GB834158A - Improvements in or relating to polyether polymers - Google Patents
Improvements in or relating to polyether polymersInfo
- Publication number
- GB834158A GB834158A GB6808/58A GB680858A GB834158A GB 834158 A GB834158 A GB 834158A GB 6808/58 A GB6808/58 A GB 6808/58A GB 680858 A GB680858 A GB 680858A GB 834158 A GB834158 A GB 834158A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- oxetane
- tetrahydrofuran
- radicals
- ethyl
- 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
- 229920000570 polyether Polymers 0.000 title 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 20
- -1 7-octenyl Chemical group 0.000 abstract 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 10
- 229920000642 polymer Polymers 0.000 abstract 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 6
- 239000003054 catalyst Substances 0.000 abstract 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 5
- 239000000203 mixture Substances 0.000 abstract 5
- VFYHHERJNPKXIX-UHFFFAOYSA-N 3,3-diethyloxetane Chemical compound CCC1(CC)COC1 VFYHHERJNPKXIX-UHFFFAOYSA-N 0.000 abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- 150000004820 halides Chemical class 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 238000002360 preparation method Methods 0.000 abstract 4
- CXURGFRDGROIKG-UHFFFAOYSA-N 3,3-bis(chloromethyl)oxetane Chemical compound ClCC1(CCl)COC1 CXURGFRDGROIKG-UHFFFAOYSA-N 0.000 abstract 3
- QOZLLNFAKXRSQL-UHFFFAOYSA-N 3-ethyl-3-(prop-2-enoxymethyl)oxetane Chemical compound C=CCOCC1(CC)COC1 QOZLLNFAKXRSQL-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 3
- 150000001298 alcohols Chemical class 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000002170 ethers Chemical class 0.000 abstract 3
- 229930195733 hydrocarbon Natural products 0.000 abstract 3
- 150000002430 hydrocarbons Chemical class 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- LSWYGACWGAICNM-UHFFFAOYSA-N 2-(prop-2-enoxymethyl)oxirane Chemical compound C=CCOCC1CO1 LSWYGACWGAICNM-UHFFFAOYSA-N 0.000 abstract 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 2
- KMNZBDMJZWVIOY-UHFFFAOYSA-N 3-methyl-3-(4-methylpent-4-enoxymethyl)oxetane Chemical compound CC(CCCOCC1(COC1)C)=C KMNZBDMJZWVIOY-UHFFFAOYSA-N 0.000 abstract 2
- DQISWQYRBSAAFP-UHFFFAOYSA-N 3-methyl-3-(pent-4-enoxymethyl)oxetane Chemical compound CC1(COC1)COCCCC=C DQISWQYRBSAAFP-UHFFFAOYSA-N 0.000 abstract 2
- CDGGFIMPNCEPBA-UHFFFAOYSA-N 3-methyl-3-(prop-2-enoxymethyl)oxetane Chemical compound C=CCOCC1(C)COC1 CDGGFIMPNCEPBA-UHFFFAOYSA-N 0.000 abstract 2
- 125000006042 4-hexenyl group Chemical group 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 2
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 239000005864 Sulphur Substances 0.000 abstract 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 150000004292 cyclic ethers Chemical class 0.000 abstract 2
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000005394 methallyl group Chemical group 0.000 abstract 2
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical class C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 abstract 2
- 229920001281 polyalkylene Polymers 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-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
- CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 abstract 1
- KVTHPKXDLVYNCH-UHFFFAOYSA-N 2-iodoethylbenzene Chemical compound ICCC1=CC=CC=C1 KVTHPKXDLVYNCH-UHFFFAOYSA-N 0.000 abstract 1
- NTMUDPWGPGZGQW-UHFFFAOYSA-N 2-oxaspiro[3.4]octane Chemical compound C1OCC11CCCC1 NTMUDPWGPGZGQW-UHFFFAOYSA-N 0.000 abstract 1
- PNLURCRXZLVRJR-UHFFFAOYSA-N 2-oxaspiro[3.5]nonane Chemical compound C1OCC11CCCCC1 PNLURCRXZLVRJR-UHFFFAOYSA-N 0.000 abstract 1
- 229910021630 Antimony pentafluoride Inorganic materials 0.000 abstract 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract 1
- 239000004150 EU approved colour Substances 0.000 abstract 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 abstract 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- BIZNEDGOZPNEPL-UHFFFAOYSA-N [3-(chloromethyl)oxetan-3-yl]methanol Chemical compound OCC1(CCl)COC1 BIZNEDGOZPNEPL-UHFFFAOYSA-N 0.000 abstract 1
