DE3704149A1 - Durch bestrahlung haertbare harze, verfahren zu ihrer herstellung und verwendung - Google Patents
Durch bestrahlung haertbare harze, verfahren zu ihrer herstellung und verwendungInfo
- Publication number
- DE3704149A1 DE3704149A1 DE19873704149 DE3704149A DE3704149A1 DE 3704149 A1 DE3704149 A1 DE 3704149A1 DE 19873704149 DE19873704149 DE 19873704149 DE 3704149 A DE3704149 A DE 3704149A DE 3704149 A1 DE3704149 A1 DE 3704149A1
- Authority
- DE
- Germany
- Prior art keywords
- resins
- bisphenol
- acid
- esterified
- resoles
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229920005989 resin Polymers 0.000 title claims abstract description 57
- 239000011347 resin Substances 0.000 title claims abstract description 57
- 238000000034 method Methods 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title claims description 3
- 230000008569 process Effects 0.000 title claims description 3
- 229930185605 Bisphenol Natural products 0.000 claims abstract description 15
- 239000002253 acid Substances 0.000 claims abstract description 13
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims abstract description 6
- 230000032050 esterification Effects 0.000 claims abstract description 5
- 238000005886 esterification reaction Methods 0.000 claims abstract description 5
- 229920002120 photoresistant polymer Polymers 0.000 claims abstract description 5
- 150000007513 acids Chemical class 0.000 claims abstract description 4
- 238000004519 manufacturing process Methods 0.000 claims abstract description 4
- 150000002148 esters Chemical class 0.000 claims abstract description 3
- 239000007795 chemical reaction product Substances 0.000 claims abstract 3
- 150000002989 phenols Chemical class 0.000 claims abstract 3
- 229920003987 resole Polymers 0.000 claims description 34
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 13
- ZCJLOOJRNPHKAV-ONEGZZNKSA-N (e)-3-(furan-2-yl)prop-2-enoic acid Chemical compound OC(=O)\C=C\C1=CC=CO1 ZCJLOOJRNPHKAV-ONEGZZNKSA-N 0.000 claims description 7
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 claims description 5
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 3
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 3
- 150000001805 chlorine compounds Chemical class 0.000 claims description 3
- 229930016911 cinnamic acid Natural products 0.000 claims description 3
- 235000013985 cinnamic acid Nutrition 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 241000723347 Cinnamomum Species 0.000 claims description 2
- 235000017803 cinnamon Nutrition 0.000 claims description 2
- 238000001465 metallisation Methods 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 16
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 9
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 4
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 238000007086 side reaction Methods 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229940106691 bisphenol a Drugs 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 1
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 1
- BLPUXJIIRIWMSQ-QPJJXVBHSA-N 2-[(e)-3-phenylprop-2-enylidene]propanedioic acid Chemical compound OC(=O)C(C(O)=O)=C\C=C\C1=CC=CC=C1 BLPUXJIIRIWMSQ-QPJJXVBHSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- KXHPPCXNWTUNSB-UHFFFAOYSA-M benzyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1=CC=CC=C1 KXHPPCXNWTUNSB-UHFFFAOYSA-M 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- -1 hydroxymethyl bisphenol Chemical compound 0.000 description 1
- CEQFOVLGLXCDCX-WUKNDPDISA-N methyl red Chemical compound C1=CC(N(C)C)=CC=C1\N=N\C1=CC=CC=C1C(O)=O CEQFOVLGLXCDCX-WUKNDPDISA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
- 229940031826 phenolate Drugs 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
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
