DE1006152B - Verfahren zum Haerten von Epoxyharzen - Google Patents
Verfahren zum Haerten von EpoxyharzenInfo
- Publication number
- DE1006152B DE1006152B DEC10407A DEC0010407A DE1006152B DE 1006152 B DE1006152 B DE 1006152B DE C10407 A DEC10407 A DE C10407A DE C0010407 A DEC0010407 A DE C0010407A DE 1006152 B DE1006152 B DE 1006152B
- Authority
- DE
- Germany
- Prior art keywords
- epoxy
- epoxy resins
- adducts
- groups
- resin
- 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.)
- Pending
Links
- 239000003822 epoxy resin Substances 0.000 title claims description 22
- 229920000647 polyepoxide Polymers 0.000 title claims description 22
- 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 title claims description 17
- 238000000034 method Methods 0.000 title claims description 6
- 150000001412 amines Chemical class 0.000 claims description 10
- 239000004593 Epoxy Substances 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 125000003700 epoxy group Chemical group 0.000 description 9
- 239000004848 polyfunctional curative Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 6
- 238000009833 condensation Methods 0.000 description 6
- 230000005494 condensation Effects 0.000 description 6
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 5
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000003944 halohydrins Chemical class 0.000 description 3
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- DEQUKPCANKRTPZ-UHFFFAOYSA-N (2,3-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1O DEQUKPCANKRTPZ-UHFFFAOYSA-N 0.000 description 1
- WAUNMVYXQAKNLE-UHFFFAOYSA-N 2,2-diphenylpropan-1-ol Chemical compound C=1C=CC=CC=1C(CO)(C)C1=CC=CC=C1 WAUNMVYXQAKNLE-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000012670 alkaline solution Substances 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
- 238000005266 casting Methods 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 206010041232 sneezing Diseases 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004383 yellowing Methods 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
- C08G59/5006—Amines aliphatic
-
- 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
- C08G59/182—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 using pre-adducts of epoxy compounds with curing agents
- C08G59/184—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 using pre-adducts of epoxy compounds with curing agents with amines
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)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL200828D NL200828A (enrdf_load_stackoverflow) | 1954-12-11 | ||
| NL97242D NL97242C (enrdf_load_stackoverflow) | 1954-12-11 | ||
| DEC10407A DE1006152B (de) | 1954-12-11 | 1954-12-11 | Verfahren zum Haerten von Epoxyharzen |
| CH344843D CH344843A (de) | 1954-12-11 | 1955-09-29 | Zu einem Kunstharz härtbare Mischung |
| FR1136454D FR1136454A (fr) | 1954-12-11 | 1955-09-30 | Procédé de durcissement de résines époxydes |
| GB3389655A GB790083A (en) | 1954-12-11 | 1955-11-25 | Improvements in or relating to hardening agents for epoxide resins |
| US552698A US2906723A (en) | 1954-12-11 | 1955-12-13 | Epoxy resin compositions of improved heat hardening characteristics and the process of their production |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEC10407A DE1006152B (de) | 1954-12-11 | 1954-12-11 | Verfahren zum Haerten von Epoxyharzen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1006152B true DE1006152B (de) | 1957-04-11 |
Family
ID=7014752
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEC10407A Pending DE1006152B (de) | 1954-12-11 | 1954-12-11 | Verfahren zum Haerten von Epoxyharzen |
Country Status (5)
| Country | Link |
|---|---|
| CH (1) | CH344843A (enrdf_load_stackoverflow) |
| DE (1) | DE1006152B (enrdf_load_stackoverflow) |
| FR (1) | FR1136454A (enrdf_load_stackoverflow) |
| GB (1) | GB790083A (enrdf_load_stackoverflow) |
| NL (2) | NL97242C (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1098199B (de) * | 1958-10-10 | 1961-01-26 | Bayer Ag | Verfahren zum Beschleunigen der Haertung von Epoxyharzen |
| DE1117871B (de) * | 1959-04-29 | 1961-11-23 | Shell Int Research | Verfahren zum Haerten von Polyepoxyden |
| DE1153524B (de) * | 1959-11-10 | 1963-08-29 | Bayer Ag | Herstellen stabiler Loesungen oder Dispersionen basischer Polyadditionsprodukte aus Epoxyharzen und mehrwertigen Aminen |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3297608A (en) * | 1963-05-31 | 1967-01-10 | Exxon Research Engineering Co | Method for curing epoxy resins under water |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH295069A (de) * | 1949-10-25 | 1953-12-15 | Bataafsche Petroleum | Verfahren zur Herstellung einer zu harzartigen Produkten härtbaren Mischung. |
-
0
- NL NL200828D patent/NL200828A/xx unknown
- NL NL97242D patent/NL97242C/xx active
-
1954
- 1954-12-11 DE DEC10407A patent/DE1006152B/de active Pending
-
1955
- 1955-09-29 CH CH344843D patent/CH344843A/de unknown
- 1955-09-30 FR FR1136454D patent/FR1136454A/fr not_active Expired
- 1955-11-25 GB GB3389655A patent/GB790083A/en not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH295069A (de) * | 1949-10-25 | 1953-12-15 | Bataafsche Petroleum | Verfahren zur Herstellung einer zu harzartigen Produkten härtbaren Mischung. |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1098199B (de) * | 1958-10-10 | 1961-01-26 | Bayer Ag | Verfahren zum Beschleunigen der Haertung von Epoxyharzen |
| DE1117871B (de) * | 1959-04-29 | 1961-11-23 | Shell Int Research | Verfahren zum Haerten von Polyepoxyden |
| DE1153524B (de) * | 1959-11-10 | 1963-08-29 | Bayer Ag | Herstellen stabiler Loesungen oder Dispersionen basischer Polyadditionsprodukte aus Epoxyharzen und mehrwertigen Aminen |
Also Published As
| Publication number | Publication date |
|---|---|
| CH344843A (de) | 1960-02-29 |
| FR1136454A (fr) | 1957-05-23 |
| NL200828A (enrdf_load_stackoverflow) | |
| GB790083A (en) | 1958-02-05 |
| NL97242C (enrdf_load_stackoverflow) |
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