GB680997A - Compositions of matter containing glycidyl ethers and diamines and resinous productsobtained therefrom - Google Patents
Compositions of matter containing glycidyl ethers and diamines and resinous productsobtained therefromInfo
- Publication number
- GB680997A GB680997A GB5232/49A GB523249A GB680997A GB 680997 A GB680997 A GB 680997A GB 5232/49 A GB5232/49 A GB 5232/49A GB 523249 A GB523249 A GB 523249A GB 680997 A GB680997 A GB 680997A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diamine
- diamino
- reacting
- methyl
- epichlorhydrin
- 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
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 title abstract 5
- 150000004985 diamines Chemical class 0.000 title abstract 4
- 239000000203 mixture Substances 0.000 title abstract 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 6
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 5
- 239000004593 Epoxy Substances 0.000 abstract 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 abstract 4
- 239000000047 product Substances 0.000 abstract 4
- 150000005846 sugar alcohols Polymers 0.000 abstract 4
- YZTDHNFXEQKPGK-UHFFFAOYSA-N 1,6-diaminohexane-2,5-dione Chemical compound C(CCC(=O)CN)(=O)CN YZTDHNFXEQKPGK-UHFFFAOYSA-N 0.000 abstract 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 3
- 150000001721 carbon Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000007859 condensation product Substances 0.000 abstract 3
- 150000002170 ethers Chemical class 0.000 abstract 3
- -1 glycidyl radical Chemical class 0.000 abstract 3
- 150000002576 ketones Chemical class 0.000 abstract 3
- 238000000465 moulding Methods 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 229910015900 BF3 Inorganic materials 0.000 abstract 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 abstract 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract 2
- 239000004386 Erythritol Substances 0.000 abstract 2
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- 229930195725 Mannitol Natural products 0.000 abstract 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 abstract 2
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract 2
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 abstract 2
- 235000019414 erythritol Nutrition 0.000 abstract 2
- 229940009714 erythritol Drugs 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 239000000594 mannitol Substances 0.000 abstract 2
- 235000010355 mannitol Nutrition 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 abstract 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 abstract 2
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 2
- 239000000843 powder Substances 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 239000000600 sorbitol Substances 0.000 abstract 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 abstract 1
- OPCJOXGBLDJWRM-UHFFFAOYSA-N 1,2-diamino-2-methylpropane Chemical compound CC(C)(N)CN OPCJOXGBLDJWRM-UHFFFAOYSA-N 0.000 abstract 1
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 abstract 1
- QSSWKPVVDJURMQ-UHFFFAOYSA-N 2,2,4,4,6-pentamethyl-1,3-diazinane Chemical compound CC1CC(C)(C)NC(C)(C)N1 QSSWKPVVDJURMQ-UHFFFAOYSA-N 0.000 abstract 1
- CGCVLTOGUMLHNP-UHFFFAOYSA-N 2,3-dimethylbutane-2,3-diamine Chemical compound CC(C)(N)C(C)(C)N CGCVLTOGUMLHNP-UHFFFAOYSA-N 0.000 abstract 1
- ZTPWMHSGQNDCQW-UHFFFAOYSA-N 2,4,6-triethyl-2,4-dimethyl-1,3-diazinane Chemical compound CC1(NC(CC(N1)(CC)C)CC)CC ZTPWMHSGQNDCQW-UHFFFAOYSA-N 0.000 abstract 1
- FPEMDPUWASXYQD-UHFFFAOYSA-N 2,4-diethyl-2,4,5,6-tetramethyl-1,3-diazinane Chemical compound CC1(NC(C(C(N1)(CC)C)C)C)CC FPEMDPUWASXYQD-UHFFFAOYSA-N 0.000 abstract 1
- JWTVQZQPKHXGFM-UHFFFAOYSA-N 2,5-dimethylhexane-2,5-diamine Chemical compound CC(C)(N)CCC(C)(C)N JWTVQZQPKHXGFM-UHFFFAOYSA-N 0.000 abstract 1
- PCXAQLMRLMZKRL-UHFFFAOYSA-N 2-methylpentane-2,4-diamine Chemical compound CC(N)CC(C)(C)N PCXAQLMRLMZKRL-UHFFFAOYSA-N 0.000 abstract 1
- OAAMCNOOFRTQOG-UHFFFAOYSA-N 3,4-dimethylhexane-2,4-diamine Chemical compound NC(CC)(C(C(C)N)C)C OAAMCNOOFRTQOG-UHFFFAOYSA-N 0.000 abstract 1
