DE1115922B - Verfahren zur Herstellung von Giessharzkoerpern auf Basis von Epoxyharzen - Google Patents
Verfahren zur Herstellung von Giessharzkoerpern auf Basis von EpoxyharzenInfo
- Publication number
- DE1115922B DE1115922B DES64893A DES0064893A DE1115922B DE 1115922 B DE1115922 B DE 1115922B DE S64893 A DES64893 A DE S64893A DE S0064893 A DES0064893 A DE S0064893A DE 1115922 B DE1115922 B DE 1115922B
- Authority
- DE
- Germany
- Prior art keywords
- resin
- epoxy resins
- epoxy
- production
- heat resistance
- 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.)
- Pending
Links
- 239000003822 epoxy resin Substances 0.000 title claims description 22
- 229920000647 polyepoxide Polymers 0.000 title claims description 22
- 229920005989 resin Polymers 0.000 title claims description 18
- 239000011347 resin Substances 0.000 title claims description 18
- 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 title claims description 12
- 238000000034 method Methods 0.000 title claims description 7
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 239000005056 polyisocyanate Substances 0.000 claims description 5
- 229920001228 polyisocyanate Polymers 0.000 claims description 5
- -1 aliphatic hydroxyl compound Chemical class 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 7
- 239000004593 Epoxy Substances 0.000 description 6
- 238000005266 casting Methods 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 5
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 4
- 125000003700 epoxy group Chemical group 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 241000428199 Mustelinae Species 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 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 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 1
- 238000004870 electrical engineering Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- FLBJFXNAEMSXGL-UHFFFAOYSA-N het anhydride Chemical compound O=C1OC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl FLBJFXNAEMSXGL-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical class O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/40—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes epoxy resins
-
- 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/1816—Catalysts containing secondary or tertiary amines or salts thereof having carbocyclic 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
- C08G18/58—Epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Polyurethanes Or Polyureas (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE593093D BE593093A (enrdf_load_stackoverflow) | 1959-09-12 | ||
| DES64893A DE1115922B (de) | 1959-09-12 | 1959-09-12 | Verfahren zur Herstellung von Giessharzkoerpern auf Basis von Epoxyharzen |
| CH779960A CH411347A (de) | 1959-09-12 | 1960-07-08 | Verfahren zur Herstellung von Epoxydharzkörpern mit erhöhter Warmformbeständigkeit |
| FR835665A FR1264969A (fr) | 1959-09-12 | 1960-08-11 | Procédé de préparation de corps de résines époxy présentant une stabilité améliorée de leur forme sous l'effet de la chaleur |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DES64893A DE1115922B (de) | 1959-09-12 | 1959-09-12 | Verfahren zur Herstellung von Giessharzkoerpern auf Basis von Epoxyharzen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1115922B true DE1115922B (de) | 1961-10-26 |
Family
ID=7497582
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DES64893A Pending DE1115922B (de) | 1959-09-12 | 1959-09-12 | Verfahren zur Herstellung von Giessharzkoerpern auf Basis von Epoxyharzen |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE593093A (enrdf_load_stackoverflow) |
| CH (1) | CH411347A (enrdf_load_stackoverflow) |
| DE (1) | DE1115922B (enrdf_load_stackoverflow) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1963899A1 (de) * | 1969-12-20 | 1971-06-24 | Henkel & Cie Gmbh | Verfahren zur Herstellung von trifunktionellen Isocyanaten |
| DE2359386A1 (de) * | 1972-11-29 | 1974-06-20 | Hitachi Ltd | Duroplast, duroplastkomposition und herstellungsverfahren dafuer |
| DE2444458A1 (de) * | 1973-09-19 | 1975-04-24 | Hitachi Ltd | Wicklung fuer elektrische rotierende maschinen und verfahren zur herstellung |
| US4564651A (en) * | 1983-06-27 | 1986-01-14 | Siemens Aktiengesellschaft | Method for the manufacture of reaction resin molding materials |
| US5021536A (en) * | 1988-03-09 | 1991-06-04 | Bayer Aktiengesellschaft | Storage stable resin reaction mixtures, and the preparation and use thereof |
| US5286765A (en) * | 1989-09-15 | 1994-02-15 | Bayer Aktiengesellschaft | Process for the preparation of foundry cores and molds |
| US6051632A (en) * | 1993-08-17 | 2000-04-18 | Bayer Aktiengesellschaft | Free-flowing compression molding compositions and processes for their production and use |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1067766A (fr) * | 1951-12-21 | 1954-06-18 | Nat Res Dev | Produits résineux synthétiques à base de résines d'épichlorhydrine |
| DE1055808B (de) * | 1957-11-07 | 1959-04-23 | Collo Rheincollodium G M B H | Verfahren zur Herstellung von homogenen Formkoerpern |
-
0
- BE BE593093D patent/BE593093A/xx unknown
-
1959
- 1959-09-12 DE DES64893A patent/DE1115922B/de active Pending
-
1960
- 1960-07-08 CH CH779960A patent/CH411347A/de unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1067766A (fr) * | 1951-12-21 | 1954-06-18 | Nat Res Dev | Produits résineux synthétiques à base de résines d'épichlorhydrine |
| DE1055808B (de) * | 1957-11-07 | 1959-04-23 | Collo Rheincollodium G M B H | Verfahren zur Herstellung von homogenen Formkoerpern |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1963899A1 (de) * | 1969-12-20 | 1971-06-24 | Henkel & Cie Gmbh | Verfahren zur Herstellung von trifunktionellen Isocyanaten |
| DE2359386A1 (de) * | 1972-11-29 | 1974-06-20 | Hitachi Ltd | Duroplast, duroplastkomposition und herstellungsverfahren dafuer |
| DE2444458A1 (de) * | 1973-09-19 | 1975-04-24 | Hitachi Ltd | Wicklung fuer elektrische rotierende maschinen und verfahren zur herstellung |
| US4564651A (en) * | 1983-06-27 | 1986-01-14 | Siemens Aktiengesellschaft | Method for the manufacture of reaction resin molding materials |
| US5021536A (en) * | 1988-03-09 | 1991-06-04 | Bayer Aktiengesellschaft | Storage stable resin reaction mixtures, and the preparation and use thereof |
| US5286765A (en) * | 1989-09-15 | 1994-02-15 | Bayer Aktiengesellschaft | Process for the preparation of foundry cores and molds |
| US6051632A (en) * | 1993-08-17 | 2000-04-18 | Bayer Aktiengesellschaft | Free-flowing compression molding compositions and processes for their production and use |
Also Published As
| Publication number | Publication date |
|---|---|
| BE593093A (enrdf_load_stackoverflow) | |
| CH411347A (de) | 1966-04-15 |
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