GB1002185A - Improvements in and relating to epoxy resins - Google Patents
Improvements in and relating to epoxy resinsInfo
- Publication number
- GB1002185A GB1002185A GB39584/61A GB3958461A GB1002185A GB 1002185 A GB1002185 A GB 1002185A GB 39584/61 A GB39584/61 A GB 39584/61A GB 3958461 A GB3958461 A GB 3958461A GB 1002185 A GB1002185 A GB 1002185A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- epoxy
- phosphoric acid
- ethylene oxide
- epoxypropane
- 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
- 229920000647 polyepoxide Polymers 0.000 title abstract 4
- 239000003822 epoxy resin Substances 0.000 title 1
- 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 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 10
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 229910052698 phosphorus Inorganic materials 0.000 abstract 3
- 239000011574 phosphorus Substances 0.000 abstract 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000008064 anhydrides 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
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 2
- 239000004848 polyfunctional curative Substances 0.000 abstract 2
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 abstract 1
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 1
- PRJNEUBECVAVAG-UHFFFAOYSA-N 1,3-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1 PRJNEUBECVAVAG-UHFFFAOYSA-N 0.000 abstract 1
- GELKGHVAFRCJNA-UHFFFAOYSA-N 2,2-Dimethyloxirane Chemical compound CC1(C)CO1 GELKGHVAFRCJNA-UHFFFAOYSA-N 0.000 abstract 1
- 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
- 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
- YGDRAHDIGNDNNT-UHFFFAOYSA-N 3,6-bis(ethenyl)-7-oxabicyclo[4.1.0]hepta-2,4-diene Chemical compound C1=CC(C=C)=CC2OC21C=C YGDRAHDIGNDNNT-UHFFFAOYSA-N 0.000 abstract 1
- SLJFKNONPLNAPF-UHFFFAOYSA-N 3-Vinyl-7-oxabicyclo[4.1.0]heptane Chemical compound C1C(C=C)CCC2OC21 SLJFKNONPLNAPF-UHFFFAOYSA-N 0.000 abstract 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 abstract 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- LMMDJMWIHPEQSJ-UHFFFAOYSA-N bis[(3-methyl-7-oxabicyclo[4.1.0]heptan-4-yl)methyl] hexanedioate Chemical compound C1C2OC2CC(C)C1COC(=O)CCCCC(=O)OCC1CC2OC2CC1C LMMDJMWIHPEQSJ-UHFFFAOYSA-N 0.000 abstract 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 1
- BQQUFAMSJAKLNB-UHFFFAOYSA-N dicyclopentadiene diepoxide Chemical compound C12C(C3OC33)CC3C2CC2C1O2 BQQUFAMSJAKLNB-UHFFFAOYSA-N 0.000 abstract 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
- 150000002118 epoxides Chemical class 0.000 abstract 1
- JDVIRCVIXCMTPU-UHFFFAOYSA-N ethanamine;trifluoroborane Chemical compound CCN.FB(F)F JDVIRCVIXCMTPU-UHFFFAOYSA-N 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- UCAOGXRUJFKQAP-UHFFFAOYSA-N n,n-dimethyl-5-nitropyridin-2-amine Chemical compound CN(C)C1=CC=C([N+]([O-])=O)C=N1 UCAOGXRUJFKQAP-UHFFFAOYSA-N 0.000 abstract 1
- 229920001228 polyisocyanate Polymers 0.000 abstract 1
- 239000005056 polyisocyanate Substances 0.000 abstract 1
- 229920005862 polyol Polymers 0.000 abstract 1
- 150000003077 polyols Chemical class 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids
- C07F9/1411—Esters of phosphorous acids with hydroxyalkyl compounds with further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- 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
- C08G59/18—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
- C08G59/4071—Curing agents not provided for by the groups C08G59/42 - C08G59/66 phosphorus containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Emergency Medicine (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68364A US3256240A (en) | 1960-11-10 | 1960-11-10 | Compositions comprising a polyepoxide, a chloro-hydroxy hydrocarbon phosphate and anepoxy resin curing agent |
| US7914760A | 1960-12-29 | 1960-12-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1002185A true GB1002185A (en) | 1965-08-25 |
Family
ID=26748893
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB39584/61A Expired GB1002185A (en) | 1960-11-10 | 1961-11-06 | Improvements in and relating to epoxy resins |
Country Status (6)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3981832A (en) * | 1971-02-11 | 1976-09-21 | Fokker-V.F.W. B.V. | Fire-protecting epoxy resins |
| NL7101806A (US20110009641A1-20110113-C00256.png) * | 1971-02-11 | 1972-08-15 | ||
