DE1057332B - Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis - Google Patents
Waermehaertbare Form-, UEberzugs- und Klebmasse auf EpoxyharzbasisInfo
- Publication number
- DE1057332B DE1057332B DEN14052A DEN0014052A DE1057332B DE 1057332 B DE1057332 B DE 1057332B DE N14052 A DEN14052 A DE N14052A DE N0014052 A DEN0014052 A DE N0014052A DE 1057332 B DE1057332 B DE 1057332B
- Authority
- DE
- Germany
- Prior art keywords
- epoxy resin
- epoxy
- resin
- weight
- novolak
- 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 28
- 229920000647 polyepoxide Polymers 0.000 title claims description 28
- 238000000465 moulding Methods 0.000 title claims description 12
- 230000001070 adhesive effect Effects 0.000 title claims description 7
- 239000000853 adhesive Substances 0.000 title claims description 6
- 238000000576 coating method Methods 0.000 title claims description 6
- 239000011248 coating agent Substances 0.000 title claims description 5
- 229920003986 novolac Polymers 0.000 claims description 17
- 229920005989 resin Polymers 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 14
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000004593 Epoxy Substances 0.000 claims description 7
- 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 claims description 7
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 6
- 150000002897 organic nitrogen compounds Chemical class 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 125000003700 epoxy group Chemical group 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- -1 Phenol aldehyde Chemical class 0.000 claims description 2
- 239000000843 powder Substances 0.000 description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 229910017464 nitrogen compound Inorganic materials 0.000 description 2
- 150000002830 nitrogen compounds Chemical class 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-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
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical class OC1CC=CC=C1 MIHINWMALJZIBX-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229920003987 resole Polymers 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
- C08G59/18—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
- C08G59/68—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 catalysts used
- C08G59/686—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 catalysts used containing nitrogen
-
- 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
- C08G59/50—Amines
- C08G59/5093—Complexes of amines
-
- 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
- C08G59/50—Amines
- C08G59/56—Amines together with other curing agents
-
- 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)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL210236 | 1956-08-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1057332B true DE1057332B (de) | 1959-05-14 |
Family
ID=19750786
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEN14052A Pending DE1057332B (de) | 1956-08-30 | 1957-08-28 | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis |
Country Status (5)
Country | Link |
---|---|
CH (1) | CH366669A (enrdf_load_stackoverflow) |
DE (1) | DE1057332B (enrdf_load_stackoverflow) |
FR (1) | FR1189137A (enrdf_load_stackoverflow) |
GB (1) | GB806259A (enrdf_load_stackoverflow) |
NL (2) | NL89336C (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1151934B (de) | 1958-05-29 | 1963-07-25 | Shell Int Research | Epoxyharz-, Form- oder UEberzugsmassen, die aus 2 oder 3 koernigen, voneinander verschiedenen Bestandteilen bestehen |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3154554A (en) * | 1959-07-09 | 1964-10-27 | Boehringer Sohn Ingelheim | Tertiary amines |
DE1138542B (de) * | 1959-11-23 | 1962-10-25 | Reichhold Chemie Ag | Formmassen, die Epoxydverbindungen und Novolake enthalten |
