DE2460768C3 - Härtbare wärmebeständige ungesättigte Polyesterharze, insbesondere zur Verwendung in der Elektroindustrie - Google Patents
Härtbare wärmebeständige ungesättigte Polyesterharze, insbesondere zur Verwendung in der ElektroindustrieInfo
- Publication number
- DE2460768C3 DE2460768C3 DE19742460768 DE2460768A DE2460768C3 DE 2460768 C3 DE2460768 C3 DE 2460768C3 DE 19742460768 DE19742460768 DE 19742460768 DE 2460768 A DE2460768 A DE 2460768A DE 2460768 C3 DE2460768 C3 DE 2460768C3
- Authority
- DE
- Germany
- Prior art keywords
- unsaturated polyester
- polyester resins
- alcohols
- residues
- carboxylic acids
- 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
- 229920006337 unsaturated polyester resin Polymers 0.000 title claims description 22
- 150000001735 carboxylic acids Chemical class 0.000 claims description 22
- 229920005989 resin Polymers 0.000 claims description 22
- 239000011347 resin Substances 0.000 claims description 22
- 150000001298 alcohols Chemical class 0.000 claims description 20
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 10
- 229920006305 unsaturated polyester Polymers 0.000 claims description 9
- 239000004135 Bone phosphate Substances 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- SPAMRUYRVYMHPV-UHFFFAOYSA-N 3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical group C1=CCCC2C(=O)NC(=O)C21 SPAMRUYRVYMHPV-UHFFFAOYSA-N 0.000 claims description 7
- 150000003949 imides Chemical group 0.000 claims description 7
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 6
- 239000000178 monomer Substances 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 6
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000001530 fumaric acid Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- 239000011976 maleic acid Substances 0.000 claims description 3
- 150000005846 sugar alcohols Polymers 0.000 claims description 3
- HENCHDCLZDQGIQ-UHFFFAOYSA-N 3-[3,5-bis(2-carboxyethyl)-2,4,6-trioxo-1,3,5-triazinan-1-yl]propanoic acid Chemical compound OC(=O)CCN1C(=O)N(CCC(O)=O)C(=O)N(CCC(O)=O)C1=O HENCHDCLZDQGIQ-UHFFFAOYSA-N 0.000 claims description 2
- 238000004870 electrical engineering Methods 0.000 claims description 2
- -1 acids Alcohols Chemical class 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 125000005462 imide group Chemical group 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 5
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 5
- 238000005470 impregnation Methods 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
- 230000004580 weight loss Effects 0.000 description 4
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 3
- 239000010754 BS 2869 Class F Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 description 3
- 238000001879 gelation Methods 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 3
- SGWZVZZVXOJRAQ-UHFFFAOYSA-N 2,6-Dimethyl-1,4-benzenediol Chemical compound CC1=CC(O)=CC(C)=C1O SGWZVZZVXOJRAQ-UHFFFAOYSA-N 0.000 description 2
- 125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- BCNBMSZKALBQEF-UHFFFAOYSA-N 1,3-dimethylpyrrolidin-2-one Chemical compound CC1CCN(C)C1=O BCNBMSZKALBQEF-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 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
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 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
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction 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
- 238000007086 side reaction Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000004250 tert-Butylhydroquinone Substances 0.000 description 1
- 235000019281 tert-butylhydroquinone Nutrition 0.000 description 1
- 150000003512 tertiary amines Chemical class 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
