DE1046877B - Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis - Google Patents
Waermehaertbare Form-, UEberzugs- und Klebmasse auf EpoxyharzbasisInfo
- Publication number
- DE1046877B DE1046877B DEN14053A DEN0014053A DE1046877B DE 1046877 B DE1046877 B DE 1046877B DE N14053 A DEN14053 A DE N14053A DE N0014053 A DEN0014053 A DE N0014053A DE 1046877 B DE1046877 B DE 1046877B
- Authority
- DE
- Germany
- Prior art keywords
- epoxy resin
- epoxy
- weight
- phenol
- resin
- 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 31
- 229920000647 polyepoxide Polymers 0.000 title claims description 31
- 238000000465 moulding Methods 0.000 title claims description 11
- 238000000576 coating method Methods 0.000 title claims description 6
- 239000000853 adhesive Substances 0.000 title claims description 5
- 230000001070 adhesive effect Effects 0.000 title claims description 5
- 239000011248 coating agent Substances 0.000 title claims description 5
- 239000000203 mixture Substances 0.000 claims description 20
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 14
- -1 phenol aldehyde Chemical class 0.000 claims description 13
- 229920005989 resin Polymers 0.000 claims description 12
- 239000011347 resin Substances 0.000 claims description 12
- 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 9
- 239000004593 Epoxy Substances 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 125000003700 epoxy group Chemical group 0.000 claims description 4
- 239000007859 condensation product Substances 0.000 claims description 3
- 229920001169 thermoplastic Polymers 0.000 claims description 3
- 239000004416 thermosoftening plastic Substances 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 150000007522 mineralic acids Chemical class 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 1
- 229920003986 novolac Polymers 0.000 description 16
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 11
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 239000001294 propane Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 150000002989 phenols Chemical class 0.000 description 5
- 238000009835 boiling Methods 0.000 description 4
- ROLMZTIHUMKEAI-UHFFFAOYSA-N 4,5-difluoro-2-hydroxybenzonitrile Chemical compound OC1=CC(F)=C(F)C=C1C#N ROLMZTIHUMKEAI-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical class CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
- 150000005208 1,4-dihydroxybenzenes Chemical class 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
- FUFZNHHSSMCXCZ-UHFFFAOYSA-N 5-piperidin-4-yl-3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole Chemical compound FC(F)(F)C1=CC=CC(C=2N=C(ON=2)C2CCNCC2)=C1 FUFZNHHSSMCXCZ-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 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
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000003947 ethylamines Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N monoethyl amine Natural products CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- RCHKEJKUUXXBSM-UHFFFAOYSA-N n-benzyl-2-(3-formylindol-1-yl)acetamide Chemical compound C12=CC=CC=C2C(C=O)=CN1CC(=O)NCC1=CC=CC=C1 RCHKEJKUUXXBSM-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
- 238000002360 preparation method Methods 0.000 description 1
- 150000003232 pyrogallols Chemical class 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 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
- C08G59/68—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
- C08G59/681—Metal alcoholates, phenolates or carboxylates
- C08G59/682—Alcoholates
-
- 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
- C08G59/681—Metal alcoholates, phenolates or carboxylates
- C08G59/685—Carboxylates
-
- 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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL210234 | 1956-08-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1046877B true DE1046877B (de) | 1958-12-18 |
Family
ID=19750784
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEN14053A Pending DE1046877B (de) | 1956-08-30 | 1957-08-28 | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis |
Country Status (5)
| Country | Link |
|---|---|
| CH (1) | CH366667A (enrdf_load_stackoverflow) |
| DE (1) | DE1046877B (enrdf_load_stackoverflow) |
| FR (1) | FR1186297A (enrdf_load_stackoverflow) |
| GB (1) | GB806188A (enrdf_load_stackoverflow) |
| NL (2) | NL94293C (enrdf_load_stackoverflow) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1169114B (de) * | 1959-05-08 | 1964-04-30 | Otto Muehlschlegel Dipl Ing | Verwendung von Epoxyharzen zur Verbindung und/oder Formung von Konstruktionsteilen |
| DE3135010A1 (de) * | 1981-09-04 | 1983-03-24 | Hoechst Ag, 6000 Frankfurt | "bindemittel auf der grundlage von mischkondensaten aus epoxydharzen, resolen und aminen, verfahren zu dessen herstellung und zur elektrophoretischen abscheidung sowie elektrophoresebad" |
| US7997023B2 (en) | 2008-09-05 | 2011-08-16 | Moore Larry E | Gun with mounted sighting device |
| US8006428B2 (en) | 2008-10-10 | 2011-08-30 | Moore Larry E | Gun-mounted sighting device |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE588383A (enrdf_load_stackoverflow) * | 1959-03-09 | |||
| IT649945A (enrdf_load_stackoverflow) * | 1960-05-12 | |||
| US3264230A (en) * | 1961-12-29 | 1966-08-02 | Union Carbide Corp | Epoxide compositions containing tin curing catalysts |
| US3284383A (en) * | 1961-12-29 | 1966-11-08 | Union Carbide Corp | Epoxide compositions |
-
0
- NL NL210234D patent/NL210234A/xx unknown
- NL NL94293D patent/NL94293C/xx active
-
1957
- 1957-08-28 CH CH4990357A patent/CH366667A/de unknown
- 1957-08-28 DE DEN14053A patent/DE1046877B/de active Pending
- 1957-08-28 FR FR1186297D patent/FR1186297A/fr not_active Expired
- 1957-08-28 GB GB2710757A patent/GB806188A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1169114B (de) * | 1959-05-08 | 1964-04-30 | Otto Muehlschlegel Dipl Ing | Verwendung von Epoxyharzen zur Verbindung und/oder Formung von Konstruktionsteilen |
| DE3135010A1 (de) * | 1981-09-04 | 1983-03-24 | Hoechst Ag, 6000 Frankfurt | "bindemittel auf der grundlage von mischkondensaten aus epoxydharzen, resolen und aminen, verfahren zu dessen herstellung und zur elektrophoretischen abscheidung sowie elektrophoresebad" |
| US7997023B2 (en) | 2008-09-05 | 2011-08-16 | Moore Larry E | Gun with mounted sighting device |
| US8006428B2 (en) | 2008-10-10 | 2011-08-30 | Moore Larry E | Gun-mounted sighting device |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1186297A (fr) | 1959-08-19 |
| CH366667A (de) | 1963-01-15 |
| NL94293C (enrdf_load_stackoverflow) | |
| NL210234A (enrdf_load_stackoverflow) | |
| GB806188A (en) | 1958-12-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1046877B (de) | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis | |
| DE1520897B2 (de) | Verfahren zur Herstellung eines Epoxyäthers | |
| DE1061067B (de) | Verfahren zur Herstellung einer Pressmasse aus Epoxyharz und einem 4, 4'-Diaminodiarylalkan | |
| DE2738097A1 (de) | Glycidylaether-zusammensetzung und ein verfahren zu ihrer herstellung | |
| DE1057331B (de) | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis | |
| EP0004999B1 (de) | Verfahren zur Herstellung von stark profilierten Formteilen | |
| DE1057332B (de) | Waermehaertbare Form-, UEberzugs- und Klebmasse auf Epoxyharzbasis | |
| DE1570415C3 (de) | Verfahren zur Herstellung polymerer Borverbindungen | |
| DE1495793C3 (de) | Verfahren zum Herstellen von Epoxidpolyaddukten | |
| DE1141446B (de) | Verfahren zur Herstellung von haertbaren Kunstharzen | |
| EP0152760A2 (de) | Säurehärtbare Mischung für schwindungsarme Furankitte und Verfahren zu deren Herstellung | |
| DE2519406A1 (de) | Verfahren zur herstellung von harzen vom novolak-typ, nach diesem verfahren hergestellte harze, sie enthaltende lacke und mit den harzen impraegnierte gegenstaende | |
| DE1151934B (de) | Epoxyharz-, Form- oder UEberzugsmassen, die aus 2 oder 3 koernigen, voneinander verschiedenen Bestandteilen bestehen | |
| DE1022005B (de) | Verfahren zur Herstellung von Novolakharzen | |
| DE1040235B (de) | Verfahren zum Haerten von harzartigen Polyepoxyverbindungen durch Phenol-aldehydkondensationsprodukte | |
| DE1643304C3 (de) | Verfahren zur Herstellung eines Epoxynovolakharzes | |
| DE862504C (de) | Kunstharzpressstoff | |
| DE883651C (de) | Verfahren zur Herstellung harzartiger Kondensationsprodukte aus Phenolen, Formaldehyd und aromatischen Aminen | |
| DE749798C (de) | Verfahren zur Herstellung von unloeslichen und unschmelzbaren Giessharzen | |
| DE1139649B (de) | Verfahren zur Herstellung von Epoxydharzen | |
| DE892828C (de) | Verfahren zur Herstellung von harzartigen Kondensationsprodukten | |
| DE1193667B (de) | Verfahren zur Herstellung von kaltgepressten Elektroisolierkoerpern mit verbesserterKriech-stromfestigkeit, die Phenolharz als Bindemittel, und Polyisocyanate enthalten | |
| DE2363357B2 (de) | Verfahren zur herstellung von haertbaren kondensationsharzen des phenols und/oder kresols | |
| DE525494C (de) | Verfahren zur Herstellung harzartiger Phenolaldehydkondensationsprodukte | |
| EP0805830A1 (de) | Wässerige aminoplastharze mit verbesserter waschbarkeit für die herstellung von holzwerkstoffen |