KR960034265A - 콘택트 렌즈 제조용 상호침투 중합체 망상구조물 - Google Patents
콘택트 렌즈 제조용 상호침투 중합체 망상구조물 Download PDFInfo
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- KR960034265A KR960034265A KR1019960009423A KR19960009423A KR960034265A KR 960034265 A KR960034265 A KR 960034265A KR 1019960009423 A KR1019960009423 A KR 1019960009423A KR 19960009423 A KR19960009423 A KR 19960009423A KR 960034265 A KR960034265 A KR 960034265A
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- 229920000642 polymer Polymers 0.000 title claims 28
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000004925 Acrylic resin Substances 0.000 claims abstract 7
- 239000000203 mixture Substances 0.000 claims 14
- 125000002947 alkylene group Chemical group 0.000 claims 8
- 239000001257 hydrogen Substances 0.000 claims 8
- 229910052739 hydrogen Inorganic materials 0.000 claims 8
- 229920002396 Polyurea Polymers 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 150000001412 amines Chemical class 0.000 claims 7
- 239000012948 isocyanate Substances 0.000 claims 7
- 150000002513 isocyanates Chemical class 0.000 claims 7
- -1 acrylate ester Chemical class 0.000 claims 6
- 239000003999 initiator Substances 0.000 claims 6
- 150000003254 radicals Chemical class 0.000 claims 6
- 239000011541 reaction mixture Substances 0.000 claims 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 5
- 239000000126 substance Substances 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 150000004985 diamines Chemical class 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 claims 4
- 230000000379 polymerizing effect Effects 0.000 claims 3
- 229920001451 polypropylene glycol Polymers 0.000 claims 3
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical class CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims 2
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 claims 2
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical group CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 claims 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical group NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims 2
- 239000005058 Isophorone diisocyanate Substances 0.000 claims 2
- JUIBLDFFVYKUAC-UHFFFAOYSA-N [5-(2-ethylhexanoylperoxy)-2,5-dimethylhexan-2-yl] 2-ethylhexaneperoxoate Chemical group CCCCC(CC)C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C(CC)CCCC JUIBLDFFVYKUAC-UHFFFAOYSA-N 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 229920000768 polyamine Polymers 0.000 claims 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 claims 2
- 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
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 229920002125 Sokalan® Polymers 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- FHRUQOOVHXMESF-UHFFFAOYSA-N benzoyl benzenecarboperoxoate;2-hydroperoxy-2-methylpropane Chemical compound CC(C)(C)OO.C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 FHRUQOOVHXMESF-UHFFFAOYSA-N 0.000 claims 1
- 235000019400 benzoyl peroxide Nutrition 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- 125000004386 diacrylate group Chemical group 0.000 claims 1