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/06—Unsaturated polyesters
-
- 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
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/685—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
- C08G63/6854—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/6858—Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- 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
- H01B3/421—Polyesters
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)
- Macromonomer-Based Addition Polymer (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Organic Insulating Materials (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742460768 DE2460768C3 (de) | 1974-12-21 | 1974-12-21 | Härtbare wärmebeständige ungesättigte Polyesterharze, insbesondere zur Verwendung in der Elektroindustrie |
| ES442941A ES442941A1 (es) | 1974-12-21 | 1975-11-25 | Procedimiento para la fabricacion de resinas de poliester nosaturadas, endurecibles, resistentes al calor, especialmentepara su empleo en la industria electrica. |
| NL7514640A NL169598C (nl) | 1974-12-21 | 1975-12-16 | Werkwijze ter bereiding van onverzadigde polyesterharsen. |
| IT5275375A IT1060455B (it) | 1974-12-21 | 1975-12-17 | Procedimento per la fabbricazione di resine di poliesteri temprabili refrattarie insature in particolare per impiegh nell industria elettrica |
| FR7538899A FR2295051A1 (fr) | 1974-12-21 | 1975-12-18 | Procede de preparation de resines de polyesters insatures durcissables, stables a la chaleur et utilisables en particulier dans l'industrie electrique |
| JP50150753A JPS5189592A (en) | 1974-12-21 | 1975-12-19 | Kokasei tainetsuseifuhowahoriesuterujushinoseiho |
| GB5201875A GB1522659A (en) | 1974-12-21 | 1975-12-19 | Hardenable unsaturated polyester resins |
| SE7514478A SE417832B (sv) | 1974-12-21 | 1975-12-19 | Forfarande for framstellning av herdbara och vermebestendiga polyesterhartser samt en genom forfarandet framstelld produkt |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742460768 DE2460768C3 (de) | 1974-12-21 | 1974-12-21 | Härtbare wärmebeständige ungesättigte Polyesterharze, insbesondere zur Verwendung in der Elektroindustrie |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2460768A1 DE2460768A1 (de) | 1976-07-01 |
| DE2460768B2 DE2460768B2 (de) | 1981-04-09 |
| DE2460768C3 true DE2460768C3 (de) | 1982-04-08 |
Family
ID=5934198
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19742460768 Expired DE2460768C3 (de) | 1974-12-21 | 1974-12-21 | Härtbare wärmebeständige ungesättigte Polyesterharze, insbesondere zur Verwendung in der Elektroindustrie |
Country Status (8)
| Country | Link |
|---|---|
| JP (1) | JPS5189592A (enExample) |
| DE (1) | DE2460768C3 (enExample) |
| ES (1) | ES442941A1 (enExample) |
| FR (1) | FR2295051A1 (enExample) |
| GB (1) | GB1522659A (enExample) |
| IT (1) | IT1060455B (enExample) |
| NL (1) | NL169598C (enExample) |
| SE (1) | SE417832B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2856050C2 (de) * | 1978-12-23 | 1995-01-19 | Herberts Gmbh | Verfahren zur Herstellung von ungesättigten, Imidgruppen enthaltenden Polyestern und ihre Verwendung |
| JPH01129013A (ja) * | 1987-11-12 | 1989-05-22 | Nitto Denko Corp | 不飽和ポリエステルイミド樹脂の製法 |
| JP2551602B2 (ja) * | 1987-11-12 | 1996-11-06 | 日東電工株式会社 | 不飽和ポリエステルイミド樹脂の製法 |
| JP2001502003A (ja) * | 1996-10-08 | 2001-02-13 | サイテク・テクノロジー・コーポレーシヨン | 架橋剤組成物およびそれを用いた低光沢のエポキシコーティング |
| DE19711410A1 (de) | 1997-03-19 | 1998-09-24 | Beck & Co Ag Dr | Tränk-, Verguß- und Überzugsmassen für elektrotechnische und/oder elektronische Bauteile sowie für Trägermaterialien für flächige Isolierstoffe |
