NO742725L - - Google Patents
Info
- Publication number
- NO742725L NO742725L NO742725A NO742725A NO742725L NO 742725 L NO742725 L NO 742725L NO 742725 A NO742725 A NO 742725A NO 742725 A NO742725 A NO 742725A NO 742725 L NO742725 L NO 742725L
- Authority
- NO
- Norway
- Prior art keywords
- epoxy
- epoxy resin
- equivalents
- amine
- mass
- Prior art date
Links
- 239000003822 epoxy resin Substances 0.000 claims description 34
- 229920000647 polyepoxide Polymers 0.000 claims description 34
- 239000004593 Epoxy Substances 0.000 claims description 31
- 150000001412 amines Chemical class 0.000 claims description 20
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 14
- 150000004985 diamines Chemical class 0.000 claims description 12
- 239000000049 pigment Substances 0.000 claims description 11
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 5
- 150000003512 tertiary amines Chemical class 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 claims description 3
- 230000002787 reinforcement Effects 0.000 claims description 3
- 229920001187 thermosetting polymer Polymers 0.000 claims description 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 description 27
- 239000000843 powder Substances 0.000 description 23
- 239000011248 coating agent Substances 0.000 description 17
- 230000008719 thickening Effects 0.000 description 17
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 16
- 239000000203 mixture Substances 0.000 description 16
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 14
- -1 polyethylene Polymers 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 12
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 11
- 238000003756 stirring Methods 0.000 description 11
- 239000004698 Polyethylene Substances 0.000 description 10
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 10
- 229920000573 polyethylene Polymers 0.000 description 10
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 8
- 238000001816 cooling Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000004848 polyfunctional curative Substances 0.000 description 8
- 239000004925 Acrylic resin Substances 0.000 description 7
- 239000011888 foil Substances 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 238000005096 rolling process Methods 0.000 description 7
- 239000004408 titanium dioxide Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 229910052681 coesite Inorganic materials 0.000 description 6
- 229910052906 cristobalite Inorganic materials 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 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 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229910052682 stishovite Inorganic materials 0.000 description 6
- 229910052905 tridymite Inorganic materials 0.000 description 6
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 5
- 241000428199 Mustelinae Species 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 238000000227 grinding Methods 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 235000012239 silicon dioxide Nutrition 0.000 description 5
- 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 4
- 229910001873 dinitrogen Inorganic materials 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- 229920006337 unsaturated polyester resin Polymers 0.000 description 3
- 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 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 230000009969 flowable effect Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000001960 triggered effect Effects 0.000 description 2
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical group CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- HSUODFYJTNEEGW-UHFFFAOYSA-N 1-n-cyclohexylpropane-1,2-diamine Chemical compound CC(N)CNC1CCCCC1 HSUODFYJTNEEGW-UHFFFAOYSA-N 0.000 description 1
- DPQHRXRAZHNGRU-UHFFFAOYSA-N 2,4,4-trimethylhexane-1,6-diamine Chemical compound NCC(C)CC(C)(C)CCN DPQHRXRAZHNGRU-UHFFFAOYSA-N 0.000 description 1