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
- C08G59/1455—Monocarboxylic acids, anhydrides, halides, or low-molecular-weight esters thereof
- C08G59/1461—Unsaturated monoacids
-
- 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
- C08G59/40—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
- C08G59/62—Alcohols or phenols
- C08G59/621—Phenols
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/46—Manufacturing multilayer circuits
- H05K3/4644—Manufacturing multilayer circuits by building the multilayer layer by layer, i.e. build-up multilayer circuits
- H05K3/4673—Application methods or materials of intermediate insulating layers not specially adapted to any one of the previous methods of adding a circuit layer
- H05K3/4676—Single layer compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Emergency Medicine (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Epoxy Resins (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19873704149 DE3704149A1 (de) | 1987-02-11 | 1987-02-11 | Durch bestrahlung haertbare harze, verfahren zu ihrer herstellung und verwendung |
| SE8800023A SE469474B (sv) | 1987-02-11 | 1988-01-07 | Genom bestraalning haerdbara hartser, foerfarande foer framstaellning av dessa hartser och anvaendning daerav |
| DK56288A DK56288A (da) | 1987-02-11 | 1988-02-04 | Harpikser, som kan haerdes ved bestraaling, fremgangsmaade til fremstilling deraf samt deres anvendelse |
| NO880592A NO169720C (no) | 1987-02-11 | 1988-02-10 | Fremgangsmaate for fremstilling av herdbare harpikser og anvendelse av disse |
| SE9102977A SE9102977L (sv) | 1987-02-11 | 1991-10-14 | Genom bestraalning haerdbara hartser, foerfarande foer deras framstaellning och anvaendning |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19873704149 DE3704149A1 (de) | 1987-02-11 | 1987-02-11 | Durch bestrahlung haertbare harze, verfahren zu ihrer herstellung und verwendung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE3704149A1 true DE3704149A1 (de) | 1988-08-25 |
| DE3704149C2 DE3704149C2 (enExample) | 1990-09-27 |
Family
ID=6320703
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19873704149 Granted DE3704149A1 (de) | 1987-02-11 | 1987-02-11 | Durch bestrahlung haertbare harze, verfahren zu ihrer herstellung und verwendung |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE3704149A1 (enExample) |
| DK (1) | DK56288A (enExample) |
| NO (1) | NO169720C (enExample) |
| SE (2) | SE469474B (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0365844A3 (de) * | 1988-10-28 | 1991-02-06 | Siemens Aktiengesellschaft | Gut aushärtbarer Photolack |
| DE4038895A1 (de) * | 1990-12-06 | 1992-06-11 | Harald Dr Mueller | Schrumpfungsarme, thermostabile photoresists |
| EP0558149A1 (en) * | 1992-02-27 | 1993-09-01 | Shell Internationale Researchmaatschappij B.V. | Epoxy resin and epoxy resin composition |
| CN100358953C (zh) * | 2005-05-23 | 2008-01-02 | 容大油墨（惠州）有限公司 | 一种液态感光防焊油墨及其电路板 |
| US10508169B2 (en) | 2015-02-02 | 2019-12-17 | Nippon Shokubai Co., Ltd. | Curable resin and producing process therefor |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100342950B1 (ko) * | 1997-11-11 | 2002-10-19 | 가부시키가이샤 닛폰 쇼쿠바이 | 경화성수지및수지조성물 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3230560A1 (de) * | 1981-08-20 | 1983-05-05 | Hussain Kashif Dr. 8003 Zürich El-Ghatta | Polymere und verfahren zu deren herstellung |
| EP0167051A1 (de) * | 1984-06-29 | 1986-01-08 | Siemens Aktiengesellschaft | Thermostabiles, durch Bestrahlung vernetzbares Polymersystem auf der Basis von Bisphenolen und Epichlorhydrin sowie Verfahren zu seiner Verwendung |
-
1987
- 1987-02-11 DE DE19873704149 patent/DE3704149A1/de active Granted
-
1988
- 1988-01-07 SE SE8800023A patent/SE469474B/sv not_active IP Right Cessation
- 1988-02-04 DK DK56288A patent/DK56288A/da not_active Application Discontinuation
