DE2632047C3 - Verwendung von Polyesterurethanlacken - Google Patents
Verwendung von PolyesterurethanlackenInfo
- Publication number
- DE2632047C3 DE2632047C3 DE2632047A DE2632047A DE2632047C3 DE 2632047 C3 DE2632047 C3 DE 2632047C3 DE 2632047 A DE2632047 A DE 2632047A DE 2632047 A DE2632047 A DE 2632047A DE 2632047 C3 DE2632047 C3 DE 2632047C3
- Authority
- DE
- Germany
- Prior art keywords
- wire
- mol
- wires
- enamelled
- enamel
- 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.)
- Expired
Links
- 229920000728 polyester Polymers 0.000 title claims description 19
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 title claims description 8
- 239000003973 paint Substances 0.000 title description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- 239000012948 isocyanate Substances 0.000 claims description 9
- -1 aromatic isocyanates Chemical class 0.000 claims description 7
- 150000003673 urethanes Chemical class 0.000 claims description 7
- 238000004804 winding Methods 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000002966 varnish Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 210000003298 dental enamel Anatomy 0.000 description 12
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 239000008096 xylene Substances 0.000 description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 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
- 239000002253 acid Substances 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229910000679 solder Inorganic materials 0.000 description 4
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 3
- IHEDBVUTTQXGSJ-UHFFFAOYSA-M 2-[bis(2-oxidoethyl)amino]ethanolate;titanium(4+);hydroxide Chemical compound [OH-].[Ti+4].[O-]CCN(CC[O-])CC[O-] IHEDBVUTTQXGSJ-UHFFFAOYSA-M 0.000 description 3
- 239000001361 adipic acid Substances 0.000 description 3
- 235000011037 adipic acid Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 239000004922 lacquer Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- OQBLGYCUQGDOOR-UHFFFAOYSA-L 1,3,2$l^{2}-dioxastannolane-4,5-dione Chemical compound O=C1O[Sn]OC1=O OQBLGYCUQGDOOR-UHFFFAOYSA-L 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- HPVRZSQOEHEUKJ-UHFFFAOYSA-N 1-methoxyhexan-2-one Chemical compound CCCCC(=O)COC HPVRZSQOEHEUKJ-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- HCGFUIQPSOCUHI-UHFFFAOYSA-N 2-propan-2-yloxyethanol Chemical compound CC(C)OCCO HCGFUIQPSOCUHI-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- YYLLIJHXUHJATK-UHFFFAOYSA-N Cyclohexyl acetate Chemical compound CC(=O)OC1CCCCC1 YYLLIJHXUHJATK-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
- 150000007513 acids Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000000903 blocking effect 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
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 101150038956 cup-4 gene Proteins 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 238000004534 enameling Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- VQPKAMAVKYTPLB-UHFFFAOYSA-N lead;octanoic acid Chemical compound [Pb].CCCCCCCC(O)=O VQPKAMAVKYTPLB-UHFFFAOYSA-N 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 239000011527 polyurethane coating Substances 0.000 description 1
- 238000010944 pre-mature reactiony Methods 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
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical class O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
- JMXKSZRRTHPKDL-UHFFFAOYSA-N titanium ethoxide Chemical compound [Ti+4].CC[O-].CC[O-].CC[O-].CC[O-] JMXKSZRRTHPKDL-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 150000003739 xylenols Chemical class 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
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- 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
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2938—Coating on discrete and individual rods, strands or filaments
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31605—Next to free metal