- MOBNLCPBAMKACS-UHFFFAOYSA-N 2-(1-chloroethyl)oxirane Chemical compound CC(Cl)C1CO1 MOBNLCPBAMKACS-UHFFFAOYSA-N 0.000 description 1
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 1
- CUFXMPWHOWYNSO-UHFFFAOYSA-N 2-[(4-methylphenoxy)methyl]oxirane Chemical compound C1=CC(C)=CC=C1OCC1OC1 CUFXMPWHOWYNSO-UHFFFAOYSA-N 0.000 description 1
- HPILSDOMLLYBQF-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)butoxymethyl]oxirane Chemical compound C1OC1COC(CCC)OCC1CO1 HPILSDOMLLYBQF-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 1
- FEUISMYEFPANSS-UHFFFAOYSA-N 2-methylcyclohexan-1-amine Chemical compound CC1CCCCC1N FEUISMYEFPANSS-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- IGSBHTZEJMPDSZ-UHFFFAOYSA-N 4-[(4-amino-3-methylcyclohexyl)methyl]-2-methylcyclohexan-1-amine Chemical compound C1CC(N)C(C)CC1CC1CC(C)C(N)CC1 IGSBHTZEJMPDSZ-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical group CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- XFUOBHWPTSIEOV-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohexane-1,2-dicarboxylate Chemical compound C1CCCC(C(=O)OCC2OC2)C1C(=O)OCC1CO1 XFUOBHWPTSIEOV-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- KEIQPMUPONZJJH-UHFFFAOYSA-N dicyclohexylmethanediamine Chemical compound C1CCCCC1C(N)(N)C1CCCCC1 KEIQPMUPONZJJH-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000007590 electrostatic spraying Methods 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- ZETYUTMSJWMKNQ-UHFFFAOYSA-N n,n',n'-trimethylhexane-1,6-diamine Chemical compound CNCCCCCCN(C)C ZETYUTMSJWMKNQ-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000011265 semifinished product Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—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
- C08G59/50—Amines
-
- 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
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
- C08G59/4021—Ureas; Thioureas; Guanidines; Dicyandiamides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2338430A DE2338430C3 (de) | 1973-07-28 | 1973-07-28 | Heißhärtbare, eingedickte Epoxidharzmassen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO742725L true NO742725L (de) | 1975-02-24 |
Family
ID=5888267
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO742725A NO742725L (de) | 1973-07-28 | 1974-07-26 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3914204A (de) |
| BE (1) | BE818146R (de) |
| DE (1) | DE2338430C3 (de) |
| DK (1) | DK177174A (de) |
| ES (1) | ES423524A1 (de) |
| FR (1) | FR2238736B2 (de) |
| NL (1) | NL7410209A (de) |
| NO (1) | NO742725L (de) |
| SE (1) | SE7409680L (de) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3256442A (en) * | 1961-12-08 | 1966-06-14 | Perrin Stryker | Flexible sheet containing a high proportion of rigid material |
| ES444862A1 (es) * | 1976-02-03 | 1977-09-16 | Pellicer Carlos F | Procedimiento para la obtencion de un producto ignifugo de resina epoxi. |
| US4260727A (en) * | 1979-07-23 | 1981-04-07 | Henkel Corporation | Epoxy-amine adducts for use in electrodeposition |
| US4360649A (en) * | 1980-04-30 | 1982-11-23 | Sumitomo Chemical Company, Limited | Curable composition |
| US4608300A (en) * | 1983-06-21 | 1986-08-26 | Ciba-Geigy Corporation | Fibre composite materials impregnated with a curable epoxide resin matrix |
| DE3340788A1 (de) * | 1983-11-11 | 1985-05-23 | Skw Trostberg Ag, 8223 Trostberg | Haerter fuer epoxidharzmassen |
| US5223172B1 (en) * | 1983-11-11 | 1998-09-29 | Sueddeutsche Kalkstickstoff | Hardener for epoxide resin masses |
| EP0253272B1 (de) * | 1986-07-11 | 1992-09-23 | Hoechst Aktiengesellschaft | Additionsverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung |
| JPS6375044A (ja) * | 1986-09-17 | 1988-04-05 | Toto Ltd | 連続気孔多孔体の製造方法 |
| JPH07100766B2 (ja) * | 1987-06-25 | 1995-11-01 | ソマール株式会社 | エポキシ樹脂粉体塗料組成物 |
