GB872306A - Epoxide compositions and their production - Google Patents
Epoxide compositions and their productionInfo
- Publication number
- GB872306A GB872306A GB10743/58A GB1074358A GB872306A GB 872306 A GB872306 A GB 872306A GB 10743/58 A GB10743/58 A GB 10743/58A GB 1074358 A GB1074358 A GB 1074358A GB 872306 A GB872306 A GB 872306A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- epoxy
- heating
- hydrogen
- alkyl
- 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 8
- 150000002118 epoxides Chemical class 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 5
- 238000010438 heat treatment Methods 0.000 abstract 5
- -1 polyoxy Polymers 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 229910052739 hydrogen Chemical group 0.000 abstract 4
- 239000001257 hydrogen Chemical group 0.000 abstract 4
- 229920005862 polyol Polymers 0.000 abstract 4
- 150000003077 polyols Chemical class 0.000 abstract 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 150000008064 anhydrides Chemical class 0.000 abstract 2
- 125000004956 cyclohexylene group Chemical group 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 abstract 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- 150000003628 tricarboxylic acids Chemical class 0.000 abstract 2
- PYHWULKPIOPCSA-UHFFFAOYSA-N 2-(7-oxabicyclo[4.1.0]heptan-4-ylmethoxy)-2-oxoacetic acid Chemical compound C1C(COC(=O)C(=O)O)CCC2OC21 PYHWULKPIOPCSA-UHFFFAOYSA-N 0.000 abstract 1
- GRWFFFOEIHGUBG-UHFFFAOYSA-N 3,4-Epoxy-6-methylcyclohexylmethyl-3,4-epoxy-6-methylcyclo-hexanecarboxylate Chemical compound C1C2OC2CC(C)C1C(=O)OCC1CC2OC2CC1C GRWFFFOEIHGUBG-UHFFFAOYSA-N 0.000 abstract 1
- YXALYBMHAYZKAP-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCC1CC2OC2CC1 YXALYBMHAYZKAP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 abstract 1
- 239000002841 Lewis acid Substances 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 1
- 239000001361 adipic acid Substances 0.000 abstract 1
- 235000011037 adipic acid Nutrition 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 abstract 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 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000007859 condensation product Substances 0.000 abstract 1
- 125000005725 cyclohexenylene group Chemical group 0.000 abstract 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 229910001507 metal halide Inorganic materials 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 230000004048 modification Effects 0.000 abstract 1
- 238000012986 modification Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000005702 oxyalkylene group Chemical group 0.000 abstract 1
- 229920001568 phenolic resin Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 abstract 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4284—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with other curing agents
-
- 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
- C08G59/62—Alcohols or phenols
-
- 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
- C08G59/62—Alcohols or phenols
- C08G59/621—Phenols
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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US650554A US2890195A (en) | 1957-04-04 | 1957-04-04 | Compositions comprising a diepoxide and a polyhydric compound |
Publications (1)
Publication Number | Publication Date |
---|---|
GB872306A true GB872306A (en) | 1961-07-05 |
Family
ID=24609386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10743/58A Expired GB872306A (en) | 1957-04-04 | 1958-04-03 | Epoxide compositions and their production |
Country Status (5)
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0028583A2 (de) * | 1979-11-05 | 1981-05-13 | Ciba-Geigy Ag | Verfahren zur Herstellung von Epoxidharzgiesskörpern |
GB2148900A (en) * | 1983-08-19 | 1985-06-05 | Ici Plc | Curable compositions |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3050478A (en) * | 1958-07-28 | 1962-08-21 | Glidden Co | Solidifiable fluid compositions prepared from enedioyl acids, epoxidized hydrocarbondrying oil, and conjugated dienes |
US3126298A (en) * | 1959-06-03 | 1964-03-24 | Method of coating with a composition | |
BE594234A (US07642317-20100105-C00010.png) * | 1959-08-21 | |||
US3062770A (en) * | 1960-03-21 | 1962-11-06 | Standard Oil Co | Composition consisting essentially of (alpha) a reaction product of trimellitic anhydride and alkylene oxide and (beta) an epoxy resin |
US3242108A (en) * | 1961-04-04 | 1966-03-22 | Union Carbide Corp | Compositions for producing polyurethane resins and resinous foams and products prepared therefrom |
US3213067A (en) * | 1961-12-07 | 1965-10-19 | Allied Chem | Method of preparing unsaturated polyester resins from alkylene oxides and ethylenically unsaturated dicarboxylic acid anhydrides |
BE625783A (US07642317-20100105-C00010.png) * | 1961-12-07 | |||