- 125000005442 diisocyanate group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 230000009477 glass transition Effects 0.000 claims 1
- 230000000149 penetrating effect Effects 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 claims 1
- 239000004584 polyacrylic acid Substances 0.000 claims 1
- 235000011178 triphosphate Nutrition 0.000 claims 1
- 239000001226 triphosphate Substances 0.000 claims 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/02—Polyureas
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
- G02B1/043—Contact lenses
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- 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
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3228—Polyamines acyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5024—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/637—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers characterised by the in situ polymerisation of the compounds having carbon-to-carbon double bonds in a reaction mixture of saturated polymers and isocyanates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2210/00—Compositions for preparing hydrogels
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2270/00—Compositions for creating interpenetrating networks
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/04—Polymer mixtures characterised by other features containing interpenetrating networks
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/903—Interpenetrating network
Abstract
본 발명은 폴리아크릴 수지 망상구조물과 상호침투된 리우레아 망상구조물 및 이로부터 제조한 콘택트 렌즈와 같은 제품에 관한 것이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (30)
- 상대적 중량비 약 60/40 내지 약 100/0의 다음 일반식 디아민 A와 B로 이루어지며 반응성 혼합물 중에 약 20 내지 60중량%로 존재하는 아민 혼합물 ⒜, 아민 혼합물과 반응하여 폴리우레아 망상구조물을 형성시키기에 충분한 양으로 반응 혼합물 중에 존재하는 유기 디이소시아네이트 또는 폴리이소시아네이트⒝, 반응성 혼합물 중에 약 10 내지 50중량%의 양으로 존재하는 다음 일반식(C) 또는 (D)의 아크릴산 에스테르⒞, 아크릴산 에스테르⒞를 중합시켜 폴리아크릴을 망상구조물을 형성시키기에 충분한 양으로 존재하는 유리 라디칼 개시제⒟, 아민 혼합물⒜을 가교결합시키기에 충분한 양으로 존재하는 트리아민⒠을 포함하여 폴리우레아:폴리아크릴 수지의 비가 약 50 : 50 내지 약 90 : 10이고 반응성 혼합물 중의 성분의 중량의 합이 100%인 중합가능 성분들의 반응성 혼합물을 중합시켜 수득한 단일 유리 전이온도를 나타내는 균질한 상호침투 중합체 망상구조물.상기 식에서, f1은 1 내지 75의 정수이고, R은 탄소수 3의 알킬렌이며 각각의 R은 동일하고, f는 1 내지 150의 정수이고, R10내지 R14는 각각 독립적으로 수소 또는 저급 알킬이고, Z1과 Z2는 각각 독립적으로 화학 결합 또는 저급 알킬렌이고, R3는 수소 또는 저급 알킬이고, m은 0 내지 150의 정수이고, Z3과 Z5는 각각 독립적으로 저급 알킬렌이고, Z4와 Z6은 각각 독립적으로 화학결합 또는 저급 알킬렌이고, R4은 수소, 저급 알킬 또는이고, R7은 저급 알킬렌 또는 화학결합 또는 -CH2(OCH2CH2)q이고, q는 0 내지 200의 정수이다.
- 제1항에 있어서, 디아민 B가 다음 구조식의 폴리옥시프로필렌 디아민인 상호침투 중합체 망상구조물.
- 제1항에 있어서, 트리아민이 반응 혼합물 중에 총 아민 등가물의 30 내지 50%의 양으로 존재하는 상호침투 중합체 망상구조물.
- 제1항에 있어서, 트리아민이 디에틸렌 트리아민 또느 폴리옥시프로필렌 트리아민인 상호침투 중합체 망상구조물.
- 제1항에 있어서, 이소시아네이트가 메틸렌-비스(4,4`-사이클로헥실이소시아네이트) 또는 이소포론 디이소시아네이트인 상호침투 중합체 망상구조물.
- 제1항에 있어서, 유리 라디칼 개시제가 2,5-디메틸-2,5-디-(2-에틸헥사노일퍼옥시)헥산, 벤조일, 퍼옥사이드 3급-부틸 하이드로퍼옥사이드, 3급-부틸 퍼옥사이드 또는 라우릴 퍼옥사이드인 상호침투 중합체 망상구조물.
- 제1항에 있어서, 폴리우레아/폴리아크릴 수지 중량비가 약 80 : 20내지 약 70 : 30인 상호침투 중합체 망상구조물.
- 제1항에 있어서, 폴리우레아/폴리아크릴 수지 주량비가 약 75 : 25인 상호침투 중합체 망상구조물.
- 제1항에 있어서, 이소시아네이트가 반응 혼합물 중에 약 15 내지 약 50중량%의 양으로 존재하는 상호침투 중합체 망상구조물.
- 제9항에 있어서, 이소시아네이트가 약 25 내지 약 40중량%의 양으로 존재하는 상호침투 중합체 망상구조물.
- 제1항에 있어서, 유리 라디칼 개시제가 반응 혼합물 중에 약 0.01 내지 약 1중량%의 양으로 존재하는 상호침투 중합체 망상구조물.
