DE1150807B - Haerten von fluessigen Epoxyharzen - Google Patents
Haerten von fluessigen EpoxyharzenInfo
- Publication number
- DE1150807B DE1150807B DEL38527A DEL0038527A DE1150807B DE 1150807 B DE1150807 B DE 1150807B DE L38527 A DEL38527 A DE L38527A DE L0038527 A DEL0038527 A DE L0038527A DE 1150807 B DE1150807 B DE 1150807B
- Authority
- DE
- Germany
- Prior art keywords
- parts
- aniline
- resin
- epoxy resins
- mixture
- 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
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 title claims description 7
- 239000004848 polyfunctional curative Substances 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 9
- 239000007859 condensation product Substances 0.000 claims description 6
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 3
- DYDNPESBYVVLBO-UHFFFAOYSA-N formanilide Chemical compound O=CNC1=CC=CC=C1 DYDNPESBYVVLBO-UHFFFAOYSA-N 0.000 claims description 2
- 239000000725 suspension Substances 0.000 claims description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 39
- 229920005989 resin Polymers 0.000 description 27
- 239000011347 resin Substances 0.000 description 27
- 239000000203 mixture Substances 0.000 description 18
- 239000003822 epoxy resin Substances 0.000 description 10
- 229920000647 polyepoxide Polymers 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 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 6
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 6
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 239000012442 inert solvent Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001448 anilines Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 230000007096 poisonous effect Effects 0.000 description 2
- 235000013824 polyphenols Nutrition 0.000 description 2
- 238000011417 postcuring Methods 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 239000006286 aqueous extract Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 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
- 238000005266 casting Methods 0.000 description 1
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 1
- 235000005487 catechin Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 229950001002 cianidanol Drugs 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- -1 cresyl phosphite Chemical compound 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- NLRKCXQQSUWLCH-UHFFFAOYSA-N nitrosobenzene Chemical compound O=NC1=CC=CC=C1 NLRKCXQQSUWLCH-UHFFFAOYSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1016260A GB960869A (en) | 1960-03-22 | 1960-03-22 | Improvements in or relating to liquid epoxide resin compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1150807B true DE1150807B (de) | 1963-06-27 |
Family
ID=9962674
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEL38527A Pending DE1150807B (de) | 1960-03-22 | 1961-03-22 | Haerten von fluessigen Epoxyharzen |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE601644A (enrdf_load_stackoverflow) |
| DE (1) | DE1150807B (enrdf_load_stackoverflow) |
| ES (1) | ES265892A1 (enrdf_load_stackoverflow) |
| GB (1) | GB960869A (enrdf_load_stackoverflow) |
| NL (1) | NL262658A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3539659A (en) * | 1967-11-22 | 1970-11-10 | Vanderbilt Co R T | Liquid amine curing agents for polyepoxides |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2511913A (en) * | 1950-06-20 | Compositions of resinous epoxides | ||
| DE1038752B (de) * | 1956-04-04 | 1958-09-11 | Ciba Geigy | Verwendung eines Arylamin-Formaldehyd-Harzes als Haertungsmittel fuer Epoxyharze |
| DE1041244B (de) * | 1957-07-11 | 1958-10-16 | Solvay Werke Gmbh | Verfahren zum Haerten von Epoxyharzen |
-
0
- NL NL262658D patent/NL262658A/xx unknown
- BE BE601644D patent/BE601644A/xx unknown
-
1960
- 1960-03-22 GB GB1016260A patent/GB960869A/en not_active Expired
-
1961
- 1961-03-21 ES ES0265892A patent/ES265892A1/es not_active Expired
- 1961-03-22 DE DEL38527A patent/DE1150807B/de active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2511913A (en) * | 1950-06-20 | Compositions of resinous epoxides | ||
| DE1038752B (de) * | 1956-04-04 | 1958-09-11 | Ciba Geigy | Verwendung eines Arylamin-Formaldehyd-Harzes als Haertungsmittel fuer Epoxyharze |
| DE1041244B (de) * | 1957-07-11 | 1958-10-16 | Solvay Werke Gmbh | Verfahren zum Haerten von Epoxyharzen |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3539659A (en) * | 1967-11-22 | 1970-11-10 | Vanderbilt Co R T | Liquid amine curing agents for polyepoxides |
Also Published As
| Publication number | Publication date |
|---|---|
| GB960869A (en) | 1964-06-17 |
| ES265892A1 (es) | 1961-07-01 |
| BE601644A (enrdf_load_stackoverflow) | |
| NL262658A (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69701807T2 (de) | Hitzehärtende phenolharzzusammensetzung | |
| DE2262025A1 (de) | Epoxyharzmassen und verfahren zu ihrer herstellung | |
| DE2025343C2 (de) | Gemische aus Aminomethylphenolen und deren Ausgangsverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Vernetzungsmittel | |
| DE1770446A1 (de) | Neue Addukte aus Polyepoxiden und cycloaliphatischen diprimaeren Diaminen,Verfahren zu ihrer Herstellung und Anwendung | |
| EP0184106B1 (de) | Harzlösungen für Kitte und Beschichtungsmassen, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE2552518A1 (de) | Thermoplastische klebstoffmasse und verfahren zu ihrer herstellung | |
| DE1026956B (de) | Verfahren zur Herstellung von Glycidylaethern von Phenolen | |
| DE3803508C2 (de) | Kalthärtendes, warm nachvernetzbares Harz auf Epoxidbasis | |
| DE2854827A1 (de) | Verfahren zum aushaerten von epoxidharzen | |
| DE2738097A1 (de) | Glycidylaether-zusammensetzung und ein verfahren zu ihrer herstellung | |
| DE2025159A1 (de) | Verfahren zur Herstellung von Formkörpern und Überzügen | |
| DE1150807B (de) | Haerten von fluessigen Epoxyharzen | |
| DE1041246B (de) | Verfahren zur Herstellung kalt- oder warmgehaerteter modifizierter Epoxyharze | |
| DE1906515A1 (de) | Haertbare Mischungen aus Epoxidharzen und cyclischen Harnstoffderivaten | |
| DE1046877B (de) | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis | |
| DE1057332B (de) | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis | |
| DE3934428A1 (de) | Haertbare epoxidharze | |
| DE1113566B (de) | Verfahren zur Herstellung von Kunststoffen auf Grundlage von Polyepoxyden | |
| DE1795288A1 (de) | Haertbare Masse | |
| AT227950B (de) | Flüssiger Härter für Epoxydharze | |
| DE1040235B (de) | Verfahren zum Haerten von harzartigen Polyepoxyverbindungen durch Phenol-aldehydkondensationsprodukte | |
| DE1643304C3 (de) | Verfahren zur Herstellung eines Epoxynovolakharzes | |
| DE1184496B (de) | Herstellen von Formteilen aus Formmassen, die Novolake und Polyglycidylaether enthalten | |
| DE1089544B (de) | Verfahren zum Haerten von endstaendige Epoxydgruppen enthaltenden Epoxyharzen | |
| DE19901419A1 (de) | Kunststoffmischung, sowie Verfahren zu ihrer Herstellung |