ES2080300T3 - Copolimeros de monoepoxido de butadieno/anhidrido maleico. - Google Patents
Copolimeros de monoepoxido de butadieno/anhidrido maleico.Info
- Publication number
- ES2080300T3 ES2080300T3 ES91905731T ES91905731T ES2080300T3 ES 2080300 T3 ES2080300 T3 ES 2080300T3 ES 91905731 T ES91905731 T ES 91905731T ES 91905731 T ES91905731 T ES 91905731T ES 2080300 T3 ES2080300 T3 ES 2080300T3
- Authority
- ES
- Spain
- Prior art keywords
- epb
- dioxolane
- reaction
- solvent
- maleic anhydride
- 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 - Lifetime
Links
- GXBYFVGCMPJVJX-UHFFFAOYSA-N Epoxybutene Chemical compound C=CC1CO1 GXBYFVGCMPJVJX-UHFFFAOYSA-N 0.000 title abstract 2
- 229920001577 copolymer Polymers 0.000 title abstract 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 abstract 4
- 239000007810 chemical reaction solvent Substances 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- 239000000539 dimer Substances 0.000 abstract 2
- 238000011065 in-situ storage Methods 0.000 abstract 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000007334 copolymerization reaction Methods 0.000 abstract 1
- 150000008282 halocarbons Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 125000000468 ketone group Chemical group 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 229920013730 reactive polymer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/04—Anhydrides, e.g. cyclic anhydrides
- C08F222/06—Maleic anhydride
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyethers (AREA)
- Epoxy Resins (AREA)
Abstract
LOS COPOLIMEROS SE PRODUCEN CUANDO SE COPOLIMERIZA 3,4-EPOXI-1BUTENO (EPB) CON ANHIDRIDO MALEICO. LA COPOLIMERIZACION LA INICIAL RADICALES LIBRES Y CONSISTE EN LA 1,2-PROPAGACION Y LA 1,5-PROPAGACION DEL EPB. CUANDO SE UTILIZA UN ETER COMO EL SOLVENTE DE REACCION, EL PRODUCTO ES SOLUBLE Y SE COMPONE ESENCIALMENTE DE (A) UN MONOMERO DERIVADO DEL ANHIDRIDO MALEICO Y (B) DOS MONOMEROS DERIVADOS DEL EPB. CUANDO EL SOLVENTE DE REACCION ES UNA CETONA, EL PRODUCTO DE POLIMERO TAMBIEN ES SOLUBLE Y CONTIENE ADICIONALMENTE (C) UNA UNIDAD DERIVADA DE UN DIOXOLANO FORMADO IN SITU. CUANDO LA REACCION SE LLEVA A CABO ANTE LA PRESENCIA DE UN SOLVENTE NO POLAR (EJ. UN HIDROCARBURO O UN HALOCARBURO), O PURO (EJ. EN AUSENCIA DE UN SOLVENTE), EL PRODUCTO DE POLIMERO ES INDISOLUBLE EN SOLVENTES ORGANICOS COMUNES Y CONTIENE (D) UN DIMERO DE EPB SIMETRICO. EL DIMERO NO SE FORMA APARENTEMENTE, O SE FORMA SOLO HASTA UN PUNTO MUY LIMITADO, CUANDO SE LLEVA A CABO LA POLIMERIZACION EN SOLVENTES DE REACCION POLARES. LOS PRODUCTOS DE POLIMERO CON UNA UNIDAD DE DIOXOLANO SE PUEDE PREPARA UTILIZANDO EL DIOXOLANO PREVIAMENTE FORMADO EN LA MEZCLA DE POLIMERIZACION. ASI, ESTA INVENCION NO QUEDA LIMITADA A LA PREPARACION IN SITU DEL DIOXOLANO A PARTIR DE UNA MEZCLA DE REACCION QUE CONTENGA CETONA. LOS PRODUCTOS DE ESTA INVENCION SE PUEDEN MOLDEAR A MODO DE PELICULAS CLARAS Y SE PUEDEN UTILIZAR TAMBIEN COMO POLIMEROS REACTIVOS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/498,183 US5013806A (en) | 1990-03-23 | 1990-03-23 | Butadiene monoepoxide/maleic anhydride copolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2080300T3 true ES2080300T3 (es) | 1996-02-01 |
Family
ID=23979929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES91905731T Expired - Lifetime ES2080300T3 (es) | 1990-03-23 | 1991-03-14 | Copolimeros de monoepoxido de butadieno/anhidrido maleico. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5013806A (es) |
| EP (1) | EP0524198B1 (es) |
| JP (1) | JP3155274B2 (es) |
| AT (1) | ATE131180T1 (es) |
| CA (1) | CA2078552C (es) |
| DE (1) | DE69115266T2 (es) |
| DK (1) | DK0524198T3 (es) |
| ES (1) | ES2080300T3 (es) |
| GR (1) | GR3018461T3 (es) |
| WO (1) | WO1991014720A1 (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5304611A (en) * | 1992-12-30 | 1994-04-19 | Eastman Kodak Company | Copolymers of vinyl dioxolanes and imidized derivatives of maleic anhydride |
| US5302680A (en) * | 1992-12-30 | 1994-04-12 | Eastman Kodak Company | Copolymers of epoxybutadiene and maleimides |
