CS212437B1 - Method of making the quick hardenable epoxide composition for the injection pouring - Google Patents
Method of making the quick hardenable epoxide composition for the injection pouring Download PDFInfo
- Publication number
- CS212437B1 CS212437B1 CS78737A CS73778A CS212437B1 CS 212437 B1 CS212437 B1 CS 212437B1 CS 78737 A CS78737 A CS 78737A CS 73778 A CS73778 A CS 73778A CS 212437 B1 CS212437 B1 CS 212437B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- epoxy resin
- compsns
- pressure
- composition
- parts
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 26
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 150000002118 epoxides Chemical class 0.000 title 1
- 238000002347 injection Methods 0.000 title 1
- 239000007924 injection Substances 0.000 title 1
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 15
- 239000003822 epoxy resin Substances 0.000 claims abstract description 14
- 238000001746 injection moulding Methods 0.000 claims abstract description 9
- VYKXQOYUCMREIS-UHFFFAOYSA-N methylhexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21C VYKXQOYUCMREIS-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000000049 pigment Substances 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 21
- 239000004593 Epoxy Substances 0.000 claims description 8
- 239000004971 Cross linker Substances 0.000 claims description 7
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 claims description 5
- 150000003512 tertiary amines Chemical class 0.000 claims description 5
- 239000011256 inorganic filler Substances 0.000 claims description 3
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000012744 reinforcing agent Substances 0.000 claims 1
- 239000000499 gel Substances 0.000 abstract description 5
- 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 abstract description 5
- 239000000126 substance Substances 0.000 abstract description 5
- 238000000465 moulding Methods 0.000 abstract description 4
- 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 abstract description 2
- 239000003431 cross linking reagent Substances 0.000 abstract description 2
- 239000000945 filler Substances 0.000 abstract description 2
- 239000004841 bisphenol A epoxy resin Substances 0.000 abstract 1
- 238000010292 electrical insulation Methods 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 238000004132 cross linking Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 6
- 238000005266 casting Methods 0.000 description 6
- 235000013312 flour Nutrition 0.000 description 5
- 239000010453 quartz Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000004804 winding Methods 0.000 description 4
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 2
- 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 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- MKZHJJQCUIZEDE-UHFFFAOYSA-N 1-[(2-hydroxy-3-naphthalen-1-yloxypropyl)-propan-2-ylamino]-3-naphthalen-1-yloxypropan-2-ol Chemical compound C1=CC=C2C(OCC(O)CN(CC(O)COC=3C4=CC=CC=C4C=CC=3)C(C)C)=CC=CC2=C1 MKZHJJQCUIZEDE-UHFFFAOYSA-N 0.000 description 1
- 239000010754 BS 2869 Class F Substances 0.000 description 1
- 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 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 239000002879 Lewis base Substances 0.000 description 1
- 101100022176 Mus musculus Gstz1 gene Proteins 0.000 description 1
- 241000428199 Mustelinae Species 0.000 description 1
- RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 1
- 241000255632 Tabanus atratus Species 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 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 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 ethylenetriamine Chemical compound 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920006295 polythiol Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000010125 resin casting Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08G59/68—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 catalysts used
- C08G59/686—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 catalysts used containing nitrogen
