GB953206A - Preparation of self-extinguishing epoxide resin polymers - Google Patents
Preparation of self-extinguishing epoxide resin polymersInfo
- Publication number
- GB953206A GB953206A GB2304059A GB2304059A GB953206A GB 953206 A GB953206 A GB 953206A GB 2304059 A GB2304059 A GB 2304059A GB 2304059 A GB2304059 A GB 2304059A GB 953206 A GB953206 A GB 953206A
- Authority
- GB
- United Kingdom
- Prior art keywords
- antimony
- added
- resin
- ether
- bromine
- 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
- 239000003822 epoxy resin Substances 0.000 title abstract 6
- 229920000647 polyepoxide Polymers 0.000 title abstract 6
- 229920000642 polymer Polymers 0.000 title 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 9
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 6
- 229910052794 bromium Inorganic materials 0.000 abstract 5
- 229920005989 resin Polymers 0.000 abstract 5
- 239000011347 resin Substances 0.000 abstract 5
- YKUYKENINQNULY-UHFFFAOYSA-N 2-[(4-bromophenoxy)methyl]oxirane Chemical compound C1=CC(Br)=CC=C1OCC1OC1 YKUYKENINQNULY-UHFFFAOYSA-N 0.000 abstract 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 4
- 229910052787 antimony Inorganic materials 0.000 abstract 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 4
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 abstract 3
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- -1 hydroxy acid ester Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- 229910000410 antimony oxide Inorganic materials 0.000 abstract 2
- 125000003700 epoxy group Chemical group 0.000 abstract 2
- 239000004744 fabric Substances 0.000 abstract 2
- 239000011521 glass Substances 0.000 abstract 2
- 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 abstract 2
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 abstract 2
- YGBFTDQFAKDXBZ-UHFFFAOYSA-N tributyl stiborite Chemical compound [Sb+3].CCCC[O-].CCCC[O-].CCCC[O-] YGBFTDQFAKDXBZ-UHFFFAOYSA-N 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- VADKRMSMGWJZCF-UHFFFAOYSA-N 2-bromophenol Chemical compound OC1=CC=CC=C1Br VADKRMSMGWJZCF-UHFFFAOYSA-N 0.000 abstract 1
- RQRREPLGINXKFY-UHFFFAOYSA-N BrC1(C(C(C2=CC=CC=C2)OC(C2(C(O2)(Br)Br)Br)C2=CC=CC=C2)(O1)Br)Br Chemical class BrC1(C(C(C2=CC=CC=C2)OC(C2(C(O2)(Br)Br)Br)C2=CC=CC=C2)(O1)Br)Br RQRREPLGINXKFY-UHFFFAOYSA-N 0.000 abstract 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 abstract 1
- VZOTVEFYVWBGDG-UHFFFAOYSA-N C(=O)(OCCCC)C(O)C(O)C(=O)OCCCC.[Sb] Chemical compound C(=O)(OCCCC)C(O)C(O)C(=O)OCCCC.[Sb] VZOTVEFYVWBGDG-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 abstract 1
- 150000001463 antimony compounds Chemical class 0.000 abstract 1
- 239000007900 aqueous suspension Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 230000031709 bromination Effects 0.000 abstract 1
- 238000005893 bromination reaction Methods 0.000 abstract 1
- 150000001649 bromium compounds Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 1
- WBTCZEPSIIFINA-MSFWTACDSA-J dipotassium;antimony(3+);(2r,3r)-2,3-dioxidobutanedioate;trihydrate Chemical compound O.O.O.[K+].[K+].[Sb+3].[Sb+3].[O-]C(=O)[C@H]([O-])[C@@H]([O-])C([O-])=O.[O-]C(=O)[C@H]([O-])[C@@H]([O-])C([O-])=O WBTCZEPSIIFINA-MSFWTACDSA-J 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 150000002894 organic compounds Chemical class 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229960005235 piperonyl butoxide Drugs 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 230000008929 regeneration Effects 0.000 abstract 1
- 238000011069 regeneration method Methods 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium 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
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
- C08G59/145—Compounds containing one epoxy group
-
- 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
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1405—Polycondensates modified by chemical after-treatment with inorganic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Epoxy Resins (AREA)
- Reinforced Plastic Materials (AREA)
- Laminated Bodies (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL253369D NL253369A (en:Method) | 1959-07-04 | ||
BE592576D BE592576A (en:Method) | 1959-07-04 | ||
