 title claims 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 title claims 3
- 239000004094 surface-active agent Substances 0.000 title claims 3
- 230000003197 catalytic effect Effects 0.000 title 1
- 230000000087 stabilizing effect Effects 0.000 title 1
- 239000002253 acid Substances 0.000 claims 9
- 238000000034 method Methods 0.000 claims 6
- 239000003054 catalyst Substances 0.000 claims 5
- 239000000178 monomer Substances 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 5
- 229920002554 vinyl polymer Polymers 0.000 claims 5
- -1 hydroxide peroxide Chemical class 0.000 claims 4
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 claims 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims 3
- GAYAMOAYBXKUII-UHFFFAOYSA-L cobalt(2+);dibenzoate Chemical compound [Co+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 GAYAMOAYBXKUII-UHFFFAOYSA-L 0.000 claims 3
- 238000005187 foaming Methods 0.000 claims 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- ZKXWKVVCCTZOLD-UHFFFAOYSA-N copper;4-hydroxypent-3-en-2-one Chemical group [Cu].CC(O)=CC(C)=O.CC(O)=CC(C)=O ZKXWKVVCCTZOLD-UHFFFAOYSA-N 0.000 claims 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 150000002978 peroxides Chemical class 0.000 claims 2
- 239000005011 phenolic resin Substances 0.000 claims 2
- 229920001568 phenolic resin Polymers 0.000 claims 2
- 238000006116 polymerization reaction Methods 0.000 claims 2
- 239000000376 reactant Substances 0.000 claims 2
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 claims 2
- QMWZWSKVFJAAAA-SREVYHEPSA-N (Z)-4-(2-methylhexan-2-yloxy)-4-oxobut-2-enoic acid Chemical compound CCCCC(C)(C)OC(=O)\C=C/C(O)=O QMWZWSKVFJAAAA-SREVYHEPSA-N 0.000 claims 1
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 claims 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 claims 1
- FXLKYDLHIKYUAB-UHFFFAOYSA-N 3-oxobutanoic acid;vanadium Chemical compound [V].CC(=O)CC(O)=O FXLKYDLHIKYUAB-UHFFFAOYSA-N 0.000 claims 1
- YMCIVAPEOZDEGH-UHFFFAOYSA-N 5-chloro-2,3-dihydro-1h-indole Chemical compound ClC1=CC=C2NCCC2=C1 YMCIVAPEOZDEGH-UHFFFAOYSA-N 0.000 claims 1
- 239000004342 Benzoyl peroxide Substances 0.000 claims 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims 1
- 239000004604 Blowing Agent Substances 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- 229910021577 Iron(II) chloride Inorganic materials 0.000 claims 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 claims 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 claims 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 235000019400 benzoyl peroxide Nutrition 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- JAWGVVJVYSANRY-UHFFFAOYSA-N cobalt(3+) Chemical compound [Co+3] JAWGVVJVYSANRY-UHFFFAOYSA-N 0.000 claims 1
- ILZSSCVGGYJLOG-UHFFFAOYSA-N cobaltocene Chemical compound [Co+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 ILZSSCVGGYJLOG-UHFFFAOYSA-N 0.000 claims 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims 1
- MRIZMKJLUDDMHF-UHFFFAOYSA-N cumene;hydrogen peroxide Chemical compound OO.CC(C)C1=CC=CC=C1 MRIZMKJLUDDMHF-UHFFFAOYSA-N 0.000 claims 1
- JBSLOWBPDRZSMB-BQYQJAHWSA-N dibutyl (e)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C\C(=O)OCCCC JBSLOWBPDRZSMB-BQYQJAHWSA-N 0.000 claims 1
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 claims 1
- OGVXYCDTRMDYOG-UHFFFAOYSA-N dibutyl 2-methylidenebutanedioate Chemical compound CCCCOC(=O)CC(=C)C(=O)OCCCC OGVXYCDTRMDYOG-UHFFFAOYSA-N 0.000 claims 1
