GB905725A - Improvements in or relating to an epoxy resin composition - Google Patents
Improvements in or relating to an epoxy resin compositionInfo
- Publication number
- GB905725A GB905725A GB4409459A GB4409459A GB905725A GB 905725 A GB905725 A GB 905725A GB 4409459 A GB4409459 A GB 4409459A GB 4409459 A GB4409459 A GB 4409459A GB 905725 A GB905725 A GB 905725A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diamine
- methyl
- pentanediamine
- butylidene
- bis
- 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
- 239000000203 mixture Substances 0.000 title abstract 5
- 229920000647 polyepoxide Polymers 0.000 title abstract 4
- 239000003822 epoxy resin Substances 0.000 title 1
- -1 methyl isobutyl Chemical group 0.000 abstract 10
- 150000004658 ketimines Chemical class 0.000 abstract 5
- 150000002576 ketones Chemical class 0.000 abstract 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 abstract 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 abstract 2
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 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 abstract 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 150000003141 primary amines Chemical class 0.000 abstract 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- CJAGRJAFLCPABV-UHFFFAOYSA-N 2-(4-methylpentan-2-ylideneamino)-n-[2-(4-methylpentan-2-ylideneamino)ethyl]ethanamine Chemical compound CC(C)CC(C)=NCCNCCN=C(C)CC(C)C CJAGRJAFLCPABV-UHFFFAOYSA-N 0.000 abstract 1
- FPHDXPRLWRPJNS-UHFFFAOYSA-N 2-(propan-2-ylideneamino)-n-[2-(propan-2-ylideneamino)ethyl]ethanamine Chemical compound CC(C)=NCCNCCN=C(C)C FPHDXPRLWRPJNS-UHFFFAOYSA-N 0.000 abstract 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical class CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 abstract 1
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 abstract 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 229930194542 Keto Chemical group 0.000 abstract 1
- UAGJVSRUFNSIHR-UHFFFAOYSA-N Methyl levulinate Chemical compound COC(=O)CCC(C)=O UAGJVSRUFNSIHR-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 abstract 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003368 amide group Chemical group 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000000468 ketone group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- PTYYERSOSUWRAT-UHFFFAOYSA-N n,n'-bis[2-(butan-2-ylideneamino)ethyl]ethane-1,2-diamine Chemical compound CCC(C)=NCCNCCNCCN=C(C)CC PTYYERSOSUWRAT-UHFFFAOYSA-N 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 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
-
- 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
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
- C08G59/4042—Imines; Imides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US78404258A | 1958-12-31 | 1958-12-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB905725A true GB905725A (en) | 1962-09-12 |
Family
ID=25131170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4409459A Expired GB905725A (en) | 1958-12-31 | 1959-12-29 | Improvements in or relating to an epoxy resin composition |
Country Status (4)
| Country | Link |
|---|---|
| CH (1) | CH431965A (cg-RX-API-DMAC10.html) |
| FR (1) | FR1243743A (cg-RX-API-DMAC10.html) |
| GB (1) | GB905725A (cg-RX-API-DMAC10.html) |
| NL (2) | NL246904A (cg-RX-API-DMAC10.html) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3468830A (en) * | 1966-08-26 | 1969-09-23 | Pall Corp | Curing of epoxide resins with the reaction product of an organic amine and an aldehyde,and curing and resin compositions and process |
| US4017438A (en) | 1974-12-16 | 1977-04-12 | Ppg Industries, Inc. | Ketimine-blocked primary amine group-containing cationic electrodepositable resins |
| US4748083A (en) * | 1986-01-29 | 1988-05-31 | Sika Ag, Vorm. Kaspar Winkler & Co. | Moisture curable composition |
| EP2133381A1 (de) * | 2008-06-13 | 2009-12-16 | Sika Technology AG | Wasserverdünnbares Amin und dessen Anwendungen |
| CN103524716A (zh) * | 2013-08-31 | 2014-01-22 | 苏州保力瑞生物材料科技开发有限公司 | 一种酮亚胺及其制备方法 |
| CN111253834A (zh) * | 2020-03-19 | 2020-06-09 | 滨州学院 | 一种潮湿固化环氧涂料及其制备方法 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1236194B (de) * | 1962-03-01 | 1967-03-09 | Basf Ag | Verfahren zur Herstellung von Formkoerpern auf der Basis von Polyaddukten |
| DE2418041C3 (de) * | 1974-04-13 | 1982-04-29 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Verfahren zur Herstellung von elastifizierten Formteilen nach Flächengebilden |
-
0
- NL NL128837D patent/NL128837C/xx active
- NL NL246904D patent/NL246904A/xx unknown
-
1959
- 1959-12-29 GB GB4409459A patent/GB905725A/en not_active Expired
- 1959-12-29 FR FR814337A patent/FR1243743A/fr not_active Expired
- 1959-12-29 CH CH8243559A patent/CH431965A/de unknown
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3468830A (en) * | 1966-08-26 | 1969-09-23 | Pall Corp | Curing of epoxide resins with the reaction product of an organic amine and an aldehyde,and curing and resin compositions and process |
| US4017438A (en) | 1974-12-16 | 1977-04-12 | Ppg Industries, Inc. | Ketimine-blocked primary amine group-containing cationic electrodepositable resins |
| US4748083A (en) * | 1986-01-29 | 1988-05-31 | Sika Ag, Vorm. Kaspar Winkler & Co. | Moisture curable composition |
| EP0234047A3 (de) * | 1986-01-29 | 1988-11-09 | Sika AG, vorm. Kaspar Winkler & Co. | Durch Einwirkung von Feuchtigkeit aushärtende Zusammensetzung |
| EP2133381A1 (de) * | 2008-06-13 | 2009-12-16 | Sika Technology AG | Wasserverdünnbares Amin und dessen Anwendungen |
| WO2009150212A1 (de) * | 2008-06-13 | 2009-12-17 | Sika Technology Ag | Wasserverdünnbares amin und dessen anwendungen |
| US8524807B2 (en) | 2008-06-13 | 2013-09-03 | Sika Technology Ag | Water soluble amine and uses thereof |
| CN102037051B (zh) * | 2008-06-13 | 2014-12-24 | Sika技术股份公司 | 水可稀释的胺及其应用 |
| CN103524716A (zh) * | 2013-08-31 | 2014-01-22 | 苏州保力瑞生物材料科技开发有限公司 | 一种酮亚胺及其制备方法 |
| CN103524716B (zh) * | 2013-08-31 | 2016-02-03 | 苏州保力瑞生物材料科技开发有限公司 | 一种酮亚胺及其制备方法 |
| CN111253834A (zh) * | 2020-03-19 | 2020-06-09 | 滨州学院 | 一种潮湿固化环氧涂料及其制备方法 |
| CN111253834B (zh) * | 2020-03-19 | 2022-05-24 | 滨州学院 | 一种潮湿固化环氧涂料及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1243743A (fr) | 1960-10-14 |
| NL246904A (cg-RX-API-DMAC10.html) | |
| NL128837C (cg-RX-API-DMAC10.html) | |
| CH431965A (de) | 1967-03-15 |
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