GB2304059A GB953206A (en) | 1959-07-04 | 1959-07-04 | Preparation of self-extinguishing epoxide resin polymers |
FR831673A FR1262180A (fr) | 1959-07-04 | 1960-06-30 | Préparation de polymères résineux époxydés à auto-extinction |
CH751960A CH466566A (de) | 1959-07-04 | 1960-07-01 | Verfahren zur Herstellung eines selbsterlöschenden, aromatisch gebundenes Brom enthaltenden, gehärteten Epoxyharz-Formkörpers |
DE19601520708 DE1520708A1 (de) | 1959-07-04 | 1960-07-02 | Herstellen von Formteilen aus Formmassen,die halogenhaltige Epoxyharze enthalten |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2304059A GB953206A (en) | 1959-07-04 | 1959-07-04 | Preparation of self-extinguishing epoxide resin polymers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB953206A true GB953206A (en) | 1964-03-25 |
Family
ID=10189130
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2304059A Expired GB953206A (en) | 1959-07-04 | 1959-07-04 | Preparation of self-extinguishing epoxide resin polymers |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE592576A (en:Method) |
CH (1) | CH466566A (en:Method) |
DE (1) | DE1520708A1 (en:Method) |
GB (1) | GB953206A (en:Method) |
NL (1) | NL253369A (en:Method) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2249523A (en) * | 1991-04-10 | 1992-05-13 | Jactone Products Ltd | Fire barrier material |
-
0
- BE BE592576D patent/BE592576A/xx unknown
- NL NL253369D patent/NL253369A/xx unknown
-
1959
- 1959-07-04 GB GB2304059A patent/GB953206A/en not_active Expired
-
1960
- 1960-07-01 CH CH751960A patent/CH466566A/de unknown
- 1960-07-02 DE DE19601520708 patent/DE1520708A1/de active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2249523A (en) * | 1991-04-10 | 1992-05-13 | Jactone Products Ltd | Fire barrier material |
GB2249523B (en) * | 1991-04-10 | 1995-01-11 | Jactone Products Ltd | Fire barrier material |
Also Published As
Publication number | Publication date |
---|---|
BE592576A (en:Method) | |
NL253369A (en:Method) | |
CH466566A (de) | 1968-12-15 |
DE1520708A1 (de) | 1969-08-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB781416A (en) | Process for curing polyepoxides | |
GB788350A (en) | Improvements in or relating to a process for the production of glycidyl ethers of polyhydric phenols | |
GB855205A (en) | Improvements in curing of polyepoxides | |
EP0303901A2 (en) | Method for reducing the aliphatic halide content of epoxy resins | |
GB953206A (en) | Preparation of self-extinguishing epoxide resin polymers | |
GB1527154A (en) | Unsaturated epoxides as coupling agents for carbon fibres and unsaturated matrix resins | |
GB986204A (en) | Epoxy compounds and flame-retardant resins therefrom | |
GB1328853A (en) | Process for preparation of epoxy resin adhesive composition | |
GB880423A (en) | Improvements in or relating to a process for preparing glycidyl polyethers of polyhydric phenols | |
GB1153688A (en) | Curing Epoxy Resins and the resulting cured Resins; and Curable Epoxy Resin Compositions and their use | |
GB791303A (en) | Process for preparing compositions containing glycidyl ethers | |
GB913794A (en) | Improvements in epoxy resins | |
US3309384A (en) | Preparation of low viscosity epoxide resins | |
GB928009A (en) | Process for the preparation of halogenated glycidyl ethers | |
US3251861A (en) | Di- and triepoxtoe derivatives of trivinylcyclohexane | |
US3404126A (en) | Process of preparing color improved glycidyl polyethers of polyhydric phenols | |
GB1108390A (en) | Process for preparing hardened epoxy resins | |
GB952357A (en) | Process for the purification of epoxy resins | |
GB1122146A (en) | Process for preparing hardened epoxy resins | |
US3288761A (en) | Curable mistures of diepoxy compounds and dicarboxylic acid anhydrides | |
CA2035957A1 (en) | Process for reducing the undesirable halide content of epoxy resins | |
GB1389937A (en) | Process for the production of cured moulded articles made from epoxy resins | |
US3790602A (en) | Accelerated process for diaryl sulfone glycidyl ethers | |
GB788887A (en) | Improvements in or relating to the production of glycidyl ethers of polyhydric phenols | |
US3591554A (en) | Curable polyepoxides produced by metal hydride or alkoxide catalyst |