GB1454345A - Process for the manufacture of polyethers containing ionic bonds - Google Patents
Process for the manufacture of polyethers containing ionic bondsInfo
- Publication number
- GB1454345A GB1454345A GB572974A GB572974A GB1454345A GB 1454345 A GB1454345 A GB 1454345A GB 572974 A GB572974 A GB 572974A GB 572974 A GB572974 A GB 572974A GB 1454345 A GB1454345 A GB 1454345A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- bisphenol
- reacting
- radical
- epoxide
- 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 abstract 4
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 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 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 6
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 4
- 229940106691 bisphenol a Drugs 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 150000002118 epoxides Chemical group 0.000 abstract 4
- 239000004215 Carbon black (E152) Substances 0.000 abstract 3
- 125000001246 bromo group Chemical group Br* 0.000 abstract 3
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 3
- 229930195733 hydrocarbon Natural products 0.000 abstract 3
- 125000002346 iodo group Chemical group I* 0.000 abstract 3
- 150000002989 phenols Chemical class 0.000 abstract 3
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 2
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 abstract 2
- -1 epoxide compound Chemical class 0.000 abstract 2
- 239000003822 epoxy resin Substances 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 150000002894 organic compounds Chemical class 0.000 abstract 2
- 229920000647 polyepoxide Polymers 0.000 abstract 2
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 2
- 150000005846 sugar alcohols Polymers 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 abstract 1
- CPEONABTMRSIKA-UHFFFAOYSA-N 1,4$l^{2}-oxazinane Chemical compound C1COCC[N]1 CPEONABTMRSIKA-UHFFFAOYSA-N 0.000 abstract 1
- SLHJJBZBHQIKBB-UHFFFAOYSA-N 2-(2-chloroethoxymethyl)oxirane Chemical compound ClCCOCC1CO1 SLHJJBZBHQIKBB-UHFFFAOYSA-N 0.000 abstract 1
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- 238000007259 addition reaction Methods 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000003957 anion exchange resin Substances 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 239000011324 bead Substances 0.000 abstract 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 abstract 1
- 150000001717 carbocyclic compounds Chemical class 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000000084 colloidal system Substances 0.000 abstract 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 abstract 1
- 150000001925 cycloalkenes Chemical class 0.000 abstract 1
- 238000006704 dehydrohalogenation reaction Methods 0.000 abstract 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 150000003022 phthalic acids Chemical class 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 230000001681 protective effect Effects 0.000 abstract 1
- 238000005956 quaternization reaction Methods 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 229930195734 saturated hydrocarbon Natural products 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 238000010557 suspension polymerization reaction Methods 0.000 abstract 1
- 229930195735 unsaturated hydrocarbon Natural products 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
- C08G59/62—Alcohols or phenols
- C08G59/621—Phenols
- C08G59/623—Aminophenols
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/54—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
-
- 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
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/48—Polymers modified by chemical after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Hydrology & Water Resources (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paper (AREA)
- Epoxy Compounds (AREA)
- Polyethers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH208673A CH584245A5 (enExample) | 1973-02-14 | 1973-02-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1454345A true GB1454345A (en) | 1976-11-03 |
Family
ID=4225565
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB572974A Expired GB1454345A (en) | 1973-02-14 | 1974-02-07 | Process for the manufacture of polyethers containing ionic bonds |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4000116A (enExample) |
| JP (1) | JPS5821646B2 (enExample) |
| CA (1) | CA1016691A (enExample) |
| CH (1) | CH584245A5 (enExample) |
| DE (1) | DE2406367C2 (enExample) |
| FR (1) | FR2217374B1 (enExample) |
| GB (1) | GB1454345A (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH642670A5 (de) * | 1979-12-21 | 1984-04-30 | Ciba Geigy Ag | Verfahren zur herstellung von vernetzten kunststoffen und ihre verwendung. |