- QMCVOSQFZZCSLN-VAWYXSNFSA-N dihexyl (e)-but-2-enedioate Chemical compound CCCCCCOC(=O)\C=C\C(=O)OCCCCCC QMCVOSQFZZCSLN-VAWYXSNFSA-N 0.000 claims 1
- QMCVOSQFZZCSLN-QXMHVHEDSA-N dihexyl (z)-but-2-enedioate Chemical compound CCCCCCOC(=O)\C=C/C(=O)OCCCCCC QMCVOSQFZZCSLN-QXMHVHEDSA-N 0.000 claims 1
- TVWTZAGVNBPXHU-FOCLMDBBSA-N dioctyl (e)-but-2-enedioate Chemical compound CCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCC TVWTZAGVNBPXHU-FOCLMDBBSA-N 0.000 claims 1
- WTIFDVLCDRBEJK-VAWYXSNFSA-N diphenyl (e)-but-2-enedioate Chemical compound C=1C=CC=CC=1OC(=O)/C=C/C(=O)OC1=CC=CC=C1 WTIFDVLCDRBEJK-VAWYXSNFSA-N 0.000 claims 1
- DFKBFBPHOGVNGQ-QPLCGJKRSA-N ditridecyl (z)-but-2-enedioate Chemical compound CCCCCCCCCCCCCOC(=O)\C=C/C(=O)OCCCCCCCCCCCCC DFKBFBPHOGVNGQ-QPLCGJKRSA-N 0.000 claims 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 claims 1
- 230000000887 hydrating effect Effects 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 125000001905 inorganic group Chemical group 0.000 claims 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 claims 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 claims 1
- VRIVJOXICYMTAG-IYEMJOQQSA-L iron(ii) gluconate Chemical group [Fe+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O VRIVJOXICYMTAG-IYEMJOQQSA-L 0.000 claims 1
- SQZZGEUJERGRIN-UHFFFAOYSA-N manganese;pentane-2,4-dione Chemical compound [Mn].CC(=O)CC(C)=O SQZZGEUJERGRIN-UHFFFAOYSA-N 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 150000001451 organic peroxides Chemical class 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000003223 protective agent Substances 0.000 claims 1
- 238000007342 radical addition reaction Methods 0.000 claims 1
- 238000010526 radical polymerization reaction Methods 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 150000003623 transition metal compounds Chemical class 0.000 claims 1
- KOKKJWHERHSKEB-UHFFFAOYSA-N vanadium(3+) Chemical compound [V+3] KOKKJWHERHSKEB-UHFFFAOYSA-N 0.000 claims 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/18—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/06—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polyethers, polyoxymethylenes or polyacetals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2266/00—Composition of foam
- B32B2266/02—Organic
- B32B2266/0214—Materials belonging to B32B27/00
- B32B2266/0285—Condensation resins of aldehydes, e.g. with phenols, ureas, melamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2405/00—Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2401/00 or C08J2403/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2451/00—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Polyethers (AREA)
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 한개의 면판을 가진 건축용 적층 판매의 횡단면도이고,
제2도는 두개의 면판을 가진 건축용 적층 판매의 횡단면도이다.
Claims (13)
- 일반식이 H-(폴리옥시알킬렌쇄)t-R(여기서, R는 유기 또는 무기기이고, t는 R에 반응한 폴리옥시 알킬렌 쇄의 수이다), 공지의 양보다 다량의 유리기 과산화물 개시제인 유기 또는 무기 과화합물 및 금속 촉매의 존재하 또는 이 금속 촉매의 부재하에 환상 질소 비닐 단량체 및 에스테르화된 불포화 이염기산을 유리기 부가 중합법에 의하여 반응시키는 것이 특징인 다공성 발포체의 제조방법.
- 특허 청구의 범위 제1하에 기재에 있어서, 환상 질소 비닐 단량체가 다음의 일반식을 가지며, 에스테르화된 불포화이염산은 그의 산 부분에 4 또는 5개의 탄소 원자를 갖는 것이 특징인 방법.이 식에서, n은 3,4 또는 5이다.
- 전술한 특허청구의 범위 제1 또는 2항 기재에 있어서, 에스테르화된 불포화 이 염기산이 다음의 일반식을 갖는 것이 특징인 방법.CuH2u-2(CO2vH2Cv+1)2상기 식에서, u는 2 또는 3이고, v는 3내지 18의 정수인데, 이 염기산으로서는 푸마르산 디부틸, 말레산디부틸, 푸마르산디헥실, 메틸렌말로산디아밀, 이타콘산디부틸, 말레산디메틸아밀, 말레산디이소옥틸, 말레산디페닐, 말레산디헥실, 말레산디옥틸 또는 말레산디트리데실이 바람직하다.