- 125000002015 acyclic group Chemical group 0.000 abstract 1
- 230000001476 alcoholic effect Effects 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 abstract 1
- 125000005336 allyloxy group Chemical group 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 229910052787 antimony Inorganic materials 0.000 abstract 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 1
- VBVBHWZYQGJZLR-UHFFFAOYSA-I antimony pentafluoride Chemical compound F[Sb](F)(F)(F)F VBVBHWZYQGJZLR-UHFFFAOYSA-I 0.000 abstract 1
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 abstract 1
- 229910052796 boron Inorganic materials 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 1
- 235000010216 calcium carbonate Nutrition 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 abstract 1
- 239000011951 cationic catalyst Substances 0.000 abstract 1
- 238000010538 cationic polymerization reaction Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 238000004132 cross linking Methods 0.000 abstract 1
- 150000005676 cyclic carbonates Chemical class 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 150000002440 hydroxy compounds Chemical class 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical class [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 abstract 1
- 239000001095 magnesium carbonate Substances 0.000 abstract 1
- 235000011160 magnesium carbonates Nutrition 0.000 abstract 1
- 235000012245 magnesium oxide Nutrition 0.000 abstract 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical class [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 abstract 1
- 150000002924 oxiranes Chemical class 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- OBCUTHMOOONNBS-UHFFFAOYSA-N phosphorus pentafluoride Chemical group FP(F)(F)(F)F OBCUTHMOOONNBS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004014 plasticizer Substances 0.000 abstract 1
- 239000002685 polymerization catalyst Substances 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- 235000012222 talc Nutrition 0.000 abstract 1
- 229910052718 tin Inorganic materials 0.000 abstract 1
- 239000004408 titanium dioxide Substances 0.000 abstract 1
- 235000010215 titanium dioxide Nutrition 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 235000014692 zinc oxide Nutrition 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/16—Cyclic ethers having four or more ring atoms
- C08G65/20—Tetrahydrofuran
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US64471657A | 1957-03-08 | 1957-03-08 | |
| US713538A US3287330A (en) | 1958-02-06 | 1958-02-06 | Polyether polymers having unsaturated side chains |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB834158A true GB834158A (en) | 1960-05-04 |
Family
ID=27094540
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB6808/58A Expired GB834158A (en) | 1957-03-08 | 1958-03-03 | Improvements in or relating to polyether polymers |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE1420683B1 (enrdf_load_html_response) |
| FR (1) | FR1202252A (enrdf_load_html_response) |
| GB (1) | GB834158A (enrdf_load_html_response) |
| NL (2) | NL225631A (enrdf_load_html_response) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3354133A (en) * | 1964-09-18 | 1967-11-21 | Phillips Petroleum Co | Vulcanizable copolymers of tetrahydrofuran with unsaturated epoxy compouns prepared i the presence of organoantimony hexachloride |
| US3361724A (en) * | 1963-06-04 | 1968-01-02 | Courtaulds Ltd | Polyether elastomer containing sulfur crosslinks and the method for its production |
| US3362941A (en) * | 1964-09-28 | 1968-01-09 | Olin Mathieson | Copolymers of tetrahydrofuran and oxetane compounds |
| US3417064A (en) * | 1963-05-27 | 1968-12-17 | Union Carbide Corp | Polymers of 1,2-alkylene oxides |
| US3442875A (en) * | 1966-01-19 | 1969-05-06 | Exxon Research Engineering Co | Monoepoxide polymers |
| WO1995019383A1 (en) * | 1994-01-18 | 1995-07-20 | Eastman Chemical Company | Polyether glycols and alcohols derived from 3,4-epoxy-1-butene |
