DE2115854C3 - Verfahren zur Herstellung von noch vernetzungsfähigen Addukten aus Triglycidylisocyanurat - Google Patents
Verfahren zur Herstellung von noch vernetzungsfähigen Addukten aus TriglycidylisocyanuratInfo
- Publication number
- DE2115854C3 DE2115854C3 DE2115854A DE2115854A DE2115854C3 DE 2115854 C3 DE2115854 C3 DE 2115854C3 DE 2115854 A DE2115854 A DE 2115854A DE 2115854 A DE2115854 A DE 2115854A DE 2115854 C3 DE2115854 C3 DE 2115854C3
- Authority
- DE
- Germany
- Prior art keywords
- triglycidyl isocyanurate
- production
- adducts
- crosslinked
- reaction
- 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
- OUPZKGBUJRBPGC-UHFFFAOYSA-N 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound O=C1N(CC2OC2)C(=O)N(CC2OC2)C(=O)N1CC1CO1 OUPZKGBUJRBPGC-UHFFFAOYSA-N 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000000034 method Methods 0.000 title claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000007795 chemical reaction product Substances 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 7
- 229920003986 novolac Polymers 0.000 claims description 6
- 239000004593 Epoxy Substances 0.000 claims description 5
- 125000003700 epoxy group Chemical group 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 150000002894 organic compounds Chemical class 0.000 claims description 3
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- -1 aliphatic amines Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000002924 oxiranes Chemical group 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
- C08L63/06—Triglycidylisocyanurates
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)
- Epoxy Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2115854A DE2115854C3 (de) | 1971-04-01 | 1971-04-01 | Verfahren zur Herstellung von noch vernetzungsfähigen Addukten aus Triglycidylisocyanurat |
| US00236339A US3766296A (en) | 1971-04-01 | 1972-03-20 | Adducts of triglycidyl isocyanurate with novolaks able to form cross links |
| ES401301A ES401301A1 (es) | 1971-04-01 | 1972-03-29 | Procedimiento para la obtencion de productos de adicion re-ticulables de triglicidilisocianurato. |
| CH484472A CH571545A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-04-01 | 1972-03-30 | |
| FR7211290A FR2132259B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-04-01 | 1972-03-30 | |
| GB1495272A GB1383847A (en) | 1971-04-01 | 1972-03-30 | Cross-linkable adducts of triglycidylisocyanurate |
| AT278372A AT320814B (de) | 1971-04-01 | 1972-03-30 | Vernetzungsfähige Addukte aus Triglycidylisocyanurat zur Herstellung von Überzügen |
| AT132774A AT328589B (de) | 1971-04-01 | 1972-03-30 | Vernetzungsfahige addukte aus triglycidylisocyanurat zur herstellung von verklebungen |
| AT132874*1A AT322217B (de) | 1971-04-01 | 1972-03-30 | Verfahren zur herstellung vernetzungsfaehiger addukte aus triglycidylisocyanurat und haertern |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2115854A DE2115854C3 (de) | 1971-04-01 | 1971-04-01 | Verfahren zur Herstellung von noch vernetzungsfähigen Addukten aus Triglycidylisocyanurat |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2115854A1 DE2115854A1 (de) | 1972-10-12 |
| DE2115854B2 DE2115854B2 (de) | 1978-02-02 |
| DE2115854C3 true DE2115854C3 (de) | 1978-10-05 |
Family
ID=5803551
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2115854A Expired DE2115854C3 (de) | 1971-04-01 | 1971-04-01 | Verfahren zur Herstellung von noch vernetzungsfähigen Addukten aus Triglycidylisocyanurat |
Country Status (7)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4506063A (en) * | 1984-02-22 | 1985-03-19 | The Dow Chemical Company | Advanced epoxy resins containing triazine or both triazine and oxazoline groups |
| US4611036A (en) * | 1984-12-10 | 1986-09-09 | Dainippon Ink And Chemicals, Inc. | Epoxy resin composition |
-
1971
- 1971-04-01 DE DE2115854A patent/DE2115854C3/de not_active Expired
-
1972
- 1972-03-20 US US00236339A patent/US3766296A/en not_active Expired - Lifetime
- 1972-03-29 ES ES401301A patent/ES401301A1/es not_active Expired
- 1972-03-30 AT AT132874*1A patent/AT322217B/de not_active IP Right Cessation
- 1972-03-30 GB GB1495272A patent/GB1383847A/en not_active Expired
- 1972-03-30 AT AT278372A patent/AT320814B/de not_active IP Right Cessation
- 1972-03-30 FR FR7211290A patent/FR2132259B1/fr not_active Expired
- 1972-03-30 CH CH484472A patent/CH571545A5/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FR2132259B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1980-04-04 |
| US3766296A (en) | 1973-10-16 |
| GB1383847A (en) | 1974-02-12 |
| DE2115854B2 (de) | 1978-02-02 |
| AT320814B (de) | 1975-02-25 |
| ES401301A1 (es) | 1975-02-16 |
| DE2115854A1 (de) | 1972-10-12 |
| FR2132259A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1972-11-17 |
| CH571545A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-01-15 |
| AT322217B (de) | 1975-05-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) |