GB2055843A (en) * | 1979-07-20 | 1981-03-11 | Ciba Geigy Ag | Curable epoxide resin mixtures and their use in corrosion resistant coatings |
US20100227981A1 (en) * | 2009-03-04 | 2010-09-09 | Air Products And Chemicals, Inc. | Epoxide-based composition |
US9080007B2 (en) * | 2013-02-28 | 2015-07-14 | Air Products And Chemicals, Inc. | Anhydride accelerators for epoxy resin systems |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2458796A (en) * | 1946-08-08 | 1949-01-11 | Ciba Ltd | Phenol oxide resin lacquers and their manufacture |
-
0
- NL NL210236D patent/NL210236A/xx unknown
- NL NL89336D patent/NL89336C/xx active
-
1957
- 1957-08-28 FR FR1189137D patent/FR1189137A/fr not_active Expired
- 1957-08-28 CH CH4990557A patent/CH366669A/de unknown
- 1957-08-28 GB GB2710857A patent/GB806259A/en not_active Expired
- 1957-08-28 DE DEN14052A patent/DE1057332B/de active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2458796A (en) * | 1946-08-08 | 1949-01-11 | Ciba Ltd | Phenol oxide resin lacquers and their manufacture |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1151934B (de) | 1958-05-29 | 1963-07-25 | Shell Int Research | Epoxyharz-, Form- oder UEberzugsmassen, die aus 2 oder 3 koernigen, voneinander verschiedenen Bestandteilen bestehen |
Also Published As
Publication number | Publication date |
---|---|
FR1189137A (fr) | 1959-09-29 |
NL89336C (enrdf_load_stackoverflow) | |
NL210236A (enrdf_load_stackoverflow) | |
CH366669A (de) | 1963-01-15 |
GB806259A (en) | 1958-12-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1152255B (de) | Verfahren zum Herstellen von Pressteilen aus Pressmassen, die Epoxyde enthalten | |
DE1057332B (de) | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis | |
DE2611536A1 (de) | Polyaminophenol-epoxyharzhaertungsmittel | |
DE1495946C3 (de) | Verfahren zur Herstellung von Epoxid polyaddukten | |
DE1046877B (de) | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis | |
DE1057331B (de) | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis | |
DE1570373A1 (de) | Verfahren zur Verminderung des Hydroxylgruppen-Gehaltes von Epoxydharzen | |
DE1570415C3 (de) | Verfahren zur Herstellung polymerer Borverbindungen | |
DE1151934B (de) | Epoxyharz-, Form- oder UEberzugsmassen, die aus 2 oder 3 koernigen, voneinander verschiedenen Bestandteilen bestehen | |
AT311050B (de) | Verfahren zur Herstellung von Kunststoffen und Lackharzen auf der Grundlage von basischen, stickstoffhaltigen Glycidylverbindungen und Dicarbonsäureanhydriden | |
DE1643304C3 (de) | Verfahren zur Herstellung eines Epoxynovolakharzes | |
AT233261B (de) | Verfahren zur Härtung von Epoxyharzen | |
DE1244407B (de) | Verfahren zur Herstellung von wasserloeslichen Kondensationsprodukten | |
DE1041244B (de) | Verfahren zum Haerten von Epoxyharzen | |
DE2604195C2 (de) | Verfahren zur Herstellung von Melamin-Formaldehydharzen | |
AT229588B (de) | Verfahren zur Herstellung von neuen Glycidyläthern | |
DE1150807B (de) | Haerten von fluessigen Epoxyharzen | |
DE1570419C3 (de) | Verfahren zur Herstellung polymerer Borverbindungen | |
AT337455B (de) | Verfahren zur herstellung von geharteten produkten auf der grundlage von polyepoxiden | |
DE888293C (de) | Verfahren zur Herstellung durch Hitze haertbarer, chemikalienfeste UEberzuege ergebender Harnstoff-Formaldehydharze | |
DE2264286C3 (de) | Verwendung von 1,3,6,8-Tetraaza- tricyclo-4,4,11·6 .l3·8 - dodecan als Härter bei der Herstellung von Epoxidpolyaddukten | |
DE525494C (de) | Verfahren zur Herstellung harzartiger Phenolaldehydkondensationsprodukte | |
DE1139649B (de) | Verfahren zur Herstellung von Epoxydharzen | |
CH542897A (de) | Verfahren zur Herstellung von Kunststoffen und Lackharzen aus basischen, stickstoffhaltigen Glycidylverbindungen und Dicarbonsäureanhydriden | |
DE1238213B (de) | Verfahren zur Herstellung von Formkoerpern auf der Basis von Epoxyd-Polyaddukten |