- KSFZHJKCQJAHKL-UHFFFAOYSA-N 3-methylheptane-3,5-diamine Chemical compound CCC(N)CC(C)(N)CC KSFZHJKCQJAHKL-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005083 Zinc sulfide Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 239000012670 alkaline solution Substances 0.000 abstract 1
- 150000005215 alkyl ethers Chemical class 0.000 abstract 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 abstract 1
- 229910000410 antimony oxide Inorganic materials 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 239000001273 butane Substances 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 abstract 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 125000003700 epoxy group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 235000013312 flour Nutrition 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 238000007689 inspection Methods 0.000 abstract 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 abstract 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 abstract 1
- WOTPFVNWMLFMFW-ISLYRVAYSA-N para red Chemical compound OC1=CC=C2C=CC=CC2=C1\N=N\C1=CC=C(N(=O)=O)C=C1 WOTPFVNWMLFMFW-ISLYRVAYSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000012262 resinous product Substances 0.000 abstract 1
- 229910001388 sodium aluminate Inorganic materials 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 abstract 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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
- C08G59/5006—Amines aliphatic
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21D—SHAFTS; TUNNELS; GALLERIES; LARGE UNDERGROUND CHAMBERS
- E21D20/00—Setting anchoring-bolts
- E21D20/02—Setting anchoring-bolts with provisions for grouting
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mining & Mineral Resources (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Structural Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- Epoxy Resins (AREA)
- Epoxy Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12152A US2500600A (en) | 1948-02-28 | 1948-02-28 | Compositions of matter containing epoxy ethers and diamines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB680997A true GB680997A (en) | 1952-10-15 |
Family
ID=21753627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5232/49A Expired GB680997A (en) | 1948-02-28 | 1949-02-25 | Compositions of matter containing glycidyl ethers and diamines and resinous productsobtained therefrom |
Country Status (7)
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1008909B (de) * | 1955-04-28 | 1957-05-23 | Albert Ag Chem Werke | Haertungsmittel fuer Epoxyharze |
| US2866768A (en) * | 1955-03-18 | 1958-12-30 | Honeywell Regulator Co | Epoxy molding composition and method of molding with same |
| DE1100948B (de) * | 1956-06-09 | 1961-03-02 | Basf Ag | Verfahren zur Herstellung von Formkoerpern und UEberzuegen durch Umsetzung von Polyglycidylaethern |
| US4193905A (en) | 1976-12-10 | 1980-03-18 | Ciba-Geigy Corporation | Curable epoxide resin mixtures containing diaminopropanes |
| US4652625A (en) * | 1986-02-18 | 1987-03-24 | Texaco Inc. | N-aminopropyl derivatives of 2,4-diamino-2-methylpentane as epoxy curing agents |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB652024A (en) * | 1948-11-26 | 1951-04-11 | Courtaulds Ltd | Improvements in and relating to the production of thermoplastic resins and of threads, fibres, filaments and like products therefrom |
| US2594979A (en) * | 1949-01-19 | 1952-04-29 | Gen Electric | Resinous compositions and their use |
| BE494250A (US20100223739A1-20100909-C00005.png) * | 1949-03-02 | |||
| BE498918A (US20100223739A1-20100909-C00005.png) * | 1949-10-25 | 1900-01-01 | ||
| US2709664A (en) * | 1950-10-13 | 1955-05-31 | Master Mechanics Co | Process for forming chemical resistant synthetic resin coatings on metal and product thereof |
| BE510386A (US20100223739A1-20100909-C00005.png) * | 1951-04-05 | 1900-01-01 | ||
