DE1446735A1 - Verfahren zur Herstellung von Kunstharzen fuer UEberzugsmassen - Google Patents
Verfahren zur Herstellung von Kunstharzen fuer UEberzugsmassenInfo
- Publication number
- DE1446735A1 DE1446735A1 DE19571446735 DE1446735A DE1446735A1 DE 1446735 A1 DE1446735 A1 DE 1446735A1 DE 19571446735 DE19571446735 DE 19571446735 DE 1446735 A DE1446735 A DE 1446735A DE 1446735 A1 DE1446735 A1 DE 1446735A1
- Authority
- DE
- Germany
- Prior art keywords
- polyisocyanate
- wire
- equivalent
- polyester
- 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
- 238000000034 method Methods 0.000 title claims description 11
- 229920003002 synthetic resin Polymers 0.000 title claims description 9
- 239000000057 synthetic resin Substances 0.000 title claims description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 238000000576 coating method Methods 0.000 title description 14
- 239000011248 coating agent Substances 0.000 title description 10
- 150000001875 compounds Chemical class 0.000 title description 4
- 239000000463 material Substances 0.000 claims description 39
- 229920001228 polyisocyanate Polymers 0.000 claims description 31
- 239000005056 polyisocyanate Substances 0.000 claims description 31
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- 150000002148 esters Chemical class 0.000 claims description 7
- 150000005846 sugar alcohols Polymers 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 239000011247 coating layer Substances 0.000 claims description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 229920005862 polyol Polymers 0.000 claims description 4
- 150000003077 polyols Chemical class 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- 125000005442 diisocyanate group Chemical group 0.000 claims description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 description 20
- 239000002904 solvent Substances 0.000 description 19
- 238000005299 abrasion Methods 0.000 description 17
- 239000010410 layer Substances 0.000 description 17
- 238000012360 testing method Methods 0.000 description 12
- 210000003298 dental enamel Anatomy 0.000 description 10
- 229910000679 solder Inorganic materials 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000004020 conductor Substances 0.000 description 6
- 229920001225 polyester resin Polymers 0.000 description 6
- 239000004645 polyester resin Substances 0.000 description 6
- 238000009835 boiling Methods 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
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 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 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 3
- 238000005476 soldering Methods 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 2
- 150000003739 xylenols Chemical class 0.000 description 2
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical compound ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- MGIAHHJRDZCTHG-UHFFFAOYSA-N benzene-1,3-dicarboxylic acid;terephthalic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C=C1.OC(=O)C1=CC=CC(C(O)=O)=C1 MGIAHHJRDZCTHG-UHFFFAOYSA-N 0.000 description 1
- LHQLJMJLROMYRN-UHFFFAOYSA-L cadmium acetate Chemical compound [Cd+2].CC([O-])=O.CC([O-])=O LHQLJMJLROMYRN-UHFFFAOYSA-L 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000009189 diving Effects 0.000 description 1
- 239000002320 enamel (paints) Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940046892 lead acetate Drugs 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 239000011787 zinc oxide Substances 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
- H01B3/302—Polyurethanes or polythiourethanes; Polyurea or polythiourea
-
- 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
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
- C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
- C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols
- C08G18/4219—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols from aromatic dicarboxylic acids and dialcohols in combination with polycarboxylic acids and/or polyhydroxy compounds which are at least trifunctional
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
-
- 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
- H01B3/42—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 polyesters; polyethers; polyacetals
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)
- Organic Insulating Materials (AREA)
- Insulated Conductors (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US588557A US2935487A (en) | 1956-05-31 | 1956-05-31 | Polyester-polyisocyanate insulating materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1446735A1 true DE1446735A1 (de) | 1969-10-09 |
Family
ID=24354323
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19571446735 Pending DE1446735A1 (de) | 1956-05-31 | 1957-05-31 | Verfahren zur Herstellung von Kunstharzen fuer UEberzugsmassen |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US2935487A (en, 2012) |
| BE (1) | BE557685A (en, 2012) |
| DE (1) | DE1446735A1 (en, 2012) |
| GB (1) | GB820343A (en, 2012) |
| NL (1) | NL111500C (en, 2012) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1994020966A1 (de) * | 1993-03-12 | 1994-09-15 | Dr. Beck & Co. Ag | Verzinnbare drahtbeschichtungsmittel sowie verfahren zum kontinuierlichen beschichten von drähten |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3115479A (en) * | 1955-12-08 | 1963-12-24 | R oconr | |
| DE1096031B (de) * | 1958-08-04 | 1960-12-29 | Bayer Ag | Verfahren zur Herstellung von Kunststoff-Formkoerpern und UEberzuegen |
| FR1236526A (fr) * | 1959-04-24 | 1960-07-22 | Onera (Off Nat Aerospatiale) | Colle |
| US3210215A (en) * | 1959-11-02 | 1965-10-05 | Ici Ltd | Process for coating substrates with compositions comprising vinyl chloride polymers and polyisocyanate modified polyesters of aliphatic acids and diols with carbon: oxygen content of at least 5:2 |
| US3210439A (en) * | 1959-11-02 | 1965-10-05 | Ici Ltd | Coating and adhesive compositions comprising vinyl chloride polymers and polyisocyanate modified polyesters of aliphatic acids and diols with carbon:oxygen content of at least 5:2 |
| US3133340A (en) * | 1959-11-10 | 1964-05-19 | Goodyear Tire & Rubber | Printer's roll comprising a polyurethane and method for producing same |
| IT649529A (en, 2012) * | 1960-05-25 | 1900-01-01 | ||
| DE1181844B (de) * | 1960-07-30 | 1964-11-19 | Bayer Ag | Lackloesungen |
| US3223672A (en) * | 1960-12-28 | 1965-12-14 | American Can Co | Polyurethane solution and method of making same |
| US3248371A (en) * | 1961-03-10 | 1966-04-26 | Wyandotte Chemicals Corp | Cross-linking blocked two-step prepolymer polyurethane coating compositions |
| US3249578A (en) * | 1965-02-10 | 1966-05-03 | Schenectady Chemical | Coating compositions of a dibasic polycarboxylic acid/tris (2-hydroxyethyl) isocyanurate polyester and a phenolformaldehyde resin |
| US3214489A (en) * | 1961-09-22 | 1965-10-26 | Goodrich Co B F | Polycarbonate plasticized polyurethanes |
| US3213055A (en) * | 1962-07-26 | 1965-10-19 | Westinghouse Electric Corp | Diisocyanate modified epoxy polyesteramide coating resins and electrical conductors insulated therewith |
| DE1299416B (de) * | 1963-04-02 | 1969-07-17 | Takeda Chemical Industries Ltd | Waessrige Klebstofldispersionen zum Verkleben von Kautschuk mit faserigen Materialien |
| US3532661A (en) * | 1966-03-09 | 1970-10-06 | Gen Constr Elect Mec | Impregnating varnish for electric motors wound with wire enamelled with polyester-imide |
| DE2632047C3 (de) * | 1976-07-16 | 1987-01-22 | Dr. Beck & Co Ag, 2000 Hamburg | Verwendung von Polyesterurethanlacken |
| US4581093A (en) * | 1980-12-15 | 1986-04-08 | Whittaker Corporation | Branched polyester adhesive compositions and method employing same |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL57709C (en, 2012) * | 1940-07-02 | |||
| US2606162A (en) * | 1948-01-30 | 1952-08-05 | Ici Ltd | Compositions comprising polyisocyanate modified polyesters and vinyl chloride polymers |
| GB650358A (en) * | 1948-10-08 | 1951-02-21 | Owen Burchell Edgar | Film-forming copolyesters and films thereof |
| BE501717A (en, 2012) * | 1950-03-09 | 1900-01-01 |
-
0
- BE BE557685D patent/BE557685A/xx unknown
- NL NL111500D patent/NL111500C/xx active
-
1956
- 1956-05-31 US US588557A patent/US2935487A/en not_active Expired - Lifetime
-
1957
- 1957-05-13 GB GB15124/57A patent/GB820343A/en not_active Expired
- 1957-05-31 DE DE19571446735 patent/DE1446735A1/de active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1994020966A1 (de) * | 1993-03-12 | 1994-09-15 | Dr. Beck & Co. Ag | Verzinnbare drahtbeschichtungsmittel sowie verfahren zum kontinuierlichen beschichten von drähten |
Also Published As
| Publication number | Publication date |
|---|---|
| GB820343A (en) | 1959-09-16 |
| US2935487A (en) | 1960-05-03 |
| NL111500C (en, 2012) | |
| BE557685A (en, 2012) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1446735A1 (de) | Verfahren zur Herstellung von Kunstharzen fuer UEberzugsmassen | |
| DE1520007A1 (de) | Verfahren zur Herstellung von Polyestern | |
| AT213987B (de) | Verfahren zur Herstellung von Emaildraht | |
| DE1515751A1 (de) | Emaillierter verseilter Leiterstrang fuer Rohrkabel | |
| DE642191C (de) | Verfahren zum UEberziehen von Eisen- und Stahlgegenstaenden mit einer Schutzschicht | |
| DE1164588B (de) | UEberzugsmittel bzw. daraus hergestellte Lacke fuer elektrische Leiter | |
| DE2347206A1 (de) | Verfahren zum aufbringen von aluminiumschutzueberzuegen auf eisensubstraten und mit solchen ueberzuegen versehene substrate | |
| DE3048348C2 (de) | Verfahren zum Herstellen von isolierten direkt verzinnbaren Wickeldrähten | |
| AT253644B (de) | Eingefärbte Isolierschicht für elektrische Leiter | |
| DE970286C (de) | Selbstausheilender Kondensator | |
| DE347781C (de) | Verfahren zur Herstellung eines schuetzenden UEberzuges auf Gegenstaenden aus Magnesium | |
| AT149272B (de) | Verfahren zur Herstellung isolierter elektrischer Leiter. | |
| DE1170096B (de) | Drahtlacke fuer loetbare lackierte Draehte | |
| DE2522386C3 (de) | Elektroisolierlack | |
| DE931666C (de) | Verfahren zum Lackieren elektrischer Leiter mit ofentrocknenden Lacken | |
| AT134791B (de) | Isolierter Leiter. | |
| DE1494452C2 (de) | Hochwärmebeständige Überzüge liefernder Elektroisolierlack | |
| DE2030857A1 (de) | Verfahren und Präparat zur Entfernung von Umhüllungen von Drahten | |
| DE895180C (de) | Verfahren zur Herstellung von oelfreien elektrischen Lackdraehten | |
| DE924287C (de) | Verfahren zur Herstellung von harzartigen Kondensationsprodukten | |
| DD148193A1 (de) | Verfahren zur herstellung korrosionsverhindernder ueberzuege mit flussmitteleigenschaften | |
| DE495202C (de) | Elektrischer Kondensator, bei dem das Dielektrikum in fluessigem Zustande auf die leitenden Belaege aufgebracht ist und nach dem Trocknen auf diesen einen festen UEberzug bildet | |
| DE2528143A1 (de) | Kaltgewalztes emaillierstahlblech | |
| DE478435C (de) | Verfahren zum Lackieren von Draehten | |
| DE1036962B (de) | Verfahren zur Herstellung eines gegen Difluorchlormethan widerstandsfaehigen isolierten elektrischen Leiters |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| SH | Request for examination between 03.10.1968 and 22.04.1971 |