- 제1항에 있어서, 상대적 중량비 약 60/40 내지 약 100/0의 다음 일반식 폴리아민 A와 B로 이루어지며 반응성 혼합물 중에 약 20 내지 60중량%로 존재하는 아민 혼합물 ⒜, 아민 혼합물과 반응하여 폴리우레아 망상구조물을 형성시키기에 충분한 양으로 반응 혼합물 중에 존재하는 유기 디이소시아네이트 또는 폴리이소시아네이트⒝, 반응성 혼합물 중에 약 10 내지 50중량%의 양으로 존재하며 다음 일반식(C1)의 제1아크릴레이트와 다음 일반식(C2)의 디아크릴레이트 또는 다음 일반식(D)의 트리아크릴레이트인 제2아크릴레이트와의 혼합물(여기서, 제1아크릴레이트: 제2아크릴레이트의 비는 약 80 : 20 내지 약 95 : 5이다)로 이루어지는 아크릴산 에스테르⒞, 아크릴산 에스테르⒞를 중합시켜 폴리아크릴을 망상구조물으 형성시키기에 충분한 양으로 존재하는 유리 라디칼 개시제⒟, 및 아민 혼합물⒜을 가교결합시키기에 충분한 양으로 존재하는 트리아민⒠을 포함하여 폴리우레아: 폴리아크릴 수지의 비가 약 90 : 10내지 약 50 : 50인 반응성 혼합물을 중합시켜 형성한 상호침투 중합체 망상구조물.상기 식에서 f1은 1 내지 75의 정수이고, R은 탄소수 3의 알킬렌이며 각각의 R은 동일하고, f는 1 내지 150의 정수이고, R10내지 R14는 각각 독립적으로 수소 또는 저급 알킬이고, Z1과 Z2는 각각 독립적으로 화학결합 또는 저급 알킬렌이고, R3, R4, R5, R8및 R9는 각각 독립적으로 수소 또는 저급 알킬이고, R6은 저급 알킬이고, R7은 화학결합 또는 저급 알킬렌이고, m과 n은 각각 독립적으로 0 내지 30의정수이고, p는 1 내지 3의 정수이다.
- 제12항에 있어서, B가 다음 구조식의 폴리옥시프로필렌디아민인 상호침투 중합체 망상구조물.
- 제12항에 있어서, 트리아민이 반응성 혼합물 중에 충 아민 등가물의 약 30 내지 50%의 양으로 존재하는 상호침투 중합체 망상구조물.
- 제14항에 있어서, 트리아민이 디에틸렌 트리아민 또는 폴리옥시프로필렌 트리아민인 상호침투 중합체 망상구조물.
- 제12항에 있어서, 이소시아네이트가 메틸렌-비스(4,4`-사이클로헥실이소시아네이트) 또는 이소포론 디이소시아네이트인 상호침투 중합체 망상구조물.
- 제12항에 있어서, 유리 라디카 개시제가 2,5-디메틸-2,5-디-(2-에틸헥사노일퍼옥시)헥산, 벤조일 퍼옥사이드, 3급-부틸하이드로퍼옥사이드, 3급-부틸퍼옥사이드 또는 라우릴 퍼옥사이드인 상호침투 중합체 망상구조물.
- 제12항에 있어서, 폴리우레아/폴리아크릴 수지 중량비가 약 70 : 30내지 약 80:20인 상호침투 중합체 망상구조물.
- 제12항에 있어서, 폴리우레아/폴리아크릴 수지 주량비가 약 75/25인 상호침투 중합체 망상구조물.
- 제12항에 있어서, 이소시아네이트가 반응 혼합물 중에 약 15 내지 약 50중량%의 양으로 존재하는 상호침투 중합체 망상구조물.
- 제20항에 있어서, 이소시아네이트가 약 25 내지 약 40중량%의 양으로 존재하는 상호침투 중합체 망상구조물.
- 제12항에 있어서, 유리 라디칼 개시제가 반응 혼합물 중에 약 0.01 내지 약 1중량%의 양으로 존재하는 상호침투 중합체 망상구조물.
- 제12항에 있어서, R3,R4,R5및 R9가 CH3인 상호침투 중합체 망상구조물.
- 제12항에 있어서, R3,R5, 및 R9가 CH3이고, m이 0이며, R4가 수소이고, n이 2인 상호침투 중합체 망상구조물.
- 제12항에 있어서, R3, R5, 및 R9가 CH3이고, m이 4이며, R4가 수소이고, n이 2인 상호침투 중합체 망상구조물.
- 제12항에 있어서, m이 4이고, R4가 수소이며, p가 3이고, R6이 에틸이며, R7이 에틸렌이고, R3과 R8이 CH3인 상호침투 중합체 망상구조물.
- 제1항 내지 제26항 중의 어느 한 항의 상호침투 중합체 망상구조물로 이루어진 제품.
- 제27항에 있어서, 콘택트 렌즈인 제품.