| US2772186A (en) * | 1951-06-28 | 1956-11-27 | Hartford Nat Bank & Trust Co | Method of applying an epoxy resin to a base and curing said resin |
| DE1017622B (de) * | 1951-12-07 | 1957-10-17 | Sandoz Ag | Verfahren zur Herstellung von wasserloeslichen basischen, stickstoffhaltigen Kondensationsprodukten |
| US2761078A (en) * | 1952-03-29 | 1956-08-28 | Wetmore Hodges | Electrical motor pump or compressor |
| US2795680A (en) * | 1952-05-16 | 1957-06-11 | Sprague Electric Co | Printed resistors and inks |
| US2730427A (en) * | 1952-08-13 | 1956-01-10 | American Cyanamid Co | Shrinkage control of cellulosic and wool textiles with diglycidyl ether compounds |
| US2842497A (en) * | 1953-01-05 | 1958-07-08 | Shell Dev | Phosphorus esters containing diarylamines and polyepoxypolyhydroxy polyethers |
| NL186180B (nl) * | 1953-03-25 | Basf Ag | Werkwijze voor de bereiding van oplosmiddelarme moffellakken, alsmede gevormd voortbrengsel, dat met toepassing daarvan is bekleed. | |
| BE527446A (US20100223739A1-20100909-C00005.png) * | 1953-03-30 | |||
| US2772248A (en) * | 1953-05-04 | 1956-11-27 | Interchem Corp | Water-soluble epoxy-amine resins |
| US2904447A (en) * | 1954-04-15 | 1959-09-15 | Ciba Ltd | Process for pigment printing of flexible flat structures |
| US2924264A (en) * | 1954-07-17 | 1960-02-09 | Moser Glaser & Co Ag | Laminated body and method of making the same |
| BE541648A (US20100223739A1-20100909-C00005.png) * | 1955-04-07 | 1900-01-01 | ||
| US2909448A (en) * | 1955-03-07 | 1959-10-20 | Shell Dev | Salts of polyamine polyepoxide adducts and their use as curing agents for polyepoxides |
| DE1019461B (de) * | 1955-03-15 | 1957-11-14 | Basf Ag | Haerten von im Mittel mehr als eine Epoxygruppe im Molekuel enthaltenden Verbindungen |
| DE1022004B (de) * | 1955-05-05 | 1958-01-02 | Union Carbide Corp | Verwendung von Polyaminen als Haertungsmittel fuer haertbare harzartige, mehr als eine Epoxydgruppe im Molekuel enthaltende Verbindungen |
| DE1105613B (de) * | 1955-08-08 | 1961-04-27 | Licentia Gmbh | Verfahren zur Herstellung von Bindemitteln fuer Schichtpressstoffe auf Epoxyharzbasis |
| DE1025884B (de) * | 1955-09-21 | 1958-03-13 | Henkel & Cie Gmbh | Verfahren zur Herstellung von als Haerter geeigneten Aminen |
| DE1086236B (de) * | 1955-10-07 | 1960-08-04 | Du Pont | Verfahren zur Herstellung von als Aushaertemittel fuer Epoxyharze geeigneten N, N'-Bis-[(1-aminocycloalkyl)-methyl]-piperazinen |
| US2940161A (en) * | 1955-10-11 | 1960-06-14 | Western Electric Co | Methods of making encapsulated electrical devices |
| NL211636A (US20100223739A1-20100909-C00005.png) * | 1955-10-28 | |||
| DE1041246B (de) * | 1956-02-14 | 1958-10-16 | Reichhold Chemie Ag | Verfahren zur Herstellung kalt- oder warmgehaerteter modifizierter Epoxyharze |
| US2904618A (en) * | 1956-07-30 | 1959-09-15 | Sprague Electric Co | Sealed housing and indexing means for electrical components |
| US2970983A (en) * | 1956-09-10 | 1961-02-07 | Shell Oil Co | Epoxy-containing condensates of polyepoxides and acidic materials, their preparation and polymers |
| DE1076365B (de) * | 1957-09-25 | 1960-02-25 | Bayer Ag | Verfahren zum Haerten von Polyepoxyverbindungen |
| CA659234A (en) * | 1957-10-24 | 1963-03-12 | R. Hinkley James | Epoxy dipping compounds |
| NL235079A (US20100223739A1-20100909-C00005.png) * | 1958-01-13 | 1900-01-01 | ||
| DE1271247B (de) * | 1958-06-23 | 1968-06-27 | Gen Electric | Innenisolation auf Epoxydharzbasis fuer einen aus Teilleitern bestehenden Leiterstab einer dynamoelektrischen Wechselstrommaschine |
| DE1084025B (de) * | 1959-03-20 | 1960-06-23 | Leuna Werke Iawalter Ulbrichti | Verfahren zum Haerten von epoxydgruppenhaltigen Harzen |
| US3087060A (en) * | 1959-06-30 | 1963-04-23 | Robert J Omohundro | Scintillation counter |
| US3154460A (en) * | 1960-02-29 | 1964-10-27 | William R Graner | Anti-fouling coating |
| CH398641A (de) * | 1961-05-04 | 1966-03-15 | Ciba Geigy | Verfahren zur Herstellung von neuen halogenhaltigen Polyaminen |