| US5310839A (en) * | 1992-12-30 | 1994-05-10 | Eastman Chemical Company | Copolymers of vinyl dioxolanes and maleimides |
| WO1994015975A1 (en) * | 1992-12-30 | 1994-07-21 | Eastman Chemical Company | Copolymers of epoxybutadiene and imidized derivatives of maleic anhydride |
| WO1995019382A1 (en) * | 1994-01-18 | 1995-07-20 | Eastman Chemical Company | Polyether polymers derived from 3,4-epoxy-1-butene |
| US6107425A (en) * | 1998-02-06 | 2000-08-22 | Shipley Company, L.L.C. | Narrow molecular weight distribution polymers and use of same as resin binders for negative-acting photoresists |
| US6146495A (en) | 1998-08-31 | 2000-11-14 | Nalco Chemical Company | Kraft process for the production of wood pulp by adding a copolymer of 1,2-dihydroxy-3-butene antiscalant |
| US20090112888A1 (en) * | 2007-10-25 | 2009-04-30 | Rand Warsaw | Method of providing database access to non-programmers |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2540072A (en) * | 1948-08-19 | 1951-01-30 | Hercules Powder Co Ltd | Preparation of copolymer of chloromaleic anhydride and butadiene |
| US2582708A (en) * | 1948-10-01 | 1952-01-15 | Standard Oil Dev Co | Lubricating oil additives |
| US2570601A (en) * | 1950-11-13 | 1951-10-09 | Universal Oil Prod Co | Production of resins from butadiene monoxide and from mixtures of butadiene monoxide and vinyl compounds |
| US3230207A (en) * | 1961-03-01 | 1966-01-18 | Nippon Carbide Kogyo Kk | Process for polymerizing olefin oxides with a catalyst consisting of a zinc alkyl and an oxide or hydroxide of a group iia metal |
| DE1173658B (de) * | 1962-05-11 | 1964-07-09 | Huels Chemische Werke Ag | Verfahren zur Herstellung von fluessigen Epoxypolydiolefinen |
| US3398126A (en) * | 1965-03-24 | 1968-08-20 | Allied Chem | Propylene oxide-butadiene monoxide copolymers cross-linked with maleic anhydride |
| US3530103A (en) * | 1965-06-03 | 1970-09-22 | Stauffer Chemical Co | Copolymers of carbon bisulfide and certain monoolefinic monomers |
| US3851015A (en) * | 1972-02-17 | 1974-11-26 | Aquitaine Petrole | Method for copolymerizing monomers of different types |
| USRE29028E (en) * | 1973-06-26 | 1976-11-02 | Hoechst Aktiengesellschaft | Heat-curable pulverulent coating agent consisting of a mixture of copolymers containing glycidyl groups, dicarboxylic acid anhydrides and curing anhydrides |
| US3944533A (en) * | 1973-08-25 | 1976-03-16 | Bayer Aktiengesellschaft | Polyalkenamers of wide molecular-weight distribution |
| US3998126A (en) | 1974-09-03 | 1976-12-21 | Ross Rudd | Delayed bolt action for firearm |
| DE3712265A1 (de) * | 1987-04-10 | 1988-10-20 | Giulini Chemie | Verfahren zur herstellung von copolymerisaten mit hohem polymerisationsgrad |
-
1990
- 1990-03-23 US US07/498,183 patent/US5013806A/en not_active Expired - Fee Related
-
1991
- 1991-03-14 WO PCT/US1991/001589 patent/WO1991014720A1/en not_active Ceased
- 1991-03-14 EP EP91905731A patent/EP0524198B1/en not_active Expired - Lifetime
- 1991-03-14 AT AT91905731T patent/ATE131180T1/de not_active IP Right Cessation
- 1991-03-14 JP JP50619491A patent/JP3155274B2/ja not_active Expired - Fee Related
- 1991-03-14 CA CA002078552A patent/CA2078552C/en not_active Expired - Fee Related
- 1991-03-14 DK DK91905731.5T patent/DK0524198T3/da active
- 1991-03-14 ES ES91905731T patent/ES2080300T3/es not_active Expired - Lifetime
- 1991-03-14 DE DE69115266T patent/DE69115266T2/de not_active Expired - Fee Related
-
1995
- 1995-12-19 GR GR950403594T patent/GR3018461T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO1991014720A1 (en) | 1991-10-03 |
| EP0524198B1 (en) | 1995-12-06 |
| DK0524198T3 (da) | 1996-01-08 |
| EP0524198A1 (en) | 1993-01-27 |
| ATE131180T1 (de) | 1995-12-15 |
| DE69115266T2 (de) | 1996-05-02 |
| JP3155274B2 (ja) | 2001-04-09 |
| US5013806A (en) | 1991-05-07 |
| GR3018461T3 (en) | 1996-03-31 |
| DE69115266D1 (en) | 1996-01-18 |
| JPH06504798A (ja) | 1994-06-02 |
| CA2078552C (en) | 1997-07-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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