| AT394197B (de) * | 1989-08-23 | 1992-02-10 | Vianova Kunstharz Ag | Verfahren zur herstellung von bindemitteln fuer kathodisch abscheidbare lacke |
| US5545278A (en) * | 1989-10-25 | 1996-08-13 | Thiokol Corporation | Method for increasing fiber strength translation in composition pressure vessels using matrix resin formulations containing anhydride curing agents and surface-active agents |
| US5593770A (en) * | 1989-10-25 | 1997-01-14 | Thiokol Corporation | Chemorheologically tailored matrix resin formulations containing anhydride curing agents |
| DE4410785A1 (de) * | 1994-03-28 | 1995-10-05 | Hoechst Ag | Amin-modifizierte Epoxidharz-Zusammensetzung |
| FR2743362B1 (fr) * | 1996-01-05 | 1998-02-06 | Vetrotex France Sa | Composition d'ensimage pour fils de verre, procede utilisant cette composition et produits resultants |
| US20030015823A1 (en) * | 2001-07-18 | 2003-01-23 | Hydranautics | Method for forming a thick section, thermoset, solid casting |
| GB2462996B (en) * | 2005-07-19 | 2011-10-12 | Hexcel Composites Ltd | A moulding material |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2909448A (en) * | 1955-03-07 | 1959-10-20 | Shell Dev | Salts of polyamine polyepoxide adducts and their use as curing agents for polyepoxides |
| US3515698A (en) * | 1967-05-24 | 1970-06-02 | Hercules Inc | High molecular weight polymers containing the reaction product of an aliphatic amine and a mono- or dioxirane as antistatic agent |
| CH565216A5 (de) * | 1970-06-12 | 1975-08-15 | Schering Ag |
-
1973
- 1973-07-28 DE DE2338430A patent/DE2338430C3/de not_active Expired
-
1974
- 1974-02-22 ES ES423524A patent/ES423524A1/es not_active Expired
- 1974-03-29 DK DK177174*A patent/DK177174A/da not_active IP Right Cessation
- 1974-07-19 US US490058A patent/US3914204A/en not_active Expired - Lifetime
- 1974-07-25 SE SE7409680A patent/SE7409680L/xx unknown
- 1974-07-26 BE BE146995A patent/BE818146R/xx active
- 1974-07-26 NO NO742725A patent/NO742725L/no unknown
- 1974-07-29 FR FR7426243A patent/FR2238736B2/fr not_active Expired
- 1974-07-29 NL NL7410209A patent/NL7410209A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK177174A (de) | 1975-04-01 |
| DE2338430B2 (de) | 1976-09-02 |
| BE818146R (fr) | 1975-01-27 |
| NL7410209A (nl) | 1975-01-30 |
| FR2238736B2 (de) | 1978-05-19 |
| DE2338430A1 (de) | 1975-02-27 |
| FR2238736A2 (de) | 1975-02-21 |
| SE7409680L (de) | 1975-01-29 |
| DE2338430C3 (de) | 1978-10-12 |
| ES423524A1 (es) | 1976-05-16 |
| US3914204A (en) | 1975-10-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO742725L (de) | ||
| CN108603009B (zh) | 环氧树脂组合物、成型材料及纤维增强复合材料 | |
| US3728302A (en) | Heat hardenable thickened epoxy resin masses | |
| TWI752973B (zh) | 作為快速環氧固化劑之室溫離子液體 | |
| US20030135011A1 (en) | Epoxy resin composition and prepreg made with the epoxy resin composition | |
| JP2015180753A (ja) | 硬化性エポキシ樹脂組成物及びこれから製造された複合材 | |
| JPH05247322A (ja) | エポキシ樹脂組成物およびその硬化物、並びに硬化方法 | |
| JP7230056B2 (ja) | フェナルカミンエポキシ硬化剤およびこれを含有するエポキシ樹脂組成物 | |
| US20090005516A1 (en) | Curing Agent for Epoxy Resins | |
| CN105408385B (zh) | 具有高断裂韧性的可硬化组合物 | |
| US20130261228A1 (en) | Curable compositions | |
| JP2003238657A (ja) | エポキシ樹脂組成物、樹脂硬化物、プリプレグおよび繊維強化複合材料 | |
| US2965609A (en) | Process for curing polyepoxides and resulting products | |
| JP2016507622A5 (de) | ||
| JP3433878B2 (ja) | エポキシ樹脂組成物、それからなるフィルム状接着剤およびエポキシ樹脂組成物の調製方法 | |
| CN102191000B (zh) | 粘合剂组合物 | |
| DE2131929C3 (de) | Heißhärtbare, eingedickte Epoxidharzmassen | |
| RU2772286C1 (ru) | Эпоксидная композиция холодного отверждения | |
| JP2000119375A (ja) | 複合材料用低温硬化型エポキシ樹脂組成物 | |
| JPH09316302A (ja) | エポキシ樹脂組成物およびその調製方法 | |
| JP3354707B2 (ja) | エポキシ樹脂組成物 | |
| JP7230433B2 (ja) | エポキシ樹脂組成物、成形材料の製造方法、成形材料、繊維強化複合材料及び繊維強化複合材料の製造方法 | |
| JP3413285B2 (ja) | エポキシ樹脂組成物及びフィルム状接着剤 | |
| JPH0717734B2 (ja) | 繊維強化プラスチック用樹脂組成物 | |
| JPH09110963A (ja) | エポキシ樹脂組成物 |