| FR2910012B1 (fr) * | 2006-12-15 | 2009-03-06 | Cray Valley S A Sa | Resines polyesters insatures fonctionnalises par imides cycloaliphatiques insaturees, pour revetements et compositions de moulage |
-
1974
- 1974-12-21 DE DE19742460768 patent/DE2460768C3/de not_active Expired
-
1975
- 1975-11-25 ES ES442941A patent/ES442941A1/es not_active Expired
- 1975-12-16 NL NL7514640A patent/NL169598C/xx not_active IP Right Cessation
- 1975-12-17 IT IT5275375A patent/IT1060455B/it active
- 1975-12-18 FR FR7538899A patent/FR2295051A1/fr active Granted
- 1975-12-19 JP JP50150753A patent/JPS5189592A/ja active Granted
- 1975-12-19 GB GB5201875A patent/GB1522659A/en not_active Expired
- 1975-12-19 SE SE7514478A patent/SE417832B/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE2460768A1 (de) | 1976-07-01 |
| ES442941A1 (es) | 1977-08-01 |
| FR2295051B1 (enExample) | 1980-05-23 |
| GB1522659A (en) | 1978-08-23 |
| FR2295051A1 (fr) | 1976-07-16 |
| JPS5546405B2 (enExample) | 1980-11-22 |
| NL7514640A (nl) | 1976-06-23 |
| SE7514478L (sv) | 1976-06-22 |
| NL169598C (nl) | 1982-08-02 |
| DE2460768B2 (de) | 1981-04-09 |
| SE417832B (sv) | 1981-04-13 |
| IT1060455B (it) | 1982-08-20 |
| NL169598B (nl) | 1982-03-01 |
| JPS5189592A (en) | 1976-08-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1770643A1 (de) | Verfahren zur Herstellung von ungesaettigten Polyesterharzmassen | |
| DE2460768C3 (de) | Härtbare wärmebeständige ungesättigte Polyesterharze, insbesondere zur Verwendung in der Elektroindustrie | |
| DE1795857C3 (de) | Verfahren zur Herstellung von Formkörpern aus ungesättigten Polyestern | |
| GB1559254A (en) | Polyester and polyesterimide resins and insulating resins compositions prepared therefrom | |
| DE2720004A1 (de) | Copolyester sowie verfahren zu ihrer herstellung | |
| DE1127585B (de) | Verfahren zum Herstellen von Formkoerpern fuer elektrische Isolationen durch Aushaerten von ungesaettigten Polyestern aus gemischt aliphatisch-aromatischen AEthern mit freien Hydroxygruppen und ungesaettigten Dicarbonsaeuren | |
| DE3115380C2 (de) | Verfahren zur Herstellung ungesättigter Polyester | |
| DE2302842B2 (de) | Formmassen auf Basis ungesättigter Polyester, anpolymerisierbarer Vinylmonomerer und Celluloseester | |
| DE1520174A1 (de) | Verfahren zur Herstellung isolierter Spulen | |
| DE2003077B2 (de) | Neue härtbare Mischungen aus PoIyglycidylverbindungen, sauren Polyestern, aliphatisch-cycloaliphatischen Dicarbonsäuren und Polycarbonsäureanhydriden | |
| DE2849120A1 (de) | Elektrisch isolierende ueberzugszusammensetzung | |
| DE2904184A1 (de) | Formmasse und die daraus hergestellten spritzguss-formkoerper | |
| DE1495878A1 (de) | Lufttrocknende UEberzugsmassen | |
| EP0013397B1 (de) | Verfahren zur Herstellung von ungesättigten, Imidgruppen enthaltenden Polyestern und ihre Verwendung | |
| DE1112299B (de) | Verfahren zur Polymerisation von ungesaettigten Verbindungen | |
| AT212898B (de) | Elektrische Leiter mit Polyesterharz-Isolierungen und Verfahren zu deren Herstellung | |
| DE1017789B (de) | Verfahren zur Herstellung von Polymerisationsprodukten | |
| AT202776B (de) | Verfahren zur Herstellung eines Polyesterharzes | |
| DE4122765A1 (de) | Ungesaettigte ester, ein verfahren zu ihrer herstellung und ihre verwendung | |
| DE860714C (de) | Verfahren zur Herstellung von Alkydharzen | |
| AT247490B (de) | Lack und Anstrichmittel | |
| DE1595271A1 (de) | Copolyester und Verfahren zu deren Herstellung | |
| DE3229618A1 (de) | Ungesaettigte, homo- und/oder copolymerisierbare polyester, verfahren zu ihrer herstellung und ihre verwendung | |
| DE1445287C3 (de) | Verfahren zur Herstellung von ungesättigten Polyestern | |
| AT229040B (de) | Verfahren zur Herstellung von hochmolekularen Polyestern |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) |