US3227603A (en) * | 1962-03-02 | 1966-01-04 | Sun Chemical Corp | Laminating adhesives, laminating process and laminated products |
US3484398A (en) * | 1965-03-18 | 1969-12-16 | Dexter Corp | Powdered epoxy resin compositions |
CH539628A (de) * | 1970-07-07 | 1973-07-31 | Reichhold Albert Chemie Ag | Verfahren zur Umsetzung von Hydroxylgruppen und Sulfhydrylgruppen enthaltenden Verbindungen mit überschüssigen Mengen Polyepoxiden allein oder im Gemisch mit Monoepoxiden |
US4434286A (en) | 1980-11-03 | 1984-02-28 | Union Carbide Corporation | Curable epoxy resin containing compositions |
EP0080500A4 (en) * | 1981-06-05 | 1983-09-30 | Gen Electric | HEAT-CURABLE EPOXY COMPONENT. |
US4401775A (en) * | 1982-06-24 | 1983-08-30 | Rca Corporation | Epoxy encapsulating formulation |
JPS60123526A (ja) * | 1983-12-06 | 1985-07-02 | Mitsubishi Electric Corp | エポキシ樹脂組成物 |
US5597886A (en) * | 1994-03-10 | 1997-01-28 | Ciba-Geigy Corporation | Heat-curable epoxy resin systems having a good reactivity/stability ratio |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA530335A (en) * | 1956-09-11 | Union Carbide And Carbon Corporation | Diepoxides | |
US2543419A (en) * | 1949-05-11 | 1951-02-27 | Rohm & Haas | Polycyclic di-epoxy ethers |
NL78770C (US07642317-20100105-C00010.png) * | 1950-09-30 | |||
US2609357A (en) * | 1950-11-13 | 1952-09-02 | Rohm & Haas | Preparation of thermoset resins |
BE518763A (US07642317-20100105-C00010.png) * | 1952-03-29 | |||
US2720500A (en) * | 1952-10-17 | 1955-10-11 | Alkydol Lab Inc | Polyesters from polycarboxylic acids, polyhydric alcohols, and glycidyl ethers of monoh ydrocarbon substituted monohydric phenol |
US2716123A (en) * | 1953-08-13 | 1955-08-23 | Dbepoxides of cycloaliphatic esters | |
US2750395A (en) * | 1954-01-05 | 1956-06-12 | Union Carbide & Carbon Corp | Diepoxides |
-
0
- BE BE566442D patent/BE566442A/xx unknown
-
1957
- 1957-04-04 US US650554A patent/US2890195A/en not_active Expired - Lifetime
-
1958
- 1958-04-03 GB GB10743/58A patent/GB872306A/en not_active Expired
- 1958-04-03 DE DEU5255A patent/DE1096037B/de active Pending
- 1958-04-04 FR FR1204495D patent/FR1204495A/fr not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0028583A2 (de) * | 1979-11-05 | 1981-05-13 | Ciba-Geigy Ag | Verfahren zur Herstellung von Epoxidharzgiesskörpern |
EP0028583A3 (en) * | 1979-11-05 | 1981-08-26 | Ciba-Geigy Ag | Process for producing epoxy resin castings |
GB2148900A (en) * | 1983-08-19 | 1985-06-05 | Ici Plc | Curable compositions |
Also Published As
Publication number | Publication date |
---|---|
DE1096037B (de) | 1960-12-29 |
US2890195A (en) | 1959-06-09 |
BE566442A (US07642317-20100105-C00010.png) | |
FR1204495A (fr) | 1960-01-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB872306A (en) | Epoxide compositions and their production | |
US3397254A (en) | Carboxy terminated polyesters prepared from tribasic acid anhydrides and hydroxy terminated polyesters | |
US3201360A (en) | Curable mixtures comprising epoxide compositions and divalent tin salts | |
US3247163A (en) | Curable compositions of a polyepoxide and a reaction product of an amine and an acrylate | |
GB1402966A (en) | Copolyester compositions | |
US3218369A (en) | Blend of brominated polygylcidyl ether, a liquid epoxycyclohexane resin and a liquidaliphatic polyglycidyl ether | |
US2884406A (en) | Production of cured epoxide resins | |
US3784583A (en) | Latent organic phosphonium salt catalysts for curing glycidyl ether epoxy resins | |
GB852409A (en) | Improvements in and relating to curing epoxy resins | |
JPH01193317A (ja) | 熱硬化性液状組成物 | |
US3793247A (en) | Curable epoxide resin compositions containing boron-trichloride-tertiary amine complexes | |
US3403131A (en) | Epoxide resin-acid anhydride compositions containing a hydroxyalkylated aromatic amine accelerator | |
US3352810A (en) | Epoxy resin compositions | |
US3242104A (en) | Process for polymerizing 1, 2-epoxides and tetrahydropyrans | |
US2918444A (en) | Polyepoxide compositions | |
US2934521A (en) | Epoxide resin compositions | |
US3873493A (en) | Process for making reinforced thermosets from epoxy-functional copolymers and crosslinking agents | |
Weiss | Anhydride curing agents for epoxy resins | |
US3438911A (en) | Reduction of hydroxyl group content of epoxy resins | |
US3799900A (en) | Process for the preparation of modified glycidyl isocyanurate resins | |
US3247283A (en) | Curable compositions comprising dicyclopentadiene dioxide, diglycidyl ether of a polyhydric phenol, polycarboxylic acid anhydride and organic polyol and resins made therefrom | |
US2917493A (en) | Polyepoxide compositions | |
US3560411A (en) | Epoxyalkyl esters of endo-methylene hexahydrophthalic acid | |
US3351610A (en) | Curable compositions containing a 1, 2-epoxy compound and a ditertiary cycloaliphatic amine | |
US3496142A (en) | Epoxide resin compositions comprising a polycarboxylic acid anhydride hardener and a substituted amide accelerator |