- 1988-02-10 NO NO880592A patent/NO169720C/no unknown
-
1991
- 1991-10-14 SE SE9102977A patent/SE9102977L/xx not_active Application Discontinuation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3230560A1 (de) * | 1981-08-20 | 1983-05-05 | Hussain Kashif Dr. 8003 Zürich El-Ghatta | Polymere und verfahren zu deren herstellung |
| EP0167051A1 (de) * | 1984-06-29 | 1986-01-08 | Siemens Aktiengesellschaft | Thermostabiles, durch Bestrahlung vernetzbares Polymersystem auf der Basis von Bisphenolen und Epichlorhydrin sowie Verfahren zu seiner Verwendung |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0365844A3 (de) * | 1988-10-28 | 1991-02-06 | Siemens Aktiengesellschaft | Gut aushärtbarer Photolack |
| DE4038895A1 (de) * | 1990-12-06 | 1992-06-11 | Harald Dr Mueller | Schrumpfungsarme, thermostabile photoresists |
| DE4038895C2 (de) * | 1990-12-06 | 1998-07-02 | Harald Dr Mueller | Licht- und strahlungsempfindliche Gemische |
| EP0558149A1 (en) * | 1992-02-27 | 1993-09-01 | Shell Internationale Researchmaatschappij B.V. | Epoxy resin and epoxy resin composition |
| CN100358953C (zh) * | 2005-05-23 | 2008-01-02 | 容大油墨（惠州）有限公司 | 一种液态感光防焊油墨及其电路板 |
| US10508169B2 (en) | 2015-02-02 | 2019-12-17 | Nippon Shokubai Co., Ltd. | Curable resin and producing process therefor |
Also Published As
| Publication number | Publication date |
|---|---|
| NO880592L (no) | 1988-08-12 |
| DE3704149C2 (enExample) | 1990-09-27 |
| NO169720C (no) | 1992-07-29 |
| DK56288A (da) | 1988-08-12 |
| NO169720B (no) | 1992-04-21 |
| DK56288D0 (da) | 1988-02-04 |
| NO880592D0 (no) | 1988-02-10 |
| SE8800023D0 (sv) | 1988-01-07 |
| SE469474B (sv) | 1993-07-12 |
| SE9102977L (sv) | 1993-04-15 |
| SE9102977D0 (sv) | 1991-10-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69702910T2 (de) | Novolak-harze zur verwendung als adhäsionspromotoren in epoxidharzgemischen | |
| EP0035969B1 (de) | Zusammensetzung aus kationisch polymerisierbarem Material und einem Katalysator | |
| DE2459471A1 (de) | Mischungen aus epoxidharzen, polycarbonsaeureanhydriden und polyesterdicarbonsaeuren | |
| EP0057162A1 (de) | Verfahren zur Erzeugung von Abbildungen | |
| DE3303473A1 (de) | Neues epoxyharz und verfahren zur herstellung desselben | |
| DE3704149C2 (enExample) | ||
| EP0347669A2 (de) | Verfahren zur Herstellung von aromatischen Polyethersulfonen | |
| EP0143075B1 (de) | Verfahren zur Herstellung von N-Glycidylverbindungen | |
| DE4030283A1 (de) | Verfahren zur herstellung cyclischer carbonate | |
| DE69302768T2 (de) | Verfahren zur Herstellung von Biphenolskelett aufweisenden Epoxyharzen | |
| EP0184149B1 (de) | Poly(phenylenether) und Verfahren zu ihrer Herstellung | |
| EP0205124B1 (de) | Verfahren zur Herstellung phosphorhaltiger Polyarylenäther | |
| EP0479192A2 (de) | Modifizierte Polyarylenether-Blockcopolymere | |
| EP0135477B1 (de) | Polyglycidyläther | |
| DE60314319T2 (de) | Hydroxymethyl-substituierte polyfunktionelle Phenole | |
| DE3410385C2 (de) | Oxidatives Kupplungsverfahren zur Herstellung eines Polyphenylenoxids | |
| EP0391370B1 (de) | Neue Epoxidharze | |
| DE2217239C3 (de) | Verfahren zur Herstellung von Glycidyläthern ein- bzw. mehrwertiger Phenole | |
| EP0226543A2 (de) | Verbessertes Verfahren zur Herstellung von Glycidylverbindungen | |
| DE19613063A1 (de) | Phosphormodifizierte Epoxidharze und ein Verfahren zu ihrer Herstellung | |
| EP0297030B1 (de) | Epoxidgruppenhaltige Polycycloacetale | |
| EP0206099A1 (de) | Phosphorhaltige Polyarylenäther und Verfahren zu ihrer Herstellung | |
| EP0412934A2 (de) | Modifizierte Polyarylenethersulfone | |
| DE19613061A1 (de) | Phosphormodifizierte Epoxidharze aus Epoxiden und phosphorhaltigen Verbindungen | |
| DE2555183C3 (de) | Verfahren zur Herstellung von p-Nitrobenzyl-7-phenoxy- und -7-phenylacetamidodeacetoxycephalosporanat |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |