DE1283420B - Thixotrope UEberzugsmittel - Google Patents
Thixotrope UEberzugsmittelInfo
- Publication number
- DE1283420B DE1283420B DEM39379A DEM0039379A DE1283420B DE 1283420 B DE1283420 B DE 1283420B DE M39379 A DEM39379 A DE M39379A DE M0039379 A DEM0039379 A DE M0039379A DE 1283420 B DE1283420 B DE 1283420B
- Authority
- DE
- Germany
- Prior art keywords
- cation
- thixotropic
- weight
- clay
- parts
- 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
- 239000011248 coating agent Substances 0.000 title claims description 15
- 230000009974 thixotropic effect Effects 0.000 title claims description 10
- 239000004927 clay Substances 0.000 claims description 23
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 17
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 claims description 16
- 238000000576 coating method Methods 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 12
- 239000004593 Epoxy Substances 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 150000008065 acid anhydrides Chemical class 0.000 claims description 6
- 238000007598 dipping method Methods 0.000 claims description 6
- 239000013008 thixotropic agent Substances 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 150000003512 tertiary amines Chemical class 0.000 claims description 5
- 150000001767 cationic compounds Chemical class 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 claims description 4
- 229910001411 inorganic cation Inorganic materials 0.000 claims description 4
- 229920001187 thermosetting polymer Polymers 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 239000011256 inorganic filler Substances 0.000 claims 1
- 229910003475 inorganic filler Inorganic materials 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 49
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical class O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 10
- 239000000440 bentonite Substances 0.000 description 9
- 229910000278 bentonite Inorganic materials 0.000 description 9
- 239000003822 epoxy resin Substances 0.000 description 9
- 239000003973 paint Substances 0.000 description 9
- 229920000647 polyepoxide Polymers 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 150000008064 anhydrides Chemical class 0.000 description 8
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 7
- 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 7
- 238000001723 curing Methods 0.000 description 7
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 7
- 238000007654 immersion Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000000049 pigment Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- AHDSRXYHVZECER-UHFFFAOYSA-N 2,4,6-tris[(dimethylamino)methyl]phenol Chemical compound CN(C)CC1=CC(CN(C)C)=C(O)C(CN(C)C)=C1 AHDSRXYHVZECER-UHFFFAOYSA-N 0.000 description 6
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 6
- 239000010445 mica Substances 0.000 description 6
- 229910052618 mica group Inorganic materials 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 5
- 125000001453 quaternary ammonium group Chemical group 0.000 description 5
- 229940014800 succinic anhydride Drugs 0.000 description 5
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 4
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 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 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000008240 homogeneous mixture Substances 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
- 230000009969 flowable effect Effects 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052901 montmorillonite Inorganic materials 0.000 description 2
- CABDEMAGSHRORS-UHFFFAOYSA-N oxirane;hydrate Chemical compound O.C1CO1 CABDEMAGSHRORS-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VRHVIMKDGPTATK-UHFFFAOYSA-N 3-(2-ethylhex-1-enyl)oxolane-2,5-dione Chemical compound CCCCC(CC)=CC1CC(=O)OC1=O VRHVIMKDGPTATK-UHFFFAOYSA-N 0.000 description 1
- UJWPNMNCNGQIJP-UHFFFAOYSA-N 3-pent-1-enyloxolane-2,5-dione Chemical compound CCCC=CC1CC(=O)OC1=O UJWPNMNCNGQIJP-UHFFFAOYSA-N 0.000 description 1
- -1 Alkyl succinic anhydride Chemical compound 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-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
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000005341 cation exchange Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- VICYBMUVWHJEFT-UHFFFAOYSA-N dodecyltrimethylammonium ion Chemical compound CCCCCCCCCCCC[N+](C)(C)C VICYBMUVWHJEFT-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000005292 vacuum distillation 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
- C08G59/18—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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
-
- 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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4215—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Epoxy Resins (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA659234A CA659234A (en) | 1957-10-24 | Epoxy dipping compounds | |
| US692039A US3021234A (en) | 1957-10-24 | 1957-10-24 | Epoxy coating composition and method of coating electrical article therewith |
| GB33235/58A GB906423A (en) | 1957-10-24 | 1958-10-17 | Improved epoxy resin dipping compounds |
| DEM39379A DE1283420B (de) | 1957-10-24 | 1958-10-23 | Thixotrope UEberzugsmittel |
| JP3035558A JPS376466B1 (OSRAM) | 1957-10-24 | 1958-10-24 |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA659234T | |||
| US692039A US3021234A (en) | 1957-10-24 | 1957-10-24 | Epoxy coating composition and method of coating electrical article therewith |
| GB33235/58A GB906423A (en) | 1957-10-24 | 1958-10-17 | Improved epoxy resin dipping compounds |
| DEM39379A DE1283420B (de) | 1957-10-24 | 1958-10-23 | Thixotrope UEberzugsmittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1283420B true DE1283420B (de) | 1968-11-21 |
Family
ID=74095575
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEM39379A Pending DE1283420B (de) | 1957-10-24 | 1958-10-23 | Thixotrope UEberzugsmittel |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3021234A (OSRAM) |
| JP (1) | JPS376466B1 (OSRAM) |
| CA (1) | CA659234A (OSRAM) |
| DE (1) | DE1283420B (OSRAM) |
| GB (1) | GB906423A (OSRAM) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3109969A (en) * | 1959-07-11 | 1963-11-05 | Philips Corp | Capacitor for use at high operating voltages |
| US3256114A (en) * | 1962-01-23 | 1966-06-14 | Aerojet General Co | Method for preloading ultrasonic transducer |
| US3211581A (en) * | 1962-07-31 | 1965-10-12 | William John Van Schelven | Construction block of compressed salts encapsulated with epoxy resin |
| US3396138A (en) * | 1964-08-21 | 1968-08-06 | Tile Council Of America | Organic acid resistant compositions from epoxy resin, polyamines and clay |
| US5045588A (en) * | 1972-05-08 | 1991-09-03 | The United States Of America As Represented By The Secretary Of The Navy | High polymer suspension |
| US4127695A (en) * | 1975-10-07 | 1978-11-28 | Matsushita Electric Industrial Co., Ltd. | Method of insulating electromagnetic coils |
| US4980005A (en) * | 1987-03-13 | 1990-12-25 | The Boeing Company | Method for producing an aerospace structure having a cast-in-place noncompressible void filler |
| US4861643A (en) * | 1987-03-13 | 1989-08-29 | The Boeing Company | Aerospace structure having a cast-in-place noncompressible void filler |
| US4980401A (en) * | 1988-10-31 | 1990-12-25 | Hinden Edwin R | Chemical resistant tile and brick mortar |
| MX390080B (es) * | 2014-05-16 | 2025-03-20 | Vesuvius U S A Corp | Sistema de aglutinante de refractario. |
| KR102012788B1 (ko) * | 2015-09-23 | 2019-08-21 | 주식회사 엘지화학 | 접착 필름, 반도체 장치의 제조 방법 및 반도체 장치 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2622987A (en) * | 1951-04-10 | 1952-12-23 | Nat Lead Co | Coating composition and the vehicle therefor containing a compound of a clay and an onium base |
| CH305116A (de) * | 1950-11-27 | 1955-02-15 | Alfred Hauser Ernst | Verfahren zur Herstellung eines gelbildenden organophilen Tones. |
| CH312514A (de) * | 1950-11-27 | 1955-12-31 | Nat Lead Co | Verfahren zur Herstellung eines gelbildenden organophilen Tones. |
| FR1114888A (fr) * | 1953-08-28 | 1956-04-17 | Ciba Geigy | Procédé de durcissement de composés polyépoxydes |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL73196C (OSRAM) * | 1948-02-28 | |||
| GB678936A (en) * | 1948-10-20 | 1952-09-10 | Westinghouse Electric Int Co | Improvements in or relating to the treating of electrical windings with insulating varnishes |
| BE501783A (OSRAM) * | 1950-03-11 | 1900-01-01 | ||
| US2666719A (en) * | 1950-03-28 | 1954-01-19 | Petrolite Corp | Resinous coated article and method of making same |
| US2824851A (en) * | 1953-08-24 | 1958-02-25 | Minnesota Mining & Mfg | Acrylic acid derivatives of epoxide resins and method of curing same |
| US2850707A (en) * | 1954-04-15 | 1958-09-02 | Sylvania Electric Prod | Electromagnetic coils |
| DE1072801B (de) * | 1954-04-29 | 1960-01-07 | Westinghouse Electric Corporation, East Pittsburgh. Pa. (V. St. A.j | Form- und Überzugsmasse |
| BE541648A (OSRAM) * | 1955-04-07 | 1900-01-01 | ||
| US2804404A (en) * | 1955-10-04 | 1957-08-27 | Gen Motors Corp | Method of impregnating electrical windings |
-
0
- CA CA659234A patent/CA659234A/en not_active Expired
-
1957
- 1957-10-24 US US692039A patent/US3021234A/en not_active Expired - Lifetime
-
1958
- 1958-10-17 GB GB33235/58A patent/GB906423A/en not_active Expired
- 1958-10-23 DE DEM39379A patent/DE1283420B/de active Pending
- 1958-10-24 JP JP3035558A patent/JPS376466B1/ja active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH305116A (de) * | 1950-11-27 | 1955-02-15 | Alfred Hauser Ernst | Verfahren zur Herstellung eines gelbildenden organophilen Tones. |
| CH312514A (de) * | 1950-11-27 | 1955-12-31 | Nat Lead Co | Verfahren zur Herstellung eines gelbildenden organophilen Tones. |
| US2622987A (en) * | 1951-04-10 | 1952-12-23 | Nat Lead Co | Coating composition and the vehicle therefor containing a compound of a clay and an onium base |
| FR1114888A (fr) * | 1953-08-28 | 1956-04-17 | Ciba Geigy | Procédé de durcissement de composés polyépoxydes |
Also Published As
| Publication number | Publication date |
|---|---|
| US3021234A (en) | 1962-02-13 |
| JPS376466B1 (OSRAM) | 1962-06-29 |
| CA659234A (en) | 1963-03-12 |
| GB906423A (en) | 1962-09-19 |
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