| NL283760A (US20100223739A1-20100909-C00005.png) * | 1961-09-29 | |||
| US3257442A (en) * | 1961-11-21 | 1966-06-21 | United States Borax Chem | Aminoalkyl glycol monoborate esters |
| BE631373A (US20100223739A1-20100909-C00005.png) * | 1962-04-27 | |||
| NL137052C (US20100223739A1-20100909-C00005.png) * | 1962-07-30 | |||
| US3347802A (en) * | 1964-07-31 | 1967-10-17 | Dow Chemical Co | Water soluble polymer of diglycidyl ether and an alkylenediamine hydrohalide |
| US3462383A (en) * | 1966-03-07 | 1969-08-19 | Dow Chemical Co | Wet strength additives for cellulosic products |
| US3931116A (en) * | 1972-08-14 | 1976-01-06 | Witco Chemical Corporation | Curable amine-terminated polyurethane-urea-epoxide lacquers |
| US4252936A (en) * | 1979-01-24 | 1981-02-24 | The United States Of America As Represented By The United States Department Of Energy | Use of 2,5-dimethyl-2,5-hexane diamine as a curing agent for epoxy resins |
| US5300541A (en) * | 1988-02-04 | 1994-04-05 | Ppg Industries, Inc. | Polyamine-polyepoxide gas barrier coatings |
| US5038555A (en) * | 1989-02-28 | 1991-08-13 | Ppg Industries, Inc. | Twistable chemically treated glass fibers, fabrics and coated articles |
| US5731090A (en) † | 1996-07-29 | 1998-03-24 | Morton International, Inc. | Urethane laminating adhesives useful for retort pouches |
| US5840825A (en) * | 1996-12-04 | 1998-11-24 | Ppg Incustries, Inc. | Gas barrier coating compositions containing platelet-type fillers |
| US5728439A (en) * | 1996-12-04 | 1998-03-17 | Ppg Industries, Inc. | Multilayer packaging material for oxygen sensitive food and beverage |
| US7442727B2 (en) * | 2003-06-04 | 2008-10-28 | Degussa Ag | Pyrogenically prepared, surface modified aluminum oxide |
| SG178630A1 (en) * | 2005-05-12 | 2012-03-29 | Georgia Tech Res Inst | Coated metal oxide nanoparticles and methods for producing same |
| US8405069B2 (en) * | 2006-11-10 | 2013-03-26 | Georgia Tech Research Corporation | Printable thin-film transistors with high dielectric constant gate insulators and methods for producing same |
| CN111116369B (zh) * | 2019-10-10 | 2020-11-24 | 苏州巨峰新材料科技有限公司 | 一种活性酯化合物及其制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2136928A (en) * | 1934-12-10 | 1938-11-15 | Ig Farbenindustrie Ag | Manufacture of amines of high molecular weight, which are rich in nitrogen |
| DE676117C (de) * | 1934-12-11 | 1939-05-26 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung hochmolekularer Polyamine |
| BE456650A (US20100223739A1-20100909-C00005.png) * | 1943-06-16 |
-
0
- NL NL73196D patent/NL73196C/xx active
- BE BE487600D patent/BE487600A/xx unknown
-
1948
- 1948-02-28 US US12152A patent/US2500600A/en not_active Expired - Lifetime
-
1949
- 1949-02-23 CH CH274530D patent/CH274530A/de unknown
- 1949-02-25 GB GB5232/49A patent/GB680997A/en not_active Expired
- 1949-02-26 DE DEP35103A patent/DE975516C/de not_active Expired
- 1949-02-28 FR FR981842D patent/FR981842A/fr not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2866768A (en) * | 1955-03-18 | 1958-12-30 | Honeywell Regulator Co | Epoxy molding composition and method of molding with same |
| DE1008909B (de) * | 1955-04-28 | 1957-05-23 | Albert Ag Chem Werke | Haertungsmittel fuer Epoxyharze |
| DE1100948B (de) * | 1956-06-09 | 1961-03-02 | Basf Ag | Verfahren zur Herstellung von Formkoerpern und UEberzuegen durch Umsetzung von Polyglycidylaethern |
| US4193905A (en) | 1976-12-10 | 1980-03-18 | Ciba-Geigy Corporation | Curable epoxide resin mixtures containing diaminopropanes |
| US4652625A (en) * | 1986-02-18 | 1987-03-24 | Texaco Inc. | N-aminopropyl derivatives of 2,4-diamino-2-methylpentane as epoxy curing agents |
Also Published As
| Publication number | Publication date |
|---|---|
| NL73196C (US20100223739A1-20100909-C00005.png) | |
| BE487600A (US20100223739A1-20100909-C00005.png) | |
| FR981842A (fr) | 1951-05-30 |
| CH274530A (de) | 1951-04-15 |
| DE975516C (de) | 1961-12-14 |
| US2500600A (en) | 1950-03-14 |
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