PL78042B2 - - Google Patents
Download PDFInfo
- Publication number
- PL78042B2 PL78042B2 PL15613172A PL15613172A PL78042B2 PL 78042 B2 PL78042 B2 PL 78042B2 PL 15613172 A PL15613172 A PL 15613172A PL 15613172 A PL15613172 A PL 15613172A PL 78042 B2 PL78042 B2 PL 78042B2
- Authority
- PL
- Poland
- Prior art keywords
- epoxy resins
- hardening
- epoxy
- agents
- curing
- Prior art date
Links
- 239000003822 epoxy resin Substances 0.000 claims description 20
- 229920000647 polyepoxide Polymers 0.000 claims description 20
- 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 claims description 16
- 238000000034 method Methods 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 229920001021 polysulfide Polymers 0.000 claims description 6
- SBOJXQVPLKSXOG-UHFFFAOYSA-N o-amino-hydroxylamine Chemical class NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
- 229920000768 polyamine Polymers 0.000 claims description 4
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 239000005077 polysulfide Substances 0.000 claims description 3
- 150000008117 polysulfides Polymers 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- VKEIPALYOJMDAC-UHFFFAOYSA-N 3,3,3-trichloroprop-1-ene Chemical compound ClC(Cl)(Cl)C=C VKEIPALYOJMDAC-UHFFFAOYSA-N 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- 239000000463 material Substances 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 7
- 238000004132 cross linking Methods 0.000 description 7
- 230000009975 flexible effect Effects 0.000 description 5
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- -1 2,4-diaminophenoxy Chemical group 0.000 description 2
- 239000013043 chemical agent Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
- KMKWGXGSGPYISJ-UHFFFAOYSA-N 4-[4-[2-[4-(4-aminophenoxy)phenyl]propan-2-yl]phenoxy]aniline Chemical compound C=1C=C(OC=2C=CC(N)=CC=2)C=CC=1C(C)(C)C(C=C1)=CC=C1OC1=CC=C(N)C=C1 KMKWGXGSGPYISJ-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-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
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Landscapes
- Epoxy Resins (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL15613172A PL78042B2 (enExample) | 1972-06-20 | 1972-06-20 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL15613172A PL78042B2 (enExample) | 1972-06-20 | 1972-06-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL78042B2 true PL78042B2 (enExample) | 1975-04-30 |
Family
ID=19959019
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL15613172A PL78042B2 (enExample) | 1972-06-20 | 1972-06-20 |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL78042B2 (enExample) |
-
1972
- 1972-06-20 PL PL15613172A patent/PL78042B2/pl unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2840173T3 (es) | Adhesivo de resina epoxídica con alta resistencia a la compresión | |
| KR100420896B1 (ko) | 에폭시수지용 경화제 및 에폭시수지 조성물 | |
| JP2010132924A (ja) | ポリマーブレンド、ならびにこのポリマーブレンドを用いる組成物および方法 | |
| KR20100017712A (ko) | 과잉 에폭시 수지를 포함하는 에폭시 열경화성 조성물 및 이의 제조 방법 | |
| JPH09504328A (ja) | 反応性稀釈剤アルドイミンオキサゾリジン類 | |
| BR112019011857B1 (pt) | Endurecedor para adesivos de resina epóxi para endurecimento a frio com endurecimento rápido | |
| NO823255L (no) | Fremgangsmaate ved herding av polyepoxyder med polymercaptaner plus katalytisk co-herdemiddel | |
| CN112714776A (zh) | 包含含脲二酮的材料、多硫醇和酸性稳定剂的聚合物材料、两部分组合物以及方法 | |
| TW201518268A (zh) | 含有硫醇基之化合物及單液型環氧樹脂組成物 | |
| CN105408385B (zh) | 具有高断裂韧性的可硬化组合物 | |
| BR112013002590A2 (pt) | endurecedor de resinas de epóxi | |
| CN101589090B (zh) | 被硫杂丙环封端的聚硫醚聚合物 | |
| JP2021505735A (ja) | ポリチオエーテルスルフィドを調製する方法 | |
| BR112016009727B1 (pt) | processo para a preparação de uma mistura de eteramina, e, composição | |
| US3363026A (en) | Epoxy resin containing a curing catalyst mixture of a polymercaptan and a fused ringamine | |
| PL78042B2 (enExample) | ||
| BR112015028273B1 (pt) | Método para produção de uma resina, resina e uso de tal resina | |
| CN107141446A (zh) | 氨基甲酸酯基硫醇类环氧固化剂及其制备方法和应用 | |
| DE1570382A1 (de) | Neue Epoxydharzmassen | |
| KR101032588B1 (ko) | 수지 조성물 | |
| CA2788739C (en) | Epoxy resin composition with reduced toxicity | |
| JP5327087B2 (ja) | １液型熱硬化性エポキシ樹脂組成物 | |
| CA1058350A (en) | Rapidly-hardenable resin and use thereof | |
| RU2717938C1 (ru) | Защитные эпоксидные композиции | |
| KR790000933B1 (ko) | 수성에폭시 수지도료 |