| US4085247A (en) * | 1971-02-11 | 1978-04-18 | Fokker-Vfw B. V. | Fire-protecting epoxy resin reinforced with glass fiber |
| AU2004236479B2 (en) * | 2003-05-09 | 2010-12-23 | Prometheus Developments Limited | A method of producing polymeric material |
| WO2016149700A1 (en) | 2015-03-19 | 2016-09-22 | Zephyros, Inc. | Esterified acids for use in polymeric materials |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2732367A (en) * | 1956-01-24 | ruuivj | ||
| US2372244A (en) * | 1941-09-24 | 1945-03-27 | Standard Oil Co | Esters of acids of phosphorus |
| US2541027A (en) * | 1948-05-11 | 1951-02-13 | Shell Dev | Compositions of matter containing epoxy ethers and phosphorus-containing compounds |
| US2568784A (en) * | 1950-07-18 | 1951-09-25 | Victor Chemical Works | Reaction products of olefin oxides and p2o5 or p2s5 and the method of forming the same |
| US2634824A (en) * | 1951-01-22 | 1953-04-14 | Dow Chemical Co | Method for recovery of hydrogen cyanide |
| US2830069A (en) * | 1953-05-04 | 1958-04-08 | Exxon Research Engineering Co | Process of preparing phosphoric acid esters |
| US2849418A (en) * | 1953-11-10 | 1958-08-26 | Du Pont | Thermosetting epoxide polymer mixtures, method of making same and coatings containing same |
| US2938877A (en) * | 1954-01-08 | 1960-05-31 | Carlisle Chemical Works | Stabilized halogen-containing resins |
| GB757043A (en) * | 1954-02-10 | 1956-09-12 | Du Pont | Improvements in polymeric materials and methods of preparing them |
| US2917491A (en) * | 1956-06-01 | 1959-12-15 | Union Carbide Corp | Diepoxide polymers |
| US2909559A (en) * | 1958-02-03 | 1959-10-20 | Union Carbide Corp | Polymeric phosphate esters and their production |
| BE598179A (US20110009641A1-20110113-C00256.png) * | 1959-12-14 |
-
0
- NL NL271256D patent/NL271256A/xx unknown
- FR FR1310093D patent/FR1310093A/fr not_active Expired
- BE BE610068D patent/BE610068A/xx unknown
-
1960
- 1960-11-10 US US68364A patent/US3256240A/en not_active Expired - Lifetime
-
1961
- 1961-11-06 GB GB39584/61A patent/GB1002185A/en not_active Expired
- 1961-11-08 CH CH1292761A patent/CH419606A/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR1310093A (US20110009641A1-20110113-C00256.png) | 1963-03-04 |
| US3256240A (en) | 1966-06-14 |
| CH419606A (fr) | 1966-08-31 |
| NL271256A (US20110009641A1-20110113-C00256.png) | |
| BE610068A (US20110009641A1-20110113-C00256.png) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2951825A (en) | Glycidyl derivatives of amino phenols | |
| US3201360A (en) | Curable mixtures comprising epoxide compositions and divalent tin salts | |
| US3787451A (en) | Epoxides of alkoxy-substituted tri(hydroxyphenyl)alkanes | |
| ES407331A1 (es) | Metodo para preparar una composicion resinosa curable. | |
| GB947950A (en) | New dicarboxylic acid anhydrides and process for their preparation | |
| GB1422728A (en) | Copolyester compositions | |
| US3116301A (en) | Epoxyesters of 3, 4-dihydropyran-2-carboxylic acids | |
| GB818218A (en) | A process for the production of cured epoxide resins | |
| GB1123960A (en) | Organosilicon epoxides | |
| US2848426A (en) | Polyerpoxy polyethers, their preparation and polymers | |
| GB855205A (en) | Improvements in curing of polyepoxides | |
| ES447709A1 (es) | Un metodo para la preparacion de una composicion resinosa. | |
| GB1002185A (en) | Improvements in and relating to epoxy resins | |
| GB1005241A (en) | Thio-derivatives of polyacid anhydrides and resinous compositions derived therefrom | |
| GB1487609A (en) | Phosphono-spiro-bisphenols a process for their manufacture and their use | |
| GB1108543A (en) | Latently curable resin compositions and novolak compounds for use as curing agents in these compositions | |
| GB904549A (en) | Preparation of epoxy ethers and formation of cured resinous products therefrom | |
| GB991910A (en) | Improvements in and relating to epoxide compositions | |
| US3284383A (en) | Epoxide compositions | |
| US3264230A (en) | Epoxide compositions containing tin curing catalysts | |
| US3247283A (en) | Curable compositions comprising dicyclopentadiene dioxide, diglycidyl ether of a polyhydric phenol, polycarboxylic acid anhydride and organic polyol and resins made therefrom | |
| US4689376A (en) | Heat-hardenable epoxide resin mixtures | |
| US3714198A (en) | Polyglycidyl esters | |
| US3220981A (en) | Ethylenically unsaturated epoxy sulfones | |
| US3328318A (en) | Epoxide compositions |