- 제1항에 있어서, A가인 상호침투 중합체 망상구조물.
- 제12항에 있어서, A가인 상호침투 중합체 망상구조물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/415001 | 1995-03-31 | ||
US08/415,001 US5674942A (en) | 1995-03-31 | 1995-03-31 | Interpenetrating polymer networks for contact lens production |
Publications (1)
Publication Number | Publication Date |
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KR960034265A true KR960034265A (ko) | 1996-10-22 |
Family
ID=23643940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019960009423A KR960034265A (ko) | 1995-03-31 | 1996-03-30 | 콘택트 렌즈 제조용 상호침투 중합체 망상구조물 |
Country Status (17)
Country | Link |
---|---|
US (1) | US5674942A (ko) |
EP (1) | EP0735097B1 (ko) |
JP (1) | JPH08292404A (ko) |
KR (1) | KR960034265A (ko) |
CN (1) | CN1134502C (ko) |
AT (1) | ATE219123T1 (ko) |
AU (1) | AU694329B2 (ko) |
BR (1) | BR9601194A (ko) |
CA (1) | CA2173096A1 (ko) |
DE (1) | DE69621689T2 (ko) |
HU (1) | HUP9600830A3 (ko) |
IL (1) | IL117585A0 (ko) |
MX (1) | MX9601227A (ko) |
NO (1) | NO961284L (ko) |
NZ (1) | NZ286249A (ko) |
SG (1) | SG47097A1 (ko) |
ZA (1) | ZA962560B (ko) |
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-
1996
- 1996-03-20 IL IL11758596A patent/IL117585A0/xx unknown
- 1996-03-22 NZ NZ286249A patent/NZ286249A/xx unknown
- 1996-03-29 EP EP96302228A patent/EP0735097B1/en not_active Expired - Lifetime
- 1996-03-29 HU HU9600830A patent/HUP9600830A3/hu unknown
- 1996-03-29 AU AU50394/96A patent/AU694329B2/en not_active Ceased
- 1996-03-29 CA CA002173096A patent/CA2173096A1/en not_active Abandoned
- 1996-03-29 BR BR9601194A patent/BR9601194A/pt not_active Application Discontinuation
- 1996-03-29 SG SG1996006869A patent/SG47097A1/en unknown
- 1996-03-29 ZA ZA9602560A patent/ZA962560B/xx unknown
- 1996-03-29 NO NO961284A patent/NO961284L/no unknown
- 1996-03-29 DE DE69621689T patent/DE69621689T2/de not_active Expired - Lifetime
- 1996-03-29 JP JP8099553A patent/JPH08292404A/ja active Pending
- 1996-03-29 AT AT96302228T patent/ATE219123T1/de not_active IP Right Cessation
- 1996-03-29 MX MX9601227A patent/MX9601227A/es not_active Application Discontinuation
- 1996-03-30 CN CNB96108989XA patent/CN1134502C/zh not_active Expired - Fee Related
- 1996-03-30 KR KR1019960009423A patent/KR960034265A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
NO961284L (no) | 1996-10-01 |
ZA962560B (en) | 1997-09-29 |
US5674942A (en) | 1997-10-07 |
NO961284D0 (no) | 1996-03-29 |
BR9601194A (pt) | 1998-01-06 |
CA2173096A1 (en) | 1996-10-01 |
HUP9600830A2 (en) | 1997-01-28 |
DE69621689T2 (de) | 2002-11-28 |
MX9601227A (es) | 1997-04-30 |
HUP9600830A3 (en) | 1999-03-01 |
IL117585A0 (en) | 1996-07-23 |
AU5039496A (en) | 1996-10-10 |
ATE219123T1 (de) | 2002-06-15 |
DE69621689D1 (de) | 2002-07-18 |
CN1138062A (zh) | 1996-12-18 |
EP0735097B1 (en) | 2002-06-12 |
NZ286249A (en) | 1997-08-22 |
HU9600830D0 (en) | 1996-05-28 |
JPH08292404A (ja) | 1996-11-05 |
CN1134502C (zh) | 2004-01-14 |
SG47097A1 (en) | 1998-03-20 |
AU694329B2 (en) | 1998-07-16 |
EP0735097A1 (en) | 1996-10-02 |
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