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)
- Paints Or Removers (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2632047A DE2632047C3 (de) | 1976-07-16 | 1976-07-16 | Verwendung von Polyesterurethanlacken |
| IT4993877A IT1079079B (it) | 1976-07-16 | 1977-06-22 | Poliestereuretani induribili per la produzione di fili per avvolgere direttamente stagnabili |
| CH793777A CH625823A5 (en, 2012) | 1976-07-16 | 1977-06-28 | |
| GB2736277A GB1554351A (en) | 1976-07-16 | 1977-06-30 | Production of enamelled wires |
| AT471677A AT357243B (de) | 1976-07-16 | 1977-07-01 | Verwendung von haertbaren polyesterurethanen zur herstellung von direkt verzinnbaren wickel- draehten |
| ES460673A ES460673A1 (es) | 1976-07-16 | 1977-07-12 | Procedimiento para la utilizacion de uretanos de poliester endurecibles para la fabricacion de hilos de bobinado, di- rectamente esta/ables. |
| BR7704554A BR7704554A (pt) | 1976-07-16 | 1977-07-12 | Processo para preparacao de arames de amarracao isolados por laca |
| FR7721794A FR2358452A1 (fr) | 1976-07-16 | 1977-07-13 | Polyesterurethannes durcissables pour la preparation de fils laques directement etamables |
| NL7707913A NL180017C (nl) | 1976-07-16 | 1977-07-15 | Werkwijze voor het vervaardigen van met lak geisoleerde wikkeldraden. |
| SE7708255A SE429275B (sv) | 1976-07-16 | 1977-07-15 | Anvendning av herdbara polyesteruretaner for framstellning av lackisolerade tradar |
| JP8464477A JPS5311930A (en) | 1976-07-16 | 1977-07-16 | Setting polyesterrurethane lacquer for producing electric wire capable of being directly tinned |
| US05/816,775 US4131693A (en) | 1976-07-16 | 1977-07-18 | Hardenable polyesterurethane composition for producing a directly tinnable wire |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2632047A DE2632047C3 (de) | 1976-07-16 | 1976-07-16 | Verwendung von Polyesterurethanlacken |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2632047A1 DE2632047A1 (de) | 1978-01-26 |
| DE2632047B2 DE2632047B2 (de) | 1981-07-09 |
| DE2632047C3 true DE2632047C3 (de) | 1987-01-22 |
Family
ID=5983186
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2632047A Expired DE2632047C3 (de) | 1976-07-16 | 1976-07-16 | Verwendung von Polyesterurethanlacken |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4131693A (en, 2012) |
| JP (1) | JPS5311930A (en, 2012) |
| AT (1) | AT357243B (en, 2012) |
| BR (1) | BR7704554A (en, 2012) |
| CH (1) | CH625823A5 (en, 2012) |
| DE (1) | DE2632047C3 (en, 2012) |
| ES (1) | ES460673A1 (en, 2012) |
| FR (1) | FR2358452A1 (en, 2012) |
| GB (1) | GB1554351A (en, 2012) |
| IT (1) | IT1079079B (en, 2012) |
| NL (1) | NL180017C (en, 2012) |
| SE (1) | SE429275B (en, 2012) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4254168A (en) * | 1979-07-27 | 1981-03-03 | Minnesota Mining And Manufacturing Company | Chip-resistant pigmented polyurethane protective coating |
| US4260717A (en) * | 1980-01-10 | 1981-04-07 | Ehrhart Wendell A | High performance urethane coating which is a solvent solution of a polyester containing hydroxyl groups and an aliphatic diisocyanate |
| US4338234A (en) * | 1980-06-04 | 1982-07-06 | Ppg Industries, Inc. | Sizing composition and sized glass fibers and strands produced therewith |
| US4338233A (en) * | 1981-06-15 | 1982-07-06 | Ppg Industries, Inc. | Aqueous sizing composition and sized glass fibers and method |
| US4435474A (en) | 1981-06-15 | 1984-03-06 | Ppg Industries, Inc. | Aqueous sizing composition and sized glass fibers and method |
| US4477496A (en) * | 1981-06-15 | 1984-10-16 | Ppg Industries, Inc. | Process for preparing sized glass fiber roving |
| US4410645A (en) * | 1981-06-15 | 1983-10-18 | Ppg Industries, Inc. | Aqueous sizing composition and sized glass fibers and method |
| JPS5850518A (ja) * | 1981-09-22 | 1983-03-25 | Minolta Camera Co Ltd | 一眼レフレツクスカメラのミラ−装置 |
| US4457970A (en) * | 1982-06-21 | 1984-07-03 | Ppg Industries, Inc. | Glass fiber reinforced thermoplastics |