-
- 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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4215—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof cycloaliphatic
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Insulating Materials (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU77MU578A HU175640B (hu) | 1977-02-03 | 1977-02-03 | Sposob poluchenija shpricevaemoj, bystrozatverdejuhhej komposicii iz ehpoksidnoj smoly |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS212437B1 true CS212437B1 (en) | 1982-03-26 |
Family
ID=10999745
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS78737A CS212437B1 (en) | 1977-02-03 | 1978-02-03 | Method of making the quick hardenable epoxide composition for the injection pouring |
Country Status (8)
| Country | Link |
|---|---|
| CS (1) | CS212437B1 (de) |
| DD (1) | DD134111A1 (de) |
| DE (1) | DE2804135A1 (de) |
| FR (1) | FR2379558A1 (de) |
| HU (1) | HU175640B (de) |
| IT (1) | IT1113104B (de) |
| PL (1) | PL204404A1 (de) |
| YU (1) | YU24678A (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY201234A (en) * | 2016-03-15 | 2024-02-13 | Huntsman Adv Mat Licensing Switzerland Gmbh | A process for the preparation of insulation systems for electrical engineering, the articles obtained therefrom and the use thereof |
-
1977
- 1977-02-03 HU HU77MU578A patent/HU175640B/hu not_active IP Right Cessation
-
1978
- 1978-01-31 DE DE19782804135 patent/DE2804135A1/de not_active Withdrawn
- 1978-02-01 DD DD78203513A patent/DD134111A1/de unknown
- 1978-02-02 PL PL20440478A patent/PL204404A1/xx unknown
- 1978-02-02 FR FR7802870A patent/FR2379558A1/fr active Granted
- 1978-02-02 IT IT19929/78A patent/IT1113104B/it active
- 1978-02-02 YU YU00246/78A patent/YU24678A/xx unknown
- 1978-02-03 CS CS78737A patent/CS212437B1/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL204404A1 (pl) | 1978-09-25 |
| IT7819929A0 (it) | 1978-02-02 |
| IT1113104B (it) | 1986-01-20 |
| FR2379558B3 (de) | 1980-10-10 |
| HU175640B (hu) | 1980-09-28 |
| DD134111A1 (de) | 1979-02-07 |
| FR2379558A1 (fr) | 1978-09-01 |
| YU24678A (en) | 1982-06-30 |
| DE2804135A1 (de) | 1978-08-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE3480402D1 (en) | Process for the preparation of moulding masses from reactive resins | |
| EP0463866A2 (de) | Faserverstärkte Harzzusammensetzung | |
| EP0736053B1 (de) | Kinetisch überprüfte -i(in-situ) erzeugung von katalytischen spezien zur härtung von epoxy/amin-zusammensetzungen | |
| US4677144A (en) | Epoxy resin composition | |
| US4130511A (en) | Curable epoxide resin compositions | |
| KR890004087B1 (ko) | 에폭시 수지 조성물 | |
| US3036041A (en) | Reaction products of epoxylated compositions and process | |
| US5171769A (en) | Filled thixotropic resin compositions comprising epoxy resin, curing agent, sugar-aldehyde and filler | |
| US4652597A (en) | Epoxy resin composition | |
| US3530095A (en) | Curable mixtures of epoxide resins and cyclic urea derivatives | |
| US3717593A (en) | A composition comprising a 1,2-polyepoxide and piperidine derivitive as curing agent | |
| EP0385949B1 (de) | Zusammensetzungen | |
| US3620983A (en) | {11 -methylglycidyl-isocyanurates | |
| HK1004277B (en) | Compositions | |
| US3554968A (en) | Storage-stable hot-curable compositions of polyepoxides and acyl substituted urea derivatives | |
| US2967843A (en) | Epoxy resin composition having high heat stability | |
| US3692705A (en) | Epoxy phthalimide resins | |
| US3671592A (en) | Modification of alicyclic or aliphatic diepoxy compounds | |
| EP0813945B1 (de) | Herstellung von Formkörpern aus einer Einkomponenten-Expoxidharzmischung mit Hilfe der automatischen Druckgeliertechnik | |
| US4670534A (en) | Epoxy resin composition | |
| JPH0350244A (ja) | 反応射出成形用エポキシ樹脂組成物 | |
| US3558558A (en) | Curable mixtures of epoxide resins and alkyl substituted ureas | |
| JPH04227621A (ja) | 重合可能な液状組成物 | |
| US3767617A (en) | Polycarboxylic acid curing agent for polyepoxide resin mixtures | |
| JPS58500858A (ja) | エポキシ成形配合物 |