| WO2003059989A1 (en) * | 2002-01-10 | 2003-07-24 | Invista Technologies S.À.R.L. | Copolymers of tetrahydrofuran, ethylene oxide and an additional cyclic ether |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3133905A (en) * | 1960-05-23 | 1964-05-19 | Goodyear Tire & Rubber | Polyhydroxyl terminated polyethers |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1027400B (de) * | 1956-11-02 | 1958-04-03 | Bayer Ag | Verfahren zur Herstellung von ungesaettigten Mischpolymerisaten des Tetrahydrofurans |
-
0
- NL NL110981D patent/NL110981C/xx active
- NL NL225631D patent/NL225631A/xx unknown
-
1958
- 1958-03-03 GB GB6808/58A patent/GB834158A/en not_active Expired
- 1958-03-07 FR FR1202252D patent/FR1202252A/fr not_active Expired
- 1958-03-08 DE DE19581420683D patent/DE1420683B1/de active Pending
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3417064A (en) * | 1963-05-27 | 1968-12-17 | Union Carbide Corp | Polymers of 1,2-alkylene oxides |
| US3361724A (en) * | 1963-06-04 | 1968-01-02 | Courtaulds Ltd | Polyether elastomer containing sulfur crosslinks and the method for its production |
| US3354133A (en) * | 1964-09-18 | 1967-11-21 | Phillips Petroleum Co | Vulcanizable copolymers of tetrahydrofuran with unsaturated epoxy compouns prepared i the presence of organoantimony hexachloride |
| US3362941A (en) * | 1964-09-28 | 1968-01-09 | Olin Mathieson | Copolymers of tetrahydrofuran and oxetane compounds |
| US3442875A (en) * | 1966-01-19 | 1969-05-06 | Exxon Research Engineering Co | Monoepoxide polymers |
| WO1995019383A1 (en) * | 1994-01-18 | 1995-07-20 | Eastman Chemical Company | Polyether glycols and alcohols derived from 3,4-epoxy-1-butene |
| CN1056628C (zh) * | 1994-01-18 | 2000-09-20 | 伊斯特曼化学公司 | 从3,4-环氧-1-丁烯衍生的聚醚二元醇和醇 |
| WO2003059989A1 (en) * | 2002-01-10 | 2003-07-24 | Invista Technologies S.À.R.L. | Copolymers of tetrahydrofuran, ethylene oxide and an additional cyclic ether |
| US6989432B2 (en) | 2002-01-10 | 2006-01-24 | Invista North America S.A.R.L. | Copolymers of tetrahydrofuran, ethylene oxide and an additional cyclic ether |
| CN1293120C (zh) * | 2002-01-10 | 2007-01-03 | 因维斯塔技术有限公司 | 四氢呋喃、环氧乙烷和其他环醚的共聚物 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1420683B1 (de) | 1971-01-07 |
| NL110981C (enrdf_load_html_response) | |
| FR1202252A (fr) | 1960-01-08 |
| NL225631A (enrdf_load_html_response) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11440995B2 (en) | Method for preparing aliphatic polythioether | |
| US3158581A (en) | Polymeric epoxides | |
| US3645917A (en) | Polyethers containing azidomethyl side chains | |
| Tanaka et al. | Curing reactions | |
| GB834158A (en) | Improvements in or relating to polyether polymers | |
| RU2015102570A (ru) | Полибутадиен с эпоксигруппами | |
| US4833183A (en) | Poly [3-(substituted)-3(hydroxymethyl)oxetane] and method of preparing same | |
| US3158591A (en) | Copolymers of epihalohydrins and ethylenically unsaturated epoxides | |
| KR20160006198A (ko) | 경화성 에폭시 수지 조성물 및 그의 경화물, 디올레핀 화합물 및 그의 제조 방법, 및 디에폭시 화합물의 제조 방법 | |
| US3388079A (en) | High molecular weight polyethers containing silane groupings | |
| US3506597A (en) | Polymerization of olefin oxides | |
| JP5213547B2 (ja) | エポキシ基含有エステル化合物を含む硬化性組成物、該組成物の製造方法およびエポキシ基含有エステル化合物 | |
| Nishikubo et al. | Synthesis of polyester by novel addition reaction of active di‐ester with di‐epoxy compound | |
| JPH024613B2 (enrdf_load_html_response) | ||
| JPH0725877B2 (ja) | エポキシ樹脂 | |
| US3205207A (en) | Sulfur vulcanizable oxetane and oxetane-oxirane copolymers | |
| US3313740A (en) | Expoxide polymerization catalysts, their preparation and their use | |
| JPH02621A (ja) | ２，２−ビス−〔３−（アリルもしくはプロペニル）−４−ヒドロキシフエニル〕化合物のグリシジルエーテルおよびそれから得られる樹脂 | |
| US3287330A (en) | Polyether polymers having unsaturated side chains | |
| JP3858471B2 (ja) | オキセタニル基を有する高分子量重合体の製造方法 | |
| JP2000169552A (ja) | カチオン硬化性樹脂組成物 | |
| US3442876A (en) | Novel rubbery polyoxyalkylene copolymers | |
| US3476718A (en) | Polymers of epoxy cyclic sulfones | |
| US3794687A (en) | Substituted bis(fluoroalkylsulfonyl)halomethanes | |
| US2883395A (en) | Epoxy-substituted organosilicon compounds and method for preparing the same |