| US4362853A (en) * | 1980-10-24 | 1982-12-07 | Ciba-Geigy Corporation | Resinous salts, their preparation, and their use in coatings |
| JPS57204206A (en) * | 1981-06-09 | 1982-12-14 | Kyoritsu Yuki Kogyo Kenkyusho:Kk | Cationic high molecular coagulant |
| US4507446A (en) * | 1982-03-23 | 1985-03-26 | Ciba-Geigy Corporation | Water-soluble or water-dispersible resinous sulphur or phosphorus containing salts, their preparation, and their use in coatings |
| US4775591A (en) * | 1987-06-01 | 1988-10-04 | General Electric Company | Ionomer compositions and method for their preparation |
| JPH04122775A (ja) * | 1990-09-14 | 1992-04-23 | Dai Ichi Kogyo Seiyaku Co Ltd | 樹脂の導電性改質方法 |
| JPH0940759A (ja) * | 1995-07-28 | 1997-02-10 | Asahi Denka Kogyo Kk | エポキシ樹脂硬化性組成物 |
| CN111423903A (zh) * | 2020-04-22 | 2020-07-17 | 金湖金凌新材料科技有限公司 | 一种新型的多支化阳离子聚醚反相破乳剂的制备方法以及多支化阳离子聚醚反相破乳剂 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3436373A (en) * | 1965-04-16 | 1969-04-01 | Union Carbide Corp | Phenol-formaldehyde-aliphatic amine condensation products |
| US3462382A (en) * | 1966-07-15 | 1969-08-19 | Koppers Co Inc | Tris - substituted resorcinol compound and the modification of rubber therewith |
| GB1208474A (en) * | 1968-04-29 | 1970-10-14 | Agfa Gevaert Nv | Electroconductive layers for use in electrographic and electrophotographic recording elements |
| US3790606A (en) * | 1970-09-30 | 1974-02-05 | Diamond Shamrock Corp | Alkoxylated mannich compositions and derivatives thereof |
-
1973
- 1973-02-14 CH CH208673A patent/CH584245A5/xx not_active IP Right Cessation
-
1974
- 1974-01-28 CA CA191,037A patent/CA1016691A/en not_active Expired
- 1974-02-07 GB GB572974A patent/GB1454345A/en not_active Expired
- 1974-02-07 US US05/440,633 patent/US4000116A/en not_active Expired - Lifetime
- 1974-02-11 DE DE2406367A patent/DE2406367C2/de not_active Expired
- 1974-02-13 FR FR7404866A patent/FR2217374B1/fr not_active Expired
- 1974-02-14 JP JP49018057A patent/JPS5821646B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US4000116A (en) | 1976-12-28 |
| JPS5821646B2 (ja) | 1983-05-02 |
| FR2217374A1 (enExample) | 1974-09-06 |
| CH584245A5 (enExample) | 1977-01-31 |
| DE2406367C2 (de) | 1984-05-10 |
| CA1016691A (en) | 1977-08-30 |
| DE2406367A1 (de) | 1974-08-29 |
| JPS49113898A (enExample) | 1974-10-30 |
| USB440633I5 (enExample) | 1976-02-10 |
| FR2217374B1 (enExample) | 1978-06-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4358578A (en) | Process for reacting a phenol with an epoxy compound | |
| US2965607A (en) | Ethers of epoxy-substituted phenols and their polymers | |
| US3843605A (en) | 3-(trihydrocarbylphosphoranylidene)-2,5-pyrrolidinediones as latent catalysts for promoting the reaction between phenols and epoxy resins | |
| US3632836A (en) | Solid curable polyepoxides modified with hydrolyzed liquid polyepoxides | |
| GB1492869A (en) | Process of reacting epoxides with phenols and/or carboxylic acids and epoxy resin composition | |
| US3385908A (en) | Flame retardant phenolic polyglycidyl ether resin compositions | |
| US4634757A (en) | Fusion product | |
| US4692504A (en) | Deactivation of phosphonium salt catalyst | |
| US2848426A (en) | Polyerpoxy polyethers, their preparation and polymers | |
| US4661644A (en) | Brominated epoxyaromatic compounds | |
| US3787508A (en) | Solid,curable polyepoxides modified with hydrolyzed liquid polyepoxides | |
| KR900004796A (ko) | 포스포늄 촉매를 함유하는 에폭시 수지 | |
| US4000116A (en) | Process for the manufacture of polyethers containing ionic bonds | |
| US3878132A (en) | Epoxy resins which are glycidyl ethers of glycerine | |
| US3092610A (en) | Polyepoxy ethers of polyhydric phenols and cured products obtained therefrom | |
| US3360486A (en) | Production of epoxide resins from aromatic amines in the presence of a hydroxyl group-containing promoter | |
| AU542371B2 (en) | Preparation of glycidyl polyethers of polyphenols | |
| US4689376A (en) | Heat-hardenable epoxide resin mixtures | |
| GB1045187A (en) | Bisphenolic lactones | |
| GB1002185A (en) | Improvements in and relating to epoxy resins | |
| GB1485345A (en) | Process for the manufacture of glycidyl ethers of monohydric or polyhydric phenols which have improved properties | |
| US3530096A (en) | Reduction of hydroxyl group content of epoxide resins | |
| GB1381011A (en) | Methylolglycidyl ethers of polyhydric phenol ethers a process for their manufacture and cursable mixtures containing them | |
| US3459828A (en) | Epoxy resins containing a polyglycidyl ether and the reaction product of an hydroxy terminated monoglycidyl ether with a diisocyanate | |
| US3351673A (en) | Process for preparing composite epoxide resins |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |