KR850700250A - 트리아진 및 옥사졸린의 양 그룹을 함유하는 하이드록시 방향족 올리고머의 제조방법 및 상기 올리고머로부터 에폭시 수지를 제조하는 방법 - Google Patents
트리아진 및 옥사졸린의 양 그룹을 함유하는 하이드록시 방향족 올리고머의 제조방법 및 상기 올리고머로부터 에폭시 수지를 제조하는 방법Info
- Publication number
- KR850700250A KR850700250A KR1019850700240A KR850700240A KR850700250A KR 850700250 A KR850700250 A KR 850700250A KR 1019850700240 A KR1019850700240 A KR 1019850700240A KR 850700240 A KR850700240 A KR 850700240A KR 850700250 A KR850700250 A KR 850700250A
- Authority
- KR
- South Korea
- Prior art keywords
- component
- groups
- group
- epoxy resin
- cyanogen
- Prior art date
Links
Classifications
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C261/00—Derivatives of cyanic acid
- C07C261/02—Cyanates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/30—Only oxygen atoms
- C07D251/34—Cyanuric or isocyanuric esters
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/066—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with chain extension or advancing agents
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/26—Di-epoxy compounds heterocyclic
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- C08G59/3236—Heterocylic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Epoxy Resins (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Carbon And Carbon Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Adornments (AREA)
- Steroid Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (8)
- ( I )( A ) 분자당 평균 하나 이상의 방향족 하이드록실 그룹을 갖는 물질 최소한 1종을 ( B ) 방향족 하이드록실 그룹당 최소한 0.01 내지 0.95몰의 시아노겐 할라이드 또는 시아노겐 할라이드의 혼합물과 (C ) 방향족 하이드실 그룹당 0.01 내지 1.1몰의 적절한 염기 존재하에 반응을 거의 완결시키는데 충분한 온도 및 시간에서 반응시킨 후, 수득되는 시아네이트 혼합물을 회수하고;. ( II ) 단계 ( I )로부터 수득된 생성물을 ( D ) 에폭시 수지와(에폭시 그룹 대 시아네이트 그룹의 몰비가 1 : 1 내지 1: 100이다), 적절한 공올리고머화 촉매 존재하에 공올리고머화반응을 거의 완결시키는 온도 및 시간에서 공올리고머화시킴을 특징으로 하여, 트리아진 및 옥사졸린의 양 그룹을 함유하는 하이드록시방향족 올리고머를 제조하는 방법.
- 제1항에 있어서, 성분( A ) 및 ( B )가 방향족 하이드록실그룹당 0.05 내지 0.55몰의 시아노겐 할라이드 또는 시아노겐 할라이드의 혼합물을 제공하는 량으로 존재하고, 성분( C )가 방향족 하이드록실 그룹의 몰당 0.05내지 0.6몰의 염기를 제공하는 량으로 존재하고, 에폭시그룹 대 시아네이트 그룹의 몰비가 1 : 10내지 1 : 40인 방법.
- 제2항에 있어서, 성분( A )가 명세서내의 일반식( I ),( II ) 또는 ( III )의 화합물이고, 성분( B )가 시아노겐 클로라이드, 시아노겐 브로마이드 또는 이의 혼합물이고, 성분( C )가 트리알킬아민이고, 성분( D )가 명세서내의 일반식( IV ) 또는 ( V )의 화합물인 방법.
- 제3항에 있어서, 성분(A)가 일반식( II )의 화합물이고, 성분( C )가 트리에틸아민이고, 성분( D )가 일반식( IV ) 의 에폭시 수지인 방법.
- 제4항에 있어서, 성분( A )에서 A는 탄소수 1내지 12의 2가 탄화수소 그룹이고, n은 1이며, 성분( D )에서 A는 각기 독립적으로 탄소수 1 내지 12의 2가 탄화수소 그룹이고, n은 1이며 m2는 0 내지 40의 평균값을 갖는 방법.
- 제5항에 있어서, 성분(A)에서 A는 이소프필리덴 그룹이고, 성분(D)에서 A는 이소프로필리덴그룹이고 m2는 0.1내지 20의 평균값을 갖는 방법.
- 하이드록시방향족 물질을 에피할로히드린과 반응시키고, 염기성-작용물질과 계속하여 탈할로겐화수소화 반응시키고, 최종적으로 수득되는 글리시딜 에테르생성물을 회수함으로써 통상적 방법으로 에폭시화하여 에폭시수지를 제조하는 방법에 있어서, 하이드록시 방향족 물질이 제1항의 단계 ( II )로부터 수득되는 공올리고머화 생성물인 방법.
- 제7항에 있어서, 에피할로히드린이 에피클로로히드린이고 염기성-작용 물질이 알칼리 금속 수산화물인 방법.※참고사항:최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/576,304 US4487915A (en) | 1984-02-02 | 1984-02-02 | Hydroxy aromatic oligomers containing triazine and oxazoline groups and epoxy resins prepared therefrom |
US576,304 | 1984-02-02 | ||
PCT/US1984/001724 WO1985003514A1 (en) | 1984-02-02 | 1984-10-25 | Processes for preparing hydroxyaromatic oligomers containing both triazine and oxazoline groups and for preparing epoxy resins from the oligomers |
US576304 | 1990-08-31 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890700111A Division KR890005041B1 (ko) | 1984-02-02 | 1984-10-25 | 하이드록시 방향족 올리고머로부터 에폭시수지를 제조하는 방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR850700250A true KR850700250A (ko) | 1985-12-26 |
KR890001621B1 KR890001621B1 (ko) | 1989-05-11 |
Family
ID=24303859
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890700111A KR890005041B1 (ko) | 1984-02-02 | 1984-10-25 | 하이드록시 방향족 올리고머로부터 에폭시수지를 제조하는 방법 |
KR1019850700240A KR890001621B1 (ko) | 1984-02-02 | 1984-10-25 | 트리아진 및 옥사졸린 그룹을 함유하는 하이드록시방향족 올리고머의 제조방법 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890700111A KR890005041B1 (ko) | 1984-02-02 | 1984-10-25 | 하이드록시 방향족 올리고머로부터 에폭시수지를 제조하는 방법 |
Country Status (17)
Country | Link |
---|---|
US (1) | US4487915A (ko) |
EP (1) | EP0150278B1 (ko) |
JP (2) | JPS61500317A (ko) |
KR (2) | KR890005041B1 (ko) |
AT (1) | ATE40390T1 (ko) |
AU (1) | AU553539B2 (ko) |
BR (1) | BR8407285A (ko) |
CA (1) | CA1259993A (ko) |
DE (1) | DE3476407D1 (ko) |
DK (1) | DK445785D0 (ko) |
ES (1) | ES537220A0 (ko) |
FI (1) | FI72328C (ko) |
IL (1) | IL73359A (ko) |
NO (1) | NO161622C (ko) |
NZ (1) | NZ210040A (ko) |
WO (1) | WO1985003514A1 (ko) |
ZA (1) | ZA848470B (ko) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4546131A (en) * | 1985-01-15 | 1985-10-08 | The Dow Chemical Company | Polymer modified cyanate mixture and epoxy resins thereof |
US4555554A (en) * | 1985-02-15 | 1985-11-26 | The Dow Chemical Company | Oligomeric vinyl ester resin compositions containing triazine groups and imino carbamate linkages |
US4555553A (en) * | 1985-02-15 | 1985-11-26 | The Dow Chemical Company | Hydroxyaromatic oligomers of a mixed cyanate and aromatic polyamine and epoxy resins thereof |
US4611022A (en) * | 1985-06-24 | 1986-09-09 | The Dow Chemical Company | Polymer modified polyphenol compositions and thermosettable resins thereof |
US4629763A (en) * | 1985-06-24 | 1986-12-16 | The Dow Chemical Company | Polymer modified polyphenol compositions and thermosettable resins thereof |
US4629762A (en) * | 1985-06-24 | 1986-12-16 | The Dow Chemical Company | Polymer modified polyphenol compositions and thermosettable resins thereof |
US4629764A (en) * | 1985-06-24 | 1986-12-16 | The Dow Chemical Company | Polymer modified polyphenol compositions and thermosettable resins thereof |
US4699933A (en) * | 1985-11-04 | 1987-10-13 | The Dow Chemical Company | Polyurethanes containing triazine or both triazine and oxazoline, triazine and imino carbamate or triazine and other N-heterocyclic groups |
US4665149A (en) * | 1985-11-08 | 1987-05-12 | The Dow Chemical Company | Triazine containing epoxy resins having improved thermal stability |
US5130385A (en) * | 1986-01-23 | 1992-07-14 | Allied-Signal Inc. | Cyanato group containing phenolic resins, and phenolic triazines derived therefrom |
US4978727A (en) * | 1986-01-23 | 1990-12-18 | Allied-Signal | Cyanato group containing phenolic resins, phenolic triazines derived therefrom |
US5124414A (en) * | 1986-01-23 | 1992-06-23 | Allied-Signal Inc. | Process for preparing phenolic cyanate resins |
US4970276A (en) * | 1986-01-23 | 1990-11-13 | Allied-Signal Inc. | Phenolic triazine copolymers based on pure cyanato novolacs |
US4661553A (en) * | 1986-02-24 | 1987-04-28 | The Dow Chemical Company | Vinyl esters of polyepoxides of polyphenol cyanate mixture and polymaleimide co-oligomers |
US4663398A (en) * | 1986-02-24 | 1987-05-05 | The Dow Chemical Company | Co-oligomerization product of a mixed cyanate and a polymaleimide and epoxy resins thereof |
US5126412A (en) * | 1987-10-05 | 1992-06-30 | Allied-Signal Inc. | Cyanato group containing phenolic resins, and phenolic triazines derived therefrom |
US4988780A (en) * | 1988-08-15 | 1991-01-29 | Allied-Signal | Flame resistant article made of phenolic triazine and related method using a pure cyanato novolac |
US4933423A (en) * | 1989-04-07 | 1990-06-12 | Shell Oil Company | Thermosetting resin compositions |
US5001213A (en) * | 1989-04-07 | 1991-03-19 | Shell Oil Company | Thermosetting resin compositions |
GB9318872D0 (en) * | 1993-09-11 | 1993-10-27 | Unisersity Fo Leeds The | Polymer resin |
US5912308A (en) * | 1994-11-30 | 1999-06-15 | Alliedsignal Inc. | Multifunctional cyanate ester and epoxy blends |
US20010020071A1 (en) | 1997-10-10 | 2001-09-06 | Capote Miguel Albert | High performance cyanate-bismaleimide-epoxy resin compositions for printed circuits and encapsulants |
CN110330445A (zh) * | 2019-07-18 | 2019-10-15 | 扬州天启新材料股份有限公司 | 一种三酚a型氰酸酯及其制备方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2810706A (en) * | 1953-07-01 | 1957-10-22 | American Cyanamid Co | Oxirane triazine resinous compositions and processes of preparing the same |
US2741607A (en) * | 1954-02-23 | 1956-04-10 | Shell Dev | Triglycidyl cyanurate and polymers thereof |
US2809942A (en) * | 1955-10-21 | 1957-10-15 | Devoe & Raynolds Co | Process for making polyglycidyl cyanurates |
US2864805A (en) * | 1955-12-05 | 1958-12-16 | Devoe & Raynolds Co | Epoxide resins |
US2971942A (en) * | 1956-10-01 | 1961-02-14 | Devoe & Raynolds Co | Epoxide resins |
US3708483A (en) * | 1968-10-31 | 1973-01-02 | Dow Chemical Co | Synthesis of polymers from s-triazines and perfluoro-vinyl ethers |
US3676397A (en) * | 1970-10-12 | 1972-07-11 | Dow Chemical Co | Oxazolidinone-containing epoxy resins and process for their preparation |
FR2124413B1 (ko) * | 1971-02-03 | 1975-10-24 | Minnesota Mining & Mfg | |
JPS5847422B2 (ja) * | 1977-10-04 | 1983-10-22 | 三菱電機株式会社 | 熱硬化性樹脂材料 |
JPS5626925A (en) * | 1979-08-10 | 1981-03-16 | Sumitomo Chem Co Ltd | Production of epoxy resin |
JPS5874720A (ja) * | 1981-10-30 | 1983-05-06 | Hitachi Ltd | 耐熱性樹脂の製法 |
-
1984
- 1984-02-02 US US06/576,304 patent/US4487915A/en not_active Expired - Fee Related
- 1984-10-25 KR KR1019890700111A patent/KR890005041B1/ko not_active IP Right Cessation
- 1984-10-25 BR BR8407285A patent/BR8407285A/pt unknown
- 1984-10-25 KR KR1019850700240A patent/KR890001621B1/ko not_active IP Right Cessation
- 1984-10-25 AU AU35527/84A patent/AU553539B2/en not_active Ceased
- 1984-10-25 WO PCT/US1984/001724 patent/WO1985003514A1/en active IP Right Grant
- 1984-10-25 JP JP59503945A patent/JPS61500317A/ja active Granted
- 1984-10-26 CA CA000466385A patent/CA1259993A/en not_active Expired
- 1984-10-30 NZ NZ210040A patent/NZ210040A/xx unknown
- 1984-10-30 DE DE8484113037T patent/DE3476407D1/de not_active Expired
- 1984-10-30 AT AT84113037T patent/ATE40390T1/de not_active IP Right Cessation
- 1984-10-30 ZA ZA848470A patent/ZA848470B/xx unknown
- 1984-10-30 ES ES537220A patent/ES537220A0/es active Granted
- 1984-10-30 IL IL73359A patent/IL73359A/xx unknown
- 1984-10-30 EP EP84113037A patent/EP0150278B1/en not_active Expired
-
1985
- 1985-09-26 FI FI853711A patent/FI72328C/fi not_active IP Right Cessation
- 1985-10-01 NO NO85853873A patent/NO161622C/no unknown
- 1985-10-01 DK DK445785A patent/DK445785D0/da not_active Application Discontinuation
-
1987
- 1987-07-15 JP JP62176923A patent/JPS63118318A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
BR8407285A (pt) | 1986-02-18 |
NO161622B (no) | 1989-05-29 |
DE3476407D1 (en) | 1989-03-02 |
FI853711L (fi) | 1985-09-26 |
EP0150278A2 (en) | 1985-08-07 |
NO853873L (no) | 1985-10-01 |
ZA848470B (en) | 1986-06-25 |
KR890005041B1 (ko) | 1989-12-08 |
IL73359A0 (en) | 1985-01-31 |
EP0150278A3 (en) | 1986-02-12 |
ES8607348A1 (es) | 1985-12-16 |
IL73359A (en) | 1988-07-31 |
DK445785A (da) | 1985-10-01 |
AU3552784A (en) | 1985-08-27 |
US4487915A (en) | 1984-12-11 |
ES537220A0 (es) | 1985-12-16 |
JPH0571046B2 (ko) | 1993-10-06 |
NO161622C (no) | 1989-09-06 |
JPS63118318A (ja) | 1988-05-23 |
CA1259993A (en) | 1989-09-26 |
ATE40390T1 (de) | 1989-02-15 |
DK445785D0 (da) | 1985-10-01 |
EP0150278B1 (en) | 1989-01-25 |
NZ210040A (en) | 1988-07-28 |
AU553539B2 (en) | 1986-07-17 |
FI72328B (fi) | 1987-01-30 |
JPS6261210B2 (ko) | 1987-12-21 |
KR890001621B1 (ko) | 1989-05-11 |
FI853711A0 (fi) | 1985-09-26 |
JPS61500317A (ja) | 1986-02-27 |
KR890702423A (ko) | 1989-12-23 |
FI72328C (fi) | 1987-05-11 |
WO1985003514A1 (en) | 1985-08-15 |
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