DE2200717B2 - Härtungsmittel für Epoxidharze und deren Verwendung - Google Patents
Härtungsmittel für Epoxidharze und deren VerwendungInfo
- Publication number
- DE2200717B2 DE2200717B2 DE2200717A DE2200717A DE2200717B2 DE 2200717 B2 DE2200717 B2 DE 2200717B2 DE 2200717 A DE2200717 A DE 2200717A DE 2200717 A DE2200717 A DE 2200717A DE 2200717 B2 DE2200717 B2 DE 2200717B2
- Authority
- DE
- Germany
- Prior art keywords
- weight
- parts
- epoxy resins
- curing agents
- mixed
- 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.)
- Withdrawn
Links
- 239000003822 epoxy resin Substances 0.000 title claims description 27
- 229920000647 polyepoxide Polymers 0.000 title claims description 27
- 239000003795 chemical substances by application Substances 0.000 title claims description 16
- 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 11
- 150000001412 amines Chemical class 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 10
- 229920000768 polyamine Polymers 0.000 claims description 10
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- -1 amine hydrogen Chemical class 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 239000000047 product Substances 0.000 description 12
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000012778 molding material Substances 0.000 description 11
- 238000010521 absorption reaction Methods 0.000 description 10
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 235000013162 Cocos nucifera Nutrition 0.000 description 6
- 244000060011 Cocos nucifera Species 0.000 description 6
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 4
- 238000005266 casting Methods 0.000 description 3
- ZETYUTMSJWMKNQ-UHFFFAOYSA-N n,n',n'-trimethylhexane-1,6-diamine Chemical compound CNCCCCCCN(C)C ZETYUTMSJWMKNQ-UHFFFAOYSA-N 0.000 description 3
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 2
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 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 2
- 238000009835 boiling Methods 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 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
- 230000009257 reactivity Effects 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- FVCWZBVQRLEGDH-UHFFFAOYSA-N 1,2,2-trimethylcyclohexan-1-amine Chemical compound CC1(C)CCCCC1(C)N FVCWZBVQRLEGDH-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
- 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 class C1OC1COC(CCC)OCC1CO1 HPILSDOMLLYBQF-UHFFFAOYSA-N 0.000 description 1
- FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- XUQVTMWQDBPSQP-UHFFFAOYSA-N 3-(2-propoxyethoxy)propane-1,1-diamine Chemical compound CCCOCCOCCC(N)N XUQVTMWQDBPSQP-UHFFFAOYSA-N 0.000 description 1
- GLRGDPDTBLJQJD-UHFFFAOYSA-N 3-(4-propoxybutoxy)propane-1,1-diamine Chemical compound CCCOCCCCOCCC(N)N GLRGDPDTBLJQJD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- YOOSAIJKYCBPFW-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)butoxy]propan-1-amine Chemical compound NCCCOCCCCOCCCN YOOSAIJKYCBPFW-UHFFFAOYSA-N 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
- 229930185605 Bisphenol Natural products 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ZJDVQXFDVNWZIJ-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) 2,2,3-trimethylhexanedioate Chemical compound C1OC1COC(=O)C(C)(C)C(C)CCC(=O)OCC1CO1 ZJDVQXFDVNWZIJ-UHFFFAOYSA-N 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
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 150000005846 sugar alcohols Polymers 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
-
- 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
- C08G59/5093—Complexes of 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
- C08G59/50—Amines
- C08G59/56—Amines together with other curing agents
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 (14)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE793700D BE793700A (fr) | 1972-01-07 | Durcisseurs pour les resines epoxydiques | |
| DE2200717A DE2200717B2 (de) | 1972-01-07 | 1972-01-07 | Härtungsmittel für Epoxidharze und deren Verwendung |
| ES407370A ES407370A1 (es) | 1972-01-07 | 1972-10-06 | Procedimiento para la preparacion de materiales de moldeo de resinas epoxidicas. |