- 전술한 임의의 항의 특허 청구의 범위에 있어서, t는 1 내지 50의 정수이고, 폴리옥시알킬렌 부가물의 분자량은 약 1000이상, 바람직하게는 이 부가물의 폴리옥시알킬렌 쇄가 산화에틸렌, 1,2-에폭시프로판, 에폭시부탄 또는 이들의 혼합물로부터 유된 것이 특징인 방법.
- 전술한 임의의 항의 특허청구의 범위에 있어서, 폴리옥시알킬렌 부가물을 이 부가물의 히드록실기와 반응할 수 있는 초산무수물 등의 보호제를 사용하여 유리기 중합 반응 전 또는 후에 처리하여 그 부가물의 히드록실가를 50미만, 바람직하게는 10미만으로 감소시키는 것이 특징인 방법.
- 전술한 임의의 항에 특허 청국의 범위에 있어서, 과화합물이 과벤조산 삼급-부틸, 히드록페록시드화 삼급-부틸, 히드로페록시드화 쿠멘, 과산화 라우로일, 과사화벤조일, 과산화 디-삼급-부틸 또는 과산화디쿠밀 등의 유기 과산화물 또는 유기 히드록페록시드화물인 것이 특징인 방법.
- 전술한 임의의 항의 특허 청구의 범위에 있어서 금속 촉매가 아세틸아세톤산구리(Ⅱ), 아세틸아세톤산철(Ⅱ) 또는 아세틸 아세톤산철(Ⅲ), 또는 황산철(Ⅱ), 황산철(Ⅲ), 황산철(Ⅱ)와 염화철(Ⅲ), 아세틸 아세톤산망간(Ⅱ)과 아세틸아세톤 망간(Ⅲ), 벤조산코발트(Ⅱ)와 아세틸아세톤산코발트(Ⅲ), 초산구리(I)과 아세틸아세톤산구리(Ⅱ) 또는 아세틸아세톤산 바나듐(Ⅲ)과 아세틸아세톤산산화바나듐(Ⅳ)의 혼합물, 또는 페로센, 아세틸페로센, 벤조일페로센, 코발토센, 1,1'-디아세틸페로센, 1,1'-페로센비스-(디페닐-포시핀), 니켈로센, 이염화하프노센 또는 페르센카르복스알데히드등의 원자번호 21내지 30인 천이 금속 화합물인 것이 특징인 방법.
- 전술한 임의의 항의 특허 청구의 범위에 있어서, 금속 촉매가 페로세이고, 과화합물이 과벤조산 삼급-부틸인 것이 특징인 방법.
- 전술한 임의의 하의 특허 청구의 범위에 있어서, 환상 질소비닐 단량체 및 에스테르화된 불포화 이 염기산이 모두 중합 반응혼합물의 약 5내지 40중량%를 구성하고, 과화합물은 환상 질소비닐 단량체 및 에스테프화된 불포화 이염기산의 총량에 대하여 약 2내지 30중량%를 구성하며, 금속 촉매는 과화합물 1g당 약 0.001내지 0.06g을 구성하고, 환상 질소비닐 단량체와 에스테르화된 불포화 이염기산의 몰비가 1:1인 것이 특징인 방법.
- 전술한 임의의 항의 특허청구의 범위에 따라 얻은 주성분으로 구 반드시 구성된 것이 특징인 페놀발포체 계면 활성제.
- 페놀 수지 발포 반응물질, 발포제 및 특허 청구의범위 제11항 또는 특허 청구의범위 제1항 내지 제11항에 따라 제조한 주성분인 계면 활성제의 반응 생성물로 이루어진 것이 특징인 발포재료.
- 특허청구의 범위 제11항 기재에 있어서, 페놀 수지 발포체 형성 반응물질이 페놀 및 0-크레졸-페놀블록 중합체인 것이 특징인 방법.