| FI865050A0 (fi) * | 1985-05-08 | 1986-12-11 | Reinmar John & Rainer | Belaeggningsmassa foer elastiska underlag, dess anvaendning och foerfarande foer framstaellning av skyddsbelaeggningar. |
| JPH02178372A (ja) * | 1988-12-29 | 1990-07-11 | Toutoku Toryo Kk | 絶縁電線用塗料 |
| DE4201376C1 (en, 2012) * | 1992-01-20 | 1993-01-28 | Herberts Gmbh, 5600 Wuppertal, De | |
| US20030094876A1 (en) * | 2001-11-20 | 2003-05-22 | Chun-Pu Hsu | Stator structure with composite windings |
| US20030155817A1 (en) * | 2002-01-04 | 2003-08-21 | Borde Benjamin La | Super conducting action motor (acronym SCAM): electrical apparatus for generating a one-directional (ie reactionless) force, with applications in space vehicle propulsion |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE495849A (en, 2012) * | 1949-05-30 | |||
| NL102992C (en, 2012) * | 1955-07-07 | |||
| US3115479A (en) * | 1955-12-08 | 1963-12-24 | R oconr | |
| NL111500C (en, 2012) * | 1956-05-31 | |||
| US2982754A (en) * | 1957-11-08 | 1961-05-02 | Schenectady Varnish Company In | Polyisocyanate-modified polyester of terephthalic or isophthalic acid, and electrical conductor coated therewith |
| NL106889C (en, 2012) * | 1957-09-25 | 1900-01-01 | ||
| BE571625A (en, 2012) * | 1957-10-01 | 1900-01-01 | ||
| US2970119A (en) * | 1958-02-21 | 1961-01-31 | Eastman Kodak Co | Polyester-urethanes derived from dialkylmalonic compounds and textile fabric coated therewith |
| US3252944A (en) * | 1962-08-27 | 1966-05-24 | Gen Motors Corp | Urethane coating composition for electrical conductors and method |
| CH475326A (de) * | 1965-03-17 | 1969-07-15 | Bayer Ag | Lacklösung |
| CH505167A (de) * | 1968-12-09 | 1971-03-31 | Ciba Geigy Ag | Verfahren zur Herstellung von kristallinen Polyurethan-Kunststoffprodukten auf Basis von Diisocyanaten und linearen Polyestern |
| US3764375A (en) * | 1971-04-23 | 1973-10-09 | Gen Electric | Polyurethane wire coating method |
| US3763079A (en) * | 1971-06-01 | 1973-10-02 | Du Pont | Polyurethanes based on mixed aromatic aliphatic polyesters |
| DE2404740C2 (de) * | 1974-02-01 | 1982-04-29 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Filmen und Überzügen und Beschichtungsmittel |
| DE2545912A1 (de) * | 1975-10-14 | 1977-04-28 | Wiedeking Chem Fab | Loetbarer drahtlack |
-
1976
- 1976-07-16 DE DE2632047A patent/DE2632047C3/de not_active Expired
-
1977
- 1977-06-22 IT IT4993877A patent/IT1079079B/it active
- 1977-06-28 CH CH793777A patent/CH625823A5/de not_active IP Right Cessation
- 1977-06-30 GB GB2736277A patent/GB1554351A/en not_active Expired
- 1977-07-01 AT AT471677A patent/AT357243B/de not_active IP Right Cessation
- 1977-07-12 ES ES460673A patent/ES460673A1/es not_active Expired
- 1977-07-12 BR BR7704554A patent/BR7704554A/pt unknown
- 1977-07-13 FR FR7721794A patent/FR2358452A1/fr active Granted
- 1977-07-15 NL NL7707913A patent/NL180017C/xx not_active IP Right Cessation
- 1977-07-15 SE SE7708255A patent/SE429275B/xx not_active IP Right Cessation
- 1977-07-16 JP JP8464477A patent/JPS5311930A/ja active Granted
- 1977-07-18 US US05/816,775 patent/US4131693A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| GB1554351A (en) | 1979-10-17 |
| SE429275B (sv) | 1983-08-22 |
| ES460673A1 (es) | 1978-05-16 |
| SE7708255L (sv) | 1978-01-17 |
| NL7707913A (nl) | 1978-01-18 |
| ATA471677A (de) | 1979-11-15 |
| NL180017C (nl) | 1986-12-16 |
| AT357243B (de) | 1980-06-25 |
| CH625823A5 (en, 2012) | 1981-10-15 |
| DE2632047A1 (de) | 1978-01-26 |
| JPS5533831B2 (en, 2012) | 1980-09-03 |
| US4131693A (en) | 1978-12-26 |
| FR2358452A1 (fr) | 1978-02-10 |
| FR2358452B1 (en, 2012) | 1983-07-29 |
| IT1079079B (it) | 1985-05-08 |
| DE2632047B2 (de) | 1981-07-09 |
| NL180017B (nl) | 1986-07-16 |
| BR7704554A (pt) | 1978-03-28 |
| JPS5311930A (en) | 1978-02-02 |
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| OD | Request for examination | ||
| 8263 | Opposition against grant of a patent | ||
| C3 | Grant after two publication steps (3rd publication) |