| CH1740572A CH572951A5 (enExample) | 1972-01-07 | 1972-11-29 | |
| IT33518/72A IT972862B (it) | 1972-01-07 | 1972-12-22 | Indurenti per resine epossidiche |
| US00318109A US3853812A (en) | 1972-01-07 | 1972-12-26 | Mixed amine-phenol hardeners for epoxy resins |
| AT6073*#A AT335184B (de) | 1972-01-07 | 1973-01-03 | Hartungsmittel fur epoxidharze und hartung von epoxidharzen hiemit |
| NL7300123A NL7300123A (enExample) | 1972-01-07 | 1973-01-04 | |
| SE7300126A SE402464B (sv) | 1972-01-07 | 1973-01-04 | Sett att herda epoxidhartser med associationsprodukter av aminforeningar samt herdningsmedel |
| GB68873A GB1406722A (en) | 1972-01-07 | 1973-01-05 | Curing agents for epoxy-compounds |
| FR7300344A FR2167734B1 (enExample) | 1972-01-07 | 1973-01-05 | |
| DE2304579A DE2304579A1 (de) | 1972-01-07 | 1973-01-31 | Haertungsmittel fuer epoxidharze |
| ES413328A ES413328A2 (es) | 1972-01-07 | 1973-04-04 | Procedimiento para la preparacion de materiales de moldeo deresinas epoxidicas. |
| US05/487,742 US3954762A (en) | 1972-01-07 | 1974-07-11 | Mixed amine-phenol hardeners for epoxy resins |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2200717A DE2200717B2 (de) | 1972-01-07 | 1972-01-07 | Härtungsmittel für Epoxidharze und deren Verwendung |
| DE2304579A DE2304579A1 (de) | 1972-01-07 | 1973-01-31 | Haertungsmittel fuer epoxidharze |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2200717A1 DE2200717A1 (de) | 1973-07-12 |
| DE2200717B2 true DE2200717B2 (de) | 1978-11-23 |
Family
ID=62567068
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2200717A Withdrawn DE2200717B2 (de) | 1972-01-07 | 1972-01-07 | Härtungsmittel für Epoxidharze und deren Verwendung |
| DE2304579A Pending DE2304579A1 (de) | 1972-01-07 | 1973-01-31 | Haertungsmittel fuer epoxidharze |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2304579A Pending DE2304579A1 (de) | 1972-01-07 | 1973-01-31 | Haertungsmittel fuer epoxidharze |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3853812A (enExample) |
| AT (1) | AT335184B (enExample) |
| BE (1) | BE793700A (enExample) |
| CH (1) | CH572951A5 (enExample) |
| DE (2) | DE2200717B2 (enExample) |
| ES (2) | ES407370A1 (enExample) |
| FR (1) | FR2167734B1 (enExample) |
| GB (1) | GB1406722A (enExample) |
| IT (1) | IT972862B (enExample) |
| NL (1) | NL7300123A (enExample) |
| SE (1) | SE402464B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2951603A1 (de) * | 1979-12-21 | 1981-07-02 | Chemische Werke Hüls AG, 4370 Marl | Haertbare epoxidharzmischungen |
| DE3233565A1 (de) * | 1982-09-10 | 1984-03-15 | Hoechst Ag, 6230 Frankfurt | Haertungsmittel fuer epoxidharze und verfahren zum haerten von epoxidharzen |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3954762A (en) * | 1972-01-07 | 1976-05-04 | Schering Ag. | Mixed amine-phenol hardeners for epoxy resins |
| US4185132A (en) * | 1975-11-26 | 1980-01-22 | H. B. Fuller Company | Method of marking paved surfaces using a curable two-part epoxy composition comprising curable liquid epoxide and amine co-curative |
| US4088633A (en) * | 1975-11-26 | 1978-05-09 | H. B. Fuller Company | Method of marking paved surfaces and curable two-part epoxy systems therefor |
| US4221890A (en) * | 1977-09-30 | 1980-09-09 | Thermal-Chem, Inc. | Epoxy resin composition and method for making same |
| ZA794091B (en) * | 1978-08-29 | 1980-10-29 | Ici Ltd | New epoxy resin and use as build-up suppressant coating in polymerisation reactors and in vinyl halide polymerisations |
| US4414377A (en) * | 1981-06-03 | 1983-11-08 | Ciba-Geigy Corporation | Epoxide resin compositions containing esters as diluents and cure accelerators |
| US4593056A (en) * | 1985-06-21 | 1986-06-03 | Union Carbide Corporation | Epoxy/aromatic amine resin systems containing aromatic trihydroxy compounds as cure accelerators |
| EP0253272B1 (de) * | 1986-07-11 | 1992-09-23 | Hoechst Aktiengesellschaft | Additionsverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US4695605A (en) * | 1986-10-01 | 1987-09-22 | Ashland Oil, Inc. | Sag resistant, high performance epoxy structural adhesives |