- 최소한 1개의 면판과 이 면판에 접착되는 특허청구의 범위 제13항 또는 제14항에 기재한 발포 재료로된 적층 구조판.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US113841 | 1979-01-21 | ||
| US11384180A | 1980-01-21 | 1980-01-21 | |
| US113,841 | 1980-01-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR830005273A true KR830005273A (ko) | 1983-08-13 |
| KR840000592B1 KR840000592B1 (ko) | 1984-04-24 |
Family
ID=22351828
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019810000178A KR840000592B1 (ko) | 1980-01-21 | 1981-01-21 | 페놀 발포체를 안정화시키기 위한 폴리옥시알킬렌 계면 활성제의 제조방법 |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0039756B1 (ko) |
| JP (1) | JPS56112915A (ko) |
| KR (1) | KR840000592B1 (ko) |
| AT (1) | ATE14132T1 (ko) |
| CA (1) | CA1148956A (ko) |
| DE (1) | DE3171158D1 (ko) |
| DK (1) | DK23781A (ko) |
| FI (1) | FI69088C (ko) |
| IE (1) | IE51168B1 (ko) |
| NO (1) | NO810175L (ko) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4365024A (en) * | 1981-07-10 | 1982-12-21 | The Celotex Corporation | Polyoxyalkylene/unsaturated diester reaction product for cellular foam stabilization |
| JP3204424B2 (ja) * | 1993-02-18 | 2001-09-04 | 三菱化学フォームプラスティック株式会社 | ポリプロピレン系樹脂発泡粒子 |
| DE10156135A1 (de) * | 2001-11-16 | 2003-06-05 | Basf Ag | Pfropfpolymerisate mit Stickstoffheterocyclen enthaltenden Seitenketten |
| DE10156134A1 (de) | 2001-11-16 | 2003-05-28 | Basf Ag | Pfropfpolymerisate mit cyclische N-Vinylamide enthaltenden Seitenketten |
| DE10156133A1 (de) | 2001-11-16 | 2003-05-28 | Basf Ag | Pfropfpolymerisate mit Stickstoffheterocyclen enthaltenden Seitenketten |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1161423B (de) * | 1962-05-23 | 1964-01-16 | Bayer Ag | Verfahren zur Herstellung von Pfropf-polymerisaten |
| BE758609A (fr) * | 1969-11-06 | 1971-04-16 | Bayer Ag | Procede de preparation de corps moules en matieres mousses |
| US3763277A (en) * | 1971-07-01 | 1973-10-02 | Union Carbide Corp | Process for the preparation of inter-polymers of poly(ethylene oxide) |
| LU65552A1 (ko) * | 1972-06-20 | 1973-12-27 | ||
| GB1439741A (en) * | 1974-01-31 | 1976-06-16 | Air Prod & Chem | Copolyers of polyfunctional polyether polyols and cyclic nitrogen ous and ester monomers |
| US4204020A (en) * | 1977-09-29 | 1980-05-20 | The Celotex Corporation | Phenolic foam laminated structural panel |
| US4140842A (en) * | 1977-09-29 | 1979-02-20 | The Celotex Corporation | Phenolic foam and surfactant useful therein |
-
1980
- 1980-10-30 CA CA000363637A patent/CA1148956A/en not_active Expired
-
1981
- 1981-01-09 IE IE38/81A patent/IE51168B1/en unknown
- 1981-01-13 DE DE8181100201T patent/DE3171158D1/de not_active Expired
- 1981-01-13 AT AT81100201T patent/ATE14132T1/de not_active IP Right Cessation
- 1981-01-13 EP EP81100201A patent/EP0039756B1/en not_active Expired
- 1981-01-20 NO NO810175A patent/NO810175L/no unknown
- 1981-01-20 FI FI810154A patent/FI69088C/fi not_active IP Right Cessation
- 1981-01-20 DK DK23781A patent/DK23781A/da not_active Application Discontinuation
- 1981-01-20 JP JP712381A patent/JPS56112915A/ja active Pending
- 1981-01-21 KR KR1019810000178A patent/KR840000592B1/ko active
Also Published As
| Publication number | Publication date |
|---|---|
| IE810038L (en) | 1981-07-21 |
| DE3171158D1 (en) | 1985-08-08 |
| FI810154L (fi) | 1981-07-22 |
| EP0039756A2 (en) | 1981-11-18 |
| EP0039756B1 (en) | 1985-07-03 |
| CA1148956A (en) | 1983-06-28 |
| NO810175L (no) | 1981-07-22 |
| ATE14132T1 (de) | 1985-07-15 |
| FI69088C (fi) | 1985-12-10 |
| DK23781A (da) | 1981-07-22 |
| EP0039756A3 (en) | 1982-02-24 |
| IE51168B1 (en) | 1986-10-29 |
| JPS56112915A (en) | 1981-09-05 |
| KR840000592B1 (ko) | 1984-04-24 |
| FI69088B (fi) | 1985-08-30 |
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