| DE19631370A1 (de) * | 1996-08-02 | 1998-02-05 | Hoechst Ag | Härtungsmittel für Epoxidharz-Systeme |
| US20040072927A1 (en) * | 2002-10-14 | 2004-04-15 | Hachikian Zakar Raffi | Two-part epoxy adhesives with improved flexibility and process for making and using same |
| WO2006005723A1 (en) * | 2004-07-09 | 2006-01-19 | Huntsman Advanced Materials (Switzerland) Gmbh | Amine compositions |
| EP2408837A1 (en) * | 2009-03-17 | 2012-01-25 | Dow Global Technologies LLC (formerly Known As Dow Global Technologies Inc.) | Curable compositions containing cyclic diamine and cured products therefrom |
| NL1038883C2 (en) * | 2011-06-23 | 2013-01-02 | Holland Novochem Technical Coatings B V | Novel liquid curing agents and surfactants. |
| FR3072671B1 (fr) * | 2017-10-19 | 2022-03-04 | Saint Gobain Weber | Kit pour mortier de jointoiement de carrelage |
| WO2019138059A1 (en) * | 2018-01-11 | 2019-07-18 | Holland Novochem Technical Coatings B.V. | Curing agent and coating composition |
| WO2022004695A1 (ja) * | 2020-06-30 | 2022-01-06 | 東亞合成株式会社 | 被覆電線シール用組成物及び被覆電線のシール方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2908664A (en) * | 1956-06-11 | 1959-10-13 | Devoe & Raynolds Co | Modified epoxide resins |
| FR1322661A (fr) * | 1961-05-26 | 1963-03-29 | Ciba Geigy | Durcissement de résines époxy et agents durcisseurs pour ce durcissement |
| US3366600A (en) * | 1964-06-02 | 1968-01-30 | Grace W R & Co | Process for preparing amine-phenol curing agent epoxy resin compositions |
| NL145576B (nl) * | 1966-03-19 | 1975-04-15 | Philips Nv | Hardersysteem voor epoxy-verbindingen. |
| US3518220A (en) * | 1966-12-27 | 1970-06-30 | Shell Oil Co | Powdered heat-curable epoxy resin compositions of (1) an adduct of a polyepoxide and an aromatic amine and (2) 3-aminopyridine |
| CH513943A (de) * | 1968-07-10 | 1971-10-15 | Basf Ag | Verfahren zur Herstellung von Formkörpern oder Überzügen aus Polyepoxid-Mischungen |
| US3637902A (en) * | 1969-08-26 | 1972-01-25 | Celanese Coatings Co | Epoxide resins cured with amine-glycidyl ester adducts in admixture with a phenolic accelerator |
| US3763102A (en) * | 1972-05-03 | 1973-10-02 | Basf Ag | Production of moldings and coatings by the reaction of a polyepoxide and a polyamine |
-
0
- BE BE793700D patent/BE793700A/xx unknown
-
1972
- 1972-01-07 DE DE2200717A patent/DE2200717B2/de not_active Withdrawn
- 1972-10-06 ES ES407370A patent/ES407370A1/es not_active Expired
- 1972-11-29 CH CH1740572A patent/CH572951A5/xx not_active IP Right Cessation
- 1972-12-22 IT IT33518/72A patent/IT972862B/it active
- 1972-12-26 US US00318109A patent/US3853812A/en not_active Expired - Lifetime
-
1973
- 1973-01-03 AT AT6073*#A patent/AT335184B/de not_active IP Right Cessation
- 1973-01-04 SE SE7300126A patent/SE402464B/xx unknown
- 1973-01-04 NL NL7300123A patent/NL7300123A/xx not_active Application Discontinuation
- 1973-01-05 GB GB68873A patent/GB1406722A/en not_active Expired
- 1973-01-05 FR FR7300344A patent/FR2167734B1/fr not_active Expired
- 1973-01-31 DE DE2304579A patent/DE2304579A1/de active Pending
- 1973-04-04 ES ES413328A patent/ES413328A2/es not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2951603A1 (de) * | 1979-12-21 | 1981-07-02 | Chemische Werke Hüls AG, 4370 Marl | Haertbare epoxidharzmischungen |
| DE3233565A1 (de) * | 1982-09-10 | 1984-03-15 | Hoechst Ag, 6230 Frankfurt | Haertungsmittel fuer epoxidharze und verfahren zum haerten von epoxidharzen |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2167734B1 (enExample) | 1976-05-14 |
| NL7300123A (enExample) | 1973-07-10 |
| SE402464B (sv) | 1978-07-03 |
| BE793700A (fr) | 1973-07-05 |
| ES407370A1 (es) | 1976-02-16 |
| CH572951A5 (enExample) | 1976-02-27 |
| US3853812A (en) | 1974-12-10 |
| DE2200717A1 (de) | 1973-07-12 |
| ATA6073A (de) | 1976-06-15 |
| FR2167734A1 (enExample) | 1973-08-24 |
| AT335184B (de) | 1977-02-25 |
| IT972862B (it) | 1974-05-31 |
| ES413328A2 (es) | 1977-06-16 |
| GB1406722A (en) | 1975-09-17 |
| DE2304579A1 (de) | 1974-08-01 |
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| OI | Miscellaneous see part 1 | ||
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